EP0222507B1 - Shaped articles of crosslinked polymers - Google Patents
Shaped articles of crosslinked polymers Download PDFInfo
- Publication number
- EP0222507B1 EP0222507B1 EP86307817A EP86307817A EP0222507B1 EP 0222507 B1 EP0222507 B1 EP 0222507B1 EP 86307817 A EP86307817 A EP 86307817A EP 86307817 A EP86307817 A EP 86307817A EP 0222507 B1 EP0222507 B1 EP 0222507B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cross
- layer
- polymer
- linking agent
- psi
- 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
- 229920006037 cross link polymer Polymers 0.000 title claims description 3
- 239000000203 mixture Substances 0.000 claims abstract description 32
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 25
- 239000004020 conductor Substances 0.000 claims abstract description 22
- 229920002313 fluoropolymer Polymers 0.000 claims abstract description 17
- 230000005855 radiation Effects 0.000 claims abstract description 14
- 238000004132 cross linking Methods 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000005977 Ethylene Substances 0.000 claims abstract description 6
- 229920000642 polymer Polymers 0.000 claims description 33
- 238000002844 melting Methods 0.000 claims description 17
- 230000008018 melting Effects 0.000 claims description 17
- 241000699670 Mus sp. Species 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 5
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 claims description 3
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 claims description 3
- 238000010292 electrical insulation Methods 0.000 claims description 3
- 230000001678 irradiating effect Effects 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 239000013047 polymeric layer Substances 0.000 abstract 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 10
- 229910052731 fluorine Inorganic materials 0.000 description 10
- 239000011737 fluorine Substances 0.000 description 10
- 238000009413 insulation Methods 0.000 description 10
- 238000012360 testing method Methods 0.000 description 5
- 238000005299 abrasion Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 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
- 238000013508 migration Methods 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- 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
- CDZMWAHBQLPCHD-UHFFFAOYSA-N 3-(4-carboxyphenyl)-1,1,3-trimethyl-2h-indene-5-carboxylic acid Chemical compound C12=CC(C(O)=O)=CC=C2C(C)(C)CC1(C)C1=CC=C(C(O)=O)C=C1 CDZMWAHBQLPCHD-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- -1 diallyl ester Chemical class 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- GRPURDFRFHUDSP-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,2,4-tricarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C(C(=O)OCC=C)=C1 GRPURDFRFHUDSP-UHFFFAOYSA-N 0.000 description 1
- VOSUIKFOFHZNED-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,3,5-tricarboxylate Chemical compound C=CCOC(=O)C1=CC(C(=O)OCC=C)=CC(C(=O)OCC=C)=C1 VOSUIKFOFHZNED-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- 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
-
- 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
- H01B3/443—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 vinylhalogenides or other halogenoethylenic compounds
Definitions
- This invention relates to insulated electrical conductors.
- insulated wires include wires coated with a layer of a radiation cross-linked fluorocarbon polymer, particularly an ethylene/tetrafluoroethylene copolymer (often referred to as an ETFE polymer), which are extensively used for the wiring in aircraft.
- ETFE polymer ethylene/tetrafluoroethylene copolymer
- Military Specification No. MiL-W-22759 sets various standards for such standards for such insulated wires. Reference may be made for example to U.S. Patents Nos. 3 763 222,3 840 619,3 894118,3 911 192, 3 970 770, 985 716,3 995 091,4 031 167,4 155 823 and 4 353 961.
- Such wires have the significant disadvantage that if the outer surface of the insulation is damaged, subsequent flexing of the wire causes the damage to propagate through the insulation, at a rate which is highly undesirable. This disadvantage is especially serious when the insulated wire is to be used in an aircraft or in other high performance situations where the consequences of insulation failure can be so serious. A quantitative measure of this disadvantage can be obtained from a notch propagation test such as that described below.
- insulation which comprises an inner layer of a polymer which has little cross-linking and an outer layer of polymer which has a relatively high level of cross-linking. Furthermore, this improvement is obtained with little or no substantial deterioration of other important properties of the insulation, for example, resistance to scrape abrasion, resistance to crossed wire abrasion and resistance to cut-through.
