JPH025309A - Self-adhesive type insulated wire - Google Patents

Self-adhesive type insulated wire

Info

Publication number
JPH025309A
JPH025309A JP14259988A JP14259988A JPH025309A JP H025309 A JPH025309 A JP H025309A JP 14259988 A JP14259988 A JP 14259988A JP 14259988 A JP14259988 A JP 14259988A JP H025309 A JPH025309 A JP H025309A
Authority
JP
Japan
Prior art keywords
resin
polymer compound
radical
weight
self
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
JP14259988A
Other languages
Japanese (ja)
Other versions
JP2698378B2 (en
Inventor
Izumi Ishikawa
石川 泉
Shigemi Takahashi
重美 高橋
Sueji Chabata
茶畑 末治
Teruo Yamazawa
山沢 照夫
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.)
Fujikura Ltd
Original Assignee
Fujikura 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 Fujikura Ltd filed Critical Fujikura Ltd
Priority to JP63142599A priority Critical patent/JP2698378B2/en
Publication of JPH025309A publication Critical patent/JPH025309A/en
Application granted granted Critical
Publication of JP2698378B2 publication Critical patent/JP2698378B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Organic Insulating Materials (AREA)
  • Insulated Conductors (AREA)

Abstract

PURPOSE:To reduce a deterioration of the adhesive strength with the rise of temperature and to improve the flexibility of an attached membrane by spreading or baking a paint made by mixing a specific amount of an amino resin or a phenol resin to a polyhydroxy ether with a led-in sulfonic radical, or a mixture of such a polyhydroxy ether and a high polymer compound including an active OH radical, on a conductor. CONSTITUTION:To 100 pts.wt. of polyhydroxy ether with a led-in sulfonic radical, or a mixture of such a polyhydroxy ether and a high polymer compound including 3wt.% or more of active OH radical, 10 to 80 pts.wt. of amino resin or a paint made by mixing less then 50 pts.wt. of phenol resin to said amino resin is spread or baked on a conductor directly or through an insulating membrane. In this case, the mean molecular weight of the polyhydroxy ether and the high polymer compound is made 10000 or higher respectively. As the polyhydroxy ether with led-in sulfonic radical, YPS-007.A30, YPS-030.A30, or the like is available. As the high polymer compound including an active OH radical, phenoxy resin, polyvinyl acetal resin, or the like can be used.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は電気通信機等の機器コイル用電線として広範囲
な目的に使用される自己接着性絶縁電線に関するもので
あり、コイル巻回後加熱接着したらのの耐熱軟化性を向
上せしめたものである。
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a self-adhesive insulated wire that is used for a wide range of purposes as an electric wire for equipment coils such as telecommunications equipment, and is heat-bonded after coil winding. This product has improved heat softening resistance of Tarano.

〔従来の技術〕[Conventional technology]

この種の自己接着性絶縁電線としては、従来からポリビ
ニルブチラール樹脂あるいはフェノキシ樹脂(高重合度
エポキシ樹脂を含む)等の直鎮状高分子化合物を適当な
溶剤に溶かしてなる塗料を、他の絶縁皮膜を介して塗布
焼付けを施すか、あるいはこれらの樹脂にエポキシ樹脂
、アミン樹脂、安定化イソシアナート樹脂等の中から、
そのいくつかを適宜組合わけ配合してなる塗料を前記同
様、他の絶縁皮膜を介して塗布焼付けを施したものであ
る。
This type of self-adhesive insulated wire has traditionally been made using a paint made by dissolving a straight polymer compound such as polyvinyl butyral resin or phenoxy resin (including highly polymerized epoxy resin) in an appropriate solvent, and applying it to other insulating wires. Either apply and bake through a film, or add to these resins from among epoxy resins, amine resins, stabilized isocyanate resins, etc.
A paint made by appropriately mixing and blending some of these is coated and baked through another insulating film as described above.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

