EP0103487B1 - Electrical insulation - Google Patents

Electrical insulation Download PDF

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Publication number
EP0103487B1
EP0103487B1 EP83305380A EP83305380A EP0103487B1 EP 0103487 B1 EP0103487 B1 EP 0103487B1 EP 83305380 A EP83305380 A EP 83305380A EP 83305380 A EP83305380 A EP 83305380A EP 0103487 B1 EP0103487 B1 EP 0103487B1
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Prior art keywords
radical
polymer
aromatic
carbon atoms
article according
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German (de)
French (fr)
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EP0103487A2 (en
EP0103487A3 (en
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Stephen Leroy Tondre
Hans Edmund Lunk
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Raychem Corp
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Raychem Corp
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/44Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
    • H01B3/441Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from alkenes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/17Protection against damage caused by external factors, e.g. sheaths or armouring
    • H01B7/29Protection against damage caused by extremes of temperature or by flame
    • H01B7/295Protection against damage caused by extremes of temperature or by flame using material resistant to flame

Definitions

  • This invention relates to insulation for electrical articles.
  • electrical insulation must meet a variety of electrical and physical requirements under normal service conditions. In addition, for many purposes the insulation must meet test requirements which are intended to ensure that if the insulation is exposed to very high temperatures, e.g. in a fire, it will not evolve excessive amounts of toxic products or smoke. These requirements are particularly severe for electrical cable which is to be used in aircraft and similar equipment.
  • the term "cable” is used herein to include a single electrically insulated elongate conductor often referred to in the art as "wire"), an article comprising a plurality of separate elongate conductors each of which is separately insulated, and an article comprising a plurality of elongate conductors which are physically joined together but electrically insulated from each other by insulating material, e.g. ribbon cable.
  • Fluorocarbon polymers especially ethylene/tetrafluoroethylene (ETFE) copolymers such as Tefzel, are used extensively for electrical insulation, in particular for aircraft wire. Particularly when crosslinked, such polymers can exhibit an excellent combination of physical and electrical properties under normal service conditions.
  • EFE ethylene/tetrafluoroethylene
  • Tefzel ethylene/tetrafluoroethylene copolymers
  • U.S. Patents Nos. 3,580,829, 3,738,923, 3,763,222, 3,840,619, 3,894,118, 3,911,192, 3,947,525, 3,970,770, 3,985,716, 3,995,091, 4,031,167, 4,155,823, 4,121,001, and 4,176,027 Other polymers which have been used for electrical insulation include other olefin polymers (both homopolymers and copolymers) and various high-melting aromatic polymers.
  • Examples of the use of such polymers include the wire and cable described in EP-A-56510 in which an ethylene tetrafluoroethylene or a tetrafluoroethylene coated polyimide primary insulation is provided with a solution coated polyimide topcoat followed by a layer of polyvinylidine fluoride.
  • Another form of cable is described in US ⁇ A ⁇ 3,217,084, in which a tape of polyethylene terephthalate or polycarbonate is wrapped under tension around a solid polyethylene or polypropylene insulating layer.
  • the olefin polymer forming the inner layer preferably has a tensile (Young's) modulus of at least 138 MPa (20,000 p.s.i.) especially at least 207 MPa (30,000 p.s.i.) and particularly at least 276 MPa (40,000 p.s.i.) in order to minimize wrinkling of the outer layer when the article, e.g. in the form of a wire, is bent.
  • a tensile (Young's) modulus of at least 138 MPa (20,000 p.s.i.) especially at least 207 MPa (30,000 p.s.i.) and particularly at least 276 MPa (40,000 p.s.i.) in order to minimize wrinkling of the outer layer when the article, e.g. in the form of a wire, is bent.
  • the insulation of the article to the invention provides a valuable combination of physical and electrical properties.
