SESSION: OxidativeMonPM1-R1 |
Abe International Symposium (4th Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings) |
Mon. 21 Oct. 2024 / Room: Marika A | |
Session Chairs: Shigeru Hirano; Yoshiaki Harakawa; Student Monitors: TBA |
Neuroprotection is essential for therapy not only in acute stage of stroke, but also in chronic progressive neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS), Parkinson’s disease (PD), and Alzheimer’s disease (AD). Free radical scavenger can be such a neuroprotective reagent with inhibiting death signals and potentiating survival signals under cerebral pathological conditions. Edaravone, a free radical scavenger, is the first clinical drug for neuroprotection in the world which has been used from 2001 in most ischemic stroke patients in Japan and other countries. Edaravone scavenges hydroxyl radicals both in hydrophilic and hydrophobic conditions, and showed beneficial clinical effects both on acute ischemic stroke and ALS.
Regenerative therapy with stem cells is another important challenge to cure neurological diseases. Bone marrow stromal cells and fatty-tissue derived stem cells have been used for ischemic stroke and neurodegenerative diseases. Because a cell therapy with MUSE cell was successful for ALS model mice, we conducted a human study for ALS patients with MUSE cell from 2021 April (Phase 1+2), having a good result. Tentative results will be presented.
Acne vulgaris is one of the most common skin diseases with varying etiologies. Acne vulgaris is most often seen on the face and back, and especially acne on the face is associated with a change in appearance, which may lead to psychogenic stress. Treatment includes cosmetic treatments such as chemical peels and phototherapy, but generally they are treated with topical medications, vitamins, or antibiotics for a certain period of time. Acne, including rough skin, is caused by oxidative stress due to fatigue, irregular lifestyle, and ultraviolet rays, which leads to the deterioration of the skin barrier function. SOD activity and malondialdehyde (MDA) concentrations in tissue and blood levels depend on the severity of the acne. Especially in severe acne, low SOD activity and high MDA levels have been reported, clearly indicating that oxidative stress is involved in acne vulgaris. Twendee X, an antioxidant supplement consisting of eight active ingredients of vitamins, amino acids, and CoQ10, has passed drug-level safety testing and is safe for use in children and adults. Since Twendee X significantly reduces blood oxidative stress in healthy individuals, it is feasible to provide oxidative stress care in acne vulgaris. In addition, each of the ingredients in Twendee X may have the potential to reduce the recurrence and aggravation of acne. We will report on the potential of Twendee X as an antioxidant treatment for acne vulgaris, using the results of a questionnaire we have conducted to date.
Backgrounds: Oxidative stress is produced at the wound site, and excessive oxidative stress causes poor wound healing which can lead to dysfunction of the organ. The vocal fold is a vibratory mucosa in the voice box, and creates voice by high frequency vibration such as 100Hz to 800Hz. It can be injured by excessive voicing (vocal abuse), traume, and inflammation. It should be important to control oxidative stress during wound healing of the vocal fold to maintain the vibratory function keeping voice.
Materials and methods: Patients that underwent surgery to the vocal fold due to vocal fold lesions were enrolled in this study. They were seprated into 2 groups: a group treated by anti-oxidant, Twendee X, before and after the surgery (TWX group), and another group with no anti-oxidanta therapy (Control). Post-operative vocal functions were evaluated up to 3 months. The study was approved by institutional IRB.
Results: TWX group showed better vibratory properties with better phonatory function as compared to the control group.
Conclusion: TWX proved to be effective to improve wound healing of the vocal fold after surgery possibly due to reduction of post-operative oxidative stress.
Mitochondria, a powerplant of the cell, have developed an elaborate communication network within the cell communication with the nucleus and other subcellular organelles using a broad array of signaling molecules, including the components of the TCA cycle, reactive oxygen species, and other messenger molecules. This mitocellular communication ensures an orchestrated response to everchanging energy demands and energetic stress, ultimately preserving cell survival. Using small molecules mild mitochondrial complex I inhibitors, we demonstrated that activation of mitocellular communication promotes health and lifespan in chronologically aged wild-type mice and in wild-type mice fed with a high fat diet, a model of accelerated aging. Efficacy of this approach was demonstrated based on increased survival, improved energy homeostasis in brain and periphery, reduced oxidative stress, multiple behavior and cognitive tests, and biochemistry and systems biology approaches. These methods allowed to identify key mechanisms essential for health- and life-extending therapeutics. Most importantly, such an approach results in the activation of multiple neuroprotective mechanisms mimicking a polypharmacy approach that is necessary to treat complex human conditions. Consistent with the hypothesis that improved aging will result in a delay of the onset of age-related neurodegenerative diseases, we demonstrated that treatment with mitochondria-targeted molecules blocked the ongoing neurodegeneration and cognitive dysfunction in multiple mouse models of Alzheimer’s Disease. Taken together, our data suggest that activation of mitocellular communication could be achieved with mild mitochondrial complex I inhibitors. This approach could be beneficial to promote health and longevity restoring mitochondria function and energy balance in brain and periphery [1-3].
SESSION: OxidativeMonPM2-R1 |
Abe International Symposium (4th Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings) |
Mon. 21 Oct. 2024 / Room: Marika A | |
Session Chairs: Haruhiko Inufusa; Kumiko Sugiyama; Student Monitors: TBA |
Fatty acid liver disease is a growing health problem associated with the increasing prevalence of obesity and diabetes. Elevated free fatty acid (FFA) concentrations are linked with the onset of peripheral and hepatic insulin resistance and, while their precise action in the liver remains unclear, it leads to liver steatosis. Although steatosis represents a reversible state of excess intra-hepatic lipid, it is also associated with increased susceptibility to oxidative stress and inflammation thought to trigger its progression to irreversible liver injury characterized by steatohepatitis, cirrhosis and hepato-carcinoma. The current molecular mechanisms of this progression remain poorly understood. However, the “two hit” hypothesis represents the most commonly accepted model. In this model, steatosis represents the first “hit”, sensitizing cells to subsequent stress with a dysregulation of energy production and accumulation of ROS. The second “hit” may take many forms, including drugs, hypoxia or cytokines, eventually leading to inflammation or steatohepatitis. Few in vitro models exist that can recapitulate this progression and its dynamics. Twendee X (TwX) is a potent anti-oxidant and that it is capable of reducing H2O2-induced and acetaldehyde-induced oxidative stress in native HepG2 cells. We have established the FFA-induced lipid accumulation in HepG2 cells, as well as ascertained that the model induced significant oxidative stress and perturbed mitochondrial bioenergetics. We also established the effect of TwX treatment in dose response in both preventive- or curative-treatment designs, and further obtained evidence of intracellular signaling pathways involved both in the FFA-induced oxidative stress and in TwX activity in regulating and normalizing these pathways.
A collection of numerous casses and stories worldwide will be described on the effect of Twendee X and MTControl on the people’s life. They range from improving the quality of life of normal healthy people at various stages of their life and more importantly on people that suffer from various diseases before, during or after treatments. This collection help develop scientific placebo based studies on the effect of Twendee. The success stories are numerous and impressive.
Background: Multiple Chemical Sensitivity (MCS) is a rising concern worldwide, particularly in Japan, where the number of individuals with high chemical sensitivity has increased by 500% over the past decade, with the current prevalence estimated to be 1 in 7 people. The exposure to fragrances in households continues to rise, as fragrance chemicals are found in nearly every household product. Limonene, an ingredient common to 77% of fragrance products, converts to formaldehyde in the air, which potentially implicates it in MCS pathology due to the generation of oxidative stress.[1][2]
Purpose: This study aims to investigate the relationship between a fragrance ingredient, formaldehyde generation, oxidative stress, and MCS pathology.
Methods: Over 40 Japanese detergents and fabric softeners were assessed for common ingredients, with limonene identified as the most prevalent. Gas detection methods were employed to measure the amount of formaldehyde generated from limonene.
Results: Heating limonene to 37°C produced formaldehyde concentrations exceeding indoor air quality standards, when the concentration of limonene was around 400 ppm (in the range of an easily detectable to strong odor). The concentration of formaldehyde surpasses permissible regulatory indoor standards and could increase oxidative stress in airway tissue and the blood.[3] This toxic effect potentially suggests a pathological mechanism for triggering MCS symptoms.
Conclusions: These findings highlight the potential role of common fragrance ingredients in formaldehyde generation in households. The formaldehyde concentration reached exceeded indoor safe standards, which presents a necessity to investigate the relationship with MCS pathology further, mediated by changes in oxidative stress levels in airway tissue and blood.[4]
Dysphagia is a big issue for a large number of patients with cerebrovascular and other neurodegenerative diseases. Animal models are essential for understanding the pathophysiology of these conditions and developing effective treatments. In this study, we developed an animal model with attenuated pharyngeal constriction during swallowing using denervation of the pharyngeal branch of the vagus nerve. Our findings suggest that the pharyngeal area and pharyngeal transit duration during the pharyngeal stage of swallowing were increased compared to those in sham-operated and control animals. We investigated the potential of the anti-oxidant Twendee X in preventing oxidative stress caused by denervation-induced muscle damage, which could suppress muscle atrophy. Hence, we tested the effect of oral application of the Twendee X on swallowing function in the dysphagia model animals.
Our results indicate that Twendee X administration resulted in less increase in the pharyngeal area and pharyngeal transit duration compared to those in the dysphagia animal model. The thyropharyngeal muscles were also thicker than those in the nerve-sectioned animals. Overall, our findings suggest that Twendee X may have a possible role in preventing oxidative stress by the denervation of the pharyngeal constrictor muscle, leading to the suppression of denervation-induced muscle atrophy. Further studies are necessary to ascertain the clinical effects of Twendee X on bulbar paralysis in stroke patients. This study provides important insights into the potential use of Twendee X as a treatment for dysphagia patients.
SESSION: OxidativeMonPM3-R1 |
Abe International Symposium (4th Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings) |
Mon. 21 Oct. 2024 / Room: Marika A | |
Session Chairs: Fuhua Yang; Koji Fukui; Student Monitors: TBA |
Many types of antioxidant supplements are available in the private market in Japan. However, it is difficult to know which type and how much to take, as it is possible to take too many of some vitamins. Since it is difficult for general consumers to make a choice, it is important to provide information based on scientific evidence. This study investigated the effects of continuous administration of a blended supplement, Twendee X (TwX) to aging mice. When 18-month-old C57BL/6 mice were given TwX for 1 month, behavioral tests showed that special cognition and short-term memory significantly improved compared to the age-matched controls. There were no significant differences in secreted neurotrophic factors, such as nerve growth factor and brain-derived neurotrophic factor in the brain. In treadmill durability tests before and after administration, the rate of increase in running distance after administration was significantly higher than that of the untreated group. These results suggest continuous intake of TwX may improve cognition and suppress age-related muscle decline. There is no problem with overdosing, so we think it's a good idea to take the blended supplement continuously.
Reactive oxygen species (ROS) and free radicals work to maintain homeostasis in the body, and excessive ROS can damage the body's proteins, lipids, and DNA. Oxidative stress (OS) is the term commonly used to describe the imbalance between the generation of free radicals in the body and the ability of cells to counteract them. Accumulation of OS is aging, and OS also represents an important role for physiological homeostasis. Deviations from sustained redox signaling homeostasis are also now known to cause disease. The important relationship between OS and various diseases has been established, and OS is now at the forefront of research to elucidate pathogenesis. Despite this, so-called antioxidant therapy for diseases is still not widely used.
There are many types of ROS and free radicals, and each type has different properties. The widespread use of antioxidant therapy requires a level of antioxidants that can counter these. It is not clear whether OS induced the disease or was secondary to tissue damage derived from the onset of the disease. Although the exact role of oxidants in disease pathogenesis is not always clear, OS has received significant attention as a factor in human disease and is the focus of extensive research. This field will contribute to the prevention and treatment of diseases in the future.
Sinusitis is a disease that is accompanied by a runny or stuffy nose, pain in the cheeks, between the eyes, and in the head, and olfactory disturbances These symptoms can lead to a decreased quality of life due to lack of concentration and discomfort. The main cause is viral or bacterial infections, such as the common cold. Since the sinuses are connected to the nasal cavity, it is known that infection can also cause inflammation of the sinuses. When the body is invaded by a virus or bacteria, it employs highly active reactive oxygen species (ROS) to eliminate them. This causes inflammation. Therefore, ROS are elevated in areas of inflammation, resulting in increased oxidative stress. In patients with chronic sinusitis, reduced glutathione and uric acid concentrations have been reported, suggesting that chronic sinusitis is likely to play a role in oxidative stress. Twendee X is an antioxidant supplement that contains a balanced blend of eight ingredients with strong antioxidant potential. It has passed drug-level safety testing and is safe for use by both children and adults. This study reviewed the relevance of oxidative stress in sinusitis and the results of a questionnaire on symptom changes in humans with sinusitis before and after taking Twendee X. The results suggest that intervention with antioxidant supplements could improve or prevent symptoms of sinusitis.
Background: In recent years, fragrance pollution triggered by common household items has become a global concern, contributing to the increasing prevalence of Multiple Chemical Sensitivity (MCS) worldwide [1]. Despite the rising prevalence, there is a lack of researchers and diagnostic criteria for MCS, hindering effective diagnosis and treatment.
Purpose: This study proposes several investigations and experimental methods to elucidate the factors contributing to MCS and discusses the current status of diagnostic criteria for MCS, which remain unidentified.
Methods: We estimated the number of individuals affected by MCS based on existing studies [2] and identified fragrance ingredients commonly used in everyday products. Additionally, we explored methods to visualize invisible fragrances and considered how physicians should diagnose MCS.
Conclusions: At present, more than 16 million people in Japan (about 1 in 7) are estimated to suffer from “MCS” or have “High Sensitivity” or “Semi-High Sensitivity” to Chemical Substances. Recent developments in microencapsulation technology suggests that sustained fragrance release may contribute to the increase in MCS prevalence by continuously emitting hazardous substances [3], similar to allergic reactions seen in individuals with pollen allergies. Therefore, MCS should be recognized as a condition that anyone can develop, similar to pollen allergies. To prevent MCS, essential measures such as refraining from releasing fragrances in shared spaces are indispensable.
SESSION: OxidativeMonPM4-R1 |
Abe International Symposium (4th Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings) |
Mon. 21 Oct. 2024 / Room: Marika A | |
Session Chairs: Haruhiko Inufusa; Student Monitors: TBA |
Amyotrophic lateral sclerosis (ALS) is a disease that causes muscle weakness in the extremities, muscle atrophy, and dysphagia due to motor neuron degeneration. It is a neurologically intractable disease that mainly develops in middle age or later, eventually leading to respiratory failure due to paralysis of respiratory muscles, resulting in death within 3-5 years. Familial ALS is found in approximately 10% of all ALS cases and was reported to be caused by a point mutation in the gene for Cu/Zn SOD (SOD1), an antioxidant enzyme. It is hypothesized that oxidative stress damage caused by SOD1 abnormalities is deeply involved in the pathogenesis of ALS, and that oxidative stress may play an important role in the progression and worsening of the disease in ALS. Recently, the use of Edaravone, a radical scavenger, was approved for treatment in Japan the first time. Edaravone was developed as a treatment for acute cerebral infarction and is useful for cranial nerve and blood vessel protection by inhibiting inflammation in the brain. It also significantly improves motor and cognitive deficits for Alzheimer's disease in neurodegenerative disorders, reduces Aβ/p-Tau accumulation, and alleviates neuronal loss, oxidative stress, and neuroinflammation. Similarly, Twendee X, a known antioxidant supplement, also significantly improves motor and cognitive impairment and reduces Aβ/p-Tau accumulation by inhibiting oxidative stress in the brain, protecting mitochondria, and maintaining neurogenesis and autophagy function. It is composed of eight active ingredients consisting of vitamins, amino acids, and CoQ10, and has passed drug-level safety testing. Studies have shown that Twendee X has the potential for symptomatic relief of systemic scleroderma, an intractable therapeutic disease. Twendee X is not a pharmaceutical product and can be used safely on a daily basis. Twendee X is expected to be one of the most promising antioxidant therapies for ALS. Treatment experience for one patient of ALS also presented.
The vocal fold vibrates in high frequency to create voice sound. The vocal fold has a sophisticated histological “layered structure” that enables such vibration. As the vibration causes fricative damage to the mucosa, excessive voicing can cause inflammation or injury to the mucosa. Chronic inflammation or repeated injury to the vocal fold occasionally induces scar formation in the mucosa, which can result in severe dysphonia, which is difficult to treat. Oxidative stress has been proven to be an important factor in aggravating the injury, which can lead to scarring. It is important to avoid excessive oxidative stress during the wound healing period. Excessive accumulation of reactive oxygen species (ROS) has been found in the injured vocal folds of rats during the early phase of wound healing. Antioxidants proved to be useful in preventing the accumulation of ROS during the period with less scar formation in the long-term results. Oxidative stress is also revealed to contribute to aging of the vocal fold, in which the mucosa becomes thin and stiff with a reduction in vibratory capacity. The aged voice can be characterized as weak and breathy. It has been confirmed that ROS gradually increases in rat vocal fold mucosa with age, which may cause further damage to the vocal fold. Antioxidants have also proved effective in avoiding aging of the vocal fold in rat models. Recently, human trials have shown significant effects of the antioxidant Twendee X for maintaining the voice of professional opera singers. In conclusion, it is suggested that oxidative stress has a great impact on the damage or deterioration of the vocal folds, and the use of antioxidants is effective for preventing damage of the vocal fold and maintaining the voice.
SESSION: GeochemistryMonPM1-R2 |
Ross International Symposium (3rd Intl. Symp. on Geochemistry for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Marika B1 | |
Session Chairs: Alexandra Navrotsky; Student Monitors: TBA |
Framework structures, which feature three-dimensional networks of relatively rigid polyhedral units that share corners with one another, encompass a wide range of natural and synthetic compounds of importance in Earth science, chemistry, physics, and materials science. Examples include feldspars, zeolites, garnets, perovskites and hybrid materials such as metal-organic frameworks (MOFs). The inherent flexibility of the framework gives rise to many interesting phenomena that control the stabilities of the materials. These phenomena include extensive polymorphism, negative volumes of fusion, very low to negative thermal expansion, a P-T region of pressure induced amorphization, and polyamorphism. These properties serve as inspirations that form the basis of many technological materials such as photovoltaics, sensors, catalysts, lasers, molecular sieves, etc. The Ross group studies the structure-property relations of framework materials using a combination of methods including X-ray diffraction, Raman spectroscopy and inelastic neutron spectroscopy to explore how the flexible structural framework is related to their thermodynamic, elastic and physical properties[1-5]. This talk will present an overview of how structural changes influence mechanical functionality and ongoing ultimately lead to the development of novel materials based on this important group of materials.
Composition, temperature and pressure are the main knobs to turn in synthesizing, characterizing, and using new materials. Though the geologic and planetary science communities have embraced pressure as a natural and necessary variable, it has been underutilized in materials research. FORCE, the Facility for Open Research in a Compressed Environment, is a new initiative and laboratory at ASU, housing unique multianvil equipment and research. FORCE enables synthesis of relatively large samples over a wide pressure – temperature range and combines both experimental and computational studies relevant to structure, bonding, and phase transitions. It is a user facility for the broad scientific community. FORCE and its capabilities will be described and several examples of current materials research linking high pressure, thermochemistry, and important functional materials will be presented. Specifically, rare earth monoxides, metastable at ambient conditions, have been investigated, while current work focuses on sulfides, selenides, tellurides and arsenides.
Nanostructured transition metal nitrides represent a sustainable alternative to conventional materials in a variety of applications, including catalysis, coatings, electrochemical devices, and lithium-ion batteries [1]. Nanoparticles exhibit thermodynamic parameters that can differ significantly from those of bulk materials due to the decrease in dimension [2] and dependence of energetic stability on the surface energy. The investigation of how the thermodynamic parameters of transition metal nitrides differ between bulk and nanoparticles provides the foundation for optimizing these materials for diverse applications. However, compared to other properties (e.g., magnetic, conductive, electronic) that have been measured, thermodynamic investigation is still in its nascent stages. In this study, we employ high temperature oxidative melt solution calorimetry [3] and differential scanning calorimetry to ascertain thermodynamic properties (enthalpy of formation, surface energetics and enthalpy of decomposition) and to identify and discuss stability differences between bulk and nanophases as well as trends among different transition metal (Ti, Fe, Co, and Ni) nitride phases.
Geosystems especially in the Earth’s crust often feature rhythmic patterns such as banded formations, layered and folded structures, diapirs or cockade ores that can cover scales from just microns, and even sub-microns, up to several kilometers. This subject has been examined from a thermochemical-mechanical perspective since times.
As well for a long time, physics was limited to characterizing continuous changes in closed systems. The concept of self-organization (I. Prigogine, 1977), however, enables to describe discontinuities as sequential spontaneous structure/texture formation. For this reason, the earlier approach in closed systems with given boundary conditions of existing "ideal gases" is abandoned and instead open systems with distributed components and properties (W. Ebeling, 1976) as well as available free energy are introduced. For allowing spontaneous structure/texture formation, the open systems should be far from thermodynamic equilibrium.
In closed systems, changes inevitably cause an increase in complexity and disorder (increase in entropy). Contrarily, the concept of self-organization in open systems lays the foundation for changes going together with increasing order and complexity at the same time, i.e. by means of export of entropy and energy dissipation. Here, phase transitions play an essential role. Precipitate patterns mediated by solute reactions have been discussed in detail since the 1980s (P. Ortoleva, 1982). As a further characteristic of open systems, the scale invariance is formulated by H. Haken 1978 with his synergetics concept.
As the earth system is considered as an open system including geochemical processes and geomaterials of all scales that changes because of the supply and withdrawal of energy, ordered structures and patterns are typical features in geological systems.
In this talk, radiolarite, malachite, reef limestone and banded iron-manganese deposits will be addressed as illustrating examples. Using the example of a recent early diagenetic new mineral formation, the findings of experimental, theoretical, and numerical analyses will be discussed. Finally, generalized results will be considered for future investigation.
SESSION: GeochemistryMonPM2-R2 |
Ross International Symposium (3rd Intl. Symp. on Geochemistry for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Marika B1 | |
Session Chairs: Megan Householder; Larissa Dobrzhinetskaya; Student Monitors: TBA |
Planets that orbit stars other than our sun are called exoplanets and over 5,500 have been confirmed in our galaxy. Hot Jupiters are a type of exoplanet that orbit very close to their star and are tidally locked, with a permanent daytime and nighttime side. Being the hottest exoplanets, they emit the most radiation and thus are a prime target for the James Webb Space Telescope. Silicates are a ubiquitous feature of aerosols on hot giant exoplanets. [1] WASP 17-b is a hot Jupiter with an orbital period of 3.7 days whose atmosphere was recently observed by James Webb Space Telescope to be dominated by quartz (SiO2) nanocrystals, although magnesium-rich silicates were expected to be seen. [2] In the brown dwarf VHS 1256-1257b, the best fit models for spectroscopic observations were clouds of enstatite (MgSiO3), forsterite (Mg2SiO4), and quartz. [3] Despite key silicate features in spectroscopy, it is not possible to determine complete atmospheric composition and cloud formation by astronomical observations alone, and particle formation in atmospheres must be modeled. Major factors in modeling atmospheres are nucleation and condensation, which are exponentially dependent on the species’ surface energy, with higher surface energies drastically hindering nucleation rates. Although the need for reliable surface energy measurements is evident, surface energies of several key species in hot giant exoplanets are not yet constrained by experiment. In this work, surface energies of likely exoplanet atmosphere condensates, including zinc sulfide (ZnS), crystalline, and amorphous enstatite were measured using oxide melt solution calorimetry of appropriate nanoparticles. These are then input into a nucleation code that gives nucleation rates for these species. [4,5] The surface energy of crystalline SiO2 is much lower than that of the crystalline magnesium-rich silicates, supporting the observation of silica in the atmosphere of WASP-17b, while the surface energy of amorphous enstatite is similar to that of quartz. [4,6] This suggests that initial nucleation of MgSiO3 in VHS 1256-1257b could form the amorphous phase. This research provides experimental surface energy data of high relevance to a broad range of exoplanet atmospheres.
Geopolymers are inorganic, polyaluminosilicate or chemically-bonded ceramics centered around the nominal formula M2O•Al2O3•4SiO2•11H2O where M = Group I elements and the amount of water is variable, depending on the particle size and specific surface area of the aluminosilicate clay. They are refractory, inorganic polymers formed from both aluminum and silicon sources containing AlO4-and SiO4 tetrahedral units, under highly alkaline conditions at ambient temperatures. Therefore, they are a rigid, hydrated, materials containing group I, charge-balancing cations which result in an amorphous, cross-linked, impervious, acid-resistant, 3-D structure.1,2 Geopolymer composites are stable to 1000°C above which they crystallize into ceramic composites. They can be reinforced with ceramic, metal, polymeric or biological particulates, chopped fibers, weaves or meshes. They can be prefabricated in polymeric molds or 3D/4D printed. Other new inorganic polymers are being identified, such as acid-based Al2O3•SiO2•P2O5 made by high shear mixing metakaolin with phosphoric acid; magnesium potassium phosphate (MgKPO4); magnesium borate (MgO•B2O3); yttrium silicates and zinc silicates.3
To produce 1 ton of geopolymer liberates only 0.25 tons of CO2 whereas 1 ton of CO2 is liberated for manufacturing 1 ton of cement. In civil engineering, the term “geopolymers” refers to the product resulting from high shear mixing of class F fly ash mixed with ground, granulated, blast furnace, slag, waste products. The solid is also amorphous or crystalline, but it is based on the calcium silicate hydrate (CSH), C(A)SH, KASH, NASH) binder phases, forming cements not geopolymer. In this structure, the silicate or aluminate tetrahedra form 2D layers sharing only two or sometimes three corners, and are separated by layers of Ca(OH)2. CSH is the main binder phase in Portland cement. One main difference between the cements versus geopolymers is that geopolymers are chemically stable up to 1,000°C, after which they crystallize into ceramic, retaining some mechanical strength. Cements contain significantly more water and steadily decompose with increasing temperature, losing their mechanical strength.4
Geopolymers have wide potential applications as: fire-resistant structures or coatings, corrosion-resistant coatings; stronger and tougher replacements for cements and concretes; ceramic composites exhibiting “graceful failure” or pseudo-ductility; geopolymers containing glass frit can undergo amorphous self-healing when heated below 950°C (ASH-G) or behave as amorphous, self-healed ceramics when crystallized above 950°C; ASH-G composites for molten salt encapsulation for thermal energy storage or micro nuclear reactor applications; (a, b,g and neutron) nuclear radiation shielding; electromagnetic pulse interference (EMI) shielding; water purification filters; refractory glues between ceramics, metals, glass and/or wood; non-burnable building insulation; as a substitute for cements or concrete when made from revalorized mine tailings; removal of heavy metals (As, Hg) or PFAS from water.
Unusual microdiamonds discovered in metamorphic rocks of continental affinities during the 1990th in Kazakhstan, China, Norway and Germany provided new geochemical data that led to revisions in the understanding of the plate tectonic subduction and exhumation processes [1,2,3,4].
Diamond, due to its chemical inertness, is considered the perfect “geological container” where gas, fluid, and solid inclusions can be preserved. High-resolution Scanning and Transmission Electron Microscopy, Focused Ion Beam technology, Synchrotron X-ray diffraction, Fourier Transformed Infra-Red, and Raman spectroscopic studies exemplify the remarkable interaction between 21st-century science and technology. These advancements have led to a paradigm shift regarding microdiamonds formation in geological environments of metamorphic belts previously believed to be “forbidden” for their crystallization.
Our studies revealed that nanoscale gas and fluid inclusions in microdiamonds consist of light and heavy elements such as Cl, S, H, K, Cr, Ba, Ti, Pb, Mo, Co, Al [5,6]. The presence of the negative crystals of diamonds filled with a C-O-H fluid provided evidence that such a fluid was in equilibrium with the diamond at T= 800-1200oC and P=7-9 GPa and it can be considered as the diamond-forming media [5,6]. Studies of microdiamond carbon isotopes characteristics suggest that the diamond was formed from “organic” carbon (average δ13C = -10 to – 33 o%) [6]. The measurements of noble gases in microdiamonds from the Kokchetav terrane of Kazakhstan indicate that the ³He/⁴He ratio is consistent with values associated with geochemical interactions between a continental crust slab and a mantle plume [6].
We have conducted a series of successful experimental reproductions of diamonds crystallization from C-O-H-rich fluids at geological conditions close to those of their host rocks [6]. Studies of microdiamonds from recently discovered UHPM terranes continue to release new geochemical observations on organic carbon cycling into deep mantle, geochemical crust-mantle interaction and rejuvenation of the mantle which are critical components for understanding of mantle dynamics.
In the last 10 years the phenomenon known bradyseism in the Campi Flegrei (CF), has been active, with different earthquakes swarms. This continuous low-magnitude seismic activity, has created problems in the densely populated area of CF, which includes the western portion of Naples. The seismic activity is accompanied by uprising of soils (about 2 cm/month). Some researchers are creating panic in the citizenry as they make hypothesis about the fact that a potential, catastrophic, Plinian eruption might occur any time. Such catastrophists hypothesize that bradyseism occurs due to up-rising of magma. The fact is that there is no proofs or evidence of such magma rising to explain the bradyseism phenomenon. With an international research group [1, and ref therein] we have made an interpretation of the bradyseism which occurs cyclically in the CF, at least in the last 4.000 years, never producing a catastrophic eruption. The only exception was the very small Monte Nuovo phreatic eruption of 1538 AD.
We obtained data during long-term monitoring of the CF volcanic district which has led to the development of a model based on lithological-structural and stratigraphic features that produce anisotropic and heterogeneous permeability features showing large variations both horizontally and vertically. These data are inconsistent with a model in which bradyseism is driven exclusively by shallow magmatic intrusions. Instead, CF bradyseism events are driven by cyclical magmatic-hydrothermal activity. Bradyseism events are characterized by cyclical, constant invariant signals repeating over time, such as area deformation along with a spatially well-defined seismogenic volume. These similarities have been defined as “bradyseism signatures” that allow us to relate the bradyseism with impending eruption precursors. Bradyseism is governed by an impermeable shallow layer (B-layer known as pozzolana), which is the cap of an anticlinal geological structure culminating at Pozzuoli, where maximum uplift is recorded. This B-layer acts as a throttling valve between the upper aquifer and the deeper hydrothermal system that experiences short (1-102 yr) timescale fluctuations between lithostatic/hydrostatic pressure. The hydrothermal system also communicates episodically with a cooling and quasi-steady-state long timescale (103-104 yr) magmatic system (at depth of 8 km) enclosed by an impermeable carapace (A layer).
Connectivity between hydrostatic and lithostatic reservoirs is episodically turned on and off causing alternatively subsidence (when the systems are connected) or uplift (when they are disconnected), depending on whether permeability by fractures is established or not. Earthquake swarms are the manifestation of hydrofracturing which allows fluid expansion; this same process promotes silica precipitation (and sulphides) that seals cracks and serves to isolate the two reservoirs.
Faults and fractures promote outgassing and reduce the vertical uplift rate depending on fluid pressure gradients and spatial and temporal variations in the permeability field. The mini-uplift episodes also show “bradyseism signatures” and are well explained in the context of the short timescale process.
This interpretation is supported by the fact that earthquake hypocenters at CF are never registered at depths between 4 and 8 km. 90% of the earthquake hypocenters (with M mostly between 1 and 2.5) occur at depths between 1.5 to 3.5 km. We know from deep boreholes that in the CF, that the B-layer; known as “pozzolana” is occurring at depth between 2-3 km [2]. The hydrothermal fluids, fracturing the impermeable layer, pass from lithostatic to hydrostatic pressure; hence they boil, depositing different sulphide mineralizations (pyrite, chalcopyrite, galena, scheelite and others) along the fractured system in the pozzolana B-layer [3-4]. When this occurs, the negative bradyseism begins, and the soil starts to go down slowly.
With the present state-of-the art knowledge of bradyseism, there is no evidence that a catastrophic plinian eruption might occur. Nevertheless millions of people are scared by the phenomenon. What should the Government do? 1. Proceed and prepare for a worst-case potential scenario as a precaution. As there is not evidence of any magma rising up at the moment, create ample, escape roads from which at least 1 million people should be able to escape quickly from the Red Zone of CF; 2. Establish an international panel of researchers and experts to advise the Government and citizenry of CF about seismic activity; 3. Carry out seismological screening of old houses in the Red Zone of CF and identify those not properly built to withstand the continuous small magnitude earthquakes continuously occurring in the Red Zone of CF.
SESSION: GeochemistryMonPM3-R2 |
Ross International Symposium (3rd Intl. Symp. on Geochemistry for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Marika B1 | |
Session Chairs: Megan Householder; Benedetto De Vivo; Student Monitors: TBA |
The first and second laws of thermodynamics are the fundamental laws that govern the states of a system, large or small, and its interactions with its surroundings. The changes of states inside the system, i.e., internal processes, are guided by the entropy change of each internal process. The recently termed zentropy theory stipulates that the entropy of a system is the sum of statistical entropy among all conceivable configurations of the system, i.e., the Gibbs entropy or Shannon information entropy, and the statistical average of entropy of each configuration, i.e., the quantum entropy (https://doi.org/10.1088/1361-648X/ad4762). It is demonstrated that when the quantum entropy of each configuration can be predicted by quantum mechanics, the properties of the system can be quantitively predicted without any additional models and fitted model parameters, showing remarkable agreement with experimental observations, including singularity at critical points. For complex systems such as biology, society, planet, and galaxy, the properties of configurations in them could not be predicted by quantum mechanics, it is proposed to learn the properties of each configuration from observations using the zentropy theory. It is anticipated that based on the zentropy theory, a science-based foundation model for artificial intelligence in the flattened configuration space can be developed so their properties can be predicted including emergent behaviors and instability with singularity so concerted efforts can be organized to utilize them or mitigate them.
Superconductivity in the vicinity of room temperature has the potential to revolutionize numerous technologies and sustainability as well as our understanding of condensed matter. Zero electrical resistance and expulsion of magnetic field below a critical temperature are critical tests of superconductivity. As for the original high-Tc cuprate superconductors, accurate crystal structures are also required for complete characterization of the materials [1]. Inspired by theoretical predictions for hydrogen-rich materials under pressure [2], previous work from our group has established the existence of near-room temperature superconductivity at megabar pressures [3], now reproduced by numerous other groups [4]. Recently reported evidence for superconductivity at ambient P-T conditions in nitrogen-doped lutetium hydride (Lu-N-H) has been promising but controversial [5]. Our group has conducted independent electrical resistivity and magnetic susceptibility measurements on the material that confirm the remarkable properties of the material as well as the difficulty of synthesis [6]. First-principles DFT and DFT+U calculations provide important insights into the behavior of this remarkable class of materials [7]. There are prospects for similar high Tc superconductivity in related compounds, including complex quaternary and higher order chemical systems.
processes. Due to its physical properties, rock crystal was frequently used as a lithic raw material for the production of tools and weapons in prehistoric times. Recently, the first mining sites where the material was aquired in large quantities, were discovered. One of them is situated near Eggishorn Mountain in the Upper Valais (Switzerland) at an elevation of 2600 m above sea level. The archaeological finds and features date to the Early Mesolithic (almost 10,000 years ago) and to a younger phase of the Neolithic.
The talk presents the results of a petrographic characterisation of the material occurring at the investigated site. It provides a description of the fluid inclusions within the quartz crystals and an overview over the related mineral paragenesis.
This gives interesting new insights into the formation of the analysed fissure and allows comparing rock crystal artefacts found in other archaeological sites to this particular source. The results form the basis for further investigations concerning mobility patterns and trade networks in the past.
The Alpine area presents many small copper deposits, mostly exploited since Late Medieval times. This led to the widespread assumption that these ores were exploited much before and that most circulating prehistoric metal objects were produced with local copper sources. This assumption was largely validated for the Bronze Age through the use of lead isotope tracers, and well supported by the archaeological and archaeometallurgical evidences. However, the scarcity of available lead isotope data for pre-Bronze Age metals precluded to date the reconstruction of the metal flow in the 4th and 3rd millennia BC [1-2].
Based on 49 new analyses of archaeologically important artefacts, it is now shown that the Northern Italian Eneolithic (or Copper Age, approximately 3500-2200 BC) includes three chronologically distinct periods of metal production: Balkanic, Tuscanian, and Alpine copper [3].
The Alpine ores were massively exploited only starting from the middle of the 3rd millennium BC, in connection or slightly earlier than the Beaker event.
SESSION: GeochemistryMonPM4-R2 |
Ross International Symposium (3rd Intl. Symp. on Geochemistry for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Marika B1 | |
Session Chairs: Larissa Dobrzhinetskaya; Student Monitors: TBA |
Natural processes such as earthquakes, volcanism, and mountain building are driven by plate tectonics, which are fundamentally influenced by the deformation of rocks and minerals under various environmental conditions. Understanding the rheology of rock-forming minerals is thus crucial for deciphering the geodynamics of Earth. Our current understanding of mineral rheology is primarily derived from laboratory experiments and theoretical models based on simplified synthetic systems. However, the properties of minerals are significantly affected by structural defects and impurities, making the extrapolation to natural, chemically complex systems uncertain. Crystal defects such as dislocations, chemical impurities and vacancies play a crucial role in influencing the elastic properties of minerals and their rheology, introducing deviations from the idealized, flawless structure. These defects act as perturbations that impede the smooth transmission of mechanical forces within the crystal structure, consequently influencing its overall elasticity and, in turn, impacting the material's macroscopic mechanical properties. In addition to defects and vacancies, minerals often contain fluid, melt and solid inclusions that can reach significant volumetric abundances and strongly affect the elastic properties (and thus the mechanical properties and rheology) of the host crystal. The investigation of mineral inclusions does offer a unique opportunity to study their impact on the rheology of the host mineral in situ. This approach holds great potential for enhancing our comprehension of the rheology of mineral assemblages and, consequently, the dynamics of our planet.
The compressional behaviour of microporous materials (in particular, zeolites and feldspathoids) compressed in a fluid can be substantially governed by the potential crystal-fluid interaction, due to the selective sorption of new molecular species (or solvated ions) through the structural cavities in response to the applied (hydrostatic) pressure.
When no crystal-fluid interaction takes place, the experimental findings and computational modelling performed so far show that the effects of the applied pressure, at the atomic scale, are mainly accommodated by the tilting of the (quasi-rigid) (Si,Al,P)O4 tetrahedra, around the bridging oxygen atoms that act as hinges between tetrahedra [1]. Tilting of tetrahedra was proved to be the dominant mechanism at low-mid P-regime, then followed by distortion and compression of these polyhedra, which become dominant at the mid-high P-regime (i.e., once titling is not sufficient anymore to accommodate the deformation energy) [2]. Specific mechanisms of deformation at the atomic scale, in response to compression, are controlled by the topology of the framework of tetrahedra. For example, the continuous increase of channels ellipticity, with increasing pressure, is one of the most common deformation mechanisms in zeolitic frameworks, but inversion of ellipticity occurs only in response to a phase transition, with a drastic structure rearrangement (e.g., reconstructive in character). On the other hand, the compressibility of the cavities (in the form of channels or cages) is governed by the so-called extraframework population (made by ions and small molecules), leading to different bulk compressibility in isotypic structures [3]. The elastic parameters available for zeolites (natural or synthetic) show that microporosity does not necessarily imply high compressibility, and most of the zeolites appear to be less compressible than many other Crustal minerals [1,3]. A high compressibility is somehow expected for porous framework structures due to the tetrahedral tilting, but the bonding configuration between the framework of tetrahedra and the stuffed species affects the overall compressional behaviour, making this class of host-guest structures less compressible than other rock-forming silicates.
When compressed in penetrating fluids, some zeolites experience a P-induced intrusion of new monoatomic species or molecules from the fluids themselves. Materials having well-stuffed cavities at room P-T conditions tend to hinder the penetration of new species. Crystal-fluid interactions in zeolites have observed using pressure-fluids made by: monoatomic species (e.g., He, Ar, Kr, Xe), small (e.g., H2O, CO2) or more complex molecules (e.g., C2H2, C2H4, C2H6O, C2H6O2, BNH6, electrolytic MgCl2·21H2O solution), with potential geological and technological implications [4,5]. Diverse variables govern the P-mediated sorption phenomena: the “free diameters” of the framework cavities, nature and bonding configuration of the extraframework population, kinetic diameter of the potentially-penetrating molecules, rate of P-increase, temperature at which the experiment is conducted and surface/volume ratio of the crystallites under investigations.
My research is focused on sustainable metallurgical processes that concerns energy, resource and environment. For metallurgical processes, one fundamental question is how much heat needed when reactants enter into the furnace regardless of minerals and electronic wastes. Calorimetry method is the main approach that I will use to explore the heat effect measurement in the metallurgical processes.
The history and evolution of our species has always been closely linked with environmental factors. During the last years, the dramatic consequences of climate change and catastrophic events had an impact on humanity on a global level. In combination with methodologies from a variety of partner disciplines, Prehistoric Archaeology is the only academic field that analyses the interdependence between human societies and changing environmental conditions from a long-term perspective and based on the study of material culture. Therefore, it leads to a better understanding of the use of resources throughout time and space and is able to contribute to the solution of several problems that we are facing today. The last time human beings were subject to equally rapid changes, was towards the end of the last ice age (Late Glacial Interstadial), around 14,500 years ago. This period was marked by the disappearance of large reindeer herds in Central Europe and important innovations such as the widespread use of bow and arrow or domesticated dogs for hunting. The lecture gives an overview over the various ways in which interactions with natural resources have influenced human history and evolution. Based on several case studies, it shows how people adapted to new climatic conditions and challenges in the past. Finally, it presents strategies developed by prehistoric societies aimed at a more efficient and sustainable use of resources that could also lead to practical implications in the presence.
SESSION: MathematicsMonPM1-R3 |
Rowlands International Symposium (7th Intl. Symp. on Sustainable Mathematics Applications) |
Mon. 21 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Mike Mikalajunas; Student Monitors: TBA |
Physics, at the fundamental level, is concerned only with a single system, that of the fermion or fundamental particle, and it is possible to conceive the actions of the entire universe as those of a single fermion. We have had a quantum mechanical equation for the fermion – the Dirac equation for nearly a hundred years – but no one has imagined that that equation alone could even lead to all the developments encoded in the Standard Model of particle physics. This is partly because the equation is not normally expressed in its most significantly meaningful form, but it is also because ‘derivation’ is generally taken to mean a deductive mathematical consequence given certain conditions rather than an unfolding of the innate structure that is built into the equation as a result of more fundamental principles. The equation is not necessarily the source of these principles, rather the codification of them. In fact, given these additional considerations, it is possible to see the equation in its most physically meaningful form as the source of all current aspects of the Standard Model and even some things beyond it. In addition, the full statement of the equation is not necessary for these derivations, only the definition of the fermion creation operator that the equation requires. So, the question that we will be answering is the more restricted one of whether physics can be defined by a single operator, rather than a single equation.
The usual concept of an electron worldline in Minkowski space assumes that particles have smooth time-like curves representing the movement of a centre of mass. Events are then points on the worldline and can occur with arbitrarily small inter-event spacing. Mass by itself is not a direct kinematic feature of such curves. Instead, mass and energy are input from dynamical behaviour. An alternative model, explored in this paper is to assume that mass represents an upper bound on the frequency of special events on the worldline. This imposes a lower bound on the measure of causal regions between such events and produces two characteristic scales associated with particle mass. The scales are classical analogs of the de Broglie and Compton scales respectively. The model provides a direct basis for Feynman's original non-relativistic path-integral approach to quantum mechanics[1] as well as his relativistic chessboard model[2] and its extension to 3+1 dimensions[3].
In this talk I will be presenting the main highlights of what I consider a very important development in the Medical Sciences for acquiring a much better understanding of the human body by demonstrating how the unique mathematical properties of SDF would play a very significant role in the development of more advanced and reliable theoretical models for the human body. This would require performing a complete analysis only on those "general" analytical solutions that can be obtained using the very unique computational feature of SDF on the Naiver-Stokes equations for the "Mechanical" aspect of the human body that is largely influenced from the general Mechanical properties of fluids and on the Schrodinger equation for the “Chemical” aspect of the human body.
Currently there exist no such advanced theoretical models of the human body that would be based entirely on general analytical solutions of PDEs because of the severe limitation of Calculus which if successfully resolved by the method of SDF would become immeasurable in terms of reducing our excessive dependency on the use of experimental models in favor of a more universal algebraic theory for the Physical and Biological Sciences.
Peter Rowlands appears to be the only physicist who has written a book on foundational laws in physics [1]. He identifies four fundamental symmetries that are foundational to physics: space, time, mass and charge. A group relationship, a zero-totality condition and a nilpotent Dirac equation are the primary mathematical structures used to build the foundational laws. [2]. The duality between space-time and mass-charge is so exact that any reversal of role between discrete space and continuous time also produces a corresponding reversal of role between continuous mass and discrete charge [3]. One of us has argued that his ‘principle of duality’ is so ubiquitous in both mathematics and physics that it should be promoted into a ‘law’ based on the quantum mechanical law of entanglement [4]. Rowlands identifies three distinct mathematical processes: (A) conjugation, (B) complexification and (C) dimesionalization. Their corresponding physical manifestations are dualistic in nature: (a) conserved/nonconserved, conjugated/nonconjugated, + / –, (b) real/complex (the relativistic duality) and (c) the discrete/continuous, or the dimensional/nondimensional options. A classic case of the discrete/continuous representation is the well-known continuous wave/discrete particle duality. Rowlands’ principle of duality UNITES the theory of general relativity (GR), which is a theory about gravity not a theory of gravity, and quantum mechanics (QM). It does not UNIFY them [5].
SESSION: MathematicsMonPM2-R3 |
Rowlands International Symposium (7th Intl. Symp. on Sustainable Mathematics Applications) |
Mon. 21 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Louis Kauffman; Mohamed Said Moulay; Student Monitors: TBA |
In [1] and [2] models of elementary particles are proposed based on combinatorial substructures for quarks.
These papers succeed in given combinatorial models for many particle interactions. In [3] a vector version of the Harari, Shupe models is
given, in which each particle is a four-vector and particle interactions correspond to vector identities. The Lambek model can be matched directly with the Shupe model, but contains
extra information that allows the vectorial work. In [4] a so-called Helon model is given by Bilson-Thompson that uses framed three braids and can be seen as a generalization of the Rishon models of Harari and Schupe. In fact, we find (joint work with David Chester and Xerxes Arsiwalla) that the Lambek model is a nearly perfect intermediary between the Helon model and the Rishon model. There is a direct correspondence between Lambek's four-vectors and the braids in the Helon model, up to a slight readjustment. This means that we are in possession of a dictionary that lets us discuss and compare the structures in these models and to examine possible generalizations of them. We also can use this point of view to see some of the limitations of the Helon model that arise from the non-commutativity of the Artin Braid Group. The talk will present these structures, and our speculations about generalizations and relationships with other topological work such as found in the papers of the author [5], the work of Witten [6] and alternate topological intepretations such as [7], [8], [9] and [10].
Negative signed numbers can represent a variety of concepts depending on the specific context in physics. Sometimes, their meaning is ambiguous, and in quantum equations, the physical interpretation of these quantities can be uniquely challenging. For example, the Dirac equation is well-known to have both positive and negative signed solutions. Today, physicists still debate the physical significance of the negative signed solutions. One way to confer meaning to these ambiguous negative signed quantities is to express them in an expanded dimensional canvas. But how might such a canvas be conceived?
Part 1 of this paper sketches a new approach showing considerable promise. The fundamental symmetry of positivity and negativity seem to be built into the very fabric of the universe at subatomic scales. In consonance with Rowlands’ concept of totality zero, these fundamental symmetries can be shown to naturally admit an alternative explanation for conceptualising the shape and content of space at subatomic scales. The approach posited is that a recursive pseudo Riemannian cobordism (PRC) of manifolds can describe the shape of space using an expanded nD + 1 space coordinate system. The advantage of this system is that it confers physicality on abstract nD mathematical spaces that are conventionally assumed to map the structure of reality. The revised shape of space admits physical content consistent with experimental findings in an altogether different way. The physical system of two surfaces connected by a small, variable length, recursive dimension, constitutes a recursive cobordism, a modification of the one conceptualised by P. Yodzis.
The new frame of thinking distinguishes between the content of space – light and matter – and the shape of space in which that content exists. Two elementary particles – analogous to the photon and electron - are described as embedded deterministic objects in this space.
By adding a small, variable length +1 dimension that runs perpendicular to every direction in nD space, the emergent nD + 1 space physical system allows us to account for the ubiquitous negative signed quantities that emerge in certain quantum equations. It also admits a qualitative, deterministic expression of Maxwell’s equations, the Schrödinger equation and the Dirac equation.
This naturally leads to a deeper understanding of Rowlands' fundamental parameters of space, time, mass and charge, and delivers new insight into our understanding of condensed matter physics. Most tellingly, the approach opens the way to conceptualising subatomic particles, such as photons and electrons, as real physical objects existing in 3D + 1 space rather than appearing as statistical probabilities in abstract 3D space.
Negative signed numbers can represent a variety of concepts depending on the specific context in physics. Sometimes, their meaning is ambiguous, and in quantum equations, the physical interpretation of these quantities can be uniquely challenging. One way to confer meaning to these ambiguous negative signed quantities is to express them in an expanded dimensional canvas.
In Part 1, a new approach showing considerable promise was introduced. Part 2 of this paper extends this approach. It was noted that positive and negative signed quantities seem to be built into the very fabric of the universe at subatomic scales. In consonance with Rowlands’ concept of totality zero, certain fundamental symmetries were shown to naturally admit an alternative explanation for conceptualising the shape and content of space at subatomic scales. The new approach posited that a pseudo Riemannian cobordism (PRC) of manifolds can describe the shape of space using an expanded nD + 1 space coordinate system. The advantage of this system is that it confers physicality on an otherwise abstract mathematical space. The revised shape of space admits physical content consistent with experimental findings in an altogether different way. Two particles – the fundamental particle of light analogous to the photon and the fundamental particle of matter, analogous to the electron, were described.
In Part 2, the structure and dynamics of two additional particles analogous to the proton and neutron will be described in a PRC. The topology of these particles provides compelling answers to certain questions that have long eluded quantum theorists. In particular, the structure and dynamics of particles analogous to quarks and their force carrying gluons can be described deterministically, and this offers significant advantages. The elusive reasoning that gives rise to the strong interaction, the property of confinement, and the origin of fractional colour charges can all be seen as inevitable consequences of the new understanding. This completes the cobordism manifold picture of subatomic particles that constitute the atom.
This new approach opens the way to reconceptualising protons and neutrons as real physical objects existing in 3D + 1 space rather than appearing as statistical excitations associated with an infinitely extensive quantum field in 3D space. This naturally leads to a deeper understanding of subatomic reality, the fundamental parameters of space, time, mass and charge, and delivers new insight into our understanding of condensed matter physics.
In the development of the theory, an approach with strict observance of the principles of physical reality, causality, and logical understanding is used. The main goals were clarifying the space-time nature of the physical vacuum, and identifying the physical models of stable elementary particles. The proposed physical model of the physical vacuum corresponds to the etheric substance predicted by the ancient Greek physicists Plato and Aristotle and maintained until the beginning of the 20th century, but a similar model has not been suggested before. It is a specific grid with oscillation properties made up of two types of sub-elementary particles with sizes in the scale about 1x10-20 (m) and called the Cosmic Lattice. The elements of the Cosmic Lattice are held by a Supergravitational Law (SG) which differs from Newtonian gravity in that SG forces are inversely proportional to the cube of the distance. Therefore, they are super-strong at the microscopic level. Their experimental manifestation is the attractive and repulsive Casimir forces between two bodies with highly polished surfaces. It is inferred that the sub-particles forming the Cosmic Lattice also build elementary particles as helical structures. Experimental results from particle colliders and in particular the characteristics of the first unstable particles such as pions and kaons and their decay were used to infer initially the shape of protons and neutrons. The narrow standard deviation of mass and lifetime of the pions and kaons lead to the conclusion that the protons and neutrons from which they emerge have some toroidal shape in which they are locked. Therefore, with a single cut, they come out with a very narrow standard deviation. From the additional decay of pions, it was inferred that the elementary particles are made of helical structures left-handed and right-handed, while handedness defines the sign of charge as a specific modulation of the Cosmic Lattice. The electron is a 3-body system of helical structures whose oscillation and rotational motion interact with the oscillating properties of the Cosmic Lattice and exhibit quantum mechanical features. The proton and neutron are with the same substructure but with different shapes. The proton is a twisted toroid like a 3-D Hippoped curve, while the neutron is double-folded. At the neutron, the electrical charge is locked by the SG forces at the near field, but in motion, it exhibits a magnetic moment. In the atomic nuclei, they are held by a balance between repulsive Coulomb forces and attracted SG forces. Using their shapes and following the building trend of the nuclei a complete match to the shape of the Periodic Table of Elements is obtained. Chemical valences, bond direction, and isotope stability are apparent. In theory, this is called the Atlas of Atomic Structures. The validation of the Atlas is supported by experimental results from 16 different fields of physics. The physical dimensions of the proton, neutron, and electron are identified.
The theory offers a hypothetical scenario for the creation of sub-elementary and elementary particles through a unique crystallization that takes place on the surface and surrounding of a superdense protomatter known as a black hole indirectly observed at the center of galaxies. This leads to a very different view of the universe and to an explanation of the serious inconsistencies with the Big Bang model. Instead of this single burst, it is concluded that galaxies have cycles of active existence and hidden unobservable phases of recycling and crystallization of elementary particles ending with the birth of a new visible galaxy with a new Cosmic Lattice. In such a case, the redshift of the galaxies appears not to be Doppler but of a cosmological nature as a result of a weak difference in their Cosmic Lattices, which depends on the individual mass of the galaxies. The theory was first published in 2001, cataloged in the National Library of Canada in 2002, and published as a book, scientific papers and reported in many scientific conferences.
SESSION: GlassMonPM3-R3 |
Oktik International Symposium (2nd Intl. Symp. on Sustainable Glass and Polymers Processing and Applications) |
Mon. 21 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Sener Oktik; Peter Simurka; Student Monitors: TBA |
This presentation will explore the innovative Research and Technology Development (R&TD) activities at Şişecam, with a particular focus on the significant contributions made during the tenure of Prof. Dr. Şener Oktik, who led the Şişecam Research and Technology Development Department from 2012 to 2020. Under his leadership, substantial advancements were achieved in research capabilities and the cultivation of a robust innovation culture.
Building on these advancements, at Şişecam, the integration of Innovation, Product Development Engineering, and Production Technology Engineering and Design are seamlessly integrated under one organizational structure. This unique approach has given Şişecam a significant competitive edge, enabling it to excel in the global market. A central focus of Şişecam's R&TD activities is the development of technologies that enhance the sustainability of both production processes and final glass products. As a material recognized for its inherent sustainability, glass presents significant potential for further innovation, and ongoing efforts are dedicated to exten these boundaries.
The 2023 estimate of global primary energy consumption is ~183 230 TWh (~108 billion barrel of oil equivalent) and the share of fossil fuels, renewable are 83%, 14% and 3% respectively [1]. The distribution of global primary energy consumption by sectors in 2023 can be given as an average of industry 33% buildings 33% transportation 30% agriculture 3% and others 1% [2]. After a 6% decrease d during the COVID-19 the annual carbon dioxide emission exhibited 1-2% increase reaching to a 37.5 Giga tons in 2023. . The top three sectors in CO2 emissions are reported to be electricity and heat (16Gt), transport (8 Gt) and manufacturing and construction (6 Gt) [3]. The simulations for 2050 of primary energy demand diverge significantly from ~53% increase from today’s value (high scenario) to only around 10% decrease (low scenario). CO2 emissions in 2050 follows a similar diverged pattern with values from over 45Gt to the net zero [4]. It is reported that 3% of global greenhouse gas emissions associated with activities related to the value chain of glass industries. It is estimated one tonne of glass recycling avoids approximately 580kg/ CO2 through the supply chain[5]. Reports on global glass productions in 2023 suggest that glass production capacity was 226 million metric tons [6]. Despite the recovery after economic slowdown related to COVID, the growths have been moderate with the highest increase in flat glass which was less than %0.5 from 2022 to 2023 [3,7]. The reports estimate the YoY global glass market growth of 15 billion $ between 2022 (220 billion $) and 2023 (235 billion $). Drivers of the relatively high growth of the global market for flat glass were innovations for product differentiations in different industries particularly in solar industries [8,9]. The glass sector continues to develop new ways to continue the improvements in sustainability, with research and development identifying clear options for manufacturers to secure their long-term futures and achieve net-zero emissions targets. Most of the glass manufacturing sector still relies predominantly on the combustion of natural gas, with up to 75% of energy consumption in glass production coming from the operation of furnaces. Biofuel offers a supplementary fuel option but is it not the long-term solution, as the long-term solution is likely to be mixed of energy such as renewable electricity, hydrogen and biofuel, depending on availability, sustainability and cost of the energy. Another key tool already employed and that is being continually developed by glass manufacturers to increase their sustainability is waste heat recovery technology. Pre-heating raw materials and recycled glass generally result in a 10-15% energy saving throughout the overall glass production process [8]. In this context, it is understandable that manufactures are seeking clarity on the availability and cost of electricity and hydrogen and other energy sources before making large investments. Along the changes. However, the appetite is clearly shared in the glass manufacturing industry to secure the long-term future for the production of one of the oldest materials in the world in new and innovative ways. [4,8]. Continuous improvement of the optical, mechanical, electrical and chemical properties of glass surfaces together with deposition technologies and functions supplied by passive and active layers on glass are leading an expected growth at a CAGR of 5.0% towards 2028 reaching close to 25 Billion$ [9,10]. Coated glass with soft or hard-coated low-e and solar low-e layers are the most popular products. Active or passive coating systems (smart coatings) in which the light and heat transmission/emission properties are modulated by applied voltage, light or heat intensity have been maturing for large volume commercial productions[11,12, 13]. The global market for smart coatings in construction and transportation sectors is predicted to be around ~9 billion $ in 2023 and expected to grow by CAGR of between 18and 20% to over 30 billion $ in by 2030[14,15]. This brief review is aimed to update the status of “What does the glass sector need to do “ in flat glass production and multifunctional coatings on glass towards net zero emission targets.
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SESSION: GlassMonPM4-R3 |
Oktik International Symposium (2nd Intl. Symp. on Sustainable Glass and Polymers Processing and Applications) |
Mon. 21 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Sener Oktik; Zhuoer Jiang; Student Monitors: TBA |
Weathering phenomena occurring during storage of tableware glasses with different chemical compositions were examined using Scanning Electron Microscopy (SEM) and Electron Diffraction X-ray analysis (EDX). The tumblers of different chemical compositions of tableware glass, crystalline type, were prepared in a small tank furnace. They were packed in paper boxes and placed in the warehouse. Samples were removed after 4 months, two years, and 4 years. The inner surface of the samples was analyzed with SEM and EDX. In addition, concentration profiles of the glass wall were measured using EDX. The comparison of the SiO2 change is discussed in connection with the glass weathering resistance of different glass compositions. The presence of large amounts of corrosion products, microcracks in the surface layer, and a significant difference in SiO₂ content between the surface and the bulk glass indicates low weathering resistance in glass with less than 1% Al₂O₃ and without ZnO, ZrO₂, or TiO₂.
Alongside many other industries, the glass industry is also a major CO2 emitter. With various approaches such as electric melting, hydrogen or ammonia combustion or post-processing measures such as CCS, the industry is driving forward the reduction of CO2 emissions to a more sustainable glass production. However, these efforts must be seen in the overall context, firstly because they are unlikely to be sufficient enough and implemented quickly enough to meet the global climate targets and secondly because they ignore a significant area of CO2 emissions which is the raw materials itself.
With a look at the glass industry in Germany, Europe and the world, the presentation will provide an insight into the various problems that arise when switching energy usage from the combustion of natural gas to hydrogen, ammonia or electricity. It will compare the potential and disadvantages of the various approaches and compare the cost of these technologies with the result.
Furthermore, as already mentioned, the general approach of switching to hydrogen-oxygen combustion or purely electric melting falls short when it comes to achieving greater sustainability, a reduction in energy consumption and, above all, a reduction in CO2 emissions. These approaches do not take into account completely CO2-free glass production, as a significant proportion of the CO2 still comes from the raw materials themselves, nor do they call into question the general approach to large-scale glass melting and therefore also the design of the melting furnaces.
The approach presented provides an insight into the development of completely CO2-free container glass production and shows the levers for achieving this. A concept for CO2-free glass production is presented. Key points such as melting kinetics and glass melting behavior in a modified combustion atmosphere, melting and shaping behavior of carbonate-free glass and the effect of furnace layout on space utilization are discussed.
Animal skin,as a natural polymer material with abundant sources,was used to make various leather items in early human society.Ancient books,archives,and other cultural relics made from them carry profound cultural value.Studying the internal structure of them can provide good theoretical support for the protection and inheritance of cultural relics[1].For example,artifacts such as parchment and Chinese shadow puppets that have not been tanned with tanning agents are called untanned hide artifacts.This system combined traditional production methods and modern processing techniques to study the performance changes of untanned hide during the production process.
The research method for untanned hide referred to IDAP(Improved Damage Assesment of Parchment)[2],and quantitative and qualitative measurement methods such as SEM and FTIR[3] were used to measure the effects of different pretreatment methods and chemical reagents on material properties.
The treatment methods for the samples in this study include saponification or emulsification reactions for defatting the raw skin,and adding different depilatory reagents, including alkaline reagents such as sodium sulfide or gastric protease,to the pretreated samples.
The analysis of infrared spectra in the study can reveal the effects of different chemical reagents on the peak shift of untanned Pete's characteristic,and SEM scanning can observe the changes in its intrinsic fiber configuration.The wet heat shrinkage temperature and stress-strain curve reflect the changes in its mechanical properties.
Vanadium nitride (VN) plays an important role in high-strength steel production due to the unique precipitation strengthening and grain refinement effects [1]. high-purity VN is widely used in the fields of advanced materials, batteries and catalysts since high electrical conductivity, high thermal conductivity and good chemical stability [2, 3]. The traditional method for preparing VN is the carbon thermal reduction method [4]. Nowadays, thermal processing precursor method is highly anticipated for preparing high-quality VN due to lower reaction temperature, simple process, and short production process [5]. This method includes two steps, which the precursors containing the shell of vanadium and core of carbon powders are formed and then the precursors are reduced and nitrided in the N2 atmosphere to obtain VN.
However, carbon powders are difficult to disperse in the solution uniformly owing to the huge surface tension and adsorption properties, and the precursors prepared subsequently are agglomerate. This is the main reason that the reaction is insufficient during the nitrogen reduction process, which affects the quality of VN.
In response to the above issue, Polyvinyl pyrrolidone (PVP) and the other two dispersants are used to optimize the structure of the precursors in order to prepare high quality VN. Under optimum condition of 1150 °C, the VN with nitrogen content of 17.94% is prepared by adding 5% PVP. When the reaction temperature exceeds 400 °C, the precursors of adding 5% PVP are easily converted to V7O13, V3O5, V2O3 and VN at the same temperature. The precursors of adding 5% PVP have lower Ea during reduction and nitration process, which are easier to be reduced and nitridated. In comparison with the process without adding dispersants, the addition of carbon powders is reduced by 9% and the nitriding time is decreased by 75%, which reduce CO2 emission, the energy consumption for generation and the production cost.
SESSION: LawsMonPM1-R4 |
Dibra International Symposium (4th Intl Symp on Laws & their Applications for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Minos | |
Session Chairs: Haruhiko Inufusa; Samuel Berger; Student Monitors: TBA |
Judicial systems around the world may be divided in two major groups: common and civil law system. Common Law systems are mainly used in UK, USA, Canada and the civil law systems are used in Europe and other countries. There are also countries or states/provinces that have mix systems like Quebec where criminal matters use mainly common law system and civil matters use civil law systems and in manty cases both methods of both systems are used interchangeably. A somewhat indirect product of the systems is the way that the judges are appointed or elected. In this paper a comparative analysis of both systems and their elected or appointed judges is carried out with all his advantaged and disadvantages.
Medical malpractice cases are inherently difficult for many reasons. First, the attorney that handles the case is not trained to analyze medical data, practices and procedures. Hiring a doctor to review a complex case is cost prohibitive and may prove unproductive for a number of reasons such as professional curtesy, looking at the case from the doctor’s prospective biases the opinion and findings of the doctor, and due to similar training and practices sees nothing wrong with the quality of treatment (i.e., every doctor has to see 50 patients a day to make extra money so we cut corners, we all do it so I can’t blame Joe).
A data scientist with a background in biology and working on medical applications becoming familiar with HIPAA, SOAP Notes, etc. can provide the technical background necessary to make the necessary findings and develop a case while not having any of the bad habits and ties to the profession. Also, a data scientist is trained to examine the all the data and find the relationships. In many ways the training makes them perfect for this specific kind of analysis. Data scientists also are trained to be methodical and detailed.
In the case of the wonderful Ms. Migen Dibra, having a data science background makes one well trained to analyze and assess all of the medical studies given to the FDA for the drug “label” approvals, which can be most revealing.
This lecture will cover these important subjects as well as go through the case of Ms. Migen Dibra who died prematurely.
In developed countries, medical care should not only provide standard treatment but should also take the patient's condition and needs into full consideration. This presentation will clarify the basic human rights of patients and their rights when receiving medical care, and make it clear that the attending physician should be held accountable when those rights are violated.
1. Second opinion
There is a standard treatment for malignant diseases in each country, but there are generally no significant differences among developed countries. The treatment of malignant diseases is constantly evolving, and there are effective treatment options that are not selected for standard treatment. If a patient requests a second opinion from a third-party institution, the attending physician is obligated to provide the necessary data. Conversely, if a patient obtains a second opinion from a third-party institution, the attending physician is obligated to respect and accept the second opinion. It is normal for the attending physician to consult with the patient regarding the difference in treatment and efficacy between the patient's treatment and that of the attending physician.
2. The right to optimal treatment of malignant diseases
Chemotherapy and immunotherapy for advanced malignant diseases may cause regression of the malignant disease itself, but when administered systemically, they also have significant side effects on other normal organs. Particularly in cases where malignant disease has invaded or metastasized to other organs, careful attention must be paid to the side effects. If the side effects are judged to be greater than the therapeutic effect, it is necessary to choose a treatment method with fewer side effects than chemotherapy or immunotherapy. In other words, patients have the right to receive a treatment that has fewer side effects and prolongs life.
As an oncological surgeon, I had worked at Kindai University Hospital (Osaka Japan) for 25 years. Ms. Migan requested me providing various examinations in Japan and treatment proposals for her malignant disease since August 2022. I found in medical record that there had been the fatal error in monitoring the disease, ignored second opinion, and the administration of the wrong chemotherapy / immunotherapy in November 2023 and February 2024. These were real evidence that violation of patient’s right. A monitoring system to ensure proper medical treatment for patients is needed in the medical community. Future legislation protecting the rights and interests of patients is also needed in the legal field as well.
To facilitate the sharing of medical and health information across jurisdictions, harmonizing related practices appears to be essential. It is highly likely that governments and legal professionals will consider establishing international treaties or agreements for this purpose. However, it remains questionable whether they can effectively harmonize the actual practices of medical and healthcare professionals.
A more practical and swift approach, suitable for jurisdictions with diverse personal information protection laws, would involve implementing measures that ensure the collection of evidence demonstrating prior and express informed consent, and the ability for patients and other data subjects to withdraw consent. These measures should also aim to minimize the burden on both medical and healthcare service providers and the data subjects. Furthermore, if these measures become de facto standards—and ideally evolve into de jure standards—they would help domestic courts recognize practices compliant with these standards as lawful.
To design measures that face less resistance across various jurisdictions, efforts should be made to minimize conflicts with existing personal information protection legislation. A key aspect of this involves maintaining a straightforward informed consent process. Typically, this process includes disclosing the scope and purpose of using certain personal information and securing either implied or express consent from the data subject. The author suggests reforms in the practice of obtaining informed consent for sharing medical and health data, recommending the use of a common ITC platform to provide information and secure informed consent.
SESSION: PharmaceuticalMonPM2-R4 |
Leuenberger International Symposium on Pharmaceutical Sciences and Industrial Applications for Sustainable Development |
Mon. 21 Oct. 2024 / Room: Minos | |
Session Chairs: Hans Leuenberger; Norbert Schwarzer; Student Monitors: TBA |
Interestingly, there are many unresolved mysteries. Thus, if the result of a pharmacological effect cannot be explained, it is most convenient to declare this fact as a “placebo effect”! In Germany a comprehensive Acupuncture study showed to be effective [1], however, skeptical scientists [2] pretend that these Acupuncture results have fallen under the “placebo effect”. This statement is irrelevant to those that have been healed. It is important to strengthen the “Placebo Effect” instead of using opioids [3]! The focus of this contribution is to develop different hypotheses to explain the mystery of the placebo effect! Is the placebo effect a physical resonance effect of the human body with the drug substance if both systems can be described by an Einstein - Debye model of harmonic oscillators? Is the cause of the Placebo effect the human propensity of self-healing which can be triggered by methods such as Tai Chi, the Nishino Breathing Method, by Qi Gong and by other methods such pleasant music, vibrations, pleasant figures, shapes, pleasant environment such as healthy power spots at sacred sites i.e. places of worship such as monasteries, temples etc. Interestingly, such power spots can be detected by experienced and talented dowsers. In this context, dowsing and the search for water, applied kinesiology [4] also is considered as pseudoscience, and part of alternative medicine. However, it is difficult to explain why sensitive dowsers and practitioners in kinesiology using “muscle testing” instead of a “pendulum” as instrument for dowsing usually agree in testing the positive effect of supplements, drugs or food. Hahnemann realized that the more he diluted a substance dissolved in water the pharmacological effect became more pronounced, even in the case that due to the continuous dilution statistically no molecule of the active ingredient is present. This incredible phenomenon leads to the conclusion that homoeopathy [5] is a pseudoscientific system. However, five reasons are mentioned, why homeopathic preparations were reported to be successful: 1) placebo effect; The therapeutic effect of consultation; Unassisted natural healing [5]; Unrecognized treatments; Regression towards the mean [5]. This long list leads to the tentative conclusion that homeopathy seems to be effective. Modern advocates of homeopathy have proposed the concept of “water memory”, according to which water "remembers" the substances mixed and transmits the effect when consumed. In 1988, Jacques Benveniste published a paper in the journal Nature while working at INSERM supporting the idea of Hahnemann. However, he was forced to withdraw his paper against his will. Interestingly, Nobel Laureate Luc Montagnier, who was credited with identifying the AIDS virus, subsequently took up Benveniste's work on water memory. He and several other scientists claimed to have successfully replicated Benveniste's experiments. Thus, additional research is needed so that Hahnemann’s work is officially recognized. Hypnotic medicine describes the use of hypnosis in psychotherapy. Unfortunately, the efficacy of hypnotherapy is not well supported by scientific evidence. Hypnotherapy was used to sedate a patient before surgery. Interestingly, there is evidence of hypnosis in ancient cultures. Galenic Pharmacy was originally describing Pharmaceutical Technology according to Galen (born in 131, in Pergamon, Greece. Galen was a physician, pharmacist, natural scientist, nutritional scientist and philosopher. The remedies of Galen did not consist of a single substance but of a combination of different herbs and other products like the contemporary Traditional Chinese Medicine (TCM). The efficacy of the Galen recipes included remedies against human poisons since the emperors were interested in their chance of surviving poisoning. TCM also is considered as alternative medicine. Humanity needs to realize that there is a close correlation between a healthy and a peaceful society. Nations at war lead to a sick society and to collateral damage. The World Health Organization, WHO, takes care of a sustainable global/planetary health system. In this context, it makes sense that WHO also takes care of a sustainable peaceful world. Ideally such a peace initiative should be proposed by the 2024 SIPS summit and supported by Nobel Laureates attending this SIPS summit in Crete. Will computational science and Artificial Intelligence close the gap between the exact natural sciences, the technological sciences and the humanities/social sciences and lead us to appreciate the knowledge of ancient cultures? Can we stimulate open mindedness, transdisciplinary sciences, love for peace and tolerance under the umbrella of a strict ethical Codex?
It was not easy to find detailed information on the life of Nicolas of Flue such as the book1 “Brother Klaus, Man of Two Worlds” by Christina Yates. She was educated at a Quaker co-educational Boarding school in Somerset, England. In Geneva, Switzerland, she worked from 1926-1927 at the Friends International Centre established during the early years of the League of Nations, today: United Nations. Quakers2 were known to refuse to participate in war, to swear oaths and were opposed to slavery. Anabaptists also refused to participate in a war being prosecuted by Catholic and Protestant authorities. In this context, the father of Niklaus Leuenberger3, head of the peasant revolt in 1653, was also an Anabaptist.
In 1947, in recognition of their dedication to peace, Quakers1 were awarded the Nobel Peace Prize. Quakers2 introduced the Bill of Rights to the U.S. Constitution, trial by jury, equal rights for men and women, and public education. From 1953 - 1970 Christina Yates was teaching English at the Ecole d’Humanite following Paul Geheeb’s educational principles4 in the Bernese Oberland. During this time, she spent several years studying extensive French and German literature on the life of Nicolas of Flue. Her book consists of 4 parts, describing his “Life” (I), citing “Eyewitnesses” (II), describing “The Other Dimension” (III) and “Brother Klaus Today” (IV). Part III is related to the Man of the Two worlds: Klaus, he has experienced war, -brutal hand to hand combat with pike and lance - as brave soldier being promoted to the rank of a captain, he also sat on the bench with magistrates accepting bribes. Knowing the deficiencies of his own community, he suffered from depression until he retired as hermit in a wooden shack in the Ranft close to his former home. Brother Klaus had several visions triggering the curiosity1 of C.G. Jung (Carl Jung - Wikipedia). Christina describes the controversy regarding the incrediblefasting of Brother Klaus, since the local people wondered if he was receiving food secretly. Albrecht von Bonstetten, a nobleman, describes Brother Klaus as of “low birth” since he had no higher education. Thus, Klaus needed the support of Brother Ulrich1 for writing letters to authorities. Ulrich was an educated man, who established in an “arrow shot” distance1 his own hermit cell. Thus, Brother Klaus was happy that his youngest son enrolled as student at the University of Basel.
