US20050272872A1 - Dynamic vulcanization of fluorocarbon elastomers - Google Patents

Dynamic vulcanization of fluorocarbon elastomers Download PDF

Info

Publication number
US20050272872A1
US20050272872A1 US11171719 US17171905A US2005272872A1 US 20050272872 A1 US20050272872 A1 US 20050272872A1 US 11171719 US11171719 US 11171719 US 17171905 A US17171905 A US 17171905A US 2005272872 A1 US2005272872 A1 US 2005272872A1
Authority
US
Grant status
Application
Patent type
Prior art keywords
thermoplastic
comprises
elastomer
according
tfe
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11171719
Inventor
Edward Park
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Freudenberg-NOK GP
Original Assignee
Freudenberg-NOK GP
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F214/00Copolymers 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
    • C08F214/18Monomers containing fluorine
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/24Crosslinking, e.g. vulcanising, of macromolecules
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/14Copolymers of propene
    • C08L23/142Copolymers of propene at least partially crystalline copolymers of propene with other olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/14Copolymers of propene
    • C08L23/147Copolymers of propene with monomers containing other atoms than carbon or hydrogen atoms
    • 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
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/06Polyamides derived from polyamines and polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G
    • C08J2327/00Characterised 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
    • C08J2327/02Characterised 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
    • C08J2327/12Characterised 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2312/00Crosslinking
    • 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
    • C08L27/16Homopolymers or copolymers or vinylidene fluoride
    • 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
    • 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
    • C08L27/20Homopolymers or copolymers of hexafluoropropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C08L67/025Polyesters derived from dicarboxylic acids and dihydroxy compounds containing polyether sequences
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/12Polyester-amides

Abstract

Processable rubber compositions contain a vulcanized fluorocarbon elastomer dispersed in a matrix of a non-fluorine containing thermoplastic polymeric material. In one embodiment the matrix forms a continuous phase and the vulcanized elastomeric material is in the form of particles forming a non-continuous phase. The compositions are made by combining a curative, an uncured fluorocarbon elastomer, and a thermoplastic material, and heating the mixture at a temperature and for a time sufficient to effect vulcanization of the elastomeric material, while mechanical energy is applied to mix the mixture during the heating step. Shaped articles such as seals, gaskets, O-rings, and hoses may be readily formed from the rubber compositions according to conventional thermoplastic processes such as blow molding, injection molding, and extrusion.

