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  • C08L27/12—Compositions 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
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  • C08L27/02—Compositions 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
  • C08L27/12—Compositions 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
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  • C08L27/02—Compositions 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
  • C08L27/12—Compositions 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
  • C08L27/20—Homopolymers or copolymers of hexafluoropropene
• • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
  • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
  • F16J—PISTONS; CYLINDERS; SEALINGS
  • F16J15/00—Sealings
  • F16J15/02—Sealings between relatively-stationary surfaces
  • F16J15/06—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces
  • F16J15/10—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing
  • F16J15/102—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing characterised by material
• • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
  • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
  • F16J—PISTONS; CYLINDERS; SEALINGS
  • F16J15/00—Sealings
  • F16J15/16—Sealings between relatively-moving surfaces
  • F16J15/32—Sealings between relatively-moving surfaces with elastic sealings, e.g. O-rings
  • F16J15/3284—Sealings between relatively-moving surfaces with elastic sealings, e.g. O-rings characterised by their structure; Selection of materials
• • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
  • F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
  • F16J—PISTONS; CYLINDERS; SEALINGS
  • F16J3/00—Diaphragms; Bellows; Bellows pistons
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  • C08J2327/00—Characterised by the use 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; Derivatives of such polymers
  • C08J2327/02—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment
  • C08J2327/12—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
  • C08J2327/16—Homopolymers or copolymers of vinylidene fluoride
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  • C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
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  • C08J2479/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2461/00 - C08J2477/00
  • C08J2479/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
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Definitions

• This invention relates to curable fluoroelastomers having a low tendency to swell.
• Fluoroelastomers are characterized by excellent physical and chemical properties, such as high heat resistance, oil resistance and chemical resistance, and are therefore widely used as sealing materials.
• fluoroelastomers include copolymers containing units of vinylidene fluoride (VF2) and units of at least one other copolymerizable fluorine-containing monomer, such as hexafluoropropylene (HFP), tetrafluoroethylene (TFE), chlorotrifluoroethylene (CTFE), vinyl fluoride (VF), and fluorovinyl ethers, such as a perfluoro(alkyl vinyl ether) (PAVE).
• PAVE perfluoro(methyl vinyl ether), perfluoro(ethyl vinyl ether) and perfluoro(propyl vinyl ether).
• elastomers are cured, i.e., vulcanized or crosslinked.
• fluoroelastomers this is generally accomplished by mixing uncured polymer (i.e. fluoroelastomer rubber) with a polyfunctional curing agent and heating the resulting mixture.
• uncured polymer i.e. fluoroelastomer rubber
• a polyfunctional curing agent i.e. fluoroelastomer rubber
• a chemical reaction of the curing agent takes place with active sites along the polymer backbone or side chains, whereby a crosslinked polymer composition having a three-dimensional network structure is obtained.
• Conventional curing agents for fluoroelastomers include a radical-generating agent, such as an organic peroxide in combination with a multifunctional crosslinking co-agent.
• a metal oxide is added to this combination to improve the curing reaction (i.e., both the curing intensity and the curing rate).
• a disadvantage of using a metal oxide is that the cured fluoroelastomers obtainable in this way, when exposed to organic acids or acidic media comprising hydrocarbon blends (fuel, oil) for some time or at elevated temperatures, show very high volume swelling (e.g. 20-200 vol %) which can lead to sealing failure. Such swelling can be prevented or at least minimized by eliminating metal oxides from the compositions.
• WO 2014088919 (A1) describes a curable fluoroelastomer composition
• the preparation of the fluoroelastomer composition comprises the steps of: A) providing a peroxide-curable fluoroelastomer; B) providing a polyamide having a melting temperature or glass transition temperature; C) mixing the peroxide-curable fluoroelastomer with the polyamide at a temperature greater than whichever is the higher of the melting temperature and glass transition temperature of the polyamide, D) cooling the polymer mixture to solidify the polyamide, and E) adding a peroxide curing agent and a multifunctional co-agent to the polymer mixture at a temperature lower than whichever is the lower of the melting temperature and glass transition temperature of the polyamide.
• the preparation method described is used to incorporate the polyamide into the fluoroelastomer in molten form.
• the fluoroelastomer composition is present as a polymer blend, i.e., the polyamide is present in the fluoroelastomer in a molecularly distributed or microscopically dispersed form. It has been found in practical trials that such fluoroelastomer compositions cure well even in the absence of metal oxides so that a low tendency to swell and good heat resistance can be achieved with them. A disadvantage of these compositions, however, is that they exhibit a non-satisfactory compression set.
• the object of the present invention is to provide a fluoroelastomer composition showing not only a low tendency to swell and good heat resistance but also a good compression set.
• curable fluoroelastomer composition comprising:
• the fluoroelastomer composition according to the invention comprising as an additive the nitrogen-containing polymer in particle form with an average particle size in the range from 0.15 to 70 ⁇ m and/or in fiber form with an average fiber diameter in the range from 0.15 to 70 ⁇ m, surprisingly exhibits both a low tendency to swell and good heat resistance and a good compression set expressed by a significantly improved tensile strength even after heat aging, for example at 250° C.
