JPH04245110A - Self-fusible insulative electric wire and coil using the same - Google Patents

Self-fusible insulative electric wire and coil using the same

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Publication number
JPH04245110A
JPH04245110A JP3009768A JP976891A JPH04245110A JP H04245110 A JPH04245110 A JP H04245110A JP 3009768 A JP3009768 A JP 3009768A JP 976891 A JP976891 A JP 976891A JP H04245110 A JPH04245110 A JP H04245110A
Authority
JP
Japan
Prior art keywords
layer
foaming agent
foaming
fusible
resin
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.)
Granted
Application number
JP3009768A
Other languages
Japanese (ja)
Other versions
JP3151836B2 (en
Inventor
Hironori Matsuura
裕紀 松浦
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.)
Sumitomo Electric Industries Ltd
Original Assignee
Sumitomo Electric Industries 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 Sumitomo Electric Industries Ltd filed Critical Sumitomo Electric Industries Ltd
Priority to JP00976891A priority Critical patent/JP3151836B2/en
Publication of JPH04245110A publication Critical patent/JPH04245110A/en
Application granted granted Critical
Publication of JP3151836B2 publication Critical patent/JP3151836B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To provide a thin fusible layer which is foamed at a predetermined low temperature and enhanced in fusing strength and space factor by forming the fusible layer including a foaming agent and a foaming assistant on the metal conductor via an insulative layer. CONSTITUTION:An insulative layer 2 is formed on a metal conductor 1, and a fusible layer 3 including a foaming agent and a foaming assistant is formed on the layer 2. Such a foaming agent as to be dissolved with application of heat and generate nitrogen gas or carbon dioxide gas is used as the foaming agent to be included, and an azo, nitroso or hydrazide foaming agent is used as an organic foaming agent. A vulcanization accelerator capable of promoting thermal decomposition of the foaming agent, a PVC stabilizer or the like is used as the foaming assistant. Each predetermined quantity of the foaming agent and foaming assistant is dissolved or dispersed in a solution of a fusible resin, thus forming a fusible coating material, which is applied and baked on the layer 2, followed by energization heating or hot-air drying, for foaming the layer 3. Consequently, the fusible layer is foamed at a predetermined low temperature for thinness, thus enhancing fusing strength and a space factor of the conductor.

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、融着性に優れた自己融
着性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 a self-bonding insulated wire with excellent melting properties.

【0002】0002

【従来の技術】自己融着性絶縁電線は、コイル作成時含
浸ワニスを使用することなく電線間の固着が可能なため
、作業工程が短縮されるという利点を有している。しか
しながら、自己融着性絶縁電線の使用は、増加しつつあ
るものの以下の二つの問題があるので使用される用途が
限定され未だほんの一部にとどまっている。
2. Description of the Related Art Self-bonding insulated wires have the advantage of shortening the work process because wires can be bonded together without the use of impregnated varnish when making a coil. However, although the use of self-bonding insulated wires is increasing, the following two problems have limited the applications in which they can be used, and only a few of them are still used.

【0003】まず第一に、自己融着性絶縁電線の最も重
要な特性である融着力が不十分である。特に融着時の流
動性に乏しいブチラール樹脂及びフェノキシ樹脂は融着
力の不足が大きく、また、流動性に優れるポリアミド樹
脂においても融着力が十分とは言えないという問題点が
あった。さらに、自己融着性絶縁電線をコイル状にした
場合、コイルの形状によっては線間密度の小さな部分が
発生して電線どうしの接着が少なくなり融着力が不足す
るという問題もあった。
First of all, the most important characteristic of self-bonding insulated wires, the fusing strength, is insufficient. In particular, butyral resins and phenoxy resins, which have poor fluidity during fusion bonding, have a significant lack of fusion bonding strength, and even polyamide resins, which have excellent fluidity, have a problem in that their fusion bonding strength is not sufficient. Further, when the self-bonding insulated wire is formed into a coil, there is a problem in that depending on the shape of the coil, there may be portions with low inter-wire density, resulting in less adhesion between the wires and insufficient fusing force.