Description

    CROSS-REFERENCE TO RELATED APPLICATION
  • This application is a divisional of U.S. patent application Ser. No. 10/620,213 filed on Jul. 15, 2003, the disclosure of which is incorporated herein by reference.
  • FIELD OF THE INVENTION
  • The present invention relates to thermoprocessable compositions containing cured fluorocarbon elastomers. It also relates to seal and gasket type material made from the compositions and methods for their production by dynamic vulcanization techniques.
  • BACKGROUND OF THE INVENTION
  • Cured elastomeric materials have a desirable set of physical properties typical of the elastomeric state. They show a high tendency to return to their original sized and shape following removal of a deforming force, and they retain physical properties after repeated cycles of stretching, including strain levels up to 1000%. Based on these properties, the materials are generally useful for making shaped articles such as seals and gaskets.
  • Because they are thermoset materials, cured elastomeric materials can not generally be processed by conventional thermoplastic techniques such as injection molding, extrusion, or blow molding. Rather, articles must be fashioned from elastomeric materials by high temperature curing and compression molding. Although these and other rubber compounding operations are conventional and known, they nevertheless tend to be more expensive and require higher capital investment than the relatively simpler thermoplastic processing techniques. Another drawback is that scrap generated in the manufacturing process is difficult to recycle and reuse, which further adds to the cost of manufacturing such articles.
  • In today's automobile engines, the high temperatures of use have led to the development of a new generation of lubricants containing a high level of basic materials such as amines. Articles made from elastomeric materials, such as seals and gaskets, are in contact with such fluids during use, and are subject to a wide variety of challenging environmental conditions, including exposure to high temperature, contact with corrosive chemicals, and high wear conditions during normal use. Accordingly, it is desirable to make such articles from materials that combine elastomeric properties and stability or resistance to the environmental conditions.
  • To meet the demands of the new lubricant technology, a line of fluorocarbon elastomers has been developed highly resistant to the basic compounds found in the lubricating oils and greases. Specifically, cured elastomers based on copolymers of tetrafluoroethylene and propylene have met great commercial success. As a thermoset material, the cured fluorocarbon rubber is subject to the processing disadvantages noted above.
  • It would be desirable to provide an elastomeric or rubber composition that would combine a high level of chemical resistance with the advantages of thermoplastic processability. It would further be desirable to provide methods for formulating chemically resistant rubbers having such advantageous properties.
  • SUMMARY OF THE INVENTION
  • These and other advantages are achieved with a processable rubber composition containing a vulcanized elastomeric material dispersed in a matrix of a thermoplastic polymeric material. The elastomeric material comprises a synthetic, non-crystalline fluorine-containing polymeric material that exhibits elastomeric properties when crosslinked or vulcanized. In a preferred embodiment, the material contains repeating units derived from tetrafluoroethylene, at least one C2-4 olefin, and optionally one or more additional fluorine-containing monomers. In another, the material contains repeating units derived from vinylidene fluoride, hexafluoropropylene, and optional other fluorine-containing monomers. In one embodiment the matrix forms a continuous phase and the vulcanized elastomeric material is in the form of particles forming a non-continuous phase.
  • A method for making a rubber composition comprises combining a curative, an elastomeric material as described above, and a thermoplastic material, and heating the mixture at a temperature and for a time sufficient to effect vulcanization of the elastomeric material, while mechanical energy is applied to mix the mixture during the heating step. The thermoplastic material comprises a polymeric material that softens and flows upon heating.
  • Shaped articles may be readily formed from the rubber compositions according to conventional thermoplastic processes such as blow molding, injection molding, and extrusion. Examples of useful articles include seals, gaskets, O-rings, and hoses.
  • Further areas of applicability of the present invention will become apparent from the detailed description provided hereinafter. It should be understood that the detailed description and specific examples, while indicating preferred embodiments of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is an atomic force micrograph of a microtomed cross section of shaped article of the invention.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The following description of the preferred embodiment(s) is merely exemplary in nature and is in no way intended to limit the invention, its application, or uses.
  • Processable rubber compositions are provided that contain a vulcanized elastomeric material dispersed in a matrix. The vulcanized elastomeric material is the product of vulcanizing, crosslinking, or curing a fluorocarbon elastomer. The matrix is made of a thermoplastic material containing at least one non-fluorine containing thermoplastic polymer. The processable rubber compositions may be processed by conventional thermoplastic techniques to form shaped articles having physical properties that make them useful in a number of applications calling for elastomeric properties. In particular preferred embodiments, shaped articles made from the processable compositions typically exhibit a Shore A hardness of 50 or more, preferably Shore A 70 or more, typically in the range of Shore A 70 to Shore A 90. In addition or alternatively, the tensile strength of the shaped articles will preferably be 4 MPa or greater, preferably 8 MPa or greater, typically about 8-13 MPa. In still other embodiments, shaped articles may be characterized as having a modulus at 100% of at least 2 MPa, preferably at least about 4 MPa, and typically in the range of about 4-8 MPa. In other embodiments, elongation at break of articles made from the processable compositions of the invention will be 10% or greater, preferably at least about 50%, more preferably at least about 150%, and typically in the range of 150-300 %. Shaped articles of the invention may be characterized as having at least one of hardness, tensile strength, modulus, and elongation at break in the above noted ranges.
  • In one embodiment, the fluorocarbon elastomer is a polymeric material containing repeating units derived from tetrafluoroethylene and from at least one C2-4 olefin. In another embodiment, it contains repeating units derived from hexafluoropropylene, vinylidene difluoride, and optionally tetrafluoroethylene or other fluorine-containing monomer. In yet another embodiment, it contains repeating units derived from tetrafluoroethylene, perfluorovinylether, and optional other monomers. The matrix is made of a thermoplastic polymeric material.
  • In one aspect, the rubber compositions are made of two-phases where the matrix forms a continuous phase, and the vulcanized elastomeric material is in the form of particles forming a non-continuous, disperse, or discrete phase. In another aspect, the elastomeric material and the matrix form co-continuous phases.
  • In preferred embodiments, the compositions contain 35% by weight or more, and preferably 40% by weight or more of the elastomer phase, based on the total weight of elastomer and thermoplastic material. In other embodiments, the compositions contain 50% by weight or more of the elastomer phase. The compositions are homogenous blends of two phases that are sufficiently compatible that the compositions may readily be formed into shaped articles having sufficient elastomer properties, such as tensile strength, modulus, elongation at break, and compression set to be industrially useful as seals, gaskets, O-rings, hoses, and the like.
  • The elastomer phase may be present in the form of particles in a continuous thermoplastic phase, as a 3-D network forming a co-continuous phase with the thermoplastic material, or as a mixture of both. The particles or 3-D network of the elastomer phase preferably have minimum dimensions of 10 μm or less, and more preferably 1 μm or less.
  • The rubber composition of the invention may be made by dynamic vulcanization of a fluorocarbon elastomer in the presence of a thermoplastic component. In this embodiment, a method is provided for making the rubber composition, comprising combining a curative agent, an elastomeric material, and a thermoplastic material to form a mixture. The mixture is heated at a temperature and for a time sufficient to effect vulcanization or cure of the fluorocarbon elastomer in the presence of the thermoplastic material. Mechanical energy is applied to the mixture of elastomeric material, curative agent and thermoplastic material during the heating step. Thus the method of the invention provides for mixing the elastomer and thermoplastic components in the presence of a curative agent and heating during the mixing to effect cure of the elastomeric component. Alternatively, the elastomeric material and thermoplastic material may be mixed for a time and at a shear rate sufficient to form a dispersion of the elastomeric material in a continuous or co-continuous thermoplastic phase. Thereafter, a curative agent may be added to the dispersion of elastomeric material and thermoplastic material while continuing the mixing. Finally, the dispersion is heated while continuing to mix to produce the processable rubber composition of the invention.
  • The compositions of the invention are readily processable by conventional plastic processing techniques. In another embodiment, shaped articles are provided comprising the cured, fluorocarbon elastomers dispersed in a thermoplastic matrix. Shaped articles of the invention include, without limitation, seals, O-rings, gaskets, and hoses.
  • In a preferred embodiment, shaped articles prepared from the compositions of the invention exhibit an advantageous set of physical properties that includes a high degree of resistance to the effects of chemical solvents. In these embodiments, it is possible to provide articles for which the hardness, tensile strength, and/or the elongation at break change very little or change significantly less than comparable cured fluorocarbon elastomers or other known thermoplastic vulcanizates, when the articles are exposed for extended periods of time such as by immersion or partial immersion in organic solvents or fuels.
  • The fluorocarbon elastomer undergoes dynamic vulcanization in the presence of thermoplastic non-curing polymers to provide compositions with desirable rubber-like properties, but that can be thermally processed by conventional thermoplastic methods such as extrusion, blow molding, and injection molding. The elastomers are generally synthetic, non-crystalline polymers that exhibit rubber-like properties when crosslinked, cured, or vulcanized. As such, the cured elastomers, as well as the compositions of the invention made by dynamic vulcanization of the elastomers, are observed to substantially recover their original shape after removal of a deforming force, and show reversible elasticity up to high strain levels.
  • Preferred fluorocarbon elastomers include commercially available copolymers of one or more fluorine containing monomers, chiefly vinylidene fluoride (VDF), hexafluoropropylene (HFP), tetrafluoroethylene (TFE), and perfluorovinyl ethers (PFVE). Preferred PFVE include those with a C1-8 perfluoroalkyl group, preferably perfluoroalkyl groups with 1 to 6 carbons, and particularly perfluoromethyl vinyl ether and perfluoropropyl vinyl ether. In addition, the copolymers may also contain repeating units derived from olefins such as ethylene (Et) and propylene (Pr). The copolymers may also contain relatively minor amounts of cure site monomers (CSM), discussed further below. Preferred copolymer fluorocarbon elastomers include VDF/HFP, VDF/HFP/CSM, VDF/HFP/TFE, VDF/HFP/TFE/CSM, VDF/PFVE/TFE/CSM, TFE/Pr, TFE/Pr/VDF, TFE/Et/PFVE/VDF/CSM, TFE/Et/PFVE/CSM and TFE/PFVE/CSM. The elastomer designation gives the monomers from which the elastomer gums are synthesized. The elastomer gums have viscosities that give a Mooney viscosity in the range generally of 15-160 (ML1+10, large rotor at 121° C.), which can be selected for a combination of flow and physical properties. Elastomer suppliers include Dyneon (3M), Asahi Glass Fluoropolymers, Solvay/Ausimont, Dupont, and Daikin.
  • In one embodiment, the elastomeric material may be described as a copolymer of tetrafluoroethylene and at least one C2-4 olefin. As such, the elastomeric material comprises repeating units derived from tetrafluoroethylene and at least one C2-4 olefin. Optionally, the elastomeric material may contain repeating units derived from one or more additional fluorine-containing monomers.
  • In a preferred embodiment, the elastomeric material comprises repeating units derived from 10-90 mole % tetrafluoroethylene, 10-90 mole % C2-4 olefin, and up to 30 mole % of one or more additional fluorine-containing monomers. Preferably, the repeating units are derived from 25-90 mole % tetrafluoroethylene and 10-75 mole % C2-4 olefin. In another preferred embodiment, the repeating units are derived from 45-65 mole % tetrafluoroethylene and 20-55 mole % C2-4 olefin.
  • In particularly preferred embodiments, the molar ratio of tetrafluoroethylene units to C2-4 olefin repeating units is from 60:40 to 40:60. In another embodiment, the elastomeric material comprises alternating units of C2-4 olefins and tetrafluoroethylene. In such polymers the molar ratio of tetrafluoroethylene to C2-4 olefin is approximately 50:50.
  • In another embodiment, the elastomeric materials 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. Elastomeric materials based on copolymers of tetrafluoroethylene and propylene are commercially available, for example from Asahi under the Aflas® trade name.
  • A preferred additional monomer in the vulcanized elastomeric material is vinylidene-difluoride. Other fluorine-containing monomers that may be used in the elastomeric materials of the invention include without limitation, perfluoroalkyl vinyl compounds, perfluoroalkyl vinylidene compounds, and perfluoroalkoxy vinyl compounds. Hexafluoropropylene (HFP) is an example of perfluoroalkyl vinyl monomer. Perfluoromethyl vinyl ether is an example of a preferred perfluoroalkoxy vinyl monomer. For example, rubbers based on copolymers of tetrafluoroethylene, ethylene, and perfluoromethyl vinyl ether are commercially available from Dupont under the Viton® ETP trade name.
  • In another embodiment, the elastomeric materials are curable fluorocarbon elastomers containing repeating units derived from fluoromonomers vinylidene fluoride (VDF) and hexafluoropropylene (HFP). In some embodiments, the elastomers further contain repeating units derived from tetrafluoroethylene. The elastomeric materials may be cured or crosslinked as described below to provide cured materials with rubber-like properties.
  • Chemically, in this embodiment the elastomeric material is made of copolymers of VDF and HFP, or of terpolymers of VDF, HFP, and tetrafluoroethylene (TFE), with optional cure site monomers. In preferred embodiments, they contain about 66 to about 70% by weight fluorine. The elastomers are commercially available, and are exemplified by the Viton® A, Viton® B, and Viton® F series of elastomers from DuPont Dow Elastomers. Grades are commercially available containing the gum polymers alone, or as curative-containing pre-compounds.
  • In another embodiment, the elastomers can be described chemically as copolymers of TFE and PFVE, optionally as a terpolymer with VDF. The elastomer may further contain repeating units derived from cure site monomers.
  • Fluorocarbon elastomeric materials used to make the processable rubber compositions of the invention may typically be prepared by free radical emulsion polymerization of a monomer mixture containing the desired molar ratios of starting monomers. Initiators are typically organic or inorganic peroxide compounds, and the emulsifying agent is typically a fluorinated acid soap. The molecular weight of the polymer formed may be controlled by the relative amounts of initiators used compared to the monomer level and the choice of transfer agent if any. Typical transfer agents include carbon tetrachloride, methanol, and acetone. The emulsion polymerization may be conducted under batch or continuous conditions. Such fluoroelastomers are commercially available as noted above.
  • The fluorocarbon elastomers may also contain up to 5 mole % and preferably up to 3 mole % of repeating units derived from so-called cure site monomers that provide cure sites for vulcanization as discussed below. In one embodiment, the cure site repeating units are derived from bromine-containing olefin monomers. If used, preferably the repeating units of a bromine-containing olefin are present in a level to provide at least about 0.05% bromine in the polymer, preferably 0.3% bromine or more. In a preferred embodiment, the total weight of bromine in the polymer is 1.5 wt. % or less.
  • Bromine-containing olefin monomers useful to provide cure sites for fluoropolymers are disclosed for example in U.S. Pat. No. 4,035,565, the disclosure of which is incorporated by reference. Non-limiting examples of bromine-containing monomers include bromotrifluoroethylene and 4-bromo-3,3,4,4-tetrafluoro-1-butene. Additional non-limiting examples include vinyl bromide, 1-bromo-2,2-difluoroethylene, perfluoroalkyl 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-5,5,6,6-tetrafluorohexene, 4-bromoperfluorobutene-1, and 3,3-difluoroallyl bromide. As noted above, it is usually preferred that enough of the bromo-olefin repeating units be present to provide from about 0.3-1.5 wt. % bromine in the copolymer.
  • Other cure monomers may be used that introduce low levels, preferably less than or equal about 5 mole %, more preferably less than or equal about 3 mole %, of functional groups such as epoxy, carboxylic acid, carboxylic acid halide, carboxylic ester, carboxylate salts, sulfonic acid groups, sulfonic acid alkyl esters, and sulfonic acid salts. Such monomers and cure are described for example in Kamiya et al., U.S. Pat. No. 5,354,811, the disclosure of which is hereby incorporated by reference.
  • The thermoplastic material making up the matrix includes at least one component that is a non-fluorine containing thermoplastic polymer. The polymeric material softens and flows upon heating. In one aspect, a thermoplastic material is one the melt viscosity of which can be measured, such as by ASTM D-1238 or D-2116, at a temperature above its melting point
  • The thermoplastic material of the invention may be selected to provide enhanced properties of the rubber/thermoplastic combination at elevated temperatures, preferably above 100° C. and more preferably at about 150° C. and higher. Such thermoplastics include those that maintain physical properties, such as at least one of tensile strength, modulus, and elongation at break to an acceptable degree at the elevated temperature. In a preferred embodiment, the thermoplastics possess physical properties at the elevated temperatures that are superior (i.e. higher tensile strength, higher modulus, and/or higher elongation at break) to those of the cured fluorocarbon elastomer (rubber) at a comparable temperature.
  • The thermoplastic polymeric material used in the invention may be a thermoplastic elastomer. Thermoplastic elastomers have some physical properties of rubber, such as softness, flexibility and resilience, but may be processed like thermoplastics. A transition from a melt to a solid rubber-like composition occurs fairly rapidly upon cooling. This is in contrast to conventional elastomers, which harden slowly upon heating. Thermoplastic elastomers may be processed on conventional plastic equipment such as injection molders and extruders. Scrap may generally be readily recycled.
  • Thermoplastic elastomers have a multi-phase structure, wherein the phases are generally intimately mixed. In many cases, the phases are held together by graft or block copolymerization. At least one phase is made of a material that is hard at room temperature but fluid upon heating. Another phase is a softer material that is rubber like at room temperature.
  • Some thermoplastic elastomers have an A-B-A block copolymer structure, where A represents hard segments and B is a soft segment. Because most polymeric material tend to be incompatible with one another, the hard and soft segments of thermoplastic elastomers tend to associate with one another to form hard and soft phases. For example, the hard segments tend to form spherical regions or domains dispersed in a continuous elastomer phase. At room temperature, the domains are hard and act as physical crosslinks tying together elastomeric chains in a 3-D network. The domains tend to lose strength when the material is heated or dissolved in a solvent.
  • Other thermoplastic elastomers have a repeating structure represented by (A-B)n, where A represents the hard segments and B the soft segments as described above.
  • Many thermoplastic elastomers are known. Non-limiting examples of A-B-A type thermoplastic elastomers include polystyrene/polysiloxane/polystyrene, polystyrene/polyethylene-co-butylene/polystyrene, polystyrene/polybutadiene polystyrene, polystyrene/polyisoprene/polystyrene, poly-α-methyl styrene/polybutadiene/poly-α-methyl styrene, poly-α-methyl styrene/polyisoprene/poly-α-methyl styrene, and polyethylene/polyethylene-co-butylene/polyethylene.
  • Non-limiting examples of thermoplastic elastomers having a (A-B)n repeating structure include polyamide/polyether, polysulfone/polydimethylsiloxane, polyurethane/polyester, polyurethane/polyether, polyester/polyether, polycarbonate/polydimethylsiloxane, and polycarbonate/polyether. Among the most common commercially available thermoplastic elastomers are those that contain polystyrene as the hard segment. Triblock elastomers are available with polystyrene as the hard segment and either polybutadiene, polyisoprene, or polyethylene-co-butylene as the soft segment. Similarly, styrene butadiene repeating co-polymers are commercially available, as well as polystyrene/polyisoprene repeating polymers.
  • In a preferred embodiment, a thermoplastic elastomer is used that has alternating blocks of polyamide and polyether. Such materials are commercially available, for example from Atofina under the Pebax® trade name. The polyamide blocks may be derived from a copolymer of a diacid component and a diamine component, or may be prepared by homopolymerization of a cyclic lactam. The polyether block is generally derived from homo- or copolymers of cyclic ethers such as ethylene oxide, propylene oxide, and tetrahydrofuran.
  • The thermoplastic polymeric material may also be selected from among solid, generally high molecular weight, plastic materials. Preferably, the materials are crystalline or semi-crystalline polymers, and more preferably have a crystallinity of at least 25 percent as measured by differential scanning calorimetry. Amorphous polymers with a suitably high glass transition temperature are also acceptable as the thermoplastic polymeric material. The thermoplastic also preferably has a melt temperature or glass transition temperature in the range from about 80° C. to about 350° C., but the melt temperature should generally be lower than the decomposition temperature of the thermoplastic vulcanizate.
  • Non-limiting examples of thermoplastic polymers include polyolefins, polyesters, nylons, polycarbonates, styrene-acrylonitrile copolymers, polyethylene terephthalate, polybutylene terephthalate, polyamides, polystyrene, polystyrene derivatives, polyphenylene oxide, polyoxymethylene, and fluorine-containing thermoplastics.
  • Polyolefins are formed by polymerizing α-olefins such as, but not limited to, ethylene, propylene, 1-butene, 1-hexene, 1-octene, 2-methyl-1-propene, 3-methyl-1-pentene, 4-methyl-1-pentene, 5-methyl-1-hexene, and mixtures thereof. Copolymers of ethylene and propylene or ethylene or propylene with another α-olefin such as 1-butene, 1-hexene, 1-octene, 2-methyl-1-propene, 3-methyl-1-pentene, 4-methyl-1-pentene, 5-methyl-1-hexene or mixtures thereof are also contemplated. These homopolymers and copolymers, and blends of them, may be incorporated as the thermoplastic polymeric material of the invention.
  • Polyester thermoplastics contain repeating ester linking units in the polymer backbone. In one embodiment, they contain repeating units derived from low molecular weight diols and low molecular weight aromatic diacids. Non-limiting examples include the commercially available grades of polyethylene terephthalate and polybutylene terephthalate. Alternatively, the polyesters may be based on aliphatic diols and aliphatic diacids. Exemplary here the copolymers of ethylene glycol or butanediol with adipic acid. In another embodiment, the thermoplastic polyesters are polylactones, prepared by polymerizing a monomer containing both hydroxyl and carboxyl functionality. Polycaprolactone is a non-limiting example of this class of thermoplastic polyester.
  • Polyamide thermoplastics contain repeating amide linkages in the polymer backbone. In one embodiment, the polyamides contain repeating units derived from diamine and diacid monomers such as the well known nylon 66, a polymer of hexamethylene diamine and adipic acid. Other nylons have structures resulting from varying the size of the diamine and diacid components. Non-limiting examples include nylon 610, nylon 612, nylon 46, and nylon 6/66 copolymer. In another embodiment, the polyamides have a structure resulting from polymerizing a monomer with both amine and carboxyl functionality. Non-limiting examples include nylon 6 (polycaprolactam), nylon 11, and nylon 12.
  • Other polyamides made from diamine and diacid components include the high temperature aromatic polyamides containing repeating units derived from diamines and aromatic diacids such as terephthalic acid. Commercially available examples of these include PA6T (a copolymer of hexanediamine and terephthalic acid), and PA9T (a copolymer of nonanediamine and terephthalic acid), sold by Kuraray under the Genestar tradename. For some applications, the melting point of some aromatic polyamides may be higher than optimum for thermoplastic processing. In such cases, the melting point may be lowered by preparing appropriate copolymers. In a non-limiting example, in the case of PA6T, which has a melting temperature of about 370° C., it is possible to in effect lower the melting point to below a moldable temperature of 320° C. by including an effective amount of a non-aromatic diacid such as adipic acid when making the polymer.
  • In another preferred embodiment, an aromatic polyamide is used based on a copolymer of an aromatic diacid such as terephthalic acid and a diamine containing greater than 6 carbon atoms, preferably containing 9 carbon atoms or more. The upper limit of the length of the carbon chain of the diamine is limited from a practical standpoint by the availability of suitable monomers for the polymer synthesis. As a rule, suitable diamines include those having from 7 to 20 carbon atoms, preferably in the range of 9 to 15 carbons, and more preferably in the range from 9 to 12 carbons. Preferred embodiments include C9, C10, and C11 diamine based aromatic polyamides. It is believed that such aromatic polyamides exhibit an increase level of solvent resistance based on the oleophilic nature of the carbon chain having greater than 6 carbons. If desired to reduce the melting point below a preferred molding temperature (typically 320° C. or lower), the aromatic polyamide based on diamines of greater than 6 carbons may contain an effective amount of a non-aromatic diacid, as discussed above with the aromatic polyamide based on a 6 carbon diamine. Such effective amount of diacid should be enough to lower the melting point into a desired molding temperature range, without unacceptably affecting the desired solvent resistance properties.
  • Other non-limiting examples of high temperature thermoplastics include polyphenylene sulfide, liquid crystal polymers, and high temperature polyimides. Liquid crystal polymers are based chemically on linear polymers containing repeating linear aromatic rings. Because of the aromatic structure, the materials form domains in the nematic melt state with a characteristic spacing detectable by x-ray diffraction methods. Examples of materials include copolymers of hydroxybenzoic acid, or copolymers of ethylene glycol and linear aromatic diesters such as terephthalic acid or naphthalene dicarboxylic acid.
  • High temperature thermoplastic polyimides include the polymeric reaction products of aromatic dianhydrides and aromatic diamines. They are commercially available from a number of sources. Exemplary is a copolymer of 1,4-benzenediamine and 1,2,4,5-benzenetetracarboxylic acid dianhydride.
  • In a preferred embodiment, the matrix comprises at least one non-fluorine containing thermoplastic, such as those described above. Thermoplastic fluorine-containing polymers may be selected from a wide range of polymers and commercial products. The polymers are melt processable—they soften and flow when heated, and can be readily processed in thermoplastic techniques such as injection molding, extrusion, compression molding, and blow molding. The materials are readily recyclable by melting and re-processing.
  • The thermoplastic polymers may be fully fluorinated or partially fluorinated. Fully fluorinated thermoplastic polymers include copolymers of tetrafluoroethylene and perfluoroalkyl vinyl ethers. The perfluoroalkyl group is preferably of 1 to 6 carbon atoms. Other examples of copolymers are PFA (copolymer of TFE and perfluoropropyl vinyl ether) and MFA (copolymer of TFE and perfluoromethyl vinyl ether). Other examples of fully fluorinated thermoplastic polymers include copolymers of TFE with perfluoroolefins of 3 to 8 carbon atoms. Non-limiting examples include FEP (copolymer of TFE and hexafluoropropylene).
  • Partially fluorinated thermoplastic polymers include E-TFE (copolymer of ethylene and TFE), E-CTFE (copolymer of ethylene and chlorotrifluoroethylene), and PVDF (polyvinylidene fluoride). A number of thermoplastic copolymers of vinylidene fluoride are also suitable thermoplastic polymers for use in the invention. These include, without limitation, copolymers with perfluoroolefins such as hexafluoropropylene, and copolymers with chlorotrifluoroethylene.
  • Thermoplastic terpolymers may also be used. These include thermoplastic terpolymers of TFE, HFP, and vinylidene fluoride.
  • These and other fluorine-containing thermoplastic materials are commercially available. Suppliers include Dyneon (3M), Daikin, Asahi Glass Fluoroplastics, Solvay/Ausimont and DuPont
  • Useful curative agents include diamines, peroxides, and polyol/onium salt combinations. Diamine curatives have been known since the 1950's. Diamine curatives are relatively slow curing, but offer advantages in several areas. Such curatives are commercially available, for example as Diak-1 from DuPont Dow Elastomers.
  • Preferred peroxide curative agents are organic peroxides, preferably dialkyl peroxides. In general, an organic peroxide may be selected to function as a curing agent for the composition in the presence of the other ingredients and under the temperatures to be used in the curing operation without causing any harmful amount of curing during mixing or other operations which are to precede the curing operation. A dialkyl peroxide, which decomposes at a temperature above 49° C. is especially preferred when the composition is to be subjected to processing at elevated temperatures before it is cured. In many cases one will prefer to use a di-tertiarybutyl peroxide having a tertiary carbon atom attached to a peroxy oxygen. Non-limiting examples include 2,5-dimethyl-2,5-di(tert-butylperoxy)-3-hexyne; 2,5-dimethyl-2,5-di(tert-butylperoxy) hexane; and 1,3-bis-(t-butylperoxyisopropyl)benzene. Other non-limiting examples of peroxide curative agent include dicumyl peroxide, dibenzoyl peroxide, tertiary butyl perbenzoate, di[1,3-dimethyl-3-(t-butylperoxy)butyl]carbonate, and the like.
  • One or more crosslinking co-agents may be combined with the peroxide. Examples include triallyl cyanurate; triallyl isocyanurate; tri(methallyl)-isocyanurate; tris(diallylamine)-s-triazine, triallyl phosphite; N,N-diallyl acrylamide; hexaallyl phosphoramide; N,N,N′,N′-tetraallyl terephthalamide; N,N,N′,N′-tetraallyl malonamide; trivinyl isocyanurate; 2,4,6-trivinyl methyltrisiloxane; and tri(5-norbornene-2-methylene) cyanurate.
  • Suitable onium salts are described, for example, in U.S. Pat. Nos. 4,233,421; 4,912,171; and 5,262,490, each of which is incorporated by reference. Examples include triphenylbenzyl phosphonium chloride, tributyl alkyl phosphonium chloride, tributyl benzyl ammonium chloride, tetrabutyl ammonium bromide, and triarylsulfonium chloride.
  • Another class of useful onium salts is represented by the following formula:
    Figure US20050272872A1-20051208-C00001

