WO2018151421A1 - Polymer composition for high-voltage cable, and cable comprising insulation layer and sheath layer which are formed therefrom - Google Patents

Polymer composition for high-voltage cable, and cable comprising insulation layer and sheath layer which are formed therefrom Download PDF

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WO2018151421A1
WO2018151421A1 PCT/KR2018/000587 KR2018000587W WO2018151421A1 WO 2018151421 A1 WO2018151421 A1 WO 2018151421A1 KR 2018000587 W KR2018000587 W KR 2018000587W WO 2018151421 A1 WO2018151421 A1 WO 2018151421A1
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parts
weight
content
polymer composition
resin
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French (fr)
Korean (ko)
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주동욱
김인하
박찬웅
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엘에스전선 주식회사
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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
    • H01B3/307Other macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0853Vinylacetate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/16Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/003Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • C09K21/02Inorganic materials
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K21/00Fireproofing materials
    • C09K21/02Inorganic materials
    • C09K21/04Inorganic materials containing phosphorus
    • 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
    • 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
    • H01B7/02Disposition of insulation
    • 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
    • H01B7/02Disposition of insulation
    • H01B7/0208Cables with several layers of insulating material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B9/00Power cables
    • H01B9/02Power cables with screens or conductive layers, e.g. for avoiding large potential gradients

Definitions

  • the present invention relates to a cable comprising a polymer composition for a high voltage cable and an insulating layer and a sheath layer formed therefrom.
  • the present invention satisfies the high insulation resistance characteristics required for high voltage cables and at the same time has a high degree of flexibility in conflict with the polymer composition and excellent properties such as oil resistance, wear resistance, heat resistance, cold resistance, flame resistance, etc.
  • a cable comprising an formed insulating layer and a sheath layer.
  • High-voltage cable for electric vehicles corresponds to 150 °C class 600V, and there are products of various specifications depending on the cross-sectional area of the conductor.
  • Insulators and sheaths of high-voltage cables for electric vehicles are applied to ethylene vinyl acetate (EVA) resin having high vinyl acetate (VA) content or polyolefin elastomer (POE) having low melting point (Tm).
  • EVA ethylene vinyl acetate
  • POE polyolefin elastomer
  • insulators and sheaths meet the existing international standard ISO 6722-1, but are based on the existing international standard ISO 6722-1 from the European Union of Leading Automobile Manufacturers, the LV 216, especially cables with metal shielding layers. It is difficult to satisfy insulation resistance, oil resistance, etc. required by LV 216-2.
  • the volume resistance of an insulator required by the ISO 6722-1 standard is 10 9 ⁇ ⁇ mm
  • the volume resistance of the insulator required by the LV 216 standard is 10 13 ⁇ ⁇ mm
  • the sheath usually protects the cable from the external environment.
  • priority is given to securing the mechanical properties such as strength and hardness.
  • the sheath also requires insulation performance according to the insulator.
  • insulators and sheaths applied with ethylene vinyl acetate (EVA) resin having a high vinyl acetate (VA) content or polyolefin elastomer (POE) having a low melting point have a volume resistance of the insulator required by the LV 216 standard.
  • EVA ethylene vinyl acetate
  • POE polyolefin elastomer
  • automotive cables should satisfy the oil resistance characteristics for various oils, but when the resin of the polymer composition is changed to ensure insulation resistance and flexibility of the insulator, oil resistance, flame retardancy, etc. are greatly affected, and crosslinking according to the resin Mechanical properties such as abrasion resistance, heat resistance, etc. are greatly influenced by the method and the degree of crosslinking, and it is very difficult for all these properties to meet the LV 216 standard.
  • a polymer composition and an insulating layer formed therefrom that satisfy the high insulation resistance characteristics required by the LV 216 standard and at the same time have a high degree of flexibility and have excellent properties such as oil resistance, abrasion resistance, heat resistance, cold resistance, and flame resistance. And a cable including a sheath layer is urgently needed.
  • an object of the present invention is to provide a cable comprising a polymer composition which satisfies the characteristics such as excellent oil resistance, abrasion resistance, heat resistance, cold resistance, flame resistance, and the like, and an insulating layer and a sheath layer formed therefrom.
  • a polymer composition for a high voltage cable comprising a base resin and an additive, the base resin comprising a polypropylene resin, a polyolefin elastomer, ethylene propylene diene rubber, and ethylene vinyl acetate resin grafted with maleic anhydride,
  • the insulating layer and the sheath layer formed from the polymer composition provide a polymer composition having a volume resistance of more than 10 13 ⁇ ⁇ mm.
  • the content of the polypropylene resin is 15 to 25 parts by weight
  • the content of the polyolefin elastomer is 30 to 50 parts by weight
  • the content of the ethylene propylene diene rubber is 20 to 40 parts by weight based on 100 parts by weight of the base resin.
  • the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 8 to 13 parts by weight, to provide a polymer composition.
  • the content of the polypropylene resin is 17 to 24 parts by weight
  • the content of the polyolefin elastomer is 37 to 45 parts by weight
  • the content of the ethylene propylene diene rubber is 27 to 31 parts by weight
  • the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 9 to 10 parts by weight, to provide a polymer composition.
  • the content of the polypropylene resin is 22 to 32 parts by weight
  • the content of the polyolefin elastomer is 25 to 35 parts by weight
  • the content of the ethylene propylene diene rubber is 27 to 35 parts by weight
  • the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 8 to 13 parts by weight, to provide a polymer composition.
  • the content of the polypropylene resin is 24 to 29 parts by weight
  • the content of the polyolefin elastomer is 29 to 33 parts by weight
  • the content of the ethylene propylene diene rubber is 29 to 33 parts by weight
  • the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 10 to 11 parts by weight, to provide a polymer composition.
  • the polypropylene resin has a melting point (Tm) of 140 to 145 ° C and a specific gravity of 0.860 to 0.880, and the polyolefin elastomer has a melting point (Tm) of 90 to 100 ° C and a specific gravity of 0.890 to 0.910.
  • Tm melting point
  • Tm melting point
  • the ethylene propylene diene rubber has a specific gravity of 0.870 to 0.890 and a Mooney viscosity (ML1 + 4 (125 °C)) is characterized in that 20 to 40, to provide a polymer composition.
  • the additive provides a polymer composition, characterized in that it comprises at least one additive selected from the group consisting of flame retardants, crosslinking aids, antioxidants and lubricants.
  • the flame retardant includes magnesium hydroxide or aluminum hydroxide, and based on 100 parts by weight of the base resin, the content of the flame retardant is 80 to 100 parts by weight, to provide a polymer composition.
  • the content of the flame retardant provides a polymer composition, characterized in that 87 to 95 parts by weight based on 100 parts by weight of the base resin.
  • the crosslinking aid includes a crosslinking multifunctional organic monomer of the base resin, and the content of the crosslinking aid is 2 to 5 parts by weight based on 100 parts by weight of the base resin. .
  • the additive provides a polymer composition, characterized in that it comprises one or more additives selected from the group consisting of flame retardants, flame retardant aids, crosslinking aids, antioxidants and lubricants.
  • the flame retardant includes magnesium hydroxide or aluminum hydroxide
  • the flame retardant aid comprises a flame retardant, based on 100 parts by weight of the base resin, the content of the flame retardant is 95 to 110 parts by weight, the content of the flame retardant aid Silver is 0.6 to 1.2 parts by weight, to provide a polymer composition.
  • the content of the flame retardant is from 100 to 105 parts by weight
  • the content of the flame retardant aid is characterized in that the polymer composition, which provides 0.8 to 1.1 parts by weight.
  • the crosslinking aid includes a crosslinking multifunctional organic monomer of the base resin, and the content of the crosslinking aid is 2 to 5 parts by weight based on 100 parts by weight of the base resin. .
  • conductors An insulating layer surrounding the conductor and formed from the polymer composition of any one of claims 1 to 3; A metal shielding layer surrounding the insulating layer; And a sheath layer surrounding the metal shielding layer and formed from the polymer composition of any one of claims 1, 4 and 5.
  • the polymer composition for a high voltage cable of the present invention has a superior effect of satisfying the high insulation resistance required at the same time as the LV 216 standard by applying a base resin containing a specific resin at a specific compounding ratio, and at the same time having a high flexibility. Indicates.
  • the polymer composition for a high voltage cable of the present invention is applied to the base resin containing a specific resin in a specific compounding ratio, and excellent oil resistance, wear resistance, heat resistance, cold resistance required by the LV 216 standard through the application of a specific flame retardant, crosslinking method, crosslinking agent, etc. It shows an excellent effect of satisfying properties such as and flame retardancy.
  • FIG. 1 schematically shows a cross-sectional structure of one embodiment of a high voltage cable comprising an insulating layer and a sheath layer formed from a polymer composition according to the present invention.
  • FIG. 1 schematically shows a cross-sectional structure of one embodiment of a high voltage cable comprising an insulating layer and a sheath layer formed from a polymer composition according to the present invention.
  • the high voltage cable according to the present invention includes a conductor 10, an insulation layer 20 formed around the conductor 10 and formed from the polymer composition of the present invention, and a metal shield surrounding the insulation layer 20.
  • the layer 30 and the metal shielding layer 40 may include a sheath layer 40 formed from the polymer composition of the present invention.
  • the conductor 10 may apply a copper stranded wire combined with copper fine wires to secure flexibility of the cable, and the metal shielding layer 40 may be made of a metal material such as copper or aluminum to shield electromagnetic waves generated from the cable conductors. Can be done.
  • the polymer composition forming the insulating layer 20 and the sheath layer 40 may include a base resin, a flame retardant, a crosslinking aid, and the like dispersed in the resin, and may further include other additives such as an antioxidant and a lubricant. have.
  • the base resin includes a blending resin of polypropylene (PP) resin, polyolefin elastomer (POE) resin, ethylene propylene diene rubber (EPDM) and ethylene vinyl acetate (EVA) resin grafted with maleic anhydride. can do.
  • PP polypropylene
  • POE polyolefin elastomer
  • EPDM ethylene propylene diene rubber
  • EVA ethylene vinyl acetate
  • the polypropylene (PP) resin has a high melting point (Tm) of its own, excellent insulation resistance properties, oil resistance, and the like, and may include a propylene homopolymer and / or a propylene copolymer, and the propylene homopolymer may have a total monomer weight.
  • the propylene copolymer is propylene and ethylene or ⁇ -olefin having 4 to 12 carbon atoms, for example, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, Comonomers selected from 1-dodecene and combinations thereof, preferably copolymers with ethylene. This is because copolymerization of propylene and ethylene shows hard and flexible properties.
  • the propylene copolymer may include a random propylene copolymer and / or a block propylene copolymer, and the random propylene copolymer refers to a propylene copolymer in which an propylene monomer and another olefin monomer are arbitrarily alternately arranged.
