Method for manufacturing fluoroelastomers

Patent metadata

Field	Value
Publication number	US-10030087-B2
Application number	US-201214114799-A
Country	US
Kind code	B2
Filing date	May 2, 2012
Priority date	May 3, 2011
Publication date	Jul 24, 2018
Grant date	Jul 24, 2018

Abstract

The invention pertains to a process for manufacturing a fluoroelastomer [fluoroelastomer (A)] having a heat of fusion of less than 5 J/g as measured by ASTM D-3418-08, said method comprising emulsion polymerizing vinylidene fluoride (VDF) in the presence of at least one additional fluorinated monomer, in an aqueous polymerization medium, said method comprising polymerizing VDF and said additional fluorinated monomer(s) in the presence of a redox radical initiator system comprising: —at least one organic oxidizing agent [agent (O)]; —at least one organic reducing agent [agent (R)]; wherein agent (O) is fed to said polymerization medium separately from agent (R), so that agent (O) comes in contact with agent (R) exclusively in said polymerization medium comprising VDF and optional additional monomer(s), to fluoroelastomers having low amount of chain defects and low amount of polar end groups, notably obtainable from said process, and to curable compositions therefrom.

First claim

The invention claimed is:

1. A fluoroelastomer (A) comprising recurring units derived from vinylidene fluoride and from at least one additional fluorinated monomer, said fluoroelastomer further comprising:
end groups of formula —CF 2 H and/or —CF 2 CH 3 in an amount of at most 60 mmoles per kg of fluoroelastomer; and
polar end groups of formula —CF 2 CH 2 OH in an amount of at most 5 mmoles per kg of fluoroelastomer.

2. The fluoroelastomer of claim 1 , in which VDF is copolymerized with at least one comonomer selected from:
(a) C 2 -C 8 perfluoroolefins;
(b) C 2 -C 8 hydrogenated fluoroolefins;
(c) C 2 -C 8 chloro and/or bromo and/or iodo-fluoroolefins;
(d) (per)fluoroalkylvinylethers (PAVE) of formula CF 2 ═CFOR f , wherein R f is a C 1 -C 6 (per)fluoroalkyl group;
(e) (per)fluoro-oxy-alkylvinylethers of formula CF 2 ═CFOX, wherein X is a C 1 -C 12 ((per)fluoro)-oxyalkyl group comprising catenary oxygen atoms;
(f) (per)fluorodioxoles having formula:

wherein R f3 , R f4 , R f5 , R f6 , equal or different from each other, are independently selected among fluorine atoms and C 1 -C 6 (per)fluoroalkyl groups, optionally comprising one or more than one oxygen atom; and
(g) (per)fluoro-methoxy-vinylethers (MOVE) having formula:
CFX 2 ═CX 2 OCF 2 OR″ f

wherein R″ f is selected among C 1 -C 6 (per)fluoroalkyls, linear or branched; C 5 -C 6 cyclic (per)fluoroalkyls; and C 2 -C 6 (per)fluorooxyalkyls, linear or branched, comprising from 1 to 3 catenary oxygen atoms, and X 2 ═F, H.

3. The fluoroelastomer of claim 1 , further comprising recurring units derived from:
(CSM-1) iodine or bromine containing monomers of formula:

wherein
each of A Hf , equal to or different from each other and at each occurrence, is independently selected from F, Cl, and H;
B Hf is any of F, Cl, H and OR Hf B , wherein R Hf B is a branched or straight chain alkyl radical which can be partially, substantially or completely fluorinated or chlorinated;
each of W Hf equal to or different from each other and at each occurrence, is independently a covalent bond or an oxygen atom;
E Hf is a divalent group having 2 to 10 carbon atoms, optionally fluorinated;
R Hf is a branched or straight chain alkyl radical, which can be partially, substantially or completely fluorinated; and
X Hf is a halogen atom selected from the group consisting of iodine and bromine;

which may be inserted with ether linkages; or
(CSM-2) ethylenically unsaturated compounds comprising cyanide groups, possibly fluorinated.

4. The fluoroelastomer of claim 1 , further comprising recurring units derived from a bis-olefin [bis-olefin (OF)] having general formula:

wherein R 1 , R 2 , R 3 , R 4 , R 5 and R 6 , equal or different from each other, are H or C 1 -C 5 alkyl; Z is a linear or branched C 1 -C 18 alkylene or cycloalkylene radical, optionally containing oxygen atoms, optionally fluorinated, or a (per)fluoropolyoxyalkylene radical.

5. The fluoroelastomer of claim 1 , wherein the end groups of formula —CF 2 H and/or —CF 2 CH 3 are present in an amount of at most 40 mmoles per kg of fluoroelastomer; and wherein the polar end groups of formula —CF 2 CH 2 OH are present in an amount of at most 3 mmoles per kg of fluoroelastomer.

