JPH01161607A - Self-melting insulated wire - Google Patents
Self-melting insulated wireInfo
- Publication number
- JPH01161607A JPH01161607A JP31933387A JP31933387A JPH01161607A JP H01161607 A JPH01161607 A JP H01161607A JP 31933387 A JP31933387 A JP 31933387A JP 31933387 A JP31933387 A JP 31933387A JP H01161607 A JPH01161607 A JP H01161607A
- Authority
- JP
- Japan
- Prior art keywords
- self
- resin
- weight
- parts
- insulated wire
- 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
- 238000002844 melting Methods 0.000 title abstract 3
- 239000000203 mixture Substances 0.000 claims abstract description 14
- 239000003822 epoxy resin Substances 0.000 claims abstract description 12
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 9
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 7
- 239000013034 phenoxy resin Substances 0.000 claims abstract description 7
- 229920006287 phenoxy resin Polymers 0.000 claims abstract description 7
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 7
- 239000004020 conductor Substances 0.000 claims abstract description 5
- 239000012212 insulator Substances 0.000 claims abstract description 5
- 239000005011 phenolic resin Substances 0.000 claims abstract description 3
- 229920005989 resin Polymers 0.000 claims description 12
- 239000011347 resin Substances 0.000 claims description 12
- 239000011247 coating layer Substances 0.000 claims description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 3
- 229920001568 phenolic resin Polymers 0.000 claims description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 2
- HMOZDINWBHMBSQ-UHFFFAOYSA-N 2-[3-(4,5-dihydro-1,3-oxazol-2-yl)phenyl]-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC(C=2OCCN=2)=C1 HMOZDINWBHMBSQ-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 7
- 150000001875 compounds Chemical class 0.000 abstract description 5
- 239000004640 Melamine resin Substances 0.000 abstract description 4
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 abstract description 3
- 238000005299 abrasion Methods 0.000 abstract description 3
- 125000003700 epoxy group Chemical group 0.000 abstract description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 2
- 230000008018 melting Effects 0.000 abstract 1
- 230000004927 fusion Effects 0.000 description 5
- 238000004804 winding Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- VOOLKNUJNPZAHE-UHFFFAOYSA-N formaldehyde;2-methylphenol Chemical compound O=C.CC1=CC=CC=C1O VOOLKNUJNPZAHE-UHFFFAOYSA-N 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 239000004135 Bone phosphate Chemical class 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ODFJOVXVLFUVNQ-UHFFFAOYSA-N acetarsol Chemical group CC(=O)NC1=CC([As](O)(O)=O)=CC=C1O ODFJOVXVLFUVNQ-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229920005546 furfural resin Polymers 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012793 heat-sealing layer Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- -1 naphtha Chemical compound 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- ABBSXDLFMMKRKR-UHFFFAOYSA-N phosphorous acid;triphenylene Chemical compound OP(O)O.C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 ABBSXDLFMMKRKR-UHFFFAOYSA-N 0.000 description 1
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Organic Insulating Materials (AREA)
- Insulated Conductors (AREA)
Abstract
Description
【発明の詳細な説明】
(発明の技′術分野)
本発明は、自己潤滑性に優れる自己゛融着性絶縁電線に
関する。DETAILED DESCRIPTION OF THE INVENTION (Technical Field of the Invention) The present invention relates to a self-bonding insulated wire with excellent self-lubricating properties.
(発明の技術的背景およびその問題点)従来から電気機
器、通信機器のコイル成型工程における省力化、簡略化
、あるいは機器等のワニス含浸処理工程における安全衛
生および環境汚染対策の見地から、導体上に絶縁物層を
介して熱融着性の塗膜を設けてなるいわゆる自己融着性
絶縁ti線か使用されている。(Technical background of the invention and its problems) Conventionally, from the viewpoint of labor saving and simplification in the coil forming process of electrical equipment and communication equipment, and safety and health and environmental pollution prevention in the varnish impregnation process of equipment, etc., A so-called self-bonding insulated Ti wire, which is formed by providing a heat-fusible coating film with an insulating layer interposed therebetween, is used.
