KR102563549B1 - Pvc composition, as well as electric wire and cable using the same - Google Patents
Pvc composition, as well as electric wire and cable using the same Download PDFInfo
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- KR102563549B1 KR102563549B1 KR1020160087831A KR20160087831A KR102563549B1 KR 102563549 B1 KR102563549 B1 KR 102563549B1 KR 1020160087831 A KR1020160087831 A KR 1020160087831A KR 20160087831 A KR20160087831 A KR 20160087831A KR 102563549 B1 KR102563549 B1 KR 102563549B1
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- chloride resin
- terephthalic acid
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- 239000000203 mixture Substances 0.000 title abstract description 7
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 40
- -1 terephthalic acid ester Chemical class 0.000 claims abstract description 38
- KKEYFWRCBNTPAC-UHFFFAOYSA-N benzene-dicarboxylic acid Natural products OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000011342 resin composition Substances 0.000 claims abstract description 33
- 229920002379 silicone rubber Polymers 0.000 claims abstract description 27
- 239000004945 silicone rubber Substances 0.000 claims abstract description 27
- 239000004014 plasticizer Substances 0.000 claims abstract description 24
- 239000011347 resin Substances 0.000 claims abstract description 18
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000004800 polyvinyl chloride Substances 0.000 claims description 20
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 20
- PEIIRIVDOVFUIW-UHFFFAOYSA-N bis(7-methyloctyl) benzene-1,4-dicarboxylate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCC(C)C)C=C1 PEIIRIVDOVFUIW-UHFFFAOYSA-N 0.000 claims description 6
- DUQLDVZUQAAAMU-UHFFFAOYSA-N bis(8-methylnonyl) benzene-1,4-dicarboxylate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=C(C(=O)OCCCCCCCC(C)C)C=C1 DUQLDVZUQAAAMU-UHFFFAOYSA-N 0.000 claims description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 239000004020 conductor Substances 0.000 abstract description 11
- 239000010410 layer Substances 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 9
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical group CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 9
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 8
- BJAJDJDODCWPNS-UHFFFAOYSA-N dotp Chemical compound O=C1N2CCOC2=NC2=C1SC=C2 BJAJDJDODCWPNS-UHFFFAOYSA-N 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229920002545 silicone oil Polymers 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000003504 terephthalic acids Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- IHBCFWWEZXPPLG-UHFFFAOYSA-N [Ca].[Zn] Chemical compound [Ca].[Zn] IHBCFWWEZXPPLG-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 150000002531 isophthalic acids Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- LAQFLZHBVPULPL-UHFFFAOYSA-N methyl(phenyl)silicon Chemical compound C[Si]C1=CC=CC=C1 LAQFLZHBVPULPL-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical class OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/441—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from alkenes
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- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/02—Disposition of insulation
- H01B7/0208—Cables with several layers of insulating material
- H01B7/0216—Two layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
- H01B7/28—Protection against damage caused by moisture, corrosion, chemical attack or weather
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
- C08L2203/202—Applications use in electrical or conductive gadgets use in electrical wires or wirecoating
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- Spectroscopy & Molecular Physics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
- Insulated Conductors (AREA)
Abstract
(과제)
본 발명은, 가소제로서 테레프탈산 에스테르를 사용하여도 내후성 및 내블리드성이 양호한 염화비닐수지 조성물, 및 이것을 사용한 전선 및 케이블을 제공하는 것이다.
(해결수단)
전선(10)은, 도체(1)의 외주에, 가소제로서 테레프탈산 에스테르를 함유하며 염화비닐수지 100질량부에 대하여 상기 테레프탈산 에스테르를 100질량부 이하, 실리콘고무를 0.1질량부 이상 함유하는 염화비닐수지 조성물로 이루어지는 절연층(2)을 구비한다.(assignment)
The present invention provides a vinyl chloride resin composition having good weather resistance and bleed resistance even when terephthalic acid ester is used as a plasticizer, and electric wires and cables using the same.
(solution)
The electric wire 10 is a vinyl chloride resin containing terephthalic acid ester as a plasticizer on the outer periphery of the conductor 1 and containing 100 parts by mass or less of the terephthalic acid ester and 0.1 part by mass or more of silicone rubber with respect to 100 parts by mass of the vinyl chloride resin. An insulating layer 2 made of a composition is provided.
Description
본 발명은, 염화비닐수지 조성물, 및 이것을 사용한 전선 및 케이블에 관한 것이다.
The present invention relates to a polyvinyl chloride resin composition and electric wires and cables using the same.
염화비닐수지(PVC)는, 저비용이며 난연성(難燃性)을 구비하는 재료로, 유연성(柔軟性)을 부여하기 위한 가소제(可塑劑)를 첨가함으로써 전선피복재(電線被覆材)로서 사용된다.Polyvinyl chloride resin (PVC) is a low-cost, flame retardant material, and is used as a wire covering material by adding a plasticizer for imparting flexibility.