  • the polypropylene (PP) resin may have a melting point (Tm) of 140 to 145 ° C and a specific gravity of 0.860 to 0.880. If the melting point of the polypropylene (PP) resin is less than 140 °C or specific gravity is less than 0.860, the insulation resistance properties of the insulation and sheath composition, mechanical properties such as wear resistance, heat resistance, etc. may be insufficient, while melting point is more than 145 °C or specific gravity If it is greater than 0.880, the flexibility of the insulation and sheath composition may be greatly reduced.
  • Tm melting point
  • the content of the polypropylene (PP) resin may be 15 to 25 parts by weight, preferably 17 to 24 parts by weight based on 100 parts by weight of the base resin.
  • the content of the polypropylene (PP) resin may be 22 to 32 parts by weight, preferably 24 to 29 parts by weight based on 100 parts by weight of the base resin.
  • the insulation resistance characteristics of the insulating layer 20 and the sheath layer 40, mechanical properties such as wear resistance, heat resistance, etc. may be insufficient. If it exceeds the reference content, the flexibility of the insulating layer 20 and the sheath layer 40 may be greatly reduced.
  • the polyolefin elastomer (POE) may further improve insulation resistance, oil resistance, and the like of the polymer composition, and may have a melting point (Tm) of 90 to 100 ° C. and specific gravity of 0.890 to 0.910. If the melting point of the polyolefin elastomer (POE) is less than 90 °C or specific gravity is less than 0.890, the mechanical properties such as insulation resistance characteristics, wear resistance, heat resistance, oil resistance, etc. of the polymer composition may be insufficient, while the melting point is more than 100 °C or specific gravity If it is more than 0.910, the flexibility, cold resistance, etc. of the polymer composition may be greatly reduced.
  • Tm melting point
  • the content of the polyolefin elastomer (POE) may be 30 to 50 parts by weight, preferably 37 to 45 parts by weight based on 100 parts by weight of the base resin, the sheath
  • the content of the polyolefin elastomer (POE) may be 25 to 35 parts by weight, preferably 29 to 33 parts by weight based on 100 parts by weight of the base resin.
  • the insulation resistance characteristics, oil resistance, etc. of the polymer composition may be insufficient, whereas when the polyolefin elastomer (POE) is exceeded, the flexibility, cold resistance, etc. of the polymer composition may be greatly reduced. .
  • the ethylene propylene diene rubber (EPDM) may further improve the flexibility, cold resistance, etc. of the polymer composition, specific gravity may be 0.870 to 0.890, Mooney viscosity (ML1 + 4 (125 ° C)) may be 20 to 40.
  • specific gravity of the ethylene propylene diene rubber (EPDM) is less than 0.870 or the Mooney viscosity (ML1 + 4 (125 ° C.)) is less than 20, the mechanical properties such as insulation resistance, wear resistance, and heat resistance of the polymer composition may be insufficient.
  • the specific gravity is greater than 0.890 or the Mooney viscosity (ML1 + 4 (125 ° C.)) is greater than 40, flexibility, flexibility, and cold resistance of the polymer composition may be insufficient.
  • the content of the ethylene propylene diene rubber may be 20 to 40 parts by weight, preferably 27 to 31 parts by weight based on 100 parts by weight of the base resin.
  • the content of the ethylene propylene diene rubber may be 27 to 35 parts by weight, preferably 29 to 33 parts by weight based on 100 parts by weight of the base resin. .
  • the content of the ethylene propylene diene rubber (EPDM) is lower than the reference content, the flexibility, cold resistance, etc. of the polymer composition may be lowered, whereas when the content of the ethylene propylene diene rubber (EPDM) is lower than the reference content, the mechanical properties such as insulation resistance and wear resistance of the polymer composition, Heat resistance and the like can be greatly reduced.
  • EPDM ethylene propylene diene rubber
  • the maleic anhydride-grafted ethylene vinyl acetate (EVA) resin may increase the compatibility of the base resin and the inorganic flame retardant to improve the flame retardancy and mechanical properties of the polymer composition.
  • the content of the maleic anhydride-grafted ethylene vinyl acetate (EVA) resin is 8 to 13 parts by weight, preferably 9 based on 100 parts by weight of the base resin.
  • the content of the maleic anhydride-grafted ethylene vinyl acetate (EVA) resin may be from about 10 parts by weight to 10 parts by weight, based on 100 parts by weight of the base resin. It may be 10 parts by weight, preferably 10 to 11 parts by weight.
  • the flame resistance, flexibility, and cold resistance of the polymer composition may be lowered, whereas the insulation resistance of the polymer composition that is higher than the reference content is decreased. Properties, mechanical properties such as abrasion resistance, heat resistance, and the like can be greatly reduced.
  • the flame retardant dispersed in the base resin may improve the flame retardancy of the insulating composition, and may include, for example, metal hydroxides such as magnesium hydroxide and aluminum hydroxide, and to improve dispersibility in the base resin. It may be surface-treated with a hydrophobic material such as silane, and the polymer composition forming the sheath layer 40 may further include a flame retardant as a flame retardant aid, the flame retardant in the resin compatible with the base resin Flame retardants can be added in the form of highly dispersed masterbatches.
  • the content of the flame retardant may be 80 to 100 parts by weight, preferably 87 to 95 parts by weight based on 100 parts by weight of the base resin, and the sheath layer 40
  • the content of the flame retardant may be 95 to 110 parts by weight, preferably 100 to 105 parts by weight based on 100 parts by weight of the base resin
  • the content of the flame retardant aid is based on 100 parts by weight of the base resin. 0.6 to 1.2, preferably 0.8 to 1.1 parts by weight.
  • the flame retardancy of the polymer composition may be insufficient, whereas when the content of the flame retardant and the flame retardant aid is exceeded, mechanical properties such as insulation resistance and wear resistance of the polymer composition may be greatly reduced. have.
  • the crosslinking aid may be added for irradiation crosslinking of the base resin, and may include, for example, a polyfunctional organic monomer.
  • the content of the crosslinking aid may be It may be 2 to 5 parts by weight, preferably 3 to 5 parts by weight based on 100 parts by weight of the base resin, and in the case of the polymer composition forming the sheath layer 40, the amount of the crosslinking aid is based on 100 parts by weight of the base resin. 2 to 5, preferably 3 to 4 parts by weight.
  • the crosslinking degree of the base resin may significantly lower the insulation resistance characteristics, mechanical properties such as wear resistance, heat resistance, etc., of the base resin, but exceeds the reference content. In the case of flexibility, cold resistance, etc. of the polymer composition may be lowered.
  • an antioxidant may be further added to ensure long-term heat resistance of the polymer composition, and the lubricant may be further added to improve compatibility of the base resin with other additives.
  • Prescription 1 Prescription 2 Prescription 3
  • Prescription 4 Prescription 5
  • Prescription 6 Prescription 7
  • Prescription 8 Prescription 9
  • Prescription 10 Resin 1 23 18 19 23 40 28 27 25 26 20 Resin 2 38 44 26 38 20 30 32 32 30 25 Resin 3 30 28 35 35 31 31 32 33 45 Resin 4 9 10 20 9 5 11 10 11 11 10 Resin 5 30
  • Flame retardant 1 90 90 90 90 105 100 120 110 Flame Retardant 2 0.8 1.0 1.1 0.9 Crosslinking aid 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3 3
  • Resin 1 Polypropylene (melting point: 141 ° C; specific gravity: 0.870)
  • Resin 2 polyolefin elastomer (melting point: 97 ° C; specific gravity: 0.902)
  • Resin 3 Ethylene propylene diene rubber (specific gravity: 0.880; Mooney viscosity (ML1 + 4 (125 ° C)): 21 ⁇ 29)
  • Resin 4 Ethylene vinyl acetate grafted with maleic anhydride
  • Resin 5 Ethylene vinyl acetate (melting point: 62 ° C; vinyl acetate content: 33 wt%)
  • -Flame retardant 1 Magnesium hydroxide coated with vinyl silane (BET specific surface area: 4.0 ⁇ 6.0 m2 / g)
  • TMPTMA trimethylolpropane trimethacrylate
  • the cable specimens of each of Examples and Comparative Examples were soaked in a beaker containing gasoline for 20 hours at room temperature, and then taken out, and the cable outer diameter was measured after 30 minutes. If the outer diameter after immersion exceeds 15% of the increased diameter compared to the outer diameter before immersion, it is less than the standard.
  • Insulation resistance was measured for each of the cable specimens of Examples and Comparative Examples according to the LV 216 standard. Insulation resistance measurement method was applied according to ISO 6722-1, but with 70% 1% saline instead of 70 °C water, and the insulation resistance between the sheath layer and the metal shielding layer was measured when evaluating the insulation resistance. The measured insulation resistance should exceed 10 13 ⁇ ⁇ mm.
  • Tensile strength at the time of 2% elongation was measured for each of the insulated specimens of the Examples and Comparative Examples using a UTM facility.
  • the level of flexibility is determined by comparing the tensile strength value at the time of 2% elongation of the prescription meeting the existing ISO standard.
  • each cable specimen according to the example and the comparative example was suspended according to the conductor size according to the conductor size, stayed for 4 hours in the oven at -40 °C, and wound around the rod of the specified standard to see if cracks occurred. Check it. If no cracking occurs, no breakdown shall occur during the application of a voltage of 1 kV in water for one minute.
  • a 0.45 mm diameter needle was reciprocated perpendicularly to the specimen with 7 N load applied to each of the cable specimens of Examples and Comparative Examples. If the sheath layer wears and the needle contacts the shielding layer, the evaluation is complete and the round trip frequency should be 1,500 or more.
  • each cable specimen and burner fix each cable specimen and burner at 45 ° angle from the ground, and arrange the specimen and burner to be perpendicular to each other. It must be digested within.
  • the cable specimen of Comparative Example 1 did not satisfy the flame retardancy because the sheath layer was formed from the polymer composition of Formulation 1 containing no flame retardant aid, the cable specimen of Comparative Example 2 is an insulating layer and sheath
  • the layers were formed from the polymer compositions of Formulations 6 and 5, each containing an excessive amount of polypropylene resin, resulting in poor heat resistance due to unstable properties after crosslinking due to the properties of the polypropylene, and deteriorated flexibility, and the cable specimen of Comparative Example 3 was a sheath layer.
  • the cable specimens of Examples 1 to 3 of the present invention satisfy all of the high insulation resistance properties and the flexibility in conflict with the standard required by the LV 216 standard. It was also confirmed that the physical properties were excellent.

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Abstract

The present invention relates to a polymer composition for a high-voltage cable, and a cable comprising an insulation layer and a sheath layer which are formed from the composition. Particularly, the present invention relates to a polymer composition which satisfies high insulation resistance characteristics required for a high-voltage cable and simultaneously satisfies a high level of flexibility in a trade-off relationship therewith, and which has excellent properties such as oil resistance, wear resistance, heat resistance, cold resistance and flame resistance. The present invention also relates to a cable comprising an insulation layer and a sheath layer which are formed from the polymer composition.

