KR100239581B1 - Insulating material for electric wire - Google Patents
Insulating material for electric wire Download PDFInfo
- Publication number
- KR100239581B1 KR100239581B1 KR1019960078045A KR19960078045A KR100239581B1 KR 100239581 B1 KR100239581 B1 KR 100239581B1 KR 1019960078045 A KR1019960078045 A KR 1019960078045A KR 19960078045 A KR19960078045 A KR 19960078045A KR 100239581 B1 KR100239581 B1 KR 100239581B1
- Authority
- KR
- South Korea
- Prior art keywords
- weight
- parts
- density polyethylene
- flame retardant
- resin composition
- Prior art date
Links
- 239000011810 insulating material Substances 0.000 title 1
- 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 claims abstract description 46
- 239000003063 flame retardant Substances 0.000 claims abstract description 46
- 239000000779 smoke Substances 0.000 claims abstract description 42
- 229920005989 resin Polymers 0.000 claims abstract description 32
- 239000011347 resin Substances 0.000 claims abstract description 32
- 239000000203 mixture Substances 0.000 claims abstract description 31
- 239000011342 resin composition Substances 0.000 claims abstract description 29
- 231100000252 nontoxic Toxicity 0.000 claims abstract description 14
- 230000003000 nontoxic effect Effects 0.000 claims abstract description 14
- 239000006229 carbon black Substances 0.000 claims abstract description 12
- 239000011248 coating agent Substances 0.000 claims abstract description 9
- 238000000576 coating method Methods 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 9
- 239000003112 inhibitor Substances 0.000 claims abstract description 9
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 8
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 14
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 14
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 14
- 239000000347 magnesium hydroxide Substances 0.000 claims description 14
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 14
- 239000004594 Masterbatch (MB) Substances 0.000 claims description 12
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 12
- 239000004707 linear low-density polyethylene Substances 0.000 claims description 12
- -1 zinc borate compound Chemical class 0.000 claims description 12
- 239000004700 high-density polyethylene Substances 0.000 claims description 10
- 229920001684 low density polyethylene Polymers 0.000 claims description 10
- 239000004702 low-density polyethylene Substances 0.000 claims description 10
- 229920001903 high density polyethylene Polymers 0.000 claims description 8
- 239000005078 molybdenum compound Substances 0.000 claims description 7
- 150000002752 molybdenum compounds Chemical class 0.000 claims description 7
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- 229920001179 medium density polyethylene Polymers 0.000 claims description 5
- 239000004701 medium-density polyethylene Substances 0.000 claims description 5
- 230000003078 antioxidant effect Effects 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 3
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 claims description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 claims description 2
- 229940018557 citraconic acid Drugs 0.000 claims description 2
- 229920004889 linear high-density polyethylene Polymers 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- MZHULIWXRDLGRR-UHFFFAOYSA-N tridecyl 3-(3-oxo-3-tridecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCC MZHULIWXRDLGRR-UHFFFAOYSA-N 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 229920002943 EPDM rubber Polymers 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 abstract description 13
- 239000011247 coating layer Substances 0.000 description 12
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 11
- 238000004891 communication Methods 0.000 description 9
- 238000004132 cross linking Methods 0.000 description 9
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 229910000000 metal hydroxide Inorganic materials 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 238000012545 processing Methods 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 5
- 230000007774 longterm Effects 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 206010003497 Asphyxia Diseases 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000001739 density measurement Methods 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
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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
- H01B3/42—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 polyesters; polyethers; polyacetals
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/16—Halogen-containing compounds
- C08K2003/164—Aluminum halide, e.g. aluminium 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/16—Halogen-containing compounds
- C08K2003/166—Magnesium halide, e.g. magnesium chloride
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Insulated Conductors (AREA)
Abstract
a) 비극성 폴리올레핀계 수지, 극성 수지 또는 이들의 혼합물 100 중량부,a) 100 parts by weight of a non-polar polyolefin resin, a polar resin or a mixture thereof,
b) 무독성 비할로겐계 난연제 70 내지 120 중량부b) 70 to 120 parts by weight of non-toxic non-halogen flame retardant
c) 보조난연제 10 내지 20 중량부c) 10 to 20 parts by weight of auxiliary flame retardant
d) 연기밀도억제제 20 내지 100 중량부d) 20 to 100 parts by weight of smoke density inhibitor
e) 상용화제 5 내지 30 중량부 및e) 5 to 30 parts by weight of a compatibilizer and
f) 카본블랙 5 내지 10 중량부를 함유하는 케이블 피복용 난연 수지 조성물이 개시되었다. 이 전선 케이블 피복용 난연 수지 조성물은 연소시 발생되는 연기밀도를 획기적으로 감소시킴으로서 화재시 발생되는 연기에 의한 인적, 물적 피해를 최대한 감소시킬 수 있는 특징을 가지고 있다.f) The flame retardant resin composition for cable coating containing 5-10 weight part of carbon black was disclosed. The flame-retardant resin composition for coating the wire cable has a feature that can significantly reduce the physical and physical damage caused by the smoke generated by the fire by significantly reducing the smoke density generated during the combustion.
Description
본 발명은 전선 케이블 피복용 난연 수지 조성물, 보다 상세하게는 전선 케이블 피복용으로 사용될 수 있는 연기 발생량이 매우 적은 비할로겐계 무독성 난연 수지 조성물에 관한 것이다.The present invention relates to a flame retardant resin composition for wire cable sheathing, and more particularly to a non-halogen non-toxic flame retardant resin composition having a very low smoke generation amount which can be used for wire cable sheathing.
