US20060189760A1 - Fluoroelastomer compositions - Google Patents

Fluoroelastomer compositions Download PDF

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US20060189760A1
US20060189760A1 US11305107 US30510705A US2006189760A1 US 20060189760 A1 US20060189760 A1 US 20060189760A1 US 11305107 US11305107 US 11305107 US 30510705 A US30510705 A US 30510705A US 2006189760 A1 US2006189760 A1 US 2006189760A1
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cured
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tfe
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Margherita Albano
Marco Apostolo
Vincenzo Arcella
Enrico Marchese
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Solvay Specialty Polymers Italy SpA
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Solvay Specialty Polymers Italy SpA
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/10Homopolymers or copolymers of unsaturated ethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08L27/18Homopolymers or copolymers or tetrafluoroethene

Abstract

Fluoropolymers comprising a fluoroelastomer matrix incorporating therein particles of a semicrystalline fluoropolymer formed of tetrafluoroethylene (TFE) homopolymers or copolymers, wherein the average particle sizes of the semicrystalline fluoropolymer latex range from 10 to 100 nm.

Description

  • This application is a continuation of U.S. patent application Ser. No. 10/843,440 filed on May 12, 2004, which is a continuation of U.S. application Ser. No. 10/118,066, filed on Apr. 4, 2002, which is a continuation of U.S. application Ser. No. 09/511,949 filed on Feb. 23, 2000, all of which are incorporated by reference herein.
  • The present invention relates to fluoropolymers essentially formed by a mixture of a fluoroelastomer and a semicrystalline fluoropolymer usable for sealing manufactured articles in the electronic, optical and pharmaceutical industry.
  • More specifically the present invention relates to fluoropolymers formed by a mixture of a fluoroelastomer and a semicrystalline fluoropolymer, characterized by improved mechanical properties combined with good properties of elastic retention (lower compression set) and very good surface appearance without roughness. It is well known that one of the fluoroelastomer uses is the preparation of O-rings for seals: for this application it is essential that the O-ring surface is smooth.
  • The use of fluoroelastomers containing polytetrafluoroethylene (PTFE) particles to improve the properties of abrasion-resistance and of hot tearing the obtained manufactured articles is known in the prior art. As described in Japanese patent 57-107,336, the fluoroelastomer abrasion-resistance is improved by physically mixing solid curable fluoroelastomers with PTFE powders having a low molecular weight, in the range 500-200,000 as average molecular weight by number (Mn). Said PTFE is prepared by thermal decomposition at a temperature between 450° C. and 600° C. for prolonged times or by irradiation with ionic radiation of high molecular weight PTFE. An alternative method for obtaining PTFE having a low molecular weight is that to polymerize TFE in the presence of chain transfer agents. The fluoroelastomer and the PTFE powders are mixed in Banbury or in calender.
  • In U.S. Pat. No. 4,879,362 and U.S. Pat. No. 4,904,726 mixtures of fluoroelastomers with resins of PTFE modified with the addition of comonomers such as hexafluoropropene (HFP), perfluoropropylvinylether (PPVE), etc., are used, in order to avoid PTFE fibrillation problems without losing the reinforcement properties that the PTFE gives to the obtained fluoroelastomers. The comonomer results much more present on the polymeric particle surface, so as to allow an uniform distribution in the fluoroelastomer without the formation of visible agglomerates. The latter should be the cause of fibrillation phenomena.
  • In EP 708,797 fluoroelastomer compositions formed by a fluoroelastomer and by a semicrystalline fluorinated filler in the form of micropowder which are obtained in curing compounds not containing metal species, are described. Said compositions give a low release of metal species under conditions where an high purity is required, but they show poor mechanical properties. Tests carried out by the Applicant (see the comparative Examples), have shown that the surface of the manufactured articles obtained from said fluoroelastomer compositions shows roughness. It is well known that in the O-ring preparation, typical fluoroelastomer application, surfaces having a low roughness in order to obtain good sealing properties, are required. The semicrystalline fluorinated filler is based on PTFE or PTFE modified with a comonomer and obtained by emulsion or suspension polymerization. The high molecular weight PTFE is subjected to irradiation, as above said, in order to reduce the molecular weight. This makes easier the PTFE milling produced by a suspension process; it eliminates the fibrillation and reduces the PTFE agglomeration obtained by an emulsion process.
  • The need was felt to have available fluoroelastomer compositions comprising a semicrystalline fluorinated filler having improved properties compared with those of the prior art and specifically with the following property combination:
      • improved mechanical properties
      • good elastic retention properties (lower compression set-very good seal)
      • very good surface appearance roughness free.
  • The Applicant has unexpectedly and surprisingly found that it is possible to obtain the combination of the above mentioned properties, by incorporating in the fluoroelastomer matrix PTFE particles or its copolymers having well defined sizes as specified hereinafter.
  • It is therefore an object of the present invention fluoropolymers comprising a fluoroelastomer matrix incorporating therein particles of a semicrystalline fluoropolymer latex formed by tetrafluoroethylene (TFE) homopolymers, or TFE copolymers with one or more monomers containing at least one ethylene unsaturation in amounts ranging from 0.01% to 10% by moles, preferably from 0.05% to 5% by moles, wherein the average particle sizes of the semicrystalline fluoropolymer latex range from 10 to 100 nm, preferably from 10 to 60 nm. Also semycrystalline fluoropolymers wherein the latex particle sizes have the above mentioned value for at least 60% by weight, preferably 70% by weight of the semicrystalline fluoropolymer, can be used.
  • The invention compositions are obtainable by mixing the semicrystalline fluoropolymer latex with the fluoroelastomer latex and subsequent coagulation. Alternatively the invention compositions can be polymerized in the same reactor in two subsequent steps: in a first step the semicrystalline fluoropolymer with the mentioned nanometric sizes is polymerized and in a second step the fluoroelastomer is polymerized. By operating in this way the fluoroelastomer should cover the semicrystalline fluoropolymer latex particles, allowing to obtain a very good dispersion of the latter in the fluoroelastomer.
  • The semicrystalline fluoropolymer amount inside the fluoroelastomer matrix is in the range 2%-40% by weight, preferably 5-30% by weight, more preferably 10-20% by weight on the total of the polymeric mixture.
  • The semicrystalline fluoropolymer particles having the above mentioned sizes are obtainable for example by a polymerization process in an aqueous microemulsion of perfluoropolyoxyalkylenes as described for example in the European patent application EP 99112083.3 in the name of the Applicant, herein incorporated by reference. Microemulsion polymerization methods can also be used, wherein the oil phase is formed by polymerizable unsaturated monomers, as described in U.S. Pat. No. 5,523,346 and in U.S. Pat. No. 5,616,648.
  • The fluoroelastomers can be prepared by copolymerization of the monomers in aqueous emulsion, according to well known methods in the prior art, in the presence of radical initiators (for example alkaline or ammonium persulphates, perphosphates, perborates, percarbonates), optionally in combination with ferrous, cuprous or silver salts, or of other easily oxidizable metals. In the reaction medium also surfactants of various kind, among which the fluorinated surfactants are particularly preferrred, are usually present.
  • Alternatively the fluoroelastomers can be prepared in bulk or in suspension, in an organic liquid in which a suitable radical initiator is present, according to well known techniques.
  • The polymerization reaction is generally carried out at temperatures in the range 25°-150° C., under a pressure up to 10 MPa.
  • The fluoroelastomers are preferably prepared in microemulsion of perfluoropolyoxyalkylens, according to U.S. Pat. No. 4,789,717 and U.S. Pat. No. 4,864,006.
  • The Applicant has found that in order to obtain the results of the present invention it is essential that the semi-crystalline fluoropolymer filler latex has the mentioned nanometric sizes, while the size of the latex of the fluoroelastomer is not critical.
  • When the semi-crystalline fluorinated filler is based on modified PTFE, for its preparation comonomers having an ethylene unsaturation both of hydrogenated and fluorinated type, can be used. Among those hydrogenated, ethylene, propylene, acrylic monomers, for example methylmethacrylate, (meth)acrylic acid, butylacrylate, hydroxyethylhexyl-acrylate, styrene monomers can be mentioned.
  • Among the fluorinated comonomers we can mention:
      • perfluoroolefins C3-C8, such as hexafluoropropene (HFP), hexafluoroisobutene;
      • hydrogenated fluorolefins C2-C8, such as vinyl fluoride (VF), vinylidene fluoride (VDF), trifluoroethylene, perfluoroalkylethylene CH2═CH—Rf, wherein Rf is a perfluoroalkyl C1-C6;
      • chloro- and/or bromo- and/or iodo-fluoroolefins C2-C8, such as chlorotrifluoroethylene (CTFE);
      • (per)fluoroalkylvinylethers (PAVE) CF2═CFORf, wherein Rf is a (per)fluoroalkyl C1-C6, for example CF3, C2F5, C3F7;
      • (per)fluoro-oxyalkylvinylethers CF2═CFOX, wherein X is: an alkyl C1-C12, or an oxyalkyl C1-C12, or a (per)fluorooxyalkyl C1-C12 having one or more ether groups, for example perfluoro-2-propoxy-propyl; fluorodioxoles, preferably perfluorodioxoles.
  • PAVEs are preferred comonomers, specifically perfluoromethyl-, ethyl-, propylvinylether and fluorodioxoles, preferably perfluorodioxoles.
  • The fluoroelastomers used in the present invention belong to the following classes:
    • (1) VDF-based copolymers, wherein VDF is copolymerized with at least one comonomer selected from the following: perfluoroolefins C2-C8, such as tetrafluoroethylene (TFE) hexafluoropropene (HFP); chloro- and/or bromo- and/or iodo-fluoroolefins C2-C8, such as chlorotrifluoroethylene (CTFE) and bromotrifluoroethylene; (per)fluoroalkylvinylethers (PAVE) CF2═CFORf, wherein Rf is a (per)-fluoroalkyl C1-C6, for example trifluoromethyl, bromodifluoromethyl, pentafluoropropyl; perfluorooxyalkylvinylethers CF2═CFOX, wherein X is a perfluorooxyalkyl C1-C12 having one or more ether groups, for example perfluoro-2-propoxy-propyl; non fluorinated olefins (Ol) C2-C8, for example ethylene and propylene;
    • (2) TFE-based copolymers, wherein TFE is copolymerized with at least one comonomer selected from the following: (per)fluoroalkylvinylethers (PAVE) CF2═CFORf, wherein Rf is as above defined; perfluoro-oxyalkylvinylethers CF2═CFOX, wherein X is as above defined; fluoroolefins C2-C8 containing hydrogen and/or chloro and/or bromo and/or iodo atoms; non fluorinated olefins (Ol) C2-C8; perfluorovinylethers containing hydrocyanic groups as described in U.S. Pat. No. 4,281,092, U.S. Pat. No. 5,447,993, U.S. Pat. No. 5,789,489.
  • Preferably the invention fluoroelastomers contain perfluorinated monomers, and preferably the base structure of these fluoroelastomers is selected from the copolymers of class (2), wherein TFE is polymerized with one or more perfluorinated comonomers as above mentioned.
  • Within the above defined classes, preferred compositions by moles of the monomers forming the base structure of the fluoroelastomer are the following:
      • (a) vinylidene fluoride (VDF) 45-85%, hexa-fluoropropene (HFP) 15-45%, tetrafluoroethylene (TFE) 0-30%;
      • (b) vinylidene-fluoride (VDF) 50-80%, perfluoroalkylvinylether (PAVE) 5-50%, tetrafluoroethylene (TFE) 0-20%;
      • (c) vinylidene fluoride (VDF) 20-30%, non fluorinated olefins (Ol) C2-C8 10-30%, hexafluoropropene (HFP) and/or perfluoroalkylvinylether (PAVE) 18-27%, tetrafluoroethylene (TFE) 10-30%;
      • (d) tetrafluoroethylene (TFE) 50-80%, perfluoroalkylvinylether (PAVE) 20-50%;
      • (e) tetrafluoroethylene (TFE) 45-65%, non fluorinated olefins (Ol) C2-C8 20-55%, vinylidene fluoride 0-30%;
      • (f) tetrafluoroethylene (TFE) 32-60% by moles, non fluorinated olefins (Ol) C2-C8 10-40%, perfluoroalkylvinylether (PAVE) 20-40%;
      • (g) tetrafluoroethylene (TFE) 33-75%, perfluoroalkylvinylether (PAVE) 15-45%, vinylidene fluoride (VDF) 5-30%.
  • Specific particularly preferred compositions are:
      • (d) TFE 50-80%, PAVE 20-50%;
      • (g) TFE 33-75%, PAVE 15-45%, VDF 5-30%.
  • Optionally the fluoroelastomers comprise also monomer units deriving from a bis-olefin having general formula:
    Figure US20060189760A1-20060824-C00001

