JPH10340637A - Insulated wire - Google Patents
Insulated wireInfo
- Publication number
- JPH10340637A JPH10340637A JP9149697A JP14969797A JPH10340637A JP H10340637 A JPH10340637 A JP H10340637A JP 9149697 A JP9149697 A JP 9149697A JP 14969797 A JP14969797 A JP 14969797A JP H10340637 A JPH10340637 A JP H10340637A
- Authority
- JP
- Japan
- Prior art keywords
- inner layer
- resin
- outer layer
- layer
- resistance
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 13
- 229920001083 polybutene Polymers 0.000 claims abstract description 11
- -1 polypropylene Polymers 0.000 claims description 10
- 229910000000 metal hydroxide Inorganic materials 0.000 claims description 9
- 150000004692 metal hydroxides Chemical class 0.000 claims description 9
- 239000004743 Polypropylene Substances 0.000 claims description 8
- 229920001155 polypropylene Polymers 0.000 claims description 8
- 238000005299 abrasion Methods 0.000 abstract description 9
- 239000011342 resin composition Substances 0.000 abstract description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 4
- 239000004020 conductor Substances 0.000 abstract description 2
- 229910052802 copper Inorganic materials 0.000 abstract description 2
- 239000010949 copper Substances 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 2
- 238000010030 laminating Methods 0.000 abstract 1
- 239000003063 flame retardant Substances 0.000 description 9
- 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 8
- 230000000052 comparative effect Effects 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 4
- 229920005672 polyolefin resin Polymers 0.000 description 4
- 230000002087 whitening effect Effects 0.000 description 4
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 3
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 3
- 239000000347 magnesium hydroxide Substances 0.000 description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 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 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Insulated Conductors (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、耐摩耗性、難燃
性、耐加熱変形性等の特性に優れた2層構造の絶縁電線
に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a two-layer insulated wire having excellent properties such as abrasion resistance, flame retardancy, and heat deformation resistance.
【0002】[0002]
【従来の技術】例えば自動車用の絶縁電線に使用される
絶縁被覆材としては、適度な柔軟性や難燃性の面から、
ポリ塩化ビニル樹脂が従来より多く採用されている。と
ころが、この電線は、車両の廃車処分に伴って焼却廃棄
されると、焼却炉内で絶縁被覆が燃えることから塩化水
素ガスを発生し、焼却炉を傷めたり、大気中に排出され
て環境汚染の原因となるという問題点を有している。2. Description of the Related Art For example, as an insulating covering material used for insulated wires for automobiles, from the viewpoint of appropriate flexibility and flame retardancy,
Polyvinyl chloride resin is used more often than ever. However, when this wire is incinerated and disposed of with the scrapping of vehicles, the insulation coating burns in the incinerator, generating hydrogen chloride gas, damaging the incinerator or being discharged into the atmosphere, resulting in environmental pollution. Has the problem of causing
【0003】そこで、近年、塩素等のハロゲン成分を含
まない難燃性の樹脂組成物を絶縁被覆材として使用する
電線が研究されており、その構成はポリオレフィン系樹
脂に金属水酸化物を混合したものが一般的である。[0003] Therefore, in recent years, electric wires using a flame-retardant resin composition containing no halogen component such as chlorine as an insulating coating material have been studied, and the structure thereof is a mixture of a polyolefin resin and a metal hydroxide. Things are common.
【0004】[0004]
【発明が解決しようとする課題】しかしながら、従来の
この種の難燃性樹脂組成物では、ポリ塩化ビニルと比べ
ると柔軟性や屈曲性が劣り、しかも難燃性を与えるため
に多量の金属水酸化物を混合するため、耐摩耗性や引張
強さ等の機械的強度が低下するという問題があった。However, conventional flame-retardant resin compositions of this type are inferior in flexibility and flexibility as compared with polyvinyl chloride, and have a large amount of metallic water to provide flame retardancy. Mixing the oxide has a problem that mechanical strength such as wear resistance and tensile strength is reduced.
【0005】そこで、例えば特開平6−176631号
公報に示されるように、内層で難燃剤を多量に配合した
難燃オレフィン材料を使用し、外層では難燃剤配合量の
少ないまたは全く含有しないオレフィン樹脂を使用する
2層構造の絶縁電線が考えられている。Therefore, as shown in, for example, JP-A-6-176631, a flame-retardant olefin material containing a large amount of a flame retardant is used in the inner layer, and an olefin resin containing little or no flame retardant is contained in the outer layer. Are considered.