    where
      • Q is nitrogen or phosphorus;
      • Z is a hydrogen atom or
      •  is a substituted or unsubstituted, cyclic or acyclic alkyl group having from 4 to about 20 carbon atoms that is terminated with a group of the formula —COOA where A is a hydrogen atom or a NH4 + cation or Z is a group of the formula —CY2 COOR′ where Y is a hydrogen or halogen atom, or is a substituted or unsubstituted alkyl or aryl group having from 1 to about 6 carbon atoms that may optionally contain one or more quaternary heteroatoms and where R′ is a hydrogen atom, a NH4 + cation, an alkyl group, or is an acyclic anhydride, e.g., a group of the formula —COR where R is an alkyl group or is a group that itself contains organo-onium (i.e., giving a bis-organo-onium); preferably R′ is hydrogen; Z may also be a substituted or unsubstituted, cyclic or acyclic alkyl group having from 4 to about 20 carbon atoms that is terminated with a group of the formula —COOA where A is a hydrogen atom or is a NH4 + cation;
      • R1, R2, and R3 are each, independently, a hydrogen atom or an alkyl, aryl, alkenyl, or any combination thereof, each R1, R2, and R3 can be substituted with chlorine, fluorine, bromine, cyano, —OR″, or —COOR″ where R″ is a C1 to C20 alkyl, aryl, aralkyl, or alkenyl, and any pair of the R1, R2, and R3 groups can be connected with each other and with Q to form a heterocyclic ring; one or more of the R1, R2, and R3 groups may also be a group of the formula Z where Z is as defined above;
      • X is an organic or inorganic anion (for example, without limitation, halide, sulfate, acetate, phosphate, phosphonate, hydroxide, alkoxide, phenoxide, or bisphenoxide); and
      • n is a number equal to the valence of the anion X.
  • The polyol crosslinking agents may be any of those polyhydroxy compounds known in the art to function as a crosslinking agent or co-curative for fluoroelastomers, such as those polyhydroxy compounds disclosed in U.S. Pat. Nos. 4,259,463 (Moggi et al.), U.S. Pat. No. 3,876,654 (Pattison), U.S. Pat. No. 4,233,421 (Worm), and U.S. Defensive Publication T107,801 (Nersasian). Preferred polyols incude aromatic polyhydroxy compounds, aliphatic polyhydroxy compounds, and phenol resins.
  • Representative aromatic polyhydroxy compounds include any one of the following: di-, tri-, and tetrahydroxybenzenes, -naphthalenes, and -anthracenes, and bisphenols of the Formula
    Figure US20050272872A1-20051208-C00002

    wherein A is a difunctional aliphatic, cycloaliphatic, or aromatic radical of 1 to 13 carbon atoms, or a thio, oxy, carbonyl, or sulfonyl radical, A is optionally substituted with at least one chlorine or fluorine atom, x is 0 or 1, n is 1 or 2, and any aromatic ring of the polyhydroxy compound is optionally substituted with at least one atom of chlorine, fluorine, or bromine atom, or carboxyl or an acyl radical (e.g., —COR, where R is H or a C1 to C8 alkyl, aryl or cycloalkyl group) or alkyl radical with, for example, 1 to 8 carbon atoms. It will be understood from the above bisphenol formula III that the —OH groups can be attached in any position (other than number one) in either ring. Blends of two or more such compounds can also be used. A preferred bisphenol compound is Bisphenol AF, which is 2,2-bis(4-hydroxyphenyl)hexafluoropropane. Other non-limiting examples include 4,4′-dihydroxydiphenyl sulfone (Bisphenol S) and 2,2-bis(4-hydroxyphenyl) propane (Bisphenol A). Aromatic polyhydroxy compound, such as hydroquinone may also be used as curative agents. Further non-limiting examples include catechol, resorcinol, 2-methyl resorcinol, 5-methyl resorcinol, 2-methyl hydroquinone, 2,5-dimethyl hydroquinone, and 2-t-butyl hydroquinone, 1,5-dihydroxynaphthalene and 9,10-dihydroxyanthracene.
  • Aliphatic polyhydroxy compounds may also be used as a polyol curative. Examples include fluoroaliphatic diols, e.g. 1,1,6,6-tetrahydrooctafluorohexanediol, and others such as those described in U.S. Pat. No. 4,358,559 (Holcomb et al.) and references cited therein. Derivatives of polyhydroxy compounds can also be used such as those described in U.S. Pat. No. 4,446,270 (Guenthner et al.) and include, for example, 2-(4-allyloxyphenyl)-2-(4-hydroxyphenyl)propane. Mixtures of two or more of the polyhydroxy compounds can be used.
  • Phenol resins capable of crosslinking a rubber polymer can be employed as the polyol curative agent. Reference to phenol resin may include mixtures of these resins. U.S. Pat. Nos. 2,972,600 and 3,287,440 are incorporated herein in this regard. These phenolic resins can be used to obtain the desired level of cure without the use of other curatives or curing agents.
  • Phenol resin curatives can be made by the condensation of alkyl substituted phenols or unsubstituted phenols with aldehydes, preferably formaldehydes, in an alkaline medium or by condensation of bi-functional phenoldialcohols. The alkyl substituents of the alkyl substituted phenols typically contain 1 to about 10 carbon atoms. Dimethylolphenols or phenolic resins, substituted in para-positions with alkyl groups containing 1 to about 10 carbon atoms, are preferred. Useful commercially available phenol resins include alkylphenol-formaldehyde resin, and bromomethylated alkylphenol-formaldehyde resins.
  • In one embodiment, phenol resin curative agents may be represented by the general formula
    Figure US20050272872A1-20051208-C00003

