JP3364372B2 - Insulated wire - Google Patents

Insulated wire

Info

Publication number
JP3364372B2
JP3364372B2 JP24514495A JP24514495A JP3364372B2 JP 3364372 B2 JP3364372 B2 JP 3364372B2 JP 24514495 A JP24514495 A JP 24514495A JP 24514495 A JP24514495 A JP 24514495A JP 3364372 B2 JP3364372 B2 JP 3364372B2
Authority
JP
Japan
Prior art keywords
insulated wire
mol
anhydride
insulating
ethylene glycol
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 - Lifetime
Application number
JP24514495A
Other languages
Japanese (ja)
Other versions
JPH0973817A (en
Inventor
節夫 寺田
利樹 山田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dainichiseika Color and Chemicals Mfg Co Ltd
Ukima Chemicals and Color Mfg Co Ltd
Original Assignee
Dainichiseika Color and Chemicals Mfg Co Ltd
Ukima Chemicals and Color Mfg Co 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 Dainichiseika Color and Chemicals Mfg Co Ltd, Ukima Chemicals and Color Mfg Co Ltd filed Critical Dainichiseika Color and Chemicals Mfg Co Ltd
Priority to JP24514495A priority Critical patent/JP3364372B2/en
Publication of JPH0973817A publication Critical patent/JPH0973817A/en
Application granted granted Critical
Publication of JP3364372B2 publication Critical patent/JP3364372B2/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)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、半田付け性及び耐
熱性に優れる絶縁電線に関する。
TECHNICAL FIELD The present invention relates to an insulated wire having excellent solderability and heat resistance.

【0002】[0002]

【発明が解決しようとする課題】従来、絶縁皮膜を剥離
することなく、直接半田付けが出来る絶縁電線として、
ポリウレタン絶縁電線が広く使用されている。しかしな
がら、近年においては、電気機器の小型化及び高性能化
に伴い、機器の使用雰囲気温度が上昇する場合が多く、
電気機器の使用材料である絶縁電線の耐熱性化が要求さ
れている。従って、従来のポリウレタン絶縁電線では耐
熱性の要求に満足できない用途が現われてきている。ま
た、一方では絶縁電線の端末処理の簡便さから、ポリウ
レタン絶縁電線と同様に絶縁皮膜を剥離することなく半
田付けの出来る絶縁電線が望まれている。
Conventionally, as an insulated wire that can be directly soldered without peeling off the insulating film,
Polyurethane insulated wire is widely used. However, in recent years, with the miniaturization and high performance of electric devices, the operating ambient temperature of the devices often rises,
Heat resistance of insulated wires, which is a material used for electric equipment, is required. Therefore, the conventional polyurethane insulated wire has come to be used in applications that cannot satisfy the heat resistance requirement. On the other hand, an insulated wire that can be soldered without peeling off the insulating film is desired, as in the case of the polyurethane insulated wire, because of the ease of end treatment of the insulated wire.

【0003】上記ポリウレタン絶縁電線に変るものとし
て、同様に絶縁皮膜を剥離することなく半田付けの出来
るポリエステルイミド絶縁電線やポリエステルイミドウ
レタン絶縁電線等が開発され一部用途に使用されている
が、ポリエステルイミド絶縁電線では耐熱性は充分なも
のの半田付け性はポリウレタン絶縁電線に大きく劣り、
ポリエステルイミドウレタン絶縁電線では半田付け性は
ほぼ満足し得るものの耐熱性においては要求を充分には
満足していない。従って、半田付け性及び耐熱性を兼ね
備えた絶縁電線の開発が強く要求されている。
As a substitute for the above-mentioned polyurethane insulated wire, polyesterimide insulated wire or polyesterimide urethane insulated wire which can be soldered without peeling off the insulating film has been developed and used for some applications. Although imide-insulated wires have sufficient heat resistance, their solderability is significantly inferior to polyurethane-insulated wires.
Polyester imide urethane insulated electric wire can almost satisfy the solderability, but does not sufficiently satisfy the demand for heat resistance. Therefore, development of an insulated wire having both solderability and heat resistance is strongly required.