• the fluoroelastomer composition contains nitrogen-containing polymer selected from polyamide, polyimide, mixtures and/or copolymers thereof, each in particle form with an average particle size in the range from 0.15 to 70 ⁇ m and/or in fiber form with an average fiber diameter in the range from 0.15 to 70 ⁇ m.
• the nitrogen-containing polymer preferably has an average particle size in the range from 0.2 to 50 ⁇ m, more preferably in the range from 0.3 to 30 ⁇ m, more preferably in the range from 0.4 to 20 ⁇ m, more preferably in the range from 0.4 to 12.5 ⁇ m, in particular in the range from 0.4 to 8 ⁇ m, and/or, if present in fiber form, has an average fiber diameter in the range from 0.2 to 50 ⁇ m, more preferably in the range from 0.3 to 30 ⁇ m, more preferably in the range from 0.4 to 20 ⁇ m, more preferably in the range from 0.4 to 12.5 ⁇ m, in particular in the range from 0.4 to 8 ⁇ m.
• the mean particle size is determined according to ISO 13320 and the average fiber diameter is determined by image analysis.
• the fluoroelastomer composition has an amount of metal oxide functioning as an acid acceptor, in particular zinc oxide, magnesium oxide, calcium oxide and/or lead oxide (PbO/Pb 3 O 4 ) of less than 1.5 wt %, and/or an amount of metal hydroxide functioning as an acid acceptor, in particular calcium hydroxide, of less than 1.5 wt %, and/or an amount of metal salt functioning as an acid acceptor, in particular hydrotalcite, calcium and/or magnesium stearate of less than 5 wt %, wherein the quantities are based in each case on the total weight of the fluoroelastomer composition.
• metal oxide functioning as an acid acceptor in particular zinc oxide, magnesium oxide, calcium oxide and/or lead oxide (PbO/Pb 3 O 4 ) of less than 1.5 wt %
• metal hydroxide functioning as an acid acceptor in particular calcium hydroxide, of less than 1.5 wt %
• metal salt functioning as an acid acceptor in particular hydrotalcite, calcium and/or magnesium
• the fluoroelastomer composition contains a curable fluoroelastomer.
• the amount of fluoroelastomer in the fluoroelastomer composition is 40 wt % to 95 wt %, in particular 50 wt % to 90 wt %, based in each case on the total weight of the fluoroelastomer composition.
• fluoroelastomers are suitable for use as a curable elastomer.
• Suitable fluoroelastomers include, in particular, those classified as FKM, FFKM and FTPM in ASTM-D 1418, “Standard Practice for Rubber and Rubber Lattice Nomenclature”.
• FKM fluoroelastomers that use vinylidene fluoride as comonomer.
• Various types of fluoroelastomers are commercially available.
• a first type may be described chemically as a copolymer of hexafluoropropylene and vinylidene fluoride. These fluoroelastomers tend to have an advantageous combination of overall properties. Some commercial embodiments are available with about 66 wt % fluorine.
• Another type of FKM may be described chemically as a terpolymer of tetrafluoroethylene, hexafluoropropylene and vinylidene fluoride. Such elastomers tend to have high heat resistance and good resistance to aromatic solvents.
• FKM fluorinated vinyl ether and vinylidene fluoride.
• elastomers tend to have improved low temperature performance. In various embodiments, they are available with 62-68 wt % fluorine.
• fluoroelastomer is described as a terpolymer of tetrafluoroethylene, propylene and vinylidene fluoride. Such fluoroelastomers tend to have improved base resistance. Some commercial embodiments contain about 67 wt % fluorine.
• fluoroelastomer may be described as a pentapolymer of tetrafluoroethylene, hexafluoropropylene, ethylene and a fluorinated vinyl ether and vinylidene fluoride. Such elastomers typically have improved base resistance and improved low temperature performance.
• FFKM fluoroelastomers Another category of fluoroelastomers is referred to as FFKM. Such elastomers can be referred to as perfluoroelastomers because the polymers are fully fluorinated and do not contain any carbon-hydrogen bonding.
• FFKM fluoroelastomers are generally characterized by excellent fluid resistance. They were originally introduced by DuPont under the registered trade name Kalrez®. Further suppliers are Daikin and Ausimont.
• FTPM fluoroelastomers
• Typical of this category are the copolymers of propylene and tetrafluoroethylene.
• the category is characterized by high resistance to basic materials, such as amines.
• Suitable fluoroelastomers include commercially available copolymers of one or more fluorine-containing monomers, mainly vinylidene fluoride (VDF), hexafluoropropylene (HFP), tetrafluoroethylene (TFE), and perfluorovinyl ether (PFVE).
