JPH04245110A - Self-fusible insulative electric wire and coil using the same - Google Patents
Self-fusible insulative electric wire and coil using the sameInfo
- Publication number
- JPH04245110A JPH04245110A JP3009768A JP976891A JPH04245110A JP H04245110 A JPH04245110 A JP H04245110A JP 3009768 A JP3009768 A JP 3009768A JP 976891 A JP976891 A JP 976891A JP H04245110 A JPH04245110 A JP H04245110A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- foaming agent
- foaming
- fusible
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000004088 foaming agent Substances 0.000 claims abstract description 28
- 238000005187 foaming Methods 0.000 claims abstract description 27
- 239000004020 conductor Substances 0.000 claims abstract description 6
- 229910052751 metal Inorganic materials 0.000 claims abstract description 4
- 239000002184 metal Substances 0.000 claims abstract description 4
- 238000003466 welding Methods 0.000 claims description 4
- 229920005989 resin Polymers 0.000 abstract description 27
- 239000011347 resin Substances 0.000 abstract description 27
- 238000000576 coating method Methods 0.000 abstract description 10
- 239000011248 coating agent Substances 0.000 abstract description 9
- 238000004073 vulcanization Methods 0.000 abstract description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract description 4
- 239000007789 gas Substances 0.000 abstract description 4
- 238000010438 heat treatment Methods 0.000 abstract description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 2
- 239000001569 carbon dioxide Substances 0.000 abstract description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract description 2
- 229910001873 dinitrogen Inorganic materials 0.000 abstract description 2
- 238000007602 hot air drying Methods 0.000 abstract description 2
- 125000000018 nitroso group Chemical group N(=O)* 0.000 abstract description 2
- 239000006077 pvc stabilizer Substances 0.000 abstract description 2
- 238000005979 thermal decomposition reaction Methods 0.000 abstract description 2
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 230000001737 promoting effect Effects 0.000 abstract 1
- 230000004927 fusion Effects 0.000 description 19
- 230000000052 comparative effect Effects 0.000 description 17
- 239000010410 layer Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 10
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 9
- 229920001187 thermosetting polymer Polymers 0.000 description 8
- 239000011787 zinc oxide Substances 0.000 description 8
- 235000014692 zinc oxide Nutrition 0.000 description 8
- 239000004604 Blowing Agent Substances 0.000 description 7
- 239000013034 phenoxy resin Substances 0.000 description 7
- 229920006287 phenoxy resin Polymers 0.000 description 7
- 239000012790 adhesive layer Substances 0.000 description 6
- 239000003973 paint Substances 0.000 description 6
- -1 aldehyde-amine Chemical compound 0.000 description 4
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 4
- 229920006122 polyamide resin Polymers 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 239000004962 Polyamide-imide Substances 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000001099 ammonium carbonate Substances 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- PPQREHKVAOVYBT-UHFFFAOYSA-H dialuminum;tricarbonate Chemical compound [Al+3].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O PPQREHKVAOVYBT-UHFFFAOYSA-H 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- WCRDXYSYPCEIAK-UHFFFAOYSA-N dibutylstannane Chemical compound CCCC[SnH2]CCCC WCRDXYSYPCEIAK-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- OCWMFVJKFWXKNZ-UHFFFAOYSA-L lead(2+);oxygen(2-);sulfate Chemical compound [O-2].[O-2].[O-2].[Pb+2].[Pb+2].[Pb+2].[Pb+2].[O-]S([O-])(=O)=O OCWMFVJKFWXKNZ-UHFFFAOYSA-L 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229920003055 poly(ester-imide) Polymers 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 239000009719 polyimide resin Substances 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- CZGWDPMDAIPURF-UHFFFAOYSA-N (4,6-dihydrazinyl-1,3,5-triazin-2-yl)hydrazine Chemical compound NNC1=NC(NN)=NC(NN)=N1 CZGWDPMDAIPURF-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- UJPKMTDFFUTLGM-UHFFFAOYSA-N 1-aminoethanol Chemical compound CC(N)O UJPKMTDFFUTLGM-UHFFFAOYSA-N 0.000 description 1