  • the outer layer provides excellent resistance to physical abuse.
  • the inner layer is more flexible than the outer layer and thus provides insulation which is more flexible, for a particular dielectric strength, than insulation which is composed only of the aromatic polymer.
  • the aromatic polymers often have poor resistance to stress-cracking which can seriously reduce their dielectric strength, the olefin polymers do not suffer from this disadvantage, and the inner jacket will therefore provide continuous insulation even in environments which cause stress-cracking of the outer jacket.
  • olefin polymer as used herein is defined as being a polymer of one or more unsubstituted and/or substituted olefins. Where the polymer includes substituted olefins as monomers or comonomers they are preferably polar monomers and especially fluorine-containing monomers, e.g. tetrafluoroethylene, or a carboxylic ester, in particular an alkyl acrylate, e.g. methyl or ethyl acrylate, or a vinyl ester, e.g. vinyl acetate.
  • the olefin is preferably a fluorocarbon polymer as explained below.
  • the inner layer is composed of a cross-linked fluorocarbon layer.
  • the combination of an inner layer of a cross-linked fluorocarbon polymer and an outer layer of an aromatic polymer results in a completely unexpected reduction in the smoke evolved under standard test conditions.
  • electrical wire which, when tested for smoke evolution by ASTM E 662-79 (flaming mode) has a D m value of less than 50, preferably less than 35, where D m is the maximum specific optical density.
  • fluorocarbon polymer is used herein to denote a polymer or mixture of polymers which contains more than 10%, preferably more than 25%, by weight of fluorine.
  • the fluorocarbon polymer may be a single fluorine-containing polymer, a mixture of two or more fluorine-containing polymers, or a mixture of one or more fluorine-containing polymers with one or more polymers which do not contain fluorine.
  • the fluorocarbon polymer comprises at least 50%, particularly at least 75% especially at least 85%, by weight of one or more thermoplastic crystalline polymers each containing at least 25% by weight of fluorine, a single such crystalline polymer being preferred.
  • Such a fluorocarbon polymer may contain, for example, a fluorine-containing elastomer and/or a polyolefin, preferably a crystalline polyolefin, in addition to the crystalline fluorine-containing polymer or polymers.
  • the fluorine-containing polymers are generally homo- or copolymers of one or more fluorine-containing olefinically unsaturated monomers, or copolymers of one or more such monomers with one or more olefins.
  • the fluorocarbon polymer usually has a melting point of at least 150°C, and will often have a melting point of at least 250°C, e.g.
  • the melting point being defined for crystalline polymers as the temperature above which no crystallinity exists in the polymer (or when a mixture of crystalline polymers is used, in the major crystalline component in the mixture).
  • the polymeric composition, prior to cross-linking has a viscosity of less than 10 4 Pa.s (10 5 poise) at a temperature not more than 60°C above its melting point.
  • a preferred fluorocarbon polymer is a copolymer of ethylene and tetrafluoroethylene and optionally one or more other comonomers (known as ETFE polymers), especially a copolymer comprising 35 to 60 mole percent of ethylene, 35 to 60 mole percent of tetrafluoroethylene and up to 10 mole percent of one or more other comonomers.
  • ETFE polymers comonomers
  • polymers which can be used include copolymers of ethylene and chlorotrifluoroethylene; polyvinylidene fluoride; copolymers of vinylidene fluoride with one or both of hexafluoropropylene and tetrafluoroethylene, or with hexafluoroisobutylene; and copolymers of tetrafluoroethylene and hexafluoropropylene.
  • Either or both of the inner and outer insulating layers can optionally contain suitable additives such as pigments, antioxidants, thermal stabilisers, acid acceptors and processing aids.
  • Such polymers include polyketones, polyether ketones, polyether ether ketones and polyether sulfones, polyether ketone/sulfone copolymers and polyether imides. Blends of different polymers can be used.
