JPH0287607A - Resin-molded coil - Google Patents
Resin-molded coilInfo
- Publication number
- JPH0287607A JPH0287607A JP24127888A JP24127888A JPH0287607A JP H0287607 A JPH0287607 A JP H0287607A JP 24127888 A JP24127888 A JP 24127888A JP 24127888 A JP24127888 A JP 24127888A JP H0287607 A JPH0287607 A JP H0287607A
- Authority
- JP
- Japan
- Prior art keywords
- polyamideimide
- insulating
- insulating film
- resin
- polyurethane
- 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
Links
- 239000004962 Polyamide-imide Substances 0.000 claims abstract description 29
- 229920002312 polyamide-imide Polymers 0.000 claims abstract description 29
- 229920002635 polyurethane Polymers 0.000 claims abstract description 26
- 239000003822 epoxy resin Substances 0.000 claims abstract description 25
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 25
- 229920005989 resin Polymers 0.000 claims abstract description 24
- 239000011347 resin Substances 0.000 claims abstract description 24
- 239000004814 polyurethane Substances 0.000 claims abstract description 23
- -1 aromatic tricarboxylic acid Chemical class 0.000 claims abstract description 10
- 239000004020 conductor Substances 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 3
- 238000005219 brazing Methods 0.000 claims description 2
- 239000003973 paint Substances 0.000 abstract description 18
- 229920001228 polyisocyanate Polymers 0.000 abstract description 11
- 239000005056 polyisocyanate Substances 0.000 abstract description 11
- 238000000576 coating method Methods 0.000 abstract description 6
- 239000011248 coating agent Substances 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract description 3
- 229920005862 polyol Polymers 0.000 abstract description 3
- 150000003077 polyols Chemical class 0.000 abstract description 3
- 239000002243 precursor Substances 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 10
- 238000009413 insulation Methods 0.000 description 8
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 5
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 150000004985 diamines Chemical class 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 4
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- 230000000873 masking effect Effects 0.000 description 3
- 150000003628 tricarboxylic acids Chemical class 0.000 description 3
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 2
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 238000005476 soldering Methods 0.000 description 2
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- ITWBWJFEJCHKSN-UHFFFAOYSA-N 1,4,7-triazonane Chemical compound C1CNCCNCCN1 ITWBWJFEJCHKSN-UHFFFAOYSA-N 0.000 description 1
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
- VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- PWAXUOGZOSVGBO-UHFFFAOYSA-N adipoyl chloride Chemical compound ClC(=O)CCCCC(Cl)=O PWAXUOGZOSVGBO-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 125000005462 imide group Chemical group 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Insulated Conductors (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はコイルに樹脂を含浸モールドさせ、これを加熱
硬化して成形する樹脂モールドコイルに関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a resin-molded coil in which a coil is impregnated with resin and molded, and then heated and cured to be molded.
(従来の技術)
樹脂モールドコイルは、例えばプラスチックボビンに絶
縁電線を所定のターン数に巻線した後、樹脂を注入し、
恒温槽等で加熱硬化する事により作製する。(Prior art) Resin molded coils are made by, for example, winding an insulated wire around a plastic bobbin to a predetermined number of turns, and then injecting resin into the coil.
Manufactured by heating and curing in a constant temperature bath, etc.
絶縁電線には半田付により端末はくりの出来るポリウレ
タン絶縁電線が使用される事が多い。又モールドする樹
脂としては、エポキシ樹脂が価格、品質の面より選択さ
れる場合が多い。Polyurethane insulated wires, whose terminals can be peeled off by soldering, are often used as insulated wires. Furthermore, as the resin for molding, epoxy resin is often selected from the viewpoints of price and quality.
代表的な樹脂モールドコイルである自動車のイグニッシ
ョンコイル、テレビのフライバックトランス等は2次側
に数十ミクロンの細い絶縁電線を使用し、コイルに数千
ボルトの高電圧をかける。Typical resin-molded coils, such as automobile ignition coils and television flyback transformers, use thin insulated wires of several tens of microns on the secondary side, and apply high voltages of several thousand volts to the coils.