【0004】第二の問題点は、融着層の膜厚が厚いため
、モーターのコアに占める電線の断面積の割合を表わす
占積率が小さいという点である。近年、機器の小型化に
伴い、コイル、モーターも小型になり小さなスペースに
より多くの絶縁電線を詰めこみ電線の占積率の向上が望
まれている。従って融着層の膜厚は、融着力を損なわな
い限りできるだけ薄い方が占積率の向上につながり好ま
しい。しかしながら現在用いられている融着層の膜厚は
絶縁層の1/2〜1/3ほど有り非常に厚く占積率が向
上できないという問題があった。
The second problem is that because the adhesive layer is thick, the space factor, which represents the ratio of the cross-sectional area of the electric wire to the core of the motor, is small. In recent years, with the miniaturization of equipment, coils and motors have also become smaller, and it is desired to pack more insulated wires into a small space and improve the space factor of the wires. Therefore, it is preferable that the thickness of the fusion layer be as thin as possible without impairing the fusion bonding strength, as this will improve the space factor. However, the thickness of the currently used fusion layer is approximately 1/2 to 1/3 that of the insulating layer, which is very thick, and there is a problem in that the space factor cannot be improved.

【0005】[0005]

【発明が解決しようとする課題】これらの問題点に対し
て融着層が融着時発泡する自己融着性絶縁電線が提案さ
れた。この自己融着性絶縁電線を使用すると、融着層が
発泡し融着層皮膜厚が2〜3倍になることから、樹脂の
流れ性が改善され融着力が向上する。また融着層の薄膜
化が可能となり占積率が向上する。しかしながら、通電
加熱による融着の場合は、融着層の発泡が発生するが、
150℃前後での熱風乾燥による融着の場合融着層の発
泡が不十分という問題点が新たに生じた。
SUMMARY OF THE INVENTION To address these problems, a self-bonding insulated wire in which the bonding layer foams during bonding has been proposed. When this self-bonding insulated wire is used, the welding layer foams and the thickness of the welding layer increases by two to three times, thereby improving the flowability of the resin and increasing the welding strength. Furthermore, the fusion layer can be made thinner, and the space factor can be improved. However, in the case of fusion bonding by electrical heating, foaming of the fusion layer occurs;
In the case of fusing by hot air drying at around 150°C, a new problem arose that the fusing layer was insufficiently foamed.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上記問題
を解決するために鋭意検討を重ねた結果、発泡剤を含有
する融着層に発泡助剤を添加することにより150℃前
後の低温でも融着層を発泡させることができる自己融着
性絶縁電線を発明した。
[Means for Solving the Problems] As a result of intensive studies in order to solve the above problems, the present inventors have found that by adding a foaming aid to the adhesive layer containing a foaming agent, the temperature at around 150° C. We have invented a self-bonding insulated wire whose adhesive layer can be foamed even at low temperatures.

【0007】即ち、本発明は金属導体上に絶縁層を介し
て発泡剤と発泡助剤を含有する融着層を形成させたこと
を特徴とした自己融着性絶縁電線である。
That is, the present invention is a self-bonding insulated wire characterized in that a melting layer containing a foaming agent and a foaming aid is formed on a metal conductor via an insulating layer.

【0008】以下本発明を詳細に説明する。本発明で用
いる発泡助剤は発泡剤の熱分解を促進するものならいか
なるものでも使用でき例えば、加硫促進剤、充填剤、加
硫促進助剤、PVC用安定剤、老防、加硫剤、尿素化合
物などが挙げられる。
The present invention will be explained in detail below. The foaming aid used in the present invention can be anything that promotes thermal decomposition of the foaming agent, such as vulcanization accelerator, filler, vulcanization accelerator, PVC stabilizer, anti-aging agent, and vulcanizing agent. , urea compounds, etc.

