JPH10116521A - Fluoro-rubber covered wire - Google Patents
Fluoro-rubber covered wireInfo
- Publication number
- JPH10116521A JPH10116521A JP8270746A JP27074696A JPH10116521A JP H10116521 A JPH10116521 A JP H10116521A JP 8270746 A JP8270746 A JP 8270746A JP 27074696 A JP27074696 A JP 27074696A JP H10116521 A JPH10116521 A JP H10116521A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- pts
- fluoro
- coating layer
- 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
- 229920001973 fluoroelastomer Polymers 0.000 title claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 15
- 239000004020 conductor Substances 0.000 claims abstract description 12
- 229920006172 Tetrafluoroethylene propylene Polymers 0.000 claims abstract description 10
- 239000004927 clay Substances 0.000 claims abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 7
- 239000011247 coating layer Substances 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 6
- 238000001125 extrusion Methods 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 4
- 150000001451 organic peroxides Chemical class 0.000 abstract description 3
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 230000015556 catabolic process Effects 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000007765 extrusion coating Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- -1 for example Polymers 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 3
- 239000004636 vulcanized rubber Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- UBRWPVTUQDJKCC-UHFFFAOYSA-N 1,3-bis(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC(C(C)(C)OOC(C)(C)C)=C1 UBRWPVTUQDJKCC-UHFFFAOYSA-N 0.000 description 1
- DNJRKFKAFWSXSE-UHFFFAOYSA-N 1-chloro-2-ethenoxyethane Chemical compound ClCCOC=C DNJRKFKAFWSXSE-UHFFFAOYSA-N 0.000 description 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 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- JJRUAPNVLBABCN-UHFFFAOYSA-N 2-(ethenoxymethyl)oxirane Chemical compound C=COCC1CO1 JJRUAPNVLBABCN-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
- ROHTVIURAJBDES-UHFFFAOYSA-N 2-n,2-n-bis(prop-2-enyl)-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N(CC=C)CC=C)=N1 ROHTVIURAJBDES-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
Landscapes
- Insulated Conductors (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、耐熱性に優れた被
覆電線の改良に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improved coated electric wire having excellent heat resistance.
【0002】[0002]
【従来の技術】電線の被覆材料としては、安価なクロロ
プレン、クロロスルフォン化ポリエチレンが汎用されて
いるが、耐熱性が不十分であるために高温環境下、例え
ば連続使用環境温度が100℃を越えるような環境では
耐熱性に優れたフッ素ゴムが用いられている。フッ素ゴ
ム例えばテトラフルオロエチレン−プロピレン系共重合
体は、高度な熱安定性を有する含フッ素エラストマーで
あり、この共重合体を導体の外側に押出被覆し、架橋す
ることで耐熱性に特に優れた電線を得ることができる。2. Description of the Related Art Inexpensive chloroprene and chlorosulfonated polyethylene are widely used as covering materials for electric wires. However, due to insufficient heat resistance, the temperature in a high temperature environment, for example, a continuous use environment temperature exceeds 100 ° C. In such an environment, fluorine rubber having excellent heat resistance is used. Fluororubber, for example, tetrafluoroethylene-propylene copolymer, is a fluorine-containing elastomer having a high degree of thermal stability, and is particularly excellent in heat resistance by extrusion-coating this copolymer on the outside of a conductor and crosslinking. An electric wire can be obtained.
【0003】[0003]
【発明が解決しようとする課題】しかし、テトラフルオ
ロエチレン−プロピレン系共重合体は粘度が高いため
に、導体上へ押出被覆する際の加工成形性に劣り、電線
外観が不良となったり、薄肉被覆が困難であるなどの種
々の欠点があった。また、これら加工成形性を改善しよ
うとすると機械的強度、電気特性の低下が生じるという
問題があった。However, since the tetrafluoroethylene-propylene copolymer has a high viscosity, it is inferior in processability when extrusion-coated on a conductor, resulting in poor electric wire appearance or thin wall. There were various disadvantages such as difficulty in coating. In addition, there is a problem that the mechanical strength and the electrical characteristics are lowered when trying to improve the processability.
【0004】本発明の目的は、表面外観が良好で、かつ
高温環境下においても優れた機械的強度、電気特性を有
するフッ素ゴム被覆電線を提供することにある。An object of the present invention is to provide a fluorine rubber-coated electric wire having a good surface appearance and excellent mechanical strength and electric characteristics even in a high temperature environment.