これらの内、前記直鎖状化合珈だけからなる塗料を伯の
絶縁物を介して塗布焼付けを施す゛場合には、当該樹脂
と絶縁皮膜の熱劣化にのみ注意して焼付条件を選定すれ
ば、絶縁皮膜の焼付けとIi1時に、その条件で接着皮
膜の焼付けも可能なため、焼付作業性に1ぐれる反面、
コイルに巻回接着後の接着強度は、機器内温度の上昇と
共に接着皮膜が軟化し、著しく低下するためコイルに変
形を生じる等の欠点があった。
Among these, when applying and baking a paint made only of the linear compound silicone through a metal insulator, the baking conditions should be selected with consideration only to thermal deterioration of the resin and insulating film. , since it is possible to bake the adhesive film under the same conditions at the time of baking the insulating film and Ii1, the baking workability is improved, but on the other hand,
The adhesive strength after winding and bonding around a coil deteriorates significantly as the adhesive film softens as the temperature inside the device increases, resulting in deformation of the coil.

これらの欠点を改善するため、前記直鎖状高分子化合物
にエポキシ樹脂、アミノ樹脂、安定化イソシアナート樹
脂等の中から単独もしくはそのいくつかを適宜組合わせ
配合してなる塗料を他の絶縁皮膜を介して焼付ける場合
があるが、この場合においても前記直鎖状高分子化合物
のガラス移転温度(1g)が70〜110℃前後と低い
ため、たとえエポキシ樹脂、アミン樹脂、安定化イソシ
アナートで架橋しても、コイルに巻回接着後の接着力が
温度上昇と共に著しく低下するなどの欠点を充分に解決
出来ない状態であった。
In order to improve these drawbacks, a paint made by blending the above-mentioned linear polymer compound singly or in appropriate combinations of epoxy resins, amino resins, stabilized isocyanate resins, etc., is used to form other insulating coatings. However, even in this case, the glass transition temperature (1 g) of the linear polymer compound is low at around 70 to 110°C, so even if epoxy resin, amine resin, or stabilized isocyanate is used, Even with crosslinking, it was not possible to satisfactorily solve the problem that the adhesive force after being wound around a coil and bonded decreased significantly as the temperature rose.

この問題を解決づるために、近年スルホン基を導入した
ポリヒドロキシエーテルを前記直鎖状高分子化合物に代
えて用いられ゛つつある。このスルホン基を導入したポ
リヒドロキシエーテルは、ガラス移転)jシiffが1
00〜150℃と耐熱性が良いため、温度上昇による巻
回接着後の接着強度の低下【よ抑えられるbのの8スデ
ージ(半硬化状態)での接着被膜の可撓性が乏lノく、
絶縁電線としたときの曲げ性に劣るなどの欠点があった
In order to solve this problem, polyhydroxy ethers having introduced sulfone groups have recently been used in place of the above-mentioned linear polymer compounds. This polyhydroxyether into which a sulfone group has been introduced has a glass transfer) j iff of 1
Since it has good heat resistance of 00 to 150℃, it can suppress the decrease in adhesive strength after winding and bonding due to temperature rise.The flexibility of the adhesive film at 8 degrees (semi-cured state) is poor. ,
It had drawbacks such as poor bendability when used as an insulated wire.

よって、本発明はさ同棲着後の接着強度の温度」−胃に
伴“)低下が微かで、かつ可撓性、曲げ性の良好な自己
接着性絶縁電線を提供することを目的どする。
SUMMARY OF THE INVENTION Therefore, an object of the present invention is to provide a self-adhesive insulated wire that exhibits a slight decrease in adhesive strength after the wire is attached to the wire and has good flexibility and bendability.

〔課題を解決するための手段〕[Means to solve the problem]

本発明では、平均分子間が10000以上のスルホン基
を導入したポリヒドロキシエーテルまたは、これと平均
分子1iが10000以上で粘付OH基を3小吊%以上
含有する高分子化合物の混合物100小吊部に対して、
アミン樹脂の10〜80重司部あるいはこれとフェノー
ル樹脂の50重量部以下を配合した塗料を導体上に直接
あるいは絶縁皮膜を介して塗布、焼付けることをその解
決手段とした。
In the present invention, a mixture of polyhydroxyether into which a sulfone group having an average molecular weight of 10,000 or more and a polymer compound having an average molecular weight of 10,000 or more and containing a sticky OH group of 3 or more percent is used. For the department,
The solution was to apply and bake a paint containing 10 to 80 parts by weight of amine resin or 50 parts by weight or less of phenol resin onto the conductor directly or through an insulating film.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

本発明で用いられる平均分子mが10000以上のスル
ホン基を導入したポリヒドロキシエーテルとしては下記
の一般式で表わされるものである。
The polyhydroxyether having a sulfone group and having an average molecular m of 10,000 or more used in the present invention is represented by the following general formula.

