JPH01166410A - Multicore parallel adhesive wire - Google Patents

Multicore parallel adhesive wire

Info

Publication number
JPH01166410A
JPH01166410A JP32458687A JP32458687A JPH01166410A JP H01166410 A JPH01166410 A JP H01166410A JP 32458687 A JP32458687 A JP 32458687A JP 32458687 A JP32458687 A JP 32458687A JP H01166410 A JPH01166410 A JP H01166410A
Authority
JP
Japan
Prior art keywords
resin
adhesive
parts
core wires
weight
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
JP32458687A
Other languages
Japanese (ja)
Inventor
Izumi Ishikawa
石川 泉
Sueji Chabata
茶畑 末治
Michio Koike
小池 三千雄
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 JP32458687A priority Critical patent/JPH01166410A/en
Publication of JPH01166410A publication Critical patent/JPH01166410A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To enhance adhesive force between core wires as well as facilitate the separation therebetween by incorporating a specified amount of either one or more of higher fatty acid, terminal reactive silicone oil or terminal reactive fluorine oil into an adhesive resin composition. CONSTITUTION:As an adhesive resin composition is used either alone or in combination of two or more of polyamide, polyvinyl butyral, epoxy resin or the like, or a composition incorporating either alone or two or more of amino resin, stabilized isocyanate, triazine resin, phenol resin or the like into the above mentioned resin. Into 100 pts.wt. of this composition is incorporated 0.1-20 pts.wt. of either alone or two or more of higher fatty acid, terminal reactive silicone oil, terminal reactive fluorine oil so as to obtain the adhesive resin composition. Therefore, besides sufficient adhesive force between core wires, the separation of the core wires at the terminal of a multicore parallel adhesive wire can be easily performed, thereby, upon the separation, eliminating any breakage in the insulating layers of the core wires. Furthermore, the surfaces of adhesive layers have surface lubrication property so as to be hard to generate machining flaw upon winding the wire.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、電気、通信機器等の機器コイル用′Irl
l1lとして使用される多芯平行接着線に関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field)
This relates to a multi-core parallel adhesive wire used as l1l.

(従来の技術) 第1図は、このような多芯平行接着線の例を示すもので
、図中符号1は絶縁芯線である。この絶縁芯線1は導体
2上にポリウレタン、ポリビニルホルマール、ポリエス
テル、ポリエステルイミド、ポリヒダントン、ポリアミ
ドイミド、ポリエステルアミドイミド、ポリヒダントイ
ンエステスル、ポリエステルアミドなどからなる絶縁塗
料を塗布し焼付けて絶縁層3を形成してなるものである
(Prior Art) FIG. 1 shows an example of such a multicore parallel bonded wire, and the reference numeral 1 in the figure is an insulated core wire. This insulated core wire 1 is formed by applying an insulating paint made of polyurethane, polyvinyl formal, polyester, polyester imide, polyhydanthone, polyamide imide, polyester amide imide, polyhydantoin ester, polyester amide, etc. onto the conductor 2 and baking it to form an insulating layer 3. This is what happens.

この絶縁芯線1は複数本(ここでは5本)が平行にかつ
一列に束ねられ、接着WIJ4で接着され一体化されて
多芯平行接着線とされている。接着層4を構成する接着
樹脂組成物としては、ポリビニルブチラール、エポキシ
樹脂、ポリエステル、ポリヒドロキシエーテル、ポリビ
ニルホルマール、ポリアミドなどの樹脂もしくはこれに
アミノ樹脂、イソシアネート、トリヒドロキシエチルイ
ソシアネート、トリアジン樹脂、フェノール樹脂、フェ
ノールホルムアルデヒド樹脂などを配合した樹脂組成物
が用いられる。
A plurality of insulated core wires 1 (here, five wires) are bundled in parallel in a line, and bonded and integrated with adhesive WIJ4 to form a multicore parallel bonded wire. The adhesive resin composition constituting the adhesive layer 4 is a resin such as polyvinyl butyral, epoxy resin, polyester, polyhydroxy ether, polyvinyl formal, polyamide, or an amino resin, isocyanate, trihydroxyethyl isocyanate, triazine resin, or phenol resin. A resin composition containing phenol formaldehyde resin or the like is used.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

このような多芯平行接着線にあっては、その端末処理な
どの際に、絶縁芯線1間の分離が必要になるが、接着層
4が強固に芯線1に接着しているため芯線1の分離作業
が困難であり、時には第2図に示すように絶縁F43が
接着層4に取られ、絶縁層3が損傷して導体2が露出す
ることもある。
In such a multicore parallel bonded wire, it is necessary to separate the insulated core wires 1 when processing the terminals, but since the adhesive layer 4 is firmly bonded to the core wire 1, the core wires 1 are separated. Separation is difficult, and sometimes the insulation F43 is taken by the adhesive layer 4, as shown in FIG. 2, and the insulation layer 3 is damaged and the conductor 2 is exposed.

