초록

VDF-based curable fluoroelastomers having glass transition temperature lower than-35° C. and an amount of--COF end groups in the polymer lower than the sensitivity limit of the method using the FT-IR spectroscopy described in the present application.

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The invention claimed is: 1. Cured fluoroelastomers comprising VDF-based curable fluoroelastomers, said fluoroelastomers comprising the monomer of formula (a) CF3OCF2OCF═CF2, said fluoroelastomers having a glass transition temperature lower than-35° C., an improved combination of mechanical a

The invention claimed is: 1. Cured fluoroelastomers comprising VDF-based curable fluoroelastomers, said fluoroelastomers comprising the monomer of formula (a) CF3OCF2OCF═CF2, said fluoroelastomers having a glass transition temperature lower than-35° C., an improved combination of mechanical and compression set properties at range of temperatures up to 250° C., high thermal resistance, high molecular weight, and an amount of--COF end groups lower than the sensitivity limit of the method described herein: at the end of the polymerization, the polymer is isolated by coagulation by freezing and subsequent defrosting; it is washed twice with demineralized water and is dried in a stove until a constant weight; the--COF end groups are determined by FT-IR spectroscopy, wherein on a polymer film having a thickness from 50 to 300 micron a scanning between 4,000 cm-1 and 400 cm-1 is initially carried out, the film being then kept for 12 hours in an environment saturated with ammonia vapours, and recording the IR spectrum under the same conditions of the initial IR spectrum; elaborating the two spectra by subtracting to the signals of the spectrum of the untreated specimen (initial spectrum) the corresponding signals of the specimen spectrum after exposure to ammonia vapours, drawing the difference spectrum, normalized by the following equation: the optical densities related to the--COF end groups, reacted with the ammonia vapours, are measured; the optical densities are converted into mmoles/kg of polymer by using the extinction coefficients reported in Table 1, page 73 of the report by M. Pianca et Al. "End groups in fluoropolymers", J. Fluorine Chem. 95 (1999), 71-84; obtaining the concentrations of the residual--COF end groups expressed as mmoles of end groups--COF/Kg of polymer: in the fluoroelastomer spectrum no bands related to COF groups (1900-1830 cm-1) are detectable, the method sensitivity limit being 0.05 mmoles/Kg. 2. The cured fluoroelastomers according to claim 1, wherein the curable fluoroelastomers further comprise units deriving from bis-olefins of general formula: wherein: R1, R2, R3, R4, R5, R6, equal to or different from each other, are H or C1-C5 alkyls; Z is a C1-C18 linear or branched alkylene or cycloalkylene radical, optionally containing oxygen atoms, or a (per) fluoropolyoxyalkylene radical. 3. The cured fluoroelastomers according to claim 2, wherein the amount of bis-olefins is from 0.01 to 1.0% by moles per 100 moles of the monomeric units, constituting the basic fluoroelastomer structure, the monomer total sum being 100%. 4. The cured fluoroelastomers according to claim 2, wherein in formula (I), Z is a C4-C12 perfluoroalkylene radical, R1, R2, R3, R4, R5, R6 are hydrogen; when Z is a (per) fluoropolyoxyalkylene radical, it comprises units selected from the following: --CF2CF2O--,--CF2CF(CF3)O--,--CFX1O--wherein X1=F, CF3,--CF2CF2CF2O--,--CF2--CH2CH2O--,--C3F6O--. 5. The cured fluoroelastomers according to claim 2, wherein Z has formula: -(Q)hd p--CF2O--(CF2CF2O)m(CF2O) n--CF2-(Q)p-(II) wherein: Q is a C1-C10 alkylene oroxyalkylene radical; p is 0 or 1; m and n are numbers such that the m/n ratio is between 0.2 and 5 and the molecular weight of said (per) fluoropolyoxyalkylene radical is in the range 500-10,000. 6. The cured fluoroelastomers according to claim 5, wherein Q is selected from:--CH2OCH2--;--CH2O(CH2CH2O)sCH2--, s being=1-3. 7. The cured fluoroelastomers according to claim 2, wherein the bis-olefin has formula: CH2═CH--(CF2)t0-CH═CH 2 wherein t0 is an integer from 6 to 10. 8. The cured fluoroelastomers according to claim 2, wherein the bis-olefin has formula: CH2═CH--(CF2)6--CH═CH 2 (b). 9. The cured fluoroelastomers according to claim 1, wherein the curable fluoroelastomers further comprise iodine in amounts between 0.001% and 5% by weight with respect to the total polymer weight. 