JPS6055931B2 - colored insulated wire - Google Patents

colored insulated wire

Info

Publication number
JPS6055931B2
JPS6055931B2 JP10019478A JP10019478A JPS6055931B2 JP S6055931 B2 JPS6055931 B2 JP S6055931B2 JP 10019478 A JP10019478 A JP 10019478A JP 10019478 A JP10019478 A JP 10019478A JP S6055931 B2 JPS6055931 B2 JP S6055931B2
Authority
JP
Japan
Prior art keywords
weight
parts
rubber
insulated wire
colored
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.)
Expired
Application number
JP10019478A
Other languages
Japanese (ja)
Other versions
JPS5528218A (en
Inventor
亮一 伊藤
孝一 吉田
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 JP10019478A priority Critical patent/JPS6055931B2/en
Publication of JPS5528218A publication Critical patent/JPS5528218A/en
Publication of JPS6055931B2 publication Critical patent/JPS6055931B2/en
Expired legal-status Critical Current

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  • Insulated Conductors (AREA)

Description

【発明の詳細な説明】 本発明は着色被覆を有するゴムやプラスチック絶縁電
線に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a rubber or plastic insulated wire having a colored coating.

従来、ゴムやプラスチックの絶縁電線の識別には(1
)絶縁体に着色剤を混合する。
Traditionally, rubber and plastic insulated wires were identified using (1)
) Mix the coloring agent into the insulation.

(2)合成ゴムを有機溶剤で溶かした着色剤を含む塗料
を塗布する。2つの方法が採用されてきた。
(2) Apply a paint containing a colorant made by dissolving synthetic rubber in an organic solvent. Two methods have been adopted.

(1)は着色剤の異なる多数の配合を製造する必要があ
り、材料管理が煩雑になる。また、短尺品の場合には押
出機の清掃、段取等のロスタイムが多くなる。(2)の
場合には有機溶剤が飛散するため材料の損失があるうえ
、環境汚染の問題が派生する。 これを克服するものと
してアクリルエステルオリゴマのような液状ポリマがあ
げられる。
In (1), it is necessary to manufacture a large number of formulations with different colorants, which makes material management complicated. Furthermore, in the case of short products, there is a lot of loss time such as cleaning and setup of the extruder. In the case of (2), the organic solvent is scattered, which causes material loss, and also poses the problem of environmental pollution. Liquid polymers such as acrylic ester oligomers can be used to overcome this problem.

ところが一般に1 硬化速度が大きいものは可撓性に乏
しい。
However, in general, materials with a high curing speed have poor flexibility.

2 可撓性にすぐれたものは硬化速度がおそい。2. Materials with excellent flexibility have a slow curing speed.

傾向があり、絶縁電線上被覆への適用はほとんど行われ
なかつた。 したがつて材料損失が少なく、硬化速度が
大きく、硬化物が可撓性にすぐれており、絶縁体との接
着が良好であり、絶縁体の特性に悪影響しない材料が要
求される。
As a result, it has rarely been applied to coatings on insulated wires. Therefore, there is a need for a material that has low material loss, a high curing speed, excellent flexibility of the cured product, good adhesion to the insulator, and does not adversely affect the properties of the insulator.

本発明の目的は、前記した従来技術の欠点を解消し、
ゴム、プラスチック絶縁電線の識別を経済的かつ技術的
に容易に達成できる新規な着色絶縁電線を提供すること
にある。 本発明の要旨は、導体周上のゴムあるいはプ
ラスチック絶縁体上に、アクリルウレタンオリゴマを主
体とする着色塗料を被覆し、これを硬化して構成したこ
とを特徴とする着色絶縁電線にある。
The purpose of the present invention is to eliminate the drawbacks of the prior art described above,
An object of the present invention is to provide a new colored insulated wire that can economically and technically easily identify rubber and plastic insulated wires. The gist of the present invention resides in a colored insulated wire characterized by coating a rubber or plastic insulator on the circumference of a conductor with a colored paint mainly composed of acrylic urethane oligomer and curing the coated paint.