케이블은 크게 통신 케이블 및 전선 케이블 두가지로 분류할 수 있다. 통신 케이블 피복재료로는 전기적 특성, 기계적 특성 등이 우수한 저밀도, 중밀도 및 고밀도 폴리에틸렌이 주로 사용되나 국내외 여러나라에서의 통신 케이블의 빈번한 화재 발생으로 수년전부터 난연화가 추진되어 현재는 비할로겐계 무독성 난연 수지 조성물을 사용한 통신 케이블의 사용이 국내에서도 활발한 상태이다.Cables can be broadly classified into two types: communication cables and wire cables. Low-density, medium-density and high-density polyethylene are mainly used as the coating material for communication cables.They are flame-retardant for many years due to frequent fires in communication cables in many countries at home and abroad. The use of a communication cable using a resin composition is also active in Korea.
전선 케이블의 경우 누전이나 외부 불꽃에 의한 화재발생시 그 위험성은 통신 케이블에 비해 매우 심각하다. 따라서, 전선 케이블 피복재료로 폴리염화비닐계 난연수지 조성물이 사용되고 있는데, 이 폴리염화비닐계 난연수지 조성물은 압출 가공시나 화재로 인한 연소시 인체에 매우 치명적인 다량의 연기 및 분해가스가 발생하며, 내열성 및 내한성이 약하여 여름철 제품의 변형과 기계적 물성 저하가 발생하고, 저온 및 상온에서 취약한 내충격성으로 인해 수십년 동안 장기간 사용을 위한 케이블의 장기 신뢰성에 커다란 결점이 되고 있다. 이에 전선 케이블의 피복층의 경우에도 압출가공시와 화재시 유독가스를 발생시키지 않고 연기밀도 발생량이 적은 비할로겐계 난연제를 사용한 무독성 난연 수지 조성물의 사용이 본격화 되어야만 할 것이다.In the case of wire cables, the risk of a short circuit or a fire caused by an external flame is more serious than a communication cable. Therefore, polyvinyl chloride-based flame retardant resin composition is used as the wire cable coating material, and the polyvinyl chloride-based flame retardant resin composition generates a large amount of smoke and decomposition gas, which is extremely fatal to the human body during extrusion processing or combustion due to fire, and heat resistance. And because the cold resistance is weak, deformation of the summer product and mechanical properties are deteriorated, and the weak impact resistance at low temperatures and room temperature has been a major drawback in the long-term reliability of the cable for long-term use for decades. Accordingly, even in the case of the coating layer of the wire cable, the use of a non-toxic flame retardant composition using a non-halogen-based flame retardant having a small amount of smoke density generation without generating toxic gas during extrusion processing and fire should be in earnest.
통신 케이블의 피복층의 경우, 비할로겐계 무독성 난연수지 조성물과 관련된 종래의 기술은 다음과 같다.In the case of the coating layer of the communication cable, the related art related to the non-halogen-based nontoxic flame retardant resin composition is as follows.
1) 대한민국 특허 공고번호 제 96-6148 호에는 비극성 및 극성의 폴리올레핀계 수지 혼합물, 수산화금속 화합물, 적인, 상용화제, 표면처리제 및 기타 첨가제로 구성되는 것을 특징으로 하는 통신 케이블 피복용 난연성 수지 조성물이 기술되어 있다. 여기에 기재된 실시예에 따른 무독성 난연 수지 조성물은 우수한 상온 인장특성과 산소지수를 보여주었으나, 가열후 인장 특성 시험시 온도조건이 낮고 가열시간이 낮아 더욱 더 우수한 장시간 내열성을 요구하는 전선 케이블 피복층의 경우에는 사용이 다소 어려운 점이 있다. 연기밀도 측정시 측정시편의 두께에 대한 구체적인 언급이 없으며, 또한 상기 조성물을 사용하여 케이블을 제조한 경우 피복층의 두께가 증가함에 따라 연소시 연기 밀도가 급격히 증가하는 단점이 있다.1) Korean Patent Publication No. 96-6148 discloses a flame retardant resin composition for coating a telecommunication cable, comprising a non-polar and polar polyolefin resin mixture, a metal hydroxide compound, a red, a compatibilizer, a surface treatment agent, and other additives. Described. The non-toxic flame retardant resin composition according to the embodiments described herein showed excellent room temperature tensile properties and oxygen index, but when the tensile properties test after heating, the low temperature conditions and low heating time of the wire cable coating layer requiring more excellent long-term heat resistance In this case, it is somewhat difficult to use. There is no specific reference to the thickness of the measurement specimen when measuring the smoke density, and when the cable is manufactured using the composition, the smoke density increases rapidly during combustion as the thickness of the coating layer increases.
2) 일본 공개특허 제 63-56544/1988호, 일본 공개특허 제 184704호/1987호, 일본 공개특허 제 74138/1984호2) Japanese Patent Laid-Open No. 63-56544 / 1988, Japanese Patent Laid-Open No. 184704/1987, and Japanese Patent Laid-Open No. 74138/1984
저밀도 폴리에틸렌, 에틸렌 에틸 아크릴레이트 공중합체, 에틸렌 비닐 아세테이트 공중합체 혼합물을 베이스 수지로하고 수산화알루미늄(Al(OH)3)이나 수산화마그네슘(Mg(OH)2), 적인 등의 난연제로 이루어진 가교용 조성물을 제안하고 있으나 실제로 수가교나 조사가교를 하는 경우 높은 온도, 수분 등의 영향으로 내부 통신선의 기계적 강도 손상 및 열산화를 유발시켜 통신선으로서의 기능을 할 수 없다. 또한 조사가교는 그 특성상 피복층의 두께증가에 따라 균일한 가교 특성을 보이지 못하는 단점이 있다. 난연 조성물로 제조된 케이블 피복층내의 수산화 금속화합물은 수분과 열, 압력에 민감하여 수가교와 고온, 고압을 요하는 가류관내 화학가교에는 적합하지 않다.A composition for crosslinking comprising a low density polyethylene, ethylene ethyl acrylate copolymer, ethylene vinyl acetate copolymer mixture as a base resin, and a flame retardant such as aluminum hydroxide (Al (OH) 3 ), magnesium hydroxide (Mg (OH) 2 ), and red However, in the case of water crosslinking or irradiating crosslinking, it is impossible to function as a communication line by causing mechanical strength damage and thermal oxidation of the internal communication line under the influence of high temperature and moisture. In addition, irradiated crosslinking has a disadvantage in that it does not show uniform crosslinking characteristics as the thickness of the coating layer increases. The metal hydroxide compound in the cable coating layer made of the flame retardant composition is sensitive to moisture, heat, and pressure, and is not suitable for chemical crosslinking in vulcanization tubes requiring water crosslinking, high temperature, and high pressure.