    wherein:
    R1, R2, R3, R4, R5, R6, equal to or different from each other, are H or alkyls C1-C5;
    Z is a linear or branched, alkylene or cycloalkylene C1-C18 radical, optionally containing oxygen atoms, preferably at least partially fluorinated, or a (per)fluoropolyoxyalkylene radical, as described in EP 661,304 in the name of the Applicant.
  • The unit amount in the chain deriving from said bis-olefins is generally in the range 0.01-1.0 by moles, preferably 0.03-0.5 by moles, still more preferably 0.05-0.2% by moles for 100 moles of the other above mentioned monomer units forming the fluoroelastomer base structure.
  • The fluoropolymers of the present invention can be cured by peroxidic route, wherefore they preferably contain along the chain and/or in terminal position of the macromolecules iodine and/or bromine atoms. The introduction of such iodine and/or bromine atoms can be achieved by addition, in the reaction mixture, of brominated and/or iodinated cure-site comonomers, such as bromo and/or iodo olefins having from 2 to 10 carbon atoms (as described for example in U.S. Pat. No. 4,035,565 and U.S. Pat. No. 4,694,045), or iodo and/or bromo fluoroalkylvinylethers (as described in U.S. Pat. No. 4,745,165, U.S. Pat. No. 4,564,662 and EP 199,138), in such amounts so that the content of cure-site comonomers in the final product is generally in the range 0.05-2 moles for 100 moles of the other base monomer units.
  • Other usable iodinated compounds are the triodinated deriving from triazines as described in European patent application EP 860,436 and in the European patent application EP 99114823.0.
  • Alternatively or also in association with the cure-site comonomers it is possible to introduce iodine and/or bromine end atoms by addition to the reaction mixture of iodinated and/or brominated chain transfer agents, such as for example the compounds of formula Rf(I)x(Br)y, wherein Rf is a (per)fluoroalkyl or a (per)fluorochloroalkyl having from 1 to 8 carbon atoms, while x and y are integers between 0 and 2, with 1≦x+y≦2 (see for example U.S. Pat. No. 4,243,770 and U.S. Pat. No. 4,943,622). It is also possible to use, as chain transfer agents, alkaline or earth-alkaline metal iodides and/or bromides, according to U.S. Pat. No. 5,173,553.
  • In association with the chain transfer agents containing iodine and/or bromine, other chain transfer agents known in the prior art, such as ethyl acetate, diethylmalonate, etc., can be used.
  • Curing by peroxidic route is carried out, according to known techniques, by addition of a suitable peroxide capable to generate radicals by thermal decomposition. Among the most commonly used we mention: dialkylperoxides, such as for example di-terbutyl-peroxide and 2,5-dimethyl-2,5-di-(terbutylperoxy)hexane; dicumyl peroxide; dibenzoyl peroxide; diterbutyl perbenzoate; di [1,3-dimethyl-3-(terbutylperoxy)-butyl]carbonate. Other peroxidic systems are described, for example, in European patent applications EP 136,596 and EP 410,351.
  • To the compound (curable blend) other products are then added, such as:
    • (a) curing coagents, in an amount generally in the range 0.5-10%, preferably 1-7% by weight with respect to the polyymer; among them, triallyl-cyanurate; triallyl-isocyanurate (TAIC); tris(diallylamine)-s-triazine; triallylphosphite; N,N-diallyl-acrylamide; N,N,N′,N′-tetraallylmalonamide; trivinyl-isoyanurate; 2,4,6-trivinyl-methyltrisiloxane, etc., are commonly used; TAIC is particularly preferred; other preferred crosslinking agents are bis-olefins described in the European patent application EP 769,520. Other crosslinking agents which can be used are the triazines described in the European patent applications EP 860,436 and WO97/05122.
    • (b) optionally a metal compound, in an amount in the range 1-15%, preferably 2-10%, by weight with respect to the polymer, selected from oxides or hydroxides of divalent metals, such as for example, Mg, Zn, Ca or Pb, optionally associated to a weak acid salt, such as for example stearates, benzoates, carbonates, oxalates or phosphites of Ba, Na, K, Pb, Ca;
    • (c) optionally acid acceptors of the non metal oxide type, such as 1,8 bis dimethyl amino naphthalene, octadecylamine etc. as described in EP 708,797.
    • (d) other conventional additives, such as thickening fillers, pigments, antioxidants, stabilizers and the like.
  • When the fluoroelastomer matrix contains cyano groups, the fluoropolymer curing of the present invention is carried Out by using as crosslinking agents tin organic compounds or di-aromatic aminic compounds, as described in U.S. Pat. No. 4,394,489, U.S. Pat. No. 5,767,204, U.S. Pat. No. 5,789,509. This type of curing can be associated to a curing of peroxidic type, when the fluoroelastomer matrix contains iodine or bromine atoms, preferably end atoms, as described in U.S. Pat. No. 5,447,993.
  • The present invention will be better illustrated by the following Examples, which have a merely indicative but not limitative purpose of the scope of the invention itself.
  • EXAMPLE 1
  • a) Preparation of the Semicrystalline Fluoropolymer
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 272 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 59 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 59 ml of a 30% by volume NH4OH aqueous solution;
      • 118 ml of demineralized water;
      • 36 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. 0.48 bar of C2H6 were fed into the autoclave and the pressure was increased and maintained constant at 11 bar during the whole polymerization with TFE.
  • 6.5 g of ammonium persulphate (APS) as initiator agent were then introduced into the autoclave. After 37 minutes of reaction, the autoclave was cooled and the latex discharged. The latex characteristics are reported in Table 1.
  • b) Preparation of the Fluoroelastomer
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 67 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 14.5 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 14.5 ml of a 30% by volume NH4OH aqueous solution;
      • 29 ml of demineralized water;
      • 9 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)m(CF2O)CF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The following mixture of monomers was then fed:
    perfluoromethylvinylether (PMVE) 60% by moles
    tetrafluoroethylene (TFE) 40% by moles