【0004】[0004]

【課題を解決するための手段】本発明者は、上記課題に
つき鋭意検討した結果、多価アルコールと無水トリメリ
ット酸及び/又は無水ピリメリット酸とポリイソシアネ
ートとを反応させて得られる、分子中にウレタン結合、
アミド結合及びイミド結合を有する樹脂を含む絶縁塗料
を導体上に塗布及び焼付けしてなる絶縁層を有すること
を特徴とする絶縁電線が得られる事を見出し、本発明を
達成するに至った。
Means for Solving the Problems As a result of extensive studies on the above problems, the present inventor has found that polyhydric alcohols and anhydrous trimellitic acid
Urethane bond in the molecule, which is obtained by reacting polyamic acid with formic acid and / or pyrimellitic anhydride .
The inventors have found that an insulated wire having an insulating layer obtained by applying and baking an insulating coating material containing a resin having an amide bond and an imide bond on a conductor is obtained, and the present invention has been accomplished.

【0005】特定の樹脂を含む絶縁塗料を用いることに
よって、優れた半田付け性及び耐熱性を兼ね備えた絶縁
電線が提供される。
By using an insulating coating material containing a specific resin, an insulated wire having excellent solderability and heat resistance is provided.

【0006】[0006]

【発明の実施の形態】次に発明の実施の形態を挙げて本
発明を更に詳しく説明する。本発明で使用する絶縁塗料
は、多価アルコール20〜45モル%と多価カルボン酸
又はその誘導体30〜5モル%、及びこれら両者を加え
たモル数に対し0.8〜1.10の比となるモル%のポ
リイソシアネートとを反応させて得られる樹脂を含む絶
縁塗料である。上記多価アルコールとしてはエチレング
リコールが、多価カルボン酸又はその誘導体としては無
水トリメリット酸及び/又は無水ピロリット酸が、そ
してポリイソシアネートとしてはジフェニルメタンジイ
ソシアネートが好ましい。
BEST MODE FOR CARRYING OUT THE INVENTION Next, the present invention will be described in more detail with reference to embodiments of the invention. The insulating coating used in the present invention has a polyhydric alcohol of 20 to 45 mol% and a polycarboxylic acid or its derivative of 30 to 5 mol%, and a ratio of 0.8 to 1.10. It is an insulating coating material containing a resin obtained by reacting a polyisocyanate of which mol% is The ethylene glycol as a polyhydric alcohol, polycarboxylic acid or trimellitic anhydride and / or pyromellitic anhydride benefits acids as derivatives thereof, and diphenylmethane diisocyanate are preferred as polyisocyanates.

【0007】本発明に用いられる塗料は、ジフェニルメ
タンジイソシアネートとエチレングリコール及び無水ト
リメリット酸及び/又は無水ピロリット酸とを反応さ
せて得られるものであり、イソシアネート基とアルコー
ル基との間にウレタン結合を、イソシアネート基と無水
トリメリット酸及び/又は無水ピロリット酸の酸無水
物構造との間にイミド結合を、更にイソシアネート基と
無水トリメリット酸及び/又は無水ピロリット酸のカ
ルボキシル基との間にアミド結合を有するものと考えら
れる。
[0007] Paint used in the present invention are those obtained by reacting a diphenylmethane diisocyanate and ethylene glycol and trimellitic acid and / or pyromellitic anhydride benefits anhydride, urethane between the isocyanate group and the alcohol group coupling the carboxyl group of an imide bond, and further isocyanate groups and trimellitic anhydride and / or pyromellitic anhydride benefits acids between the acid anhydride structure of the isocyanate groups and trimellitic anhydride and / or pyromellitic anhydride benefits acid It is considered to have an amide bond between and.