この自己融着性絶縁電線の熱融着層としては、ポリビニ
ールブチラール樹脂、ポリアミド樹脂、フェノキシ樹脂
等が多用されているが、このような熱可塑性樹脂は、1
50℃までに軟化してしまうので、実際上コイルに過負
荷電流が流れた場合や、高温雰囲気中に置かれた場合に
融着強度が著るしく低下してしまうという難点があった
。Polyvinyl butyral resin, polyamide resin, phenoxy resin, etc. are often used as the heat sealing layer of this self-bonding insulated wire.
Since it softens by 50° C., there is a problem in that the fusion strength is significantly reduced when an overload current flows through the coil or when it is placed in a high temperature atmosphere.
また、アルコール可溶性ナイpン樹脂は高温において、
高い接着力を有しているが、実際の使用にあたってその
絶縁電線の温度に対する寿命である接着層の熱劣化特性
は105℃程度と低い。In addition, alcohol-soluble Nipun resin at high temperatures
Although it has high adhesive strength, the thermal deterioration property of the adhesive layer, which is the lifespan of the insulated wire in actual use, is as low as about 105°C.
さらに、ポリスルホン樹脂は高温における接着力は問題
ないがフィル成診時に十分な接着力を保持するためには
250℃以上のMmで長時間の作業を必要とし、作業性
が悪いという欠点を有している。Furthermore, although polysulfone resin has no problems with adhesive strength at high temperatures, it requires long hours of work at Mm of 250°C or higher in order to maintain sufficient adhesive strength during fill diagnosis, and has the disadvantage of poor workability. ing.
本出願人は、耐熱性、自己融着性に優れる組成物につい
て研究を重ねた結果、lリアリレート樹脂を用いた。も
の(特開昭59−60906号)、および2・2′(1
・3−フエニレン)ビス(2−オキサゾリン)(以下P
BOと略す)を配合したもの(特開昭60−23394
7号)が優れた効果を生むことを見い出している。しか
しながら、これらの組成物は自己潤滑性が充分でなく、
得られる絶縁電線の作業性、耐摩耗性に問題があった。The present applicant used l-realylate resin as a result of repeated research on compositions with excellent heat resistance and self-bonding properties. (Japanese Unexamined Patent Publication No. 59-60906), and 2.2' (1
・3-phenylene)bis(2-oxazoline) (hereinafter P
(abbreviated as BO) (JP-A-60-23394)
No. 7) has been found to produce excellent effects. However, these compositions do not have sufficient self-lubricating properties;
There were problems with the workability and wear resistance of the resulting insulated wire.
エナメル線等の巻線作業を迅速化させるため、近年では
高速自動巻取機の使用が一般化している。In order to speed up the winding work of enameled wire, etc., the use of high-speed automatic winding machines has become common in recent years.
このような機械巻きトおいては、エナメル線の自己潤滑
性が良好でないと、不要な張力等がかかり、得られる製
品の電気特性が著しく低下する0このため、絶縁電線に
張力等に対する良好な機械特性を付与する目的で、2重
被覆層の外層にナイロン樹脂を用いる方法がとられてい
るが、この方法では耐熱性が著しく低下してしまうとい
う欠点があった。また、絶縁電線の被覆層にシリコーン
オイルを添加した組成物を納いる方法もあるが、シリコ
ーンオイルの添加量は得られる被′lIi層の外観が悪
くなること等から制限されるため、耐加工性は不充分で
あった。In such mechanical winding, if the enameled wire does not have good self-lubricating properties, unnecessary tension will be applied and the electrical properties of the resulting product will deteriorate significantly. For the purpose of imparting mechanical properties, a method has been adopted in which a nylon resin is used as the outer layer of the double coating layer, but this method has the disadvantage that heat resistance is significantly reduced. There is also a method of adding a composition containing silicone oil to the coating layer of the insulated wire, but the amount of silicone oil added is limited because the appearance of the resulting coated layer becomes poor, so it is difficult to process. Sexuality was insufficient.
(発明の目的)
以上の点に着目し、耐熱性、自己融着性が良好で、かつ
耐加工性、自己潤滑性に優れる自己融着性絶縁1!線を
提供することを目的とした。(Objective of the Invention) Focusing on the above points, we created a self-bonding insulation that has good heat resistance and self-bonding properties, as well as excellent workability and self-lubricating properties! Intended to provide a line.