    so as to increase the pressure to 25 bar.
      • 0.32 g of ammonium persulphate (APS) as initiator agent;
      • 26 g of 1,6-diiodoperfluorohexane (C6F12I2) as chain transfer agent;
      • 5 g of bis-olefin of formula CH2═CH—(CF2)6—CH═CH2; the addition was carried out in 20 portions, each of 0.25 g, starting from the polymerization beginning and for every increase in the monomer conversion,
      • were then introduced in the autclave.
  • The 25 bar pressure was maintained constant for the whole duration of the polymerization by feeding a mixture formed by:
    perfluoromethylvinylether (PMVE) 40% by moles
    tetrafluoroethylene (TFE) 60% by moles
  • After 137 minutes of reaction, the autoclave was cooled and the latex discharged. The latex properties are reported in Table 1.
  • c) Mixing of the Latexes Preparation of the Final Polymer
  • 635.6 ml of the latex obtained in Example 1a are mixed with 1517 ml of the Example 1b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for every litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 2, were obtained.
  • EXAMPLE 2 (COMPARATIVE)
  • a) Preparation of the Semicrystalline Fluoropolymer
  • In a 50 l autoclave, equipped with a stirrer working at 245 rpm, 32 l of demineralized water, 12 g of ammonium prfluorooctanoate and 140 g of paraffin with melting point 52-56° C. were introduced, after evacuation.
  • The autoclave was then heated to 89° C. and progressively increased up to 102.1° C. with a rate of 1° C. per minute for the whole reaction duration. 350 mbar of ethane were fed into the autoclave and the pressure was increased and maintained at 20 bar by continuously feeding TFE during the polymerization.
  • 3.5 g of ammonium prsulphate (APS) as initiator agent and subsequently further 2 g of an APS aqueous solution at a flow-rate of 50 cc/min were introduced in the autoclave.
  • After 73 minutes of reaction, the autoclave was cooled and the latex discharged. The latex characteristics are reported in Table 1.
  • b) Preparation of the Fluoroelastomer
  • The fluoroelastomer latex was obtained as described in Example 1b.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 428.5 ml of the latex obtained in Example 2a are mixed with 1517 ml of the Example 2b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for every litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 2, were obtained.
  • EXAMPLE 3 (COMPARATIVE)
  • a) Preparation of the Semicrystalline Fluoropolymer
  • The PTFE latex was obtained in the presence of a microemulsion as in Example 1a. The latex was subsequently coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 150° C. in an air-circulation oven for 24 hours.
  • b) Preparation of the Fluoroelastomer
  • The perfluoroelastomer latex was obtained as described in Example 1b. The latex was subsequently coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 100° C. in an air-circulation oven for 12 hours.
  • c) Mechanical Mixing—Preparation of the Final Polymer
  • 425 g of fluoroelastomer of Example 3b were mixed with 75 g of PTFE powder obtained from Example 3a in an open mixer with rollers heated at 60° C. In the mixing process the perfluoroelastomer is introduced first with the rollers completely near the one to the other and mixed until a continuous polymer film is obtained. The PTFE powder was then added until obtaining an uniform mixing. The obtained mixture was characterized as reported in Table 2.
  • EXAMPLE 4 (COMPARATIVE)
  • 425 g of fluoroelastomer obtained in Example 3b were mixed in an open mixer with 75 g of PTFE MP 1600 by Du Pont by using the procedure described in Example 3c. The mixture properties are reported in Table 2.
  • EXAMPLE 5
  • a) Preparation of the Semicrystalline Fluoropolymer
  • In a 50 l autoclave, equipped with a stirrer working at 245 rpm, after evacuation, 32 l of demineralized water, 140 g of a paraffin with melting point 52°-56° C. and 300 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 65 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 65 ml of a 30% by volume NH4OH aqueous solution;
      • 130 ml of demineralized water;
      • 40 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and the temperature was progressively increased up to 96° C. with a rate of 0.6° C./min for the whole reaction duration. 370 mbar of C2H6 were fed into the autoclave and the pressure was increased and maintained constant at 20 bar during the whole polymerization by feeding TFE.
  • 2.5 g of ammonium persulphate (APS) as initiator agent were then introduced into the autoclave and subsequently by feeding, starting from 10% of conversion, 0.54 g of APS every 10% of monomer conversion. After 64 minutes of reaction, the autoclave was cooled and the latex discharged. The latex characteristics are reported in Table 3.
  • b) Preparation of the Fluoroelastomer
  • The fluoroelastomer latex was obtained as described in Example 1b, except that the amount of 1,6-diiodoperfluorohexane was of 30 g instead of 26 g.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 347 ml of the latex obtained in Example 5a are mixed with 1197 ml of the Example 5b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 4, were obtained.
  • EXAMPLE 6
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 260 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 56.3 ml of a perfluoropolyoxyalkylene having an acid end group of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 56.3 ml of a 30% by volume NH4OH aqueous solution;
      • 112.7 ml of demineralized water;
      • 34.7 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. 0.48 bar of ethane were fed into the autoclave and the pressure was increased and maintained constant at 11 bar by continuously feeding TFE during the polymerization.
  • 6.5 g of ammonium persulphate (APS) were then introduced into the autoclave as initiator. After 15 minutes of reaction, the autoclave was cooled, degassed and discharged. The latex characteristics are reported in Table 3. Subsequently 2368 ml (corresponding to 449.9 g of polymer) of the latex are introduced again in the 10 litre reactor to which 4132 litres of demineralized water are added. The autoclave is then brought to 90° C. and maintained for one hour at said temperature in order to decompose all the residual initiator agent.
  • Subsequently the temperature is increased to 80° C. and maintained constant for the whole duration of the polymerization. The following mixture of monomers was then fed:
    perfluoromethylvinylether (PMVE) 60% by moles
    tetrafluoroethylene (TFE) 40% by moles