このため、従来は絶縁芯線1表面に予めワックス、ロウ
、WJ′Wi油−などの離型剤を塗布しておき、ついで
接着樹脂組成物を塗布して絶縁芯線1・・・を接着一体
化する方法がとられている。
For this reason, conventionally, a release agent such as wax, wax, or WJ'Wi oil is applied to the surface of the insulated core wire 1 in advance, and then an adhesive resin composition is applied to bond and integrate the insulated core wires 1... A method is being taken to do so.

しかしながら、この離型剤の塗布によるものでは、絶縁
芯線1・・・間の接着強度が低下したり、ばらついたり
する不都合が生じ、また多芯平行接着線の外観不良を招
く不都合も生じる。
However, this application of a mold release agent has disadvantages in that the adhesive strength between the insulated core wires 1 is reduced or varies, and also causes a defect in the appearance of the multi-filamentary parallel bonded wire.

〔問題点を解決するための手段〕[Means for solving problems]

この発明では、接着層をなず接着樹脂組成物として高級
脂肪酸、末端反応性シリコーンオイル、末端反応性フッ
素油を含有したものを用いることにより、上記問題点を
解決するようにした。
In this invention, the above-mentioned problems are solved by using an adhesive resin composition containing a higher fatty acid, a terminally reactive silicone oil, and a terminally reactive fluorine oil as the adhesive layer.

この発明の多芯平行接着線は、その接着層をなす接着樹
脂組成物として、ポリアミド、ポリビニルブチラール、
エポキシ樹脂、ポリエステル、ポリヒドロキシエーテル
のいずれか1種もしくは2種以上組合せた樹脂もしくは
これに、 アミノ樹脂、安定化イソシアネート、トリアジン樹脂、
フェノール樹脂、フェノールホルムアルデヒド樹脂のい
ずれか1種もしくは2種以上を配合してなる組成物10
0重量部に対し、高級脂肪酸、末端反応性シリコーンオ
イル、末端反応性フッ素油のいずれか1種もしくは2種
以上を0.1〜20重司部配合してなるものを用いるも
のであり、従来から用いられている接着樹脂組成物に高
級脂肪酸、末端反応性シリコーンオイル、末端反応性フ
ッ素油を配合したものを用いる点に特徴がある。
The multicore parallel adhesive wire of the present invention uses polyamide, polyvinyl butyral, polyvinyl butyral, polyamide, polyvinyl butyral,
Epoxy resin, polyester, polyhydroxy ether, or a combination of two or more of them, amino resin, stabilized isocyanate, triazine resin,
Composition 10 containing one or more of phenol resin and phenol formaldehyde resin
A product containing 0.1 to 20 parts by weight of one or more of higher fatty acids, terminally reactive silicone oils, and terminally reactive fluorine oils per 0 parts by weight is used. It is characterized by the fact that it uses an adhesive resin composition that is used in combination with a higher fatty acid, a terminally reactive silicone oil, and a terminally reactive fluorine oil.

この発明における接着樹脂組成物のベースポリマーとし
ては、ポリアミド(ナイロン)、ポリビニルブチラール
、エポキシ樹脂、ポリエステル、ポリヒドロキシエーテ
ルのいずれか1種もしくは2種以上のブレンドポリマー
あるいはこれに耐熱性向上の目的でアミノ樹脂、安定化
イソシアネート、トリアジン樹脂、フェノール樹脂、フ
ェノールホルムアルデヒド樹脂の熱硬化性樹脂の1種も
しくは2種以上を配合したものが用いられる。熱硬化性
樹脂を配合した時のベースポリマー中におけるその配合
割合は重量比で1〜80%程度とされる。
The base polymer of the adhesive resin composition in this invention may be one or more blended polymers of polyamide (nylon), polyvinyl butyral, epoxy resin, polyester, and polyhydroxy ether, or a blend polymer of two or more thereof, or a blend polymer of two or more of polyamide (nylon), polyvinyl butyral, epoxy resin, polyester, and polyhydroxy ether, or a blend polymer of two or more of polyamide (nylon), polyvinyl butyral, epoxy resin, polyester, and polyhydroxy ether, or One or a mixture of two or more of thermosetting resins such as amino resin, stabilized isocyanate, triazine resin, phenol resin, and phenol formaldehyde resin is used. When the thermosetting resin is blended, the blending ratio in the base polymer is about 1 to 80% by weight.