【0008】本発明に用いられる塗料を塗布焼付けして
なる絶縁層を有する絶縁電線は、ウレタン結合の存在が
優れた半田付け性を、イミド結合及びアミド結合の存在
が、優れた耐熱性を示すものと考えられる。上記の絶縁
塗料を調製するには、先ず、適当な溶媒中にて、ジフェ
ニルメタンジイソシアネートとエチレングリコールとを
常温にて反応させた後、無水トリメリット酸及び/又は
無水ピロリット酸を加えて加熱反応させればよい。
The insulated wire having an insulating layer formed by coating and baking the coating material used in the present invention exhibits excellent solderability due to the presence of urethane bonds, and excellent heat resistance due to the presence of imide bonds and amide bonds. It is considered to be a thing. In order to prepare the above-mentioned insulating paint, first, in a suitable solvent, diphenylmethane diisocyanate and ethylene glycol are reacted at room temperature, and then trimellitic anhydride and / or pyrolitic anhydride are added and reacted by heating. Just do it.

【0009】塗料を得るその他の方法としては、ジフェ
ニルメタンジイソシアネートとエチレングリコール、及
び無水トリメリット酸及び/又は無水ピロリット酸を
常温にて一括配合後、加熱反応させてもよい。ジフェニ
ルメタンジイソシアネートと無水トリメリット酸及び/
又は無水ピロリット酸を加熱反応後、エチレングリコ
ールを反応させることも可能である。
[0009] As another method for obtaining a paint, diphenylmethane diisocyanate and ethylene glycol, and after batch mixing trimellitic anhydride and / or pyromellitic anhydride benefits acid at room temperature, may be heated and reacted. Diphenylmethane diisocyanate and trimellitic anhydride and /
Or after heating the reaction of pyromellitic anhydride benefits acids, it is also possible to react the ethylene glycol.

【0010】エチレングリコールの一部を、本発明の目
的を損わない範囲で他のポリオール、例えば、グリセリ
ン、トリメチロールプロパン、トリス(2−ヒドロキシ
エチル)イソシアヌレート(THEIC)等に置き換え
ることも可能である。
It is also possible to replace a part of ethylene glycol with other polyols such as glycerin, trimethylolpropane, tris (2-hydroxyethyl) isocyanurate (THEIC), etc. within a range not impairing the object of the present invention. Is.

【0011】無水トリメリット酸の一部を、本発明の目
的を損わない範囲で他のポリカルボン酸、例えば、テレ
フタル酸、イソフタル酸、無水フタル酸等の芳香族ジカ
ルボン酸等に置き換えることも可能である。
It is also possible to replace a part of trimellitic anhydride with another polycarboxylic acid, for example, an aromatic dicarboxylic acid such as terephthalic acid, isophthalic acid, phthalic anhydride, etc. within a range not impairing the object of the present invention. It is possible.

【0012】本発明に用いる絶縁塗料に使用する溶剤
は、溶媒となるNMP、DMAC、DMF等に、キシレ
ン、ソルベントナフサ等の希釈剤を組合せることが好ま
しいが、フェノール類、クレゾール類、グリコールエー
テル類、アルコール類、ケトン類等通常の焼き付け塗料
に用いられる溶剤を使用するか一部加えてもよい。
The solvent used in the insulating coating material used in the present invention is preferably NMP, DMAC, DMF or the like, which is a solvent, in combination with a diluent such as xylene or solvent naphtha, but phenols, cresols, glycol ethers are preferred. Solvents used in ordinary baking paints such as alcohols, alcohols and ketones may be used or partly added.

【0013】本発明に用いる絶縁塗料には、本発明の特
徴を害しない範囲であれば、ポリアミド、ポリエステ
ル、ポリスルホン、ポリビニルホルマール、エポキシ等
の熱可塑性樹脂、ポリエステル、ポリエステルイミド、
ポリウレタン、ポリアミドイミド、メラミン樹脂、フェ
ノール樹脂等の熱硬化性樹脂、ジフェニルメタンジイソ
シアネート等のポリイソシアネートより得られる安定化
ポリイソシアネート化合物、染料、顔料、潤滑剤、その
他塗料用添加剤等を添加することも可能である。また、
必要に応じて、ナフテン酸やオクテン酸の金属塩、アル
キルアミン類やイミダゾール類等のアミン類、有機錫化
合物を触媒として添加することも可能である。
The insulating coating material used in the present invention is a thermoplastic resin such as polyamide, polyester, polysulfone, polyvinyl formal, or epoxy, polyester, polyester imide, as long as the characteristics of the present invention are not impaired.
Stabilized polyisocyanate compounds obtained from thermosetting resins such as polyurethane, polyamide imide, melamine resin, phenol resin, etc., polyisocyanates such as diphenylmethane diisocyanate, dyes, pigments, lubricants, and other additives for paints may also be added. It is possible. Also,
If necessary, metal salts of naphthenic acid and octenoic acid, amines such as alkylamines and imidazoles, and organic tin compounds can be added as catalysts.