3) 미국 특허 4,575,184/1986년3) US Patent 4,575,184 / 1986
에틸렌 비닐아세테이트 공중합체를 베이스 수지로하고 수산화 금속화합물, 마그네슘 카보네이트, 칼슘 카보네이트, 아연보레이트 등의 난연제와 연기밀도 억제제를 함유한 조사가교용 무독성 난연 수지 조성물을 이용하여 광섬유 케이블을 제조한 발명이다. 그러나 전술한바와같이 피복층이 두꺼운 통신 및 전선 케이블 내에서는 균일한 가교도를 유지할 수 있으며 이로 인한 기계적 강도 불량 및 가교시의 높은 열로 인해 수산화금속화합물계 난연제 분해를 촉진하여 난연성을 유지할 수 없다. 또한 실시예에서 보여주는 연기밀도는 플래밍 (FLAMING) 방법에 의한 측정이며 피복층의 두께도 0.8 mm 의 매우 얇은 상태에서 측정된 것으로서 화재발생시의 실지 조건과 유사한 엄격한 방법에 의해 측정되지 못한 단점이 있다. 또한 위 조성물에 의해 제조된 피복층의 기계적 강도는 너무 낮은 결점을 가지고 있다.An optical fiber cable is prepared by using a non-toxic flame retardant resin composition for irradiation crosslinking comprising a ethylene vinyl acetate copolymer as a base resin and containing a flame retardant such as a metal hydroxide compound, magnesium carbonate, calcium carbonate, and zinc borate, and a smoke density inhibitor. However, as described above, even in the communication and wire cable with a thick coating layer, it is possible to maintain a uniform degree of crosslinking, and thus, due to poor mechanical strength and high heat during crosslinking, metal hydroxide compound-based flame retardant decomposition may not be promoted to maintain flame retardancy. In addition, the smoke density shown in the embodiment is measured by the flamming method, and the thickness of the coating layer was also measured in a very thin state of 0.8 mm, which was not measured by a strict method similar to the actual conditions at the time of fire. In addition, the mechanical strength of the coating layer produced by the above composition has a drawback that is too low.
위 발명들에 의한 무독성 난연 피복층은 우수한 산소지수를 보여주나 공통적으로 피복층의 증가에 따라 연소시 다량의 연기를 발생시키는 결점을 가지고 있다.The non-toxic flame retardant coating layer according to the above inventions shows an excellent oxygen index, but has a drawback of generating a large amount of smoke during combustion in accordance with the increase of the coating layer in common.
화재시 발생되는 연기는 신속한 대피를 어렵게 함으로써 질식으로 인한 많은 인명피해를 발생시키고 또한 연소시 발생되는 가스는 수분과 접촉하여 산성을 띄는 수분을 만들기 때문에 각종 금속을 부식시켜 화재로 인한 직접적인 1 차 재산피해 뿐만이 아닌 2 차적인 재산피해까지 발생시킨다. 그리하여 실내용 전기제품, 사무기기제품, 건축재료, 케이블 피복재료 등에 관해 화재시 발생되는 연기밀도에 관한 보다 더 엄격한 규제가 각국에서 추진중에 있다.Smoke generated during a fire makes it difficult to evacuate quickly, causing a lot of casualties due to suffocation, and the gas generated during combustion creates moisture that shows acidic contact with moisture. Not only damage, but also secondary property damage. Thus, stricter regulations on smoke density in the event of fire are being pursued in each country for indoor electrical appliances, office equipment products, building materials and cable sheathing materials.
따라서, 본 발명의 목적은 종래의 난연 수지 조성물과 비교하여 연소시 발생되는 연기밀도를 획기적으로 감소시킴으로서 화재시 발생되는 연기에 의한 인적, 물적 피해를 최대한 감소시킬 수 있는 연소시 낮은 연기밀도를 갖는 무독성의 전선 케이블 피복용 난연 수지 조성물을 제공하는데 있다.Accordingly, an object of the present invention has a low smoke density during combustion that can greatly reduce the physical and physical damage caused by the smoke generated by the fire by dramatically reducing the smoke density generated during combustion compared to the conventional flame retardant resin composition. It is to provide a non-toxic flame retardant resin composition for wire cable coating.
상기와 같은 목적을 달성하기위해 노력한 결과, 본 발명자들은 비극성 폴리올레핀계 수지와 극성 수지의 베이스 수지에, 상용화제, 비할로겐계 난연제, 보조난연제, 연기밀도 억제제를 첨가함으로써, 연소시 낮은 연기밀도를 갖는 무독성의 전선 케이블 피복용 난연 수지 조성물을 얻을 수 있음을 알아내고, 본 발명을 완성하게 되었다.As a result of our efforts to achieve the above object, the present inventors have added a compatibilizer, a non-halogen flame retardant, a secondary flame retardant, and a smoke density inhibitor to a non-polar polyolefin resin and a base resin of a polar resin, thereby providing low smoke density during combustion. It was found out that a non-toxic flame retardant resin composition for electric wire cable coating can be obtained, and completed the present invention.