このベースポリマーに添加される高級脂肪酸としては、
炭素数4〜34程度の脂肪酸およびその誘導体が用いら
れ、飽和脂肪酸としてはカプロン酸、カプリル酸、カプ
リン酸、ラウリン酸、パルミチン酸、ステアリン酸、ア
ラキン酸、ベヘン酸などが例示され、誘導体としてはこ
れらのエステル、酸ハロゲン化物が用いられ、また不飽
和脂肪酸としてはオレイン酸、リノール酸などが例示さ
れ、誘導体としてはこれらのエステル、酸ハロゲン化物
が用いられる。
The higher fatty acids added to this base polymer include:
Fatty acids having about 4 to 34 carbon atoms and their derivatives are used. Examples of saturated fatty acids include caproic acid, caprylic acid, capric acid, lauric acid, palmitic acid, stearic acid, arachidic acid, and behenic acid. These esters and acid halides are used, and examples of the unsaturated fatty acids include oleic acid and linoleic acid, and as the derivatives, these esters and acid halides are used.

また、ベースポリマーに添加される末端反応性シリコー
ンオイルとしては、 一般式(I) (ただし、Heはメチル基を示し、Xは、−(CHz 
) l 0H1−(C1lz ) l NlI2、−I
f、−CIl=CI+2、−C3If 60C2H40
il、−C2HB O−Cl1z、 −Ctl−CH゛
。′ OC1+。
In addition, the terminal-reactive silicone oil added to the base polymer has the general formula (I) (where He represents a methyl group and X represents -(CHz
) l 0H1-(C1lz) l NlI2, -I
f, -CIl=CI+2, -C3If 60C2H40
il, -C2HB O-Cl1z, -Ctl-CH゛. 'OC1+.

等の反応性の基を示し、m、nは1以上の整数である。m and n are integers of 1 or more.

)で表される、両末端に反応性の基を有する化合物、も
しくは 一般式(II) で表される(ただし、He、 X 、 III 、 n
は(I)式と同様である。)、片末端に反応性の基を有
する化合物である。
), or a compound having a reactive group at both ends, or a compound represented by the general formula (II) (where He, X, III, n
is the same as formula (I). ), is a compound having a reactive group at one end.

この末端反応性シリコーンオイルの代表的な具体例を示
すと、両末端に反応性の基を有するものでは、チッソ株
式会社製サイラブレーンFM1111、同1121、同
1125、同223L同2241、同2242、同33
11、同3321、同3325、同441L同4421
、同4425、同5511、同552L同5525、信
越化学工業株式会社製シリコーンオイルX−22−16
0AS、同X−22−160A、 jiJX−22−1
608,同X−22−160G、 同X−22−161
AS、同X−22−161A1X−22−16181同
X−22−161Cなどであり、片末端に反応性の雄を
有するものでは、チッソ株式会社製サイラブレーンFM
O411、同0421、同0511、同0521、同0
525、同0711、同0721、同0725等であり
、これらを1種または2種以上組み合わせて用いられる
Typical specific examples of this terminal-reactive silicone oil include those having reactive groups at both ends: Silablane FM1111, 1121, 1125, 223L, 2241, 2242, manufactured by Chisso Corporation; Same 33
11, 3321, 3325, 441L 4421
, 4425, 5511, 552L 5525, Silicone oil X-22-16 manufactured by Shin-Etsu Chemical Co., Ltd.
0AS, X-22-160A, jiJX-22-1
608, X-22-160G, X-22-161
AS, X-22-161A1
O411, 0421, 0511, 0521, 0
525, 0711, 0721, 0725, etc., and these may be used alone or in combination of two or more.

