JPH05258613A - Insulated electric cable - Google Patents

Insulated electric cable

Info

Publication number
JPH05258613A
JPH05258613A JP5281092A JP5281092A JPH05258613A JP H05258613 A JPH05258613 A JP H05258613A JP 5281092 A JP5281092 A JP 5281092A JP 5281092 A JP5281092 A JP 5281092A JP H05258613 A JPH05258613 A JP H05258613A
Authority
JP
Japan
Prior art keywords
polyamide
mechanical strength
electric cable
insulated electric
heat 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
Application number
JP5281092A
Other languages
Japanese (ja)
Inventor
Kenji Asano
健次 浅野
Kazunori Suzuki
和則 鈴木
Akio Mitsuoka
昭雄 光岡
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi Cable Ltd
Original Assignee
Hitachi Cable Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hitachi Cable Ltd filed Critical Hitachi Cable Ltd
Priority to JP5281092A priority Critical patent/JPH05258613A/en
Publication of JPH05258613A publication Critical patent/JPH05258613A/en
Pending legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyamides (AREA)
  • Paints Or Removers (AREA)
  • Organic Insulating Materials (AREA)
  • Insulated Conductors (AREA)

Abstract

PURPOSE:To provide an insulated electric cable with high heat resistance and mechanical strength by applying a paint containing mainly specified polyamide prepared by reaction of terephthalic acid, hexamethylenediamine, caprolactam to a conductor and baking it. CONSTITUTION:A polyamide having a chemical structure shown as the formula and melting point 290-300 deg.C is prepared by reaction of terephthalic acid, hexamethylenediamine, and caprolactam. A paint mainly containing the polyamide is applied to a conductor directly or having another insulator between them and baked. As a result an insulated electric cable bearing polyamide overcoat which has high heat resistance, that is softening resistance and deterioration resistance, and mechanical strength, that is flexibility and reciprocal wear resistance.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、絶縁電線に関するもの
である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an insulated wire.

【0002】[0002]

【従来の技術】近年、電気機器の小形化、コイル巻線作
業の高速化、コイル不良率の低減等を目的として機械巻
線性に優れたエナメル線への要望はますます高まってい
る。機械巻線性の改善には線の仕上げ外径を細くするこ
と、しなやかさをますこと、皮膜の機械強度を高めるこ
と、エナメル線に滑り性を与える(自己潤滑化)こと等
が行われている。
2. Description of the Related Art In recent years, there has been an increasing demand for enameled wires with excellent mechanical winding properties for the purpose of downsizing electrical equipment, speeding up coil winding work, and reducing the coil defect rate. To improve the mechanical winding property, the outer diameter of the wire is made thinner, the flexibility is increased, the mechanical strength of the coating is increased, and the enamel wire is made slippery (self-lubricating). ..

【0003】従来、エナメル線皮膜の強度を高める方法
の一つとして、ポリアミドをエナメル皮膜の上層に焼付
ける方法が一般に行われてきた。ポリアミドとしては
6.6ナイロン(融点250℃)、6ナイロン(融点2
15℃)、6.10ナイロン(融点210℃)、11ナ
イロン(融点185℃)、12ナイロン(融点178
℃)等が用いられるが、機械強度と皮膜の軟化性(高融
点ほど軟化しにくい)の点から特に6.6ナイロンが多
く用いられている。
Conventionally, as one of the methods for increasing the strength of the enamel wire coating, a method of baking polyamide on the upper layer of the enamel coating has been generally performed. As polyamide, 6.6 nylon (melting point 250 ° C.), 6 nylon (melting point 2)
15 ° C), 6.10 nylon (melting point 210 ° C), 11 nylon (melting point 185 ° C), 12 nylon (melting point 178)
However, 6.6 nylon is particularly often used from the viewpoint of mechanical strength and film softening property (higher melting point is less likely to soften).

【0004】エナメル線としては皮膜の機械的強度がや
や劣るポリエステル線やポリウレタン線にこのポリアミ
ドオーバコートの手法が主に適用されている。
As the enamel wire, the method of this polyamide overcoat is mainly applied to a polyester wire and a polyurethane wire whose coating film has a slightly poor mechanical strength.

【0005】[0005]

【発明が解決しようとする課題】H種エステルイミド線
は皮膜の機械的強度がやや劣るため、このポリアミドオ
ーバコートとすることも考えられるが、6.6ナイロン
の耐熱性が劣るため、F〜H種機器用としては実用する
ことができなかった。
Since the H-type ester imide wire has a slightly inferior mechanical strength of the film, it may be possible to use this polyamide overcoat. However, since the heat resistance of 6.6 nylon is inferior, F- It could not be put to practical use for H class equipment.