The differentiation between noble families and free people evolved only later, since the noble family “von Schweinsberg - Attinghausen” (https://en.wikipedia.org/wiki/Schweinsberg_Castle) of the Canton of Uri and Bern sided with the free farmers playing an important role in the foundation of Switzerland. The birth of the concept of the “armed political Swiss neutrality” can be summarized with the following statements1 by Brother Klaus: “O dear friends, don’t make your fence too wide, the better to remain in peace, calm and unity in your honorable and hard-won liberty. Don’t burden yourselves with foreign affairs, don’t join up with foreign rulers, guard against dissension and self-seeking. Protect your fatherland and cleave it to it. Do not foster intentional love of fighting, but if anyone attacks you, then fight bravely for freedom and fatherland”. Edgar Bonjour‘s extensive work consists of nine volumes on the history of the Swiss neutrality5. A sustainable healthy world only can be realized in the case of peace. Thus, the author of this abstract supports the idea of Prof Marcel Tanner that the World Health Organization (WHO) also addresses a peaceful planet thanks to the creation of the WHO Peace Initiative by using the tools of the International Council of Harmonization by establishing a special ICH-EPC team7 with the goal of Easing and Preventing Conflicts (EPC).
There are more and more approaches to try and understand the world of feeling such as love, hate, fear, anger and so on plus consciousness in general, sub- and un-consciousness via quantum concepts. A standard drawback to such attempts seems to result from the old problem that our current quantum theory is not of metric origin or – in other words – does not appear to be fully compatible with Einstein’s General Theory of Relativity [1]. This lack of a true Quantum Gravity Theory does seem to be the major obstacle for all our attempts to understand consciousness. After all, it well could be that our feelings and consciousness in general, potentially embedding both quantum and cosmic scales, require a truly scale invariant and thus, metric theory.
In order to overcome these difficulties, we explicitly tried to avoid to “push” any existing theory into the comprehension of the human mind and all its derivatives but, instead, started our consideration with the assumption that everything, including consciousness, may consist of attributes or properties. Subjecting these properties to a general Hamilton extremal principle, thereby using the Riemann theory and Hilbert techniques, we – most surprisingly – ended up in generalized Einstein-Field-Equations [2, 3, 4]. These equations do not only contain the full Theory of General Relativity [1], but – lo and behold – also include all main quantum equations, be it for bosonic or fermionic entities. The whole ensemble undoubtedly has the characteristics of a Quantum Gravity Theory and the best part of it is, that it was already there for about 109 years [5].
In this talk, we are going to apply our approach onto the interesting field of love and the topic of feelings in general [3, 6]. Thereby, we will not only consider the aspect of feelings of an individual but also investigate phenomena coming into play where ensembles of human beings entangle. This reaches from observations of so-called mass formations to the simple question whether an economic entity - a company - can be good [4]?
There are more and more approaches to try and understand the world of feeling such as love, hate, fear, anger and so on plus consciousness in general, sub- and un-consciousness via quantum concepts. A standard drawback to such attempts seems to result from the old problem that our current quantum theory is not of metric origin or – in other words – does not appear to be fully compatible with Einstein’s General Theory of Relativity [1]. This lack of a true Quantum Gravity Theory does seem to be the major obstacle for all our attempts to understand consciousness. After all, it well could be that our feelings and consciousness in general, potentially embedding both quantum and cosmic scales, require a truly scale invariant and thus, metric theory.
In order to overcome these difficulties, we explicitly tried to avoid to “push” any existing theory into the comprehension of the human mind and all its derivatives but, instead, started our consideration with the assumption that everything, including consciousness, may consist of attributes or properties. Subjecting these properties to a general Hamilton extremal principle, thereby using the Riemann theory and Hilbert techniques, we – most surprisingly – ended up in generalized Einstein-Field-Equations [2, 3, 4]. These equations do not only contain the full Theory of General Relativity [1], but – lo and behold – also include all main quantum equations, be it for bosonic or fermionic entities. The whole ensemble undoubtedly has the characteristics of a Quantum Gravity Theory and the best part of it is, that it was already there for about 109 years [5].
In this talk, we are going to apply our approach onto the interesting field of love and the topic of feelings in general [3, 6]. Thereby, we will not only consider the aspect of feelings of an individual but also investigate phenomena coming into play where ensembles of human beings entangle. This reaches from observations of so-called mass formations to the simple question whether an economic entity - a company - can be good [4]?
SESSION: LawsMonPM3-R4 |
Dibra International Symposium (4th Intl Symp on Laws & their Applications for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Minos | |
Session Chairs: Berin Romagnolo; Shinto Teramoto; Student Monitors: TBA |
Businesses, governments, and individuals have significant immigration needs in the global economy. But they have competing interests. Businesses are desperate to find the most talented human resources and most lucrative markets, and individuals are desperate to find the most rewarding employment and environments for themselves and their families. Governments desire to attract the greatest talents and increase economic activity while also protecting its local workforce. Is it possible to balance their interests and have everyone’s core needs met? Is it possible to achieve justice for all?
Foreign entrepreneurs and international businesses must have routes to establish and operate businesses in new global markets, generating revenue and offering employment opportunities locally and globally. Individuals need feasible ways to obtain visas in a timely manner to accept global employment assignments and to establish themselves in new settings. Countries must develop realistic and reliable paths for foreign experts and workers to establish and build businesses in order to drive research and innovation, and to solidify their strength and place in the global economy.
This session will explore the competing interests and encourage a lively discussion regarding paths to meet the needs of all those involved.
Therapeutic Jurisprudence (“TJ”) is an approach to law which highlights “wellbeing” as an important component of the legal system [1]. Inspired by an excellent article by Harmony Decosimo at Suffolk University[2], the aim of this paper is to prove that applying law in a TJ manner is a simple and “ready to use” tool to fulfill the revised ABA Standards for the development of a professional identity in the legal profession [3] that state that: “Professional identity focuses on what it means to be a lawyer and the special obligations lawyers have to their clients and society and that the development of a professional identity should involve an intentional exploration of the values, guiding principles, and well-being practices considered foundational to successful legal practice”. To this purpose we will present a set of TJ legal values creating the “lens” through which professionals can apply the law in a “better and more fulfilling way” and a collection of examples of different legal roles that can give tangible ideas of professional identity formation.
The concept of sustainability has been somehow politized in terms of unilaterally extracting it from its core basis. Following the definition of FLOGEN Sustainability Framework the 3 criteria of sustainability that must be reached simultaneously are economic growth, environmental protection, and social development. As per this definition there are 3 factors that can help or hinder sustainability: Science and Technology, Governance and Management and education of civil society. In this paper a depoliticized sensible approach to a balance in environment and energy considerations of sustainability will be presented, depoliticizing its concept.
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As the global community grapples with the escalating challenges posed by climate change, the imperative to mitigate carbon emissions becomes increasingly urgent. Carbon capture and storage (CCS) technology stands at the forefront of climate solutions, offering a transformative approach to reducing carbon dioxide (CO2) emissions from industrial processes and energy production. This paper delves into the multifaceted world of CCS, exploring its pivotal role in addressing climate change and fostering clean energy transitions, integrating hydrogen technology as well.
The global push for reducing carbon emissions has highlighted CCS as a key technology. Greece, with its commitment to sustainable development, is making significant strides in this area. This paper aims to examine Greece's contributions and initiatives in advancing CCS technology, focusing on technical challenges, legal frameworks, policy recommendations, economic and regulatory incentives, and innovations in CCS technology. The study employs a comprehensive review of technical advancements, legal documents, policy papers, and economic analyses. It also incorporates interviews with experts and case studies of successful CCS projects in Greece.
By investigating Greece’s role in advancing CCS and its collaborations on the European stage, this paper underscores the significance of CCS as a critical tool in combating climate change. Greece’s proactive engagement with experts, alignment with EU directives, and establishment of a robust legal framework position it as a leader in CCS advancements within Europe and on the global stage. As CCS technology continues to evolve, it remains a beacon of hope in the collective efforts to secure a sustainable and greener world.
SESSION: LawsMonPM4-R4 |
Dibra International Symposium (4th Intl Symp on Laws & their Applications for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Minos | |
Session Chairs: Mariadina Lili-Kokkori; Student Monitors: TBA |
This paper explores how disputes are being channelled, gradually with the support of technology, to a menu of dispute resolution options, which for civil cases often favour non-binding processes that enable an amicable settlement prior to exploring a more costly, confrontational, and formal adjudicative process. Accordingly, this paper first examines how Dispute System Design seeks to identify the most suitable dispute resolution option, contributing to a greater variety of process pluralism and improving dispute prevention to avoid unnecessary escalation. Secondly, it examines how (English) courts and Alternative Dispute Resolution (ADR) processes steer disputants towards informal settlement options. Thirdly, the paper discusses how dispute resolution providers are leveraging data and technology to increase access and provide greater efficiency in the dispute resolution process. Lastly, the paper argues that as the number of litigants in person increases, there is a growing risk of alienating those who need the most protection from the civil justice system, thus adequate safeguards ought to be incorporated to prevent weaker parties from receiving second-class justice.
This paper reviews the largest marketplaces from the Dark Web, which have become a haven for illegal activities—ranging from drug sales to cybercrime—and unearths their dispute avoidance and resolution mechanisms that aim to increase trust in these dark markets. Illegal trading on the Dark Web owes its success from the enhanced security and transparency as well as for effective dispute resolution processes, which are unreviewable by traditional courts. The dispute system design of these processes include anonymity, informality, user-support, community involvement in decisions, adherence to transaction terms and dark market rules, encrypted communications, and blockchain-based enforcement. While these processes lack due process guarantees and are often skewed towards experienced vendors, they are very effective, transparent, and incentivise parties to settle. The paper discusses the adaptability of civil justice principles in these unregulated digital spaces, which ironically undermine the rule of law by fostering trust in illegal transactions and offers insights into how these innovative processes can inform the development of more robust online dispute resolution systems within the legal system.
The lack of Ethics in the academic world is a serious problem. The criticism of Jonathan Swift in Gulliver Travels (1726), is still valid [1]. In this sense, we remain in middle age. This is not the only obsolete thing nowadays: In the year 2000, The Roman Right of Roman Emperors is still used. Arminius revolt [2] was against the Roman code of laws, essentially. Maybe what makes the Roman ridiculous is the punishment system: jail for everything. The time of jail varies since 1-2 days to entire life. Also signing a confession (even if innocent) may result in condemnation.
Criticizing the authorities is always a risky task: Galileu Galilei was incarcerated for defending that the Earth orbits the Sun (and not the inverse). To avoid trouble, Copernicus asked to have his book published after his death. Criticizing “authorities” always is a risky task, because then “authorities” are no longer “authorities” and lose their political power, money and other assets.
In the 20th Century Cecilia Payne was forced to change her conclusions in her PHD Thesis [3]. No Nobel Prize to her! By another hand, influential people are able to publish wrong papers. Everett was advised by John Weller [4], a very influential figure in the politics of Physics. Thus, the Many World hypothesis [4] was published (but it obviously violates the principle of conservation of energy!). Such absurd papers are published and can receive large number of citations. By another hand, Oliver Heaviside also almost was banned from scientific life [5]. No Nobel Prize for him!
There are Lobby for some authors. Thus, be careful about “invited papers”, which may even admit completely wrong ideas! The two more relevant corrupt issues are the “networking” and the Ponzi scheme. Correct papers are rejected, whereas wrong papers are accepted and even published several times. Editors and Referees are “rigorous” with some authors, and lenient with others. The Ponzi (or pyramid) scheme makes that the PHD candidate always have to confirm the thesis of the advisor.
Here it is discussed on how we can escape from such corrupt system. The Fourier series were presented in 1807, but Poisson, Legendre and others denied its publication [6]. Soon after Fourier published a book (by his own) in 1822, Fourier was elected for the Royal Society [7] (but 15 years were missed)! Conclusion: The soapbox oratory is the ultimate solution [8].
Climate change has a major impact on human rights and is a global pressing issue. Yet, several gaps remain as to the obligations of states and other stakeholders in light of the climate crisis. It is thus unsurprising to observe the current trend to turn to international and regional tribunals to interpret or clarify the scope and content of rights and obligations in relation to climate change. The interconnection between human rights principles and climate change are clear, from ensuring accountability and an effective remedy, to preventing the negative impact of climate change on the enjoyment of human rights. Against this background, this presentation will explore the diverse links between human rights and climate change, specifically in relation to mitigation, adaptation and remedying climate change harms. First, the paper will focus on exploring the impact of human rights on climate action. It twill then dwell upon exploring the initiatives in the international scene, from regional courts to United Nations bodies, which clarify the rights and obligations relating to human rights and the climate emergency. Finally, the paper will analyse the right to an effective remedy in relation to harms caused by climate change.
SESSION: MineralMonPM1-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Mon. 21 Oct. 2024 / Room: Lida | |
Session Chairs: Georgios N. Anastassakis; Vladimir Andric; Student Monitors: TBA |
The following personnels will give a welcoming speech to Anastassakis International Symposium:
Following a brief description of the background, a life timeline of industrial and scientific activity for 35 years will be presented. First, there will be presented the scientific work done, experiences gained and memories of working for 2 years as engineer in LARCO GMM SA Ferronickel Company.
The scientific activity at National Technical University of Athens (NTUA) will follow along with the scientific achievements, the experience gained as visiting researcher in Columbia University, evaluator of the Research Excellence Center of MiMer, member of Scientific Bodies and Committees in the field of Mineral Processing, etc.
The establishment during thirty-five years as professor, researcher and Scientist of many collaborations with the best universities and professors in the world and lifetime lessons will be presented.
Global competition for resources will become fierce in the coming decade. Dependence on mineral raw materials may soon replace today's dependence on oil. The EU's ambition to become the first climate-neutral economy by 2050, and its ability to sustain the green and digital transition and achieve strategic autonomy, all rely heavily on reliable, secure, and resilient access to raw materials. The European Commission defined strategic and critical raw materials based on objective criteria including their economic importance and their supply risk (CRMs). In an important move to secure the supply of essential raw materials, the European Critical Raw Materials Act (CRMA) entered into force on 23 May 2024, introducing the concept of strategic raw materials (SRMs), which are key for some strategic technologies and vulnerable to shortages and setting specific ambitious benchmarks for extraction, processing, recycling, and supply diversification through strategic partnerships with mineral rich countries for 2030. Greece is a EU country with a significant mineral resources in terms of quality, quantity and variety of ores, minerals and aggregates. Also, there is satisfactory legislation framework, funding opportunities and a political support to start and implement investments in the sector. Greece’s mineral potential is largely contained in State-owned areas and includes resources with CRMs. Our strategic goal is to unlock the existing mineral potential and reform the Greek mining industry. The national steps for raw materials sector according to MOEE΄s action plan 2024 and EU CRMA are described in detail.
Based on recent studies, the Greek Mining Industry has an important contribution to the Greek Gross Product, providing a competitive advantage for the Greek economy, and supplying raw materials that are key prerequisites for important economic-industrial activities as well as raw materials necessary to the EU economy and international market.
It possesses a remarkable share to the reduction of the dependence of EU economy from imported raw materials and an important role to the country’s exports. The contribution of the Greek Extractive Industry to the employment, especially in the province is a noteworthy fact.
Some of the ores and minerals produced in Greece are highly ranked at international level. Just to mention some:
Magnesite: larger exporter in Europe
Perlite: 1st world wide
Bauxite: largest producer in Europe, key for the remarkable national aluminum industry
Bentonite: 1st in Europe, 2nd world wide
Marble: Global leader, famous for its quality
Concerning the future:
Greek Extractive Industry has the potential to increase its share to the Greek GDP from 3% today to 7%, thanks to the variety of ores and minerals existing in the country and their significant reserves.
Additionally, the existing potential of Critical Raw Materials Act (CRMA) is expected to provide the country with a comparative advantage and economic benefits. As a proof:
Finally, concerning the green transition, specific exploration research is on progress aiming at the discovery of suitable geological formations to ensure appropriate Carbon Capture Utilization System (CCUS) installation.
SESSION: MineralMonPM2-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Mon. 21 Oct. 2024 / Room: Lida | |
Session Chairs: Georgios N. Anastassakis; Eirini Evangelou; Student Monitors: TBA |
This study presents the primary results from field campaigns conducted in the Messara Basin, Crete, emphasizing the hydrogeological conditions and sustainability challenges in the region (Pictures 4-14). Geological maps at scales of 1:50,000 and 1:200,000 (Pictures 1-2) were foundational in understanding the basin’s geological framework and were used for hydrolithological classification, providing a detailed analysis of the hydrolithological characteristics linked to the region's geological features. Groundwater levels in the basin exhibit significant seasonal variations, largely due to over-exploitation for irrigation, raising critical sustainability concerns. Effective groundwater management requires systematic data collection and precise utilization of primary data (Picture 3). Despite the involvement of various authorities in localized groundwater management, the absence of a comprehensive, large-scale framework hinders the creation of a detailed master plan. Addressing this gap necessitates systematic fieldwork aimed at delineating the boundaries of groundwater systems.
The lack of a detailed hydrogeological map complicates the management of the region’s essential groundwater resources, which are crucial for irrigation. Changes in groundwater head were studied, identifying areas of generalized groundwater depressions, with maximum changes analyzed from May 2021 to October 2023 (Pictures 6-10). Additionally, data from the European Ground Motion Service (EGMS) were analyzed to detect induced land subsidence in the basin (Pictures 11-12). These findings were combined with areas of groundwater depressions for further investigation. The recent poor hydrological conditions over the past four years have exacerbated the sustainability crisis, posing significant economic and social challenges to the future of the Messara Basin.
The world is couming bulimically raw materials and the demand for metals skyrockets. Securing raw materials, processing industrial minerals, enabling higher recycling rates targeting zero residuals production, utilizing advanced manufacturing techniques together with established mass production and forming methods, tailoring materials and alloys to service conditions, mastering extreme environments set the prerequisites for the ongoing shift, both digital and green. Hence, raw materials, recycling, metals and alloys tailored to even the most extreme conditions underline today’s importance in the geopolitical chess board. At the same time, the 4th industrial revolution affects also the minerals industry value chain. All these challenges bring the School of Mining & Metallurgical Engineering (SMME) again at the epicenter of academia and industry. Dedicated to actively addressing societal needs through the lens of sustainability, responsible resource management, and a profound respect for local communities, the SMME adapts to these challenges and prepares future leaders in the field.
Xanthates is a family of highly efficient collectors, widely used in the industry of sulphide minerals flotation, which, however is considered toxic and hazardous to the environment, and can pose significant risks to aquatic life and human health. The need for its replacement by other more environmental friendly reagents is of vital importance towards a more sustainable extractive industry.
Organosolv lignin is natural, biodegradable material that possesses a low carbon footprint compared to the conventional reagents. The study investigates the potentiality of the use of organosolv lignin as collector in the flotation of metalic sulphide minerals (sphalerite, pyrite/arsenopyrite) from greek mixed sulphides. Critical parameters under investigation was the collector dosage and composition, while the efficiency of the collector formula was evaluated according to the achieved selectivity, grade and recovery. To simulate and evaluate the performance of the optimum formula under realistic operating conditions, locked cycle flotation tests were carried out and the results are discussed.
The generation of WEEE in Europe has been increasing steadily over the last decades and is expected to reach 14 million tonnes by 2021. Its composition, although highly dependent on the type of equipment treated, consists of a significant amount of plastics, ferrous and non-ferrous metals, and a small but relevant amount of precious metals and so-called rare earths. The recovery of valuable materials from WEEE is of particular interest due to the different legislation in place and the high concentration of WEEE, which is, in many cases, higher than that of primary ores. WEEE treatment and recovery lines start with manual sorting of easily identifiable equipment or components, followed by a shredding process to reduce the particle size and release the components. This is followed by physical concentration processes focused on the recovery of materials, the by-product is a plastic material with heterogeneous granulometry. The finest fraction of this plastic by-product contains relevant concentrations of different metals, whose concentration depends on the efficiency of the treatment plant. In the case of the treatment plan studied, these concentrations were approximately 33.0 g/kg of aluminium and 28.8 g/kg of copper.
The present study raised the possibility of generating a secondary treatment line, based on densimetric and gravimetric treatments to achieve the recovery of these valuable metals under the following perspectives: the generation of a dense product of metal concentrate and the obtaining of a light plastic waste that can be used as a by-product.
The first approach developed for this treatment was based on the direct use of a wet shaking table as a simple but precise gravimetric treatment. The results obtained after the setting of its operating parameters based on both technical manuals and the equipment operator's own experience showed a metallic concentrate product with aluminum and copper concentrations of 250 g/kg and 360 g/kg respectively and valuable yields of 15% for aluminum and 50% for copper. An intermediate-density product with potential for aluminum recovery (concentration of 100 g/kg and valuable yield of 50 %) was also observed. By the visual study of this treatment, it was observed that a large percentage of the wet shaking table classification surface was focused solely on the classification by density of the plastic fraction, which, in comparison with metals, has very low densities generally not exceeding 2.00 g/cm3.
Based on this assumption, a preliminary material roughing treatment was proposed that would allow the precise recovery of plastics according to their density and, on the other hand, allow the vibrating table to work with a better quality material for separation. For this roughing process, the LARCODEMS dense media separator was used with two cutting densities, 1.00 g/cm3 (using water) for the precise recovery of light plastics suitable for energy recovery and 1.33 g/cm3 (using a calcium chloride brine) for the separation of the majority of plastics, minimizing the loss of valuable metals that could be encapsulated in the plastic material. After this pre-treatment, the pre-concentrated product would be placed on the vibrating table. The results obtained show that after the two roughing processes, the material to be treated was reduced to 26% of the raw material, obtaining a concentrated metallic product of 315 g/kg aluminum and 490 g/kg copper, with a valuable yield of 37% and 66% respectively. The intermediate density (aluminium-rich) product improved its properties with a concentration of approximately 230 g/kg and a recovery of 44%.
The results obtained show how the roughing process prior to concentration significantly improves the operation of the shaking table. The results obtained after this process show an improvement in the concentration of aluminum and copper of 25 and 35% respectively and their recovery of 145% and 32% respectively. Finally, the material recovered after first roughing, with a density of less than 1.00 g/cm3, can be used for further energy recovery.
SESSION: MineralMonPM3-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Mon. 21 Oct. 2024 / Room: Lida | |
Session Chairs: Vladimir Andric; Vasiliki Dova; Student Monitors: TBA |
Ferrous ores play a remarkable role in the development of human activities, over the decades; iron is of the most common and crucial elements in construction field; from household appliance to automotive and aerospace equipment [1-2]. This statement is highly supported, by the fact that the iron content in ferrous ores has been diminished throughout the years. With that being said, it was considered of high importance to explore new physicochemical methods of separation and recovery of pure iron from hematite ores with significantly low percentages in iron [3].
In this scientific paper, the separation and recovery of fine iron particles from artificial mixtures of hematite and limestone is being studied, as the demand for iron has become more and more imperative. Limestone is met in great percentages in hematite ores as gangue mineral, which led to its usage in the artificial textures. Sodium oleate and dodecylamine are used as collector reagents in the testing procedure.
The testing procedure includes preliminary tests in single minerals, in order to define the most effective operation points of the aforementioned mixture (pH, collector dosage, conditioning time). Afterwards, hematite and limestone are both subjected to flotation tests separately, in order to determine their behavior, in presence of sodium oleate and dodecylamine, as collector reagents. The results are really promising, as hematite’s recovery is particularly high; 84.5% and 93.5% using sodium oleate and dodecylamine, respectively. On the other hand, limestone in single-minerals tests has remarkable behavior, as the usage of sodium oleate leads to 93.5% recovery; while 98.5% recovery is achieved by using dodecylamine as collector reagent.
Over the last five decades, nearly 6 million tonnes of oil have contaminated our oceans solely from tanker spills, according to Ritchie et al., 2022, posing severe environmental and economic risks. Despite the development of various methods to contain oil spills, even advanced technologies have limitations associated with environmental and economic factors. Conventional cleanup methods face limitations, such as smoke production from in situ burning and dependency on calm seas for booms and skimmers. Oil absorption using industrial minerals, like perlite or bentonite, although cost-effective still poses challenges regarding collection and treatment of the remaining product and byproducts. The proposed innovative solution integrates perlite absorption with bioremediation methods, by utilizing an inorganic carrier acting as a “living sponge”, hosting oil-degrading microorganisms. Perlite’s lightweight and buoyant nature, enhanced by bioremediation functionalities, allows it to float on water and facilitate easy deployment, making it reliable for immediate oil spill response, resulting in non-toxic residues, while supporting global sustainability goals by preserving marine ecosystems and promoting economic competitiveness.
The lead complex of benzohydroxamic (Pb-BHA), as an effective collector, has realized the mixed flotation of wolframite and scheelite to a certain extent. The Pb-BHA complex can be adsorbed on the surface of wolframite and scheelite by bonding with the O on the surface of tungsten minerals through the lead ion in the structure. However, current research cannot explain the detailed difference between wolframite and scheelite in flotation behavior and kinetic, and it is of great significance for the design of corresponding reagents and the development of efficient flotation flowsheets in actual ores. In this paper, the flotation behavior and kinetics of two tungsten minerals under the Pb-BHA system are systematically studied. The flotation rate constant K for scheelite(0.20) is higher than wolframite(0.16), which is the reason why the tungsten minerals lost in the actual tailings are mainly wolframite. Subsequently, the internal reasons for the difference in their flotation behaviors are analyzed through adsorption experiments, solution chemical analysis, and quantum chemical calculation. The quantum chemical calculation showed that the ΔE(|EHOMO(mineral)-ELUMO(Pb-BHA)|) for wolframite is lower than scheelite but the adsorption capacity of Pb-BHA on scheelite surface is higher than wolframite. The contradiction is further explained by the different interaction characteristics between water molecules and mineral surfaces. The pre-hydration degree of two tungsten mineral surfaces affects the adsorption of Pb-BHA, further influencing the hydrophobicity of the two mineral surfaces.
The main purpose of this paper is to investigate the existence of super cycles, i.e. long waves, in global energy production and consumption between 1900 and 2016. The statistical data indicate the presence of long waves in global energy production and consumption between 1956 and 1999. According to the econometric estimates, the peak of the cycle is in 1975, immediately after the 1973 global oil price shock. If the paper's econometric estimates are statistically valid, one might expect another super cycle in global primary energy production and consumption between 2000 and 2043, with the peak of the cycle occurring around 2020. In addition, policy makers and other stakeholders in the energy sector could utilise the results of this paper in forecasting future global energy supply and demand. To generalize the findings of this article, potential avenues for further research include broadening the analyses for specific energy products, most notably coal, oil and natural gas.
SESSION: MineralMonPM4-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Mon. 21 Oct. 2024 / Room: Lida | |
Session Chairs: Irineu A.S. de Brum; Georgios N. Anastassakis; Student Monitors: TBA |
The continuous rapid growth in the use of lithium-ion batteries (LiBs) for electric vehicles (EVs) and portable electronic devices has resulted in even increasing demands for lithium and other metals related to their production. This, in turn, has led to the generation of continuously increasing and alarming number of spent LiBs. [1] Spent LiBs contain heavy metals like cobalt, nickel, and manganese, thereby posing a significant environmental hazard if not managed accordingly [2]. However, these metals along with lithium are considered valuable and their recovery is deemed beneficial. Recycling of spent LiBs helps minimize pollution from their toxic components, while simultaneously recovering the contained valuable metals. [3] This paper provides a comprehensive view on the current state of LiB recycling technologies for recovering valuable metals, highlighting the strengths and weaknesses of each approach in terms of efficiency and feasibility. Specifically, pyrometallurgical and hydrometallurgical processes, as well as direct recycling [4] are thoroughly discussed and evaluated, addressing problems and challenges. Moreover, the current and future market trends and regulatory landscape will be presented and examined. Additionally, recent advancements and prospects in the field are discussed.
Copper is one of the most demanded minerals by the global industrial sector, with approximately 20 million tons mined worldwide each year. Silver, another important technical and precious metal, sees production around 26 kt/y. The general trend of declining average grades in these deposits has made mining low-grade ores a reality for many mines worldwide. The sensor-based sorting has emerged as a significant pre-concentration solution for these cases. This study investigates the applicability of this technique to copper ore samples from the Cerro do Andrade deposit, located in Caçapava do Sul, southern Brazil. The primary product of interest is copper (Cu), with silver (Ag) as a by-product. Pre-concentration tests are ongoing at the UFRGS Mineral Processing Laboratory (LAPROM) using a dual-energy X-ray transmission (DE-XRT) sensor sorter. Were analyzed 32 ore samples (64-16 mm size fraction). Relative density histograms and false-color images were generated. This data, along with Cu and Ag grades, was assessed in Excel to estimate recoveries (metallurgical and mass), concentration factors, and Cu and Ag grades in tailings fractions. Some scenarios of tailings generation and reuse were also explored. The analyzed samples had an average of 0.83% Cu and 7.31 g/t Ag. Pre-concentration simulations yielded Cu grades in the product ranging from 0.9% to 1.0% and Ag grades of 7.8 to 8.8 g/t in the Range A. Waste grades varied from 0.02-0.20% Cu and 0.7-2.2 g/t Ag. Range B exhibited more stable Cu and Ag grades in the product (around 0.9% Cu and 11 g/t Ag). Mass recoveries ranged from 92-77% in the Range A and reached 70% in the Range B. Metallurgical recoveries remained high: 99-95% Cu in the Range A and above 94% in the Range B. Silver recoveries were also promising (99-93% in Range A, 90% in Range B). Considering a feed of 1,000 kt/y, estimated ROM mass after pre-concentration ranged from 833-675 kt/y of product and 167-325 kt/y of coarse tailings. Currently, these preliminary results hold great promise, demonstrating the potential for achieving significant outcomes through the implementation of sensor-based sorting pre-concentration in the Andrade Project.
Laterites are valuable European sources to produce the critical battery metals cobalt, nickel, and manganese. In this study the wet-chemical leaching of pyrometallurgically treated laterites from the LARCO Ferronickel Plant in Greece was tested. It was shown that leaching with peroxydisulfate at 50°C allows to almost fully recover residual amounts of Co, Ni, and Mn from the rotary kiln dust and electric arc furnace (EAF) slag. The results of this study shows that EAF treatment followed by leaching the EAF slag is the most promising way. In sum, there were obtained ~ 65% overall yield of Co, ~95% overall yield Ni and ~100 % overall yield of Mn. In addition, up to 37% of chromium were mobilized and 98% of titanium, rendering this approach highly promising in terms of energy and resource efficiency and likewise overall process economy. As the successful development and application of this method in the field can increase the outcome of the plant by nearly ~50 million €/year.
To date, the main problem in the development of the mineral resource base has been the deterioration in the quality and technological properties of processed minerals. This has led to a significant decrease in the efficiency of traditional beneficiation techniques. These techniques are unable to meet industry standards in terms of the content of useful components, processing complexity, and environmental requirements.
The key factors determining the technological complexity of processing strategic raw minerals include: the dispersed connection between minerals of valuable components and waste rock, high complexity and variability in material composition, and the complexity of the morphology and separation of ore bodies involved in the processing. All these aspects significantly affect the efficiency of beneficiation processes and profitability of the final product.
The main directions for solving this problem are improving flotation beneficiation processes. The flexibility and versatility of flotation technologies allows increasing their efficiency through improving reagent regimes and intensification methods with the preceding grinding stage. Confirmation of the effectiveness of these solutions is possible through the use of complex numerical criteria based on experimental and theoretical studies of the physical and chemical properties of raw materials.
For numerical evaluation of the intensifying impacts during the grinding process, a semi-empirical criterion has been proposed, which characterizes the proportionality between the required specific energy for destruction and the relative reduction in the characteristic fineness of the product. This criterion is based on interpreting the Gibbs–Helmholtz equation in terms of the equivalence of energies expended on reducing the fineness and forming a new surface area. In grinding operations, the increase in the newly formed surface area is proportional to the energy spent breaking a certain amount of material, as described by Bond's law.
To establish the influence of variations in grinding and flotation technologies on beneficiation efficiency, a method for characterizing the distribution of materials by flotability has been proposed. This method allows for the numerical characterization of changes in the flotation ability of materials. The method is based on a probabilistic-kinetic approach to studying flotation, and it involves abstractly allocating flotability classes to materials according to their flotation properties. Each fraction of material is assigned a flotability value, which is proportional to the flotation constant rate of that fraction. The flotation index value represents the proportionality between the flotation recovery probability and the constant value of the fraction's flotation rate. Initial data for determining flotability functions are obtained from experimental studies of flotation kinetic enrichment using the γ model. The values of the flotation function characterize the distribution of materials into certain flotation classes and collectively represent a step function with an exponent b.
Thus, the criterion for intensifying the grinding process's efficiency will allow us to justify the most cost-effective ratio of particle size and energy consumption for the proposed ore preparation solutions. Parameters of floatability functions will allow estimating the effectiveness of new reagent regimens on the flotability of various ore components. Establishing correlations between these parameters will enable us to characterize the impact of intensified grinding on the efficiency of flotation processes.
This work was carried out within the grant of the Russian Science Foundation (Project № 23-47-00109).
SESSION: SISAMMonPM1-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Mon. 21 Oct. 2024 / Room: Knossos | |
Session Chairs: Michael Coey; Student Monitors: TBA |
By cooling a superconductor in a magnetic field the field configuration can be permanently frozen in the material. Offering this field configuration by a continuous magnetic track allows superconducting magnetic levitation along this track. Due to the attracting and repelling forces it is passively stable without any electronic control to suspend a vehicle which can hang under the track or is standing upright. Due to this intrinsic stability, the levitation itself does not consume any energy. These are perfect conditions for a rail-bound system like Hyperloop, an individual transport with cabins for 4 to 5 passengers, requested call by call. Also mass transportation is possible. The vehicles will be levitated without friction or noise over a track constructed of rare-earth permanent magnets. In this presentation we will report on SupraTrans II, a research and test facility for such a transport system using bulk high-temperature superconductors in the levitation and guidance system, in combination with a permanent magnetic track, which had originally been set up at IFW Dresden and can now be visited at KIT Karlsruhe. A vehicle for 2 passengers, equipped with linear drive propulsion, noncontact energy supply, second braking system, and various test and measurement systems is running on an 80 m long oval driveway. In the presentation, the principle of superconducting levitation by flux pinning in bulk high-temperature superconductors will be described. Based on this, an overview of the SupraTrans II research facility and future directions of superconductivity-based magnetic levitation and bearing for automation technology, transportation, and medical treatment under enhanced gravity will be given. Also the physics behind the “Back to the Future“ superconducting hoverboard, recently presented by Lexus, will be described.
By cooling a superconductor in a magnetic field the field configuration can be permanently frozen in the material. Offering this field configuration by a continuous magnetic track allows superconducting magnetic levitation along this track. Due to the attracting and repelling forces it is passively stable without any electronic control to suspend a vehicle which can hang under the track or is standing upright. Due to this intrinsic stability, the levitation itself does not consume any energy. These are perfect conditions for a rail-bound system like Hyperloop, an individual transport with cabins for 4 to 5 passengers, requested call by call. Also mass transportation is possible. The vehicles will be levitated without friction or noise over a track constructed of rare-earth permanent magnets. In this presentation we will report on SupraTrans II, a research and test facility for such a transport system using bulk high-temperature superconductors in the levitation and guidance system, in combination with a permanent magnetic track, which had originally been set up at IFW Dresden and can now be visited at KIT Karlsruhe. A vehicle for 2 passengers, equipped with linear drive propulsion, noncontact energy supply, second braking system, and various test and measurement systems is running on an 80 m long oval driveway. In the presentation, the principle of superconducting levitation by flux pinning in bulk high-temperature superconductors will be described. Based on this, an overview of the SupraTrans II research facility and future directions of superconductivity-based magnetic levitation and bearing for automation technology, transportation, and medical treatment under enhanced gravity will be given. Also the physics behind the “Back to the Future“ superconducting hoverboard, recently presented by Lexus, will be described.
Two aspects of magneto-optics are reviewed that have hardly be considered in the past: (i) For Magneto-optical Kerr Effect (MOKE) magnetometry it will be shown that the obtained hysteresis loops need to be interpreted very carefully as they are measured locally, determined by the internal (not applied) magnetic field and by local magnetization processes [1]. MOKE hysteresis loops are therefore in most cases significantly different from integrally measured loops on the same specimen. (ii) For wide-field MOKE microscopy numerous magneto-optical effects will be discussed that lead to intensity-based domain contrasts in the absence of analyser and compensator, which are the main optical components in conventional MOKE microscopy [2]. This includes the Transverse Kerr effect, a novel 45°-dichroic effect (Oppeneer effect), the Magnetic Linear Dichroism effect, and the Dichroic Gradient effect. All these effects require linearly polarized light for illumination. A further effect is the Magnetic Circular Dichroism effect that requires circularly polarised illumination.
Two aspects of magneto-optics are reviewed that have hardly be considered in the past: (i) For Magneto-optical Kerr Effect (MOKE) magnetometry it will be shown that the obtained hysteresis loops need to be interpreted very carefully as they are measured locally, determined by the internal (not applied) magnetic field and by local magnetization processes [1]. MOKE hysteresis loops are therefore in most cases significantly different from integrally measured loops on the same specimen. (ii) For wide-field MOKE microscopy numerous magneto-optical effects will be discussed that lead to intensity-based domain contrasts in the absence of analyser and compensator, which are the main optical components in conventional MOKE microscopy [2]. This includes the Transverse Kerr effect, a novel 45°-dichroic effect (Oppeneer effect), the Magnetic Linear Dichroism effect, and the Dichroic Gradient effect. All these effects require linearly polarized light for illumination. A further effect is the Magnetic Circular Dichroism effect that requires circularly polarised illumination.
SESSION: SISAMMonPM2-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Mon. 21 Oct. 2024 / Room: Knossos | |
Session Chairs: Christian Teichert; Student Monitors: TBA |
Amorphous magnetic wires can exhibit unique magnetic properties, such as magnetic bistability [1] and/or Giant Magneto-Impedance, GMI, effect associated with excellent magnetic softness [2]. Additionally, amorphous materials are also characterized by superior mechanical and corrosion properties [3]. Such combination of physical properties makes the amorphous wires attractive for a variety of industrial applications, such as magnetic and magnetoelastic sensors or tunable metamaterials [2,4]. One of the latest trends in the development of amorphous magnetic wires is to reduce their size and expand their functionality through protective coatings. Among the most effective solutions for the production of thin amorphous magnetic wires is the so-called Taylor-Ulitovsky method, allowing the preparation of microwires with rather extended diameters range from 100 nm to 100 µm coated with an insulating, flexible and biocompatible glass coating [4]. The performance of GMI effect based sensors and devices can be significantly improved by using materials with higher GMI effect. Typically, the highest GMI ratio of about 200-300% is observed in Co-rich magnetic wires with vanishing magnetostriction coefficients, λs [2]. While, in carefully processed magnetic microwires, GMI ratios of up to 650% have been obtained [4]. However, the reported GMI ratios are still below the theoretically predicted 3000% [2]
Consequently, in this paper we provide our latest attempt on optimization of the magnetic softness and GMI effect in Co-rich glass-coated magnetic microwires.We studied the effect of annealing on the hysteresis loops and the GMI ratio of Co-rich microwires. Surprisingly, after conventional annealing, in most of Co-rich microwires, magnetic hardening and transformation of a linear hysteresis loop into a rectangular one with a higher coercive force are observed. However, stress-annealing allows preventing magnetic hardening and remarkably improve GMI ratio. Properly stress-annealed samples present almost unhysteretic loops with coercivity about 2 A/m and magnetic anisotropy field about 35A/m. A remarkable GMI ratio improvement up to 735% is observed after annealing of Co-rich microwires at appropriate conditions. Observed magnetic softening and GMI ratio improvement have been discussed considering the internal stresses relaxation, induced magnetic anisotropy and a change in the magnetostriction coefficient sign and values with increasing of annealing temperature.
Permanent magnets (PM) are vital components of the green transition. However, the criticality of rare-earth elements (REE) [1] needed for their manufacture makes them of great strategic, geopolitical, and socio-economic importance, making it an urgent need to develop alternative REE-free magnets. The best-performing PMs are based on REEs, while lower-performance PMs use ferrites. [2] Due to the high performance of REE magnets, most modern devices employ them, as they are lighter and lead to better efficiency. Unfortunately, REEs are critical raw materials owing to their supply risk and price volatility, and also their harmful environmental impacts. [3,4] One of the main solutions focuses on improving the performance of alternative rare-earth-free or rare-earth-lean magnets co-designed with motors or generators for greater efficiency.
This study focuses on a consolidation of ferrite-based permanent magnets by means of novel Pressure-less Spark Plasma Sintering Technique (PSPS). PSPS process uses the Joule heating effect to elevate the temperature in the heating die, which is transferred to the sample via thermal radiation. The method allows very high heating rates (up to 900 °/min) and short retention times in a matter of minutes. Thus, the grain growth is suppressed.
The starting material for the study was recycled Sr-ferrite powder obtained from the injection bonded magnets’ production waste. Processing and consolidation parameters were tailored to achieve dense magnets. The phase composition, microstructural analysis and magnetic properties of starting powders and sintered magnets were evaluated.
Acknowledgement: This research has received funding from the European Union’s Horizon 2020 Research and Innovation Programme under grant agreement No. 101003575 (ERA-MIN3, project GENIUS), and Slovenian national research agency (P2-0087, P2-0405, P2-0412).
Bulk metallic glasses (BMGs) have been intensively investigated because of their special mechanical properties as amorphous materials and their unique glass transition state. However, the atomic-scale origins of their behavior have not been unequivocally clarified. To explain their properties, structural models of BMGs and their small-scale deformation behavior have been proposed but not yet confirmed due to the inability of conventional measurement approaches to characterize samples at the relevant scale. For example, local structural analysis of glasses at the atomic scale using methods such as transmission electron microscopy or neutron/x-ray scattering is challenging due to the material’s disordered nature. In contrast, scanning probe microscopes and nanoindenters possess the potential of direct nanometer-scale observation local glass structure and mechanical properties. But even with these approaches, extraction of meaningful data is challenging due to the difficulty to prepare clean, atomically flat surfaces of BMG. This is because a surface roughness of some nanometers, standard with most sample preparation techniques, may alter the results of local testing if the volumes probed are nanometer-sized as well.
In this talk, we will be reviewing our recent progress in developing novel imprinting and fabrication methods of metallic glasses that can produce both atomically flat surfaces with sub-nanometer-scale features and samples with well-defined nanometer- and micron-sized total volumes as well as their subsequent use for the study of their nanometer-scale structural and mechanical properties. Imprinting is realized via thermoplastic forming of BMGs [1,2] and, alternately, by magnetron sputtering of general metallic glasses [3]. The capability of imprinting at an atomic scale enriches the range of applications of BMGs and brings a new way to directly characterize heterogeneity, relaxation, and crystallization in BMGs [4, 5]. It also allows to study onset of yielding and the local plastic flow mechanisms of BMGs in the limit of very small activation volumes (about 1000 atoms). The experiments revealed a much higher yield stress compared to the value obtained by conventional nanoindentation testing, followed by homogeneous plastic flow [6]. These atomic-scale results are contrasted to the larger-scale model that explains plastic deformation of BMG as originating from the finite STZs activation. Finally, current work is aimed at producing large numbers (>1000) of well defined, uniform micron- or nanometer-scaled pillars that can be used to explore the deformation behavior of BMGs under compression as a function of sample volume and compression rate in a statistically relevant manner.
The scientific and technological exploration of three-dimensional magnetic nanostructures is an emerging research field with exciting novel physical phenomena, originating from the increased complexity in spin textures, topology, and frustration in three dimensions. The concept of chirality which requires three dimensions, is essential to understand e.g., fundamental interactions in cosmology and particle physics, the evolution of life in biology, or molecular chemistry, but has recently also attracted enormous interest in the magnetism community. Tailored three-dimensional nanomagnetic structures, including in artificial spin ice systems or magnonics will enable novel applications in magnetic sensor and information processing technologies with improved energy efficiency, processing speed, functionalities, and miniaturization of future spintronic devices.
Another approach to explore and harness the full three-dimensional space is to use curvature as a design parameter, where the local curvature impacts physical properties across multiple length scales, ranging from the macroscopic to the nanoscale at interfaces and inhomogeneities in materials with structural, chemical, electronic, and magnetic short-range order. In quantum materials, where correlations, entanglement, and topology dominate, the local curvature opens the path to novel phenomena that have recently emerged and could have a dramatic impact on future fundamental and applied studies of materials. Particularly, magnetic systems hosting non-collinear and topological states and 3D magnetic nanostructures strongly benefit from treating curvature as a new design parameter to explore prospective applications in the magnetic field and stress sensing, micro-robotics, and information processing and storage.
Exploring 3d nanomagnetism requires advances in modelling/theory, synthesis/fabrication, and state-of-the-art nanoscale characterization techniques to understand, realize and control the properties, behavior, and functionalities of these novel magnetic nanostructures.
I will summarize and review the challenges but also the opportunities ahead of us in the future exploration of nanomagnetism in three dimensions.
This work was funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Materials Sciences and Engineering Division under Contract No. DE-AC02-05-CH11231 (NEMM program MSMAG).
SESSION: SISAMMonPM3-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Mon. 21 Oct. 2024 / Room: Knossos | |
Session Chairs: Ludwig Schultz; Student Monitors: TBA |
Intermetallic compounds of 4f and 3d elements, especially Fe and Co were intensively investigated in the 20th century, and the roles of crystal structure, exchange and crystal field were elucidated. Important consequences were rational design permanent magnets with strong uniaxial anisotropy using an appropriate light rare earth (SmCo5, Nd2Fe14B), uniaxial ferrimagnets with compensation (TbCo3) and cubic ferrimagnets with strong magnetostriction but no net anisotropy (Tb0.3Dy0.7)Fe2. Analogous compounds with the nonmagnetic rare earth yttrium were invaluable for isolating the 3d contribution to the magnetism. When high-quality metallic thin films began to be produced by sputtering 1970s, it was found that some 4f-3d binaries could be deposited as amorphous films which exhibited perpendicular magnetic anisotropy. Ferrimagnetic Gd-Fe-Co magneto-optic recording media with compensation point writing were an interesting, if commercially limited development [1]. Amorphous alloys with strongly anisotropic rare earth elements tend to have magnetic ground-states where the rare earth moments freeze along randomly-oriented axes, with a net magnetic moment — parallel or antiparallel to that of Fe or Co [2], and a new series of random noncollinear magnetic structures was discovered.
A revival of interest in these materials has been spurred by several developments. One is the reappraisal of transverse magnetotransport (anomalous, spin and orbital Hall effects) in terms of real- or reciprocal-space Berry curvature. Atomic-scale simulations of atomic and magnetic structures have improved greatly in the past 50 years. Also, the observation in 2013 of ultra-fast single-pulse all-optical toggle switching in thin films of perpendicular ferrimagnetic amorphous Gdx(FeCo)1-x with x ≈ 0.25 opened new perspectives for magneto-optic applications, and understanding of the transient collapse of magnetization and anisotropy [3]. Proposals for using these thin films for as magnetic switches modulate an optical signal at frequencies of up 100 GHz raises the possibility of multiplexing the existing global fibre-optic communication system and increasing its capacity by a factor of five.
A new study of spin and orbital magnetism and magnetotransport in amorphous R1-xCox will be presented, which allows a reassessment of the noncollinear magnetic structures of amorphous alloys with a heavy rare earth, Th, Dy or Er and its temperature dependence and field dependence in the vicinity of the magnetic compensation point Tcomp. The corresponding amorphous yttrium alloys are remarkably soft ferromagnets despite the strong random anisotropy experienced by the cobalt, which is exchange-averaged to vanishing point on account of the exchange field and extrapolated Curie temperatures in excess of 1000 K for x ≈ 0.9. This makes the amorphous Y1-xCox alloys ideal materials with which to explore new ideas of orbital electronics, where the orbital polarization of the electrons is the key to magnetoelectronics, via the orbital Hall effect (OHE), rather than the spin polarization as in conventional spintronics [5] and effects may be are much larger. The orbital moment in random close-packed amorphous cobalt may exceed 0.5 Bohr magnetons per atom. The quantities of cobalt and rare earth metals required for the new thin-film functionality are miniscule, of order a milligram for a wafer with a trillion orbital switches.
Intermetallic compounds of 4f and 3d elements, especially Fe and Co were intensively investigated in the 20th century, and the roles of crystal structure, exchange and crystal field were elucidated. Important consequences were rational design permanent magnets with strong uniaxial anisotropy using an appropriate light rare earth (SmCo5, Nd2Fe14B), uniaxial ferrimagnets with compensation (TbCo3) and cubic ferrimagnets with strong magnetostriction but no net anisotropy (Tb0.3Dy0.7)Fe2. Analogous compounds with the nonmagnetic rare earth yttrium were invaluable for isolating the 3d contribution to the magnetism. When high-quality metallic thin films began to be produced by sputtering 1970s, it was found that some 4f-3d binaries could be deposited as amorphous films which exhibited perpendicular magnetic anisotropy. Ferrimagnetic Gd-Fe-Co magneto-optic recording media with compensation point writing were an interesting, if commercially limited development [1]. Amorphous alloys with strongly anisotropic rare earth elements tend to have magnetic ground-states where the rare earth moments freeze along randomly-oriented axes, with a net magnetic moment — parallel or antiparallel to that of Fe or Co [2], and a new series of random noncollinear magnetic structures was discovered.
A revival of interest in these materials has been spurred by several developments. One is the reappraisal of transverse magnetotransport (anomalous, spin and orbital Hall effects) in terms of real- or reciprocal-space Berry curvature. Atomic-scale simulations of atomic and magnetic structures have improved greatly in the past 50 years. Also, the observation in 2013 of ultra-fast single-pulse all-optical toggle switching in thin films of perpendicular ferrimagnetic amorphous Gdx(FeCo)1-x with x ≈ 0.25 opened new perspectives for magneto-optic applications, and understanding of the transient collapse of magnetization and anisotropy [3]. Proposals for using these thin films for as magnetic switches modulate an optical signal at frequencies of up 100 GHz raises the possibility of multiplexing the existing global fibre-optic communication system and increasing its capacity by a factor of five.
A new study of spin and orbital magnetism and magnetotransport in amorphous R1-xCox will be presented, which allows a reassessment of the noncollinear magnetic structures of amorphous alloys with a heavy rare earth, Th, Dy or Er and its temperature dependence and field dependence in the vicinity of the magnetic compensation point Tcomp. The corresponding amorphous yttrium alloys are remarkably soft ferromagnets despite the strong random anisotropy experienced by the cobalt, which is exchange-averaged to vanishing point on account of the exchange field and extrapolated Curie temperatures in excess of 1000 K for x ≈ 0.9. This makes the amorphous Y1-xCox alloys ideal materials with which to explore new ideas of orbital electronics, where the orbital polarization of the electrons is the key to magnetoelectronics, via the orbital Hall effect (OHE), rather than the spin polarization as in conventional spintronics [5] and effects may be are much larger. The orbital moment in random close-packed amorphous cobalt may exceed 0.5 Bohr magnetons per atom. The quantities of cobalt and rare earth metals required for the new thin-film functionality are miniscule, of order a milligram for a wafer with a trillion orbital switches.
Rare Earths (RE) permanent magnets are essential components for Europe's successful green and digital transition However, the entire value chain of RE magnetic materials depends on imports, which are highly vulnerable in current global supply chain models.
To mitigate this situation, EU Regulation plans that at least 25% of the EU's annual consumption of permanent magnets should be covered by recycling capacities by 2030. Researchers in the EU H2020 project SUSMAGPRO consortium have shown that hydrogen can be used as a very efficient recycling method to extract NdFeB magnet powder from various EOL Components in the IP protected Hydrogen-based Processing of Magnet Scrap (HPMS).
On exposure to hydrogen the sintered NdFeB magnets break down into a friable, demagnetised, hydrogenated powder containing an interstitial hydride of Nd2Fe14BHX (10 microns) and smaller particles (< 1 micron) from the grain-boundary phase NdH2.7. This process delivers a sustainable source of magnetic material for the production of sintered, polymer bonded and metal-injection moulded magnets [1].
The talk will present numerous results along the whole value chain of magnet recycling, including automatic dismantling of magnet containing products, magnets extraction, HPMS recycling, production of recycled magnets and demonstrator testing [1-5].
It will also discuss best practices and bottlenecks of the processes as an outlook for successful design-for-recycling of future applications.
Rare Earths (RE) permanent magnets are essential components for Europe's successful green and digital transition However, the entire value chain of RE magnetic materials depends on imports, which are highly vulnerable in current global supply chain models.
To mitigate this situation, EU Regulation plans that at least 25% of the EU's annual consumption of permanent magnets should be covered by recycling capacities by 2030. Researchers in the EU H2020 project SUSMAGPRO consortium have shown that hydrogen can be used as a very efficient recycling method to extract NdFeB magnet powder from various EOL Components in the IP protected Hydrogen-based Processing of Magnet Scrap (HPMS).
On exposure to hydrogen the sintered NdFeB magnets break down into a friable, demagnetised, hydrogenated powder containing an interstitial hydride of Nd2Fe14BHX (10 microns) and smaller particles (< 1 micron) from the grain-boundary phase NdH2.7. This process delivers a sustainable source of magnetic material for the production of sintered, polymer bonded and metal-injection moulded magnets [1].
The talk will present numerous results along the whole value chain of magnet recycling, including automatic dismantling of magnet containing products, magnets extraction, HPMS recycling, production of recycled magnets and demonstrator testing [1-5].
It will also discuss best practices and bottlenecks of the processes as an outlook for successful design-for-recycling of future applications.
SESSION: SISAMMonPM4-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Mon. 21 Oct. 2024 / Room: Knossos | |
Session Chairs: Jean-Marie Dubois; Ludwig Schultz; Student Monitors: TBA |
So-called “nanoglasses” are considered as non-crystalline solids which exhibit a glass-like atomic structure and contain a considerable number of internal interfaces. This metastable state of matter can be synthesized by RF magnetron thin film sputter deposition as an alternative to other methods including inert gas condensation and chemical decomposition on a nanoscale. Using sputtering targets of VIT105 and Au-based BMG as well as Fe-Sc the resulting nanostructures can be varied from monolithic amorphous to nanoglass and to columnar amorphous nanostructures at varying Argon base pressure. Remarkably, the BMG based nanoglass specimen clearly exhibit an anomaly of the specific heat typical for the glassy state. While generally glassy structures lack ductility, the nanoglass state exhibits superior mechanical properties achieving a remarkable level of plastic deformation in nanoindentation experiments. Further details, also in relation to a recent theoretical approach as well as measurements of electrical and magnetic properties will be presented and discussed.
So-called “nanoglasses” are considered as non-crystalline solids which exhibit a glass-like atomic structure and contain a considerable number of internal interfaces. This metastable state of matter can be synthesized by RF magnetron thin film sputter deposition as an alternative to other methods including inert gas condensation and chemical decomposition on a nanoscale. Using sputtering targets of VIT105 and Au-based BMG as well as Fe-Sc the resulting nanostructures can be varied from monolithic amorphous to nanoglass and to columnar amorphous nanostructures at varying Argon base pressure. Remarkably, the BMG based nanoglass specimen clearly exhibit an anomaly of the specific heat typical for the glassy state. While generally glassy structures lack ductility, the nanoglass state exhibits superior mechanical properties achieving a remarkable level of plastic deformation in nanoindentation experiments. Further details, also in relation to a recent theoretical approach as well as measurements of electrical and magnetic properties will be presented and discussed.
SESSION: SolidStateChemistryMonPM1-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Takao Mori; Kyoung-Shin Choi; Student Monitors: TBA |
This symposium honors Prof. Mercouri Kanatzidis for his transformative contributions to inorganic chemistry and materials science. As a Professor of Chemistry at Northwestern University and Senior Scientist at Argonne National Laboratory, he has mentored hundreds of students and fellows worldwide. Kanatzidis is recognized for pioneering breakthroughs in chalcogenide materials, thermoelectrics, and halide perovskites. His development of chemical sorbents for radioactive waste, nanostructuring strategies in thermoelectrics, and the introduction of halide perovskites in solar cells have revolutionized these fields. With over 1,500 publications, 200,000 citations, 60 patents, and numerous prestigious awards, including induction into the National Academy of Sciences and the naming of the mineral "kanatzidisite" in his honor, his work continues to shape the future of advanced materials and energy technologies.
When producing a multi-layer photoelectrode for solar fuel production, selecting appropriate bulk materials to use as a semiconductor, a catalyst, and a protection layer is important. However, optimizing the surface of each component and the interfaces between the components is just as critical to maximize the overall performance of the photoelectrode. Our research team has been at the forefront of demonstrating and elucidating the impact of the photoelectrode surfaces and interfaces on the overall performance of the photoelectrodes. For example, our team has shown that when a ternary oxide containing two different metal ions, such as BiVO4, is used as a photoanode, the surface metal composition (i.e., the surface Bi:V ratio) may not necessarily be the same as the bulk metal composition (Bi:V = 1:1) and it can also be intentionally modified. We showed that changes in the surface composition while using the same underlying bulk photoelectrode can have an immense impact on the band edge positions and work function, which have a direct impact on electron-hole separation and photocurrent generation, even for the same facet exposed on the surface.[1] This observation made us wonder how varying the surface composition of the same photoelectrode can impact the photoelectrode/catalyst junction when the same catalyst layer is deposited on the photoelectrode. In order to explicitly demonstrate and investigate how the detailed features of the photoanode/OEC interface affect interfacial charge transfer and photocurrent generation for water oxidation, we prepared two BiVO4(010)/FeOOH photoanodes with different Bi:V ratios at the outermost layer of the BiVO4 interface (close to stoichiometric vs Bi-rich) while keeping all other factors in the bulk BiVO4 and FeOOH layers identical. The resulting two photoanodes show striking differences in the photocurrent onset potential and the photocurrent density for water oxidation.[2] In this presentation, we explain the atomic origin of the experimentally observed difference by revealing the impact of the surface Bi:V ratio on the hydration of the BiVO4surface and bonding with the FeOOH layer, which in turn affect the band alignments between BiVO4 and FeOOH.
2D multilayered perovskites introduced by Calabrese (JACS 1991) share similarities with 3D perovskites including direct electronic band gap, sizeable optical absorption, small effective masses, Rashba-like effects. Calabrese’s Ruddlesden-Popper phases were completed more recently by "Alternative cations in the interlayer" (Soe, JACS 2017) and Dion-Jacobson (Mao, JACS 2018) phases, leading to a consistent classification of multilayered perovskites in relation with the chemistry of the compounds or the crystallographic order along the stacking axis (Blancon, Nature Nano 2020). 2D multilayered thus afford extensive chemical engineering possibilities, and exhibit other features related to tuneable quantum and dielectric confinements, strong lattice anisotropy, strong exciton interactions, more complex combinations of atomic orbitals and lattice dynamics.
Exploring the potential of 2D perovskites for PV and the association of 2D and 3D perovskites in solar cell architectures is a long-term joint project with colleagues in US (Prof. A. Mohite, LANL then Rice Univ., Prof. M. Kanatzidis Northwestern Univ.) that we started years ago including the first breakthrough on 2D perovskite for PV (Tsai Nature 2016). This approach is in line with Snaith’s recent viewpoint (Science 2024) about perovskite solar cell architecture trends: “a growing consensus is forming about the requirements for an ideal perovskite interface: the elimination or repair of surface interface defects, the design of a rational energy landscape to satisfy selective carrier collection, the minimization of strain and stress, and the improvement of physical robustness and adhesion”.
This will be illustrated by recent combined experimental and theoretical studies on excitons, formation of edge states, hot carrier effects and carrier localization (Blancon Science 2017, Blancon Nature Comm. 2018, Li. Nature Nano 2022, Zhang Nature Phys. 2023). 2D multilayered perovskites have exhibited very early improved device stability under operation. More, combined in 2D/3D bilayer structures using new versatile growth methods, excellent solar cell device stability can be achieved (Sidhik, Science 2022). Band alignment calculations nicely explain the difference of performances for ni-p or p-i-n devices. Our lattice mismatch concept (Kepenekian, Nanoletters 2018) shall provide further guidance for the choice of the proper 2D/3D combinations, leading to enhanced stability for 3D-based solar cells (Sidhik, Science 2024).
Development of thermoelectric (TE) materials & devices is important, for energy saving via waste heat power generation and IoT power sources [1]. There are a variety of device forms which can be envisioned to be useful. I will present several high-performance materials systems we have been developing such as Mg3Sb2-type materials, skutterudites, Heusler alloys, magnetic chalcogenides, etc., and mainly on the development of various TE modules. An initial realistic 8 pair bulk module of our doped Mg-Sb materials exhibited an efficiency of 7.3%@320oC, with estimated efficiency from the actual materials being ~11%, and a variant exhibited high performance room temperature power generation and cooling [2]. Recently, a modified single element device of Mg3Sb2 was able to achieve a TE efficiency ~12% [3]. Design and construction of two different design thin film TEG devices [4] and hybrid flexible TEGs will also be presented. It is also critical to have accurate evaluation of TEGs and we have recently laid out some best practices thereof [5].
SESSION: SolidStateChemistryMonPM2-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Alain Tressaud; Vinayak Dravid; Student Monitors: TBA |
Characterization and analysis by scanning transmission and transmission electron microscopy (S/TEM) is pervasive in modern materials research. The ongoing work in our group is inspired by innovations in high throughout assays and related automation from biotech. It combines novel design and nanofabrication of in-situ stages with smart imaging to utilize electron exposure in a commensurate manner. It is tailored to “ration” both electrons and time, spatially and temporally, utilizing AI/ML methods.
The presentation will cover emerging opportunities in advanced microscopy. In addition to typical static observations of structures and defect phenomena in functional materials (thermoelectrics, energy storage, photovoltaics etc.), it will cover innovative nanofabricated ultra-thin (UT) window fluidic cells for nanoscale discrimination of reactants and products in catalysis with spectroscopy. The presentation will also explore the feasibility of AI/ML-enabled data acquisition approach for rapid and high throughput materials discovery, as well as monitoring of in-situ phenomena in the temporal domain.
The presentation will show role of microscopy for energy, environment and sustainability research and innovations for broader societal good.
Thermoelectric energy converters are mostly investigated to recover waste heat from sources such as power plants, factories, vehicles or even transform heat from human bodies into electric power. Besides the energy efficiency of these devices, the selection of materials and processes are also important towards the high-priority pathway of environmentally friendly, earth-abundant, and low-cost materials. Therefore, systems such as silicides attract much attention since they exhibit very promising thermoelectric properties meeting at the same time relative environmental priorities. Furthermore, the proper use of materials as well as the possible reuse/recycling of expensive lost materials from several industries are also main priorities. PV industry is a typical example where high purity Si is required and, at the same time, large amount is wasted as kerf during wafer cutting.
In this work, our efforts to synthesize thermoelectric silicides based on recycled Si-kerf are presented. n-type and p-type Mg2Si- based materials as well as p-type Higher Manganese Silicides were prepared using commercial and recyclable Si. The materials were fully characterized in terms of structure and thermoelectric properties and selected compositions were used for prototype module fabrication.
The traditional understanding in materials science considers single crystals nearly perfect in their ordered structures, represented by a unit cell that informs their mechanical and electronic properties. Our studies challenge this paradigm by demonstrating large deviations from the predictions made by the unit cell model to materials properties in systems such as halide perovskites, ion conductors, and organic semiconductors.
Utilizing Raman spectroscopy, our efforts focus on the detailed examination of thermal motions and their implications on single crystals. The discrepancies between experimental observations and theoretical predictions are explored, particularly emphasizing the interaction between vibrational modes and their impact on material properties.
A significant aspect of this research is detailed in our recent publication, where we propose a new model for second-order Raman scattering to account for the nonmonotonic temperature dependence observed in perovskite single crystals. This model, supported by numerical simulations, identifies low-frequency anharmonic features as key players in light scattering processes, highlighting a transition between two minima of a double-well potential surface. Our findings provide a more accurate understanding of the structural dynamics within disordered crystals and suggest broader applications for designing materials with enhanced electronic and optical functionalities.
Inorganic fluorine-based compounds are found today as nano-components in many applications, including energy storage and conversion, photonics, electronics, medicinal chemistry, and more [1]. The strategic importance of nano-fluorinated materials can be illustrated by several examples drawn from various scientific fields. In the field of energy storage, fluorinated carbon nanoparticles (F-CNPs) are tested as active materials in primary lithium batteries, while 3d-transition metal fluorides and oxyfluorides, mainly iron-, cobalt- and titanium- based have been proposed as electrodes in secondary batterie(reversible) s. In all-solid-state batteries, materials derived from fluorite- (CaF2) or tysonite- (LaF3) structural types can be used as solid electrolytes, provided the F- anions are highly mobile. Nanocrystalline rare-earth fluorides are currently used for their photoluminescent properties at the micro- or nanoscale.
Functionalized nanoparticles and nanostructured compounds based on solid-state inorganic fluorides are used in many other advanced fields, including fluorinated graphene quantum dots (FGQDs), solar cells (DSSC, QDSSC), transparent conducting films (TCF), solid state lasers, nonlinear optics (NLO), UV absorbers, etc.
Their role is also decisive in medicine and biotechnologies [2], where doped rare-earth fluoride nanocrystals serve as luminescent biomarkers thanks to their up- and down-conversion properties, allow fluorine labeling of nanoparticles and in-vivo 19F NMR. Relevant nanotherapeutics include photodynamic therapy (PDT), luminescent thermometry, radiotracers for positron emission tomography (PET), theranostic nano-agents that incorporate both imaging probes and therapeutic media, and are therefore capable of carrying out both diagnosis and therapy within the same nano-object.
SESSION: SolidStateChemistryMonPM3-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Jiaqing He; Kanishka Biswas; Student Monitors: TBA |
Two most imminent scientific and technological problems that mankind is facing now are energy and climate. The energy production and utilization in modern society is mostly based on the combustion of carbonaceous fuels like coal, petroleum and natural gas the combustion of which produces CO2, which alters earth’s carbon cycle. 30 billion of tons of CO2 per year get emitted globally as waste from the carbonaceous fuel burning and industrial sector, which if converted to valuable chemicals have the potential to change the economy of the world. We, in our lab, are trying to address both issues and are keen upon translating our innovative technologies from the lab to the industrial and commercial scale. In this talk, I will discuss about our recent discoveries of materials based on intermetallics, chalcogenides, oxides, organic-inorganic hybrids, etc as efficient catalysts for the conversion of CO2 to chemicals/fuels.[1-15] We are capturing CO2 from industrial flue stream and converting it to value added chemicals/fuels such as methanol, CO, methane, dimethyl ether, C2-C5 & C5-C11 gasoline hydrocarbons. I will also cover our activities to produce green hydrogen via electrochemical pathway.[16] The utilization of hydrogen and other fuels like methanol/ethanol through fuel cells also will be discussed.[17] Catalyst design is at the heart of all these technologies, and we have developed customized catalyst systems for targeted product conversions as per the need of different industries. Development of these catalyst via various methods, the driving force behind the enhancement in activity and the mechanistic pathways will be explained with the support of various in-situ (DRIFTS, IR, XAFS), ex-situ (XPS, XRD, IR, XAFS) and theoretical (DFT calculation) studies. The talk also will cover the industrial viability of these catalysts.
Fundamental understanding of the nature of chemical bonding and its influence on the electronic structure is paramount to chemistry, solid state physics and materials science. CuBiI4 has a fascinating structure where Cu and Bi are surrounded by a tetrahedral and octahedral halogen framework respectively. From fundamental inorganic chemistry concepts, it is expected to have symmetry-allowed d-p overlap in the tetrahedral co-ordination and we see here strong Cu (d)- I (p) strong interaction. This rare interaction generates an antibonding state in the valence band just below the Fermi energy in the electronic structure. Electrons filling up the antibonding band weaken the bond and subsequently the crystal lattice becomes soft and anharmonic giving rise to ultra-low thermal conductivity.1 In the latter part of my talk, I will be talking about achieving an ultralow value and unusual glass-like temperature dependence of lattice thermal conductivity in a large single crystal of layered halide perovskite Cs3Bi2I6Cl3.2 Here, Bi-Cl interaction also forms a s-p antibonding state below the Fermi level which renders a soft lattice. While strong anharmonicity originates from the low energy and localized rattling-like vibration of Cs atoms, synchrotron X-ray pair-distribution function analysis further evidences the presence of local structural distortions in the Bi-halide octahedra. We propose that hierarchical chemical bonding, presence of antibonding states near Fermi level and low energy vibrations from selective sublattice in crystalline inorganic halide perovskites open an intriguing avenue for thermal transport research with their unfathomed lattice dynamics and potential applications.3, 4
The performance of thermoelectric materials is mainly governed by the materials’ electrical and thermal conductivity properties and a number of new materials and structures have been exploited in order to optimize the energy conversion efficiency. Especially, nanostructure engineering via dopants, precipitates or phase/twin/grain boundaries is found to be effective in increasing the conversion efficiency by reducing the thermal conductivity. However, a direct correlation of these nanostructures to the material’s property is yet to be elucidated. Nowadays, with the rapid development of aberration-corrected transmission electron microscopy (TEM), the resolution of electron microscopes takes a leap forward to sub-angstrom and sub-eV, which allows a direct access to a material’s structure and chemical composition at an atomic scale.
The presentation will start with a brief and realistic coverage of the emerging and maturing themes in the context of energy sources, efficiency, charge storage and distribution. It will illustrate GeTe as one example of emerging excitements in nanostructured materials and systems for thermoelectric materials. It will highlight the role of advanced and classical electron microscopy in unravelling the hierarchical architecture of the constituents and their intimate interplay in governing key phenomena in thermoelectric materials.
Birefringent crystals serve as crucial elements in optical devices, as they exhibit anisotropic refractive indices along different crystal directions. This optical anisotropy stems from the anisotropies of both structural geometry and spatial electron distribution. Consequently, the planar structural building units are excellent choices for constructing birefringent crystals. However, achieving an anisotropic crystal structure (especially a coplanar geometry) poses a significant challenge. Herein, we propose a novel hydrogen bond-click reaction concept to unravel the giant birefringence in (C5H6ON)+(NO3)–, (4HPN) for the first time. We demonstrate that the interactions between the planar hydrogen bond donor (4-hydroxypyridinium, C5H6ON+ cation) and planar hydrogen bond acceptor (NO3– anion) ensure the coplanarity during the crystal packing, generating the desired optical anisotropy. At 546 nm, several as-obtained (001)-single crystal wafers (#1–4) measure varying from 0.331 to 0.358; and two manually cut chips (#5,6) read = 0.469, 0.494, respectively. These values are smaller than the DFT calculated maximal value ( = nY – nX = 0.593 at 546 nm). Since 4HPN has heavy (001)-growth habit, the maximal ∆n has not been observed yet. Nevertheless, the observed ∆n values on 4HPN with an Eg = 3.70 eV already surpass that of the commercialized benchmark crystals, e.g., YVO4 ( = 0.232, = 3.1 eV) and CaCO3 (∆nobv = 0.174, = 5.4 eV), commonly used in the UV to visible and near IR spectral range. 4HPN also exhibits a strong second harmonic generation (SHG = 9.55 × KDP measured at 1064 nm). This unique concept offers a promising avenue for the design and development of birefringent crystals with potential applications in optical communication, sensing and signal processing devices.
SESSION: SolidStateChemistryMonPM4-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Mon. 21 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Elisabeth Djurado; Manjunatha Reddy G N; Student Monitors: TBA |
Research on solution-processable semiconductors has achieved significant fundamental and technological advancements over the last decade, in large part due to improvements in characterization techniques to understand these materials at different length scales. Notable example include hybrid perovskites and organic semiconductors, which have garnered interest for a wider energy paradigm and sustainability. Recent upserge in the solar-to-enelectrical energy conversion further expands the application space for these materials. Hoever, some fundamental questions regarding to the solar cell efficiencies of are related to morphology, defects, local disorder and interfaces between the semiconductor thin films and charge transport layers. To this end, understanding structure-stability-property relationships in emerging photovoltaics brings new opportunities and challenges to characterization techniques. Synergy between length and timescales of characterization techniques is particularly important.[1,2] We will present how local structures/morphology and interactions can be resolved by state-of-the-art magnetic resonance spectroscopy and imaging techniques at high fields.[3-4] Specifically, recent in situ and ex situ capabilities for examining thin films at micron-to-submicron thicknesses will be discussed. Gaining access to the local interfacial structures enables a number of questions to be addressed including a better picture of stacked semiconductor layers in electronic devices, diffusion of electrodes into photo-active layers, and film formation kinetics and molecules aggregation, surfaces/bulk passivation, and instability and degradation reactions and kinetics.[5-7]
The development of highly active earth-abundant catalysts for solar water splitting is critical for the innovation of noncarbon-based renewable fuels [1]. It is therefore important to determine the mechanisms of these water oxidation catalysts, such as nickel-iron layered double hydroxides ([NiFe]-LDHs), which exhibit low overpotentials, excellent long-term stability, and high current densities and Faradaic efficiencies [2]. In principle, mechanistic insight can pave the way for the development of new materials with enhanced activity.
We have developed a new, magnetic resonance-based technique to monitor the reaction kinetics of [NiFe]-LDH relative to other well-studied catalysts. This technique allows for nanomolar detection of oxygen isotopes and yields important information about the mechanism of these catalysts. Membrane inlet mass spectrometry and differential electrochemical mass spectrometry were instrumental in determining electrochemical properties in situ; however, they are indeed limited in their collection efficiency and quantification of oxygen on the minute timescale [4,5]. Results were paired with computational and kinetic modeling in order to differentiate key O–O bond-forming steps. Nickel-iron-based catalysts were shown to operate by a novel oxo-oxo coupling mechanism, distinct from hydroxide attack proposed for other systems—consistent with previous findings [3]. We present our initial findings and share our efforts at incorporating pulsed EPR experiments for these systems.
Solid oxide cells (SOCs) are efficient electrochemical systems for electrical power generation in fuel cell mode (SOFC) and hydrogen production in electrolysis mode (SOEC). One solution to increase the lifetime consists of decreasing the operating temperature to 650-750 °C but the electrode reaction kinetics become relatively insufficient [1]. One of the main challenges is to improve the oxygen electrode efficiency by enhancing the oxygen reduction/evolution reaction (ORR/OER). To tackle this issue, it is important to choose suitable materials with adequate physicochemical properties and to optimize the microstructure and architecture to further increase the electrochemical performances [2].
This work aims to design novel optimized oxygen electrodes with improved mixed ionic-electronic properties to be used as more efficient oxygen electrodes in SOCs. Indeed, it is of high importance to control the electrode microstructure and composition to obtain large surface areas. These properties are essential to increase the number of active sites for the ORR/OER and to enhance the ionic transfer at the electrode/electrolyte interface.