Description

고전압 케이블용 고분자 조성물 및 이로부터 형성된 절연층 및 시스층을 포함하는 케이블A cable comprising a polymer composition for a high voltage cable and an insulating layer and a sheath layer formed therefrom
본 발명은 고전압 케이블용 고분자 조성물 및 이로부터 형성된 절연층 및 시스층을 포함하는 케이블에 관한 것이다. 구체적으로, 본 발명은 고전압 케이블에서 요구되는 높은 절연저항 특성을 만족하는 동시에 이와 상충관계에 있는 고도의 유연성을 만족하고, 내유성, 내마모성, 내열성, 내한성, 난연성 등의 특성도 우수한 고분자 조성물 및 이로부터 형성된 절연층 및 시스층을 포함하는 케이블에 관한 것이다.The present invention relates to a cable comprising a polymer composition for a high voltage cable and an insulating layer and a sheath layer formed therefrom. Specifically, the present invention satisfies the high insulation resistance characteristics required for high voltage cables and at the same time has a high degree of flexibility in conflict with the polymer composition and excellent properties such as oil resistance, wear resistance, heat resistance, cold resistance, flame resistance, etc. A cable comprising an formed insulating layer and a sheath layer.
전기자동차용 고전압 케이블은 150℃급 600V에 해당하며 도체의 단면적에 따라 다양한 규격의 제품이 존재한다.High-voltage cable for electric vehicles corresponds to 150 ℃ class 600V, and there are products of various specifications depending on the cross-sectional area of the conductor.
종래 전기자동차용 고전압 케이블의 절연체 및 시스는 유연성을 확보하기 위하여 비닐 아세테이트(VA) 함량이 높은 에틸렌 비닐 아세테이트(EVA) 수지 또는 융점(Tm)이 낮은 폴리올레핀 엘라스토머(POE) 등을 적용하였다.Insulators and sheaths of high-voltage cables for electric vehicles are applied to ethylene vinyl acetate (EVA) resin having high vinyl acetate (VA) content or polyolefin elastomer (POE) having low melting point (Tm).
이러한 절연체 및 시스는 기존 국제 규격인 ISO 6722-1을 만족하지만 유럽의 유수 자동차 메이커 연합에서 기존 국제 규격인 ISO 6722-1을 기반으로 하여 새로 만든 국제 규격인 LV 216, 특히 금속차폐층을 갖는 케이블에 대한 규격인 LV 216-2에서 요구하는 절연저항 특성, 내유성 등을 만족하기 어렵다.These insulators and sheaths meet the existing international standard ISO 6722-1, but are based on the existing international standard ISO 6722-1 from the European Union of Leading Automobile Manufacturers, the LV 216, especially cables with metal shielding layers. It is difficult to satisfy insulation resistance, oil resistance, etc. required by LV 216-2.
예를 들어, ISO 6722-1 규격에서 요구하는 절연체의 체적저항은 10 9 Ω·㎜이나 LV 216 규격에서 요구하는 절연체의 체적저항은 10 13 Ω·㎜이고, 시스는 대개 외부 환경으로부터 케이블을 보호하기 위해 강도, 경도 등 기계적 특성의 확보를 우선시 하나, LV 216 규격에서는 시스 또한 절연체에 준하여 절연성능이 요구되며, 그 외에도 다양한 특성의 평가방법 및 판정기준이 변경되었다.For example, the volume resistance of an insulator required by the ISO 6722-1 standard is 10 9 Ω · mm, but the volume resistance of the insulator required by the LV 216 standard is 10 13 Ω · mm, and the sheath usually protects the cable from the external environment. In order to secure mechanical properties such as strength and hardness, priority is given to securing the mechanical properties such as strength and hardness. In addition, the sheath also requires insulation performance according to the insulator.
따라서, 종래 유연성을 확보하기 위해 비닐 아세테이트(VA) 함량이 높은 에틸렌 비닐 아세테이트(EVA) 수지 또는 융점이 낮은 폴리올레핀 엘라스토머(POE) 등을 적용한 절연체 및 시스는 LV 216 규격에서 요구하는 절연체의 체적저항을 만족할 수 없었고, 체적저항은 만족시키기 위해 융점(Tm)이 높은 자재로 대체하면 절연저항 특성은 개선될 수 있으나 절연체 및 시스의 유연성이 악화되어 전기자동차 배터리 케이블 제품으로서 적용하기 어려운 문제가 있다.Therefore, insulators and sheaths applied with ethylene vinyl acetate (EVA) resin having a high vinyl acetate (VA) content or polyolefin elastomer (POE) having a low melting point in order to secure the flexibility of the related art have a volume resistance of the insulator required by the LV 216 standard. In order to satisfy the volume resistance, if the material has a high melting point (Tm), the insulation resistance may be improved, but the flexibility of the insulator and the sheath may deteriorate, making it difficult to apply as an electric vehicle battery cable product.
또한, 자동차용 케이블은 다양한 오일에 대한 내유 특성을 만족하여야 하나, 절연체의 절연저항 특성과 유연성 확보를 위해 고분자 조성물의 수지를 변경하는 경우 내유성, 난연성 등이 큰 영향을 받게 되고, 수지에 따른 가교 방식과 가교도에 따라 내마모성 등의 기계적 특성, 내열성 등이 큰 영향을 받게 되어, 이들 모든 물성이 LV 216 규격을 만족시키는 것은 매우 어렵다.In addition, automotive cables should satisfy the oil resistance characteristics for various oils, but when the resin of the polymer composition is changed to ensure insulation resistance and flexibility of the insulator, oil resistance, flame retardancy, etc. are greatly affected, and crosslinking according to the resin Mechanical properties such as abrasion resistance, heat resistance, etc. are greatly influenced by the method and the degree of crosslinking, and it is very difficult for all these properties to meet the LV 216 standard.
따라서, LV 216 규격에서 요구하는 높은 절연저항 특성을 만족하는 동시에 이와 상충관계에 있는 고도의 유연성을 만족하고, 내유성, 내마모성, 내열성, 내한성, 난연성 등의 특성도 우수한 고분자 조성물 및 이로부터 형성된 절연층 및 시스층을 포함하는 케이블이 절실히 요구되고 있는 실정이다.Therefore, a polymer composition and an insulating layer formed therefrom that satisfy the high insulation resistance characteristics required by the LV 216 standard and at the same time have a high degree of flexibility and have excellent properties such as oil resistance, abrasion resistance, heat resistance, cold resistance, and flame resistance. And a cable including a sheath layer is urgently needed.
본 발명은 LV 216 규격에서 요구하는 높은 절연저항 특성을 만족하는 동시에 이와 상충관계에 있는 고도의 유연성을 만족하는 고분자 조성물 및 이로부터 형성된 절연층 및 시스층을 포함하는 케이블을 제공하는 것을 목적으로 한다.It is an object of the present invention to provide a cable comprising a polymer composition which satisfies the high insulation resistance properties required by the LV 216 standard and at the same time has a high degree of flexibility, and an insulation layer and a sheath layer formed therefrom. .
또한, 본 발명은 LV 216 규격에서 요구하는 우수한 내유성, 내마모성, 내열성, 내한성, 난연성 등의 특성을 만족하는 고분자 조성물 및 이로부터 형성된 절연층 및 시스층을 포함하는 케이블을 제공하는 것을 목적으로 한다.In addition, an object of the present invention is to provide a cable comprising a polymer composition which satisfies the characteristics such as excellent oil resistance, abrasion resistance, heat resistance, cold resistance, flame resistance, and the like, and an insulating layer and a sheath layer formed therefrom.
상기 과제를 해결하기 위해, 본 발명은,In order to solve the above problems, the present invention,
고전압 케이블용 고분자 조성물로서, 베이스 수지 및 첨가제를 포함하고, 상기 베이스 수지는 폴리프로필렌 수지, 폴리올레핀 엘라스토머, 에틸렌 프로필렌 디엔 고무 및 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지를 포함하고, 상기 고분자 조성물로부터 형성된 절연층 및 시스층은 체적저항이 10 13 Ω·㎜을 초과하는, 고분자 조성물을 제공한다.A polymer composition for a high voltage cable, comprising a base resin and an additive, the base resin comprising a polypropylene resin, a polyolefin elastomer, ethylene propylene diene rubber, and ethylene vinyl acetate resin grafted with maleic anhydride, The insulating layer and the sheath layer formed from the polymer composition provide a polymer composition having a volume resistance of more than 10 13 Ω · mm.
여기서, 상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 15 내지 25 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 30 내지 50 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 20 내지 40 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 8 내지 13 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.Here, the content of the polypropylene resin is 15 to 25 parts by weight, the content of the polyolefin elastomer is 30 to 50 parts by weight, the content of the ethylene propylene diene rubber is 20 to 40 parts by weight based on 100 parts by weight of the base resin. And the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 8 to 13 parts by weight, to provide a polymer composition.
또한, 상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 17 내지 24 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 37 내지 45 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 27 내지 31 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 9 내지 10 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.In addition, based on 100 parts by weight of the base resin, the content of the polypropylene resin is 17 to 24 parts by weight, the content of the polyolefin elastomer is 37 to 45 parts by weight, the content of the ethylene propylene diene rubber is 27 to 31 parts by weight And the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 9 to 10 parts by weight, to provide a polymer composition.
한편, 상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 22 내지 32 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 25 내지 35 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 27 내지 35 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 8 내지 13 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.On the other hand, based on 100 parts by weight of the base resin, the content of the polypropylene resin is 22 to 32 parts by weight, the content of the polyolefin elastomer is 25 to 35 parts by weight, the content of the ethylene propylene diene rubber is 27 to 35 parts by weight And the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 8 to 13 parts by weight, to provide a polymer composition.
여기서, 상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 24 내지 29 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 29 내지 33 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 29 내지 33 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 10 내지 11 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.Here, based on 100 parts by weight of the base resin, the content of the polypropylene resin is 24 to 29 parts by weight, the content of the polyolefin elastomer is 29 to 33 parts by weight, the content of the ethylene propylene diene rubber is 29 to 33 parts by weight And the content of the ethylene vinyl acetate resin grafted with maleic anhydride is 10 to 11 parts by weight, to provide a polymer composition.
그리고, 상기 폴리프로필렌 수지는 융점(Tm)이 140 내지 145℃이고 비중이 0.860 내지 0.880이며, 상기 폴리올레핀 엘라스토머는 융점(Tm)이 90 내지 100℃이고 비중이 0.890 내지 0.910인 것을 특징으로 하는, 고분자 조성물을 제공한다.The polypropylene resin has a melting point (Tm) of 140 to 145 ° C and a specific gravity of 0.860 to 0.880, and the polyolefin elastomer has a melting point (Tm) of 90 to 100 ° C and a specific gravity of 0.890 to 0.910. To provide a composition.