  • Preferred aromatic polymers are crystalline polymers with a melting point of at least 250°C, particularly at least 300°C.
  • the polymer comprises, and preferably consists essentially of, units of the general formula the units being the same or different, wherein Ar represents a divalent aromatic radical and Q represents ⁇ 0 ⁇ , ⁇ S ⁇ , ⁇ S0 2 ⁇ , ⁇ CO ⁇ , -NH-CO or -COO-, or Ar represents a polyvalent radical and Q represents each bond of the Q radical preferably being bonded directly to an aromatic carbon atom.
  • the aromatic polymer is a crystalline polyarylene ether comprising recurring units of the formula where E is the residue of a dihydric phenol and E' is the residue of an aromatic compound having an electron withdrawing group in at least one of the positions ortho and para to the valence bonds, the E and E' radicals being linked to the -0- radicals through aromatic carbon atoms.
  • E is a radical of the formula wherein R is a divalent radical; x is 0 or 1; Y is a radical selected from halogen atoms, alkyl radicals containing 1 to 4 carbon atoms and alkoxy radicals containing 1 to 4 carbon atoms; yisO, 1,2,3 or 4; Y' is a radical selected from halogen atoms, alkyl radicals containing 1 to 4 carbon atoms and alkoxy radicals containing 1 to 4 carbon atoms; z is 0, 1, 2, 3 or 4, and E' is a radical of the formula wherein R' is a sulfone, carbonyl, vinyl, sulfoxide, azo, saturated fluorocarbon, organic phosphine oxide or ethylidene radical.
  • polysulfones are those in which y and z are 0, x is 1, R' is a sulfone radical and R is a radical of the formula wherein each of R" and R"' is independently selected from the group consisting of hydrogen; alkyl radicals containing 1 to 4 carbon atoms; halogen-substituted alkyl radical containing 1 to 4 carbon atoms; aryl, alkaryl and aralkyl radicals containing 6 to 10 carbon atoms; and halogen-substituted aryl, alkaryl and aralkyl radicals containing 6 to 10 carbon atoms.
  • the polymer is a polyether imide or polysulfone imide which comprises recurring units of the formula where Q is -0- or -S0 2 , Z is a trivalent aromatic radical, R is a divalent aromatic radical and R' is a divalent organic radical.
  • Preferred aromatic polymers consist essentially of repeating units having one of the following formulae wherein each of x, m and n is 0 or 1, with n being 0 when x is 1, p is an integer from 1 to 4, with m being 1 and x being 0 when p is greater than 1, e.g.,
  • the insulated articles of the present invention can be produced by conventional techniques; the inner layer usually contacts the conductor, and the inner and outer layers generally constitute the total insulation of the article; however, other insulating layers can be present.
  • the olefin polymer is preferably cross-linked by radiation, and cross-linking can be effected before or after the aromatic polymer (which is generally not cross-linked by radiation) is applied.
  • the inner layer will usually be of annular cross- section of thickness for example 76.2 to 381 micrometres (3 to 15 mils), preferably 101.6 to 177.8 micrometres (4 to 7 mils) and the outer insulating layer will be a melt extruded layer which surrounds and contacts the inner insulating layer and preferably has a wall thickness of from 101.6 to 177.8 micrometres.
  • the cable can comprise a plurality of conductors, each of which has an inner insulating layer around it, with the conductors being joined together and further insulated by the outer insulating layer.
  • the invention is illustrated by the following Examples, Examples 1, 2, 3 and 8 of which are comparative.
  • a 20 AWG stranded (19/32) conductor was extrusion-coated with an inner insulating layer having the composition and thickness shown in the Table. Except in Examples 1 and 2, the inner insulating layer was then extrusion-coated with an outer insulating layer having the composition and thickness shown in the Table.
  • the coated conductor was irradiated to a dosage of about 10 Megarads to cross-link the inner coating; in these Examples, the inner coating also contained, when it was irradiated, a suitable amount of a radiation cross-linking agent.
  • the outer coating was substantially unaffected by this irradiation.
  • the coated conductor was annealed at 180°C for 1 hour.
  • PEEK, Ultem and PES are substantially linear aromatic polymers.