    so as to increase the pressure to 25 bar.
      • 0.32 g of ammonium persulphate (ADS) as initiator agent;
      • 22.3 g of 1,6-diiodoperfluorohexane (C6F12I2) as chain transfer agent;
      • 4.28 g of bis-olefin of formula CH2═CH—(CF2)6—CH═CH2; the addition was carried out in 20 portions, each of 0.214 g, starting from the polymerization beginning and for every 5% increase in the monomer conversion,
      • were then introduced in the autoclave.
  • The 25 bar pressure was maintained constant for the whole duration of the polymerization by feeding a mixture formed by:
    perfluoromethylvinylether (PMVE) 40% by moles
    tetrafluoroethylene (TFE) 60% by moles
  • After 45 minutes of reaction corresponding to 2550 g of elastomer, the autaoclave was cooled and the latex discharged. The latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. The obtained polymer was characterized as shown in Table 4.
  • EXAMPLE 7
  • a) Preparation of the Semicrystalline Fluoropolymer
  • The PTFE latex was obtained as described in Example 5a. The latex characteristics are reported in Table 3.
  • b) Preparation of the Fluoroelastomer
  • The fluoroelastomer latex was obtained as described in Example 5b. The characteristics are reported in Table 3.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 463 ml of the latex obtained in Example 7a are mixed with 1127 ml of the Example 7b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. The obtained polymer was characterized as shown in Table 4.
  • EXAMPLE 8
  • The polymer obtained in Example 7c was crosslinked with bis-olefin of formula CH2═CH— (CF2)6—O═CH2, instead of TAIC. The compound characteristics are reported in Table 4.
  • EXAMPLE 9
  • a) Preparation of the Semicrystalline Fluoropolymer
  • The PTFE latex was obtained as reported in Example 1a. The latex characteristics are reported in Table 5.
  • b) Preparation of the Fluoroelastomer
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, 6.5 l of demineralized water and 26 g of ammonium perfluorooctanoate were introduced, after evacuation.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The following mixture of monomers was then fed:
    perfluoromethylvinylether (PMVE) 60% by moles
    tetrafluoroethylene (TFE) 40% by moles

    so as to increase the pressure to 25 bar.
      • 6.5 g of ammonium persulphate (APS) as initiator agent;
      • 25 g of 1,6-diiodoperfluorohexane (C6F12I2) as chain transfer agent;
      • 5 g of bis-olefin of formula CH2═CH—(CF2)n—CH═CH2; the addition was carried out in 20 portions, each of 0.25 g, starting from the polymerization beginning and for every 5% increase in the monomer conversion,
      • were then introduced in the autoclave.
  • The 25 bar pressure was maintained constant for the whole duration of the polymerization by feeding a mixture formed by:
    perfluoromethylvinylether (PMVE) 40% by moles
    tetrafluoroethylene (TFE) 60% by moles
  • After 500 minutes of reaction, the autoclave was cooled and the latex discharged. The latex properties are reported in Table 5.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 551.5 ml of the latex obtained in Example 9a are mixed with 1393.5 ml of the Example 9b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 6, were obtained.
  • EXAMPLE 10
  • a) Preparation of the Semicrystalline Fluoropolymer
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 65.1 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 14.1 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 14.1 ml of a 30% by volume NH4OH aqueous solution;
      • 28.2 ml of demineralized water;
      • 8.7 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The autoclave was pressurized to the pressure of 0.56 bar with ethane and then to the pressure of 25 bar with a monomer mixture constituted by 10% by moles of perfluoromethylvinylether (PMVE) and 90% by moles of tetrafluoroethylene (TFE)
  • 1.3 g of ammonium persulphate (APS) as initiator agent were then introduced in the autoclave. During the reaction the pressure is maintained at 25 bar by continuously feeding the following monomer mixture: 3.5% by moles of PMVE and 96.5% of TFE.
  • After 60 minutes of reaction, the autoclave was cooled and the latex discharged. The latex characteristics are reported in Table 7.
  • b) Preparation of the Fluoroelastomer
  • In a 22 l autoclave, equipped with a stirrer working at 460 rpm, after evacuation, 15 l of demineralized water and 154.5 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 33.46 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 33.46 ml of a 30% by volume NH4OH aqueous solution;
      • 66.93 ml of demineralized water;
      • 20.65 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The following mixture of monomers was then fed:
    perfluoromethylvinylether (PMVE) 60% by moles
    tetrafluoroethylene (TFE) 40% by moles

    so as to increase the pressure to 25 bar.
      • 0.75 g of ammonium persulphate (APS) as initiator agent;
      • 69.24 g of 1,6-diiodoperfluorohexane (C6F12I2) as chain transfer agent;
      • 11.09 g of bis-olefin of formula CH2═CH—(CF2)6—CH═CH2; the addition was made in 20 portions, each of 0.554 g, starting from the polymerization beginning and for every 5% increase in the monomer conversion,
      • were then introduced in the autoclave.
  • The 25 bar pressure was maintained constant for the whole duration of the polymerization by feeding a mixture formed by:
    perfluoromethylvinylether (PMVE) 40% by moles
    tetrafluoroethylene (TFE) 60% by moles
  • After 110 minutes of reaction, the autoclave was cooled and the latex discharged. The latex properties are reported in Table 7.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 238 ml of the latex obtained in Example 10a are mixed with 1187 ml of the Example 10b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 8, were obtained.
  • EXAMPLE 11
  • In a 5 l autoclave, equipped with stirrer working at 630 rpm, after evacuation, 3.5 l of demineralized water and 35 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 7.58 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 7.58 ml of a 30% by volume NH4OH aqueous solution;
      • 15.16 ml of demineralized water;
      • 4.68 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The autoclave was pressurized to the pressure of 0.56 bar with ethane and then to the pressure of 25 bar with a monomer mixture formed by 10% by moles of perfluoromethylvinylether (PMVE) and 90% by moles of tetrafluoroethylene (TFE).
  • In the autoclave 0.7 g of ammonium persulphate (APS) as initiator agent were then introduced. During the reaction the pressure is maintained at 25 bar by continuously feeding the following monomer mixture: 3.5% by moles of PMVE and 96.5% of TFE.
  • After 10 minutes of reaction, the autoclave was cooled, degassed and discharged. The latex characteristics are reported in Table 7. Subsequently 747 ml (corresponding to 225 g of polymer) of the latex are introduced again in the 5 litres reactor to which 2.703 litres of demineralized water are added. The autoclave is then heated up to 90° C. and maintained for one hour at said temperature in order to decompose all the residual initiator agent. Subsequently the temperature is brought to 80° C. and maintained constant for the whole duration of the polymerization. The following mixture of monomers was then fed:
    perfluoromethylvinylether (PMVE) 60% by moles
    tetrafluoroethylene (TFE) 40% by moles