구체적으로 본 발명의 전선 케이블용 난연 수지 조성물은 하기 성분을 함유한다:Specifically, the flame retardant resin composition for electric wire cables of the present invention contains the following components:
a) 비극성 폴리올레핀계 수지, 극성 수지 또는 이들의 혼합물 100 중량부,a) 100 parts by weight of a non-polar polyolefin resin, a polar resin or a mixture thereof,
b) 무독성 비할로겐계 난연제 70 내지 120 중량부b) 70 to 120 parts by weight of non-toxic non-halogen flame retardant
c) 보조난연제 10 내지 20 중량부c) 10 to 20 parts by weight of auxiliary flame retardant
d) 연기밀도억제제 20 내지 100 중량부d) 20 to 100 parts by weight of smoke density inhibitor
e) 상용화제 5 내지 30 중량부 및e) 5 to 30 parts by weight of a compatibilizer and
f) 카본블랙 5 내지 10 중량부.f) 5 to 10 parts by weight of carbon black.
본 발명의 난연 수지 조성물의 a) 베이스 수지로서는 비극성 폴리올레핀계 수지, 극성 수지 또는 이들의 혼합물을 사용하였다. 비극성 수지 단독만을 사용할 경우에는 수산화금속 화합물, 연기밀도 억제제의 충진이 불량하게 되어 기계적 강도 및 내한성이 크게 저하되므로, 극성 수지와의 혼합물을 사용하는 것이 바람직하다.As the a) base resin of the flame retardant resin composition of the present invention, a nonpolar polyolefin resin, a polar resin, or a mixture thereof was used. In the case where only the nonpolar resin is used alone, since the filling of the metal hydroxide compound and the smoke density inhibitor becomes poor, the mechanical strength and the cold resistance are greatly reduced, it is preferable to use a mixture with the polar resin.
사용된 비극성 폴리올레핀계 수지로는 ASTM D1238 에 의해 측정된 용융지수 (MI) 가 2.8 내지 5.0 g/10 분인 저밀도 폴리에틸렌, 선형저밀도 폴리에틸렌, 중밀도 폴리에틸렌, 고밀도 폴리에틸렌, 에틸렌-프로필렌 고무, 에틸렌-프로필렌-디엔 고무 등의 수지가 사용될 수 있으며, 극성 수지로는 비닐아세테이트 함량이 41 % 이하이고 MI가 5 g/10 분이하인 에틸렌 비닐 아세테이트 공중합체, 에틸 아크릴레이트 함량이 35 % 이하이며 MI 가 5 g/10 분 이하인 에틸렌 에틸 아크릴레이트 공중합체 또는 이들의 혼합물이 사용될 수 있다.Non-polar polyolefin resins used include low density polyethylene, linear low density polyethylene, medium density polyethylene, high density polyethylene, ethylene-propylene rubber, ethylene-propylene- having a melt index (MI) of 2.8 to 5.0 g / 10 min, as measured by ASTM D1238. A resin such as a diene rubber may be used, and as the polar resin, an ethylene vinyl acetate copolymer having a vinyl acetate content of 41% or less and a MI of 5 g / 10 minutes or less, an ethyl acrylate content of 35% or less and a MI of 5 g / Ethylene ethyl acrylate copolymers or mixtures thereof that are 10 minutes or less can be used.
본 발명에서 b) 비할로겐계 난연제로서는 수산화마그네슘과 수산화알루미늄을 단독 또는 혼합 사용하였다. 수산화 마그네슘은 수산화 알루미늄에 비해 동일한 함량에서 산소지수가 양호한 편이고 분해온도가 300℃ 이상으로 인해 가공온도가 높은 열가소성수지에 적합하며 분해온도가 200℃ 로 낮은 수산화 알루미늄에 비해 주로 사용되어지고 있다. 그러나 수산화 마그네슘이 함유된 수지 조성물의 연소시 발생되는 연기밀도는 수산화 알루미늄이 함유된 수지 조성물의 연소시 발생되는 연기밀도에 비해 상당히 높은 단점을 가지고 있다.In the present invention, b) magnesium hydroxide and aluminum hydroxide were used alone or in combination as a non-halogen flame retardant. Magnesium hydroxide has a good oxygen index at the same content as aluminum hydroxide, and is suitable for thermoplastic resins having a high processing temperature due to the decomposition temperature of 300 ° C. or higher. However, the smoke density generated during the combustion of the resin composition containing magnesium hydroxide has a significantly higher disadvantage than the smoke density generated during the combustion of the resin composition containing aluminum hydroxide.
따라서, 본 발명에서는 평균 입자크기가 0.6 ∼ 2.0 ㎛ 인 수산화알루미늄을 사용하여 연기밀도를 낮추었으며 부족한 가공성 및 불량한 압출외관을 극복하기 위해 평균 입자크기가 0.6 ∼ 2.0 ㎛ 인 수산화마그네슘을 혼합 사용하는 것이 바람직하다. 상기 수산화금속화합물들의 첨가량은 베이스 수지 100 중량부에 대해 70 내지 120 중량부가 적당하다. 120 중량부 초과에서는 기계적 특성이 저하되고 연소시 연기밀도가 증가하게 된다. 상기 두가지의 수산화금속화합물의 혼합물내 수산화알루미늄이 차지하는 비율은 40 내지 60 % 일때가 양호하다. 그 미만인 경우 연기밀도가 증가되며 60 % 초과일 경우 가공성이 급격히 나빠지게 된다.Therefore, in the present invention, it is possible to lower the smoke density by using aluminum hydroxide having an average particle size of 0.6 to 2.0 μm, and to mix magnesium hydroxide having an average particle size of 0.6 to 2.0 μm to overcome poor processability and poor extrusion appearance. desirable. The addition amount of the metal hydroxide compounds is suitably 70 to 120 parts by weight based on 100 parts by weight of the base resin. If it exceeds 120 parts by weight, the mechanical properties are lowered and the smoke density is increased during combustion. The proportion of aluminum hydroxide in the mixture of the two metal hydroxide compounds is preferably 40 to 60%. If it is less than that, smoke density increases, and when it exceeds 60%, workability will worsen rapidly.