Here, we report recent advances in the design of the state-of-the-art La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF) [3, 4], La2-xPrxNiO4+δ (LPNO), [5, 6] with 0 ≤ x ≤ 2, and Pr6O11 [7] oxygen electrodes with grain size and porosity at the nanometre length scales. These active functional layers are fabricated using electrostatic spray deposition (ESD), a unique bottom-up method capable of depositing films with original morphologies by a nano-texturing approach.
This talk will show our latest electrochemical performance results of these innovative oxygen electrodes investigating the role of the nanostructure and the electrode/electrolyte interface. The correlation between microstructure, composition, grain size, interfaces, and electrochemical properties is discussed in detail for the different investigated oxygen electrodes.
Our investigations suggest that the ESD process is a suitable low-cost method to manufacture unique optimized porous and nanostructured oxygen electrodes with reproducibility. Three MIEC oxygen electrodes have shown one of the lowest values of polarization resistances in the literature and excellent performances in single-cell tests. To conclude, the suitability of these mixed ionic and electronic conductors (MIEC) with innovative and controlled microstructure as durable air electrodes for SOECs has been proven to be promising.
Direct exposure to solar irradiation (ultraviolet, visible, and infrared) is correlated with several harmful implications, such as biological damage in humans and material adulteration [1]. A wide variety of products, especially pharmaceutically active compounds, food, and soft drinks are sensitive to UV light and visible light exposure. Products exposed to sunlight may suffer from ramifications such as the increase in temperature, which results in the deterioration of their quality. Appropriate packaging materials have been developed to protect products from light exposure during transportation or storage [2].
Sensor-based logistics (SBL) uses various sensors to offer real-time data about different environmental conditions such as temperature, light exposure, relative humidity, and barometric pressure. The accumulative dose of light exposure can be defined with optoelectronic devices or with chemical probes that undergo various physicochemical transformations (oxidation/reduction, decomposition, photocleavage, dimerization, polymerization, etc.) upon exposure to UV irradiation [3]. This approach has been extensively followed to detect the exposure level of human skin to UV irradiation of solar light.
This work unveils a novel application of a common packing material, “bubble wraps” (Aeroplast), as a tool to measure visible sunlight exposure [4]. We have synthesized and meticulously characterized a layered metal selenide photocatalyst with the general formula (DMAH)2xMnxSn3–xSe6 (DMSe-1) (x= 1.3-1.7; DMAH+=dimethylammonium), featuring a narrow band gap of 0.76 eV. Subsequently, a photochemically sensitive probe based on this new catalyst, an indicator dye, and a reducing agent was prepared to assess exposure to visible light directly. The probe is introduced into air-filled bubble wrap compartments, where it undergoes photocatalytic degradation to provide a chromatic response to sunlight exposure. The probe's sensitivity to variable irradiation dose is customizable by adjusting the amount of the photocatalyst, while the color intensity is directly proportional to the absorbed irradiation dose.
The results from the new photoactive material show a strong correlation with those from standard sunlight pyranometers (r = 0.98, p=0.05), proving that bubble wraps, in addition to their protective function, can effectively serve as a visible light sensor with an average error of <15%. Furthermore, the study's findings mark a significant step forward in the use of metal chalcogenides as visible light sensors, offering promising prospects for the development of new light-sensitive materials.
SESSION: CompositeMonPM1-R8 |
Monteiro International Symposium on Composite, Ceramic & Nano Materials Processing, Characterization & Applications (10th Intl. Symp.) |
Mon. 21 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Sergio Monteiro; Henry Alonso Colorado Lopera; Student Monitors: TBA |
Following a brief description of personal background, a timeline of academic, administrative and scientific activities during 60 years will be presented. Initially, as a graduate student, contributing to the creation of the Master and Doctoral Program in Metallurgical Engineering at the Federal University of Rio de Janeiro, COPPE/UFRJ. Following a post doctorate at the University of Stuttgart, Germany, assumed administrative positions as Head of Department, Coordinator of COPPE, Under-Rector for Research of UFRJ and Under-Secretary of the Ministry of Education in Brasilia, Brazil. Since MSc and PhD graduate period, at the Department of Materials Science and Engineering of the University of Florida, has published more than 2,300 articles associated with more than 20,000 citations and a H index of 72 (Google Scholar). Received several awards, including ASM Fellowship, Brazilian Army Medal as well as several TMS distinctions. Consultant of the main Brazilian R&D agencies and Executive Editor of Elsevier’s Journal of Materials Research and Technology. Finally life-learned lessons will be described.
Pollution has profound impacts on human health, the environment, and Earth's systems, including climate regulation. Its reach is global, affecting our well-being through contaminated food, water, and air. Material engineers and scientists play a crucial role in addressing these challenges through innovative materials and manufacturing techniques. One promising sustainable solution involves utilizing eco-friendly materials sourced from nature.
In this presentation, we delve into natural fibers, exploring their fundamentals to practical applications for engineering. Natural fibers are more environmentally conscious and sustainably produced. These fibers and their composites offer a sustainable alternative, being both environmentally conscious and responsibly manufactured. They can be transformed into functional materials suitable for various uses, displaying their versatility and potential.
Most of the fibers have been used for centuries by ancient communities, forming a fascinating field known as cultural materials research. It will focused on fibers sourced from the Andes Mountains and the Amazon River region, in the traditional uses, microstructure, properties, and their potential applications in modern materials engineering.
Plastics are a necessity in today’s economy, being present in all the industrial and domestic sectors. The worldwide production of plastics about 200 million tons in 2000, 400 million tons in 2022 with an annual growth rate of 11% per annum. Basically, they are produced from petrol products and the disposal of pervasive plastic waste is a growing worldwide concern, and these materials generates large amounts of greenhouse emission which contributes to global pollution. This study examined the combined effects of coupling agent developed locally and Pineapple Leaf Fiber (PALF) different % loading on the mechanical and thermal characteristics of recycling polypropylene (r-PP) which was produced using twin screw extruder melt compounding. The PP grafted with maleic anhydride (MA) (PP -g-MA) was used as a coupling agent to improve the interfacial adhesion between recycling PP with PALF. The extent of grafting level was confirmed with FTIR. The results demonstrated the dependence of thermal stability and tensile properties on the grafting level of PP-g-MA, and weight percentage of PALF. Thus, it could be deduced that combination of PALF at high weight percentage (5, 10 and 15wt%) and PP-g-MA with high grafting level can significantly improve the thermal stability of recycling PP. The morphological analysis indicated better adhesion between PALF and recycling PP, in composites containing PP-g-MA with high grafting level. Overall, Recycling PP/PALF/PP-g-MA composites with improved interfacial adhesion and thermal stability and young’s modulus were successfully prepared, in the presence of PP-g-MA with high grafting level.
The processing of solid wood generates a large amount of waste, which alternatively to disposal and burning in the open air, these can be used in the manufacture of wood products. Among the various stages of production of particleboards, the homogenization process requires consumption of energy, time and labor, and its eventual suppression would certainly result in a reduction in the cost of manufacturing these materials. As there are several properties resulting from the characterization of panels, obtained in equipment generally available in large research centers and branch companies, the relation of properties through mathematical models makes it possible to reduce the volume of tests, as recommended by the Brazilian standard [1]. This research aimed, with the use of a mix of wood shavings (fine particle formed in processes such as planing and thinning wood) in the integral form (without dimensional classification) of Pinus elliottii and Pinus taeda woods (12% moisture content) and of the urea-formaldehyde adhesive, to evaluate the feasibility of producing medium and high density particleboards, the influence of density (medium and high) of composites on the physical and mechanical properties as well as evaluating the possibility of estimating properties as a function of others by linear regression models, also considering colorimetric parameters. Six medium and six high density particleboards were produced considering the use of 15% adhesive content, with the proper use of only 11% adhesive. The physical and mechanical properties were obtained according to the assumptions and calculation methods of the Brazilian standard [2], with the requirements being evaluated based on this and some international standards. In general, the density of the panels was significant in practically 50% of the determined properties. The particleboards can be classified as P2 by the Brazilian standard [2], it should be noted that in some properties the values exceeded the P7 class. The results of thermal conductivity show the potential for application of the panels in buildings. The surface roughness was considered intermediate (class N7 of Brazilian standard [3]). From the regression models, only four of the twenty generated had a coefficient of determination close to 70%, however, because they are all considered significant, a greater number of samples and experimental conditions should be considered for more robust conclusions, should be the objective of future research.
SESSION: CompositeMonPM2-R8 |
Monteiro International Symposium on Composite, Ceramic & Nano Materials Processing, Characterization & Applications (10th Intl. Symp.) |
Mon. 21 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Sergio Monteiro; Thomaz Jacintho Lopes; Student Monitors: TBA |
This research summarizes results regarding a vegetable natural fiber from Colombia, produced in the leaves of the fique plant, a species from the genus Furcraea andina. Fique is a strong natural fiber used for centuries for local indigenous peoples in Colombia, and later used for farmers and locals to produce crafts, clothes, shoes, and bags, among other traditional objects. Recently, fique has been used in combination with clays and cements as a construction material, and also as a reinforcement in polymer matrix composite in a strong collaboration between Colombia and Brazil, particularly for ballistic protection and other dynamic applications. Tensile tests and scanning electron microscopy characterization is presented here, with a discussion of possibilities for fique in engineering.
Polymeric materials are essentially insulating, but they have unique properties such as low density, high resistance to corrosion, ease of processing and lower cost compared to metallic and ceramic materials. Polymethyl methacrylate (PMMA), a polymer commercially known as acrylic, is known as a low-cost material with very interesting properties to be applied in engineering, such as transparency, mechanical resistance, electrical insulation and good thermal stability [1] [2]. Since the discovery of graphene, polymeric composite materials based on graphene and its derivatives have been explored in both academic and industrial research, due to the possible dispersion of carbon in the polymeric material, offering thermal and electrical properties to the polymer. The structure of graphene is made up of a two-dimensional sheet with a network of hexagons, formed by carbon atoms with sp^2 hybridization [3]. Graphene oxide can be obtained by functionalizing graphene through its exfoliation, presenting intercalated regions with sp^2 and sp^3 hybridized carbons, as well as hydroxyl and epoxy functional groups on its basal planes, which increase its interaction with the polymer matrix. This interaction improves the mechanical fit at the interface between the filler and the matrix, and its two-dimensional geometry may be responsible for increasing the stiffness of the composite [4].
Therefore, microcomposite films of PMMA and rGO with different concentrations were produced. The physicochemical changes were evaluated by differential scanning calorimetry (DSC) and fourier transform infrared spectroscopy (FT-IR). The morphological characteristics were observed by scanning electron microscopy (SEM).
The DSC test showed that the addition of filler to the polymer made the material (microcomposite) more thermally stable and indicated greater rigidity of the PMMA macromolecules in the microcomposites as the concentration of rGO increased. FT-IR analysis revealed the characteristic groupings of both PMMA and rGO, indicating that the matrix interacted with the filler, as was also observed in the topography of the material by SEM. These factors indicate that the higher the concentration of rGO, the greater the chance that PMMA, being an insulating material, will be transformed into a semiconductor/conductor material.
The genus Sporobolus (Poaceae Chloridoideae) consists of approximately 160 species of tropical and subtropical grasses. In Brazil, this genus is represented by 28 species, among which Sporobolus indicus stands out, a perennial species, made up of two varieties (indicus and pyramidalis), distributed throughout the national territory. In a 1979 botanical survey, in degraded pastures, in the northeast (Paragominas) and south (Santana do Araguaia) of the state of Pará, Brazil, Sporobolus indicus is not listed as a frequent species, although it is present in Santana do Araguaia. That said, this work aims to present a study on a polyester composite reinforced by Sporobolus indicus fibers. The composites were manufactured with fiber in different lengths, 5, 10 and 15 mm, added discontinuously. A tensile test was carried out following the ASTM D 638M standard. A composite of the same matrix was also manufactured with the aforementioned fiber, unidirectionally aligned. The tensile test was carried out according to the ASTM D 3039 standard, in order to compare results. It was possible to notice the behavior of the composite by varying the length of the reinforcement introduced into the matrix. The mechanical resistance showed growth proportional to the growth of the fibers, with the values found for the composite reinforced with discontinuous fibers being 11.33, 12.10 and 14.95 MPa, respectively, in increasing order according to the size of the fibers, while the results for the specimens reinforced with unidirectionally aligned fibers were 18.84 MPa. This occurs due to the alignment of the reinforcement within the mold, where in a length of 5 mm, many fibers were arranged transversely to the direction of application of the load on the specimen, not cooperating with the resistance and causing failure mechanisms. At a length of 15 mm, the fibers were distributed longitudinally in the center of the specimen, coinciding with the direction of load application and enabling greater tensile strength.
Due to the development of novel technologies, there emerges a demand in the industrial sector for new materials with enhanced properties. In this context, new applications are being explored for structural composites, typically involving continuous fibers characterized by low density, high strength, and high elasticity modulus, such as carbon fibers, extensively utilized in industries such as automotive, food, aerospace, household goods, and others. However, environmental concerns are also on the rise, prompting the substitution of synthetic fibers with lignocellulosic fibers (LF) like jute fibers, sugarcane bagasse, coconut, banana, among others. The use of natural fibers instead of synthetic fibers brings about various benefits to the industrial sector. Apart from being a renewable source, LF is biodegradable and cost-effective, given their common discard and lack of market value. Within the realm of many fibers scrutinized in composite materials, one finds the fibers extracted from the açaí palm stem (FEFAPS). According to Embrapa (Brazilian Agricultural Research Corporation), Brazil stands as the leading producer, consumer, and exporter of açaí globally, with consumption primarily concentrated in the northern regions of the country. A study conducted by Embrapa indicates a 675% increase in the planted area of açaí cultivars (Euterpe oleracea) for upland regions developed through agricultural research in the past 12 years. Within this backdrop, this study aims at producing polymeric composites with polyester matrix reinforced with FEFAPS at varying weight concentrations (0, 10, 20, and 30%). Tensile tests were conducted following ASTM D3039 standards, alongside impact energy assessment via Charpy testing based on ASTM D6110-18 norms, and thermogravimetric analyses (TGA) under inert N2 atmosphere, ranging from 30°C to 600°C with a heating rate of 10°C/min. For morphological evaluation, the fracture surfaces post-tensile tests were scrutinized utilizing Scanning Electron Microscopy (SEM). The tensile test results depict a linear increase in maximum tensile strength of composites with FFSAPT addition, reaching up to 48 MPa. Regarding Charpy impact tests, a progressive rise in absorbed energy until rupture was observed, with 30% composites exhibiting growth of up to 2301% compared to pure polyester. Thermal analysis demonstrated no alteration in thermal resistance with FEFAPS inclusion, with degradation onset temperatures hovering around 300°C. Lastly, SEM micrographs exhibited weak interaction between fibers and the matrix, a characteristic trait of lignocellulosic fiber-reinforced composites. In conclusion, this study establishes the successful application of FEFAPS in polymeric composites, ushering in a new perspective for their utilization and the valorization of residues generated during açaí ice cream production, commonly employed in Brazil.
SESSION: CompositeMonPM3-R8 |
Monteiro International Symposium on Composite, Ceramic & Nano Materials Processing, Characterization & Applications (10th Intl. Symp.) |
Mon. 21 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Afonso Rangel Garcez De Azevedo; Henry Alonso Colorado Lopera; Student Monitors: TBA |
This study explores the importance of simulations conducted with MCNP5 and the modifications implemented in 316 steel to optimize energy efficiency in nuclear power production. Molybdenum (Mo) is investigated as a promising additive due to its low absorption cross-section for thermal neutrons, which enhances neutron participation in fission and heat generation. Using the MCNP5 code, simulations were performed to analyze a hypothetical UO2 fuel element with different enrichment zones to evaluate its performance[1-3]. The results indicate that incorporating molybdenum into the fuel cladding alloy significantly impacts neutron production, suggesting that this addition might affect energy generation efficiency. In summary, this study highlights the potential of molybdenum as an additive to improve nuclear fuel performance[4-8], promoting safer, more efficient, and sustainable nuclear energy. The comparison of the results from the two simulations allowed for the assessment of the impact of molybdenum inclusion on the criticality of the simulated fuel. Conversely, if the inclusion of molybdenum does not positively influence or even reduce the fuel's criticality, this suggests that such a strategy is not viable for optimizing nuclear fuel performance. Therefore, the results of this analysis have significant implications for the development of more efficient and environmentally sustainable nuclear fuels. The effective multiplication factor (keff) obtained for the clad rod under study was keff=1.12086 ± 0.00064, while the reference value without doping was keff=1.04355 ± 0.00076, resulting in a relative percentage deviation of approximately 6.897%. Doping 316 steel with molybdenum nanoparticles presented a significant alteration in neutron production, suggesting that this addition may compromise energy generation efficiency.
The advancement of materials research for the nuclear industry is growing as energy demand increases [1],[2]. As a result, new materials are being explored to improve the efficiency of nuclear applications. Molybdenum has been studied for decades as an alloying element due to its low thermal neutron absorption cross-section and high strength under nuclear reactor temperature conditions [3],[4]. A critical reactor condition is understanding how fuel rods behave during the fission reaction of UO2 pellets [5],[6] and, consequently, how heat transfer occurs in this process. To understand these key characteristics, a study was conducted on the criticality of a fuel rod clad with Zircaloy doped with molybdenum nanoparticles [7],[8] using MCNP code simulations. Simulations of the fuel element were performed with a 3.2%, 2.5%, and 1.9% UO2 enrichment distribution based on a hypothetical PWR reactor model [6]. A hypothetical fuel element for a hypothetical PWR reactor was simulated using the MCNP5 software. The element consisted of 25 fuel rods with UO2 pellets with three enrichment zones (3.2%, 2.5%, and 1.9%), as shown in Figure 1, and a height of 3.6 m. The kcode was used in the simulation to calculate the criticality of the simulated fuel. 10,000 neutrons per cycle and a total of 100 cycles were used, with 50 of them being passive. To achieve the objective of the work, the first simulation was performed with pure Zircaloy-4, and this result was considered as the reference standard criticality for the fuel element. The second simulation was performed with this alloy doped with 10% molybdenum.The result obtained for the effective multiplication factor (kef f ) with the coated rod under study was equal to kef f = 1.314503 ± 0.0007, which when compared to the reference value without doping kef f = 1.39207 ± 0.00072, a relative percentage deviation of approximately |δ| ≈ 5.57% is obtained. Doping Zircaloy with molybdenum nanoparticles does not significantly alter neutron production. This enables the improvement of the alloy without loss of energy production efficiency. The results of the simulations indicate that the doping of Zircaloy with molybdenum nanoparticles does not significantly alter the neutron production of the fuel rod. This is an important finding, as it suggests that the addition of molybdenum nanoparticles can improve the properties of the Zircaloy alloy without sacrificing its efficiency in terms of energy production. The relative percentage deviation of |δ| ≈ 5.57% between the kef f values for the doped and undoped rods is considered to be small. This suggests that the doping of Zircaloy with molybdenum nanoparticles does not have a significant impact on the criticality of the fuel rod. Overall, the results of this study suggest that the doping of Zircaloy with molybdenum nanoparticles is a promising approach for improving the properties of the alloy without sacrificing its efficiency in terms of energy production. Further research is needed to confirm these findings and to explore the potential benefits of molybdenum doping in more detail.
This study explored the influence of incorporating silicon carbide (SiC) nanoparticles into Stainless Steel 316 on the performance of nuclear fuel using computational simulations with the MCNP5 software[1]. The findings revealed that the introduction of SiC had minimal impact on the effective multiplication factor (keff), suggesting that this modification could be a viable approach to enhancing fuel characteristics without compromising efficacy[2-3]]. Furthermore, the integration of SiC could provide added advantages such as improved thermal stability and resistance to corrosion. These results underscore the potential of SiC as a promising additive for enhancing the safety and efficiency of nuclear fuel elements in reactors, opening avenues for future advancements and research in nuclear energy[4-5]. The results for the effective multiplication factor (keff) with a rod coated and doped with 10% SiC showed keff = 1.12759 ± 0.00064. Compared to the undoped reference value of keff = 1.12086 ± 0.00064, there is a relative increase in criticality of approximately 0.6%. The computational simulation using MCNP5 with kcode provided a detailed analysis of nuclear fuel criticality. The data indicate that doping Stainless Steel 316 with SiC nanoparticles increased the effective multiplication factor (keff) by about 0.6%. This suggests that adding SiC significantly affects neutron production, which is crucial for the safety and efficiency of nuclear reactors[6]. These results point to potential improvements in nuclear fuel performance. Including SiC may offer additional benefits such as greater thermal stability, corrosion resistance, and reduced deformation, contributing to the safety and longevity of fuel elements[7-8]. Moreover, maintaining energy production without compromising neutron efficiency is promising, allowing for advancements in the materials used in nuclear reactor construction. Therefore, the neutron results obtained in this simulation highlight SiC's potential as an effective additive to enhance nuclear fuel properties, paving the way for future research and developments in nuclear energy.
This study explores the significance of simulations performed in MCNP5 and the modifications applied to 316 steel to enhance energy efficiency in nuclear power production. Graphene Nanotubes (GNTs) are examined as promising additives owing to their low absorption cross-section for thermal neutrons, facilitating increased neutron involvement in fission and heat generation. Using the MCNP5 code[1], simulations were carried out to analyze a hypothetical UO2 fuel element with varying enrichment zones to assess its performance[2,3]. The findings underscore the substantial impact of incorporating graphene nanotubes[4] into the fuel cladding alloy on neutron production, implying a potential compromise in energy generation efficiency. The comparison between the results of two simulations allowed us to assess the impact of including graphene nanotubes[5,6] on the criticality of the simulated fuel. If the addition of these nanotubes [7] results in an improvement in criticality, this may indicate superior performance of the nuclear reactor, with higher fuel efficiency and reduced nuclear waste generation. On the other hand, if the inclusion does not positively affect or even reduces criticality, this suggests that this strategy is not viable for optimizing nuclear fuel performance [8]. Therefore, the results of this analysis have significant implications for the development of more efficient and environmentally sustainable nuclear fuels. The result of the effective multiplication factor (keff) for the studied clad rod was keff=1.12086 ± 0.00064, while the reference value without doping was keff=1.13565 ± 0.00076, resulting in a relative percentage deviation of approximately Δ = -1.32%. Doping 316 steel with graphene nanotubes causes a significant alteration in neutron production, which may compromise efficiency in energy generation.
SESSION: CompositeMonPM4-R8 |
Monteiro International Symposium on Composite, Ceramic & Nano Materials Processing, Characterization & Applications (10th Intl. Symp.) |
Mon. 21 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Sergio Monteiro; Student Monitors: TBA |
One of the most important applications of material processing has been the protection of humans and their facilities during times of war. With the creation of firearms, there arose a need for the enhancement of this protection, now known as ballistic protection. Materials for ballistic protection and their processing are the focus of research around the world. One of the biggest challenges is to develop materials light enough for personal protection. A promising material for this kind of application is silicon carbide, that absorbs approximately 55% of the energy by breaking upon projectile impact. However, one of the challenges in processing this material lies in the temperature required for sintering. Temperatures above 2000°C and small volume of economically accessible furnaces hinder parameter control and limit the size of the pieces. The additive manufacturing process, that up to now has been successfully applied to produce polymer and metal pieces, is now being studied as a possible processing method for ceramic materials. In this review, we discuss the evolution of additive manufacturing with a focus on the processing of ceramic materials and, primarily, silicon carbide, with the purpose of presenting existing technologies in the market and the stages of the process, as well as a brief comparison between the characteristics of materials submitted to conventional processing and additive manufacturing.
In this research, the relevance of polymers in our daily lives, in the industrial market, in the development of new technologies, and the harmfulness of the waste generated by these polymers to human health and the environment are observed. By applying and analyzing techniques such as thermal analysis, microscopy, spectroscopy, and diffraction, we explore a composite that contains polymers, organic residues, and metallic residues. Thermal analysis, microscopy, spectroscopy, and diffraction highlight essential behaviors of the material for a process focused on sustainability. Understanding the characteristics of this type of material is crucial for developing processes that transform polluting materials into relevant and economically viable products, with the aim of mitigating human health impacts and environmental impacts. This research validates the use of thermal analysis, microscopy, spectroscopy, and diffraction techniques to characterize and understand complex polluting composites and enhance their applications in new processes and consequently in new sustainable products worldwide, respecting and preserving the environment for future generations.
The embira bark fiber is routinely used in Brazil to construct simple structures because of its ease of extraction, flexibility, and considerable strength. It plays an important role, somewhat similar to duct tape, and is commonly used for temporary repairs and tying objects. The flexible bark is removed from the tree by making two cuts into it and manually pulling off the fibrous structure. Three similar but distinct embira bark fibers are characterized structurally and mechanically: embira branca, embira capa bode, and embira chichá. The bark separates readily into strips with thicknesses between 0.3 and 1 mm, enabling it to be twisted and bent without damage. The structure consists of aligned cellulose fibers bound by lignin and hemicellulose. Thus, it is a natural composite. The tensile strength of the three fibers varies in the range of 25 to 100 MPa, with no clear difference between them. There is structural and strength consistency among them. The mechanical strength of embira branca is measured with other lignocellulosic fibers X-ray diffraction identifies two major components: the monoclinic crystalline structure of cellulose and an amorphous phase; the crystallinity index is approximately 50%.
Nowadays, sustainability and good use of resources and waste are necessary. So, this work seeks to synthesize a ceramic material from natural waste, as well as its characterization and biological evaluation after all the steps that anticipate in vivo application. In this way, brushite, which is a dihydrate dicalcium phosphate mineral that is a calcium phosphate present in the natural mineralization of tissues, can be obtained synthetically from chicken eggshells. It is used as a biomaterial for different applications such as medical treatment, especially orthopedic treatment and bone repair, agrobiological inorganic fertilizers. Brushite has the property of adsorbing ions and changing its active sites with calcium, such as Zn and Ag ions, which can enhance the biocompatible and bactericidal potential of the biomaterial, respectively. In this work, we started with the synthesis of bruxite nanopowders (previously performed) that was characterization by microscopy and physical-chemistry analysis (MEV-topography, MET-nanoscale, FTIR-chemistry-group, XRD Rietveld- material identity). The cytotoxicity was then tested by in vitro microbiological analysis in a nutrient medium using 3 species of bacteria was made ISO-10993-5- ceramic tests. The results shows that was possible to obtain bruxite through the results of chemical-physical characterization and the initial results in vitro indicate that it is a biocompatible nanoceramic.
Thanks to Faperj 203.409/2023 - SEl-260003/016585/2023 for supporting the research, to CAPES, CNPQ and to the student Ronald Palandi Cardoso for helping with the cultivation of microorganisms and to Prof. Yutao Xing for helping with the MET analysis.
SESSION: IronMonPM1-R9 |
Leite International Symposium (10th Intl. Symp. on Advanced Sustainable Iron & Steel Making) |
Mon. 21 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Marcos De Campos; GS Mahobia; Student Monitors: TBA |
Sergio Leite de Andrade has worked in the steel industry for more than half a century. As a metallurgical engineer, he has been actively involved in the field since his university days. Throughout his professional career at Usiminas, he has held 15 positions, including serving as CEO for six years and later as Chairman of the Board of Directors. He is currently an Advisor of the Board of Directors and Vice-President of Strategic Affairs at Usiminas.
In addition to his roles at Usiminas, Sergio has been actively involved in steel industry institutions since the 20th century. He currently serves as President of the Board of Directors of Instituto Aço Brasil and President of the Board of Directors of the Brazilian Association of Metallurgy, Materials, and Mining (ABM).
With the green hydrogen starting at 4.45 US$/kg, [1] hydrogen usage seems difficult. Not only the green hydrogen is very expensive, even the gray hydrogen is uneconomical. However, hydrogen production is a possibility when there is oversupply of electric energy.
In California, renewables as solar and wind already able to provide almost 100% of the energy, avoiding fossil fuels as coal and natural gas [2]. Both windy days or sunny days offer the possibility of in-excess production of energy [2], which can be employed for cheap hydrogen production.
Usually, DRI – Direct Reduction of Iron – request high quality iron ore [3], offering a possibility for Brazil in this market. Vale is considering a hub for HBI (hot briquetted iron) in Porto do Açu in Brazil [4]. Other possible hubs are planned for Saudi Arabia, Oman and Dubai, due to the possibility of cheap natural gas [5].
This study addresses economic issues of hydrogen usage in steelmaking.
Although the denomination “steelmaking” is much more common in English, the world “siderurgy” also exists in English. The name “siderurgy” comes from the old Greek world for iron: sideros. Steelmaking and Ironmaking revolutionized the history of humankind: There are distincts quality of life for the 4 main hystorical ages: stone age, copper age [1], bronze age, and iron age.
Nowadays it became clear that the Old Egyptians were less advanced in metallurgy - or ironmaking - than their neighbors: The Tut-ankh-amon dagger is meteoritic (due to high nickel) and, besides, it probably was imported from Mittani or Hittite lands [2], thats is, present day Turkey .
The transition of bronze to iron and steel was very important for quality of life: In the iron age, furniture could be easily manufactured, and also ships and boats. This revolutionized the commerce. Bronze was very expensive due to the scarce and essential alloying element tin (11-12% in bronze). Instead, iron ore can be found almost everywhere.
It is reviewed the complex process that gave origin to smelting [3,4], for steel and iron production: Magnetite maybe the first ore used for reduction. The origin of first smelting techniques are still uncertain [5]. More and more it became clear that Black Sea regions started the iron smelting process, possibly in areas related to the Chalybes [6], near present day Trebzon.
The iron and steel industry contributes about 7 % of the total carbon dioxide emission globally and about 35% of all CO2 produced in the manufacturing sector[1, 2]. About 1.9 tons of CO2 is produced per ton of crude steel [3, 4]. Carbon from coke or coal is the primary source of heat energy in blast furnaces and rotary hearth furnaces used worldwide. Carbon in the form of graphite electrodes is also used in electric arc furnaces. Thus, it is easy to comprehend that carbon is used extensively in the entire steel making route, making it a high contributor to global CO2 production. Using hydrogen gas as a reductant in place of carbonaceous material offers significant advantages like zero greenhouse gas (GHG) emissions, faster reduction at lower temperatures, and the absence of a complicated boudouard (C-O) reaction. Most hydrogen reduction studies have been carried out on commercial-grade iron ores containing more than 65% Fe, and limited studies are available on the hydrogen reduction of low-grade ores containing less than 50% Fe [3, 5].
The hydrogen reducibility of pellets made from a low-grade multimetallic magnetite ore (Fe content ~45%) was investigated in the present study. Pellets were reduced in a horizontal tube furnace at temperatures ranging from 973 K to 1173 K for 1 to 60 minutes. Pure Hydrogen (H2) gas (99.9%) at three flow rates of 0.25 L/min, 0.5 L/min, and 1 L/min were blown during the reduction process. A maximum reduction degree of 93.55%, metallization ratio of 0.925, and H2 gas utilization of 8.92% were obtained at a temperature and a reduction time of 1173 K and 60 minutes, respectively. In order to optimize the hydrogen utilization, a reduction temperature of 1173 K, a reduction time of 45 minutes, and a gas flow rate of 0.25 L/min were selected, resulting in a reduction degree and metallization ratio of 89% and 0.86, respectively. The cold crushing strength (CCS) of the reduced pellets initially decreased and then increased slightly, exhibiting behavior similar to high-grade ores. SiO2, Al2O3, and MgO are found to control the porosity of the pellets, which directly affected the CCS and reducibility of the pellets.
SESSION: IronMonPM2-R9 |
Leite International Symposium (10th Intl. Symp. on Advanced Sustainable Iron & Steel Making) |
Mon. 21 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Jose Adilson De Castro; Alena Upolovnikova; Student Monitors: TBA |
The role of mathematical models in improving the technology of blast furnace smelting is shown [1]. Examples of new developments of the Institute of Metallurgy of the Ural Branch of the Russian Academy of Sciences in the field of digital models of blast furnace production are given, in particular, two-dimensional and three-dimensional mathematical models of the thermal state of various zones of the blast furnace, the condition of the refractory lining and filling of the furnace, the forecast of the silicon content in cast iron [2, 3].
New developments in the field of analysis and control of various thermophysical and physico-chemical phenomena occurring in various zones of the blast furnace allow us to raise the technology and methods of conducting blast furnace melting to a fundamentally new level, allowing us to save fuel and energy resources.
The possibility of using a digital model at a keeping up with the process when using sensor readings through the database management system of the blast furnace shop of the metallurgical enterprise is shown.
The work was performed within the framework of the State Assignment of Institute of Metallurgy UB RAS.
This paper considers the possibility of using and improving the 2-D models of gas dynamics and heat transfer of the blast furnace process, taking into account the injection of synthesis gas (with different amounts of hydrogen in it) [1-2]. The analysis of existing mathematical models of gas dynamics and heat exchange of a blast furnace is carried out and arguments are given justifying the need to take into account the characteristics of synthesis gas in the mathematical model.
In a blast furnace, additional hydrogen in synthesis gas can be used as a partial replacement for coke, which will reduce the amount of carbon dioxide emissions into the atmosphere and increase the energy efficiency of the process. The use of synthesis gas in a blast furnace has a number of advantages and disadvantages. However, when analyzing the current environmental situation, it should be noted that the technology of using synthesis gas has great prospects.
Calculations using an improved two-dimensional mathematical model have shown a more accurate assessment of the heat transfer characteristics in the blast furnace process using synthesis gas. The results of the study can be used to effectively optimize the parameters of technological processes in blast furnace production.
The work was performed within the framework of the State Assignment of Institute of Metallurgy UB RAS.
The present study investigates the advantages and feasibility of the shaft furnace in direct reduction processes, highlighting its energy efficiency and flexibility in the choice of reducing agents. The complexity of the processes involved within the furnace is addressed, dividing it into four distinct zones. Although mathematical models have been developed to predict direct reduction, their application is limited due to the simplification required in the face of the complexity of the phenomena. The integration of the shaft furnace with partial replacement of the charge by self-reducing pellets is explored, demonstrating a potential increase in process efficiency and reduction in CO2 emissions. This study proposes a multiphase and multicomponent mathematical model to predict the internal temperature distribution of the furnace, validated by simulations on an industrial scale. The results indicate a significant increase in productivity and metalization when using self-reducing pellets, as well as, a reduction in carbon emissions when partially replacing conventional reducing gas with hydrogen. The findings highlight the importance of optimizing operational parameters to maximize the benefits of the shaft furnace in direct iron production.
This study investigates the potential of combined injection of hydrogen as fuel and pulverized charcoal (PCH) in the operation of blast furnaces, aiming to reduce carbon emissions and increase energy efficiency. Through a detailed computational model, we analyzed various operational scenarios with different rates of PCH and hydrogen injection. The results demonstrate that the partial or total replacement of pulverized coal (PC) with PCH can significantly increase blast furnace productivity, reducing coke consumption and carbon emissions. An improvement in internal material distribution and temperature was also observed, with an acceleration in burden descent and a modification in the temperature pattern in the raceway region. Furthermore, it was found that progressive increases in PCH and hydrogen injection can lead to substantial increases in blast furnace productivity, with additional reductions in coke consumption and carbon emissions. These results highlight the potential of combined hydrogen and PCH injection as a viable strategy to promote sustainability and efficiency in the steel industry, aligned with decarbonization and circular economy objectives.
SESSION: IronMonPM3-R9 |
Leite International Symposium (10th Intl. Symp. on Advanced Sustainable Iron & Steel Making) |
Mon. 21 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Marcos De Campos; Bhaskar Topalle; Student Monitors: TBA |
The development of effective technological methods for controlling non-metallic inclusions is a promising direction for improving the complex of properties and quality characteristics of steels. One of the factors regulating the quantity, morphology and distribution of sulfide inclusions over the metal volume is the sulfur content. To organize the production of steel with low sulfur content (up to 0.003 - 0.005%), the desulfurization process is carried out in ladle-furnace installations with the formation of the main slags of the CaO-SiO2-Al2O3 system and deep deoxidation of steel with aluminum. At the same time, one of the main oxide inclusions in steel deoxidized with aluminum is corundum (Al2O3), which deteriorates the properties of steel and leads to “overgrowth” of the inner surface of the immersion nozzle during continuous casting. This negative effect of corundum in steel can be neutralized by removing it into the main liquid slag formed in the ladle-furnace by reducing the activity of Al2O3. However, in practice, an excessive increase in the basicity of refining slag to reduce the activity of Al2O3 is usually accompanied by heterogenization of the slag, an increase in its melting temperature and a decrease in refining properties. One of the promising directions for reducing the activity coefficient of Al2O3 in basic refining slags may be the use of rare earth metal oxides. The use of REM oxides ensures a decrease in their melting point, an increase in fluid mobility, an increase in the coefficient of interphase distribution of sulfur and a decrease in the coefficient of interphase distribution of REM. The paper presents the results of a study of the influence of cerium oxide in the slags of the CaO-SiO2-Al2O3-MgO-CeO2 system on the physicochemical properties. New data were obtained on the influence of temperature, cerium oxide and the basicity of the formed slags on the equilibrium interphase distribution of cerium.
The research was supported by a grant from the Russian Science Foundation.
The production of Tyre cord grades requires not only a very good surface quality in the wire rods but also a very high degree of steel cleanliness. The reason is that the application is safety critical and the end use in Tyre demands a very high level of cleanliness.
There is both fine drawing and also patenting involved in the manufacturing process which means that both gas content and the inclusion content need to be extremely low. Achieving lower gas content as well as inclusion levels is a challenge in the tyre cord manufacturing process. Careful inclusion engineering, selective use of synthetic slags, high process reduction ratios in rolling and use of rectangular bloom sections are all critical to Tyre cord manufacturing. This paper discussed all the critical parameters that need to be controlled in the manufacturing of Tyre Cord steel.
Since essentially the Tyre Cord is a high carbon steel, all precautions that are necessary to avoid segregation like low superheat, optimum casting speed, and optimum rolling & soaking parameters as to be maintained. Since Al₂O₃ inclusions have to be as low as possible, the selection of the right synthetic slag and Sulphur control while tapping are key to the success of manufacturing these grades. In case sulfur is not low (<0.01%) in tapping, then external heat metal desulfurization is a must before refining.
India is poised to emerge as a global hub in car manufacturing, which will be requiring huge quantities of Tyre cord steels for the local usage of Tyre. This presents a unique opportunity for Indian special steel makers to not only be part of the global supply chain but also to significantly reduce the carbon footprint of steel by eliminating the emissions in the transportation of steel from Abroad.
This project discusses the potential of producing Tyre cord steel in India and the opportunity to reduce the carbon footprint by manufacturing near to local Markets.
Among the priority tasks for the development of the country's metallurgical complex, the problem of improving the quality and reducing the cost of metal products remains relevant. Improving the quality characteristics of structural steels is carried out at all technological stages of steel production. The thermodynamics of the phosphorus oxidation reaction, macrokinetics of oxidation processes, phase composition, structure and physicochemical properties of multicomponent slags of the CaO-SiO2-FeO-MnO-P2O5-MgO and CaO-SiO2-B2O3-Al2O3 system, including viscosity, equilibrium interphase distribution of sulfur and boron during out-of-furnace processing of steel.
The results of fundamental research form the basis for the development of innovative technological solutions that provide:
- smelting of intermediate steel in oxygen converters and modern EAFs under magnesium slag of rational composition with a guaranteed low phosphorus content and high durability of the refractory lining of steel-smelting units;
-deep desulfurization and direct microalloying of structural steel grades with boron in ladle-furnace installations using environmentally friendly boron-containing slag.
The introduction of developed innovative technological solutions ensured the production of low-carbon boron-containing structural steels of a new generation, sparingly alloyed with manganese, with low phosphorus and sulfur content and a complex of increased mechanical properties, incl. for large-diameter pipes of strength category X80 without heat treatment with the prospect of reaching strength category X100-X120.
The discussion of sustainable development is directly related to the materials sector, in the first instance because materials are essential for socioeconomic development and in the second instance because of the environmental impacts related to the extraction and management of the sector. Everything from buildings and infrastructure to technology and consumer goods relies on materials. Environmental pressures push the industry and the commerce sector to adopt a more eco friendly stance. Companies are rethinking how they operate to be greener. They're looking for ways to use materials that are less harmful to the environment. This might mean using recycled materials or finding alternatives to traditional materials that are more sustainable. This matters because it helps us deal with big issues like pollution and climate change. As a result, the materials sector has been undergoing adjustments to accommodate the new reality. In this sense, the adoption of sustainable practices in the materials sector is a basic condition to combat the social, economic and environmental problems of present and future generations. In view of the theme presented, the work aims to analyze the evolution of materials over the years in the face of market pressures and the green economy.
SESSION: IronMonPM4-R9 |
Leite International Symposium (10th Intl. Symp. on Advanced Sustainable Iron & Steel Making) |
Mon. 21 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Dimas Coura; Dhanraj Patil; Student Monitors: TBA |
The steel industry is responsible for 5% of total energy consumption and contributes 6% of CO2 emissions worldwide [1]. Brazil produces around 30% of the world's charcoal and a large part of this is used to produce pig iron, ferroalloys and silicon metal. There is a large proportion of artisanal production in the country and pressure for sustainable production systems has led to the development of new clean technologies with higher yields [2]. There are a total of 21 types of carbonization furnaces, of which there are 172 patents with various improvements to the carbonization process [3].
Residues from rice, maize, soy, wheat and other crops such as bambo have high energy potential, and these sources can contribute to increasing electricity generation [4]. The carbonization process has evolved, as has furnace productivity, and making full use of the energy contained in biomass has reached technological limits [5]. With finite natural resources and an industry that is intensive for the development of society, it is necessary to develop alternatives in the direction of the circular economy [6].
This article carries out an analysis of the availability of maize waste and bamboo biomass in Brazil, as well as a review of the optimized carbonization process, where there is use of the gases generated and co-products from the pyrolysis process. The article also evaluates a charcoal generation process that can be adapted to the conditions of biomass availability in the regions of Brazil.
In a submerged electric arc furnace, contact shoes/ clamps/ pads are large copper/ copper alloys components, that are pressed against the electrode casing to conduct electric current into the electrode from the furnace transformer/s connections. Submerged electric arc furnaces normally use Soderberg electrodes in which the solid electrode paste becomes molten and then baked to solid by the increasing heat as the paste moves down inside the electrode casing and passes by the contact shoe area. To bake the paste properly and uniformly across the cross-sectional area of the electrode, the appropriate level of current and its uniform distribution among all the contact shoes of the same electrode, are required, to provide the heating, to solidify the electrode paste at the correct rate. Lower current level at any contact shoe may result in poor baking in the zone of that contact shoe, which may force to reduce the slipping rate to prevent the baked paste level dropping too below the electrode contact shoes or it may result in a green break in extreme case. The contact of the contact shoe with the electrode is not fixed, as the electrode must be supplemented from the top, which continues to get consumed at the bottom; this makes the working conditions of the contact shoes worse. Contact shoes are designed for long and trouble-free operation with optimum electrical contact. Also, to avoid hot spots around the contact shoes or overloading of any contact shoe, the equalization of current in each contact shoe of an electrode is essential. High unequal contact shoe current may indicate poor contact shoe service pressure, over slipping of the electrode so green electrode beneath the contact shoe, furnace zone wise charge mix problem/ under carbon, electrode breakage, issues with the transformer secondary winding, cooling circuit problem of that contact shoe, electrode casing problem, cavitation in the electrode, arcing of contact shoe, double earthing issues etc. This paper focuses and describes the procedure for accurate measurement of individual contact shoe current as well as accurate derivation of electrode-wise current and furnace transformer phase wise current; so that from the recorded trends the above noted problems can be predicted and longer breakdown for defective contact shoe replacement can be substituted with no required replacement / planned maintenance, resulting in higher availability and more efficient operation.
The main challenges in sintering technology within the iron and steel industry involve enhancing productivity and maintaining the quality of sintered ore. Key concerns include uneven heat distribution and high emissions, with sintering and blast furnace processes contributing significantly to overall industry emissions. To address these issues, various methods have been explored, such as double ignition, altering gas compositions, recycling hot flue gases, and using additional gaseous fuels. Among these strategies, modifying the inlet gas conditions is seen as a practical approach. This study examines the effects of oxygen injection during the iron ore sintering process on parameters such as temperature profile, sintering time, yield, and productivity. Lab-scale trials were conducted using a pot sinter setup, with oxygen injected from the top of the sinter bed, while keeping other variables constant. Results showed a significant increase in the duration of high temperatures, which promoted the formation of stronger sinter with improved structural properties. The injection of oxygen also helped maintain the burn-through temperature and increased the mean particle size of the sinter. Thermographic analysis indicated that the flame front expanded upward with oxygen injection, enhancing the efficiency of the sintering process.
SESSION: EnvironmentalMonPM1-R10 |
11th Intl. Symp. on Environmental, Policy, Management, Health, Economic, Financial, Social Issues Related to Technology & Scientific Innovation |
Mon. 21 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Alda Osmeni; Carolyn Merchant; Student Monitors: TBA |
In the Renaissance of fifteenth and sixteenth century Europe, nature was conceptualized as a living organism. Like humans, it had a body, soul, and spirit. The body was the earth mother, the planets the soul, and the fixed stars the spirit. Beyond that was God. In the seventeenth century, the metaphor changed to that of a machine made of dead particles controlled according to the laws of momentum and energy. Nature could be predicted and controlled, ultimately leading to the pollution and depletion of resources. However, through conservation and restoration, much of the damage could be undone. I believe that through a new ethic of partnership with nature, we can take, but also give back to the earth. Such an ethic would allow human lives and nature’s life to continue in an ongoing dynamic relationship.
In the Renaissance of fifteenth and sixteenth century Europe, nature was conceptualized as a living organism. Like humans, it had a body, soul, and spirit. The body was the earth mother, the planets the soul, and the fixed stars the spirit. Beyond that was God. In the seventeenth century, the metaphor changed to that of a machine made of dead particles controlled according to the laws of momentum and energy. Nature could be predicted and controlled, ultimately leading to the pollution and depletion of resources. However, through conservation and restoration, much of the damage could be undone. I believe that through a new ethic of partnership with nature, we can take, but also give back to the earth. Such an ethic would allow human lives and nature’s life to continue in an ongoing dynamic relationship.
The rivers and seas are vital ecosystems, in which various forms of life develop. Sediments act as a substrate for pollutants, including microplastics (MP) and heavy metals (HM) and other elements, which can have adverse effects on aquatic organisms and ecosystems. Contamination of river sediments by these pollutants can pose risks to human and animal health via the food chain or direct exposure, thus aggravating ecological imbalances.
The distinctive character of MPs is their small size, defined as particles with a dimension of 0.1 to 5 mm. Heavy metals, widespread contaminants in the environment, continually affect sediments and bodies of water. MPs, due to their non-degradable nature, and heavy metals act as persistent pollutants, and their combined pollution also poses a new threat to our lives.
This work describes an analytical methodology for sampling and analysis of microplastic pollution, including steps such as sample collection, chemical treatment, density separation and filtration[1]. Another objective of this study was also to prepare a protocol for isolating microplastics from organic matter in a river sediment system. Microplastic evaluation was carried out by optical microscopy and FTIR spectroscopy[2].
We used X-ray fluorescence spectroscopy (XRF) to assess heavy metals and other elements present in sediments prepared as pressed pellets and loose powders, applying two different sets of standards[3]. In this way a comparative study was carried out using two different sets of standards to determine the quantity of heavy metals and other elements.
In 1926, Vito Volterra presented the Pray-Predator model to evalute the effect of time on the population of species [1].
In mathematics, the Lotka-Volterra equations are a couple of first-order, nonlinear, differential equations, which can be used for describing chaotic systems. Lotka-Volterra equations are typically used for describing the dynamics of biological systems, when two species interact: one as prey and the other as predator.
The model can be used to evalute the economy. The idea of Adam Smith of the “Invisible hand” [2] is completely wrong.
Unfortunately, Adam Smith reasoning has dominated the economy for centuries, maybe.
Here it is shown that some economic crisis [3], as 1929 [4] and 1987 [ 5], may have been origin on the excess of capital.
The reasoning presented here can be used to understand variations of price of commodities, as discussed previously [6].
Thus “bubbles” in economy [7] can be predicted, thus mitigating the nephast effect of possible stock market crisis. The Lotke -Volterra equations [8] can be used for the prediction of such “bubbles”.
SESSION: RecyclingMonPM2-R10 |
10th Intl. Symp. on Sustainable Materials Recycling Processes & Products |
Mon. 21 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Jie Liu; Fang Wang; Student Monitors: TBA |
The leather industry produces footwear, leather textiles, technical leather, and leather for haberdashery. The main auxiliary chemicals are compounds of trivalent and hexavalent chromium. Stabilization of appropriately treated natural hide, as a by-product of slaughterhouses, is carried out with 80% complex compounds of trivalent chromium, which creates strong coordination bonds with peptide groups of the skin protein - collagen, and thus achieves the desired useful properties of stabilized raw hide - leather. However, the use of chromium also carries risks. In relation to the shoes that we wear, it is important that the shoe material contains only trivalent chromium. According to standards, the maximum content of Cr VI in footwear is 3 ppm and 50 ppm Cr III of leachable chromium. Our contribution looks at both valences of chromium, the conditions under which trivalent chromium is oxidized to its toxic hexavalent form, and its relationship to the footwear and to our health.
The beamhouse plays a pivotal role in leather manufacturing. However, the conventional lime-sulfide system (LSS) used in the beamhouse causes significant environmental pollution due to the extensive use of chemical agents. In recent years, most research has focused on biological treatments, with enzymes emerging as a promising environmentally friendly alternative. In this study, we employed the salt-enzyme system (SES) to utilize MgCl2-assisted neutral protease to streamline processes and reduce pollution in the beamhouse. Additionally, response surface methodology (RSM) was utilized to optimize the experimental conditions for enhancing unhairing, fiber opening, and bating efficiency. In terms of environmental benefits, compared to LSS, SES exhibits a significant decrease in COD, NH3-N, and TS by 9.59%, 26.27%, and 76.94%, respectively, highlighting its efficacy as an environmentally sustainable alternative. The environmental impacts of the beamhouse stage (LCA) approach by comparing two scenarios. The results showed that all the environmental significantly lower than those linked to LSS. The utilization of MgCl2-assisted neutral protease in a one-step beamhouse aligns with the trend of environmentally friendly and green production for the leather industry.
According to archaeological records, there are a number of well-established dating methods. However, there is a lack of identification of specific type of artifacts, especially collagen-based materials with complex structure. Leather cultural relics, one of representative of collagen-based cultural relics, are precious physical historical materials for the study of ancient social history[1-3]. Leather cultural relic is an important carrier for inheriting human civilization and witnessing historical development. Therefore, the research on the identification and aging mechanism of leather cultural relic is of great significance. In this work, with leathers tanned by tara and quebracho as cultural relics model, the pyrolysis characteristics and kinetics of vegetable-tanned leather were investigated by thermogravimetry (TG) analysis at three different heating rates and the pyrolysis products were analyzed by TG coupled with Fourier transform infrared spectrometry and mass spectrometry (TG-FTIR-MS) analysis, whose micro-loss characteristic is in line with the particularity of cultural relics. The pyrolysis kinetics of the untanned sheepskin and vegetable-tanned leathers were investigated by using both methods of modified Kissinger-Akahira-Sunose (MKAS) and Friedman (FR). The gaseous products mainly consist of CH4, NH3, H2O, CO, HNCO, CO2, and pyrrole. The results were obtained that the appearance of CO and the intensity changes of CH4 and NH3 may provide secure and reliable identification of leather tanned by hydrolyzed and condensed tannins. The leather aging mechanism was revealed, and a new identification method was obtained, which might provide an important theoretical basis for the proper preservation and restoration of collagen-based cultural relics.
Collagen is a naturally occurring polymer with unique triple helical structure, which is the main structural component of leather [1]. The thermal stability of leather has important implications for practical applications and is affected by many factors. In the present work, the effect of re-tanning and fat-liquoring, two important post-tanning operations [2], on thermal degradation behaviors, kinetics and mechanisms of chrome-tanned leather (CTL) was investigated by using thermogravimetry (TG) and TG-Fourier transform infrared (TG-FTIR). The activation energy (Ea) values for the thermal degradation of chrome-tanned, re-tanned and fat-liquored leathers at different conversions were calculated using modified Kissinger-Akahira-Sunose (MKAS) method [3]. It was found that the average value of Ea decreased after re-tanning and fat-liquoring operations. The thermal degradation mechanism was predicted and compared based on single-step and multi-step reaction models with the combination of isoconversional and master plots methods. The results suggested that a two-parallel-reaction model could match the An model better than single-step one. TG-FTIR results showed that CO2, H2O, NH3 and pyrrole were main evolved gaseous products during CTL thermal degradation and confirmed an enhancement of gas release after re-tanning and fat-liquoring operations.
SESSION: RecyclingMonPM3-R10 |
10th Intl. Symp. on Sustainable Materials Recycling Processes & Products |
Mon. 21 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Mingrui Zhang; Qijue Chen; Student Monitors: TBA |
There is growing interest on the utilization of animal by-products and wastes based on sustainability and recycling of natural biomaterials. Animal by-products and wastes mainly refer to skin, bones, and tendons that contain proteins and other macromolecules[1]. Animal raw hides represent a remarkable portion of the weight of sheep (11.0–11.7%), which are abundant sources of epithelial tissue that contains a high concentration of collagen[2]. As the primary ingredients to produce leather products, these raw materials undergo trimming to achieve uniform shapes before commencing the tanning process, which may generate considerable proteinaceous waste[3]. Reportedly, one ton of wet salted hides/skins yields approximately 200kg finished leather along with 350 kg non-tanned solid waste, 250 kg tanned solid waste, and 200 kg wastewater loss[4]. Hence, there remains a considerable of lamb trimming wastes of tannery for the collagen recycle. Plant-based enzymes including papain and bromelain have been utilized for extracting gelatin or collagen from un-tanned bovine trimming waste. Given the potential of ficin enzyme for collagen hydrolysis[5], harnessing this enzyme to extract collagen from discarded sheep trimming waste could be beneficial. In addition, with aided ultrasound, entangled collagen fibrils can be opened then separated, contributing to post-treatment with acids or enzymes as well as reduced extraction periods.
Based on aided ultrasound technology, the aim of this research is to design a sustainable method for extracting collagen from untreated tannery trimming waste using ficin enzyme derived from ficin leaves. The structural and biochemical characteristics of the extracted collagen from this green method and conventional methods (acetic acid) will be fully discussed.
A simple and effective method for the extraction of collagen from untanned tannery trimming waste using acetic acid and ficin enzyme obtained from ficin leaves was developed in this study. Although acetic acid and ficin enzyme both are effective for the extraction of collagen but enzymatic hydrolysis can extract more collagen than the acid hydrolysis method. Collagen obtained from the enzymatic hydrolysis process maintained its predominant triple helix structure and had amorphousness which was confirmed by the FTIR and XRD analysis. However, the collagen obtained from enzymatic hydrolysis was thermally less stable compared to the collagen obtained by acid hydrolysis. Hence, it can be concluded that ficin enzyme- assisted hydrolysis method can aid in the implementation of circular economy approach in the leather industry by extracting collagen from the trimming waste in an environment-friendly way.
Leather manufacturing is increasingly prioritizing environmentally friendly processes, emphasizing clean production to reduce environmental impacts [1-3]. The present work was focused to explore the application of an α-amylase/neutral protease system (ANS) in a simplified one-step process for unhairing, fiber opening, and bating to replace the traditional, chemically beamhouse of lime-sulfide system (LSS). With response surface methodology (RSM), a mathematical model was established to optimize operational conditions, with the concentrations of 0.3 wt.% α-amylase and 0.5 wt.% neutral protease at 28.4℃ for 16.6 hours. The effectiveness of the process on unhairing and fiber opening was studied through scanning electron microscopy (SEM), and the impact on bating was evaluated by the removal rates of carbohydrate and proteoglycan. The leather produced using the optimized ANS exhibited comparable physical properties to those traditionally processed, with higher hydrothermal shrinkage temperature and better softness. Environmentally, the optimized ANS process achieved significant reductions in pollutants, more than 90% of chemical oxygen demand (COD), NH3-N, and Cl-, and 73.91% of total solids (TS) by. An economic analysis further revealed a direct cost savings of 30.98% with the ANS of that with the LSS, alongside indirect benefits of enhanced production efficiency and simplified wastewater treatment. Notably, the one-step enzymatic beamhouse substantially decreases the electricity and water usage, potentially reducing the greenhouse gas emissions by 44.6%. The ANS is proposed to be a sustainable and cost-effective alternative for leather manufacturing with environmentally friendly practices.
The assembly of medium-scale collagen in native tissues promotes excellent performance and multiple functions. The preparation of collagen fibers and fiber bundles from collagen-rich tissues through acid swelling[1,2] and the utilization of combined chemical and physical treatments have been documented[3]. Homogenization and grinding were employed to enhance collagen nanofibrillation, albeit with high energy consumption. In this study, two simple and controllable liquid exfoliation methods were used to extract collagen fine structures directly from bovine Achilles tendons. One method utilized a sodium hydroxide (NaOH)/urea water system to extract collagen fibers with diameters ranging from 26~230 nm through freeze-thaw cycles and ultrasound. The other method involved the use of a urea/GuHCl deep eutectic solvent to extract interstitial collagen fibers with diameters ranging from 102~159 nm directly from bovine Achilles tendons. In situ observation under polarized optical microscopy (POM) and molecular dynamics simulations revealed the effects of these two methods on tendon collagen. FTIR results confirmed that these original fibers retained the typical structural characteristics of type I collagen. Subsequently, these extracted collagen fibers were used as building blocks to prepare independent collagen membranes, which exhibited good transparency, strong mechanical properties, excellent barrier performance, and cell compatibility.
The development of natural fibre biodegradable composites are gaining much attention due to lower environmental impact, driven by the issues with synthetic fiber-based polymer composites manufacture, disposal, and recycling. Nowadays, pineapple leaf fibre (PALF) are playing significant role in composites exhibiting superior performance than other cellulose fibres for a variety of uses in the automotive, biomedical, furniture, and packaging industries, among others. This study examined the combined effects of in-house coupling agent production and pineapple leaf fibre (PALF) loading on the mechanical and thermal characteristics of biodegradable polymers polylactic acid (PLA) and poly(butylene adipate-co-tere-phthalate) (PBAT), which were manufactured by melt compounding. The PLA grafted with maleic anhydride (MA) (PLA-g-MA) was used as a coupling agent to improve the interfacial adhesion between PLA and PBAT with PALF. The results demonstrated the dependence of thermal stability and tensile properties on the grafting level of MA, and also on the concentrations of PALF. Thus, it could be deduced that combination of PALF at high concentrations (5, 10 and 15 wt%) and PLA-g-MA with high grafting level can significantly improve the thermal stability of PLA and PBAT. On the other hand, at high grafting level, there was an improvement in tensile modulus of biocomposite. The morphological analysis indicated better adhesion between PALF and PLA with PBAT, in composites containing PLA-g-MA with high grafting level. Overall, PLA/PBAT/PALF/PLA-g-MA green composites with improved interfacial adhesion, thermal stability and mechanical properties were successfully optimised to replace non-biodegradable conventional plastics with added advantages of biodegradability.
SESSION: RecyclingMonPM4-R10 |
10th Intl. Symp. on Sustainable Materials Recycling Processes & Products |
Mon. 21 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Jiaqi Li; Student Monitors: TBA |
Mineral exploration generates a significant amount of waste, whose improper disposal can cause adverse environmental impacts. This work investigates the use of mining waste in the manufacture of interlocking paving blocks, with the aim of promoting sustainability in civil construction and reducing environmental liabilities. For this purpose, the waste was processed through gravimetric separation methods, using a shaking table and Humphrey spiral, aiming to separate the sand from the iron contained in the waste. Gravimetric methods are based on the difference in density between minerals to promote separation. The shaking table, a device that uses vibratory movements combined with a water flow, separates particles according to their density and size. In this process, heavier particles, such as iron, are directed to one end, while lighter particles, such as sand, are collected at the other end. The Humphrey spiral, in turn, uses the centrifugal force generated by the spiral flow to separate particles of different densities, with the sand being collected on the outer parts of the spiral. After separation, the resulting sand was analyzed for its granulometry through sieving. This process involves passing the sand through a series of sieves with different openings, classifying the particles according to their size. Adequate granulometry is crucial to ensure the quality of interlocking blocks, directly influencing their strength and durability. The processed sand was then used in the production of interlocking paving blocks, employing a vibratory press. This equipment compacts the mixture of sand, cement, and water, forming high-density, high-strength blocks. Interlocking blocks are a sustainable and efficient alternative for paving, offering ease of installation and maintenance, as well as allowing rainwater drainage. To evaluate the quality of the produced blocks, standard compressive strength tests were carried out. These tests consist of subjecting the blocks to compressive forces until rupture occurs, measuring the maximum strength supported. The interlocking blocks manufactured with the processed waste sand achieved a compressive strength of 25 MPa, meeting the normative requirements for paving. The results demonstrate that it is feasible to use mining waste, properly processed, in the manufacture of interlocking paving blocks, contributing to the reduction of environmental impacts and promoting sustainability in civil construction. The application of gravimetric separation methods proved effective in obtaining sand of adequate quality, and the produced blocks showed satisfactory performance in compressive strength tests. This study reinforces the importance of innovative solutions for the management of mining waste, promoting material recycling and the circular economy. Furthermore, the use of waste in civil construction can represent an economically viable alternative, reducing costs with raw materials and minimizing the environmental liabilities associated with mining.
Mineral exploration generates a significant amount of waste, whose improper disposal can cause adverse environmental impacts. This work investigates the use of mining waste processed by gravimetric separation methods, aiming at the production of sustainable construction materials and the elimination of dams, pits, and dry stacks. The waste was subjected to separation processes using a shaking table and a Humphrey spiral, with the objective of separating the clay, sand, and iron contained in the residual material.
Gravimetric methods are based on the difference in density between minerals to promote separation. The shaking table uses vibratory movements combined with a water flow to separate particles according to their density and size. In this process, heavier particles, such as iron, are directed to one end, while lighter particles, such as sand and clay, are collected at the other end. The Humphrey spiral, in turn, uses the centrifugal force generated by the spiral flow to separate particles of different densities, collecting the sand in the outer parts of the spiral and the clay in the intermediate areas.
After separation, the resulting sand was analyzed for its granulometry through sieving. This process involves passing the sand through a series of sieves with different openings, classifying the particles according to their size. Adequate granulometry is crucial to ensure the quality of interlocking blocks, directly influencing their strength and durability.
The processed sand was then used in the production of interlocking paving blocks, employing a vibratory press. This equipment compacts the mixture of sand, cement, and water, forming high-density and high-strength blocks. Interlocking blocks are a sustainable and efficient alternative for paving, offering ease of installation and maintenance, as well as allowing rainwater drainage.
To evaluate the quality of the produced blocks, standard compressive strength tests were carried out. These tests consist of subjecting the blocks to compressive forces until rupture occurs, measuring the maximum strength supported. The interlocking blocks manufactured with the processed waste sand achieved a compressive strength of 14,87 MPa, meeting the normative requirements for paving.
In addition to using sand, the separated clay was used in the manufacture of soil-cement blocks for building construction. The clay was mixed with soil and cement, compacted in specific molds, and cured to achieve adequate strength for civil construction. These soilcement blocks offer advantages in terms of sustainability and cost-benefit, contributing to more ecological constructions.
The iron separated from the waste was pelletized to supply the metallurgical industry. Pelletization involves agglomerating iron fines into pellets, which are then used as raw material in steel production. This process not only adds value to mining waste but also reduces the need for virgin iron ore extraction, promoting sustainability in the metallurgical industry.
The results of this study demonstrate the feasibility of using processed mining waste in the production of sustainable construction materials and supplying the metallurgical industry. The application of gravimetric separation methods proved effective in obtaining materials of adequate quality, and the manufactured products showed satisfactory performance in strength tests. This study reinforces the importance of innovative solutions for mining waste management, promoting material recycling and the circular economy, eliminating the need for dams, pits, and dry stacks.
The need to transition to a clean energy economy has received significant global attention in recent years. This has led to pledges by different nations to get to net-zero emissions. For example, the United States targets achieving net-zero emissions by 2050. Of the different strategies for meeting the targets, significant emphasis has been placed on the electrification of transportation systems. This requires advancement in two key components: traction drives and batteries in electric vehicles (EVs). Recycling of the critical metals contained in these components is one aspect of the advancement strategies. Despite several years of research in recycling permanent magnets and batteries, there are still hurdles to overcome towards making a significant impact.
This talk will, therefore, focus on approaches employed in the recycling of critical metals from permanent magnets in EV traction drives and batteries. It will include a discussion of the key limitations and the opportunities to overcome those. Some innovative approaches developed in the Critical Materials Innovation Hub and Ames National Laboratory will be presented. Particularly, we present the novel acid-free dissolution recycling (ADR) approach for recovering rare earth elements from e-waste. We will also present the newly developed Batteries Recycling and Water Splitting (BRAWS) technology that uses water as the only solvent for recycling Li-ion batteries, uses CO2 as feedstock and produces green hydrogen as a co-product.
SESSION: OxidativeTuePM1-R1 |
Abe International Symposium (4th Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings) |
Tue. 22 Oct. 2024 / Room: Marika A | |
Session Chairs: Fuhua Yang; Haruhiko Inufusa; Student Monitors: TBA |
Depression and other neuropsychiatric diseases are brain disorders that affect daily life. They are triggered by stress from changes in environment, relationships, finances, chronic illness, and other life obstacles. The number of patients with depression is on the rise worldwide, and in recent years, due to the COVID-19 pandemic, there is concern about a further increase. Oxidative stress (OS) plays an important role in depressive disorders in recent studies, including decreased serum antioxidant levels in depressed patients. Increased reactive oxygen species (ROS) and OS-induced dysfunction are associated with the etiology and progression of depression. However, at present, depression is commonly treated with many antipsychotic drugs, and few therapies have targeted oxidative stress. Twendee X®︎ (TwX), an antioxidant combination supplement with dementia-preventive effects for mild cognitive impairment (MCI) in Japanese, provides mitochondrial protection, maintains neurogenesis in the hippocampal dentate gyrus, increases brain autophagy and telomeres, in addition to antioxidant properties that cannot be achieved with a single ingredient. It is composed of eight vitamins, amino acids, and CoQ10, and has passed the same safety standards required of pharmaceuticals. In addition to lowering blood oxidative stress, TwX has been reported to improve quality of life, including defecation status and sleep quality, by acting on the gut microbiota. These various effects suggest that TwX is promising in terms of providing a new treatment option for neuropsychiatric disorders such as depression. Antioxidant therapy using effective antioxidant supplements is promising in terms of diversifying treatment methods in the treatment of depression, even in view of its different positioning from pharmaceuticals.
Free radicals continue to be produced in our body. Free radicals attack lipids and produce lipid hydroperoxide. Aggregated lipid peroxides are known to be a risk factor for developing various diseases such as arteriosclerosis and cancer. Antioxidant enzymes such as SOD and CAT that exist in the body are not sufficient to prevent these problems. Therefore, we consume antioxidants such as vitamins. Therefore, in this study, we reexamined the antioxidant activity of Twendee X, which is commonly sold as a multi-supplement [1]. In this experiment, electron spin resonance (ESR) was used to measure antioxidant activity. ESR is the only measurement method that can directly measure radicals. The results showed that Twendee X has very strong antioxidant activity. The ingredients contained in Twendee X are mainly water-soluble vitamins and amino acids. Despite this, it is surprising that Twendee X has the ability to scavenge hydroxyl radicals and superoxide radicals. This time, we will present a comparison of its antioxidant effect with other antioxidants. As future research progresses, we may be able to discover new combinations of vitamins and amino acids that strongly scavenge many types of radicals. Furthermore, if the relationship between individual radicals and disease and fatigue is clarified, it may become possible to create custom-made supplements.
Vocalization is a complex laryngeal function that involves intricate neuronal networks in the brain. This function depends on vocal fold vibration, which requires adequate subglottic pressure, vocal fold adduction, and tension. However, excessive use of vocal folds can damage the tissue structure of the vocal folds, as well as the laryngeal and respiratory muscles, possibly due to oxidative stress. Therefore, we conducted a study investigating whether vocal loading could lead to functional deterioration of the vocal-related muscles.
Thus, we achieved an animal model, in which excessive vocal fold use induces hoarseness, produced by repetitive forced vocalization triggered by electrical stimulation of the midbrain periaqueductal grey in guinea pigs.
To examine oxidative stress of the laryngeal and respiratory muscles of vocal-loaded animals, we then compared the formation of malondialdehyde protein adducts of the laryngeal and respiratory muscles for a representative vocal-loaded animal with a control animal. The intralaryngeal and expiratory respiratory muscles showed higher levels of malondialdehyde in a vocal-loaded animal.
While additional experiments are required to substantiate this hypothesis, these results may give a new perspective on evaluating vocal fatigue in individuals who use their voices excessively. They may also help identify potential interventions or treatments for vocal disorders.
After the onset of ischemia in an organ, treatments allow blood to flow back into the organs (reperfusion). Typical reperfusion procedures include thrombotherapy for cerebral infarction and catheterization for myocardial infarction. When blood begins to re-enter an ischemic organ, a large amount of oxidative stress is generated from the damaged area. In the case of cerebral infarction, prolonged oxidative stress causes inflammation of the surrounding normal cranial nerve tissue, leading to functional impairment and vascular dementia. In the case of myocardial infarction, it is known that even if catheterization allows blood to return to the heart, a large amount of oxidative stress is generated from the damaged myocardium, resulting in heart failure and death 5 to 7 days after the infarction.
There are limited methods of anti-oxidant treatment for reperfusion. Although Edaravone (RADICUT BAG I.V. Infusion) is covered by health insurance in Japan for cerebral infarction, it is only allowed to be administered once within 24 hours after the onset of cerebral infarction due to its strong side effects. Antioxidant therapy has been tested in myocardial infarction, but no significant effects have been reported.
We have developed an antioxidant combination supplemental, Twendee X (TwX), and TwX has been reported that it can reduce cerebral infarction damage in a mouse model of cerebral infarction. A small number of cerebral infarction patients have reported the improvements of sequelae and reduction of the severity symptoms at the time of infarction. In myocardial infarction, one patient with ST-segment elevation myocardial infarction who had been taking TwX before the onset of the disease was discharged from the hospital on the fifth day without symptoms of heart failure after catheterization. As a safe antioxidant therapy, TwX may be useful in reperfusion disease.
SESSION: OxidativeTuePM2-R1 |
Abe International Symposium (4th Intl. Symp. on Oxidative Stress for Sustainable Development of Human Beings) |
Tue. 22 Oct. 2024 / Room: Marika A | |
Session Chairs: Haruhiko Inufusa; Yuki Sato; Student Monitors: TBA |
Airway reflexes such as coughing, sneezing, and the expiration reflex are essential in preventing foreign body from staying in the airway. These defensive reflexes should be appropriately activated against foreign bodies entering both the upper and lower airways. However, excessive responses to airway stimulation can lead to further airway distress and result in complications such as an overactive cough reflex and sneezing.
Allergic airway diseases, such as asthma and allergic rhinitis (AR), are typically chronic and are occasionally characterized by excessive and prolonged Th2 responses to inhaled allergens. They are assumed to be linked to oxidative stress. Asthma is associated with decreased antioxidant defenses, such as superoxide dismutase, catalase, and glutathione. Patients with AR have systemically elevated oxidative stress and systemically elevated serum total antioxidant status levels. Concomitant use of nasal steroids and antihistamines significantly decreases total oxidative stress in AR patients. Significant improvement in clinical outcome was observed in subjects who received antioxidants along with intranasal steroid fluticasone furoate. Other treatments that have been reported to improve symptoms of respiratory allergic diseases by enhancing antioxidant status include hydrogen-rich saline, crocin, curcumin, and silymarin.
Interleukin (IL)-4 and IL-13 are critical cytokines in the induction of the pathogenic Th2 responses. They induce periostin in the airway tract that is highly expressed in chronic inflammatory diseases―asthma, atopic dermatitis, eosinophilc chronic sinusitis/chronic rhinosinusitis with nasal polyp, and allergic conjunctivitis.
In this presentation, we will briefly review previous studies regarding airway disorders linked to oxidative stress. We will also introduce our recent project regarding airway hyperresponsiveness and the involvement of periostin in respiratory allergic diseases using periostin-knockout mice and respiratory allergic models. Further studies are necessary to evaluate the possibility of anti-oxidative treatment for the hypersensitivity caused by allergic airway inflammation.
This lecture will discuss the data showing that mammals, including the humans, have two major sources of melatonin that exhibit different functions. The best-known source of melatonin, herein referred to as Source #1, is the pineal gland. In this organ, melatonin production is circadian with maximal synthesis and release occurring during the daily dark period [1]. Of the total amount of melatonin produced in mammals, we speculate that less than 5% is produced by the pineal gland [2]. he regulation of the synthesis of pineal melatonin primarily involves the sympathetic innervation of the pinealocytes. Once synthesized, pineal melatonin is released into both the capillaries that perfuse the gland as well as into the cerebrospinal fluid (CSF) of the third ventricle, with both of these fluids exhibiting elevated levels of melatonin at night. The amplitude of the nocturnal rise in CSF melatonin is generally an order of magnitude greater than in the blood [3]. These melatonin rhythms have the primary function of influencing the circadian clock at the level of the suprachiasmatic nucleus (the CSF melatonin) and the clockwork in all peripheral organs (the blood melatonin) via receptor-mediated actions. A second source of melatonin (Source # 2) is produced in multiple tissues throughout the body, probably being synthesized in the mitochondria of these cells [4]. This constitutes the bulk of the melatonin produced in mammals and is concerned with metabolic regulation. Although this review emphasizes the action of melatonin from this source in determining redox homeostasis, it has other critical metabolic effects as well. The possible synthesis of melatonin in mitochondria is of particular interest since these organelles are a primary site of free radical generation [5]. Extrapineal melatonin synthesis does not exhibit a circadian rhythm and it is not released into the blood but acts locally in its cell of origin and possibly in a paracrine matter on adjacent cells [6]. The factors that control/influence melatonin synthesis in extrapineal cells have yet to be identified. We propose, however, that the concentration of melatonin in these cells is determined by the subcellular redox state and that it may be inducible under stressful conditions as is well documented in plant cells [7].