• VDF vinylidene fluoride
• HFP hexafluoropropylene
• TFE tetrafluoroethylene
• PFVE perfluorovinyl ether
• Preferred PFVE include those having a C1-8 perfluoroalkyl group, preferably perfluoroalkyl groups having 1 to 6 carbon atoms, and especially perfluoromethyl vinyl ether and perfluoropropyl vinyl ether.
• copolymers may also contain repeating units derived from olefins, such as ethylene (Et) and propylene (Pr).
• olefins such as ethylene (Et) and propylene (Pr).
• the fluoroelastomer is a so-called base-resistant fluoroelastomer.
• base-resistant fluoroelastomers also include fluoro-olefin copolymers.
• Particularly preferred is a copolymer of tetrafluoroethylene having at least one C2-4 olefin and so-called cure site monomers (CSM).
• the fluoroelastomer may contain repeating units derived from one or more additional fluorine-containing monomers.
• the cured elastomeric material comprises repeating units derived from tetrafluoroethylene and at least one C2-4 olefin, and further comprises peroxide crosslinking sites.
• the fluoroelastomer comprises repeating units derived from 10-90 mol % tetrafluoroethylene, 10-90 mol % C2-4 olefin and up to 30 mol % from one or more additional fluorine-containing monomers.
• the repeating units are derived from 25-90 mol % tetrafluoroethylene and 10-75 mol % C2-4 olefin.
• the repeating units are derived from 45-65 mol % tetrafluoroethylene and 20-55 mol % C2-4 olefin.
• the molar ratio of tetrafluoroethylene units to C2-4 olefin repeating units is from 60:40 to 40:60.
• the fluoroelastomer comprises alternating units of C2-4 olefins and tetrafluoroethylene. In such polymers, the molar ratio of tetrafluoroethylene to C2-4 olefin is about 50:50.
• the fluoroelastomers are provided as block copolymers having an A-B-A structure, wherein A represents a block of polytetrafluoroethylene and B represents a block of polyolefin.
• a preferred C2-4 olefin is propylene.
• Fluoroelastomers based on copolymers of tetrafluoroethylene and propylene are commercially available, for example, from Asahi under the registered trade name Aflas®.
• a preferred additional monomer in the fluoroelastomer is vinylidene difluoride.
• Other fluorine-containing monomers that can be used in the fluoroelastomers of the present invention include, without limitation, perfluoroalkyl vinyl compounds, perfluoroalkyl vinylidene compounds, and perfluoroalkoxy vinyl compounds.
• Hexafluoropropylene is an example of a perfluoroalkyl vinyl monomer.
• Perfluoromethyl vinyl ether is an example of a preferred perfluoroalkoxy vinyl monomer.
• rubbers based on copolymers of tetrafluoroethylene, ethylene, and perfluoromethyl vinyl ether are commercially available from DuPont under the registered trade name Viton® ETP.
• Fluoroelastomers used to prepare the processable rubber compositions of the invention can be typically prepared by radical emulsion polymerization of a monomer mixture containing the desired molar ratios of the starting monomers.
• Initiators are typically organic or inorganic peroxide compounds, and the emulsifier is typically a fluorinated acid soap.
• the molecular weight of the polymer formed can be controlled by the relative amounts of initiators used as compared to the monomer content and the choice of the transfer agent, if any.
• Typical transfer agents include carbon tetrachloride, methanol and acetone.
• Emulsion polymerization can be carried out under discontinuous or continuous conditions. Such fluoroelastomers are commercially available as indicated above.
• the fluoroelastomers used in the compositions and methods of the invention preferably contain repeating units derived from one or more fluorine-containing olefinic monomers.
• the fluoroelastomers are curable according to the invention.
• the fluoroelastomers are radically and/or ionically curable.
• Radically curable fluoroelastomers are to be understood as meaning fluoroelastomers that contain so-called crosslinking sites.
• the radically curable fluoroelastomers contain repeating units as crosslinking sites, based on so-called cure site monomers (CSM) which are described in more detail below.
• CSM cure site monomers
• the repeating units are based on the corresponding monomers in the sense that the structure of the polymer results from copolymerization of the monomers and the resulting structure is the addition polymerization product of the monomers.
• the cured fluoroelastomers at least some of the repeating units derived from the cure site monomers are crosslinked.
• crosslinking is achieved by the reaction of multifunctional crosslinking co-agents with radicals at the crosslinking sites which is induced, for example, by the action of an organic peroxide of the radical cure system.
• the radically curable fluoroelastomers contain up to 5 mol %, for example from 0.05 to 5 mol % repeating units that are based on the so-called cure site monomers.
• the crosslinking sites are based on halogen-containing olefin monomers, the halogen being chlorine, bromine, iodine, or combinations thereof.
• the repeating units of a halogen-containing olefin are preferably present in an amount to provide at least about 0.05% wt % halogen in the fluoroelastomer, preferably 0.3% wt % halogen or more.
• the total weight of halogen in the fluoroelastomer is 1.5 wt % or less.
• the cure site monomers produce crosslinking sites in the fluoroelastomer which preferably react at high speed with radical initiators, such as peroxides. They react faster than other parts of the elastomer. Crosslinking is thus preferably effected at the crosslinking sites. This crosslinking effect is at least partially responsible for the elastomeric properties in the elastomer.