【0006】ところがこのような例では、高温下におい
て絶縁電線が変形し易いという問題があった。However, such an example has a problem that the insulated wire is easily deformed at a high temperature.
【0007】そこで、本発明の目的は、焼却時に有害ガ
スを発生せず、しかも柔軟性や屈曲性に優れるととも
に、十分な難燃性を備えつつ耐摩耗性や耐加熱変形性に
も優れる絶縁電線を提供するところにある。Accordingly, an object of the present invention is to provide an insulating material which does not generate harmful gas during incineration, has excellent flexibility and bendability, has sufficient flame retardancy, and has excellent wear resistance and heat deformation resistance. To provide the wires.
【0008】[0008]
【課題を解決するための手段】本発明に係る絶縁電線
は、導電芯線の外周に内層と外層とからなる絶縁層を被
覆した絶縁電線であって、内層はポリプロピレン/ポリ
ブテンアロイ化樹脂重量部に対して金属水酸化物を50
〜400重量部配合してなる樹脂組成物からなると共
に、外層はポリアミド樹脂からなり、内層及び外層の厚
さ寸法比が内層/外層=6/4〜9/1であるところに
特徴を有する。る。The insulated wire according to the present invention is an insulated wire in which an outer peripheral layer of a conductive core is covered with an insulating layer composed of an inner layer and an outer layer, and the inner layer is formed of a polypropylene / polybutene alloy resin by weight. On the other hand, 50
The outer layer is made of a polyamide resin, and the thickness ratio of the inner layer and the outer layer is such that the inner layer / outer layer = 6/4 to 9/1. You.
【0009】本発明で、内層にポリプロピレン/ポリブ
テンアロイ化樹脂を使用するのは、これ以外の硬い樹脂
では柔軟性や耐寒性が不足するためである。金属水酸化
物としては、水酸化マグネシウム、水酸化アルミニウ
ム、水酸化カルシウム等が好適である。これらの金属水
酸化物の粒径はポリマーへの分散性、作業性、電線特性
等の点から平均粒径0.1〜5μmのものが好ましい
が、この範囲を越えても本発明の所期の目的は達成する
ことができる。また、金属水酸化物の凝集防止、ポリマ
ーへの分散性向上及びポリマーへの接着性向上の目的
で、シランカップリング剤、チタネートカップリング
剤、脂肪酸及びその金属塩等を用いて表面処理を施した
ものを用いることが好ましい。In the present invention, the reason why the polypropylene / polybutene alloyed resin is used for the inner layer is that the other hard resins are insufficient in flexibility and cold resistance. As the metal hydroxide, magnesium hydroxide, aluminum hydroxide, calcium hydroxide and the like are preferable. The average particle size of these metal hydroxides is preferably from 0.1 to 5 μm from the viewpoint of dispersibility in a polymer, workability, electric wire characteristics, and the like. The objective of can be achieved. In addition, for the purpose of preventing aggregation of the metal hydroxide, improving dispersibility in the polymer, and improving adhesion to the polymer, surface treatment is performed using a silane coupling agent, a titanate coupling agent, a fatty acid and a metal salt thereof, and the like. It is preferable to use those that have been used.
【0010】内層において、ポリプロピレン/ポリブテ
ンアロイ化樹脂100重量部に対して金属水酸化物を5
0〜400重量部配合させたが、これは50重量部以下
では電線の難燃性が不足し、逆に400重量部以上にな
ると電線の耐白化性や柔軟性、更に耐摩耗性、引張強さ
等が不足するためである。In the inner layer, 5 parts of metal hydroxide are added to 100 parts by weight of the polypropylene / polybutene alloyed resin.
0 to 400 parts by weight, but if the amount is less than 50 parts by weight, the flame retardancy of the wire is insufficient, and if the amount is more than 400 parts by weight, the whitening resistance and flexibility, the abrasion resistance, and the tensile strength of the wire are further reduced. This is due to lack of quality.