さらに、末端反応性フッ素油としては、一般式(III
) 1100c (C112) JCs  Ha  ’7−
a   +* (III )(ただし、Jは2〜15の
整数、aは0〜6の整数である。) で表わされる含フツ素化合物であり、具体的には同村製
油製HF−ICなどが用いられる。
Furthermore, as the terminal-reactive fluorine oil, general formula (III
) 1100c (C112) JCs Ha '7-
It is a fluorine-containing compound represented by a + * (III) (J is an integer of 2 to 15, a is an integer of 0 to 6), and specifically, HF-IC manufactured by Domura Oil Co., Ltd. used.

これら高級脂肪酸、末端反応性シリコーンオイルおよび
末端反応性フッ素油は、単独もしくは2種以上混合して
上記ベースポリマーに添加して用いられる、これらのベ
ースポリマーの配合量はベースポリマー100重信部に
対して0.1〜20重ω部とされ、0.11fit部未
満では得られる多芯平行接着線の端末の線分は性および
表面潤滑性が得られず、20重缶部を越えると芯線間の
接着力不足や多芯平行接着線の外観不良を招いて不都合
を来たす。
These higher fatty acids, terminally reactive silicone oils, and terminally reactive fluorine oils are used alone or as a mixture of two or more of them and are added to the above base polymer.The blending amount of these base polymers is based on 100 parts by weight of the base polymer. If the fit is less than 0.11 fit, the terminal segments of the multifilamentary parallel bonded wire will not have good properties and surface lubricity, and if it exceeds 20 fit, the line between the core wires will This causes inconveniences such as insufficient adhesive strength and poor appearance of multi-core parallel adhesive lines.

この発明の多芯平行接着線の製造方法としては1、E記
ベースポリマーに所定量の高級脂肪酸、末端反応性シリ
コーンオイル、末端反応性フッ素油のいずれか1種を配
合してなる接着樹脂組成物を、クレゾール、シクロヘキ
サノン、ピロリドン、フェノール、キシレン、ソルベン
トナフサなどの溶剤とシンナーの混合物に溶解して接着
ワニスとし、この接着ワニスを芯線上に塗布、焼付けて
Bステージ(半硬化状態)としたのち、これらの芯線を
複数本平行に並べて加熱あるいは溶剤活性化等の手段に
より相互に接着し一体化する方法や複数本の芯線を平行
に並べておき、これに上記接着ワニスを塗布、焼付けて
、接着し一体化する方法などがある。
The method for manufacturing the multi-filamentary parallel adhesive wire of the present invention is as follows: 1. An adhesive resin composition prepared by blending a predetermined amount of higher fatty acid, terminal-reactive silicone oil, or terminal-reactive fluorine oil with base polymer E. The material is dissolved in a mixture of solvent and thinner such as cresol, cyclohexanone, pyrrolidone, phenol, xylene, and solvent naphtha to make an adhesive varnish, and this adhesive varnish is applied onto the core wire and baked to obtain a B stage (semi-hardened state). Thereafter, a method of arranging a plurality of these core wires in parallel and adhering them to each other and integrating them by means such as heating or solvent activation, or arranging a plurality of core wires in parallel, applying the above-mentioned adhesive varnish to this and baking it, There are methods such as gluing and integrating.

このような多芯平行接着線にあっては、接着層をなす接
着樹脂組成物中に特定量の高級脂肪酸、末端反応性シリ
コーンオイル、末端反応性フッ素油が含有されているの
で、芯線間の接着力が十分となるにもかかわらず、多芯
平行接着線の末端での芯線の分離が容易に行われ、分離
の際に芯線の絶縁層が破損するようなこともなくなる。
In such multicore parallel adhesive wires, the adhesive resin composition forming the adhesive layer contains specific amounts of higher fatty acids, terminally reactive silicone oil, and terminally reactive fluorine oil, so that the bond between the core wires is Although the adhesive force is sufficient, the core wires can be easily separated at the ends of the multi-core parallel bonded wire, and the insulating layer of the core wires will not be damaged during separation.

また、接e層表面も表面潤滑性を有し、巻線時に加工傷
がつきにくくなる。
Furthermore, the surface of the contact layer also has surface lubricity, making it difficult for processing scratches to occur during winding.

〔実施例〕〔Example〕

(実施例1) ポリビニルブチラール樹脂の100重量部に、信越化学
■製シリコーンX−22−160ASの5重信部、シク
ロヘキサノン1501ffi部、ソルベントナフサ10
0重口部、キシレン50重量部を加え60℃で2時間混
合したのち90℃で3゜5時間撹拌し、透明な接着ワニ
スを得た。
(Example 1) To 100 parts by weight of polyvinyl butyral resin, 5 parts of silicone
0 parts by weight and 50 parts by weight of xylene were added and mixed at 60°C for 2 hours, followed by stirring at 90°C for 3.5 hours to obtain a transparent adhesive varnish.