• Non-limiting examples of cure site monomers include brominated, chlorinated and iodinated olefins; brominated, chlorinated and iodinated unsaturated ethers; and non-conjugated dienes.
• the radically curable fluoroelastomers are peroxide-curable fluoroelastomers, preferably comprising at least one halogenated crosslinking site or a reactive double bond resulting from the presence of a copolymerized unit of a non-conjugated diene.
• the double bond of the cure site monomer is referred to herein as an olefin.
• Functional groups associated with the cure sites thus include a carbon-bromine (C—Br) bond, a carbon-iodide (C—I) bond, a carbon-chlorine (C—Cl) bond, and an olefin.
• halogenated crosslinking sites are provided by copolymerized cure site monomers and/or by halogen atoms present at the terminal positions of the fluoroelastomer polymer chain.
• the halogenated crosslinking sites are referred to as repeating units stemming from a cure site monomer.
• Copolymerized cure site monomers, reactive double bonds and halogenated end groups are capable of reacting by forming crosslinks, in particular under catalysis or initiation by the action of peroxides.
• the repeating units of an uncured fluoroelastomer that are based on cure site monomers contain one or more of these functional groups.
• cured elastomers at least some of the functional groups are reacted with the curing system.
• the elastomer contains repeating units stemming from cure site monomers.
• Brominated cure site monomers may contain other halogens, preferably fluorine.
• bromo trifluoroethylene 4-bromo-3,3,4,4-tetrafluorobut-1-ene and others, such as vinyl bromide, 1-bromo-2,2-difluoroethylene, perfluoroallyl bromide, 4-bromo-1,1,2-trifluorobutene, 4-bromo-1,1,3,3,4,4-hexafluorobutene, 4-bromo-3-chloro-1,1,3,4,4-pentafluorobutene, 6-bromo-6-tetrafluorohexene, 4-bromo perfluorobut-1-ene and 3,3-difluorallyl bromide.
• Brominated unsaturated ether cure site monomers usable in the invention include ethers, such as 2-bromo perfluoroethylperfluorovinyl ethers and fluorinated compounds of the CF2 Br—Rf—O—CF—CF2 (Rf is perfluoroalkylene) class, such as CF2 BrCF2OCF—CF2 and fluorovinyl ethers of the ROCF—CFBr or ROCBr—CF2 class, where R is a lower alkyl group or fluoroalkyl group, such as CH3OCF—CFBr or CF3CH2OCF—CFBr.
• ethers such as 2-bromo perfluoroethylperfluorovinyl ethers and fluorinated compounds of the CF2 Br—Rf—O—CF—CF2 (Rf is perfluoroalkylene) class, such as CF2 BrCF2OCF—CF2 and fluorovinyl ethers of
• Iodinated olefins can also be used as cure site monomers.
• Suitable iodinated monomers include iodinated olefins of the formula: CHR—CH—Z—CH2-CHR—I where R is —H or —CH3, Z is a C1-018 (per)fluoroalkylene radical, linear or branched, optionally containing one or more ether oxygen atoms, or a (per)fluoropolyoxyalkylene radical as described in U.S. Pat. No. 5,674,959.
• Suitable iodinated cure site monomers are unsaturated ethers of formula I(CH2CF2CF2)nOCF—CF2, and ICH2CF2O[CF(CF3)CF2O]nCF—CF2 and the like, as described in U.S. Pat. No. 5,717,036.
• suitable iodinated cure site monomers can be used, including iodo-ethylene, 4-iodo-3,3,4,4-tetrafluorobutene-1,3-chloro-4-iodo-3,4,4-trifluoromethyl, 2-iodo-1,1,2,2-tetrafluoro-1-(vinyloxy)ethane, 2-iodo-1-(perfluorovinyloxy)-1,1,2,2-tetrafluoroethylene, 1,1,2,3,33-hexafluoro-2-iodone-1-(perfluorovinyloxy) propane; 2-iodo ethyl vinyl ether; 3,3,4,5,5,5-hexafluoro-4-iodopentene; and iodo-trifluoroethylene as described in U.S. Pat. No. 4,694,045.
• non-conjugated diene cure site monomers examples include 1,4-pentadiene, 1,5-hexadiene, 1,7-octadiene and others, such as those disclosed in Canadian Patent 2,067,891.
• a suitable triene is 8-methyl-4-ethylidene-1,7-octadiene.
• cure site monomers include 4-bromo-3,3,4,4-tetrafluorobut-1-ene; 4-iodo-3,3,4,4-tetrafluorobut-1-ene, and bromo-trifluoroethylene.
• cure site monomers and repeating units derived therefrom and containing iodine, bromine or mixtures thereof are present at the ends of the fluoroelastomeric chains as a result of the use of chain transfer or molecular weight regulating agents during the preparation of the fluoroelastomers.
• Such agents include iodine-containing compounds that yield iodine bound at one or both ends of the polymer molecules.