- the present invention provides an insulated electrical conductor, especially a wire, which comprises:
- the M 100 values given herein are modulus values measured at a temperature above the melting point of the polymer by the procedure described in detail below, and therefore reflect the level of cross-linking in the layer.
- a preferred method of making such an insulated conductor comprises:
- the polymeric component in the polymeric compositions used in the present invention preferably comprises, and more preferably consists essentially of, a melt-shapeable crystalline polymer having a melting point of at least 200 ° C, preferably at least 250 ° C, or a mixture of such polymers.
- melting point is used herein to denote the temperature above which no crystallinity exists in the polymer (or, when a mixture of crystalline polymers is used, in the major crystalline component of the mixture).
- 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 co-polymers 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 has a melting point of at least 200 ° C, and will often have a melting point of at least 250°C, e.g. up to 300°C.
- the polymeric composition has a viscosity of less than 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, 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.
- polymers which can be used include copolymers of ethylene and chlorotrifluoroethylene; copolymers of vinylidene fluoride with one or both of hexafluoropropylene and tetrafluoroethylene, or with hexafluoroisobutylene; and copolymers of tetrafluoroethylene and hexafluoropropylene.
- the polymeric composition can optionally contain suitable additives such as pigments, antioxidants, thermal stabilisers, acid acceptors and processing aids.
- the first and second compositions preferably contain the same polymeric components, and more preferably are substantially the same in all respects except for the level of cross-linking.
- the conductor is preferably a metal (e.g. copper) wire, which may be stranded or solid.
- the wire may be for example from 10 to 26 AWG in size.
- the first layer preferably contacts the conductor.
- the second member is preferably also in the form of a layer which has the same general shape as the first layer or which serves to join together a number of wires each of which is surrounded by a first layer, thus forming a ribbon cable.
- the layers are preferably in direct contact, but may be joined together by a layer of adhesive.
- the first and second members are preferably formed by melt-extrusion, particularly by sequential extrusion, which may be tubular or pressure extrusion, so that the layers are hot when first contacted, in order to promote migration of the cross-linking agent.
- the polymeric compositions should preferably be selected so that at least the outer layer has a tensile strength of at least 3,000 psi (210 kg/cm 2 ); and since a higher tensile strength is usually desired in the cross-linked product and there is frequently a loss of tensile strength during the irradiation step, a higher initial tensile strength is preferred, e.g. greater than 6,000 psi (420 kg/cm 2 ), preferably at least 7,000 psi (490 kg/cm2), particularly at least 8,000 psi (560 kg/cm2).
- the thickness of the inner layer is generally 0.0075 to 0.038 cm (0.003 to 0.015 inch), preferably 0.0075 to 0.0225 cm (0.003 to 0.009 inch).
- the thickness of the outer layer is generally 0.01 to 0.063 cm (0.004 to 0.025 inch), preferably 0.01 to 0.023 cm (0.005 to 0.009 inch).
- Preferred radiation cross-linking agents contain carbon-carbon unsaturated groups in a molar percentage greater than 15, especially greater than 20, particularly greater than 25.
- the cross-linking agent contains at least two ethylenic double bonds, which may be present, for example, in allyl, methallyl, propargyl or vinyl groups.
- cross- linking agents are triallyl cyanurate (TAC) and triallyl isocyanurate (TAIC); other specific cross-linking agents include triallyl trimellitate, triallyl trimesate, tetrallyl pyromellitate, the diallyl ester of 1,1,3-trimethyl-5-carboxy-3-(p-carboxyphenyl) indan.
- TAC triallyl cyanurate
- TAIC triallyl isocyanurate
- Other cross-linking agents which are known for incorporation into fluorocarbon polymers prior to shaping, for example those disclosed in U.S. Patents referenced above, can also be used. Mixtures of cross-linking agents can be used.
- the first composition as extruded contains little or no cross- linking agent (e.g. 0 to 2% by weight, preferably 0%), and the second composition as extruded contains more than is desired during the cross-linking step, e.g. at least 5%, preferably 5 to 25%, particularly 7 to 12%, by weight.