【0005】[0005]
【課題を解決するための手段】上記目的を達成するため
に、本発明においては、導体の外側に、テトラフルオロ
エチレン−プロピレン系共重合体100重量部に対し
て、焼成クレーを20〜40重量部、MTカーボンを5
〜20重量部、有機過酸化物を0.5〜2重量部、多ア
リル化合物を5〜10重量部を配合してなるフッ素ゴム
組成物からなる押出被覆層が形成されており、かつ該被
覆層が架橋されていることを特徴とする被覆電線が提供
される。In order to achieve the above object, in the present invention, 20 to 40 parts by weight of a calcined clay is added to the outside of a conductor with respect to 100 parts by weight of a tetrafluoroethylene-propylene copolymer. Part, MT carbon 5
An extruded coating layer comprising a fluororubber composition comprising about 20 to 20 parts by weight, 0.5 to 2 parts by weight of an organic peroxide, and 5 to 10 parts by weight of a polyallyl compound. A coated wire is provided, wherein the layers are crosslinked.
【0006】[0006]
【発明の実施の形態】以下に本発明の実施の形態を説明
する。図1は、本発明の被覆電線の一実施例を示す概略
断面図であり、導体1上に半導電性ポリエステルテープ
からなる内部導電層2、フッ素ゴム組成物を押出被覆し
て架橋された押出被覆層3の順に設けられている。な
お、図1では導体1の上に内部導電層2を介して押出被
覆層3が設けられているが、図2のように導体1直上に
押出被覆層3を設けてもよく、いずれの場合も押出被覆
層3の上に、主に耐熱性を考慮してフッ素ゴムなどから
なるシース4を設けても良い。また、図3に示すように
導体上に押出被覆層3を設けた被覆電線を複数本撚り合
わせ、ガラス繊維などからなる介在5を設けた上をシー
ス4で覆ったケーブルとしても良い。Embodiments of the present invention will be described below. FIG. 1 is a schematic cross-sectional view showing one embodiment of a coated electric wire of the present invention, in which an inner conductive layer 2 made of a semiconductive polyester tape is coated on a conductor 1 by extrusion coating with a fluororubber composition. The coating layers 3 are provided in this order. In FIG. 1, the extruded coating layer 3 is provided on the conductor 1 via the internal conductive layer 2, but the extruded coating layer 3 may be provided directly on the conductor 1 as shown in FIG. Also, a sheath 4 made of fluoro rubber or the like may be provided on the extruded coating layer 3 mainly in consideration of heat resistance. Alternatively, as shown in FIG. 3, a cable in which a plurality of insulated wires each having an extruded coating layer 3 provided on a conductor are twisted, and an intervening member 5 made of glass fiber or the like is provided and covered with a sheath 4 may be used.
【0007】本発明におけるフッ素ゴム組成物のベース
樹脂として用いられるテトラフルオロエチレン−プロピ
レン系共重合体は、テトラフルオロエチレンと、プロピ
レンとの共重合体である。テトラフルオロエチレン/プ
ロピレンのモル比は、95/5〜30/70モル%、好
ましくは90/10〜45/55モル%である。主成分
のテトラフルオロエチレンとプロピレンに加えて、これ
らと共重合可能な成分、例えばエチレン、ブテン−1、
イソブテン、アクリル酸及びそのアルキルエステル、メ
タクリル酸及びそのアルキルエステル、フッ化ビニル、
フッ化ビニリデン、ヘキサフルオロプロペン、クロロエ
チルビニルエーテル、グリシジルビニルエーテル、クロ
ロトリフルオロエチレン、パーフルオロアルキルビニル
エーテル等を適当に含有させたものでもよい。市販のテ
トラフルオロエチレン−プロピレン系共重合体として
は、日本合成ゴム(株)製のアフラスなどがあり、柔軟
性などの電線の必要特性を十分考慮し、市販品の各種グ
レードから適宜選択し、単独または数種をブレンドして
用いることができる。The tetrafluoroethylene-propylene copolymer used as the base resin of the fluororubber composition in the present invention is a copolymer of tetrafluoroethylene and propylene. The molar ratio of tetrafluoroethylene / propylene is 95/5 to 30/70 mol%, preferably 90/10 to 45/55 mol%. In addition to the main components tetrafluoroethylene and propylene, components copolymerizable therewith, for example, ethylene, butene-1,
Isobutene, acrylic acid and its alkyl ester, methacrylic acid and its alkyl ester, vinyl fluoride,
It may contain vinylidene fluoride, hexafluoropropene, chloroethyl vinyl ether, glycidyl vinyl ether, chlorotrifluoroethylene, perfluoroalkyl vinyl ether or the like. Commercially available tetrafluoroethylene-propylene-based copolymers include AFLAS manufactured by Nippon Synthetic Rubber Co., Ltd., taking into account the required properties of electric wires such as flexibility, and appropriately selecting from various grades of commercially available products. A single compound or a mixture of several compounds can be used.