본 발명에서는 난연성의 보완을 위해 c) 보조 난연제로서 적인을 사용하였는데, 이 적인은 그 자체로서는 가공시 자체발화 및 폭발의 위험성이 있어서 ASTM D1238 에 의한 용융지수 (MI) 가 2 내지 5 g/10분의 저밀도폴리에틸렌, 선형저밀도 폴리에틸렌, 고밀도 폴리에틸렌 또는 에틸렌 비닐 아세테이트 공중합체, 에틸렌 에틸아크릴레이트 공중합체, 혹은 이들의 혼합물 100 중량부에 대해 10 내지 30 중량부의 적인 마스터뱃치를 제조하여 사용하였다. 사용된 적인 마스터 뱃치는 베이스 수지 100 중량부에 대해 10 내지 20 중량부를 사용하였다. 20 중량부 초과에서는 급격히 연기밀도가 증가 하였다.In the present invention, in order to supplement the flame retardancy, c) was used as an auxiliary flame retardant, which itself has a risk of self-ignition and explosion during processing, so that the melt index (MI) according to ASTM D1238 is 2 to 5 g / 10. 10 to 30 parts by weight of the masterbatch was prepared by using 100 parts by weight of low density polyethylene, linear low density polyethylene, high density polyethylene or ethylene vinyl acetate copolymer, ethylene ethyl acrylate copolymer, or mixtures thereof. The used master batch used 10 to 20 parts by weight based on 100 parts by weight of the base resin. Above 20 parts by weight, the smoke density rapidly increased.
본 발명에서는 d) 연기밀도 억제제를 사용하여 연소시 발생될 수 있는 연기량을 최대한 낮추었다. 본 발명에서 사용된 연기밀도 억제제로서는 평균 입자크기 1 ∼ 3 ㎛ 의 아연 보레이트, 몰리브데늄 화합물(MoO3) 또는 이들의 혼합물을 사용하였다. 상기 사용된 아연 보레이트, 몰리브데늄 화합물 또는 이들의 혼합물은 베이스 수지 100 중량부에 대해 20 내지 100 중량부가 적당하며, 바람직하기로는 40 내지 100 중량부이다. 100 중량부 초과에서는 기계적 특성이 급격히 저하되며 20 중량부 미만에서는 연기밀도 억제의 기능을 하지 못한다.In the present invention, d) the smoke density inhibitor was used to minimize the amount of smoke that can be generated during combustion. As the smoke density inhibitor used in the present invention, zinc borate, molybdenum compound (MoO 3 ) or a mixture thereof having an average particle size of 1 to 3 μm was used. The zinc borate, molybdenum compound or mixtures thereof used above is suitably 20 to 100 parts by weight, preferably 40 to 100 parts by weight, relative to 100 parts by weight of the base resin. If it is more than 100 parts by weight, the mechanical properties are drastically reduced, and if it is less than 20 parts by weight, it does not function as a smoke density suppressor.
또한 a) 베이스 수지로 사용된 비극성 수지와 극성 수지와의 상용성을 개선시켜 계면에서의 결합력을 높임과 동시에 난연제의 충진성을 높혀주고 조성물의 기계적 강도를 유지하기 위하여 본 발명에서는 e) 상용화제로 말레인산, 메타아크릴산, 시트라콘산, 아크릴산 또는 그 무수물 등의 관능기 함량이 2.0 내지 4.0 중량부이고 밀도는 0.920 내지 0.950 g/cm3이며 MI 가 0.3 내지 5.0 g/10분인 저밀도 폴리에틸렌, 선형 저밀도 폴리에틸렌, 중밀도 폴리에틸렌, 또는 고밀도 폴리에틸렌인 관능기가 그라프트된 접착성 폴리에틸렌 수지를 베이스 수지 100 중량부에 대해 5 내지 30 중량부 사용하였다.In addition, a) in order to improve the compatibility between the non-polar resin and the polar resin used as the base resin to increase the bonding strength at the interface and at the same time to increase the filling of the flame retardant and to maintain the mechanical strength of the composition, e) as a compatibilizer Low density polyethylene, linear low density polyethylene having a functional group content of 2.0 to 4.0 parts by weight, a density of 0.920 to 0.950 g / cm 3, and a MI of 0.3 to 5.0 g / 10 minutes, such as maleic acid, methacrylic acid, citraconic acid, acrylic acid or anhydride thereof; 5 to 30 parts by weight of an adhesive polyethylene resin grafted with a functional group of medium density polyethylene or high density polyethylene was used based on 100 parts by weight of the base resin.
본 발명에서 사용된 f) 카본블랙은 옥외 폭로시 자외선 차단제로서 케이블의 장기 내후성을 향상시킬 목적으로 사용되는데 평균 입자크기 25 nm 이하인 내후성 증진용 카본블랙을 사용하여 베이스 수지의 MI 가 5 내지 10 g/10분 인 저밀도폴리에틸렌, 선형저밀도 폴리에틸렌, 고밀도 폴리에틸렌 100 중량부에 대해 20 내지 40 중량부로 카본블랙 마스터 뱃치를 제조하여 사용하였으며, 사용된 카본블랙 마스터 뱃치는 베이스 수지 100 중량부에 대해 5 내지 10 중량부를 사용하였다.F) Carbon black used in the present invention is used for the purpose of improving the long-term weather resistance of the cable as a sunscreen when exposed to the outdoors, and the MI of the base resin is 5 to 10 g by using carbon black for improving weather resistance having an average particle size of 25 nm or less. 20 to 40 parts by weight based on 100 parts by weight of low density polyethylene, linear low density polyethylene, and 100 parts by weight of high density polyethylene were prepared and used, and the carbon black master batch used was 5 to 10 parts by weight of 100 parts by weight of the base resin. Parts by weight were used.