    so as to increase the pressure to 25 bar.
      • 0.175 g of ammonium persulphate (APS) as initiator agent;
      • 11.14 g of 1,6-diiodoperfluorohexane (C6F12I2) as chain transfer agent;
      • 2.14 g of bis-olefin of formula CH2═CH—(CF2)6—CH═CH2; the addition was carried out in 20 portions, each of 0.107 g, starting from the polymerization beginning and for every 5% increase in the monomer conversion,
      • were then introduced in the autoclave.
  • The 25 bar pressure was maintained constant for the whole duration of the polymerization by feeding a mixture formed by:
    perfluoromethylvinylether (PMVE) 40% by moles
    tetrafluoroethylene (TFE) 60% by moles
  • After 95 minutes of reaction corresponding to 1275 g of produced elastomer, the autoclave was cooled and the latex discharged.
  • The latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. The obtained polymer was characterized as shown in Table 8.
  • EXAMPLE 12 (COMPARATIVE)
  • a) Preparation of the Semicrystalline Fluoropolymer
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 16.25 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 3.52 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 3.52 ml of a 30% by volume NH4OH aqueous solution;
      • 7.04 ml of demineralized water;
      • 2.17 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The autoclave was pressurized to the pressure of 0.56 bar with ethane and then to the pressure of 25 bar with a monomer mixture formed by 10% by moles of perfluoromethylvinylether (PMVE) and 90% by moles of tetrafluoroethylene (TFE).
  • In the autoclave 1.3 g of ammonium persulphate (APS) as initiator agent were then introduced.
  • During the reaction the pressure is maintained at 25 bar by continuously feeding the following monomer mixture: 3.5% by moles of PMVE and 96.5% of TFE.
  • After 65 minutes of reaction, the autoclave was cooled and the latex discharged. The latex characteristics are reported in Table 7.
  • b) Preparation of the Fluoroelastomer
  • The perfluoroelastomer latex was obtained as reported in Example 10b. The latex characteristics are reported in Table 7.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 233.7 ml of the latex obtained in Example 12a are mixed with 1187 ml of the Example 12b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 8, were obtained.
  • EXAMPLE 13
  • a) Preparation of the Semicrystalline Fluoropolymer
  • The PTFE latex is obtained as reported in Example 9a. The latex properties are reported in Table 9.
  • b) Preparation of the Fluoroelastomer
  • In a 10 l autoclave, equipped with stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 65.1 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 14.1 ml of a perfluoropolyoxyalkylene, having an acid end group of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 14.1 ml of a 30% by volume NH4OH aqueous solution;
      • 28.2 ml of demineralized water;
      • 8.7 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The following mixture of monomers was then fed:
    vinylidene fluoride (VDF) 28% by moles
    tetrafluoroethylene (TFE) 15% by moles
    hexafluoropropene (HFP) 57% by moles

    so as to increase the pressure to 30 bar.
      • 1.3 g of ammonium persulphate (APS) as initiator agent;
      • 16.17 g of diiodomethane (CH2I2) as chain transfer agent fed with the following procedure: 20% at the reaction beginning, 40% when the conversion is equal to 20% and 40% when the conversion is equal to 80%;
      • 9 g of bis-olefin of formula CH2═CH—(CF2)6—CH═CH2; the addition was made in 20 portions, each of 0.45 g, starting from the polymerization beginning and for every 5% increase in the monomer conversion,
      • were then introduced in the autclave.
  • The 30 bar pressure was maintained constant for the whole duration of the polymerization by feeding a mixture formed by:
    vinylidene fluoride (VDF) 50% by moles
    tetrafluoroethylene (TFE) 25% by moles
    hexafluoropropene (HFP) 25% by moles
  • After 270 minutes of reaction, the autoclave was cooled and the latex discharged. The latex properties are reported in Table 9.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 552 ml of the latex obtained in Example 14a are mixed with 1412 ml of the Example 14b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 10, were obtained.
  • EXAMPLE 14
  • a) Preparation of the Semicrystalline Fluoropolymer
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 130 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 28.15 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 28.15 ml of a 30% by volume NH4OH aqueous solution;
      • 56.3 ml of demineralized water;
      • 17.4 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The autoclave was pressurized to the pressure of 0.56 bar with ethane and then to the pressure of 20 bar by feeding a monomer mixture formed by 1.8% by moles of perfluoropropylvinylether (PPVE) and 98.2% by moles of tetrafluoroethylene (TFE).
  • In the autoclave 1.3 g of ammonium persulphate (APS) were then introduced as initiator. During the reaction the pressure is maintained at 20 bar by continuously feeding the following monomer mixture: 1.8% of PPVE and 98.2% of TFE.
  • After 18 minutes of reaction, the autoclave was cooled and the latex discharged. The latex characteristics are reported in Table 9.
  • b) Preparation of the Fluoroelastomer
  • In a 10 l autoclave, equipped with a stirrer working at 545 rpm, after evacuation, 6.5 l of demineralized water and 65.1 ml of a perfluoropolyoxyalkylene microemulsion were introduced: the latter was previously obtained by mixing:
      • 14.1 ml of a perfluoropolyoxyalkylene, having an acid end group, of formula:
        CF2ClO(CF2—CF(CF3)O)n(CF2O)mCF2COOH
      • wherein n/m=10, having average molecular weight of 600;
      • 14.1 ml of a 30% by volume NH4OH aqueous solution;
      • 28.2 ml of demineralized water;
      • 8.7 ml of Galden® D02 of formula:
        CF3O(CF2—CF(CF3)O)n(CF2O)mCF3
      • wherein n/m=20, having average molecular weight of 450.
  • The autoclave was then heated up to 80° C. and maintained at said temperature for the whole reaction duration. The following mixture of monomers was then fed:
    perfluoromethylvinylether (PMVE) 60% by moles
    tetrafluoroethylene (TFE) 40% by moles

    so as to increase the pressure to 25 bar.
      • 0.32 g of ammonium persulphate (APS) as initiator agent;
      • 17 g of 1,6-diiodoperfluorohexane (C6F12I2) as chain transfer agent;
      • 5 g of bis-olefin of formula CH2═CH—(CF2)6—CH═CH2; the addition was effected in 20 portions, each of 0.25 g, starting from the polymerization beginning and for every 5% increase in the monomer conversion,
      • were then introduced in the autoclave.
  • The 25 bar pressure was maintained constant for the whole duration of the polymerization by feeding a mixture formed by:
    perfluoromethylvinylether (PMVE) 40% by moles
    tetrafluoroethylene (TFE) 60% by moles
  • After 80 minutes of reaction, the autoclave was cooled and the latex discharged. The latex properties are reported in Table 9.
  • c) Mixing of the Latexes—Preparation of the Final Polymer
  • 528 ml of the latex obtained in Example 15a are mixed with 1218 ml of the Example 15b latex. After mixing, the latex is coagulated with an aluminum sulphate solution (6 g of Al2(SO4)3 for each litre of latex) and dried at 80° C. in an air-circulating oven for 10 hours. 500 g of polymer, characterized as shown in Table 10, were obtained.
    TABLE 1
    Latex con- Particle MFI(1) Mooney
    centration diameter ASTM (1 + 10)121° C.
    (g/l) (nm) D 1238 ASTM D 1646
    Example 1a 118 12 82.7
    Example 1b 280 54 27
    Example 2a 175 197 0.2
    (comp.)
    Example 2b 280 54 27
    (comp.)