- CQSQUYVFNGIECQ-UHFFFAOYSA-N 1-n,4-n-dimethyl-1-n,4-n-dinitrosobenzene-1,4-dicarboxamide Chemical compound O=NN(C)C(=O)C1=CC=C(C(=O)N(C)N=O)C=C1 CQSQUYVFNGIECQ-UHFFFAOYSA-N 0.000 description 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 1
- ICGLPKIVTVWCFT-UHFFFAOYSA-N 4-methylbenzenesulfonohydrazide Chemical compound CC1=CC=C(S(=O)(=O)NN)C=C1 ICGLPKIVTVWCFT-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- OMRGOCGKDHSKAY-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)[O-].[NH4+].[S] Chemical compound C(C1=CC=CC=C1)(=O)[O-].[NH4+].[S] OMRGOCGKDHSKAY-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229910000004 White lead Inorganic materials 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 229940118662 aluminum carbonate Drugs 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
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- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- VJRITMATACIYAF-UHFFFAOYSA-N benzenesulfonohydrazide Chemical compound NNS(=O)(=O)C1=CC=CC=C1 VJRITMATACIYAF-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- MOOAHMCRPCTRLV-UHFFFAOYSA-N boron sodium Chemical compound [B].[Na] MOOAHMCRPCTRLV-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 1
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- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
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- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
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- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
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- 239000004576 sand Substances 0.000 description 1
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- XJKVPKYVPCWHFO-UHFFFAOYSA-N silicon;hydrate Chemical compound O.[Si] XJKVPKYVPCWHFO-UHFFFAOYSA-N 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
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- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
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- Paints Or Removers (AREA)
- Insulated Conductors (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、融着性に優れた自己融
着性絶縁電線に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a self-bonding insulated wire with excellent melting properties.
【0002】0002
【従来の技術】自己融着性絶縁電線は、コイル作成時含
浸ワニスを使用することなく電線間の固着が可能なため
、作業工程が短縮されるという利点を有している。しか
しながら、自己融着性絶縁電線の使用は、増加しつつあ
るものの以下の二つの問題があるので使用される用途が
限定され未だほんの一部にとどまっている。2. Description of the Related Art Self-bonding insulated wires have the advantage of shortening the work process because wires can be bonded together without the use of impregnated varnish when making a coil. However, although the use of self-bonding insulated wires is increasing, the following two problems have limited the applications in which they can be used, and only a few of them are still used.
【0003】まず第一に、自己融着性絶縁電線の最も重
要な特性である融着力が不十分である。特に融着時の流
動性に乏しいブチラール樹脂及びフェノキシ樹脂は融着
力の不足が大きく、また、流動性に優れるポリアミド樹
脂においても融着力が十分とは言えないという問題点が
あった。さらに、自己融着性絶縁電線をコイル状にした
場合、コイルの形状によっては線間密度の小さな部分が
発生して電線どうしの接着が少なくなり融着力が不足す
るという問題もあった。First of all, the most important characteristic of self-bonding insulated wires, the fusing strength, is insufficient. In particular, butyral resins and phenoxy resins, which have poor fluidity during fusion bonding, have a significant lack of fusion bonding strength, and even polyamide resins, which have excellent fluidity, have a problem in that their fusion bonding strength is not sufficient. Further, when the self-bonding insulated wire is formed into a coil, there is a problem in that depending on the shape of the coil, there may be portions with low inter-wire density, resulting in less adhesion between the wires and insufficient fusing force.