または、 H であり、またR1は ○ 式において、Aは であり、R2は または、 であり、Bは ○R2 H3 のいずれかであり、J、m、nはJ≧Q、m≧1゜n≧
1の整数である。) このポリヒドロキシエーテルの平均分子潰を1oooo
以上としたのは、充分な耐熱性を得るためであり、10
000未)1では、接着強度の温度上背による低下が大
きくなって不都合である。このような平均分子m 10
000以上のスルホン基を導入したポリヒドロキシエー
テルの具体的なものとしては、YPS−007^30 
、 YPS−030Δ30(東部化成社、商品名)など
がある。
Or, H and R1 is ○ In the formula, A is , R2 is or , B is ○R2 H3 , and J, m, and n are J≧Q, m≧1゜n≧
It is an integer of 1. ) The average molecular weight of this polyhydroxyether is 1oooo
The above setting was made in order to obtain sufficient heat resistance, and 10
000) 1 is disadvantageous because the adhesive strength decreases greatly due to temperature changes. Such an average molecule m 10
A specific example of a polyhydroxy ether with 000 or more sulfone groups introduced is YPS-007^30.
, YPS-030Δ30 (Tobu Kasei Co., Ltd., trade name).

また、平均分子量がi oooo以上で活性OH基を3
小舅%以上含右する高分子化合物としては、71ノキシ
樹脂(エビク【コルヒドリンビスフェノール△縮合物)
、ポリビニルポルマール樹脂、ポリビニルブチラール樹
脂などのポリビニルアセタール樹脂が挙げられる。ここ
で、平均分子量を10000以上としたのは充分な可ど
う性を得んがためであり、また活性0f−1基の含有率
を3小量%以上としたのは充分な耐熱性を得るためであ
る。
In addition, if the average molecular weight is ioooo or more and the active OH group is 3
Examples of polymeric compounds containing 71% or more include 71noxy resin (corhydrin bisphenol △ condensate)
, polyvinyl acetal resins such as polyvinyl polymer resin and polyvinyl butyral resin. Here, the reason why the average molecular weight is set to 10,000 or more is to obtain sufficient flexibility, and the content of active 0f-1 groups is set to 3% or more to obtain sufficient heat resistance. It's for a reason.

この高分子化合物の具体例としては、エビコー1〜0f
−53−all−35、1255−11X−30(油化
シェルエポキシ社商品名) 、 PKIIC,PKII
II、 PKIIJ (U CC社商品名)、  YP
−50、YP−50EK35  、  YP−50C3
25B、  YP60八C25(束都化成社、商品名)
Specific examples of this polymer compound include Ebiko 1 to 0f.
-53-all-35, 1255-11X-30 (product name of Yuka Shell Epoxy Co., Ltd.), PKIIC, PKII
II, PKIIJ (product name of UCC company), YP
-50, YP-50EK35, YP-50C3
25B, YP608C25 (Tokuto Kaseisha, product name)
.

デンカブチラール12000−L 、 13000−1
 。
Denka Butyral 12000-L, 13000-1
.

曾3000−2  、 13000−4  、  $3
000−に 、雲4000−1  。
Zeng 3000-2, 13000-4, $3
000-, cloud 4000-1.

番4000−2 、暑5000−A 、 16000−
C、デンカホルマール嘗201番30.書100.12
00 (電気化学工業商品名)、などが例示される。
No. 4000-2, Hot 5000-A, 16000-
C, Denka Formal 201 No. 30. Book 100.12
00 (Deki Kagaku Kogyo brand name), etc. are exemplified.

