JP3267327B2 - Solderable insulated wire - Google Patents

Solderable insulated wire

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Publication number
JP3267327B2
JP3267327B2 JP11538392A JP11538392A JP3267327B2 JP 3267327 B2 JP3267327 B2 JP 3267327B2 JP 11538392 A JP11538392 A JP 11538392A JP 11538392 A JP11538392 A JP 11538392A JP 3267327 B2 JP3267327 B2 JP 3267327B2
Authority
JP
Japan
Prior art keywords
insulated wire
weight
parts
monomer
conductor
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 - Fee Related
Application number
JP11538392A
Other languages
Japanese (ja)
Other versions
JPH05290638A (en
Inventor
善久 加藤
美由樹 菅
英行 菊池
紀雄 高畑
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
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Filing date
Publication date
Application filed by Hitachi Cable Ltd filed Critical Hitachi Cable Ltd
Priority to JP11538392A priority Critical patent/JP3267327B2/en
Publication of JPH05290638A publication Critical patent/JPH05290638A/en
Application granted granted Critical
Publication of JP3267327B2 publication Critical patent/JP3267327B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は半田付け性絶縁電線に関
し、特に、絶縁被覆の材料として紫外線架橋樹脂組成物
を用いた半田付け性絶縁電線に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a solderable insulated wire, and more particularly to a solderable insulated wire using a UV-crosslinked resin composition as a material for insulating coating.

【0002】[0002]

【従来の技術】薄い皮膜の電線を得る手段として、液状
材料を塗布硬化させる方法がよく知られており、この代
表的な例としてエナメル線があげられる。
2. Description of the Related Art As a means for obtaining a thin-film electric wire, a method of applying and curing a liquid material is well known, and a typical example thereof is an enameled wire.

【0003】液状材料としては、熱硬化型,紫外線硬化
型,電子線硬化型などがあり、エナメル線の多くは熱硬
化型の材料(熱硬化型ワニス)が使用されている。熱硬
化型ワニスには、エポキシ系,シリコーン系,ポリウレ
タン系,ポリエステル系,ポリアミイドイミド系,ポリ
イミド系,ポリエステルイミド系,ホルマール系などが
ある。これらの中でウレタン系の熱硬化型ワニスを用い
たエナメル線は、他のエナメルにない特徴として、被膜
を剥さず、更にフラックスを使用しないでそのまま半田
付ができることが知られている。
As the liquid material, there are a thermosetting type, an ultraviolet curing type, an electron beam curing type, and the like. Most of the enamel wires are made of a thermosetting material (thermosetting varnish). The thermosetting varnish includes epoxy, silicone, polyurethane, polyester, polyamidimide, polyimide, polyesterimide, and formal. Among these, it is known that an enameled wire using a urethane-based thermosetting varnish can be soldered as it is without peeling off a coating and without using a flux, as a feature not found in other enamels.

【0004】近年、コンピュータ,オーディオ,自動
車,航空機をはじめ人工衛星などの小型化,軽量化に伴
いそれらに用いられる電線・ケーブルも細径・薄肉化が
一層進められるようになってきている。その一つの方法
として被膜の薄肉化がある。押出方式による薄肉化は被
膜が薄くなればなるほど被覆材料と導体との温度差によ
り生じる歪が影響し易く伸びの低下を引き起こす原因と
なり易い。このため、導体に予熱を施すことが行われる
が、導体が細くなると予熱の熱により強度が低下し、更
に、押出時の材料圧力によって断線することがあり好ま
しくない。
In recent years, with the miniaturization and weight reduction of computers, audios, automobiles, aircraft, artificial satellites, and the like, wires and cables used for them have been further reduced in diameter and thickness. One method is to reduce the thickness of the coating. In the thinning by the extrusion method, the thinner the coating, the more easily the strain caused by the temperature difference between the coating material and the conductor is apt to affect, and it is likely to cause a decrease in elongation. For this reason, the conductor is preheated. However, if the conductor becomes thinner, the strength decreases due to the heat of preheating, and furthermore, the wire may be disconnected due to the material pressure at the time of extrusion, which is not preferable.