본 발명에서는 또한 조성물 제조와 케이블제조시 열안정을 부여하고 고전압 송전 및 배전시 도체 저항에 의해 자체열 발생이 심한 전선 케이블에서 피복층의 노화를 방지하고 장기 열안정성을 부여하기 위하여 산화방지제를 사용하였다. 사용된 산화방지제로서는 옥타데실 3,5-디-t-부틸-4-히드로신나메이트, 펜타에리트리틸-테트라키스[3-(3,5-디-t-부틸-4-히드록시-페닐)프로피오네이트], 디(트리데실)티오디프로피오네이트, 2,4-티오-비스(6-t-부틸-3-메틸 페놀)을 사용하였으며 베이스 수지 100 중량부에 대해 0.5 내지 4 중량부를 사용하는게 바람직하다.In the present invention, an antioxidant was used to impart thermal stability to the composition and cable manufacturing, and to prevent aging of the coating layer and to provide long-term thermal stability in the wire cable, which is highly self-heating due to conductor resistance during high voltage transmission and distribution. . Antioxidants used include octadecyl 3,5-di-t-butyl-4-hydrocinnamate, pentaerythryl-tetrakis [3- (3,5-di-t-butyl-4-hydroxy-phenyl ) Propionate], di (tridecyl) thiodipropionate, 2,4-thio-bis (6-t-butyl-3-methyl phenol) was used and 0.5 to 4 wt% based on 100 parts by weight of the base resin It is preferable to use a part.
본 발명의 저연기밀도의 무독성 난연 수지 조성물을 얻기 위해서는 헨셀믹서, 리본 블렌더, 브이 블랜더 등을 사용하여 원료를 혼합하거나 각기 다른 원료 공급장치로 정해진 비율로 원료를 공급하여 사용할 수 있고 가공기기로는 가공조건에 따라 1 축 압출기, 2 축 압출기 또는 일반적으로 하나의 공급구 이외에 압출기 일부를 공급구로 사용할 수 있는 2 축 압출기, 니더 (kneader), 믹서, 벤버리 (banbury) 믹서를 사용하여 용융 혼합하여 펠렛 형상화하였다. 가공조건에 따라 수지조성물의 물성이 변화하므로 주로 하나의 공급구 이외에 압출기 일부를 공급구로 사용할 수 있는 2 축 압출기를 주로 이용하여 스크류 회전수, 공급량 및 가공온도를 변화시켜 가공조건을 최적화 시켰다.In order to obtain the low smoke density non-toxic flame retardant resin composition of the present invention, a raw material may be mixed using a Henschel mixer, a ribbon blender, a V blender, or the like, or the raw materials may be supplied at different ratios using different raw material supply devices. Depending on the processing conditions, melt mixing may be carried out using a twin screw extruder, a twin screw extruder, or a twin screw extruder, kneader, mixer, or banbury mixer, in which a part of the extruder can be used as a feed in addition to a single feed port. Pellets were shaped. Since the physical properties of the resin composition change depending on the processing conditions, the screw rotation speed, supply amount and processing temperature are optimized by using a twin screw extruder that can use a part of the extruder as a supply port in addition to one supply port.
이렇게 제조된 저연기밀도의 무독성 난연 수지 조성물은 일정한 수분제거 공정을 거친후 압축 시편을 제조하여 미국 표준규격 (ASTM) 에 준하여 기계적 물성 및 기타 연기밀도, 산소지수를 측정하였다.The low smoke density non-toxic flame retardant resin composition thus prepared was subjected to a constant water removal process to prepare compressed specimens, and measured mechanical properties, other smoke densities, and oxygen indexes according to the American Standard.
1) 인장강도1) tensile strength
ASTM D 638 에 규정된 방법에 의하여 파단강도 및 신율을 측정하였다.The breaking strength and elongation were measured by the method specified in ASTM D 638.
2) 가열후 인장강도 및 신율2) Tensile strength and elongation after heating
120℃ 온도가 유지되는 오븐에서 압축시편을 7 일간 에이징한 후 파단강도 및 신율을 측정하였다.After compressing the compressed specimens in an oven maintained at 120 ° C. for 7 days, the breaking strength and elongation were measured.
3) 산소지수3) oxygen index
ASTM D 2683 에 규정된 방법에 의거하여 산소지수를 측정하였다.Oxygen index was measured according to the method specified in ASTM D 2683.
4) 연기밀도 측정4) Smoke density measurement
ASTM E 662 에 규정된 비플레밍 방법에 의하여 연기밀도를 측정하였으며 시편의 두께는 0.5 mm 와 4.0 mm 두가지를 적용하였다.Smoke density was measured by the non-flemming method specified in ASTM E 662, and the specimen thicknesses were 0.5 mm and 4.0 mm.
실시예와 비교예에서 사용한 원부재료는 다음과 같다.Raw materials used in Examples and Comparative Examples are as follows.