가소제로서는, 저렴하고 PVC와의 상용성(相溶性)이 높은 디-2-에틸헥실프탈레이트(DOP)가 주로 사용되지만(예를 들면 특허문헌1 참조), 근년 REACH 규정과 더불어 RoHS 지령의 사용금지물질로 지정될 우려도 있어, 이후의 사용이 꺼려지고 있다.As a plasticizer, di-2-ethylhexyl phthalate (DOP), which is inexpensive and has high compatibility with PVC, is mainly used (see, for example, Patent Document 1), but in recent years, along with the REACH regulation, it is a substance prohibited by the RoHS directive There is a possibility that it will be designated as , so its use is discouraged.
DOP의 대체후보로서는, DOP 다음으로 전선피복재로서 사용실적이 있는 디이소노닐프탈레이트(DINP)를 들 수 있지만(예를 들면 특허문헌2 참조), DINP는 고무 용도로도 사용되어 공급부족을 일으킬 가능성이 있기 때문에, 그 외의 가소제의 실용화가 요구되고 있다.As an alternative candidate for DOP, there is diisononyl phthalate (DINP), which has a track record of use as a wire covering material next to DOP (see, for example, Patent Document 2), but DINP is also used for rubber purposes, which may cause a supply shortage. Because of this, practical use of other plasticizers is required.
그 외의 가소제로서는, DOP, DINP와 동등한 PVC와의 상용성을 구비하는 테레프탈산 에스테르 구조의 가소제가 있다(예를 들면 특허문헌3∼4 참조).
As other plasticizers, there is a plasticizer having a terephthalic acid ester structure having compatibility with PVC equivalent to that of DOP and DINP (for example, see
그러나 하기 일반식(1)로 나타내는 테레프탈산 에스테르는, 하기 일반식(2)로 나타내는 프탈산 에스테르와 비교하여 내후성(耐候性)이 떨어지기 때문에, 전선 용도로 옥외에서 사용하는 데에는 문제가 있다(각 식 중의 R은 알킬쇄를 나타낸다).However, since the terephthalic acid ester represented by the following general formula (1) has inferior weather resistance compared to the phthalic acid ester represented by the following general formula (2), there is a problem in using it outdoors for wire applications (each formula R in represents an alkyl chain).
(화학식1)(Formula 1)
(화학식2)(Formula 2)
또한 첨가제 중에는, PVC나 테레프탈산 에스테르와 상용(相溶)되기 어려워, 조성물의 표면에 블리드(bleed)하여 끈적임을 발생시키는 문제가 있는 것이 있다.In addition, among additives, there is a problem that it is difficult to be compatible with PVC or terephthalic acid ester and bleeds to the surface of the composition to generate stickiness.
그래서 본 발명은, 가소제로서 테레프탈산 에스테르를 사용하여도 내후성 및 내블리드성이 양호한 염화비닐수지 조성물, 및 이것을 사용한 전선 및 케이블을 제공하는 것을 목적으로 한다.
Accordingly, an object of the present invention is to provide a vinyl chloride resin composition having good weather resistance and bleed resistance even when terephthalic acid ester is used as a plasticizer, and electric wires and cables using the same.
상기 목적을 달성하기 위한 본 발명에 의하면, 이하의 염화비닐수지 조성물, 및 이것을 사용한 전선 및 케이블이 제공된다.According to the present invention for achieving the above object, the following polyvinyl chloride resin composition and electric wires and cables using the same are provided.
[1] 가소제로서 테레프탈산 에스테르를 함유하는 염화비닐수지 조성물에 있어서, 염화비닐수지 100질량부에 대하여, 상기 테레프탈산 에스테르를 100질량부 이하, 실리콘고무를 0.1질량부 이상 함유하는 염화비닐수지 조성물.[1] A vinyl chloride resin composition containing a terephthalic acid ester as a plasticizer, which contains 100 parts by mass or less of the terephthalic acid ester and 0.1 part by mass or more of a silicone rubber based on 100 parts by mass of the vinyl chloride resin.
[2] 염화비닐수지 100질량부에 대하여, 상기 테레프탈산 에스테르를 10∼100질량부 함유하는 상기 [1]에 기재되어 있는 염화비닐수지 조성물.[2] The vinyl chloride resin composition according to the above [1], containing 10 to 100 parts by mass of the terephthalic acid ester with respect to 100 parts by mass of the vinyl chloride resin.
[3] 염화비닐수지 100질량부에 대하여, 상기 실리콘고무를 0.1∼5질량부 함유하는 상기 [1] 또는 상기 [2]에 기재되어 있는 염화비닐수지 조성물.[3] The vinyl chloride resin composition according to [1] or [2] above, containing 0.1 to 5 parts by mass of the silicone rubber based on 100 parts by mass of the vinyl chloride resin.
[4] 상기 테레프탈산 에스테르는, 1개당 알킬쇄의 탄소수가 8∼10인 테레프탈산 에스테르인 상기 [1] 내지 [3] 중의 어느 하나에 기재되어 있는 염화비닐수지 조성물.[4] The vinyl chloride resin composition according to any one of [1] to [3], wherein the terephthalic acid ester is a terephthalic acid ester having 8 to 10 carbon atoms in each alkyl chain.