従って、絶縁電線には半田付の出来るポリウレタン絶縁
電線、モールド樹脂にはV−を特性のよいエポキシ樹脂
が不可欠の組み合せとなっている。Therefore, it is essential to use a polyurethane insulated wire that can be soldered as the insulated wire, and an epoxy resin with good V- characteristics as the molding resin.
(発明が解決しようとする課題)
先にも述べたように、樹脂モールドコイルテハ絶縁電線
としてポリウレタン絶縁電線モールド樹脂としてエポキ
シ樹脂が一般的に使用される。(Problems to be Solved by the Invention) As mentioned above, epoxy resin is generally used as a resin for molding a polyurethane insulated wire as a resin-molded coiled wire.
最近、機器の小型化、高性能化が進み、機器の使用雰囲
気温度が上昇し、使用部品の耐熱性が要求されてきた。Recently, equipment has become smaller and more sophisticated, the ambient temperature in which the equipment is used has increased, and the parts used have been required to have higher heat resistance.
エポキシ樹脂モールドコイルも使用雰囲気温度が高くな
って来た。Epoxy resin molded coils are also being used at higher ambient temperatures.
そのため、エポキシ樹脂モールドコイル中のポリウレタ
ン絶縁電線の絶縁皮膜が熱変形を生じるようになり、ひ
どい場合は、導体同志が接触し、レアーショートを起こ
すという問題点が生じて来た。As a result, the insulation film of the polyurethane insulated wire in the epoxy resin molded coil begins to undergo thermal deformation, and in severe cases, the conductors come into contact with each other, causing a layer short circuit.
ポリウレタン絶縁電線のかわりに、イミド成分やインシ
アヌル環構造を分子中に導入し耐熱性を向上させた耐熱
ウレタン絶縁電線を使用したが予想に反して熱変形温度
は大きく向上しなかった。Instead of polyurethane insulated wire, we used heat-resistant urethane insulated wire, which has improved heat resistance by introducing imide components and incyanuric ring structures into the molecule, but contrary to expectations, the heat distortion temperature did not improve significantly.
一方、ポリエステル絶縁電線や、ポリエステルイミド絶
縁電線をポリウレタン絶縁電線のかわりに使用すると、
皮膜の熱変形は起らないが絶縁電線が半田付出来ないた
め、製造工程での生産性が低くエポキシ樹脂モールドコ
イルの生産コストが高くなる。On the other hand, if polyester insulated wire or polyester imide insulated wire is used instead of polyurethane insulated wire,
Although thermal deformation of the film does not occur, the insulated wire cannot be soldered, resulting in low productivity in the manufacturing process and high production costs for epoxy resin molded coils.
このため、半田付が出来、エポキシ樹脂モールドコイル
にした時、熱変形の起りにくい絶縁電線が要求されてい
る。For this reason, there is a demand for insulated wires that can be soldered and are less prone to thermal deformation when made into epoxy resin molded coils.
(発明の構成)
本発明は導体上にろう着性を有するポリウレタン絶縁皮
膜、ポリアミドイミド絶縁皮膜を順次設は今度膜厚に対
してポリアミドイミド絶縁皮膜厚の占める割合が40%
以下である二重構造の絶縁電線をコイル状に巻線した後
、エポキシ樹脂をモールドした事を特徴とする樹脂モー
ルドコイルである。(Structure of the Invention) In the present invention, a polyurethane insulating film having brazeability and a polyamide-imide insulating film are sequentially formed on a conductor, and the ratio of the polyamide-imide insulating film thickness to the film thickness is 40%.
This is a resin molded coil characterized by having the following double structure insulated wire wound into a coil shape and then molded with epoxy resin.
本発明においてろう着性を有するポリウレタン1絶縁皮
膜とは、安定化ポリイソシアネートとポリオールを主成
分呑するポリウレタン絶縁塗料を塗加、フェノール樹脂
、メラミン樹脂、ポリアミド樹脂等の一般に絶縁塗料の
添加樹脂として用いられるものを組み合せたものを包含
する。In the present invention, the polyurethane 1 insulating film with brazing properties refers to polyurethane insulating coatings containing stabilized polyisocyanates and polyols as main components, and generally used as additive resins for insulating coatings such as phenolic resins, melamine resins, and polyamide resins. It includes combinations of those used.