【0005】そこで、被膜厚を薄くできる熱硬化型の材
料を電線の被覆材料として使用できれば非常に有効とな
ることが考えられるが、これらは塗布焼付工程を通常5
回以上繰り返して行う必要があること、多くのものが5
0%以上有機溶剤が占める材料のため大掛かりな安全設
備が必要なこと、焼付けによるためポリエチレンやポリ
塩化ビニルなどのように被覆が容易でないこと、更に、
皮剥性に劣るなど電子機器などの配線用電線,或いはケ
ーブルの被覆には好ましくない。
Therefore, it would be very effective if a thermosetting material capable of reducing the film thickness could be used as a covering material for electric wires.
Need to be repeated more than once, many are 5
Excessive safety equipment is required due to the material occupied by 0% or more of the organic solvent, and coating is not as easy as polyethylene and polyvinyl chloride due to baking.
It is not preferable for coating of wiring wires or cables of electronic equipment and the like because of poor peelability.

【0006】現在、この薄肉被覆の手段として注目され
ているのが無溶剤で液状の紫外線架橋樹脂組成物であ
り、光ファイバの被覆材として利用され、ウレタンアク
リレート系,シリコーンアクリレート系,フッ素アクリ
レート系などの材料が使用されている。これらの紫外線
架橋樹脂組成物は、紫外線を利用したラジカル重合,イ
オン重合,カチオン重合など(主としてラジカル重合)
により硬化させられ、液状であることから薄肉被覆が容
易で硬化速度が早く生産性が高いという利点を有してい
る。また、熱硬化性ワニスに比べ安全性が高く、任意の
膜厚を得るのに1回ないし数回の塗布により得ることが
でき、更に、無色透明な樹脂組成物とすることで熱硬化
性ワニス比べ着色が容易である利点も有している。
[0006] At present, attention has been paid to a solvent-free, liquid ultraviolet-crosslinking resin composition which is used as a coating material for optical fibers, and is used as a coating material for an optical fiber, such as urethane acrylate, silicone acrylate, and fluorine acrylate. Such materials are used. These UV-crosslinkable resin compositions are used for radical polymerization, ionic polymerization, cationic polymerization, etc. utilizing ultraviolet rays (mainly radical polymerization).
It has the advantage that it is easy to thin coat because it is liquid and the curing speed is high and the productivity is high. In addition, it is higher in safety than thermosetting varnish, and can be obtained by one or several coatings to obtain an arbitrary film thickness. It also has the advantage that coloring is easier.

【0007】[0007]

【発明が解決しようとする課題】しかし、従来の絶縁電
線によると、被覆材料である紫外線架橋樹脂組成物の半
田付け温度が極めて高いため、導体の細いものにあって
は熱によって断線が生じたり、高温によって基材へ熱の
影響を及ぼすという不都合がある。また、導体上に樹脂
のかす(炭化物)が残り易く、適性な半田付性が得られ
ないか,或いは全く半田が付かないという問題がある。
However, according to the conventional insulated wire, since the soldering temperature of the ultraviolet-crosslinking resin composition as the coating material is extremely high, a thin conductor may be broken by heat. In addition, there is a disadvantage that the high temperature causes heat to be exerted on the substrate. In addition, there is a problem that resin residue (carbide) is easily left on the conductor, so that proper solderability is not obtained or no solder is attached.

【0008】従って、本発明の目的は半田付け温度の低
温化が図れると共に、導体上に樹脂の炭化物が残ること
がない半田付け性絶縁電線を提供することである。
It is therefore an object of the present invention together with the attained low temperature of soldering temperature is to provide a soldering insulated wire never carbides of the resin remains on the conductor.