The telomere length is suggested and used as a biomarker of human aging simply due to previously telomeres has been suggested to predict longevity. Oxidative stress is presumably one of the major causes of telomere shortening,
Our findings supported the idea of a possible correlation between the TL and biomarkers of oxidative stress in aging. The study has remarkable scope in medical science as the findings on correlation of TL with biomarkers of oxidative stress in aging are novel and they will help in further research against oxidative stress.
During aging, telomeres shorten classically due to cell turnover. Telomere length is mainly maintained by telomerase. This enzyme is present in the embryonic stem cells in high concentrations and declines with age. It is still unclear to what extent there is telomerase in adult stem cells, but considering these are the founder cells to the cells of all tissues in a body, understanding the telomere dynamics and expression of telomerase in adult stem cells is very important.
Telomere length has been implicated as one of the markers for aging related diseases and neoplastic transformation in both in vivo and in vitro studies. During carcinogenesis telomeres shorten due to high cell turnover and repeats are added by active telomerase or alternative lengthening of telomeres (ALT). This gradual shortening is replication driven and does not necessarily explain the presence of ultra-short telomeres.
Ultra-short telomeres are observed when there is a sudden shortening in telomeres not related with cell division and may arise from breaks in telomeres due to oxidative damage and replication slippage. Telomeres have important functions but do shorten through-out life, ultimately causing cellular problems.
Our group has compared different methods that available to evaluate telomere length, with a special focus on the telomere length dynamics in different tissues, both the overall telomere length and telomere length of individual chromosomes in age related disorders.
Thus, our results showed that telomere profiling may be use as an important clinical parameter and supported the idea of a possible correlation between the ultra-short telomeres as biomarkers of aging. Overall telomere science showed that single or a small group of ultra-short telomeres are more influential in senescence associated disease progression rather than shortening that reflected as average telomere length, therefore it is important to identify the presence and load of ultra-short telomeres in diseases.
Our results suggest the using Universal STELA is an accurate method for evaluation of extreme-short telomeres. Compared to golden standard well known TRF assay, that measures mean telomere length, U-STELA is developed to overcome several problems detecting abrupt telomere shortening in a single chromosome out of 92 chromosome ends same time. The novel approach in U-STELA is to anneal a linker or telorette to the G rich 3’ overhang of the telomere which is a product of restriction digestion after DNA isolation. Telorette enables stable PCR of telomeric regions without template slippage ensuring successful completion of PCR.
At present, the human population is consuming approximately “1.7 earth gross domestic products (earth GDPs)“ per year. It is obvious that this cannot sustain human and planetary life and health. The two major challenges to be met for preserving a healthy human life on a healthy planet are sustainable generation und use of energy and food [1].
Humanity in the Anthropocene faces enormous challenges in terms of: the global population of 8 billion today and 10 billion predicted for 2080; the human impact on biodiversity and climate change; and the need for a more resilient health care system. Yet, humanity also disposes of unprecedented knowledge, technologies, and tools to meet these challenges: the converging and mutually beneficial revolutions in bio- and information technology; and – despite remaining shortcomings – the increasing international cooperation in science, economics, and politics [2].
Nutrition and agriculture stand at the center of both the necessities and opportunities to deliver better human, animal, and planetary health by facilitating sustainable global food and feed supply for populations and livestock [3]; personalized and precision nutrition for enhanced individual human health [4]; and unlocking the wealth of natural bioactives [5]. Human nutrition needs to sustain life, enhance health, and help prevent disease. Nutrition should furthermore prolong human health span in view of extended life span, improve individual well-being, and help enhance performance. While doing that, it should sustainably use planetary resources and minimize irreparable impact on environment and climate [2].
To meet these seemingly overwhelming and possibly conflicting challenges, nutrition science is advancing towards a translational systems science supporting: a more sustainable food system "from farm to fork" [3]; a more efficient yet affordable health care system; and nutritional and dietary strategies tailored to different ethnicities as well as consumer and patient groups [6]. A more sustainable food system requires first and foremost reduction of food waste. We also need enhanced leverage of the plant kingdom for macronutrients, in particular the typically animal-derived protein, and for micronutrients and other bioactive compounds [5]. Efficient yet affordable health care should include (general, medical, and clinical) nutrition and prevention as a complement to pharmaceutical repair and cure. Tailored nutrition requires translational and comparable clinical studies with deeply phenotyped subjects, representative of population groups [7].
SESSION: PhysicalTuePM1-R2 |
Lipkowski International Symposium (4th Intl. Symp. on Physical Chemistry & Its Applications for Sustainable Development) |
Tue. 22 Oct. 2024 / Room: Marika B1 | |
Session Chairs: Junji Saida; Bogdan Palosz; Student Monitors: TBA |
If we use lithium batteries, non-stoichiometry of bonding lithium is clearly evident ((inclusion, or intercalation). Single crystals of silicon, the basis of modern electronics, receive their desired characteristics after successful doping by respective additives, again in non-stoichiometric proportions. Zeolites are the next example and the ‘organic’ option is among the precious, in terms of possible applications, materials known in the chemical literature since 1970ths
Porous molecules are not a rarity, biological chemistry may serve as the valuable source of this sort of matter, like starch component, amylose, and the products of its enzymatic degradation – cyclodextrins. And in recent decades numerous synthetic molecules possessing internal pores have been reported: calixarenes, cucurbiturils, cavitands, crowns, to mention just a few examples.
The paper will concentrate on physico-chemical characteristic of porous materials, including flexibility of their crystal structures which allows ‘engineering’ of sorption/desorption procedures aimed at optimization of solid materials towards a given practical use. Structural and thermochemical experimental data will be discussed jointly with the examples of practical application: separation of organic mixtures in extraction and chromatographic systems, storage of selected species and stabilization of unstable or reactive species.
The illustration will be selected from two major classes of porous materials: solvates of coordination compounds in the form of inclusion compounds and selected molecular hosts (cyclodextrins) presenting infinite number of possible chemical modifications thus enabling design and control of structure/properties relationships.
Studies of fine structural effects accompanying sorption/desorption processes will be discussed from the above mentioned point of view and as aimed at engineering of materials of desired properties.
Supramolecular hydrates will be mentioned as a special class of porous materials.
There is a full consensus that structure of nano-crystals differs from bulk crystals because the atoms on the surface have fewer bonds than in the volume and, consequently, the interatomic bond lengths on the surface are different from those inside the grain. Despite this common knowledge when it comes to characterize experimentally real nanomaterials it is common to make "tacit assumption" of a periodic atomic network representing the structure of a single nanocrystal ignoring lack of information about its actual structure and poor knowledge of tools which may serve for identification of their internal atomic structure.
Practical application of any material is not determined by in-depth knowledge of its atomic structure. However, it is certain that the lack of this knowledge is a significant limitation in predicting and exploiting the properties of nano-materials that may come from their unique but not well recognized atomic structure. To open new perspectives for exploring unique nano-properties one needs to create novel tools serving specifically structural studies of nanomaterials: identification of their shape, determination of surface strains, and learning about their internal atomic structure. Therefore it is worth considering creation of a sub-branch of crystallography dedicated specifically to structural studies of nanomaterials and to name it nano-crystallography.
A review of various crystallographic methods and programs existing for reciprocal and real space analysis of diffraction data to study the atomic structure of nanocrystals will be presented with a focus on accuracy and resolution of diffraction measurements and limitations of numerical methods used to elaborate the experimental diffraction data [1].
Application of DFT and molecular dynamics simulations which were used to model the real structure of nanocrystals, to conduct virtual diffraction experiments, and identify the shape and surface structure of a few nm size grains of CdSe, diamond, and SiC [2-4] will be discussed. Preliminary results of application of Machine Learning to identify the shape and surface structure of nanograins will be presented.
This is quite a paradox that more than a century after introduction of the spherical Independent Atom Model (IAM, 1914 [1]), 99.7% of all ca. 1.5mln known crystal structures have still been refined using IAM which suffers from severe methodological deficiencies. Far better results can be obtained when new approaches of Quantum Crystallography(QCr) utilising aspherical atomic scattering factors are applied. In short, QCr is crystallography beyond IAM.
In this contribution, I will present details of aspherical Hansen-Coppens [2] pseudoatom refinement of electron density and the main ideas of Hirshfeld Atom refinement. My lecture will be complemented by several examples of our QCr [3-9] studies including: (1) multipole refinement of electron density in crystals of minerals including minerals under pressure, (2) Hirshfeld Atom Refinement (HAR) of ice structures against X-ray, electron diffraction and neutron diffraction data, (3) HAR refinement of H-atom positions in small molecule organic compounds and hydrides, and, if I still have some time, I will present: (4) Experimental HAR studies of relativistic effects and electron correlation in gold derivatives.
A century after the Braggs, it is possible to obtain H-atom positions from X-ray diffraction studies which are equally reliable as those from neutron diffraction. It is also possible to get reliable positions of H-atoms in the closest neighborhood of very heavy atoms, to study tiny redistribution of electron density in minerals under pressure, or to estimate consequences of relativistic effects using X-ray diffraction data. So users of X-ray crystallography can do far better than just routinely refining poor IAM model against precise, accurate and very often very dear diffractometer/synchrotron/ XFEL X-ray data. QCr approaches can also improve quality of macromolecular studies, powder -S-ray diffraction results, PDF, XANES, EXAFS, CryoEM, electron diffraction etc. In consequence, one can improve scientific results and stimulate progress in all fields of science/technology/medicine which utilize structural and electronic results.
In R-Ni-In system for R=Tb-Tm, the compounds with the stoichiometry near to 2:2:1 crystallize in two different crystal structures:
The both structures consists of the different types of atomic planes perpendicular to the c-axis. One containing only the rare earth atoms and other composed by the Ni and In atoms. The rare earth atoms are located at C2 point symmetry positions, which have different orientation in the two structures. The C2 axes in the tetragonal structure are perpendicular to each other, while in orthorhombic one are parallel to each other.
Magnetic and neutron diffraction data indicate that these compounds are antiferromagnet with the different magnetic structures. The dependence of the Néel temperature on the de Gennes function is fulfilled for nonstoichiometric and not fulfilled for stoichiometric one. The magnetic moments are localized only on the R elements. For nonstoichiometric compounds the magnetic orders are described by the propagation vector k=[kx,kx,1/2] for kx equal ¼ for Tb, Er and Tm and 0.3074 for R=Ho [1]. For stoichiometric magnetic order is described by k=[1/2,1//2,1/2] for R=Tb [2], k=[1/2,0,1/2] for R=[Er and Tm [3] and k=[0.24,1,0.52] for R=Ho [2]. Direction of the magnetic moments are parallel to the c-axis for R=Tb and Ho in both systems and lie in ab plane in nonstoichiometric one and is parallel to the b-axis for stoichiometric one for R=Er and Tm. The change of the direction of the magnetic moments are connected with the change of the sign of the Stevens operator αJ from negative For R=Tb and Ho to positive for Er and Tm. Those confirm influence of the crystal electric field (CEF) in stabilizing of the magnetic structure. In both systems the antiferromagnetic coupling along the short c-axis is observed.
The difference in the magnetic structures observed in (001) plane results from the difference in the distribution in plane the two structural elements: square TbIn ( CsCl- type) and triangle TbNi2 (AlB2- type).
For R2Ni1.78In the distribution of these elements form the chain along the [110] direction, while for R2Ni2In form chain along a-axis and alternating chain from triangles and squares along b- axis. Competition of two interactions: RKKY and crystal electric field (CEF) lead to complicated magnetic structures [4].
SESSION: MoltenTuePM2-R2 |
10th Intl. Symp. on Sustainable Molten Salt, Ionic & Glass-forming Liquids & Powdered Materials |
Tue. 22 Oct. 2024 / Room: Marika B1 | |
Session Chairs: Ramesh Gardas; Fan Meng; Amr Henni; Student Monitors: TBA |
Two task-specific ionic liquids (TSILs) were encapsulated into the framework of a Zeolite imidazolate framework-8 (ZIF-8) to enhance its CO2 capture capacity and CO2/N2 selectivity at post-combustion conditions. 1-Ethyl-3-methylimidazolium amino-acetate {[EMIM][glycine (Gly)]} and 1-Ethyl-3-methylimidazolium (S)-2-aminopropionate {[EMIM][alanine (Ala)]} were selected as TSILs. TSIL@ZIF-8 composite sorbents were prepared by varying the loading of TSIL, and properties such as sorbent thermal stability, porous structure and crystal nature of the composite were investigated. The incorporation of TSIL into ZIF-8 led to a dramatic rise in CO2 uptake particularly at pressures lower than 1.0 bar. At this low-pressure range, CO2 uptake was greater than in pristine ZIF-8 for all TSIL loadings and TSIL@ZIF-8 composites with 30 wt.% [Emim][Gly] reached a CO2 uptake capacity of 0.76 mmol·g-1 solid at 0.1 bar, and 0.88 mmol/g-solid at 0.2 bar at 303 K. These values were 13 and 7 times higher that CO2 uptake in pristine ZIF-8 at identical conditions. TSIL functionalized composites also exhibited much higher selectivity than pristine ZIF-8 at all pressures. For instance, at 30 wt.% [EMIM][Gly] loading, CO2/N2 ideal selectivities at 313 K were 28 and 19 at 0.1 and 0.2 bar, respectively. This synthesized composite sorbent, with significantly high CO2 uptake, better CO2/N2 selectivity at the low-pressure region (<1.0 bar), and low isosteric heat of adsorption (Qst), confirms that TSIL@ZIF-8 composites can be potential candidates for post-combustion CO2 capture processes and opens the door for the further development of suitable TSIL@MOF composite sorbent to be deployed in the CO2 capture process.
Ionic liquids, a novel class of molten salts, exhibit a distinctive array of properties that set them apart from traditional molecular liquids. These properties include negligible vapor pressure, a wide thermal and electrochemical window, non-flammability, high ionic conductivity, and exceptional solvating capabilities for a diverse range of compounds. Their emergence as "organic solvent alternatives" has spurred significant interest in both academic and industrial spheres. The dynamic research landscape surrounding ionic liquids is expanding rapidly, owing to their versatile applicability, which stems from the ease with which their physical properties can be fine-tuned through modifications in cation-anion combinations or attached moieties. This talk will offer an overview of ionic liquids, emphasizing their unique thermophysical attributes crucial for applications such as metal ion extraction, CO2 capture, fuel desulfurization, and aqueous biphasic systems for extracting value-added products. Furthermore, it will delve into the influence of these thermophysical properties on the efficacy of such applications, while also highlighting current research trajectories exploring ionic liquids as solvents within the chemical industry.
This state-of-the-art review examines the synergistic effects and applications of binary mixtures of ionic liquids (ILs), delineating their potential as versatile solvents in various fields. Binary mixtures of ILs have gathered compelling attention due to their uncommon properties and interactions, offering tailored solutions for various scientific and industrial applications [1].
The review surveys the synthesis and characterization of binary mixtures of ILs, featuring the diverse combinations of anions and cations employed to obtain desired properties. The physicochemical properties of binary mixtures, including conductivity, viscosity, thermal stability, phase behaviour and solvation behaviour, are examined to expound the synergistic effects of mixing different ILs [2]. In addition, the review analyses the thermodynamic aspects of binary mixtures, investigating miscibility, phase transitions, and phase diagrams to comprehend their complex behaviour under changing conditions.
A detailed analysis of the applications of binary mixtures of ILs reveals their versatility in extraction, separation processes, catalysis, green chemistry, and energy storage. In catalysis, binary mixtures of ILs show enhanced selectivity, catalytic activity, and recyclability compared to individual ILs, effectively synthesizing fine chemicals and organic compounds [3]. In separation and extraction processes, binary mixtures of ILs exhibit better performance in the selective recovery of industrial effluents, electronic waste, and metals from ores, contributing to environmental protection and sustainable resource management.
Moreover, binary mixtures of ILs have exhibited promising uses in energy storage, serving as electrolytes in supercapacitor systems and advanced batteries. Their thermal stability, high ionic conductivity, and wide electrochemical stability window make them excellent candidates for enhancing the safety and performance of energy storage devices, promising the development of next-generation energy technologies [4].
The review also discusses the role of binary mixtures of ILs in fostering green chemistry practices by replacing perilous organic solvents in various chemical processes. Their nontoxicity, low volatility, and recyclability help reduce environmental pollution and minimize waste generation, coinciding with sustainable chemistry and technology principles.
Finally, the review pinpoints future research directions and issues in the field of binary mixtures of ILs, highlighting the need for further investigation of their fundamental characteristics, improvement for specific uses, and incorporation in industrial processes [5-6]. In conclusion, this state-of-the-art review provides valuable perceptivity concerning the synergistic effects and applications of binary mixtures of ILs, emphasizing their immense potential as sustainable solvents for diverse scientific and industrial endeavours.
SESSION: MathematicsTuePM1-R3 |
Rowlands International Symposium (7th Intl. Symp. on Sustainable Mathematics Applications) |
Tue. 22 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Svetlin Georgiev; Peter Rowlands; Student Monitors: TBA |
Mineral-, metal- and mine-rich Sweden was a leading powerhouse of Chemistry in the mid- eighteenth to mid-nineteenth centuries with, still most in the world, 20 of the then known elements discovered by Swedes (n = 12), and another telling world record presented by the mineral gadolinite found in 1882 in the village of Ytterby on an island in the Stockholm archipelago, from which eight elements were originally identified; in increasing atom number order, and first isolation in parenthesis, nr 21 Scandium (Nilson 1879), 39 Yttrium (Wöhler 1838), 64 Gadolinium (de Marignac 1880), 65 Terbium (Mosander 1843), 67 Holmium (Cleve 1878), 68 Erbium (Mosander 1843), 69 Thulium (Cleve 1879) and 70 Ytterbium (von Welsbach 1906).
The shining star in this Eldorado was Jöns Jacob Berzelius (1779-1848), “the father of modern Chemistry”. He was initially trained and worked as a physician, which widened his scope, and from his enormous production here only will be mentioned that he discovered four elements; determined all then known atomic weights and innumerable other chemical properties and conditions; developed the subject of Electrochemistry; coined the terms ”allotrope”, ”catalysis”, ”polymer”, ”isomer”, ”protein” and others; and formulated the still valid distinction between ”organic” and ”inorganic” Chemistry.
Fundamentally, he also invented the unambiguous system of chemical notation still used today, i.e. the first letter(s) of the Latin name of the atoms with a numerical suffix of the amount of them in the compound, e.g. CaCO3, calcium carbonate, containing one Calcium, one Carbon and three Oxygen atoms. No other factors are involved, so the consequence would be that the layering between the atoms is dependent upon their sizes and proportions, i.e. stoichiometric, which was Berzelius’ main hypothesis. But nobody knew the fabric of an atom, and he also, somewhat prophetically, suggested that electric forces might be involved to bind the atoms together. However, in the mid-19th century, Kekulé in Germany, Frankland in Great Britain and others developed the theory of "combining power", in which compounds were joined owing to an attraction between positive and negative poles, and from there the ‘valence’ concept has mushroomed to a plethora of localized varieties which have taken over the whole body from the real atoms in a tail-wags-the-dog way. A “network”, a “skeletal”, a “ball-and-stick” chemical formula is a phantom figure of an artificial structure and reduces the true atom build to a point or a mere intersection. It is high time to return to the stoichiometry of the atoms themselves!
Since many years I have been studying an alternative to the Standard Model, following the original differential Lie algebra as outlined in his Norwegian Ph.D. Thesis Over en Classe geometriske Transformationer at Christiania (now Oslo) University in 1871.1,2 I could spend days praising the geniality and innovation of this work. However, the main point here is that it has no direct connections with his continuous groups or root space classifications that the Standard Model has been tied up with to annoying near-fit, but that it is a tangential line congruence algebra that together with the Bohr Aufbau system allows a precise reproduction of the periodic table and its molecular combinations.3-5 Regrettably, though, no one understood Lie ́s thesis: it got excellent marks but soon went into oblivion in the faculty archives. 100 years later I went there and got a photo copy of it (now one can get it electronically), and 1984 I together with professor R.M. Santilli translated it into English (internet open access available at hadronicpress.com/lie.pdf ).2
The aim of this communication is to review and discuss the findings from their chemical model and formula implications. Now that we have the natural figures of all atoms the phantom diagrams of their inferred force lines should be replaced by their real structure.
As it is well known, Isaac Newton had to develop the differential calculus, (jointly with Gottfried Leibniz), with particular reference to the historical definition of velocities as the time derivative of the coordinates, $v = dr/dt$, in order to write his celebrated equation $m a = F(t, r, v)$, where $a = dv/dt$ is the acceleration and $F(t, r, v)$ is the Newtonian force acting on the mass $m$. Being local, the differential calculus solely admitted the characterization of massive points. The differential calculus and the notion of massive points were adopted by Galileo Galilei and Albert Einstein for the formulation of their relativity, thus acquiring a fundamental role in 20th century sciences.
In his Ph. D. thesis of 1966 at the University of Turin, Italy, the Italian-American scientist Ruggero Maria Santilli pointed out that Newtonian forces are the most widely known in dynamics, including action-at-a-distance forces derivable derivable from a potential, thus representable with a Hamiltonian, and other forces that are not derivable from a potential or a Hamiltonian, since they are contact dissipative and non-conservative forces caused by the motion of the mass $m$ within a physical medium. Santilli pointed out that, due to their lack of dimensions, massive points can solely experience action-at-a-distance Hamiltonian forces.
On this ground, Santilli initiated a long scientific journey for the generalization of Newton's equation into a form permitting the representation of the actual extended character of massive bodies whenever moving within physical media, as a condition to admit non-Hamiltonian forces. Being a theoretical physicist, Santilli had a number of severe physical conditions for the needed representation. One of them was the need for a representation of extended bodies and their non-Hamiltonian forces to be invariant over time as a condition to predict the same numerical values under the same conditions but at different times.
The resulting new calculus, today known as Santilli IsoDifferential Calculus, or IDC for short, stimulated a further layer of studies that finally signaled the achievement of mathematical and physical maturity. In particular, we note: the isotopies of Euclidean, Minkowskian, Riemannian and symplectic geometries; the isotopies of classical Hamiltonian mechanics, today known as the Hamilton-Santilli isomechanics, and the isotopies of quantum mechanics, today known as the isotopic branch of Hadronic mechanics.
The main purpose in this lecture is to represent some recent researches of Santilli iso-mathematics in the area of the plane geometry. This lecture is devoted to the iso-plane geometry. It summarizes the most recent contributions in this area.
Straight iso-lines are introduced. Iso-angle between two iso-vectors is defined. They are introduced iso-lines and they are deducted the main equations of iso-lines. They are given criteria for iso-perpendicularity and iso-parallel of iso-lines. Iso-reflections, iso-rotations, iso-translations and iso-glide iso-reflections are introduced. We define iso-circles and they are given the iso- parametric iso-representations of the iso-circles. We introduce iso-ellipse, iso-parabola and iso-hyperbola and they are given some of their basic properties. The lecture is provided with suitable examples.
Nonlocal elasticity and strain gradient elasticity theories are challenging generalized continuum theories to model crystals at small scales like the Ångström-scale (see,e.g., [1,2]), where classical elasticity is not valid and leads to unphysical singularities. The theory of first strain gradient elasticity in its modern form dates back to Toupin [3] and Mindlin [4]. A mathematical modeling of the elastic properties of cubic crystals with centrosymmetry at small scales by means of the Toupin-Mindlin anisotropic first strain gradient elasticity theory is presented [2]. In this framework, two constitutive tensors are involved, a constitutive tensor of fourth-rank of the elastic constants and a constitutive tensor of sixth-rank of the gradient-elastic constants. The 3+11 material parameters (3 elastic and 11 gradient-elastic constants), 3 characteristic lengths and 1+6 isotropy conditions are derived. The 11 gradient-elastic constants are given in terms of the 11 gradient-elastic constants in Voigt notation. The numerical values of the obtained quantities are computed for some representative cubic materials using an interatomic potential (MEAM) [2, 5]. Moreover, the isotropy conditions of strain gradient elasticity are given and discussed. A generalization of the Voigt average towards the sixth-rank constitutive tensor of the gradient-elastic constants is given to determine the 5 isotropic gradient-elastic constants [2].
In this work, a nonlocal elasticity model of Klein-Gordon type, characterized by nonlocality in space and time, is developed for the investigation of wave propagation in isotropic elastic media [1, 2]. Nonlocal elasticity theory having a close link to the underlying microstructure has the advantage to capture effects at small scales [3]. Specifically, nonlocal elasticity is valid down to the Ångström-scale and it can be considered as a generalized continuum theory of Ångström-mechanics as it has been shown in [4]. For the first time in the framework of nonlocal elasticity theory, the proposed nonlocal elasticity model of Klein-Gordon type possessing one characteristic internal time scale parameter in addition to the characteristic internal length scale parameter describes spatial and temporal nonlocal effects at small scales.
The dispersion relations of the considered isotropic nonlocal model of Klein-Gordon type are analytically determined predicting in addition to the acoustic modes (low-frequency modes), optic modes (high-frequency modes) as well as frequency band-gaps between the acoustic and optic modes. The ranges of the frequency band-gaps for longitudinal and transverse waves are determined. Moreover, the phase and group velocities are calculated for the acoustic and optic branches of longitudinal and transverse waves showing that all four modes exhibit normal dispersion with positive group velocity.
The proposed nonlocal model of Klein-Gordon type possessing only 4 constitutive parameters (2 elastic constants, 1 length scale and 1 time scale) provides an appropriate framework for the modelling of accurate frequency band-gaps and overall physically realistic dispersive wave propagation.
SESSION: MathematicsTuePM2-R3 |
Rowlands International Symposium (7th Intl. Symp. on Sustainable Mathematics Applications) |
Tue. 22 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Peter Rowlands; Mike Mikalajunas; Student Monitors: TBA |
This course is a continuation of the first course that was given in Panama last year at the SIPS 2023 conference. Our primary objective for this year will always remain the same by providing a more transparent solution on the current major limitation of Calculus in terms of not being able to establish some form of a unified theory of analytical integration.
The complete mathematical solution that was presented at the last SIPS Workshop was described in the form of Specialized Differential Forms or SDF for short with some major applications in the field of the Physical Sciences that would include Fluid Dynamics, Mechanics of Material, Quantum Mechanics and even in Cosmology. We will be demonstrating at this Workshop how the unique mathematical properties of SDF would play a major role in the development of more reliable theoretical models of the human body by working only with the general analytical solutions of the Navier-Stokes equations for the Mechanical aspect and the Schrödinger equations for the Chemical aspect of the human body.
Currently there exist no such theoretical models of the human body that would be based entirely on general analytical solutions of PDEs because of the severe limitation of Calculus which if successfully resolved by the method of SDF would become immeasurable in terms of reducing our excessive dependency on the use of experimental models in the Physical and Biological sciences.
This course is a continuation of the first course that was given in Panama last year at the SIPS 2023 conference. Our primary objective for this year will always remain the same by providing a more transparent solution on the current major limitation of Calculus in terms of not being able to establish some form of a unified theory of analytical integration.
The complete mathematical solution that was presented at the last SIPS Workshop was described in the form of Specialized Differential Forms or SDF for short with some major applications in the field of the Physical Sciences that would include Fluid Dynamics, Mechanics of Material, Quantum Mechanics and even in Cosmology. We will be demonstrating at this Workshop how the unique mathematical properties of SDF would play a major role in the development of more reliable theoretical models of the human body by working only with the general analytical solutions of the Navier-Stokes equations for the Mechanical aspect and the Schrödinger equations for the Chemical aspect of the human body.
Currently there exist no such theoretical models of the human body that would be based entirely on general analytical solutions of PDEs because of the severe limitation of Calculus which if successfully resolved by the method of SDF would become immeasurable in terms of reducing our excessive dependency on the use of experimental models in the Physical and Biological sciences.
There is an ongoing debate as to whether our biologic origin is dualistic or monistic. Theoretically, there should be unequivocal scientific evidence for one state or the other being the primary source of the evolutionary origin of serial Symbiogenesis. The essence of this article is that the process of Symbiogenesis- the assimilation of factors in the environment that have posed existential threats as the physiologic basis for consciousness provides that hypothetical evidence. Peter Rowlands’ Rewrite Mathematics is an algorithmic homolog of Epigenetic Inheritance that explains the how and why of mathematics running true to physiology. However, it only accounts for synchronic or ‘real time’ consciousness, not for diachronically emergent nonlocal consciousness. It is how and why Gödel’s Incompleteness Theorems are incomplete….they overlook Gödel’s nonlocal consciousness that was necessary for formulating the formal math.
It has been proposed that life is a Singularity (1). The primary means of sustaining that state biologically is Symbiogenesis, the assimilation of factors in the environment that pose existential threats. But why not just destroy them? Answer: Because then there would be no history to reference in order to evolve effectively. Moreover, given that, Symbiogenesis must have evolved from a Singularity as its reference point, generating a ‘holism’. This hypothetically answers the question as to where mathematics emerged from as follows. Tegmark (“Our Mathematical Universe”) stipulates that math is inherent to the Cosmos; since Symbiogenesis passively assimilates the math inherent to the Cosmos, incorporating it into physiology as the basis of consciousness, there is a seamless integration of math both physiologically and consciously. For example, Rowlands’ Rewrite Math (“Foundations of Physical Law”) mirrors the mechanism of Epigenetic Inheritance, Rowlands’ zero ‘attractor’ behaving like the cell does, a new datum assessed by the existing data set behaving in the same way as the egg and sperm of the parent, facilitating adaptation to change. Lou Kauffman’s ‘Knot Math’ similarly resembles embryogenesis, the twisting of the circle generating knots, the twisting of the embryo generating the stages of its development. Proof of a true ‘knot’ is the ability to unknot it to re-form the circle; homologously, the cell must undergo meiosis to form the egg or sperm in order to then reproduce. And Soft Logic Math as the family of real numbers and ‘zeroes’ reflects how physiology has evolved as a two-tiered system, the real numbers being the horizontal accumulation of data, the family of zeroes as the vertical generation of physiologic traits ontogenetically and phylogenetically. This intimate relationship between the Singularity, Symbiogenesis and evolution can also be seen as a Fibonacci sequence, the Singularity (1) + Symbiogenesis (2) = Evolution (3), or 1 + 2 = 3, out of which emerges empathy as a product. These fundamental insights provide for sustainability of life based on the ubiquity of the Fibonacci sequence.
SESSION: MathematicsTuePM3-R3 |
Rowlands International Symposium (7th Intl. Symp. on Sustainable Mathematics Applications) |
Tue. 22 Oct. 2024 / Room: Marika B2 | |
Session Chairs: TBA Student Monitors: TBA |
This review paper examines the status of artificial intelligence (AI) technology in Ethiopian STEM (Science, Technology, Engineering and Mathematics) schools and the possibility of implementing AI programs in the future. Many developed and developing countries are using AI to help grow and improve their economies and to leverage their technology and services. The primary use of AI technology in schools is generally to make more creative the teenagers learning in mathematics and science. This article aims to provide alternative directions on implementing artificial intelligence programs in Ethiopian STEM schools, with an emphasis on learning from developed countries and sharing best practices. Primary and secondary data are used: Secondary data are analyzed on theory-based evidence while primary data are analyzed based on structured questionnaires. In order to achieve the goal, select journals, research and other related websites are reviewed. The findings of this review indicate that in STEM schools, there are many teenagers with specific interests and abilities in mathematics and coding. This knowledge is needed for artificial intelligence. The encouragement and reflection on the advantages of basic AI concepts for youths is necessary as it can help to engage talented students in learning. This paper thoroughly analyzes relevant research and interview data to highlight key insights, status, challenges, and future directions for AI implementation in Ethiopian STEM schools.
SESSION: PharmaceuticalTuePM1-R4 |
Leuenberger International Symposium on Pharmaceutical Sciences and Industrial Applications for Sustainable Development |
Tue. 22 Oct. 2024 / Room: Minos | |
Session Chairs: Ibrahim Karim; Hassan Tarabishi; Student Monitors: TBA |
The application of environmental solutions using the science of BioGeometry in government projects in Switzerland has resulted in a significant reduction of physical and psychological symptoms caused by electromagnetic and chemical pollution. Based on a solid new physics of quality, these results have been sustained for over twenty years. The purpose of this paper is to introduce the possibility of applying BioGeometry to pharmacology to reduce the side-effects of pharmaceutical drugs. The application of BioGeometry design principles to water and feed in chicken farming in Canada have produced healthy chemical-free products for several years. Saltwater planting experiments in Egypt have shown the effect of using BioGeometry design principles for water and §plant containers. BioGeometry-designed bottles have given water and other liquids prolonged freshness with health benefits. Based on a wide range of research, the introduction of the BioGeometry harmonizing energy quality into all kinds of pharmaceutical as well as other products can insure a widespread effect of the BioGeometry benefits with a significant reduction of drug side-effects. This will surely play an important role in this age of pandemics.
The success of BioGeometry in environmental research projects over the years has prompted us to extend this invitation to do interdisciplinary integrative research that promises to introduce a new era of pharmaceutical products that will greatly enhance human, animal and plant health.
Water, something that we often take for granted, has a fourth phase [1] that holds mysteries crucial to understanding many natural phenomena. This theory on structured water fourth phase was often met with skepticism and labelled as pseudo-science but recently, finds acceptance as researches advances with more evidences through more sensitive equipment and modern super-computer quantum energy calculations.
The concept of Structured Water (SW) fourth phase between solid and liquid is defined as cluster of water molecules joined by strong H-bonds to form relative stable ringed-structures molecular called Coherent Domains (CD) with characteristics that differs from classical notions of bulk liquid water. Based on the Quantum Electrodynamics (QED) field theory, the two phases, unstructured/non-coherent bulk water and structured/coherent (CD) water, exist together in liquid water at variable proportion depending on water conditions and environment [2-6]. The Coherent Domains (CD) are created when water molecules oscillate between two electronic configurations in phase with a resonating electromagnetic field (EMF) [7-8], which can create a quantum resonating cavity in the Coherent Domain (CD) trapping specific frequencies/waves [9-10]. In other words, bulk water may convert into (SW) water by resonating with and collecting coherent (EMF) fields generated from either in vivo or environmental sources [11]. The trapped non-vanishing (EMF) field doesn’t dissipate and tends to resonate with other CDs coherently. This phenomenon is referred to as Water Memory (WM) by Dr. Luc Montagnier [12]. Similarly, at hydrophilic surfaces, structured water (CD) is formed as dense lattice of hexagonal-ringed molecules expelling contaminates out of those tight H-bonded layers of hexagonal rings, firstly referred to as Exclusion Zone (EZ) by Dr. Gerald Pollack. The honey comb structure forms 60 degree shifted layers up to 1 mm in thickness capable of accommodating helix structure [13-14].
Recent (SW) studies employing Transmission Electron Microscope (TEM), Atomic Force Microscopy (AFM), and Scanning Tunneling Microscopy (STM) to detect and image structured water (CD) in liquid water and on metal surfaces [15-18]. AFM images revealed water supra-molecules of various sizes and shapes potentially comprising millions to billions of clustered H-bonded water molecules with soft, gel-like properties. Each supra-molecules rod-like or spiral-helical structures comprised of much smaller “spheres” resembling pentamers and hexagonal ring structure (CD). The spheres’ (CD) outer shell is electron-dense, indicating that the outer shells are a cloud or cold vortex of quasi-free electrons. These structures remain stable for weeks or months at room temperature and pressure [19]. As CD spheres approach a hydrophilic surface, they flatten out into a liquid crystalline lattice, known as Exclusion Zone (EZ), composed of tight layers of H-bonded, hexagonal-ringed water molecules [20]. The cold vortices of quasi-free electrons in the outer shell of the (CD) sphere are converted into quasi-free electrons within the (EZ) layers that interfaced with the hydrophilic surface [6,7,20]. When the H-bond strength increases to provide more structure to water, it becomes less fluid, with higher viscosity but the pentamers and hexagonal ring structure (CD) spheres or rods is less dense than liquid bulk water (similar to ice). However, the tight lattice structured water at hydrophilic surfaces is more dense than liquid bulk water [21].
In structured coherent domain the molecular electrons fluctuate between being strongly bound (ionization potential 12.60 eV) and an excited configuration (12.06 eV) in which one electron per molecule is “quasi-free”. Additionally, the trapped (EMF) radiation inside the (CD) had an equivalent of (0.26 eV) [19,22]. Even weak energy sources like red light (~680nm) have enough energy (1.8 eV) to bring the quasi-free electrons over the threshold of ionization potential. Infrared and other weak frequencies emitting subtle (EMF) electromagnetic and magnetic fields are able to increase structured water (EZ) [23-24]. However, many studies showed that, microwave frequencies (2.45 GHz) of older cell phones and (20-60 GHz) of newer 5G reduce water structure (EZ) layers since they destroy covalent bonds and disrupt H-bonding dynamics in water [25-27].
(SW) is not just H2O but rather pentamers or hexagonal ring structure with 3 x -eH3O2 which bears noticeable negative charge (-100 mV to -200mV) due to losing protons +H to the adjacent bulk water forming positively charged hydronium ions +H3O, lowering its pH < 7 and serving as energy reservoir [28]. A quantum computational model study of anionic and neutral hexamer structures showed that a set of two hexamer rings could be stacked on top of another with quasi-free electrons in the π orbitals. The computational spectral signature of (SW) hexagonal rings was 271 nm [29], which matched the experimental spectral signature of (EZ) water 270 nm [30-31].
There is a well known but forgotten heat measuring apparatus, an isothermal microcalorimeter (Fast4U Calorimeter built by Calbact AG) that can be used to obtain the dynamic heat-flow produced during a bacterial infection. It allows susceptibility testing to be done in shorter time than with conventional methods.
The result of a heat-flow curve produced e.g. the one produced at the threshold level by 105 CFU one gets what otherwise uses multiple steps.
The influence of antibiotics on heat-flow curves will be shown. These modifications indicate the effect caused by the resistivity.
Deciding to invest in any company/ business requires that you educate yourself so that you know as much as possible prior to committing your capital and time.
We will discuss a process to determine if an investment in either an existing pharmaceutical company or start-up is a viable choice based on your time horizon, goals, and expectations. We will discuss the importance of the management’s goals, the company’s financial situation and the time needed to realize your goal for the investment.
The goal of the discussion is to give you some of the tools needed, so that you can determine for yourself if the investment makes sense for your individual situation,
You will be able to decide for yourself whether you want to invest the time to do the research or to hire a professional to research your options.
SESSION: LawsTuePM2-R4 |
Dibra International Symposium (4th Intl Symp on Laws & their Applications for Sustainable Development) |
Tue. 22 Oct. 2024 / Room: Minos | |
Session Chairs: Shulamit Almog; Besfort Rrecaj; Student Monitors: TBA |
The official entry into force of the EU’s AI Act has brought forth a new regulatory reality, for the development and application of Artificial Intelligence technologies, within the jurisdictions of Europe. With a strong focus on the transparent and explainable character of these systems, the AI Act adopts a risk-based approach that categorizes them based on the possibility of harm they may endanger, for persons and for the general public. This new reality creates newfound challenges for businesses, as they are bound to employ all the more AI technologies within their work, regardless of their scale. And these technologies use data as their fuel; this fuel, though, has the abovementioned strong regulatory framework to conform with, in order for the business utilizing these technologies to be able to profit from them in accordance with the law. Therefore, the analysis of the AI Act’s provisions related to business activity, and especially those regarding the correct and safe collection, processing and exchange of data is of paramount importance for businesses to be able to develop in this new era, as well as to guarantee that this deployment doesn’t intervene with the rights guaranteed to natural persons interacting with these businesses within the European legal order(s). It is this hard balancing that creates a new set of issues around the liability of developers, deployers and users of AI systems, that must be thoroughly and punctually assessed within this new framework and its upcoming legal follow-ups centered especially on liability.
On April 8, 2024, the European Court of Human Rights (ECtHR) delivered a landmark decision in Verein KlimaSeniorinnen Schweiz and Others v. Switzerland, finding that States have a legal duty to take action to mitigate climate change. Ruling in favor of a Swiss association of over 2,000 Swiss women, the Court found that the Swiss government violated the human rights of its citizens by failing to do enough to combat climate change.
The original complaint, presented to the Court by four women and a Swiss association Verein KlimaSeniorinnen Schweiz, centered around the impact of climate change on their living conditions and health. They argued that the government's inaction on climate change put them at risk of heatwave-related deaths, with their age and gender making them particularly vulnerable. While the Court deemed the four individual applicants inadmissible, stating that they did not meet the victim-status requirements under Article 34 of the Convention, it recognized the right of the applicant association to file a complaint.
Ultimately, the Court determined that the Swiss Confederation had neglected its duty to fulfill its positive obligations under the Convention concerning the right to respect for private and family life of the Convention, interpreting it as freedom from environmental threats to one's personal life, and a violation of the right to access to the Court. Failure by Switzerland to revise its policies may lead to additional legal actions at the domestic level, potentially resulting in court-imposed financial penalties.
This presentation will seek to analyze future ramification of the said decision and possible future legal actions by individuals against regarding their right to a healthy environment and how will this translate into positive duties of state to take concrete actions to mitigate the effects of climate change. It will also touch upon the basic articles of the European Convention on Human Rights encroaching actions regarding climate changes.
The presentation introduces the Homeric oeuvre into the law and literature canon. It argues for a reading of Homer's The Iliad and The Odyssey as primordial narratives on the significance of the rule of law. It delineates moments of correspondence between the transition from myth to tragedy and the gradual transition from a social existence lacking formal law to an institutionalized legal system as practiced in the polis. It suggests the Homeric epics are a significant milestone in the way justice and injustice were conceptualized, and testify to a growing awareness in Homer's time that mechanisms that protect both individuals and the collective from acts of unbridled rage are necessary for the continued existence of communities.
There is a quote goes like that "Your comfort zone will destroy you" but whenever unemployed youths get the opportunity to earn money without any effort except an investment. In return, such unemployed people and youth living in a developing country shall receive double or triple investment benefits through crypto-currencies or tokens i.e. Bitcoin Cash (BCH), Ether (ETH), Binance Coin (BNB), Tether (USDT), Solana (SOL) where the local government banned such transaction of coins.
Law enforcing agencies cannot take immediate actions as the transaction is made secretly with local money transfer apps and funding from Black Money. People living in a developing country shall always take detrimental life risk to have a safe and secure future with huge money for their successors. Being scammed again and again, those needy people will try to change their present economic status by any means where the laws and regulations don't make any sense to them.
Unemployment, bribery, lack of standard life, greed for earning speedy money and converting one's black money to white money, all these elements are forcing Bangladeshi people to invest in crypto-currencies.
SESSION: PharmaceuticalTuePM3-R4 |
Leuenberger International Symposium on Pharmaceutical Sciences and Industrial Applications for Sustainable Development |
Tue. 22 Oct. 2024 / Room: Minos | |
Session Chairs: Hassan Tarabishi; Martin Bultmann; Student Monitors: TBA |
The application of environmental solutions using the science of BioGeometry in government projects in Switzerland has resulted in a significant reduction of physical and psychological symptoms caused by electromagnetic and chemical pollution. The study done by the Building Biology Information Organisation (x) GIBB and Dr. Med. Yvonne Gilli, Member of Parliament showed that the effects on the emotional and mental level were more significant than those on the physical level which had shown a 60% reduction in symptoms. A new taste for life, the will to undertake activities as well as the significant reduction of aggression in interaction with others were among the many lost traits that were restored. The mayor said on television that peace had had prevailed on the community. A complete reduction of epileptic seizures was very surprising. The frequent buzzing headaches were greatly reduced. Based on a solid new physics of quality, these results have been sustained for over twenty years. Those results led to several post-graduate PhD research on the effect of BioGeometry design on different brain problems like depression (X), hyperactivity and autism (x). The results obtained in more than two decades of research with, were applied in the creation of architecture that played an active part in creating a healing environment for special abilities, the new term used to collectively describe those brain disturbances. In this paper, the stressful effect of different shapes on the brain will be examined (x), and some examples of research in this field will be presented. These promising results have been applied in the design of the new project for the integration of special abilities to be carried out by the Egyptian government’s presidential projects.
Energized structured water (SW) consists of relative stable h-bonded cyclic rings with quasi-free electron swarm and readily available protons. Structured water (SW) in contact with hydrophilic biological surfaces, like cell or mitochondria membranes, proteins and DNA turns into biological structured water (BSW) or exclusion zone (EZ), adheres to the surface and is the main charge contributor due to its energized quasi-free electrons and adjacent proton +H or hydronium ion +H3O. Thus, playing a major rule in cell redox reactions, respiratory functions and in maintaining healthy cellular functions [1-5]. Negatively charged (SW) unexpectedly adheres to negatively charged lipid membrane surfaces and forms exclusion zone (EZ) [6]. According to Quantum Electrodynamics (QED) theory, resonance attraction forces (SW) is generated when coherent domains (CD) oscillate in phase with resonant waves emitted from the lipid membranes [7].
Aquaporins in cell and mitochondria membranes are more permeable for SW/BSW than liquid bulk water enhancing the functionality of mitochondria and cell [8-10]. Mitochondrial heat energy (53-54°C) equivalent to FIR of 10174 nm [11] is absorbed by BSW, increasing EZ layers and providing additional energized quasi-free electrons for cellular activities, acting like an energy store [12-13]. Near-infrared and red-light wavelengths, directly from the sun or indirectly through Schumann Resonance (SR) frequencies (7.8, 14.1, 20.3, 26.3 and 32.5 Hz) [11,14], has higher energy to penetrate the body and increase (EZ) layers in the cells. Interestingly, Schumann Resonance (SR) frequencies agree with the human brain electroencephalogram (EEG) frequencies. These waves can carry & transmit specific resonating information (EMF) to the coherent domains (CDs) in the hexagonal ring-layers of (BSW) initiating specific cellular functions similar to old radio receivers that use hexagonal silicon quartz crystal [15]. Furthermore, Dr. Luc Montagnier demonstrated that weak EMF at 7.8 Hz for 18 hours could transfer specific DNA (EMF) to SW in another tube, where DNA signals were detectable even at extreme dilutions, referred to as water memory (WM). This water, when exposed to specific DNA (EMF) digital acoustic files, can reproduce the same DNA strain in a PCR reactor, called Water Transduction (WT) [16-17]. Qi or Ki, transmitted by a trained person, through special breathing techniques by Nishino, in near-infrared wavelengths (0.8-2.7 µm), can manipulate muscle contraction and suppress cancer cell growth in vitro [18]. The explanation lies in the influence of NIF on (EZ) water in the cells. Water respiration (WR) energy theory is based on a cascade of redox reactions including reactive oxygen species (ROS), which is considered the main cause for age-related diseases. However, when superconductivity, a characteristic of BSW, is considered, redox reactions in vivo could occur at superconductive speeds without causing detectable (ROS) damages [19-23]. Along with BSW, cells require a four-fold excess of oxygen to prevent ROS accumulation injury [19]. Specific (EMF) wavelengths, such as infrared radiation energize BSW maintaining good O2 levels within cells.
Neutrophils inactivate pathogens through NADPH oxidase producing Radical Oxygen Species (ROS) in a process called respiratory burst, which increases oxygen consumption by 10-15-fold [19,24-25]. Myeloperoxidase MPO then produces localized small quantities of HOCl as biocide. Studies found that (SW) increases Natural Killer cell activity from 8% to 25% and doubling phagocytic activity [26]. In a close manner, our innovative PLUS biocide, which consist mainly of (SW) water< 99.7% and HOCl with traces of other (ROS) biocides totally equivalent to 250 ppm free chlorine, inactivates pathogens and enhances cell functionality/metabolism. PLUS's physiological effect can’t be solely attributed to 250 ppm free chlorine. Its wide spectrum and fast eliminations of pathogens incl. viruses, Chlorine resistant bacteria and spores > 99,9999% qualifies PLUS as a “chemical sterilant”. Simultaneously, due to its (SW) water, enhance and support cell granulation and speed up damaged area recovery (e.g. wounds & burns), safe on dermatological cells/skin and non-bleach. PLUS is produced in a unique reactor by electrolysis of NaCl salted purified water, producing hydroxylated water with hydronium ions +H3O and hydroxyl radicals •OH. These reform into (SW) water with stronger H-bonds that favor cyclic rings enhancing electrical conductivity and dielectric constant [27-29]. PLUS, generation process involves a combination of synergetic technologies like ionizing energy, electromagnetic field (EMF), resonance, catalytic TiO2 and ceramics membrane, ozone + hydrogen peroxide reactions to form stable gentle biocide with energized (SW) & HOCl. Plus is stable with pH 7 unlike chemically produced HOCl stable at pH 4-5. Additionally, its UV spectrum differs from chemically produced HOCl with 2 peaks around 240 and 290 nm. Plus, safe and effective regime of disinfection opens doors for new holistic biocide supporting human health and animals’ wellbeing.
Though all industries can harvest low-hanging fruit in terms of sustainability (environmental, economic, social) in various aspects like waste-reduction, material/water/energy-consumption etc., pharma-specific SWOT analysis reveal internal and external obstacles for significant improvement: e.g. regulatory aspects, data handling, implementation of innovation.
Conservative and risk-avoiding internal/external regulatory bodies with different views and foci result in a downward spiral narrowing down the operational window, fostering only applying legacy approaches and create a hindering environment for implementing innovative technologies.
On the other hand, regulatory bodies are right asking for thorough understanding of products and processes (e.g. ICH Q8-10) which comprises the ability to rationally explain formulation and process.
Data, information, knowledge play a major role in creating that knowledge and wisdom around products, the human body and our industry in the widest sense. With vast amount of (unstructured) data available, supercomputing power, NN, AI, KBS are necessary prerequisites for harvesting knowledge. Plus, educating next generation scientists in best practices of (DOE-)data-evaluation, modelling, simulation becomes even more important to achieve next big steps in sustainability.
Nowadays, the number of poorly water soluble drug candidates has increased tremendously. More than 40% of newly discovered drugs are poorly water soluble. It has to be kept in mind that up to now there is no universal science-based formulation design for low water soluble drugs [1]. Co-crystal formation is one of the methods for improving their solubility [2]. This presentation is about the formulation development of SDP-17, a co-crystal drug substance at Shionogi [3]. In the formulation research of this co-crystal, a series of formulation development challenges were found, such as ① crystal transition to a hydrate crystal with low solubility, ② increase in mutagenic impurities, and ③ crystal transition to a metastable form of the co-crystal. By ingenuity in the formulation design and process selection, all of these challenges were overcome and the co-crystal drug substance was successfully formulated. In this presentation, the history of the development of this formulation will be introduced along with some of the challenges and how to address with data.
SESSION: PharmaceuticalTuePM4-R4 |
Leuenberger International Symposium on Pharmaceutical Sciences and Industrial Applications for Sustainable Development |
Tue. 22 Oct. 2024 / Room: Minos | |
Session Chairs: Go Kimura; Student Monitors: TBA |
Smart Cities are being built everywhere in a competitive display of the extravagant possibilities of modern technology. An incomplete understanding of global warming results in making a zero-carbon footprint as the goal of environmental urban planning. The goal is reached by replacing combustion engine cars with electrically driven versions. This limited vision of considering oil as the only culprit in global warming.
The practical experience from applying BioGeometry solutions to areas plagued by a stressful situation resulting from electromagnetic radiation clearly shows the harmful effects on human, animal and plant life. In the research projects done in Hemberg, St. Gallen (x) and Hirschberg Appenzell IR, Switzerland, in collaboration with the government Authority for Mobile communication and environment and Swisscom the government mobile communication provider, it was clearly shown that by infusing the electromagnetic radiation with BioGeometry life force energy quality (x) a significant improvement in human, animal and plant health was achieved. Electromagnetic radiation causes heat. Tests on mobile phone emission with Infra-Red technology showed a reduction in the raised temperature from the device electromagnetic radiation when infused with BioGeometry Life force solutions. It is widely ignored that electromagnetic radiation from modern technology contributes to global warming. Replacing carbon emission with electricity is not only harmful to living systems in general but will also increase the effect on global warming.
Artificial Intelligence running smart cities will employ sensors on every level from the smallest to the largest and will depend on an information technology that will produce a huge increase in electromagnetic radiation in the environment. Urban settlements in history were always located around water springs, lakes and rivers that carried life force into the agriculture. They were also planned on the energetic patterns of the earth. Roman planning based on life force earth patterns can be found everywhere in Europe. Zurich with its thousand natural water fountains is good example. New Smart cities showcase extravagant shapes with total disregard to the natural life force patterns of the earth, Carbon emissions from all types of life on earth form part of the energetic life forcr exchange in nature. Carbon emissions of modern technology however, do not contain life force and are not absorbed into the natural cycle and stagnate in the atmosphere contributing to global warming. Natural electromagnetic activity of the earth is part of the life force of all living species and contains an inner regulation and optimising of temperature. Electromagnetic radiation from modern technology is disturbing the natural counterpart in nature and causing global warming.
BioGeometry offers a fresh look at climate change by infusing carbon emissions and electromagnetic radiation with life force resulting in their integration in nature an harmonizing their effect on the temperature of their environment. The high intensity of carbon and electromagnetic will become a healing environment. This is the practical solution that we applied successfully in the Swiss projects.
There are many reports about health symptoms apparently caused by geopathic stress-sometimes collectively known as “sick building syndrome”.
There is often a correlation with active zones detected by dowsers.
This paper aims to describe the story of a society of mostly scientists, founded in 1977, namely known as GFBG, whose aim it was to discover a purely scientific, objective method based on sensors to find a causal relationship between the symptoms and the agent causing them.
Dowsers with a proven record of success in finding sources of water, active zones were able to be localized and corresponding physically known signals (i.e. signals of electromagnetic origin) were analysed.
It was found that, whereas some dowsers could indeed identify sources of electromagnetic signals, the inverse relation was not true: Some dowsers could detect active zones even from within a faraday cage.
Some 30 year after the foundation of the society, it has become clear that the active zones have no clearly identified connection to any person suffering from geopathic stress. To identify such an active zone reliably, a trained dowser is required and can not be replaced by a physical instrument.
Unfortunately, empirically detected results which do not conform with a known scientific model are not easily accepted by many members of the scientific community, due to the prevalence of the physicalist/materialist assumptions.
It is estimated that 17% of the global electricity production is used by a broad array of industrial refrigeration systems, collectively known as the Cold Chain. This global refrigeration industry encompasses a wide range of disciplines, including the healthcare industry, where refrigeration preserves medicines and pharmaceuticals, including vaccines, and the food sector, where temperature-controlled warehouses, trucks and shipping containers maintain food safety. The need for industrial refrigeration is expected to grow in the coming years due to global warming.
The pharmaceutical industry, in particular, has very stringent temperature storage requirements, and some of the required storage temperatures can be extremely low, leading to significant refrigeration system power use. Performance enhancements, reduction in energy consumption and greenhouse gas emission, and improved equipment maintenance intervals can be achieved by using physics-based thermodynamic modeling methods [2-5] to develop a digital twin for a range of industrial refrigeration systems. Implementations have been demonstrated for stand-alone, single-loop commercial vapor compression refrigeration systems (refrigerators or commercial cooling units, e.g., vaccine storage units) and for multi-loop, multi-compressor industrial refrigeration systems used in temperature-controlled warehouses up to several hundred thousand square feet in size. Such digital twins enable real-time performance monitoring by computing mass- and energy-balances using measured data, and the calculated results can be trended and used by machine learning algorithms to identify common equipment failures and alert personnel to operational problems.
Examples are presented illustrating how the trended calculated results enable root-cause identification of operational inefficiencies as well as reduction in system performance due to equipment degradation and improper hardware selection.
SESSION: NonferrousTuePM1-R5 |
Stelter International Symposium (10th Intl. Symp. on Sustainable Non-ferrous Smelting & Hydro/Electrochemical Processing) |
Tue. 22 Oct. 2024 / Room: Lida | |
Session Chairs: Alexandros Charitos; Lars Felkl; Student Monitors: TBA |
Recyco, part of the Aperam group, built its pyrometallurgical recycling expertise by recovering valuable elements from stainless steel meltshop dusts. Since 2019, a real evolution of the site started, following the receival of an extended environmental permit allowing the treatment of a broader range of wastes, including hazardous ones. This capability expansion goes along with the development of new processes and products, and is now a real asset for the ongoing transformation of Aperam into a climate-neutral stainless steel producer.
The production of high Ni containing alloys from a multitude of different wastes is described in this paper. This case study is an excellent example of cooperation between R&D and operations, supported by internal customers and aided by sourcing, legal and environmental teams. The development started with preliminary design and simulation of the process using thermodynamic simulations [1, 2]. Slag design and reduction equilibria studies were an important part of the fundamental investigation. Lab-scale experiments supported this development, before a step-by-step transfer to operations, following learning cycles and inspired by the minimalist approach [1], was performed. These cycles are closed by the comparison of the experimental and industrial results to the thermodynamic simulations, and the generated knowledge has been used as the basis for an in-house developed process model of our operation. This model now allows us to simulate the behavior of new wastes in our process, reducing the risk of downtime and production being out of speciation.
The produced alloys are in line with our meltshop specifications replacing primary nickel. As these alloys have a significantly lower CO2 footprint than primary Ni units normally used, Recyco is transforming into an important player in reducing Aperam’s scope 3 emissions.
A wide variety of metals of considerable relevance to the European high-tech industry, and therefore also for our society, are supplied by the nonferrous metal industry. As the technologies became rapidly more complex in the last decades, the number and kind of metals and alloys utilized were getting more specialized and unique. With this technological innovation, the demand for minor elements increases steadily. Since their primary production, in most cases, can only be achieved economically as a by-product, it is difficult to respond to peaks in demand for minor elements. This, in turn, underlines the great need for recycling to compensate for these gaps.
In this context, together with the industry partners of the Christian Doppler Laboratory, methods for determining the distribution of metals in the phases and compounds that occur in industrial intermediates, by-products, and residues are developed and applied, and the possibilities of influencing the behavior in hydro- and pyrometallurgical processes are investigated. This subsequently enables the development of extraction methods for selected elements.
Since residual industrial materials can differ significantly in their behaviour, various innovative processes using chemical and physical properties for separation are used. These include, for example, chlorination of valuables or artificial mineral production by targeted crystallization during the cooling of slags. The paper gives an overview of the activities of the Christian Doppler Laboratory and will then focus on the area of artificial mineral growth to enrich chromium in special spinel phases.
In consideration of the growing production of stainless steel, which averaged at about 6 %/year between 2012 and 2021 and reached 58.3 Mio t/year in 2021, the accumulation of the corresponding residues such as dust increases as well [1]. During the production of stainless steel via electrical arc furnace (EAF), which is the most commonly applied production route, approximately between 10-20 kg of dust accrue per ton of steel [2]. This dust contains a quite significant amount of Cr and Ni. If no recycling of those dusts is carried out, these metals are lost for further operations and potentially interact in a harmful way with the environment in case of present leachable components, such as CrVI+. This would lead to economic loss as well as ecological harm. All of todays in industry applied processes to recover valuable metals from such dusts are of pyrometallurgical nature, which are carbon based and quite energy intensive.
Hydrometallurgical operations for the recovery of metals from Cr-Ni-rich AOD and EAFD have been examined by Aromaa et all. and Stefanova et all. but with the goal to selectively extract Zn [3, 4]. Therefore, after thoroughly charactering the dust including X‑Ray diffraction (XRD), scanning electron microscope-energy dispersive X‑ray (SEM‑EDX), Elemental analysis with inductively coupled plasma‑optical emission spectroscopy (ICP‑OES) and thermogravimetric analysis (TGA), five different acids (hydrochloric, sulphuric, nitric, vinegar and citric acid) were investigated in their potential to leach Cr and Ni. Out of the five acids used, hydrochloric acid was the most promising candidate to conduct a parameter variation with. In the conducted follow-up experiments, a clear trend of increased extraction rates can be observed for higher temperatures and longer leaching times. To counter specific problems observed in previous experiments, a double walled reaction vessel including a lid with four openings for stirrer, reflux condenser, acid addition and pH‑electrode was used. Through applying these methods, the FeCr2O4 and NiFe2O4 spinel phases, which contain the metals of interest, were able to be leached in a satisfactory amount. The paper summarizes the results of the characterization in conjunction with the obtained extraction rates and conclusions on the mineralogical phases and their leachabilities under different conditions.
During secondary copper production both internal slags and a final copper slag is produced. In contrast to the final copper slag, which is a process by-product, internal slags are typically recycled to the preceding aggregate. Therefore also the part of copper and other valuable elements like nickel, tin, lead and zinc reporting to the final slag is kept low. On the other hand, other elements which influence the process negatively like aluminium and chromium are also recirculated and lead to an increase of density, melting temperature and therefore also viscosity of the resulting slags. This results in a more complicated slag treatment and influences aggregate capacity, i.e. (black copper smelter and the converter) and copper loss to slag, negatively.
This study is investigating a slag treatment (slag reduction) of high-copper bearing slags from secondary copper production to meet the described challenges by avoiding internal slag recirculation. But besides that, the process results to additional value in that the secondary slag produced through appropriate fluxing (i.e., through slag design) can be easily used for construction purposes. For this investigation an in-depth knowledge about not only the thermodynamics but also kinetics of this process is required.
This study is built on three pillars: Thermodynamical modelling, kinetic investigations and experimental tests in a medium scale. The thermodynamical modelling is conducted using FactSage™ with inclusion of the copper database. An open-system approach is used to model the reduction process by hydrogen. Through that several simulation steps are taken into account, where the hydrogen is added in fractions which are forming a thermochemical equilibrium with the slag and the resulting metal phase. After reaching equilibrium (during each step) the gas phase is removed and a new gas phase is formed by a new addition of hydrogen and the creation of a new thermodynamical equilibrium.
Kinetics investigations were performed by using thermogravimetric methods with the combined analysis of the off-gas stream using mass spectrometry for the achieved ratio of hydrogen to steam. This ratio can be used as a measure for the reduction progress. Firstly, the slag under investigation is mixed with hematite (Fe2O3) and silica (SiO2) to achieve a secondary slag near fayalitic composition (45-50 wt.-% FeO and 35 wt.-% SiO2). The non-fluxed slag would for be rich in alumina but contains also a non-negligible proportion of chromium(III)-oxide. Both compounds are known for increasing slag viscosity. The chemical composition of the resulting metal phase and the secondary slag is analysed using SEM-EDX.
The experimental trials in medium scale are performed with around 0.5-0.75 kg slag material, depending on the mass of needed fluxes. Here the gas is injected via a lance in the molten slag system at given temperature. Via weighing before and after the experiment the mass loss during reduction, i.e., due to zinc and lead fuming can be estimated. By means of chemical analysis of the achieved metal phase as well as of the resulting secondary slag the reduction degree in this scale can be evaluated. The main goal is to achieve a secondary slag which contains less than 1 wt.-% of copper and other valuable elements and a secondary slag with an iron oxide content and silica content of 45-50 wt.-% and 35 wt.-%, respectively.
It can be seen that the majority of slag reduction is completed within a few minutes and is therefore faster than when using carbon monoxide as a typical reducing agent, as long as diffusion can be neglected. In reality, this is not the case: due to the distance e.g., between the lance tip and the outer diameter of the reaction vessel, the necessary reduction time is extended, as the process is increasingly diffusion-controlled.
With increasing temperature, an accelerated reduction can be observed due to a reduced viscosity of the slag and an improved mobility of the hydrogen, whereby the reduction of the hematite added as an additive can be considered complete even before the reduction of the slag.
SESSION: NonferrousTuePM2-R5 |
Stelter International Symposium (10th Intl. Symp. on Sustainable Non-ferrous Smelting & Hydro/Electrochemical Processing) |
Tue. 22 Oct. 2024 / Room: Lida | |
Session Chairs: Vangelis Palavos-Chesper; Paul Schönherr; Student Monitors: TBA |
The composition of the metal melt plays an important role in the production of high-quality aluminum castings. A melt with high hydrogen content often leads to defects and macro porosity [1]. Gas purging treatment and the use of melting salts for degassing are commonly used to reduce the hydrogen content. However, a consistent solidification of the entire cast part cannot always be realized. In these cases, undesired macro porosity may occur due to hydrogen excess in comparison to the amount of porous seeds in the melt.
In recent years, the Institute of Nonferrous Metallurgy and Purest Materials has identified two ways of positively influencing this hydrogen porosity. On the one hand, it was found out that it is possible to use a special melt additive to adjust the ratio between the hydrogen dissolved in the melt and the existing pore nuclei so that the hydrogen released during solidification is finely distributed in the casting [2]. On the other hand, it was shown that the use of reactive filter materials can positively influence the precipitation of the atomically dissolved hydrogen and thus generate denser castings [3,4]. Both processes are presented and the efficiency and influence of the respective filter materials and additives is explained.
Increasingly, scientific and technological developments are moving to a more environmentally friendly direction [1]. Therefore, the necessary adaptation of state-of-the-art processes with modified systems to an overall cleaner and more energy efficient state is imminent and requires a lot of research work, a more detailed look at processes and new test equipment. This is particularly true for the metallurgical industry, where carbon is needed not only as an energy source but also for reduction, and where the transition to greener processes has to work in tandem with the difficulties of recycling new complex multi-metal wastes such as magnets, batteries, e-waste and complex slag systems.
The Institute of Nonferrous Metallurgy and Purest Materials (INEMET) aims to look more closely at utilizing hydrogen as a key challenge for the near future with regard to metallurgical process decarbonization [2]. This is planned as a substitute for fossil fuels, e.g., natural gas for smelting copper cathodes prior to casting; nonetheless the influence of hydrogen on the copper melt, furnace refractory, fluid-dynamics, heat transfer and process control have to be assessed. In addition, the utilization of hydrogen for the molten phase reduction, e.g., in the reduction metal oxides, e,g. SnO2 in the context of a smelting process or of iron ore in the context of fluidized bed gas-solid processes is planned. [3].
The use of atmospheric thermal plasma jets as an alternative to conventional gas burners is also being investigated. The ability to use different gas compositions enables new ways of heating and treating slags, scrap and ores and is identified as a key technology in modern metallurgy [4]. Thermal plasma can be used to form species such as atomic hydrogen or even H+, which can reduce any metal oxide, allowing processes that cannot be decarbonized with molecular H2 to be carried out completely without CO2 emissions [5]. The fuming behavior of melt components can differ in these systems hence opening further pathways for metal refining.
Various new sensors are being installed and used to improve the measurement capabilities and to combine all the sensor data to gain better process knowledge. For example, new phase-differentiating melt height measurements are being tested with radar sensors. The aim is to identify the height of the slag and metal phases in a smelting unit operation. In addition, acoustic measurements may aid to analyze process fluid-dynamics. To link the different parameters of the experiments, a digital twin (on-line process model receiving experimental data) of the Institute's TSL is being built. Developments realized within the EU-HORIZON Mine.io project will be analyzed in detail.
In order to enable new process designs for industrial use, the key expertise lies in scaling up from laboratory scale to pilot scale experimental campaigns. To this end, new experimental fields are being designed within a newly planned furnace hall.
All in all, the directions for future-oriented pyrometallurgical research have been set and will be realized and carried out hand in hand throughout the university, by undergraduate/ graduate students, technical/ academic staff and industry alike.
The metallurgical industry is continuously seeking sustainable methods for the valorization of materials, such as tin residues, which arise as a byproduct during production processes for example in soldering printed circuit boards. This study focuses on the utilization of green, non-fossil reducing agents, specifically biomasses, for the recovery of tin from industrial residues. These can contain valuable amounts of tin and other valuable metals (e.g. Ag and Cu) that can be recovered and reused, essentially making its valorization not only environmentally imperative, but also economically beneficial. When treated correctly the produced secondary slag can become a valuable base product for cement production. This study aims to prove exemplary pathways for holistic valorization of two distinct tin residues.
Biomasses, abundant and renewable, from agricultural, forestry and other organic sources, are considered carbon-neutral due to the fact that they absorb as much carbon during their “life”, as they release when utilized. This more climate friendly status holds especially true for low-grade byproducts. In pyrometallurgy, the use of biomasses as reducing agents is a rapidly growing field of research, providing greener alternatives to the traditional reducing agents such as coke [1][2][3]. This work, is also aimed to explore the effectiveness of different biomasses in the reduction of tin oxides from the residues to their metallic form [4].
With regard to the experimental procedure, various biomass types such as straw, wood, coconut shells etc. were used [5] and compared against traditional coke. The reduction process was carried out in crucible experiments under inert gas in completely molten systems, while optimizing the parameters of temperature, reaction time and tin residue / biomass ratio as well as fluxing, in order to minimize the concentration of impurities in the metallic phases.
For some residues a prior leaching step is explored and compared against direct pyrometallurgical treatment. Neutral and acidic leaching was investigated with the purpose of decreasing Cl and S amounts which are potentially undesired in the following pyrometallurgical step.
In conclusion, the study demonstrates the feasibility of using biomass reducing agents as greener reducing agents for the valorization of tin residues. The approach aligns with the principles of circular economy and offers a pathway towards more sustainable metallurgical processes. The successful recovery of tin using biomasses could lead to a reduction in the industry’s carbon footprint and contribute to the conservation of natural resources.
Zinc (Zn) is utilized in many industrial applications, such as batteries, cosmetics, pharmaceuticals, and metal production. Due to urbanization and the depletion of high-grade ore deposits, efficient resource management is required from both primary and secondary resources. In terms of the latter, the most widely used recycling method of Zn-containing scrap is the Waelz process, particularly for electric arc furnace dust (EAFD). The Waelz process is a pyrometallurgical technique where the Zn scrap is loaded into a rotary kiln with a carbon-containing reducing agent at 1200-1300 oC to extract Zn [1]. Zn subsequently vaporizes and oxidizes in the gas stream to form particulate ZnO, which is then collected on bag filters.
In Europe, approximately 250,000 tons/year of Zn is recovered via the Waelz process. However, the process also generates nearly 800,000 tons/year of slag. Utilization of the “Waelz Slag” is hindered due to the lack of environmental compatibility [2], mainly because of the complex chemical and mineralogical composition. As a result, Waelz slag is largely landfilled, even though the iron content exceeds that of high-grade iron ores (~25% iron).
Numerous studies have investigated the recycling potential of Waelz slag by different methods, such as in a vertical retort [1], in a top-blown rotary converter, and as a charge to an electric arc steelmaking furnace. However, these studies were either theoretical, or in the early stages of development. Nevertheless, the main component of Waelz slag is iron (Fe), followed by Zn, manganese (Mn), and lead (Pb). Of these, Fe and Zn represent the target elements for downstream utilization.
The project’s primary goals are to generate pig iron, slag (ideal for the building materials sector), and Zn-rich fly ash (for Zn recovery). Information from a number of analytical techniques, including X-ray fluorescence (XRF), X-ray diffraction (XRD), inductively coupled plasma optical emission spectroscopy (ICP-OES), and mineral liberation analysis (MLA), were employed to augment parameters for simulation of one-kilogram experiments conducted in an induction furnace using FactSage 8.2.
The study employs an iterative approach where the result of each experiment serves as a guide for the subsequent experiments. The highest total iron recovery is 83.18%. A combination of the FactSage and Einstein-Roscoe viscosity models was used to determine slag viscosity, implying that viscosity depends more on composition than temperature. Addition of 16% SiO2 and 3% Al2O3 shows a high slag viscosity and delayed Mn reduction, possibly due to insufficient Si dissolved in the metal phase and the system being furnace cooled, giving time for nucleation of Mn-containing phases. The calculated actual oxygen partial pressure on all experiments ranges from 10-8 to 10-21. XRD analysis of dust recovery filter paper confirmed the presence of Zn. The slag produced in this study has similar compositions to those studied by Grudinsky et al. that can be used as concrete material to enhance its properties [3]. Overall, the study opens the way for holistic valorization of Waelz slag, resulting in more sustainable Zn resource management.
SESSION: NonferrousTuePM3-R5 |
Stelter International Symposium (10th Intl. Symp. on Sustainable Non-ferrous Smelting & Hydro/Electrochemical Processing) |
Tue. 22 Oct. 2024 / Room: Lida | |
Session Chairs: Junnile Romero; Student Monitors: TBA |
Tin is one of the earliest metals used in human history. The amount of tin produced and consumed worldwide in the last ten years has been estimated to be between 300,000 - 400,000 tons annually [1]. Not only is tin an essential constituent of tin bronze, it is also a critical component of alloys for making solders, which are essential for the major drivers of green energy transition; electric and autonomous vehicles, solar PV, semiconductors, etc. [2]. Tin from cassiterite, SnO2 (main source of tin), has over the years been processed via the pyrometallurgical route. Sulfurization and roasting are primary steps in the process, which are carried out to thermally enrich SnO2 content in case of low-grade concentrates. Afterwards SnO2 is treated in reactors, where carbon-based reducing agents are used to reduce tin to the metallic form at high temperatures [3], after which the resulting tin produced is further refined to obtain a marketable grade [4]. The carbothermic reduction of cassiterite, has however, seen several drawbacks such as the generation of environmentally harmful waste gases (e.g., CO2), high energy and equipment costs, as well as low selectivity with regard to impurities contained in the ore which are difficult to be separated at elevated temperatures [5].
A hydrometallurgical extraction route is proposed as a potential alternative processing method for tin extraction from cassiterite to achieve a higher degree of sustainability. This is because it ensures the reuse of chemicals in the process loop and allows for a higher metal recovery at a significantly lower energy consumption and greenhouse emissions [6]. Three different acids, (methanesulfonic acid, sulfuric acid, and oxalic acid) were investigated for their potential to leach tin from cassiterite, and they all proved futile, which supports already existing literature regarding the high chemical stability of cassiterite. A pre-treatment step was deemed necessary to render tin water soluble for subsequent hydrometallurgical processes.
A reduction of cassiterite in a hydrogen-controlled environment to produce SnO slag, from which tin can easily be leached in acid or alkaline media was investigated. The formation of SnO slag can be accompanied with the production of a tin metal phase depending on the H2/concentrate ratio used. During experimentation, a high purity tin nugget (99.5 wt.%) was produced at a reduction temperature of 1300 ⁰C at 30 g H2/ kg concentrate. The slag formed was soluble in sulfuric acid solution, from which tin extraction is being examined. Other pre-treatment options such as soda roasting and alkaline fusion are being investigated with regard to technological, economic and environmental feasibility.
Roasting processes in the pyrometallurgical production of non-ferrous metals are very complex, taking into account the chemical and mineralogical composition of the raw materials, as well as the complexity of the chemical reactions which take place in the roasting aggregate. Laboratory-scale characterization of the initial materials, intermediates, and final products gives researchers the possibility to propose the most likely possible reaction mechanism in order to guide the roasting process towards the desired products. On the other hand, studying the microstructure of materials helps to understand the reasons for the lack of the roasting process efficiency for a certain application case. More recently, the development and application of advanced thermodynamic software additionally helps to predict more accurately the phase distribution and overall dynamics of the roasting process, prior to experimental laboratory tests, thus increasing the probability of successful replication on a larger scale.