[5] 가소제로서 테레프탈산 에스테르를 함유하는 염화비닐수지 조성물에 있어서, 염화비닐수지 100질량부에 대하여, 상기 테레프탈산 에스테르를 100질량부 이하, 실리콘고무를 0.1질량부 이상 함유하는 염화비닐수지 조성물로 이루어지는 절연층을 구비한 전선.[5] A polyvinyl chloride resin composition containing terephthalic acid ester as a plasticizer, based on 100 parts by mass of the vinyl chloride resin, 100 parts by mass or less of the terephthalic acid ester and 0.1 part by mass or more of a silicone rubber Composed of a vinyl chloride resin composition containing Electrical wire with an insulating layer.
[6] 가소제로서 테레프탈산 에스테르를 함유하는 염화비닐수지 조성물에 있어서, 염화비닐수지 100질량부에 대하여, 상기 테레프탈산 에스테르를 100질량부 이하, 실리콘고무를 0.1질량부 이상 함유하는 염화비닐수지 조성물로 이루어지는 시스를 구비한 케이블.[6] A polyvinyl chloride resin composition containing terephthalic acid ester as a plasticizer, based on 100 parts by mass of the vinyl chloride resin, 100 parts by mass or less of the terephthalic acid ester and 0.1 part by mass or more of a silicone rubber Composed of a vinyl chloride resin composition containing Cable with sheath.
[7] 상기 [5]에 기재되어 있는 전선을 구비한 상기 [6]에 기재되어 있는 케이블.
[7] The cable described in [6] above, provided with the wire described in [5] above.
본 발명에 의하면, 가소제로서 테레프탈산 에스테르를 사용하여도 내후성 및 내블리드성이 양호한 염화비닐수지 조성물, 및 이것을 사용한 전선 및 케이블이 제공된다.
According to the present invention, a vinyl chloride resin composition having good weather resistance and bleed resistance even when terephthalic acid ester is used as a plasticizer, and electric wires and cables using the same are provided.
도1은, 본 발명의 실시형태에 관한 전선의 일례를 모식적으로 나타내는 횡단면도이다.
도2는, 본 발명의 실시형태에 관한 케이블의 일례를 모식적으로 나타내는 횡단면도이다.1 is a cross-sectional view schematically showing an example of an electric wire according to an embodiment of the present invention.
Fig. 2 is a cross-sectional view schematically showing an example of a cable according to an embodiment of the present invention.
〔염화비닐수지 조성물〕[Vinyl chloride resin composition]
본 발명의 실시형태에 관한 염화비닐수지 조성물은, 가소제로서 테레프탈산 에스테르를 함유하는 염화비닐수지 조성물로서, 염화비닐수지 100질량부에 대하여, 상기 테레프탈산 에스테르를 100질량부 이하, 실리콘고무를 0.1질량부 이상 함유한다.A vinyl chloride resin composition according to an embodiment of the present invention is a vinyl chloride resin composition containing a terephthalic acid ester as a plasticizer, and 100 parts by mass or less of the terephthalic acid ester and 0.1 part by mass of a silicone rubber with respect to 100 parts by mass of the vinyl chloride resin contain more than
본 발명자는, 테레프탈산 에스테르가 내후성이 떨어지는 이유로는, 테레프탈산 에스테르는 에스테르의 카르복실기가 열린 구조여서, 외부로부터 침투되는 물과의 접촉이 용이하게 되어 가수분해성이 높기 때문이라고 생각했다.The present inventors considered that the reason why terephthalic acid esters have poor weatherability is that terephthalic acid esters have an open carboxyl group structure, so that contact with water penetrating from the outside is easy and hydrolysis is high.
그래서 테레프탈산 에스테르를 사용할 때의 내후성의 열화를 억제하기 위하여, 다양한 첨가제에 대하여 첨가를 검토한 결과, 발수성(撥水性)이 뛰어난 실리콘고무를 첨가함으로써 내후성을 개선할 수 있다는 것을 발견하였다.Therefore, as a result of examining the addition of various additives in order to suppress the deterioration of weather resistance when using terephthalic acid ester, it was found that weather resistance can be improved by adding silicone rubber having excellent water repellency.
한편 액상(液狀)의 실리콘오일에는, 내후성은 개선되지만, PVC나 테레프탈산 에스테르와 상용되기 어려워, 조성물의 표면에 블리드하여 끈적임을 발생시킨다는 문제가 있었다.On the other hand, liquid silicone oil has improved weather resistance, but has a problem that it is difficult to be compatible with PVC or terephthalic acid ester and bleeds to the surface of the composition to cause stickiness.
그 때문에 내후성과 함께 내블리드성도 고려하여 검토한 결과, 고형상(固形狀)의 실리콘고무가 이들을 양립시킬 수 있다는 것을 발견하고, 본 발명의 염화비닐수지 조성물을 개발하기에 이르렀다.Therefore, as a result of examining in consideration of weather resistance as well as bleed resistance, it was found that a solid silicone rubber can make these compatible, and the polyvinyl chloride resin composition of the present invention was developed.