(実施例2) ポリアミド樹脂の100重量部に、チッソ@J製シリコ
ーンFMO521の5重信部、m−クレゾールの400
重量部を加え120℃で6時間撹拌したのら、160℃
で2時間撹拌し、かっ色透明な接着ワニスを得た。
(Example 2) To 100 parts by weight of polyamide resin, 5 parts of silicone FMO521 manufactured by Chisso@J and 400 parts of m-cresol were added.
After adding parts by weight and stirring at 120°C for 6 hours, the mixture was heated to 160°C.
The mixture was stirred for 2 hours to obtain a brown transparent adhesive varnish.

(実施例3) ポリビニルブチラール樹脂100項五部に、信越化学■
製シリコーンX−22−1618の5川9部、イソシア
ネートMDIの20重回部、シクロへキサノン20Of
flff1部、キシレン100重量部を加え、90℃で
1時間撹拌して透明な接着ワニスを得た。
(Example 3) Shin-Etsu Chemical ■5 parts of polyvinyl butyral resin 100 items
5 parts of silicone X-22-1618, 20 parts of isocyanate MDI, 20 parts of cyclohexanone
1 part of flff and 100 parts by weight of xylene were added and stirred at 90°C for 1 hour to obtain a transparent adhesive varnish.

(実施例4) フェノキシ樹脂100重量部に、チッソ■製シリコーン
FMO421の5重ω部、イソシアネートMD1の25
重量部、シクロへキサノン200重聞部、キシレン15
0重R部を加え、80℃で撹拌して透明な接着ワニスを
得た。
(Example 4) To 100 parts by weight of phenoxy resin, 5 parts of silicone FMO421 manufactured by Chisso ■ and 25 parts of isocyanate MD1 were added.
Parts by weight, 200 parts of cyclohexanone, 15 parts of xylene
0 weight R part was added and stirred at 80°C to obtain a transparent adhesive varnish.

(実施例5) エポキシ樹脂20重量部に、チッソ■製シリコ−:/F
M3321(7)4重fLilFMO511(7)2f
fi吊部、m−クレゾールの450重量部を加え70℃
で3時間、次いで160℃で4時間加熱撹拌し、50℃
とした後、ポリアミド樹脂601ffi部を加え、1.
5時間撹拌してかっ色透明な接着ワニスを得た。
(Example 5) 20 parts by weight of epoxy resin was added to Chisso's Silico:/F.
M3321 (7) Quadruple fLilFMO511 (7) 2f
450 parts by weight of m-cresol was added to the fi hanging part and heated at 70°C.
for 3 hours, then heated and stirred at 160°C for 4 hours, and heated to 50°C.
After that, 601ffi parts of polyamide resin was added, and 1.
After stirring for 5 hours, a brown transparent adhesive varnish was obtained.

(実施例6) ポリアミド樹脂の100重量部に、チッソ■製シリコー
ンFMO525の10重開部、クレゾールの550重h
1部を加え70℃で8時間、撹拌してかっ色透明の接着
ワニスを得た。
(Example 6) 100 parts by weight of polyamide resin, 10 parts by weight of silicone FMO525 manufactured by Chisso ■, and 550 parts by weight of cresol.
1 part was added and stirred at 70°C for 8 hours to obtain a brown transparent adhesive varnish.

(実施例7) ポリビニルブチラール樹脂の100fflffi部に、
ヘキストン+1パ2社製へキストワックスS(モンタン
ワックス酸)の5重ω部、シクロへキサノン200重ω
部、ソルベントナフサ100重R部、を加え135℃で
4時間加熱してかっ色透明な接着ワニスを得た。
(Example 7) 100fflffi parts of polyvinyl butyral resin,
5-fold ω part of Hexistone + 1 Pa2 manufactured by Hexistwax S (montan wax acid), cyclohexanone 200-fold ω part
100 parts by weight of solvent naphtha were added and heated at 135° C. for 4 hours to obtain a brown transparent adhesive varnish.