여기서, 상기 에틸렌 프로필렌 디엔 고무는 비중이 0.870 내지 0.890이고 무니점도(ML1+4(125℃))가 20 내지 40인 것을 특징으로 하는, 고분자 조성물을 제공한다.Here, the ethylene propylene diene rubber has a specific gravity of 0.870 to 0.890 and a Mooney viscosity (ML1 + 4 (125 ℃)) is characterized in that 20 to 40, to provide a polymer composition.
나아가, 상기 첨가제는 난연제, 가교조제, 산화방지제 및 활제로 이루어진 그룹으로부터 선택된 1종 이상의 첨가제를 포함하는 것을 특징으로 하는, 고분자 조성물을 제공한다.Further, the additive provides a polymer composition, characterized in that it comprises at least one additive selected from the group consisting of flame retardants, crosslinking aids, antioxidants and lubricants.
여기서, 상기 난연제는 수산화마그네슘 또는 수산화알루미늄을 포함하고, 상기 베이스 수지 100 중량부를 기준으로, 상기 난연제의 함량은 80 내지 100 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.Here, the flame retardant includes magnesium hydroxide or aluminum hydroxide, and based on 100 parts by weight of the base resin, the content of the flame retardant is 80 to 100 parts by weight, to provide a polymer composition.
또한, 상기 난연제의 함량은 상기 베이스 수지 100 중량부를 기준으로 87 내지 95 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.In addition, the content of the flame retardant provides a polymer composition, characterized in that 87 to 95 parts by weight based on 100 parts by weight of the base resin.
그리고, 상기 가교조제는 상기 베이스 수지의 조사가교용 다관능 유기모노머를 포함하고, 상기 가교조제의 함량은 상기 베이스 수지 100 중량부를 기준으로 2 내지 5 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.The crosslinking aid includes a crosslinking multifunctional organic monomer of the base resin, and the content of the crosslinking aid is 2 to 5 parts by weight based on 100 parts by weight of the base resin. .
한편, 상기 첨가제는 난연제, 난연보조제, 가교조제, 산화방지제 및 활제로 이루어진 그룹으로부터 선택된 1종 이상의 첨가제를 포함하는 것을 특징으로 하는, 고분자 조성물을 제공한다.On the other hand, the additive provides a polymer composition, characterized in that it comprises one or more additives selected from the group consisting of flame retardants, flame retardant aids, crosslinking aids, antioxidants and lubricants.
여기서, 상기 난연제는 수산화마그네슘 또는 수산화알루미늄을 포함하고, 상기 난연보조제는 적인 난연제를 포함하며, 상기 베이스 수지 100 중량부를 기준으로, 상기 난연제의 함량은 95 내지 110 중량부이고, 상기 난연보조제의 함량은 0.6 내지 1.2 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.Here, the flame retardant includes magnesium hydroxide or aluminum hydroxide, the flame retardant aid comprises a flame retardant, based on 100 parts by weight of the base resin, the content of the flame retardant is 95 to 110 parts by weight, the content of the flame retardant aid Silver is 0.6 to 1.2 parts by weight, to provide a polymer composition.
또한, 상기 베이스 수지 100 중량부를 기준으로, 상기 난연제의 함량은 100 내지 105 중량부이고, 상기 난연보조제의 함량은 0.8 내지 1.1 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.In addition, based on 100 parts by weight of the base resin, the content of the flame retardant is from 100 to 105 parts by weight, the content of the flame retardant aid is characterized in that the polymer composition, which provides 0.8 to 1.1 parts by weight.
그리고, 상기 가교조제는 상기 베이스 수지의 조사가교용 다관능 유기모노머를 포함하고, 상기 가교조제의 함량은 상기 베이스 수지 100 중량부를 기준으로 2 내지 5 중량부인 것을 특징으로 하는, 고분자 조성물을 제공한다.The crosslinking aid includes a crosslinking multifunctional organic monomer of the base resin, and the content of the crosslinking aid is 2 to 5 parts by weight based on 100 parts by weight of the base resin. .
한편, 도체; 상기 도체를 감싸고 제1항 내지 제3항 중 어느 한 항의 고분자 조성물로부터 형성된 절연층; 상기 절연층을 감싸는 금속차폐층; 및 상기 금속차폐층을 감싸고 제1항, 제4항 및 제5항 중 어느 한 항의 고분자 조성물로부터 형성된 시스층을 포함하는 케이블을 제공한다.Meanwhile, conductors; An insulating layer surrounding the conductor and formed from the polymer composition of any one of claims 1 to 3; A metal shielding layer surrounding the insulating layer; And a sheath layer surrounding the metal shielding layer and formed from the polymer composition of any one of claims 1, 4 and 5.
본 발명의 고전압 케이블용 고분자 조성물은 특정 수지를 특정 배합비로 포함하는 베이스 수지를 적용함으로써 LV 216 규격에서 요구하는 높은 절연저항 특성을 만족하는 동시에 이와 상충관계에 있는 고도의 유연성을 만족하는 우수한 효과를 나타낸다.The polymer composition for a high voltage cable of the present invention has a superior effect of satisfying the high insulation resistance required at the same time as the LV 216 standard by applying a base resin containing a specific resin at a specific compounding ratio, and at the same time having a high flexibility. Indicates.
또한, 본 발명의 고전압 케이블용 고분자 조성물은 특정 수지를 특정 배합비로 포함하는 베이스 수지를 적용하고 특정 난연제, 가교방식, 가교제 등의 적용을 통해 LV 216 규격에서 요구하는 우수한 내유성, 내마모성, 내열성, 내한성, 난연성 등의 특성을 만족하는 우수한 효과를 나타낸다.In addition, the polymer composition for a high voltage cable of the present invention is applied to the base resin containing a specific resin in a specific compounding ratio, and excellent oil resistance, wear resistance, heat resistance, cold resistance required by the LV 216 standard through the application of a specific flame retardant, crosslinking method, crosslinking agent, etc. It shows an excellent effect of satisfying properties such as and flame retardancy.
도 1은 본 발명에 따른 고분자 조성물로부터 형성된 절연층 및 시스층을 포함하는 고전압 케이블의 하나의 실시예에 관한 단면 구조를 개략적으로 도시한 것이다.1 schematically shows a cross-sectional structure of one embodiment of a high voltage cable comprising an insulating layer and a sheath layer formed from a polymer composition according to the present invention.
이하, 본 발명의 바람직한 실시예들을 상세히 설명하기로 한다. 그러나, 본 발명은 여기서 설명된 실시예들에 한정되지 않고 다른 형태로 구체화될 수도 있다. 오히려, 여기서 소개되는 실시예들은 개시된 내용이 철저하고 완전해질 수 있도록, 그리고 당업자에게 본 발명의 사상이 충분히 전달될 수 있도록 하기 위해 제공되어지는 것이다. 명세서 전체에 걸쳐서 동일한 참조번호들은 동일한 구성요소들을 나타낸다.Hereinafter, preferred embodiments of the present invention will be described in detail. However, the invention is not limited to the embodiments described herein but may be embodied in other forms. Rather, the embodiments introduced herein are provided so that the disclosure may be made thorough and complete, and to fully convey the spirit of the present invention to those skilled in the art. Like numbers refer to like elements throughout.
도 1은 본 발명에 따른 고분자 조성물로부터 형성된 절연층 및 시스층을 포함하는 고전압 케이블의 하나의 실시예에 관한 단면 구조를 개략적으로 도시한 것이다.1 schematically shows a cross-sectional structure of one embodiment of a high voltage cable comprising an insulating layer and a sheath layer formed from a polymer composition according to the present invention.
도 1에 도시된 바와 같이, 본 발명에 따른 고전압 케이블은 도체(10), 상기 도체(10)를 감싸고 본 발명의 고분자 조성물로부터 형성된 절연층(20), 상기 절연층(20)을 감싸는 금속차폐층(30) 및 상기 금속차폐층(40)을 감싸고 본 발명의 고분자 조성물로부터 형성된 시스층(40)을 포함할 수 있다.As shown in FIG. 1, the high voltage cable according to the present invention includes a conductor 10, an insulation layer 20 formed around the conductor 10 and formed from the polymer composition of the present invention, and a metal shield surrounding the insulation layer 20. The layer 30 and the metal shielding layer 40 may include a sheath layer 40 formed from the polymer composition of the present invention.
상기 도체(10)는 케이블의 유연성 확보를 위해 구리 세선이 연합된 구리 연선을 적용할 수 있고, 상기 금속차폐층(40)은 케이블 도체로부터 발생한 전자파를 차폐하기 위해 구리, 알루미늄 등의 금속 소재로 이루어질 수 있다.The conductor 10 may apply a copper stranded wire combined with copper fine wires to secure flexibility of the cable, and the metal shielding layer 40 may be made of a metal material such as copper or aluminum to shield electromagnetic waves generated from the cable conductors. Can be done.
상기 절연층(20) 및 상기 시스층(40)을 형성하는 고분자 조성물은 베이스 수지와 상기 수지 내에 분산된 난연제, 가교조제 등을 포함하고, 추가로 산화방지제, 활제 등의 기타 첨가제를 포함할 수 있다.The polymer composition forming the insulating layer 20 and the sheath layer 40 may include a base resin, a flame retardant, a crosslinking aid, and the like dispersed in the resin, and may further include other additives such as an antioxidant and a lubricant. have.
여기서, 상기 베이스 수지는 폴리프로필렌(PP) 수지, 폴리올레핀 엘라스토머(POE) 수지, 에틸렌 프로필렌 디엔 고무(EPDM) 및 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트(EVA) 수지의 블렌딩 수지를 포함할 수 있다.Here, the base resin includes a blending resin of polypropylene (PP) resin, polyolefin elastomer (POE) resin, ethylene propylene diene rubber (EPDM) and ethylene vinyl acetate (EVA) resin grafted with maleic anhydride. can do.
*상기 폴리프로필렌(PP) 수지는 자체적인 융점(Tm)이 높아 절연저항 특성, 내유성 등이 우수하고, 프로필렌 단독중합체 및/또는 프로필렌 공중합체를 포함할 수 있으며, 상기 프로필렌 단독중합체는 단량체 총 중량을 기준으로 99 중량% 이상, 바람직하게는 99.5 중량% 이상의 프로필렌의 중합에 의해 형성되는 폴리프로필렌을 의미한다.* The polypropylene (PP) resin has a high melting point (Tm) of its own, excellent insulation resistance properties, oil resistance, and the like, and may include a propylene homopolymer and / or a propylene copolymer, and the propylene homopolymer may have a total monomer weight. Polypropylene formed by polymerization of at least 99% by weight, preferably at least 99.5% by weight, of propylene.