    where Q is a divalent radical selected from the group consisting of —CH2— and —CH2—O—CH2—; m is zero or a positive integer from 1 to 20 and R′ is hydrogen or an organic radical. Preferably, Q is the divalent radical —CH2—O—CH2—, m is zero or a positive integer from 1 to 10, and R′ is hydrogen or an organic radical having less than 20 carbon atoms. In another embodiment, preferably m is zero or a positive integer from 1 to 5 and R′ is an organic radical having between 4 and 12 carbon atoms. Other preferred phenol resins are also defined in U.S. Pat. No. 5,952,425, which is incorporated herein by reference.
  • In a preferred embodiment, plasticizers, extender oils, synthetic processing oils, or a combination thereof may be used in the compositions of the invention. The type of processing oil selected will typically be consistent with that ordinarily used in conjunction with the specific rubber or rubbers present in the composition. The extender oils may include, but are not limited to, aromatic, naphthenic, and paraffinic extender oils. Preferred synthetic processing oils include polylinear α-olefins. The extender oils may also include organic esters, alkyl ethers, or combinations thereof. As disclosed in U.S. Pat. No. 5,397,832, it has been found that the addition of certain low to medium molecular weight organic esters and alkyl ether esters to the compositions of the invention lowers the Tg of the thermoplastic and rubber components, and of the overall composition, and improves the low temperatures properties, particularly flexibility and strength. These organic esters and alkyl ether esters generally have a molecular weight that is generally less than about 10,000. Particularly suitable esters include monomeric and oligomeric materials having an average molecular weight below about 2000, and preferably below about 600. In one embodiment, the esters may be either aliphatic mono- or diesters or alternatively oligomeric aliphatic esters or alkyl ether esters.
  • In addition to the elastomeric material, the thermoplastic polymeric material, and curative, the processable rubber compositions of this invention may include other additives such as stabilizers processing aids, curing accelerators, fillers, pigments, adhesives, tackifiers, and waxes. The properties of the compositions and articles of the invention may be modified, either before or after vulcanization, by the addition of ingredients that are conventional in the compounding of rubber, thermoplastics, and blends thereof.
  • A wide variety of processing aids may be used, including plasticizers and mold release agents. Non-limiting examples of processing aids include Caranuba wax, phthalate ester plasticizers such as dioctylphthalate (DOP) and dibutylphthalate silicate (DBS); fatty acid salts such zinc stearate and sodium stearate, polyethylene wax, and keramide. In some embodiments, high temperature processing aids are preferred. Such include, without limitation, linear fatty alcohols such as blends of C10-C28 alcohols, organosilicones, and functionalized perfluoropolyethers. In some embodiments, the compositions contain about 1 to about 15% by weight processing aids, preferably about 5 to about 10% by weight.
  • Acid acceptor compounds are commonly used as curing accelerators or curing stabilizers. Preferred acid acceptor compounds include oxides and hydroxides of divalent metals. Non-limiting examples include Ca(OH)2, MgO, CaO, and ZnO.
  • Non-limiting examples of fillers include both organic and inorganic fillers such as, barium sulfate, zinc sulfide, carbon black, silica, titanium dioxide, clay, talc, fiber glass, fumed silica and discontinuous fibers such as mineral fibers, wood cellulose fibers, carbon fiber, boron fiber, and aramid fiber (Kevlar). Some non-limiting examples of processing additives include stearic acid and lauric acid. The addition of carbon black, extender oil, or both, preferably prior to dynamic vulcanization, is particularly preferred. Non-limiting examples of carbon black fillers include SAF black, HAF black, SRP black and Austin black. Carbon black improves the tensile strength, and an extender oil can improve processability, the resistance to oil swell, heat stability, hysteresis, cost, and permanent set. In a preferred embodiment, fillers such as carboxy block may make up to about 40% by weight of the total weight of the compositions of the invention. Preferably, the compositions comprise 1-40 weight % of filler. In other embodiments, the filler makes up 10 to 25 weight % of the compositions.
  • The vulcanized elastomeric material, also referred to herein generically as a “rubber”, is generally present as small particles within a continuous thermoplastic polymer matrix. A co-continuous morphology is also possible depending on the amount of elastomeric material relative to thermoplastic material, the cure system, and the mechanism and degree of cure of the elastomer and the amount and degree of mixing. Preferably, the elastomeric material is fully crosslinked/cured.
  • Full crosslinking can be achieved by adding an appropriate curative or curative system to a blend of thermoplastic material and elastomeric material, and vulcanizing or curing the rubber to the desired degree under vulcanizing conditions. In a preferred embodiment, the elastomer is crosslinked by the process of dynamic vulcanization. The term dynamic vulcanization refers to a vulcanization or curing process for a rubber (here a fluorocarbon elastomer) contained in a thermoplastic composition, wherein the curable rubber is vulcanized under conditions of sufficiently high shear at a temperature above the melting point of the thermoplastic component. The rubber is thus simultaneously crosslinked and dispersed within the thermoplastic matrix. Dynamic vulcanization is effected by applying mechanical energy to mix the elastomeric and thermoplastic components at elevated temperature in the presence of a curative in conventional mixing equipment such as roll mills, Moriyama mixers, Banbury mixers, Brabender mixers, continuous mixers, mixing extruders such as single and twin-screw extruders, and the like. An advantageous characteristic of dynamically cured compositions is that, notwithstanding the fact that the elastomeric component is fully cured, the compositions can be processed and reprocessed by conventional plastic processing techniques such as extrusion, injection molding and compression molding. Scrap or flashing can be salvaged and reprocessed.
  • Heating and mixing or mastication at vulcanization temperatures are generally adequate to complete the vulcanization reaction in a few minutes or less, but if shorter vulcanization times are desired, higher temperatures and/or higher shear may be used. A suitable range of vulcanization temperature is from about the melting temperature of the thermoplastic material (typically 120° C.) to about 300° C. or more. Typically, the range is from about 150° C. to about 250° C., a preferred range of vulcanization temperatures is from about 180° C. to about 220° C. It is preferred that mixing continue without interruption until vulcanization occurs or is complete.
  • If appreciable curing is allowed after mixing has stopped, an unprocessable thermoplastic vulcanizate may be obtained. In this case, a kind of post curing step may be carried out to complete the curing process. In some embodiments, the post curing takes the form of continuing to mix the elastomer and thermoplastic during a cool-down period.
  • After dynamic vulcanization, a homogeneous mixture is obtained, wherein the rubber is in the form of small dispersed particles essentially of an average particle size smaller than about 50 μm, preferably of an average particle size smaller than about 25 μm. More typically and preferably, the particles have an average size of about 10 μm or less, preferably about 5 μm or less, and more preferably about 1 μm or less. In other embodiments, even when the average particle size is larger, there will be a significant number of cured elastomer particles less than 1 μm in size dispersed in the thermoplastic matrix.
  • The size of the particles referred to above may be equated to the diameter of spherical particles, or to the diameter of a sphere of equivalent volume. It is to be understood that not all particles will be spherical. Some particles will be fairly isotropic so that a size approximating a sphere diameter may be readily determined. Other particles may be anisotropic in that one or two dimensions may be longer than another dimension. In such cases, the preferred particle sizes referred to above correspond to the shortest of the dimensions of the particles.
  • In some embodiments, the cured elastomeric material is in the form of particles forming a dispersed, discrete, or non-continuous phase wherein the particles are separated from one another by the continuous phase made up of the thermoplastic matrix. Such structures are expected to be more favored at relatively lower loadings of cured elastomer, i.e. where the thermoplastic material takes up a relatively higher volume of the compositions. In other embodiments, the cured material may be in the form of a co-continuous phase with the thermoplastic material. Such structures are believed to be favored at relatively higher volume of the cured elastomer. At intermediate elastomer loadings, the structure of the two-phase compositions may take on an intermediate state in that some of the cured elastomer may be in the form of discrete particles and some may be in the form of a co-continuous phase.
  • Where some of the cured elastomer is in a co-continuous phase with the thermoplastic, the particle size referred to above is understood to refer to the dimensions of features in two-dimensional cross sections such as FIG. 1.
  • FIG. 1 is an atomic force micrograph of a shaped article produced by injection molding a processable rubber composition according to the invention (see Example 19). The micrograph shows hard and soft regions of the article at a resolution such that features of dimensions 1 μm and less may readily be seen. Lighter portions 2 represent soft areas, which are made of the cured fluorocarbon elastomer. Darker portions 4 represent hard areas corresponding to the thermoplastic material. In a feature not shown in Figure, associated with the soft areas are small hard points that show as dark dots in the micrographs. The dark dots correspond to filler such as carbon black that is present along with the elastomer during the dynamic vulcanization process.
  • Some features 6 of the micrograph suggest the elastomer is present as a particle surrounded by a “sea” of thermoplastic material. For these cases, the structure can be interpreted as the cured fluorocarbon elastomer particles being present as discrete, non-continuous phase dispersed in a continuous thermoplastic phase. Other features 8 of the micrograph may be better interpreted as showing a cross section of an elastomer phase dispersed as a 3-D network in the thermoplastic matrix, suggesting co-continuous phases. For both features 6 and 8, it is evident that the dimensions of the structures are on the order of 10 μm or less, with many particles or other structures having a size of 1 μm or less.
  • From two-dimensional cross sections, it may be difficult to determine whether the elastomer phase is in the form of particles surrounded by a continuous thermoplastic phase, or is rather present as a three-dimensional network forming a co-continuous phase, or is present as a mixture of both. Nevertheless, the cross sections demonstrate that the dimensions of the “particles” are much smaller than those that can be achieved by simply mixing ground rubber particles into a thermoplastic material as a filler.
  • The homogenous nature of the compositions, the small particle size indicative of a large surface area of contact between the phases, and the ability of the compositions to be formed into shaped articles having sufficient hardness, tensile strength, modulus, elongation at break, or compression set to be useful in industrial applications, indicate a relatively high degree of compatibility between the elastomer and thermoplastic phases. It is believed such compatibility results from the dynamic vulcanization process. During the process, the elastomeric particles are being crosslinked or cured while the two phases are being actively mixed and combined. In addition, the higher temperature and the presence of reactive crosslinking agent may lead to some physical or covalent linkages between the two phases. At the same time, the process leads to a finer dispersion of the discrete or co-continuous elastomer phase in the thermoplastic than is possible with simple filling.
  • The progress of the vulcanization may be followed by monitoring mixing torque or mixing energy requirements during mixing. The mixing torque or mixing energy curve generally goes through a maximum after which mixing can be continued somewhat longer to improve the fabricability of the blend. If desired, one can add additional ingredients, such as the stabilizer package, after the dynamic vulcanization is complete. The stabilizer package is preferably added to the thermoplastic vulcanizate after vulcanization has been essentially completed, i.e., the curative has been essentially consumed.
  • The processable rubber compositions of the invention may be manufactured in a batch process or a continuous process.
  • In a batch process, predetermined charges of elastomeric material, thermoplastic material and curative agents are added to a mixing apparatus. In a typical batch procedure, the elastomeric material and thermoplastic material are first mixed, blended, masticated or otherwise physically combined until a desired particle size of elastomeric material is provided in a continuous phase of thermoplastic material. When the structure of the elastomeric material is as desired, a curative agent may be added while continuing to apply mechanical energy to mix the elastomeric material and thermoplastic material. Curing is effected by heating or continuing to heat the mixing combination of thermoplastic and elastomeric material in the presence of the curative agent. When cure is complete, the processable rubber composition may be removed from the reaction vessel (mixing chamber) for further processing.
  • It is preferred to mix the elastomeric material and thermoplastic material at a temperature where the thermoplastic material softens and flows. If such a temperature is below that at which the curative agent is activated, the curative agent may be a part of the mixture during the initial particle dispersion step of the batch process. In some embodiments, a curative is combined with the elastomeric and polymeric material at a temperature below the curing temperature. When the desired dispersion is achieved, the temperature may be increased to effect cure. In one embodiment, commercially available elastomeric materials are used that contain a curative pre-formulated into the elastomer. However, if the curative agent is activated at the temperature of initial mixing, it is preferred to leave out the curative until the desired particle size distribution of the elastomeric material in the thermoplastic matrix is achieved. In another embodiment, curative is added after the elastomeric and thermoplastic material are mixed. In a preferred embodiment, the curative agent is added to a mixture of elastomeric particles in thermoplastic material while the entire mixture continues to be mechanically stirred, agitated or otherwise mixed.
  • Continuous processes may also be used to prepare the processable rubber compositions of the invention. In a preferred embodiment, a twin screw extruder apparatus, either co-rotation or counter-rotation screw type, is provided with ports for material addition and reaction chambers made up of modular components of the twin screw apparatus. In a typical continuous procedure, thermoplastic material and elastomeric material are combined by inserting them into the screw extruder together from a first hopper using a feeder (loss-in-weight or volumetric feeder). Temperature and screw parameters may be adjusted to provide a proper temperature and shear to effect the desired mixing and particle size distribution of an uncured elastomeric component in a thermoplastic material matrix. The duration of mixing may be controlled by providing a longer or shorter length of extrusion apparatus or by controlling the speed of screw rotation for the mixture of elastomeric material and thermoplastic material to go through during the mixing phase. The degree of mixing may also be controlled by the mixing screw element configuration in the screw shaft, such as intensive, medium or mild screw designs. Then, at a downstream port, by using side feeder (loss-in-weight or volumetric feeder), the curative agent may be added continuously to the mixture of thermoplastic material and elastomeric material as it continues to travel down the twin screw extrusion pathway. Downstream of the curative additive port, the mixing parameters and transit time may be varied as described above. By adjusting the shear rate, temperature, duration of mixing, mixing screw element configuration, as well as the time of adding the curative agent, processable rubber compositions of the invention may be made in a continuous process. As in the batch process, the elastomeric material may be commercially formulated to contain a curative agent, generally a phenol or phenol resin curative.