1. LLDPE, 대림산업 주식회사 제품 : 상품명 LL-04 (밀도 : 0.920 g/cm3, MI : 1.0 g/10 분)1. LLDPE, Daelim Industrial Co., Ltd. Product: Name LL-04 (density: 0.920 g / cm 3, MI : 1.0 g / 10 min)
2. EVA, 미쓰이 듀퐁 : 상품명 EVA 260 (밀도 : 0.950 g/cm3, MI : 6 g/10 분, VA 함량 28 %)2.EVA, Mitsui Dupont: trade name EVA 260 (density: 0.950 g / cm 3 , MI: 6 g / 10 min, VA content 28%)
3. EEA, 네스테 : 상품명 NCPE 5710 (밀도 : 0.930 g/cm3, MI : 1.0 g/10 분, EA 함량 15 %)3.EEA, Neste: trade name NCPE 5710 (density: 0.930 g / cm 3 , MI: 1.0 g / 10 min, EA content 15%)
4. Mg(OH)2, 교화화학 공업사 : 상품명 KISUMA 5A4. Mg (OH) 2 , Kyowa Chemical Industry: trade name KISUMA 5A
5. Al(OH)3, 알코아 : H-7105.Al (OH) 3 , Alcoa: H-710
6. 아연보레이트, 험프레이 화학 제품 : 상품명 ZB-3256. Zinc borate, Humprey Chemicals: ZB-325
7. MoO3, 쉐린 윌리암스 : 상품명 KEMGARD 9817.MoO 3 , Cherin Williams: trade name KEMGARD 981
8. 적인 마스터 뱃치, 일본화학공업 TP-10을 사용 대림산업주식회사에서 제조8. Master batch, manufactured by Daelim Industrial Co., Ltd. using TP-10
9. 카본블랙 마스터 뱃치, 카봇 Vulcan 9A32 사용, 대림산업주식회사 제조9. Carbon Black Master Batch, using Cabot Vulcan 9A32, manufactured by Daelim Industrial Co., Ltd.
10. 접착성 폴리에틸렌, 대림산업주식회사 제품 : 상품명 SX-810 (무수말레인산으로 그라프트된 고밀도 폴리에틸렌)10. Adhesive Polyethylene, Daelim Industrial Co., Ltd. Product Name: SX-810 (High density polyethylene grafted with maleic anhydride)
11. 열안정제, 요시토미 : 상품명 YOSHINOX SR11. Heat stabilizer, Yoshitomi: trade name YOSHINOX SR
이하 본 발명의 실시예 및 비교예를 통하여 본 발명을 상세히 설명하나 본 발명이 하기 실시예 및 비교예에 의해 한정되는 것은 아니다.Hereinafter, the present invention will be described in detail through examples and comparative examples of the present invention, but the present invention is not limited to the following examples and comparative examples.
실시예Example
실시예 1Example 1
에틸렌 비닐 아세테이트 공중합체를 베이스 수지로하여 수산화마그네슘 75 중량부, 아연보레이트 25 중량부, 적인 마스터뱃치 10 중량부, 산화방지제 0.8 중량부와 카본블랙 7.0 중량부를 투입하여 밤버리 믹서, 롤밀을 이용하여 실지 수지온도가 200℃ 이하가 되도록 난연성 조성물을 제조한후 ASTM D 1928 에 의거하여 압축성형 시편을 제조한다. 제조된 시편을 ASTM D 638 방법으로 상온에서의 파단강도, 신율을 측정하였고 120℃ 가 유지되는 열풍 건조기에서 일주일간 가열 노화한후 파단강도 및 신율을 측정하였다. ASTM E 662 에 의거하여 압축시편을 일정한 형태로 제조 (0.5 × 76 × 76 mm, 4.0 × 76 × 76 mm)하여 복사열에 의해 발생되는 연기밀도 (non-flaming 방법)를 측정하였다. 또한 길이 125 ± 5 mm, 폭 6.5 mm ± 0.3 mm, 두께 3 mm 의 산소지수 측정용 시편을 제조하여 ASTM D 2638 방법에 의거하여 측정 비교하였다.75 parts by weight of magnesium hydroxide, 25 parts by weight of zinc borate, 10 parts by weight of a masterbatch, 0.8 parts by weight of antioxidant and 7.0 parts by weight of carbon black were added using an ethylene vinyl acetate copolymer as a base resin. After the flame retardant composition was prepared so that the actual resin temperature was 200 ° C. or lower, compression molded specimens were prepared according to ASTM D 1928. Tensile strength and elongation at room temperature were measured by the ASTM D 638 method, and the breaking strength and elongation were measured after a week of heat aging in a hot air dryer maintained at 120 ° C. Compression specimens were prepared in a uniform form (0.5 × 76 × 76 mm, 4.0 × 76 × 76 mm) according to ASTM E 662 to measure smoke density (non-flaming method) generated by radiant heat. In addition, a specimen for measuring oxygen index of 125 ± 5 mm in length, 6.5 mm ± 0.3 mm in width and 3 mm in thickness was prepared and measured according to the ASTM D 2638 method.
상기 실시예 1 에 의한 조성물의 물성측정 결과는 하기의 표 1 과 같다.Physical property measurement results of the composition according to Example 1 are shown in Table 1 below.
실시예 2Example 2
수산화마그네슘 대신 수산화알루미늄를 사용한 것을 제외하고 실시예 1 과 동일하게 실시하였으며 그 결과는 하기의 표 1 과 같다.Except for using aluminum hydroxide instead of magnesium hydroxide was carried out in the same manner as in Example 1 and the results are shown in Table 1 below.
실시예 3Example 3
에틸렌비닐아세테이트 공중합체 대신 에틸렌 에틸 아크릴레이트 공중합체를 사용하고, 아연보레이트 대신 몰리브데늄 화합물(MoO3)을 사용하여 실시한 것을 제외하고 실시예 1 과 동일하며 물성측정 결과는 표 1 과 같다.Ethylene ethyl acrylate copolymer is used instead of ethylene vinyl acetate copolymer, and the molybdenum compound (MoO 3 ) instead of zinc borate was used in the same manner as in Example 1 and the physical properties measurement results are shown in Table 1.