【0009】[0009]

【課題を解決するための手段】本発明は上記問題点に鑑
み、半田付け温度の低温化が図れると共に、導体上に樹
脂の炭化物が残ることがないようにするため、光重合性
モノマとして官能基がメタクロイル基でなるモノマのみ
を使用し、当該モノマを樹脂組成物中に15wt%〜7
0wt%含有した紫外線架橋樹脂組成物を、導体の外周
に絶縁被覆として施した半田付け性絶縁電線を提供する
ものである。
SUMMARY OF THE INVENTION In view of the above problems, the present invention provides a functionalized photopolymerizable monomer to reduce the soldering temperature and to prevent the resin carbide from remaining on the conductor. Only a monomer whose group is a methacroyl group is used, and the monomer is contained in the resin composition in an amount of 15 wt% to 7 wt%.
An object of the present invention is to provide a solderable insulated wire in which a UV-crosslinked resin composition containing 0 wt% is applied as an insulating coating on the outer periphery of a conductor.

【0010】上記紫外線架橋樹脂組成物は、基本的に光
重合性オリゴマ,光重合性モノマ,光開始剤などからな
る。光重合性オリゴマとして、エポキシアクリレート
系,エポキシ化油アクリレート系,ウレタンアクリレー
ト系,ポリエステルウレタンアクリレート系,ポリエー
テルウレタンアクリレート系,不飽和ポリエステル系,
ポリエステルアクリレート系,ポリエーテルアクリレー
ト系,ビニル/アクリレート系,ポリエン/チオール
系,シリコーンアクリレート系,ポリブタジエンアクリ
レート系,ポリスチルエチルアクリレート系,ポリカー
ボネートジアクリレート系などや、これらのフッ素化
物,また、不飽和二重結合をもつアクリロイル基(CH
2 =CHCOO−)やメタクロイル基(CH2 =C(C
3 )CO−),アリル基(CH2 =CHCH2 −),
ビニル基(CH2 =CH−)などの官能基を2個以上有
しているもの、更には、これらを複数組み合わせたもの
が好ましい。最も望ましいものはウレタン系のアクリレ
ートオリゴマで、特に、官能基がメタクロイル基のもの
が良い。
[0010] The ultraviolet crosslinked resin composition basically comprises a photopolymerizable oligomer, a photopolymerizable monomer, a photoinitiator and the like. Photopolymerizable oligomers include epoxy acrylates, epoxidized oil acrylates, urethane acrylates, polyester urethane acrylates, polyether urethane acrylates, unsaturated polyesters,
Polyester acrylates, polyether acrylates, vinyl / acrylates, polyenes / thiols, silicone acrylates, polybutadiene acrylates, polystilethyl acrylates, polycarbonate diacrylates, etc. An acryloyl group having a heavy bond (CH
2 CHCHCOO-) or a methacryloyl group (CH 2 CC (C
H 3) CO-), an allyl group (CH 2 = CHCH 2 -) ,
A compound having two or more functional groups such as a vinyl group (CH 2 CHCH—), and a combination of a plurality of such compounds are preferable. Most preferred are urethane-based acrylate oligomers, particularly those whose functional groups are methacryloyl groups.

【0011】光重合性モノマとしては、官能基がメタク
ロイル基でなるモノマのみを使用する必要がある。官能
基がメタクロイル基でなるモノマの紫外線架橋樹脂組成
物中における含有割合は15wt%〜70wt%の範囲
である。15wt%より少ないと半田付性が著しく低下
し、70wt%より多くなるとオリゴマの特性が阻害さ
れるほか硬化性、機械特性、材料粘度等の特性バランス
をとることが困難となる。更に、1分子当りのモノマの
官能基数は少ない方が良く、単官能であると極めて優れ
た半田付性を提供することができる。
As the photopolymerizable monomer, it is necessary to use only a monomer whose functional group is a methacryloyl group. The content ratio of the monomer having a functional group of a methacryloyl group in the ultraviolet crosslinked resin composition is in a range of 15 wt% to 70 wt% . If the amount is less than 15% by weight, the solderability is remarkably reduced. If the amount is more than 70% by weight, the properties of the oligomer are impaired, and it is difficult to balance properties such as curability, mechanical properties and material viscosity. Further, it is better that the number of functional groups of the monomer per molecule is small, and if it is monofunctional, extremely excellent solderability can be provided.