상기 프로필렌 공중합체는 프로필렌과 에틸렌 또는 탄소수 4 내지 12의 α-올레핀, 예를 들어, 1-부텐, 1-펜텐, 4-메틸-1-펜텐, 1-헥센, 1-옥텐, 1-데센, 1-도데센 및 이들의 조합으로부터 선택되는 공단량체 등, 바람직하게는 에틸렌과의 공중합체를 포함할 수 있다. 프로필렌과 에틸렌을 공중합시키면 단단하면서 유연한 성질을 나타내기 때문이다.The propylene copolymer is propylene and ethylene or α-olefin having 4 to 12 carbon atoms, for example, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, Comonomers selected from 1-dodecene and combinations thereof, preferably copolymers with ethylene. This is because copolymerization of propylene and ethylene shows hard and flexible properties.
상기 프로필렌 공중합체는 랜덤 프로필렌 공중합체 및/또는 블록 프로필렌 공중합체를 포함할 수 있고, 상기 랜덤 프로필렌 공중합체는 프로필렌 단량체와 다른 올레핀 단량체가 임의로 교호 배열되어 이루어진 프로필렌 공중합체를 의미한다.The propylene copolymer may include a random propylene copolymer and / or a block propylene copolymer, and the random propylene copolymer refers to a propylene copolymer in which an propylene monomer and another olefin monomer are arbitrarily alternately arranged.
상기 폴리프로필렌(PP) 수지는 융점(Tm)이 140~145℃이고, 비중이 0.860 내지 0.880일 수 있다. 상기 폴리프로필렌(PP) 수지의 융점이 140℃ 미만이거나 비중이 0.860 미만인 경우 절연 및 시스 조성물의 절연저항 특성, 내마모성 등의 기계적 특성, 내열성 등이 불충분할 수 있는 반면, 융점이 145℃ 초과이거나 비중이 0.880 초과인 경우 절연 및 시스 조성물의 유연성이 크게 저하될 수 있다.The polypropylene (PP) resin may have a melting point (Tm) of 140 to 145 ° C and a specific gravity of 0.860 to 0.880. If the melting point of the polypropylene (PP) resin is less than 140 ℃ or specific gravity is less than 0.860, the insulation resistance properties of the insulation and sheath composition, mechanical properties such as wear resistance, heat resistance, etc. may be insufficient, while melting point is more than 145 ℃ or specific gravity If it is greater than 0.880, the flexibility of the insulation and sheath composition may be greatly reduced.
상기 절연층(20)을 형성하는 고분자 조성물의 경우, 상기 폴리프로필렌(PP) 수지의 함량은 상기 베이스 수지 100 중량부를 기준으로 15 내지 25 중량부, 바람직하게는 17 내지 24 중량부일 수 있고, 상기 시스층(40)을 형성하는 고분자 조성물의 경우, 상기 폴리프로필렌(PP) 수지의 함량은 상기 베이스 수지 100 중량부를 기준으로 22 내지 32 중량부, 바람직하게는 24 내지 29 중량부일 수 있다.In the case of the polymer composition for forming the insulating layer 20, the content of the polypropylene (PP) resin may be 15 to 25 parts by weight, preferably 17 to 24 parts by weight based on 100 parts by weight of the base resin. In the case of the polymer composition forming the sheath layer 40, the content of the polypropylene (PP) resin may be 22 to 32 parts by weight, preferably 24 to 29 parts by weight based on 100 parts by weight of the base resin.
상기 폴리프로필렌(PP) 수지의 함량이 상기 기준함량 미달인 경우 상기 절연층(20) 및 상기 시스층(40)의 절연저항 특성, 내마모성 등의 기계적 특성, 내열성 등이 불충분할 수 있는 반면, 상기 기준함량 초과인 경우 상기 절연층(20) 및 상기 시스층(40)의 유연성이 크게 저하될 수 있다.When the content of the polypropylene (PP) resin is less than the reference content, the insulation resistance characteristics of the insulating layer 20 and the sheath layer 40, mechanical properties such as wear resistance, heat resistance, etc. may be insufficient. If it exceeds the reference content, the flexibility of the insulating layer 20 and the sheath layer 40 may be greatly reduced.
상기 폴리올레핀 엘라스토머(POE)는 고분자 조성물의 절연저항 특성, 내유성 등을 등을 추가로 향상시킬 수 있으며, 융점(Tm)이 90 내지 100℃이고, 비중이 0.890 내지 0.910일 수 있다. 상기 폴리올레핀 엘라스토머(POE)의 융점이 90℃ 미만이거나 비중이 0.890 미만인 경우 고분자 조성물의 절연저항 특성, 내마모성 등의 기계적 특성, 내열성, 내유성 등이 불충분할 수 있는 반면, 융점이 100℃ 초과이거나 비중이 0.910 초과인 경우 고분자 조성물의 유연성, 내한성 등이 크게 저하될 수 있다.The polyolefin elastomer (POE) may further improve insulation resistance, oil resistance, and the like of the polymer composition, and may have a melting point (Tm) of 90 to 100 ° C. and specific gravity of 0.890 to 0.910. If the melting point of the polyolefin elastomer (POE) is less than 90 ℃ or specific gravity is less than 0.890, the mechanical properties such as insulation resistance characteristics, wear resistance, heat resistance, oil resistance, etc. of the polymer composition may be insufficient, while the melting point is more than 100 ℃ or specific gravity If it is more than 0.910, the flexibility, cold resistance, etc. of the polymer composition may be greatly reduced.
상기 절연층(20)을 형성하는 고분자 조성물의 경우, 상기 폴리올레핀 엘라스토머(POE)의 함량은 상기 베이스 수지 100 중량부를 기준으로 30 내지 50 중량부, 바람직하게는 37 내지 45 중량부일 수 있고, 상기 시스층(40)을 형성하는 고분자 조성물의 경우, 상기 폴리올레핀 엘라스토머(POE)의 함량은 상기 베이스 수지 100 중량부를 기준으로 25 내지 35 중량부, 바람직하게는 29 내지 33 중량부일 수 있다.In the case of the polymer composition forming the insulating layer 20, the content of the polyolefin elastomer (POE) may be 30 to 50 parts by weight, preferably 37 to 45 parts by weight based on 100 parts by weight of the base resin, the sheath In the case of the polymer composition forming the layer 40, the content of the polyolefin elastomer (POE) may be 25 to 35 parts by weight, preferably 29 to 33 parts by weight based on 100 parts by weight of the base resin.
상기 폴리올레핀 엘라스토머(POE)의 함량이 상기 기준함량 미달인 경우 고분자 조성물의 절연저항 특성, 내유성 등이 불충분할 수 있는 반면, 상기 기준함량 초과인 경우 고분자 조성물의 유연성, 내한성 등이 크게 저하될 수 있다.When the content of the polyolefin elastomer (POE) is less than the reference content, the insulation resistance characteristics, oil resistance, etc. of the polymer composition may be insufficient, whereas when the polyolefin elastomer (POE) is exceeded, the flexibility, cold resistance, etc. of the polymer composition may be greatly reduced. .
상기 에틸렌 프로필렌 디엔 고무(EPDM)는 고분자 조성물의 유연성, 내한성 등을 추가로 향상시킬 수 있으며, 비중이 0.870 내지 0.890이고, 무니점도(ML1+4(125℃))가 20 내지 40일 수 있다. 상기 에틸렌 프로필렌 디엔 고무(EPDM)의 비중이 0.870 미만이거나 무니점도(ML1+4(125℃))가 20 미만인 경우 고분자 조성물의 절연저항 특성, 내마모성 등의 기계적 특성, 내열성 등이 불충분할 수 있는 반면, 비중이 0.890 초과이거나 무니점도(ML1+4(125℃))가 40 초과인 경우 고분자 조성물의 유연성, 굴곡성, 내한성 등이 불충분할 수 있다.The ethylene propylene diene rubber (EPDM) may further improve the flexibility, cold resistance, etc. of the polymer composition, specific gravity may be 0.870 to 0.890, Mooney viscosity (ML1 + 4 (125 ° C)) may be 20 to 40. When the specific gravity of the ethylene propylene diene rubber (EPDM) is less than 0.870 or the Mooney viscosity (ML1 + 4 (125 ° C.)) is less than 20, the mechanical properties such as insulation resistance, wear resistance, and heat resistance of the polymer composition may be insufficient. When the specific gravity is greater than 0.890 or the Mooney viscosity (ML1 + 4 (125 ° C.)) is greater than 40, flexibility, flexibility, and cold resistance of the polymer composition may be insufficient.
*상기 절연층(20)을 형성하는 고분자 조성물의 경우, 상기 에틸렌 프로필렌 디엔 고무(EPDM)의 함량은 상기 베이스 수지 100 중량부를 기준으로 20 내지 40 중량부, 바람직하게는 27 내지 31 중량부일 수 있고, 상기 시스층(40)을 형성하는 고분자 조성물의 경우, 상기 에틸렌 프로필렌 디엔 고무(EPDM)의 함량은 상기 베이스 수지 100 중량부를 기준으로 27 내지 35 중량부, 바람직하게는 29 내지 33 중량부일 수 있다.In the case of the polymer composition forming the insulating layer 20, the content of the ethylene propylene diene rubber (EPDM) may be 20 to 40 parts by weight, preferably 27 to 31 parts by weight based on 100 parts by weight of the base resin. In the case of the polymer composition forming the sheath layer 40, the content of the ethylene propylene diene rubber (EPDM) may be 27 to 35 parts by weight, preferably 29 to 33 parts by weight based on 100 parts by weight of the base resin. .
상기 에틸렌 프로필렌 디엔 고무(EPDM)의 함량이 상기 기준함량 미달인 경우 고분자 조성물의 유연성, 내한성 등이 저하될 수 있는 반면, 상기 기준함량 초과인 경우 고분자 조성물의 절연저항 특성, 내마모성 등의 기계적 특성, 내열성 등이 크게 저하될 수 있다.When the content of the ethylene propylene diene rubber (EPDM) is lower than the reference content, the flexibility, cold resistance, etc. of the polymer composition may be lowered, whereas when the content of the ethylene propylene diene rubber (EPDM) is lower than the reference content, the mechanical properties such as insulation resistance and wear resistance of the polymer composition, Heat resistance and the like can be greatly reduced.
상기 말레산 무수물이 그라프트된 에틸렌 비닐 아세테이트(EVA) 수지는 상기 베이스 수지와 무기계 난연제의 상용성을 증대시켜 고분자 조성물의 난연성 및 기계적 특성을 향상시킬 수 있다.The maleic anhydride-grafted ethylene vinyl acetate (EVA) resin may increase the compatibility of the base resin and the inorganic flame retardant to improve the flame retardancy and mechanical properties of the polymer composition.