10. The cured fluoroelastomers according to claim 9, wherein the iodine atoms are in the chain and/or in end position. 11. The cured fluoroelastomers according to claim 9, wherein alternatively or in combination with the iodine, bromine, in the chain and in end position is present. 12. The cured fluoroelastomers according to claim 1, wherein the curable fluoroelastomers further comprise in admixture a semicrystalline (per) fluoropolymer, in an amount in per cent by weight referred to the total of the dry weight of the mixture fluoroelastomer+semicrystalline (per) fluoropolymer, from 0% to 70%. 13. The cured fluoroelastomers according to claim 12, wherein the semicrystalline (per) fluoropolymer is formed of tetrafluoroethylene (TFE) homopolymers, or TFE copolymers with one or more monomers containing at least one unsaturation of ethylene type, in an amount from 0.01% to 10% by moles, said comonomers having an ethylene unsaturation both of hydrogenated and fluorinated type. 14. The cured fluoroelastomers according to claim 13, wherein the hydrogenated comonomers are selected from ethylene, propylene, acrylic monomers, styrene monomers. 15. The cured fluoroelastomers according to claim 13, wherein the fluorinated comonomers are selected from the following: C3-C8, perfluoroolefins; C2-C8 hydrogenated fluoroolefins; perfluoroalkylethylene CH2═CH-Rf, wherein Rf is a C1-C6 perfluoroalkyl; C2-C8 chloro-and/or bromo-and/or iodo-fluoroolefins; CF2═CFORf (per) fluoroalkylvinylethers (PAVE), wherein Rf is a C1-C6 (per) fluoroalkyl; CF2═CFOX (per) fluoro-oxyalkylvinylethers, wherein X is: a C1-C12 alkyl, or a C1-C12 oxyalkyl, or a C1-C12 (per) fluoro-oxyalkyl having one or more ether groups, or fluorodioxoles. 16. The cured fluoroelastomers according to claim 12, wherein the comonomers are PAVEs and fluorodioxoles. 17. The cured fluoroelastomers according to claim 1, wherein the curable fluoroelastomers further comprise the following monomers (per cent by moles): A) from 1% to 99% of the monomer of formula: CF2═CFOCF2OCF3 (a) B) from 1% to 99% of one or more perfluorinated comonomers having at least one ethylene type unsaturation; said one or more comonomers comprising vinyliderie fluoride (VDF) in an amount from 1% to 85% on the total of the monomer moles so that the polymer is fluoroelastomeric; the sum of the monomer molar percentages being 100%. 18. The cured fluoroelastomers according to claim 17, wherein, when the copolymer does not contain other comonomers (B) besides VDF, the monomer amount of formula (a) is not lower than about 15% by moles. 19. The cured fluoroelastomers according to claim 17, wherein comonomers B) are selected from the following: C2-C8 perfluoroolefins; perfluoroalkylvinylethers of formula CF2═CFORf wherein Rf is a C1-C2 perfluoroalkyl. 20. The cured fluoroelastomers according to claim 19, wherein comonomer B) is selected from tetrafluoroethylene (TFE) and/or perfluoromethylvinylether (MVE). 21. The cured fluoroelastomers according to claim 17, having the following monomer compositions (in % by moles), the sum of the monomer molar percentages being 100%: monomer of formula (a): 15-40%, VDF: 60-85%, bis-olefin of formula (b) 0.01-1%; monomer of formula (a): 15-40%, VDF: 60-85%, TFE: 5-40%, bis-olefin of formula (b) 0.01-1%; monomer of formula (a): 5-40%, MVE: 5-30%, VDF: 50-85%, bis-olefin of formula (b) 0.01-1%; monomer of formula (a): 5-40%, MVE: 5-30%, VDF: 50-85%, TFE: 5-40%, bis-olefin of formula (b) 0.01-1%; monomer of formula (a): 40-99%, VDF: 1-60%, bis-olefin of formula (b) 0.01-1%; monomer of formula (a): 40-99%, MVE: 0-30%, VDF: 1-60%, bis-olefin of formula (b) 0.01-1%; monomer of formula (a): 40-99%, MVE: 0-30%, VDF: 1-60%, TFE: 5-40%, bis-olefin of formula (b) 0.01-1%. 22. The cured fluoroelastomers of claim 1, wherein the curable fluoroelastomers have a glass transition temperature lower than-40° C. 23. The cured fluoroelastomers of claim 2, wherein the C1-C18 linear or branched alkylene or cycloalkylene radical comprises oxygen atoms. 24. The cured fluoroelastomers of claim 2, wherein the C1-C18 linear or branched alkylene or cycloalkylene radical is partially fluorinated. 25. The cured fluoroelastomers of claim 3, wherein the unit amount in the chain deriving from the bis-olefins of formula (I) is from 0.03 to 0.5% by moles of the monomeric units, constituting the basic fluoroelastomer structure, the monomer total sum being 100%. 