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  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Organic Insulating Materials (AREA)
  • Insulated Conductors (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Abstract

Electrical insulation comprises (1) an inner layer of a cross-linked polymer, e.g. an ethylene/tetrafluoroethylene copolymer, an ethylene/chlorotrifluoroethylene polymer or a vinylidene fluoride polymer, and (2) an outer layer of an aromatic polymer having a glass transition temperature of at least 100 DEG C, e.g. a polyether ether ketone, a polyether ketone or a polyether sulfone. Such insulation combines excellent properties under normal service conditions with low smoke evolution on burning, and is therefore particularly useful for aircraft wire and cable.

Description

  • This invention relates to insulation for electrical articles.
  • Electrical insulation must meet a variety of electrical and physical requirements under normal service conditions. In addition, for many purposes the insulation must meet test requirements which are intended to ensure that if the insulation is exposed to very high temperatures, e.g. in a fire, it will not evolve excessive amounts of toxic products or smoke. These requirements are particularly severe for electrical cable which is to be used in aircraft and similar equipment. The term "cable" is used herein to include a single electrically insulated elongate conductor often referred to in the art as "wire"), an article comprising a plurality of separate elongate conductors each of which is separately insulated, and an article comprising a plurality of elongate conductors which are physically joined together but electrically insulated from each other by insulating material, e.g. ribbon cable.
  • Fluorocarbon polymers, especially ethylene/tetrafluoroethylene (ETFE) copolymers such as Tefzel, are used extensively for electrical insulation, in particular for aircraft wire. Particularly when crosslinked, such polymers can exhibit an excellent combination of physical and electrical properties under normal service conditions. In this connection, reference may be made to U.S. Patents Nos. 3,580,829, 3,738,923, 3,763,222, 3,840,619, 3,894,118, 3,911,192, 3,947,525, 3,970,770, 3,985,716, 3,995,091, 4,031,167, 4,155,823, 4,121,001, and 4,176,027. Other polymers which have been used for electrical insulation include other olefin polymers (both homopolymers and copolymers) and various high-melting aromatic polymers.
  • Examples of the use of such polymers include the wire and cable described in EP-A-56510 in which an ethylene tetrafluoroethylene or a tetrafluoroethylene coated polyimide primary insulation is provided with a solution coated polyimide topcoat followed by a layer of polyvinylidine fluoride. Another form of cable is described in US―A―3,217,084, in which a tape of polyethylene terephthalate or polycarbonate is wrapped under tension around a solid polyethylene or polypropylene insulating layer.
  • We have discovered that insulation which has improved properties and which can be efficiently manufactured comprises an inner layer of a cross-linked melt-extruded olefin polymer covered by a layer of a melt extruded aromatic polymer having a glass transition temperature of at least 100°C. Accordingly, the present invention provides an insulated electrical article, especially an insulated electrical wire or cable comprising:
    • (a) a conductor;
    • (b) a melt-shaped, preferably melt-extruded, inner insulating layer which preferably contacts the conductor and comprises a first organic polymer component which is a cross-linked olefin polymer, particularly an ETFE copolymer, and
    • (c) a melt-shaped, preferably melt-extruded, outer insulating layer which contacts the inner insulating layer and which comprises a second organic polymer component which is a substantially linear aromatic polymer having a glass transition temperature of at least 100°C, preferably at least 130°C.
  • The olefin polymer forming the inner layer preferably has a tensile (Young's) modulus of at least 138 MPa (20,000 p.s.i.) especially at least 207 MPa (30,000 p.s.i.) and particularly at least 276 MPa (40,000 p.s.i.) in order to minimize wrinkling of the outer layer when the article, e.g. in the form of a wire, is bent.
  • The insulation of the article to the invention provides a valuable combination of physical and electrical properties. The outer layer provides excellent resistance to physical abuse. The inner layer is more flexible than the outer layer and thus provides insulation which is more flexible, for a particular dielectric strength, than insulation which is composed only of the aromatic polymer. Furthermore, the aromatic polymers often have poor resistance to stress-cracking which can seriously reduce their dielectric strength, the olefin polymers do not suffer from this disadvantage, and the inner jacket will therefore provide continuous insulation even in environments which cause stress-cracking of the outer jacket.