This paper presents the results of microstructural investigation of three different materials which are used in non-ferrous metallurgy as primary or secondary raw materials: 1) copper-iron sulphide flotation concentrate (Republic of Serbia), 2) lead and arsenic containing dust from copper smelter (Republic of Kazakhstan), and 3) gold containing residues from gold winning plant (Republic of Uzbekistan).
Samples of sulphide copper concentrate were roasted at 425°C, 675°C and 950°C in an air atmosphere for 1 hour. The experimental characterization included chemical and quantitative microstructural analysis of the initial sample, XRD and SEM/EDS analyses of the initial sample and roasted products. Thermodynamic prediction of the equilibrium compositions and phase distribution at elevated temperatures was done using HSC Chemistry software (ver. 6.1) under the incomplete and complete roasting conditions.
Samples of lead- and arsenic-containing dust from copper smelter were subjected to sulphatising roasting in a pilot-scale fluidised bed furnace at temperatures of 400-550°C for 1 hour. The data of the initial dust and calcine samples investigation by scanning electron microscopy and X-ray spectral microanalysis (SEM and XRMS) allowed to detect and eliminate the cause of insufficient efficiency of impurity removal into the gas phase. The samples were also studied by chemical analysis and X-Ray diffraction analysis.
In the next example under consideration, the starting material and products of oxidative roasting of sulphide- and carbonaceous-bearing gold plant residues at 500-700°C were investigated. In addition to the methods of chemical analysis, optical studies, X-ray phase analysis and diagnostic leach, the use of the scanning electron microscope study equipped with a dual-detector X-ray microanalysis system provided the most complete information explaining the cause of incomplete gold recovery at the downstream roasting stage of cyanidation.
Application of the scanning electron microscopy method with local X-ray spectral analysis allows not only to establish the percentual content of minerals in the investigated sample, but also to determine the elemental distribution within the mineral, the degree of mineral liberation in individual particles of the sample, as well as to determine the association of the mineral/component of interest with other minerals, the quality of its surface, size and shape. This information helps the scientists and experts to optimise metallurgical processes, particularly, as the results have shown, the roasting process.
Vanadium is a valuable and rare resource widely used in chemical manufacturing, military affairs, aerospace, metallurgical industry and other fields [1], and China is rich in vanadium resources, accounting for 34% of the world's total, ranking first in the world. Vanadium mainly in the form of vanadium-titanium magnetite and vanadium-bearing coal [2]. As a new type of energy storage technology, vanadium redox flow battery has been widely studied due to its advantages of environmental protection, long-life, safety and flexible power design [3]. Vanadium electrolyte is an important component of vanadium batteries, and it is directly related to the performance and cycle life of vanadium batteries [4]. Solvent extraction is widely used for the extraction of vanadium. It can prepare electrolyte from vanadium-containing solution, eliminating the steps of vanadium precipitation, impurity removal and dissolution, which meets the requirements of energy saving and environmental protection. Based on the above, we propose a clean and short process for the preparation of vanadium electrolyte from vanadium shale leaching solution by solvent extraction.
An oxidative stripping system, with the low concentrations of hydrogen peroxide and sodium hypochlorite was introduced to facilitate vanadium recovery and further separation of impurities from the leach solution. In order to investigate the mechanism, FTIR and Raman spectroscopy were used to investigate the changes in valence bonding before and after extraction and stripping. The concentration of vanadium and other impurities in the vanadium-rich liquid was investigated by ICP to determine whether it complied with national standards(GB/T 37204-2018).
After reduction and enrichment, a high purity vanadium electrolyte with low concentration of impurities was prepared. The prepared electrolyte exhibits acceptable electrochemical and charge/discharge properties. The method saves a large amount of preparation cost than the traditional method and does not produce ammonia, nitrogen or harmful gases. The technology is economically reasonable and eco-friendly, and is expected to be applied to large-scale production and promote the development of vanadium redox flow battery and new energy.
This study explores a sustainable approach to pyro-metallurgical recovery of metallic raw materials from mixed sulfidic fine-grained waste streams, named as Theisenschlamm [1, 2]. As part of the FINEST project (https://finest-project.de/), Subproject 3 "FINEST Disperse Metals," our focus is on optimizing the secure blending of fine and ultra-fine-grained material flows to recover valuable metals through a multi-stage pyro-metallurgical recycling process. Specifically, we investigate the utilization of calcium- and zinc-rich industrial residues as alternative feeds for the pyro-metallurgical metal recovery process.
Using FactSage™ 8.2 software, we simulate and evaluate the behavior of the slag systems throughout both the oxidation and reduction stages of the process. Ternary phase diagrams are constructed for the key components of the slag systems, providing insights into phase equilibria, solidification behavior, and the stability of various phases under different thermal conditions [3].
A significant aspect of this work involves calculating the viscosity of the slag during the high-temperature processing stages, as this property is critical for ensuring efficient metal separation and refining [4]. Viscosity calculations are performed using the Einstein-Roscoe model, integrated with the Quasi-chemical model from FactSage™ platform, to predict the flow behavior of the slag in relation to its composition and temperature. These findings offer a deeper understanding of the impact of alternative flux materials on slag characteristics, contributing to process optimization.
This detailed modeling-driven approach not only facilitates the refinement of metal recovery processes from complex waste streams but also promotes sustainable circular economy practices by reducing dependence on traditional flux materials and enhancing resource efficiency in pyro-metallurgical recycling [5].
SESSION: NonferrousTuePM4-R5 |
Stelter International Symposium (10th Intl. Symp. on Sustainable Non-ferrous Smelting & Hydro/Electrochemical Processing) |
Tue. 22 Oct. 2024 / Room: Lida | |
Session Chairs: Alexandros Charitos; Michael Stelter; Student Monitors: TBA |
What kind of motoring is both sustainable and resilient? And what specific societal shift will allow us to move into it? Until now, motoring has not been fully considered as a means of environmental resiliency in production. Too often it is seen as a problem rather than the means toward shifting sectors into a more sustainable future. This is a blind spot because motoring is at the heart of production, manufacturing, and economics, and a foundational aspect of our systems of resiliency in wider society. Those systems dependent on motoring are matters of urban planning, infrastructure, policy, food and disaster systems, social and community disaster relief, etc., and yet many advocates of sustainability and resiliency within those sectors assume motoring is an obstacle rather than a portal into the change they desire. This paper examines that assumption and offers a model whereby we can turn this dissonance into collaboration, ultimately arguing that a cognitive shift about what motoring is and can do is necessary across sections if we wish to develop a sustainable future.
Motoring, which is any form of movement powered by energy that is not one’s own, includes internal combustion, diesel, electric, hydrogen, gas, steam, and solar sources, and is a necessary part of our systems of communication, nourishment, and disaster services. It could also become a tool towards resilience rather than its obstacle, though the necessary shift, as this paper argues, will be a cognitive one. For motoring to promote resiliency, we must have a clear understanding of what it means for motoring to be ecological, which means getting beyond the current either/or debate about fuel sources and focusing on use patterns and planetary motoring needs. In that respect, this paper establishes ecological motoring as that which “meets the motoring needs of all within the means of the living planet,” a definition inspired by and modelled upon the Doughnut model of economics by Kate Raworth. To move towards ecological motoring—motoring that is sustainable and resilient—we need to understand these motoring needs from a different cognitive perspective, which means releasing old judgements and debates, and reconfiguring our understanding of the needs and uses of motoring for the planet. Using the opensource tools and workbooks of the Doughnut Economics Action Lab (DEAL) as its methodology, this paper proposes four main quadrants of ecological motoring—system, materials, energy exchange, and scope—which can be understood as motoring’s core components of resiliency at various nested scales among sectors of society. Towards demonstrating these findings, it looks at the case study of Riversimple and shows how we might be able to shift (regardless what the fuel source of our company is) towards a more sustainable and lucrative reality by using these four quadrants.
Developing sustainable processes to minimize greenhouse gases is an ongoing effort in various industries around the world. Wind energy or electrical vehicles are two prominent technologies driving the green transition. Neodymium-iron-boron (NdFeB) permanent magnets with a rare earth element (REE) content of around 30 wt.% are typically used within electric motors. Large wind turbines can contain more than a ton of rare earths. The above mentioned factors are causing an increasing demand for these metals whilst industrial nations being heavily dependent on producing countries in Asia. Developing new recycling methods to recover REE from scrap materials (termed as long-loop recycling processes) is an internationally growing topic.
A pyrometallurgical recycling process for waste NdFeB permanent magnets named as slag extraction method is discussed in detail here. Recently, it was found that selective oxidation of REE by metal oxides is promising to recover REE in a slag phase while iron, boron, alloying elements (e.g., cobalt) or coating elements (e.g., nickel) are efficiently collected in an iron phase. This efficient separation of impurities leads to a concentration of REE in a single-stage process providing a significant advantage over direct chemical leaching of permanent magnets. Moreover, the remaining iron phase contains >3 wt.% cobalt and can be utilized to further extract other valuable metals.
In this approach boron oxide was added as flux and ferric oxide as oxidant to produce a slag with concentrations >85 wt.% RE2O3. Beside sintered also polymer-bonded NdFeB magnets were investigated in this study which are typically not treatable by direct leaching due to high organic content. Different crucible materials such as graphite, clay-graphite or alumina were tested. Experiments were performed at temperatures between 1300 °C and 1500 °C under inert argon atmosphere. High REE extraction rates of >99 % could be achieved at 1400 °C and 2 h dwell time. In the slag phase, the concentration of impurities such as iron, nickel or cobalt were <1 wt.% detected by ICP-OES and SEM-EDX. The use of clay-graphite crucibles leads to Al and Si contaminations in the slag phase which were avoided in pure graphite crucibles. The developed process can be used as pre-concentration step prior to hydrometallurgical refining of REE. To further optimize the process parameters and provide a scalable technology, kinetic studies are currently conducted.
In this present work, a computational fluid dynamics (CFD) model is devised to study and understand the flow hydrodynamics and chemical reactions occurring between the liquid molten concentrate containing cassiterite and gas phase containing hydrogen.
This study is motivated by the goal for CO2-neutral production and recovery of valuable non-ferrous metals, e.g. copper, tin and zinc. The metallurgical industry is facing major challenges in transforming existing processes in terms of substitution of fossil fuels, considering costs and safety of plant operation and maintaining product quality. [1] Hydrogen is considered as a promising substituent to fossil fuels as reducing agent in high-temperature metallurgical applications, like smelting in top-submerged-lance (TSL) processes. [2] However, replacing traditional systems with hydrogen has a major influence on the process itself. Hence, numerical models enable a more detailed understanding of hydrodynamics between gas and slag phase as well as thermochemical interactions at the reactive interphase.
In order to study the effect of hydrogen, a CFD model has been developed according to an experimental setup. [3] In the experiment a lance was introduced into the molten cassiterite though which a mixture of hydrogen and argon is injected into the molten concentrate. A one-fluid approach has been used to understand the interactions and track the interface between the gas and slag phase. Simulations have been carried out to investigate the influence of varying interphase reaction rates and gas flow rates on the flow hydrodynamics and the reduction performance.
The rare earth elements (REE) play an important role in modern technology due to its wide applicability in various sectors of the world economy. The REE configures a select group of elements with exceptional properties physicochemical, catalytic, electrical, magnetic, and optical attributes [1]. Usually, the REEs are obtained from ore concentrates. However, secondary sources, such as effluents resulting from acid mining drainage (AMD) [2], could be an alternative to the conventional mining and represent an important source of these elements [3].
The current work addresses the study of the recovery of rare earth elements (REE) from acid mine drainage (AMD) by using cationic exchange resin. The acid water was obtained from one closed uranium mine at Caldas Municipality (Brazil). The total REE concentration was approx. 0,90 mmol/L, i.e, the sum of the concentrations of lights REE (LREE) and heavies REE (HREE), total impurities 12,9 mmol/L (Al; Ca; Mg; Mn and Zn), sulfate 10 mmol/L, fluoride 5,26 mmol/L, iron <0.09 mmol /L, and the pH around 3.4.
The loading experiments were carried out in columns at a temperature of 25±1⁰C and the cation exchange resins used were Dowex 50WX8, Lewatit MDS 200H, and Purolite C160. The best results for loading capacity and percentages of efficient removal (%) for total REE and impurities were obtained for the resin Lewatit MDS 200H with 0,566 mmol/g (92%) (LREE = 0,501 + HREE = 0,065) and 1,64 mmol/g (60%), respectively. The selectivity of the resins for the REE can be described as LREE > HREE. Regarding the impurities (Ca, Mn, Mg, Zn, and Al), the resin presents greater loading for calcium and aluminum. The elution experiments with inorganic and organic acids showed that hydrochloric acid and EDTA were more appropriate for the desorption and/or separation of the REE.
SESSION: SISAMTuePM1-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Tue. 22 Oct. 2024 / Room: Knossos | |
Session Chairs: Mariana Calin; Jean-Marie Dubois; Student Monitors: TBA |
Multicomponent alloys have attracted definitely increasing interest for the last three decades since the first synthesis of multicomponent bulk metallic glasses (BMGs) by copper mold casting in 1990. The multicomponent alloys reported to date are classified to BMGs, BMG composites, high entropy (HE) BMGs and HE alloys. When we focus on engineering applications, the most widely commercialized alloys are BMGs. Their BMGs are roughly classified into nonmagnetic Zr-based and ferromagnetic Fe-based types. The former type is typically composed of Zr-Al-Ni-Cu and Zr-Al-Ni-Cu-(Ti,Nb) systems and the latter type is Fe-Cr-(P,B,C,Si), Fe-(Cr,Nb)-P-B and Fe-(Cr,Nb)-(P,B,Si) systems. The commercialization articles have been usually produced by die casting from liquid for the Zr-based BMGs, while the Fe-based glass-type alloys have been produced by high-pressure gas atomization or ultrahigh water atomization. The former BMGs have been used as various structural materials such as casing, housing, pin spring, hinge, clinic instruments, ratch cover writing tools, precise gears, knives, optical mirrors, sporting goods and ornaments, etc., while the latter glassy powders are used to produce soft magnetic composite (SMC) by mixing with resin et al. The SMCs exhibit unique soft magnetic properties with the features of low core losses, good high-frequency permeability characteristics and high electrical resistivity in high-frequency range from 100 kHz to 5 MHz. High glass-forming ability enables the mass production of good spherical glassy powders over the whole particle size range even by low-cost water atomization process. Owing to their unique production process and good soft magnetic properties, the SMCs have been used as high performance of inductors and reactors with low core losses even in a high frequency range up to 3 MHz in various kinds of fields such as smartphone, smartwatch, tablet-type computer, notebook PC, DC/DC converter, point of load power supply, digital camera, automobile AV equipment, car navigation system and RFID sheet, etc. Thus, Zr- and Fe-based BMGs are expected to increase academic and technological interests as functional materials in recent information communication technology owing to the unique properties that cannot be obtained for ordinary crystalline structural and magnetic materials.
Multicomponent alloys have attracted definitely increasing interest for the last three decades since the first synthesis of multicomponent bulk metallic glasses (BMGs) by copper mold casting in 1990. The multicomponent alloys reported to date are classified to BMGs, BMG composites, high entropy (HE) BMGs and HE alloys. When we focus on engineering applications, the most widely commercialized alloys are BMGs. Their BMGs are roughly classified into nonmagnetic Zr-based and ferromagnetic Fe-based types. The former type is typically composed of Zr-Al-Ni-Cu and Zr-Al-Ni-Cu-(Ti,Nb) systems and the latter type is Fe-Cr-(P,B,C,Si), Fe-(Cr,Nb)-P-B and Fe-(Cr,Nb)-(P,B,Si) systems. The commercialization articles have been usually produced by die casting from liquid for the Zr-based BMGs, while the Fe-based glass-type alloys have been produced by high-pressure gas atomization or ultrahigh water atomization. The former BMGs have been used as various structural materials such as casing, housing, pin spring, hinge, clinic instruments, ratch cover writing tools, precise gears, knives, optical mirrors, sporting goods and ornaments, etc., while the latter glassy powders are used to produce soft magnetic composite (SMC) by mixing with resin et al. The SMCs exhibit unique soft magnetic properties with the features of low core losses, good high-frequency permeability characteristics and high electrical resistivity in high-frequency range from 100 kHz to 5 MHz. High glass-forming ability enables the mass production of good spherical glassy powders over the whole particle size range even by low-cost water atomization process. Owing to their unique production process and good soft magnetic properties, the SMCs have been used as high performance of inductors and reactors with low core losses even in a high frequency range up to 3 MHz in various kinds of fields such as smartphone, smartwatch, tablet-type computer, notebook PC, DC/DC converter, point of load power supply, digital camera, automobile AV equipment, car navigation system and RFID sheet, etc. Thus, Zr- and Fe-based BMGs are expected to increase academic and technological interests as functional materials in recent information communication technology owing to the unique properties that cannot be obtained for ordinary crystalline structural and magnetic materials.
Recent studies of glass-forming metallic systems have revealed intriguing complexity, e.g. unusual shifts in radial distribution functions with temperature change or upon mechanical loading in the elastic or plastic regime. Nearest neighbour distances and medium-range order structural arrangements appear to change, e.g. shorten upon heating or become larger with decreasing temperature. Concomitantly, temperature changes as well as static or dynamic mechanical loading within the nominally elastic regime can trigger significant changes in glass properties, which are directly correlated with local non-reversible configurational changes due to non-affine elastic or anelastic displacements. All these findings strongly suggest that the characteristics of the atomic structure decisively determine the properties of the glass and of nanostructured materials derived from glass-forming systems.
Residual stress engineering is widely used in the design of new advanced lightweight materials. For metallic glasses the attention has been on structural changes and rejuvenation processes. High energy scanning x-ray diffraction strain mapping reveals large elastic fluctuations in metallic glasses after deformed under triaxial compression. Transmission electron microscopy proves that structural rejuvenation under room temperature deformation relates to the shear band formation that closely correlates to the underlying distribution of elastic heterogeneities. Micro-indentation hardness mapping hints at an unsymmetrical hardening/softening after compression and further reveals the competing effects of stress and structure modulation. Molecular dynamics simulations provide an atomistic understanding of the correlation between shear banding and fluctuations in the local strain/stress heterogeneity. Thus, stress engineering and elastic heterogeneity together with structure modulation is a promising approach for designing metallic glasses with enhanced ductility and strain hardening ability.
Recent studies of glass-forming metallic systems have revealed intriguing complexity, e.g. unusual shifts in radial distribution functions with temperature change or upon mechanical loading in the elastic or plastic regime. Nearest neighbour distances and medium-range order structural arrangements appear to change, e.g. shorten upon heating or become larger with decreasing temperature. Concomitantly, temperature changes as well as static or dynamic mechanical loading within the nominally elastic regime can trigger significant changes in glass properties, which are directly correlated with local non-reversible configurational changes due to non-affine elastic or anelastic displacements. All these findings strongly suggest that the characteristics of the atomic structure decisively determine the properties of the glass and of nanostructured materials derived from glass-forming systems.
Residual stress engineering is widely used in the design of new advanced lightweight materials. For metallic glasses the attention has been on structural changes and rejuvenation processes. High energy scanning x-ray diffraction strain mapping reveals large elastic fluctuations in metallic glasses after deformed under triaxial compression. Transmission electron microscopy proves that structural rejuvenation under room temperature deformation relates to the shear band formation that closely correlates to the underlying distribution of elastic heterogeneities. Micro-indentation hardness mapping hints at an unsymmetrical hardening/softening after compression and further reveals the competing effects of stress and structure modulation. Molecular dynamics simulations provide an atomistic understanding of the correlation between shear banding and fluctuations in the local strain/stress heterogeneity. Thus, stress engineering and elastic heterogeneity together with structure modulation is a promising approach for designing metallic glasses with enhanced ductility and strain hardening ability.
SESSION: SISAMTuePM2-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Tue. 22 Oct. 2024 / Room: Knossos | |
Session Chairs: Hans Fecht; Student Monitors: TBA |
The European Union has set itself the goal of achieving climate neutrality by 2050, a milestone that depends on the continent's ability to develop and implement clean energy and mobility solutions in a way that is both economically viable and environmentally sustainable. The amount of critical raw materials (CRM) needed to facilitate this energy transition is significant. In addition, industrial and household appliances will need to meet stringent energy efficiency standards to support this transition. The most energy-efficient electric motors and generators contain rare earth permanent magnets. While EU companies are world leaders in the production of electric motors, they are completely dependent on imports for the entire value chain of rare earth magnet materials. (Bernd Schaferet.al, A Report of the Rare Earth Magnets and Motors Cluster, Berlin 2021).
Rare earth elements (REEs) are essential components of these permanent magnets, which are critical for many applications that are vital to Europe's future. It is well known that REEs from China have been the main source for Europe, that supplies are uncertain, and that the Chinese production chain is generally unsustainable. At the same time, the demand for REEs for the production of new PMs is expected to double in 15 years.
In light of this data, our work focuses on the collection of EOL magnets and the sustainable recycling and reprocessing of PM from sources, concentrating on the most common and readily available source of economically recyclable electric motors: domestic appliances. We are developing new dismantling and recovery processes for PM on high-availability scrap and reprocessing lines. In HPMS (Hydrogen Processing of Magnetic Scrap)1,2 we use an already established method of hydrogenation followed by grinding, degassing, and coating of sensitive powders. The HDDR (Hydrogenation-Disproportionation-Desorption-Regeneration)3 process has been implemented to simplify and minimize the steps in the recycling process.
Initial, ongoing pilot trials for the production of sintered and bonded magnets from recycled magnets confirm the waste-free, economic processing and future independence from unstable REE sources. For the production of sintered magnets, a new sustainable process of rapid consolidation is used, while for bonded magnets the most sensitive part to protect the reactive powders is the coating with a few monolayers of chemically bound coating precursor. In addition to magnetic measurements, various analytical techniques (SEM, HRTEM, XPS) are used to characterize the powders obtained by HPMS and HDDR processes, as well as the final magnets.
*This work is part of the “INSPIRES” project financed by EIT RawMaterials, Proposal Number 20090 (project website: https://eitrawmaterials.eu/project/inspires/).
Magnetic wires have attracted considerable attention due to their rather attractive magnetic properties such as giant magneto-impedance (GMI) effect or magnetic bistability, potentially suitable for several prospective applications (magnetic and magnetoelastic sensors, magnetic memory and logic, electronic surveillance, etc.) [1,2]. Glass-coated magnetic microwires prepared using the Taylor-Ulitovsky technique with thin metallic nucleus (typically with diameters 0.1 to 100 μm) covered by flexible, insulating and biocompatible glass are therefore quite interesting for sensor applications [2]. This technique allows preparation of magnetic wires with amorphous or crystalline structure of metallic nucleus. In the case of glass-coated microwires the magnetoelastic anisotropy contribution becomes relevant since the preparation process involves not only the rapid quenching itself, but also simultaneous solidification of the metallic nucleus surrounded by non-magnetic glass-coating with rather different thermal expansion coefficients [3].
The purpose of this paper is present last results on tailoring of soft magnetic properties and GMI effect in glass-coated microwires paying special attention to achievement of high GMI effect and on optimization of domain wall dynamics.
The impact of post-processing on soft magnetic properties and the giant magnetoimpedance (GMI) effect of Fe- and Co-based glass-coated microwires is evaluated. A remarkable improvement of magnetic softness and GMI effect is observed in Fe-rich glass-coated microwires subjected to stress annealing. Annealed and stress-annealed Co-rich microwires present rectangular hysteresis loop and single and fast domain wall propagation. However, Co-based stress-annealed microwires present higher magnetoimpedance ratio. Observed stress-induced anisotropy and related changes of magnetic properties are discussed considering internal stresses relaxation and “back-stresses”. Consequently, stress annealing of ferromagnetic microwires allows achievement of interesting combination of magnetic properties.
The present situation of the market and applications of rare-earths is reviewed. It is given special attention for discussing the possibility of substitution of rare-earth magnets by other families of magnets.
Three are the main commercial applications of rare-earths: i) luminescent phosphors, ii) magnets, and iii) catalysis.
For catalysis, the cheap rare-earths as cerium and lanthanum are employed. Luminescent phosphors are essential in many applications, as lasers and, for example, erbium is used in optical fibers. However, in spite of its relevance, erbium is not expensive as Tb and Dy.
In LED applications, the rare-earths are used as thin films, and , thus the demand in volume is not very significant when compared with the demand for magnets. The use of white LED (light emission diode) significantly reduced the demand for europium after 2015, but this application is still relevant. In the 1960s and up the 1980s, Europium was the most expensive rare-earth, due to extreme demand.
The rare-earth market is nowadays driven by Tb, Dy, Nd and Pr, which are employed in rare-earth iron permanent magnets of the RE2Fe14B family (RE=rare earth). For applications in high temperature, dysprosium and terbium are added, and this made the demand and price of Dy and Tb be skyrocketing.
SmCo magnets have the problem of using the expensive element cobalt. Nowadays the demand and price of cobalt increased conbseiderably due to application in rechargeable battteries, and thus, SmCo use in large scale is avoided, but they remain relevant for high temperature applications (above 150oC).
Possible alternatives for rare-earth permanents magnets are discussed. Among the few options for replacement are the ferrite magnets (BaFe12O19 or SrFe12O19), the Alnico magnes based on shape anisotropy and maybe iron nitrogen. Economic and technical feasibility of these families of magnets are discussed.
Its is given a brief overview about recent mining projects in Brazil, which are focusing on ionic clays, with the objective of extracting the scarce and expensive elements terbium and dysprosium.
Entire scientific disciplines are governed by the interactions between atoms and molecules. On surfaces, forces extending into the vacuum direct the behavior of many scientifically and technologically important phenomena such as corrosion, adhesion, thin film growth, nanotribology, and surface catalysis. To advance our knowledge of the fundamentals governing these subjects, it would be useful to simultaneously map electron densities and quantify force interactions between the surface of interest and a probe with atomic resolution. When attempting to use scanning probe microscopy (SPM) towards this goal, significant limitations in both imaging and mapping persist despite their ability to image surfaces and map their properties down to the atomic level. Most commonly, SPM qualitatively records only one property at a time and at a fixed distance from the surface. To overcome these limitations, we have integrated significant extensions to existing SPM approaches, which we will shortly summarize in this talk.
The work started in 2009, when we expanded noncontact atomic force microscopy (NC-AFM) with atomic resolution to three dimensions by adding the capability to quantify the tip-sample force fields near a surface with picometer and piconewton resolution [1, 2]. In 2013, we added electronic information through the recording of the tunneling current simultaneously with the force interaction. Using copper oxide as an example of a catalytically active surface, this allowed to study the role of surface defects as active sites [3]. With the goal of yielding information on energy barriers in on-surface chemical reactions, we further extended this approach in 2022 to gain insight into the energetics of molecular motions on surfaces, with benzene and iodobenzene as model systems. And most recently, we introduced the method to study single-molecule chemistry with the example of cobalt phthalocyanine (CoPc) molecules, which have shown great potential to favorably catalyze the formation of methanol from CO2 and hydrogen [4, 5]. Thereby, the binding strength of the intermediate CO to the cobalt atom at the center of the CoPcs catalyst molecule has been recognized as a key descriptor affecting catalytic efficiency, with the ideal CO-Co binding strength being neither too strong nor too weak. Using a CO-terminated tip, the CO-CoPc equilibrium distances and potential energies at equilibrium distances were recovered across the molecule [6]. Currently ongoing work aims at systematically changing the substituents/side chains of the CoPc or the substrate the CoPc molecules sit on to clarify the effect of these changes on the CO-Co binding strength and eventually enable a fine tuning of the binding strength, which may open new avenues to optimize the catalytic reaction.
SESSION: SISAMTuePM3-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Tue. 22 Oct. 2024 / Room: Knossos | |
Session Chairs: Spomenka Kobe; Hans Fecht; Student Monitors: TBA |
Score I: Consolidation Of Ti And Ti-6Al-4V-Chips Achieving Bulk Nanomaterials [1]. The two most important Severe Plastic Deformation (SPD) methods [2] - Equal Channel Angular Pressing (ECAP) and High Pressure Torsion (HPT) - were used for recycling and/or upcycling of titanium chips. To check the quality of the consolidated materials, results of mechanical testing, texture analysis, and of optical and electron microscopy were compared with those of the bulk counterparts. It is concluded that full consolidation i.e. the recycling of chips using SPD is possible at temperatures which not only are significantly lower than those of melting but also than those of sintering while reaching the same density. However, the chips must be prevented from mutual sliding as plastic deformation is essential for successful consolidation. Still, small sizes of chips, enhanced pressures, as well as elevated temperatures prove as beneficial to successful for consolidation.
Score II: Effect Of High Pressure Torsion On The Magnetic Properties Of Two Fe-Based Metallic Glasses. Recently, High Pressure Torsion (HPT) was applied not only for achieving massive samples out of Fe-based metallic glasses but also for their crystallization [3,4], in order to increase the saturation magnetization. Magnetic measurements by means of Vibrating Sample Magnetometry (VSM) of the two Fe-based metallic glasses Vitroperm Fe73.9Cu1Nb3Si15.5B6.6 and Makino Fe81.2Co4Si0.5B9.5P4Cu0.8 were undertaken. In contrast to the Vitroperm alloy, the Makino alloy showed – after applying at least 4 turns of HPT - an increase of magnetization by 10%, and a complete removal of HPT-induced increase of the coercivity related to deformation induced internal stresses. These effects occurred strictly in parallel to a HPT-induced crystallization which was not observed in the Vitroperm alloy [5]. It can be concluded that SPD processing of soft magnetic amorphous alloys appears as a viable alternative to the addition of nanocrystallizing elements, at least unless the material specific crystal systems are too complex to enable SPD induced crystallization [5].
Score I: Consolidation Of Ti And Ti-6Al-4V-Chips Achieving Bulk Nanomaterials [1]. The two most important Severe Plastic Deformation (SPD) methods [2] - Equal Channel Angular Pressing (ECAP) and High Pressure Torsion (HPT) - were used for recycling and/or upcycling of titanium chips. To check the quality of the consolidated materials, results of mechanical testing, texture analysis, and of optical and electron microscopy were compared with those of the bulk counterparts. It is concluded that full consolidation i.e. the recycling of chips using SPD is possible at temperatures which not only are significantly lower than those of melting but also than those of sintering while reaching the same density. However, the chips must be prevented from mutual sliding as plastic deformation is essential for successful consolidation. Still, small sizes of chips, enhanced pressures, as well as elevated temperatures prove as beneficial to successful for consolidation.
Score II: Effect Of High Pressure Torsion On The Magnetic Properties Of Two Fe-Based Metallic Glasses. Recently, High Pressure Torsion (HPT) was applied not only for achieving massive samples out of Fe-based metallic glasses but also for their crystallization [3,4], in order to increase the saturation magnetization. Magnetic measurements by means of Vibrating Sample Magnetometry (VSM) of the two Fe-based metallic glasses Vitroperm Fe73.9Cu1Nb3Si15.5B6.6 and Makino Fe81.2Co4Si0.5B9.5P4Cu0.8 were undertaken. In contrast to the Vitroperm alloy, the Makino alloy showed – after applying at least 4 turns of HPT - an increase of magnetization by 10%, and a complete removal of HPT-induced increase of the coercivity related to deformation induced internal stresses. These effects occurred strictly in parallel to a HPT-induced crystallization which was not observed in the Vitroperm alloy [5]. It can be concluded that SPD processing of soft magnetic amorphous alloys appears as a viable alternative to the addition of nanocrystallizing elements, at least unless the material specific crystal systems are too complex to enable SPD induced crystallization [5].
Achieving a climate-neutral and circular economy by 2050 is a significant goal for Europe, emphasising innovation in clean energy and e-mobility. A major role in this transformation have permanent magnets (PM), vital in electric vehicles and renewable energy technologies. Despite their specialised market, they have a strategic impact on the EU's mobility sector and its dependence on imports. Given their critical role in numerous industrial and consumer applications, there is a pressing need for innovative approaches in their production and recycling.
For over 30 years, our research group at the Jožef Stefan Institute has led research and innovations in PMs, focusing on enhancing magnetic properties and efficient use of critical material resources. The most recent activities towards these goals are commonly referred to as grain-boundary engineering, focused on manipulating the non-magnetic two-dimensional-like grain boundary regions between the magnetic matrix grains to enhance the overall coercivity of the entire magnet. Simultaneously, we have explored various recycling and reprocessing strategies to enable the sustainable reuse of magnet waste into new functional magnets with only a little or negligible loss of overall magnetic performance.
In this presentation, we will discuss several case studies illustrating how atomic-level structural and chemical analysis enhances our understanding of key physical and chemical mechanisms, which are essential for optimising magnetic performance and developing effective recycling strategies. For that purpose, we employed Advanced Transmission Electron Microscopy along with specialised analytical techniques such as Electron Energy-Loss Spectroscopy and Electron Holography, which provides quantitative magnetic characterisation at nanometer resolution. Among other findings, we will highlight how various grain-boundary structural refinement strategies during spark plasma sintering (SPS) influence the coercivity of Nd–Fe–B bulk magnets [1,2]. Additionally, we will discuss innovative electrochemical recycling techniques for sintered Nd–Fe–B PMs [3,4]. These techniques, which include direct recovery of the matrix phase and pure metal winning, are still emerging but have already shown promising results in our studies.
Achieving a climate-neutral and circular economy by 2050 is a significant goal for Europe, emphasising innovation in clean energy and e-mobility. A major role in this transformation have permanent magnets (PM), vital in electric vehicles and renewable energy technologies. Despite their specialised market, they have a strategic impact on the EU's mobility sector and its dependence on imports. Given their critical role in numerous industrial and consumer applications, there is a pressing need for innovative approaches in their production and recycling.
For over 30 years, our research group at the Jožef Stefan Institute has led research and innovations in PMs, focusing on enhancing magnetic properties and efficient use of critical material resources. The most recent activities towards these goals are commonly referred to as grain-boundary engineering, focused on manipulating the non-magnetic two-dimensional-like grain boundary regions between the magnetic matrix grains to enhance the overall coercivity of the entire magnet. Simultaneously, we have explored various recycling and reprocessing strategies to enable the sustainable reuse of magnet waste into new functional magnets with only a little or negligible loss of overall magnetic performance.
In this presentation, we will discuss several case studies illustrating how atomic-level structural and chemical analysis enhances our understanding of key physical and chemical mechanisms, which are essential for optimising magnetic performance and developing effective recycling strategies. For that purpose, we employed Advanced Transmission Electron Microscopy along with specialised analytical techniques such as Electron Energy-Loss Spectroscopy and Electron Holography, which provides quantitative magnetic characterisation at nanometer resolution. Among other findings, we will highlight how various grain-boundary structural refinement strategies during spark plasma sintering (SPS) influence the coercivity of Nd–Fe–B bulk magnets [1,2]. Additionally, we will discuss innovative electrochemical recycling techniques for sintered Nd–Fe–B PMs [3,4]. These techniques, which include direct recovery of the matrix phase and pure metal winning, are still emerging but have already shown promising results in our studies.
SESSION: SISAMTuePM4-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Tue. 22 Oct. 2024 / Room: Knossos | |
Session Chairs: Carlo Burkhardt; Student Monitors: TBA |
In contrast to classical ex-situ spectro-microscopic techniques, in-situ characterizations and the combined application of complementary methods on identical samples not only provide for a more comprehensive insight into the structures and phenomena of interest, but also allow to study their kinetic development under the impact of external stimuli [1-3].
The talk will present a short review of our recent endeavors along this line and will specifically report on findings on the helimagnetic Heusler compound Mn1.4PtSn. Lorentz transmission electron microscopy (LTEM) was used to study the evolution of magnetic phases as a function of (strength and direction of) an external magnetic field. The combination of (i) real space textures as derived from LTEM with (ii) magnetic scattering patterns obtained from complementary small angle resonant X-ray scattering (REXS) and (iii) micromagnetic simulations allowed us to substantially deepen our understanding of the nature and stability of the magnetic phases in Mn1.4PtSn as a consequence of the competing magnetic interactions at work. We could show that due to the material’s uniaxial magnetic anisotropy, a stripe domain phase derived from a chiral soliton lattice rather than the previously assumed helical phase forms the ground state of the system. The studies also reveal the occurrence a previously overlooked fan state and provide a detailed understanding as to why and how antiskyrmions are formed along a kinetic pathway that is defined through a particular sequence of to be applied external magnetic fields.
Furthermore, by measuring the anomalous Hall effect in-situ in the microscope and simultaneously with the LTEM investigations, we could show that the field-induced formation of antiskyrmions does not cause any additional contribution to the Hall effect thereby indicating the lack of any topological Hall effect in the system.
In contrast to classical ex-situ spectro-microscopic techniques, in-situ characterizations and the combined application of complementary methods on identical samples not only provide for a more comprehensive insight into the structures and phenomena of interest, but also allow to study their kinetic development under the impact of external stimuli [1-3].
The talk will present a short review of our recent endeavors along this line and will specifically report on findings on the helimagnetic Heusler compound Mn1.4PtSn. Lorentz transmission electron microscopy (LTEM) was used to study the evolution of magnetic phases as a function of (strength and direction of) an external magnetic field. The combination of (i) real space textures as derived from LTEM with (ii) magnetic scattering patterns obtained from complementary small angle resonant X-ray scattering (REXS) and (iii) micromagnetic simulations allowed us to substantially deepen our understanding of the nature and stability of the magnetic phases in Mn1.4PtSn as a consequence of the competing magnetic interactions at work. We could show that due to the material’s uniaxial magnetic anisotropy, a stripe domain phase derived from a chiral soliton lattice rather than the previously assumed helical phase forms the ground state of the system. The studies also reveal the occurrence a previously overlooked fan state and provide a detailed understanding as to why and how antiskyrmions are formed along a kinetic pathway that is defined through a particular sequence of to be applied external magnetic fields.
Furthermore, by measuring the anomalous Hall effect in-situ in the microscope and simultaneously with the LTEM investigations, we could show that the field-induced formation of antiskyrmions does not cause any additional contribution to the Hall effect thereby indicating the lack of any topological Hall effect in the system.
It was recently presented a model [1-3] able to predict the magnetic anisotropy of any sample, This is called the "Simultanoeus Fitting Method" SFM.
According the SFM method, the magnetic anisotropy can be determined, since magnetic measurements are performed at the (_|_) perpendicular and (//) parallel directions (relative to the alignment direction). The method assumes samples with alignment in one preferential direction, thus with uniaxial anisotropy. This kind of anisotropy is typically found in samples prepared by powder metallurgy, where the alignbment is obtained by applying magnetic fields in grains with single domain size.
Using the SFM, the crystallographic texture of samples can be determined directly from magnetic measurements, avoiding complicated, laborious and expensive techniques as EBSD - Electron BackSacterred Diffraction.
A symmetrical distribution as for example the Gaussian, is used for describing the crystallographic texture.
Other distribution functions can also be used, since they are symmetrical. This includes Cauchy -Lorentz, Voigt and Pearson VII as possibilities.
It is experimentally found that f=cos(theta)^n or Gaussian distributions describe very well the texture of the samples.
The model allows the re-evaluation of experimental data. Here it is discussed how to apply the model in very different samples.
These samples are SmFeN (magnetocrystalline anisotropy), Alnico, (shape anisotropy [4,5]) and cobalt-needle samples.
In cobalt needle samples the shape anisotropy and the magnetocrystalline anisotropy may have the same order of magnitude.
It is discussed the question of dominant anisotropy.
SESSION: SolidStateChemistryTuePM1-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Tue. 22 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Reshef Tenne; Ram Seshadri; Student Monitors: TBA |
Colloidal lead halide perovskite (LHP) nanocrystals (NCs), with bright and spectrally narrow photoluminescence (PL) tunable over the entire visible spectral range, are of immense interest as classical and quantum light sources. Fast (bright) and statistically pure single-photon emission is key for many quantum technologies, from optical quantum computing to quantum key distribution and quantum imaging. The brightness of an emitter is ultimately described by Fermi’s golden rule, with a radiative rate proportional to its oscillator strength (intrinsic emitter property) times the local density of photonic states (photonic engineering, i.e. cavity). With perovskite NCs, we present a record-low sub-100 ps radiative decay time for CsPb(Br/Cl)3, almost as short as the reported exciton coherence time, by the NC size increase to 30 nm. The characteristic dependence of radiative rates on QD size, composition, and temperature suggests the formation of giant transition dipoles, as confirmed by effective-mass calculations for the case of the giant oscillator strength. Importantly, the fast radiative rate is achieved along with the single-photon emission despite the NC size being ten times larger than the exciton Bohr radius.
NC self-assembly is a versatile platform for materials engineering, particularly for attaining collective phenomena with perovskite NCs, such as superfluorescence in perovskite NC superlattices. Thus far, LHP NCs have been co-assembled with building blocks that acted solely as spacers to promote the tuning of the mutual arrangement of LHP nanocubes [2]. However, the functionality of the second SL component can give rise to the enhancement of the LHP NCs properties or the emergence of new collective effects. We present the formation of multicomponent SLs made from the CsPbBr3 NCs of two different sizes. The diversity of obtained SLs encompassed the binary ABO6-, ABO3-, and NaCl-type structures, all of which contained orientationally and positionally confined NCs. For the selected model system, the ABO6-type SL, we observed efficient NC coupling and Förster-like energy transfer from strongly confined 5.3 nm CsPbBr3 NCs to weakly confined 17.6 nm CsPbBr3 NCs. Exciton spatiotemporal dynamics measurements reveal that binary SLs exhibit enhanced exciton diffusivity compared to one-component SLs across the entire temperature range (from 5 K to 298 K). Observed incoherent NC coupling and controllable excitonic transport within the solid NC SLs hold promise for potential applications in optoelectronic devices.
We also will present a novel library of phospholipid-based capping ligands for LHP NCs [4].
Among the 2D-materials, misfit layered compounds make a special class with incommensurate and non-stoichiometric lattice made of an alternating layer with rocksalt structure, like LaS (O) and a layer with hexagonal (octahedral) structure, like TaS2 (T). The lack of lattice commensuration between the two slabs leads to a built-in strain, which can be relaxed via bending. Consequently, nanotubes have been produced from numerous MLC compounds over the last decade and their structure was elucidated.
Owing to their large surface area, nanostructures are generally metastable and tend to recrystallize into microscopic (macroscopic) crystallites via different mechanisms, like Ostwald ripening, or chemically decompose and then recrystallize. The stability of nanostructures at elevated temperatures has been investigated quite scarcely, so far. As for the chemical selectivity, entropic effects are expected to dictate random distribution of the chalcogen atoms on the anion sites of the MLC nanotubes at elevated temperatures. Surprisingly, the sulfur atoms were found to bind exclusively to the rare-earth atom (Ln= La, Sm) of the rocksalt slab, and the selenium to the tantalum of the hexagonal TX2 slab [1].
In other series of experiments, the lack of utter symmetry in the multiwall nanotubes leads to exclusions of certain X-ray (0kl) reflections, which was used to distinguish them from the bulk crystallites. The transformation of Ln-based MLC nanotubes into microscopic flakes was followed as a function of the synthesis temperature (800-1200 °C) and synthesis time (1-96 h) [2, 3]. Furthermore, sequential high-temperature transformations of the (O-T) lattice into (O-T-T) and finally (O-T-T-T) phases via deintercalation of the LnS slab was observed. This autocatalytic process is reminiscent of the deintercalation of alkali atoms from different layered structure materials. Annealing at higher temperatures and for longer periods of time leads eventually to the decomposition of the ternary MLC into binary metal-sulfide phases as well as partial oxidation of the product. This study sheds light on the complex mechanism of high-temperature chemical stability of nanostructures.
An examination of materials discovery processes suggest that there can be a long lag between the creation of compounds and the discovery of their utility that would permit them to be described as materials. The goal of materials-by-design therefore is therefore dictated primarily by the ability to screen materials for function. This is the first step en route to a paradigm of dialing up the optimal material structure and composition to serve a particular function. Several issues that make even this task of screening somewhat complex. The first is that many properties of interest are not tractably calculated in a reliable way, because the underlying science is as-yet not established. The second is that materials optimization is frequently based on much more than a single performance criterion. In this talk, I will describe computational proxies that have allowed us to establish guidelines to find better phosphor materials for solid-state white lighting, better magnetocaloric materials, and some recent work on low-k dielectrics. Separately, I will describe the computational screening of all inorganic photovoltaic materials.
Halide perovskites have emerged as a new class of semiconductors with excellent properties such as large tunable band-gaps, large absorption coefficients, long diffusion lengths, low effective mass and long radiative lifetimes. These have resulted in record efficiencies for photovoltaics surpassing that of Si. However, a major challenge for these materials is realizing long-term stability under light, temperature and humidity. In contrast, 2D perovskites are a sub-class of 3D perovskites, have demonstrated excellent stability compared to the 3D perovskites.
In this talk I will describe our work over the past five years on 3D and 2D perovskites ranging from novel fundamental light-induced structural behaviors and its impact on charge transport, solvent chemistry and the synergy between 2D and 3D perovskites in achieving durable and high-efficiency photovoltaic devices. Finally, if time permits, I will also present some new results, which offer an exciting prospects for developing single photon emitters using a new solid state platform, which allows for ultra stable quantum emitters with high purity photons with unity quantum yield.
SESSION: SolidStateChemistryTuePM2-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Tue. 22 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Wendy Queen; Christopher Wolverton; Student Monitors: TBA |
LHP NCs are of broad interest as classical light sources (LED/LCD displays) and quantum light sources (quantum sensing and imaging, quantum communication, optical quantum computing). The surface-functionalization of such labile ionic materials poses a formidable challenge, which we address with the library of designer phospholipid capping ligands [1]. Lattice-matched primary-ammonium phospholipids enhance the structural and colloidal integrity of hybrid organic–inorganic NCs [FAPbBr3 and MAPbBr3 (FA, formamidinium; MA, methylammonium)] and lead-free metal halide NCs. The molecular structure of the organic ligand tail governs the long-term colloidal stability and compatibility with solvents of diverse polarity, from hydrocarbons to alcohols. These NCs exhibit photoluminescence (PL) quantum yield of more than 96% in solution and solids, as well as hours-long stability at a single-particle level, with minimal PL intermittency, as well as bright and high-purity (about 95%) single-photon emission. The brightness of such a quantum emitter is ultimately described by Fermi’s golden rule, where a radiative rate proportional to its oscillator strength (intrinsic emitter property) and the local density of photonic states (photonic engineering, i.e. cavity). With perovskite NCs, we present a record-low sub-100 ps radiative decay time for CsPb(Br/Cl)3 NCs by the NC size increase to 30 nm, owing to the giant oscillator strength [2]. Notably, the fast radiative rate is achieved along with the single-photon emission. When such bright and coherent QDs are assembled into superlattices, collective properties emerge, such as superradiant emission from the inter-NC coupling [3]. In the most recent work [4], we present the formation of multicomponent SLs made from the CsPbBr3 NCs of two different sizes. The diversity of obtained SLs encompassed the binary ABO6-, ABO3-, and NaCl-type structures, all of which contained orientationally and positionally confined NCs. We observed efficient NC coupling and Förster-like energy transfer from strongly confined 5.3 nm CsPbBr3 NCs to weakly confined 17.6 nm CsPbBr3 NCs. Exciton spatiotemporal dynamics measurements reveal that binary SLs exhibit enhanced exciton diffusivity compared to one-component SLs.
Among several classes of porous materials, metal-organic frameworks (MOFs) are particularly attractive due to their unprecedented internal surface areas (up to 7800 m2/g),[1] easy chemical tunability, and strong, selective binding of a host of guest species. Through judicious selection of MOF building blocks, which include metal ions and organic ligands, one can readily modify their properties for a variety of potential applications. Despite these attractive features, there are still challenges in the field that limit our ability to use MOFs as a solution for a wide range of industrial problems. For instance, some MOFs have limited mechanical and chemical stability, particularly in highly humid, acidic or basic environments. Overcoming this problem could lead to extended lifetimes and hence increased feasibility for their use in areas where such conditions are required.
In response to these needs, we have recently begun to combine MOFs and polymers in an effort to boost MOF performance and extend their stability.[2] Our recent work demonstrates that selected polymers can significantly enhance MOF performance in a number of important liquid and gas separations[3-6] as well as extend catalyst lifetimes in selected reactions.[7] In addition to this, controlled polymerization processes were employed to enhance the mechanical stability[8] of large pore frameworks and extend the chemical stability of a number structurally diverse MOFs not only in humid environments, but also in acidic and basic media.[9] We hope such work can help bring these frameworks a few steps closer to their deployment into a range of ecologically and economically important applications. In this presentation our recent work devoted to modification of MOFs and their application in several globally relevant separations will be outlined.
Metal-Organic Frameworks (MOFs) have attracted a tremendous research interest because of their significant potential for practical applications in areas such as gas storage and separation, drug delivery, sensing, catalysis, etc.1 The crystalline nature of these materials allows them to be characterized via single – crystal X-ray diffraction, which provides valuable insight of their structural features. MOFs with fine-tuned properties can be prepared through a process called post synthesis modification. PSM allows the introduction/exchange of functional groups of a MOF and is preferable to proceed in a single-crystal-to-single-crystal (SCSC) fashion because with this way direct structural information can be provided for the achieved structural modifications via single crystal x-ray crystallography. Several types of SCSC transformations have been reported which include insertion/exchange of organic ligands, exchange of lattice solvent molecules or terminally ligated molecules, transmetallations, metalation of the framework, etc.2
We shall report two families of trivalent rare earth (RE3+) MOFs based on a hexanuclear (RE3+)6 SBU and their exchanged analogues. The first one involves 8-connected 2-D MOFs based on an angular dicarboxylic ligand 4,4'-(hydroxymethylene)dibenzoic acid (H2BCPM), UCY-17(RE). A series of exchanged analogues UCY-17(Tb)/L produced from linker installation SCSC reactions of UCY-17(Tb) with selected dicarboxylic ligands shall also be discussed. The SCSC installation of the dicarboxylic ligands resulted not only to the turn-on of the thermometric properties of these materials but also to a variety of different thermometric performances.3 The second family of compounds with the general formula ((CH3)2NH2)2[Y6(μ3-ΟΗ)8(bpydc)6] is based on the linear dicarboxylic ligand H2bpydc= [2,2'-bipyridine]-5,5'-dicarboxylic acid. Its subsequent metalation with transition metal ions was achieved giving rise to a series of exchanged analogues with various metal ions. Gas sorption measurements of the metalated analogues reveal lower Brunauer - Emmett Teller (BET) surface areas consistent with the complexation of metal ions to the accessible nitrogen atoms of the bpydc2- ligand whereas the CO2 uptake of the metalated analogues is increased. Furthermore, gas sensing studies of the pristine and metalated compounds revealed a variety of different gas sensing capabilities. Thus, SCSC transformation reactions allowed not only the targeted modification of the structures of the two MOFs but also the modulation of their temperature and gas sensing properties.
Discovery and design of novel thermoelectric materials is particularly challenging, due to the complex (and often contraindicated) set of materials properties that must be simultaneously optimized. Here we discuss our efforts at developing and applying data-driven computational techniques that enable an accelerated discovery of novel thermoelectrics. These techniques involve a combination of high-throughput density functional theory (DFT) calculations, inverse design approaches, and machine learning and artificial intelligence based methods. We discuss several recent examples of these methods: (i) inverse design strategies based on a materials database screening to design a solid with a desired band structure [1], (ii) inverse design strategies to identify compounds with ultralow thermal conductivity [2] (iii) an effective strategy of weakening interatomic interactions and therefore suppressing lattice thermal conductivity based on chemical bonding principles [3], and (iv) the development of crystal graph based neural network techniques to accelerate high-throughput computational screening for materials with ultralow thermal conductivity. [4,5]
SESSION: SolidStateChemistryTuePM3-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Tue. 22 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Daniela Marongiu; Francesco Quochi; Student Monitors: TBA |
Thermoelectricity is the process of directly converting heat into electricity and vice versa, offering an environmentally sustainable means to generate electricity from wasted heat. To enhance the efficiency of this conversion, it's essential to precisely control various structural aspects beyond just the crystal structure. These aspects include defects, grain size, orientation, and interfaces.
In recent years, solution-based techniques have garnered significant interest as a cost-effective and easily scalable approach for manufacturing high-performance thermoelectric materials. In this method, a powdered material is first prepared in a solution and then subjected to purification and thermal processing to produce the desired dense polycrystalline material. Unlike traditional methods, solution-based syntheses offer an exceptional level of control over various particle properties, including size, shape, crystal structure, composition, and surface chemistry. This precise control over the properties of the powder creates distinct opportunities for crafting thermoelectric materials with precisely tailored microstructural characteristics. In this presentation, we will highlight the opportunities and challenges that this synthetic strategy can bring, in particular we will focus on metal chalcogenides.
Halide double perovskites are gaining increasing attention for various optoelectronic applications, such as photovoltaics, light-emitting diodes, and sensors, due to their unique properties. They offer advantages over traditional lead-based perovskites, including enhanced stability and reduced toxicity. Lanthanides, with their distinct electronic configurations, enhance functionality by introducing luminescence, magnetism, and stability. This study focuses on synthesizing and characterizing ytterbium- and erbium-based halide double perovskites for near-infrared (NIR) optical amplifiers and lasers, contributing to advancements in solid-state photonics.
Polycrystalline powders of double perovskites Cs2NaxAg1-xLnyBizIn1-y-zCl6 (0≤𝑥≤1, 0≤𝑦≤1, 0≤𝑧≤1) were synthesized by solvent evaporation of acidic solutions containing precursor salts. Comprehensive characterization of the materials was conducted using techniques such as powder X-ray Diffraction (pXRD), Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), optical absorption spectroscopy, Raman spectroscopy, photoluminescence excitation (PLE) spectroscopy, photoluminescence quantum yield (PLQY) spectroscopy, and time-resolved photoluminescence (PL) spectroscopy with sub-nanosecond resolution. Additionally, single crystals of Cs2NaYbCl6 were grown using a vertical Bridgman furnace and characterized both structurally and spectroscopically.
pXRD analysis confirmed a single cubic phase in all samples, while precise control over materials composition was demonstrated via ICP-OES analysis. Materials rich in indium exhibited PLQYs reaching 90% for warm-white emission from self-trapped excitons and 10% for lanthanide emission. Using NIR-PL lifetime measurements and resonant absorption spectroscopy, we determined the lanthanide photophysical parameters, including radiative lifetimes and absorption/emission cross-section spectra, within the halide octahedral crystal field. Modeling optical gain enabled estimation of the figure-of-merit (FOM) of lanthanide-based double perovskites as NIR optical gain media. Structural and spectroscopic data on Cs2NaYbCl6 powder were confirmed in Cs2NaYbCl6 single crystals.
In summary, halide double perovskites demonstrated minimal lanthanide luminescence concentration quenching for Er and Yb concentrations up to 100 at.% (𝑦≈1), attributed to the significant interionic distances within the double perovskite matrix. Evidence suggested a reduction in phonon-assisted relaxation within low-lying Er(III) electronic multiplets in Er-based double perovskites. Additionally, Er-based lasing at 1570 nm under 1530 nm optical pumping demonstrated an excellent FOM, distinguishing the halide double perovskite (HDP) crystal matrix from conventional crystal matrices such as yttrium aluminum garnet (YAG). Successful growth of high-purity single crystals is essential for advancing lanthanide-based halide double perovskites in the development of a new class of NIR solid-state lasers.
Hybrid halide perovskites are a novel class of semiconductor materials with promising and versatile optoelectronic properties, enabled by their chemically adjustable structures and dimensionality. The diversity in the metal ions, halide anions, and organic spacers enables a wide range of materials with highly tunable properties and variable dimensionalities. These materials are studied for various applications such as solar cells, detectors, and light-emitting diodes. The ability to control and adjust the optical properties for a required application is significant. Thus, an improved understanding of the structure and optical mechanisms is crucial.
Specific low-dimensionality hybrid halide perovskites exhibit white-light emission at room temperature, associated with self-trapped excitons (STE), making them ideal candidates for illumination applications. We study the correlation between structural and chemical motifs of low dimensionality (2D, 1D) halide perovskites and their STE emission.
Specifically, we have studied how exchanging the halide anions while maintaining the structure affects the STE properties in a unique 1D perovskite structure based on edge-sharing dimers. These structures exhibit strong, broad emission with PLQY of approximately 40%. By changing the halide from I to Br and Cl, we can see the widening of the bandgap, as expected. However, the broad emission shows an anti-correlated behavior, resulting in red-shifted emission for the Cl sample, with a significantly larger stokes shift. We further study how mixing Br and Cl in a single structure affects the broad emission properties and how different synthetic approaches can be utilized for the fabrication of these compounds.
In the context of solar cell technology, 2D Ruddlesden-Popper perovskite phases have been utilized alongside polycrystalline (PC) 3D hybrid perovskites (HPs) as ultrathin passivation layers to enhance stability and charge extraction. The majority of the reported 3D/2D heterostructures consist of PC thin films deposited on top of PC 3D HPs. This method offers limited control over the orientation and crystalline phase, leading to a high concentration of defects at grain boundaries and interfaces. These defects promote the presence of traps for charge carriers, ion migration, and water permeation.
On the other hand, pure 2D HPs have been considered less suitable for photovoltaic applications due to their large exciton binding energies, which theoretically hinder charge separation and result in significant energy losses. Surprisingly, the presence of large polarons - charge carriers coupled to lattice deformations - prevents the formation of excitons [1]. One of the first explanations was based on exciton dissociation caused by polycrystalline grains boundaries, suggesting that the formation of free carriers actually requires a defective material [2]. However, fundamental studies performed on singles crystals showed that exciton dissociation into unbound carriers is an intrinsic phenomenon, taking place also in single crystals with low defect densities [3]. This can enable more possibilities for 2D single crystals for optoelectronic applications, including photovoltaic ones.
Despite the potential benefits, the use of single crystal (SC) HPs for both 2D/3D heterostructures and pure 2D film devices remains challenging and, at the moment, the best performances are attributed to polycrystalline films possibly with a 2D passivating layer on top. Indeed, the best performing single crystal solar cells show an efficiency gap with respect to the polycrystalline counterpart which is attributed to the high surface charge trap density that results from the contamination of residual crystal growth solution, strongly affecting the surface quality and charge recombination.
In this study, we investigate single crystal 2D perovskites and 2D/3D heterostructures. We demonstrate the growth of 2D HP single crystal thin films using various additives and analyze their optical and structural properties together with the electrical characterization. We also present single crystal 2D/3D thin film heterostructures and propose several strategies for interface engineering. Additionally, we provide a critical comparison of the photophysics and transport properties between single crystal and polycrystalline samples.
SESSION: SolidStateChemistryTuePM4-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Tue. 22 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Omar Farha; Student Monitors: TBA |
The realization of ultralow thermal conductivity in a well-ordered structure is crucial for crystalline materials which consider heat conduction properties to be primary in design. We report herein an extremely low (0.32‒0.25 Wm-1K-1) and glassy temperature dependence (300‒600 K) of lattice thermal conductivity in a monoclinic K2Ag4Se3. By applying a unified theory of thermal transport, we reveal that K2Ag4Se3 features a complex phonon scattering mechanism. Delocalized vibrational correlations lead to synergistic inhibition of both propagating and wave-like heat conduction through polarization transmission. Density functional theory calculations reveal that long-range correlated Se vibrations, enhanced by delocalized hole carriers, promote interlayer lattice shearing. This shearing induces dynamically competitive expressions of different orders of anharmonicity, ultimately leading to full-spectrum phonon bunching as the temperature increases. These correlated interactions cause Se anions to vibrate together as a cluster in the low frequency region, resulting in short phonon lifetimes, low group velocities, and a large scattering phase space, which ultimately suppresses both intra- and inter-band phonon transfers. Moreover, these findings have been experimentally confirmed through low-temperature heat capacity measurements and in situ Raman spectroscopy. The insights gained from this work will advance the design of crystalline materials with tailored thermal properties.
As chemists and materials scientists, it is our duty to synthesize and utilize materials for a multitude of applications that promote the development of society and the well-being of its citizens. Since the inception of metal-organic frameworks (MOFs), researchers have proposed a variety of design strategies to rationally synthesize new MOF materials, studied their porosity and gas sorption performances, and integrated MOFs onto supports and into devices. MOFs are a class of porous, crystalline materials composed of metal-based nodes and organic ligands that self-assemble into multi-dimensional lattices. In contrast to conventional porous materials, an abundantly diverse set of molecular building blocks allows for the realization of MOFs with a broad range of properties. Efforts have explored the relevance of MOFs for applications including, but not limited to, heterogeneous catalysis, guest delivery, water capture, destruction of nerve agents, gas storage, and separation. For example, we have developed an extensive understanding of how the physical architecture and chemical properties of MOFs affect material performance in applications such as catalytic activity for chemical warfare agent detoxification. Recently, start-up companies have undertaken MOF commercialization within industrial sectors. ION-X™ is used in this talk as an example to show case the way NuMat Technologies is innovating at the intersection of molecular design and precision engineering, to build the products driving the industries of tomorrow.
SESSION: AdvancedMaterialsTuePM1-R8 |
8th Intl Symposium on New & Advanced Materials and Technologies for Energy, Environment, Health and Sustainable Development |
Tue. 22 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Tetiana Prikhna; Fernand D. S. Marquis; Student Monitors: TBA |
Materials have always played a most important and crucial role in the development of human civilizations, throughout the Ages. So much so that they were named after them such as the stone, the bronze and the iron ages. Sustainable development is a comprehensive and complex system of systems requiring multidisciplinary and interdisciplinary science and technology inputs with economic, environmental, and social objectives and goals. In broad terms, sustainable development is achieved when the present needs and challenges are met without placing in jeopardy the ability of future generations to meet their own needs and challenges. The trade space is very wide, and the multitude of trade-offs generate considerable challenges and make it often difficult to achieve an effective balance, most beneficial to all concerned. During the last sixty years the planet’s population has grown exponentially, from 2 to almost 8 billion people, and the technological progress achieved has been tremendous, especially in the industrialized countries. These trends are expected to continue, even at faster rates. However, all these associated technological activities in the pursuit of better living standards have created a considerable depletion of resources and pollution of land, water, air, and natural resources, for the global population. During this period considerable achievements have been obtained in the development and deployment of transformative materials such as light weight metallic alloys, metal matrix composites, intermetallic and carbon fiber composites, and hybrid materials. Nano, nano-structured and nano-hybrid materials systems and nanotechnologies are now being deployed with considerable impact on energy, environment, health and sustainable development. This presentation presents perspectives on the evolution and global impact of transformative materials with a focus on Nanomaterials and Nanotechnologies, and with examples from several domains of sustainable development.
Nanodispersed iron oxides (contained mainly magnetit) obtained by the electroerosion dispersion (EED) technology was used to produce developed by M. Monastyrov feed additive Nano-Fe+TM. The efficiency of feed premixe Nano-Fe+TM was studied for growing broiler chickens. The method of increasing the productivity of agricultural animals and birds is to introduce iron nanopowder into the feeding ration by spraying feed with a suspension of iron nanopowder with a particle size of 20-30 nm in doses of 0.08-0.1 mg/kg of live weight per day. At the poultry faсtory, Nano-Fe+TM (suspension of iron oxides in glycerin) was diluted in water at a rate of 10 ml/10 l. The solution was sprayed on the feed of the birds before feeding at a rate of 10 l/1 ton of feed. The following results were obtained when using Nano-Fe+TM: the live weight gain of chickens increased by 5÷17%; the growth rate of broilers increased by 10÷20%; the protection of poultry from diseases increased by 10÷20%; the effects of stress from vaccination, regrouping, etc. decreased.
Closed-cell Aluminum foam is a particular type of lightweight metallic material that can sustain considerable deformation under nearly constant stress which is known as plateau stress. Thus, under dynamic loading, aluminum foams can be used for energy absorption. However, these foams have a low plateau stress and are generally unsuitable for carrying structural loads. To improve foam mechanical properties graphene reinforcement has been used to enhance its dynamic mechanical response for applications at room temperature and high temperatures. Preliminary investigation was conducted at room temperature on graphene reinforced aluminum foam by Sinha et al. [1].
For this investigation, aluminum foams reinforced with graphene concentration varying between 0.2 – 0.62 wt.%, manufactured using the liquid metallurgy route were studied. The compressive dynamic behavior of this foam has been studied over a range of high strain rates up to 2200 s-1 using the Split Hopkinson Pressure Bar (SHPB) apparatus [2]. The mechanical response was studied at high temperatures of 473K, 623K, and compared to room temperature of 298K. Amongst the four different graphene compositions (0.20wt.%, 0.40wt.%, 0.50wt.% and 0.62 wt.%) studied, 0.62 wt.% displayed the maximum value of peak stress, plateau stress, and energy absorption. The experimental data obtained in the present study is supported using an empirical model.
It is observed that at high temperature, the values of peak and plateau stress decreased when compared with the values obtained at room temperature for reinforced foam. However, the high strain rate response of the reinforced foam at high temperature was equal or better than the response of unreinforced foam under similar loading conditions at room temperature.
Tissue wounds afflict millions of individuals annually, giving rise to significant social and economic concerns. Previous investigations have demonstrated the remarkable potential of hydrogels in wound healing owing to their exceptional capabilities in absorbing wound exudate, moisturizing, facilitating oxygen permeation, and possessing a three-dimensional porous structure[1]. However, natural polymer-based hydrogel dressings for wounds often suffer from susceptibility to bacterial growth and subsequent infection, which represents a major obstacle impeding the wound healing process.
Photothermal therapy (PTT) is a strategy to achieve antibacterial effect through rapid hyperthermia produced by a photothermal agent under near-infrared (NIR) light radiation (700-1100 nm). Compared with conventional antibacterial methods, PTT offers distinct advantages including heightened sterilization potency, reduced treatment duration, and diminished risk of drug-resistant bacteria[2]. We previously synthesized stable tricomplex molecules (PA@Fe) assembled by protocatechualdehyde (PA) and ferric iron, which were subsequently embedded in a gelatin hydrogel (Gel-PA@Fe). The embedded PA@Fe served as a crosslinker to improve the mechanical and adhesive properties of hydrogels through coordination bonds and dynamic Schiff base bonds, meanwhile acting as a photothermal agent to convert NIR light into heart to kill bacteria effectively[3]. The hydrogel was endowed with exceptional hemostatic and antioxidant properties by grafting serotonin onto the gelatin molecular chain, resulting in the preparation of a composite hydrogel (GelS-PA@Fe). As a mediator of blood coagulation, serotonin can interact with catechol-containing PA and chemical hemostatic agents, thereby enhancing the adhesion of more blood cells to the hydrogel surface. The free radical scavenging rate of GelS-PA@Fe (80.49%) exhibited a 1.5-fold increase compared to that of the Gel-PA@Fe hydrogel, indicating enhanced efficacy in neutralizing free radicals. Importantly, the introduction of serotonin did not compromise the biocompatibility and photothermal antibacterial properties of the GelS-PA@Fe hydrogel. Our results indicated the great potential of GelS-PA@Fe hydrogel in promoting infected wound healing.
SESSION: AdvancedMaterialsTuePM2-R8 |
8th Intl Symposium on New & Advanced Materials and Technologies for Energy, Environment, Health and Sustainable Development |
Tue. 22 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Sanjeev Khanna; Andriani Manataki; Student Monitors: TBA |
Molten Carbonate Fuel Cells (MCFCs) are a relatively recent development in fuel cell technology, with applications ranging from small to large scale power generation systems. The interconnect is the part of the MCFC to which the anode and cathode are attached and through which the electrical current generated by the cell is conducted. Therefore, the interconnect must not only be mechanically strong and resistant to oxygen and hydrogen, but also maintain high electrical conductivity and corrosion resistance (including on the surface of the interconnect) at high temperatures (550...650°C) for long periods.
Interconnections (0.3-0.5 mm thick) made of stainless steel (which contains 16-18% Cr and has a high density γ ~ 8 g/cm3) lose surface electrical conductivity due to oxidation. MAX phases Ti2AlC3 and Ti2AlC have two times lower density (γ ~ 4.1 - 4.3 g/cm3) than stainless steel, are stable in oxygen and hydrogen atmosphere at high temperature, and have high electrical conductivity. Therefore, the MAX phase based coatings are potentially promising for this application. OT4-1 titanium alloy substrates with protective coatings are being developed for use as interconnects for MCFCs to replace 316L stainless steel.
Ti-Al-C, (Ti,Mo)-Al-C and (Ti,Cr)-Al-C coatings were deposited on OT4-1 alloy substrates by hybrid magnetron sputtering and cathodic arc evaporation. For magnetron sputtering, a MAX phase (Ti2AlC - 63 wt.% and Ti3AlC2 - 37 wt.%) target prepared by hot pressing of TiC, Al and TiH2 under 20 МPа, at 1350 °С for 10 min was used. Simultaneously with magnetron sputtering of the MAX phase target, chromium or molybdenum was deposited using a cathodic arc plasma source. Three types of coatings were deposited: Ti-Al-C magnetron-only and hybrid (Ti,Mo)-Al-C and (Ti,Cr)-Al-C. The thickness of the deposited coatings was 5-11 µm.
X-ray diffraction analysis showed that all deposited coatings are close to amorphous state. The SEM-EDX study indicated that the average composition of the coatings obtained from the MAX phase based target was Ti2Al1.0-1.1C1.1-1.3 (close to 211), for the coating with additions of Mo: Ti2 Mo2.1Al0.9C2.8 (close to 413) and Cr: Ti2Cr2.6Al0.8C1.5. The nanohardness of the coatings varied from 11 to 15 GPa and the Young's modulus from 188 to 240 GPa.
The (Ti,Cr)-Al-C coating showed the highest stability against electrochemical corrosion in 3.5 wt.% NaCl aqueous solution at 20 °C: corrosion potential Ecorr = 0.044 V, corrosion current density icorr = 2.48×10-9 A/cm2, anodic current density ianodic (at 0.25 V vs. SCE) = 5.18×10-9 A/cm2. This coating also showed the highest long-term oxidation resistance and after heating in air at 600 °C, 1000 h its electrical conductivity s= 9.84×106 S/m was slightly higher than before heating s= 4.35×105 S/m, the nanohardness and Young's modulus are in the range of 15 GPa and 240 GPa, respectively. The increase in electrical conductivity after long-term heating at 600 °C can be explained by the observed crystallization of the amorphous phase in the structure of the coating.
Thus, the hybrid deposited (Ti,Cr)-Al-C coatings exhibit high corrosion and oxidation resistance while maintaining electrical conductivity and can be used to protect titanium alloy interconnects in lightweight MCF cells.
Acknowledgments The work was supported by the III-7-22 (0785) Project of the National Academy of Sciences of Ukraine "Development of wear-resistant electrically conductive composite materials and coatings based on MAX phases for the needs of electrical engineering, aviation, and hydrogen energy"; by the NATO project SPS G6292 “Direct liquid fuelled molten carbonate fuel cell for energy security (DIFFERENT)”, and by the MES Ukraine project №0122U001258 “Development of nanotechnological methods to prevent corrosion of structural materials in thermal and nuclear power plants”.
In oil and gas fields, once exploration or production phase concludes, the wells undergo plugging and abandonment (P&A), a crucial phase in their lifecycle. P&A aims to seal wells to prevent environmental contamination and hazards. In Norway, increased attention to this phase arises as more than 7000 wells are heading for plugging and abandonment in the North Sea till 2050. Compliance with specific NORSOK standards dictates the use of well-barrier materials tailored to stringent requirements.
Historically, cement has served as the primary well-barrier material for P&A activities. However, inherent drawbacks such as shrinkage, poor bonding, and susceptibility to gas migration have spurred exploration into alternative materials offering enhanced mechanical strength and sealing performance. Among these alternatives, bismuth-based alloys stand out as promising candidates.
This article is a literature review, aiming to disseminate international innovative endeavors from industry and academia alike, addressing the efforts made to achieve well integrity and environmental protection, using bismuth-based alloys as well barrier materials. At the beginning, the article examines diverse practices employed by 15 different industry stakeholders utilizing the same material. To date, bismuth-based plugs have been deployed as environmental plugs and for annular sealing, utilizing the intense heat mostly generated by an exothermic reaction from a thermite blend. The combination of these materials has made bismuth alloy plugs promising candidates as well-barrier materials, particularly because they may be deployed without the need for rigs, section milling, perforation, or casing removal. This significantly reduces both the time and cost of P&A operations. The paper describes various new technologies and field operations, highlighting how bismuth-based plugs are emerging as a novel solution that enhances well integrity and safety while also lowering operational costs. Furthermore, the paper provides a comprehensive overview of academic research focused on the BiSn alloy, detailing laboratory mechanical testing, microstructural analysis, and numerical simulations to assess its suitability for well applications. Overall, this article effectively communicates the significance of P&A operations, the necessity for advanced well barrier materials, and ongoing collaborative efforts between industry and academia to meet the challenges of integrity that a well may face. It contributes to the advancement of environmentally responsible well-abandonment practices and to the enhancement of the knowledge of the bismuth-based sealing methods used in this area.
Cubic boron nitride (cBN) has long been used to create superhard tool materials [1, 2] due to its high hardness (up to 60 GPa) and chemical inertness with respect to many steels, which makes it valuable for cutting tools [3]. The most commercially known cBN-bonding systems are cBN-Al, cBN-TiC (TiCN), and cBN-Co&Al.
The main problem in high-speed machining of parts for these cutting materials is chemical wear, where temperatures in the cutting zone can reach up to 1000-1100 °C, leading to a decrease in strength and an increase in ductility of cubic boron nitride composites. One solution to this problem is to add inert components to the structure bonds, such as refractory carbides, borides, and nitrides of p- and d-elements. For cutting tools based on cubic boron nitride, the best wear resistance and service life for high-speed turning of Inconel 718 is achieved at a cBN content of 45-60% with ceramic bonds of Ti (C,N) or TiN.
Within the framework of the project "Development of the Center for Collective Use of the Institute of Materials Science of the National Academy of Sciences of Ukraine" (2023.05/0007, National Research Foundation of Ukraine), the structure and properties of superhard composite materials BL with a cBN content of 60 %, obtained in the cBN(Al)-SiB4-WC system under high pressure and temperature, were investigated. The experiments were carried out using the high-pressure apparatus "toroid-30".After reaching a pressure of 7.7 GPa, the composite material was sintered in the temperature range of 1600-2300 °C (time heater for 1 min). As a result, ceramic inserts, which were then ground with diamond wheels to achieve dimensions of d = 9.52 mm and h = 3.18 mm, in accordance with ISO 1832-2017 for cutting inserts - RNGN 090300T.