(発明の概要)
本発明は即ち、(イ)フェノキシ樹脂と、(ロ)エポキ
シ樹脂と、e92・2′−(l・3−フエニレン)ビス
(2−オキサゾリン)あるいはその誘導体と、に)フェ
ノール系樹脂および/またはメラミン樹脂トノ混合物に
、(ホ)エチレン−酢酸ビニル−ビニルアルコール共重
合体を前記(イ)からに)の混合物100重量部に対し
て0.O1〜20重量部配合してなる被覆層を導体上に
直接もしくは他の絶縁物を芥して設けてなる自己融着性
絶縁電線に関する。(Summary of the Invention) The present invention comprises (a) a phenoxy resin, (b) an epoxy resin, e92,2'-(l,3-phenylene)bis(2-oxazoline) or a derivative thereof, and (a) phenol. (v) ethylene-vinyl acetate-vinyl alcohol copolymer is added to the mixture of resin and/or melamine resin based on 100 parts by weight of the mixture of (b) to (b). The present invention relates to a self-bonding insulated wire in which a coating layer containing 1 to 20 parts by weight of O is provided directly on a conductor or by removing another insulator.
本発明に使用される(イ)のフェノキシ樹脂としては、
分子中に水酸基を含有する化合物であり、分子j12G
、ooo〜30,000の例えば、P K HHlPK
HJ(米国ユニオンカーバイド社製:商品名)等がある
。As the phenoxy resin (a) used in the present invention,
It is a compound containing a hydroxyl group in the molecule, and the molecule j12G
, ooo ~ 30,000, e.g., P K HHlPK
There are HJ (trade name, manufactured by Union Carbide Company, USA), etc.
本発明に使用する(口)の工メキシ樹脂としては、分子
中にエポキシ基を2個以上含有する化合物であり、例え
ばビスフェノール型エポキシ樹脂、ポリオール型エポキ
シ樹脂、ノボラック型エポキシa脂、多価カルボンra
型二lキシ樹脂、)リアジン型エポキシ他脂、ポリオレ
フィン型エポキシ樹脂、脂m型エポキシm脂のいずれも
使用することができる。The engineered mexyl resin used in the present invention is a compound containing two or more epoxy groups in the molecule, such as bisphenol-type epoxy resin, polyol-type epoxy resin, novolak-type epoxy resin, polyhydric carbonate resin, etc. ra
Any of type 2l xy resin, riazine type epoxy resin, polyolefin type epoxy resin, and fat type epoxy resin can be used.
本発明に使用される(ハ)のPBOは、の構造を有し、
酸又は活性水素を有する化合物とオキ号ゾリン環が開票
反応を起し、副生物を生成することなくエステルアミド
結合で三次元架橋構造を形成する性質を有している。The PBO (c) used in the present invention has a structure of
It has the property of causing a ticket-opening reaction between an acid or a compound containing active hydrogen and the oxozoline ring to form a three-dimensional crosslinked structure with esteramide bonds without producing any by-products.
また、PBOの誘導体は、PBOと多価カルボン酸とを
無溶剤または溶媒中でトリフェニレンホスファイトを触
媒として少くとも100℃以上の温度で反応させること
により得られるo P B Oと反応させる多価カルボ
ン酸は、PBOとの開環反応およびエポキシ樹脂との硬
化反応に寄与するもので、本発明に使用するものとして
は、テレフタル酸、無水マレイン酸等の二塩基酸や二塩
基酸無水物、トリメリット酸等の三塩基酸やその無水物
、ピロメリット酸等の四塩基酸やその無水物等がある@
また、組成物の熱軟化温度を上げる目的でに)の7エノ
ール系樹脂またはメラミン樹脂を単独で、あるいは混合
して添加する。本発明に使用するフx / −k fF
、 g 脂としては、フェノール−ホルムアルデヒド樹
脂、クレゾール−ホルムアルデヒド樹脂、クレゾール−
フルフラール樹脂等が、メラミン樹脂としては、メラミ
ン−ホルムアルデヒド樹脂、ブチル化メラミン!脂等が
ある。Further, the derivative of PBO is a polyhydric derivative obtained by reacting PBO and a polyhydric carboxylic acid with o PBO obtained by reacting PBO and a polyhydric carboxylic acid without a solvent or in a solvent using triphenylene phosphite as a catalyst at a temperature of at least 100 ° C. Carboxylic acids contribute to the ring-opening reaction with PBO and the curing reaction with epoxy resins, and those used in the present invention include dibasic acids such as terephthalic acid and maleic anhydride, dibasic acid anhydrides, Tribasic acids such as trimellitic acid and their anhydrides, tetrabasic acids such as pyromellitic acid and their anhydrides, etc. 7-enol resins or melamine (for the purpose of increasing the thermal softening temperature of the composition) Add the resins alone or in a mixture. fF used in the present invention x/-k fF
, g As the fat, phenol-formaldehyde resin, cresol-formaldehyde resin, cresol-formaldehyde resin,
Furfural resin etc., melamine resin, melamine-formaldehyde resin, butylated melamine! There is fat etc.