  • The compositions and articles of the invention will contain a sufficient amount of vulcanized elastomeric material (“rubber”) to form a rubbery composition of matter, that is, they will exhibit a desirable combination of flexibility, softness, and compression set. Preferably, the compositions should comprise at least about 25 parts by weight rubber, preferably at least about 35 parts by weight rubber, more preferably at least about 40 parts by weight rubber, even more preferably at least about 45 parts by weight rubber, and still more preferably at least about 50 parts by weight rubber per 100 parts by weight of the rubber and thermoplastic polymer combined. The amount of cured rubber within the thermoplastic vulcanizate is generally from about 5 to about 95 percent by weight, preferably from about 35 to about 95 percent by weight, more preferably from about 40 to about 90 weight percent, and more preferably from about 50 to about 80 percent by weight of the total weight of the rubber and the thermoplastic polymer combined.
  • The amount of thermoplastic polymer within the processable rubber compositions of the invention is generally from about 5 to about 95 percent by weight, preferably from about 10 to about 65 percent by weight and more preferably from about 20 to about 50 percent by weight of the total weight of the rubber and the thermoplastic combined.
  • As noted above, the processable rubber compositions and shaped articles of the invention include a cured rubber and a thermoplastic polymer. Preferably, the thermoplastic vulcanizate is a homogeneous mixture wherein the rubber is in the form of finely-divided and well-dispersed rubber particles within a non-vulcanized matrix. It should be understood, however, that the thermoplastic vulcanizates of the this invention are not limited to those containing discrete phases inasmuch as the compositions of this invention may also include other morphologies such as co-continuous morphologies. In especially preferred embodiments, the rubber particles have an average particle size smaller than about 50 μm, more preferably smaller than about 25 μm, even more preferably smaller than about 10 μm or less, and still more preferably smaller than about 5 μm.
  • Advantageously, the shaped articles of the invention are rubber-like materials that, unlike conventional rubbers, can be processed and recycled like thermoplastic materials. These materials are rubber like to the extent that they will retract to less than 1.5 times their original length within one minute after being stretched at room temperature to twice its original length and held for one minute before release, as defined in ASTM D1566. Also, these materials satisfy the tensile set requirements set forth in ASTM D412, and they also satisfy the elastic requirements for compression set per ASTM D395.
  • The reprocessability of the rubber compositions of the invention may be exploited to provide a method for reducing the costs of a manufacturing process for making shaped rubber articles. The method involves recycling scrap generated during the manufacturing process to make other new shaped articles. Because the compositions of the invention and the shaped articles made from the compositions are thermally processable, scrap may readily be recycled for re-use by collecting the scrap, optionally cutting, shredding, grinding, milling, otherwise comminuting the scrap material, and re-processing the material by conventional thermoplastic techniques. Techniques for forming shaped articles from the recovered scrap material are in general the same as those used to form the shaped articles—the conventional thermoplastic techniques include, without limitation, blow molding, injection molding, compression molding, and extrusion.
  • The re-use of the scrap material reduces the costs of the manufacturing process by reducing the material cost of the method. Scrap may be generated in a variety of ways during a manufacturing process for making shaped rubber articles. For example, off-spec materials may be produced. Even when on-spec materials are produced, manufacturing processes for shaped rubber articles tend to produce waste, either through inadvertence or through process design, such as the material in sprues of injection molded parts. The re-use of such materials through recycling reduces the material and thus the overall costs of the manufacturing process.
  • For thermoset rubbers, such off spec materials usually can not be recycled into making more shaped articles, because the material can not be readily re-processed by the same techniques as were used to form the shaped articles in the first place. Recycling efforts in the case of thermoset rubbers are usually limited to grinding up the scrap and the using the grinds as raw material in a number products other than those produced by thermoplastic processing technique
  • The description of the invention is merely exemplary in nature and, thus, variations that do not depart from the gist of the invention are intended to be within the scope of the invention. Such variations are not to be regarded as a departure from the spirit and scope of the invention.
  • EXAMPLES
  • In Examples 1-10, the following materials are used:
  • AFLAS MZ is a copolymer elastomer of tetrafluoroethylene and propylene, sold by Asahi Glass Company. It is supplied by Asahi pre-formulated with a phenol crosslinking compound.
  • AFLAS SZ is another grade of TFE/propylene elastomer pre-formulated with a phenol crosslinking compound.
  • AFLAS SP is a copolymer elastomer of tetrafluoroethylene and propylene. It is formulated without a crosslinking compound.
  • Hytrel is Hytrel 4556, 5526 or 8139, a thermoplastic elastomer comprising blocks of polyester and blocks of polyether, sold by DuPont.
  • MT Black is a carbon black filler.
  • MgO is magnesium oxide, which acts as an acid accepting curing accelerator.
  • Ca(OH)2 is calcium hydroxide, another acid accepting curing accelerator.
  • Pebax is Pebax MX 1205, 4033, MV 1074, or MH 1657, grades of a thermoplastic elastomer having blocks of polyamide and blocks of polyether, sold by Atofina.
  • Nylon is ultramid A (nylon 66), ultramid B (nylon 6) or ultramid C (PA 6/66 copolymer).
  • Polyester is PET (polyethylene terephthalate) from Eastman Chemical (Eastar) or PBT (polybutylene terephthalate) from BASF (Ultradur).
  • Polypropylene is Profax from Himont (now Basell).
  • Examples 1-10 demonstrate dynamic vulcanization of copolymers of tetrafluoroethylene and propylene in the presence of a variety of thermoplastic elastomers and semicrystalline thermoplastic materials. The AFLAS materials are used at a level of 100 parts, and the thermoplastic materials are used at levels between 25 parts per hundred AFLAS to 125 parts per hundred parts of the AFLAS material.
  • To demonstrate a batch process, the ingredients are mixed in a Brabender mixer according to the following procedure. The thermoplastic material (Hytrel, Pebax, nylon, polyester, or polypropylene) is melted in a Brabender mixer and stirred. To the molten stirring thermoplastic material is added the AFLAS MZ or AFLAS SZ, along with the MT Black. Mixing continues at the melting point of the thermoplastic material for a further 10-20 minutes, preferably at a temperature of about 120-180° C. Then, the curing accelerators MgO and Ca(OH)2 are added and the mixing and heating continued for a further 10 minutes. The vulcanized material is cooled down and removed from the Brabender mixer. Shaped articles may be prepared from the vulcanized composition by conventional compression molding, injection molding, extrusion, and the like. Plaques may be fabricated from the vulcanized composition for measurement of physical properties.
  • For Examples 11-15, using AFLAS SP, process is similar, except that the peroxide crosslinking material is added at the same time as the curing accelerators MgO and Ca(OH)2 are added.
  • Examples 16a-e—Continuous Process in a Twin Screw Extruder
  • The ingredients for Examples 16a-e are the same as for Examples 7a-e. The barrel of a W&P ZSK-25 model twin screw extruder was heated at 240° C. A mixture of chopped AFLAS SZ elastomer and Pebax plastic pellets was added into the main hopper using a K-tron feeder while turning the screw at 150 rpm. A mixture of the carbon black (MT Black), MgO, Ca(OH)2 and peroxide powder was added using a K-tron side feeder through the downstream side feeding part of the extruder. Strands were extruded through a 2-hole die through a water cooling tank, and cut into pellets with the pelletizer.
    Example 1a Example 1b Example 1c Example 1d Example 1e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS MZ 100.0 195.7 100.0 158.1 100.0 129.4 100.0 115.7 100.0 104.6
    Hytrel 25.0 48.9 50.0 79.0 75.0 97.1 100.0 115.7 125.0 130.8
    MT Black 30.0 58.7 30.0 47.4 30.0 38.8 30.0 34.7 30.0 31.4
    MgO 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Ca(OH)2 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Example 2a Example 2b Example 2c Example 2d Example 2e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS MZ 100.0 195.7 100.0 158.1 100.0 129.4 100.0 115.7 100.0 104.6
    Pebax 25.0 48.9 50.0 79.0 75.0 97.1 100.0 115.7 125.0 130.8
    MT Black 30.0 58.7 30.0 47.4 30.0 38.8 30.0 34.7 30.0 31.4
    MgO 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Ca(OH)2 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Example 3a Example 3b Example 3c Example 3d Example 3e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS MZ 100.0 195.7 100.0 158.1 100.0 129.4 100.0 115.7 100.0 104.6
    Nylon 25.0 48.9 50.0 79.0 75.0 97.1 100.0 115.7 125.0 130.8
    MT Black 30.0 58.7 30.0 47.4 30.0 38.8 30.0 34.7 30.0 31.4
    MgO 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Ca(OH)2 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Example 4a Example 4b Example 4c Example 4d Example 4e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS MZ 100.0 195.7 100.0 158.1 100.0 129.4 100.0 115.7 100.0 104.6
    Polyester 25.0 48.9 50.0 79.0 75.0 97.1 100.0 115.7 125.0 130.8
    MT Black 30.0 58.7 30.0 47.4 30.0 38.8 30.0 34.7 30.0 31.4
    MgO 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Ca(OH)2 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Example 5a Example 5b Example 5c Example 5d Example 5e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS MZ 100.0 195.7 100.0 158.1 100.0 129.4 100.0 115.7 100.0 104.6
    Polyproplene 25.0 48.9 50.0 79.0 75.0 97.1 100.0 115.7 125.0 130.8
    MT Black 30.0 58.7 30.0 47.4 30.0 38.8 30.0 34.7 30.0 31.4
    MgO 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Ca(OH)2 3.0 5.9 3.0 4.7 3.0 3.9 3.0 3.5 3.0 3.1
    Example 6a Example 6b Example 6c Example 6d Example 6e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Hytrel 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 7a Example 7b Example 7c Example 7d Example 7e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Pebax 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.7 3.0 5.7 3.0 5.7 3.0 5.7 3.0 5.7
    isocyanurate
    Example 8a Example 8b Example 8c Example 8d Example 8e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Nylon 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 9a Example 9b Example 9c Example 9d Example 9e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Polyester 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 10a Example 10b Example 10c Example 10d Example 10e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Polypropylene 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 11a Example 11b Example 11c Example 11d Example 11e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Hytrel 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 12a Example 12b Example 12c Example 12d Example 12e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Pebax 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 13a Example 13b Example 13c Example 13d Example 13e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Nylon 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 14a Example 14b Example 14c Example 14d Example 14e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Polyester 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
    Example 15a Example 15b Example 15c Example 15d Example 15e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    AFLAS SP 100.0 190.9 100.0 154.8 100.0 127.0 100.0 113.8 100.0 103.0
    Polypropylene 25.0 47.7 50.0 77.4 75.0 95.2 100.0 113.8 125.0 128.8
    MT Black 30.0 57.3 30.0 46.4 30.0 38.1 30.0 34.1 30.0 30.9
    MgO 3.0 5.7 3.0 4.6 3.0 3.8 3.0 3.4 3.0 3.1
    Ca(OH)2 6.0 11.5 6.0 9.3 6.0 7.6 6.0 6.8 6.0 6.2
    1,3-bis (t-butyl 1.0 1.9 1.0 1.5 1.0 1.3 1.0 1.1 1.0 1.0
    peroxyisopropyl)
    benzene
    triallyl 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9 3.0 5.9
    isocyanurate
  • Examples 17-18
  • Viton F605C is a VDF/HFP/TFE terpolymer elastomer from DuPont Dow Elastomers.
  • Genestar PA9T is C9 diamine based aromatic polyamide. It is a high temperature polyamide based on a copolymer of terephthalic acid and nonanediamine, commercially available from Kuraray.
  • Dyneon FE 5840 is a terpolymer elastomer of VDF/HFP/TFE, from Dyneon (3M).
  • Dyneon BRE 7231X is a base resistant elastomer, based on a terpolymer of TFE, propylene, and VDF, commercially available from Dyneon (3M).
  • Rhenofit CF is a calcium hydroxide crosslinker for fluoroelastomers, from Rhein Chemie.
  • Elastomag 170 is a high activity powdered magnesium oxide from Rohm and Haas.
  • MT Black (N990) is carbon black.
  • Struktol WS-280 is a silane coupling agent from Struktol.
  • Technoflon FPA-1 is a functionalized perfluoropolyether from Ausimont.
  • Examples 17-19 were carried out in a batch process in a Brabender mixer. The thermoplastic polymer is melted in the batch mixer at about 240° C. The elastomer is then added. The blend of elastomer and thermoplastic is stirred about 10-15 minutes at 50 rpm. Then the curative, curing accelerator, processing aids, and carbon black are added while continuing to stir. Stirring is continued until the mixture is homogenously mixed and cure is complete (typically an additional 10 minutes at 240° C. and 50 rpm). Material is cooled, removed from the mixer, and fabricated into plaques for tensile strength measurements.
    Example 17a Example 17b Example 17c Example 17d Example 17e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    Viton F605C Terpolymer 100.0 232.8 100.0 202.3 100.0 160.4 100.0 132.8 100.0 113.3
    Genestar PA9T 25.0 58.2 50.0 101.2 100.0 160.4 150.0 199.2 200.0 226.7
    Rhenofit CF 6.0 14.0 6.0 12.1 8.0 9.6 6.0 8.0 6.0 6.8
    Elastomag 170 3.0 7.0 3.0 6.1 3.0 4.8 3.0 4.0 3.0 3.4
    MT Black (N990) 30.00 69.8 30.00 60.7 30.00 48.1 30.00 39.8 30.00 34.0
    Struktol WS-280 1.00 2.3 1.00 2.0 1.00 1.6 1.00 1.3 1.00 1.1
    Technoflon FPA-1 1.00 2.3 1.00 2.0 1.00 1.6 1.00 1.3 1.00 1.1
    Example 18a Example 18b Example 18c Example 18d Example 18e
    Ingredient pphr g pphr g pphr g pphr g pphr g
    Dyneon FE 5840 70.0 185.3 70.0 158.2 70.0 122.4 70.0 99.8 70.0 84.3
    Dyneon BRE 7231X 30.0 79.4 30.0 67.3 30.0 52.6 30.0 42.8 30.0 36.1
    Genestar PA9T 25.0 66.2 50.0 113.0 100.0 174.9 150.0 213.9 200.0 240.8
    Rhenofit CF 0.0 15.9 6.0 13.6 8.0 10.6 6.0 8.6 6.0 7.2
    Elastomag 170 3.0 7.9 3.0 6.8 3.0 5.2 3.0 4.3 3.0 3.6
    Austin Black 30.00 26.5 30.00 22.6 30.00 17.6 30.00 14.3 30.00 12.0
    Struktol WS-280 1.00 2.6 1.00 2.3 1.00 1.7 1.00 1.4 1.00 1.2
    Technoflon FPA-1 1.00 2.6 1.00 2.3 1.00 1.7 1.00 1.4 1.00 1.2
  • Example 19
  • For Example 19, 100 parts of Viton F605 was dynamically vulcanized with 125 parts of Nylon 66 according to the conditions of Examples 17-18. The fluorocarbon elastomer made up 44.4% by weight of the total elastomer and thermoplastic combined. The processable rubber composition was molded into a tensile bar for testing of tensile strength and elongation at break.
  • The middle portion of the tensile bar was cut out of the bar and encased in a ½ inch block of epoxy. The block was taken down to liquid nitrogen temperature, and the shaped article was microtomed to produce a specimen for analysis with an atomic force microscope (AFM).
  • The AFM was used in intermittent contact mode, permitting phase and topography images to be obtained simultaneously. Resolution was 1024 data points per scan line and 1024 lines per image. The scan rate was 2 Hz, and the X and Y axis were set at 20 μm by 20 μm. A built-in image analyzer allowed the total for each domain to be calculated. The amount of cured rubber phase was analyzed to be 42.4% by area of the cross section shown in FIG. 1.
  • FIG. 1 shows a pictorial representation of a 10 μm×10 μm section of an AFM scan illustrating the two-phase structure of the shaped article of Example 19. The darker areal portion is a harder area, corresponding to the thermoplastic; the lighter portions are softer areas, corresponding to the rubbery cured elastomer material. Yet darker dots believed to represent filler particles present predominantly in the cured elastomer phase have been omitted for clarity.