【0006】本発明は以上の点に鑑みなされたものであ
り、耐熱性、機械的強度の向上を可能としたポリアミド
オーバコートの絶縁電線を提供することを目的とするも
のである。
The present invention has been made in view of the above points, and it is an object of the present invention to provide a polyamide overcoat insulated wire capable of improving heat resistance and mechanical strength.

【0007】[0007]

【課題を解決するための手段】上記目的は、導体上にテ
レフタル酸、ヘキサメチレンジアミン、カプロラクタム
を反応させた下記化2の化学構造を有する融点290〜
300℃のポリアミドを主体とする塗料を直接もしくは
他の絶縁物を介し塗布焼付けてなることにより、達成さ
れる。
[Means for Solving the Problems] The above object is to have a melting point of 290 to 290, which has a chemical structure of the following chemical formula 2 in which terephthalic acid, hexamethylenediamine and caprolactam are reacted on a conductor.
This can be achieved by coating and baking a paint mainly composed of polyamide at 300 ° C. directly or through another insulating material.

【0008】[0008]

【化2】 [Chemical 2]

【0009】[0009]

【作用】上記手段を設けたので、耐熱性、機械的強度が
向上するようになる。
Since the above means is provided, heat resistance and mechanical strength are improved.

【0010】上記化2の構造を有する材料としては「ウ
ルトラミッドT」(西独国、BASF社)等がある。ウ
ルトラミッドTの融点は295℃で従来の6.6ナイロ
ンに比べ約45℃高く、また平衡吸水量(23℃)も
6.6ナイロンの8.2%に対し5.7%と低い。
As a material having the structure of the above chemical formula 2, there is "Ultramid T" (BASF, West Germany) and the like. The melting point of Ultramid T is 295 ° C, which is about 45 ° C higher than that of conventional 6.6 nylon, and the equilibrium water absorption (23 ° C) is 5.7%, which is lower than 8.2% of 6.6 nylon.

【0011】なお、表面の滑り性付与のため、低分子ポ
リエチレン、テフロンオリゴマー、脂肪酸ポリエステル
等を0.1〜10重量添加してもよい。
In order to impart surface slipperiness, low molecular weight polyethylene, Teflon oligomer, fatty acid polyester, etc. may be added in an amount of 0.1 to 10 parts by weight.

【0012】また、低分子ポリエチレンの末端にカルボ
ン酸(R−COOH)、当該ポリアミドの末端をアミノ
基(−NH2)と反応させて分散安定性を向上させても
よい。
Further, the dispersion stability may be improved by reacting the terminal of the low molecular weight polyethylene with a carboxylic acid (R-COOH) and the terminal of the polyamide with an amino group (-NH 2 ).

【0013】[0013]

【実施例】次に本発明を実施例により具体的に説明す
る。本実施例では導体上にテレフタル酸、ヘキサメチレ
ンジアミン、カプロラクタムを反応させた下記化3の化
学構造を有する融点290〜300℃のポリアミドを主
体とする塗料を直接もしくは他の絶縁物を介し塗布焼付
けた。
EXAMPLES Next, the present invention will be specifically described by way of examples. In this example, a paint mainly composed of a polyamide having a chemical structure of the following chemical formula 3 and having a melting point of 290 to 300 ° C., which is obtained by reacting terephthalic acid, hexamethylenediamine, and caprolactam on a conductor, is directly applied or baked through another insulating material. It was

【0014】[0014]

【化3】 [Chemical 3]

【0015】このようにすることにより、耐熱性、機械
的強度が向上するようになって、耐熱性、機械的強度の
向上を可能としたポリアミドオーバコートの絶縁電線を
得ることができる。
By doing so, heat resistance and mechanical strength are improved, and a polyamide overcoated insulated wire capable of improving heat resistance and mechanical strength can be obtained.

【0016】表1には実施例および比較例について塗料
配合によるエナメル線特性を検討した結果が示されてい
る。
Table 1 shows the results of examining the enameled wire characteristics of the coating compositions for the examples and comparative examples.

【0017】[0017]

【表1】 [Table 1]

【0018】同表で実施例および比較例は導体径1.0
mm、皮膜厚は35μmのH種エステルイミド線(以下
EIWと称す)を用い、上層のポリアミド層は皮膜厚3
〜4μmとなるように焼付けて供試線とした。エナメル
線の特性はJIS−C3003に準拠して測定した。以
下表1に基づいて説明する。
In the table, the conductor diameter is 1.0 in the examples and comparative examples.
mm, the film thickness is 35 μm, and an H-type ester imide wire (hereinafter referred to as EIW) is used, and the upper polyamide layer has a film thickness of 3
The test line was baked to have a thickness of ˜4 μm. The characteristics of the enameled wire were measured according to JIS-C3003. A description will be given below based on Table 1.

