Fluoroelastomers having low temperature characteristics and solvent resistance
The present invention is based on quad-fluoropolymer suitable for the preparation of a fluoroelastomer. The fluoropolymer comprises repeating units derived from 10 to 40 mol % of tetrafluoroethylene, 40 to 65 mol % of vinylidene fluoride, 1 to 30 mol % of a perfluorinated vinyl ether of the formula CF 2 ═CFOCF 2 CF 2 CF 2 OCF 3 , 1 to 20 mol % of perfluoromethyl vinylether.
1. A fluoropolymer suitable for the preparation of a fluoroelastomer, said fluoropolymer comprising repeating units derived from:
(a) 10 to 40 mol % of tetrafluoroethylene;
(b) 40 to 65 mol % of vinylidene fluoride;
(c) 1 to 30 mol % of a perfluorinated vinyl ether of the formula CF 2 ═CFOCF 2 CF 2 CF 2 OCF 3 ; and
(d) 1 to 20 mol % of perfluoromethyl vinylether.
2. The fluoropolymer of claim 1 , wherein components (c) and (d) combined comprise at least 13 mol %.
3. The fluoropolymer of claim 1 , wherein (c) is 7 to 30 mol % and (d) is 1 to 15 mol %.
4. The fluoropolymer of claim 3 , wherein component (c) is pre-emulsified into a water based system containing a fluorinated surfactant.
5. The fluoropolymer of claim 4 , wherein said fluorinated surfactant includes non-telogenic fluoroemulsifiers.
6. The fluoropolymer of claim 1 , wherein (c) is 1 to 7 mol % and (d) is 10 to 20 mol %.
7. The fluoropolymer of claim 6 , wherein component (c) is introduced into a polymerization system as a hot aerosol without any fluoroemulsifiers.
8. The fluoropolymer of claim 1 , wherein said fluoropolymer has a bimodal or multimodal molecular weight.
9. The fluoropolymer of claim 1 , further comprising a cure site monomer.
10. The fluoropolymer of claim 9 , wherein said cure site monomer is 1-bromo-2,2-difluoroethylene (CF 2 ═CHBr, BDFE), 4-bromo-3,3,4,4-tetrafluorobutene-1 (CH 2 ═CHCF 2 CF 2 Br, BTFB), bromotrifluoroethylene (CF 2 ═CFBr, BTFE), 4-iodo-3,3,4,4-tetrafluorobutene-1 (CH 2 ═CHCF 2 CF 2 I, ITFB), perfluoro (2-bromoethyl vinyl ether) (CF 2 ═CFOCF 2 CF 2 Br, BEVE), perfluoro (3-iodopropyl viny ether) (CF 2 ═CFO(CF 2 ) 3 I, or combinations thereof.
11. The fluoropolymer of claim 1 , further comprising a chain transfer agent.
12. The fluoropolymer of claim 11 , wherein iodine, bromine, or both are chemically bound to polymer chain ends using said chain transfer agent derived from one or more bromine or iodine of the formula:
R f Br x and R f I x (Formula A) wherein R f is a X-valent fluoroalkylradical C 1 -C 12 , optionally containing chlorine atoms, while X is 1 or 2, or
RBr n I m (Formula B) wherein R represents a fluoro hydrocarbon, chlorofluoro hydrocarbon or a hydrocarbon and each of n and m is 0.1 or 2, or combinations thereof.
13. A fluoroelastomer comprising repeating units derived from:
(a) 10 to 40 mol % of tetrafluoroethylene;
(b) 40 to 65 mol % of vinylidene fluoride;
(c) 1 to 30 mol % of a perfluorinated vinyl ether of the formula CF 2 ═CFOCF 2 CF 2 CF 2 OCF 3 ; and
(d) 1 to 20 mol % of perfluoromethyl vinylether.
14. A fluoroelastomer of claim 13 , wherein components (c) and (d) combined comprise at least 13 mol %.
15. The fluoroelastomer of claim 13 , wherein (c) is 7 to 30 mol % and (d) is 1 to 15 mol %.
16. The fluoroelastomer of claim 13 , wherein (c) is 1 to 7 mol % and (d) is 10 to 20 mol %.
17. The fluoroelastomer of claim 13 , wherein said fluoroelastomer has a T g of about −25° C. or lower.
18. The fluoroelastomer of claim 13 , wherein said fluororelastomer has a solvent swell according to ASTM D471-98 in FUEL K (CM85) of about 60% or less.
19. The fluoroelastomer of claim 13 , wherein said cure composition is a peroxide cure composition containing brominated units, iodinated units, or combinations thereof.