Claims (72)

  1. 1-11. (canceled)
  2. 12. A processable rubber composition comprising a cured fluorocarbon elastomer dispersed in a thermoplastic matrix,
    wherein the thermoplastic matrix comprises a non-fluorine containing thermoplastic polymer, and
    wherein the cured fluorocarbon elastomer is present as a discrete phase or a phase co-continuous with the matrix, and
    wherein the dimensions of the elastomer phase are less than 10 μm, as measured by atomic force microscopy on cryogenically microtomed cross-sections of shaped articles formed from the processable rubber composition,
    wherein the thermoplastic matrix comprises an amorphous polymer with a glass transition temperature of greater than or equal to 150° C. or a semi-crystalline polymer with a melting point greater than or equal to 150° C.
  3. 13. A composition according to claim 12, wherein the dimensions of the elastomer phase are less than or equal to 1 μm.
  4. 14. A composition according to claim 12, wherein the cured fluorocarbon elastomer is present at least in part as particles dispersed in a continuous thermoplastic phase.
  5. 15. A composition according to claim 12, wherein the cured fluorocarbon elastomer is present at least in part in a dispersed phase co-continuous with the thermoplastic phase.
  6. 16. A composition according to claim 12, wherein the cured fluorocarbon elastomer comprises repeating units derived from tetrafluoroethylene and propylene.
  7. 17-18. (canceled)
  8. 19. A composition according to claim 12, wherein the cured fluorocarbon elastomer comprises repeating units derived from vinylidene fluoride and hexafluoropropylene.
  9. 20-21. (canceled)
  10. 22. A composition according to claim 12, wherein the cured fluorocarbon elastomer comprises repeating units derived from tetrafluoroethylene and perfluoroalkylvinyl ethers,
    wherein the perfluoroalkyl vinyl ether contains 1 to 6 carbons in the perfluoroalkyl group
  11. 23-24. (canceled)
  12. 25. A processable rubber composition made by a process comprising the step of dynamically vulcanizing a fluorocarbon elastomer in the presence of a non-fluorine-containing thermoplastic material,
    wherein the thermoplastic material has a glass transition temperature of greater than or equal to 150° C. or a melting point greater than or equal to 150° C.
  13. 26. A composition according to claim 25, made by a process comprising the steps of:
    combining an uncured or partially cured fluorocarbon elastomer, a curative agent capable of reacting with the fluorocarbon elastomer to effect cure, and a non-fluorine-containing thermoplastic material;
    mixing the combination; and
    applying heat to the combination during the mixing step.
  14. 27. A composition according to claim 25, made by a process comprising the steps of:
    mixing the elastomer and thermoplastic components in the presence of the curative agent, and
    heating during mixing to effect cure of the elastomeric components.
  15. 28. A composition according to claim 25 made by a process comprising the steps of:
    mixing the elastomer material and thermoplastic material for a time and at a shear rate sufficient to form a dispersion of the elastomeric material in a continuous thermoplastic phase;
    adding a curative to the dispersion while continuing the mixing; and
    heating the dispersion while continuing to mix the curative, elastomeric material, and thermoplastic material.
  16. 29. A composition according to claim 25, wherein the curative agent comprises a polyol.
  17. 30. A composition according to claim 25, wherein the curative agent comprises a peroxide.
  18. 31. A method for making a rubber composition comprising:
    forming a mixture by combining a curative, an uncured or partially cured elastomeric material, and a thermoplastic material; and
    heating the mixture at a temperature and for a time sufficient to effect vulcanization of the elastomeric material, wherein mechanical energy is applied to mix the mixture during the heating step;
    wherein the elastomeric material comprises a fluorocarbon elastomer; and
    wherein the thermoplastic material comprises a non-fluorine-containing polymeric material with a glass transition temperature greater than or equal to 150° C. or a melting point greater than or equal to 150° C.
  19. 32. A method according to claim 31 comprising:
    mixing the elastomer and thermoplastic components in the presence of a curative agent, and
    heating during mixing to effect cure of the elastomeric component.
  20. 33. A method according to claim 31 comprising:
    mixing the elastomeric material and the thermoplastic material for a time and at a shear rate sufficient to form a dispersion of the elastomeric material in a continuous thermoplastic phase;
    adding a curative to the dispersion while continuing the mixing; and
    heating the dispersion while continuing to mix the curative, elastomeric material, and thermoplastic material.
  21. 34. A method according to claim 31, wherein the fluorine-containing elastomer comprises repeating units derived from:
    10-90 mole % tetrafluoroethylene;
    10-90 mole % propylene; and
    up to 30 mole % of an additional fluorine containing monomer.
  22. 35. A method according to claim 34, wherein the additional monomer comprises vinylidene difluoride.
  23. 36. A method according to claim 31, wherein the fluorocarbon elastomer comprises repeating units deriving from vinylidene fluoride and hexafluoropropylene.
  24. 37. A method according to claim 36, wherein the fluorocarbon elastomer further comprises repeating units derived from tetrafluoroethylene.
  25. 38. A method according to claim 31, wherein the fluorocarbon elastomer is selected from the group consisting of:
    VDF/HFP,
    VDF/HFP/TFE,
    VDF/PFVE/TFE,
    TFE/Pr,
    TFE/Pr/VDF,
    TFE/Et/PFVE/VDF,
    TFE/Et/PFVE, and
    TFE/PFVE.
  26. 39. A method according to claim 38, wherein the fluorocarbon elastomer also comprises cure site monomers.
  27. 40. A method according to claim 31, wherein the curative agent comprises an amine.
  28. 41. A method according to claim 31, wherein the curative comprises a polyol.
  29. 42. A method according to claim 31, wherein the curative comprises a peroxide.
  30. 43. A method according to claim 31, wherein the thermoplastic material comprises a thermoplastic elastomer.
  31. 44. A method according to claim 43, wherein the thermoplastic elastomer comprises blocks of polyamide and blocks of polyether.
  32. 45. A method according to claim 43, wherein the thermoplastic elastomer comprises blocks of polyether and blocks of polyester.
  33. 46. A method according to claim 31, wherein the thermoplastic material comprises a polyamide, a polyester, or a polyolefin.
  34. 47. A method according to claim 31, comprising a continuous process.
  35. 48. A method according to claim 47, carried out in a twin screw extruder.
  36. 49. A method according to claim 31, comprising a batch process.
  37. 50. A method according to claim 31, wherein the combination comprises at least about 35 parts by weight vulcanized elastomeric material per 100 parts of the vulcanized elastomeric material and thermoplastic material combined.
  38. 51. A method according to claim 31, wherein the combination comprises at least about 45 parts by weight vulcanized elastomeric material per 100 parts of the vulcanized elastomeric material and thermoplastic material combined.
  39. 52. A method according to claim 31, wherein the combination comprises at least about 50 parts by weight vulcanized elastomeric material per 100 parts of the vulcanized elastomeric material and thermoplastic material combined.
  40. 53. A shaped article comprising a cured fluorocarbon elastomer dispersed in a matrix comprising a thermoplastic material, wherein the thermoplastic material comprises a non-fluorine-containing thermoplastic polymer having a glass transition temperature greater than or equal to 150° C. or a melting point greater than or equal to 150° C.
  41. 54. A shaped article according to claim 53, wherein the hardness of the article is Shore A 50 or greater, the tensile strength of the article is 4 MPa or greater, the modulus at 100% of the article is 4 Mpa or greater, or the elongation at break of the article is 10% or greater.
  42. 55. A shaped article according to claim 53, wherein the cured fluorocarbon elastomer is present at a level of at least 35% by weight based on the total weight of cured fluorocarbon elastomer and thermoplastic polymer.
  43. 56. A shaped article according to claim 53 wherein the cured fluorocarbon elastomer is present at a level of at least 50% by weight based on the total weight of cured fluorocarbon elastomer and thermoplastic polymer.
  44. 57-58. (canceled)
  45. 59. An article according to claim 53, wherein the fluorocarbon elastomer is selected from the group consisting of:
    VDF/HFP,
    VDF/HFP/TFE,
    VDF/PFVE/TFE,
    TFE/Pr,
    TFE/Pr/VDF,
    TFE/Et/PFVE/VDF,
    TFE/Et/PFVE, and
    TFE/PFVE.
  46. 60. An article according to claim 53, wherein the thermoplastic polymer comprises a thermoplastic elastomer.
  47. 61. An article according to claim 60, wherein the thermoplastic elastomer comprises a polyamide block and a polyester block.
  48. 62. An article according to claim 60, wherein the thermoplastic elastomer comprises a polyester block and a polyether block.
  49. 63. An article according to claim 53, wherein the thermoplastic polymer comprises a polyamide.
  50. 64. An article according to claim 63, wherein the polyamide comprises an aromatic polyamide.
  51. 65. An article according to claim 64, wherein the aromatic polyamide comprises repeating units derived from a diamine containing more than 6 carbons and an aromatic diacid.
  52. 66. An article according to claim 64, wherein the aromatic polyamide comprises repeating units derived from nonanediamine and an aromatic diacid.
  53. 67. A seal according to claim 53.
  54. 68. An O-ring according to claim 53.
  55. 69. A gasket according to claim 53.
  56. 70. A hose according to claim 53.
  57. 71. A continuous process for making a processable rubber composition comprising:
    combining a fluorocarbon elastomer, curative agent, a thermoplastic material comprising a non-fluorine containing thermoplastic polymer in a twin screw extruder,
    mixing the combination in the twin screw extruder for a time and at a temperature sufficient to effect cure of the fluorocarbon elastomer, and
    extruding the cured mixture wherein the thermoplastic polymer comprises an amorphous polymer with a glass transition temperature greater than or equal to 150° C. or a semi-crystalline polymer having a melting point greater than or equal to 150° C.
  58. 72. A process according to claim 71 comprising:
    injecting a combination of the fluorocarbon elastomer and thermoplastic material into the twin screw extruder with a first feeder, and
    injecting the curative agent into the screw extruder with a second feeder downstream from the first feeder.
  59. 73. A process according to claim 71, wherein the fluorocarbon elastomer and curative agent are formulated together into a pre-compound.
  60. 74. A process according to claim 71, wherein the fluorocarbon elastomer comprises repeating units derived from tetrafluoroethylene and propylene.
  61. 75. A process according to claim 71, wherein the fluorocarbon elastomer comprises repeating units derived from vinylidene fluoride and hexafluoropropylene.
  62. 76. A process according to claim 71, wherein the fluorocarbon elastomer is selected from the group consisting of:
    VDF/HFP,
    VDF/HFP/TFE,
    VDF/PFVE/TFE,
    TFE/Pr,
    TFE/Pr/VDF,
    TFE/Et/PFVE/VDF,
    TFE/Et/PFVE, and
    TFE/PFVE.
  63. 77. A process according to claim 71, wherein the thermoplastic material comprises a thermoplastic elastomer.
  64. 78. A process according to claim 77, wherein the thermoplastic elastomer comprises polyamide blocks and polyester blocks.
  65. 79. A process according to claim 77, wherein the thermoplastic elastomer comprises blocks of polyester and blocks of polyether.
  66. 80. A process according to claim 71, wherein the thermoplastic material comprises an aromatic polyamide.
  67. 81. An process according to claim 80, wherein the aromatic polyamide comprises repeating units derived from a diamine containing more than 6 carbons and an aromatic diacid.
  68. 82. An process according to claim 80, wherein the aromatic polyamide comprises repeating units derived from nonanediamine and an aromatic diacid.
  69. 83. A method for reducing costs of a manufacturing process for making shaped rubber articles from a processable rubber composition, comprising
    recycling scrap material generated during the manufacturing process to make new shaped articles comprising the processable rubber composition,
    wherein the processable rubber composition is the product of dynamic vulcanization of a fluorocarbon elastomer in the presence of a thermoplastic material, wherein the thermoplastic material comprises a non-fluorine containing thermoplastic polymer.
  70. 84. A method according to claim 83, wherein the manufacturing process comprises forming the shaped articles by a thermoplastic processing technique.
  71. 85. A method according to claim 83, wherein the thermoplastic processing technique is selected from the group consisting of blow molding, injection molding, compression molding, and extrusion.
  72. 86-95. (canceled)
US11171719 2003-07-15 2005-06-30 Dynamic vulcanization of fluorocarbon elastomers Abandoned US20050272872A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US10620213 US7022769B2 (en) 2003-07-15 2003-07-15 Dynamic vulcanization of fluorocarbon elastomers
US11171719 US20050272872A1 (en) 2003-07-15 2005-06-30 Dynamic vulcanization of fluorocarbon elastomers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11171719 US20050272872A1 (en) 2003-07-15 2005-06-30 Dynamic vulcanization of fluorocarbon elastomers

Publications (1)

Publication Number Publication Date
US20050272872A1 true true US20050272872A1 (en) 2005-12-08

Family

ID=34062736

Family Applications (2)

Application Number Title Priority Date Filing Date
US10620213 Active 2023-08-14 US7022769B2 (en) 2003-07-15 2003-07-15 Dynamic vulcanization of fluorocarbon elastomers
US11171719 Abandoned US20050272872A1 (en) 2003-07-15 2005-06-30 Dynamic vulcanization of fluorocarbon elastomers

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US10620213 Active 2023-08-14 US7022769B2 (en) 2003-07-15 2003-07-15 Dynamic vulcanization of fluorocarbon elastomers

Country Status (1)

Country Link
US (2) US7022769B2 (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050165168A1 (en) * 2004-01-26 2005-07-28 Park Edward H. Dynamic vulcanization of elastomers with in-situ polymerization
US20050167928A1 (en) * 2004-02-04 2005-08-04 Park Edward H. Dynamic seal using vulcanization of fluorocarbon elastomers
US20050281973A1 (en) * 2004-06-21 2005-12-22 Park Edward H Pre-molding heat treatment of dynamic vulcanizates of fluorocarbon elastomers
US20060004126A1 (en) * 2004-06-30 2006-01-05 Park Edward H Thermoplastic vulcanizate with functional fillers
US20060142491A1 (en) * 2004-12-27 2006-06-29 Freudenberg-Nok General Partnership Thermoplastic vulcanizate with high temperature processing aid
US20060141324A1 (en) * 2004-12-27 2006-06-29 Kelley Dana A Manifold gasket accommodating differential movement of fuel cell stack
US20070004865A1 (en) * 2005-06-29 2007-01-04 Freudenberg-Nok General Partnership Dynamic vulcanization of fluorocarbon elastomers containing peroxide cure sites
US20070004862A1 (en) * 2005-06-30 2007-01-04 Freudenberg-Nok General Partnership Base resistant FKM-TPV elastomers
US20080157439A1 (en) * 2006-12-27 2008-07-03 Freudenberg-Nok General Partnership Methods for preparing articles from processable and dimensionally stable elastomer compositions
US7449524B2 (en) 2005-01-05 2008-11-11 Freudenberg-Nok General Partnership Dynamic vulcanization with fluorocarbon processing aids
US7449523B2 (en) 2004-12-27 2008-11-11 Freudenberg-Nok General Partnership Fluorocarbon elastomer compositions containing wear reducing additives
US7658387B2 (en) 2005-06-27 2010-02-09 Freudenberg-Nok General Partnership Reinforced elastomeric seal
US7863365B2 (en) 2006-12-20 2011-01-04 Freudenberg-Nok General Partnership Robust magnetizable elastomeric thermoplastic blends

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7351471B2 (en) * 2000-12-06 2008-04-01 3M Innovative Properties Company Fluoropolymer coating compositions with multifunctional fluoroalkyl crosslinkers for anti-reflective polymer films
US7151134B2 (en) * 2003-06-17 2006-12-19 Freudenberg-Nok General Partnership Dynamic vulcanization of polyurethane elastomeric material in the presence of thermoplastics
US20050155690A1 (en) * 2004-01-16 2005-07-21 Park Edward H. Bonding of dynamic vulcanizates of fluorocarbon elastomers
US7153908B2 (en) * 2004-02-04 2006-12-26 Freudenberg-Nok General Partnership Peroxide cured fluorocarbon elastomer compositions
US7623933B2 (en) * 2005-06-10 2009-11-24 Time Warner Cable Inc. Methods and apparatus for controlling display in a networked device
US20070021564A1 (en) * 2005-07-13 2007-01-25 Ellul Maria D Peroxide-cured thermoplastic vulcanizates
US7872075B2 (en) * 2005-10-07 2011-01-18 Exxonmobil Chemical Patents Inc. Peroxide-cured thermoplastic vulcanizates and process for making the same
US8263695B2 (en) * 2005-12-20 2012-09-11 Arkema Inc. Polyvinylidene fluoride having an increased melting point
US20070167574A1 (en) * 2006-01-13 2007-07-19 Freudenberg-Nok General Partnership Fluorocarbon rubber with enhanced low temperature properties
US20110054543A1 (en) * 2009-08-31 2011-03-03 Warsaw Orthopedic, Inc. Locking mechanism
KR20150048900A (en) * 2011-06-09 2015-05-07 가부시끼가이샤 리켄 Seal ring
US20140155551A1 (en) * 2012-12-03 2014-06-05 E I Du Pont De Nemours And Company Peroxide curable fluoroelastomer compositions
EP3164455A4 (en) * 2014-07-01 2018-02-21 Halliburton Energy Services, Inc. Improved high temperature mechanical properties of elastomers with semi-crystalline polymers for downhole applications

