Controlled free-radical copolymerization of trifluoroethylene

Patent metadata

Field	Value
Publication number	US-9708419-B2
Application number	US-201314396528-A
Country	US
Kind code	B2
Filing date	Apr 25, 2013
Priority date	Apr 26, 2012
Publication date	Jul 18, 2017
Grant date	Jul 18, 2017

Abstract

The invention concerns a method for preparing block copolymers, comprising a step of controlled free-radical copolymerisation of trifluoroethylene with at least one additional monomer, different from trifluoroethylene, in the presence of a chain transfer agent, said chain transfer agent being a xanthate compound, a trithiocarbonate compound or a monoiodide compound. The invention also concerns the block copolymers likely to be obtained by this method.

First claim

The invention claimed is:

1. A thermoplastic block copolymer, comprising:
a poly(vinylidene fluoride) homopolymer block and a copolymer block comprising vinylidene fluoride and trifluoroethylene units and optionally additional units; or
a copolymer block comprising vinylidene fluoride and trifluoroethylene units and a copolymer block comprising vinylidene fluoride and trifluoroethylene units and additional units,
said thermoplastic block copolymer having a xanthate or trithiocarbonate or monoiodinated end group.

2. A thermoplastic block copolymer according to claim 1 having trifluoroethylene and vinylidene fluoride units and additional units, and having a xanthate or trithiocarbonate or monoiodinated end group.

3. The copolymer as claimed in claim 2 , in which the xanthate or trithiocarbonate end group is an —S—C(═S)—Z group, —Z representing an —O—R 2 group in which R 2 represents an alkyl or aryl group comprising from 1 to 10 carbon atoms or —Z representing an —S—R 3 group in which R 3 represents an aliphatic group comprising from 1 to 20 carbon atoms.

4. The copolymer as claimed in claim 3 , in which the xanthate or trithiocarbonate end group is an —S—C(═S)—O—C 2 H 5 or —S—C(═S)—S—C 12 H 25 group.

5. A process for preparing a copolymer (c), comprising reacting a copolymer (a) as claimed in claim 2 with at least one comonomer (b).

6. The process as claimed in claim 5 , in which the comonomer (b) is a fluorinated monomers or a combination thereof.

7. The process according to claim 6 , wherein the comonomer (b) is 2,3,3,3-tetrafluoropropene, vinyl fluoride, 2-chloro-1,1-difluoroethylene, 2-bromo-1,1-difluoroethylene, hexafluoropropene, 3,3,3-trifluoropropene, 3,3,3-trifluoro-2-chloropropene, 1,1,1,3-tetrafluoropropene, 3,3,3-trifluoro-2-bromopropene, 1H-pentafluoropropene, 2H-pentafluoropropene, perfluoromethyl vinyl ether, perfluoroethyl vinyl ether, perfluoropropyl vinyl ether, α-trifluoromethacrylic acid and its derivatives; vinyl acetate, N-vinylpyrrolidone, methacrylates, acrylates, acrylamide, N-vinylcarbazole, acrylonitrile, allyl alcohol, allyl acetate, allyl halide or allyl glycidyl ether units; or are combinations thereof.

8. The process as claimed in claim 5 , comprising preparing the copolymer (a) by controlled free-radical copolymerization, comprising copolymerization of a trifluoroethylene monomer with at least one additional monomer, different than trifluoroethylene, in the presence of an initiator and of a chain transfer agent, said chain transfer agent being a xanthate compound, a trithiocarbonate compound or a monoiodinated compound, in which the copolymer prepared is a block copolymer and in which the molar ratio of the amount of chain transfer agent to the amount of monomers is from 0.001 to 0.020, and the initial molar ratio of the amount of the TrFE monomer to the amount of the comonomers is from 10% to 90%, preferably from 20% to 50%.

9. A film or membrane comprising at least one copolymer as claimed in claim 2 .

10. A piezoelectric device comprising a film as claimed in claim 9 .

11. A ferroelectric device comprising a film as claimed in claim 9 .

12. A pyroelectric device comprising a film as claimed in claim 9 .

13. A coating comprising a film as claimed in claim 9 .

14. The copolymer as claimed in claim 1 , in which the additional units are fluorinated units or combinations thereof.

15. The block copolymer as claimed in claim 14 , in which: the additional units are 2,3,3,3-tetrafluoropropene, vinyl fluoride, 2-chloro-1,1-difluoroethylene, 2-bromo-1,1-difluoroethylene, hexafluoropropene, 3,3,3-trifluoropropene, 3,3,3-trifluoro-2-chloropropene, 1,1,1,3-tetrafluoropropene, 3,3,3-trifluoro-2-bromopropene, 1H-pentafluoropropene, 2H-pentafluoropropene, perfluoromethyl vinyl ether, perfluoroethyl vinyl ether, perfluoropropyl vinyl ether, α-trifluoromethacrylic acid and its derivatives; vinyl acetate, N-vinylpyrrolidone, methacrylates, acrylates, acrylamide, N-vinylcarbazole, acrylonitrile, allyl alcohol, allyl acetate, allyl halide or allyl glycidyl ether units; or are combinations thereof.