【0004】第二の問題点は、融着層の膜厚が厚いため
、モーターのコアに占める電線の断面積の割合を表わす
占積率が小さいという点である。近年、機器の小型化に
伴い、コイル、モーターも小型になり小さなスペースに
より多くの絶縁電線を詰めこみ電線の占積率の向上が望
まれている。従って融着層の膜厚は、融着力を損なわな
い限りできるだけ薄い方が占積率の向上につながり好ま
しい。しかしながら現在用いられている融着層の膜厚は
絶縁層の1/2〜1/3ほど有り非常に厚く占積率が向
上できないという問題があった。The second problem is that because the adhesive layer is thick, the space factor, which represents the ratio of the cross-sectional area of the electric wire to the core of the motor, is small. In recent years, with the miniaturization of equipment, coils and motors have also become smaller, and it is desired to pack more insulated wires into a small space and improve the space factor of the wires. Therefore, it is preferable that the thickness of the fusion layer be as thin as possible without impairing the fusion bonding strength, as this will improve the space factor. However, the thickness of the currently used fusion layer is approximately 1/2 to 1/3 that of the insulating layer, which is very thick, and there is a problem in that the space factor cannot be improved.
【0005】[0005]
【発明が解決しようとする課題】これらの問題点に対し
て融着層が融着時発泡する自己融着性絶縁電線が提案さ
れた。この自己融着性絶縁電線を使用すると、融着層が
発泡し融着層皮膜厚が2〜3倍になることから、樹脂の
流れ性が改善され融着力が向上する。また融着層の薄膜
化が可能となり占積率が向上する。しかしながら、通電
加熱による融着の場合は、融着層の発泡が発生するが、
150℃前後での熱風乾燥による融着の場合融着層の発
泡が不十分という問題点が新たに生じた。SUMMARY OF THE INVENTION To address these problems, a self-bonding insulated wire in which the bonding layer foams during bonding has been proposed. When this self-bonding insulated wire is used, the welding layer foams and the thickness of the welding layer increases by two to three times, thereby improving the flowability of the resin and increasing the welding strength. Furthermore, the fusion layer can be made thinner, and the space factor can be improved. However, in the case of fusion bonding by electrical heating, foaming of the fusion layer occurs;
In the case of fusing by hot air drying at around 150°C, a new problem arose that the fusing layer was insufficiently foamed.
【0006】[0006]
【課題を解決するための手段】本発明者らは、上記問題
を解決するために鋭意検討を重ねた結果、発泡剤を含有
する融着層に発泡助剤を添加することにより150℃前
後の低温でも融着層を発泡させることができる自己融着
性絶縁電線を発明した。[Means for Solving the Problems] As a result of intensive studies in order to solve the above problems, the present inventors have found that by adding a foaming aid to the adhesive layer containing a foaming agent, the temperature at around 150° C. We have invented a self-bonding insulated wire whose adhesive layer can be foamed even at low temperatures.
【0007】即ち、本発明は金属導体上に絶縁層を介し
て発泡剤と発泡助剤を含有する融着層を形成させたこと
を特徴とした自己融着性絶縁電線である。That is, the present invention is a self-bonding insulated wire characterized in that a melting layer containing a foaming agent and a foaming aid is formed on a metal conductor via an insulating layer.
【0008】以下本発明を詳細に説明する。本発明で用
いる発泡助剤は発泡剤の熱分解を促進するものならいか
なるものでも使用でき例えば、加硫促進剤、充填剤、加
硫促進助剤、PVC用安定剤、老防、加硫剤、尿素化合
物などが挙げられる。The present invention will be explained in detail below. The foaming aid used in the present invention can be anything that promotes thermal decomposition of the foaming agent, such as vulcanization accelerator, filler, vulcanization accelerator, PVC stabilizer, anti-aging agent, and vulcanizing agent. , urea compounds, etc.