• Methylene iodide; 1,4-diiodine-perfluoro-n-butane, and 1,6-diiodine-3,3,4,4-tetrafluorohexane are representative of such agents.
• Other iodinated chain transfer agents include 1,3-diiodine-perfluoropropane; 1,4-diiodine-perfluorobutane, 1,6-diiodine-perfluorohexane, 1,3-diiodine-2-chloroperfluoropropane; 1,2-di(iododifluoromethyl)perfluorocyclobutane, monoiodperfluoroethane; monoiodperfluorobutane; and 2-iodo-1-hydroperfluoroethane.
• Diiodinated chain transfer agents are particularly preferred.
• brominated chain transfer agents include 1-bromo-2-iodoperfluoroethane, 1-bromo-3-iodoperfluoropropane; 1-iodo-2-bromo-1,1-difluoroethane and others as disclosed in U.S. Pat. No. 5,151,492.
• Non-limiting examples of peroxide-curable fluoroelastomers include VDF/HFP/CSM, VDF/HFP/TFE/CSM, VDF/PFVE/TFE/CSM, TFE/Pr/CSM, TFE/Pr/VDF/CSM, PFVE/VDF/CSM, TFE/Et/PFVE/CSM and TPE/PFVE/CSM, with CSM representing at least one cure site monomer.
• the name of the elastomer indicates the monomers from which the elastomeric rubbers are synthesized.
• the elastomeric rubbers have viscosities that result in a Mooney viscosity of generally 15-160 (ML1+10, large rotor at 121° C.).
• Elastomeric suppliers include Dyneon (3M), Asahi glass fluoropolymers, Solvay/Ausimont, DuPont and Daikin.
• the radical curing system (B) preferably contains a radical initiator and a crosslinking co-agent. It is believed that the radical initiator acts by first extracting a hydrogen or halogen atom from the fluoroelastomer to produce a free radical that can be crosslinked.
• the above-described cure site monomers are believed to provide sites that react with the radical initiator at an accelerated rate so that the subsequent crosslinking described below occurs primarily at the crosslinking sites.
• These crosslinking sites contain the free radicals which can react with the unsaturated sites of the crosslinking co-agents.
• Crosslinking co-agents contain at least two unsaturated, preferably olefinically unsaturated sites.
• the radical initiators have a peroxide functionality.
• Numerous organic peroxides are known as examples of radical initiators and are commercially available.
• the radical initiators, including the organic peroxides can be activated over a wide temperature range.
• the activation temperature can be described using a parameter known as half-life (T1/2). Typical values for half-lives of, for example, 0.1 hours, 1 hour and 10 hours are given in degrees Celsius. For example, at 0.1 hours at 143° C., a T1/2 indicates that at this temperature, half of the radical initiator will decompose within 0.1 hours.
• Organic peroxides having a T1/2 at 0.1 hours of 118° C. to 228° C. are commercially available.
• Such peroxides have a half-life of at least 0.1 hours at the stated temperatures.
• the T1/2 values indicate the kinetics of the initial reaction when crosslinking the fluoroelastomers, i.e. the decomposition of the peroxide forming a radical-containing intermediate.
• Non-limiting examples of commercially available organic peroxides for initiating curing of fluoroelastomers include butyl-4,4-di-(tert-butylperoxy)valerate; tert-butyl peroxybenzoate; di-tert-amyl peroxide; dicumyl peroxide; di(tert-butylperoxyisopropyl)benzene; 2,5-dimethyl-2,5-di(tert-butylperoxy)hexane; tert-butylcumylperoxide; 2,5-dimethyl-2,5-di(tert-butylperoxy)hex-3-ine; di-tert-butylperoxide; 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxonane, 1,1,3,3-tetramethylbutyl hydroperoxide; diisopropylbenzene monohydroperoxide; cumylhydroperoxide
• Non-limiting examples of crosslinking co-agents include triallyl cyanurate; triallyl isocyanurate; tri(methallyl)-isocyanurate; tris(diallylamine)-s-triazine; N, N, N N′-tetraallyl terephthalamide; N, N, N′, N′-tetraallylmalonamide, trivinyl isocyanurate; 2,4,6-trivinylmethyltrisiloxane; and tri(5-norbornene-2-methylene)cyanurate.
• the crosslinking co-agents preferably contain at least two sites of olefinic unsaturation. The unsaturated sites react with the free radical produced on the fluoroelastomer molecule and crosslink the elastomer.
• a commonly used crosslinking agent is triallyl isocyanurate (TAIC).
• Ionically curable fluoroelastomers are those that can be cured with amines, preferably diamines and/or polyols, preferably bisphenols. Ionically curable fluoroelastomers are well known and described in the literature, for example in Albert L. Moore, Fluoroelastomers Handbook: The Definitive User's Guide and Databook.
• fluoroelastomer In addition to the fluoroelastomer, curing system, and nitrogen-containing polymer, other additives, such as stabilizers, processing aids, curing accelerators, fillers, pigments, dyes, adhesives, tackifiers and waxes may be added to the fluoroelastomer composition of the present invention.