- the time for which the layers should be maintained in contact prior to cross-linking depends upon the extent of migration which is needed and the temperature during such contact, which is preferably 5 to 150 ° C below the melting point of the polymer (or the lower melting polymer if there are two or more polymers in the layers).
- the inner layer preferably contains 0 to 3% by weight of cross- linking agent and the outer layer preferably contains 3 to 10% by weight of crosslinking agent.
- the dosage employed in the irradiation step is generally below 50 Mrads to ensure that the polymer is not degraded by excessive irradiation, and the dosages preferably employed will of course depend upon the extent of cross-linking desired, balanced against the tendency of the polymer to be degraded by high doses of irradiation. Suitable dosages are generally in the range 2 to 40 Mrads, for example 2 to 30 Mrads, preferably 3 to 20 Mrads, especially 5 to 25 or 5 to 20 Mrads, particularly 5 to 15 Mrads.
- the ionising radiation can for example be in the form of accelerated electrons or gamma rays. Irradiation is generally carried out at about room temperature, but higher temperatures can also be used.
- the inner layer preferably has an Mice value of at least 2.8 kg/cm2 (40 psi) and especially from 3.5 to 10.5 kg/cm 2 (50 to 150 psi).
- the elongation of the inner layer is preferably at least 100%, particularly at least 125%, e.g. at least 150%, especially 200 to 300%.
- the outer layer is preferably cross-linked so that it has an Mice value of at least 28 kg/cm 2 (400 psi), particularly at least 31.5 kg/cm 2 (450 psi), with yet higher values of at least 42 kg/cm 2 (600 psi) being valuable in many cases.
- the elongation of the outer layer is preferably 40 to 150%, particularly 50 to 120%.
- the Notch Propagation Values are measured on a piece of insulated wire about 30 cm (12 inch) long.
- a notch is made in the insulation, about 5 cm (2 inch) from one end, by means of a razor blade at right angles to the axis of the wire.
- the depth of the notch is controlled by mounting the razor blade between two metal blocks so that it protrudes by a distance which is 0.01 cm (0.004) inch or., if the insulation comprises two layers and the outer layer has a thickness t which is less than 0.018 cm (0.007 inch) thick, by a distance which is (t-0.0051) cm [(t-0.002) inch].
- the end of the wire closer to the notch is secured to a horizontal mandrel whose diameter is three times the outer diameter of the insulation.
- a 0.675 kg (1.5 Ib) weight is secured to the other end of the wire so that the wire hangs vertically.
- the mandrel is then rotated clockwise, at about 60 revolutions a minute, until most of the wires has wrapped around the mandrel.
- the mandrel is then rotated, counterclockwise, until the wire has unwrapped and most of the wire has again been wrapped around the mandrel.
- the mandrel is then rotated clockwise until the wire has unwrapped and most of the wire has again been wrapped around the mandrel. This sequence is continued until visual observation of the notched area shows the conductor to be exposed.
- the M 100 values are determined by a static modulus test as described in U.S. Patent No. 4,353,961 carried out at about 40°C above the melting point of the polymer, (e.g. at about 320 ° C for ETFE polymers).
- the tensile strengths and elongations are determined in accordance with ASTM D 638-72 (i.e. at 23 ° C) at a testing speed of 50 mm (2 inch) per minute.
- cross-wire abrasion values are measured by the tests described in U.S. Patent No. 4,353,961.
- Example 1 is a comparative Example.
- a 20 AWG (19/32) stranded tin-coated copper wire was insulated by melt-extruding over it, by sequential extrusion, an inner insulating layer 0.01 to 0.0125 cm (0.004 to 0.005 inch) thick and an outer insulating layer .018 to 0.020 cm (0.007 to 0.008 inch) thick.
- the layers were composed of the following compositions:
- the polymeric insulation was cross-linked by irradiating it to a dosage of 14 Mrads.