【0009】加硫促進剤ではグアジニン系、アルデヒト
−アンモニア系、スルフェンアミド系、チウラム系、ザ
ンテート系、アルデヒト−アミン系、チアゾール系、チ
オ尿素系、ジチオカルバメート系などが、充填剤では、
シリカ、炭酸マグネシウム、炭酸カルシウム、ケイ酸マ
グネシウム、炭酸アルミニウム、タルク、硫酸バリウム
、硫酸アルミニウム、硫酸カルシウムなどが、加硫促進
助剤では、亜鉛華、活性亜鉛華、炭酸亜鉛、酸化マグネ
シウム、一酸化鉛、塩基性炭酸鉛、水酸化カルシウム、
ステアリン酸、オレイン酸、ラウリン酸、ジエチレング
ルコール、ジ−n−ブチルアミン、ジシクロヘキシルア
ミン、ジエタノールアミン、有機アミンなどが、PVC
用安定剤は三塩基性硫酸鉛、ジブチルすずジラウレート
、ジブチルすずジマレート、ステアリン酸亜鉛、ステア
リン酸カドミウム、ステアリン酸バリウム、ステアリン
酸カルシウムなどが、老防では、ナフチルアミン系、ジ
フェニルアミン系、P−フェニレン系、キノリン系、モ
ノフェノール系、ポリフェノール系、チオビスフェノー
ル系、亜りん酸エステル系などが加硫剤では、タイク、
イオウ安息香酸アンモニウムなどが挙げられる。
Vulcanization accelerators include guanidine, aldehyde-ammonia, sulfenamide, thiuram, xanthate, aldehyde-amine, thiazole, thiourea, and dithiocarbamate, and fillers include:
Silica, magnesium carbonate, calcium carbonate, magnesium silicate, aluminum carbonate, talc, barium sulfate, aluminum sulfate, calcium sulfate, etc. are used as vulcanization accelerators, zinc white, activated zinc white, zinc carbonate, magnesium oxide, monoxide, etc. Lead, basic lead carbonate, calcium hydroxide,
Stearic acid, oleic acid, lauric acid, diethylene glycol, di-n-butylamine, dicyclohexylamine, diethanolamine, organic amines, etc.
Stabilizers include tribasic lead sulfate, dibutyltin dilaurate, dibutyltin dimalate, zinc stearate, cadmium stearate, barium stearate, calcium stearate, etc. Anti-aging stabilizers include naphthylamine type, diphenylamine type, P-phenylene type, Vulcanizing agents include quinoline, monophenol, polyphenol, thiobisphenol, and phosphite esters.
Examples include ammonium sulfur benzoate.

【0010】その他薬品として無水フタル酸、サリチル
酸、安息香酸、三酸化アンチモン、白色ワセリン、酸化
チタン、酸化カドミウム、ホウ砂、グリセリン、ジブチ
ルチンジマレートなどがあげられる。これらの中でも、
亜鉛華、三塩基性硫酸鉛、加硫促進剤などが好ましい。
[0010] Other chemicals include phthalic anhydride, salicylic acid, benzoic acid, antimony trioxide, white petrolatum, titanium oxide, cadmium oxide, borax, glycerin, dibutyltin dimalate, and the like. Among these,
Zinc white, tribasic lead sulfate, vulcanization accelerators and the like are preferred.

【0011】これらの発泡助剤の添加量は、発泡剤に対
し5重量部〜200重量部が好ましく、より好ましくは
50重量部〜150重量部である。発泡助剤の添加量が
少ないと発泡剤を分解させる効果が小さく発泡温度の低
下が少なくなる。逆に発泡助剤の添加量が多いと、絶縁
電線作成時に融着層が発泡する。
The amount of these foaming aids added is preferably from 5 parts by weight to 200 parts by weight, more preferably from 50 parts by weight to 150 parts by weight, based on the foaming agent. If the amount of the foaming aid added is small, the effect of decomposing the foaming agent will be small and the drop in foaming temperature will be small. On the other hand, if the amount of foaming aid added is large, the fusion layer will foam during the production of an insulated wire.