20. The fluoroelestomer of claim 13 , further comprising a cure site.
21. The fluoroelastomer of claim 20 , wherein said cure site is derived from 1-bromo-2,2-difluoroethylene (CF 2 ═CHBr, BDFE), 4-bromo-3,3,4,4-tetrafluorobutene-1 (CH 2 ═CHCF 2 CF 2 Br, BTFB), bromotrifluoroethylene (CF 2 ═CFBr, BTFE), 4-iodo-3,3,4,4-tetrafluorobutene-1 (CH 2 ═CHCF 2 CF 2 I, ITFB), perfluoro (2-bromoethyl vinyl ether) (CF 2 ═CFOCF 2 CF 2 Br, BEVE), perfluoro (3-iodopropyl viny ether) (CF 2 ═CFO(CF 2 ) 3 I, or combinations thereof.
22. The fluroelastomer of claim 13 , further comprising a functional end group.
23. The fluoroelastomer of claim 22 , wherein said functional end group is derived from one or more bromine or iodine of the formula:
R f Br x and R f I x (Formula A) wherein R f is a X-valent fluoroalkylradical C 1 -C 12 , optionally containing chlorine atoms, while X is 1 or 2, or
RBr n I m (Formula B) wherein R represents a fluoro hydrocarbon, chlorofluoro hydrocarbon or a hydrocarbon and each of n and m is 0.1 or 2, or combinations thereof.
24. A fluoroelastomer composition comprising repeating units derived from:
(a) 10 to 40 mol % of tetrafluoroethylene;
(b) 40 to 65 mol % of vinylidene fluoride;
(c) 1 to 30 mol % of a perfluorinated vinyl ether of the formula CF 2 ═CFOCF 2 CF 2 CF 2 OCF 3 ; and
(d) 1 to 20 mol % of perfluoromethyl vinylether, wherein components (c) and (d) combined comprise at least about 13 mol % and said fluoroelastomer has a T g of about −25° C. or lower.
25. The fluoroelastomer of claim 24 , wherein said fluororelastomer has a solvent swell according to ASTM D471-98 in FUEL K (CM85) of about 60% or less.
26. A method of making a fluoropolymer as defined in claim 1 , comprising free radical polymerization of tetrafluoroethylene, vinylidene fluoride, a perfluorinated vinyl ether of the formula CF 2 ═CFOCF 2 CF 2 CF 2 OCF 3 , and perfluoromethyl vinylether in amounts appropriate so as to obtain a fluoropolymer having the composition as defined in claim 1 .
27. The method of claim 26 , wherein the free radical polymerization is an aqueous suspension polymerization or aqueous emulsion polymerization.
28. The method of claim 26 , wherein the perfluorinated vinyl ether is pre-emulsified and added before polymerization.
29. The method of claim 26 , wherein said fluoropolymer is prepared as a core-shell material.
30. The method of claim 26 , wherein said polymerization is performed in the presence of I or Br salts.
31. The method of claim 26 , wherein the fluoropolymer further comprises a cure site monomer.
32. The method of claim 31 , wherein said cure site monomer is 1-bromo-2,2-difluoroethylene (CF 2 ═CHBr, BDFE), 4-bromo-3,3,4,4-tetrafluorobutene-1 (CH 2 ═CHCF 2 CF 2 Br, BTFB), bromotrifluoroethylene (CF 2 ═CFBr, BTFE), 4-iodo-3,3,4,4-tetrafluorobutene-1 (CH 2 ═CHCF 2 CF 2 I, ITFB), perfluoro (2-bromoethyl vinyl ether) (CF 2 ═CFOCF 2 CF 2 Br, BEVE), perfluoro (3-iodopropyl viny ether) (CF 2 ═CFO(CF 2 ) 3 I, or combinations thereof.
33. The method of claim 26 , wherein the fluoropolymer further comprises a chain transfer agent.
34. The method of claim 33 , wherein iodine, bromine, or both are chemically bound to polymer chain ends using said chain transfer agent derived from one or more bromine or iodine of the formula:
R f Br x and R f I x (Formula A) wherein R f is a X-valent fluoroalkylradical C 1 -C 12 , optionally containing chlorine atoms, while X is 1 or 2, or
RBr n I m (Formula B) wherein R represents a fluoro hydrocarbon, chlorofluoro hydrocarbon or a hydrocarbon and each of n and m is 0.1 or 2, or combinations thereof.
35. A method for forming a fluoroelastomer comprising vulcanizing the fluoropolymer of claim 1 with a cure composition.
36. A method according to claim 35 , wherein an organic peroxide is utilized for vulcanization of said fluoropolymer.