【0008】また、本発明におけるフッ素ゴム組成物に
は、焼成クレー(Al2 O3 ・2SiO2 )が含有され
ているために、導体上に押出成形する際の加工性に優
れ、電気特性が特に優れるものとなる。タルクでは電気
特性が劣り、またシリカを配合するとベース樹脂粘度の
上昇、電気特性の低下といった問題が生じる。その配合
量は、ベース樹脂100重量部に対して、20〜40重
量部、特に好ましくは30〜40重量部である。20重
量部未満では被覆層の成形性に劣り、40重量部を越え
ると引張強度などの機械的強度、耐熱性が低下する。Further, since the fluororubber composition of the present invention contains calcined clay (Al 2 O 3 .2SiO 2 ), it has excellent workability when extruded on a conductor and has excellent electrical characteristics. It will be particularly excellent. Talc has inferior electrical properties, and the addition of silica causes problems such as an increase in base resin viscosity and a decrease in electrical properties. The compounding amount is 20 to 40 parts by weight, particularly preferably 30 to 40 parts by weight, based on 100 parts by weight of the base resin. If the amount is less than 20 parts by weight, the moldability of the coating layer is inferior. If the amount exceeds 40 parts by weight, mechanical strength such as tensile strength and heat resistance are reduced.
【0009】さらに、本発明のフッ素ゴム組成物には、
ベース樹脂100重量部に対して、MTカーボンが5〜
20重量部、好ましくは5〜10重量部配合される。M
Tカーボンがこの範囲の配合量で配合されていると、被
覆層の成形性が改善される。配合量が多すぎると電気特
性に悪影響を及ぼす。Further, the fluororubber composition of the present invention comprises:
MT carbon is 5 to 100 parts by weight of the base resin.
20 parts by weight, preferably 5 to 10 parts by weight are blended. M
When T carbon is blended in the blending amount in this range, the moldability of the coating layer is improved. If the amount is too large, the electrical properties are adversely affected.
【0010】本発明の被覆層の樹脂は架橋されているこ
とが必須であり、フッ素ゴム組成物には架橋剤が配合さ
れる。架橋剤としては、有機過酸化物を好適に用いるこ
とができ、例えば、ジクミルパーオキサイド、2,5−
ジメチル−2,5−ジ(t−ブチルパーオキシド)ヘキ
シン、1,3−ビス−(t−ブチルパーオキシイソプロ
ピル)ベンゼン、1,1−ジ−t−ブチルパーオキシ−
3,3,5−トリメチルシクロヘキサン等が挙げられ
る。その配合量は、ベース樹脂100重量部に対して、
0.5〜2重量部が適当である。It is essential that the resin of the coating layer of the present invention is crosslinked, and a crosslinking agent is blended in the fluororubber composition. As the cross-linking agent, an organic peroxide can be suitably used. For example, dicumyl peroxide, 2,5-
Dimethyl-2,5-di (t-butylperoxide) hexine, 1,3-bis- (t-butylperoxyisopropyl) benzene, 1,1-di-t-butylperoxy-
3,3,5-trimethylcyclohexane and the like. The amount is based on 100 parts by weight of the base resin.
0.5 to 2 parts by weight is suitable.
【0011】また、フッ素ゴム組成物には架橋助剤とし
て多アリル化合物を配合する。多アリル化合物として
は、フタル酸ジアリル、ジアヌル酸トリアリル、トリア
リルイソシアヌレート、ジアリルメラミン等が挙げら
れ、好ましくはトリアリルイソシアヌレートを用いるこ
とができる。その配合量はベース樹脂100重量部に対
して、5〜10重量部が適当である。Further, a polyallyl compound is compounded in the fluororubber composition as a crosslinking aid. Examples of the polyallyl compound include diallyl phthalate, triallyl dianurate, triallyl isocyanurate, diallyl melamine and the like, and preferably triallyl isocyanurate can be used. The compounding amount is suitably 5 to 10 parts by weight based on 100 parts by weight of the base resin.