【0012】本発明で用いる発泡剤は、加熱することに
より分解し窒素ガス、炭酸ガス、一酸化炭素、アンモニ
アガス等を発生するものを言い有機発泡剤、無機発泡剤
が使用できる。有機発泡剤としては、例えば、アゾ系で
はアゾジカルボンアミド(A.D.C.A)、アゾビス
イソブチロニトリル(A.I.B.N)、ニトロソ系で
は、ジニトロソペンタメチレンテトラミン(D.P.T
)、N,N’ジニトロソ−N,N’−ジメチルテレフタ
ルアミド(D.N.D.M.T.A)、ヒドラジド系で
は、P−トルエンスルホニルヒドラジド(T.S.H)
、P,P−オキシビスベンゼンスルホニルヒドラジド(
O.B.S.H)、ベンゼンスルホニルヒドラジド(B
.S.H)、その他にトリヒドラジノトリアジン(T.
H.T)、アセトン−P−スルホニルヒドラゾンなどが
あり分解温度、発生ガス量が異なるものが市販されてい
る。これらを単独あるいは、ニ種類以上合わせて融着塗
料へ溶解あるいは分散させて使用できる。
The blowing agent used in the present invention is one that decomposes when heated to generate nitrogen gas, carbon dioxide gas, carbon monoxide, ammonia gas, etc. Organic blowing agents and inorganic blowing agents can be used. Examples of organic blowing agents include azo dicarbonamide (A.D.C.A.) and azobisisobutyronitrile (A.I.B.N.) for azo systems, and dinitrosopentamethylenetetramine (for nitroso systems). D.P.T.
), N,N'dinitroso-N,N'-dimethylterephthalamide (D.N.D.M.T.A), and in the hydrazide series, P-toluenesulfonylhydrazide (T.S.H)
, P,P-oxybisbenzenesulfonyl hydrazide (
O. B. S. H), benzenesulfonyl hydrazide (B
.. S. H), and trihydrazinotriazine (T.
H. T), acetone-P-sulfonylhydrazone, etc., and those having different decomposition temperatures and amounts of gas generated are commercially available. These can be used alone or in combination of two or more types dissolved or dispersed in the adhesive coating.

【0013】一方無機発泡剤としては、重炭酸ナトリウ
ム、炭酸アンモニウム、重炭酸アンモニウム、ホウ化水
素ナトリウム、ソジウムボロンハイドライド、シリコン
オキシハイドライドなどが例示されるが一般的に無機発
泡剤は、ガス発生速度が有機発泡剤より緩慢でありガス
発生の調整が難しいので有機発泡剤が好ましい。
On the other hand, examples of inorganic blowing agents include sodium bicarbonate, ammonium carbonate, ammonium bicarbonate, sodium borohydride, sodium boron hydride, and silicon oxyhydride. Organic blowing agents are preferred because their speed is slower than that of organic blowing agents and gas generation is difficult to control.

【0014】発泡剤の添加量は、融着樹脂に対し0.1
PHR〜50PHRが好ましく、より好ましくは1PH
R〜25PHRである。発泡剤の添加量が少ないと発泡
が見られず、発泡剤の添加量が多いと融着層の機械的強
度が不足する。
[0014] The amount of foaming agent added is 0.1 to the fusion resin.
PHR ~ 50PHR is preferable, more preferably 1PH
R~25PHR. If the amount of foaming agent added is small, no foaming will be observed, and if the amount of foaming agent added is large, the mechanical strength of the adhesive layer will be insufficient.