16. The block copolymer as claimed in claim 1 , comprising:
a poly(vinylidene fluoride) homopolymer block and a copolymer block comprising vinylidene fluoride, trifluoroethylene and 2,3,3,3-tetrafluoropropene units; or
a copolymer block comprising vinylidene fluoride and trifluoroethylene units and a copolymer block comprising vinylidene fluoride, trifluoroethylene and 2,3,3,3-tetrafluoropropene units; or
a poly(vinylidene fluoride) homopolymer block and a copolymer block consisting of vinylidene fluoride and trifluoroethylene units.

17. The process for preparing a copolymer according to claim 1 by controlled free-radical copolymerization, comprising copolymerization of a trifluoroethylene monomer with at least one additional monomer, different than trifluoroethylene, in the presence of an initiator and of a chain transfer agent, said chain transfer agent being a xanthate compound, a trithiocarbonate compound or a monoiodinated compound, in which the copolymer prepared is a block copolymer and the monomers present during the copolymerization step comprise vinylidene fluoride, trifluoroethylene, and at least one additional monomer, and in which the molar ratio of the amount of chain transfer agent to the amount of monomers is from 0.001 to 0.020, and the initial molar ratio of the amount of the TrFE monomer to the amount of the comonomers is from 10% to 90%.

18. The process as claimed in claim 1 , in which the additional monomers are 2,3,3,3-tetrafluoropropene, vinyl fluoride, 2-chloro-1,1-difluoroethylene, 2-bromo-1,1-difluoroethylene, hexafluoropropene, 3,3,3-trifluoropropene, 3,3,3-trifluoro-2-chloropropene, 1,1,1,3 tetrafluoropropene, 3,3,3-trifluoro-2-bromopropene, 1H-pentafluoropropene, 2H-pentafluoropropene, perfluoromethyl vinyl ether, perfluoroethyl vinyl ether, perfluoropropyl vinyl ether, α-trifluoromethacrylic acid or its derivatives; vinyl acetate, N-vinylpyrrolidone, methacrylates, acrylates, acrylamide, N-vinylcarbazole, acrylonitrile, allyl alcohols, allyl acetate, allyl halides, allyl glycidyl ether; or are combinations thereof.

19. The process as claimed in claim 1 , in which the chain transfer agent is a xanthate or trithiocarbonate compound which is a compound of formula R 1 —S—C(═S)—Z, in which R 1 represents an aliphatic group comprising from 1 to 20 carbon atoms, —Z represents an —O—R 2 group in which R 2 represents an alkyl or aryl group comprising from 1 to 10 carbon atoms or —Z represents an —S—R 3 group in which R 3 represents an aliphatic group comprising from 1 to 20 carbon atoms.

20. The process as claimed in claim 19 , in which the xanthate or trithiocarbonate compound is O-ethyl-S-(1-methyloxycarbonyl)ethyl xanthate.

21. The process as claimed in claim 1 , in which the chain transfer agent is a monoiodinated compound which is a 1-iodofluoroalkane.

22. The process according to claim 21 , wherein the monoiodinated compound is a compound of formula R F —(CH 2 CF 2 ) N —I, in which n is an integer ranging from 1 to 500, and R F represents a perfluorocarbon group.

23. The process according to claim 22 , wherein R F is CF 3 , C 2 F 5 , C 3 F 7 or C m F 2m+1 , m being an even integer ranging from 4 to 20.

Assignees

• Arkema France
• Enscm
• Ecole Nat Superieure De Chime De Montpellier

Inventors

• Ameduri Bruno
• Alaaeddine Ali

Classifications

• C08F214/18 Primary

  Monomers containing fluorine · CPC title

• C08F293/005

  using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent · CPC title

• C08F2438/00

  Living radical polymerisation · CPC title

• C09D127/16

  Homopolymers or copolymers of vinylidene fluoride · CPC title

• C08F214/182

  Monomers containing fluorine not covered by the groups C08F214/20 - C08F214/28 · CPC title