• additives such as stabilizers, processing aids, curing accelerators, fillers, pigments, dyes, adhesives, tackifiers and waxes may be added to the fluoroelastomer composition of the present invention.
• processing aids may be used, including plasticizers and mold release agents.
• processing aids include carnauba wax, ester plasticizers, such as dioctyl sebacate (DOS), fatty acid salts, such as zinc stearate and sodium stearate, polyethylene wax and ceramide.
• high temperature processing aids are preferred. They include, without limitation, linear fatty alcohols, such as mixtures of C10-C28 alcohols, organosilicones and functionalized perfluoropolyethers.
• the compositions contain from about 0.5 to about 15 wt % processing aids, preferably from about 0.5 to about 10 wt %.
• the fluoroelastomer composition of the present invention preferably contains no to minor amounts of the commonly preferred acid acceptor compounds comprising oxides and hydroxides of divalent metals.
• Non-limiting examples include Ca(OH)2, MgO, CaO and ZnO.
• the compositions of the invention are substantially free of acid acceptors, especially the aforementioned acid acceptors, “substantially free” meaning less than 0.1 (preferably 0) parts by weight per 100 parts by weight of fluoroelastomer.
• Non-limiting examples of fillers include both organic and inorganic fillers, such as barium sulfate, carbon black, graphite, plastic powders, such as PTFE powder, silica, titanium dioxide, glass fiber, fumed silica, graphenes and fibers, such as mineral fibers, plastic fibers, such as ultra-high molecular weight polyethylene fibers, carbon fibers, carbon nano tubes (CNTs), boron fibers.
• fillers such as plastic powders, for example PTFE powder, graphite and CNT, are used to improve wear resistance and other properties of moldings intended for use as dynamic seal members, for example.
• fillers such as carbon black
• the compositions preferably comprise from 1 to 50 wt % filler. In other embodiments, the filler accounts for 10 to 30 wt % of the compositions.
• the fluoroelastomer, the curing system, the nitrogen-containing polymer, and any other components can be incorporated into a curable fluoroelastomer composition by methods conventional in the rubber industry, for example by means of an internal mixer or rolling mill at a temperature below the melting temperature of the nitrogen-containing polymer.
• Other ingredients that may be added include those commonly used in fluoroelastomer compositions as described above.
• the resulting curable composition may then be shaped (e.g., molded or extruded) and cured to form a fluoroelastomer article. Curing typically takes place at about 150 to 200° C. for 1 to 60 minutes.
• the nitrogen-containing polymers contained in the fluoroelastomer composition are selected according to the invention from polyamide, polyimide, mixtures and/or copolymers thereof. These polymers can be amorphous, semicrystalline or crystalline and linear, branched, crosslinked or uncrosslinked.
• the amount of nitrogen-containing polymer in the fluoroelastomer composition is 0.1 wt % to 30 wt %, preferably from 0.1 wt % to 15 wt %, more preferably from 0.1 wt % to 10 wt %, even more preferably from 0.1 wt % to 5 wt % based in each case on the total weight of fluoroelastomer and nitrogen-containing polymer.
• Particularly suitable nitrogen-containing polymers are those having a melting temperature determined according to ASTM D3418-08 or decomposition temperature of more than 180° C., preferably from 180° C. to 1000° C., preferably greater than 190° C., for example from 190° C. to 1000° C., more preferably greater than 200° C., for example from 200° C. to 1000° C., most preferably greater than 215° C., for example from 215° C. to 1000° C.
• the nitrogen-containing polymer is solid at the curing temperature of the fluoroelastomer, meaning that the curing temperature of the fluoroelastomer is lower than the greater of the melting temperature, glass transition temperature and decomposition temperature of the polymer.
• Polyamides useful in the practice of the invention include: aliphatic polyamides, such as nylon 6, nylon 7, nylon 6/6, nylon 6/10, nylon 6/12, nylon 11, nylon 12, aromatic and partially aromatic polyamides, such as p-aramid, m-aramid, polyphthalamides, and aliphatic, aromatic, and/or partially aromatic polyamide copolymers, such as copoly(amide-ether), copoly(amide-ester).
• aliphatic polyamides such as nylon 6, nylon 7, nylon 6/6, nylon 6/10, nylon 6/12, nylon 11, nylon 12, aromatic and partially aromatic polyamides, such as p-aramid, m-aramid, polyphthalamides, and aliphatic, aromatic, and/or partially aromatic polyamide copolymers, such as copoly(amide-ether), copoly(amide-ester).
• a polyamide having an amine end group content greater than 30 mEq/kg may be desirable.
• polyamides examples include polyhexamethylene adipamide (6,6 nylon), polyhexamethylene azelamide (6,9 nylon), polyhexamethylene sebacamide (6,10 nylon), and polyhexamethylene dodecanamide (6,12 nylon), the polyamide being prepared by ring-opening of lactams, i.e., polycaprolactam, polylauriclactam, poly-11-aminoundecanoic acid and poly-bis(p-aminocyclohexyl)methane dodecanoamide.