安定化ポリイソシアネートの例としてはトルエンジイソ
シアネート3モルとトリメチロールプロパン1モルとよ
り得られたポリイソシアネートをフェノール類をマスキ
ング剤に使用して安定化させたバイエル社製のデスモジ
ュールAPステーブル。An example of the stabilized polyisocyanate is Desmodur AP Stable manufactured by Bayer, which is a polyisocyanate obtained from 3 moles of toluene diisocyanate and 1 mole of trimethylolpropane, which is stabilized using phenols as a masking agent.
日本ポリウレタン社製のコロネートAPステーブル、ジ
フェニルメタンジイソシアネートをキシレノール類をマ
スキング剤とした日本ポリウレタン社製のミリオネート
MS−50、ジフェニルメタンジイソシアネートとトリ
メチロールプロパンより得られたポリイソシアネートを
キシレノール類でマスクした日本ポリウレタン社製のコ
ロネート2503等がある。Coronate AP Stable manufactured by Nippon Polyurethane Co., Ltd., Millionate MS-50 manufactured by Nippon Polyurethane Co., Ltd., which uses diphenylmethane diisocyanate as a masking agent with xylenol compounds, and Japan Polyurethane, which uses polyisocyanate obtained from diphenylmethane diisocyanate and trimethylolpropane as a masking agent with xylenol compounds. There are Coronate 2503 and other products made by the company.
ポリオールとしては、例えば無水フタル酸、アジピン酸
、無水フタル酸、テレフタル酸、イソフタル酸などの2
塩基酸の一種又は二種以上、エチレングリコール、プロ
ピレングリコール等の2価アルコール及びグリセリン、
トリメチロールプロパン、2−ヒドロキシエチルイソシ
アヌレート等の3価アルコールの一種又は二種以上より
得られるポリエステルポリオールが使用出来る。Examples of polyols include phthalic anhydride, adipic acid, phthalic anhydride, terephthalic acid, and isophthalic acid.
One or more basic acids, dihydric alcohols such as ethylene glycol and propylene glycol, and glycerin,
Polyester polyols obtained from one or more trihydric alcohols such as trimethylolpropane and 2-hydroxyethyl isocyanurate can be used.
これに相当するものとして日本ポリウレタン社製のニノ
ボラン2006 、住友−バイニル社製のデス上ヘン8
00等がある。Equivalent products include Ninoboran 2006 manufactured by Nippon Polyurethane Co., Ltd., and Desjohen 8 manufactured by Sumitomo-Vinyl Co., Ltd.
There are 00 etc.
そのほかにイミド基を分子骨格中に導入したエステルイ
ミドを使用する事も可能である。In addition, it is also possible to use ester imide in which an imide group is introduced into the molecular skeleton.
ポリアミドイミド絶縁皮膜は、ポリアミドイミド絶縁塗
料を塗布焼付したもので、ポリアミドイミド絶縁塗料と
は、ポリアミドイミド樹脂或いはポリアミドイミド前駆
体樹脂を主成分とする絶縁塗料であり、その一部をエポ
キシ樹脂、フェノール樹脂、ポリイソシアネート、安定
化ポリイソシアネート等の一般に絶縁塗料の添加樹脂と
して用いられるものを組合せたものを包含する。A polyamide-imide insulating film is obtained by applying and baking a polyamide-imide insulating paint. A polyamide-imide insulating paint is an insulating paint whose main component is a polyamide-imide resin or a polyamide-imide precursor resin, and some of it is made of epoxy resin, It includes combinations of resins commonly used as additives for insulating coatings, such as phenolic resins, polyisocyanates, and stabilized polyisocyanates.