【0009】加硫促進剤ではグアジニン系、アルデヒト
−アンモニア系、スルフェンアミド系、チウラム系、ザ
ンテート系、アルデヒト−アミン系、チアゾール系、チ
オ尿素系、ジチオカルバメート系などが、充填剤では、
シリカ、炭酸マグネシウム、炭酸カルシウム、ケイ酸マ
グネシウム、炭酸アルミニウム、タルク、硫酸バリウム
、硫酸アルミニウム、硫酸カルシウムなどが、加硫促進
助剤では、亜鉛華、活性亜鉛華、炭酸亜鉛、酸化マグネ
シウム、一酸化鉛、塩基性炭酸鉛、水酸化カルシウム、
ステアリン酸、オレイン酸、ラウリン酸、ジエチレング
ルコール、ジ−n−ブチルアミン、ジシクロヘキシルア
ミン、ジエタノールアミン、有機アミンなどが、PVC
用安定剤は三塩基性硫酸鉛、ジブチルすずジラウレート
、ジブチルすずジマレート、ステアリン酸亜鉛、ステア
リン酸カドミウム、ステアリン酸バリウム、ステアリン
酸カルシウムなどが、老防では、ナフチルアミン系、ジ
フェニルアミン系、P−フェニレン系、キノリン系、モ
ノフェノール系、ポリフェノール系、チオビスフェノー
ル系、亜りん酸エステル系などが加硫剤では、タイク、
イオウ安息香酸アンモニウムなどが挙げられる。Vulcanization accelerators include guanidine, aldehyde-ammonia, sulfenamide, thiuram, xanthate, aldehyde-amine, thiazole, thiourea, and dithiocarbamate, and fillers include:
Silica, magnesium carbonate, calcium carbonate, magnesium silicate, aluminum carbonate, talc, barium sulfate, aluminum sulfate, calcium sulfate, etc. are used as vulcanization accelerators, zinc white, activated zinc white, zinc carbonate, magnesium oxide, monoxide, etc. Lead, basic lead carbonate, calcium hydroxide,
Stearic acid, oleic acid, lauric acid, diethylene glycol, di-n-butylamine, dicyclohexylamine, diethanolamine, organic amines, etc.
Stabilizers include tribasic lead sulfate, dibutyltin dilaurate, dibutyltin dimalate, zinc stearate, cadmium stearate, barium stearate, calcium stearate, etc. Anti-aging stabilizers include naphthylamine type, diphenylamine type, P-phenylene type, Vulcanizing agents include quinoline, monophenol, polyphenol, thiobisphenol, and phosphite esters.
Examples include ammonium sulfur benzoate.
【0010】その他薬品として無水フタル酸、サリチル
酸、安息香酸、三酸化アンチモン、白色ワセリン、酸化
チタン、酸化カドミウム、ホウ砂、グリセリン、ジブチ
ルチンジマレートなどがあげられる。これらの中でも、
亜鉛華、三塩基性硫酸鉛、加硫促進剤などが好ましい。[0010] Other chemicals include phthalic anhydride, salicylic acid, benzoic acid, antimony trioxide, white petrolatum, titanium oxide, cadmium oxide, borax, glycerin, dibutyltin dimalate, and the like. Among these,
Zinc white, tribasic lead sulfate, vulcanization accelerators and the like are preferred.
【0011】これらの発泡助剤の添加量は、発泡剤に対
し5重量部〜200重量部が好ましく、より好ましくは
50重量部〜150重量部である。発泡助剤の添加量が
少ないと発泡剤を分解させる効果が小さく発泡温度の低
下が少なくなる。逆に発泡助剤の添加量が多いと、絶縁
電線作成時に融着層が発泡する。The amount of these foaming aids added is preferably from 5 parts by weight to 200 parts by weight, more preferably from 50 parts by weight to 150 parts by weight, based on the foaming agent. If the amount of the foaming aid added is small, the effect of decomposing the foaming agent will be small and the drop in foaming temperature will be small. On the other hand, if the amount of foaming aid added is large, the fusion layer will foam during the production of an insulated wire.