• polyamides prepared by copolymerization of two of the above polymers or by terpolymerization of the above polymers or their components, such as adipic acid isophthalic acid hexamethylenediamine copolymer.
• polyamides are condensation products of one or more dicarboxylic acids and one or more diamines and/or one or more aminocarboxylic acids and/or ring-opening polymerization products of one or more cyclic lactams.
• Aliphatic polyamides useful in the practice of the present invention can be formed from aliphatic and alicyclic monomers, such as diamines, dicarboxylic acids, lactams, aminocarboxylic acids and their reactive equivalents.
• a suitable aminocarboxylic acid is 1,1-aminododecanoic acid.
• Suitable lactams are caprolactam and laurolactam. Linear, branched and cyclic monomers may be used.
• Carboxylic acid monomers that can be used to prepare aliphatic polyamides include aliphatic carboxylic acids, such as adipic acid, pimelic acid, suberic acid, azelaic acid, decanedioic acid, dodecanedioic acid, tridecanedioic acid, tetradecanedioic acid and pentadecanedioic acid.
• aliphatic carboxylic acids such as adipic acid, pimelic acid, suberic acid, azelaic acid, decanedioic acid, dodecanedioic acid, tridecanedioic acid, tetradecanedioic acid and pentadecanedioic acid.
• Diamines can be selected from diamines having four or more carbon atoms, including but not limited to tetramethylenediamine, hexamethylenediamine, octamethylenediamine, decamethylenediamine, dodecamethylenediamine, 2-methylpentamethylenediamine, 2-ethyltetramethylenediamine, 2-methyloctamethylenediamine, trimethylhexamethylenediamine, meta-xylylenediamine and/or mixtures thereof.
• Aromatic and partially aromatic polyamides are homopolymers, dipolymers, terpolymers or higher order polymers formed from monomers containing aromatic groups.
• One or more aromatic carboxylic acids may be terephthalic acid or a mixture of terephthalic acid with one or more other carboxylic acids, such as isophthalic acid, phthalic acid, 2-methylterephthalic acid and naphthalic acid.
• the one or more aromatic carboxylic acids may be mixed with one or more aliphatic dicarboxylic acids.
• an aromatic diamine such as meta-xylylenediamine can be used to provide a partially aromatic polyamide.
• Block copoly(amide) copolymers are also suitable as polyamide components. If the block copoly(amide) copolymer comprises e.g. a polyether oligomer or a polyalkylene ether, for example poly(ethylene oxide), then the block copolymer is a copoly(amide-ether). If the block copoly(amide) copolymer comprises an ester, for example a polylactone, such as polycaprolactone, then the block copolymer is a copoly(amide-ester). Preferably, the block copoly(amide) copolymer is a block copoly(amide-ester), a block copoly(amide-ether), or a mixture thereof.
• the block copoly(amide) copolymer comprises e.g. a polyether oligomer or a polyalkylene ether, for example poly(ethylene oxide), then the block copolymer is a copoly(amide-ether). If the block copoly(amide) copo
• Preferred polyamides are homopolymers or copolymers, the term copolymer referring to polyamides having two or more amide and/or diamide molecular repeat units.
• the polyamide component may comprise one or more aliphatic or semiaromatic polyamides, for example poly(pentamethylene decanediamide), poly(pentamethylene dodecanediamide), poly (e-caprolactam/hexamethylene hexanediamide), poly(e-caprolactam/hexamethylene-decanediamide), poly-(12-amino-dodecanamide), poly(l2-amino-dodecanamide/tetramethylene terephthalamide)dodecanediamide); poly(tetramethylene hexanediamide), poly(e-caprolactam), poly(hexamethylene hexanediamide), poly((hexamethylene)dodecanediamide) and poly(hexamethylene tetradecanediamide
• the polyamide may also be a mixture of two or more polyamides.
• Preferred polyamides have a melting temperature high enough not to impair the scope of application for the curable fluoroelastomer compositions.
• polyamides formed by ring opening or condensation of aminocarboxylic acids.
• Polyamides suitable for use in the invention are widely commercially available, for example Zytel®, Kevler® available from E.I. du Pont de Nemours and Company, Wilmington, Del., U.S.A., Durethan®, available from Lanxess, Germany, and Ultramid® resins, available from BASF, U.S.A., Twaron®, available from TEIJIN, The Netherlands.
• Polyimides in the sense of the invention include polymers whose most important structural feature is the imide group.
• Polyimides containing further structural elements, such as ester groups, amide groups, etc., such as polyetherimides (PEI) and polyamideimides (PAI), are also to be understood as polyimides according to the invention.