【0012】光開始剤は特に限定するものではなく、例
えば、アセトフェノン系,ベンゾイン系,ベンゾヘェノ
ン系,チオキサンソン系等といった公知の光開始剤を用
いることができる。アセトフェノン系としては2−ヒド
ロキシ−2−メチル−1−フェニルプロパン−1−オ
ン,1−ヒドロキシシクロヘキシルフェニルケトン,2
−メチル−1−〔4−(メチルチオ)フェニル〕−2−
モルホリプロパン等があり、ベンゾフェノン系としては
ベンゾイン,ベンゾインメチルエーテル,ベンゾインイ
ソプロピルエーテル,ベンゾインイソブチルエーテル,
2,2−ジメトキシ−2−フェニルアセトフェノン等が
ある。また、ベンゾフェノン系としてはベンゾフェノ
ン,ベンゾイル安息香酸メチル,3,3’−ジメチル−
4−メトキシベンゾフェノン等があり、チオキサンソン
系としては2.4−ジエチルチオキサンソン,2.4−
ジクロロチオキサンソン等が挙げられる。
The photoinitiator is not particularly limited. For example, known photoinitiators such as acetophenone, benzoin, benzophenone, and thioxanthone can be used. As acetophenones, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexylphenyl ketone, 2
-Methyl-1- [4- (methylthio) phenyl] -2-
Morphopropane and the like, and benzophenones include benzoin, benzoin methyl ether, benzoin isopropyl ether, benzoin isobutyl ether,
2,2-dimethoxy-2-phenylacetophenone and the like. Benzophenones include benzophenone, methyl benzoylbenzoate, 3,3'-dimethyl-
4-methoxybenzophenone and the like, and thioxanthone-based compounds such as 2.4-diethylthioxanthone and 2.4-
And dichlorothioxanthone.

【0013】このような紫外線架橋樹脂組成物は、この
他に必要に応じて光開始助剤,接着防止剤,チクソ付与
剤,充填剤,可塑剤,非反応性ポリマー,着色剤,難燃
剤,難燃助剤,軟化防止剤,離型剤,乾燥剤,分散剤,
潤滑剤,沈澱防止剤,増粘剤,帯電防止剤,静電防止
剤,防かび剤,防鼠剤,防蟻剤,艶消し剤,ブロッキン
グ防止剤,皮張り防止剤等,その他諸々の無機化合物,
有機化合物を組み合わせて用いることができる。
Such an ultraviolet-crosslinkable resin composition may further contain, if necessary, a photoinitiator, an antiadhesive, a thixotrope, a filler, a plasticizer, a non-reactive polymer, a colorant, a flame retardant, Flame retardant aid, softening inhibitor, release agent, desiccant, dispersant,
Lubricants, anti-settling agents, thickeners, anti-static agents, anti-static agents, fungicides, rodents, termites, matting agents, anti-blocking agents, anti-skinning agents, etc. Compound,
Organic compounds can be used in combination.

【0014】[0014]

【実施例】図1より図4には、本発明の適用対象となる
絶縁電線の断面構造が示されている。図1における絶縁
電線は、導体1と、その外周に施された絶縁被覆2より
構成され、図2における絶縁電線は、撚り合わされた複
数の導体1と、その外周に施された絶縁被覆2より構成
され、図3における絶縁電線は、複数の導体1と、当該
複数の導体1を個々に被覆する絶縁被覆2と、これらの
を被覆するシース3より構成され、図4における絶縁電
線は複数の導体1を撚り合わせて成る複数の撚り合わせ
線心と、当該撚り合わせ線心を個々に被覆する絶縁被覆
2と、これらを被覆するシース3より構成されている。
1 to 4 show a cross-sectional structure of an insulated wire to which the present invention is applied. The insulated wire in FIG. 1 is composed of a conductor 1 and an insulating coating 2 provided on the outer periphery thereof, and the insulated wire in FIG. 2 is constituted by a plurality of twisted conductors 1 and an insulating coating 2 provided on the outer periphery thereof. The insulated wire in FIG. 3 is composed of a plurality of conductors 1, an insulating coating 2 that individually covers the plurality of conductors 1, and a sheath 3 that covers them. The insulated wire in FIG. It comprises a plurality of twisted cores formed by twisting conductors 1, an insulating coating 2 for individually covering the twisted cores, and a sheath 3 for coating these.