【0012】本発明で用いる発泡剤は、加熱することに
より分解し窒素ガス、炭酸ガス、一酸化炭素、アンモニ
アガス等を発生するものを言い有機発泡剤、無機発泡剤
が使用できる。有機発泡剤としては、例えば、アゾ系で
はアゾジカルボンアミド(A.D.C.A)、アゾビス
イソブチロニトリル(A.I.B.N)、ニトロソ系で
は、ジニトロソペンタメチレンテトラミン(D.P.T
)、N,N’ジニトロソ−N,N’−ジメチルテレフタ
ルアミド(D.N.D.M.T.A)、ヒドラジド系で
は、P−トルエンスルホニルヒドラジド(T.S.H)
、P,P−オキシビスベンゼンスルホニルヒドラジド(
O.B.S.H)、ベンゼンスルホニルヒドラジド(B
.S.H)、その他にトリヒドラジノトリアジン(T.
H.T)、アセトン−P−スルホニルヒドラゾンなどが
あり分解温度、発生ガス量が異なるものが市販されてい
る。これらを単独あるいは、ニ種類以上合わせて融着塗
料へ溶解あるいは分散させて使用できる。The blowing agent used in the present invention is one that decomposes when heated to generate nitrogen gas, carbon dioxide gas, carbon monoxide, ammonia gas, etc. Organic blowing agents and inorganic blowing agents can be used. Examples of organic blowing agents include azo dicarbonamide (A.D.C.A.) and azobisisobutyronitrile (A.I.B.N.) for azo systems, and dinitrosopentamethylenetetramine (for nitroso systems). D.P.T.
), N,N'dinitroso-N,N'-dimethylterephthalamide (D.N.D.M.T.A), and in the hydrazide series, P-toluenesulfonylhydrazide (T.S.H)
, P,P-oxybisbenzenesulfonyl hydrazide (
O. B. S. H), benzenesulfonyl hydrazide (B
.. S. H), and trihydrazinotriazine (T.
H. T), acetone-P-sulfonylhydrazone, etc., and those having different decomposition temperatures and amounts of gas generated are commercially available. These can be used alone or in combination of two or more types dissolved or dispersed in the adhesive coating.
【0013】一方無機発泡剤としては、重炭酸ナトリウ
ム、炭酸アンモニウム、重炭酸アンモニウム、ホウ化水
素ナトリウム、ソジウムボロンハイドライド、シリコン
オキシハイドライドなどが例示されるが一般的に無機発
泡剤は、ガス発生速度が有機発泡剤より緩慢でありガス
発生の調整が難しいので有機発泡剤が好ましい。On the other hand, examples of inorganic blowing agents include sodium bicarbonate, ammonium carbonate, ammonium bicarbonate, sodium borohydride, sodium boron hydride, and silicon oxyhydride. Organic blowing agents are preferred because their speed is slower than that of organic blowing agents and gas generation is difficult to control.
【0014】発泡剤の添加量は、融着樹脂に対し0.1
PHR〜50PHRが好ましく、より好ましくは1PH
R〜25PHRである。発泡剤の添加量が少ないと発泡
が見られず、発泡剤の添加量が多いと融着層の機械的強
度が不足する。[0014] The amount of foaming agent added is 0.1 to the fusion resin.
PHR ~ 50PHR is preferable, more preferably 1PH
R~25PHR. If the amount of foaming agent added is small, no foaming will be observed, and if the amount of foaming agent added is large, the mechanical strength of the adhesive layer will be insufficient.