• polyimides or polyamide-imides can be obtained by polycondensation of at least one aromatic tetracarboxylic (di)anhydride or an aromatic tricarboxylic acid, preferably selected from the group consisting of 3,4,3′,4′-benzophenone-tetracarboxylic dianhydride, 1,2,4,5-benzene tetracarboxylic dianhydride, 3,4,3′4′-biphenyl-tetracarboxylic dianhydride, oxydiphthalic dianhydride, sulfonyldiphthalic dianhydride and 1,1,1,3,3,3-hexafluoro-2,2-propylidene diphthalic dianhydride, 1,3,4-benzene tricarboxylic acid and at least one aromatic diisocyanate, preferably selected from the group consisting of toluene-2,4-diisocyanate, toluene-2,6-diisocyanate, 4,4
• Particularly preferred polyimides include:
• R corresponds to one or more, identical or different, radicals selected from the group consisting of L1, L2, L3 and L4.
• This polymer is commercially available under the name P84 or P84 type 70 from Evonik Fibers and is registered under CAS number: 9046-51-9.
• This polymer is commercially available as P84HT from Evonik Fibers and is registered under CAS number: 134119-41-8.
• polyamide-imides are the polymers sold under the trade names Torion® and Kermel® and having the composition indicated below:
• radical R corresponds to one or more, identical or different, radicals selected from the group consisting of L2, L3 and L4.
• Polyimides suitable for use in the invention are widely commercially available, for example Polyimide P84® NT polyimide available from Evonik, Germany, Kapton®, Vespel® available from E.I. du Pont de Nemours and Company, Wilmington, Del., U.S.A., and Torion®, available from Solvay, Belgium.
• the fluoroelastomer composition in cured state has a volume swelling in 20% acetic acid after 168 h/95° C., measured according to DIN ISO 1817, of from 0 to 25 vol %, more preferably from 0 to 15 vol %, in particular from 0 to 10 vol %.
• the fluoroelastomer composition in cured state has a compression set after 168 h/200° C., measured according to DIN ISO 815, of from 0 to 70 percent, for example 1 to 70 percent, more preferably from 0 to 60 percent, for example 1 to 60 percent, in particular from 0 to 40 percent, for example 1 to 40 percent.
• the fluoroelastomer composition according to the invention is perfectly suitable for preparing seals, in particular O-rings, frame seals, radial shaft seals, bellow-type and valve stem seals.
• a further subject matter of the present invention is a seal comprising a fluoroelastomer composition according to one or more of the embodiments described herein as well as its use in acidic media.
• Comparative mixture FKM mixture free of metal oxides.
• the crosslinked material shows a marked decrease in tensile strength after air aging at 250° C. for 168 h with respect to CE2.
• Comparative mixture FKM mixture containing metal oxides, contains 1.5 phr ZnO.
• the crosslinked material shows high swelling after storage in acetic acid.
• the tensile strength is comparable to CE2 after air aging.
• the tensile strength is comparable to CE2 after air aging. Swelling in acetic acid shows an improvement over CE1.
• the measured compression sets are comparable to CE1 and CE2. Swelling in acetic acid shows an improvement over CE1.
• Polyaramid-containing mixture FKM mixture free of metal oxides having 6 phr polyaramid powder.
• the measured compression sets are comparable to CE1 and CE2. Swelling in acetic acid shows an improvement over CE1.
• Polyimide-containing mixture FKM mixture free of metal oxides having 6 phr polyimide 1 powder.
• the tensile strength after air aging at 250° C. for 168 h is comparable to CE2 and the measured compression sets are comparable to CE1 and CE2. Swelling in acetic acid shows an improvement over CE1.
• Polyimide-containing mixture FKM mixture free of metal oxides having 6 phr polyimide 2 powder.
• the tensile strength after air aging at 250° C. for 168 h is comparable to CE2 and the measured compression sets are comparable to CE1 and CE2. Swelling in acetic acid shows an improvement over CE1.
• Polyimide-containing mixture FKM mixture free of metal oxides having another FKM base polymer and 6 phr polyimide 2 powder.
• the tensile strength after air aging at 250° C. for 168 h is comparable to CE2 and the measured compression sets are comparable to CE1 and CE2. Swelling in acetic acid shows an improvement over CE1.
• Polyimide-containing mixture FKM mixture free of metal oxides having another FKM base polymer and 30 phr polyimide 1 powder.
• the measured compression sets are comparable to CE1 and CE2.
• Polyimide-containing mixture FKM mixture free of metal oxides having another FKM base polymer and 30 phr polyimide 2 powder.
• polyimide-containing mixtures EI1, EI2 and EI3 demonstrate the best properties with regard to air aging and swelling in acetic acid, as well as no significant deterioration in compression set over CE1 and CE2.
• the recitation of “at least one of A, B, and C” should be interpreted as one or more of a group of elements consisting of A, B, and C, and should not be interpreted as requiring at least one of each of the listed elements A, B, and C, regardless of whether A, B, and C are related as categories or otherwise.
• the recitation of “A, B, and/or C” or “at least one of A, B, or C” should be interpreted as including any singular entity from the listed elements, e.g., A, any subset from the listed elements, e.g., A and B, or the entire list of elements A, B, and C.

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