(테레프탈산 에스테르)(terephthalic acid ester)
본 발명의 실시형태에 관한 염화비닐수지 조성물에서 가소제로서 사용되는 테레프탈산 에스테르로는, 1개당 알킬쇄의 탄소수가 8∼10(C8∼C10)인 테레프탈산 에스테르가 적합하다. C8 미만으로는 필요한 내열성(耐熱性)을 얻기 어렵다. 알킬쇄의 탄소수가 적을수록, 즉 분자량이 작을수록 가열에 의한 가소제의 휘발이 촉진되어, 염화비닐수지 조성물이 경화되기 때문이다. 한편 C11 이상이면, 가소제의 에스테르 합성에 필요한 알코올의 입수가 곤란하여 비용이 늘어나기 때문에 실용성이 떨어져, C10 이하인 것이 바람직하다.As the terephthalic acid ester used as a plasticizer in the vinyl chloride resin composition according to the embodiment of the present invention, terephthalic acid esters having 8 to 10 (C8 to C10) carbon atoms in each alkyl chain are suitable. If it is less than C8, it is difficult to obtain required heat resistance. This is because as the number of carbon atoms in the alkyl chain decreases, that is, as the molecular weight decreases, volatilization of the plasticizer by heating is promoted, and the vinyl chloride resin composition is cured. On the other hand, if it is C11 or more, it is difficult to obtain alcohol necessary for ester synthesis of the plasticizer and the cost increases, so practicality is poor, and C10 or less is preferable.
테레프탈산 에스테르의 알킬쇄는, 직쇄 구조(直鎖 構造)이어도 분기쇄 구조(分岐鎖 構造)이어도 좋지만, 분기쇄 구조인 것이 바람직하다. 구체적으로는, C8인 것으로서 디-2-에틸헥실테레프탈레이트(DOTP), C9인 것으로서 디이소노닐테레프탈레이트(DINTP), C10인 것으로서 디이소데실테레프탈레이트(DIDTP)를 들 수 있지만, 이들에 한정되는 것은 아니다.The alkyl chain of the terephthalic acid ester may have either a straight chain structure or a branched chain structure, but it is preferably a branched chain structure. Specifically, although di-2-ethylhexyl terephthalate (DOTP) as C8, diisononyl terephthalate (DINTP) as C9, and diisodecyl terephthalate (DIDTP) as C10, it is limited to these. it is not going to be
본 발명의 실시형태에 있어서 상기 테레프탈산 에스테르의 첨가량은, 염화비닐수지 100질량부에 대하여 100질량부 이하로 한다. 10질량부 이상 첨가하는 것이 바람직하다. 실리콘고무를 첨가함으로써 테레프탈산 에스테르의 첨가에 대한 효과가 발휘되지만, 테레프탈산 에스테르의 첨가량이 100질량부를 넘으면, 가소제 자체가 블리드하여 표면에 끈적임이 발생한다.In the embodiment of the present invention, the addition amount of the terephthalic acid ester is 100 parts by mass or less with respect to 100 parts by mass of the vinyl chloride resin. It is preferable to add 10 parts by mass or more. Although the addition of silicone rubber exerts an effect on the addition of terephthalic acid ester, if the added amount of terephthalic acid ester exceeds 100 parts by mass, the plasticizer itself bleeds and stickiness occurs on the surface.
(실리콘고무)(silicone rubber)
본 발명의 실시형태에 관한 염화비닐수지 조성물에 사용되는 실리콘고무로서는, 예를 들면 디메틸 실리콘고무, 메틸페닐 실리콘고무, 비닐페닐 실리콘고무, 메틸비닐페닐 실리콘고무가 적합하다.As the silicone rubber used in the vinyl chloride resin composition according to the embodiment of the present invention, dimethyl silicone rubber, methylphenyl silicone rubber, vinylphenyl silicone rubber, and methylvinylphenyl silicone rubber are suitable, for example.
본 발명의 실시형태에 있어서 상기 실리콘고무의 첨가량은, 염화비닐수지 100질량부에 대하여 0.1질량부 이상이 필요하다. 첨가량 0.1질량부 미만으로는 필요한 내후성을 얻을 수 없다. 또한 첨가량은 5질량부 이하인 것이 바람직하다. 5질량부를 넘으면, 가공성에 문제가 생기기 쉽다.In the embodiment of the present invention, the addition amount of the silicone rubber is required to be 0.1 parts by mass or more with respect to 100 parts by mass of the vinyl chloride resin. If the addition amount is less than 0.1 parts by mass, the necessary weather resistance cannot be obtained. Moreover, it is preferable that the addition amount is 5 parts by mass or less. When it exceeds 5 parts by mass, it is easy to cause problems in workability.
(염화비닐수지)(Polyvinyl chloride resin)
염화비닐수지로서는, 염화비닐의 단독 중합체(즉, 폴리염화비닐) 외에, 염화비닐과 공중합 가능한 다른 모노머와의 공중합체 및 이들의 혼합물을 들 수 있다. 염화비닐과 공중합 가능한 모노머로서는, 아세트산비닐, 염화비닐리덴, (메타)아크릴산, 아크릴로니트릴 등을 들 수 있다.Examples of the vinyl chloride resin include homopolymers of vinyl chloride (ie, polyvinyl chloride), copolymers of vinyl chloride with other monomers copolymerizable with them, and mixtures thereof. As a monomer copolymerizable with vinyl chloride, vinyl acetate, vinylidene chloride, (meth)acrylic acid, acrylonitrile, etc. are mentioned.