【0014】本発明の絶縁電線を製造するには、上記の
塗料を適当な溶媒にて作業に適した粘度に調整後、軟銅
線等の導体上に常法に従って塗布、焼付けして絶縁層と
する。
In order to produce the insulated wire of the present invention, the above-mentioned paint is adjusted with a suitable solvent to a viscosity suitable for work, and then coated and baked on a conductor such as annealed copper wire according to a conventional method to form an insulating layer. To do.

【0015】更に、本発明の絶縁電線は、上記の塗料を
塗布、焼付けした絶縁層の上層に、他の諸特性を付与さ
せるために一般的に行なわれているごとく、他の絶縁塗
料を塗布、焼付けした絶縁層を設けることも可能であ
る。例えば、耐熱性を更に要求される場合にはポリイミ
ド系絶縁塗料またはポリアミドイミド系塗料、巻線性を
要求される場合には6,6−ナイロンのようなポリアミ
ド系塗料、コイル形状自己保持化を要求される場合には
自己融着塗料、例えば、ポリビニルブチラール、エポキ
シ、フェノキシ、ポリエステル、ポリアミド、ポリスル
ホン系塗料がある。
Further, the insulated wire of the present invention is coated with the above-mentioned paint, and is coated with another insulating paint, as is generally done in order to give various characteristics to the upper layer of the insulating layer. It is also possible to provide a baked insulating layer. For example, when heat resistance is further required, polyimide-based insulating paint or polyamide-imide-based paint, when winding property is required, polyamide-based paint such as 6,6-nylon, coil shape self-holding is required. If so, there are self-fusing coatings such as polyvinyl butyral, epoxy, phenoxy, polyester, polyamide, polysulfone based coatings.

【0016】[0016]

【実施例】以下の実施例において、本発明の内容を説明
するが本発明はこれら実施例に限定されるものではな
い。 実施例1 エチレングリコール2.0モルと無水トリメリット酸
3.0モルをN−メチル−2−ピロリドン(以下NMP
と略記する)中にて室温にて0.5時間反応させた後、
ジフェニルメタンジイソシアネート4.8モルを加え加
温し120℃にて3時間反応させて得られた絶縁塗料
を、0.2mmの軟銅線上に皮膜厚0.015mmとな
るように常法に従って焼き付け、絶縁電線を得た。
The contents of the present invention will be described in the following examples, but the present invention is not limited to these examples. Example 1 2.0 mol of ethylene glycol and 3.0 mol of trimellitic anhydride were mixed with N-methyl-2-pyrrolidone (hereinafter referred to as NMP).
(Hereinafter abbreviated as)) at room temperature for 0.5 hours,
The insulating coating obtained by adding 4.8 mol of diphenylmethane diisocyanate and heating and reacting at 120 ° C. for 3 hours is baked on a 0.2 mm soft copper wire according to a conventional method so that the film thickness becomes 0.015 mm, Got

【0017】実施例2 エチレングリコール3.0モルと無水トリメリット酸
2.0モルをNMP中にて室温にて0.5時間反応させ
た後、ジフェニルメタンジイソシアネート4.8モルを
加え加温し120℃にて3時間反応させて得られた絶縁
塗料を、実施例1と同様にして焼き付け、絶縁電線を得
た。
Example 2 3.0 mol of ethylene glycol and 2.0 mol of trimellitic anhydride were reacted in NMP at room temperature for 0.5 hours, and then 4.8 mol of diphenylmethane diisocyanate was added and heated to 120. The insulating paint obtained by reacting at 3 ° C. for 3 hours was baked in the same manner as in Example 1 to obtain an insulated electric wire.