- Example 1 The procedure of Example 1 was followed except that the composition of the inner layer was
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- Spectroscopy & Molecular Physics (AREA)
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- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Insulated Conductors (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
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Abstract
Description
- This invention relates to insulated electrical conductors.
- It is known to use cross-linked polymeric compositions as electrical insulation on a wire or other conductor. Known insulated wires include wires coated with a layer of a radiation cross-linked fluorocarbon polymer, particularly an ethylene/tetrafluoroethylene copolymer (often referred to as an ETFE polymer), which are extensively used for the wiring in aircraft. Military Specification No. MiL-W-22759 sets various standards for such standards for such insulated wires. Reference may be made for example to U.S. Patents Nos. 3 763 222,3 840 619,3 894118,3 911 192, 3 970 770, 985 716,3 995 091,4 031 167,4 155 823 and 4 353 961. Such wires have the significant disadvantage that if the outer surface of the insulation is damaged, subsequent flexing of the wire causes the damage to propagate through the insulation, at a rate which is highly undesirable. This disadvantage is especially serious when the insulated wire is to be used in an aircraft or in other high performance situations where the consequences of insulation failure can be so serious. A quantitative measure of this disadvantage can be obtained from a notch propagation test such as that described below.
- We have discovered that this disadvantage can be substantially mitigated by insulation which comprises an inner layer of a polymer which has little cross-linking and an outer layer of polymer which has a relatively high level of cross-linking. Furthermore, this improvement is obtained with little or no substantial deterioration of other important properties of the insulation, for example, resistance to scrape abrasion, resistance to crossed wire abrasion and resistance to cut-through.
- In one aspect, the present invention provides an insulated electrical conductor, especially a wire, which comprises:
- (1) an electrical conductor; and
- (2) electrical insulation which comprises:
- (a) an inner electrically insulating layer which (i) is composed of a first melt-processed, cross-linked polymer composition wherein the polymer comprises a fluorocarbon polymer having a melting point of at least 200°C, and (ii) has a first M100 value of 0 to 17.5 kg/cm2 (0 to 250 psi); and
- (b) an outer electrically insulating layer which (i) is separated from the conductor by the inner layer, (ii) is composed of a second melt-processed cross-linked polymeric composition wherein the polymer comprises a fluorocarbon polymer having a melting point of at least 200°C, and (iii) has a second Mice value which is at least 24.5 kg/cm2 (350 psi).
- The M100 values given herein are modulus values measured at a temperature above the melting point of the polymer by the procedure described in detail below, and therefore reflect the level of cross-linking in the layer.
- A preferred method of making such an insulated conductor comprises:
- (1) melt-extruding around the wire a first electrically insulating composition which comprises a fluorocarbon polymer having a melting point of at least 200°C and 0-2% by weight of a radiation cross-linking agent, thereby forming a first insulating layer;
- (2) melt-extruding around the first insulating layer a second electrically insulating composition which comprises a fluorocarbon polymer having a melting point of at least 200°C and at least 5% by weight of a radiation cross-linking agent, thereby forming a second insulating layer;
- (3) maintaining contact between the first and second layers under conditions such that part of the radiation cross-linking agent migrates from the second layer into the first layer; and
- (4) without further addition of radiation cross-linking agent to the layers, irradiating the first and second layers to effect cross-linking thereof so that the first insulating layer has a first Mice value of less than 17.5 kg/cm2 and the second insulating layer has a second M100 value which is at least 24.5 kg/cm2.
- The polymeric component in the polymeric compositions used in the present invention preferably comprises, and more preferably consists essentially of, a melt-shapeable crystalline polymer having a melting point of at least 200°C, preferably at least 250°C, or a mixture of such polymers. The term "melting point" is used herein to denote the temperature above which no crystallinity exists in the polymer (or, when a mixture of crystalline polymers is used, in the major crystalline component of the mixture). 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. Preferably 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 co-polymers 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 has a melting point of at least 200°C, and will often have a melting point of at least 250°C, e.g. up to 300°C. Preferably the polymeric composition has a viscosity of less than 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, 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; copolymers of vinylidene fluoride with one or both of hexafluoropropylene and tetrafluoroethylene, or with hexafluoroisobutylene; and copolymers of tetrafluoroethylene and hexafluoropropylene.