【0011】本発明において、外層にはポリアミド樹脂
を使用しているが、これはポリアミド樹脂以外の柔らか
い樹脂を使用すると、耐加熱変形性や耐摩耗性が不足す
るためである。さらに、難燃性を高めるために、ハイド
ロタルサイト類やシリカ、カーボンブラック、ホウ酸亜
鉛、リン化合物等の難燃助剤を添加してもよく、また、
酸化防止剤、滑剤、分散剤、銅害防止剤、架橋剤、架橋
助剤或いは着色剤等を添加してもよく、また、各種の架
橋方法にてポリマーの架橋を行ってもよい。In the present invention, a polyamide resin is used for the outer layer. This is because the use of a soft resin other than the polyamide resin results in insufficient heat deformation resistance and wear resistance. Furthermore, in order to enhance the flame retardancy, a flame retardant auxiliary such as hydrotalcites, silica, carbon black, zinc borate, and a phosphorus compound may be added.
An antioxidant, a lubricant, a dispersant, a copper damage inhibitor, a cross-linking agent, a cross-linking aid or a colorant may be added, and the polymer may be cross-linked by various cross-linking methods.
【0012】内層及び外層の厚さ寸法比を内層/外層=
6/4〜9/1としたのは、6/4以下では絶縁電線の
柔軟性が不足し、逆に9/1以上では耐摩耗性や引張強
さが不足するためである。The thickness dimension ratio of the inner layer and the outer layer is defined as inner layer / outer layer =
The reason why the ratio is 6/4 to 9/1 is that if the ratio is 6/4 or less, the insulated wire has insufficient flexibility, and if it is 9/1 or more, the wear resistance and the tensile strength are insufficient.
【0013】[0013]
【発明の効果】以上述べたように、本発明の絶縁電線に
よれば、ポリプロピレン/ポリブテンアロイ化樹脂は通
常用いられているポリオレフィン樹脂に比べて難燃性、
柔軟性に優れるから、内層においてこれらの特性を高め
ることができる。As described above, according to the insulated wire of the present invention, the polypropylene / polybutene alloyed resin is more flame-retardant than the commonly used polyolefin resin.
Because of excellent flexibility, these properties can be enhanced in the inner layer.
【0014】一方外層に用いるポリアミド樹脂は、一般
的にオレフィン樹脂よりも高価なものなので、これに難
燃化処方を施して汎用電線に用いるのは経済面で不適で
あった。しかし内層において難燃性が高められた結果、
外層では耐加熱変形性や耐摩耗性に優れるという特性を
活かし、なおかつ経済性に優れているポリアミド樹脂を
使用することが可能となった。On the other hand, since the polyamide resin used for the outer layer is generally more expensive than the olefin resin, it is economically unsuitable to apply it to a flame-retardant formulation and use it for general-purpose electric wires. However, as a result of increased flame retardancy in the inner layer,
In the outer layer, it has become possible to use a polyamide resin which is excellent in economical efficiency while taking advantage of the property of being excellent in heat deformation resistance and abrasion resistance.
【0015】[0015]
【実施例】以下、本発明のいくつかの実施例について説
明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS Some embodiments of the present invention will be described below.
【0016】本発明の実施例1として、ポリプロピレン
/ポリブテンアロイ化樹脂、ポリアミド樹脂、水酸化ア
ルミニウム、水酸化マグネシウム、並びに難燃助剤とし
てのシリカ及び赤リンを表1に示す割合で混練した樹脂
組成物を作製した。As Example 1 of the present invention, a resin obtained by kneading a polypropylene / polybutene alloyed resin, a polyamide resin, aluminum hydroxide, magnesium hydroxide, and silica and red phosphorus as flame retardant aids in the proportions shown in Table 1. A composition was made.
【0017】一方、比較例1〜8として、ポリプロピレ
ン/ポリブテンアロイ化樹脂、エチレン−酢酸ビニル共
重合体(酢酸ビニル含量=20%)、エチレン−エチル
アクリレート共重合体(エチルアクリレート含量=25
%)、高密度ポリエチレン(融点=135℃,ショアD
硬さ=63)、低密度ポリエチレン(融点=98℃,シ
ョアD硬さ=48)、直鎖状低密度ポリエチレン(融点
=110℃,ショアD硬さ=58)、ポリアミド樹脂、
水酸化アルミニウム、水酸化マグネシウム、シリカ、赤
リンを表2及び表3に示す割合で混練した樹脂組成物を
作製した。On the other hand, as Comparative Examples 1 to 8, polypropylene / polybutene alloyed resin, ethylene-vinyl acetate copolymer (vinyl acetate content = 20%), ethylene-ethyl acrylate copolymer (ethyl acrylate content = 25
%), High density polyethylene (melting point = 135 ° C, Shore D)
Hardness = 63), low density polyethylene (melting point = 98 ° C., Shore D hardness = 48), linear low density polyethylene (melting point = 110 ° C., Shore D hardness = 58), polyamide resin,
A resin composition was prepared by kneading aluminum hydroxide, magnesium hydroxide, silica, and red phosphorus at the ratios shown in Tables 2 and 3.