염화비닐수지는, 평균중합도가 1000∼2500인 것을 사용하는 것이 바람직하다. 평균중합도가 1000∼2000인 것이 내열성, 내한성(耐寒性), 성형성(成形性)의 면에서 더 바람직하다. 중합도가 낮아지면 성형성은 향상되지만 내열성, 내한성이 저하된다. 반대로 중합도가 높아지면 내열성, 내한성은 향상되지만 성형성이 나빠진다.As the vinyl chloride resin, it is preferable to use one having an average polymerization degree of 1000 to 2500. Those having an average polymerization degree of 1000 to 2000 are more preferable from the viewpoint of heat resistance, cold resistance, and moldability. When the polymerization degree is lowered, moldability is improved, but heat resistance and cold resistance are lowered. Conversely, when the degree of polymerization increases, heat resistance and cold resistance improve, but moldability deteriorates.
염화비닐수지는, 필요에 따라 중합도가 다른 것을 2종류 이상 블렌드(blend)하여 사용하여도 좋다.The vinyl chloride resin may be used in a blend of two or more types having different degrees of polymerization, if necessary.
(그 외의 성분)(other ingredients)
본 발명의 실시형태에 있어서는, 본 발명의 효과를 얻을 수 있는 한, 상기 성분 이외에, PVC 이외의 폴리머, 무기충전제, 안정제, 산화방지제, 가소제, 활제(滑劑), 착색제, 자외선흡수제, 광안정제, 가교제, 가교조제 등의 첨가제를 다양하게 배합할 수 있다.In the embodiment of the present invention, as long as the effects of the present invention can be obtained, in addition to the above components, polymers other than PVC, inorganic fillers, stabilizers, antioxidants, plasticizers, lubricants, colorants, ultraviolet absorbers, light stabilizers , cross-linking agent, additives such as cross-linking aid can be mixed in various ways.
예를 들면 내열성·내한성·절연성 등을 향상시키고자 하는 경우에는, 필요에 따라 프탈산 에스테르, 이소프탈산 에스테르, 트리멜리트산 에스테르, 피로멜리트산 에스테르, 에폭시화 대두유 등의 다른 가소제를 블렌드하여 사용하여도 좋다.For example, when it is desired to improve heat resistance, cold resistance, insulation, etc., other plasticizers such as phthalic acid esters, isophthalic acid esters, trimellitic acid esters, pyromellitic acid esters, and epoxidized soybean oil may be blended and used as necessary. good night.
〔전선〕〔wire〕
본 발명의 실시형태에 관한 전선은, 도체(導體)와, 도체의 외주(外周)에 피복(被覆)되며 본 발명의 실시형태에 관한 상기 염화비닐수지 조성물로 이루어지는 절연층(絶緣層)을 구비하는 것을 특징으로 한다.An electric wire according to an embodiment of the present invention includes a conductor and an insulating layer coated on an outer circumference of the conductor and made of the above-described polyvinyl chloride resin composition according to the embodiment of the present invention. It is characterized by doing.
도1은, 본 발명의 실시형태에 관한 전선의 일례를 모식적으로 나타내는 횡단면도이다.1 is a cross-sectional view schematically showing an example of an electric wire according to an embodiment of the present invention.
도1에 나타나 있는 바와 같이 본 실시형태에 관한 전선(10)은, 도체(1)와, 도체(1)의 외주에 피복된 절연층(2)을 구비한다. 피복되는 도체(1)로서는, 예를 들면 외경이 0.15∼7mmφ 정도인 도체를 사용할 수 있다. 주석도금 연동선(tin-plated 軟銅線)을 꼬아 만든 도체 등을 적합하게 사용할 수 있지만, 이에 한정되는 것은 아니다. 도체(1)는, 도1과 같이 1개인 경우로 한정되지 않고 복수 개이더라도 좋다.As shown in Fig. 1, an
절연층(2)은, 본 발명의 실시형태에 관한 상기의 염화비닐수지 조성물로 구성되어 있다. 압출피복(壓出被覆) 등의 성형수단에 의하여 절연층으로서 피복함으로써 전선(10)을 얻을 수 있다. 필요에 따라 전자선 조사 등의 방법에 의하여 가교처리를 하여도 좋다.The insulating
본 실시형태에 있어서는, 도1에서와 같이 절연층을 단층으로 구성하였지만, 다층구조로 하는 것도 가능하다. 이 경우에 적어도 최외층(最外層)은, 상기 염화비닐수지 조성물을 사용하여 형성한다.In this embodiment, although the insulating layer is constituted by a single layer as in Fig. 1, it is also possible to make it a multilayer structure. In this case, at least the outermost layer is formed using the above-mentioned vinyl chloride resin composition.