According to the X-ray phase analysis, the phase composition of the cBN(Al)-SiB4-WC system composites does not change significantly with sintering temperature. The main phase is cubic boron nitride (cBN), whose lattice period varies depending on the sintering conditions. At high temperatures, rhombohedral silicon boride SiB4 decomposes, and as a result of its interaction with tungsten carbide WC, two new phases are formed: hexagonal tungsten boride W2B5 (a = 0.2993(2) nm, c = 1.395(1) nm) and tetragonal tungsten silicide WSi2 (a = 0.3208(1) nm, c = 0.7841(3) nm). An excess of boron and carbon forms micron-sized clusters of B-C compounds. Aluminum, when added in small quantities, oxidizes to α-Al2O3, which prevents the oxidation of other components. Thus, the material is a ceramic-matrix composite consisting of cBN, W2B5, WSi2, as well as B-C and α-Al2O3 compounds. Electron microscopy of the obtained material at a sintering temperature of 2000 °C showed that a homogeneous porous structure was formed. The density and Young's modulus of the ceramic increase with sintering temperature and reach their maximum values at 2000 °C. A further increase in temperature leads to annealing of defects, recrystallization of the structure, and partial graphitization of cBN, which worsens the material's characteristics. The materials obtained at 1800-2000 °C have the best physical and technical characteristics and are suitable for the manufacture of cutting inserts.
Thus, ceramic-matrix composites of the cBN(Al)-SiB4-WC system form high-strength, porous materials with high physical and mechanical characteristics. Compounds of tungsten boride and silicide, as well as aluminum oxide, provide oxidation resistance, which makes them suitable for processing high-alloy steels at high temperatures.
Safeguarding wounds against secondary infections and facilitating expedited wound healing are pivotal concerns in various domains, including everyday life, clinical practice, and other contexts. Compared to traditional healing therapy, electrical stimulation therapy (ES) effectively modulates cellular behavior, promotes cell proliferation and migration, and is extensively utilized in clinical treatment. In this study, MXene, nano-chitin (Ch), and polyvinyl alcohol (PVA) multifunctional hydrogels were investigated for their exceptional mechanical properties, antibacterial activity, and biocompatibility. Leveraging the self-healing property of PVA hydrogel, a novel ring splicing dressing was designed to guide the directional electric field from the wound edge towards the wound center, thereby enhancing the endogenous electric field within the wound. Experimental results using a rat skin defect model demonstrated that the hydrogel significantly accelerated the healing process with enhanced efficiency compared to conventional dressings. This study highlights a facile approach for the preparation of MXene/Ch/PVA hydrogels with enhanced wound healing capability, while introducing novel strategies for the development of electrotherapeutic dressings through its unique ring structure design.
SESSION: AdvancedMaterialsTuePM3-R8 |
8th Intl Symposium on New & Advanced Materials and Technologies for Energy, Environment, Health and Sustainable Development |
Tue. 22 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Tetiana Prikhna; Amr Henni; Student Monitors: TBA |
Ultra-high temperature (UHTC) transition metal borides can be used for a wide range of mechanical applications - as components of military and commercial equipment operating in extreme conditions, for rocket propulsion, hypersonic flights, atmospheric reentry, protective coatings on graphite, for using in abrasive, erosive, corrosive and high-temperature environments, which requires materials with significantly improved physical properties. To UHTC belongs TaB2 which exhibits high melting point (3200 °C), hardness (24.5 GPa -25.6 GPa), fracture toughness (4.5 MPa m0.5), bending strength (555 MPa), excellent chemical stability, electrical (308×104 Ω-1×m-1) and thermal (0.160 -0.161 W×cm-1×K-1 at 300-1300 oC) conductivity, good corrosion resistance [1-5]. To increase the oxidation resistance and mechanical characteristics TaB2 can be modified by silicides [1]. In the present study we investigated modification of TaB2 by MoSi2, ZrSi2 and Si3N4 in the amount of 20-30 wt.% and its sintering process under hot pressing conditions (30 MPa, 1750-1950 oC) and high pressure (4.1 GPa) - high temperature (1800 oC) conditions. The highest Vickers hardness HV=31.5 GPa and fracture toughness K1C=6 MPa×m0.5 under P= 9.8 N load was obtained for the composite sintered at 30 MPа, 1750 °C, 20 min from TaB2+20 wt.% ZrSi2, the increase of amount of ZrSi2 up to 30 wt.% leads to further increase in K1C= 6.9 MPa×m0.5, but to the reduction of microhardness down to HV=23.5 GPa. The composite sintered under 30 GPa at 1950 °C for 40 min from TaB2+20 wt.% MoSi2 showed HV=28.2 GPa and K1C= 5.42 MPa×m0.5. TaB2+30 wt.% Si3N4 sintered at 4.1 GPa, 1800 oC for 7 min had HV=18.8 GPa and K1C= 4.82 MPa×m0.5. The specific weight of the materials prepared from TaB2+20 wt.% MoSi2 was g=10.82 g/cm3, TaB2+30 wt.% Si3N4 - g=8.77 g/cm3, TaB2+20 wt.% ZrSi2 - g=9.35 g/cm3, TaB2+30 wt.% ZrSi2 - g=10.12 g/cm3.
AcknowledgementS: This work was supported by the Project of the National Academy of Sciences of Ukraine III-5-23 (0786) “Study of regularities and optimization of sintering parameters of composite materials based on refractory borides and carbides, their physical and mechanical properties in order to obtain products of complex shape for high-temperature equipment with an operating temperature of up to 2000 oC”
This work presents the encapsulation of two amino acid-based ionic liquids (AAILs), 1-Ethyl-3-methylimidazolium glycine [Emim][Gly], and 1-Ethyl-3-methylimidazolium alanine [Emim][Ala], into an highly porous metal organic framework, MOF-177, to create a state-of-the-art composite for post-combustion CO2 capture. The AAILs@MOF-177 composite sorbents were synthesized at varying loadings of AAILs. These composite sorbents were then evaluated and examined for their thermal and structural integrity, CO2 capture capability, CO2/N2 selectivity, and heat of adsorption. Thermogravimetric analysis of the composites demonstrated that the encapsulation was successful, and the slow degradation of the composites suggested that AAILs and MOF-177 interacted with each other to some extent. Both the surface area and the pore volume of the composites experienced a dramatic decrease as a direct result of the encapsulation of the AAILs. The findings of the XRD analysis also showed that an increase in the loading of AAILs greater than a particular limit produced a degradation in the structural integrity of the parent support. At pressures below 1 bar (post-combustion conditions), the AAILs encapsulated composites outperformed the pure MOF177 in terms of CO2 uptake and selectivity. The maximum CO2 uptake was found to be at 20 wt.% loading for both [Emim][Gly]@MOF-177 and [Emim][Ala]@MOF-177 at 0.2 bar, 303 K, and the uptake values were about three times higher than MOF-177. In addition, the CO2/N2 selectivity of 20-[Emim][Gly]@MOF-177 and 20-[Emim][Ala]@MOF-177 increased from 5 (pristine MOF-177) to 13 and 11, respectively. However, it was discovered that the ideal amount of AAILs was 20 wt.%, and after that, increasing the loading any further, even to 30%, did not increase the CO2 uptake. The results of this study shed light on the stability of AAILs@MOF-177 composites, as well as their overall performance in capturing CO2 and CO2/N2 selectivity under post-combustion CO2 capture conditions.
According to the latest definitions [1], High-Entropy Alloys (HEAs) are the alloys where the concentration of basic (at least 5) elements varies between 5-35%. The HEA has higher mixing entropy than the conventional alloys and intermetallic compounds and form the stabile solid solutions with disordered structure [1, 2, 3, 4, 5].
At the current stage the volume of investigations towards high entropy materials is extended from single phase solid solution structure to multi-phase structures, containing solid solution phases, intermetallic compounds, oxides, borides etc. [6, 7, 8, 9].
Promised direction in this field are the high-entropy composites, prepared based on the HEAs matrix- reinforced with hard ceramic compounds. Reinforcement of HEA matrix by Intermetallic and ceramic compounds are additional tools/and challenge to improve/or design new properties of HEA based composites. Accordance evaluation “HEA is still in earlier stages hence a detailed investigation is needed” [8]. Especially, it should be underlined that HEAs, as the composite materials, are less investigated and the studies in that direction are now quite intensive.
Accordingly, there is a huge potential to find new properties in the field of multi-component high-entropy nanostructure materials.
The analyses show that the ball milling syntheses and adiabatic explosive compaction technologies are attractive methods for the synthesis of powdered and bulk high entropy nanocomposites [10].
In the study, mechanical alloying (MA), followed by adiabatic explosive consolidation was considered for sintering of bulk high entropy nanocomposites in Fe-W-Al-Ti-Ni–B-C system. For MA the high energetic Planetary mill was used. The time of the processing was: 15; 30h. 36h; 48h and 72h. The ratio of balls to blend was 10:1. The phase composition and particle sizes of the powders were controlled by X-ray diffraction system and SEM. Industrial explosives, Ammonite, Powergel and Hexogen were used for adiabatic shock wave compaction of ball milled powder compositions. The MA nano blend was charged in Steel 3 alloy-tube container and at the first stage the pre-densification of the mixtures was performed by static press installation (intensity of loading P=500-1000 kg/cm2). The experiments were performed at room temperature. The shock wave pressure (loading intensity) varied in range: 3-20Gpa. The set conditions the explosive were detonated by electrical detonator. High pressure developed by explosive and temperature initiate the syntheses and consolidate the ball milled high entropy nanopowder composition. The compacting process accompanied with the syntheses and resulting in situ obtaining the bulk high entropy alloys. The phase analyses and structure-property of bulks HEA compact samples were studied. The obtained results and discussions are presented in the paper.
ABO3-δ perovskite-type oxides are known for their compositional flexibility, possible formation of various orderings in the cationic and anionic sublattices, and a broad range of resulting physicochemical properties. Those properties can be tuned for a particular application, including usage in reversible Solid Oxide Cells (SOCs), as well as for the oxygen storage in pressure swing-type processes.
This work summarizes general guidelines for designing effectively-working perovskite-type oxygen electrodes in SOCs, as well as presents possibility of obtaining oxygen storage materials (OSMs) with the high capacity and low operation temperature. In particular, the A-site layered RE(Ba,Sr)Co2-yMnyO5+δ (RE: selected rare-earth cations; 0 ≤ y ≤ 2) oxides are discussed in more details, as it can be shown that the properly selected Mn substitution results in the high electrocatalytic activity toward the oxygen reduction reaction (ORR), while different Mn content is preferred for the oxygen storage processes [1, 2]. Less commonly studied substitution with Cu is also shown as the effective way of altering physicochemical characteristics, and allows designing electrocatalytically-active RE(Ba,Sr)Co2-yCuyO5+δ series [3]. Furthermore, Co-free La1-x(Ba,Sr)xCuO3-δcompositions can be also designed and obtained, showing promising performance when used as the SOC oxygen electrodes [4, 5]. Notably, the recently emerging high entropy approach provides unique new opportunities, as the resulting multicomponent perovskites may exhibit properties crossing the commonly observed rule of mixtures [6].
SESSION: AdvancedMaterialsTuePM4-R8 |
8th Intl Symposium on New & Advanced Materials and Technologies for Energy, Environment, Health and Sustainable Development |
Tue. 22 Oct. 2024 / Room: Ariadni B | |
Session Chairs: TBA Student Monitors: TBA |
When considering nanocrystalline structures, we are near the microscopic world.
What is the difference between the macro and micro world?
The difference is subtle. For atoms, the macrosocopic world holds, and atoms can be assumed as rigid spheres. In metals this is expressed by a nucleus surrounded by a cloud of electrons.
Inside the atom, the electrons spin the nucleus, in a perpetuum motion. By another hand, in the macroscopic world, perpetuum motion does not exist (due to friction, for example).
Here, different philosophical approaches of quantum mechanics are discussed, as the Bohmian mechanics, the Bohr interpretation (Kopenhagen) and also the Everett many-worlds hypothesis.
Instead of a “many worlds”, it seems clear that the correct interpretation would be the “many paths”, in agreement with Feynman view.
Experiments have in general confirmed the Bohr interpretation, thus rulling out the Bohmian mechanics
Also by using the Kopenhagen interpretation, the Heisenberg uncertainty principle can be reinterpreted, showing that time is not absolute.
Also, it will be discussed that as the electron has to be defined using 5 variables (3 dimensions, spin and time) [1], it will be argued that in the microscopic world there are extra dimensions, which we can not observe in the macroscopic world. (In the macro world, we see 4 dimensions: (x,y,z time))
The concept of Flatland, as exposed in Carl Sagan Cosmos [2] will be used to clarify the different philosophical interpretations of quantum mechanics.
The hysteresis curves of a material are capable of showing the relationship between the magnetization and the applied magnetic field. These curves are crucial to understanding the magnetic properties of ferrites, which are widely used in electronic applications, such as transformers and inductors. In this work, hysteresis curves of barium and strontium ferrites, in varying proportions, were adjusted using the Hyperbolic Tangent Model. This model demonstrated a good capacity for adjusting the observed hysteresis curves, which present a characteristic sigmoidal aspect. The parameters obtained from the adjustment allowed a better understanding of the physical and magnetic properties of the analyzed samples. The Hyperbolic Tangent Model proved to be effective not only due to the high correlation coefficient achieved, but also due to its ability to reflect the nuances of the magnetic properties under different conditions. The results obtained may have significant implications for the application of these ferrites in magnetic and electronic devices, since understanding their fundamental properties is crucial to optimizing the performance of these materials in different contexts. In short, the work highlights the importance of mathematical modeling as a tool for elucidating the magnetic characteristics of barium and strontium ferrites. The results suggest that the Hyperbolic Tangent Model is a promising approach for future investigations into magnetic materials consisting of ferrites.
SESSION: MagnesiumTuePM4-R8 |
4th Intl Symp. on Magnesium Alloys & Their Applications for Sustainable Development |
Tue. 22 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Xiaodong Peng; Student Monitors: TBA |
Mg-Li alloys are the lightest metallic engineering structural materials at present, and have great application potential in 3C and autonomous smart wearable, etc. However, the engineering application of ultralight Mg-Li alloys is seriously restricted because of their low strength, poor stability and high temperature performance. It is difficult to coordinate their strength, plasticity and high temperature performance. Ultralight Mg-Li-Al-Sn, Mg-Li-Al-Mn and Mg-Li-Al-Ca alloys with high strength and good ductility have been developed in our research group. The microstructure, mechanical properties of Mg-Li-Al-X alloys were investigated systematically combing the usage of many advanced microstructure characterization methods and normal tensile tests, etc. Element segregation and strain induced precipitation reaction phenomenon was found, which is beneficial to the improvement of strength and ductility, which is beneficial to obtain high strength and good plasticity simultaneously. The results from this research provide important technological support for the controlling of microstructure and mechanical properties of Mg-Li alloys.
The global energy and transportation industries are facing increasingly pressing sustainability challenges. Magnesium (Mg) and its alloys have advantages of being lightweight, high specific strength, good damping, high castability, and machinability, which make them very promising structural materials. However, many difficulties still need to be overcome to expand the further applications of magnesium alloys. The present report aims to review the critical advances of magnesium and its alloys worldwide in 2023 to boost the multifaceted scientific research of magnesium alloys and promote its global development and application. More than 4000 papers in the Mg and Mg alloys field were published in 2023. The bibliometric analyses indicate that the microstructure, mechanical properties, and corrosion of Mg alloys are still the main research focus. Bio-Mg materials, Mg ion batteries, and hydrogen storage Mg materials have attracted much attention. This report summarizes the progress in developing structural and functional Mg and Mg alloys and provide some suggestions for future research.
SESSION: IronTuePM1-R9 |
Leite International Symposium (10th Intl. Symp. on Advanced Sustainable Iron & Steel Making) |
Tue. 22 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Dimas Coura; Gabriela Araujo Gois; Student Monitors: TBA |
The development of the steel industry in Brazil is a story of continuous growth and modernization, driven by investments in technology, expansion of production capacity and the search for new markets. However, this sector faces significant challenges in both import and export, which impact its competitiveness and sustainability. In recent decades, the industry has undergone a process of modernization, with investments in more efficient and sustainable technologies, such as the use of electric furnaces and the adoption of circular economy practices. Brazil has become one of the largest steel producers in the world, with an installed capacity of over 50 million tons per year. In addition, the steel industry is a major employer, providing thousands of direct and indirect jobs, and contributing significantly to the country's industrial GDP. In the areas of import and export, competitiveness with China and the Australia is analyzed, as they impose trade barriers, as well as tariffs, aiming to protect their local industries. Steel prices are volatile due to the interference of factors such as global demand, material costs and trade policies. Furthermore, the steel industry is one of the largest contributors to CO2 emissions into the atmosphere, and the search for more sustainable production is leading the industry to invest in greener technologies. This article discusses how the advancement of the steel industry has impacted the environment, which other countries compete with Brazil and what measures have been adopted to protect the environment.
This study points out the characteristics of Ti-6Al-4V alloys, that contains additions of 6% Al and 4% V by weight, and it also aims about the advantages of the laser welding on these alloys compared to conventional methods of welding, because they usually cause problems such as oxidation of the faces joined by the weld, porosity and overheating of the joining metals. Occurs that Ti-6Al-4V alloys are widely used in aeronautical industry and in biomedical applications, due to its excellent properties, as well as mechanical strength, corrosion resistance, toughness and biocompatibility. But due to the high cost of these alloys, conventional welding cannot be done in order to avoid losses. The laser welding method, however, is appropriate due its accuracy, high penetration, high speed and easy handling. The main characteristics of this alloy that make it so special are: lightness, mechanical strength, biocompatibility, corrosion resistance, weldability and resistance to high temperatures. The addition of aluminum and vanadium significantly improves the strength of this alloy, remaining resistant even in corrosive or high-temperature environments. For this reason, they are widely chosen for use in biomedical and aerospace devices.
The present work aims to analyze the characteristics of macauba (Acrocomia aculeata), as well as its occurrence in Brazil and its energy properties that differentiate it from other biomasses due to its extreme importance for the generation of clean energy, from sources extracted from the environment and for sustainable development. The energy potential of macaúba biomass provides the strengthening of the Brazilian domestic market, since the oil extracted from this palm tree may have differentiated applications, including in industries. Compared to other biomasses, it is noted that macauba oil is produced in greater quantity and has high agricultural profitability. In the steel mill, the use of macaúba contributes to mitigate the emission of polluting gases resulting from the burning of fuels in blast-ovens, besides having several other advantages, as well as the low amount of ash generated.
The Ni-Ti alloy exhibits exceptional properties that enhance its compatibility with the human body, notably its low density, mechanical strength, corrosion and wear resistance, shape memory effect, and superelasticity. The shape memory effect involves a thermal hysteresis due to phase transitions from martensite to austenite when the alloy is cooled and then heated above its transformation threshold, enabling it to revert to its original shape. The superelasticity effect allows the material to return to its original shape after deformation of up to 10% under applied load. In this study, three samples containing 49.5% Ti and 50.5% Ni were produced using the powder metallurgy technique. The chemical composition of these samples was analyzed. The Ni and Ti metal powder mixture was sintered in a controlled atmosphere furnace at 1118°C in the presence of an inert atmosphere with analytical argon 2.0. Following analysis under an optical microscope and scanning electron microscope (SEM), Vickers microhardness, corrosion, and wear tests were conducted to evaluate the alloy's suitability for prosthetics and orthopedic implants.
SESSION: IronTuePM2-R9 |
Leite International Symposium (10th Intl. Symp. on Advanced Sustainable Iron & Steel Making) |
Tue. 22 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Davi Santos; Luiz Leite; Student Monitors: TBA |
According to the International Energy Agency (IEA) [1], the steel sector, among heavy industries, ranks first in CO2 emissions and second in energy consumption. Iron and steel are directly responsible for 2.6 gigatons of carbon dioxide (GT CO2) emissions annually, accounting for 7% of the total global energy system. The Sixth Assessment Report (AR6) of the IPCC (United Nations Intergovernmental Panel on Climate Change) of 2023 [2], containing a comprehensive study on the climate situation of the planet, has shown in a worrying way that the goals established on December 12, 2015, in the Paris Agreement, which aims to limit global warming to less than 2, preferably 1.5 degrees Celsius, are increasingly out of reach. Brazil is the largest steel producer in Latin America and the ninth largest in the world, according to the Instituto Aço Brasil [3]. Brazil's energy park has large renewable energy sources (hydroelectric, wind, solar and biomass plants), reaching 93.1% of electricity generation in 2023, E3G [4].In this way, with the decarbonization process of steel production, combined with the use of Biochar, green hydrogen, will make Brazil a major player in the production of green steel.This study aims to evaluate the ways and processes in which Brazil has been planning its decarbonization, thus contributing to achieving the goals of the Paris agreement.
Promoting the transition from the current linear production and consumption model to a green model has become a central issue in the debates on global warming and climate change [1] [2]. The way we design and produce our products directly affects the types and intensities of impacts generated on the environment and, consequently, on the planet [3]. However, with the aim of deliberately creating products with a shorter lifespan than they could have and making consumers purchase new products in short intervals of time, obsolescence has been used by industries as a tool to increase consumption. [ 4]. This problem is particularly noticeable in the smartphone production model. This article intends to carry out a qualitative and quantitative analysis of the current production and consumption model, proposing an analysis of the factors that influence the increase in smartphone consumption, highlighting both the motivating factors and the hindering factors, also intending to identify how such practices can violate several Brazilian laws [5]. To achieve this, research developed a questionnaire via Google Forms, applied to 186 people. The results show that external motivators (such as marketing incentives and social stimuli), internal motivators (self-actualization), external impediments (economic barriers) and internal impediments (barriers of mental awareness and perception of real need) were the four determining factors that influenced or prevented new consumption.
The steelmaking industry is of fundamental importance in the energy context of Brazil, being characterized as one of the major consumers of electricity in the country. To be competitive in the global market, the steelmaking industry needs to show an excellent strategic plan. This plan includes efficient energy planning, seeking to make better use of resources, low environmental impacts and operating costs [1]. The thermoelectric power plants of coke integrated steelmaking industry demonstrate great economic potential, since they make use of the waste gases from the process [2]. The aim of this work is to analyze, from the environomic viewpoint, the thermoelectric power plant, observing the influence of hydrogen addition. The generation of hydrogen is by water electrolysis, driven by photovoltaic power. The methodology comprises of using a computational model created with Scilab [3]. For model validation, the actual data from the thermal power plant is used. Thermoeconomic modeling aims to obtain a system of cost equations that mathematically represents the cost formation process in the plant [4]. The computer simulations use seven scenarios of possible fuel mixtures, using the BFG, LDG, COG, and H2. The results indicate that up to 30% of hydrogen with BFG is possible to obtain energy and exergy efficiency equivalent to scenario zero that most represents the operation of the thermoelectric plant and still reduce the fuel cost [5]. The importance of energy management in an organization is highlighted in terms of potential financial gains and cost reductions. Scenario 0 based the real operating model showed lower exergetic efficiency 23.87%.
SESSION: EnergyTuePM3-R9 |
9th Intl. Symp. on Sustainable Energy Production: Fossil; Renewables; Nuclear; Waste handling, processing, & storage for all energy production technologies; Energy conservation |
Tue. 22 Oct. 2024 / Room: Ariadni C | |
Session Chairs: TBA Student Monitors: TBA |
With the world's population increasing from eight billion currently to approximately nine billion by the year 2040, achieving a healthy lifestyle for all people on earth will depend, in part, on the availability of affordable energy, especially electricity. This presentation considers the various choices, or options, for producing electricity and the consequences associated with each option. The options are fossil, renewable, and nuclear. The consequences associated with these three options are addressed in five different areas: public health and safety, environmental effects, economics, sustainability, and politics. All options are needed, but some options are better than others when compared in the five areas. This presentation is a brief summary of a short course entitled “Energy Choices and Consequences”, which was initially created by the author several years ago and is continuously updated. The presentation will provide updated information through September of 2024.
In the ancient time, the resources were very limited. Thus ancient people learned to use ocean currents and wind in their travels. It was a sustainable process, which lasted many centuries.
There are several examples that may be usefull for the present time.
Wind can push the ships at a significant speed. For example:
Launched in 1869, the tea clipper Cutty Sark was very famous due to its velocity. The Cutty Sark could reach 17.5 knots [1], and it was considerable one of the fastest ships of the XIX Century, however it was made obsolete by steam engines.
When the Portuguese explored the South Atlantic ocean [2,3], they found that currents pushed them from Africa, and made them arriving in Brazil.
There are also indications that Portuguese also visited North-America, and the names “Newfoundland” is translation of the Portuguese “Terra Nova”, and “Labrador” comes directly from the Portuguese name “Lavrador” [4]. The Hamy-King worldmap shows the presence fo Portuguese in North-America near the year of 1500.
Wind and ocean currents were very relevant in Ancient world, as also earlier reported by Homer.
For example, the Odyssey of Homer may, in fact, indicate a travel to the Ballearic Isands, by means of South France ocean currents. For example, the island of Calypso “Ogygya” in fact can be interpreted as Ibiza.
The war for Troy is due to the fact that, there is a 5 knot current flowing from the Dardanellos to the Agean Sea. Only in summer this strong current could be overcome by wind [6], and only during few days. The Trojans used to ask tribute and mooring fees [6], making the Greeks discontent. In fact, almost every year there as a war in Troy (and in summer time).
These ancient voyages only were possible due to competent use of wind and ocean currents.
It is discussed how the competent knowledge of wind and ocean currents could be used nowadays for saving fuel in navigation.
Regenerative practice is a new concept for the energy, other industries and all businesses that have practiced a form of resource extraction in one way or another for over a century. We have an unprecedented opportunity to contribute to climate change solutions and help restore the planet to conditions conducive to supporting all life. Regeneration is a natural outcome of resource stewardship and one that needs to be integrated into how we do business
Just as we, in business, strive to be more efficient in our use of time, material and energy, we must also become better stewards of the conditions that enable humans and all living things to thrive on the planet. We're crucial in the creation of a prosperous future. Regenerative practice is the key.
Concepts like the circular economy, bioeconomics, embodied carbon and biomimicry are discussed and practical examples of integration into business operations are provided. The key takeaway for this talk is that we all have a role in a regenerative future.
Liquid fuel cells, which promise to be a clean and efficient energy production technology, have recently attracted worldwide attention, primarily because liquid fuels offer many unique physicochemical properties including high energy density and ease of transportation, storage as well as handling. However, conventional liquid fuel cells use precious metal catalysts but result in rather low performance. Recently, a novel system using an electrically rechargeable liquid fuel (e-fuel) for energy storage and power generation has been recently proposed and demonstrated. The e-fuel is stated to be attainable from diverse kinds of materials such as inorganic materials, organic materials, and suspensions of particles. In our research, we energize fuel cells with this e-fuel. It is demonstrated that without using any catalysts for fuel oxidation, this fuel cell running on the e-fuel leads to a significant performance boost.
SESSION: EnergyTuePM4-R9 |
9th Intl. Symp. on Sustainable Energy Production: Fossil; Renewables; Nuclear; Waste handling, processing, & storage for all energy production technologies; Energy conservation |
Tue. 22 Oct. 2024 / Room: Ariadni C | |
Session Chairs: TBA Student Monitors: TBA |
The core part of the thesis is focused on experimental studies of a single solid oxide cell (SOC) operating in electrolysis mode. It is preceded by theoretical description of most important issues related to electrochemical cells, electrolysis, methods of hydrogen production, power-to-gas systems and the basic principles of operation of solid oxide cells. Three chapters are devoted to theory. The first chapter is a general introduction into the topic. It highlights the importance of energy storage technologies in current, global electric energy economy indicating the related potential role of hydrogen technologies and reversible solid oxide cells. The introduction has been further extended by a brief description of historical background on the process of electrolysis. Chapters 2, 3 and 4 contain the theoretical description. Chapter two presents an overview of most important in industry technologies of hydrogen production. These include primary methods for hydrocarbons reforming (SR, CPOX, ATR) and hydrogen generation from biomass. Next to that, general process of electrolysis is described with brief description of three main techniques: alkaline electrolysis, proton exchange electrolysis (PEM) and solid oxide electrolysis (SOE). The broadest theoretical chapter is number 3. It is devoted to detailed view on thermodynamics of solid oxide cells, cell construction solutions and materials used. There are also presented basic performance characteristics of cells working in both electrolysis (SOE) and fuel cell (SOFC) modes together with the corresponding losses and efficiencies. Chapter 4 is focused on complete power-to-gas systems including solid oxide cells. It includes description of the design, performance and evaluation of two separate hydrogen electric energy storage systems based on reversible solid oxide cells. The first is theoretical, simulated HYSYS 8.8 software, based on dedicated mathematical model. The second, on the other hand is a real system installed and operation in USA. Finally, chapter 5 is the key part that describes the experimental part of the thesis. The aim of the experiment is clearly stated, then there are presented: design of the experiment, experimental stand, the start-up procedure and graphical representation of the obtained results. The results are extensively discussed. The last chapter includes the final conclusions that are mainly focused on evaluation of the experimental procedure and guidelines for its improvement.
Additive Manufacturing (AM) is a revolutionary technology that has transformed traditional manufacturing processes. This innovative approach has opened up new possibilities across various industries, ranging from aerospace and healthcare to automotive and consumer goods. As far as metals are concerned, along with fusion-based processes such as Selective Laser Melting (SLM) or Electron Beam Melting (EBM), solid-state, friction-based additive manufacturing processes have recently been developed and have caught the attention of several researchers[1]. In this paper two variants of solid-state friction-based additive processes are presented: (i) Friction Surfacing [2] (ii) processes based on friction stir welding, known as Friction Stir Additive Manufacturing (FSAM)[3]. In the paper an experimental campaign with varying the main process parameters is presented and the obtained samples are analyzed from both mechanical properties and resource consumption performance angles. Energy and resource flows are quantified and analyzed for each process; guidelines for the environmentally friendly process selection are provided.
This talk will explore control strategies for sector coupling, focusing on how distributed flexibilities—such as flexible loads, generation facilities, energy storage, and vehicle-to-grid (V2G) technologies—can be leveraged to ensure efficient and reliable grid operation while balancing supply and demand, minimizing the need for costly grid expansion and maximising the sustainability of future grid supply systems. We examine the control of energy management systems that introduce ancillary services, with a focus on three use cases: demand-side management for beverage industries, electric park houses and energy communities. These use cases demonstrate how flexibilities in decentralized production, generation, and storage can be implemented effectively.
The talk will specifically highlight model-predictive control algorithms enabling the physical entities—such as vehicles, machines, and enterprises—to autonomously participate in primary, secondary and tertiary energy markets (spot, intra-day, and day-ahead) without human assistance. For instance, we devise how incentive-based demand response (DR) programs can facilitate beverage production lines to contribute to the stability of smart grids by adapting their power and energy consumption in accordance with grid balancing requirements. In both cases, the algorithms trade off between the flexibility revenue and reduced production.
In a second use-case, we propose a novel control algorithm to use bidirectional charging in the framework of vehicle-to-grid (V2G) technology for optimal energy transaction and investment. The energy storage components of an electric charging station, including the buffers of energy, provide the opportunity to sell energy to or buy energy from a smart grid that not only improves the stability and power quality of the grid but also offers the possibility to the charging station owner and the EV drivers to benefit from the trades in the energy market financially. Here, the portfolio optimization from financial mathematics is adopted.
Finally, we introduce an innovative top-down approach that empowers system operators to optimize grid operations, reduce costs, and enhance overall grid stability. The discussion will address also the regulatory changes necessary to support this transition, offering insights into the future of a decentralized, flexible, and efficient grid system.
SESSION: BiocharTuePM1-R10 |
2nd International Symposium on Sustainable Biochar |
Tue. 22 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Harn Wei Kua; Aida Kiani; Student Monitors: TBA |
One of the challenges of promoting accelerated carbonation curing (ACC) of concrete as a carbon sequestration strategy is ensuring that carbonation will not deteriorate mechanical strength. This study examined the mechanical strength, water sorptivity and carbonation efficiency of ten types of mortar containing dry or pre-soaked biochar subjected to internal and/or external carbonation.
The results obtained enabled a typology of ACC to be proposed, in which the carbon dioxide absorption of mortar containing various types of CO2-dosed biochar ranged between 0.022% and 0.068% per unit dosage hour. In particular, the mortar containing dry biochar dosed with carbon dioxide was the top candidate for concurrently increasing both compressive strength (54.9 MPa) and carbon dioxide absorption (0.055% per unit dosage hour).
Mortar containing pre-soaked biochar dosed with carbon dioxide was identified as a strategy that achieved the highest carbonation efficiency (0.068% per unit dosage hour), but it also reduced compressive strength (45.1 MPa). Collectively, the proposed typology offers a useful overview of the different ways by which biochar can be used to tune ACC in mortar, according to any technical constraints and/or intended functions of the carbonated concrete components.
This study investigates the use of ball milling technology to enhance the adsorption capacity of biochar for methylene blue, a model pollutant. Comparative adsorption studies were conducted on ball-milled biochar and biochar modified chemically through oxidation and alkaline treatment. [1]
Biochar, derived from the pyrolysis of biomass wastes such as wood, crop residues, and municipal waste under limited oxygen conditions at various temperatures, is a low-cost, renewable, and environmentally friendly material. Biochar is increasingly recognized for its high carbon content, cation exchange capacity, large specific surface area, and stability, making it suitable for pollutant removal, for example in wastewater treatment, biochar offers economic and ecological advantages as an adsorbent for dyes, antibiotics, and phenols. [2]
Although chemical and physical modifications (acid/alkali modifications, steam, and plasma) are effective in enhancing the surface area of biochar and adding oxygen-containing functional groups for adsorption of specific pollutants, these methods are not environmentally sustainable because they have high production costs, harsh working conditions, and generate considerable waste. [3]
Alternatively, ball milling presents a green and efficient method to enhance biochar's surface area and adsorption activity. Mechanochemical approach can reduces the grain size of solids to nanoscale particles, transferring kinetic energy to the sample powder through the impact and shear forces of colliding milling balls as well as providing new ionic and covalent functionalizations for different carbon materials. [4-5].Recent studies have shown that ball milling can even increase the oxygen content of carbon materials through exfoliation and fragmentation, though it primarily exposes existing functional groups on biochar surfaces by increasing surface area.
This study compares the adsorption ability of methylene blue on biochar chemically modified by oxidation and alkalization against that of ball-milled biochar. Experiments demonstrated that milling significantly improves biochar’s adsorption capacity without the need for chemical modification and enhances performance by increasing the number of active sites available for adsorption. The reduction in particle size and consequent increase in surface area are hypothesized to be the primary reasons for the enhanced removal efficiency. Adsorption tests were conducted on biochar samples for methylene blue removal at various pH levels (3, 7, 11) and initial concentrations (50-250 mg/L). The mechanically milled biochar consistently exhibited superior performance, achieving an adsorption capacity of 185.18 mg/g and maintaining high efficiency over six reuse cycles.
In summary, the ball milling method significantly enhances biochar's adsorption capacity for methylene blue, without extra chemical modification steps and provides a green and sustainable approach to improving biochar's effectiveness as an adsorbent for water pollutant removal. This mechanically treated biochar shows promise for practical applications in environmental remediation, offering a cost-effective and environmentally friendly alternative to chemically modified biochar and commercial activated carbon.
A comparison is presented using two microwave pyrolyzed biochars produced from agricultural biomass (shredded hemp stalk) and woody biomass (maple wood chips) for the removal of Pb (II) from aqueous solution in a batch adsorption study. Biochars were produced by microwave pyrolysis of 1.5 kg of each biomass at an average temperature of 600 ˚C in a stainless steel 309 reactor and then magnetized by mixing aqueous Fe3+/Fe2+ solutions with aqueous biochar suspensions, followed by treatment with NaOH.
The magnetic biochars were characterized and the effects of pH, adsorbent dose, temperature, contact time and initial concentration of Pb (II) solution on their adsorption performance were investigated. The physico-chemical properties of the biochars significantly influence their adsorption capacities. For the cation and system under investigation, the adsorption capacity of magnetic hemp biochar was higher than that of magnetic maple biochar. The higher adsorption efficiency of hemp biochar was correlated to its higher polarity index, pH and zeta potential.
Egypt as an agricultural country produces 30-35 million tons of agricultural residues each year, with only 7 million tons used as animal feed and 4 million as organic manure. Normally, agricultural wastes are simply left in the field to decompose to maintain long-term soil fertility or burn. Although burning is convenient, quick, and cost-effective, and allows fast preparation of the field for the next rotation, it adds a lot of gases to GHG emissions resulting in severe impacts on air quality, biodiversity, and human health. The last issue presents obstacles to human development and threatens natural resources and the environment.
The term carbonization of wastes for biochar processing includes the technologies of pyrolysis, hydrothermal carbonization, flash carbonization, and gasification. Biochar has multifunctional values that include the use for the following purposes: soil amendment to improve soil health, nutrient, and microbial carrier, immobilizing agent for remediation of toxic metals and organic contaminants in soil and water, catalyst for industrial applications, porous material for mitigating greenhouse gas emissions and odorous compounds, and feed supplement to improve animal health and nutrient intake efficiency and, thus, productivity. Biochar contributes to EU circular economy objective significantly and reduces the linear economy of using agricultural and bio-wastes for landfilling and incineration.
However, good quality biochar often requires a complex production process with a robust and effective furnace to make biochar production at high prices. Farmers can’t produce biochar by themselves; thus, it is an obstacle for poor farmers.
The present research focused on the fact that farmers can deal with their large volumes of crop residues by converting it into biochar using simple designed reactor manufactured from low cost local materials (used barrels)and some agricultural resides for heating the feedstock (slow pyrolysis).
The study includes analyses for the different types of biochar produced using different agricultural wastes. Although a significant difference was observed in specific surface area, average pore diameter, pH, CEC, and EC, the study found that different types of biochar produced have suitable properties for soil amendment and carbon sequestration.
Conclusion:
This category of unit can be suitable for clean, healthy, distributed low-tech biochar production by developing country smallholders and micro-entrepreneurs; “backyard” producers utilizing yard waste; small and urban farmers; nurseries; communal gar
SESSION: BiocharTuePM2-R10 |
2nd International Symposium on Sustainable Biochar |
Tue. 22 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Harn Wei Kua; Muhammad Afzal; Student Monitors: TBA |
Big Box biochar kilns are an alternative to open pile burning that allow for in-woods biochar production in a simple metal box with no moving parts. This approach is based on technology used by charcoal makers for centuries, but with a modern, mechanized approach. A mini-excavator or other piece of machinery is used to operate the kilns.
The Utah Biomass Resources Group (UBRG) started developing Big Box biochar kilns in 2019 with a Utah Public Lands Initiative Grant. The UBRG has focused on in-woods biochar production and application since 2011. We have focused on simple kiln technology since 2017 with our Oregon kilns which are 1.4 cubic meters in volume. Big Box kilns are 10-20 cubic meters in volume, or about 14 times the volume of Oregon kilns. We partner with the Utah Bureau of Land Management to continually test and improve the kilns and the method of production. Since first being introduced in Utah, Big Box Biochar kilns are being adopted in ten US states, including one at Harvard University, Alberta, Saskatchewan, Ireland and Indonesia.
One of Big Box biochar kiln is capable of making upwards of 30 cubic meters of biochar in a day, they cost less than $10,000 USD to build, and have no moving parts. Multiple kilns can be run in the same location by a single machine; increasing productivity to more than 100 cubic meters of biochar per day. These kilns have produced biochar in all weather conditions, using a dozen types of woody feedstock, and from pieces as large as one meter in diameter and three meters long, without any feedstock preparation. The biochar we produce from these kilns is in the 85-87% organic carbon range, H:C ratios below .3, and has ash content below 20%. This presentation will outline Big Box biochar kiln best practices including the design, transportation, placement, loading, lighting, quenching, dumping, and safety procedures.
The oral presentation is based on an investigation carried out between 2017 (a) (b) and 2018 (a). This research was carried out in a plantation of A. mangium located in the village of Planas, department of Meta (Colombia). This research’s objective was to study the effects of biochar obtained through pyrolysis of pruned biomass of Acacia mangium on the chemical properties of soils and the volume of wood in a plantation of Acacia mangium Willd in the Colombian Orinoquía. The purpose was exploring alternatives to mitigate soil degradation has been gaining importance in recent years. Biochar promises to improve properties such as soil fertility and soil conditioning. This research involved an experiment with different levels of biochar in associating it with some chemical properties and the wood yield of A. mangium. To do this, we used a design including nine treatments and three repetitions of each treatment, employing two materials: biochar from Acacia mangium W. (BAM) and synthetic fertilizer (SF). We used a Bayesian principal component analysis to reduce dimensionality, and the two extracted dimensions were labeled by treatment to visualize their grouping. We validated the grouping using cluster analysis algorithms. Volume in wood was used as the response, and the same soil variables were used to run a regression by partial least squares where the explanatory variables were characterized by relative importance. In terms of results, We found an increase in the different chemical variables of the soil analyzed in treatments with BAM and BAM + SF and an increase in the volume of the stem of the trees in treatments with BAM + SF. The analysis by partial least squares showed how the EC and SOC variables were the most important in explaining the volume of wood. With regard to the conclusions, the responses of the different variables analyzed increased with the addition of biochar, either alone or mixed with synthetic fertilizer. It was also possible to determine that the volume of A. mangium wood was influenced by soil chemical variables. These mixtures, especially those composed of the higher levels, can cause an increase in the response of the set of variables considered. Higher values found in the different variables of chemical properties may be associated with an increase in stem volume and dry weight in A. mangium trees established in plantations in the region.
This study was conducted to evaluate the efficacy of biomass and biomass-derived biochar from three different plant source such as Prosopis juliflora, Cocos nucifera (coconut fronds), Acacia moniliformis, and sugarcane bagasse. The calorific value, carbon content, sulfur content, and ash content were analyzed for all the biomass and synthesized biochar specimens. Physicochemical properties of the resulting biochar variants were thoroughly examined and the most suitable biochar was further characterized through high through put techniques FTIR, XRD, and SEM analyses. The findings indicated that biochar produced from Acacia moniliformis displayed superior characteristics in comparison to the other types of biomass investigated. These outcomes indicate the promise of Acacia moniliformis biochar as a viable sustainable energy source and emphasize its relevance in multiple aspects of sustainable energy production and environmental management.
SESSION: ConstructionTuePM3-R10 |
9th International Symposium on Sustainable Construction Materials |
Tue. 22 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Harn Wei Kua; Jing Huang; Student Monitors: TBA |
This talk is a sharing of a chapter in the recent book entitled “Biochar for Environmental Management - Science, Technology and Implementation” [1]. Focusing on the application of biochar in buildings and roads, it is more than just a review of the state-of-the-art in this aspect of biochar but aims to develop the fundamental principles and frameworks to understanding why and how biochar has the observed effect on concrete and asphalt.
This talk is divided into two segments. In the first, the overall principles on how biochar results in positive effects on concrete or asphalt is illustrated - in essence, this can be attributed to biochar's influence on the hygro-mechanical properties of these construction materials by modifying their microstructure as a result of changing the moisture distribution in them.
In the second segment, attention will be focused on the applications of biochar in concrete and asphalt. Specifically, the ways in which the filler effect, particle size, particle shape, macro- and micro-porosity, permeability, and the “reservoir effect” afforded by biochar modifies the moisture distribution in the concrete and asphalt media will be discussed. With this understanding as a background, a number of case studies on biochar concrete and asphalt research around the world will be shared.
Finally, a few key areas of future development will be discussed - including the use of biochar to augment carbon mineralization in curing green concrete, such as limestone calcined clay concrete.
Limestone calcined clay cement (LC3) is a sustainable binder that has been increasingly studied as an alternative to Ordinary Portland Cement (OPC). However, one of the technical barriers to large scale application of LC3 is its low workability. Although the creation and application of tailored superplasticizers (SPs) has become one of the most common solutions to this problem, the over-reliance on such chemicals will give rise to other problems, including high embodied energy in these SPs.
This study aims to offer a more sustainable solution by valorizing abundant waste wood, in the form of biochar, to replace 2wt% and 10wt% of OPC content in LC3; this is done to increase the overall sustainability of the LC3, while increasing compressive strength, shortening setting times and improving workability. To ensure that our results are relevant to actual construction conditions, all samples were subjected to air-curing.
It was found that all LC3 that contained biochar were significantly stronger than OPC control at 28 days. In particular, incorporating 2wt% biochar (dry or pre-soaked) could maintain compressive strength of the LC3 but yield significant better workability than OPC mortar.
A model was proposed to explain this phenomenon - specifically about how biochar modifies the water distribution by reducing the amount of gel pore water and at the same time, increasing the amount of free or bleeding water available when the LC3 samples were mechanically agitated; this enhances the movement of particles over one another during mixing or vibration, thus lowering the viscosity and improving the workability.
In summary, these results can potentially point the way to improving the sustainability of LC3 while reducing wood waste, using biochar as a pathway to waste valorization in the creation of high-performance concrete.
This study introduces the concept of Bio-LC3 in which biomass waste is upcycled into sustainable ingredients in limestone calcined clay cement (LC3) by partially replacing cement. Specifically, rice husk ash, rice husk biochar, sawdust biochar and titanium dioxide (TiO2)-coated sawdust were chosen as the partial replacement for Ordinary Portland Cement (OPC).
The novelty of this study lies in, firstly, a high replacement rate of 5-15 wt% was applied to replace OPC with the abovementioned biomass waste. Secondly, Accelerated Carbon Curing was applied to these different types of LC3 so that we could evaluate the effects of the different waste on carbon mineralization, strength, water absorption and thermal stability of LC3.
It was found that it is possible to replace 15 wt% of cement with rice husk ash or 5 wt% of cement with TiO2-coated sawdust and achieve similar compressive strength to that of carbonated LC3 control, which was in turn significantly stronger than LC3 control without carbonation. Carbonating LC3 with TiO2-coated sawdust enhanced the reaction between mineralized carbonates (calcite) and metakaolin. In contrast, carbonation of sawdust biochar reduced calcite-metakaolin and metakaolin-Portlandite (CH) reactions, thus lowering its 28-day strength. Presence of rice husk biochar enhanced capture of carbon, as well as the overall bulk thermal stability.
All in all, these results showed that it is possible to further increase the sustainability of LC3 by valorizing different types of bio-waste and develop special functions that enhance the overall usefulness of these sustainable materials.
Vanadium-bearing shale tailing is a type of solid waste with high silicon content. Due to high storage capacity, high production capacity, and low utilization rate, Vanadium-bearing shale tailing needs to be thoroughly studied to achieve resource utilization. [1] Alkali activated two-part geopolymer is a new type of inorganic polymer material made from aluminosilicate minerals. Due to environmental-friendly, excellent mechanical properties, and advantages in immobilizing heavy metals, geopolymer is the most promising inorganic polymer material to replace traditional Portland cement. [2] However, two-part geopolymer synthetic raw materials include two parts: alkali activator solution and active aluminosilicate powder. [3] The potential safety risks and operational difficulties of high concentration and high alkalinity alkaline corrosive activator solutions may limit the application of geopolymer. Therefore, researchers propose using solid alkali activators to prepare one-part geopolymer. [4] The chemical composition of Vanadium-bearing shale tailing indicates that it is suitable for synthesizing silicate based solid alkali activator.
There has been extensive research on the preparation of alkali activators from industrial solid waste, and the preparation methods can be mainly divided into three categories: fusion, hydrothermal, and thermochemical. [5] This study used thermochemical method to treat Vanadium-bearing shale tailing to prepare solid alkali activator. Then, the solid alkaline activator activates the metakaolin to synthesize one-part geopolymer.
XRD, Raman, and pH tests were used to analyze the significant effects of reaction temperature and sodium hydroxide dosage on the phase composition and activation effect of solid alkali activators. When the thermochemical activation temperature are 1073.15 K ~ 1273.15 K, the ratio of sodium hydroxide to Vanadium-bearing shale tailing are 90% ~ 100%, and the ratio of solid alkali activator to metakaolin are 66.7% ~ 100%, the compressive strength of one-part geopolymer is above 40 MPa. The main silicate phases of solid alkali activators are sodium silicate. XRD, SEM-EDS, Raman and NMR analyses indicate that sodium silicate mainly plays a role in alkali activation, and sodium silicate can be used as one-part geopolymer silicate raw material.
The one-part geopolymer synthesized by alkali activator from Vanadium-bearing shale tailing has excellent compressive performance. Solid alkali activator can replace commercial sodium silicate as a cost-effective and environmental-friendly to prepare one-part geopolymer.
SESSION: ConstructionTuePM4-R10 |
9th International Symposium on Sustainable Construction Materials |
Tue. 22 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Harn Wei Kua; Ahsen Maqsoom, Prof.; Student Monitors: TBA |
In response to the accelerated pace of urbanization and the steady rise in global population, a palpable consequence has manifested - a striking surge in CO2 emissions, emerging as the foremost catalyst behind climate change. Concrete, as one of the most widely used materials in the world aside from water, forms the foundational framework of modern society. However, the production of concrete contributes to 8% of anthropogenic carbon emissions. Despite efforts to reduce these emissions through passive strategies like decreasing clinker content, using local resources, and efficient design, the reduction levels have been limited. Consequently, CO2 emissions from the construction sector have peaked post-pandemic. This talk presents an active carbon reduction strategy for sustainable construction to tackle this challenge. This innovative approach transforms concrete into a carbon sink by utilizing CO2 at different stages of the concrete's lifecycle. Initially, CO2 acts as an activator or rheology modifier, improving the fresh properties of concrete. In the middle stages, CO2 serves as a curing agent, enhancing strength and durability through carbonation curing technology. In the later stages, CO2 functions as a surface enhancer, densifying the concrete's outer surface. This strategy also incorporates major urban solid wastes, such as incineration bottom ash, waste glass, and waste concrete, as precursors in the concrete production process.
Worker’s safety hazards results in substantial number of accidents including injuries and fatalities at the construction projects. This case study aims to apply Building Information Modeling (BIM) principles to optimize workers' safety during the design phase of a high-rise residential building. The study objective is to develop a BIM model and analyze it against construction safety hazards in order to identify risks, fire weak spots, remove structural clashes and optimize the constructability. The research methodology involved preparing a BIM model using AUTODESK Revit and analyzing it with Solibri Model Checker and IFC based fire safety analysis using Revit. The findings revealed that BIM process optimization significantly reduced accidents due to fall hazards, electrocution, caught-in or between objects, fire hazards, slips, trips, and falls. The BIM process was advantageous in terms of safety compared to traditional construction methods and could help stakeholders address safety issues, clashes, project cost, and scheduling concerns.
Soft soils provide the difficult ground conditions for construction and are characterized by low unconfined compressive strengths (<50 kPa) [1]. This study evaluated the performance of pyrolytic biochar (PBC) derived from industrial wastewater sludge in soft soils to enhance their unconfined compressive strength. Also, investigating the mechanism behind strength development was focused on. Different amounts of PBC (0%, 5%, 7.5%, 10%, and 12.5% by weight) were mixed with the soft soil, and the unconfined compressive strength (UCS) values were measured after curing periods of 1, 7, 14, and 28 days. The UCS values increased by approximately 4-5 times, while the stiffness values increased by around 5-6 times. Adding PBC also increased the alkalinity and water-holding capacity of the soil-PBC matrices, promoting pozzolanic reactions [2]. The free calcium oxide (CaO) in PBC disrupted the laminated soil structure and reacted with silica oxides (SiO2) and other aluminum silicates, resulting in a denser soil-PBC structure and the formation of Tobermorite, a hydrate mineral of calcium silicate [3]. Overall, the study concluded that PBC has the potential to be an effective alternative to traditional soil stabilizing materials, as it improves the unconfined compressive strength of soft soils.
SESSION: MedicineWedPM1-R1 |
3rd Intl. Symp. on Technological Innovations in Medicine for Sustainable Development |
Wed. 23 Oct. 2024 / Room: Marika A | |
Session Chairs: Francis V Fernandes; Krasimir Vasilev; Student Monitors: TBA |
Exposure to mutant and neglected disease resistant pathogen strains is high and presents a significant threat to public health, peace and economic mobility. The microbe outruns the R&D time-line for a new generation of drug. The microbe has changed its genome to outwit the therapy. Biological warfare poses a significant threat to a human population, operations of security personnel and emergency response specialists. Antibiotics and vaccine resistance renders the efficacy and potency of the current crop of antibiotics and treatments useless and expensive.
Such challenges need to be significantly remedied with new solutions. A moving target pathogen can be eliminated via electrodynamic treatment of an infection in a human being. A move to do away with antibiotics is in sight. Electrodynamics can eliminate the microbe independent of its mutant strategies. The electrodynamic option for fast remedy is based on deeper insights on the definitions of terms thought of as understood in Physics. This paper will define the paradigm shift in understanding of everyday terms such as temperature, Ohm’s Law, electric charge, mass, frequency and wavelength.
The electrodynamic therapy to rid pathogens is a direct result of interdisciplinary research work in physics, chemistry, pharmacy and medicine. The rationale of this original research is in the realm of empirical biophysics.
The goals are specific, and the foundation work has been completed.
The results of this work will have worldwide impact since the diseases treated by this new regimen will help millions by destroying pathogens often identified at autopsy.
Inflammatory state and immunity are the two patient conditions that need to be addressed when infectious disease hits a population or when co-infection exists in chronic disease conditions. The Magellan Therapeutic Inc. platform addresses these two patient conditions. The method employs replenishing diminished levels of a key component of the lectin pathway by cell and gene therapy. The lectin pathway is responsible for immunity as well as inflammation. Every person on Earth has probably taken a small molecule or an injection of a steroid for inflammation or antibiotics to treat infection. The waste generated from the entire cycle from disposable plastics, gowns, masks, to biowaste from liquid biopsy, patient sputum, fecal and urine is a neglected aspect of disease burden. Moreover, the cost of generating potable water from contaminants ranging from drug excretion in sewage to disturbance in soil and water pH to drug resistant pathogen mutants is largely overlooked. A discussion on nipping these issues in the bud from bench to patient is presented. The dots are connected via simple diagrams for a snapshot of the bigger picture. Solutions to the crisis are provided for debate and implementation irrespective of political viewpoints. The goal post does not move. An alternative model in new trade free parks is proposed with sustained nondilutive funding. The goal is human flourishing.
In this keynote talk, I will give an overview of recent progress from my lab on development of nanoengineered surfaces and materials that benefit many areas of application. Over the years, we developed a range plasma based methods, know-how and expertise which allow us to control that entire spectrum of materials surface properties, including chemical, physical, mechanical and topographical. The main focus of our research is on the surface modification of medical devices and biomaterials with the purpose to improve healthcare outcomes in areas such as prevention of infection, modulation of inflammation, cell therapies, tissue engineering, and medical diagnostics. I will discuss our newest discoveries and technologies, some of which have been translated onto commercial devices in collaboration with industry. However, our surface modification technologies are not limited to healthcare and medicine. We have demonstrated the utility of nanoengineered plasma polymers for solving problems in other areas such as environmental science and remediation, heath sustainability, water treatment and even wine making. In will present the engineering and chemical concepts underpinning “nanoengineering of plasma polymers” and give a range of examples of application of our technologies in various fields.
In medical practice, a high optical resolution of medical devices used to visualize cancerous tumors [1] and cells [2] and in photodynamic therapy [3,4] is an extremely important factor. High resolution is determined by the small width of the corresponding optical bands, which, in turn, is determined by the rational use of physical phenomena on which the creation of medical devices is based. The ideal physical phenomena here would be any optical resonances that have a small width and high intensity. Such a resonance is the Egorov nano-resonance [5‒8]. Egorov’s nano-resonance is one of the important consequences of the new physical theory — quantum ‒classical mechanics [5,6,9,10]. As is known, in standard quantum mechanics, a certain statistical characteristic of a microparticle (wave function) obeys a certain dynamic equation (Schrӧdinger’s equation). This statistical characteristic is an innate property of an individual microparticle. In quantum‒classical mechanics, in addition to this innate statistical characteristic of an individual microparticle, innate chaos appears in the interaction of microparticles. This chaos is called dozy chaos. In quantum mechanics, molecular (electron‒phonon) transitions are singular, and they are damped by dozy chaos in quantum‒classical mechanics [10]. Dozy chaos is present only in the transient state of electron‒phonon transitions, and it can be neglected in the initial and final adiabatic states of the transitions. Egorov’s nano-resonance is a resonance in nano-scale molecular systems between the extended motion of an electron and the motion of reorganization of the environmental nuclei in the process of electron‒phonon transitions under conditions of weak dozy chaos [8]. Based on Egorov’s nano-resonance, the resonant nature of the change in the shape of optical absorption bands in the series of polymethine dyes, in which the length of the polymethine chain changes, as well as the narrow and intense J-band of well-known J-aggregates are explained [5‒9,11]. In the framework of quantum–classical mechanics, on the basis of Egorov nano-resonance and the law of conservation of energy, an explanation is given for the strong detuning of the resonance and the associated significant parasitic transformation of the shape of the resonant optical absorption band as a result of the transition from linear to nonlinear, two-photon absorption in polymethine dyes in solutions (in selenopyrylium-terminated polymethine dye Se-3C dissolved in chloroform) [12‒14]. Based on this explanation and model band shapes of the theoretical fit to the experimental optical bands [12], the conditions for reconstructing the resonance shape of the band for two-photon absorption and its redshift are predicted [14]. The creation of quantum–classical mechanics of nonlinear optical processes in polymethine dyes will further serve as a theoretical basis for the study of nonlinear optical processes also in more complex organic systems, which are promising for applications in three-dimensional (3D) fluorescence imaging, lasing up-conversion, optical power limitation, photodynamic therapy, 3D optical data storage and so on (see [14] and refs 57‒60 therein).
SESSION: MedicineWedPM2-R1 |
3rd Intl. Symp. on Technological Innovations in Medicine for Sustainable Development |
Wed. 23 Oct. 2024 / Room: Marika A | |
Session Chairs: Vladimir Valentinovich Egorov; Student Monitors: TBA |
The new fundamental physical theory, quantum–classical mechanics (QCM), takes into account the chaotic dynamics of the transient state (TS) in electron-phonon transitions [1–3]. In the case of strong transient (dozy) chaos QCM gives the same result as the standard Franck–Condon picture of electronic-vibrational transitions [4]. Dozy chaos (DC) provides the convergence of a series of time-dependent perturbation theory which is absent in the standard quantum picture [2]. In the case of weak DC, an important result of QCM is the Egorov nano-resonance (Enr), which is associated with the appearance of a pronounced regular dynamics against the background of DC and which explains the nature of the narrow and intense optical J-band of the well-known J-aggregates [5]. The discovery of QCM and Enr opens up the possibility of creating optical spectroscopy of extended molecular systems, in which, along with DC, the effects of regular dynamics in TS are significant. DC in TS is provoked by a light electron “in order” to ensure the reorganization of a very heavy nuclear subsystem, and hence the very possibility of electronic-vibrational transitions. This organizing property of the electron undoubtedly plays an enormous role in biological processes. The next stage in the development of QCM can be to complicate the system by organizing various aggregates, where the “elementary cell” in the theory and/or the starting point for the development of the theory will be the already solved problem of elementary electron transfers in QCM [6]. The purpose of such complication and enumeration of all possible variants of aggregation will be to find the “molecule of life”, that is, the rather complex, but “minimal” structural configurations, in which elements of self-organization, both structural and dynamic, observed in theoretical optical spectra, are clearly manifested. The “atom of life” here is the electron itself which provokes DC. Thus, through the increasing complexity of the design of molecular systems, QCM opens up great prospects for the search and study of the simplest forms of life organization and related phenomena. For example, a new kind of possible materials, “living materials”, can provide us with much more comfortable living conditions [6]. Advanced artificial living beings (ALBs), created based on targeted molecular systems design and engineering, and, for example, radiation-resistant, will be able to greatly help humanity in future space exploration [6]. On planet Earth, diverse communities of ALBs will represent a virtually unlimited source of skilled labor in all areas of human activity and entirely under human control. Among other things, ALBs will give impetus to the creation of the most effective form of socio–economic and moral organization of human civilization (see [6] and references therein), which is unattainable under the currently existing egoistic paradigm of human society [7], which arose as a result of a long evolutionary process.
SESSION: PhysicalWedPM1-R2 |
Lipkowski International Symposium (4th Intl. Symp. on Physical Chemistry & Its Applications for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Marika B1 | |
Session Chairs: TBA Student Monitors: TBA |
Metallic glasses (MGs) have attracted significant interest in materials science and engineering field due to their excellent mechanical properties such as high strength, elastic modulus and hardness due to their random atomic configuration. After 1990s, numerous MGs with high glass-forming ability have been developed, which enable us to them with a bulky shape and to be applied as many kinds of mechanical parts. However, a brittle nature in bulk metallic glass (BMG) has been recognized, which appears obviously by structural relaxation through low temperature annealing and/or mechanical processing. The authors have been studying a novel method of relaxation controlling, that is, a recovery of a less relaxed state (so-called as rejuvenation), using a conventional annealing treatment [1-3]. Recently, we have succeeded to control the relaxation state preciously through a rejuvenation process, which leads to improve mechanical ductility [4,5]. In this presentation, the recent results on controlling a relaxation state and an excellent ductility in Zr-based BMGs will be reported. Our results provide insights for the effect of relaxation state and bring a novel evolution in BMG and a beneficial progress for their application.
Equilibrium constants are essential for understanding and predicting the behavior of chemical systems across various scientific disciplines [1]. Traditionally, these constants are computed via nonlinear regression of reaction isotherms, which show the dependence of the unreacted fraction of one reactant on the total concentration of another reactant [2]. However, while these equilibrium constants can be precise (with small random errors), they may also be grossly inaccurate (with large systematic errors), leading to potential misinterpretations and loss of R&D effectiveness in various areas including development of drugs and diagnostics [3, 4]. Although some statistical methods exist for assessing the accuracy of nonlinear regression [5, 6], their limited practicality for molecular scientists has resulted in their neglect by this research community. The objective of this work is to develop a practical method for quantitatively assessing the accuracy of equilibrium constants, which could be easily understood and immediately adopted by researchers routinely determining these constants. Our approach integrates error-propagation and regression-stability analyses to establish the accuracy confidence interval (ACI) — a range within which the true value of the computed parameter lies with a defined probability. In a proof-of-principle study, we applied this approach to develop a workflow for determining the ACI of the equilibrium dissociation constant of affinity complexes from a single binding isotherm. We clearly explained how the input parameters for this workflow can be determined, and finally, we have implemented this workflow in a user-friendly web application (https://aci.sci.yorku.ca) to facilitate its immediate adoption by molecular scientists, regardless of their mathematical and computer proficiency. We further conducted three case studies exemplifying the use of the ACI in the context of simultaneous assessment of precision and accuracy of determined Kd values. By understanding the ACI of equilibrium constants and other parameters computed through nonlinear regression, researchers can avoid misconceptions that arise from relying solely on precision.
The inclusion of small guest molecules into porous crystalline materials promises several exciting innovations in a wide range of areas, including separation and storage of gases or vapors, chemical sensing, and catalysis. Using now well-established principles of crystal engineering we can aspire to design porous materials with tailored structural and physical properties. However, there is still much need to develop new approaches to understanding the sometimes-complicated relationships between molecular-level structure and physico-chemical properties. In this regard, devising a range of complementary experiments to characI{Sterize materials under controlled environments such as gas pressure can be particularly challenging. This presentation will describe the development and application of a suite of new approaches to structural analysis by means of in situ X-ray diffraction,1 complemented by physico-chemical characterization using a combination of gas sorption analysis and a unique system for pressure-gradient differential scanning calorimetry.2,3 A number of examples from the recent literature will be presented.
The current period is the era of Nanoscience (Nanomaterial and Nanotechnology), where revolutions in practically all subjects of Science and Technologies relax life that reflects an extensive investigation area which encompasses Nanodevices, their unique structures, and systems with innovative possessions and novel roles linked to the prearrangement of their atoms or molecules on the 1–100 nm scale. To understand the function and activity of NPs, it is essential to expose how NPs work in almost all fields of Science and Technology, such as engineering, materials and pharmaceutical sciences, physics, chemistry, biology, and computer science. The activity or action of NPs at the microsize level, including atoms, molecules, tubes or fiber based to inhabit the electronic system, move around in orbit; this orbit may be considered a surface for the electron where the electron interacts as energy to the surrounding molecules and determine the effectiveness of the Nanoparticle. The activity of NPs may be linked with the dual nature of the particle, where size (matter) and energy are adequate. The high activity of the small size of the NPs is based on energy, which in turn is related to the surface electron as NP showed an increased surface-to-volume ratio that must be intact with outer orbit. This report demonstrates the actions of NPs in the advancement of key ethics of Nanoscience and technology in the contemporary timeline period of findings and indicators related to every field of Science.
SESSION: PhysicalWedPM2-R2 |
Lipkowski International Symposium (4th Intl. Symp. on Physical Chemistry & Its Applications for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Marika B1 | |
Session Chairs: Janusz Lipkowski; Sergey Krylov; Student Monitors: TBA |
The present article discloses a new advanced oxidation process (AOP) to control organic dye pollutants in running wastewater by H2O2/MnO4-1 [1]. The AOP is claimed as a Magneton reaction because of the presence of three oxidizing species, namely, permanganate, nascent oxygen and Urea - H2O2 complex. The new AOP (Magneton reaction) was found to be more effective and eco-friendly, with less beneficial sludge and filtrate. The experiment was conducted in a room with all dye additives, including urea, used in textile dye fabrication. H2O2 employed for the conversion of urea (the main additive of dye fixing) into eco-friendly Urea - H2O2 complex proves to be the best urea hazardous controller in dye wastewater with the degradation of dye; as the lowest chemical oxygen demand (COD) was recorded with no sludge. Oxidation kinetics is monitored at several parameters, keeping all constant and one varied. The most significant advantage of this advanced oxidation process (AOP) is its optimal performance when potassium permanganate (KMnO4) is added at various pH levels in the last enduring H2O2 in this innovation with urea, and KMnO4 (5e-) can synergistically act better with the traditional Fenton process to accomplish the resourceful speedy and septicity free degradation method. This synergistic action achieves rapid and sterile degradation, effectively reducing both the biological oxygen demand (BOD) and chemical oxygen demand (COD) of dye wastewater. Additionally, filtrate and sludge produced were found to be eco-friendly, and neutral pH supports the regular growth of plants and fish.
SESSION: GlassWedPM1-R3 |
Oktik International Symposium (2nd Intl. Symp. on Sustainable Glass and Polymers Processing and Applications) |
Wed. 23 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Sener Oktik; Aman Ullah; Student Monitors: TBA |
Indian glass and glasswork stand apart from the world of glass; Indian glass beads have been one of the greatest maritime trade items of all time. Raw materials used for glass production are unique in nature, furnace engineering has evolved from within, and the knowledge system involved for glass by-products has always been ahead of the time and a technological leap. For example, craftsmen use a natural sodic element, ‘reh’ to produce glass without any flux; the last tank furnace is still operational; they invented, innovated and have been passing air through a 3 mm diameter and 10 m long glass since 2500 BP. However, in the recent past, the indigenous glass by-product in the south has fallen, the west has been marginalised to symbolism, and the north is at the brink of extinction.
The presentation will discuss the production cycle, transformation, spread and evolutionary cycles of traditional Indian glass and glass by-products, the reasons for its disintegration, the challenges it faces and put forth a model for its sustainability.
The technology of AM has been developing for more than 30 years, and its utilization in our era covers even house construction at the final, high-quality level. In summary, in recent years, 3D printing devices have become cheaper, more reliable, and easier to use, leading to their rapid application development in various application fields. Nowadays, additive manufacturing (AM) technology is verified in many production processes as a rapid prototyping tool, except for the production of glass 3D structures, in which processing remains a challenge.
The project aims to develop a new sustainable method for repurposing pharmaceutical glass into borosilicate glass and creating innovative transparent and porous 3D glass structures. In the first stage, the glass precursor obtained from pharmaceutical glass waste through a milling process, with particle sizes below 80 μm, was used in an oxygen-methane (O2/CH4) torch (flame synthesis process) to produce solid glass microspheres (SGMs). The spherical shape of the microspheres allowed the creation of a high solid content suspension, with the SGMs making up to 70 wt% of the suspension in a photocurable resin. The second step was the fabrication of various 3D structures by a stereolithography (SLA) 3D printer (Original Prusa SL-1, Prusa Research a.s., Prague, Czech Republic) operating in the visible light range (405 nm). After burning out the organic binder and sintering treatment at a temperature range of 750-1200°C with different heating and holding regimes, various scaffolds (porous and/or transparent) were achieved.
In recent years, there has been a notable shift towards exploring renewable biomass as a viable alternative to traditional petrochemical products, driven by escalating energy demands and environmental concerns. The utilization of waste resources especially lipids has emerged as a pivotal strategy in advancing sustainable development, owing to their abundant availability, inherent functionality, potential for biodegradability, and capacity for CO2 reduction. Moreover, these resources offer a diverse array of monomers, rendering lipids and waste biomass particularly promising for the development of renewable biomaterials. This presentation will delve into the solvent-free conversion of lipids sourced from waste streams like waste cooking oil and lipids extracted from spent foul. Our focus lies in transforming these lipids into monomers and synthesizing biopolymers, with a special emphasis on polymers endowed with self-healing and reprocessing capabilities. This task poses significant challenges, particularly in maintaining mechanical and thermal properties during reprocessing, especially when utilizing biomass-derived monomers. Remarkably, our research demonstrates that the healed and reprocessed biopolymers exhibit mechanical properties and thermal stabilities comparable to the original material after undergoing self-healing and reprocessing. Furthermore, these developed polymers boast excellent thermal stability, rendering them suitable for a myriad of applications. The ability to achieve complete lipid conversion into monomers and diverse biopolymers under solvent-free conditions presents an alluring proposition, both academically and industrially.
SESSION: GlassWedPM2-R3 |
Oktik International Symposium (2nd Intl. Symp. on Sustainable Glass and Polymers Processing and Applications) |
Wed. 23 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Peter Simurka; Peter Lichvár; Student Monitors: TBA |
The prediction of defect harmfullness in continuum mechanics requires the solution of partial differential equations with specified boundary conditions. In this work, fast reduced-order models are developed to understand defect harmfulness in recycled polymers undergoing a stretch blow moulding process. Polymers underconsideration are PET. Such a process is used in bottle-to-bottle recycling [1]. The space of all possible defects is defined using a non-parametric, data-driven approach that takes into account defects seen using an infrared camera. This space is very high dimensional.
The aim of this work is to develop a non-linear dimensionality reduction approach as proposed in [2] and [3], by using a scientific machine learning. Numerical results show that the proposed reduced order models have a large validity domain in the parameter space related to the mechanical behaviour of recycled polymers. They also show computational speed-ups of around 50 compared to conventional finite element predictions. Accelerated defect damage predictionscan be used to predict potential process quality degradation.
Due to their neoteric nature, deep eutectic solvents (DES) and their mixtures surpass conventional organic and ionic liquids as solvents. DES are considered environmentally friendly alternatives to traditional organic solvents due to their low toxicity, biodegradability, and abundant natural components. They exhibit unique properties such as low volatility, high thermal stability, and tunable polarity, making them versatile in various applications, including green chemistry, extraction processes, catalysis, and electrochemistry. DES have garnered significant attention in recent years as sustainable alternatives to conventional solvents in various industrial processes [1].
Computational and experimental techniques are complementary for determining the structure, design and thermo-physical properties of liquids and their mixtures. Various researchers [2, 3] employed Density Functional Theory (DFT), Molecular Dynamics (MD), COSMO-R and Flory’s Statistical theory (FST) to estimate these properties. Though these theoretical formulations are found suitable to compute the thermo-physical properties, FST is a valuable and powerful tool because of the limited input parameters and ease of calculations. FST is a good candidate in the theoretical framework of industrial design to predict the thermodynamic properties [4].
In the present investigation, several important thermophysical properties, such as density, isothermal compressibility, and internal pressure, are predicted using Flory’s Statistical Theory (FST) for four three-component DES mixtures, at different concentrations and temperatures. The mixtures chosen for investigation are (i) choline chloride/lactic acid/ethylene glycol (Ch/LA/EG) + Water, (ii) choline chloride/lactic acid/glycerol (Ch/LA/G) + Water, (iii) choline chloride/oxalic acid/ethylene glycol (Ch/OA/EG) + Water, and (iv) choline chloride/oxalic acid/glycerol (Ch/OA/EG) + Water. ures.
The theoretically computed values of the parameters under study show good agreement with the corresponding experimental values for mixtures under investigation. Based on the obtained results, it is evident that FST can predict these physical properties for the DES mixtures under study, in the given range of concentrations and temperatures. Furthermore, additional thermophysical properties, viz., enthalpy of vaporization, cohesive energy density, and solubility parameter, are also determined for various concentrations and temperatures to understand the nature and types of molecular interactions prevalent in these mixtures. The present study provides a much deeper insight into the functionality of the given DES mixtures as an industrial solvent.
Chrompik was used as a cooling mediumfor storage of A1 nuclearpower plant spent fuel assemblies before their transport outside Slovakia. It was found that the main and crucial problem related to thermal treatment of part of Chrompik, denoted as Chrompik III with a specific activity of 137Cs approx. 1×1011 Bq/dm3 (respectively approx. 1×1012 Bq/dm3 after densification of liquid Chrompik III) is in the long-term drying and follow-up melting with origin glass frit (so called LKU). Thermal treatment process caused a strong evaporation of 137Cs, mainly during vitrification of this mixture (hereinafter referred to as the ‘vitrification mixture’). 137Cs represents a substantial part of radionuclides in this liquid solution. The vitrification process causedthe evaporation of 137Cs, which exceeded limit values according to the Slovak and international standards.
In order to suppress evaporated 137Cs during the melting–vitrification process of Chrompik III implemented by the national decommissioning and waste management organization JAVYS Inc., were in companyVUJE Inc. (both Slovakia) developed novel original additives. These additivesare additions to the vitrification mixture composed with origin glass frit and origin glass. Composition of additives is based on thermal activated (methakaolinite) geopolymer. High efficiency of additives on suppression of 137Cs evaporation, during all process of thermal treatment and first of all melting–vitrification, was observed.
The results at the end of vitrification process showed that the efficiency of retention activity is on the level approx. 99.996% of input value.