상기 절연층(20)을 형성하는 고분자 조성물의 경우, 상기 말레산 무수물이 그라프트된 에틸렌 비닐 아세테이트(EVA) 수지의 함량은 상기 베이스 수지 100 중량부를 기준으로 8 내지 13 중량부, 바람직하게는 9 내지 10 중량부일 수 있고, 상기 시스층(40)을 형성하는 고분자 조성물의 경우, 상기 말레산 무수물이 그라프트된 에틸렌 비닐 아세테이트(EVA) 수지의 함량은 상기 베이스 수지 100 중량부를 기준으로 8 내지 13 중량부, 바람직하게는 10 내지 11 중량부일 수 있다.In the case of the polymer composition forming the insulating layer 20, the content of the maleic anhydride-grafted ethylene vinyl acetate (EVA) resin is 8 to 13 parts by weight, preferably 9 based on 100 parts by weight of the base resin. In the case of the polymer composition forming the sheath layer 40, the content of the maleic anhydride-grafted ethylene vinyl acetate (EVA) resin may be from about 10 parts by weight to 10 parts by weight, based on 100 parts by weight of the base resin. It may be 10 parts by weight, preferably 10 to 11 parts by weight.
상기 말레산 무수물이 그라프트된 에틸렌 비닐 아세테이트(EVA) 수지의 함량이 상기 기준함량 미달인 경우 고분자 조성물의 난연성, 유연성, 내한성 등이 저하될 수 있는 반면, 상기 기준함량 초과인 고분자 조성물의 절연저항 특성, 내마모성 등의 기계적 특성, 내열성 등이 크게 저하될 수 있다.When the content of the ethylene vinyl acetate (EVA) resin grafted with maleic anhydride is lower than the reference content, the flame resistance, flexibility, and cold resistance of the polymer composition may be lowered, whereas the insulation resistance of the polymer composition that is higher than the reference content is decreased. Properties, mechanical properties such as abrasion resistance, heat resistance, and the like can be greatly reduced.
상기 베이스 수지에 분산되는 난연제는 절연 조성물의 난연성을 향상시킬 수 있고, 예를 들어, 수산화마그네슘, 수산화알루미늄 등의 금속수산화물을 포함할 수 있고, 상기 베이스 수지 내에서의 분산성을 향상시키기 위해 비닐실란 등의 소수성 물질로 표면처리될 수 있으며, 상기 시스층(40)을 형성하는 고분자 조성물의 경우 난연보조제로서 적인 난연제를 추가로 포함할 수 있고, 상기 적인 난연제는 상기 베이스 수지와 상용 가능한 수지 내에 적인 난연제가 고농도로 분산된 마스터배치 형태로 첨가될 수 있다.The flame retardant dispersed in the base resin may improve the flame retardancy of the insulating composition, and may include, for example, metal hydroxides such as magnesium hydroxide and aluminum hydroxide, and to improve dispersibility in the base resin. It may be surface-treated with a hydrophobic material such as silane, and the polymer composition forming the sheath layer 40 may further include a flame retardant as a flame retardant aid, the flame retardant in the resin compatible with the base resin Flame retardants can be added in the form of highly dispersed masterbatches.
상기 절연층(20)을 형성하는 고분자 조성물의 경우, 상기 난연제의 함량은 상기 베이스 수지 100 중량부를 기준으로 80 내지 100 중량부, 바람직하게는 87 내지 95 중량부일 수 있고, 상기 시스층(40)을 형성하는 고분자 조성물의 경우, 상기 난연제의 함량은 상기 베이스 수지 100 중량부를 기준으로 95 내지 110 중량부, 바람직하게는 100 내지 105 중량부일 수 있고, 난연보조제의 함량은 상기 베이스 수지 100 중량부를 기준으로 0.6 내지 1.2, 바람직하게는 0.8 내지 1.1 중량부일 수 있다.In the case of the polymer composition forming the insulating layer 20, the content of the flame retardant may be 80 to 100 parts by weight, preferably 87 to 95 parts by weight based on 100 parts by weight of the base resin, and the sheath layer 40 In the case of forming the polymer composition, the content of the flame retardant may be 95 to 110 parts by weight, preferably 100 to 105 parts by weight based on 100 parts by weight of the base resin, and the content of the flame retardant aid is based on 100 parts by weight of the base resin. 0.6 to 1.2, preferably 0.8 to 1.1 parts by weight.
상기 난연제 및 상기 난연보조제의 함량이 상기 기준함량 미달인 경우 고분자 조성물의 난연성이 불충분할 수 있는 반면, 상기 기준함량 초과인 경우 고분자 조성물의 절연저항 특성, 내마모성 등의 기계적 특성 등이 크게 저하될 수 있다.When the content of the flame retardant and the flame retardant auxiliary agent is less than the reference content, the flame retardancy of the polymer composition may be insufficient, whereas when the content of the flame retardant and the flame retardant aid is exceeded, mechanical properties such as insulation resistance and wear resistance of the polymer composition may be greatly reduced. have.
상기 가교조제는 상기 베이스 수지의 조사가교를 위해 첨가될 수 있고, 예를 들어 다관능 유기모노머를 포함할 수 있으며, 상기 절연층(20)을 형성하는 고분자 조성물의 경우 상기 가교조제의 함량은 상기 베이스 수지 100 중량부를 기준으로 2 내지 5 중량부, 바람직하게는 3 내지 5 중량부일 수 있고, 상기 시스층(40)을 형성하는 고분자 조성물의 경우 상기 가교조제의 함량은 상기 베이스 수지 100 중량부를 기준으로 2 내지 5, 바람직하게는 3 내지 4 중량부일 수 있다.The crosslinking aid may be added for irradiation crosslinking of the base resin, and may include, for example, a polyfunctional organic monomer. In the case of the polymer composition forming the insulating layer 20, the content of the crosslinking aid may be It may be 2 to 5 parts by weight, preferably 3 to 5 parts by weight based on 100 parts by weight of the base resin, and in the case of the polymer composition forming the sheath layer 40, the amount of the crosslinking aid is based on 100 parts by weight of the base resin. 2 to 5, preferably 3 to 4 parts by weight.
여기서, 상기 가교조제의 함량이 상기 기준함량 미달인 경우 상기 베이스 수지의 가교도가 불충분해 고분자 조성물의 절연저항 특성, 내나모성 등의 기계적 특성, 내열성 등이 크게 저하될 수 있는 반면, 상기 기준함량 초과인 경우 고분자 조성물의 유연성, 내한성 등이 저하될 수 있다.Here, when the content of the crosslinking aid is less than the reference content, the crosslinking degree of the base resin may significantly lower the insulation resistance characteristics, mechanical properties such as wear resistance, heat resistance, etc., of the base resin, but exceeds the reference content. In the case of flexibility, cold resistance, etc. of the polymer composition may be lowered.
상기 기타 첨가제로서 산화방지제는 고분자 조성물의 장기 내열성 확보를 위해 추가로 첨가될 수 있고, 활제는 베이스 수지와 다른 첨가제의 상용성 향상을 위해 추가로 첨가될 수 있다.As the other additive, an antioxidant may be further added to ensure long-term heat resistance of the polymer composition, and the lubricant may be further added to improve compatibility of the base resin with other additives.
[실시예]EXAMPLE
1. 제조예1. Manufacturing Example
아래 표 1에 나타난 조성으로 3L 니더(kneader) 설비를 이용하여 150℃에서 30분간 배합함으로써 고분자 조성물을 제조한 후 이로부터 45 mm 압출기를 이용하여 아래 표 2에 나타난 절연층 및 시스층을 형성함으로써 케이블 시편을 제조했다. 케이블 시편 제조시 도체는 연동선 6SQ를 적용했고, 고분자 조성물로부터 절연층 및 시스층 형성시 압출 후 조사가교를 수행했으며, 절연층과 시스층 사이에 금속차폐층이 배치된다. 아래 표 1에 기재된 함량의 단위는 중량부이고, 공통으로 첨가되는 첨가제의 일부는 기재를 생략했다.By preparing the polymer composition by mixing for 30 minutes at 150 ℃ using a 3L kneader equipment with the composition shown in Table 1 below by using the 45 mm extruder to form the insulating layer and the sheath layer shown in Table 2 below Cable specimens were prepared. When the cable specimens were manufactured, the conductor was applied with an interlocking line 6SQ, and after cross-extrusion irradiation crosslinking was performed when the insulating layer and the sheath layer were formed from the polymer composition, a metal shielding layer was disposed between the insulating layer and the sheath layer. The unit of the content shown in Table 1 below is parts by weight, and a part of the additives commonly added is omitted.
처방1Prescription 1 처방2Prescription 2 처방3Prescription 3 처방4Prescription 4 처방5Prescription 5 처방6Prescription 6 처방7Prescription 7 처방8Prescription 8 처방9Prescription 9 처방10 Prescription 10
수지1Resin 1 2323 1818 1919 2323 4040 2828 2727 2525 2626 2020
수지2Resin 2 3838 4444 2626 3838 2020 3030 3232 3232 3030 2525
수지3Resin 3 3030 2828 3535 3535 3131 3131 3232 3333 4545
수지4Resin 4 99 1010 2020 99 55 1111 1010 1111 1111 1010
수지5Resin 5 3030
난연제1Flame retardant 1 9090 9090 9090 9090 9090 105105 100100 100100 120120 110110
난연제2Flame Retardant 2 0.80.8 1.01.0 1.11.1 0.90.9
가교조제Crosslinking aid 33 33 33 33 33 33 33 33 33 33
- 수지1 : 폴리프로필렌(융점 : 141℃; 비중 : 0.870)Resin 1: Polypropylene (melting point: 141 ° C; specific gravity: 0.870)
- 수지2 : 폴리올레핀 엘라스토머(융점 : 97℃; 비중 : 0.902)Resin 2: polyolefin elastomer (melting point: 97 ° C; specific gravity: 0.902)
- 수지3 : 에틸렌 프로필렌 디엔 고무(비중 : 0.880; 무니점도(ML1+4(125℃)) : 21~29)Resin 3: Ethylene propylene diene rubber (specific gravity: 0.880; Mooney viscosity (ML1 + 4 (125 ° C)): 21 ~ 29)
- 수지4 : 말레산 무수물이 그라프트된 에틸렌 비닐 아세테이트Resin 4: Ethylene vinyl acetate grafted with maleic anhydride
- 수지5 : 에틸렌 비닐 아세테이트(융점 : 62℃; 비닐아세테이트 함량 : 33 중량%)Resin 5: Ethylene vinyl acetate (melting point: 62 ° C; vinyl acetate content: 33 wt%)
- 난연제1 : 비닐 실란이 코팅된 수산화마그네슘(BET 비표면적 : 4.0~6.0 ㎡/g)-Flame retardant 1: Magnesium hydroxide coated with vinyl silane (BET specific surface area: 4.0 ~ 6.0 ㎡ / g)
- 난연제2 : 적인 난연보조제-Flame retardant 2: fire retardant supplement
- 가교조제 : 트리메틸올프로판 트리메타크릴레이트(TMPTMA)-Crosslinking aid: trimethylolpropane trimethacrylate (TMPTMA)
실시예1Example 1 실시예2Example 2 실시예3Example 3 비교예1Comparative Example 1 비교예2Comparative Example 2 비교예3Comparative Example 3 비교예4Comparative Example 4 비교예5Comparative Example 5 비교예6Comparative Example 6
절연층Insulation layer 처방1Prescription 1 처방1Prescription 1 처방2Prescription 2 처방1Prescription 1 처방6Prescription 6 처방2Prescription 2 처방3Prescription 3 처방2Prescription 2 처방1Prescription 1
시스층Sheath layer 처방6Prescription 6 처방7Prescription 7 처방8Prescription 8 처방1Prescription 1 처방5Prescription 5 처방4Prescription 4 처방6Prescription 6 처방9Prescription 9 처방10 Prescription 10
2. 물성 평가2. Property evaluation
1) 내유성 평가1) Oil resistance evaluation
LV 216 규격에 의거하여 실시예 및 비교예 각각의 케이블 시편을 가솔린이 담긴 비이커에 침유시킨 상태로 상온에서 20 시간 동안 체류시킨 뒤 꺼내어 30분 후 케이블 외경을 측정한다. 침유 후 외경이 침유 전 외경과 비교하여 늘어난 외경이 15%를 초과하면 기준 미달이다.In accordance with the LV 216 standard, the cable specimens of each of Examples and Comparative Examples were soaked in a beaker containing gasoline for 20 hours at room temperature, and then taken out, and the cable outer diameter was measured after 30 minutes. If the outer diameter after immersion exceeds 15% of the increased diameter compared to the outer diameter before immersion, it is less than the standard.