  • The term "olefin polymer" as used herein is defined as being a polymer of one or more unsubstituted and/or substituted olefins. Where the polymer includes substituted olefins as monomers or comonomers they are preferably polar monomers and especially fluorine-containing monomers, e.g. tetrafluoroethylene, or a carboxylic ester, in particular an alkyl acrylate, e.g. methyl or ethyl acrylate, or a vinyl ester, e.g. vinyl acetate. The olefin is preferably a fluorocarbon polymer as explained below.
  • Particularly useful properties are obtained when the inner layer is composed of a cross-linked fluorocarbon layer. We have discovered that the combination of an inner layer of a cross-linked fluorocarbon polymer and an outer layer of an aromatic polymer results in a completely unexpected reduction in the smoke evolved under standard test conditions. Thus it is possible, through use of the present invention, to manufacture electrical wire which, when tested for smoke evolution by ASTM E 662-79 (flaming mode) has a Dm value of less than 50, preferably less than 35, where Dm is the maximum specific optical density.
  • The term "fluorocarbon polymer" is used herein to denote a polymer or mixture of polymers which contains more than 10%, preferably more than 25%, by weight of fluorine. Thus the fluorocarbon polymer may be a single fluorine-containing polymer, a mixture of two or more fluorine-containing polymers, or a mixture of one or more fluorine-containing polymers with one or more polymers which do not contain fluorine. In one preferred class, the fluorocarbon polymer comprises at least 50%, particularly at least 75% especially at least 85%, by weight of one or more thermoplastic crystalline polymers each containing at least 25% by weight of fluorine, a single such crystalline polymer being preferred. Such a fluorocarbon polymer may contain, for example, a fluorine-containing elastomer and/or a polyolefin, preferably a crystalline polyolefin, in addition to the crystalline fluorine-containing polymer or polymers. The fluorine-containing polymers are generally homo- or copolymers of one or more fluorine-containing olefinically unsaturated monomers, or copolymers of one or more such monomers with one or more olefins. The fluorocarbon polymer usually has a melting point of at least 150°C, and will often have a melting point of at least 250°C, e.g. up to 350°C, the melting point being defined for crystalline polymers as the temperature above which no crystallinity exists in the polymer (or when a mixture of crystalline polymers is used, in the major crystalline component in the mixture). Preferably the polymeric composition, prior to cross-linking, has a viscosity of less than 104 Pa.s (105 poise) at a temperature not more than 60°C above its melting point. A preferred fluorocarbon polymer is a copolymer of ethylene and tetrafluoroethylene and optionally one or more other comonomers (known as ETFE polymers), especially a copolymer comprising 35 to 60 mole percent of ethylene, 35 to 60 mole percent of tetrafluoroethylene and up to 10 mole percent of one or more other comonomers. Other specific polymers which can be used include copolymers of ethylene and chlorotrifluoroethylene; polyvinylidene fluoride; copolymers of vinylidene fluoride with one or both of hexafluoropropylene and tetrafluoroethylene, or with hexafluoroisobutylene; and copolymers of tetrafluoroethylene and hexafluoropropylene.
  • Either or both of the inner and outer insulating layers can optionally contain suitable additives such as pigments, antioxidants, thermal stabilisers, acid acceptors and processing aids.
  • The aromatic polymers which are used in this invention are well known to those skilled in the art, and reference may be made for example to U.S. Patents Nos. 3,025,605, 3,354,129, 3,441,538, 3,442,538, 3,446,654, 3,658,938, 3,838,097, 3,847,867, 3,953,400, 3,956,240, 4,107,147, 4,108,837, 4,111,908, 4,175,175, 4,293,670, 4,320,224, and 3,446,654 and British Patents Nos. 971,227, 1,369,210 and 1,599,106. Such polymers include polyketones, polyether ketones, polyether ether ketones and polyether sulfones, polyether ketone/sulfone copolymers and polyether imides. Blends of different polymers can be used. Preferred aromatic polymers are crystalline polymers with a melting point of at least 250°C, particularly at least 300°C. In one class of such polymers the polymer comprises, and preferably consists essentially of, units of the general formula
    Figure imgb0001
    the units being the same or different,
    wherein Ar represents a divalent aromatic radical and Q represents ―0―, ―S―, ―S02―, ―CO―, -NH-CO or -COO-, or Ar represents a polyvalent radical and Q represents
    Figure imgb0002
    each bond of the Q radical preferably being bonded directly to an aromatic carbon atom.
  • In another class of aromatic polymers the aromatic polymer is a crystalline polyarylene ether comprising recurring units of the formula
    Figure imgb0003