- The polymeric composition can optionally contain suitable additives such as pigments, antioxidants, thermal stabilisers, acid acceptors and processing aids.
- The first and second compositions preferably contain the same polymeric components, and more preferably are substantially the same in all respects except for the level of cross-linking.
- The conductor is preferably a metal (e.g. copper) wire, which may be stranded or solid. The wire may be for example from 10 to 26 AWG in size. The first layer preferably contacts the conductor. The second member is preferably also in the form of a layer which has the same general shape as the first layer or which serves to join together a number of wires each of which is surrounded by a first layer, thus forming a ribbon cable. The layers are preferably in direct contact, but may be joined together by a layer of adhesive.
- The first and second members are preferably formed by melt-extrusion, particularly by sequential extrusion, which may be tubular or pressure extrusion, so that the layers are hot when first contacted, in order to promote migration of the cross-linking agent. The polymeric compositions should preferably be selected so that at least the outer layer has a tensile strength of at least 3,000 psi (210 kg/cm2); and since a higher tensile strength is usually desired in the cross-linked product and there is frequently a loss of tensile strength during the irradiation step, a higher initial tensile strength is preferred, e.g. greater than 6,000 psi (420 kg/cm2), preferably at least 7,000 psi (490 kg/cm2), particularly at least 8,000 psi (560 kg/cm2).
- The thickness of the inner layer is generally 0.0075 to 0.038 cm (0.003 to 0.015 inch), preferably 0.0075 to 0.0225 cm (0.003 to 0.009 inch). The thickness of the outer layer is generally 0.01 to 0.063 cm (0.004 to 0.025 inch), preferably 0.01 to 0.023 cm (0.005 to 0.009 inch).
- Preferred radiation cross-linking agents contain carbon-carbon unsaturated groups in a molar percentage greater than 15, especially greater than 20, particularly greater than 25. In many cases the cross-linking agent contains at least two ethylenic double bonds, which may be present, for example, in allyl, methallyl, propargyl or vinyl groups. We have obtained excellent results with cross-linking agents containing at least two allyl groups, especially three or four allyl groups. Particularly preferred cross- linking agents are triallyl cyanurate (TAC) and triallyl isocyanurate (TAIC); other specific cross-linking agents include triallyl trimellitate, triallyl trimesate, tetrallyl pyromellitate, the diallyl ester of 1,1,3-trimethyl-5-carboxy-3-(p-carboxyphenyl) indan. Other cross-linking agents which are known for incorporation into fluorocarbon polymers prior to shaping, for example those disclosed in U.S. Patents referenced above, can also be used. Mixtures of cross-linking agents can be used.
- In the preferred method of preparing articles of the invention, in which cross-linking agent migrates from the second member to the first member, the first composition as extruded contains little or no cross- linking agent (e.g. 0 to 2% by weight, preferably 0%), and the second composition as extruded contains more than is desired during the cross-linking step, e.g. at least 5%, preferably 5 to 25%, particularly 7 to 12%, by weight. The time for which the layers should be maintained in contact prior to cross-linking depends upon the extent of migration which is needed and the temperature during such contact, which is preferably 5 to 150°C below the melting point of the polymer (or the lower melting polymer if there are two or more polymers in the layers). At the time of irradiation, the inner layer preferably contains 0 to 3% by weight of cross- linking agent and the outer layer preferably contains 3 to 10% by weight of crosslinking agent.
- The dosage employed in the irradiation step is generally below 50 Mrads to ensure that the polymer is not degraded by excessive irradiation, and the dosages preferably employed will of course depend upon the extent of cross-linking desired, balanced against the tendency of the polymer to be degraded by high doses of irradiation. Suitable dosages are generally in the range 2 to 40 Mrads, for example 2 to 30 Mrads, preferably 3 to 20 Mrads, especially 5 to 25 or 5 to 20 Mrads, particularly 5 to 15 Mrads. The ionising radiation can for example be in the form of accelerated electrons or gamma rays. Irradiation is generally carried out at about room temperature, but higher temperatures can also be used.