〔케이블〕〔cable〕
본 발명의 실시형태에 관한 케이블은, 본 발명의 실시형태에 관한 상기 염화비닐수지 조성물을 피복재료(시스(sheath), 또는 절연층 및 시스)로서 사용하는 것을 특징으로 한다.A cable according to an embodiment of the present invention is characterized in that the polyvinyl chloride resin composition according to the embodiment of the present invention is used as a covering material (sheath or insulating layer and sheath).
도2는, 본 발명의 실시형태에 관한 케이블의 일례를 모식적으로 나타내는 횡단면도이다.Fig. 2 is a cross-sectional view schematically showing an example of a cable according to an embodiment of the present invention.
도2에 나타나 있는 바와 같이 본 실시형태에 관한 케이블(20)은, 도체(1)에 절연층(2)을 피복한 상기 본 발명의 실시형태에 관한 전선(10) 3개를 종이 등의 개재물(介在物)(3)과 함께 꼬아 만든 3심 연선(三芯 撚線)과, 그 외주에 감긴 가압 테이프(4)와, 그 외주에 압출피복된 시스(5)를 구비한다. 3심 연선에 한하지 않고, 전선 1개(단심)로 하여도 좋고, 3심 이외의 다심 연선으로 하여도 좋다. 가압 테이프(4)는 생략할 수도 있고, 편조(編組)로 바꾸어도 좋다.As shown in Fig. 2, the
시스(5)는, 본 발명의 실시형태에 관한 상기의 염화비닐수지 조성물로 구성되어 있다. 본 실시형태에 있어서는 절연층(2)도, 상기의 염화비닐수지 조성물로 구성하였지만, 이것에 한정되는 것은 아니고, 그 외의 절연층용 수지 조성물(논할로겐 난연성 수지 조성물인 것이 바람직하다)로 구성되어 있어도 좋다. 시스(5)는, 필요에 따라 전자선 조사 등의 방법에 의하여 가교처리를 하여도 좋다.The
본 실시형태에 있어서는, 도2에서와 같이 시스를 단층으로 구성하였지만, 다층구조로 하는 것도 가능하다. 이 경우에 적어도 최외층은, 상기 염화비닐수지 조성물을 사용하여 형성한다.In the present embodiment, although the sheath is composed of a single layer as in Fig. 2, it is also possible to make it a multilayer structure. In this case, at least the outermost layer is formed using the above-mentioned vinyl chloride resin composition.
(실시예)(Example)
이하에, 본 발명을 실시예에 의하여 더 구체적으로 설명한다. 또한 본 발명은, 이하의 실시예에 의하여 어떠한 제한을 받는 것이 아니다.Hereinafter, the present invention will be described more specifically by examples. In addition, the present invention is not limited in any way by the following examples.
표1∼2에 실시예, 표3에 종래예 및 비교예를 나타낸다.Examples are shown in Tables 1 and 2, and conventional examples and comparative examples are shown in Table 3.
〈시험편(시트)의 제작방법〉<Method of producing test pieces (sheets)>
평균중합도가 1300인 PVC 100질량부에 대하여, 표1∼3에 나타낸 비율로 가소제, 실리콘고무, 실리콘오일, 안정제로서 칼슘-아연계 무연 안정제, 충전제로서 탄산칼슘을 혼합하였다. 그 후에 혼련(混練)(롤 온도 160℃, 5분)과 프레스(프레스 온도 180℃, 예열 3분, 가압 10MPa로 2분)에 의하여 두께가 1mm인 시트를 성형하였다. 또한 가소제는 롤로 혼련이 가능한 양으로서 40질량부 이상의 첨가가 필요하기 때문에, 테레프탈산 에스테르의 첨가량이 10질량부인 예에 있어서는 DINP(디이소노닐프탈레이트) 30질량부를 블렌드하여 제작하였다.With respect to 100 parts by mass of PVC having an average polymerization degree of 1300, a plasticizer, silicone rubber, silicone oil, a calcium-zinc-based lead-free stabilizer as a stabilizer, and calcium carbonate as a filler were mixed in the proportions shown in Tables 1 to 3. Thereafter, a sheet having a thickness of 1 mm was molded by kneading (roll temperature: 160° C., 5 minutes) and pressing (press temperature: 180° C., preheating for 3 minutes, pressing for 2 minutes at 10 MPa). In addition, since the addition of 40 parts by mass or more of the plasticizer is required as an amount that can be kneaded with a roll, in the example where the addition amount of terephthalic acid ester is 10 parts by mass, DINP (diisononylphthalate) 30 parts by mass was blended and produced.
표1∼3 중의 재료는 이하의 것을 사용하였다.As the materials in Tables 1 to 3, the following were used.