    (1)MFI has been determined at 380° C. with 3 Kg
  • TABLE 2
    EXAMPLE
    Ex. 2c Ex. 3c Ex. 4
    Ex. 1c comp. comp. comp.
    % by weight of plastomer 15 15 15 15
    ML(1 + 10)121° C. (ASTM D 1646) 58 nd 27
    Formulation:
    Elastomer (phr) 100 100 100 100
    TAIC 1.5 1.5 1.5 1.5
    Luperco 2 2 2 2
    ZnO 5 5 5 5
    ODR (177° C., 12′arc 3°)
    (ASTM D2084-81):
    ML Lbf. in. 11 nd 17 13
    MH 118 nd 115 140
    Ts2 sec 45 nd 45 51
    T′90 99 nd 90 109
    Molding in press at 180° C.
    for 10 min:
    Sheet surface smooth nd rough rough
    Mechanical properties after
    post cure at 200° C. for 1
    hour (ASTM D 412-83):
    M100 Mpa 4.9 nd 10.1 6.3
    C.R. 19.3 nd 18.5 18.7
    A.R. % 174 nd 145 174
    ShA Hardness points 69 nd 85 76
    Compression set on O-ring
    (ASTM D 395):
    200° C. for 70 hours (%) 29 nd 40 broken
    230° C. for 70 hours (%) 47 nd broken
  • TABLE 3
    Latex con- Particle MFI(1) Mooney
    centration diameter ASTM (1 + 10)121° C.
    (g/l) (nm) D 1238 ASTM D 1646
    Example 5a 216 90 2
    Example 5b 355 60 20
    Example 6 190 50 54.1
    Example 7a 216 90 2
    Example 7b 355 60 18

    (1)MFI has been determined at 380° C. with 3 Kg
  • TABLE 4
    EXAMPLE
    Ex. 5c Ex. 6 Ex. 7c Ex. 8
    % by weight of plastomer 15 15 20 20
    ML(1 + 10)121° C. (ASTM D 1646) 35 39 41 35
    Formulation:
    Elastomer (phr) 100 100 100 100
    TAIC 1.5 1.5 1.5
    BO(2) 4
    Luperco 2 2 2 4
    ZnO 5 5 5 5
    ODR (177° C., 12′arc 3°)
    (ASTM D2084-81):
    ML Lbf. in. 8 6 12 4
    MH 131 108 133 77
    Ts2 sec 45 52 60 78
    T′90 285 138 123 330
    Molding in press at 180° C.
    for 10 min:
    Sheet surface smooth smooth smooth smooth
    Mechanical properties
    after post cure at 200° C.
    for 1 h (ASTM D 412-83):
    M100 Mpa 5.6 4.5 7.9 10.1
    C.R. 16.4 16.9 18.4 18.5
    A.R. % 164 190 154 145
    ShA Hardness points 73 72 78 85
    Compression set on O-ring
    (ASTM D 395):
    200° C. for 70 hours (%) 28 49 33 43

    (2)Bisolefin of formula CH2═CH—(CF2)6—CH═CH2
  • TABLE 5
    Latex con- Particle MFI Mooney
    centration diameter ASTM (1 + 10)121° C.
    (g/l) (nm) D 1238 ASTM D 1646
    Example 9a 136 12 82.7(1)
    Example 9b 305 163 38

    (1)MFI has been determined at 380° C. with 3 Kg
  • TABLE 6
    EXAMPLE
    Ex. 9c
    % by weight of plastomer 15
    ML(1 + 10)121° C. (ASTM D 1646) 48
    Formulation:
    Elastomer (phr) 100
    TAIC 1.5
    Luperco 2
    ZnO 5
    ODR (177° C., 12′arc 3°)
    (ASTM D2084-81):
    ML Lbf. in. 11
    MH 95
    Ts2 sec 48
    T′90 103
    Molding in press at 180° C.
    for 10 min:
    Sheet surface smooth
    Mechanical properties after
    post cure at 200° C. for 1
    hour (ASTM D 412-83):
    M100 Mpa 6.3
    C.R. 22.2
    A.R. % 184
    ShA hardness points 73
    Compression set on O-ring
    (ASTM D 395):
    200° C. for 70 hours (%) 47
  • TABLE 7
    Latex con- Particle MFI Mooney
    centration diameter ASTM (1 + 10)121° C.
    (g/l) (nm) D 1238 ASTM D 1646
    Example 10a 315 60 295(1)
    Example 10b 358 54 15
    Example 11 301 26 216(2)
    Ex. 12a comp. 321 103 245(1)
    Ex. 12b comp. 358 54 15

    (1)MFI has been measured at 372° C. with 5 Kg

    (2)MFI has been measured at 372° C. with 10 Kg
  • TABLE 8
    EXAMPLE
    Ex. 12c
    Ex. 10c Ex. 11 comp.
    % by weight of plastomer 15 15 15
    ML(1 + 10)121° C. (ASTM D 1646) 27 55 28
    Formulation:
    Elastomer (phr) 100 100 100
    TAIC 1.5 1.5 1.5
    Luperco 2 2 2
    ZnO 5 5 5
    ODR (177° C., 12′arc 3°)
    (ASTM D2084-81):
    ML Lbf. in. 5 20 5
    MH 129 134 83
    Ts2 sec 54 46 54
    T′90 114 97 99
    Molding in press at 180° C.
    for 10 min:
    Sheet surface smooth smooth rough
    Mechanical properties after
    post cure at 200° C. for 1
    hour (ASTM D 412-83):
    M100 Mpa 5.7 7.1 6.6
    C.R. 16.4 19.0 18.4
    A.R. % 175 183 177
    ShA hardness points 70 79 73
    Compression set on O-ring
    (ASTM D 395):
    200° C. for 70 hours (%) 29 47
  • TABLE 9
    Latex con- Particle MFI Mooney
    centration diameter ASTM (1 + 10)121° C.
    (g/l) (nm) D 1238 ASTM D 1646
    Example 13a 136 12 29.1(1)
    Example 13b 301 72 51
    Example 14a 142 60 80(2)
    Example 14b 349 54 68

    (1)MFI has been measured at 380° C. with 3 Kg

    (2)MFI has been measured at 372° C. with 5 Kg
  • TABLE 10
    EXAMPLE
    Ex. 13c Ex. 14c
    % by weight of plastomer 15 15
    ML(1 + 10)121° C. (ASTM D 1646) 73 73
    Formulation:
    Elastomer (phr) 100 100
    TAIC 3 1.5
    Luperco 4 2
    ZnO 5 5
    ODR (177° C., 12′arc 3°)
    (ASTM D2084-81):
    ML Lbf. in. 12 30
    MH 96 130
    Ts2 sec 55 55
    T′90 115 118
    Molding in press at 180° C.
    for 10 min:
    Sheete surface smooth smooth
    Mechanical properties after
    post cure at 200° C. for 1
    hour (ASTM D 412-83):
    M100 Mpa 4 6.2
    C.R. 16.5 15.0
    A.R. % 344 164
    ShA hardness points 65 73
    Compression set on O-ring
    (ASTM D 395):
    200° C. for 70 hours (%) 32

Claims (57)