【0015】本発明で用いる融着樹脂は高温で流動性を
示すものならいかなるものでも使用可能である。例えば
、ブチラール樹脂、フェノキシ樹脂、ポリアミド樹脂そ
して他の熱可塑性樹脂が使用できる。フェノキシ樹脂で
は、ビスフェノールA,ビスフェノールS,ビスフェノ
ールFを主成分としたもの、あるいは、変性フェノキシ
が例示される。ポリアミド樹脂としては各種共重合ポリ
アミド樹脂、6−ナイロン樹脂、6,6−ナイロン樹脂
、6,10−ナイロン樹脂などが、熱可塑性樹脂として
は、共重合ポリエステル樹脂、ポリブチレンテレフタレ
ート樹脂、ポリエチレンテレフタレート樹脂、熱可塑性
ポリウレタン樹脂、ポリカーボネート樹脂、ポリフェニ
レンオキシド樹脂、ポリフェニレンスルフィド樹脂、ポ
リスルホン樹脂、ポリエーテルイミド樹脂、ポリエーテ
ルエーテルケトン樹脂、ポリエーテルケトン樹脂、ポリ
エーテルスルホン樹脂、熱可塑性ポリアミドイミド樹脂
、熱可塑性ポリイミド樹脂などが使用できる。また、上
記樹脂にメラミン樹脂、フェノール樹脂、イソシアネー
トなどを添加することにより架橋させ一部熱硬化タイプ
にすることも可能である。これら上記の樹脂のうちブチ
ラール樹脂、フェノキシ樹脂、共重合ポリアミド樹脂が
融着力、融着温度のバランスがよく現在も融着層に使わ
れており好ましい。さらに本発明では、融着層が発泡し
線間の空隙を埋められるので流動性にやや劣るブチラー
ル樹脂、フェノキシ樹脂の使用は流動性の改善の効果が
大きくより好ましい。
[0015] As the fusion resin used in the present invention, any resin can be used as long as it exhibits fluidity at high temperatures. For example, butyral resins, phenoxy resins, polyamide resins and other thermoplastic resins can be used. Examples of phenoxy resins include those containing bisphenol A, bisphenol S, and bisphenol F as main components, and modified phenoxy resins. Examples of polyamide resins include various copolyamide resins, 6-nylon resins, 6,6-nylon resins, and 6,10-nylon resins, and examples of thermoplastic resins include copolymerized polyester resins, polybutylene terephthalate resins, and polyethylene terephthalate resins. , thermoplastic polyurethane resin, polycarbonate resin, polyphenylene oxide resin, polyphenylene sulfide resin, polysulfone resin, polyetherimide resin, polyetheretherketone resin, polyetherketone resin, polyethersulfone resin, thermoplastic polyamideimide resin, thermoplastic polyimide Resin etc. can be used. Further, by adding melamine resin, phenol resin, isocyanate, etc. to the above resin, it is possible to crosslink it and make it partially thermosetting type. Among these resins mentioned above, butyral resin, phenoxy resin, and copolymerized polyamide resin are preferred because they have a good balance of fusing strength and fusing temperature and are currently used for the fusing layer. Furthermore, in the present invention, the use of butyral resin and phenoxy resin, which have slightly poor fluidity, is more preferable because the adhesive layer is foamed to fill the voids between the wires, as they have a large effect of improving fluidity.

【0016】本発明で用いる融着塗料は、前記融着樹脂
をシクロヘキサノン、キシレン、NM2P,DMAC,
SMF,クレゾール等の溶剤に10%〜50%程度の濃
度に溶解せしめ発泡剤、発泡助剤を所定量溶解あるいは
分散せしめることにより得られる。尚、分散させる場合
ディゾルバー,ボール・ミル、サンド・ミル等で分散さ
せることにより、より均一な塗料が得られる。
[0016] The fusing paint used in the present invention uses the fusing resin as cyclohexanone, xylene, NM2P, DMAC,
It is obtained by dissolving or dispersing a predetermined amount of a foaming agent or foaming aid in a solvent such as SMF or cresol to a concentration of about 10% to 50%. In addition, when dispersing, a more uniform paint can be obtained by dispersing with a dissolver, ball mill, sand mill, etc.