【0012】本発明のフッ素ゴム被覆電線は、被覆層の
樹脂が架橋されているために耐熱性の点で優れたものと
なっている。被覆層の架橋の方法としては、導体の外側
にフッ素ゴム組成物を押出成形した後、190〜220
℃で加熱して架橋するのが一般的である。The fluororubber-coated electric wire of the present invention is excellent in heat resistance because the resin of the coating layer is crosslinked. As a method for crosslinking the coating layer, after extruding the fluororubber composition on the outside of the conductor, 190 to 220
It is common to crosslink by heating at a temperature of ° C.
【0013】また、この他にフッ素ゴム組成物には、電
線被覆層において使用されている各種の添加剤、例え
ば、難燃剤、着色剤、ワックス等の滑剤、老化防止剤な
どを本発明の目的を損なわない範囲で適宜配合すること
ができる。In addition, the fluororubber composition may further contain various additives used in the wire coating layer, such as a flame retardant, a coloring agent, a lubricant such as wax, an antioxidant, and the like. Can be appropriately compounded within a range that does not impair.
【0014】[0014]
【実施例】導体(外径0.8mm銅線)上に、押出機
(15mmφ、L/D=13)を用い、シリンダー部8
5℃、ヘッド90℃の条件で表1に示したフッ素ゴム組
成物を外径が1.6mmφとなるように押出被覆し、実
施例1〜6の被覆電線を得た。なお、表2に示したフッ
素ゴム組成物を実施例1〜6と同一条件で押出被覆し、
架橋して比較例1〜7の被覆電線を得た。EXAMPLE A cylinder (8 mm diameter, 0.8 mm outer diameter) was extruded using an extruder (15 mmφ, L / D = 13).
The fluororubber composition shown in Table 1 was extrusion-coated so as to have an outer diameter of 1.6 mmφ under the conditions of 5 ° C and a head of 90 ° C to obtain coated electric wires of Examples 1 to 6. The fluororubber compositions shown in Table 2 were extrusion-coated under the same conditions as in Examples 1 to 6,
The coated electric wires of Comparative Examples 1 to 7 were obtained by crosslinking.
【0015】得られた各被覆電線につき、下記の試験法
で各種の特性を測定、評価した。 1)表面外観 以下の判定基準によって電線表面の外観を観察した。 ◎:被覆層表面が滑らかで光沢がある ○:被覆層表面が滑らかである △:被覆層表面の一部が凹凸、またはケバ立っている ×:被覆層表面の全体が凹凸、またはケバ立っているFor each of the obtained coated electric wires, various characteristics were measured and evaluated by the following test methods. 1) Surface appearance The appearance of the electric wire surface was observed according to the following criteria. ◎: The surface of the coating layer is smooth and glossy. :: The surface of the coating layer is smooth. :: Part of the surface of the coating layer is uneven or bumpy. ×: The entire surface of the coating layer is uneven or bumpy. Is
【0016】2)引張強さ、伸び 表1、2に示した各成分を40〜60℃の8インチロー
ル機により20分間混合して調整した樹脂組成物をシー
ト状に成形した後、170℃で20分プレス加硫し、試
験シートを作成した。この試験シートを用いてJIS
K 6301(加硫ゴム物理試験方法、引張試験 JI
S3号ダンベルを使用)に準拠して引張強さおよび伸び
を測定した。2) Tensile strength and elongation The resin composition prepared by mixing the components shown in Tables 1 and 2 with an 8-inch roll machine at 40 to 60 ° C. for 20 minutes to form a sheet, and then forming the sheet at 170 ° C. For 20 minutes to prepare a test sheet. JIS using this test sheet
K 6301 (Vulcanized rubber physical test method, tensile test JI
Tensile strength and elongation were measured according to S3 dumbbell).
【0017】3)硬度 JIS K 6301(加硫ゴム物理試験方法、かたさ
試験 A型を使用)に準拠して測定した。3) Hardness The hardness was measured in accordance with JIS K 6301 (Vulcanized rubber physical test method, hardness test A type).