【0018】なお、エチレン−酢酸ビニル共重合体は東
ソー社製ウルトラセン(商品名)、エチレン−エチルア
クリレート共重合体は三井デュポンポリケミカル社製エ
バフレックスEEA(商品名)、高密度ポリエチレンは
日本ポリオレフィン社製ジェイレクスHD(商品名)、
低密度ポリエチレンは日本ポリオレフィン社製ジェイレ
クスLD(商品名)、直鎖状低密度ポリエチレンは日本
ポリオレフィン社製ジェイレクスLL(商品名)、ポリ
アミド樹脂は宇部興産社製ナイロン(商品名)を使用し
た。The ethylene-vinyl acetate copolymer is Ultracene (trade name) manufactured by Tosoh Corporation, the ethylene-ethyl acrylate copolymer is Evaflex EEA (trade name) manufactured by DuPont-Mitsui Polychemicals, and high-density polyethylene is Japan. J-LEX HD (trade name) manufactured by Polyolefin,
The low-density polyethylene used was Jakelex LD (trade name) manufactured by Japan Polyolefin Co., Ltd. The linear low-density polyethylene used was Jakex LL (trade name) manufactured by Japan Polyolefin Co., Ltd., and the polyamide resin was nylon (trade name) manufactured by Ube Industries.
【0019】これらの樹脂組成物を、図1に示すよう
に、銅芯線1の外周に内層2、外層3をそれぞれの表に
示す厚みで押出して作成した薄肉電線にて、次の特性評
価を行った。 難燃性:長さ300mmの電線試料を水平に支持し、口
径10mmのブンゼンバーナーを用いて、還元炎の先端を
試料中央部の下側から30秒以内で燃焼するまで当て、
炎を静かに取り去った後、試料の燃焼の程度を調べた。 耐摩耗性:23±5℃の室温で、台上に固定した長さ
750mmの電線試料の絶縁被覆表面を軸方向に10mm以
上の長さに渡ってブレードで往復して摩耗させる。ブレ
ードを毎分50回又は60回の速さで往復させたとき、
絶縁体の摩耗により、ブレードが芯線導体に接触するま
での往復回数を測定する。次に試料を100mm移動させ
て、時計方向に90度回転し、上記の測定を繰り返す。
この測定は、同一試料で計4回行い、その最小値を摩耗
抵抗とした。 耐白化性:半径6mmの筒に静かに数回巻き付け、その
状態で表面の白化度合いを目視にて確認した。As shown in FIG. 1, these resin compositions were subjected to the following characteristic evaluation using a thin electric wire prepared by extruding an inner layer 2 and an outer layer 3 on the outer periphery of a copper core wire 1 to the thicknesses shown in the respective tables. went. Flame retardancy: A 300 mm long wire sample is supported horizontally, and the tip of the reducing flame is applied from below the center of the sample using a Bunsen burner with a diameter of 10 mm until it burns within 30 seconds.
After gently removing the flame, the degree of combustion of the sample was determined. Abrasion resistance: At room temperature of 23 ± 5 ° C., the insulating coating surface of a 750 mm long wire sample fixed on a table is reciprocated and abraded by a blade over a length of 10 mm or more in the axial direction. When the blade is reciprocated 50 or 60 times per minute,
The number of reciprocations until the blade contacts the core conductor due to wear of the insulator is measured. Next, the sample is moved 100 mm, rotated 90 degrees clockwise, and the above measurement is repeated.
This measurement was performed a total of four times with the same sample, and the minimum value was defined as abrasion resistance. Whitening resistance: The film was gently wound several times around a cylinder having a radius of 6 mm, and the degree of whitening of the surface was visually checked in that state.
【0020】評価結果を表1ないし表3に示す。The evaluation results are shown in Tables 1 to 3.
【0021】[0021]
【表1】 [Table 1]
【0022】[0022]
【表2】 [Table 2]
【表3】 まず、表1に示すように、本発明の樹脂組成物に係る実
施例1では難燃性、耐加熱変形性、耐白化性、柔軟性の
いずれも良好であった。また耐摩耗性も目標値である3
00回を大きく上回り、引張強さや伸びも良い特性値が
得られた。[Table 3] First, as shown in Table 1, in Example 1 relating to the resin composition of the present invention, all of the flame retardancy, the heat deformation resistance, the whitening resistance, and the flexibility were good. The wear resistance is also the target value of 3
The characteristic value was much higher than 00 times and good tensile strength and elongation were obtained.