Citations (91)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3037954A (en) * 1958-12-15 1962-06-05 Exxon Research Engineering Co Process for preparing a vulcanized blend of crystalline polypropylene and chlorinated butyl rubber
US3538028A (en) * 1963-10-03 1970-11-03 Bendix Corp Vulcanizater of compositions comprising a fluorine-containing copolymer and silicone gum
US3580889A (en) * 1967-08-17 1971-05-25 Du Pont Vulcanization accelerators of polycyclic ethers for fluorinated polymers
US3787341A (en) * 1972-06-12 1974-01-22 Technical Processing Inc Novel processing aids for natural and synthetic rubber compounds
US3884877A (en) * 1973-10-16 1975-05-20 Minnesota Mining & Mfg Fluoroelastomer compositions with triorganophosphorus oxide
US4035565A (en) * 1975-03-27 1977-07-12 E. I. Du Pont De Nemours And Company Fluoropolymer containing a small amount of bromine-containing olefin units
US4094949A (en) * 1975-06-09 1978-06-13 Shin-Etsu Chemical Co. Ltd. Method for preparing shaped articles of a fluorinated elastomer
US4287320A (en) * 1974-08-01 1981-09-01 Minnesota Mining And Manufacturing Company Composition of fluoroelastomer and diorganosulfuroxide
US4311628A (en) * 1977-11-09 1982-01-19 Monsanto Company Thermoplastic elastomeric blends of olefin rubber and polyolefin resin
US4328140A (en) * 1980-10-03 1982-05-04 Raybestos-Manhattan, Inc. Fluoroelastomer processing aid
US4419499A (en) * 1982-03-25 1983-12-06 Monsanto Company Compositions of urethane rubber and nylon
US4450263A (en) * 1979-08-30 1984-05-22 Minnesota Mining And Manufacturing Company Fluoropolymer gum of vinylidene fluoride, hexafluoropropene, and bromodifluoroethylene
US4451542A (en) * 1980-12-08 1984-05-29 Hitachi Maxell, Ltd. Cell with gasket comprising glass beads
US4530881A (en) * 1983-02-24 1985-07-23 Raymark Industries, Inc. Fluoroelastomer-based friction material having improved frictional properties
US4572516A (en) * 1985-06-12 1986-02-25 General Motors Corporation Low friction dynamic seal assembly with centrifugal deflection
US4624978A (en) * 1983-11-14 1986-11-25 Rogers Corporation High temperature polyimide processing aid
US4656228A (en) * 1983-09-17 1987-04-07 Bayer Aktiengesellschaft Polyamides having high notched impact strength and high fluidity in the molten state
US4696989A (en) * 1985-04-10 1987-09-29 Daikin Industries, Ltd. Fluorine-containing elastomeric copolymer
US4696976A (en) * 1984-12-07 1987-09-29 The Dow Chemical Company Vinyl urethane composite polymer containing dispersed soft copolymer particles
US4696998A (en) * 1986-07-28 1987-09-29 General Electric Company Cyclic heterocarbonates and methods for their preparation and use
US4787991A (en) * 1985-10-18 1988-11-29 Asahi Glass Company Ltd. Resin composition having lubricating properties
US4812357A (en) * 1988-09-23 1989-03-14 W. R. Grace & Co.-Conn. Printing blanket
US5006594A (en) * 1988-12-30 1991-04-09 E. I. Du Pont De Nemours And Company Fluorinated thermoplastic elastomers containing polymeric additives and process for preparing such elastomers
US5095072A (en) * 1987-12-17 1992-03-10 Nippon Zeon Co., Ltd. Thermoplastic elastomer composition
US5108780A (en) * 1991-01-28 1992-04-28 Brigham Young University Enhanced thermoplastic adhesion to fibers by using plasma discharge
US5206293A (en) * 1989-10-13 1993-04-27 Japan Synthetic Rubber Co., Ltd. Rubber composition and crosslinkable rubber composition
US5205293A (en) * 1991-10-30 1993-04-27 Koichi Sakurai Method of measuring surface blood flow
US5219931A (en) * 1989-03-04 1993-06-15 Roehm Gmbh Chemische Fabrik Thermoplastically processable solvent-resistant polymer mixtures
US5331040A (en) * 1992-10-26 1994-07-19 E. I. Du Pont De Nemours And Company Adhesive composition with functional filler
US5354811A (en) * 1991-11-20 1994-10-11 Asahi Glass Company Ltd. Fluorine-containing thermoplastic elastomer composition and process for its production
US5371143A (en) * 1989-11-16 1994-12-06 Minnesota Mining And Manufacturing Company Polymer blend composition of fluorinated elastomers, thermoplastic polymers and thermoplastics elastomers
US5384374A (en) * 1991-01-11 1995-01-24 Minnesota Mining And Manufacturing Company Curing fluorocarbon elastomers
US5391610A (en) * 1988-01-05 1995-02-21 Norton Company Moisture cured elastomeric interpenetrating network sealants
US5397832A (en) * 1993-04-20 1995-03-14 Advanced Elastomer Systems, L.P. Thermoplastic elastomer having improved low temperature properties
US5459202A (en) * 1994-06-30 1995-10-17 E. I. Du Pont De Nemours And Company Elastomer seal
US5548028A (en) * 1995-02-24 1996-08-20 E. I. Du Pont De Nemours And Company Curable elastomeric blend with vulcanized fluoroelastomer
US5585152A (en) * 1993-12-10 1996-12-17 Toyo Boseki Kabushiki Kaisha Composition of polyamide resin and polyurethane resin
US5639810A (en) * 1993-04-15 1997-06-17 Cobe Laboratories, Inc. Internally lubricated elastomers for use in biomedical applications
US5700866A (en) * 1995-08-22 1997-12-23 E. I. Du Pont De Nemours And Company Co-curable base resistant fluoroelastomer blend composition
US5723544A (en) * 1992-05-06 1998-03-03 Bayer Corporation Polyolefin ionomer as processing aid for thermoplastic polyurethane
US5747588A (en) * 1993-06-25 1998-05-05 Refac International, Ltd. Thermoplastic urethane elastometric alloys
US5792348A (en) * 1996-10-08 1998-08-11 Filtration Products Ltd. Steel reinforced filter press plates
US5910544A (en) * 1995-11-02 1999-06-08 The Yokohama Rubber Co., Ltd. Thermoplastic elastomer composition and process for production thereof and low permeability hose using the same
US5962589A (en) * 1994-12-09 1999-10-05 Daikin Industries, Ltd. Rubber compositions of low compression set
US6048939A (en) * 1997-01-09 2000-04-11 Dupont Dow Elastomers, L.L.C. Process aid for melt processible polymers
US6054537A (en) * 1992-12-10 2000-04-25 Daikin Industries, Ltd. Thermoplastic resin composition
US6066697A (en) * 1998-08-25 2000-05-23 The University Of Akron Thermoplastic compositions containing elastomers and fluorine containing thermoplastics
US6079465A (en) * 1995-01-23 2000-06-27 The Yokohama Rubber Co., Ltd. Polymer composition for tire and pneumatic tire using same
US6114441A (en) * 1997-07-25 2000-09-05 E. I. Du Pont De Nemours And Company Blends of grafted fluoropolymer and polyester
US6147158A (en) * 1999-07-06 2000-11-14 Freudenberg-Nok General Parnership Compatibilized blends of polyketones and polyolefins
US6162385A (en) * 1997-05-02 2000-12-19 Huels Aktiengesellschaft Composite comprising a polyamide-based molding composition and vulcanized fluoroelastomers
US6310141B1 (en) * 2000-06-27 2001-10-30 Dyneon Llc Fluoropolymer-containing compositions
US6312639B1 (en) * 1996-10-08 2001-11-06 Cylatec, Inc. Processing aid for thermoplastic resin compositions
US6407174B1 (en) * 1997-07-04 2002-06-18 Advanced Elastomer Systems, L.P. Propylene/ethylene/α-olefin terpolymer thermoplastic elastomer vulcanizates
US6410630B1 (en) * 1999-12-29 2002-06-25 Pelseal Technologies, Llc High solids fluoroelastomer compositions
US6429249B1 (en) * 2000-06-30 2002-08-06 Nexpress Solutions Llc Fluorocarbon thermoplastic random copolymer composition
US6437030B1 (en) * 2000-05-24 2002-08-20 Advanced Elastomer Systems, L.P. Thermoplastic vulcanizates and process for making the same
US20020122928A1 (en) * 2000-03-24 2002-09-05 Chemque, Incorporation Co-dispensed compositions for gaskets and other objects
US20020198320A1 (en) * 2001-05-22 2002-12-26 Chmielewski Craig A. Low temperature, highly chemically resistant thermoplastic vulcanizates based on perfluoroether elastomers
US6500374B1 (en) * 1996-07-23 2002-12-31 Seiko Epson Corporation Method of manufacturing bonded magnets of rare earth metal, and bonded magnet of rare earth metal
US20030026995A1 (en) * 2000-06-27 2003-02-06 Dyneon Llc Novel fluoropolymers with improved characteristics
US20030138655A1 (en) * 1999-11-29 2003-07-24 Jiro Watanabe Wiper blade
US6624251B1 (en) * 1999-12-01 2003-09-23 Freudenberg-Nok General Partnership Highly chemically resistant thermoplastic vulcanizates based on fluorocarbon polymers and seal-gasket products made with same
US6656831B1 (en) * 2000-01-26 2003-12-02 Applied Materials, Inc. Plasma-enhanced chemical vapor deposition of a metal nitride layer
US6663966B2 (en) * 2000-03-30 2003-12-16 General Electric Company Use of dendrimers as a processing aid and surface modifiers for thermoplastic resins
US6737479B2 (en) * 2000-11-17 2004-05-18 Immix Technologies, Llc Dynamically cured fluoroelastomer blends
US6774171B2 (en) * 2002-01-25 2004-08-10 L&L Products, Inc. Magnetic composition
US20040183702A1 (en) * 2003-01-23 2004-09-23 Daniel Nachtigal Magnetizable thermoplastic elastomers
US20040260023A1 (en) * 2003-06-17 2004-12-23 Park Edward Hosung Dynamic vulcanization of polyurethane elastomeric material in the presence of thermoplastics
US6872325B2 (en) * 2002-09-09 2005-03-29 General Electric Company Polymeric resin bonded magnets
US20050155690A1 (en) * 2004-01-16 2005-07-21 Park Edward H. Bonding of dynamic vulcanizates of fluorocarbon elastomers
US20050165168A1 (en) * 2004-01-26 2005-07-28 Park Edward H. Dynamic vulcanization of elastomers with in-situ polymerization
US20050167928A1 (en) * 2004-02-04 2005-08-04 Park Edward H. Dynamic seal using vulcanization of fluorocarbon elastomers
US20050171282A1 (en) * 2004-02-04 2005-08-04 Park Edward H. Peroxide cured fluorocarbon elastomer compositions
US6939477B2 (en) * 1997-06-06 2005-09-06 Ashland, Inc. Temperature-controlled induction heating of polymeric materials
US20050222337A1 (en) * 2004-03-30 2005-10-06 Park Edward H Elastomeric compositions containing fluoropolymer blends
US20050275565A1 (en) * 2003-01-23 2005-12-15 Daniel Nachtigal Magnetizable polymeric compositions
US20050281973A1 (en) * 2004-06-21 2005-12-22 Park Edward H Pre-molding heat treatment of dynamic vulcanizates of fluorocarbon elastomers
US20050288434A1 (en) * 2002-03-27 2005-12-29 Motoyuki Sugiura Olefinic thermoplastic elastomer and moldings thereof
US20060004126A1 (en) * 2004-06-30 2006-01-05 Park Edward H Thermoplastic vulcanizate with functional fillers
US7029750B2 (en) * 2003-07-14 2006-04-18 Mitsubishi Rayon Co., Ltd. Thermoplastic resin composition and production method thereof
US20060142492A1 (en) * 2004-12-28 2006-06-29 Freudenberg-Nok General Partnership Dynamic vulcanization of non-nitrile rubbers in fluoroplastic polymers
US20060142467A1 (en) * 2004-12-27 2006-06-29 Freudenberg-Nok General Partnership Fluorocarbon elastomer compositions containing wear reducing additives
US20060142491A1 (en) * 2004-12-27 2006-06-29 Freudenberg-Nok General Partnership Thermoplastic vulcanizate with high temperature processing aid
US20060148954A1 (en) * 2005-01-05 2006-07-06 Freudenberg-Nok General Partnership Dynamic vulcanization with fluorocarbon processing aids
US7098270B2 (en) * 2002-09-10 2006-08-29 Freudenberg-Nok General Partnership Fluoroelastomer composition
US20060290070A1 (en) * 2005-06-27 2006-12-28 Freudenberg-Nok General Partnership Reinforced elastomeric seal
US20070004862A1 (en) * 2005-06-30 2007-01-04 Freudenberg-Nok General Partnership Base resistant FKM-TPV elastomers
US20070004865A1 (en) * 2005-06-29 2007-01-04 Freudenberg-Nok General Partnership Dynamic vulcanization of fluorocarbon elastomers containing peroxide cure sites
US20080149881A1 (en) * 2006-12-20 2008-06-26 Freudenberg-Nok General Partnership Robust magnetizable elastomeric thermoplastic blends
US20080157439A1 (en) * 2006-12-27 2008-07-03 Freudenberg-Nok General Partnership Methods for preparing articles from processable and dimensionally stable elastomer compositions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0168020B1 (en) 1984-07-09 1989-10-18 E.I. Du Pont De Nemours And Company Fluorinated thermoplastic elastomer compositions