【0018】4)伸びの老化度 JIS K 6301(加硫ゴム物理試験方法、老化試
験 空気加熱老化試験( 220℃、96時間) )に準拠
して、試験シートの伸び残率(%)を測定した。4) Degree of aging of elongation The residual elongation (%) of the test sheet is measured according to JIS K 6301 (Vulcanized rubber physical test method, aging test, air aging test (220 ° C., 96 hours)). did.
【0019】5)体積抵抗率 1×160×160mmの試験シートを用いて、JIS
C 2123(第16項)に準拠して測定した。5) Volume resistivity Using a test sheet of 1 × 160 × 160 mm, JIS
It measured based on C2123 (Section 16).
【0020】6)交流破壊電圧 試験シートから作製された図4に示す形状の試験片の点
線が付された凹部に導電性塗料を塗布し、その凹部に直
径12mmの球状電極を置き、10分ごとに課電電圧を
1kVずつ昇圧させ、絶縁破壊に至るまでの電圧を測定
した。また、80℃の純水中に7日間浸積させた試験片
を用いて、同様に絶縁破壊に至るまでの電圧を測定し
た。6) AC Breakdown Voltage A conductive paint is applied to the dotted-lined concave portion of the test piece having the shape shown in FIG. 4 prepared from the test sheet, and a spherical electrode having a diameter of 12 mm is placed in the concave portion for 10 minutes. Each time, the applied voltage was raised by 1 kV, and the voltage up to dielectric breakdown was measured. In addition, using a test piece immersed in pure water at 80 ° C. for 7 days, a voltage until dielectric breakdown was measured in the same manner.
【0021】[0021]
【表1】 [Table 1]
【0022】[0022]
【表2】 [Table 2]
【0023】表1の結果から、被覆層としてテトラフル
オロエチレン−プロピレン系共重合体をベース樹脂とす
る特定の樹脂組成物の架橋体を用いた実施例1〜6の被
覆電線は、いずれも外観が良好で、かつ加熱試験後でも
電気特性、機械的強度に優れていることがわかる。一
方、比較例1は焼成クレーの配合量が本発明における規
定量に満たないので電線の表面外観が不良である。比較
例2は焼成クレーの配合量が規定量を越えて配合されて
いるために、加熱後の伸び残率が小さい。比較例3は焼
成クレーの代わりにタルクが配合されているので体積抵
抗率が劣り、温水浸積後の交流破壊電圧が小さい。比較
例4は、焼成クレーの代わりにシリカが配合されている
ために体積抵抗率が小さく、温水浸積後の交流破壊電圧
が小さい。比較例5はMTカーボンの配合量が多いため
に引張強さに劣り、加熱後の伸び残率、体積抵抗率が小
さく、交流破壊電圧が小さいものとなっている。比較例
6はMTカーボンの配合量が小さいために電線表面の外
観が劣るものとなっている。比較例7は焼成クレーが配
合されていないために電線表面の外観が劣るものとなっ
ている。From the results shown in Table 1, all of the coated electric wires of Examples 1 to 6 using a crosslinked product of a specific resin composition containing a tetrafluoroethylene-propylene-based copolymer as a base resin as the coating layer are shown. It is clear that the electrical properties and the mechanical strength are excellent even after the heating test. On the other hand, in Comparative Example 1, since the compounded amount of the calcined clay was less than the specified amount in the present invention, the surface appearance of the electric wire was poor. In Comparative Example 2, since the blending amount of the calcined clay exceeds the prescribed amount, the residual elongation after heating is small. Comparative Example 3 is inferior in volume resistivity and low in AC breakdown voltage after hot water immersion because talc is blended in place of calcined clay. Comparative Example 4 has a low volume resistivity and a low AC breakdown voltage after immersion in hot water because silica is mixed in place of the calcined clay. Comparative Example 5 is inferior in tensile strength due to a large amount of MT carbon, has a low residual elongation after heating, a small volume resistivity, and a small AC breakdown voltage. In Comparative Example 6, since the amount of MT carbon was small, the appearance of the electric wire surface was inferior. In Comparative Example 7, the appearance of the electric wire surface was inferior because the fired clay was not blended.
【0024】[0024]
【発明の効果】本発明のフッ素ゴム被覆電線は、その被
覆層が、特定のフッ素ゴム組成物が押出成形されて形成
されており、かつ該被覆層が架橋されているために、表
面外観が良好で、優れた機械的強度、電気特性を有して
おり、高温環境下においても好適に用いることができ
る。The fluororubber-coated electric wire of the present invention has a coating layer formed by extrusion molding of a specific fluororubber composition, and the coating layer is crosslinked, so that the surface appearance is reduced. It has good mechanical strength and excellent electrical properties, and can be suitably used even in a high-temperature environment.