【0017】本発明で用いる絶縁皮膜には、なんら制限
はなく通常使用されるのものであればいかなるものも使
用可能である。例えば、ポリビニールホルマール樹脂、
熱硬化ポリウレタン樹脂、熱硬化アクリル樹脂、エポキ
シ樹脂、熱硬化ポリエステル樹脂、熱硬化ポリエステル
イミド樹脂、熱硬化ポリエステルアミドイミド樹脂、芳
香族ポリアミド樹脂、熱硬化ポリアミドイミド樹脂、熱
硬化ポリイミド樹脂を主成分とするものが使用できる。
The insulating film used in the present invention is not limited in any way, and any commonly used insulating film can be used. For example, polyvinyl formal resin,
The main components are thermosetting polyurethane resin, thermosetting acrylic resin, epoxy resin, thermosetting polyester resin, thermosetting polyesterimide resin, thermosetting polyesteramideimide resin, aromatic polyamide resin, thermosetting polyamideimide resin, and thermosetting polyimide resin. You can use whatever you want.

【0018】これらの絶縁皮膜上に、前述の融着塗料を
発泡剤が分解しない焼き付け条件で塗布焼き付けするこ
とにより、本発明の自己融着性絶縁電線が得られる。
The self-bonding insulated wire of the present invention can be obtained by applying and baking the above-mentioned fusing paint onto these insulating coatings under baking conditions that do not decompose the foaming agent.

【0019】得られた自己融着絶縁電線を所定のコイル
状に捲き、通電加熱あるいは熱風乾燥で融着層が発泡す
る。その際、加熱温度は150℃前後の低温でも発泡が
生じる。
The obtained self-fusing insulated wire is wound into a predetermined coil shape, and the fusing layer is foamed by heating with electricity or drying with hot air. At that time, foaming occurs even when the heating temperature is as low as around 150°C.

【0020】[0020]

【実施例】以下実施例に基ずき本発明を詳細に説明する
EXAMPLES The present invention will be explained in detail based on the following examples.

【0021】〔比較例1〕フェニキシ樹脂(YP−50
:東都化成)をNM2Pに25%になるように溶解しさ
らにA.D.C.AビニホールAC3M(永和化成工業
)を10PHR添加しディゾルバーで混合攪拌し融着塗
料とした。3.0mmφの銅線に周知の方法により炉長
3mの横炉でポリエステルイミドワニス(アイソミッド
40:日触スケネクタディー)を塗布焼き付けし膜厚2
1ミクロンの1種エステルイミド線を作成した。さらに
、前述の融着塗料を炉温250℃で塗布焼き付けし8ミ
クロンの融着層を形成し自己融着性絶縁電線を作成した
。得られた自己融着性絶縁電線からヘリカルコイルを作
成し所定の温度の恒温槽に5分間放置し発泡する温度を
調べた。その結果及び、自己融着性絶縁電線の電線作成
時の外観を表1に示す。
[Comparative Example 1] Phenoxy resin (YP-50
: Toto Kasei) was dissolved in NM2P to a concentration of 25%, and further A. D. C. 10 PHR of A-vinihole AC3M (Eiwa Kasei Kogyo) was added and mixed and stirred with a dissolver to obtain a fusion coating. A polyester imide varnish (Isomid 40: Nippon Schenectady) was coated and baked on a 3.0 mmφ copper wire using a well-known method in a horizontal furnace with a furnace length of 3 m to a film thickness of 2.
A 1 micron type 1 esterimide wire was created. Further, the above-mentioned fusing paint was applied and baked at an oven temperature of 250° C. to form a fusing layer of 8 microns, thereby producing a self-fusing insulated wire. A helical coil was made from the obtained self-bonding insulated wire and left in a constant temperature bath at a predetermined temperature for 5 minutes, and the temperature at which foaming occurred was examined. Table 1 shows the results and the appearance of the self-bonding insulated wire when it was made.