6. The fluoroelastomer of claim 2 , wherein VDF is copolymerized with at least one comonomer selected from tetrafluoroethylene (TFE), hexafluoropropylene (HFP), hexafluoroisobutylene, vinyl fluoride (VF), trifluoroethylene (TrFE), chlorotrifluoroethylene (CTFE), CF 2 ═CFOCF 3 , CF 2 ═CFOC 2 F 5 , CF 2 ═CFOC 3 F 7 , CF 2 ═CFOX wherein X is a perfluoro-2-propoxypropyl group, perfluorodioxole, CF 2 ═CFOCF 2 OCF 2 CF 3 (MOVE1), CF 2 ═CFOCF 2 OCF 2 CF 2 OCF 3 (MOVE2), CF 2 ═CFOCF 2 OCF 3 (MOVE3), ethylene and propylene.

7. The fluoroelastomer of claim 1 , further comprising at least one comonomer selected from C 2 -C 8 non-fluorinated olefins.

8. A peroxide curable composition comprising the fluoroelastomer (A) according to claim 1 and at least one peroxide.

9. A ionically curable composition comprising the fluoroelastomer (A) according to claim 1 and at least one curing agent and at least one accelerator.

10. Cured articles obtained from the fluoroelastomer (A) according to claim 1 .

11. A process for manufacturing the fluoroelastomer of claim 1 having a heat of fusion of less than 5 J/g as measured by ASTM D-3418-08, said method comprising emulsion polymerizing vinylidene fluoride (VDF) in the presence of at least one additional fluorinated monomer, in an aqueous polymerization medium and-in the presence of a redox radical initiator system comprising:
at least one organic oxidizing agent [agent (O)]; and
at least one organic reducing agent [agent (R)];

wherein agent (O) is fed to said polymerization medium separately from agent (R), so that agent (O) comes in contact with agent (R) exclusively in said polymerization medium comprising VDF and optional additional monomer(s).

12. The process of claim 11 , wherein the organic oxidizing agent [agent (O)] is selected from the group consisting of:
diacylperoxides;
dialkylperoxides;
hydroperoxides;
per-acid esters and salts thereof; and
peroxydicarbonates.

13. The process of claim 12 , wherein the organic oxidizing agent [agent (O)] is selected from the group consisting of diacetylperoxide, disuccinyl peroxide, dipropionylperoxide, dibutyrylperoxide, dibenzoylperoxide, benzoylacetylperoxide, diglutaric acid peroxide, dilaurylperoxide, ditertbutylperoxide (DTBP), t-butyl hydroperoxide (TBHP), cumene hydroperoxide, tertiaryamyl-hydroperoxide, an ammonium per-acid ester, a sodium per-acid ester, a potassium per-acid ester, diisopropylperoxydicarbonate, di-n-propylperoxydicarbonate and mixtures thereof.

14. The process of claim 11 , wherein the organic reducing agent [agent (R)] is selected from the group consisting of oxalic acid, ascorbic acid, formic acid, malonic acid, citric acid, a reducing sugar, N-nitrosamine, hydroxylamines and mixtures thereof.

15. The process of claim 14 , wherein the agent (R) is ascorbic acid.

16. The process of claim 11 , wherein the redox radical initiator system comprises at least one transition metal catalyst [agent (P)].

17. The process of claim 16 , wherein agent (P) comprises at least one of Fe 2+ , Cu +1 , Co 2+ , Ag + , and Ti 2+ .

18. The process of claim 16 , wherein the agent (P) is selected from salts of Fe 2+ .

19. The process of claim 11 , wherein the redox radical initiator system comprises:
at least one organic oxidizing agent [agent (O)];
at least one organic reducing agent [agent (R)];
optionally at least one inorganic oxidizing agent [agent (IO)];

and said redox radical initiator system is substantially free from any salt of Fe 2+ , Cu +1 , Co 2+ , Ag + , Ti 2+ .

Assignees

• Chernysheva Liubov
• Kent Bradley Lane
• Comino Giovanni
• Kapelyushko Valeriy
• Solvay Specialty Polymers It

Inventors

• Chernysheva Liubov
• Kent Bradley Lane
• Comino Giovanni
• Kapelyushko Valeriy

Classifications

• C08F214/22 Primary

  Vinylidene fluoride · CPC title

• C08F214/222

  with fluorinated vinyl ethers · CPC title

• C08F214/225

  with non-fluorinated comonomers · CPC title

• C08F214/28 Primary

  Hexyfluoropropene · CPC title