【図1】本発明の被覆電線の一実施態様を示す概略断面
図である。FIG. 1 is a schematic sectional view showing an embodiment of a coated electric wire of the present invention.
【図2】本発明の被覆電線の他の一実施態様を示す概略
断面図である。FIG. 2 is a schematic sectional view showing another embodiment of the coated electric wire of the present invention.
【図3】本発明の被覆電線の他の一実施態様を示す概略
断面図である。FIG. 3 is a schematic sectional view showing another embodiment of the coated electric wire of the present invention.
【図4】交流破壊電圧の測定に用いる試験片を示す説明
図である。FIG. 4 is an explanatory view showing a test piece used for measuring an AC breakdown voltage.
1 導体 2 内部導電層 3 押出被覆層 4 シース 5 介在 DESCRIPTION OF SYMBOLS 1 Conductor 2 Internal conductive layer 3 Extrusion coating layer 4 Sheath 5 Interposition
─────────────────────────────────────────────────────
────────────────────────────────────────────────── ───
【手続補正書】[Procedure amendment]
【提出日】平成9年4月8日[Submission date] April 8, 1997
【手続補正1】[Procedure amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0021[Correction target item name] 0021
【補正方法】変更[Correction method] Change
【補正内容】[Correction contents]
【0021】[0021]
【表1】 [Table 1]
Claims (1)
−プロピレン系共重合体100重量部に対して、焼成ク
レーを20〜40重量部、MTカーボンを5〜20重量
部、有機過酸化物を0.5〜2重量部、多アリル化合物
を5〜10重量部を配合してなるフッ素ゴム組成物から
なる押出被覆層が形成されており、かつ該被覆層が架橋
されていることを特徴とするフッ素ゴム被覆電線。1. An outside of a conductor, 20 to 40 parts by weight of calcined clay, 5 to 20 parts by weight of MT carbon, and 0 to 100 parts by weight of a tetrafluoroethylene-propylene copolymer based on 100 parts by weight of a tetrafluoroethylene-propylene copolymer. 0.5 to 2 parts by weight and 5 to 10 parts by weight of a polyallyl compound to form an extruded coating layer comprising a fluororubber composition, and the coating layer is crosslinked. Fluororubber-coated electric wire.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8270746A JPH10116521A (en) | 1996-10-14 | 1996-10-14 | Fluoro-rubber covered wire |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8270746A JPH10116521A (en) | 1996-10-14 | 1996-10-14 | Fluoro-rubber covered wire |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10116521A true JPH10116521A (en) | 1998-05-06 |
Family
ID=17490407
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8270746A Pending JPH10116521A (en) | 1996-10-14 | 1996-10-14 | Fluoro-rubber covered wire |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10116521A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006236866A (en) * | 2005-02-25 | 2006-09-07 | Asahi Glass Co Ltd | Insulation coating layer for electric wires |
JP2009245927A (en) * | 2008-03-28 | 2009-10-22 | Ls Cable Ltd | Composition for manufacturing high thermal-resistance insulated material and high thermal resistance insulated wire manufactured using this |
CN113053571A (en) * | 2019-12-26 | 2021-06-29 | 住友电气工业株式会社 | Electrically insulated cables |
JPWO2024176858A1 (en) * | 2023-02-24 | 2024-08-29 |
-
1996
- 1996-10-14 JP JP8270746A patent/JPH10116521A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006236866A (en) * | 2005-02-25 | 2006-09-07 | Asahi Glass Co Ltd | Insulation coating layer for electric wires |
JP2009245927A (en) * | 2008-03-28 | 2009-10-22 | Ls Cable Ltd | Composition for manufacturing high thermal-resistance insulated material and high thermal resistance insulated wire manufactured using this |
CN113053571A (en) * | 2019-12-26 | 2021-06-29 | 住友电气工业株式会社 | Electrically insulated cables |
JP2021106131A (en) * | 2019-12-26 | 2021-07-26 | 住友電気工業株式会社 | Electrical insulation cable |
JPWO2024176858A1 (en) * | 2023-02-24 | 2024-08-29 | ||
WO2024176858A1 (en) * | 2023-02-24 | 2024-08-29 | Nok株式会社 | Fluorine rubber composition and seal for electric vehicle |
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