また、この平均分子量が10000以上で活性OH基を
3重量%以上を含有する高分子化合物のうちでも、枝分
れ構造を有し、かつその25℃で比粘度))が0.44
以下のものを使用することが特に好ましい。このような
枝分れ構造を有し、還元粘度が0.44以下の高分子化
合物を用いることによって、焼付塗膜の耐熱性を損うこ
となく可どう性が向上して好ましい。−この条件を満す
高分子化合物の具体例としてはYP−40ASH40(
東部化成社、商品名)などが挙げられる。
Furthermore, among polymer compounds having an average molecular weight of 10,000 or more and containing 3% by weight or more of active OH groups, those having a branched structure and having a specific viscosity (at 25°C) of 0.44
Particular preference is given to using the following: By using a polymer compound having such a branched structure and having a reduced viscosity of 0.44 or less, the flexibility of the baked coating film is improved without impairing the heat resistance, which is preferable. - A specific example of a polymer compound that satisfies this condition is YP-40ASH40 (
Tobu Kasei Co., Ltd., product name), etc.

また、アミノ樹脂としては尿素ホルムアルデヒド縮合物
、メラミンホルムアルデヒド縮合物、アセトグアナミン
・ホルムアルデヒド縮合物、アニリン・ホルムアルデヒ
ド縮合物、ベンゾグアナミン・ホルムアルデヒド綜合物
もしくはこれらをアルコール変性したちのが用いられ、
例えばニーパン1ts−Go、 1OR、20SB、 
20SE−60、20H8,218ν。
In addition, as the amino resin, urea formaldehyde condensate, melamine formaldehyde condensate, acetoguanamine formaldehyde condensate, aniline formaldehyde condensate, benzoguanamine formaldehyde condensate, or alcohol-denatured products of these are used.
For example, knee pants 1ts-Go, 1OR, 20SB,
20SE-60, 20H8, 218ν.

211t 、 22R、22R−60,120,122
,220,134゜435、 136.6OR、62,
69−1,163,164,165゜805、 91−
55.サイメル300. 301. 303. 325
゜350、 370.1116.1130.、1123
.1125. UFR65(三1+東圧化学社 商品名
)、ベッカミンP−138。
211t, 22R, 22R-60, 120, 122
,220,134°435, 136.6OR,62,
69-1,163,164,165゜805, 91-
55. Cymel 300. 301. 303. 325
゜350, 370.1116.1130. , 1123
.. 1125. UFR65 (San1 + Toatsu Kagakusha trade name), Beckamin P-138.

P−196−H、G−1800,G−1850,スーパ
ーベッカミン00−1.−131−60 、 !、−8
06、J−820−60,L−109−65,L−11
7−00,1,−127−60,G−821−60,L
−101−60,L−110−60、,17−508−
60,L−146−70,L−118−60,1,−1
21−60゜L−120−60,TO−139,17−
590,L−105−60,TO−126゜P−198
(人日本インキ社 商品名)等が例示される。
P-196-H, G-1800, G-1850, Super Beckamine 00-1. -131-60, ! , -8
06, J-820-60, L-109-65, L-11
7-00,1,-127-60,G-821-60,L
-101-60,L-110-60,,17-508-
60,L-146-70,L-118-60,1,-1
21-60゜L-120-60, TO-139, 17-
590, L-105-60, TO-126゜P-198
(Product name of Nippon Ink Co., Ltd.) etc. are exemplified.

さらに、フェノール樹脂としてはフェノール、クレゾー
ル、キシレノール、イソプロピルフェノール、レゾルシ
ン等のフェノール類とホルムアルデヒド、アlニア1−
アルデヒド、フルフラール等のアルデヒド類との縮合物
およびP−ビニルフェノール等のフェノール樹脂が用い
られる。このフェノール樹脂の例としては、CKH−1
634,1636,1737,1282、904,90
7,908,983,2400,941,2103゜2
432、5254. BKM−2620,BRP−59
04,CRH−0909,BにS−2600,2710
C、2750,307,316,355,CKS−71
0、813−2030,3574,3122,362,
356,3135゜CLS−3940,3950,BH
3−324、621,BLL−3085,8RL−11
3、114,116,117,134,274,285
4゜112^、120Z(昭和ユニオン合成社、商品名
)、ブライオーフェン5010.5030. TO−4
47(大日本インキ化学工業社 商品名)などが挙げら
れる。
Furthermore, phenolic resins include phenols such as phenol, cresol, xylenol, isopropylphenol, and resorcinol, as well as formaldehyde and alumina 1-
Used are aldehydes, condensates with aldehydes such as furfural, and phenolic resins such as P-vinylphenol. An example of this phenolic resin is CKH-1
634, 1636, 1737, 1282, 904, 90
7,908,983,2400,941,2103゜2
432, 5254. BKM-2620, BRP-59
04, CRH-0909, B to S-2600, 2710
C, 2750, 307, 316, 355, CKS-71
0, 813-2030, 3574, 3122, 362,
356, 3135° CLS-3940, 3950, BH
3-324, 621, BLL-3085, 8RL-11
3, 114, 116, 117, 134, 274, 285
4゜112^, 120Z (Showa Union Gosei Co., Ltd., trade name), Briophen 5010.5030. TO-4
47 (Dainippon Ink & Chemicals Co., Ltd. trade name).