【0019】〔実施例1〕ウルトラミッドT(BASF
社製)をクレゾール酸/キシロール(=8/2)に濃度
15%に溶解した塗料を、EIWの上層に4μm焼付け
た。
Example 1 Ultramid T (BASF
A coating composition prepared by dissolving (manufactured by the same company) in cresylic acid / xylol (= 8/2) at a concentration of 15% was baked at 4 μm on the upper layer of EIW.

【0020】〔実施例2〕ウルトラミッドT100重量
部に、末端に−COOH基を有する低分子ポリエチレン
(mp107℃)3重量部添加し、100〜200℃で
クレゾール中で反応した後、クレゾール酸/キシロール
(=8/2)に濃度15%に溶解した塗料を、EIWの
上層に4μm焼付けた。
Example 2 To 100 parts by weight of Ultramid T, 3 parts by weight of a low molecular weight polyethylene having a --COOH group at the end (mp107 ° C.) was added, and the mixture was reacted in cresol at 100 to 200 ° C., then cresylic acid / The paint dissolved in xylol (= 8/2) at a concentration of 15% was baked at 4 μm on the upper layer of EIW.

【0021】〔比較例1〕EIW単独である。Comparative Example 1 EIW alone.

【0022】〔比較例2〕6.6ナイロン樹脂として東
レ社製CM3001Nをクレゾール酸/キシロール(=
8/2)に濃度15%に溶解した塗料を、EIWの上層
に4μm焼付けた。
[Comparative Example 2] CM3001N manufactured by Toray Industries, Inc. as a 6.6 nylon resin was mixed with cresylic acid / xylol (=
The paint dissolved in a concentration of 15% on 8/2) was baked at 4 μm on the upper layer of EIW.

【0023】同表から明らかなように実施例1、2は耐
熱性、機械的強度に優れており、耐熱性、機械的強度に
優れたポリアミドオーバコートエナメル線を提供でき、
工業上有用である。
As is clear from the table, Examples 1 and 2 are excellent in heat resistance and mechanical strength, and can provide polyamide overcoated enameled wire excellent in heat resistance and mechanical strength.
It is industrially useful.

【0024】[0024]

【発明の効果】上述のように本発明は、導体上にテレフ
タル酸、ヘキサメチレンジアミン、カプロラクタムを反
応させた下記化4の化学構造を有する融点290〜30
0℃のポリアミドを主体とする塗料を直接もしくは他の
絶縁物を介し塗布焼付けたので、耐熱性、機械的強度が
向上するようになって、耐熱性、機械的強度の向上を可
能としたポリアミドオーバコートの絶縁電線を得ること
ができる。
As described above, the present invention has a melting point of 290 to 30 having a chemical structure represented by the following chemical formula 4 in which terephthalic acid, hexamethylenediamine and caprolactam are reacted on a conductor.
Since a paint mainly composed of polyamide at 0 ° C was applied and baked directly or through another insulating material, heat resistance and mechanical strength were improved, and polyamide capable of improving heat resistance and mechanical strength was obtained. An overcoated insulated wire can be obtained.

【0025】[0025]

【化4】 [Chemical 4]

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 H01B 3/30 M 9059−5G ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location H01B 3/30 M 9059-5G

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】導体上にテレフタル酸、ヘキサメチレンジ
アミン、カプロラクタムを反応させた下記化1の化学構
造を有する融点290〜300℃のポリアミドを主体と
する塗料を直接もしくは他の絶縁物を介し塗布焼付けて
なることを特徴とする絶縁電線。 【化1】
1. A coating mainly composed of a polyamide having a chemical structure of the following chemical formula 1 and having a melting point of 290 to 300 ° C., which is obtained by reacting terephthalic acid, hexamethylenediamine and caprolactam, on a conductor, directly or through another insulating material. An insulated wire characterized by being baked. [Chemical 1]
JP5281092A 1992-03-11 1992-03-11 Insulated electric cable Pending JPH05258613A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5281092A JPH05258613A (en) 1992-03-11 1992-03-11 Insulated electric cable

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5281092A JPH05258613A (en) 1992-03-11 1992-03-11 Insulated electric cable

Publications (1)

Publication Number Publication Date
JPH05258613A true JPH05258613A (en) 1993-10-08

Family

ID=12925205

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5281092A Pending JPH05258613A (en) 1992-03-11 1992-03-11 Insulated electric cable

Country Status (1)

Country Link
JP (1) JPH05258613A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016531107A (en) * 2013-07-25 2016-10-06 アルケマ フランス Lactam or amino acid fatty acid amides and their use as organogelators

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016531107A (en) * 2013-07-25 2016-10-06 アルケマ フランス Lactam or amino acid fatty acid amides and their use as organogelators

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