ポリアミドイミド絶縁塗料の主成分を成すポリアミドイ
ミド樹脂或いはその樹脂溶液或いはポリアミドイミド前
駆体樹脂或はその樹脂溶液の代表的な製法の例は、少な
くとも一種のトリカルボン酸無水物の酸クロライドと少
なくとも一種のジアミンとを反応させるものがある。又
、上記トリカルボン酸無水物の酸クロライドの一部を少
くとも−mのジカルボン酸ジクロライド或は少くとも、
一種のテトラカルボン酸二無水物、或は少くとも−mの
ジカルボン酸ジクロライドと少くとも一種のテトラカル
ボン酸二無水物でおきかえてもよい。A typical example of a method for producing polyamide-imide resin or its resin solution, or polyamide-imide precursor resin or its resin solution, which is the main component of polyamide-imide insulating paint, is to use at least one tricarboxylic acid anhydride acid chloride and at least one tricarboxylic acid anhydride acid chloride. Some react with diamines. Further, a part of the acid chloride of the above tricarboxylic acid anhydride is at least -m dicarboxylic acid dichloride or at least
One kind of tetracarboxylic dianhydride, or at least -m dicarboxylic dichloride may be replaced with at least one kind of tetracarboxylic dianhydride.
又、上記ジアミンの一部を少くとも一種のトリアミン、
或いは少なくとも一種のテトラミン、或いは少なくとも
一種のトリアミンと少なくとも一種のテトラミンでおき
かえてもよい。Further, a part of the above diamine may be replaced with at least one kind of triamine,
Alternatively, at least one type of tetramine, or at least one triamine and at least one tetramine may be replaced.
トリカルボン酸無水物の酸クロライドの例としては、ト
リメリット酸無水物の4−酸クロライド等がある。Examples of the acid chloride of tricarboxylic anhydride include 4-acid chloride of trimellitic anhydride.
ジカルボン酸ジクロライドの例としては、テレフタル酸
ジクロライド、イソフタル酸ジクロライド、アジピン酸
ジクロライド等がある。Examples of dicarboxylic acid dichloride include terephthalic acid dichloride, isophthalic acid dichloride, adipic acid dichloride, and the like.
ジアミンの例としては、4.4’−ジアミノジフェニル
メタン、4.4’−ジアミノジフェニルエーテルm−フ
二二レンジアミン等がある。トリアミンの例としては、
3,4.4’−1リアミノジフエニルエーテル等がある
。テトラミンの例としては、33’、4..4’−テト
ラアミノジフェニルエーテル等がある。Examples of diamines include 4,4'-diaminodiphenylmethane, 4,4'-diaminodiphenyl ether m-phenyl diamine, and the like. An example of triamine is
Examples include 3,4,4'-1 riaminodiphenyl ether. Examples of tetramines include 33', 4. .. Examples include 4'-tetraaminodiphenyl ether.
代表的な製法の他の例としては、少なくとも一種のトリ
カルボン酸無水物と少なくとも一種のジイソシアネート
とを反応させるものがある。又、上記トリカルボン酸無
水物の一部を少なくとも一種のジカルボン酸、或は少な
くとも一種のテトラカルボン酸二無水物、或は少くとも
一種のジカルボン酸と少なくとも一種のテトラカルボン
酸二無水物でおきかえてもよい。Another typical manufacturing method involves reacting at least one tricarboxylic anhydride with at least one diisocyanate. Also, a part of the above tricarboxylic anhydride is replaced with at least one dicarboxylic acid, or at least one tetracarboxylic dianhydride, or at least one dicarboxylic acid and at least one tetracarboxylic dianhydride. Good too.
又、上記ジイソシアネートの一部を少なくとも一種の3
価又はそれ以上のポリイソシアネートでおきかえてもよ
い。Further, a part of the above diisocyanate may be at least one type of 3
It may be replaced with a polyisocyanate having a polyhydric acid or higher.
トリカルボン酸無水物の例としては、トリメリット酸無
水物等がある。Examples of tricarboxylic anhydrides include trimellitic anhydride.
ジカルボン酸の例としては、イソフタル酸、テレフタル
酸、アジピン酸等がある。Examples of dicarboxylic acids include isophthalic acid, terephthalic acid, adipic acid, and the like.
テトラカルボン酸二無水物の例としては、ピロメリット
酸二無水物、ベンゾフェノンテトラカルボン酸二無水物
等がある。ジイソシアネートの例としては、ジフェニル
メタン−4,4/−ジイソシアネート、ジフェニルエー
テル−4,4′−ジイソシアネート、トリレンジイソシ
アネート、キシリレンジイソシアネート、ヘキサメチレ
ンジイソシアネート等がある。Examples of tetracarboxylic dianhydride include pyromellitic dianhydride, benzophenone tetracarboxylic dianhydride, and the like. Examples of diisocyanates include diphenylmethane-4,4/-diisocyanate, diphenyl ether-4,4'-diisocyanate, tolylene diisocyanate, xylylene diisocyanate, hexamethylene diisocyanate, and the like.