これらの樹脂の配合については、前記平均分子量が10
000以上のスルホン基を導入したポリヒドロキシエー
テルと前記平均分子1がi oo。
Regarding the formulation of these resins, the average molecular weight is 10
Polyhydroxyether into which 000 or more sulfone groups have been introduced and the average molecule 1 is i oo.

0以上で活性OH基を3重量%以上含有する高分子化合
物とを混合して使用り゛る場合の配合比率は特に限定さ
れず、得られる自己接着性絶縁電線の接着温度条件と8
温下での接着力の保持率とのかねあいにより適宜法めら
れる。通常、平均分子量が10000以上のスルホン基
を導入したポリヒド[]キシ1−チルのn1合を多くす
ると、接着温度を高くでき、かつ高温下での接着力の保
持率が高くなる。そして、前記特定のポリヒドロキシエ
ーテルまたはこれと前記高分子化合物との混合物100
重ff1部に対して前記アミノ樹脂は10〜8OIff
1部、前記フェノール樹脂は20市邑部以下が配合され
る。アミノ樹脂が10市邑部未満では高温下での接着力
を保持することが難しくなるとと6に絶縁電線としての
耐熱軟化性と耐熱劣化性との低下を招く。また、アミノ
樹脂が80市邑部を越え、フェノール樹脂が20市邑部
を越えるといずれも接着被膜の可撓性が低下して好まし
くない。
When used in combination with a polymer compound containing 0 or more active OH groups and 3% by weight or more, the blending ratio is not particularly limited, and the adhesion temperature conditions of the resulting self-adhesive insulated wire and 8
It is determined as appropriate depending on the retention rate of adhesive strength at high temperatures. Generally, when the n1 ratio of polyhydro[]xy-1-tyl into which a sulfone group having an average molecular weight of 10,000 or more is introduced is increased, the adhesion temperature can be increased and the retention rate of adhesive strength at high temperatures can be increased. and 100 of the specific polyhydroxyether or a mixture of this and the polymer compound.
The amino resin is 10 to 8 OIf per 1 part of heavy FF.
1 part, 20 or less of the phenol resin is blended. If the amino resin content is less than 10%, it becomes difficult to maintain adhesive strength at high temperatures, which leads to a decrease in heat softening resistance and heat deterioration resistance as an insulated wire. Furthermore, if the amino resin exceeds 80 degrees and the phenol resin exceeds 20 degrees, the flexibility of the adhesive coating will decrease, which is not preferable.

また、自己接着性絶縁“電線に要求される接6カおよび
接着耐熱性によっては、前記フェノール樹脂を配合しな
くと6よく、フェノール樹脂の配合がない場合には若干
接着力および接着耐熱性が低下し、可撓性が高くなるが
、従来の自己接着性絶縁電線に比へて高い接着力および
接着耐熱性を有づるものとなる。
In addition, depending on the bonding force and adhesive heat resistance required for self-adhesive insulated electric wires, it may be necessary to not include the above-mentioned phenolic resin, and if the phenolic resin is not included, the adhesive strength and adhesive heat resistance may be slightly reduced. However, it has higher adhesive strength and adhesive heat resistance than conventional self-adhesive insulated wires.