실시예 4Example 4
수산화마그네슘 대신 수산화알루미늄를 사용한 것을 제외하고 실시예 3 과 동일하며 그 결과는 표 1 과 같다.The same procedure as in Example 3 except that aluminum hydroxide was used instead of magnesium hydroxide, and the results are shown in Table 1.
비교예 1 내지 5Comparative Examples 1 to 5
하기 표 2의 조성비와 같이 베이스 수지, 수산화마그네슘 또는 수산화알루미늄을 단독으로 사용하고, 연기밀도 억제제와 상용화제를 사용하지 않은 것 이외에는 실시예 1, 2, 3, 4 와 동일하게 실시하였으며 그 결과는 표 2와 같다.As in the composition ratio of Table 2, using the base resin, magnesium hydroxide or aluminum hydroxide alone, and did not use a smoke density inhibitor and a compatibilizer was carried out in the same manner as in Examples 1, 2, 3, 4 and the results Table 2 is as follows.
상기 실시예 1, 2, 3, 4 와 비교예 1, 2, 3, 4, 5 를 비교해보면, 수산화마그네슘, 또는 수산화알루미늄의 난연제를 단독으로 사용하는 것보다 아연 보레이트 혹은 몰리브데늄 화합물과 혼합사용하는 것이 기계적 강도의 저하없이 연기밀도의 현저한 저하가 발생하였음을 알수 있다. 또한 수산화마그네슘을 사용한 것보다 수산화알루미늄을 사용한 경우가 연기밀도가 낮음을 알 수 있다.When comparing Examples 1, 2, 3, and 4 and Comparative Examples 1, 2, 3, 4, and 5, a mixture of zinc borate or molybdenum compound was used rather than using a flame retardant of magnesium hydroxide or aluminum hydroxide alone. It can be seen that the use caused a significant decrease in smoke density without a decrease in mechanical strength. In addition, it can be seen that the smoke density is lower when aluminum hydroxide is used than when magnesium hydroxide is used.
실시예 5 내지 10Examples 5-10
LLDPE 와 EVA 또는 EEA 혼합물 100 중량부를 베이스수지로하여 상용화제 25 중량부, 수산화마그네슘 또는 수산화알루미늄을 단독 또는 혼합하여 사용하였으며 아연보레이트 또는 몰리브데늄 화합물을 단독으로 사용하였다. 수산화금속화합물과 아연 보레이트 또는 몰리브데늄 화합물의 사용량은 베이스 수지 100 중량부 대비 185 중량부를 사용하였고 산화방지제 0.8 중량부를 사용하였다. 난연성 수지 조성물의 제조방법 및 물성 측정방법은 실시예 1 과 동일하며 측정된 결과는 하기 표 1과 같다.100 parts by weight of a mixture of LLDPE and EVA or EEA was used as a base resin, and 25 parts by weight of a compatibilizer, magnesium hydroxide or aluminum hydroxide was used alone or in a mixture, and zinc borate or molybdenum compound was used alone. The amount of the metal hydroxide compound and the zinc borate or molybdenum compound was used 185 parts by weight based on 100 parts by weight of the base resin and 0.8 parts by weight of antioxidant. The method for producing a flame retardant resin composition and the method for measuring physical properties are the same as in Example 1, and the measured results are shown in Table 1 below.
* 가열후 인장강도 및 신율은 EEA, EVA를 단독 사용한 조성물* Tensile strength and elongation after heating is the composition using EEA and EVA alone
시편의 경우 용융 변형으로 측정불가In case of specimen, melt measurement is not possible
본 발명에 따른 전선 케이블 피복용 난연 수지 조성물은 우수한 기계적인 물성과 함께 연소시 발생되는 연기밀도를 획기적으로 감소시킴으로서 화재시 발생되는 연기에 의한 인적, 물적 피해를 최대한 감소시킬 수 있는 특징을 가지고 있다.The flame retardant resin composition for coating a wire cable according to the present invention has the characteristics that can greatly reduce the physical and physical damages caused by the smoke generated in a fire by dramatically reducing the smoke density generated during combustion with excellent mechanical properties. .
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Cited By (4)
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KR20020063986A (en) * | 2001-01-31 | 2002-08-07 | 삼성종합화학주식회사 | Resin composition for tube or pipe in electronic and industrial field |
KR100479738B1 (en) * | 2002-03-19 | 2005-03-30 | 엘지전선 주식회사 | Polymer composition for insulating material and Locomotive wire using it |
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KR20010096666A (en) * | 2001-06-26 | 2001-11-08 | --- | Themoplastic material alternative to P.V.C |
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KR100772266B1 (en) * | 2006-02-15 | 2007-11-01 | 엘에스전선 주식회사 | Composition for preparing wire coating layer having pressure resistance property and electric wire manufactured using the same |
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Cited By (5)
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KR20020063986A (en) * | 2001-01-31 | 2002-08-07 | 삼성종합화학주식회사 | Resin composition for tube or pipe in electronic and industrial field |
KR100479738B1 (en) * | 2002-03-19 | 2005-03-30 | 엘지전선 주식회사 | Polymer composition for insulating material and Locomotive wire using it |
KR100855795B1 (en) * | 2007-02-28 | 2008-09-01 | 엘에스전선 주식회사 | Semiconducting flame retardant resin composition and electric wire manufactured using the same |
WO2014123327A1 (en) * | 2013-02-06 | 2014-08-14 | Sk Innovation Co.,Ltd. | Non-crosslinked polyethylene composition for power cable |
KR101553520B1 (en) | 2013-02-06 | 2015-09-16 | 에스케이이노베이션 주식회사 | Non-curing polyethylene composition for power cable |
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