【0015】このような絶縁電線において、本発明は絶
縁被覆2として光重合性オリゴマ光重合性モノマ
開始剤からなる紫外線架橋樹脂組成物を使用している。
光重合性モノマとして、官能基がメタクロイル基でなる
モノマが使用される
In such an insulated wire, the present invention uses, as the insulating coating 2, an ultraviolet-crosslinked resin composition comprising a photopolymerizable oligomer , a photopolymerizable monomer , and a photoinitiator.
As the photopolymerizable monomer, <br/> monomer functional group is at methacryloyl group is used.

【0016】以下、本発明の絶縁電線の実施例を詳細に
説明する。表1に示す配合の組成物を用い、以下に示す
9種類(実施例1〜7、及び比較例1、2)の絶縁電線
を得た。
Hereinafter, embodiments of the insulated wire of the present invention will be described in detail. Using the compositions having the formulations shown in Table 1, nine types of insulated wires (Examples 1 to 7 and Comparative Examples 1 and 2) shown below were obtained.

【表1】 [Table 1]

【0017】[0017]

【実施例1】ウレタンアクリレートオリゴマU−122
A(新中村化学製)100重量部,ジシクロペンタニル
メタクリレート100重量部,及び光開始剤の2,2−
ジメトキシ−2−フェニルアセトフェノン12.5重量
部より成る紫外線架橋樹脂組成物を裸軟銅線導体0.1
3(1/0.13)上に被覆した後、紫外線照射炉を通
して硬化させ、絶縁厚15μmの絶縁電線を得た。
Example 1 Urethane acrylate oligomer U-122
A (manufactured by Shin-Nakamura Chemical), 100 parts by weight of dicyclopentanyl methacrylate, and 2,2-photoinitiator
An ultraviolet-crosslinkable resin composition comprising 12.5 parts by weight of dimethoxy-2-phenylacetophenone was coated with a bare soft copper wire conductor 0.1.
3 (1 / 0.13) and cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 15 μm.

【0018】[0018]

【実施例2】ウレタンアクリレートオリゴマU−122
A100重量部,ジシクロペンタニルメタクリレート2
00重量部,及び光開始剤の2,2−ジメトキシ−2−
フェニルアセトフェノン15重量部より成る紫外線架橋
樹脂組成物を、裸軟銅線導体0.13(1/0.13)
上に被覆した後、紫外線照射炉を通して硬化させ、絶縁
厚16μmの絶縁電線を得た。
Example 2 Urethane acrylate oligomer U-122
A100 parts by weight, dicyclopentanyl methacrylate 2
00 parts by weight and the photoinitiator 2,2-dimethoxy-2-
An ultraviolet-curable resin composition comprising 15 parts by weight of phenylacetophenone was coated with bare soft copper wire conductor 0.13 (1 / 0.13).
After coating on the top, it was cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 16 μm.

【0019】[0019]

【実施例3】ウレタンアクリレートオリゴマU−122
A(新中村化学製)100重量部,ジシクロペンタニル
メタクリレート100重量部,及び光開始剤の2,2−
ジメトキシ−2−フェニルアセトフェノン12.5重量
部より成る紫外線架橋樹脂組成物を裸軟銅線導体0.1
3(1/0.13)上に被覆した後、紫外線照射炉を通
して硬化させ、絶縁厚16μmの絶縁電線を得た。
Example 3 Urethane acrylate oligomer U-122
A (manufactured by Shin-Nakamura Chemical), 100 parts by weight of dicyclopentanyl methacrylate, and 2,2-photoinitiator
An ultraviolet-crosslinkable resin composition comprising 12.5 parts by weight of dimethoxy-2-phenylacetophenone was coated with a bare soft copper wire conductor 0.1.
3 (1 / 0.13), and then cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 16 μm.