【0022】〔実施例1〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し2PHR添加し他は比較
例1と同様に行った。
[Example 1] The same procedure as in Comparative Example 1 was carried out except that zinc white was added as a foaming aid to the fusion coating of Comparative Example 1 in an amount of 2 PHR relative to the foaming agent.

【0023】〔実施例2〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し5PHR添加し他は比較
例1と同様に行った。
[Example 2] The same procedure as in Comparative Example 1 was carried out except that 5 PHR of zinc white was added as a foaming aid to the fusing paint of Comparative Example 1 based on the foaming agent.

【0024】〔実施例3〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し50PHR添加し他は比
較例1と同様に行った。
[Example 3] The same procedure as in Comparative Example 1 was carried out except that 50 PHR of zinc white was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.

【0025】〔実施例4〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し100PHR添加し他は
比較例1と同様に行った。
[Example 4] The same procedure as in Comparative Example 1 was carried out except that 100 PHR of zinc white was added as a foaming aid to the fusing paint of Comparative Example 1 based on the foaming agent.

【0026】〔実施例5〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し200PHR添加し他は
比較例1と同様に行った。
[Example 5] The same procedure as in Comparative Example 1 was carried out except that 200 PHR of zinc white was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.

【0027】〔実施例6〕比較例1の融着塗料に発泡助
剤としてBZを発泡剤に対し50PHR添加し他は比較
例1と同様に行った。
[Example 6] The same procedure as in Comparative Example 1 was carried out except that 50 PHR of BZ was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.

【0028】〔実施例7〕比較例1の融着塗料に発泡助
剤としてTLBを発泡剤に対し100PHR添加し他は
比較例1と同様に行った。
[Example 7] The same procedure as in Comparative Example 1 was carried out except that 100 PHR of TLB was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.

【0029】〔実施例8〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し300PHR添加し他は
比較例1と同様に行った。
[Example 8] The same procedure as in Comparative Example 1 was carried out except that 300 PHR of zinc white was added to the foaming agent as a foaming aid to the adhesive coating of Comparative Example 1.

【0030】[0030]

【表1】[Table 1]

【0031】[0031]

【発明の効果】以上に示したように、本発明の自己融着
性絶縁電線を用いると融着層を150℃前後の低温で発
泡させることができるという利点を有している。
As described above, the use of the self-bonding insulated wire of the present invention has the advantage that the fusion layer can be foamed at a low temperature of around 150°C.

【図面の簡単な説明】[Brief explanation of the drawing]

【図1】本発明の自己融着性絶縁電線の断面図である。FIG. 1 is a sectional view of a self-bonding insulated wire of the present invention.

【符号の説明】[Explanation of symbols]

1    導体 2    絶縁皮膜 3    自己融着層 1 Conductor 2 Insulating film 3 Self-adhesive layer

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】  金属導体上に絶縁層を介して、発泡剤
と発泡助剤を含有する融着層を形成させたことを特徴と
する自己融着性絶縁電線。
1. A self-bonding insulated wire characterized in that a welding layer containing a foaming agent and a foaming aid is formed on a metal conductor via an insulating layer.
【請求項2】  発泡助剤の添加量が発泡剤に対し5重
量部から200重量部である請求項1に記載の自己融着
性絶縁電線。
2. The self-fusing insulated wire according to claim 1, wherein the amount of the foaming aid added is from 5 parts by weight to 200 parts by weight based on the foaming agent.
【請求項3】  請求項1に記載の自己融着性絶縁電線
を用い捲線加工した後、融着層を発泡させたことを特徴
としたコイル。
3. A coil characterized in that the self-fusing insulated wire according to claim 1 is wound, and then the fusing layer is foamed.
JP00976891A 1991-01-30 1991-01-30 Self-fusing insulated wire and coil using the same Expired - Fee Related JP3151836B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP00976891A JP3151836B2 (en) 1991-01-30 1991-01-30 Self-fusing insulated wire and coil using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP00976891A JP3151836B2 (en) 1991-01-30 1991-01-30 Self-fusing insulated wire and coil using the same