ポリイソシアネートの例としては、ポリメチレンポリフ
ェニレンポリイソシアネート等がある。Examples of polyisocyanates include polymethylene polyphenylene polyisocyanate.
中でも芳香族トリカルボン酸無水物又はその誘導体と芳
香族ジインシアネートの反応より得られるポリアミドイ
ミド樹脂を用いると本発明の効果がより発揮出来好まし
い。Among them, it is preferable to use a polyamide-imide resin obtained by reacting an aromatic tricarboxylic acid anhydride or its derivative with an aromatic diincyanate because the effects of the present invention can be more effectively exhibited.
本発明においては、ポリアミドイミド絶縁皮膜厚が二重
構造の絶縁電線の今度膜厚に対して5〜40%の割合を
占める必要がある。5%未満であればエポキシ樹脂モー
ルド後の絶縁皮膜の熱変形が向上せず、4096をこえ
れば絶縁電線が半田付により端末ばくり出来ない。モー
ルドコイルに使用するエポキシ樹脂はいかなるエポキシ
樹脂でも効果を発揮するが、通常使用されるものとして
は例えば以下のものがある。In the present invention, the thickness of the polyamide-imide insulation film must account for 5 to 40% of the thickness of the double-structured insulated wire. If it is less than 5%, the thermal deformation of the insulating film after epoxy resin molding will not improve, and if it exceeds 4096, the ends of the insulated wire cannot be exposed by soldering. Although any epoxy resin can be used for the molded coil, the following are commonly used.
ビスフェノールAジグリシジルエーテル、ビスフェノー
ルFジグリシジルエーテル等のエポキシ化金物とトリエ
チレントリアミン、インホロンジアミン、フェニレンジ
アミン、ジアミノジフェニルエーテル、メチレンジアニ
リン等のポリアミン化合物の組み合せよりなるアミン硬
化タイプのエポキシ樹脂、前述のエポキシ化合物と無水
フタル酸、トリメリット酸無水物、無水マレイン酸、ピ
ロメリット酸無水物等の酸無水物fヒ金物の組み合せよ
りなる酸無水物硬化のエポキシ樹脂、前述のエポキシ化
合物にジシアンジアミド、三フッ化ホウ酸、ポリイソシ
アネート、イミダゾール類を加えたエポキシ樹脂等があ
る。An amine-curing type epoxy resin made of a combination of an epoxidized metal such as bisphenol A diglycidyl ether or bisphenol F diglycidyl ether and a polyamine compound such as triethylene triamine, inphorone diamine, phenylene diamine, diaminodiphenyl ether, or methylene dianiline, as described above. An acid anhydride-cured epoxy resin consisting of a combination of an epoxy compound and an acid anhydride f arsenic such as phthalic anhydride, trimellitic anhydride, maleic anhydride, and pyromellitic anhydride; Examples include epoxy resins containing trifluoroboric acid, polyisocyanates, and imidazoles.
もちろん、充てん剤、着色剤等を加える事ももちろん可
能である。Of course, it is also possible to add fillers, colorants, etc.
以下の実施例において本発明の詳細な説明するが本発明
はこれら実施例に限定されるものではない。以下の参考
例で比較例及び実施例に用いた絶縁塗料を示す。The present invention will be explained in detail in the following examples, but the present invention is not limited to these examples. The following reference examples show insulating paints used in comparative examples and examples.