2) 절연저항 평가2) Insulation resistance evaluation
LV 216 규격에 의거하여 실시예 및 비교예 각각의 케이블 시편에 대해 절연저항을 측정했다. 절연저항 측정방법은 ISO 6722-1을 따르되 70℃의 물 대신 70℃의 1 % 염수로 적용했고, 절연저항 평가시 시스층과 금속차폐층 사이의 절연저항을 측정한다. 측정한 절연저항이 10 13 Ω·㎜을 초과해야 한다.Insulation resistance was measured for each of the cable specimens of Examples and Comparative Examples according to the LV 216 standard. Insulation resistance measurement method was applied according to ISO 6722-1, but with 70% 1% saline instead of 70 ℃ water, and the insulation resistance between the sheath layer and the metal shielding layer was measured when evaluating the insulation resistance. The measured insulation resistance should exceed 10 13 Ω · mm.
3) 유연성 평가3) Flexibility Assessment
UTM 설비를 이용하여 실시예 및 비교예 각각의 절연 시편에 대해 2% 신율 시점의 인장강도를 측정했다. 기존 ISO 규격을 만족하는 처방의 2% 신율 시점의 인장강도 값과 비교하여 유연성 수준을 판단한다.Tensile strength at the time of 2% elongation was measured for each of the insulated specimens of the Examples and Comparative Examples using a UTM facility. The level of flexibility is determined by comparing the tensile strength value at the time of 2% elongation of the prescription meeting the existing ISO standard.
4) 내열성 평가4) Heat resistance evaluation
LV 216 규격에 의거하여 실시예 및 비교예 각각의 케이블 시편에 대해 장기/단기 내열성을 평가했고, 장기 내열성은 시편을 150℃에서 3,000 시간 동안 체류시킨 후 1분간 수중에서 1kV의 전압을 인가하는 동안 절연파괴가 일어나지 않아야 하며, 단기 내열성은 175℃에서 240 시간 동안 체류시킨 후 -25℃ 챔버에서 저온굴곡시험을 통과하여야 하고, 매우 우수(◎), 우수(○), 불량(△), 매우 불량(×)으로 평가한다.Long-term / short-term heat resistance was evaluated for each of the cable specimens of the Examples and Comparative Examples according to the LV 216 standard, and the long-term heat resistance was maintained for 1 hour after applying the voltage of 1 kV in water for 1 minute after the specimen was kept at 150 ° C. for 3,000 hours. Insulation breakage should not occur, short term heat resistance must be maintained at 175 ℃ for 240 hours, then pass low temperature bending test in -25 ℃ chamber, very good (◎), good (○), bad (△), very bad It evaluates as (x).
5) 내한성 평가5) Cold resistance evaluation
LV 216 규격에 의거하여 실시예 및 비교예 각각의 케이블 시편에 도체 사이즈에 따라 규격에 명시된 추를 매달고 -40℃ 오븐 내에서 4시간 체류시킨 후 명시된 규격의 봉에 감아서 크랙이 발생하는지 여부를 확인한다. 크랙이 발생하지 않으면 이후 1분 간 수중에서 1 kV의 전압을 인가하는 동안 절연파괴가 일어나지 않아야 한다.According to the LV 216 standard, each cable specimen according to the example and the comparative example was suspended according to the conductor size according to the conductor size, stayed for 4 hours in the oven at -40 ℃, and wound around the rod of the specified standard to see if cracks occurred. Check it. If no cracking occurs, no breakdown shall occur during the application of a voltage of 1 kV in water for one minute.
6) 내마모성 평가6) Wear resistance evaluation
ISO 6722-1 규격에 의거하여 실시예 및 비교예 각각의 케이블 시편에 7 N 하중을 인가한 채로 시편과 수직으로 0.45 mm 직경의 니들(needle)을 왕복시킨다. 시스층이 마모되어 니들이 차폐층과 접하게 되면 평가가 종료되며 왕복횟수가 1,500회 이상이어야 한다.In accordance with the ISO 6722-1 standard, a 0.45 mm diameter needle was reciprocated perpendicularly to the specimen with 7 N load applied to each of the cable specimens of Examples and Comparative Examples. If the sheath layer wears and the needle contacts the shielding layer, the evaluation is complete and the round trip frequency should be 1,500 or more.
7) 난연성 평가7) Flame retardancy evaluation
LV 216 규격에 의거하여 실시예 및 비교예 각각의 케이블 시편 및 버너를 지면에서 45°각도로 고정하고 시편과 버너 간은 서로 수직이 되도록 배치하며 버너로 30초간 시편에 불꽃을 인가한 후 70초 내에 소화되어야 한다.According to the LV 216 standard, fix each cable specimen and burner at 45 ° angle from the ground, and arrange the specimen and burner to be perpendicular to each other. It must be digested within.
상기 물성 평가 결과는 아래 표 3에 나타난 바와 같다.The physical property evaluation results are shown in Table 3 below.
spec.spec. 실시예Example 비교예Comparative example
1One 22 33 1One 22 33 44 55 66
내유성Oil resistance <15%<15% 9.79.7 10.510.5 10.210.2 10.210.2 10.710.7 17.817.8 11.411.4 10.610.6 13.813.8
절연저항Insulation Resistance Ω·㎜Ωmm 3.70E+143.70E + 14 2.10E+142.10E + 14 2.37E+142.37E + 14 7.68E+137.68E + 13 1.17E+141.17E + 14 2.37E+122.37E + 12 9.72E+139.72E + 13 9.72E+139.72E + 13 9.72E+139.72E + 13
유연성flexibility -- 0.2950.295 0.2840.284 0.2910.291 0.2890.289 0.3800.380 0.3030.303 0.4150.415 0.3100.310 0.3170.317
내열성Heat resistance ××
내한성Cold resistance No CrackNo crack No CrackNo crack No CrackNo crack No CrackNo crack No CrackNo crack No CrackNo crack No CrackNo crack No CrackNo crack CrackCrack No CrackNo crack
내마모성Wear resistance >1,500회> 1,500 times 952952 1,3741,374
난연성Flame retardant 70초 내 소화Digest in 70 seconds ×× ×× ××
상기 표 3에 기재된 바와 같이, 비교예 1의 케이블 시편은 시스층이 난연보조제가 포함되지 않은 처방1의 고분자 조성물로부터 형성되어 난연성을 만족하지 못하였고, 비교예 2의 케이블 시편은 절연층 및 시스층이 각각 폴리프로필렌 수지가 과량 포함된 처방 6 및 5의 고분자 조성물로부터 형성되어 폴리프로필렌의 특성상 가교 후 특성이 불안정하여 내열성이 불량한 것으로 확인되었고 유연성이 악화되었으며, 비교예 3의 케이블 시편은 시스층이 에틸렌 프로필렌 디엔 고무 대신 에틸렌 비닐 아세테이트 수지를 포함하는 처방 4의 고분자 조성물로부터 형성되어 난연성, 내유성, 내마모성 등을 만족하지 못하였고, 비교예 4의 케이블 시편은 절연층이 말레산 무수물이 그라프트된 에틸렌 비닐 아세테이트 수지가 과량 포함된 처방 3의 고분자 조성물로부터 형성되어 유연성이 크게 저하되었고, 비교예 5의 케이블 시편은 시스층이 난연제 1이 과량 첨가되고 난연제 2가 첨가되지 않은 처방 9의 고분자 조성물로부터 형성되어 난연성 및 내한성이 저하되었으며, 비교예 6의 케이블 시편은 시스층이 에틸렌 프로필렌 디엔 고무가 과량 포함된 처방 10의 고분자 조성물로부터 형성되어 내마모성이 규격을 만족하지 못했다.As shown in Table 3, the cable specimen of Comparative Example 1 did not satisfy the flame retardancy because the sheath layer was formed from the polymer composition of Formulation 1 containing no flame retardant aid, the cable specimen of Comparative Example 2 is an insulating layer and sheath The layers were formed from the polymer compositions of Formulations 6 and 5, each containing an excessive amount of polypropylene resin, resulting in poor heat resistance due to unstable properties after crosslinking due to the properties of the polypropylene, and deteriorated flexibility, and the cable specimen of Comparative Example 3 was a sheath layer. It was formed from the polymer composition of Formula 4 containing ethylene vinyl acetate resin instead of the ethylene propylene diene rubber, and did not satisfy flame retardancy, oil resistance, abrasion resistance, and the like. Polymer composition of formula 3 containing an excess of ethylene vinyl acetate resin Formed in the polymer composition of Comparative Example 5, the sheath layer was formed from the polymer composition of Formulation 9 in which the flame retardant 1 was excessively added and the flame retardant 2 was not added, thereby reducing the flame resistance and the cold resistance. The cable specimens were formed from the polymer composition of Formula 10 in which the sheath layer contained an excessive amount of ethylene propylene diene rubber so that the abrasion resistance did not meet the specification.
반면, 본 발명의 실시예 1 내지 3의 케이블 시편은 LV 216 규격에서 요구되는 높은 절연저항 특성 및 이와 상충관계에 있는 유연성이 모두 기준을 만족했고, 그 이외에 내유성, 내열성, 내한성, 내마모성, 난연성 등의 물성도 우수한 것으로 확인되었다.On the other hand, the cable specimens of Examples 1 to 3 of the present invention satisfy all of the high insulation resistance properties and the flexibility in conflict with the standard required by the LV 216 standard. It was also confirmed that the physical properties were excellent.