Laboratory research was also carried out on the purification of radioactive waste gases and the capture of 137Cs on the surface of natural zeolite grains, containing a natural glassy phase softened at high temperature. It was found, that 137Cs is captured on surface of these softened glassy phase.
In order to eliminate leaching radionuclide from matrix obtained from the process of vitrification, was for long-term storage proposal the process of additional covering of this matrix with a glass phase with high resistance to water, from example with basalt glass.
SESSION: MathematicsWedPM3-R3 |
Rowlands International Symposium (7th Intl. Symp. on Sustainable Mathematics Applications) |
Wed. 23 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Peter Rowlands; James Watson; Student Monitors: TBA |
Peter Rowlands's development of fundamental physics using the nilpotent concept opens up deeper questions about homological applications of the same topological relationships in other domains. I will argue that the very idea of a homological relationship between one set of phenomena conceived in terms of a Clifford algebra, and another set of phenomena, may itself be attributable to the fact that the perception of homology derives from equivalences of "nothing" at different levels. To demonstrate this, examples can be drawn from fields as diverse as AI and music.
Quantal Theory of Gravity (QTG) describes interactions between masses based on a straightforward implementation of the law of energy conservation [1]. In a manner that right away brings about the de Broglie wavelength relationship λB=h/p, QTG remains in full symbiosis with Quantum Mechanics (QM), inasmuch as being equally applicable to either light or ordinary matter in both wave-like (quantal) and the particle-like (corpuscular) limits. Such a framework leads to all of the results that were historically considered to validate the General Theory of Relativity (GTR) of Einstein. All the same, the conformance between GTR and QTG amazingly transpires only in the latter’s quantal case. QTG normally consists in a two-entity formalism. This is where a wave-like behaving test object near a host massmust get torn apart into i) an accelerating wavepacket of energy hf=γm0∞c2 operating locally (this is precisely why the proper rest mass m0∞ appears in the given equality, which in turn constitutes de Broglie’s foundational premise), and ii) a necessarily recoiling corpuscular constituent of rest mass m0∞e-a, which we call thecore or kernel, as tracked by the distant observer. The splitting occurs in accordance with the law of momentum conservation through a rest mass exchange, coming into play owing to the law of energy conservation, between the straggling core m0∞e-a and the throttled wavepacket hf.
We further derive equations of motion for both the wavepacket hf and the core m0∞e-a vis-à-vis, respectively, a fixed local observer and a remote observer situated outside of gravity where i) both observers agree that hf accelerates, ii) there exists for the local observer just the wavepacket hf with regards to a wave-like mode of interaction, and iii) the distant observer can witness the recoiling of the core (while the local observer cannot). In such a way, and without introducing any metric at the outset, we are capable of not only explaining known astrophysical observations of the 20th century that were considered to support GTR, but also of providing an explanation for the lately reported anomalous precession of the perihelion of the orbit of Saturn [2].
If the test object at hand does not delineate any wave-like behavior in gravity, such as is the case of high-energy γ-quanta, QTG predicts the nullification of gravitational bending. This finding can be explained under neither GTR nor other purely metric theories of gravity, and delineates an important aspect in regards to experimentally testing QTG against metric theories including GTR. QTG is moreover applicable to all bound fields, and provides an answer to the dark energy quandary in conformance with the empirically ascertained accelerated expansion rate of the universe.
Positive integer factorization has raised concern particularly in the security of communication technology, based on the fact that positive integers can be employed in the safety of information in cryptography. This study, revealed an infinite square table which is instrumental in the analysis of all positive integer regarding their prime factors. Formula or instructions came up following the orderly arrangement of the positive integers. Moreover, a formula to test primality of a number become obvious in this study. In this regard, positive integers particularly can all potentially be factorized. While it is a solution in mathematics, this can pose threat in the safety communication technology. Nevertheless, this is on one side a solution in cryptography for the fact that a new page is opened to advance the safety of information. Had it been the case that this study did not reveal this fact, the information technology could be at risk. Therefore, the study is about knowledge to communication technology stakeholders to consider safety modification in information systems.
We would like to draw attention in the present paper to a curious mathematical observation concerning fractional differential equations describing physical systems, whose time evolution for integer derivatives has a time-honored conservative form. This observation, although known to the general mathematical community [1, 2, 3], has not, in our view, been satisfactorily addressed. More specifically, we follow the recent exploration of Caputo-Riesz time-space-fractional nonlinear wave equation [4], in which the authors introduced an energy-type functional and proposed a finite-difference scheme to approximate the solutions of the continuous model. The relevant Klein-Gordon equation is considered, where we explore the sine-Gordon nonlinearity with smooth initial data. For the Riesz and Caputo derivative coefficients α=β=2, we naturally retrieve the exact, analytical form of breather waves expected from the literature.
Focusing on the Caputo temporal derivative variation within 1<β<2 values for α=2, however, we observe artificial dissipative effects, which lead to complete breather disappearance, over a time scale depending on the value of β. We compare such findings to single degree-of-freedom linear and nonlinear oscillators in the presence of Caputo temporal derivatives and also consider anti-damping mechanisms to counter the relevant effect. These findings also motivate some interesting directions for further study, e.g., regarding the consideration of topological solitary waves, such as kinks/antikinks and their dynamical evolution in this model.
SESSION: MathematicsWedPM4-R3 |
Rowlands International Symposium (7th Intl. Symp. on Sustainable Mathematics Applications) |
Wed. 23 Oct. 2024 / Room: Marika B2 | |
Session Chairs: Peter Rowlands; Student Monitors: TBA |
The Navier-Stokes problem in ℝ3 consists of solving the equations:
where v = v(x, t) is the velocity of the incompressible viscous fluid, p = p(x, t) is the pressure, the density ρ = 1, f = f(x, t) is the force, v0 = v0(x) is the initial velocity.
The aim of this talk is to explain and prove the author’s result concerning the Navier-Stokes problem (NSP) in ℝ3 without boundaries.
It is proved that the NSP is contradictory in the following sense:
If one assumes that the initial data and the solution to the NSP exists for all t ≥ 0, then one proves that the solution v(x, t) to the NSP has the property v(x, 0) = 0.
This paradox (the NSP paradox) shows that:
The NSP is not a correct description of the fluid mechanics problem and the NSP does not have a solution defined on all t ≥ 0.
In the exceptional case, when the data are equal to zero, the solution v(x, t) to the NSP exists for all t ≥ 0 and is equal to zero, v(x, t) ≡ 0.
The results, mentioned above, are proved in the author’s monographs [1], [5] and paper [3].
Our results solve the millennium problem concerning the Navier-Stokes equations, see [5].
These results are based on the author’s theory of integral equations with hyper-singular kernels, see [2], [4].
In paper [6], p.472, Theorem 2, there is a statement that, for f(x, t) = 0 and u0(x) sufficiently small, the solution to the NSP exists for all t ≥ 0 if m ≤ q, where m is the dimension of the space and the solution is in Lq. In our case m = 3 and q = 2, so the condition m ≤ q does not hold. Therefore, the claim in [6], p. 472, is not applicable in our case.
The Navier-Stokes problem in ℝ3 consists of solving the equations:
where v = v(x, t) is the velocity of the incompressible viscous fluid, p = p(x, t) is the pressure, the density ρ = 1, f = f(x, t) is the force, v0 = v0(x) is the initial velocity.
The aim of this talk is to explain and prove the author’s result concerning the Navier-Stokes problem (NSP) in ℝ3 without boundaries.
It is proved that the NSP is contradictory in the following sense:
If one assumes that the initial data and the solution to the NSP exists for all t ≥ 0, then one proves that the solution v(x, t) to the NSP has the property v(x, 0) = 0.
This paradox (the NSP paradox) shows that:
The NSP is not a correct description of the fluid mechanics problem and the NSP does not have a solution defined on all t ≥ 0.
In the exceptional case, when the data are equal to zero, the solution v(x, t) to the NSP exists for all t ≥ 0 and is equal to zero, v(x, t) ≡ 0.
The results, mentioned above, are proved in the author’s monographs [1], [5] and paper [3].
Our results solve the millennium problem concerning the Navier-Stokes equations, see [5].
These results are based on the author’s theory of integral equations with hyper-singular kernels, see [2], [4].
In paper [6], p.472, Theorem 2, there is a statement that, for f(x, t) = 0 and u0(x) sufficiently small, the solution to the NSP exists for all t ≥ 0 if m ≤ q, where m is the dimension of the space and the solution is in Lq. In our case m = 3 and q = 2, so the condition m ≤ q does not hold. Therefore, the claim in [6], p. 472, is not applicable in our case.
Offline tangible coding games, such as the RANGERS and TANKS problem-solving games [1] serve as a strong bridge connecting Computational Thinking Concepts to Mathematics. Offline coding games[2] and activities[3] are inspired by computer science but introduce Computational Thinking Concepts without using a computer. This approach enriches the teaching and learning of Mathematics, making abstract concepts more accessible and engaging[4].
In this presentation, participants will be introduced to coding and computational thinking concepts in a fun and playful manner through a series of engaging hands-on activities. The session will begin with interactive exercises designed to demystify coding, followed by hands-on interaction with the RANGERS and TANKS problem-solving offline coding applications. These applications provide a tangible way to explore computational thinking concepts, demonstrating how these skills are directly related to mathematical reasoning.
Following these activities, participants will engage in a reflective discussion to identify and articulate the strong connections between computational thinking concepts and Mathematics. This reflection time is crucial as it helps participants solidify their understanding and see the practical implications of intergrating these concepts into their teaching practices. The session aims to highlight the value of offline coding games in making computational thinking a natural part of Mathematics education.
SESSION: PharmaceuticalWedPM1-R4 |
Leuenberger International Symposium on Pharmaceutical Sciences and Industrial Applications for Sustainable Development |
Wed. 23 Oct. 2024 / Room: Minos | |
Session Chairs: Hans Leuenberger; Matthias Plitzko; Student Monitors: TBA |
The high level of health care capabilities and activities in many countries is very beneficial for the societies, however, the related contribution to the carbon dioxide foot print is considerable and should be reduced. Thinking about relevant reduction measures and caring about future generations may trigger the question: What could we learn from our preceding generations, from their way of living, acting, and practicing? A selection of medical and pharmaceutical practices will be presented, covering the time span from about 4000 B.C. till 20th century, encompassing practices conducted in Ancient Egypt, by the Greeks and Romans, in the Orient and medieval Europe. Examples of drugs and dosage forms that were used in ancient times are given. For comparison, practices of modern times and aspects of the pharmaceutical industry are discussed. It is then assessed how well the presented cases would match the sustainability criteria based on our view of today. Eventually, potential approaches are presented, indicating how sustainability might be achieved in pharmaceutical and medical practice today and in the future.
Background In addition to common analytical methods that involve breaking down a sample and analyzing its individual components, there are analytical tools that utilize synthesis processes instead. These methods often involve techniques such as evaporation-induced crystallization or chromatography, resulting in a structure or pattern (pattern-forming methods, PFMs). Here, we present basic research studies on homeopathy conducted using PFMs, specifically the droplet evaporation method [1], copper-chloride biocrystallization [2], and ascending chromatography [3] with physical, plant, and in vitro human blood models, respectively.
Materials and Methods
Results Our research showed that:
Discussion and Conclusions Research on homeopathic preparations requires methods that are sensitive to the sample’s coherence rather than its composition. PFMs appear to address this need and should be studied further in different experimental settings.
Spray Freeze Drying (SFD) is an innovative lyophilization technology that is now entering industrial applications in lab, pilot and manufacturing scale for aseptic processing in pharmaceutical applications, as well as for the areas of medical devices, diagnostics and fine chemicals.
SFD applies the bulkware concept from solid dosage form processing to the area of aseptic freeze drying. It yields in highly homogeneous, free flowing bulkware which can be stored and accurately dosed. Filling is done after lyophilization, with a high degree of flexibility regarding dosing, primary packaging device design and unit number.
Accordingly, the supply chain becomes highly flexible and allows for patient centricity by even providing personalized medication, but also by bringing the required medication to the market or patient very fast.
In addition, product innovation potential is achieved by e.g. enabling to process high solid concentrations up to 40%, with still fast reconstitution characteristics of the lyophilized product. Furthermore, it allows for combinatory products by filling the various lyophilized compounds as required.
Many approaches have been taken to freeze material into particles for subsequent drying under cold condition. From dripping liquids directly into liquid nitrogen [1] to spraying in an cold air flow [2, 3].
The bulk freeze drying process can be carried out at atmospheric pressure (e.g. in a fluidized bed), in conventional freeze-dryers as a layer in trays, which are positioned on the shelfs or as shown here in a dynamic system with continous mixing to provide effecient mass and heat transfer. Drying at atmospheric pressure is feasible in lab scale but have been failing so far in the scale-up due to, in the frozen state, low glass transition temperature (Tg'). Vacuum freeze drying seems to be the gold standard. While tray freeze drying requires a lot of manual handling, which is especially difficult in the light of the recently published Annex 1 of the GMP guideline [4], dynamic freeze drying offers a contained processing with nearly no manual interference.required.
Natural and social sciences are based on providing human beings with tools for sustainable living. According to Professor Hans Leuenberger[1], all sciences are related in the sense that they promote sustainability over time. In this context, the geosciences provide a wealth of knowledge about the past, present and future. Similarly, in geoscience, percolation theory is as important as in pharmaceutical sciences. One branch of the geosciences is mining, which provides human beings with economic, commercial and knowledge benefits. Well-managed mining is an activity that can provide countries with important economic resources. Fair trade promotes the sustainable development of states. Within fair trade, the correct mining of gold stands out, since this metal is linked to the growth and economic development of nations. Gold is one of the most desired mineral elements throughout history. It confers status, is synonymous with power, wealth and future aspirations. Economically successful countries base their financial stability on the gold reserves they have in their respective national banks. Therefore, it must be recognized that gold has many powers for the growth and sustainability of a country. As we have seen, for any country, gold mining is part of a fundamental economic and productive line of business. According to Professor Hans Leuenberger, all areas and human interactions must respect scientific integrity and integrity of data[1]. In the case of gold mining, as in the production of pharmaceuticals, there is regulation. Each country has a respective legal framework that establishes the conditions under which the mineral can be extracted. In order to grant a mining title to a company, minimum legal and ethical standards must be met, which can be divided into two phases: pre-extraction and post-extraction. In the first phase, the company will commit to submit all the corresponding information to the national mining authority to obtain the exploitation permit, i.e.: geological, geophysical, petrophysical and geochemical studies of the subsoil, the estimated time of duration and the probable amount of material to be extracted. During this phase a win-win situation is established between the mining company and the state, where the company can extract the gold without inconvenience and the state receives economic compensation. The second phase comprises the rehabilitation of the exploitation area, where, the mining company must try to restore the area, through processes that include the reforestation of native species, in order to mitigate the environmental damages[2]. Similarly, another type of compensation made by the company with a strong ethical code is towards the local community, through programs focused on social and community investment. On the other hand, there is another type of gold mining that does not comply with the scientific, ethical or data integrity; this is informal mining, which is carried out by some communities due to economic need and the lack of social investment, education and job opportunities. Also, a phenomenon that increases informal gold mining is the pressure exerted by criminal groups. However, in this context there are alternatives for families that depend on informal or artisanal mining to survive. An example of this occurs in Peru, where some groups of artisanal and small-scale miners are accredited by the Fairtrade International Organization[3] in the fairtrade of gold. This certification includes support for small-scale mining groups in the sense that they promote the correct extraction of gold with incentives such as improvement in working conditions, occupational safety and health. With respect to occupational health and safety of workers, Fairtrade certified mining organizations must comply with a set of criteria[4] including: the use of personal protection elements in accordance with the nature of the mine, the submission of a safety report by a competent authority, access to information and basic training in health and safety for all miners as well as the main risks and hazards and regular medical check-ups for all mine workers. The organization also supports miners in acquiring legal status and provides them with fair treatment for the difficult work they perform. Financially, Fairtrade offers the miner a minimum price for the gold extracted, which is equivalent to 95 percent of the price set by the benchmark London Bullion Market as well as a premium of two thousand dollars per kilogram of gold sold, which can be invested in local development projects, environmental protection or community care[3]. Therefore, the work done in Peru with gold mining is an example to follow worldwide, showing that there are viable alternatives for artisanal miners to be better remunerated and thus small-scale gold mining becomes more environmentally friendly for a more sustainable world.
SESSION: LawsWedPM2-R4 |
Dibra International Symposium (4th Intl Symp on Laws & their Applications for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Minos | |
Session Chairs: Florian Kongoli; Agnaldo Andrade; Student Monitors: TBA |
The objective is to inform, with a broad vision, the possibilities of acquiring, registering, legalizing and exploring a mining enterprise in Brazil. Bringing national or foreign investors legal and economic security, with the minimum necessary support, to reassure the investor in a correct and legal way, mining exploration as an excellent and profitable business to be invested in. This paper does not exhaust the topic addressed, since the Brazilian legislation on Mining Law, which is currently under the control of the National Mining Agency – ANM – as provided for in Law No. 13,575/2017, which should undergo some changes, as already under analysis in the Chamber of Deputies, Bill 957/24, which aims to bring several innovations and regulations into the legislation of the Brazilian Mining Law framework.
Currently, Brazil is the second largest producer of iron ore in the world, behind only China, which holds 21% of production, while Brazil contributes to 19%. This production plays a crucial role in the country's trade balance.
However, the extraction and processing activities of this natural resource also cause significant environmental impacts, mainly due to the generation and disposal of large quantities of waste.
Furthermore, iron ore tailings, a by-product of mining, are often deposited in dams, posing known risks to the population, as evidenced by the disasters in Mariana and Brumadinho in the State of Minas Gerais, which occurred in 2015 and 2019 respectively.
Given the need to minimize these impacts and risks, researchers and mining companies have been committed to developing studies to optimize processing, aiming to reduce the amount of waste generated and/or its use as raw material in other sectors, such as in the civil construction field.
In this sense, iron ore waste has been transformed, through technological innovation processes, into materials in order to create pavements and residential houses that can be used for the population of municipalities affected by the environmental impacts arising from mining. The paper aims to demonstrate the tax benefits that mining companies can obtain through the “Lei do Bem” (Law 11,196/2005), which grants tax benefits to companies that contribute to RD&I projects aiming at technological innovation, providing companies the benefits of the reduction in the Income Tax rate and the Social Contribution on Net Profits (CSL) to be applied to Actual Profit Method (“Lucro Real”) in total balance with environmental, social and governance (ESG) aspects.
In the 1990s, Albania moved from a centralized economy towards a free-market economy. Since then, Albania’s economic policies have been oriented towards openness to foreign investors and improvement of the business climate, which are the main promoters of economic growth. The political and economic changes went hand in hand with the legislative ones. An effective justice system is crucial for improving the business climate and increasing foreign investments. Therefore, besides enacting new laws that would strengthen the judicial system, the Albanian legislator also reintroduced arbitration that would provide the business community with a neutral forum for dispute resolution capable of being designed according to their needs.
This presentation aims to delve into the specific aspects of arbitration throughout the different political regimes in Albania, focusing particularly on the features of the new arbitration law enacted recently after decades of legal vacuum. After discussing the trends and challenges of the new Albanian arbitration law, it is concluded that it comes at a time when it is highly needed by the business community, considering the huge backlog of the Albanian courts mainly due to the judicial reform process.
Since ancient times, women have struggled to obtain due recognition for their research, facing barriers imposed by gender. In Ancient Greece, there are reports that the precursor of women in Medicine was Agnodice, a woman who dressed as a man to study and became an excellent “doctor” who was much sought after, but was accused of having deceived the people; while Hypatia of Alexandria was a great scientist, who was quartered and burned for not being Christian, having been accused of being a witch. Years later, in the Renaissance and Enlightenment, there was a scientific revolution, as society began to incorporate the ideals of scientists, although at that time most women were prevented from studying by their families. In the contemporary era, there are still difficulties to be overcome. Analyzing women in the job market, it is observed that inequality through the separation of tasks, in which women are most often responsible for tasks that involve feelings, while men perform, for the most part, tasks that involve decision-making; and the existence of a hierarchy of men under women. Although the participation of women in scientific areas such as Biosciences and Medicine is growing, areas such as Engineering, Physics and Computer Science still have a lower female representation. This sociological study highlights how important it is to fight for gender equality.
SESSION: PharmaceuticalWedPM3-R4 |
Leuenberger International Symposium on Pharmaceutical Sciences and Industrial Applications for Sustainable Development |
Wed. 23 Oct. 2024 / Room: Minos | |
Session Chairs: Hassan Tarabishi; Albert Winkler; Student Monitors: TBA |
Over the past few years, aerogels have shown great promise as delivery systems for active pharmaceutical ingredients (APIs). Aerogels are nanostructured materials with high surface area, high porosity and low density. The unique properties of aerogels provide the opportunity to incorporate various substances to obtain pharmaceutical compositions with modified release kinetics. Drug delivery systems based on aerogels provide a rapid onset of the therapeutic effect, high stability of the drug and improved bioavailability. This is due to the fact that the API is in an amorphous state in the pores of the aerogel, the average pore diameter ranges from 5 to 20 nm.
Particle-shaped aerogels are promising as nasal or inhaled drug delivery systems [1,2]. Aerogel particles can be of different sizes, for example from 2 to 50 μm, depending on the aerodynamic diameter requirements. The distinctive advantages of drug delivery systems based on biopolymer aerogels include biocompatibility, biodegradability, high mucoadhesive properties and high permeability. The successful implementation of APIs such as ibuprofen, rifabutin, loratadine, tryptophan, melatonin, clomipramine, neuropeptide Y and delta-sleep-inducing peptide into biopolymer aerogels has been successfully shown [1-5]. Experiments conducted on rats showed that API appears in the brain within 10 minutes when administered nasally, which is especially important for stroke and other dangerous diseases.
Research into the development of aerogels as drug delivery systems is accompanied by modeling to develop an in silico approach. The multiscale model approach to the creation of nasal and inhalant forms has been successfully developed [6,7]. It includes:
1 – modeling the kinetics of API release from particles in the nasal cavity (dissolution in nasal fluid) or the trachea-bronchi-lungs respiratory system;
2 – CFD modeling of particle flight and their deposition in the human nasal cavity and lungs;
3 – design of inhalers or dosing systems that ensure delivery of dry sprays to the desired location;
4 – design and 3D printing of devices that allow us to confirm calculations and study the processes of particle deposition in the nasal cavity.
At the first stage, a cellular automata approach is used, which allows modeling the transport process and the kinetics of API release from porous microparticles of biopolymer aerogels, both in the nasal cavity and in the lungs, at the nano- and microlevels [7].
The second stage uses CFD modeling (ANSYS software package, etc.), which is a promising approach in the development of innovative nasal and inhalation drug delivery systems. Combining CFD modeling with the results of medical data processing (CT and MRI) makes it possible to accurately predict the deposition zones of drug particles in various parts of the human respiratory system depending on the particle size [6].
In the complex landscape of conflict, this thesis sought to unravel the intricate effects on supply chains and trade within Syria's pharmaceutical industry, which experienced over a decade of civil war. The research was motivated by the limited existing literature on the impact of conflict on supply chains and trade in the pharmaceutical industry, particularly concerning Syria. Prior to the civil war, Syria's pharmaceutical sector demonstrated significant growth and self-sufficiency. However, the conflict brought substantial disruptions, prompting an examination of the ensuing challenges. Utilizing a qualitative approach, this study conducted semi-structured interviews with key industry stakeholders in Syria. The findings revealed that prior to the civil war, various antecedents contributed to the success of the pharmaceutical industry. However, the conflict introduced international and domestic factors that hindered the efficiency of supply chains and resulted in reduced domestic and international trade activities. In response, companies and individuals adopted adaptation strategies, showcasing the industry's resilience in the face of adversity. This research contributed valuable insights into the dynamics of conflict on supply chain and trade by contributing novel findings and enriching existing research.
It is curious that as many historians struggle to make their discipline meaningful to students, these instructors often rob the subject matter of its most fascinating and important aspects. History has long had the reputation of being among the most boring of all courses, and many young people look on their experience with the topic as a bunch of senseless and meaningless facts and dates. Some of this problem relates to the approach historians use which kills any interest their students might engender in the discipline. Among the biggest failings of the profession is a strong tendency to take humanity out of one of the most humane of all studies. In short, rather than giving students examples of moral accomplishments, history does the exact opposite. In many aspects, the historical profession is morally bankrupt by praising killers, by ignoring the peace makers, and by intimidating students rather than inspiring them. Rather than a vehicle for social change and moral action, sometimes history has degenerated to a profession of excuses and cover ups in which anything and everything is justified, forgiven, or praised.
The fossil fuel-intensive Haber-Bosch process, developed in the early 1900s by Fritz Haber and later modified for commercial production by Carl Bosch, uses natural gas to turn atmospheric nitrogen into ammonia to make nitrogen (N) fertilizers. Industrial agriculture uses N fertilizers to grow crops without manure from livestock, a process that has adversely affected food chains globally. During the past century, the use of synthetic N fertilizers has increased 20-fold while the nutrient content of produce in supermarkets has dropped by 10-50%. Research in New Zealand shows that an excess of 45 kg N-unit/ha adversely impacts the return/cost/quality ratio of crop and feed production. Applications of 200 kg N unit /ha are common in the U.S. Midwest and many other industrial countries.
Contrary to the popular belief that the green revolution increased human health, wealth and populations, the increased yields from synthetic fertilizers in agriculture have caused many problems, which took time to manifest and accept. Use of synthetic N fertilizers has a major negative impact on the sustainability of soil, air, and water and the health of livestock and humans. The inability to use groundwater in some agricultural areas is mostly (approx. 70%) due to nitrates from synthetic N fertilizers. Ground water pollution by nitrates, and excessive nitrates in lettuce, are the tip of the iceberg. The chernozem soils of the Midwest U.S. lost 40% of their organic matter, which volatilized into GHG. Overuse of N fertilizers is a major concern for GHG: nitrous oxide (N2O) has a GWP 273 times that of CO2 for a 100-year timescale. Nitrogen fertilizer production uses large amounts of natural gas and some coal and can account for more than 50% of total energy use in commercial agriculture. Human health, especially in the U.S., is also affected. Record high yields of crops, only possible with synthetic N fertilizers, reduce nutrient content of grains: 80-90% of calories in the fast-food chains are provided by corn and soy. Most of the feed for livestock is also corn and soy. Low nutrient content in grain causes livestock and humans to overingest foods in a futile attempt to meet needs for nutrients in low concentrations.
Currently, in the United States only 4% of beef calves spend their entire lives eating phytochemically rich mixes of plants on pastures and rangelands where they were born and raised. The other 96% of calves are weaned, sold, and fattened in feedlots, under conditions that violate freedoms of animal welfare. They are moved from familiar to unfamiliar locations, which causes fear and distress. They dislike any food eaten too often or in excess, yet they are fed daily the same ration so high in grain they experience nausea which causes food aversions, stress, and distress. Though individuals differ in preferences, they can’t self-select their diets, which violates their freedom to express normal behavior and avert distress and disease. These practices cause livestock to suffer various maladies, including chronic acidosis, oxidative and physiological stress, and other metabolic diseases not unlike people with metabolic syndrome, which is characterized by muscle mitochondrial dysfunction, oxidative stress, and elevated levels of cortisol, blood glucose, and insulin. Livestock and people are sustained by the medical and pharmaceutical industries to counter horrific diets, lack of exercise, and stress.
Conversely, due to their phytochemically rich diets and higher levels of physical activity, animals born, raised, and finished on farmlands and rangelands with diverse mixes of plant species have improved metabolic health. Their meat has higher levels of compounds that improve the health of livestock and humans, including polyphenols, tocopherols, carotene, and omega-3 fatty acids to name but a few.
Introducing livestock back into farming would eliminate the need for synthetic fertilizers, recreate a healthy nitrogen cycle, and reduce pollution from concentrated livestock feeding operations. These practices in the U.S. use 80% of antibiotics (70% medically important). Europe’s use of antibiotics for livestock is about half that in the U.S. By consuming animal products (meat/dairy) that have been under regular prophylactic antibiotic treatment, as well as the increase of resistance of bacteria to antibiotics in livestock, and thus humans, the efficiency of antibiotics for human medical treatment is reduced. Incorporating livestock into farming practices, and reducing N fertilizers, would improve the health of livestock, humans, and the environment; provide more nutrient-dense foods; regenerate agricultural soils; and reduce water contamination from nitrates.
SESSION: LawsWedPM4-R4 |
Dibra International Symposium (4th Intl Symp on Laws & their Applications for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Minos | |
Session Chairs: Andrea Hartmann-Piraudeau; Flutura Kola Tafaj ; Student Monitors: TBA |
Many Albanian and foreign authors have noted the coexistence of the statutes of medieval Albanian cities, an expression of the positive law of these areas, with Albanian customary law, as well as the similarities that testify to the mutual influence between the two legal systems. Researchers, such as the albanologist Milan Šufflay, have underlined that the charters of the Albanian cities, although influenced by the positive law of the Italian cities, such as the Republic of Venice or that of Ragusa, have developed original traits. This assessment has been reinforced by studies that have followed the discovery in 1997 of the 'Statutes of Shkodra' by researcher Lucia Nadin and the publication in 2009 of the full text of the Statutes and Ordinances of the Chapter of the Cathedral Church of Drishti, by Musa Ahmeti and Etleva Lala.
The purpose of this paper is to analyze, from a legal point of view, the main characteristics of the statutes of medieval Albanian cities in the domain of commercial law and to assess whether the statutory and the customary law of the Albanian kanun share commonalities and similitudes in the regimes of this branch.
Workplace conflicts are a common aspect of organizational life, significantly affecting both employees and the overall organization. This abstract delves into the various facets of workplace conflicts, including their causes, effects, and costs. It also explores the implementation of Alternative Dispute Resolution (ADR) methods, particularly focusing on mediation.
The KPMG Conflict Cost Study highlights the substantial financial burden of workplace conflicts, including increased employee turnover, higher absenteeism, and reduced productivity. According to Acas, workplace conflicts in the UK cost £28.5 billion in 2018-2019, averaging over £1,000 per employee annually. Approximately 9.7 million employees experienced conflict, with many reporting stress, anxiety, and depression (Acas, 2021).
There is a growing trend to establish structured systems for resolving workplace conflicts through mediation. Mediation is not just an alternative to legal proceedings but a crucial tool for addressing issues like trust erosion, structural problems, and social conflicts. Transformative mediation doesn't aim to avoid or suppress conflicts but ensures they are handled constructively and without harm, recognizing that well-managed conflicts can foster innovation and improvement.
Case studies from various companies demonstrate the effectiveness of mediation. For example, Company A's mediation program reduced employee turnover by 15%, saving around €200,000 annually. Company B's mediation efforts led to a 20% decrease in absenteeism, resulting in significant cost savings and increased productivity.
This session will examine workplace conflict complexities, using both qualitative and quantitative analyses to provide a comprehensive understanding of their impacts. Participants will gain insights into effective ADR strategies, especially transformative mediation. By highlighting the dynamics of conflict and practical mediation applications, this session aims to enhance the development of structured conflict resolution systems that contribute to more harmonious and productive work environments.
Self-preferencing by firms with significant market power, particularly in the digital sector, threatens consumer welfare and market competition. This paper addresses the pervasive issue of self-preferencing, focusing on its manifestation within the Google Search Engine. Google's use of the PageRank algorithm has been critiqued since its 1998 inception for favoring its own products and services over those of third parties that operate on the platform, undermining competitive dynamics and democratic principles of the web.
With the European Commission's recent proceedings against Alphabet under the Digital Markets Act (DMA), this investigation aims to determine whether Google’s search results lead to self-preferencing, thereby ensuring fair treatment of third-party services. The primary goal is to analyze the treatment of self-preferencing in recent case laws and assess the effectiveness of regulatory frameworks like the DMA in mitigating such practices. To achieve this, the paper employs a mixed-methods approach, combining a review of legal cases, an analysis of the technical mechanisms of Google's search algorithms, and an evaluation of the regulatory responses under the DMA.
Findings indicate that while the DMA provides a structured approach to curbing self-preferencing, challenges remain, especially with ensuring compliance amidst the evolving integration of AI functionalities into search engines. Effective detection and enforcement mechanisms are crucial for the DMA to achieve its intended impact on market fairness and consumer welfare. Additionally, this paper offers guidance for digital gatekeepers on compliance with Article 6(5) DMA, addressing concerns related to platform envelopment strategies that negatively impact consumers and businesses.
SESSION: MineralWedPM1-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Wed. 23 Oct. 2024 / Room: Lida | |
Session Chairs: Georgios N. Anastassakis; Carlos Petter; Student Monitors: TBA |
The vanadium shale is a unique and valuable resource of vanadium, and its efficient development can significantly contribute to the expansion of the overall available vanadium resources. However, the distribution of vanadium shale resources is widespread, with varying ore properties and significantly regional extraction characteristics. Currently, the process mineralogy data of vanadium shale is intricate and indistinct, while gangue impurity elements also hinder the detection of vanadium traces within the lattice structure. In terms of technical reliability, replicating and popularizing advanced technology proves challenging due to the unclear mechanism behind vanadium extraction from shale. The crystal lattice characteristics and vanadium extraction rules of vanadium shales are investigated based on the analysis of vanadium shales in China, providing insights into the process of vanadium coordination transformation and migration within vanadium shale. With the aid of quantum chemistry and numerical simulation methods, significant advancements have been made in enhancing the mineral genetic information of vanadium shale, thereby unveiling the fundamental mechanisms underlying key strengthening technologies for efficient extraction of vanadium from shale. The primary objective of this study is to facilitate the sustainable development of highly effective and environmentally friendly extraction techniques for utilizing vanadium resources from shale.
Recently, the European Commission carried out an assessment of 83 raw materials and identified several elements including heavy rare earths, light rare earths, platinum group metals, non-metallic elements in supply risk, and other metals in supply risk within criticality zone of high economic importance (³ 2.8) and supply risk ((³ 1) [1], which place serious pressure related to sustainable supply chains and environmental issues. This ongoing technological evolution has resulted in a rapidly growing generation of electronic waste and toxic substances, leading to significant harmful effects on the environment and human health [2]. Therefore improving the efficiency of recovery of metal from either primary mining processing or from secondary waste, as well as sustainable urban mining /recycling, is of utmost importance to both the economy and environment. Contrary to traditional recovery techniques, which are chemically intensive and often require large pH or thermal swing [3], electrochemically mediated technologies offer modular approaches as alternatives of traditional chemical / thermal swing-based separations [4,5]. In this context we present here recent considerations on hydrometallurgical and electrochemical approaches that can benefit critical materials recycling, especially for rare earth elements and other valuable transition metals. More specifically, we provide insights into the mechanisms and applications for different electrochemical techniques [6,7], namely electrodeposition, electrosorption, electrodialysis and electrocoagulation, as well as recovery techniques at an interface electrode level, using porous capacitive electrodes, intercalation electrodes and redox active electrodes. In parallel, judicious electrochemical engineering (e.g., the design of counter electrodes, types of electrical stimuli, optimizing electrochemical parameters) can significantly improve the separation and energy efficiency. In sum, the increasing demand and decreasing supply of global critical raw materials call for the development of the sustainable recovery and recycling of the valuable elements. Hydrometallurgical processes have been studied for various recycling applications, with increasing industrial-scale implementations in the last decades. There have been significant improvements but, at the same time, several issues with regard to chemical footprint, generation of wastes, slow leaching, and molecular selectivity still remain. In mitigating these challenges, electrochemical separations can be naturally coupled with existing hydrometallurgical processes, and we believe that this combination of electrochemical and hydrometallurgical separation steps, can pave a path toward sustainable materials recycling and critical element recovery.
This abstract deals with the physical separation processes of rare earth bearing placer heavy minerals. In general the Indian coast beach sand consists of the heavy minerals particularly ilmenite, rutile, garnet, sillimanite, zircon and monazite. Among these minerals monazite is considered as the primary mineral for recovery of rare earth elements. Due to high demand to the mankind on the use of mobile phones and motor vehicles etc, and the same time the requirement on the use of rare earth elements in day to day use of electronic and batter operated vehicles and mobiles, it is necessary to recover rare earth bearing minerals from primary secondary minerals. In recent it is found that rare earth elements are found not only in the primary mineral monazite, the other minerals such as garnet and sillimanite also contain rare earth elements in the placer deposits. Hence this present paper deals with the recovery of rare earth bearing placer heavy minerals by gravity, magnetic and flotation processes. The experiments on the recovery processes and the economics of the process are also discussed.
Mining is often described as a low-accumulative activity, with high production costs and low prices for finished products, which puts it in an unequal position compared to other, less demanding industries. It is frequently noted that employees in the mining sector in our region (Western Balkans) typically focus more on production costs than on realized profits. This approach has persisted for a long time, while the full potential of available resources is not sufficiently utilized.
In Serbia, around 200 mines are engaged in the exploitation of non-metallic mineral raw materials. These raw materials are found throughout Serbia and play a significant role in its economic development, serving either as final products or as raw materials for processing in various industrial sectors. Given their quantity and diversity, these raw materials are among the most important domestic natural resources. Virtually all economic sectors utilize non-metallic mineral raw materials.
Serbia's territory boasts a substantial raw material base of non-metallic mineral raw materials (NMRM). To varying extents, 47 raw materials have been explored: 16 are in constant exploitation, 16 are occasionally exploited or not currently exploited, and 15 are insufficiently explored and not exploited. Among these NMRM, raw materials for construction materials hold the greatest economic significance. Additionally, other non-metallic raw materials of great economic importance include ceramic and refractory clays, quartz sand and sandstone, magnesite, quartz raw materials, kaolin, calcite, limestone (as industrial raw materials), gypsum and its anhydrite, pozzolanic tuff, dunite (olivine), rocks for ceramics and glass ("white granites"), and boron minerals.
Beyond the mentioned NMRM, there are ecological mineral raw materials, which belong to the group of natural mineral raw materials and have a wide range of applications, particularly in environmental protection. These materials are increasingly used to remove suspended particles or dissolved substances from industrial waters—pollutants of watercourses and soil—thanks to their outstanding adsorption, ion exchange, and catalytic properties.
This paper aims to highlight the possibilities and challenges of processing NMRM into new materials with added value, based on mineral powders. These materials are produced through the micronization process, which is currently the most widely applied method. Micronization involves very fine grinding, resulting in particles with an upper size limit of a few microns.
SESSION: MineralWedPM2-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Wed. 23 Oct. 2024 / Room: Lida | |
Session Chairs: Jorge Gavronski; Carlos Petter; Student Monitors: TBA |
ESG criteria have increasingly been used by investors to measure sustainability levels for investment in a company or business. In the mining sector, most, if not all, of the available commercial software used for decision-making support, does not include sustainability indicators such as carbon footprint, water consumption, social license, and other factors commonly associated with ESG practices. In this context, the present work presents the current development state of an open-use, cloud-based computational tool called MAFMINE ESG, which aims to incorporate environmental, social, and governance (ESG) sustainability indices to the usual technical-economical parameters used into the preliminary evaluation of mining projects.
The MAFMINE ESG consists of the expansion version of “MAFMINE 3”, an already existing tool developed for the economic evaluation of mining projects (available at https://www.mafmine.com.br/v3/). The core of MAFMINE ESG consists of using parametric models supported by a relatively simple set of inputs (process targets and technical coefficients specified by the user), providing preliminary estimates of sustainability indicators as model outputs. These indicators are quantitative indices associated with one of the following ESG model parameters: emissions, water management, land use, social conflicts, automation and digitalization, and governance. For example, the following indicators are associated with the "water management" parameter: total water withdrawn, affected water sources, % of water reused/recycled, and quality and destination of effluents. The parameterization of indices is established through regression analysis, within specific validation ranges, using available databases for each parameter, such as the historical series report databases from the Intergovernmental Panel on Climate Change (IPCC) for emissions and the Global Reporting Initiative (GRI) for water management.
In addition to presenting the general structure of the software under development, this paper aims to discuss the challenges associated with selecting the indexing factors linked to each index to compare project scenarios considering the realities of different countries together with a preliminary simulation for the case of a base metals mining venture.
The industrial metallurgical processing of spodumene, for the extraction of lithium hydroxide or lithium carbonate, comprises the calcination of a-spodumene to b-spodumene at 1100 oC followed by its leaching with sulfuric acid at 250 oC. Both steps are energy-intensive, while they present a high environment footprint [1]. Recent researches aim to the replacement of calcination/H2SO4 leaching steps by a single less energy-intensive process. Whitin this framework, among other techniques, the direct hydrothermal processing of a-spodumene, aiming to its conversion to lithium intermediate products, using sodium hydroxide at high temperature and pressure conditions, has been proposed. Despite the implemented experimental work [2-4], the literature is poor concerning the thermodynamic description of the process. Furthermore, contradictory results are presented in respect of the formed reaction products. The present study is focused on the thermodynamic study of the a-spodumene ore-NaOH system, by the using of HSC 10 software, in respect of various parameters including the: temperature, pressure, stoichiometry of the reagents and the addition of CaO as an additive. The equilibrium phase diagrams of lithium and non-lithium containing phases and, as well as, Pourbaix diagrams were conducted.
Mining, a pivotal societal contributor, furnishes crucial resources for diverse industries. However, mining operations exert significant environmental impact, necessitating subsequent environmental repair and rehabilitation. The importance of addressing both environmental and social implications in mine closure planning is escalating.
Under legal mandates, mining companies must formulate thorough closure plans, specifying the site's final condition, required measures, anticipated expenses, and financial assurances for effective closure execution. Accurately estimating closure costs, though challenging, is crucial to secure sufficient funding for rehabilitation.
In Brazil, mining site closures often diverge from initial plans, with closure efforts mistaken for rehabilitation. Responding to this, regulatory bodies are fortifying requirements for new projects, enhancing mine closure laws by mandating a comprehensive Mine Closure Plan (MCP) covering decommissioning, rehabilitation, and post-closure activities.
Recognizing, evaluating, and addressing mining site risks in a standardized manner is imperative. This includes ensuring the stability of the mining area in biological, physical, and chemical aspects, averting unintended emissions, and tackling issues like acid drainage. Groundwater geochemistry, particularly concerning mine acid drainage, assumes a vital role. Closure of underground mines involves flooding and continual water level monitoring, while open-pit mines necessitate efforts to repurpose the area for new economic or social activities.
Adhering to standardized criteria is essential to effectively manage the environmental and social impact of mining activities. By prioritizing comprehensive closure planning and adherence to environmental and social considerations, the mining industry can strive to minimize its environmental footprint and champion responsible post-mining practices for a sustainable future.
In the mining industry, one of the main concerns is estimating costs in order to carry out projects efficiently and profitably. MAFMINE is a tool that provides quick and effective results for decision-making. My research was carried out using two parametric equation modeling methodologies, mainly manuals were studied (Bureau of Mines Cost Estimating System Handbook and Costs and Cost Estimation of T. Alan O'Hara and Stanley C. Suboleski), this work focuses on the area of mineral processing, the estimates for operations in processing plant. The parametric equations proposed and added in the plant area make it possible to estimate the processing costs of various circuits, which are fundamental for future plant facility design. These equations also make it possible to estimate the cost of implementations within mineral processing, which in turn allows the most appropriate option to be selected based on the characteristics of each ore. Each methodology has its own advantages and disadvantages, so it was necessary to select appropriate standardization factors. Once the cost estimation tool had been updated with the new parametric equations obtained, it was applied to specific case studies. The results obtained demonstrate the tool's reliability. In conclusion, the study of parametric equation modeling methodologies has made it possible to update a cost estimation tool in the area of mineral processing plants. The inclusion of more parametric equations to estimate mineral processing costs will enable better decisions to be made.
SESSION: MineralWedPM3-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Wed. 23 Oct. 2024 / Room: Lida | |
Session Chairs: Ori Lahav; Paul Chatzantourian; Student Monitors: TBA |
This presented work will introduce a new method for efficiently and selectively extracting pure RbCl(s) from Na+ and K+ enriched brines emanating from the phosphoric acid production industry. Utilizing the ion exchange properties of self-synthesized PES coated Zn-Hexa-Cyanoferrate (PES-Zn-HCF) material, the approach enables effective Rb+ adsorption followed by stepwise, selective desorption. The process involves passing Rb+-containing brines through a column filled with PES-Zn-HCF beads, followed by chromatography-based separation between Rb+ and Na+/K+ using a second column pre-adsorbed with NH4+. A 0.05M NH4+-solution is initially used to extract Na+ and K+ from the first column, retaining a small Rb+ mass, partly re-adsorbed in the second column. After ensuring that the eluent solution flowing out of the column is devoid of Na+ and K+, the 0.05 M NH4Cl passage is ceased and a 1 M NH4+-solution is now pumped in to extract the remaining Rb+. This solution undergoes water evaporation followed by NH3/HCl sublimation/deposition, resulting in the production of a pure RbCl(s) product and in the parallel recycling of the NH4Cl salt that is used as eluent. The study employs theoretical simulations validated by empirical results to demonstrate the method's feasibility as well as a detailed cost assessment, showing the concept to be highly cost effective.
Introduction
Games are increasingly recognized as bringing innovation in educational content. Educational games, as opposed to entertainment games, have the added imperative to infuse learning content along with game and engagement content. Games and gamification, the latter being different from the former, are often used as a tool to scale complexity of tough-to-teach topics. However, they can also be used to understand and appreciate the real-world complexity of processes, topics and actions albeit within the safety of a classroom/fictive setting. One such real-world topic, which is also of urgent concern these days, is sustainability & more specifically sustainability as an approach to counter some of the alarming trends of climate warming, biodiversity crisis, pollution of our ecosystems combined to the for raw materials and sources of energy.
Significant interventions are underway to tackle climate change and bring more sustainability to the agenda and many science and technological innovations are being championed. However, one of the most important, but often invisible/underrated, forces that we see driving change is that of “Negotiations” or “Deal-making”. One might have the most innovative technology at hand but it is only through negotiations that one might be able to get it implemented. Often these skills are only developed through years of experience and hardly taught enough formally. We propose that a sustainable future can be fast-tracked not through technological innovations alone but the essential skill of negotiations.
Educational intervention & Impact:
Gamification is intended to exemplify the complex interdependencies between different land-use areas such as forest, lakes, mountains, coastal areas and even sea-beds and subsurface. In order to enhance the sustainability agenda, land modifications come at a significant cost and are made as such to mirror reality – such as European regulations around forest use and forest replantation tariffs). The paper proposes a game designed in such a way that one needs to grow their empire (of their own sector) to thrive and earn resources and money – both of which are needed to fuel further growth. Yet, growth will result in overlapping strategies and competition for resources as well as land. While one could be more unsustainable and expand at the cost of natural resources alone, the game stands out in its message that one can use the art of making deals to meet growth objectives with minimal or limited impact to the environment. The message being imparted is then along the lines of “savvy deal-making can influence and help you meet your sustainability objectives faster and cheaper”. The game is under development and the impact is yet to be measured – but from an engagement perspective we see very high engagement from the students as well as an acceptance of a transformed mindset- i.e. looking at the world from a different perspective than then one they started out with.
Contextualisation in conference theme: The use of such a game to drive sustainability ambitions within the mining and mineral processing sector are axplored. It is one of the most pressing demands of society in their dialogue with the raw materials sector. The game will integrate the life cycle of a mining or quarrying activity, from mine area allocation, exploration drilling, acquisition of exploitation and environmental permits to full scale mine development, mineral & metal processing and waste management up to closure and land reclamation.
Africa hosts many of the largest mineral deposits in the world, with vast reserves of critical minerals and metals. High-grade deposits of gold, diamonds, and any other metal position the continent as a prime destination for mining investments. Countries like South Africa, Ghana, and Tanzania are leading gold producers with the largest companies in the sector such as Barrick Gold and AngloGold acting there, while the Democratic Republic of Congo dominates in cobalt and copper production. Production costs are relatively low in comparison to western ones due to cheaper labor costs.
This has led the mining sector to offering substantial economic growth potential in its countries alongside job creation and infrastructure development. Noravia Gold Mining has been acting in Tanzania since 2013. The country holds a major position in gold and metal extraction, everso growing the last ten years having unprecedented organization in an electronic database and license issuance based on NI 43-101 of Canadian law. At the same time the country is classed as one of the safest in Africa with a very little crime rate. Its products are transported to major markets, such as the UAE and Europe in renowned refineries such as Emirate Gold in Dubai, Umicore and Argentor in Antwerp Belgium and Balestri and Arezzo in Italy.
In the current work, details are provided regarding the potential of the extractive sector in Africa and Tanzania, the opportunities and prospects, the sociopolitical framework and some concomitant hardships and risks regarding Africa.
Finally, details are presented regarding Noravia Ltd. Referred to its mining projects, processes and application of innovative technology to simultaneously recover three different metals through censoring, with the hardware expected to be presented in Canada’s biggest mining exhibition, PDAC in March of 2025.
The presence of mineral sulfides such as pyrite, chalcopyrite etc., can pose significant challenges in gold extraction processes, regardless of the extraction route used, including the use of cyanide and thiosulfate [1]. These sulfides consume the reagents used in the aforementioned extraction processes, leading to operational problems due to the increasing ionic strength during such processes, which impacts the solubility of the oxidizing agent, particularly dissolved oxygen, which is of utmost importance for extracting gold [2]. The presence of these sulfides in gold ores represents a major challenge in gold extraction [3], as they react with leaching agents with their consequent consumption, leading to a reduction in the efficacy of gold extraction processes causing operational problems.
Therefore, this study aimed to carry out comparative tests to point to the effectiveness of the gold extraction process, from samples of gold ore subjected to three distinct forms of mineral processing: conventional crushing, in jaw crusher, crushing in high pressure grinding rolls (i.e., HPGR - High Pressure Grinding Rolls) and electrodynamic fragmentation (i.e., HVPF - High Voltage Pulse Fragmentation).
In this study, different grinding operations were used, such as the use of a jaw crusher, high pressure grinding rolls, and high voltage pulse fragmentation, aiming to determine the influence of these unit operations on the bio-oxidative process (pre-treatment) of the aforementioned mineral sulfides, as preliminary steps to the extraction of gold particles trapped in the matrices of the aforementioned sulfides, substantially reducing the consumption of gold leaching agents, thus avoiding the grinding operation, which is the most expensive unit operation of extractive metallurgy.
In the bio-oxidation process, the tests were conducted in acrylic columns, filled with 3.5 kg of ore and subjected to different mineral processing for 30 days. The columns were fed from the top with a solution of salts from the MKM medium (i.e., Modified Kelly Medium - with the following composition: (NH4)2SO4: 0.08 g.L-1; MgSO4.7H2O: 0.08 g.L-1; K2HPO4: 0.008 g.L-1), at a flow rate of 10 L/h/m², and this solution was recirculated throughout the experiment. The mineral bed was aerated with an upward flow of humidified air at a flow rate of 0.5 L/min, 3 liters of leaching solution from the MKM culture medium were used, adjusted to pH 1.8 with 5M sulfuric acid when necessary, and maintained at 30°C. The culture medium included a mixed culture of Acidithiobacillus ferrooxidans(LR lineage), Acidithiobacillus thiooxidans (FG-01), and Leptospirillum ferrooxidans (ATCC 53992), each with a population density of 107 cells/mL. For the gold extraction process, the material, after the bio-oxidation tests as bio-oxidative pre-treatment, duly exempted from acid solution residue, by successive aqueous washes, was placed in a glass column through which a descending flow of aerated cyanide solution passed, in distinct concentrations of free cyanide (usually varying from 3 to 10 g.L-1), coming from a glass reactor, with a useful volume of 5 liters. Once the cyanidation was stopped, the leachate was analyzed by atomic absorption spectrometry to measure the extraction of gold.
As initial results, the 30 day bio-oxidation experiments showed that high voltage pulse fragmentation (HVPF) was more effective in extracting copper and nickel from gold ore, compared to other crushing operations. HVPF generated microfissures that exposed the mineral sulfides to the microorganisms in the acid solution, increasing the concentrations of copper and nickel in the leachate. Crushing via HPGR showed less nickel solubilization and did not surpass the other operations at any time. These results underscore the need for continuous optimization of crushing operations for each type of ore. The cyanidation tests indicate that HVPF is the most effective operation, allowing a more efficient exposure of the gold particles to the joint action of the cyanide, complexing agent, with oxygen, oxidizing agent. The cyanidation tests revealed that processing via HVPF was the most efficient unit operation in the release of gold particles, followed by HPGR and, lastly, by the jaw crusher.
It is concluded that the operation of high voltage pulse fragmentation (HVPF) stands out as the most efficient both in the bio-oxidation process and in the cyanidation of gold ore, providing a greater extraction of gold.
SESSION: MineralWedPM4-R5 |
Anastassakis International Symposium (10th Intl. Symp. on Sustainable Mineral Processing) |
Wed. 23 Oct. 2024 / Room: Lida | |
Session Chairs: Georgios N. Anastassakis; Maciej Tora; Student Monitors: TBA |
The minerals industry is vital to national economies, energy sufficiency, and transformation worldwide. Exploiting a mineral deposit is a complex project, as it is related to technical, environmental, social, and economic aspects with significant impacts on the financial markets, societies, human life, and the global ecosystem. In this framework, sustainable exploitation and development are crucial in all mining sector activities. Considering the uncertainties related to factors that affect a mining project's viability and sustainability, the overall assessment of a mineral resource constitutes a complex and multidimensional decision-making problem [1]. In the decision analysis model, an integrated approach is required based on the spatial modelling of the mineral deposit in combination with exploitation planning and quality control [2]. In addition, evaluating alternatives in mine planning can incorporate sustainability criteria in the decision-making model [3].
In this work, a decision-making model regarding for the evaluation of a mineral deposit is developed, based on dynamic programming, and considering the whole life cycle of the extraction and processing of the mineral resource project. In this context, a quantification of sustainability and circular economy parameters is attempted through a system analysis model that combines the economic objective function, the constraints, and the cash flow analysis and optimization.
The proposed framework can be applied as an effective tool for evaluating mineral resources planning exploitation strategies, managing mining activities, and validating research and operational objectives, by always taking into consideration sustainability and circular economy standards and viable development perspectives.
The basis of this enrichment process is the difference in the densities of the minerals that make up the original raw material.
When such a mechanical mixture is immersed in a liquid with an intermediate density, the waste rock floats, while the metal-containing minerals, being heavier, sink.
Hence, the main emphasis in the development of such a high-precision enrichment process was placed on finding the optimal formulation of such a water-based working medium in close connection with the justification of a simple and energy-efficient procedure for its complete regeneration from the enrichment products and its return to the head of the process
In Poland, in 2023, renewable energy sources, such as wind turbines, solar photovoltaic panels, accounted for over 40%. installed capacity in the Polish energy mix and accounted for 27%. total energy production. Thus, Poland broke further European records in the increase in the share of renewable energy. The goals we set for ourselves are over 50%. green energy in 2030, and in 2050 we will have to reach 100%. the service life of installations of renewable energy sources: photovoltaics, wind turbines is estimated at 25-30 years[1,2]. After this time, the installation will be recycled. The article presents waste-free technologies for recycling photovoltaic panels and windmill blades developed by a consortium of universities (AGH University of Kraków) and 2LOOP TECH [3,4]. The developed technologies meet the assumptions of a closed-loop economy (circlar economy). The article presents a life cycle analysis (LCA) of PV panels and wind blades. The implementation of technology in industrial conditions implements the principle of “secondary first”.
Currently, one of the main sources of electricity generation is coal-fired power generation. Coal-fired plants generate electricity by burning coal, resulting in a large amount of waste (ash and slag) being accumulated, which has a negative impact on the environment. Involving ash and slag processing will not only reduce the environmental burden, but also provide additional marketable products. Depending on the coal deposits, combustion conditions, and waste composition, ash and slags have different physical and chemical characteristics. Very often, ash and sludge contain elements such as Fe, Si, Ti, Al, Ni, Mo, V, and many others. Various enrichment methods are used to extract these valuable components: flotation, gravity separation, magnetic separation, and leaching.The choice of beneficiation process primarily depends on the size of the material to be processed, as well as the physical and chemical properties of the components that need to be separated.
Ash-and-slag waste (ASH) from thermal power plants (TPPs) was selected to investigate the possibility of extracting iron-containing components. To justify the processing method, studies on the granulometric and chemical compositions were carried out. The material mainly consists of fine particles with a fraction greater than 90 % in the -45 micron size class. At the same time, by electron microscopy, the presence of various microspheres, including aluminosilicates and iron-bearing ones, was established. Due to the small size of these particles, it is difficult to produce concentrates with marketable quality using conventional enrichment methods.
The conducted studies on magnetic fractionation allowed us to establish that the distribution of iron is quite uniform in all fractions, but microspheres, which include magnetite associated with intermetallides, are mainly concentrated in magnetic fractions obtained at current values equal to 2, 3 and 4 A. It was assumed that iron in the compounds is in different valence forms and has different magnetic properties. At the same time, microspheres containing hematite and aluminosilicates were not found in isolated magnetic fractions. It was proposed to use high-gradient magnetic separation to separate such microspheres from finely dispersed materials.
Studies on the influence of various parameters and settings of the magnetic separator, including matrix size, field strength, and pulsation frequency, on the characteristics of extraction and concentration of the target component, were carried out at a high-gradient magnetic separator while varying technological parameters and modes. As a result of these studies, it was found that the best results were achieved with the following operating parameters: magnetic induction of 1.1 T, diameter of matrix rods of 6 mm, and pulp pulsation of 300 rpm. In order to further increase iron extraction in the concentrate, a series of experiments using flocculants were conducted. As a result of the research, a technological mode was proposed that allows for the production of iron ore with a 50% iron content and a recovery of 94.5% in one stage using a magnetic induction of 1.1 Tesla, a matrix bar diameter of 6 mm, a pulse frequency of 300 cycles per minute, and the consumption of Flotifloc flocculant of 100 grams per ton. Scanning electron microscopy revealed that under these conditions, most microspheres containing hematite and aluminosilicate minerals with sizes ranging from 2 to 15 micrometers are extracted into the magnetic fraction.
Thus, for the extraction of microspheres with different compositions and sizes, a sequential magnetic enrichment scheme is recommended: magnetic separation in a weak magnetic field and high-gradient tailings separation. This proposed solution will not only allow us to obtain materials with unique technological properties, but will also reduce the environmental impact in areas where ash dumps are located.
This work was carried out within the grant of the Russian Science Foundation (Project № 23-47-00109).
SESSION: SISAMWedPM1-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Wed. 23 Oct. 2024 / Room: Knossos | |
Session Chairs: Michael J. Zehetbauer; Student Monitors: TBA |
The research of Ludwig Schultz has covered many aspects of advanced materials, particularly related to superconductivity and magnetism. This talk will cover some recent work on metallic glasses, focusing on aspects that overlap with Ludwig’s interests.
Metallic glasses remain a particularly active research topic within research on advanced metallic materials. They have unique combinations of properties, and some individual properties that are best in class. We will assess which are the most active research directions [1]. One of these is the search for new metallic-glass-forming compositions, now reinvigorated by machine-learning approaches [2].
Another particularly active research area follows from the realization that the properties of a metallic glass can be greatly varied even at fixed composition. Most attention has been paid to ‘rejuvenation’, that is, raising the energy of the glass. We survey the methods of thermomechanical processing used to achieve rejuvenation, ranging from treatments within the elastic limit [3,4] to plastic flow under compression [5]. The beneficial effects of rejuvenation can be great: enabling bulk metallic glasses to show strain-hardening rather than strain-softening; [5]; increases in impact toughness of nearly a factor of three; and reversing the effects of annealing-induced embrittlement.
That last effect is potentially important for Fe-based metallic glasses. These show excellent soft-magnetic properties, and are of high and increasing importance in the energy transition. To optimize their magnetic properties, however, they must be annealed, and they become brittle to an extent that significantly hinders fabrication of components. If that embrittlement can be fully solved, that will greatly the more widespread use of metallic glasses in what is already their most important application area.
The research of Ludwig Schultz has covered many aspects of advanced materials, particularly related to superconductivity and magnetism. This talk will cover some recent work on metallic glasses, focusing on aspects that overlap with Ludwig’s interests.
Metallic glasses remain a particularly active research topic within research on advanced metallic materials. They have unique combinations of properties, and some individual properties that are best in class. We will assess which are the most active research directions [1]. One of these is the search for new metallic-glass-forming compositions, now reinvigorated by machine-learning approaches [2].
Another particularly active research area follows from the realization that the properties of a metallic glass can be greatly varied even at fixed composition. Most attention has been paid to ‘rejuvenation’, that is, raising the energy of the glass. We survey the methods of thermomechanical processing used to achieve rejuvenation, ranging from treatments within the elastic limit [3,4] to plastic flow under compression [5]. The beneficial effects of rejuvenation can be great: enabling bulk metallic glasses to show strain-hardening rather than strain-softening; [5]; increases in impact toughness of nearly a factor of three; and reversing the effects of annealing-induced embrittlement.
That last effect is potentially important for Fe-based metallic glasses. These show excellent soft-magnetic properties, and are of high and increasing importance in the energy transition. To optimize their magnetic properties, however, they must be annealed, and they become brittle to an extent that significantly hinders fabrication of components. If that embrittlement can be fully solved, that will greatly the more widespread use of metallic glasses in what is already their most important application area.
Nanocrystalline materials have a variety of new or improved properties compared to their single crystalline counterparts [1]. Severe plastic deformation and solute segregation to grain boundaries are useful and simple methods to produce nanocrystalline materials. Examples for nanocrystalline iron doped with various solutes (carbon, nitrogen, oxygen and boron) and various concentrations are presented. The alloys were generated by ball milling iron powder with graphite, iron boride, iron nitride and iron oxide and their grain size was determined with transmission electron microscopy. Severe plastic deformation by wire drawing of Pearlite also leads to a nanocrystalline Fe-C alloy. All alloys had a grain size of about 20 nm. Results of the thermal stability of the alloys with respect to phase separation and coarsening is provided. Based on Gibbs Adsorption Isotherm the dependence of grain size on solute concentration is explained. It will be shown that Gibbs Adsorption Isotherm can be generalized [2] from surfaces and grain boundaries to all kinds of discontinuities (dislocations, vacancies etc.).
Nanocrystalline materials have a variety of new or improved properties compared to their single crystalline counterparts [1]. Severe plastic deformation and solute segregation to grain boundaries are useful and simple methods to produce nanocrystalline materials. Examples for nanocrystalline iron doped with various solutes (carbon, nitrogen, oxygen and boron) and various concentrations are presented. The alloys were generated by ball milling iron powder with graphite, iron boride, iron nitride and iron oxide and their grain size was determined with transmission electron microscopy. Severe plastic deformation by wire drawing of Pearlite also leads to a nanocrystalline Fe-C alloy. All alloys had a grain size of about 20 nm. Results of the thermal stability of the alloys with respect to phase separation and coarsening is provided. Based on Gibbs Adsorption Isotherm the dependence of grain size on solute concentration is explained. It will be shown that Gibbs Adsorption Isotherm can be generalized [2] from surfaces and grain boundaries to all kinds of discontinuities (dislocations, vacancies etc.).
SESSION: SISAMWedPM2-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Wed. 23 Oct. 2024 / Room: Knossos | |
Session Chairs: Jürgen Eckert; Student Monitors: TBA |
Advancements in e-mobility and green power generation are crucial for fulfilling the Green Deal's objectives of creating a low-carbon society. Central to this goal are high-performing permanent magnets, such as Nd-Fe-B and Sm-Co, essential components in electric motors and generators. Consequently, intensive research into these magnets is critical to enhance their performance. However, a significant challenge is the scarce availability of these rare earth elements, designated as essential raw materials by the EU. Therefore, comprehensive approaches in resource-efficient processing, reprocessing, and recycling of these magnets are vital for the future development of permanent magnets. We are dedicated to researching and improving the viability of reprocessing and recycling Nd-Fe-B and other permanent magnets. Techniques such as electrochemical separation via anodic oxidation have successfully recycled Nd-Fe-B scrap into Nd2Fe14B matrix phase grains or break them down into rare earth-based precursors [1]. Moreover, Sm-Co permanent magnets have also shown promising recyclability through electrochemical methods [2]. Progress in scaling up recycling methods for Nd-Fe-B has been achieved through selective electrochemical and chemical approaches [3-4]. These innovative recycling and upcycling techniques pave the way for completely reengineering Nd-Fe-B magnets from the ground up, offering a break from traditional methods and potential enhancements in magnet performance metrics like energy products. Our current research also explores rapid consolidation methods, such as spark plasma sintering, which promise to advance Nd-Fe-B magnet development further [4].
Nowadays, magnetic resonance imaging (MRI) has become a powerful diagnostic tool in medical fields, e.g. in brain surgery, cardiovascular diseases and orthopedics. However, MRI diagnosis is inhibited by the presence of certain metallic implants in the body because they become magnetized in the intense magnetic field of the MRI instrument, which may produce image artifacts and therefore prevent exact diagnosis. To decrease the artifacts, medical alloys/devices with low magnetic susceptibility are required. Compared with stainless steel and Co–Cr alloys, which are conventional implant alloys, titanium (Ti)– and zirconium (Zr)-based alloys have lower magnetic susceptibility and are more suitable for clinical investigation using MRI than the others [1]
Metallic glasses have a great potential for small medical devices useful in dentistry (e.g. dental implants and suprastructures), osteosynthesis (e.g fracture fixation systems) and occlusive vascular diseases (e.g stents and aneurysm clips) [2-4]. Ti-, Zr- and precious metal-based bulk metallic glassess (BMGs) have been widely investigated as potential biomaterials especially for bone-related implant applications [2-3]. However, the major problem still facing the development of biomedical metallic glasses is the one of inducing amorphization without using any harmful alloying additions. We reviewed the biological safety and glass forming tendency in Ti of a series of alloying elements [2].
In the present paper we discuss the underlying processes for amorphous phase formation, mechanical and biochemical behavior as well as the biocompatibility of various Ni-free Ti- and Zr-based BMGs with potential for biomedicine. Moreover, we report the formation novel amorphous Ti-Zr-Nb-Hf-Si multi-principal element alloys with excellent corrosion stability in simulated body fluids and ultralow magnetic susceptibility, less than one-third of that of commercial biomedical Ti-based materials [4]. These alloys exhibit also higher X-ray linear attenuation coefficients relevant for interventional X-ray-based medical imaging. This two-fold advantage (lower magnetic susceptibility and higher radiopacity) allows the materials to be more precisely visualized via biomedical imaging methods, which is especially important for miniaturised implants.
Financial support through the European Commission (H2020-MSCA-ITN BIOREMIA GA 861046) is gratefully acknowledged.
In this study, we explore the challenge of creating anisotropic permanent magnets through the process of additive manufacturing, specifically using material extrusion (MEX). Typically, the production of anisotropic magnets requires the application of an external magnetic field, with the most cost-effective approach being the utilization of permanent magnets in a specific orientation to align the particles. However, when employing a filament-based 3D printer or material extruder, generating an adequate magnetic field presents certain difficulties. The simplest method involves printing directly atop a permanent magnet, as shown in previous studies. [1] However, this approach restricts the magnet's height due to the diminishing magnetic field with distance, eventually leading to a point where particle orientation ceases. Contrary to predictions, our observations revealed that the printed magnet not only sustains but also extends the magnetic field of the underlying permanent magnet. This results in a greater degree of anisotropy at distances further from the magnetic field source than initially anticipated. This discovery opens up new possibilities for more intricate designs, circumventing the limitations imposed by space constraints for permanent magnet placement by leveraging the magnetic field extension provided by the previously printed magnet.
Magnetic skyrmions are topologically-protected vortex-like magnetization patterns that can exist under special conditions in noncentrosymmetric structures. They might be applicable as carriers of classical and quantum information [1]. Whereas at the macroscopic level their existence is a finite-temperature phenomenon, theory predicts skyrmions with nanometer length scales at T = 0 [2].
An appropriate model, which can exhibit the respective phase, is a two-dimensional spin-1/2 Heisenberg lattice with the Dzyaloshiskii-Moriya interaction in an external field. A promising way to find the ground and excited states of the corresponding Hamiltonian is to apply a quantum algorithm. In this manner we have mapped the model-parameters phase diagram by performing the calculations with the variational quantum eigensolver (VQE) [3]. Although, due to a limited number of the working qubits, the investigated lattices have been too small to host a full skyrmion, the results clearly indicate the relation between the parameters, required for their existence.
SESSION: SISAMWedPM3-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Wed. 23 Oct. 2024 / Room: Knossos | |
Session Chairs: Saso Sturm; Student Monitors: TBA |
The green transition drives the advancement of sustainable energy conversion technologies. Nd-Fe-B permanent magnets are crucial components of energy-efficient electric motors and generator systems. Presently, state-of-the-art magnets, boasting maximum energy products as high as 450 kJ/m³, are produced through powder metallurgy routes. However, conventional sintering is energy-intensive and offers limited control over microstructure formation and the final magnet's geometry.
Rapid powder consolidation techniques, like Spark Plasma Sintering (SPS), present notable advantages over conventional methods. They offer faster and more energy-efficient sintering processes, lower sintering temperatures, and the potential for net-shape manufacture, promising a new generation of Nd-Fe-B magnets with improved functionalities. Yet, due to the strong structure-properties dependence, consolidation of microcrystalline Nd-Fe-B-type powders via SPS proved challenging. Localized overheating at particle-particle contacts, owing to the Joule effect, can disrupt the delicate phase composition of the material, resulting in a drastic loss of hard-magnetic performance [1, 2].
Through careful optimization of heating conditions and the introduction of novel concepts in processing multiphase metallic systems like Nd-Fe-B, our research has been focused on developing alternative sintering strategies for the manufacture of Nd-Fe-B magnets. Fast sintering cycles have been employed to enhance the material's high-temperature performance by suppressing grain growth during densification. We will show that rapid sintering can reduce the energy consumption required to densify an Nd-Fe-B-type powder by an order of magnitude compared to slow conventional sintering. The new powder consolidation paradigms are applicable for processing both fresh and recycled powders, offering great potential for reengineering the magnet's microstructure, and having implications for future industrial processes.
The green transition drives the advancement of sustainable energy conversion technologies. Nd-Fe-B permanent magnets are crucial components of energy-efficient electric motors and generator systems. Presently, state-of-the-art magnets, boasting maximum energy products as high as 450 kJ/m³, are produced through powder metallurgy routes. However, conventional sintering is energy-intensive and offers limited control over microstructure formation and the final magnet's geometry.
Rapid powder consolidation techniques, like Spark Plasma Sintering (SPS), present notable advantages over conventional methods. They offer faster and more energy-efficient sintering processes, lower sintering temperatures, and the potential for net-shape manufacture, promising a new generation of Nd-Fe-B magnets with improved functionalities. Yet, due to the strong structure-properties dependence, consolidation of microcrystalline Nd-Fe-B-type powders via SPS proved challenging. Localized overheating at particle-particle contacts, owing to the Joule effect, can disrupt the delicate phase composition of the material, resulting in a drastic loss of hard-magnetic performance [1, 2].
Through careful optimization of heating conditions and the introduction of novel concepts in processing multiphase metallic systems like Nd-Fe-B, our research has been focused on developing alternative sintering strategies for the manufacture of Nd-Fe-B magnets. Fast sintering cycles have been employed to enhance the material's high-temperature performance by suppressing grain growth during densification. We will show that rapid sintering can reduce the energy consumption required to densify an Nd-Fe-B-type powder by an order of magnitude compared to slow conventional sintering. The new powder consolidation paradigms are applicable for processing both fresh and recycled powders, offering great potential for reengineering the magnet's microstructure, and having implications for future industrial processes.
Since the first reports on intrinsically magnetic two-dimensional (2D) materials in 2017 [1,2], the price-to-pay for accessing their monolayers is the lack of ambient stability. We discovered in a mineral aggregate – mainly composed of hematite, magnetite, and chalcopyrite – soft layers of which macroscopic flakes easily could be peeled off that stuck to a permanent magnet. Employing mechanical exfoliation, we succeeded in thinning and transferring micrometer sized – mainly hexagonally shaped – flakes to SiO2 substrates. Energy dispersive x-ray spectroscopy (EDS) revealed magnesium and silica as major components of the flakes. Raman spectroscopy indicated the presence of hydroxide groups, pointing towards talc, a hydrated magnesium phyllosilicate mineral, namely talc (Mg3Si4O10(OH)2). Long-term EDS and Raman spectroscopy revealed that in the flakes about 10 % of the Mg atoms are substituted by Fe which clusters into about 20 nm regions according to scanning transmission electron microscopy. With atomic force microscopy, a minimum flake thickness of 1 nm was determined indicating cleavage down to a talc monolayer. Combined magnetic force microscopy (MFM) measurements in external out-of-plane fields up to 0.5 T and SQUID magnetometry measurements imply that the 2D Fe-rich talc exhibits weak ferromagnetic behavior [3]. The flakes are showing long-term stability under ambient conditions in contrast to the 2D magnets reported so far. Besides iron-rich talc, we investigate also ultrathin flakes of exotic minerals like minnesotaite (Mg3Si4O10(OH)2) as well as iron rich micas like biotite and annite [4]. As another approach towards iron-rich 2D talc flakes, we used ion implantation of iron-free talc single crystals and subsequent mechanical exfoliation.
Work has been supported by FWF, Austria via 2020 START program (grant # Y1298 N) and has been performed in collaboration with A. Matković, M. Z. Khan, K.-P. Gradwohl, L. Ludescher, M. Kratzer, M. Zimmermann, R. Bakker, J. Raith (all Montanuniversität Leoben), O. E. Peil, L. Romaner (all Materials Center Leoben), C. Gammer (Erich Schmid Institute of Materials Science, Leoben), E. Fisslthaler, D. Knez, F. Hofer (Graz University of Technology), J. Genser, A. Lugstein (Vienna University Of Technology), A. Sharma, O. Selyshchev, D.R.T. Zahn, G. Salvan (TU Chemnitz), O. Selyshchev, S. Valencia, F. Kronast (all Helmholtz-Zentrum Berlin), and U. Kentsch, N. Klingner, G. Hlawacek (all Helmholtz-Zentrum Dresden-Rossendorf).
Surface energy is an essential property of condensed matter. It determines the equilibrium shape of a piece of matter and drives its interactions with the environment, for instance its wetting and adhesion properties, or even friction against another solid. Most non-metallic liquids and solid polymers are known to exhibit relatively low surface energies, in the range of few tens to few hundreds mJ/m2. In contrast, metals show surface energies in the range of 1 to few J/m2. For example, aluminum, copper or iron have surface energies close to 1.3, 1.8 and 2.2 J/m2, respectively.