- The inner layer preferably has an Mice value of at least 2.8 kg/cm2 (40 psi) and especially from 3.5 to 10.5 kg/cm2 (50 to 150 psi). The elongation of the inner layer is preferably at least 100%, particularly at least 125%, e.g. at least 150%, especially 200 to 300%.
- The outer layer is preferably cross-linked so that it has an Mice value of at least 28 kg/cm2 (400 psi), particularly at least 31.5 kg/cm2 (450 psi), with yet higher values of at least 42 kg/cm2 (600 psi) being valuable in many cases. The elongation of the outer layer is preferably 40 to 150%, particularly 50 to 120%.
- The various physical properties referred to in this specification are measured as set out below.
- The Notch Propagation Values are measured on a piece of insulated wire about 30 cm (12 inch) long. A notch is made in the insulation, about 5 cm (2 inch) from one end, by means of a razor blade at right angles to the axis of the wire. The depth of the notch is controlled by mounting the razor blade between two metal blocks so that it protrudes by a distance which is 0.01 cm (0.004) inch or., if the insulation comprises two layers and the outer layer has a thickness t which is less than 0.018 cm (0.007 inch) thick, by a distance which is (t-0.0051) cm [(t-0.002) inch]. The end of the wire closer to the notch is secured to a horizontal mandrel whose diameter is three times the outer diameter of the insulation. A 0.675 kg (1.5 Ib) weight is secured to the other end of the wire so that the wire hangs vertically. The mandrel is then rotated clockwise, at about 60 revolutions a minute, until most of the wires has wrapped around the mandrel. The mandrel is then rotated, counterclockwise, until the wire has unwrapped and most of the wire has again been wrapped around the mandrel. The mandrel is then rotated clockwise until the wire has unwrapped and most of the wire has again been wrapped around the mandrel. This sequence is continued until visual observation of the notched area shows the conductor to be exposed. If, at this time, the conductor is broken (or some or all of the strands of a stranded wire conductor are broken) then the failure is attributable to that breakage, not to propagation of the notch through the insulation. The number of cy- des (half the number of times the rotation of the mandrel is reversed) is recorded.
- The M100 values are determined by a static modulus test as described in U.S. Patent No. 4,353,961 carried out at about 40°C above the melting point of the polymer, (e.g. at about 320°C for ETFE polymers).
- The tensile strengths and elongations are determined in accordance with ASTM D 638-72 (i.e. at 23°C) at a testing speed of 50 mm (2 inch) per minute.
- The cross-wire abrasion values, the cut-through resistance values, and the scrape abrasion values, are measured by the tests described in U.S. Patent No. 4,353,961.
- The invention is illustrated by the following Examples, in which Example 1 is a comparative Example.
- A 20 AWG (19/32) stranded tin-coated copper wire was insulated by melt-extruding over it, by sequential extrusion, an inner insulating layer 0.01 to 0.0125 cm (0.004 to 0.005 inch) thick and an outer insulating layer .018 to 0.020 cm (0.007 to 0.008 inch) thick. The layers were composed of the following compositions:
- The polymeric insulation was cross-linked by irradiating it to a dosage of 14 Mrads.