ここで、アクリルウレタンオリゴマとは末端に少なく
とも1個のアクリル酸エステル基CH2■CH−C−O
−またはメタクリル酸エステル基Cル■C−C−O−及
び分子中に少なくとも1個以上のウレタン基−COO−
NH−を有するオリゴマで分子量200〜500@度の
ものをいう。ウレタン結合はポリオールとイソシアネー
トの反応によつて生成するものである。 例えば、、カ
プロラクトンポリオール/イソボロンジイソシアネート
/ヒドロキシルアクリレートオリゴマ、アジピン酸ポリ
オール/トリレンジイソシアネート/ヒドロキシアクリ
レートオリゴマ、トリメチロールプロパンポリオール/
トリレンジイソシアネート/ヒドロキシアクリレートな
ど、またチオコール社がら市販されているUvitha
ne782(ポリエステルと芳香族ジイソシアネートか
ら生成したウレタンオリゴマをアクリル化した商品)お
よびUvithane783(ポリエステルと脂肪族ジ
イソシアネートから生成したウレタンオリゴマをアクリ
ル化した商品)などがあげられるが、これらに限定され
るものではない。
Here, acrylic urethane oligomer has at least one acrylic ester group CH2CH-C-O at the end.
- or methacrylic acid ester group C-C-O- and at least one urethane group -COO- in the molecule
An oligomer containing NH- with a molecular weight of 200 to 500 degrees. Urethane bonds are produced by the reaction of polyols and isocyanates. For example, caprolactone polyol/isoborone diisocyanate/hydroxyacrylate oligomer, adipic acid polyol/tolylene diisocyanate/hydroxyacrylate oligomer, trimethylolpropane polyol/
tolylene diisocyanate/hydroxyacrylate, etc., and Uvitha, which is commercially available from Thiokol.
Examples include, but are not limited to, ne782 (a product made by acrylating a urethane oligomer made from polyester and an aromatic diisocyanate) and Uvithane783 (a product made by acrylating a urethane oligomer made from a polyester and an aliphatic diisocyanate). do not have.

アクリルウレタンオリゴマの粘度を低下させる目的で、
反応性希釈剤例えばエチルヘキシルアクリレート、ベン
ジルアクリレート、ビニル−ピロリドン、エトキシエチ
ルアクリレート、エトキシエトキシエチルアクリレート
などを1種あるいは2種以上組合せて添加してもよい。
In order to reduce the viscosity of acrylic urethane oligomer,
Reactive diluents such as ethylhexyl acrylate, benzyl acrylate, vinyl-pyrrolidone, ethoxyethyl acrylate, and ethoxyethoxyethyl acrylate may be added alone or in combination of two or more.

勿論、従来使用されている有機溶剤を用いてもよい。こ
の場合でも従来より大巾に溶剤量を低減できる。この系
に着色剤を添加する。
Of course, conventionally used organic solvents may also be used. Even in this case, the amount of solvent can be significantly reduced compared to the conventional method. A colorant is added to this system.

着色剤は従来技術で使用されているものと同じでよい。
また必要に応じて酸化防止剤、架橋剤、光増感剤、ワッ
クス、チクソトロビー性を付与する揺変剤などを混合し
ても一向に差支えない。
Colorants may be the same as those used in the prior art.
Further, there is no problem in mixing an antioxidant, a crosslinking agent, a photosensitizer, a wax, a thixotropic agent that imparts thixotropic properties, etc., if necessary.

硬化方法としては紫外線照射、赤外線加熱、電子線照射
などのうちいずれを採用してもよい。
As a curing method, any of ultraviolet irradiation, infrared heating, electron beam irradiation, etc. may be employed.