(実施例8) ポリビニルブチラール樹脂の100重ffi部に、岡村
製油製末端反応フッ素油HF−IC5重泪部、シクロへ
キサノン200重ffi部、ソルベントナフサ100重
量部を加え135℃で4時間加熱撹拌して、かっ色透明
な接着ワニスを得た。
(Example 8) To 100 parts by weight of polyvinyl butyral resin, 200 parts by weight of terminal-reacted fluorinated oil HF-IC5 manufactured by Okamura Oil Co., Ltd., 200 parts by weight of cyclohexanone, and 100 parts by weight of solvent naphtha were added and heated at 135°C for 4 hours. After stirring, a brown transparent adhesive varnish was obtained.

上記実施例1〜8のワニスを0.1mφウレタンエナメ
ル線を7本平行に並べたものの外周に塗布焼付けた。
The varnishes of Examples 1 to 8 above were applied and baked on the outer periphery of seven 0.1 mφ urethane enameled wires arranged in parallel.

(比較例1) 0、1mφウレタンエナメル線の最外周に流動パラフィ
ンを塗布したものを7本平行にならべ、この外周にポリ
アミド樹脂100重量部i部にm−クレゾールの400
重量部を加え混合した接着ワニスを塗布焼付けた。
(Comparative Example 1) Seven 0.1 mφ urethane enameled wires coated with liquid paraffin on the outermost periphery were arranged in parallel, and 100 parts by weight of polyamide resin and 400 parts by weight of m-cresol were applied to the outer periphery of the wires.
Adhesive varnish mixed with weight parts was applied and baked.

(比較例2) 流動パラフィンの代わりに、マイクロクリスタンワック
ス2重M部をヘプタン98重闇部に溶かしたものを用い
た他は比較例1と同じ。
(Comparative Example 2) Same as Comparative Example 1 except that instead of liquid paraffin, microcrystan wax 2x M part dissolved in heptane 98x dark part was used.

(比較例3) シ!JD−ンX−22−160ASを0.05重量部と
した他は実施例1と同じ。
(Comparative Example 3) Shi! Same as Example 1 except that JD-ON X-22-160AS was used in an amount of 0.05 parts by weight.

(比較例4) シリD−ンX−22−160ASを301ffi部とし
た他は実施例1と同じ。
(Comparative Example 4) Same as Example 1 except that 301 ffi parts of Silicon D-ON X-22-160AS were used.

この場合、ワニスかにごり、均一な接着ワニスが1qら
れなかった。
In this case, the varnish was cloudy and a uniform adhesive varnish could not be obtained.

以上のようにして得られた多芯平行接着線について、芯
線間接着力、芯線弁ll!後の絶縁層の損傷の有無、可
撓性、表面の静摩擦係数を評価した。
Regarding the multi-core parallel bonded wire obtained as described above, the adhesive force between the cores, the core wire valve ll! The presence or absence of damage to the subsequent insulating layer, flexibility, and coefficient of static friction of the surface were evaluated.

結果を別表に示す。The results are shown in the attached table.

別表より明らかなように、この発明の多芯平行接着線で
は、芯線間の接着力が十分に高く、かつ芯線分離が容易
に行え、また表面の潤滑性も優れていることがわかる。
As is clear from the attached table, it can be seen that the multifilamentary parallel bonded wire of the present invention has sufficiently high adhesion between the cores, can be easily separated, and has excellent surface lubricity.

〔発明の効果〕〔Effect of the invention〕

以上説明したように、この発明の多芯平行接着線は、そ
の接着層をなす接着樹脂組成物に高級脂肪酸、末端反応
性シリコーンオイル、末端反応性フッ素油のいずれか1
種以上を特定m配合したものであるので、芯線間の接着
力が十分高くしかも芯線間の分離が容易いに行え、芯線
の絶縁層を芯線分離の際に損傷することもない。また、
接着層表面が潤滑性を有し、巻線加工時などの際に加工
10を受けることもない。さらに、従来の芯線上に離型
剤を塗布したのち、接着層を形成したものに比べて芯線
間の接着力のバラツキが小さく、また製造工程の短縮化
が可能となるなどの効果を得ることができる。  。
As explained above, the multifilamentary parallel adhesive wire of the present invention has an adhesive resin composition that forms the adhesive layer containing one of higher fatty acids, terminally reactive silicone oil, and terminally reactive fluorine oil.
Since it is a mixture of a specific number of species or more, the adhesive force between the core wires is sufficiently high, and the core wires can be easily separated, and the insulating layer of the core wires will not be damaged when the core wires are separated. Also,
The surface of the adhesive layer has lubricity and is not subjected to processing 10 during winding processing. Furthermore, compared to the conventional method in which a release agent is applied to the core wire and then an adhesive layer is formed, the variation in adhesive strength between the core wires is smaller, and the manufacturing process can be shortened. Can be done. .