【0023】これに対し、外層にポリアミド樹脂を用い
なかった比較例1,2,3,5では、耐摩耗性や引張強
さ、加熱変形率が大きく低下している。On the other hand, in Comparative Examples 1, 2, 3, and 5 in which no polyamide resin was used for the outer layer, the abrasion resistance, the tensile strength, and the heat deformation rate were significantly reduced.
【0024】また、内層にポリプロピレン/ポリブテン
アロイ化樹脂以外の樹脂を使用した比較例3では、内層
樹脂に必要な特性である柔軟性が不足している。比較例
6のように内層における金属水酸化物の量が少ないと、
電線の難燃性が不足する。また、難燃性を確保するため
に外層樹脂の金属水酸化物量を増加させると、難燃性は
向上するが、耐摩耗性や引張強さ等の特性が低下する
(比較例5)。逆に、比較例7のように内層において金
属水酸化物量が多すぎると、難燃性は向上するが、耐摩
耗性や引張強さ、柔軟性等が低下してしまう。さらに、
内層及び外層の厚さ寸法比が内層/外層=4/6以下で
は絶縁電線の柔軟性が不足し(比較例4)、逆に9/1
以上では耐摩耗性や引張強さが等が不足する(比較例
8)。In Comparative Example 3 in which a resin other than the polypropylene / polybutene alloyed resin was used for the inner layer, flexibility, which is a property required for the inner layer resin, was insufficient. When the amount of the metal hydroxide in the inner layer is small as in Comparative Example 6,
Insufficient flame retardancy of electric wires. In addition, when the amount of metal hydroxide in the outer layer resin is increased in order to ensure flame retardancy, flame retardancy is improved, but characteristics such as wear resistance and tensile strength are reduced (Comparative Example 5). Conversely, if the amount of metal hydroxide in the inner layer is too large as in Comparative Example 7, the flame retardancy is improved, but the abrasion resistance, tensile strength, flexibility and the like are reduced. further,
When the thickness dimension ratio of the inner layer and the outer layer is 4/6 or less, the flexibility of the insulated wire is insufficient (Comparative Example 4), and conversely, 9/1.
Above, the wear resistance and tensile strength are insufficient (Comparative Example 8).
【図1】絶縁電線の断面図FIG. 1 is a sectional view of an insulated wire.
1…銅芯線(導電芯線) 2…内層 3…外層 1: Copper core wire (conductive core wire) 2: Inner layer 3: Outer layer
Claims (1)
絶縁層を被覆した絶縁電線において、前記内層はポリプ
ロピレン/ポリブテンアロイ化樹脂の100重量部に対
して金属水酸化物を50〜400重量部配合してなる樹
脂組成物からなると共に、前記外層はポリアミド樹脂か
らなり、前記内層及び外層の厚さ寸法比が内層/外層=
6/4〜9/1であることを特徴とする絶縁電線。1. An insulated wire in which an outer periphery of a conductive core wire is coated with an insulating layer composed of an inner layer and an outer layer, wherein the inner layer contains 50 to 400 parts by weight of a metal hydroxide with respect to 100 parts by weight of a polypropylene / polybutene alloyed resin. And the outer layer is made of a polyamide resin, and the thickness dimension ratio of the inner layer and the outer layer is defined as inner layer / outer layer =
An insulated wire having a ratio of 6/4 to 9/1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9149697A JPH10340637A (en) | 1997-06-06 | 1997-06-06 | Insulated wire |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9149697A JPH10340637A (en) | 1997-06-06 | 1997-06-06 | Insulated wire |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH10340637A true JPH10340637A (en) | 1998-12-22 |
Family
ID=15480847
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9149697A Pending JPH10340637A (en) | 1997-06-06 | 1997-06-06 | Insulated wire |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH10340637A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113444321A (en) * | 2021-08-19 | 2021-09-28 | 山东京博石油化工有限公司 | Polypropylene-based composite foaming base material and preparation method thereof |
-
1997
- 1997-06-06 JP JP9149697A patent/JPH10340637A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113444321A (en) * | 2021-08-19 | 2021-09-28 | 山东京博石油化工有限公司 | Polypropylene-based composite foaming base material and preparation method thereof |
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