    where E is the residue of a dihydric phenol and E' is the residue of an aromatic compound having an electron withdrawing group in at least one of the positions ortho and para to the valence bonds, the E and E' radicals being linked to the -0- radicals through aromatic carbon atoms. In one preferred sub-class, E is a radical of the formula
    Figure imgb0004
    wherein R is a divalent radical; x is 0 or 1; Y is a radical selected from halogen atoms, alkyl radicals containing 1 to 4 carbon atoms and alkoxy radicals containing 1 to 4 carbon atoms; yisO, 1,2,3 or 4; Y' is a radical selected from halogen atoms, alkyl radicals containing 1 to 4 carbon atoms and alkoxy radicals containing 1 to 4 carbon atoms; z is 0, 1, 2, 3 or 4, and E' is a radical of the formula
    Figure imgb0005
    wherein R' is a sulfone, carbonyl, vinyl, sulfoxide, azo, saturated fluorocarbon, organic phosphine oxide or ethylidene radical. In this class preferred polysulfones are those in which y and z are 0, x is 1, R' is a sulfone radical and R is a radical of the formula
    Figure imgb0006
    wherein each of R" and R"' is independently selected from the group consisting of hydrogen; alkyl radicals containing 1 to 4 carbon atoms; halogen-substituted alkyl radical containing 1 to 4 carbon atoms; aryl, alkaryl and aralkyl radicals containing 6 to 10 carbon atoms; and halogen-substituted aryl, alkaryl and aralkyl radicals containing 6 to 10 carbon atoms.
  • In another class of aromatic polymers, the polymer is a polyether imide or polysulfone imide which comprises recurring units of the formula
    Figure imgb0007
    where Q is -0- or -S02, Z is a trivalent aromatic radical, R is a divalent aromatic radical and R' is a divalent organic radical.
  • Preferred aromatic polymers consist essentially of repeating units having one of the following formulae
    Figure imgb0008
    Figure imgb0009
    Figure imgb0010
    Figure imgb0011
    wherein each of x, m and n is 0 or 1, with n being 0 when x is 1, p is an integer from 1 to 4, with m being 1 and x being 0 when p is greater than 1, e.g.,
    Figure imgb0012
    Figure imgb0013
    Figure imgb0014
    Figure imgb0015
  • The insulated articles of the present invention can be produced by conventional techniques; the inner layer usually contacts the conductor, and the inner and outer layers generally constitute the total insulation of the article; however, other insulating layers can be present. The olefin polymer is preferably cross-linked by radiation, and cross-linking can be effected before or after the aromatic polymer (which is generally not cross-linked by radiation) is applied. For electrical cable, the inner layer will usually be of annular cross- section of thickness for example 76.2 to 381 micrometres (3 to 15 mils), preferably 101.6 to 177.8 micrometres (4 to 7 mils) and the outer insulating layer will be a melt extruded layer which surrounds and contacts the inner insulating layer and preferably has a wall thickness of from 101.6 to 177.8 micrometres. Alternatively, the cable can comprise a plurality of conductors, each of which has an inner insulating layer around it, with the conductors being joined together and further insulated by the outer insulating layer.
  • The invention is illustrated by the following Examples, Examples 1, 2, 3 and 8 of which are comparative.
  • Examples
  • In each of the Examples, a 20 AWG stranded (19/32) conductor was extrusion-coated with an inner insulating layer having the composition and thickness shown in the Table. Except in Examples 1 and 2, the inner insulating layer was then extrusion-coated with an outer insulating layer having the composition and thickness shown in the Table. In some of the Examples, as designated in the Table, the coated conductor was irradiated to a dosage of about 10 Megarads to cross-link the inner coating; in these Examples, the inner coating also contained, when it was irradiated, a suitable amount of a radiation cross-linking agent. The outer coating was substantially unaffected by this irradiation. The coated conductor was annealed at 180°C for 1 hour. Samples of the resulting cable were tested in accordance with the procedure of ASTM E662-79 (flaming mode), and the Table shows the values obtained for the minimum transmittance, the transmittance after 10 minutes, the time taken to reach the point of minimum transmittance, and the maximum optical density (Dm).
  • The various polymers used in the Examples are further identified below
    • Tefze/280 is a copolymer of ethylene and tetrafluoroethylene available from du Pont.
    • Halar 300 is a copolymer of ethylene and chlorotrifluoroethylene avaiable from Allied Chemical.
    • Kynar 450 is polyvinylidene fluoride available from Pennwalt.
    • PEEK is a polyether ether ketone available from ICI.
    • U/tem is a polyetherimide available from General Electric.
    • Victrex 200P is polyethersulphone available from ICI.
  • "Tefzel", "Halar", "Kynar", "Ultem" and "Victrex" are Registered Trade Marks.
  • PEEK, Ultem and PES are substantially linear aromatic polymers.
    Figure imgb0016

