초록 ▼

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,

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.

대표청구항 ▼

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 —CF2H and/or —CF2CH3 in an amount of at most 60 mmoles per kg of fluoroelastomer; andpolar end gro

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 —CF2H and/or —CF2CH3 in an amount of at most 60 mmoles per kg of fluoroelastomer; andpolar end groups of formula —CF2CH2OH 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) C2-C8 perfluoroolefins;(b) C2-C8 hydrogenated fluoroolefins;(c) C2-C8 chloro and/or bromo and/or iodo-fluoroolefins;(d) (per)fluoroalkylvinylethers (PAVE) of formula CF2═CFORf, wherein Rf is a C1-C6 (per)fluoroalkyl group;(e) (per)fluoro-oxy-alkylvinylethers of formula CF2═CFOX, wherein X is a C1-C12 ((per)fluoro)-oxyalkyl group comprising catenary oxygen atoms;(f) (per)fluorodioxoles having formula: wherein Rf3, Rf4, Rf5, Rf6, equal or different from each other, are independently selected among fluorine atoms and C1-C6 (per)fluoroalkyl groups, optionally comprising one or more than one oxygen atom; and(g) (per)fluoro-methoxy-vinylethers (MOVE) having formula: CFX2═CX2OCF2OR″f wherein R″f is selected among C1-C6 (per)fluoroalkyls, linear or branched; C5-C6 cyclic (per)fluoroalkyls; and C2-C6 (per)fluorooxyalkyls, linear or branched, comprising from 1 to 3 catenary oxygen atoms, and X2═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 AHf, equal to or different from each other and at each occurrence, is independently selected from F, Cl, and H;BHf is any of F, Cl, H and ORHfB, wherein RHfB is a branched or straight chain alkyl radical which can be partially, substantially or completely fluorinated or chlorinated;each of WHf equal to or different from each other and at each occurrence, is independently a covalent bond or an oxygen atom;EHf is a divalent group having 2 to 10 carbon atoms, optionally fluorinated;RHf is a branched or straight chain alkyl radical, which can be partially, substantially or completely fluorinated; andXHf 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 R1, R2, R3, R4, R5 and R6, equal or different from each other, are H or C1-C5 alkyl; Z is a linear or branched C1-C18 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 —CF2H and/or —CF2CH3 are present in an amount of at most 40 mmoles per kg of fluoroelastomer; and wherein the polar end groups of formula —CF2CH2OH 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), CF2═CFOCF3, CF2═CFOC2F5, CF2═CFOC3F7, CF2═CFOX wherein X is a perfluoro-2-propoxypropyl group, perfluorodioxole, CF2═CFOCF2OCF2CF3 (MOVE1), CF2═CFOCF2OCF2CF2OCF3 (MOVE2), CF2═CFOCF2OCF3 (MOVE3), ethylene and propylene. 7. The fluoroelastomer of claim 1, further comprising at least one comonomer selected from C2-C8 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)]; andat 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; andperoxydicarbonates. 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 Fe2+, Cu+1, Co2+, Ag+, and Ti2+. 18. The process of claim 16, wherein the agent (P) is selected from salts of Fe2+. 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 Fe2+, Cu+1, Co2+, Ag+, Ti2+.