ここで、導体周上の絶縁体としては、架橋ポリオレフィ
ン(ポリオレフィンとはポリエチレン、エチレンを主体
とする共重合体、三元ポリマを指し、ポリエチレン、エ
チレン−プロピレン共重合体、エチレンー酢酸ビニル共
重合体、エチレン−エチルアクリレート共重合体、エチ
レン−メチル.メタクリレート共重合体など)、天然ゴ
ム、合成ゴム、(エチレン−プロピレンゴム、フチルゴ
ム、クロロスルフォン化ポリエチレン、塩素化ポリエチ
レン、スチレンーフタジエンゴム、クロロプレンゴム、
ニトリルゴム、アクリルゴムなど)町を使用できる。こ
れらを単独もしくは組合せて使用したものを指す。次に
本発明の実施例について説明する。実施例1 Uvithane782(チオコール社製)50重量部
と・エチルヘキシルアクリレート5唾量部の混合物に対
して、酸化チタン3喧量部、フタロシアニンブルー1踵
量部、光増感剤ベンゾフェノン5重量部を混合した青色
塗料を、導体周上の天然ゴム絶縁体上に厚さ100μ程
度にうすく被覆し、2KW高圧水銀灯を高さ15anか
ら照射した。
Here, the insulator on the circumference of the conductor is a cross-linked polyolefin (polyolefin refers to polyethylene, a copolymer mainly composed of ethylene, or a terpolymer; polyethylene, ethylene-propylene copolymer, ethylene-vinyl acetate copolymer) , ethylene-ethyl acrylate copolymer, ethylene-methyl methacrylate copolymer, etc.), natural rubber, synthetic rubber, (ethylene-propylene rubber, phthyl rubber, chlorosulfonated polyethylene, chlorinated polyethylene, styrene-phtadiene rubber, chloroprene) rubber,
Nitrile rubber, acrylic rubber, etc.) can be used. Refers to those used alone or in combination. Next, examples of the present invention will be described. Example 1 3 parts by weight of titanium oxide, 1 part by weight of phthalocyanine blue, and 5 parts by weight of photosensitizer benzophenone were mixed with a mixture of 50 parts by weight of Uvithane 782 (manufactured by Thiokol) and 5 parts by weight of ethylhexyl acrylate. The blue paint obtained was thinly coated on the natural rubber insulator on the circumference of the conductor to a thickness of about 100 μm, and irradiated with a 2 KW high-pressure mercury lamp from a height of 15 ann.

照射時間は2秒である。被膜は十分硬化しており、自己
径に曲げても亀裂は発生しなかつた。着色被覆層有と無
の場合、物理特性、電気特性に何等の差が認められなか
つた。実施例2 UviU1ane783(チオコール社製)70重量部
、ビニル−ピロリドン3轍量部にメチルエチルケト)ン
3唾量部、カーボンブラック5重量部、ベンゾイルパー
オキサイド2重量部を添加した塗料を、導体周上の架橋
ポリエチレン絶縁体上に被覆し、溶剤を揮散した後電子
線(1刈σMrad)で照射した。
The irradiation time was 2 seconds. The coating was sufficiently cured and no cracks occurred even when bent to its own diameter. No difference was observed in physical properties or electrical properties between the cases with and without the colored coating layer. Example 2 A paint containing 70 parts by weight of UviU1ane 783 (manufactured by Thiokol), 3 parts by weight of vinyl-pyrrolidone, 3 parts by weight of methyl ethyl ketone, 5 parts by weight of carbon black, and 2 parts by weight of benzoyl peroxide was applied around the conductor. It was coated on a cross-linked polyethylene insulator, and after the solvent was volatilized, it was irradiated with an electron beam (1 molar σ Mrad).

照射時間は1秒である。結果は実施例1と同様であつた
The irradiation time was 1 second. The results were similar to Example 1.

比較例1 トリメチロールプロパントリアクリレート5リ重量部、
エチルヘキシルアクリレート5鍾量部に酸化チタン3鍾
量部、フタロシアニンブルー1踵量部、光増感剤ベンゾ
フェノン5重量部を添加した塗料を、実施例1と同様に
実施した。
Comparative Example 1 5 parts by weight of trimethylolpropane triacrylate,
A coating material was prepared in the same manner as in Example 1 by adding 3 parts by weight of titanium oxide, 1 part by weight of phthalocyanine blue, and 5 parts by weight of photosensitizer benzophenone to 5 parts by weight of ethylhexyl acrylate.