【0018】実施例3 エチレングリコール4.0モルと無水トリメリット酸
1.0モルをNMP中にて室温にて0.5時間反応させ
た後、ジフェニルメタンジイソシアネート4.8モルを
加え加温し120℃にて3時間反応させて得られた絶縁
塗料を、実施例1と同様にして焼き付け、絶縁電線を得
た。
Example 3 4.0 mol of ethylene glycol and 1.0 mol of trimellitic anhydride were reacted in NMP at room temperature for 0.5 hour, and then 4.8 mol of diphenylmethane diisocyanate was added and heated to 120. The insulating paint obtained by reacting at 3 ° C. for 3 hours was baked in the same manner as in Example 1 to obtain an insulated electric wire.

【0019】比較例1 エチレングリコール1.0モルと無水トリメリット酸
4.0モルをNMP中にて室温にて0.5時間反応させ
た後、ジフェニルメタンジイソシアネート4.8モルを
加え加温し120℃にて3時間反応させて得られた絶縁
塗料を、実施例1と同様にして焼き付け、絶縁電線を得
た。
Comparative Example 1 1.0 mol of ethylene glycol and 4.0 mol of trimellitic anhydride were reacted in NMP at room temperature for 0.5 hours, and then 4.8 mol of diphenylmethane diisocyanate was added and heated to 120. The insulating paint obtained by reacting at 3 ° C. for 3 hours was baked in the same manner as in Example 1 to obtain an insulated electric wire.

【0020】比較例2 半田付けの出来るポリエステルイミド塗料(弊社製商品
名FS−2)を用いて実施例1と同様にして絶縁電線を
得た。
Comparative Example 2 An insulated electric wire was obtained in the same manner as in Example 1 by using a solderable polyester imide paint (trade name: FS-2 manufactured by our company).

【0021】比較例3 ポリエステルイミドウレタン塗料(弊社製商品名FS−
141)を用いて実施例1と同様にして絶縁電線を得
た。
Comparative Example 3 Polyesterimide urethane paint (trade name FS- manufactured by our company)
An insulated wire was obtained in the same manner as in Example 1 by using 141).

【0022】以上の実施例及び比較例の各絶縁電線につ
いて、外観、可撓性、伸張ピンホール性、軟化点、絶縁
破壊電圧、耐熱衝撃性、半田付け性の各試験を行なった
結果を後記表1に示した。なお、試験方法はJIS C
3003に従って測定した。
With respect to each of the insulated wires of the above Examples and Comparative Examples, the results of the appearance, flexibility, extension pinhole property, softening point, dielectric breakdown voltage, thermal shock resistance, and solderability tests were given. The results are shown in Table 1. The test method is JIS C
It was measured according to 3003.

【0023】表1 注1)絶縁破壊電圧残存率 220℃7日劣化後の絶縁
破壊電圧の初期値に対する残存率 注2)耐熱衝撃性 20%伸張 220℃1時間 注3)半田付け性 半田浴温度400℃ 但し、比較例
1は460℃
Table 1 Note 1) Dielectric breakdown voltage residual rate 220 ° C 7 days after degrading dielectric breakdown voltage to the initial value Note 2) Thermal shock resistance 20% extension 220 ° C 1 hour Note 3) Solderability Solder bath temperature 400 ° C Comparative Example 1 is 460 ° C

【0024】表1の結果から、本発明の絶縁電線は、従
来の半田付けの出来るポリエステルイミド絶縁電線に比
べ、極めて良好な半田付け性を示している。また、ポリ
エステルイミドウレタン絶縁電線に対しては同等の半田
付け性にもかかわらず優れた耐熱性を示している。
From the results shown in Table 1, the insulated wire of the present invention shows extremely good solderability as compared with the conventional solderable polyesterimide insulated wire. Further, it has excellent heat resistance to the polyester-imide-urethane insulated electric wire, although it has the same solderability.