Patent Citations (94)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3037954A (en) * 1958-12-15 1962-06-05 Exxon Research Engineering Co Process for preparing a vulcanized blend of crystalline polypropylene and chlorinated butyl rubber
US3538028A (en) * 1963-10-03 1970-11-03 Bendix Corp Vulcanizater of compositions comprising a fluorine-containing copolymer and silicone gum
US3580889A (en) * 1967-08-17 1971-05-25 Du Pont Vulcanization accelerators of polycyclic ethers for fluorinated polymers
US3787341A (en) * 1972-06-12 1974-01-22 Technical Processing Inc Novel processing aids for natural and synthetic rubber compounds
US3884877A (en) * 1973-10-16 1975-05-20 Minnesota Mining & Mfg Fluoroelastomer compositions with triorganophosphorus oxide
US4287320A (en) * 1974-08-01 1981-09-01 Minnesota Mining And Manufacturing Company Composition of fluoroelastomer and diorganosulfuroxide
US4035565A (en) * 1975-03-27 1977-07-12 E. I. Du Pont De Nemours And Company Fluoropolymer containing a small amount of bromine-containing olefin units
US4094949A (en) * 1975-06-09 1978-06-13 Shin-Etsu Chemical Co. Ltd. Method for preparing shaped articles of a fluorinated elastomer
US4311628A (en) * 1977-11-09 1982-01-19 Monsanto Company Thermoplastic elastomeric blends of olefin rubber and polyolefin resin
US4450263A (en) * 1979-08-30 1984-05-22 Minnesota Mining And Manufacturing Company Fluoropolymer gum of vinylidene fluoride, hexafluoropropene, and bromodifluoroethylene
US4328140A (en) * 1980-10-03 1982-05-04 Raybestos-Manhattan, Inc. Fluoroelastomer processing aid
US4451542A (en) * 1980-12-08 1984-05-29 Hitachi Maxell, Ltd. Cell with gasket comprising glass beads
US4419499A (en) * 1982-03-25 1983-12-06 Monsanto Company Compositions of urethane rubber and nylon
US4530881A (en) * 1983-02-24 1985-07-23 Raymark Industries, Inc. Fluoroelastomer-based friction material having improved frictional properties
US4656228A (en) * 1983-09-17 1987-04-07 Bayer Aktiengesellschaft Polyamides having high notched impact strength and high fluidity in the molten state
US4624978A (en) * 1983-11-14 1986-11-25 Rogers Corporation High temperature polyimide processing aid
US4696976A (en) * 1984-12-07 1987-09-29 The Dow Chemical Company Vinyl urethane composite polymer containing dispersed soft copolymer particles
US4696989A (en) * 1985-04-10 1987-09-29 Daikin Industries, Ltd. Fluorine-containing elastomeric copolymer
US4572516A (en) * 1985-06-12 1986-02-25 General Motors Corporation Low friction dynamic seal assembly with centrifugal deflection
US4787991A (en) * 1985-10-18 1988-11-29 Asahi Glass Company Ltd. Resin composition having lubricating properties
US4696998A (en) * 1986-07-28 1987-09-29 General Electric Company Cyclic heterocarbonates and methods for their preparation and use
US5095072A (en) * 1987-12-17 1992-03-10 Nippon Zeon Co., Ltd. Thermoplastic elastomer composition
US5391610A (en) * 1988-01-05 1995-02-21 Norton Company Moisture cured elastomeric interpenetrating network sealants
US4812357B1 (en) * 1988-09-23 1990-03-27 Grace W R & Co
US4812357A (en) * 1988-09-23 1989-03-14 W. R. Grace & Co.-Conn. Printing blanket
US5006594A (en) * 1988-12-30 1991-04-09 E. I. Du Pont De Nemours And Company Fluorinated thermoplastic elastomers containing polymeric additives and process for preparing such elastomers
US5219931A (en) * 1989-03-04 1993-06-15 Roehm Gmbh Chemische Fabrik Thermoplastically processable solvent-resistant polymer mixtures
US5206293A (en) * 1989-10-13 1993-04-27 Japan Synthetic Rubber Co., Ltd. Rubber composition and crosslinkable rubber composition
US5371143A (en) * 1989-11-16 1994-12-06 Minnesota Mining And Manufacturing Company Polymer blend composition of fluorinated elastomers, thermoplastic polymers and thermoplastics elastomers
US5384374A (en) * 1991-01-11 1995-01-24 Minnesota Mining And Manufacturing Company Curing fluorocarbon elastomers
US5108780A (en) * 1991-01-28 1992-04-28 Brigham Young University Enhanced thermoplastic adhesion to fibers by using plasma discharge
US5205293A (en) * 1991-10-30 1993-04-27 Koichi Sakurai Method of measuring surface blood flow
US5354811A (en) * 1991-11-20 1994-10-11 Asahi Glass Company Ltd. Fluorine-containing thermoplastic elastomer composition and process for its production
US5723544A (en) * 1992-05-06 1998-03-03 Bayer Corporation Polyolefin ionomer as processing aid for thermoplastic polyurethane
US5331040A (en) * 1992-10-26 1994-07-19 E. I. Du Pont De Nemours And Company Adhesive composition with functional filler
US20030166780A1 (en) * 1992-12-10 2003-09-04 Tetsuo Shimizu Thermoplastic resin composition
US6054537A (en) * 1992-12-10 2000-04-25 Daikin Industries, Ltd. Thermoplastic resin composition
US5639810A (en) * 1993-04-15 1997-06-17 Cobe Laboratories, Inc. Internally lubricated elastomers for use in biomedical applications
US5397832A (en) * 1993-04-20 1995-03-14 Advanced Elastomer Systems, L.P. Thermoplastic elastomer having improved low temperature properties
US5747588A (en) * 1993-06-25 1998-05-05 Refac International, Ltd. Thermoplastic urethane elastometric alloys
US5585152A (en) * 1993-12-10 1996-12-17 Toyo Boseki Kabushiki Kaisha Composition of polyamide resin and polyurethane resin
US5459202A (en) * 1994-06-30 1995-10-17 E. I. Du Pont De Nemours And Company Elastomer seal
US5962589A (en) * 1994-12-09 1999-10-05 Daikin Industries, Ltd. Rubber compositions of low compression set
US6079465A (en) * 1995-01-23 2000-06-27 The Yokohama Rubber Co., Ltd. Polymer composition for tire and pneumatic tire using same
US5548028A (en) * 1995-02-24 1996-08-20 E. I. Du Pont De Nemours And Company Curable elastomeric blend with vulcanized fluoroelastomer
US5700866A (en) * 1995-08-22 1997-12-23 E. I. Du Pont De Nemours And Company Co-curable base resistant fluoroelastomer blend composition
US5910544A (en) * 1995-11-02 1999-06-08 The Yokohama Rubber Co., Ltd. Thermoplastic elastomer composition and process for production thereof and low permeability hose using the same
US6500374B1 (en) * 1996-07-23 2002-12-31 Seiko Epson Corporation Method of manufacturing bonded magnets of rare earth metal, and bonded magnet of rare earth metal
US6312639B1 (en) * 1996-10-08 2001-11-06 Cylatec, Inc. Processing aid for thermoplastic resin compositions
US5792348A (en) * 1996-10-08 1998-08-11 Filtration Products Ltd. Steel reinforced filter press plates
US6048939A (en) * 1997-01-09 2000-04-11 Dupont Dow Elastomers, L.L.C. Process aid for melt processible polymers
US6162385A (en) * 1997-05-02 2000-12-19 Huels Aktiengesellschaft Composite comprising a polyamide-based molding composition and vulcanized fluoroelastomers
US6939477B2 (en) * 1997-06-06 2005-09-06 Ashland, Inc. Temperature-controlled induction heating of polymeric materials
US6407174B1 (en) * 1997-07-04 2002-06-18 Advanced Elastomer Systems, L.P. Propylene/ethylene/α-olefin terpolymer thermoplastic elastomer vulcanizates
US6114441A (en) * 1997-07-25 2000-09-05 E. I. Du Pont De Nemours And Company Blends of grafted fluoropolymer and polyester
US6066697A (en) * 1998-08-25 2000-05-23 The University Of Akron Thermoplastic compositions containing elastomers and fluorine containing thermoplastics
US6147158A (en) * 1999-07-06 2000-11-14 Freudenberg-Nok General Parnership Compatibilized blends of polyketones and polyolefins
US20030138655A1 (en) * 1999-11-29 2003-07-24 Jiro Watanabe Wiper blade
US6624251B1 (en) * 1999-12-01 2003-09-23 Freudenberg-Nok General Partnership Highly chemically resistant thermoplastic vulcanizates based on fluorocarbon polymers and seal-gasket products made with same
US6410630B1 (en) * 1999-12-29 2002-06-25 Pelseal Technologies, Llc High solids fluoroelastomer compositions
US6656831B1 (en) * 2000-01-26 2003-12-02 Applied Materials, Inc. Plasma-enhanced chemical vapor deposition of a metal nitride layer
US20020122928A1 (en) * 2000-03-24 2002-09-05 Chemque, Incorporation Co-dispensed compositions for gaskets and other objects
US6663966B2 (en) * 2000-03-30 2003-12-16 General Electric Company Use of dendrimers as a processing aid and surface modifiers for thermoplastic resins
US6437030B1 (en) * 2000-05-24 2002-08-20 Advanced Elastomer Systems, L.P. Thermoplastic vulcanizates and process for making the same
US20030026995A1 (en) * 2000-06-27 2003-02-06 Dyneon Llc Novel fluoropolymers with improved characteristics
US6310141B1 (en) * 2000-06-27 2001-10-30 Dyneon Llc Fluoropolymer-containing compositions
US6429249B1 (en) * 2000-06-30 2002-08-06 Nexpress Solutions Llc Fluorocarbon thermoplastic random copolymer composition
US6737479B2 (en) * 2000-11-17 2004-05-18 Immix Technologies, Llc Dynamically cured fluoroelastomer blends
US20020198320A1 (en) * 2001-05-22 2002-12-26 Chmielewski Craig A. Low temperature, highly chemically resistant thermoplastic vulcanizates based on perfluoroether elastomers
US6806306B2 (en) * 2001-05-22 2004-10-19 Freduenberg-Nok General Partnership Low temperature, highly chemically resistant thermoplastic vulcanizates based on perfluroether elastomers
US6774171B2 (en) * 2002-01-25 2004-08-10 L&L Products, Inc. Magnetic composition
US20050288434A1 (en) * 2002-03-27 2005-12-29 Motoyuki Sugiura Olefinic thermoplastic elastomer and moldings thereof
US6872325B2 (en) * 2002-09-09 2005-03-29 General Electric Company Polymeric resin bonded magnets
US7098270B2 (en) * 2002-09-10 2006-08-29 Freudenberg-Nok General Partnership Fluoroelastomer composition
US20050275565A1 (en) * 2003-01-23 2005-12-15 Daniel Nachtigal Magnetizable polymeric compositions
US20040183702A1 (en) * 2003-01-23 2004-09-23 Daniel Nachtigal Magnetizable thermoplastic elastomers
US20040260023A1 (en) * 2003-06-17 2004-12-23 Park Edward Hosung Dynamic vulcanization of polyurethane elastomeric material in the presence of thermoplastics
US7029750B2 (en) * 2003-07-14 2006-04-18 Mitsubishi Rayon Co., Ltd. Thermoplastic resin composition and production method thereof
US20050155690A1 (en) * 2004-01-16 2005-07-21 Park Edward H. Bonding of dynamic vulcanizates of fluorocarbon elastomers
US20050165168A1 (en) * 2004-01-26 2005-07-28 Park Edward H. Dynamic vulcanization of elastomers with in-situ polymerization
US20050171282A1 (en) * 2004-02-04 2005-08-04 Park Edward H. Peroxide cured fluorocarbon elastomer compositions
US20050167928A1 (en) * 2004-02-04 2005-08-04 Park Edward H. Dynamic seal using vulcanization of fluorocarbon elastomers
US20050222337A1 (en) * 2004-03-30 2005-10-06 Park Edward H Elastomeric compositions containing fluoropolymer blends
US20050281973A1 (en) * 2004-06-21 2005-12-22 Park Edward H Pre-molding heat treatment of dynamic vulcanizates of fluorocarbon elastomers
US20060004126A1 (en) * 2004-06-30 2006-01-05 Park Edward H Thermoplastic vulcanizate with functional fillers
US20060142467A1 (en) * 2004-12-27 2006-06-29 Freudenberg-Nok General Partnership Fluorocarbon elastomer compositions containing wear reducing additives
US20060142491A1 (en) * 2004-12-27 2006-06-29 Freudenberg-Nok General Partnership Thermoplastic vulcanizate with high temperature processing aid
US20060142492A1 (en) * 2004-12-28 2006-06-29 Freudenberg-Nok General Partnership Dynamic vulcanization of non-nitrile rubbers in fluoroplastic polymers
US20060148954A1 (en) * 2005-01-05 2006-07-06 Freudenberg-Nok General Partnership Dynamic vulcanization with fluorocarbon processing aids
US20060290070A1 (en) * 2005-06-27 2006-12-28 Freudenberg-Nok General Partnership Reinforced elastomeric seal
US20070004865A1 (en) * 2005-06-29 2007-01-04 Freudenberg-Nok General Partnership Dynamic vulcanization of fluorocarbon elastomers containing peroxide cure sites
US20070004862A1 (en) * 2005-06-30 2007-01-04 Freudenberg-Nok General Partnership Base resistant FKM-TPV elastomers
US20080149881A1 (en) * 2006-12-20 2008-06-26 Freudenberg-Nok General Partnership Robust magnetizable elastomeric thermoplastic blends
US20080157439A1 (en) * 2006-12-27 2008-07-03 Freudenberg-Nok General Partnership Methods for preparing articles from processable and dimensionally stable elastomer compositions

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050165168A1 (en) * 2004-01-26 2005-07-28 Park Edward H. Dynamic vulcanization of elastomers with in-situ polymerization
US7351769B2 (en) 2004-01-26 2008-04-01 Freudenberg-Nok General Partnership Dynamic vulcanization of elastomers with in-situ polymerization
US20070210530A1 (en) * 2004-02-04 2007-09-13 Freudenberg-Nok General Partnership Dynamic seal using vulcanization of fluorocarbon elastomers
US20050167928A1 (en) * 2004-02-04 2005-08-04 Park Edward H. Dynamic seal using vulcanization of fluorocarbon elastomers
US8485533B2 (en) * 2004-02-04 2013-07-16 Freudenberg-Nok General Partnership Dynamic seal using vulcanization of fluorocarbon elastomers
US7413697B2 (en) 2004-06-21 2008-08-19 Freudenberg-Nok General Partnership Pre-molding heat treatment of dynamic vulcanizates of fluorocarbon elastomers
US20050281973A1 (en) * 2004-06-21 2005-12-22 Park Edward H Pre-molding heat treatment of dynamic vulcanizates of fluorocarbon elastomers
US20060004126A1 (en) * 2004-06-30 2006-01-05 Park Edward H Thermoplastic vulcanizate with functional fillers
US7449523B2 (en) 2004-12-27 2008-11-11 Freudenberg-Nok General Partnership Fluorocarbon elastomer compositions containing wear reducing additives
US20060141324A1 (en) * 2004-12-27 2006-06-29 Kelley Dana A Manifold gasket accommodating differential movement of fuel cell stack
US20060142491A1 (en) * 2004-12-27 2006-06-29 Freudenberg-Nok General Partnership Thermoplastic vulcanizate with high temperature processing aid
US7449524B2 (en) 2005-01-05 2008-11-11 Freudenberg-Nok General Partnership Dynamic vulcanization with fluorocarbon processing aids
US7658387B2 (en) 2005-06-27 2010-02-09 Freudenberg-Nok General Partnership Reinforced elastomeric seal
US20070004865A1 (en) * 2005-06-29 2007-01-04 Freudenberg-Nok General Partnership Dynamic vulcanization of fluorocarbon elastomers containing peroxide cure sites
US7662886B2 (en) 2005-06-29 2010-02-16 Freudenberg-Nok General Partnership Dynamic vulcanization of fluorocarbon elastomers containing peroxide cure sites
US20070004862A1 (en) * 2005-06-30 2007-01-04 Freudenberg-Nok General Partnership Base resistant FKM-TPV elastomers
US7718736B2 (en) 2005-06-30 2010-05-18 Freudenberg-Nok General Partnership Base resistant FKM-TPV elastomers
US7863365B2 (en) 2006-12-20 2011-01-04 Freudenberg-Nok General Partnership Robust magnetizable elastomeric thermoplastic blends
US7608216B2 (en) 2006-12-27 2009-10-27 Freudenberg-Nok General Partnership Methods for preparing articles from processable and dimensionally stable elastomer compositions
US20080157439A1 (en) * 2006-12-27 2008-07-03 Freudenberg-Nok General Partnership Methods for preparing articles from processable and dimensionally stable elastomer compositions

Also Published As

Publication number Publication date Type
US7022769B2 (en) 2006-04-04 grant
US20050014900A1 (en) 2005-01-20 application

Similar Documents

Publication Publication Date Title
US6242548B1 (en) Fluoroplastic polymers with improved characteristics
US6489420B1 (en) Fluoropolymers with improved characteristics
US5384374A (en) Curing fluorocarbon elastomers
US6048939A (en) Process aid for melt processible polymers
US5354811A (en) Fluorine-containing thermoplastic elastomer composition and process for its production
US6624251B1 (en) Highly chemically resistant thermoplastic vulcanizates based on fluorocarbon polymers and seal-gasket products made with same
US6294604B1 (en) Polymer processing additive having improved stability
US20020198320A1 (en) Low temperature, highly chemically resistant thermoplastic vulcanizates based on perfluoroether elastomers
US20050167928A1 (en) Dynamic seal using vulcanization of fluorocarbon elastomers
EP0168020A2 (en) Fluorinated thermoplastic elastomer compositions
US5371143A (en) Polymer blend composition of fluorinated elastomers, thermoplastic polymers and thermoplastics elastomers
US6642310B2 (en) Process aid for melt processable polymers
US6734252B1 (en) Melt processable thermoplastic polymer composition employing a polymer processing additive containing a fluorothermoplastic copolymer
US6465577B2 (en) Agent for minimizing size of spherulite of crystalline fluorine-containing resin and crystalline resin and crystalline fluorine-containing resin composition comprising said agent
US5869574A (en) Thermoplastic resin composition
US20040260023A1 (en) Dynamic vulcanization of polyurethane elastomeric material in the presence of thermoplastics
US6613846B2 (en) Curable fluoroelastomer compositions comprising hydro siloxanes or hydro silazanes
JP2002293831A (en) Fluorine-containing olefin polymer particle
JPH09268245A (en) Fluororesin composition, its production and molded product therefrom
US20060142492A1 (en) Dynamic vulcanization of non-nitrile rubbers in fluoroplastic polymers
US6380313B1 (en) Polymer processing additive containing a perfluorovinylether-modified flouropolymer and a melt processable thermoplastic polymer composition employing the same
US20050171282A1 (en) Peroxide cured fluorocarbon elastomer compositions
US6538069B2 (en) Polymer blends of PVDF thermoplastics blended with FKM fluoroelastomers
US20060135716A1 (en) Fluoroelastomers having low glass transition temperature
JP2004250520A (en) Fluororubber composition