  1. 1. Cured fluoropolymer compositions comprising a fluoroelastomer and a semicrystalline fluoropolymer latex formed by tetrafluoroethylene (TFE) homopolymers, or TFE copolymers with one or more monomers containing at least one unsaturation of ethylene type in amounts ranging from 0.01% to 10% by moles, obtainable by mixing the semicrystalline fluoropolymer latex with the fluoroelastomer, subsequent coagulation and drying.
  2. 2. Cured fluoropolymer compositions according to claim 1 obtainable by polymerizing in a first step the semicrystalline fluoropolymer and in a second step the fluoroelastomer.
  3. 3. Cured fluoropolymer compositions according to claim 1 wherein the semicrystalline fluoropolymer amount inside the fluoroelastomer matrix is in the range 2-40% by weight of the total of the polymeric mixture.
  4. 4. Cured fluoropolymer compositions according to claim 3 wherein the semicrystalline fluoropolymer amount inside the fluoroelastomer matrix is in the range 5-30% by weight of the total of the polymeric mixture.
  5. 5. Cured fluoropolymer compositions according to claim 1 wherein the semicrystalline polymer is based on PTFE modified with comonomers with ethylene unsaturation both of hydrogenated and fluorinated type.
  6. 6. Cured fluoropolymer compositions according to claim 5 wherein the hydrogenated comonomers are selected from the group consisting of ethylene, propylene, methylmethacrylate, methacrylic acid, butylacrylate, hydroxyethylhexylacrylate, and styrene.
  7. 7. Cured fluoropolymer compositions according to claim 5 wherein the fluorinated comonomers are selected from the group consisting of:
    perfluoroolefins C3-C8;
    hydrogenated fluoroolefins C2-C8;
    chloro- and/or bromo- and/or iodo-fluoroolefins C2-C8;
    (per)fluoroalkylvinylethers (PAVE CF2═CFORf, wherein Rf is a (per)fluoroalkyl C1-C6;
    (per)fluoro-oxyalkyvinylethers CF2═CFOX, wherein X is a alkyl C1-C12, or an oxyalkyl C1-C12, or a (per)fluoro-oxyalkyl C1-C12 having one or more ether groups; fluorodioxoles.
  8. 8. Cured fluoropolymer compositions according to claim 5 wherein the fluorinated comonomers are selected from the group consisting of perfluoromethyl-, ethyl-, propylvinylether and perfluorodioxoles.
  9. 9. Cured fluoropolymer compositions according to claim 1 wherein the fluoroelastomer is selected from the following classes:
    (1) vinylidene fluoride (VDF)-based copolymers, wherein VDF is copolymerized with at least one comonomer selected from the group consisting of: perfluoroolefins C2-C8, chloro- and/or bromo- and/or iodofluoroolefins C2-C8, (per)fluoroalkyl-vinylethers (PAVE) CF2═CFORf, wherein Rf is a (per)fluoroalkyl C1-C6, perfluoro-oxyalkylvinylethers CF2═CFOX, wherein X is a perfluoro-oxyalkyl C1-C12 having one or more ether groups, non fluorinated olefins (Ol) C2-C8;
    (2) tetrafluoroethylene (TFE)-based copolymers, wherein TFE is copolymerized with at least one comonomer selected from the group consisting of (per)fluoroalkyvinylethers (PAVE) CF2═CFORf, wherein Rf is as above defined; perfluoro-oxyalkyvinylethers CF2═CFOX, wherein X is as above defined; fluoroolefins C2-C8 containing hydrogen and/or chlorine and/or bromine and/or iodine atoms; non fluorinated olefins (Ol) C2-C8.
  10. 10. Cured fluoropolymer compositions according to claim 9 wherein the fluorelastomer is selected from the following compositions expressed by moles:
    (a) vinylidene fluoride (VDF) 45-85%, hexafluoropropene (HFP) 15-45% tetrafluoroethylene (TFE) 0-30%;
    (b) vinylidene fluoride (VDF) 50-80%, perfluoroalkylvinylether (PAVE) 5-50%, tetrafluoroethylene (TFE) 0-20%;
    (c) vinylidene fluoride (VDF) 20-30%, non fluorinated olefins (Ol) C2-C8 10-30%, hexafluoropropene (HFP) and/or perfluoroalkylvinylether (PAVE) 18-27%, tetrafluoroethylene (TFE) 10-30%;
    (d) tetrafluoroethylene (TFE) 50-80%, perfluoroalkylvinylether (PAVE) 20-50%;
    (e) tetrafluoroethylene (TFE) 45-65%, non fluorinated olefins (Ol) C2-C8 20-55%, vinylidene fluoride 0-30%
    (f) tetrafluoroethylene (TFE) 32-60%, non fluorinated olefins (Ol) C2-C8 10-40%, perfluoroalkylvinylether (PAVE) 20-40%;
    (g) tetrafluoroethylene (TFE) 33-75%, perfluoroalkylvinylether (PAVE) 15-45%, vinylidene fluoride (VDF) 5-30%.
  11. 11. Cured fluoropolymer compositions according to claim 1 wherein the fluoroelastomer comprises also monomer units deriving from a bis-olefin having the formula:
    Figure US20060189760A1-20060824-C00002
    wherein
    R1, R2, R3, R4, R5, R6, equal to or different from each other, are H or alkyl C1-C5;
    Z is a linear or branched, alkylene or cycloalkylene C1-C18 radical, optionally containing oxygen toms optionally at least partially fluorinated, or a (per)fluoropolyoxyalkylene radical.
  12. 12. Cured fluoropolymer compositions according to claim 11 wherein the unit amount in the chain deriving from the bis-olefin is in the range 0.01-1.0% by moles of the other monomer units forming the fluoroelastomer base structure.
  13. 13. Cured fluoropolymer compositions according to claim 1 wherein the fluoroelastomers are cured by peroxidic route.
  14. 14. Cured fluoropolymer compositions according to claim 1 wherein when the fluoroelastomers contain cyano groups they are cured by tin organic compounds and/or diaromatic aminic compounds.
  15. 15. Cured fluoropolymer compositions according to claim 1 wherein the fluoroelastomers are cured by tin organic compounds and/or diaromatic aminic compounds and optionally by peroxidic route if in the polymeric chain iodine and/or bromine atoms are present.
  16. 16. Cured fluoropolymer compositions according to claim 1 wherein the one or more monomers containing at least one unsaturation of ethylene type are present in amounts ranging from 0.5% to 5% by moles.
  17. 17. Cured fluoropolymer compositions according to claim 7 wherein the perfluoroolefins C3-C8 are selected from the group consisting of hexafluoropropene (HFP) and hexafluoroisobutene.
  18. 18. Cured fluoropolymer compositions according to claim 7 wherein the hydrogenated fluoroolefins C2-C8 are selected from the group consisting of vinyl fluoride (VF), vinylidene fluoride (VDF), trifluoroethylene and perfluoroalkylethylene CH2═CH—Rf, wherein Rf is a perfluoroalkyl C1-C6.
  19. 19. Cured fluoropolymer compositions according to claim 7 wherein the chlorofluoroolefin C2-C8 is chlorotrifluoroethylene (CTFE).
  20. 20. Cured fluoropolymer compositions according to claim 7 wherein the (per)fluoroalkylvinyl-ethers (PAVE) (CF3═CF)Rf) are selected from the group consisting of CF3, C2F5 and C3F7.
  21. 21. Cured fluoropolymer compositions according to claim 7 wherein the (per)fluorooxyalkyl C1-C12 having one or more ether groups is perfluoro-2-propoxy-propyl.
  22. 22. Cured fluoropolymer compositions according to claim 9 wherein the perfluoroolefin C2-C8 is selected from the group consisting of tetrafluoroethylene (TFE) and hexafluoropropene (HFP).
  23. 23. Cured fluoropolymer compositions according to claim 9 wherein the chloro- and/or bromo-fluoro-olefins C2-C8 are selected from the group consisting of chlorotrifluoroethylene (CTFE) and bromotrifluoroethylene.
  24. 24. Cured fluoropolymer compositions according to claim 9 wherein the (per)fluoroalkyl-vinylethers (PAVE) CF2—CFORf are selected from the group consisting of trifluoromethyl, bromodifluoromethyl and pentafluoropropyl.
  25. 25. Cured fluoropolymer compositions according to claim 9 wherein the perfluorooxyalkylvinylether CF2═CFOX is perfluoro-2-propoxy-propyl.
  26. 26. Cured fluoropolymer compositions according to claim 9 wherein the nonfluorinated olefins (Ol) C2-C8 are selected from the group consisting of ethylene and propylene.
  27. 27. A sealing manufactured article comprising the cured fluoropolymer compositions according to claim 1.
  28. 28. The sealing manufactured article according to claim 27, wherein the sealing manufactured article is an O-ring.