(1) 염화비닐수지(신에쓰 가가쿠 고교 가부시키가이샤(Shin-Etsu Chemical Co., Ltd.) 제품, 상품명 : TK-1300)(1) Vinyl chloride resin (manufactured by Shin-Etsu Chemical Co., Ltd., trade name: TK-1300)
(2) 가소제(2) plasticizer
· 테레프탈산 에스테르· Terephthalic acid ester
DOTP(디-2-에틸헥실테레프탈레이트)DOTP (di-2-ethylhexyl terephthalate)
DINTP(디이소노닐테레프탈레이트)DINTP (diisononyl terephthalate)
DIDTP(디이소데실테레프탈레이트)Diisodecyl terephthalate (DIDTP)
· 프탈산 에스테르· Phthalic acid ester
DINP(디이소노닐프탈레이트)DINP (diisononyl phthalate)
DOP(디-2-에틸헥실프탈레이트)DOP (di-2-ethylhexylphthalate)
(3) 실리콘고무(신에쓰 실리콘(Shin-Etsu Silicone) 제품, 상품명 : KE-76)(3) Silicone rubber (product of Shin-Etsu Silicone, trade name: KE-76)
(4) 실리콘오일(신에쓰 실리콘 제품, 상품명 : KF-96-100cs)(4) Silicone oil (Shin-Etsu silicone product, product name: KF-96-100cs)
(5) 안정제 : Ca-Zn계 무연 안정제(5) Stabilizer: Ca-Zn-based lead-free stabilizer
(6) 충전제 : 탄산칼슘(가부시키가이샤 마루토(Marutou CO., LTD) 제품, 상품명 : 소프톤1500(Softon1500))(6) Filler: Calcium carbonate (product of Marutou CO., LTD, product name: Softon 1500)
〈시험방법〉<Test Methods>
내후성은, 스가 시켄키 가부시키가이샤(Suga Test Instruments Co., Ltd.) 제품인 메탈할라이드 램프 내후촉진시험기(M6T)에 의하여 평가하였다. 시료면 방사조도 1.5kw/m2, 온도 60℃, 습도 50%, 광원-시료 간 거리 350mm, 조사시간 72시간(3분 수분무(水噴霧)+117분 조사의 120분 사이클×36회)의 조건으로 조사하고, 조사 후/조사 전의 인장시험의 신장잔율(retention of elongation)과 조사 후의 외관을 평가하였다. 인장시험은 JISK 6723에 준거하여 하였다. 신장잔율의 평가판정은, 60% 이상을 합격(○), 60% 미만을 불합격(×)으로 하였다. 또한 외관의 평가판정은, 조사 후의 시료표면에 크랙(균열)이 없는 경우를 합격(○), 있는 경우를 불합격(×)으로 하였다. 내후성판정은, 신장잔율이 합격이고 또 외관이 합격인 경우를 합격(○)으로 하고, 어느 하나가 불합격인 경우에는 불합격(×)으로 하였다. 결과를 표1∼3에 나타낸다.Weather resistance was evaluated by a metal halide lamp weathering acceleration tester (M6T) manufactured by Suga Test Instruments Co., Ltd. Sample surface irradiance 1.5kw/m 2 , temperature 60°C, humidity 50%, distance between light source and sample 350mm, irradiation time 72 hours (120-minute cycles of 3-minute water fog + 117-minute irradiation × 36 cycles) conditions, the retention of elongation in the tensile test after/before irradiation and the appearance after irradiation were evaluated. Tensile tests were conducted in accordance with JISK 6723. In the evaluation judgment of the residual elongation rate, 60% or more was passed (◯), and less than 60% was made disqualified (×). In addition, the evaluation judgment of the external appearance was made into pass (○) when there was no crack (crack) on the sample surface after irradiation, and set it as fail (x) when there was. In the determination of weather resistance, a case where the elongation residual rate was acceptable and the external appearance was acceptable was regarded as a pass (○), and a case where any of the results were unacceptable was regarded as a failure (x). The results are shown in Tables 1 to 3.
내블리드성은, 온도 70℃×습도 90%의 항온항습조(恒溫恒濕槽)에 의하여 평가하였다. 72시간 방치하고 취출한 후에, 표면에 끈적임이 없는 경우를 합격(○)으로 하고, 있는 경우를 불합격(×)으로 하였다. 결과를 표1∼3에 나타낸다.The bleed resistance was evaluated in a constant temperature and humidity chamber at a temperature of 70°C and a humidity of 90%. After being left to stand for 72 hours and taken out, the case where there was no stickiness on the surface was regarded as pass (○), and the case where there was was regarded as disqualified (X). The results are shown in Tables 1 to 3.
(표1)(Table 1)
실시예(배합량의 단위는 질량부)Examples (unit of compounding amount is parts by mass)
(표2)(Table 2)
실시예(배합량의 단위는 질량부)Examples (unit of compounding amount is parts by mass)
(표3)(Table 3)
종래예 및 비교예(배합량의 단위는 질량부)Conventional Examples and Comparative Examples (unit of blending amount is parts by mass)
참고로 실시하였던 DOP 또는 DINP를 사용한 종래예1, 2에서는, 내후성·내블리드성 모두 합격이었다.In prior art examples 1 and 2 using DOP or DINP, which were carried out for reference, both weather resistance and bleed resistance were acceptable.
실시예1 및 비교예1은 DOTP를 10질량부 첨가한 경우로서, 실리콘고무를 0.1질량부 첨가한 실시예1에서는 내후성·내블리드성 모두 합격이었지만, 실리콘고무를 첨가하지 않은 비교예1에서는 내후성시험 후에 크랙이 발생하여 외관이 불합격이었기 때문에, 내후성의 판정은 불합격이었다.In Example 1 and Comparative Example 1, 10 parts by mass of DOTP was added. In Example 1 in which 0.1 part by mass of silicone rubber was added, weather resistance and bleed resistance were all acceptable, but in Comparative Example 1 in which silicone rubber was not added, weather resistance was improved. Since cracks occurred after the test and the appearance was disqualified, weather resistance was disqualified.