このような樹脂混合物には、さらに必要に応じてリン酸
モノアルキルエステル等の右+i酸触媒を添加し、そし
てこれをm−クレゾール、フルフラール、シクロベキ1
ナノン、メヂルエチルケトン等の有機溶剤に溶かして冑
だ塗料を導体上に直接または他の絶縁皮膜を介して塗布
焼付け、本発明の自己j妄む性絶縁′電線を得る。
To such a resin mixture, a right +i acid catalyst such as phosphoric acid monoalkyl ester is further added as required, and this is mixed with m-cresol, furfural, cyclobekyl ester, etc.
The self-destructive insulated wire of the present invention is obtained by coating and baking a paint dissolved in an organic solvent such as nano or methyl ethyl ketone on the conductor directly or through another insulating film.

こうして得られた自己接着性絶縁電線は、広い4度範囲
にわたってその機能が発揮され、コイル巻回後の加熱に
よって比較的容易に接着性が(qられ、耐熱劣化性はほ
とんど認められない。
The self-adhesive insulated wire thus obtained exhibits its function over a wide range of 4 degrees, exhibits adhesiveness relatively easily by heating after winding the coil, and exhibits almost no heat deterioration resistance.

つぎに本発明を実施例をあげて説明するが、本発明はこ
れにのみ限定されるものではなく得られる接着温度下で
の接着強度、絶縁電線としての耐熱軟化性により、塗料
の配合比、材料を変更できるものである。
Next, the present invention will be explained with reference to examples, but the present invention is not limited to these examples, and the composition ratio of the paint, The material can be changed.

〔実施例〕〔Example〕

第1表に示す組成の樹脂混合物を、m−クレゾール/ツ
ルベン]−ナフサの混合溶剤(1:1)に溶解し、樹脂
濃度20市邑%の塗料を調製し、この塗料を径0.5m
mのポリニスデルエナメル線(絶縁被膜厚さ15μm)
上に塗布、焼付し、厚さ10μmの接着被膜を形成して
自己接着性絶縁電線を得た。
A resin mixture having the composition shown in Table 1 was dissolved in a mixed solvent of m-cresol/turben]-naphtha (1:1) to prepare a paint with a resin concentration of 20%.
m polynisdel enameled wire (insulating coating thickness 15 μm)
A self-adhesive insulated wire was obtained by coating and baking to form an adhesive film with a thickness of 10 μm.

これらの自己接着性絶縁電線について、自己径巻き付け
による可撓性、絶縁破壊電圧、接着力、耐熱接着力およ
び外観について測定を行った。結果を第1表に併せて示
す。
These self-adhesive insulated wires were measured for flexibility by self-diameter winding, dielectric breakdown voltage, adhesive strength, heat-resistant adhesive strength, and appearance. The results are also shown in Table 1.

なお、接着力の測定は自己接着性絶縁電線を直径5履の
マンドレルに100ターン巻付け、150℃で加熱して
巻線間を接着してヘリカルコイルとしたのち、9 rで
のヘリカルコイルの折り曲げ力を求めることに行った。
The adhesive strength was measured by winding 100 turns of self-adhesive insulated wire around a mandrel with a diameter of 5 shoes, heating it at 150°C to bond the windings together to form a helical coil, and then winding the helical coil at 9 r. I went to find the bending force.

また、耐熱接着力は前記ヘリカルコイルの折り曲げ力の
測定を90℃の雰囲気で行って求めた。さらに、第1表
中の樹脂の配合組は重1部で示した。
Further, the heat-resistant adhesive strength was determined by measuring the bending force of the helical coil in an atmosphere of 90°C. Further, the resin formulations in Table 1 are expressed in terms of 1 part by weight.

〔発明の効果〕〔Effect of the invention〕

本発明の自己接着性絶縁電線にあっては、巻回接着侵の
接着強度の温度上背に伴う低下が少なく、耐熱性が向上
するとともに接着被膜の可撓性が良く、絶縁電線として
の曲げ性も良好となる。また、接着力が高いので、従来
の自己接着性絶縁電線に比べて接着被膜の厚さを薄くし
ても良好な接着力を有し、このためコイルの占積率を高
めることができる。
In the self-adhesive insulated wire of the present invention, there is little decrease in the adhesive strength of the wound adhesive due to temperature changes, the heat resistance is improved, and the adhesive coating has good flexibility, making it easy to bend as an insulated wire. The properties are also improved. In addition, since the adhesive strength is high, it has good adhesive strength even if the thickness of the adhesive coating is made thinner than that of conventional self-adhesive insulated wires, and therefore the space factor of the coil can be increased.

