EP0103487B1 - Isolation électrique - Google Patents
Isolation électrique Download PDFInfo
- 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
- Authority
- EP
- European Patent Office
- Prior art keywords
- radical
- polymer
- aromatic
- carbon atoms
- article according
- 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.)
- Expired
Links
- 238000010292 electrical insulation Methods 0.000 title abstract description 5
- 229920000642 polymer Polymers 0.000 claims abstract description 53
- 125000003118 aryl group Chemical group 0.000 claims abstract description 22
- 229920001577 copolymer Polymers 0.000 claims abstract description 15
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000005977 Ethylene Substances 0.000 claims abstract description 10
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims abstract description 5
- 230000009477 glass transition Effects 0.000 claims abstract description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000004020 conductor Substances 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 12
- 239000011737 fluorine Substances 0.000 claims description 12
- 229920000098 polyolefin Polymers 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 4
- 229920000620 organic polymer Polymers 0.000 claims description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical group FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 3
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 claims description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001491 aromatic compounds Chemical class 0.000 claims description 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims description 2
- 229920000412 polyarylene Polymers 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 239000004416 thermosoftening plastic Substances 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Chemical group 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- ATTZFSUZZUNHBP-UHFFFAOYSA-N Piperonyl sulfoxide Chemical group CCCCCCCCS(=O)C(C)CC1=CC=C2OCOC2=C1 ATTZFSUZZUNHBP-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000001174 sulfone group Chemical group 0.000 claims 1
- 238000009413 insulation Methods 0.000 abstract description 11
- 239000004696 Poly ether ether ketone Substances 0.000 abstract description 5
- 229920002530 polyetherether ketone Polymers 0.000 abstract description 5
- 229920006393 polyether sulfone Polymers 0.000 abstract description 4
- 239000000779 smoke Substances 0.000 abstract description 4
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 abstract description 3
- 229920001643 poly(ether ketone) Polymers 0.000 abstract description 3
- 239000004695 Polyether sulfone Substances 0.000 abstract description 2
- 229920006037 cross link polymer Polymers 0.000 abstract 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 11
- 229920002313 fluoropolymer Polymers 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 8
- 239000000178 monomer Substances 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- QHSJIZLJUFMIFP-UHFFFAOYSA-N ethene;1,1,2,2-tetrafluoroethene Chemical compound C=C.FC(F)=C(F)F QHSJIZLJUFMIFP-UHFFFAOYSA-N 0.000 description 3
- -1 polyethylene terephthalate Polymers 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- 229920001780 ECTFE Polymers 0.000 description 2
- 239000002033 PVDF binder Substances 0.000 description 2
- 239000004697 Polyetherimide Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 229920006355 Tefzel Polymers 0.000 description 2
- 229920004738 ULTEM® Polymers 0.000 description 2
- JUPQTSLXMOCDHR-UHFFFAOYSA-N benzene-1,4-diol;bis(4-fluorophenyl)methanone Chemical compound OC1=CC=C(O)C=C1.C1=CC(F)=CC=C1C(=O)C1=CC=C(F)C=C1 JUPQTSLXMOCDHR-UHFFFAOYSA-N 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920002492 poly(sulfone) Polymers 0.000 description 2
- 229920001601 polyetherimide Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- QMIWYOZFFSLIAK-UHFFFAOYSA-N 3,3,3-trifluoro-2-(trifluoromethyl)prop-1-ene Chemical group FC(F)(F)C(=C)C(F)(F)F QMIWYOZFFSLIAK-UHFFFAOYSA-N 0.000 description 1
- 101100271014 Bacillus subtilis (strain 168) asnO gene Proteins 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920006370 Kynar Polymers 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920004695 VICTREX™ PEEK Polymers 0.000 description 1
- 229920004888 Victrex® 200P Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006162 poly(etherimide sulfone) Polymers 0.000 description 1
- 229920003208 poly(ethylene sulfide) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003462 sulfoxides Chemical group 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators 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
- H01B3/44—Insulators 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
- H01B3/441—Insulators 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
- H01B7/29—Protection against damage caused by extremes of temperature or by flame
- H01B7/295—Protection 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.
Landscapes
- 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)
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT83305380T ATE21462T1 (de) | 1982-09-15 | 1983-09-14 | Elektrische isolierung. |
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 (fr) | 1984-03-21 |
EP0103487A3 EP0103487A3 (en) | 1984-08-01 |
EP0103487B1 true EP0103487B1 (fr) | 1986-08-13 |
Family
ID=23657778
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP83305380A Expired EP0103487B1 (fr) | 1982-09-15 | 1983-09-14 | Isolation électrique |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0103487B1 (fr) |
JP (1) | JPS5973807A (fr) |
AT (1) | ATE21462T1 (fr) |
CA (1) | CA1214528A (fr) |
DE (1) | DE3365309D1 (fr) |
GB (1) | GB2127210B (fr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH664230A5 (de) * | 1984-02-08 | 1988-02-15 | Huber+Suhner Ag | Isolierte, elektrische leitung. |
GB8716305D0 (en) * | 1987-07-10 | 1987-08-19 | Raychem Ltd | Electrical wire |
GB8716307D0 (en) * | 1987-07-10 | 1987-08-19 | Raychem Ltd | Electrical wire |
DE3852977T2 (de) * | 1987-07-29 | 1995-07-06 | Sumitomo Electric Industries | Formkörper auf Basis einer Harzzusammensetzung. |
JP3073545B2 (ja) * | 1990-05-23 | 2000-08-07 | 株式会社フジクラ | 絶縁電線及びこれを使用したケーブル |
JPH04108810U (ja) * | 1991-03-07 | 1992-09-21 | 古河電気工業株式会社 | 絶縁電線 |
JP3233655B2 (ja) * | 1991-05-24 | 2001-11-26 | 株式会社フジクラ | 難燃性電気ケーブル |
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 (ja) * | 2008-02-18 | 2013-08-07 | 古河マグネットワイヤ株式会社 | コイル用絶縁電線 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3294604A (en) * | 1960-12-20 | 1966-12-27 | Anaconda Wire & Cable Co | Method of making electric cable having compressed insulation |
US3217084A (en) * | 1960-12-20 | 1965-11-09 | Anaconda Wire & Cable Co | 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 (fr) * | 1980-05-08 | 1981-11-18 | BICC Limited | Fils isolés et câbles électriques |
JPS57130304A (en) * | 1981-02-02 | 1982-08-12 | Chiyanpurein Cable Corp | Insulating system for wire or cable |
-
1983
- 1983-09-14 CA CA000436688A patent/CA1214528A/fr not_active Expired
- 1983-09-14 GB GB08324662A patent/GB2127210B/en not_active Expired
- 1983-09-14 AT AT83305380T patent/ATE21462T1/de not_active IP Right Cessation
- 1983-09-14 DE DE8383305380T patent/DE3365309D1/de not_active Expired
- 1983-09-14 EP EP83305380A patent/EP0103487B1/fr not_active Expired
- 1983-09-14 JP JP58170544A patent/JPS5973807A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
EP0103487A3 (en) | 1984-08-01 |
DE3365309D1 (en) | 1986-09-18 |
EP0103487A2 (fr) | 1984-03-21 |
JPS5973807A (ja) | 1984-04-26 |
CA1214528A (fr) | 1986-11-25 |
GB2127210A (en) | 1984-04-04 |
GB8324662D0 (en) | 1983-10-19 |
JPH0517642B2 (fr) | 1993-03-09 |
ATE21462T1 (de) | 1986-08-15 |
GB2127210B (en) | 1986-01-22 |
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