【0020】[0020]

【実施例4】ウレタンメタクリレートオリゴマU−12
2M(新中村化学製)100重量部,ジシクロペンタチ
ルメタクリレート25重量部,及び光開始剤の2,2−
ジメトキシ−2−フェニルアセトフェノン5重量部より
成る紫外線架橋樹脂組成物を裸軟銅線導体0.13(1
/0.13)上に被覆した後、紫外線照射炉を通して硬
化させ、絶縁厚16μmの絶縁電線を得た。
Example 4 Urethane methacrylate oligomer U-12
100 parts by weight of 2M (manufactured by Shin-Nakamura Chemical Co., Ltd.), 25 parts by weight of dicyclopentatyl methacrylate, and 2,2-
An ultraviolet-crosslinked resin composition comprising 5 parts by weight of dimethoxy-2-phenylacetophenone was added to a bare soft copper wire conductor 0.13 (1
/0.13), and then cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 16 μm.

【0021】[0021]

【実施例5】ウレタンアクリレートオリゴマU−122
A100重量部,ジシクロペンタニルメタクリレート8
0重量部,1,6−ヘキサジオールジメタクリレート
(新中村化学製)20重量部,及び光開始剤の2,2−
ジメトキシ−2−フェニルアセトフェノン12.5重量
部より成る紫外線架橋樹脂組成物を裸軟銅線導体0.1
3(1/0.13)上に被覆した後、紫外線照射炉を通
して硬化させ、絶縁厚15μmの絶縁電線を得た。
Example 5 Urethane acrylate oligomer U-122
A100 parts by weight, dicyclopentanyl methacrylate 8
0 parts by weight, 20 parts by weight of 1,6-hexadiol dimethacrylate (manufactured by Shin-Nakamura Chemical), and 2,2-
An ultraviolet-crosslinkable resin composition comprising 12.5 parts by weight of dimethoxy-2-phenylacetophenone was coated with a bare soft copper wire conductor 0.1.
3 (1 / 0.13) and cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 15 μm.

【0022】[0022]

【実施例6】ウレタンアクリレートオリゴマU−122
A100重量部,ジシクロペンタニルメタクリレート8
0重量部,トリメチロールプロパントリメタクリレート
(新中村化学製)20重量部,及び光開始剤の2,2−
ジメトキシ−2−フェニルアセトフェノン12.5重量
部より成る紫外線架橋樹脂組成物を裸軟銅線導体0.1
3(1/0.13)上に被覆した後、紫外線照射炉を通
して硬化させ、絶縁厚15μmの絶縁電線を得た。
Example 6 Urethane acrylate oligomer U-122
A100 parts by weight, dicyclopentanyl methacrylate 8
0 parts by weight, 20 parts by weight of trimethylolpropane trimethacrylate (manufactured by Shin-Nakamura Chemical Co., Ltd.), and 2,2-
An ultraviolet-crosslinkable resin composition comprising 12.5 parts by weight of dimethoxy-2-phenylacetophenone was coated with a bare soft copper wire conductor 0.1.
3 (1 / 0.13) and cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 15 μm.

【0023】[0023]

【実施例7】ウレタンアクリレートオリゴマU−122
A100重量部,ポリエチレングリコール90メタクリ
レート100重量部,及び光開始剤の2,2−ジメトキ
シ−2−フェニルアセトフェノン12.5重量部より成
る紫外線架橋樹脂組成物を裸軟銅線導体0.13(1/
0.13)上に被覆した後、紫外線照射炉を通して硬化
させ、絶縁厚15μmの絶縁電線を得た。
Example 7 Urethane acrylate oligomer U-122
A 100 parts by weight of A, 100 parts by weight of polyethylene glycol 90 methacrylate, and 12.5 parts by weight of a photoinitiator 2,2-dimethoxy-2-phenylacetophenone were mixed with a bare soft copper wire conductor 0.13 (1/1).
0.13) After coating on the top, it was cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 15 μm.