参考例1.(ポリアミドイミド絶縁塗料)トリメリット
酸無水物192、Ig(1,0モル)とジフェニールメ
タン−4,4′−ジイソシアネート250.3g(1,
0モル)とを、N−メチル−2−ピロリドン770gと
ソルベントナフサ(丸善石油化学製スワゾール# 11
000)330との混合溶剤中に加えて80°Cで3時
間反応後、165°C迄6時間で昇温し、この温度で2
時間反応させポリアミドイミド絶縁塗料を得た。樹脂の
還元比粘度は0.54であった。Reference example 1. (Polyamide-imide insulation coating) Trimellitic anhydride 192, Ig (1.0 mol) and diphenylmethane-4,4'-diisocyanate 250.3 g (1,
0 mol) and 770 g of N-methyl-2-pyrrolidone and solvent naphtha (Maruzen Petrochemical Swazol #11
000) 330 and reacted at 80°C for 3 hours, the temperature was raised to 165°C in 6 hours, and at this temperature 2
A polyamide-imide insulating paint was obtained by a time reaction. The reduced specific viscosity of the resin was 0.54.
(比較例1)
ポリウレタン絶縁塗料(日東電工社製デラコー)u−8
08=以下の例では全てこのポリウレタン絶縁塗料を使
用した)を0.3 nunφの銅導体に塗布・焼付して
、皮膜厚0.020aunのポリウレタン絶縁電線を得
た。(Comparative Example 1) Polyurethane insulation paint (Nitto Denko Corporation Delacor) u-8
08=This polyurethane insulating paint was used in all the following examples) was coated and baked on a 0.3 nunφ copper conductor to obtain a polyurethane insulated wire with a coating thickness of 0.020 aun.
上記ポリウレタン絶縁電線を2cm角のPBT製ボビン
に5層巻付した後、エポキシ樹脂(来夏ケミカル社製T
CG 1577A/B )を注入し、真空脱泡した後9
5°Cで6時間、1508Cで3時間の硬化条件で硬化
し、エポキシ樹脂でモールドしたコイルを得た。After winding the above polyurethane insulated wire in 5 layers around a 2 cm square PBT bobbin, epoxy resin (T
After injecting CG 1577A/B) and vacuum defoaming 9
It was cured at 5°C for 6 hours and at 1508C for 3 hours to obtain a coil molded with epoxy resin.
(実施例1)
ポリウレタン絶縁塗料を0.3mmφの銅導体に塗布・
焼付して皮膜厚0.015n+mとした後、参考例1で
作製したポリアミドイミド絶縁塗料上皮膜厚0.005
manになるように塗布・焼付して今度膜厚0.020
mmの絶縁電線を得た。(Example 1) Polyurethane insulation paint was applied to a 0.3 mm diameter copper conductor.
After baking to a film thickness of 0.015n+m, the polyamide-imide insulation paint epithelial film thickness prepared in Reference Example 1 was 0.005n+m.
Coat and bake so that it becomes man, and the film thickness is 0.020 this time.
An insulated wire of mm was obtained.
上記電線を用い比較例1と同様の方法でエポキシ樹脂を
モールドしたコイルを得た。A coil was obtained by molding epoxy resin using the above electric wire in the same manner as in Comparative Example 1.
(実施例2)
ポリウレタン絶縁塗料を01018mm、ポリアミドイ
ミド絶縁塗料を0.002mmの皮膜厚とした以外は実
施例1と同様の方法で、絶縁電線とエポキシモールド樹
脂を得た。(Example 2) An insulated wire and an epoxy mold resin were obtained in the same manner as in Example 1, except that the polyurethane insulating paint was 0.1018 mm thick and the polyamide-imide insulating paint was 0.002 mm thick.
(比較例2)
ポリウレタン絶縁塗料を一〇、、010 mm 、ポリ
アミドイミド絶縁塗料を0.010mmの皮膜厚とした
以外は実施例1と同様の方法で、絶縁電線とエポキシモ
ールド樹脂を得た。(Comparative Example 2) An insulated wire and an epoxy mold resin were obtained in the same manner as in Example 1, except that the polyurethane insulating paint was 10,010 mm thick and the polyamide-imide insulating paint was 0.010 mm thick.
(参照例1)
比較例1,2、実施例1,2で得たエポキシ樹脂モール
ドコイルを160°CX1時間と180°CX1時間の
2種温度条件で熱処理した。(Reference Example 1) The epoxy resin molded coils obtained in Comparative Examples 1 and 2 and Examples 1 and 2 were heat-treated under two temperature conditions: 160° C. for 1 hour and 180° C. for 1 hour.