또한 실시예2, 3 및 비교예2, 3은 DOTP의 첨가량이 40질량부, 100질량부인 경우로서, 실리콘고무를 0.1질량부 첨가한 실시예2, 3은 실시예1과 마찬가지로 합격인 반면에, 실리콘고무를 첨가하지 않은 비교예2, 3은 비교예1의 경우와 마찬가지로 외관이 불합격인 것 외에 신장잔율도 불합격이었기 때문에, 내후성의 판정은 불합격이었다.In Examples 2 and 3 and Comparative Examples 2 and 3, the amount of DOTP added was 40 parts by mass and 100 parts by mass, and Examples 2 and 3 in which 0.1 part by mass of silicone rubber was added were passed as in Example 1, whereas , Comparative Examples 2 and 3 to which silicone rubber was not added were disqualified in appearance as in the case of Comparative Example 1, and also disqualified in elongation retention, so the determination of weather resistance was disqualified.
이상으로부터, 실리콘고무 0.1질량부 이상이 내후성과 내블리드성의 양립에 필요하다는 것을 볼 수 있었다.From the above, it was found that at least 0.1 part by mass of silicone rubber is required for both weather resistance and bleed resistance.
실시예6, 11, 13 및 비교예7∼9로부터, DOTP는 100질량부를 넘으면 DOTP 자체가 블리드 해 버리기 때문에, DOTP의 첨가량은 100질량부가 한계라는 것을 알 수 있었다.From Examples 6, 11, and 13 and Comparative Examples 7 to 9, it was found that DOTP itself bleeds when the amount of DOTP exceeds 100 parts by mass, so that 100 parts by mass of DOTP is the limit.
실시예4∼9로부터, 실리콘고무를 2.5∼5질량부 첨가하여도 내후성과 내블리드성이 양립할 수 있다는 것을 알 수 있었다.From Examples 4 to 9, it was found that even when 2.5 to 5 parts by mass of silicone rubber was added, both weather resistance and bleed resistance were compatible.
실시예4∼6 및 비교예4∼6으로부터, 실리콘고무로는 내후성과 내블리드성을 양립시킬 수 있다는 것을 알 수 있었다. 그러나 실리콘오일에서는 내후성은 개선되었지만, 조성물의 표면에 블리드하여 끈적임이 발생하였다.From Examples 4 to 6 and Comparative Examples 4 to 6, it was found that both weather resistance and bleed resistance can be achieved with silicone rubber. However, although the weather resistance was improved in silicone oil, stickiness occurred due to bleeding on the surface of the composition.
실시예4, 6, 10∼13으로부터, 테레프탈산 에스테르의 알킬쇄의 탄소수C8∼C10에서 상기의 결과와 같은 경향인 것을 볼 수 있었다.From Examples 4, 6, and 10 to 13, it was found that the same tendency as the above results was observed for the number of carbon atoms C8 to C10 in the alkyl chain of terephthalic acid ester.
또한 본 발명은, 상기 실시형태 및 실시예에 한정되지 않고 여러 가지로 변형하여 실시할 수 있다.
In addition, the present invention can be implemented with various modifications without being limited to the above embodiments and examples.
1 : 도체
2 : 절연층
3 : 개재물
4 : 가압 테이프
5 : 시스
10 : 전선
20 : 케이블1: conductor
2: Insulation layer
3: inclusions
4: pressure tape
5 : Sith
10: wires
20: cable
Claims (7)
상기 테레프탈산 에스테르는 디이소노닐테레프탈레이트 또는 디이소데실테레프탈레이트로 이루어지는 전선.
An electric wire having an insulating layer made of a polyvinyl chloride resin composition (PVC) containing terephthalic acid ester as a plasticizer, wherein the polyvinyl chloride resin composition is 40 parts by mass or more and 100 parts by mass or less of the terephthalic acid ester and 0.1 part by mass or more and 5 parts by mass or less of silicone rubber based on 100 parts by mass of the vinyl resin,
The terephthalic acid ester is a wire made of diisononyl terephthalate or diisodecyl terephthalate.
상기 테레프탈산 에스테르는 디이소노닐테레프탈레이트 또는 디이소데실테레프탈레이트로 이루어지는 케이블.
A cable equipped with a sheath made of a vinyl chloride resin composition containing terephthalate as a plasticizer, wherein the vinyl chloride resin composition comprises 40 parts by mass or more of the terephthalate ester with respect to 100 parts by mass of the vinyl chloride resin , 100 parts by mass or less, containing 0.1 parts by mass or more and 5 parts by mass or less of silicone rubber,
The terephthalic acid ester is a cable made of diisononyl terephthalate or diisodecyl terephthalate.
제1항의 전선을 구비한 케이블.
According to claim 2,
A cable having the wire of claim 1.
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