本発明における前記(イ)、(ロ)、e)、に)の望ま
しい配合割合は、(−r)のフェノキシ樹脂100重量
部に対し、(ロ)のエポキシ樹脂を1〜40重量部、(
ハ)のPBOを3〜60重量部、に)のフェノール系樹
脂および/またはメラミン樹脂を10〜60重量部であ
る。この配合割合の範囲外では、熱軟化温度が低下した
り、融着力が低下したりする。In the present invention, the desirable blending ratio of (a), (b), e), and (b) is as follows: 1 to 40 parts by weight of the epoxy resin (b) to 100 parts by weight of the phenoxy resin (-r);
c) 3 to 60 parts by weight of PBO; and 10 to 60 parts by weight of phenolic resin and/or melamine resin. If the blending ratio is outside this range, the heat softening temperature will be lowered and the fusion strength will be lowered.
本発明においては得られる自己融着性絶縁電線の自己潤
滑性の効果を大きくする目的で(ホ)のエチレン−酢酸
ビニル−ビニルアルコール共重合体を配合する。(ホ)
の共重合体としては公知のものを使用することができる
が、ビニルアルコール基0.5〜15モル≦含有するも
のを配合すると、自己潤滑性向上の効果はさらに好まし
くなる。In the present invention, the ethylene-vinyl acetate-vinyl alcohol copolymer (e) is blended for the purpose of increasing the self-lubricating effect of the self-bonding insulated wire. (E)
Although any known copolymer can be used, the effect of improving self-lubricating properties becomes even more favorable when a copolymer containing 0.5 to 15 moles of vinyl alcohol groups is blended.
また、(@のエチレン−酢酸ビニル−ビニルアルコール
共重合体は前記(イ)、(す、(ハ)、に)の混合物1
00重量部に対し0.01〜20重量部配合する。In addition, the ethylene-vinyl acetate-vinyl alcohol copolymer (@) is a mixture 1 of the above (a), (su, (c), ni).
0.01 to 20 parts by weight per 00 parts by weight.
配合量が0.01重量部未満では得られる電線の自己潤
滑性が乏しく、20重量部を越えると耐熱性が低下する
。If the amount is less than 0.01 parts by weight, the resulting electric wire will have poor self-lubricating properties, and if it exceeds 20 parts by weight, the heat resistance will decrease.
なお、本発明においてヒ)から(ホ)の各成分を混練す
る際に用いる溶剤としては、クレゾール、ナフサ、シク
ロヘキサノン等があり、これらは単独で、あるいは混合
して使用する。Incidentally, in the present invention, examples of the solvent used when kneading each component (e) to (e) include cresol, naphtha, cyclohexanone, etc., and these may be used alone or in a mixture.
本発明の自己融着性絶縁電線は、各成分を溶剤とともに
混練して得た塗料を、導体上に直接もしくは他の絶縁物
を介して塗布し、通常の方法で焼付けることにより製造
する。The self-bonding insulated wire of the present invention is manufactured by kneading each component with a solvent, applying a coating material onto a conductor directly or via another insulator, and baking the coating in a conventional manner.
(発明の実施例) 本発明の実施例について説明する。(Example of the invention) Examples of the present invention will be described.
第1表に示す配合で混合し、充分攪拌して塗料を得た。The compositions shown in Table 1 were mixed and thoroughly stirred to obtain a paint.
直径1.0mの銅線上に0.04IllIKのポリエス
テルイミド被覆を設けてなるエナメル線上に、得られた
塗料を塗布し、炉温400℃、線速14@/分で焼付け
た。得られた自己融着性絶縁電線を用いて次のとおり試
験を行った。The obtained paint was applied onto an enameled wire consisting of a copper wire with a diameter of 1.0 m and a polyesterimide coating of 0.04 IllIK, and baked at an oven temperature of 400° C. and a line speed of 14 @/min. The following tests were conducted using the obtained self-bonding insulated wire.