본 명세서는 본 발명의 바람직한 실시예를 참조하여 설명하였지만, 해당 기술분야의 당업자는 이하에서 서술하는 특허청구범위에 기재된 본 발명의 사상 및 영역으로부터 벗어나지 않는 범위 내에서 본 발명을 다양하게 수정 및 변경 실시할 수 있을 것이다. 그러므로 변형된 실시가 기본적으로 본 발명의 특허청구범위의 구성요소를 포함한다면 모두 본 발명의 기술적 범주에 포함된다고 보아야 한다.Although the present specification has been described with reference to preferred embodiments of the invention, those skilled in the art may variously modify and change the invention without departing from the spirit and scope of the invention as set forth in the claims set forth below. Could be done. Therefore, it should be seen that all modifications included in the technical scope of the present invention are basically included in the scope of the claims of the present invention.

Claims (16)

  1. 고전압 케이블용 고분자 조성물로서,A polymer composition for high voltage cable,
    베이스 수지 및 첨가제를 포함하고,Base resins and additives,
    상기 베이스 수지는 폴리프로필렌 수지, 폴리올레핀 엘라스토머, 에틸렌 프로필렌 디엔 고무 및 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지를 포함하고,The base resin comprises polypropylene resin, polyolefin elastomer, ethylene propylene diene rubber and ethylene vinyl acetate resin grafted with maleic anhydride,
    상기 고분자 조성물로부터 형성된 절연층 및 시스층은 체적저항이 10 13 Ω·㎜을 초과하는, 고분자 조성물.The insulating layer and the sheath layer formed from the polymer composition have a volume resistance of more than 10 13 Ω · mm.
  2. 제1항에 있어서,The method of claim 1,
    상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 15 내지 25 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 30 내지 50 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 20 내지 40 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 8 내지 13 중량부인 것을 특징으로 하는, 고분자 조성물.Based on 100 parts by weight of the base resin, the content of the polypropylene resin is 15 to 25 parts by weight, the content of the polyolefin elastomer is 30 to 50 parts by weight, the content of the ethylene propylene diene rubber is 20 to 40 parts by weight and the The content of the ethylene vinyl acetate resin grafted maleic anhydride (grafted), characterized in that 8 to 13 parts by weight, the polymer composition.
  3. 제2항에 있어서,The method of claim 2,
    상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 17 내지 24 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 37 내지 45 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 27 내지 31 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 9 내지 10 중량부인 것을 특징으로 하는, 고분자 조성물.Based on 100 parts by weight of the base resin, the content of the polypropylene resin is 17 to 24 parts by weight, the content of the polyolefin elastomer is 37 to 45 parts by weight, the content of the ethylene propylene diene rubber is 27 to 31 parts by weight and the The content of ethylene vinyl acetate resin grafted maleic anhydride is characterized in that 9 to 10 parts by weight, the polymer composition.
  4. 제1항에 있어서,The method of claim 1,
    상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 22 내지 32 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 25 내지 35 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 27 내지 35 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 8 내지 13 중량부인 것을 특징으로 하는, 고분자 조성물.Based on 100 parts by weight of the base resin, the content of the polypropylene resin is 22 to 32 parts by weight, the content of the polyolefin elastomer is 25 to 35 parts by weight, the content of the ethylene propylene diene rubber is 27 to 35 parts by weight and the The content of the ethylene vinyl acetate resin grafted maleic anhydride (grafted), characterized in that 8 to 13 parts by weight, the polymer composition.
  5. 제4항에 있어서,The method of claim 4, wherein
    상기 베이스 수지 100 중량부를 기준으로, 상기 폴리프로필렌 수지의 함량은 24 내지 29 중량부이고, 상기 폴리올레핀 엘라스토머의 함량은 29 내지 33 중량부, 상기 에틸렌 프로필렌 디엔 고무의 함량은 29 내지 33 중량부 및 상기 말레산 무수물이 그라프트된(grafted) 에틸렌 비닐 아세테이트 수지의 함량은 10 내지 11 중량부인 것을 특징으로 하는, 고분자 조성물.Based on 100 parts by weight of the base resin, the content of the polypropylene resin is 24 to 29 parts by weight, the content of the polyolefin elastomer is 29 to 33 parts by weight, the content of the ethylene propylene diene rubber is 29 to 33 parts by weight and the The content of the ethylene vinyl acetate resin grafted maleic anhydride (grafted), characterized in that 10 to 11 parts by weight, the polymer composition.
  6. 제1항 내지 제5항 중 어느 한 항에 있어서,The method according to any one of claims 1 to 5,
    상기 폴리프로필렌 수지는 융점(Tm)이 140 내지 145℃이고 비중이 0.860 내지 0.880이며, 상기 폴리올레핀 엘라스토머는 융점(Tm)이 90 내지 100℃이고 비중이 0.890 내지 0.910인 것을 특징으로 하는, 고분자 조성물.The polypropylene resin has a melting point (Tm) of 140 to 145 ° C. and specific gravity of 0.860 to 0.880, and the polyolefin elastomer has a melting point (Tm) of 90 to 100 ° C. and specific gravity of 0.890 to 0.910.
  7. 제6항에 있어서,The method of claim 6,
    상기 에틸렌 프로필렌 디엔 고무는 비중이 0.870 내지 0.890이고 무니점도(ML1+4(125℃))가 20 내지 40인 것을 특징으로 하는, 고분자 조성물.The ethylene propylene diene rubber has a specific gravity of 0.870 to 0.890 and a Mooney viscosity (ML1 + 4 (125 ℃)) is characterized in that the 20 to 40, the polymer composition.
  8. 제1항 내지 제3항 중 어느 한 항에 있어서,The method according to any one of claims 1 to 3,
    상기 첨가제는 난연제, 가교조제, 산화방지제 및 활제로 이루어진 그룹으로부터 선택된 1종 이상의 첨가제를 포함하는 것을 특징으로 하는, 고분자 조성물.The additive is characterized in that it comprises at least one additive selected from the group consisting of flame retardants, crosslinking aids, antioxidants and lubricants.
  9. 제8항에 있어서,The method of claim 8,
    상기 난연제는 수산화마그네슘 또는 수산화알루미늄을 포함하고, 상기 베이스 수지 100 중량부를 기준으로, 상기 난연제의 함량은 80 내지 100 중량부인 것을 특징으로 하는, 고분자 조성물.The flame retardant comprises magnesium hydroxide or aluminum hydroxide, based on 100 parts by weight of the base resin, characterized in that the content of the flame retardant is 80 to 100 parts by weight, polymer composition.
  10. 제9항에 있어서,The method of claim 9,
    상기 난연제의 함량은 상기 베이스 수지 100 중량부를 기준으로 87 내지 95 중량부인 것을 특징으로 하는, 고분자 조성물.The content of the flame retardant is a polymer composition, characterized in that 87 to 95 parts by weight based on 100 parts by weight of the base resin.
  11. 제8항에 있어서,The method of claim 8,
    상기 가교조제는 상기 베이스 수지의 조사가교용 다관능 유기모노머를 포함하고, 상기 가교조제의 함량은 상기 베이스 수지 100 중량부를 기준으로 2 내지 5 중량부인 것을 특징으로 하는, 고분자 조성물.The crosslinking aid comprises a multifunctional organic monomer for irradiation crosslinking of the base resin, the content of the crosslinking aid is characterized in that 2 to 5 parts by weight based on 100 parts by weight of the base resin, polymer composition.
  12. 제1항, 제4항 및 제5항 중 어느 한 항에 있어서,The method according to any one of claims 1, 4 and 5,
    상기 첨가제는 난연제, 난연보조제, 가교조제, 산화방지제 및 활제로 이루어진 그룹으로부터 선택된 1종 이상의 첨가제를 포함하는 것을 특징으로 하는, 고분자 조성물.The additive is characterized in that it comprises at least one additive selected from the group consisting of flame retardants, flame retardant aids, crosslinking aids, antioxidants and lubricants.
  13. 제12항에 있어서,The method of claim 12,
    상기 난연제는 수산화마그네슘 또는 수산화알루미늄을 포함하고, 상기 난연보조제는 적인 난연제를 포함하며, 상기 베이스 수지 100 중량부를 기준으로, 상기 난연제의 함량은 95 내지 110 중량부이고, 상기 난연보조제의 함량은 0.6 내지 1.2 중량부인 것을 특징으로 하는, 고분자 조성물.The flame retardant includes magnesium hydroxide or aluminum hydroxide, the flame retardant aid comprises a flame retardant, based on 100 parts by weight of the base resin, the content of the flame retardant is 95 to 110 parts by weight, the content of the flame retardant aid is 0.6 To 1.2 parts by weight, the polymer composition.
  14. 제13항에 있어서,The method of claim 13,
    상기 베이스 수지 100 중량부를 기준으로, 상기 난연제의 함량은 100 내지 105 중량부이고, 상기 난연보조제의 함량은 0.8 내지 1.1 중량부인 것을 특징으로 하는, 고분자 조성물.Based on 100 parts by weight of the base resin, the content of the flame retardant is 100 to 105 parts by weight, the content of the flame retardant aid is characterized in that the polymer composition, 0.8 to 1.1 parts by weight.
  15. 제12항에 있어서,The method of claim 12,
    상기 가교조제는 상기 베이스 수지의 조사가교용 다관능 유기모노머를 포함하고, 상기 가교조제의 함량은 상기 베이스 수지 100 중량부를 기준으로 2 내지 5 중량부인 것을 특징으로 하는, 고분자 조성물.The crosslinking aid comprises a multifunctional organic monomer for irradiation crosslinking of the base resin, the content of the crosslinking aid is characterized in that 2 to 5 parts by weight based on 100 parts by weight of the base resin, polymer composition.
  16. 도체;Conductor;
    상기 도체를 감싸고 제1항 내지 제3항 중 어느 한 항의 고분자 조성물로부터 형성된 절연층;An insulating layer surrounding the conductor and formed from the polymer composition of any one of claims 1 to 3;
    상기 절연층을 감싸는 금속차폐층; 및A metal shielding layer surrounding the insulating layer; And
    상기 금속차폐층을 감싸고 제1항, 제4항 및 제5항 중 어느 한 항의 고분자 조성물로부터 형성된 시스층을 포함하는 케이블.Cable comprising a sheath layer surrounding the metal shielding layer and formed from the polymer composition of any one of claims 1, 4 and 5.
PCT/KR2018/000587 2017-02-20 2018-01-12 Polymer composition for high-voltage cable, and cable comprising insulation layer and sheath layer which are formed therefrom WO2018151421A1 (en)

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