Claims (10)

1. An insulated electrical article, comprising
(a) a conductor;
(b) a melt-shaped inner insulating layer comprising a first organic polymer component which is a cross- linked olefin polymer, and
(c) a melt-shaped outer insulating layer which contacts the inner insulating layer and which comprises a second organic polymer component which is a substantially linear aromatic polymer having a glass transition temperature of at least 100°C.
2. An article according to claim 1, wherein the olefin polymer comprises at least 75% by weight of a thermoplastic crystalline polymer containing at least 25% by weight of fluorine.
3. An article according to claim 1 or claim 2, wherein the olefin polymer consists essentially of an ethylene/tetrafluoroethylene copolymer, an ethylene/chlorotrifluoroethylene copolymer or a vinylidene fluoride polymer.
4. An article according to any one of claims 1 to 3, wherein the aromatic polymer has a glass transition temperature of at least 130°C and/or is a crystalline polymer having a melting point of at least 250°C.
5. An article according to any one of claims 1 to 4, wherein the aromatic polymer comprises units of the general formula
Figure imgb0017
the units being the same or different, wherein Ar represents a divalent aromatic radical and Q represents a radical of the formula
Figure imgb0018
or Ar represents a polyvalent aromatic radical and Q represents
Figure imgb0019
each bond of the Q radical preferably being bonded directly to an aromatic carbon atom.
6. An article according to any one of claims 1 to 5, wherein the aromatic polymer is a crystalline polyarylene ether comprising recurring units of the general formula
Figure imgb0020
wherein E is the residue of a dihydric phenol and E' is the residue of an aromatic compound having an electron-withdrawing group in at least one of the positions ortho and para to the valence bonds; the E and E' radicals being linked to the -0- radicals through aromatic carbon atoms.
7. An article according to claim 6, wherein E is a radical of the formula
Figure imgb0021
wherein R represents a divalent radical; x is 0 or 1; Y is a halogen atom, an alkyl radical containing 1 to 4 carbon atoms or an alkoxy radical containing 1 to 4 carbon atoms; y is 0 or an integer from 1 to 4; Y' is a halogen atom, an alkyl radical containing 1 to 4 carbon atoms or an alkoxy radical containing 1 to 4 carbon atoms; and z is 0 or an integer from 1 to 4, and E' is a radical of the formula
Figure imgb0022
wherein R' is a sulfone, carbonyl, vinyl, sulphoxide, azo, saturated fluorocarbon, organic phosphine oxide of ethylidene radical.
8. An article according to claim 7, wherein y and z are 0, x is 1, R' is a sulphone radical and R is a radical of the formula
Figure imgb0023
wherein each of R" and R'" is independently a hydrogen atom; an alkyl radical containing 1 to 4 carbon atoms; a halogen-substituted alkyl radical containing 1 to 4 carbon atoms; an aryl, alkaryl or aralkyl radicals containing 6 to 10 carbon atoms; or a halogen-substituted aryl, alkaryl or aralkyl radicals containing 6 to 10 carbon atoms.
9. An article according to any one of claims 1 to 4, wherein the aromatic polymer consists essentially of repeating units of the formula
Figure imgb0024
Figure imgb0025
Figure imgb0026
Figure imgb0027
wherein each of x, m and n is 0 to 1, with n being 0 when x is 1, is an integer from 1 to 4, with m being 1 and x being 0 when p is greater than 1.
10. An article according to any one of claims 1 to 9 which is in the form of an electrical wire or cable, the inner insulating layer being a melt extruded layer which surrounds and contacts the conductor and preferably has a wall thickness of from 101.5 to 177.8 micrometres and the outer insulating layer being a melt extruded layer which surrounds and contacts the inner insulating layer and preferably has a wall thickness of from 101.6 to 177.8 micrometres.
EP83305380A 1982-09-15 1983-09-14 Electrical insulation Expired EP0103487B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT83305380T ATE21462T1 (en) 1982-09-15 1983-09-14 ELECTRICAL INSULATION.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US41835582A 1982-09-15 1982-09-15
US418355 1982-09-15