- The procedure of Example 1 was followed except that the composition of the inner layer was
-
-
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT86307817T ATE48720T1 (en) | 1985-10-11 | 1986-10-09 | MOLDED PARTS MADE OF CROSSLINKED POLYMERS. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78680685A | 1985-10-11 | 1985-10-11 | |
US786806 | 1991-11-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0222507A1 EP0222507A1 (en) | 1987-05-20 |
EP0222507B1 true EP0222507B1 (en) | 1989-12-13 |
Family
ID=25139639
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86307817A Expired EP0222507B1 (en) | 1985-10-11 | 1986-10-09 | Shaped articles of crosslinked polymers |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0222507B1 (en) |
JP (1) | JPH0679451B2 (en) |
KR (1) | KR950007089B1 (en) |
AT (1) | ATE48720T1 (en) |
BR (1) | BR8604970A (en) |
CA (1) | CA1295574C (en) |
DE (1) | DE3667569D1 (en) |
ES (1) | ES2012452B3 (en) |
IL (1) | IL80269A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL87050A0 (en) * | 1987-07-10 | 1988-12-30 | Raychem Ltd | Electrical wire |
CA2187219C (en) * | 1994-04-07 | 2007-10-02 | Steven C. Zingheim | Insulated wire and cable |
AU1105801A (en) * | 1999-09-07 | 2001-04-10 | Judd Wire, Inc. | Dual layer system suitable for use as electrical insulation for wires and other conductors |
US7915532B2 (en) * | 2007-06-08 | 2011-03-29 | Westerngeco L.L.C. | Enhanced electrical seismic land cable |
JP5276891B2 (en) * | 2008-05-02 | 2013-08-28 | 株式会社クラベ | Heat and oil resistant insulated wire and method for manufacturing the same |
JPWO2016002887A1 (en) * | 2014-07-04 | 2017-04-27 | 旭硝子株式会社 | Fluororesin composition and method for producing the same, and molded product, foam molded product, and covered electric wire |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3269862A (en) | 1964-10-22 | 1966-08-30 | Raychem Corp | Crosslinked polyvinylidene fluoride over a crosslinked polyolefin |
US4101699A (en) * | 1973-11-23 | 1978-07-18 | Samuel Moore & Company | Synthetic resinous tube |
US3852518A (en) | 1973-11-29 | 1974-12-03 | Gen Cable Corp | Irradiation cross-linked composite low density/high density polyethylene insulated 600 volt power cables |
US4155823A (en) | 1976-10-12 | 1979-05-22 | Raychem Corporation | Shaped article from crosslinked fluorocarbon polymer and process therefor |
ZA776079B (en) * | 1976-10-12 | 1978-06-28 | Raychem Corp | Shaped articles of cross-linked fluorocarbon polymers |
US4353961A (en) | 1977-09-14 | 1982-10-12 | Raychem Corporation | Shaped article from crosslinked fluorocarbon polymer |
US4310597A (en) | 1978-07-10 | 1982-01-12 | Northern Telecom Limited | Low voltage electrical wire |
CA1151255A (en) * | 1980-11-06 | 1983-08-02 | Eric P. Marsden | Electrical insulated wire with flexibility and abrasion-resistant layer |
-
1986
- 1986-10-08 CA CA000520053A patent/CA1295574C/en not_active Expired - Lifetime
- 1986-10-09 EP EP86307817A patent/EP0222507B1/en not_active Expired
- 1986-10-09 ES ES86307817T patent/ES2012452B3/en not_active Expired - Lifetime
- 1986-10-09 IL IL80269A patent/IL80269A/en not_active IP Right Cessation
- 1986-10-09 AT AT86307817T patent/ATE48720T1/en not_active IP Right Cessation
- 1986-10-09 JP JP61241166A patent/JPH0679451B2/en not_active Expired - Fee Related
- 1986-10-09 DE DE8686307817T patent/DE3667569D1/en not_active Expired - Lifetime
- 1986-10-10 KR KR1019860008497A patent/KR950007089B1/en not_active IP Right Cessation
- 1986-10-10 BR BR8604970A patent/BR8604970A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
KR950007089B1 (en) | 1995-06-30 |
JPH0679451B2 (en) | 1994-10-05 |
KR870004466A (en) | 1987-05-09 |
IL80269A0 (en) | 1987-01-30 |
DE3667569D1 (en) | 1990-01-18 |
CA1295574C (en) | 1992-02-11 |
IL80269A (en) | 1991-03-10 |
JPS6293806A (en) | 1987-04-30 |
ATE48720T1 (en) | 1989-12-15 |
EP0222507A1 (en) | 1987-05-20 |
BR8604970A (en) | 1987-07-14 |
ES2012452B3 (en) | 1990-04-01 |
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