十分硬化したが自己径巻付でクラックを発生した。比較
例2 2−ヒドロキシ●ドデシルアクリレート7鍾量部、ビニ
ルピロリドン3鍾量部に酸化チタン3踵量部、フタロシ
アニンブルー1喧量部、光増感剤ベンゾフェノン5重量
部に添加した塗料を実施例1と同様に実施した。
Although it was sufficiently cured, cracks occurred due to self-diameter winding. Comparative Example 2 Example of a paint containing 7 parts by weight of 2-hydroxy dodecyl acrylate, 3 parts by weight of vinylpyrrolidone, 3 parts by weight of titanium oxide, 1 part by weight of phthalocyanine blue, and 5 parts by weight of photosensitizer benzophenone. It was carried out in the same manner as in 1.

表面は全く硬化しなかつた。完全に硬化するのに少なく
とも1分以上要した。ゴム、プラスチック絶縁電線の絶
縁体上に電極用として半導電性層を形成することがある
The surface was not hardened at all. It took at least 1 minute to completely cure. A semiconductive layer is sometimes formed on the insulator of rubber or plastic insulated wire for use as an electrode.

この場合にも本発明の被覆組成にカーボンブラックやグ
ラファイトを単独もしくは組合せて混合することによつ
て、これらの導電物質の種類、添加量に応じた体積抵抗
率を保持する塗料の調整が可能となり、これまでに述べ
た硬化方法によつて半導電層を形成できる。本発明の着
色絶縁電線によれば、特定の被覆組成を採用したことに
よつて、材料の損失となる有機溶剤を除去乃至大巾に低
減でき、さらに環境汚染も著しく軽減できる。
In this case, by mixing carbon black or graphite alone or in combination with the coating composition of the present invention, it is possible to adjust a paint that maintains volume resistivity according to the type and amount of these conductive substances. The semiconducting layer can be formed by the curing method described above. According to the colored insulated wire of the present invention, by employing a specific coating composition, organic solvents that cause material loss can be removed or greatly reduced, and environmental pollution can also be significantly reduced.

また、従来の加熱硬化に比べ紫外線、電子線照射によつ
て極めて短時間(1秒前後)に硬化することができる。
特に紫外線硬化を採用した場合の設備費、運転費などが
大巾に低減する。
Further, compared to conventional heat curing, it can be cured in an extremely short time (about 1 second) by ultraviolet ray or electron beam irradiation.
In particular, when ultraviolet curing is used, equipment costs and operating costs are significantly reduced.

もちろん加熱硬化の場合にも有機溶剤低減による材料損
失減少が見込まれる。勿論、可撓性についても着色被覆
を有しない電線に比べ、なんら遜色が無い。
Of course, in the case of heat curing, material loss can be expected to be reduced by reducing the amount of organic solvent used. Of course, the flexibility is also comparable to electric wires without colored coatings.

Claims (1)

【特許請求の範囲】[Claims] 1 導体周上にゴムあるいはプラスチック絶縁体が設け
られ、この外周に最外層としてアクリルウレタンオリゴ
マを主体とする着色塗料の被覆層が形成され、該被覆層
は硬化して構成されることを特徴とする着色絶縁電線。
1. A rubber or plastic insulator is provided on the circumference of the conductor, and a coating layer of a colored paint mainly composed of acrylic urethane oligomer is formed as the outermost layer on the outer circumference, and the coating layer is configured by curing. Colored insulated wire.
JP10019478A 1978-08-17 1978-08-17 colored insulated wire Expired JPS6055931B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10019478A JPS6055931B2 (en) 1978-08-17 1978-08-17 colored insulated wire

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10019478A JPS6055931B2 (en) 1978-08-17 1978-08-17 colored insulated wire

Publications (2)

Publication Number Publication Date
JPS5528218A JPS5528218A (en) 1980-02-28
JPS6055931B2 true JPS6055931B2 (en) 1985-12-07

Family

ID=14267485

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10019478A Expired JPS6055931B2 (en) 1978-08-17 1978-08-17 colored insulated wire

Country Status (1)

Country Link
JP (1) JPS6055931B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS582041A (en) * 1981-06-26 1983-01-07 Fujitsu Ltd Semiconductor device
JP2017130369A (en) * 2016-01-21 2017-07-27 矢崎総業株式会社 Wire and wire harness using the same

Also Published As

Publication number Publication date
JPS5528218A (en) 1980-02-28

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