融着力は、6.4■直径のマンドレルに得られた自己融
着性絶縁電線を50回巻き付けたコイルを、240℃X
30分加熱して融着硬化させた後の融着力を室温及び8
0℃で測定した。耐摩耗性は、700g荷重をかけJI
S O30031976−10・1に従って測定した
。自己潤滑性は静摩擦試験機を用いて静摩擦係数を測定
した。The fusion strength is as follows: A coil made by winding the obtained self-bonding insulated wire 50 times around a mandrel with a diameter of 6.4 mm is heated at 240℃
After heating for 30 minutes to cure the fusion bond, the fusion strength was measured at room temperature and 8
Measured at 0°C. Abrasion resistance is determined by JI with a load of 700g.
Measured according to SO30031976-10.1. Self-lubricity was determined by measuring the static friction coefficient using a static friction tester.
比較例は、第1表に示す配合で、実施例と同様にして自
己融着性絶縁[&[を製造し、試験した。As a comparative example, self-bonding insulation [&[ was manufactured and tested in the same manner as in the examples, using the formulations shown in Table 1.
比較例1及び2では、エチレン−酢酸ビニル−ビニルア
ルコール共重合体を全く添加しない場合であり、自己潤
滑性、耐摩耗性ともに低い。比較例3及び4では、エチ
レン−酢酸ビニルービニルアルコール共重合体を過剰に
添加した場合が示してあり、耐熱性、融着力の低下が見
られる。In Comparative Examples 1 and 2, no ethylene-vinyl acetate-vinyl alcohol copolymer was added, and both self-lubricity and wear resistance were low. Comparative Examples 3 and 4 show cases in which an excessive amount of ethylene-vinyl acetate-vinyl alcohol copolymer was added, and a decrease in heat resistance and fusing strength was observed.
実施例1〜7は、融着力、耐熱性を低下させずに、良好
な耐摩耗性、自己潤滑性を持っている0以下余白
(発明の効果)
本発明の自己融着性絶縁電線は、融着性、耐熱性を低下
させることなく、自己潤滑性を大幅に向上させ、機械巻
作業等に充分耐え得る特性を持つ。Examples 1 to 7 have a margin of 0 or less that has good abrasion resistance and self-lubricating properties without reducing fusing strength and heat resistance (effects of the invention). It has properties that greatly improve self-lubricating properties without reducing adhesiveness or heat resistance, and can withstand mechanical winding operations.
Claims (1)
)2・2′−(1・3−フエニレン)ビス(2−オキサ
ゾリン)あるいはその誘導体と、(ニ)フェノール系樹
脂および/またはメラミン樹脂との混合物に、(ホ)エ
チレン−酢酸ビニル−ビニルアルコール共重合体を前記
(イ)から(ニ)の混合物100重量部に対して0.0
01〜20重量部配合してなる被覆層を導体上に直接も
しくは他の絶縁物を介して設けてなる自己融着性絶縁電
線。(a) phenoxy resin, (b) epoxy resin, (c) 2,2'-(1,3-phenylene)bis(2-oxazoline) or its derivative, (d) phenolic resin and/or melamine. Add 0.0 parts by weight of (e) ethylene-vinyl acetate-vinyl alcohol copolymer to the mixture with the resin per 100 parts by weight of the mixture of (a) to (d) above.
A self-bonding insulated wire comprising a coating layer containing 1 to 20 parts by weight of 0.01 to 20 parts by weight, provided on a conductor directly or via another insulator.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31933387A JPH01161607A (en) | 1987-12-17 | 1987-12-17 | Self-melting insulated wire |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31933387A JPH01161607A (en) | 1987-12-17 | 1987-12-17 | Self-melting insulated wire |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01161607A true JPH01161607A (en) | 1989-06-26 |
Family
ID=18109007
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31933387A Pending JPH01161607A (en) | 1987-12-17 | 1987-12-17 | Self-melting insulated wire |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01161607A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103772799A (en) * | 2014-01-21 | 2014-05-07 | 安徽华海特种电缆集团有限公司 | Cable sheath material for mine |
-
1987
- 1987-12-17 JP JP31933387A patent/JPH01161607A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103772799A (en) * | 2014-01-21 | 2014-05-07 | 安徽华海特种电缆集团有限公司 | Cable sheath material for mine |
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