26. The cured fluoroelastomers of claim 4, wherein in formula (I) Z is a C4-C8 perfluoroalkylene radical. 27. The cured fluoroelastomers of claim 5, wherein the molecular weight of said (per) fluoropolyoxyalkylene radical is in the range of 700 to 2,000. 28. The cured fluoroelastomers of claim 9, wherein the curable fluoroelastomers comprise iodine in amounts between 0.01% and 2.5% by weight with respect to the total polymer weight. 29. The cured fluoroelastomers of claim 12, wherein the curable fluoroelastomers comprise 0% to 50% by weight of the semicrystalline (per) fluoropolymer. 30. The cured fluoroelastomers of claim 13, wherein the amount of tetrafluoroethylene (TFE) homopolymers or TFE copolymers with one or more monomers containing at least one unsaturation of ethylene type is 0.05% to 7% by moles. 31. The cured fluoroelastomers according to claim 15, wherein the C1-C12 (per) fluoro-oxyalkyl having one or more ether groups is perfluoro-2-propoxy-propyl. 32. The cured fluoroelastomers according to claim 15, wherein X is a periluorodioxole. 33. The cured fluoroelastomers according to claim 16, wherein the comonomers are PAVEs and per-fluorodioxoles. 34. The cured fluroelastomers of claim 17, wherein the curable fluoroelastomers comprise the following monomers (per cent by moles): A) from 5% to 99% of the monomer of formula: CF2═CFOCF2OCF3 (a) B) from 1 to 95% of one or more perfluorinated comonomers having at least one unsaturation of ethylene type. 35. The cured fluoroelastomers according to claim 19, wherein C2-C8 perfluoroolefins include TFE and hexafluoropropene. 36. The cured fluoroelastomers according to claim 19, wherein Rf is--CF3. 37. The cured fluoroelastomers according to claim 21, having the following monomer compositions, expressed in % by moles, the sum of the monomer molar percentages being 100%: monomer of formula (a): 15-40%, VDF: 60-85%, bis-olefin of formula (b): 0.01-1%; monomer of formula (a): 15-40%, VDF: 60-85%; TFE: 5-40%, bis-olefin of formula (b): 0.01-1%; monomer of formula (a): 5-40%, MVE: 5-30%, VDF: 50-85%, bis-olefin of formula (b): 0.01-1%; monomer of formula (a): 5-40%, MVE: 5-30%, VDF: 50-85%, TFE: 5-40%, bis-olefin of formula (b): 0.01-1%; monomer of formula (a): 40-99%, VDF: 1-60%, bis-olefin of formula (b): 0.01-1%; monomer of formula (a): 40-99%, MVE: 0-30%, VDF: 1-60%, bis-olefin of formula (b): 0.01-1%; monomer of formula (a): 40-99%, MVE: 0-30%, VDF: 1-60%, TFE: 5-40%, bis-olefin of formula (b): 0.01-1%. 38. Manufactured articles comprising the cured fluoroelastomers according to claim 1. 39. A method of manufacturing articles, comprising using VDF-based curable fluoroelastomers, said fluoroelastomers comprising the monomer of formula (a) CF3OCF2OCF═CF2, said fluoroelastomers having a glass transition temperature lower than-35° C., an improved combination of mechanical and compression set properties at range of temperatures up to 250° C., high thermal resistance, high molecular weight, and an amount of--COF end groups lower than the sensitivity limit of the following method: at the end of the polymerization, the polymer is isolated by coagulation by freezing and subsequent defrosting; it is washed twice with demineralized water and is dried in a stove until a constant weight; the--COF end groups are determined by FT-IR spectroscopy, wherein on a polymer film having a thickness from 50 to 300 micron a scanning between 4,000 cm-1 and 400 cm-1 is initially carried out, the film being then kept for 12 hours in an environment saturated with ammonia vapours, and recording the IR spectrum under the same conditions of the initial IR spectrum; elaborating the two spectra by subtracting to the signals of the spectrum of the untreated specimen (initial spectrum) the corresponding signals of the specimen spectrum after exposure to ammonia vapours, drawing the difference spectrum, normalized by the following equation: the optical densities related to the--COF end groups, reacted with the ammonia vapours, are measured; the optical densities are converted into mmoles/kg of polymer by using the extinction coefficients reported in Table 1, page 73 of the report by M. Pianca et Al. "End groups in fluoropolymers", J. Fluorine Chem. 95 (1999), 71-84; obtaining the concentrations of the residual--COF end groups expressed as mmoles of end groups--COF/Kg of polymer: in the fluoroelastomer spectrum no bands related to COF groups (1900-1830 cm-1) are detectable, the method sensitivity limit being 0.05 mmoles/Kg.