【0025】[0025]

【発明の効果】本発明による絶縁電線は、優れた半田付
け性と高い耐熱性を兼ね備えており、近年の電子機器類
に用いる絶縁電線に対する特性要求に充分答えることが
出来る。
INDUSTRIAL APPLICABILITY The insulated wire according to the present invention has excellent solderability and high heat resistance, and can sufficiently meet the characteristic requirements for the insulated wire used in recent electronic devices.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 山田 利樹 東京都中央区日本橋馬喰町一丁目7番6 号 大日精化工業株式会社内 (56)参考文献 特開 平2−87607(JP,A) 特開 平8−264027(JP,A) 特開 平4−85378(JP,A) 特公 平4−69402(JP,B2) (58)調査した分野(Int.Cl.7,DB名) H01B 7/02 H01B 3/30 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Toshiki Yamada 1-7-6 Nihonbashi Bakuro-cho, Chuo-ku, Tokyo Dainichi Seika Kogyo Co., Ltd. (56) Reference JP-A-2-87607 (JP, A) Special Features Kaihei 8-264027 (JP, A) JP-A-4-85378 (JP, A) JP-B 4-69402 (JP, B2) (58) Fields investigated (Int.Cl. 7 , DB name) H01B 7 / 02 H01B 3/30

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 多価アルコールと無水トリメリット酸及
び/又は無水ピリメリット酸とポリイソシアネートとを
反応させて得られる、分子中にウレタン結合、アミド結
合及びイミド結合を有する樹脂を含む絶縁塗料を導体上
に塗布及び焼付けしてなる絶縁層を有することを特徴と
する絶縁電線。
1. A polyhydric alcohol and trimellitic anhydride and
And / or pyrimellitic anhydride and polyisocyanate are reacted to obtain a urethane bond or an amide bond in the molecule.
An insulated wire having an insulating layer formed by applying and baking an insulating coating material containing a resin having an amide bond and a resin on a conductor.
【請求項2】 絶縁塗料が、多価アルコール20〜45
モル%と多価カルボン酸又はその誘導体30〜5モル
%、及びこれら両者を加えたモル数に対し0.8〜1.
10の比となるモル%のポリイソシアネートとを反応さ
せて得られる樹脂を含む絶縁塗料である請求項1に記載
の絶縁電線。
2. The insulating paint is polyhydric alcohol 20-45.
Mol% and polyvalent carboxylic acid or its derivative 30 to 5 mol%, and 0.8 to 1.
The insulated wire according to claim 1, which is an insulating coating material containing a resin obtained by reacting a polyisocyanate in a mole ratio of 10.
【請求項3】 多価アルコールがエチレングリコールで
あり、ポリイソシアネートがジフェニルメタンジイソシ
アネートである請求項1又は2に記載の絶縁電線。
Wherein the polyhydric alcohol is ethylene glycol, insulated wire according to claim 1 or 2 port polyisocyanate is diphenylmethane diisocyanate.
【請求項4】 エチレングリコールの一部をグリセリ
ン、トリメチロールプロパン又はトリス(2−ヒドロキ
シエチル)イソシアヌレートで置換する請求項3に記載
の絶縁電線。
4. The insulated wire according to claim 3, wherein a part of ethylene glycol is replaced with glycerin, trimethylolpropane or tris (2-hydroxyethyl) isocyanurate.
【請求項5】 無水トリメリット酸の一部を芳香族ジカ
ルボン酸で置換する請求項3〜4に記載の絶縁電線。
5. The insulated wire according to claim 3, wherein a part of trimellitic anhydride is replaced with an aromatic dicarboxylic acid.
JP24514495A 1995-06-27 1995-08-31 Insulated wire Expired - Lifetime JP3364372B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24514495A JP3364372B2 (en) 1995-06-27 1995-08-31 Insulated wire

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP18224195 1995-06-27
JP7-182241 1995-06-27
JP24514495A JP3364372B2 (en) 1995-06-27 1995-08-31 Insulated wire

Publications (2)

Publication Number Publication Date
JPH0973817A JPH0973817A (en) 1997-03-18
JP3364372B2 true JP3364372B2 (en) 2003-01-08

Family

ID=26501114

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24514495A Expired - Lifetime JP3364372B2 (en) 1995-06-27 1995-08-31 Insulated wire

Country Status (1)

Country Link
JP (1) JP3364372B2 (en)

Also Published As

Publication number Publication date
JPH0973817A (en) 1997-03-18

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