【0024】[0024]

【比較例1】ウレタンアクリレートオリゴマU−122
A100重量部,ジシクロペンタニルアクリレート(日
立化成製)50重量部,及び光開始剤の2,2−ジメト
キシ−2−フェニルアセトフェノン7.5重量部から成
る紫外線架橋樹脂組成物を裸軟銅線導体0.13(1/
0.13)上に被覆した後、紫外線照射炉を通して硬化
させ、絶縁厚15μmの絶縁電線を得た。
Comparative Example 1 Urethane acrylate oligomer U-122
A 100 parts by weight of A, 50 parts by weight of dicyclopentanyl acrylate (manufactured by Hitachi Chemical), and 7.5 parts by weight of 2,2-dimethoxy-2-phenylacetophenone as a photoinitiator were exposed to a bare soft copper wire conductor. 0.13 (1 /
0.13) After coating on the top, it was cured through an ultraviolet irradiation furnace to obtain an insulated wire having an insulation thickness of 15 μm.

【0025】[0025]

【比較例2】ウレタンアクリレートオリゴマU−122
A100重量部,ジシクロペンタニルメタクリレート5
0重量部,ジシクロペンタニルアクリレート50重量
部,及び光開始剤の2,2−ジメトキシ−2−フェニル
アセトフェノン10重量部から成る紫外線架橋樹脂組成
物を裸軟銅線導体0.13(1/0.13)上に被覆し
た後、紫外線照射炉を通して硬化させ、絶縁厚14μm
の絶縁電線を得た。
Comparative Example 2 Urethane acrylate oligomer U-122
A100 parts by weight, dicyclopentanyl methacrylate 5
0 parts by weight, 50 parts by weight of dicyclopentanyl acrylate, and 10 parts by weight of 2,2-dimethoxy-2-phenylacetophenone as a photoinitiator were mixed with a bare soft copper wire conductor 0.13 (1/0). .13) After coating on top, it was cured by passing through an ultraviolet irradiation furnace, and the insulation thickness was 14 μm.
Insulated wire was obtained.

【0026】次に、実施例1〜7の絶縁電線と比較例
1,2の絶縁電線に対し、半田付性,20%伸長,破壊
電圧といった電線特性の評価を行った。
Next, the insulated wires of Examples 1 to 7 and the insulated wires of Comparative Examples 1 and 2 were evaluated for wire characteristics such as solderability, 20% elongation, and breakdown voltage.

【0027】表1から明らかなように、メタクロイル基
を15%以上含有した実施例1〜7の絶縁電線はいずれ
も半田付性が良好で、且つ20%伸長,破壊電圧も良好
な値を示している。また、実施例1と実施例3では、実
施例3の方が360℃と半田付性が良好となっており、
オリゴマの官能基をメタクロイル基にするとより良好な
半田付性が得られることが判る。更に、実施例1,5,
6から、使用するモノマは多官能モノマより単官能モノ
マ単独の方が低温での半田付性が優れていることが判
る。一方、比較例1,2の絶縁電線は官能基がアクリロ
イル基のモノマを用いているため、半田が付かない等、
半田付性が低いものであった。
As is clear from Table 1, the insulated wires of Examples 1 to 7 containing 15% or more of the methacryloyl group have good solderability, 20% elongation, and good values of breakdown voltage. ing. Moreover, in Example 1 and Example 3, Example 3 has better solderability at 360 ° C.
It can be seen that better solderability can be obtained when the functional group of the oligomer is a methacryloyl group. Further, Examples 1, 5,
6, it can be seen that the monofunctional monomer alone has better solderability at low temperature than the polyfunctional monomer. On the other hand, the insulated wires of Comparative Examples 1 and 2 use a monomer of an acryloyl group as a functional group, so that no solder is attached.
The solderability was low.

【0028】[0028]

【発明の効果】以上説明した通り、本発明の半田付け性
絶縁電線によると、官能基がメタクロイル基であるモノ
マを15wt%以上含有した紫外線架橋樹脂組成物を、
導体の外周に絶縁被覆として施したため、半田付け温度
の低温化が図れると共に、導体上に樹脂の炭化物を残ら
ないようにすることができる。
As described in the foregoing, according to the solderability <br/> insulated wire of the present invention, an ultraviolet crosslinked resin composition a functional group containing more than 15 wt% of the monomer is methacryloyl group,
Since the insulating coating is provided on the outer periphery of the conductor, the soldering temperature can be reduced, and the resin carbide can be prevented from remaining on the conductor.