Publications (2)

Publication Number Publication Date
JPH04245110A true JPH04245110A (en) 1992-09-01
JP3151836B2 JP3151836B2 (en) 2001-04-03

Family

ID=11729448

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3151836B2 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0706300A3 (en) * 1994-10-03 1998-11-18 Star Micronics Co., Ltd. Electroacoustic transducer and electronic equipment using the same
WO2002099821A1 (en) * 2001-06-01 2002-12-12 The Furukawa Electric Co., Ltd. Multilayer insulated wire and transformer using the same
JP2006252852A (en) * 2005-03-09 2006-09-21 Matsushita Electric Ind Co Ltd Insulated wire
JP2009070722A (en) * 2007-09-14 2009-04-02 Fujifilm Corp Composition for insulating film formation and electronic device
JP4776048B2 (en) * 1997-10-24 2011-09-21 古河電気工業株式会社 Multilayer insulated wire and transformer using the same
WO2016017648A1 (en) * 2014-08-01 2016-02-04 住友電気工業株式会社 Self-bonding insulated wire and wire for coil
JP2016035836A (en) * 2014-08-01 2016-03-17 住友電気工業株式会社 Self-fusion insulated wire and wire for coil
JP2016081563A (en) * 2014-10-09 2016-05-16 住友電気工業株式会社 Self-fusible insulated electric wire, electric wire for coil and winding wire bundle
JP2016126903A (en) * 2014-12-26 2016-07-11 住友電気工業株式会社 Insulated wire

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63159748U (en) * 1987-04-09 1988-10-19
JPH0250654U (en) * 1989-08-31 1990-04-09
JPH0257046U (en) * 1988-10-18 1990-04-25

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63159748U (en) * 1987-04-09 1988-10-19
JPH0257046U (en) * 1988-10-18 1990-04-25
JPH0250654U (en) * 1989-08-31 1990-04-09

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0706300A3 (en) * 1994-10-03 1998-11-18 Star Micronics Co., Ltd. Electroacoustic transducer and electronic equipment using the same
JP4776048B2 (en) * 1997-10-24 2011-09-21 古河電気工業株式会社 Multilayer insulated wire and transformer using the same
WO2002099821A1 (en) * 2001-06-01 2002-12-12 The Furukawa Electric Co., Ltd. Multilayer insulated wire and transformer using the same
US7087843B2 (en) 2001-06-01 2006-08-08 The Furukawa Electric Co. Ltd. Multilayer insulated wire and transformer using the same
JP2006252852A (en) * 2005-03-09 2006-09-21 Matsushita Electric Ind Co Ltd Insulated wire
JP2009070722A (en) * 2007-09-14 2009-04-02 Fujifilm Corp Composition for insulating film formation and electronic device
WO2016017648A1 (en) * 2014-08-01 2016-02-04 住友電気工業株式会社 Self-bonding insulated wire and wire for coil
JP2016035836A (en) * 2014-08-01 2016-03-17 住友電気工業株式会社 Self-fusion insulated wire and wire for coil
CN106575549A (en) * 2014-08-01 2017-04-19 住友电气工业株式会社 Self-bonding insulated wire and wire for coil
CN110164605A (en) * 2014-08-01 2019-08-23 住友电气工业株式会社 Self-bonding insulated wire, coil electric wire and electromagnetism harness
JP2016081563A (en) * 2014-10-09 2016-05-16 住友電気工業株式会社 Self-fusible insulated electric wire, electric wire for coil and winding wire bundle
JP2016126903A (en) * 2014-12-26 2016-07-11 住友電気工業株式会社 Insulated wire

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