Claims (2)

【特許請求の範囲】[Claims] (1)平均分子量が10000以上のスルホン基を導入
したポリヒドロキシエーテルまたは、これと平均分子量
が10000以上で活性OH基を3重量%以上含有する
高分子化合物の混合物100重量部に対して、アミノ樹
脂の10〜80重量部を配合した塗料を導体上に直接あ
るいは絶縁皮膜を介して塗布,焼付けたことを特徴とす
る自己接着性絶縁電線。
(1) For 100 parts by weight of polyhydroxy ether with an average molecular weight of 10,000 or more and a sulfone group-introduced mixture, or a mixture of this and a polymer compound with an average molecular weight of 10,000 or more and containing 3% by weight or more of active OH groups, A self-adhesive insulated wire characterized in that a paint containing 10 to 80 parts by weight of a resin is applied onto a conductor directly or via an insulating film and baked.
(2)平均分子量が10000以上のスルホン基を導入
したポリヒドロキシエーテルまたは、これと平均分子量
が10000以上で活性OH基を3重量%以上含有する
高分子化合物の混合物100重量部に対して、アミノ樹
脂の10〜80重量部およびフェノール樹脂の20重量
部以下を配合した塗料を導体上に直接あるいは絶縁皮膜
を介して塗布,焼付けたことを特徴とする自己接着性絶
縁電線。
(2) With respect to 100 parts by weight of polyhydroxyether having an average molecular weight of 10,000 or more and a sulfone group introduced therein, or a mixture of this and a polymer compound having an average molecular weight of 10,000 or more and containing 3% by weight or more of active OH groups, A self-adhesive insulated wire characterized in that a paint containing 10 to 80 parts by weight of a resin and 20 parts by weight or less of a phenol resin is applied onto a conductor directly or via an insulating film and baked.
JP63142599A 1988-06-09 1988-06-09 Self-adhesive insulated wire Expired - Lifetime JP2698378B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63142599A JP2698378B2 (en) 1988-06-09 1988-06-09 Self-adhesive insulated wire

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63142599A JP2698378B2 (en) 1988-06-09 1988-06-09 Self-adhesive insulated wire

Publications (2)

Publication Number Publication Date
JPH025309A true JPH025309A (en) 1990-01-10
JP2698378B2 JP2698378B2 (en) 1998-01-19

Family

ID=15319055

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63142599A Expired - Lifetime JP2698378B2 (en) 1988-06-09 1988-06-09 Self-adhesive insulated wire

Country Status (1)

Country Link
JP (1) JP2698378B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02220310A (en) * 1989-02-20 1990-09-03 Hitachi Cable Ltd Heat-proof self welding enameled wire
JP2009067934A (en) * 2007-09-14 2009-04-02 Hitachi Magnet Wire Corp Heat-resistant self-fusing paint and heat-resistant self-fusing enamel wire

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012116954A (en) * 2010-12-01 2012-06-21 Hitachi Cable Ltd Adhesive composition, adhesive film and wiring film using the same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54132790A (en) * 1978-04-06 1979-10-16 Furukawa Electric Co Ltd:The Self-adhesive insulated wire
JPS5830003A (en) * 1981-07-24 1983-02-22 住友電気工業株式会社 Self-fusion-adhesive insulated wire

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54132790A (en) * 1978-04-06 1979-10-16 Furukawa Electric Co Ltd:The Self-adhesive insulated wire
JPS5830003A (en) * 1981-07-24 1983-02-22 住友電気工業株式会社 Self-fusion-adhesive insulated wire

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02220310A (en) * 1989-02-20 1990-09-03 Hitachi Cable Ltd Heat-proof self welding enameled wire
JP2009067934A (en) * 2007-09-14 2009-04-02 Hitachi Magnet Wire Corp Heat-resistant self-fusing paint and heat-resistant self-fusing enamel wire

Also Published As

Publication number Publication date
JP2698378B2 (en) 1998-01-19

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