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

第1図はこの発明に係わる多芯平行接着線の例を示す概
略断面図、第2図は同じく多芯平行接着線の芯線分離の
際の絶縁層損傷の状況を示1j概略断面図である。 1・・・絶縁芯線 2・・・導体 3・・・絶縁層 4・・・接@層
FIG. 1 is a schematic cross-sectional view showing an example of a multi-core parallel bonded wire according to the present invention, and FIG. 2 is a schematic cross-sectional view 1j showing the state of insulation layer damage when the cores of the multi-core parallel bonded wire are separated. . 1... Insulated core wire 2... Conductor 3... Insulating layer 4... Contact layer

Claims (1)

【特許請求の範囲】 絶縁芯線を複数本平行に接着樹脂組成物で接着してなる
多芯平行接着線において、 上記接着樹脂組成物が、 ポリアミド、ポリビニルブチラール、エポキシ樹脂、ポ
リエステル、ポリヒドロキシエーテルのいずれか1種も
しくは2種以上組合せた樹脂もしくはこれに、 アミノ樹脂、安定化イソシアネート、トリアジン樹脂、
フェノール樹脂、フェノールホルムアルデヒド樹脂のい
ずれか1種もしくは2種以上を配合してなる組成物10
0重量部に対し、 高級脂肪酸、末端反応性シリコーンオイル、末端反応性
フッ素油のいずれか1種もしくは2種以上を0.1〜2
0重量部配合してなるものであることを特徴とする多芯
平行接着線。
[Claims] A multi-filament parallel bonded wire formed by bonding a plurality of insulated core wires in parallel with an adhesive resin composition, wherein the adhesive resin composition is made of polyamide, polyvinyl butyral, epoxy resin, polyester, polyhydroxyether. Any one or a combination of two or more resins, or an amino resin, a stabilized isocyanate, a triazine resin,
Composition 10 containing one or more of phenol resin and phenol formaldehyde resin
0.1 to 2 parts by weight of one or more of higher fatty acids, terminally reactive silicone oils, and terminally reactive fluorine oils.
A multi-filamentary parallel adhesive wire characterized in that it contains 0 parts by weight.
JP32458687A 1987-12-22 1987-12-22 Multicore parallel adhesive wire Pending JPH01166410A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32458687A JPH01166410A (en) 1987-12-22 1987-12-22 Multicore parallel adhesive wire

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32458687A JPH01166410A (en) 1987-12-22 1987-12-22 Multicore parallel adhesive wire

Publications (1)

Publication Number Publication Date
JPH01166410A true JPH01166410A (en) 1989-06-30

Family

ID=18167468

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32458687A Pending JPH01166410A (en) 1987-12-22 1987-12-22 Multicore parallel adhesive wire

Country Status (1)

Country Link
JP (1) JPH01166410A (en)

Cited By (13)

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Publication number Priority date Publication date Assignee Title
US5359150A (en) * 1992-09-30 1994-10-25 Murata Mfg. Co., Ltd. Wire ribbon
US5428189A (en) * 1992-10-30 1995-06-27 Daimler-Benz Ag Cable arrangement
JP2006085906A (en) * 2004-09-14 2006-03-30 Totoku Electric Co Ltd Super heat resistant self-welding wire and super heat resistant voice coil for speaker
US8986586B2 (en) 2009-03-18 2015-03-24 Southwire Company, Llc Electrical cable having crosslinked insulation with internal pulling lubricant
US9142336B2 (en) 2004-09-28 2015-09-22 Southwire Company, Llc Method of manufacturing electrical cable, and resulting product, with reduced required installation pulling force
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US9431152B2 (en) 2004-09-28 2016-08-30 Southwire Company, Llc Method of manufacturing electrical cable, and resulting product, with reduced required installation pulling force
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Publication number Priority date Publication date Assignee Title
US5359150A (en) * 1992-09-30 1994-10-25 Murata Mfg. Co., Ltd. Wire ribbon
US5428189A (en) * 1992-10-30 1995-06-27 Daimler-Benz Ag Cable arrangement
JP2006085906A (en) * 2004-09-14 2006-03-30 Totoku Electric Co Ltd Super heat resistant self-welding wire and super heat resistant voice coil for speaker
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