Publications (3)

Publication Number Publication Date
EP0103487A2 EP0103487A2 (en) 1984-03-21
EP0103487A3 EP0103487A3 (en) 1984-08-01
EP0103487B1 true EP0103487B1 (en) 1986-08-13

Family

ID=23657778

Family Applications (1)

Application Number Title Priority Date Filing Date
EP83305380A Expired EP0103487B1 (en) 1982-09-15 1983-09-14 Electrical insulation

Country Status (6)

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EP (1) EP0103487B1 (en)
JP (1) JPS5973807A (en)
AT (1) ATE21462T1 (en)
CA (1) CA1214528A (en)
DE (1) DE3365309D1 (en)
GB (1) GB2127210B (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH664230A5 (en) * 1984-02-08 1988-02-15 Huber+Suhner Ag INSULATED, ELECTRICAL CABLE.
GB8716307D0 (en) * 1987-07-10 1987-08-19 Raychem Ltd Electrical wire
GB8716305D0 (en) * 1987-07-10 1987-08-19 Raychem Ltd Electrical wire
EP0301543B1 (en) * 1987-07-29 1995-02-08 Sumitomo Electric Industries Limited Molded article made from a resinous composition
JP3073545B2 (en) * 1990-05-23 2000-08-07 株式会社フジクラ Insulated wire and cable using this
JPH04108810U (en) * 1991-03-07 1992-09-21 古河電気工業株式会社 insulated wire
JP3233655B2 (en) * 1991-05-24 2001-11-26 株式会社フジクラ Flame retardant electrical cable
US6296935B1 (en) * 1996-08-22 2001-10-02 The Furukawa Electric Co., Ltd. Multilayer insulated wire and transformer using the same
GB2329278B (en) * 1997-07-14 2002-01-16 Delta Crompton Cables Ltd Co-axial cables
JP5258022B2 (en) * 2008-02-18 2013-08-07 古河マグネットワイヤ株式会社 Insulated wire for coil

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3217084A (en) * 1960-12-20 1965-11-09 Anaconda Wire & Cable Co Electric cable having compressed insulation
US3294604A (en) * 1960-12-20 1966-12-27 Anaconda Wire & Cable Co Method of making electric cable having compressed insulation
US4184001A (en) * 1978-04-19 1980-01-15 Haveg Industries, Inc. Multi layer insulation system for conductors comprising a fluorinated copolymer layer which is radiation cross-linked
EP0040034A1 (en) * 1980-05-08 1981-11-18 BICC Limited Insulated wires and electric cables
JPS57130304A (en) * 1981-02-02 1982-08-12 Chiyanpurein Cable Corp Insulating system for wire or cable

Also Published As

Publication number Publication date
ATE21462T1 (en) 1986-08-15
DE3365309D1 (en) 1986-09-18
GB2127210B (en) 1986-01-22
GB8324662D0 (en) 1983-10-19
GB2127210A (en) 1984-04-04
EP0103487A2 (en) 1984-03-21
CA1214528A (en) 1986-11-25
JPS5973807A (en) 1984-04-26
EP0103487A3 (en) 1984-08-01
JPH0517642B2 (en) 1993-03-09

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