  29. 29. Cured fluoropolymers comprising a fluoroelastomer matrix incorporating therein particles of a semicrystalline fluoropolymer latex formed by tetrafluoroethylene (TFE) homopolymers, or TFE copolymers with one or more monomers containing at least one unsaturation of ethylene type in amounts ranging from 0.01% to 10% by moles.
  30. 30. Cured fluoropolymers according to claim 29 obtainable by mixing the semicrystalline fluoropolymer latex with the fluoroelastomer latex and subsequent coagulation.
  31. 31. Cured fluoropolymers according to claim 29 obtainable by polymerizing in a first step the semicrystalline fluoropolymer and in a second step the fluoroelastomer.
  32. 32. Cured fluoropolymers according to claim 29 wherein the semicrystalline fluoropolymer amount inside the fluoroelastomer matrix is in the range 2-40% by weight of the total of the polymeric mixture.
  33. 33. Cured fluoropolymers according to claim 32 wherein the semicrystalline fluoropolymer amount inside the fluoroelastomer matrix is in the range 5-30% by weight of the total of the polymeric mixture.
  34. 34. Cured fluoropolymers according to claim 29 wherein the semicrystalline polymer is based on PTFE modified with comonomers with ethylene unsaturation both of hydrogenated and fluorinated type.
  35. 35. Cured fluoropolymers according to claim 34 wherein the hydrogenated comonomers are selected from the group consisting of ethylene, propylene, methylmethacrylate, methacrylic acid, butylacrylate, hydroxyethylhexylacrylate, and styrene.
  36. 36. Cured fluoropolymers according to claim 34 wherein the fluorinated comonomers are selected from the group consisting of
    perfluoroolefins C3-C8;
    hydrogenated fluoroolefins C2-C8;
    chloro- and/or bromo- and/or iodo-fluoroolefins C2-C8;
    (per)fluoroalkylvinyl ethers (PAVE) CF2═CFORf, wherein Rf is a (per)fluoroalkyl C1-C6;
    (per)fluoro-oxyalkyvinylethers CF2═CFOX, wherein X is an alkyl C1-C12, or an oxyalkyl C1-C12, or a (per)fluoro-oxyalkyl C1-C12 having one or more ether groups; fluorodioxoles.
  37. 37. Cured fluoropolymers according to claim 34 wherein the fluorinated comonomers are selected from the group consisting of perfluoromethyl-, ethyl-, propyl-vinylether and perfluorodioxoles.
  38. 38. Cured fluoropolymers according to claim 29 wherein the fluoroelastomer is selected from the following classes:
    (1) vinylidene fluoride (VDF)-based copolymers, wherein VDF is copolymerized with at least one comonomer selected from the group consisting of: perfluoroolefins C2-C8, chloro- and/or bromo- and/or iodofluoroolefins C2-C8, (per)fluoroalkyl-vinylethers (PAVE) CF2═CFORf, wherein Rf is a (per)fluoroalkyl C1-C6, perfluoro-oxyalkyvinylethers CF2═CFOX, wherein X is a perfluoro-oxyalkyl C1-C12 having one or more ether groups, non fluorinated olefins (Ol) C2-C8;
    (2) Tetrafluoroethylene (TFE)-based copolymers, wherein TFE is copolymerized with at least one comonomer selected from the group consisting of (per)fluoroalkylvinylethers (PAVE) CF2═CFORf, wherein Rf is as above defined;
    perfluoro-oxyalkyvinylethers CF2═CFOX, wherein X is as above defined; fluoroolefins C2-C8 containing hydrogen and/or chlorine and/or bromine and/or iodine atoms; non fluorinated olefins (Ol) C2-C8; perfluorovinylethers containing hydrocyanic groups.
  39. 39. Cured fluoropolymers according to claim 38 wherein the fluoroelastomers is selected from the following compositions expressed by moles:
    (a) vinylidene fluoride (VDF) 45-85%, hexafluoropropene (HFP) 15-45% tetrafluoroethylene (TFE) 0-30%;
    (b) vinylidene fluoride (VDF) 50-80%, perfluoroalkylvinylether (PAVE) 5-50%, tetrafluoroethylene (TFE) 0-20%;
    (c) vinylidene fluoride (VDF) 20-30%, non fluorinated olefins (Ol) C2-C8 10-30%, hexafluoropropene (HFP) and/or perfluoroalkylvinylether (PAVE) 18-27%, tetrafluoroethylene (TFE) 10-30);
    (d) tetrafluoroethylene (TFE) 50-80%, perfluoroalkylvinylether (PAVE) 20-50%;
    (e) tetrafluoroethylene (TFE) 45-65%, non fluorinated olefins (Ol) C2-C8 20-55%, vinylidene fluoride 0-30%;
    (f) tetrafluoroethylene (TFE) 32-60% by moles, non fluorinated olefins (Ol) C2-C8 10-40%, perfluoroalkylvinylether (PAVE) 20-40%;
    (g) tetrafluoroethylene (TFE) 33-75%, perfluoroalkylvinylether (PAVE) 15-45%, vinylidene fluoride (VDF) 5-30%.
  40. 40. Cured fluoropolymers according to claim 29 wherein the fluoroelastomer comprises also monomer units deriving from a bis-olefin having the formula:
    Figure US20060189760A1-20060824-C00003
    wherein
    R1, R2, R3, R4, R5, R6, equal to or different from each other, are H or alkyl C1-C5;
    Z is a linear or branched, alkylene or cycloalkylene C1-C18 radical, optionally containing oxygen atoms optionally at least partially fluorinated, or a (per)fluoropolyoxyalkylene radical.
  41. 41. Cured fluoropolymers according to claim 40 wherein the unit amount in the chain deriving from the bis-olefin is in the range 0.01-1.0% by moles of the other monomer units forming the fluoroelastomer base structure.
  42. 42. Cured fluoropolymers according to claim 29 wherein the fluoroelastomers are cured by peroxidic route.
  43. 43. Cured fluoropolymers according to claim 29 wherein when the fluoroelastomers contain cyano groups they are cured by tin organic compounds and/or di-aromatic aminic compounds.
  44. 44. Cured fluoropolymers according to claim 29 wherein the fluoroelastomers are cured by tin organic compounds and/or diaromatic aminic compounds and optionally by peroxidic route if in the polymeric chain iodine and/or bromine atoms are present.
  45. 45. Cured fluoropolymers according to claim 29 wherein the one or more monomers containing at least one unsaturation of ethylene type are present in amounts ranging from 0.5% to 5% by moles.
  46. 46. Cured fluoropolymers according to claim 36 wherein the perfluoroolefins C3-C8 are selected from the group consisting of hexafluoropropene (HFP) and hexafluoroisobutene.
  47. 47. Cured fluoropolymers according to claim 36 wherein the hydrogenated fluoroolefins C2-C8 are selected from the group consisting of vinyl fluoride (VF), vinylidene fluoride (VDF), trifluoroethylene and perfluoroalkylethylene CH2═CH—Rf, wherein Rf is a perfluoroalkyl C1-C6.
  48. 48. Cured fluoropolymers according to claim 36 wherein the chloro-fluoroolefin C2-C8 is chlorotrifluoroethylene (CTFE).
  49. 49. Cured fluoropolymers according to claim 36 wherein the (per)fluoroalkylvinylethers (PAVE) (CF2═CFORf) are selected from the group consisting of CF3, C2F5 and C3F7.
  50. 50. Cured fluoropolymers according to claim 36 wherein the (per)fluoro-oxyalkyl C1-C12 having one or more ether groups is perfluoro-2-propoxy-propyl.
  51. 51. Cured fluoropolymers according to claim 38 wherein the perfluoroolefin C2-C8 is selected from the group consisting of tetrafluoroethylene (TFE) and hexafluoropropene (HFP).
  52. 52. Cured fluoropolymers according to claim 38 wherein the chloro- and/or bromofluoro-olefins C2-C8 are selected from the group consisting of chlorotrifluoroethylene (CTFE) and bromotrifluoroethylene.
  53. 53. Cured fluoropolymers according to claim 38 wherein the (per)fluoroalkylvinylethers (PAVE) CF2═CFORf are selected from the group consisting of trifluoromethyl, bromodifluoromethyl and pentafluoropropyl.
  54. 54. Cured fluoropolymers according to claim 38 wherein the perfluorooxyalkylvinylether CF2═CFOX is perfluoro-2-propoxy-propyl.
  55. 55. Cured fluoropolymers according to claim 38 wherein the nonfluorinated olefins (01) C2-C8 are selected from the group consisting of ethylene and propylene.
  56. 56. A sealing manufactured article comprising the cured fluorelastomer of anyone of claims 28-54.
  57. 57. The sealing article according to claim 56, wherein the sealing article manufactured article is an O-ring.
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