Direct Defluorination and Amination of Polytetrafluoroethylene and Other Fluoropolymers by Lithium Alkylamides

Author:

Herlem Guillaume1ORCID,Roina Yaelle1,Fregnaux Mathieu2ORCID,Gonçalves Anne-Marie2,Cattey Hélène3,Picaud Fabien1ORCID,Auber Frédéric1

Affiliation:

1. Laboratoire SINERGIES, CHU Jean Minjoz, UFR Sciences & Techniques, 16 Route de Gray, 25030 Besançon CEDEX, France

2. Institut Lavoisier de Versailles, Université Paris-Saclay, UVSQ, CNRS, UMR 8180, 78035 Versailles CEDEX, France

3. Institut ICMUB—CNRS 6302, Université de Bourgogne, UFR Sciences et Techniques Mirande, 9 Avenue Alain Savary, 21000 Dijon CEDEX, France

Abstract

Polytetrafluoroethylene (PTFE) and, by extension, fluoropolymers are ubiquitous in science, life, and the environment as perfluoroalkyl pollutants (PFAS). In all cases, it is difficult to transform these materials due to their chemical inertness. Herein, we report a direct amination process of PTFE and some fluoropolymers such as polyvinylidene fluoride (PVDF) and Nafion by lithium alkylamide salts. Synthesizing these reactants extemporaneously between lithium metal and an aliphatic primary di- or triamine that also serves as a solvent leads to the rapid nucleophilic substitution of fluoride by an alkylamide moiety when in contact with the fluoropolymer. Moreover, lithium alkylamides dissolved in suitable solvents other than amines can react with fluoropolymers. This highly efficient one-pot process opens the way for further surface or bulk modification if needed, providing an easy, inexpensive, and fast experiment protocol on large scales.

Funder

Région de Bourgogne Franche-Comté

Publisher

MDPI AG

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