【図面の簡単な説明】[Brief description of the drawings]

【図1】絶縁電線の構成を示す断面図。FIG. 1 is a sectional view showing a configuration of an insulated wire.

【図2】絶縁電線の構成を示す断面図。FIG. 2 is a sectional view showing a configuration of an insulated wire.

【図3】絶縁電線の構成を示す断面図。FIG. 3 is a sectional view showing a configuration of an insulated wire.

【図4】絶縁電線の構成を示す断面図。FIG. 4 is a sectional view showing a configuration of an insulated wire.

【符号の説明】[Explanation of symbols]

1 導体 2 絶縁
被覆 3 シース
DESCRIPTION OF SYMBOLS 1 Conductor 2 Insulation coating 3 Sheath

───────────────────────────────────────────────────── フロントページの続き (72)発明者 高畑 紀雄 茨城県日立市日高町5丁目1番1号 日 立電線株式会社パワーシステム研究所内 (56)参考文献 特開 平1−97306(JP,A) (58)調査した分野(Int.Cl.7,DB名) H01B 7/02 C09D 5/25 H01B 3/22 ──────────────────────────────────────────────────続 き Continuation of the front page (72) Inventor Norio Takahata 5-1-1 Hidaka-cho, Hitachi City, Ibaraki Prefecture Power System Research Laboratories, Hitachi, Ltd. (56) References JP-A-1-97306 (JP, A) (58) Field surveyed (Int. Cl. 7 , DB name) H01B 7/02 C09D 5/25 H01B 3/22

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 導体の外周に絶縁被覆を施して成る絶縁
電線において、前記絶縁被覆は、光重合性オリゴマ、光
重合性モノマ、光開始剤を含有する紫外線架橋樹脂組成
物より成り、前記光重合性モノマとして官能基がメタク
ロイル基でなるモノマのみを使用し、当該モノマの前記
紫外線架橋樹脂組成物中における含有割合は15wt%
〜70wt%であることを特徴とする半田付け性絶縁電
線。
1. An insulated wire in which an insulating coating is applied to the outer periphery of a conductor, wherein the insulating coating is made of a UV-crosslinked resin composition containing a photopolymerizable oligomer, a photopolymerizable monomer, and a photoinitiator. As the polymerizable monomer, only a monomer whose functional group is a methacryloyl group is used, and the content ratio of the monomer in the ultraviolet-crosslinked resin composition is 15 wt%.
A solderable insulated wire characterized in that the content is up to 70 wt% .
【請求項2】 前記モノマは単官能である請求項1記載
の半田付け性絶縁電線。
2. The solderable insulated wire according to claim 1, wherein the monomer is monofunctional.
JP11538392A 1992-04-08 1992-04-08 Solderable insulated wire Expired - Fee Related JP3267327B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11538392A JP3267327B2 (en) 1992-04-08 1992-04-08 Solderable insulated wire

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11538392A JP3267327B2 (en) 1992-04-08 1992-04-08 Solderable insulated wire

Publications (2)

Publication Number Publication Date
JPH05290638A JPH05290638A (en) 1993-11-05
JP3267327B2 true JP3267327B2 (en) 2002-03-18

Family

ID=14661181

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11538392A Expired - Fee Related JP3267327B2 (en) 1992-04-08 1992-04-08 Solderable insulated wire

Country Status (1)

Country Link
JP (1) JP3267327B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5012235B2 (en) * 2007-06-11 2012-08-29 日立化成工業株式会社 Photo-curable moisture-proof insulating coating, electronic component moisture-proof insulated using this photo-curable moisture-proof insulating coating, and manufacturing method thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0197306A (en) * 1987-10-08 1989-04-14 Sumitomo Electric Ind Ltd Insulated electric wire

Also Published As

Publication number Publication date
JPH05290638A (en) 1993-11-05

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