Due to the absence of translation periodicity and to their specific atomic architecture, metallic quasicrystals (QCs hereafter) present an electronic structure that differs significantly from the one of conventional metals: a marked pseudo-gap is observed at the Fermi energy [1]. The density of mobile electrons is henceforth reduced to about 10 to 20% of the one in a classical metal like Al, and the transport properties of QCs are definitely different from the ones in a periodic metal. So is also the surface energy.
This property can be assessed experimentally using single crystal specimens, but also by computational methods for periodic crystals [2]. The power of modern computers allows nowadays the study of materials with a unit cell containing several hundreds of atoms, which covers the full range of periodic metals known so far. Yet, it is still far below the range necessary to address the surface energy of QCs. The talk will review the methods used by the author [3] to overcome this difficulty and at least estimate the surface energy of few QCs such as icosahedral AlCuFe and AlPdMn in comparison to a small number of periodic crystalline materials of related composition. The meaningful low value of the surface energy found for these QCs, in the range 0.5-0.8 J/m2, will be discussed in the light of applications of potential technological relevance such as reinforcement of polymer-matrix composites or friction against hard steel [4].
SESSION: SISAMWedPM4-R6 |
Schultz International Symposium (8th Intl. Symp. on Science of Intelligent & Sustainable Advanced Ferromagnetic and Superconducting Magnets (SISAM)) |
Wed. 23 Oct. 2024 / Room: Knossos | |
Session Chairs: Saso Sturm; Student Monitors: TBA |
High energy ball milling of powders is an extreme example of severe plastic deformation which can dramatically alter the structure and/or microstructure of materials. It was first used by John Benjamin and his colleagues in 1966, at what was the International Nickel Company, to obtain uniform distributions of oxide particles to strengthen structural materials like nickel-base superalloys. This method was later extended to produce amorphous alloys from elemental powders [1,2] or the milling of intermetallics [3]. In the synthesis of amorphous alloys from elemental powders (mechanical alloying) or by milling intermetallic compounds (mechanical milling), it was typically found that the microstructure became nanocrystalline before it became amorphous. Therefore, this suggested a mechanism for the observed amorphization, and also provided a convenient method for preparing nanocrystalline materials. This talk will present a historical perspective on the preparation by ball milling of metastable materials such as amorphous alloys, nanocrystalline materials, quasicrystalline materials [4] and microstructural changes that can have beneficial effects on properties. Work from the author’s laboratory and from the seminal research in this area by Prof. Ludwig Schultz will be emphasized.
The most used textbooks in the area of magnetic materials remain Chikazumi [1] and its north-american counterpart, Cullity [2].
Even these books are essentially correct, there are some needed corrections, also because these books are more than 50 years old, and some advances happened in this period. Some necessary corrections and amendments have been discussed in recent papers [3,4,5].
The most relevant correction is the description of exchange energy term, and also the nature and structure of the domain wall. The Bloch wall [6] is wrong . As consequence, there is no magnetic reversal by curling, which also has to be removed from textbooks [4].
The concept of heat in energy losses has also been discussed recently, and also the nature of the dissipative processes in a hysteresis cycle [5].
The Jiles-Atherton model lacks physical basis [7]. The hysteresis can be interpreted geometrically, as discussed recently [7]. The origin of Magnetic Barkhausen Noise has also been clarified recently [8].
Coercivity mechanism in Sm-Co magnets of the 2:17 type were clarified [9], and should be inserted in the textbooks.
SESSION: SolidStateChemistryWedPM1-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Michel Armand; Christophe Coperet; Student Monitors: TBA |
Most large-scale industrial processes rely on heterogeneous catalysts. Among them, supported nanoparticles represent one of the largest classes, for which the desired catalytic performances (activity, selectivity and stability) often relate to specific combination of metals, additives (promoters/poisons) and supports. The complexity of these multicomponent materials often relates to the use of conventional preparation methods in water, associated dissolution/precipitation processes. They thus raise numerous questions on the role of each components, and in particular on the role of specific compositions, interfaces and alloying in driving catalytic properties.
In this context, our group has developed synthetic methodologies to control the generation of active sites thanks to the concept of surface organometallic chemistry (SOMC). SOMC is anchored on molecular principles with the goal to understand the surface chemistry at a molecular level. It typically relies on controlling the density of functional groups like surface OH groups in oxide materials, grafting molecular precursor to generate isolated metal sites, following in many instances by a thermal treatment that removes the remaining ligands. This approach has been very successful in generating so-called single-site catalysts; it has also recently been shown to grow, in a controlled manner, nanoparticles with tailored compositions, small and nanoparticle size distribution, interfaces, and even alloying. Furthermore, these SOMC catalysts are specifically aimable to detailed characterization and operando spectroscopy, hence the possibility to derive structure-activity relationships.[1]
This lecture focuses on showing how SOMC combined with state-of-the-art Operando spectroscopies, in particular based on X-Ray Absorption (XAS) and IR, augmented with computational modelling enable to understand the structure and the dynamics of active sites. The lecture will illustrate in particular how interfaces and/or alloys in nanoparticles are created and how these specific sites/interfaces evolve under reaction conditions and contributes to the catalytic events. This lecture will focus on two specific catalytic processes, namely propane dehydrogenation and CO2 hydrogenation,[2] which are two key industrial processes relevant to current and emerging strategies. Overall, this lecture highlights how interfaces, alloying and dynamics are driving the catalytic performances and how one need to revisit (open) our views on active sites in heterogeneous catalysis.
Fundamental investigations of metal nanolayers and their applications for the oxygen evolution reaction (OER) and ocean wave energy harvesting are presented. First, nonlinear optical laser spectroscopy reveals the number of net-aligned interfacial water molecules and the energetics associated with flipping them as a function of experimental conditions (applied bias, ionic strength, pH). A spectroscopic nonlinear optical autocorrelator approach yields strong signals at wavelengths consistent with high-oxidation states oxo species that are invisible in cyclic voltammetry. Implications for strategies to lower the OER's overpotential are discussed. Second, metal nanolayers are subjected to wave action within a wave tank containing ocean water simulant. Electrical measurements using external resistors yield power curves that exceed 50 microwatts per wave event when a nanolayer deposited on a glass microscope slide is paired with a sacrificial anode. Voltages and currents are large enough to light up a blue light emitting diode with each wave event. The linear dependence of output power and wave height velocity is demonstrated. Implications for sustainable energy harvesting are discussed.
The quest for higher energy density batteries suggests the use of solid electrolytes that can harness the electro-plating and dissolution of reactive metals (Li°, Na°, K°, Mg°, Ca°) as they correspond to the highest capacity possible for the negative electrode. In liquid electrolytes, the reactivity of the organic solvent and the inevitable formation of dendrites have thwarted any effort to operate with these agressive metals. Solid electrolytes offer a safer approach to this problem. Ceramic electrolytes with high conductivity are now known for Li (Argyrodite sulfides, LAGP…) and Na (beta alumina, Nasicon…) but the building of all solid-state batteries stumbles on the loss of contact during operation and the subsequent volume change of the electrodes. Besides, the making of large thin films of the electrolyte is challenging.
Conversely, polymer electrolytes are able to be processed easily in thin films, and with their malleability and adhesiveness, keep a good contact despite the volume changes of the electrodes during operation. Most polymer electrolytes are obtained by dissolution of a low lattice energy salt into a solvating matrix, the most studied being poly(ethylene oxide) — PEO. Other solvating backbones are also known now, in the poly(ester) family with the advantage of being able to operate in contact with high voltage cathodes. As so, with a discrete salt complexed by the polymer, both anions and cations are mobile, which is a handicap, as only cations (Li+, Na+, K+, Mg++, Ca++) are exchanged at the electrode, resulting in concentration polarization. The most recent tendency is thus to tether the anions to the solvating polymer, or make an alloy of a poly(salt) with the solvating host (PEO for instance). The challenge is to design negatively charged moieties with a “handle” to link to the polymer keeping the high delocalization of the charge needed for conductivity. These so-called “single ion conductors” can operate in batteries with the reactive metals with minimal growth of deleterious dendrites.
Polymer electrolytes are presently used in the only commercial solid-state batteries, produced by Blue Solutions® in France and powering busses and cars.
A thorough discussion will be provided on these materials and their inherent electrochemistry.
The search for new high-performance hybrid metal halide phases with exotic structure types and unique functionalities has emerged recently. With the wide selection pool of metal, halide and organic component choices, targeted syntheses and rational design strategies can expedite the advancement and understanding of these materials. We have been working on a series of new metal halide families gearing towards different properties such as photoluminescence, circularly polarized luminescence and second harmonic generation. Highly luminescent systems combine emissive metal centers Mn, Cu or Sb and bulky rigid organic cations/ligands. Another strategy of controlling the symmetry is through the directional coordination via organic cationic ligands, where asymmetry arises with the complexity of bimetallic halides and cationic ligands. Neutral solvent ligands are used to trap hydroscopic rare earth metals and incorporate them into the bimetallic low-dimensional systems with group V metals. We have successfully demonstrated several new metal halide material systems with tunable and superior optoelectronic properties.
SESSION: SolidStateChemistryWedPM2-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Myung-Gil Kim; Yihui He; Student Monitors: TBA |
The well-known narrow and intense optical absorption J-band arises as a result of J-aggregation of polymethine dyes in their aqueous solutions. The J-band was discovered experimentally by Jelley and independently Scheibe in 1936. In 1938, Franck and Teller gave a theoretical explanation of the J-band based on the Frenkel exciton model. Subsequently, this explanation was developed in details by many authors. A drawback of this explanation is its inability to explain the shape of optical bands of polymethine dye monomers from which J-aggregates are formed. We give an explanation of the J-band in the framework of a new theory, quantum–classical mechanics [1–3], which includes an explanation of the shape of the bands of polymethine monomers. In quantum–classical mechanics the initial and final states of the “electron+nuclear environment” system for its “quantum” transitions are quantum in the adiabatic approximation, and the transient chaotic electron-nuclear(-vibrational) state due to chaos is classical. This chaos is called dozy chaos. The new explanation of the J-band is based on the so-called Egorov nano-resonance discovered in quantum–classical mechanics [4]. Egorov nano-resonance is a resonance between movements of the electron and the reorganization of the environmental nuclei during quantum–classical transitions in the optical chromophore under weak dozy chaos. In addition to explaining the nature of the J-band of J-aggregates, an explanation is given for the shift of the Egorov nano-resonance observed in polymethine dyes to the long-wavelength region with decreasing polarity of the solvent [5], the shape of the optical absorption bands of their dimers, H- and H*-aggregates [5], the shape of the optical absorption and luminescence bands of J-aggregates in Langmuir films [6], as well as an anomalously small Stokes shift of the J-bands of luminescence and absorption [6]. An explanation is given for the experimentally observed strong parasitic violation of the Egorov nano-resonance during the transition from one-photon to two-photon absorption, and the conditions for its restoration are predicted [7]. The idea of creating “living materials” is put forward, and a method for its practical implementation is indicated by purposefully complicating the design of molecular systems, the heuristic source of which can be the high dynamic organization of quantum-classical transitions in J-aggregates [8].
Halide perovskite semiconductors for direct X- and gamma-ray detection have currently attracted enormous attention for medical imaging and nuclear nonproliferation in homeland security, featuring excellent charge transport properties and low cost. As previously evidenced the hole carriers in perovskite semiconductors have better transport properties than electrons carriers. The unipolar sensing strategy could eliminate such challenge induced by the electron trapping issue. However, the development of unipolar detectors for perovskite semiconductors is still at an early stage where substantial efforts are requested for the device optimization. Here, our progress on the unipolar perovskite detectors were reported with the configuration of pixelated and virtual Frisch grid type aiming at their deployment for the high energy resolution gamma-ray spectroscopy. The influence of guard ring electrode on the dark reduction was also investigated. The thickness of single-crystal detectors varied from ~several mm to centimeters which were grown by melt method. The relationship of the carrier drift time and the signal amplitude in various detector configurations were analyzed to estimate the charge transport properties of the whole carrier. The energy resolution was determined based on the signal amplitude analysis. The issues in achieving high energy resolution by unipolar perovskite semiconductors were also analyzed. These results shall be of interest in the applications of high-performance room temperature gamma-ray detectors.
Chalcogenide aerogels (chalcogels) are typically synthesized with thiolysis, aggregration of nanoparticles, and metathesis of chalcometallate. Especially, the metathesis of chalcometallate enabled generalized synthesis of chalcogel with flexible choice of central metal cations and chalcometallate. Although recent developments of chalcogel achieved high surface area and unconventional surface functionality with chalcogenide, chalcogels are amorphous structures with lack of localized structural control, which hinder further tuning of pore structure, crystallinity and surface functionality. We have investigated local structure of thiostannate and thiomolybdate chalcogels. In addition to metathesis reaction, the kinetic control of chalcogel formation enables additional reaction pathways, such as condensation with coordination transformation and crystallization. The precise local structure control of thiomolybdate chalcogel enabled high performance electrocatalyst for hydrogen evolution reaction.[1] Furthermore, the coordination transformation of thiostannate enabled new synthetic route and local structure control of chalcogel.[2] For high performance aqueous radionuclide-adsorption, the well-defined crystalline Na-Mn-Sn-S chalcogel enabled efficient Cs+ and Sr2+ ion exchange reactions.[3]
Materials informatics utilizes data to establish relationships between the structures and properties of materials, enabling the exploration of the vastness of the materials space through the use of models. Trained on diverse datasets, the generative models can unlock the potential for predicting novel materials with tailored properties. However, while the key advantage of generative models is a potential to produce novel materials, often times they may be “too novel” and cannot be synthesized. In order to minimize the time and resources for experimental synthesis attempts, models that can predict the synthesizability (and, if synthesizable, synthesis recipes as well) would be immensely helpful. Thus, in this talk, I will delve into two important aspects of materials design: generation and synthesis prediction based on data and machine learning. I will also present the results of using large language models (LLMs) as strong baseline for synthesizability predictions and precursor selection problems. LLMs can also offer explanations for why certain materials are predicted as synthesizable while othere as unsynthesizable.
SESSION: SolidStateChemistryWedPM3-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Ariadni A | |
Session Chairs: In Chung; Pantelis Trikalitis; Student Monitors: TBA |
The introduction of foreign atoms or vacancies into crystal matrices forms atomic-level defects, giving rise to unique defect structures influenced by their coordination preferences and sizes relative to constituent atoms in the matrix. These defects can evolve into more complex structures like one-dimensional dislocations or nanostructures, each interacting uniquely with charge carriers and phonons, thereby significantly impacting the transport properties of bulk solids. Consequently, understanding the formation mechanisms of these defects is essential for developing highly predictable design principles and stabilizing desired defect structures within bulk crystals.
In this presentation, I will discuss our recent research on the deliberate design of multiscale defect structures across various types of crystal lattices. These structures enable independent control over crucial physical parameters that determine the thermoelectric figure of merit (ZT), such as carrier mobility, concentration, electrical conductivity, and Seebeck coefficient. Through this approach, we explore unconventional pathways to enhance ZT, promising significant advancements in thermoelectric materials.
The chemistry of metal organic frameworks (MOFs) continues to expand rapidly providing materials with diverse structures and properties. The reticular chemistry approach, where well defined structural building blocks are combined together forming crystalline open framework solids, has greatly accelerated the discovery of new and important materials. However, its full potential toward the rational design of MOFs relies on the availability of highly connected building blocks because these are greatly reducing the number of possible structures. Towards this, building blocks with connectivity greater than twelve are highly desirable but extremely rare. We report here the discovery of novel 18-connected, trigonal prismatic, ternary building blocks (tbb) and their assembly into unique MOFs, denoted as Fe-tbb-MOF-x (x: 1, 2, 3) with hierarchical micro- and mesoporosity.1 The remarkable tbb is an 18-c super-trigonal prism, with three points of extension at each corner, consisting of triangular (3-c) and rectangular (4-c) carboxylate-based organic linkers and trigonal prismatic [Fe3(μ3-Ο)(-COO)6]+ clusters. The tbb’s are linked together by an 18-c cluster made of 4-c ligands and a crystallographically distinct Fe3(μ3-Ο) trimer, forming overall a 3-D (3,4,4,6,6)-c five nodal net. The hierarchical, highly porous nature of Fe-tbb-MOF-x (x: 1, 2, 3) was confirmed by recording detailed sorption isotherms of Ar, CH4 and CO2 at 87, 112 and 195 K respectively, revealing an ultrahigh BET area (4263 - 4847 m2 g-1) and pore volume (1.95 - 2.29 cm3 g-1). Because of the observed ultrahigh porosities, the H2 and CH4 storage properties of Fe-tbb-MOF-x were investigated, revealing well-balanced high gravimetric and volumetric deliverable capacities for cryo-adsorptive H2 storage (11.6 wt%/41.4 g L-1, 77 K/100 bar – 160 K/5 bar), as well as CH4 storage at near ambient temperatures (367 mg g-1/160 cm3(STP)cm-3, 5-100 bar at 298 K), placing these materials among the top performing MOFs. The present work opens new directions to apply reticular chemistry for the construction of novel MOFs with tunable porosities, based on contracted or expanded tbb analogues.
Understanding the band-edge electronic structure and charge-transfer dynamics in size-confined nanostructures is critical for developing advanced materials used in energy conversion applications, such as green hydrogen production, organic pollutant decomposition and solar cells. [1] In this study, we present a series of high-surface-area mesoporous materials comprising continuous networks of interconnected zinc indium sulfide (ZnIn2S4) nanocrystals with tunable diameters (ranging from ~4 to ~12 nm). [2] This development enables a detailed investigation of size-dependent effects on charge-transfer dynamics and photochemical performance within these nanostructures. Using a combination of spectroscopic and (photo)electrochemical techniques as well as theoretical calculations, we elucidated the influence of nanocrystal size on the electronic structure, including band-edge positions, charge density profiles and charge-transfer kinetics. The results show that reducing the size of ZnIn2S4 nanocrystals enhances interfacial charge-transfer kinetics and charge separation rates, improving the ability of photogenerated carriers to drive water-splitting reactions. [3] Consequently, the photocatalytic H2 evolution activity of these materials is among the highest reported for single-component sulfide photocatalysts. However, for ultrasmall nanocrystals, charge transfer and separation kinetics reveal that surface sulfur vacancies, which generate mid-gap states at the interface, are significant contributors to reduced photocurrent and photocatalytic performance.
These findings offer valuable insights for the rational design of semiconductor nanostructures through synthetic engineering, aiming at the development of high-performance catalysts for zero-carbon energy applications.
On the exciting frontier of nanomaterials, we stand on the brink of a revolution. Our journey into the microscopic realm has led us to the discovery and creation of nanoscale structures, with nanowires taking center stage. These nanoscopic wonders, with their superior surface-to-volume ratio and novel properties due to their small size, are poised to reshape the energy-harvesting landscape to power IoT devices by increasing diffusive phonon scattering which decreases the heat conductivity above the amorphous limit.
Our work with Bi2Te3, crafted meticulously within anodic aluminum oxide (AAO) templates, has given birth to structures whose optical response is governed by plasmon resonances. These resonances, a product of nanowire interactions and material properties, can be harnessed to amplify thermal gradients and their associated thermoelectric power, thanks to the thermoelectric properties of Bi2Te3 nanowires.
Simultaneously, we are shining a spotlight on passive radiative cooling technology, a game-changer with the potential to revolutionize cooling methods for buildings and devices. This technology, a powerful tool in reducing carbon footprint and energy consumption, capitalizes on the morphological properties and chemical structure of AAO–Al samples to significantly alter their optical properties and cooling performance. The prowess of AAO nanostructures in thermal management applications has been demonstrated through a significant temperature reduction achieved with an AAO–Al sample.
Our exploration into the resistance of 3D-Bi2Te3 nanowire nanonetworks at low temperatures has yielded results compatible with the Anderson model for localization. The observed localization effects could potentially enhance the Seebeck coefficient in the 3D-Bi2Te3 nanowire nanonetwork compared to individual nanowires. This is particularly relevant as everyday life heavily relies on electricity, necessitating continual study to enhance power generation. Thermoelectric generators (TEGs), which use the Seebeck effect to convert waste energy into electrical energy, are a well-known method of generating electricity. The current state of TEGs, including different geometries and associated issues, as well as new TEG technologies and their challenges, have been analyzed.
Finally, in the case of triboelectric nanogenerators (TENGs), the new kids on the block, offer efficient mechanical energy harvesting through the triboelectric effect and electrostatic induction. Our research into the influence of 3D nanocavities inside polylactic acid (PLA) films on triboelectric power generation has revealed a correlation between the nanocavities and the relative permittivity of the polymer. The combination of 3D-PLA and 3D-AAO yields a fully dielectric composite film that drives power density due to an increase in the relative permittivity of the thin surface layer of the composite. The energy-storing efficiency of the developed PLA films was also studied. This work offers insight into how to use 3D nanocavities to enhance TENG performance and the useful blending of appropriate dielectric proprieties promoting self-power and intelligence of flexible electronic materials.
In conclusion, the future of energy harvesting for IoT devices is being empowered by advancements in nanomaterials. The exploration of nanoscale structures, passive radiative cooling technology, and the development of TENGs and TEGs are paving the way for more efficient and sustainable energy solutions.
SESSION: SolidStateChemistryWedPM4-R7 |
Kanatzidis International Symposium (4th Intl. Symp. on Materials/Solid State Chemistry and Nanoscience for Sustainable Development) |
Wed. 23 Oct. 2024 / Room: Ariadni A | |
Session Chairs: Pantelis Trikalitis; Gerasimos S. Armatas; Student Monitors: TBA |
Chiral metal-halide semiconductors (MHS) have recently developed as promising candidates for spin- and polarization-resolved optoelectronic devices. Although several chiral MHS with rich chemical and structural diversity have been reported lately, the fundamental mechanisms governing their chiroptical activity, namely, circularly polarized absorption and emission, remain elusive. In this talk, I will discuss our recent progress in understanding and tuning the chiroptical activity in chiral MHS. I will first discuss how the chirality is transferred from organic to inorganic component through asymmetric covalent bonding interactions. Their endowed molecular chirality was then studied by circular dichroism (CD). However, we found that the previously reported “apparent” CD in chiral MHS thin films is not an intrinsic chiroptical property, but rather, arising from an interference between the film’s linear birefringence and linear dichroism. We verify the presence of LB and LD effects in both one-dimensional and zero-dimensional chiral MHS thin films. We then establish spectroscopic methods to decouple the genuine CD from other spurious contributions, which allows a quantitative comparison of the intrinsic chiroptical activity across different chiral MHS. The relationship between the structure and the genuine chiroptical activity is then uncovered, which is well described by the chirality-induced spin–orbit coupling in the chiral structures. Meanwhile, we found that high CD signals do not necessarily lead to high circularly polarized luminescence as most of the current chiral MHS display very low photoluminescence quantum yields (PLQY). We will then discuss the reasons of low PLQY in these materials. Finally, we will show our strategies to turn on and amplify the circularly polarized luminescence in chiral MHS.
We had found it being somewhat surprising that, in the following sequence of “simple” perovskites: PbTiO3 is tetragonal (c/a = 1.064), PbVO3 is also tetragonal with quite a higher tetragonal ratio (c/a =1,229) while PbCrO3 is cubic (¡) [1]. A detailed structural and compositional analysis by X ray and electron diffraction and high-resolution electron microscopy coupled with EDS, of this High-Pressure phase, has shown that the reliability factors of the Rietveld X-ray powder refinement of PbCrO3 could be improved by considering the lead ion in a multi- minimum potential displaced from its special position. Also, the microstructure of this material is a rather complex perovskite superstructure that presents a compositional modulation, within a microdomain distribution in a slightly lead deficient material [2]. The proposed supercell is ~ap x 3ap x (~14-18)ap; with ap being the average cubic perovskite parameter [3].
SESSION: AdvancedMaterialsWedPM1-R8 |
8th Intl Symposium on New & Advanced Materials and Technologies for Energy, Environment, Health and Sustainable Development |
Wed. 23 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Fernand D. S. Marquis; Brajadulal Chattopadhyay; Student Monitors: TBA |
In the electrodynamic properties study of new AlN- 5wt.%C(diamond powder)-5wt.%Mo composite materials the values and behavior of the real and imaginary parts of the microwave permittivity were determined and the optimal technological process for materials synthesis was established. The materials with density 3.16 g/cm3 and 3.30 g/cm3 were obtained by the pressureless sintering (PS) at the temperature of 1850 °C and by the hot pressing (HP) at the temperature of 1820 °C (pressure of 15 MPa), respectively.
The microstructure and phase composition of the composite materials were studied using a scanning electron microscope and the X-ray diffractometer Ultima IV (Rigaku, Japan) with the Rietveld method for data analysis. The imaginary and real parts of the permittivity were measured by the microwave vector network analyzer Keysight PNA N5227A in the frequency range of 26 - 40 GHz.
The results of structural studies showed that sintering of composites by different methods results in almost unchanged their phase composition, and the main phases are AlN, Al3(O,N)4, Mo2C, Y3Al5O12, and C (graphite) - as in [1].
It was determined that the real part of the permittivity (ε') for both composites obtained by the PS and HP methods is practically frequency independent between 26 to 36 GHz with the value of about 8 and 27 , respectively. At the same time, the imaginary part of the permittivity (ε″) increases from 0.29 to 1 and from 3.46 to 5.56 for materials made by the PS and HP methods, respectively. When the test frequency is increased from 36 to 40 GHz, significant fluctuations in the permittivity values are observed, which is possibly related to the greater intensity of electromagnetic wave internal reflections due to the peculiarities of the formation of the materials structure.
As a result of the research, it was established that composite materials obtained by the hot pressing method are characterized by higher density and higher values of the real part of the permittivity in the frequency range 26 - 36 GHz.
To enhance the lifetime of mechanical system such as automobile, new reliability methodology – parametric Accelerated Life Testing (ALT) – suggests to produce the reliability quantitative (RQ) specifications—mission cycle—for identifying the design defects and modifying them. It incorporates: (1) a parametric ALT plan formed on system BX lifetime that will be X percent of the cumulated failure, (2) a load examination for ALT, (3) a customized parametric ALTs with the design alternatives, and (4) an assessment if the system design(s) fulfil the objective BX lifetime [1]. So, we suggest a BX life concept, quantum-transported life-stress (LS) model with a new effort idea, accelerated factor, and sample size equation. This new parametric ALT should help an engineer to discover the missing design parameters of the mechanical system influencing reliability in the design process. As the improper designs are experimentally identified, the mechanical system can recognize the reliability as computed by the growth in lifetime, LB, and the decrease in failure rate. Consequently, companies can escape recalls due to the product failures from the marketplace. As an experiment instance, two cases were investigated: 1) problematic reciprocating compressors in the French-door refrigerators returned from the marketplace and 2) the redesign of hinge kit system (HKS) in a domestic refrigerator. After a customized parametric ALT, the mechanical systems such as compressor and HKS with design alternatives were anticipated to fulfil the lifetime – B1 life 10 year.
Microbiologically incorporated cementitious materials to recuperate the activities and toughness of the concrete structures are a new aspect of research work in the current era. The uses of different chemicals and additive in concrete composites sometimes cause health problems which are environmentally unacceptable. In this study we have designed an eco-friendly bio-engineered with high strength and more durable concrete/geopolymer material by incorporating hot spring bacteria. A novel thermos-stable and high pH tolerant silica leaching protein ((M.W. ~ 28KDa) originally isolated from one of the hot spring’s bacteria BKH2 of Bakreshwar, West Bengal [1, 2] has been observed for responsible for production of high-performance structural materials. The corresponding gene of the protein has been identified and cloned into B. subtilis bacterial strain to develop an eco-friendly microbial agent [2, 3]. The transformed bacterial cells, when incorporated to the cement-sand mixture and or fly ash mixed cement-sand mixture, develop a sustainable and energy efficient material, which is useful for construction purposes [3, 4]. Improvement of compressive strength (> 30 – 40%), ultrasonic pulse velocity, sulphate and chloride ions resistant and decrement of water absorption capacity are noted in the bacteria amended mortar/concrete/geopolymer specimens. Micro-structural analyses confirmed the formation of a novel Gehlenite (Ca2Al2SiO7) phase besides calcite deposition inside the matrices of the transformed bacteria-amended cementitious materials [3-5]. This development significantly increases the true self-healing property and aims towards the production of green cement-alternative by using cent-percent fly ash which is sustainable for a prolonged period [5]. This implies lesser requirements of cement and lowers the cost of construction. This study demonstrates a new approach towards the development of Green Home technology by reducing Green House effect of cement production.
Low carbon emissions are perceived as the main target and direction in the global development. It is therefore of importance to explore new energy conversion technologies, to efficiently take advantage of the available green energy resources. Solid Oxide Cells (SOCs) are considered as one of the most promising options, since depending on the demand, they can provide both hydrogen and electricity generation in the same device. In SOCs, the main decisive factor for the efficiency is performance of the oxygen electrode, of which cobalt-containing perovskite-type materials are usually utilized due to their extraordinary electrocatalytic properties at lowered operation temperatures (500-800 °C) [1]. Meanwhile, given that the new concept of the high entropy oxides is proved to be very successful in materials science, it is of great interest to develop and study novel, multicomponent perovskites as candidate oxygen electrode materials. In fact, initial data showed promising performance, with a possibility to limit Co content [2]. Apart from the chemical content optimization, morphology of the oxygen electrode can be also enhanced, which is undoubtedly crucial to influence the oxygen reduction/evolution reaction mechanism. This can be potentially realized by the electrospinning technique, bringing new possibilities for improving the oxygen electrodes.
Taking all those concerns mentioned above into account, in this work, perovskite-type materials with varied substitution, La0.6Sr0.4Ni0.15Mn0.15Fe0.15CuyCo0.55-yO3-δ (y = 0.05-0.20) were synthesized and characterized systematically. X-ray diffraction results confirmed that all compounds are well-crystallized, without any impurities observed, and exhibit rhombohedral symmetry (R-3c). Their structures are stable at high temperatures, up to 900 °C. Only slight variations of the oxygen content with temperature were measured, suggesting mild thermal expansion behavior. High total electrical conductivity was observed for all compounds, above 200 S cm-1, and interestingly, a negative Seebeck coefficient was detected, suggesting that the main charge carriers are electrons (polarons). The electrochemical characterization in symmetrical cells (based on GDC solid electrolyte) showed an increased catalytic activity with the increasing Co content. However, even the relatively low Co content La0.6Sr0.4Ni0.15Mn0.15Fe0.15Cu0.20Co0.35O3-δ electrode demonstrated a desired, low polarization resistance value of only 0.018 Ω cm2 at 850 °C. This could be further enhanced by over 20%, if the material was obtained by the electrospinning. The excellent performance was also proved in the full cell measurements, in which a peak power density over 1.0 W cm-2 was reached at 850 °C, as well as a promising performance was measured in the electrolysis mode.
SESSION: AdvancedMaterialsWedPM2-R8 |
8th Intl Symposium on New & Advanced Materials and Technologies for Energy, Environment, Health and Sustainable Development |
Wed. 23 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Tetiana Prikhna; Fernand D. S. Marquis; Student Monitors: TBA |
REBCO (Re=Y, Eu, Gd) coated conductors (CC) based on biaxially textured, thick and homogeneous nanoengineered multilayer structures opened up new application opportunities, such as dissipation-free energy transmission in superconducting grids, highly efficient engines for electrical aviation or compact fusion reactors beyond ITER. However, current carrying capacities of CC could be further improved because they are still far from theoretical limits. As it has been shown, one of the possible robust ways to increase current carrying capacity of CC is overdoping with oxygen the REBCO structure of CC.
Treatment of GdBCO_CC under 100 bar of O2 at 600 °C for 3 h led to an increase in Jc (77K, 0 T) by 6% and a decrease in the c-parameter of Gd123 to 1.17310 nm, which may be associated not only with overdoping with oxygen, but also with silver diffusion into Gd123. No correlation was observed between Jc, Tc, c-parameter of RE123 (RE=Eu, Gd) and carrier density nH of EuBCO_CC and GdBCO_CC treated at 300-800 oC, 1-160 bar O2 for 3-12 h.
We have started investigating high oxygen pressure treatments of GdBCO and EuBCO-BHO Coated Conductors previously oxygenated with standard treatments. For our experiments we used commercially produced GdBCO and EuBCO-BHO coated conductors provided by Fujikura. The CC samples have been previously oxygenated with their standard process. For the high oxygen pressure post-treatment, GdBCO and EuBCO-BHO coated conductors with 2 mm Ag layer on the surface of GdBCO CC and without and with Ag layer on the surface of EuBCO-BHO CC were used. Therefore, before experiments the upper Cu layer (and in some cases the Ag layer) was chemically removed from CCs tapes. In the case of EuBCO-BHO_CCs the Ag upper layer was removed chemically as well, but for some experiments it was preserved as indicated. The architecture (from top) of the studied CCs was as follows: (1) FYSC : Ag (2μm)/ GdBCO (1.8μm)/ CeO2 (700 nm)/ MgO/ / Al2O3/Y2O3 /Hastelloy (75 μm); (2) FESC : EuBCO (2.5μm)+BHO Nanorods/ CeO2 (700 nm)/ /MgO/ Al2O3/Y2O3 / Hastelloy (50 μm); (3) Ag (2μm)/ EuBCO (2.5μm)+BHO Nanorods/ CeO2 (700 nm)MgO/ / Al2O3/Y2O3/ Hastelloy (50 μm).
A specially designed tube furnace was used for the oxygenation process. The oxygen pressure in the furnace varied from 1 to 160 bar, the temperature from 300 to 800 °C, and the heating rate was 5 ºC/min. After, a dwell of temperature for a certain time held at the required pressure was attained, and afterwards the heater was turned off.
Results on critical current density, superconducting transition temperature, charge carrier densities, c-lattice parameter and Auger, indicate that high oxygen pressures of 100 and 160 bar can be sustained by these materials when high temperatures are used and that this can be a route to overdope these Coated Conductors. Furthermore, we evidence that these post oxygen treatements should be done without Ag etching so that the REBCO material is not exposed to air during the high pressure treatments. Futher work is on-going to obtain the best conditions to increase the charge carrier concentration and consequently the criticial current density in a robust way.
AcknowledgementS: We acknowledge funds from MUGSUP, UCRAN20088 project from CSIC programme from the scientific cooperation with Ukraine, the Spanish Ministry of Science and Innovation and the European Regional Development Fund, MCIU/AEI/FEDER for SUPERENERTECH (PID2021-127297OB-C21), FUNFUTURE “Severo Ochoa” Program for Centers of Excellence in R&D (CEX2019-000917-S), and HTS-JOINTS (PDC2022-133208-I00), NAS of Ukraine Project III-7-24 (0788) Authors also thanks Fujikura for supplying the samples
Materials for new energy applications have recently attracted a number of research interests due to concerns about the depletion of fossil fuels and the construction of sustainable societies. In particular, lithium and sodium ion batteries (LIBs and NIBs) with higher energy density are essential for next generation energy storage devices such as electric vehicles, hybrid electric vehicles and smart grids. A large proportion of the components of these devices are generally inorganic materials in crystalline form. Since the crystal shape, outer plane, size and crystallinity drastically affect the above properties, it is necessary to control these properties simultaneously. Nowadays, all solid-state LIBs and NIBs have attracted much interest due to a number of potential advantages, including energy densities, cost, size, safety and operating temperature. However, there are still serious problems to be solved before practical use. For example, the diffusion of lithium and sodium ions at the interface between different solid materials, including active materials and electrolytes, is still poor for charge/discharge operation in batteries.
In this context, our group has been investigating "nature-mimetic flux growth" of inorganic crystals for these applications. Flux growth is a type of liquid phase crystal growth technique in which molten metals and molten metal salts are used. Fluxes act as solvents at temperatures above their melting and/or eutectic points. As the growth conditions of inorganic crystals are similar to those found in the Earth's crust, we call it "nature-mimetic". Flux grown crystals are characterised by high quality without thermal stress, idiomorphic shape with specific crystal planes and controlled shape and size.
Recently, with the aim of achieving all-crystalline (solid state) LIBs and NIBs, we have applied the flux method to battery materials. We expected that flux crystal growth would allow (I) crystal shape control of active and solid electrolyte materials, (II) construction of good interfaces in electrodes between cathodes, solid electrolytes and anodes. The second theme would be possible if electrode materials could be dissolved and densely recrystallized on their surfaces. As a result, smooth ion transport through bulk materials and their interfaces would be realized in all-crystalline (solid) state LIBs and NIBs. Our concept using the flux method would provide a new aspect to lead an innovation in all solid state LIBs and NIBs. Details of the research progress will be presented at SIPS2024.
Acknowledgement This research was partially supported by Council for Science, Technology and Innovation (CSTI), Cross-ministerial Strategic Innovation Promotion Program (SIP), the 3rd period of SIP, JST-GteX, Aichi Grant and JSPS Grant-in-Aid for Scientific Research (KAKENHI).
Today, Li-ion batteries play a vital role as energy storage devices, dominating both, the market for portable electronic products, and the electric vehicles (EV) sector. The burgeoning EV market is pushing for greater cruising ranges, which necessitates the development of novel, high-energy density cathodes and anodes. In terms of cathode materials, there are currently two noteworthy approaches. One involves further development of Ni-rich layered oxides, with Ni content above 0.9 [1], while the other one focuses on Li- and Mn-rich oxides, which possess specific structural properties [2]. Both groups of materials hold promise for significant advancements in constructing high-capacity and high-power density cells, thanks to their very high reversible discharge capacity (> 200 mAh g-1), high operating voltage (~3.7 V vs. Li/Li+), and relatively low costs. However, these oxides still face severe issues, including surface sensitivity, structural problems such as Li/Ni mixing effects, and inadequate thermal stability, which limit their practical application. Of particular concern is the presence of lithium residuals like LiOH/Li2CO3 in the active material, stemming from the synthesis process. Concerning the anode, a particularly interesting direction is combining conversion and alloying reaction mechanisms within a single compound (so called conversion-alloying materials, CAMs) [3]. However, CAMs still suffer from insufficient cycling stability and the only solution proposed in the literature so far is to employ advanced synthesis methods and additives, which are often expensive and difficult to scale. Conversely, the recently discovered high-entropy oxides (HEOs) show excellent cyclability when used as anodes in Li-ion cells, regardless of the synthesis method and resulting particle size.
Combining the above concepts, in this study we synthesized and systematically characterized selected Ni-rich LiNi0.905Co0.043Al0.052O2 (NCA905) and Li- and Mn-rich Li1.2Ni0.13Mn0.54Co0.13O2 (NMC135413) cathode materials. Cathode layers were then obtained, with high active material loadings of ca. 6 mg cm-2. Both types of cathodes were assembled initially alongside standard graphite anode, and also with the novel high-entropy Sn0.8(Co0.2Mg0.2Mn0.2Ni0.2Zn0.2)2.2O4-based anode. Various issues related to combining those electrodes into full cells were studied, including the selection of negative/positive ratio, electrode prelithiation process, and electrolyte additives. The resultant optimized full cells exhibited very good electrochemical performance. For example, the NMC135413@Graphite anode full cell delivered an initial discharge capacity of more than 186 mAh g-1 at 0.5 C current density (cathode limited), and a very high energy density of 370 Wh kg-1. A capacity retention of 80% was measured after 400 cycles, indicating very promising electrochemical characteristics.
The development of acetone gas sensors for self-diagnostic and health monitoring applications has garnered significant interest in recent years [1]. Accurate sensing of acetone levels is crucial for the noninvasive diagnosis of diabetes [2]. In healthy individuals, the acetone content in the respiratory system ranges from 0.3 to 0.9 ppm, whereas individuals with diabetes exhibit acetone concentrations exceeding 1.8 ppm [3]. Among various non-invasive diagnostic techniques, chemical sensors based on semiconductor oxides have gained popularity due to their small size, low power consumption, and ease of manufacture [5–7].
SnO2-based sensors, in particular, have been extensively researched for detecting various gases [8,9], However, achieving high sensitivity and selectivity towards trace amounts of acetone in breath remains a significant challenge. The SILAR method involves a heterogeneous interaction between the solid phase and solvated ions in the solution, creating thin films by alternately immersing the substrate into solutions containing cations and anions, followed by washing after each reaction [10].
In this study, we synthesized Fe-doped SnO2 nanoparticles using the SILAR method to develop a selective acetone gas sensor and investigate its sensing behavior under various conditions. Uniform conditions of 100 ppm gases and 175°C were employed for all gas selectivity assessments, demonstrating the feasibility of using Fe-doped SnO2 as a sensor for detecting volatile organic compounds, particularly acetone. The 0.5 mol.% Fe-doped SnO2 exhibited high response and selectivity to acetone, with a fast recovery time of approximately 20 seconds. These findings suggest that Fe-doped SnO2 sensors synthesized via the SILAR method show high selectivity to acetone vapor in an air atmosphere and rapid recovery time. Thus, doping SnO2 with Fe ions presents a promising approach for developing high-performance gas sensors selective to acetone.
SESSION: AdvancedMaterialsWedPM3-R8 |
8th Intl Symposium on New & Advanced Materials and Technologies for Energy, Environment, Health and Sustainable Development |
Wed. 23 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Sanjeev Khanna; Ali Sajid; Student Monitors: TBA |
Nano-technology delivers numerous products such as nano-ZnO, nano alumina, and nano silica, etc. to deal with corrosion in a cost-effective manner. Similarly, to address the biofouling in the aquatic environment, hybrid nanocomposites of organic-inorganic materials, photocatalytic nanomaterials, metal and metal oxide nanomaterials (nanoparticles, nanowires, nanorods), etc. are employed as viable agents to create non-toxic or low-toxic antifouling coatings. On the other hand, membrane separation technology plays a pivotal role in various industries including water treatment plants, food, medicine, pharmacy, biotechnology, etc. in addition to the domestic arena for the purification of drinking water. Such a wonderful technology is being totally disturbed by a troublesome problem and a predominant barrier called membrane fouling, which drastically limits the commercialization of the membranes and the whole membrane industrial technology as well. Hence, my keynote talk exclusively throws light on the role of nanomaterials and nanotechnologies developed for the prevention of fouling that occurs on submerged structures and membranes as well and possible solutions with increased resilience against challenges to come.
Arsenic contamination of groundwater and soil remains a significant global health concern, affecting millions of people worldwide. The primary source of arsenic exposure is contaminated drinking water, with inorganic arsenic being the most toxic form. Recent research has highlighted the long-term health effects of chronic arsenic exposure, including increased risks of cancer, cardiovascular diseases, and metabolic disorders such as diabetes. Current trends in arsenic research focus on understanding the mechanisms of toxicity, differential susceptibility, and the development of effective remediation strategies. Epigenetic alterations, omics analyses, and the study of arsenic metabolism have emerged as key areas of investigation. Notably, even low-to-moderate levels of arsenic exposure have been associated with adverse health outcomes, suggesting that current guidelines for maximum permissible limits may need reevaluation. Nano-remediation strategies have gained significant attention as promising solutions for arsenic contamination. These approaches leverage the unique properties of nanomaterials, such as high surface area and reactivity, to effectively remove arsenic from water and soil. Common nano-remediation techniques include the use of iron-based nanoparticles, carbon nanotubes, and metal oxide nanocomposites. These materials can adsorb, reduce, or oxidize arsenic species, facilitating their removal from contaminated media. Recent advancements in nano-remediation have focused on improving the efficiency, selectivity, and sustainability of these technologies. Researchers are developing novel nanocomposites with enhanced arsenic removal capacity, exploring green synthesis methods for nanoparticles, and investigating the potential of biogenic nanomaterials. Additionally, efforts are being made to address challenges associated with the scalability and environmental impact of nano-remediation techniques. In conclusion, while arsenic toxicity remains a significant public health issue, ongoing research into its sources, health effects, and remediation strategies offers promising avenues for mitigation. Nano-remediation technologies show great potential for effective arsenic removal, though further research is needed to optimize their performance and ensure their safe implementation in real-world settings.
Carbon fiber microelectrodes (CFMEs) have been used to detect neurotransmitters and other biomolecules using fast-scan cyclic voltammetry (FSCV) for the past few decades. Here, we measure neuropeptides such as Neuropeptide Y and Oxytocin, a pleiotropic peptide hormones that are important for social behavior. These neuropeptides function as anti-inflammatory agents and serves as antioxidants with protective effects during trauma. Since oxytocin and Neuropeptide Y contain tyrosine, a modified sawhorse waveform was also used to detect these neuropeptides. Additionally, we demonstrate that applying the MSW on CFMEs allows for real time measurements of exogenously applied neuropeptides on rat brain slices. These results may serve as novel assays for neuropeptide detection in a fast, sub-second timescale with possible implications for in vivo measurements and further understanding of the physiological role of these neuropeptides.
We also developed enzyme modified microelectrodes for the measurement of glutamate, which is an important excitatory amino acids and biomarker for epilepsy along with the inhibitory GABA. Since glutamate is not redox active at carbon electrodes, we modified CFMEs with glutamate oxidase enzyme to metabolize glutamate to hydrogen peroxide and alpha-ketoglurarate, which was then oxidized at carbon electrodes. The enzyme coating was optimized by varying the concentration of enzyme, chitosan binder, solvent, and deposition time. The coating was further analyzed electrochemically and imaged with scanning electron microscopy (SEM) for thickness and uniformity of surface coverages. Glutamate oxidation was found to be adsorption controlled to CFMEs and characterized at various scan rates, concentrations, and stability times as well with an approximate 100 nM limit of detection. Glutamate was co-detected in complex mixtures with several monoamines such as dopamine, serotonin, and others in addition to future in vitro, ex vivo, and in vivo studies.
SESSION: ManufacturingWedPM4-R8 |
5th Intl. Symp. on Advanced Manufacturing for Sustainable Development |
Wed. 23 Oct. 2024 / Room: Ariadni B | |
Session Chairs: Nathalia Balzana Anacleto; Student Monitors: TBA |
This article intends to demonstrate synchronous in-process control of both external size and internal structure of ball processed particulates by regulation of the power cycle. For this reason, a coupled, nonlinear, computational model of the cycle elements is laid out, modeling joint and crack occurrences influencing the structure of particulates, along plastic distortion of spatial domains in their microstructure. The physics-based structural simulation emphasizes probabilistic representations of impactor collisions, particle assembly and population growth; While a simpler stochastic model of external particle features is based on statistical formulations of impact energetics, friction and plastic deformation effects, as well as bonding and fracture transformations of the particles during the process.
The structural simulation reactions are calibrated and validated against the predictions of the stochastic model, as well as specially designed experiment data. Their real-time monitoring ability allows planning and control of the power cycle, utilizing substitute feedback from the predictions of the model, under a self-tuning regulation controller. This control scheme is tentatively implemented in low-energy planetary ball processing of Al and Ni powders for manufacturing of ignitable reactive bimetallic particulates, and the particle morphology and structureare found in concurrence with electron micrograph observations.
Promoting the transition from the current linear production and consumption model to a green model has become a central issue in the debates on global warming and climate change [1] [2]. The way we design and produce our products directly affects the types and intensities of impacts generated on the environment and, consequently, on the planet [3]. However, with the aim of deliberately creating products with a shorter lifespan than they could have and making consumers purchase new products in short intervals of time, obsolescence has been used by industries as a tool to increase consumption. [ 4]. This problem is particularly noticeable in the smartphone production model. This article intends to carry out a qualitative and quantitative analysis of the current production and consumption model, proposing an analysis of the factors that influence the increase in smartphone consumption, highlighting both the motivating factors and the hindering factors, also intending to identify how such practices can violate several Brazilian laws [5]. To achieve this, research developed a questionnaire via Google Forms, applied to 186 people. The results show that external motivators (such as marketing incentives and social stimuli), internal motivators (self-actualization), external impediments (economic barriers) and internal impediments (barriers of mental awareness and perception of real need) were the four determining factors that influenced or prevented new consumption.
SESSION: EnergyWedPM1-R9 |
9th Intl. Symp. on Sustainable Energy Production: Fossil; Renewables; Nuclear; Waste handling, processing, & storage for all energy production technologies; Energy conservation |
Wed. 23 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Harold Dodds; Flora Moon; Student Monitors: TBA |
With artificial intelligence or AI and cryptocurrency mining expanding globally at a phenomenal rate, data centers are expected to double their electricity consumption from 460 terawatt-hours (TWh) in 2022 to more than 1000 TWh in 2026 [1]. Both have significant cooling needs, with 30 to 55% of the electricity powering the cooling systems [2]. Data centers directly use water in the cooling systems to extract heat, and the humidification systems—maintain 40-60% relative humidity to prevent static electricity buildup, bathrooms, and fire sprinkler systems; and indirectly use water from using thermoelectric energy generation.
Each year, the world uses more than 4.3 trillion cubic meters (~1.1 quadrillion gallons) of water; and data centers are among the top ten consumers. In 2022, Google’s data centers alone consumed 4.3 billion gallons of water [3]. There are 7,069 hyperscale data centers in 140 countries [4]. In addition, there are hundred-thousands of data centers globally, and their water consumption adds up to a significant amount. We are in the midst of a global drought and it is not sustainable to continue supporting the data centers water needs. We urgently need to find low-water alternatives to data center cooling methods.
In 2023, the global energy mix comprised 60% fossil fuel contribution from 35% coal (10,434 TWh), 23% natural gas (634 TWh), and 2.7% oil & petroleum products (786 TWh), clean energy from 14% hydro (4,210 TWh), 9.1% nuclear (2,686 TWh), 7.8% wind (2,304 TWh), 5.5% solar (1,631 TWh), 2.4% bioenergy (697 TWh), and 0.3% or 90 TWh other renewables—mostly geothermal generation, with tidal and wave energy providing a small fraction [5].
Per the Food & Water Watch Institute, the water withdrawal intensities (and lifecycle water consumption) to produce 1 MWh of electricity using natural gas, coal, and nuclear, wind, and solar are 45.110 m3 (0.600 m3), 84.413 m3 (1.671 m3), 93.600 m3 (2.000 m3), 0.001 m3 (0.001 m3), and 0.040 m3 (0.020 m3) respectively [6]. According to the United Nations Environment Program, some 1.8 billion people will likely face absolute water scarcity by 2025 [7], and for them, power generation is the fourth priority after water for food production, safe drinking water, and sanitation.
Disregarding the global water crisis, the fossil fuel industry, and nuclear energy continue to expand their energy footprint. Recently, the electric regulatory board in the U.S. State of Georgia approved the construction of 2.4 GW of coal and gas power plants for various utilities [8]. However, there is hope from multiple fronts.
With the rapid expansion of “attribution science” [9] correlating extreme weather to climate change induced by human activity—power generation from nuclear and fossil fuels is facing backlash and litigation for economic and human losses [10].
The United States Congress has recently introduced the “Artificial Intelligence Environmental Impacts Act of 2024” mandating voluntary reporting of energy and water consumption, pollution, and electronic waste associated with the full lifecycle of artificial models and hardware, etc. [11]. This act is likely to pass and many nations will follow suit.
We urgently need an expeditiously deployable—viable clean energy—low water utilization alternative to thermoelectric power generation technology and financiers. Here’s an idea.
Install solar microgrids on the municipal water and wastewater treatment facilities to produce the cheapest clean electricity and green hydrogen; and install geothermal district cooling networks to provide heating, ventilation, and air conditioning or HVAC services. Interconnect multiple solar microgrids and district thermal energy networks to meet the data centers' energy and cooling requirements. The data centers would benefit from highly reliable cheapest clean electricity, a noise-free environment, extended operational life of electronic equipment due to the absence of combustion products from geothermal cooling, and significantly reduced operating expenditures and downtime.
Next is routing the high-quality waste heat from the data centers to chemical manufacturing plants to drive their energy efficiency and reduce energy usage. All chemical reactions occur within a temperature and pressure window, whose maintenance is energy-intensive and a source of GHG emissions. The waste heat from chemical manufacturing plants can be transported back to the municipal water & wastewater treatment facilities to aid in temperature control of wastewater during microbial decomposition of sludge, saving significant energy expenditure for this step. This route will drive energy efficiency, lower operating costs, and minimize GHG emissions at the data centers, chemical manufacturing plants, and municipal water and wastewater treatment facilities. The solar microgrids can also meet the electricity needs of the three entities. We can approach the nuclear and fossil fuel industries to finance these projects as they look to pivot.
Stirling machines have been always extensively studied. NASA has suggested Stirling machines for applications is spacecraft [1].Ford considered the Stirling machines for common passenger cars in early 1970s [2]. Stirling machines have been considered a possibility for moving submarines [3]. Many studies considered Stirling machines in connection with solar power [4]. However, with the reduction of the price of solar panels along the last decade, photovoltaic solar energy became very cheap. At the present time, the cheaper options of energy are onshore wind and photovoltaic solar [5].
Another interesting option is given by Stirling machines: As they work on basis of difference of temperature, by preserving the cold of the night and the heat of day, Stirling machines can be activated, thus producing electricity. This enables the application of Stirling machines in homes. For example, small Stirling machines can be used for charging rechargeable batteries (and cell phones), among other applications.
It is well known that nuclear fusion is regarded as the main driving phenomenon of nucleosynthesis in stars and the source of energy emissions. It is not news any more that nuclear fusion is considered to be a game changer in our quest to achieve sustainable clean energy solution. So far, the main process being experimented is the deuteron-triton reaction resulting in the alphas and neutrons. More recently, the attention is being paid to aneutronic processes such as proton -boron interactions.
In this talk, we examine the processes such as proton-boron, 3He-deuteron reactions which are cleaner in the sense that there are no neutrons nor radioactive residuals in them.
There are interesting theoretical complications regarding the plasma temperatures and the statistical physics. A progress in these aspects will contribute to better models of nuclear astrophysics of stars and also better fusion devices. We will provide an overview of the issues and possible experimental and theoretical investigations.
Li-ion batteries are becoming increasingly prolific to the point that there is concern that there is not enough of the critical elements that are significant fractions of the active material components to support massive changeover in both the transportation and electric grid systems. Thus, research is now focused on new materials that do not require cobalt, nickel, or graphite. These new materials behave quite differently in a cell than their predecessors. They may demonstrate significantly less electronic or ionic conductivity or significantly more expansion and contraction with cycling. These inherent differences of the new materials require differences in material size during their synthesis and differences in the processing resulting in highly functional electrodes. The purpose of this talk is to go over the requirements of the inactives (carbon and binder) and then show how best to combine them and at what ratio to lead to high performing electrodes, with minimal inactives that lead to thick, high-loading electrodes without defects.
SESSION: BatteryWedPM2-R9 |
9th Intl. Symp. on Sustainable Secondary Battery Manufacturing & Recycling |
Wed. 23 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Shailesh Upreti; Fail Sultanov; Mukhammed Kenzhebek; Student Monitors: TBA |
Lithium-sulfur batteries are heralded as the next-generation energy storage systems due to their exceptional theoretical discharge capacity (1675 mAh g-1) and energy density (2600 W h kg-1) [1]. However, their commercialization faces significant hurdles: the low electrical conductivity of sulfur and its compounds, substantial volume expansion during cycling, and the lithium polysulfide shuttle effect. These challenges lead to poor electrochemical performance, limited cycle life, and reduced rate capability [2,3].
In our current research aimed at overcoming these major challenges, we have developed a composite based on biomass-derived graphene-like porous carbon and MXene, which we used to modify the separator. The graphene-like porous carbon was produced by carbonizing biomass waste followed by thermochemical activation with potassium hydroxide (1:4). This process yielded carbon with an increased specific surface area of 2200 m²/g and significant mesoporosity, with an average pore size of 2-4 nm [4]. Concurrently, MXene (Ti₃C₂Tx) was synthesized by etching the aluminum layer from a titanium-based MAX phase. The chemical composition, morphological features, and microstructure of the prepared materials were thoroughly investigated using various techniques, including SEM, TEM, Raman spectroscopy, XPS, and XRD. The obtained composite was applied to a commercial Celgard separator using the doctor blade technique, with polyvinylidene fluoride dissolved in N-methyl-2-pyrrolidone as a binder.
As a result of the C/MXene separator modification, the assembled lithium-sulfur cell delivered an initial discharge capacity of 1620 mAh g⁻¹ at 0.2 C and maintained a capacity greater than 1050 mAh g⁻¹ after 100 cycles, with an average Coulombic efficiency of 97%. Further electrochemical tests of the cells are currently under investigation.
Acknowledgments
This research was funded by the Science Committee of the Ministry of Education and Science of the Republic of Kazakhstan (Grant No. AP13067625).
Lithium-ion battery (LIB) market size will grow at the compounded annual growth rate of +16%, surpassing 165 billion USD in revenue by 2030. While most of this growth is enabled by innovations in battery chemistry and performance, safety hazards remain a primary concern and a major restrain to market expansion. Safety incidences often results from errors introduced during high-volume manufacturing that, through a chain of events, leads to a thermal runaway and fire. C4V has teamed with leading Machine Learning (ML) and Artificial Intelligence (AI) experts to address the issue by developing tools that can not only track and minimize or eliminate manufacturing defects in the battery cells, but can warn users of an incipient catastrophic event ahead of time, thus preventing any damage to property or loss of life. The first generation of the DigitalDNA (DDNA) software is able to automatically capture key electrochemical data from cell cyclers installed at iM3NY, a New York based gigafactory that produces 50Ah prismatic cells.[1] DDNA automatically curates and analyse data generated at the production floor, and create actionable outputs for operator to take corrective measures in near real-time. DDNA is designed to be platform agnostic and can capture data in multiple formats. The next-generation of DDNA, with an in-built advanced data analytics algorithms can easily access and use these large data sets to train the ML models and implement AI to provide predictive insights and enable continuous improvements in electrochemical performance of LIBs. In addition, with a recent release of the Supply Chain module, DDNA can perform a full inventory control and management of +30 components that are required for battery cell production. With this module, DDNA can also track the progress of C4V’s extensive raw material qualification program currently underway for more than 50 vendors globally. By integrating best-practices in laboratory information and data management systems, DDNA enables a high level of information flow control during the 5 discrete stages of phase-gate qualification process starting with a preliminary assessments in a coin cell to a full scale evaluation in the commercial cell. When integrated with the warehouse management system and high-level business systems such as ERP, the predictive capability of the software can use the raw material utilization data intelligently to create sourcing and procurement scenarios to achieve full inventory and cost optimization.
By leveraging the fully digitized future gigafactories and the IIoT ecosystems, the future-generations of DDNA will seamlessly integrate with manufacturing execution systems to collect data at each step of the manufacturing process. By tapping into the real-time visualization of process and equipment performance data, the ML and AI analytics will be able to detect anomalies ahead of time. This ability to predict failure and perform preventive maintenance will increase equipment availability and performance and reduce disruptions and costly repairs. More importantly, DDNA will interface with the numerous in- or at-line quality control instruments implemented in a roll-to-roll process. Together with feedback control loop, access to statistically significant anomaly data set and advanced descriptive analytics, DDNA will enable processes that will reduce waste and improve yields. By quickly detecting and eliminating any debilitating defects at every step, DDNA will afford a highly reliable and safe battery products.
We envision that DDNA will mature into a comprehensive software platform that will enable Smart gigafactories and predictive manufacturing and will make intelligent decisions informed by data gathered over the entire value chain of LIB from molecules (mines) to machines (vehicles and Energy Storage Systems).
Transition metal compounds with a general formula AxMaXb (A=Li, Na, M= transition metal, X= O, S) constitute a group of potential electrode materials for a new generation of alkaline batteries.[1,2] This application is related to the fact that these compounds can reversibly intercalate high amounts of alkaline ions (1 or more moles per mole of MaXb) already at room temperature, without significant changes in their crystallographic structure. Nowadays, further development of rechargeable batteries is focused on the discovery of new, high-performance and low-cost electrode materials. Recently, Na-ion batteries have attracted much attention due to their many advantages, such as: high abundance of sodium in the Earth’s crust, its low cost and suitable redox potential (only 0.3 V above that of lithium).
The author of this work basing on her own investigations of numerous group of cathode materials has demonstrated that the electronic structure of the electrode materials plays an important role in the electrochemical intercalation process. The paper reveals correlation between crystal and electronic structure, chemical disorder, transport and electrochemical properties of layered transition metal oxides and polyanions Na2Fe2(SO4)3 cathode materials. The complex studies, including experimental as well as theoretical parts (electronic structure calculations performed using the Korringa-Kohn-Rostoker method with the coherent potential approximation KKR-CPA to account for chemical disorder), showed a strong correlation between structural, transport and electrochemical properties of these materials.
The detailed analysis presented in this work provides a strong proof that the high-entropy NaxMn0.2Fe0.2Co0.2Ni0.2Ti0.2O2 oxide with reduced content of cobalt and nickel and Na2Fe2(SO4)3 might be applicable in sodium batteries technology, especially in terms of large-scale energy storage units.
Lithium-ion batteries (LIBs) find extensive use in various electronic devices, including computers, phones, and electric vehicles. Due to their widespread applications, LIBs come in diverse shapes, sizes, and compositions. These batteries contain significant amounts of critical materials such as lithium, cobalt, and nickel. Unfortunately, without proper recycling, these valuable materials are lost when electronics reach the end of their life cycle. [1]. The increasing demand for batteries, particularly in the electric vehicle (EV) industry, has led to a surge in the need for critical metals. For example, sales of electric vehicles are expected to increase to 23-40 million in 2030 compared to 5.1 million in 2018 [2]. In response to the growing demand for batteries and the subsequent need for battery materials as well as the environmental impact of discarded batterie several governments worldwide have taken significant steps to establish a complete recycling infrastructure including collection points, incentivizing recycling facilities and promoting the use of recycled materials. Legislation has been enacted in countries such as the United States, China, and the European Union to mandate the establishment of large-scale battery recycling facilities [1] [3]. These facilities play a crucial role in creating a sustainable supply chain for critical metals. This paper provides a comprehensive overview of the recycling processes for lithium-ion batteries (LIBs), covering various scales from lab experiments to industrial implementations. All these processes are built upon three distinct technologies including hydrometallurgy, pyrometallurgy and combined hydrometallurgy and pyrometallurgy processes [4] [3] [1]. Within the developed processes, only a few have successfully scaled up to industrial pilot scales. In this paper, we will explore and compare examples of both pilot-scale and industrial-scale processes. Discussing and comparing these processes will provide valuable insights for advancing sustainable battery recycling practices.
SESSION: EnergyWedPM3-R9 |
9th Intl. Symp. on Sustainable Energy Production: Fossil; Renewables; Nuclear; Waste handling, processing, & storage for all energy production technologies; Energy conservation |
Wed. 23 Oct. 2024 / Room: Ariadni C | |
Session Chairs: Harold Dodds; Student Monitors: TBA |
Current efforts to make sustainable carbon based fuels and chemical feedstocks is a high priority research area with an urgent necessity due to climate change concerns and depleting petroleum reserves. Upgrading of cellulosic biomass derived C5-6 range feedstocks like furfural, 5-hydroxymethylfurfual and levulinic acid to bio-fuel feedstocks, biofuels or sustainable monomers is a major thrust area in this effort [1].
Levulinic acid or 2-oxopentanoic acid produced by depolymerization of cellulose to glucose followed by dehydration - rehydration under acid catalysis was used as the renewable feedstock. A low cost catalyst was prepared by pyrolyzing electrode coating material from spent Li-ion laptop battery [2], [3]. The active catalyst was identified as lithium nickel manganese cobalt oxide (LiNixMnyCozO2) with an empirical composition of the transition elements with catalytic activity in the ratio: Ni : Mn : Co : 2.02 : 1.00 : 0.73
Lithium nickel manganese cobalt oxide (LiNixMnyCozO2) on carbon catalyst is effective in the decarboxylative - dimerization of levulinic acid to a mixture of C6 and C9 fuel precursors. The highest levulinic acid conversion of 94% was observed with 10% (w/w) catalyst loading under 1.24 MPa hydrogen at 140 °C, 15h.
In conclusion we have developed an inexpensive non-noble metal based catalyst system for efficient dimerization of levulinic acid to C6 and C9 compounds through concurrent decarboxylation, with potential applications in producing sustainable fuels or fuel precursors.
SESSION: CarbonWedPM1-R10 |
7th Intl. Symp. on Sustainable Carbon and Biocoke and their Industrial Application |
Wed. 23 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Gustav Hanke; Naldo J.A. Meyer; Student Monitors: TBA |
Various metallurgical processes are still operated by utilizing fossil-based carbon sources for reduction and energy supply generating a carbon footprint which will influence future competitiveness in terms of economy and market. More and more customers look for a kind of green label on the metal product, forcing smelters to bring their CO2-output down to a certain level.
Hydrogen has been and still is the most popular option to replace fossil carbon in metallurgical processes even though the enthusiasm of previous years has changed into a more realistic view when facing available amounts and prices in near future. Electricity, in some cases could serve as energy source as well as for reduction at least offering the chance to have green electrical power sources and with this a carbon-footprint reduced production. Alternatives like biomass, biogas and charcoal have to be considered as well.
Hydrometallurgy in general is often seen as an option to reduce the carbon footprint due lower energy consumption but suffers often from high efforts for effluent treatment and low product qualities.
The presentation gives an overview about different metallurgical processes and the options to use CO2-neutral reducing agents. A detailed comparison is done for steel mill dust recycling processes showing opportunities but also challenges for alternative reducing agents.
Despite advancements in new technologies, carbon remains crucial in metallurgy. It works as energy source and, even more importantly, as reducing agent. As many modern pyrometallurgical processes still rely on carbon, it is difficult, respectively impossible in the short term, to remove it completely or to replace it by any other element. As a step towards CO2 neutrality, the use of pyrolyzed biomass (biocoke) can work as an environmental friendlier solution which is available within a short period of time. In the metallurgical processes hardly any adaptions are necessary, as solid carbon is replaced by another form of solid carbon. However, to ensure this the biocoke must fulfill some requirements, to replace the fossil coke without any drawbacks. This regards for example the grain size, porosity, reactivity and mechanical strength.
Former trials, presented at SIPS 2023, proved the general applicability in solid-liquid and solid-gas reactors and showed advantages, disadvantages and challenges when using biocoke. Since then, many new results were generated in order to further improve the properties of biocoke. Grainsize reduction, followed by briquetting using different binders, considerably influenced not only the mechanical properties, but also the reactivity and therefore increased the variety of metallurgical processes for which the biocoke could perhaps be used in near future.
Direct coal liquefaction (DCL) stands as a promising process in the realm of energy production. This process is characterized by its ability to break down the complex macromolecular structure of coal using a solvent under moderate conditions.[1] Direct liquefaction aims to yield liquid fuels with a targeted hydrogen-to-carbon ratio, which is achieved through hydrogenation reactions. Conversely, inadequate hydrogen availability can lead to the formation of undesirable residues.[2-4] The co-liquefaction of coal with other feed materials have been examined extensively. Co-liquefaction involves the simultaneous treatment of various carbonaceous materials, including coal, biomass, and plastic waste, within a shared solvent or reaction medium.[5] This innovative process capitalizes on the synergistic properties of diverse feedstocks, aiming to increase overall conversion efficiencies and generate valuable liquid products. Central to the success of co-liquefaction is an understanding of the intricate interactions between the heterogeneous components during the thermochemical conversion process.
The main driving force of the work presented in this investigation is the use of various wastes such as coal fines and plastics, and a solvent that has limited use in liquefaction processes, i.e. benzene. Co-liquefaction experiments were conducted utilizing a vitrinite-rich medium rank C bituminous coal typically utilized in coal-to-liquid processes and an inertinite-rich medium rank C bituminous discard coal fraction along with polypropylene (PP) and low-density polyethylene (LDPE) as feed materials at 450°C. Using tetralin, a hydrogen-donor solvent, and benzene, a hydrogen-poor solvent, allowed for a comprehensive assessment of liquefaction efficiency and the quantity and quality of derived products, comparing aromatic solvents with differing hydrogen-donor capabilities.
Tetralin co-liquefaction experiments involving the vitrinite-rich coal exhibited the highest carbon conversion values when co-processed with PP and LDPE, reaching 83.3 and 80.8%, respectively. Overall conversion during tetralin liquefaction involving the inertinite-rich coal was lower, attributed to the differences in maceral composition between the coals. The co-liquefaction of the inertinite-rich coal with PP and LDPE showcased conversion values of 76.4 and 72.5%, respectively. Remarkably, experiments involving LDPE revealed significantly higher conversion values compared to predicted values, indicating synergistic effects between coal and plastic materials, influencing the product yields and overall conversion. Molecular structure disparities in the feed materials notably impacted conversion outcomes.
GC-MS analysis of the liquid fractions derived from the co-liquefaction experiments of LDPE using benzene as the solvent revealed high yields of alkanes and alkenes, indicative of benzene's hydrogen-donor properties. 1H NMR analysis of the liquid yields derived from the co-liquefaction using benzene revealed an abundant presence of tetralin and its derivatives, with LDPE derived liquids exhibiting higher aliphatic-to-aromatic proton ratios compared to PP. Remarkably, experiments conducted using benzene demonstrated a high presence of aliphatic protons in the liquid fraction. Alongside the formation of biphenyl, as determined using GC-MS, the results indicate that dehydrogenation of benzene occurred. Moreover, polypropylene and low-density polyethylene were found to facilitate hydrogen transfer in the co-liquefaction process, effectively converting inertinite-rich discarded coal into liquid products when co-processed. Additionally, solid residue chars derived from inertinite-rich coal blends exhibited higher gasification reactivities during CO2 gasification experiments when compared to those containing vitrinite-rich coal. The results from this study indicate the potential of utilizing inertinite-rich coal fines and plastics such as PP and LDPE in co-liquefaction processes and subsequent gasification of residue chars.
In this investigation, polypropylene (PP) and low-density polyethylene (LDPE) were used in liquefaction experiments using tetralin and benzene as solvents. The temperature of the reaction vessel was increased to 450°C at 10 °C/min, with an isothermal reaction time of 60 minutes. This study investigated the influence of feed material and choice of solvent on conversion values and liquid yield composition during liquefaction experiments. Results showed that differences in the molecular structure of polypropylene and low-density polyethylene significantly affected conversion. Tetralin liquefaction yielded conversion values of 97.0% for PP and 23.8% for LDPE, while benzene liquefaction yielded conversion values of 98.5% for PP and 97.5% for LDPE at 450°C. Benzene liquefaction of PP and LDPE produced liquid fractions comprising alkanes and alkenes. Furthermore, it was found that benzene acted as a hydrogen-donor solvent, which was supported by the presence of biphenyl in the liquid fraction derived from benzene liquefaction. Overall, PP and LDPE demonstrated potential for high conversion to liquid products in liquefaction experiments conducted at 425–450°C.
SESSION: CarbonWedPM2-R10 |
7th Intl. Symp. on Sustainable Carbon and Biocoke and their Industrial Application |
Wed. 23 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: Juergen Antrekowitsch; Student Monitors: TBA |
Hydrogen (H2) is gaining public attention as one of the candidates for the next-generation of energy. Environmentally friendly H2 is expected to make a major contribution to sustainable societies. However, the detection of H2 gas is important in nuclear power stations, coal mines, and semiconductor manufacturing industry. The presence of H2 can be used to indicate a fire in its early state or to detect impending transformer failure in electric power plants. So, to avoid any accident, designing of new class of H2 gas sensor is important for the society. In past few decades, various materials such as semiconductor, carbon nanomaterials, metal nanoparticles and so on were explored as sensing materials for the detection of low concentration of H2 gas at room temperature conditions. Among these, carbon nanomaterials are widely investigated because of they are enormously sensitive to H2 at room temperature conditions. In recent years, carbon materials are widely investigated because of their extraordinary chemical, electrical and physical properties. In addition, carbon material have potential application in gas sensor technology.
SESSION: EnvironmentalWedPM3-R10 |
11th Intl. Symp. on Environmental, Policy, Management, Health, Economic, Financial, Social Issues Related to Technology & Scientific Innovation |
Wed. 23 Oct. 2024 / Room: Dazzle D. | |
Session Chairs: TBA Student Monitors: TBA |
The National Examination Council of Tanzania serves to sort out proper career progress of secondary school students. This study demonstrates future implication to Science, Technology, Engineering, and Mathematics (STEM) careers of candidates who sat for the Certificate of Secondary School Education (CSEE) in Mbeya city. Results collected from 58 schools, of which 32 were private schools. Number of candidates were roughly 8000 of which more than a quarter were from private schools. This study revealed that less than 40% of graduates were potential STEM careers out of which less than one third were girls. Interestingly, performance was free of gender disparity in private schools. On the other hand, boys outperformed girls in STEM subjects from public schools. Overall STEM performance showed that the smallest number of students about 13% passed physics compared to other STEM subjects in public school with number of boys being twice that of girls. Moreover, the study revealed that physics along with mathematics are the determinants of STEM career prospects. Therefore, at least 13% candidates were in the position to further studies in STEM careers from public schools.
Background: Tigray is one of the food-insecure regions with many people living under the condition of chronic hunger. Proper intervention mechanisms are vital for addressing food insecurity. Yet, food security intervention mechanisms of various levels are not researched well.
Aims/Objectives: Previous studies have rarely addressed the objectives of food security intervention mechanisms in relation to the four pillars of food security: availability, access, utilization and stability. Thus, this study aims to investigate the food security intervention mechanisms in the drought-prone rural areas of Tigray in relation with the major components of food security.
Methods: This study has employed a cross-sectional study design based on a mixed research approach with primary and secondary data. For this, 363 households from three selected drought-prone rural districts, i.e. Atsbi-wenberta, Irob and Hintalo-wejerat were studied. Primary data were collected using questionnaires and key-informant interviews. And, secondary data were collected from relevant archives and policy documents. The obtained data were analyzed descriptively and content-wise.
Results: Findings show that there were several international interventions intended to halt food insecurity sustainably through financial aid, but many of the interventions were found to be responding to humanitarian crises mainly the food shortages. Ethiopia’s Food and Nutrition Policy, Food Security Program, Food Security Strategy, and Food Security Pack program were the food security intervention mechanisms at the national level. These interventions were found to be inconsistent with each other in their intended goals. Regionally, no food security strategy or program was found intervening to the prevailing food insecurity of Tigray. More notably, the region has no food security bureau or office that deals with food security issues of the region. At a community level, food aid and PSNP transfers have been the usual food security intervention mechanisms.
Conclusions and Recommendations: The food aid and PSNP transfers were outrageously insufficient for the recipients to cope with food insecurity. Therefore, intervention mechanisms should focus on enhancing vulnerable households’ coping and adaptive capacities to deal with food security problems. In this regard, all the food security intervention mechanisms of various levels should be integrated into the common goal of achieving food security.