それぞれの温度条件で熱処理したサンプルを切断し、絶
縁皮膜の状態を顕微鏡により観察したところ、180°
CX1時間熱処理した比較例1のエポキシ樹脂モールド
コイルの絶縁皮膜には変形があったが他の180°CX
1時間熱処理した実施例1〜3のエポキシ樹脂モールド
コイル、160℃×1時間熱処理した全てのエポキシ樹
脂モールドコイルには絶縁皮膜の変形は見られなかった
。When we cut samples heat-treated under each temperature condition and observed the state of the insulating film using a microscope, we found that 180°
There was some deformation in the insulation film of the epoxy resin molded coil of Comparative Example 1 that was heat treated at CX for 1 hour, but other 180°C
No deformation of the insulation film was observed in the epoxy resin molded coils of Examples 1 to 3 that were heat-treated for 1 hour and in all the epoxy resin molded coils that were heat-treated at 160° C. for 1 hour.
結果を表1にまとめた。The results are summarized in Table 1.
(参照例2)
比較例1,2、実施例1.2で得た絶縁電線の410°
Cにおける半田付性を調べた。比較例1、実施例1.2
の絶縁電線は半田付が可能であったが、比較例2の絶縁
電線は半田付が出来なかった。(Reference Example 2) 410° of insulated wires obtained in Comparative Examples 1 and 2 and Example 1.2
The solderability of C was investigated. Comparative Example 1, Example 1.2
Although the insulated wire of Comparative Example 2 could be soldered, the insulated wire of Comparative Example 2 could not be soldered.
結果を表1にまとめた。The results are summarized in Table 1.
表 1
(発明の効果)
以上説明したように本発明の絶縁電線を使用すると、従
来のポリウレタン絶縁電線Qテ比較しエポキシ樹脂でモ
ールドしたコイルの耐熱性を向上出来る。同、従来のポ
リウレタン絶縁電線と同等の半田付性も保持しており、
イグニッションコイル、フライバックトランス等のエポ
キシ樹脂モールドコイルには最適である。Table 1 (Effects of the Invention) As explained above, when the insulated wire of the present invention is used, the heat resistance of the coil molded with epoxy resin can be improved compared to the conventional polyurethane insulated wire Q. It also maintains the same solderability as conventional polyurethane insulated wire.
Ideal for epoxy resin molded coils such as ignition coils and flyback transformers.
従って本発明の工業的価値は太きい。Therefore, the industrial value of the present invention is great.
Claims (2)
、ポリアミドイミド絶縁皮膜を順次設け、全皮膜厚に対
してポリアミドイミド絶縁皮膜厚の占める割合が5%以
上40%以下である二重構造の絶縁電線をコイル状に巻
線した後エポキシ樹脂でモールドした事を特徴とする樹
脂モールドコイル。(1) A double structure in which a polyurethane insulating film with brazing properties and a polyamide-imide insulating film are sequentially provided on the conductor, and the ratio of the polyamide-imide insulating film thickness to the total film thickness is 5% to 40%. A resin molded coil characterized by insulated wire wound into a coil and then molded with epoxy resin.
酸無水物又はその誘導体と芳香族ジイソシアネートの反
応により得られる化合物である請求項1記載の樹脂モー
ルドコイル。(2) The resin molded coil according to claim 1, wherein the polyamide-imide insulating film is a compound obtained by reacting an aromatic tricarboxylic acid anhydride or a derivative thereof with an aromatic diisocyanate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24127888A JPH0287607A (en) | 1988-09-26 | 1988-09-26 | Resin-molded coil |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24127888A JPH0287607A (en) | 1988-09-26 | 1988-09-26 | Resin-molded coil |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0287607A true JPH0287607A (en) | 1990-03-28 |
Family
ID=17071879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24127888A Pending JPH0287607A (en) | 1988-09-26 | 1988-09-26 | Resin-molded coil |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0287607A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007096073A (en) * | 2005-09-29 | 2007-04-12 | Tdk Corp | Coil device |
-
1988
- 1988-09-26 JP JP24127888A patent/JPH0287607A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007096073A (en) * | 2005-09-29 | 2007-04-12 | Tdk Corp | Coil device |
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