ORALS
SESSION:
ChemistrySatPM1-R9
| Tressaud International Symposium on Solid State Chemistry for Applications and Sustainable Development |
| Sat Oct, 26 2019 / Room: Aphrodite A (100/Gr. F) | |
| Session Chairs: Yuichi Shimakawa; Alain Demourgues; Session Monitor: TBA |
15:15: [ChemistrySatPM108]
The Fascinating World of Fluoropolymers: From the Synthesis to Applications Bruno
Ameduri1 ; Mohammad
Wehbi
2 ;
1Institute Charles Gerhardt Montpellier, Montpellier, France;
2ICGM, Montpellier, France;
Paper Id: 38
[Abstract] Fluoropolymers are valuable materials endowed with outstanding properties that allow them to be involved in many High-Tech applications [1]. This presentation aims at reporting how the design of functional fluoropolymers may influence the properties and applications. Actually, 2-trifluoromethacrylic acid (MAF) is a versatile building block for the synthesis of new functional monomers. [2] It can be homopolymerized by anionic initiation [2-3] but fails in the presence of any radical systems. However, its radical copolymerization with vinylidene fluoride (VDF) has been successful. This presentation reports overall strategies to synthesize novel functional 2-trifluoromethacrylate monomers and macromonomers, as well as their radical copolymerization with VDF, leading to various materials such as higher thermal stable thermoplastics,[4] polymer gel electrolytes for Lithium ion batteries,[5-7] and anticorrosion [8] and adhesive hybrid coatings [9] (Figure 1).
Figure 1 shows the overall strategies to synthesize novel functional 2-trifluoromethyl monomers from 2-trifluoromethacrylic acid (MAF) and their radical copolymerization with VDF (left). The figure also shows steel plates coated with poly(VDF-co-MAF Phosphonate) copolymer at the beginning of the experiment (A), after 1 h (B), and after 18 h (C). (D): uncoated steel plate used as reference sample after 1 h (right).
Tosoh FineChem Corporation (Shunan, Japan) is acknowledged for suppling MAF monomers.
References:
[1] B. Ameduri, and H. Sawada; Fluoropolymers: Applications; vol. 2, RSC, Oxford, 2016.
[2] Y. Patil and B. Ameduri, Progr. Polym. Sci., 38 (2013), 703-739.
[3] T. Narita, a) Makromol. Chem. Rapid. 6 (1985) 301-304; b) J. Fluorine Chem. 131 (2010), 812.
[4] M. Wadekar, Y. Patil, B. Ameduri, Macromolecules, 47 (2014) 47, 13-25.
[5] A. Alaeddine, J. Vergnaud, D. Vlad, J.F. Gohy, B. Ameduri, Polym. Chem. 6 (2015) 6021-6032.
[6] M. Wehbi, J. F. Gohy et al. J. Mat Chem. A, 6 (2018) 8514-8526.
[7] M. Wehbi, J. Brassine, et al., Macromolecules, 52 (2019) DOI: 10.1021/acs.macromol.9b00355.
[8] S. Banerjee, M. Wehbi et al., ACS Appl. Mater. Interface, 9 (2017) 6433-6443.
[9] M. Wehbi, S. Banerjee, et al., Macromolecules, 50 (2017) 50, 9329-9339.
15:40 Break