【0015】本発明で用いる融着樹脂は高温で流動性を
示すものならいかなるものでも使用可能である。例えば
、ブチラール樹脂、フェノキシ樹脂、ポリアミド樹脂そ
して他の熱可塑性樹脂が使用できる。フェノキシ樹脂で
は、ビスフェノールA,ビスフェノールS,ビスフェノ
ールFを主成分としたもの、あるいは、変性フェノキシ
が例示される。ポリアミド樹脂としては各種共重合ポリ
アミド樹脂、6−ナイロン樹脂、6,6−ナイロン樹脂
、6,10−ナイロン樹脂などが、熱可塑性樹脂として
は、共重合ポリエステル樹脂、ポリブチレンテレフタレ
ート樹脂、ポリエチレンテレフタレート樹脂、熱可塑性
ポリウレタン樹脂、ポリカーボネート樹脂、ポリフェニ
レンオキシド樹脂、ポリフェニレンスルフィド樹脂、ポ
リスルホン樹脂、ポリエーテルイミド樹脂、ポリエーテ
ルエーテルケトン樹脂、ポリエーテルケトン樹脂、ポリ
エーテルスルホン樹脂、熱可塑性ポリアミドイミド樹脂
、熱可塑性ポリイミド樹脂などが使用できる。また、上
記樹脂にメラミン樹脂、フェノール樹脂、イソシアネー
トなどを添加することにより架橋させ一部熱硬化タイプ
にすることも可能である。これら上記の樹脂のうちブチ
ラール樹脂、フェノキシ樹脂、共重合ポリアミド樹脂が
融着力、融着温度のバランスがよく現在も融着層に使わ
れており好ましい。さらに本発明では、融着層が発泡し
線間の空隙を埋められるので流動性にやや劣るブチラー
ル樹脂、フェノキシ樹脂の使用は流動性の改善の効果が
大きくより好ましい。[0015] As the fusion resin used in the present invention, any resin can be used as long as it exhibits fluidity at high temperatures. For example, butyral resins, phenoxy resins, polyamide resins and other thermoplastic resins can be used. Examples of phenoxy resins include those containing bisphenol A, bisphenol S, and bisphenol F as main components, and modified phenoxy resins. Examples of polyamide resins include various copolyamide resins, 6-nylon resins, 6,6-nylon resins, and 6,10-nylon resins, and examples of thermoplastic resins include copolymerized polyester resins, polybutylene terephthalate resins, and polyethylene terephthalate resins. , thermoplastic polyurethane resin, polycarbonate resin, polyphenylene oxide resin, polyphenylene sulfide resin, polysulfone resin, polyetherimide resin, polyetheretherketone resin, polyetherketone resin, polyethersulfone resin, thermoplastic polyamideimide resin, thermoplastic polyimide Resin etc. can be used. Further, by adding melamine resin, phenol resin, isocyanate, etc. to the above resin, it is possible to crosslink it and make it partially thermosetting type. Among these resins mentioned above, butyral resin, phenoxy resin, and copolymerized polyamide resin are preferred because they have a good balance of fusing strength and fusing temperature and are currently used for the fusing layer. Furthermore, in the present invention, the use of butyral resin and phenoxy resin, which have slightly poor fluidity, is more preferable because the adhesive layer is foamed to fill the voids between the wires, as they have a large effect of improving fluidity.
【0016】本発明で用いる融着塗料は、前記融着樹脂
をシクロヘキサノン、キシレン、NM2P,DMAC,
SMF,クレゾール等の溶剤に10%〜50%程度の濃
度に溶解せしめ発泡剤、発泡助剤を所定量溶解あるいは
分散せしめることにより得られる。尚、分散させる場合
ディゾルバー,ボール・ミル、サンド・ミル等で分散さ
せることにより、より均一な塗料が得られる。[0016] The fusing paint used in the present invention uses the fusing resin as cyclohexanone, xylene, NM2P, DMAC,
It is obtained by dissolving or dispersing a predetermined amount of a foaming agent or foaming aid in a solvent such as SMF or cresol to a concentration of about 10% to 50%. In addition, when dispersing, a more uniform paint can be obtained by dispersing with a dissolver, ball mill, sand mill, etc.
【0017】本発明で用いる絶縁皮膜には、なんら制限
はなく通常使用されるのものであればいかなるものも使
用可能である。例えば、ポリビニールホルマール樹脂、
熱硬化ポリウレタン樹脂、熱硬化アクリル樹脂、エポキ
シ樹脂、熱硬化ポリエステル樹脂、熱硬化ポリエステル
イミド樹脂、熱硬化ポリエステルアミドイミド樹脂、芳
香族ポリアミド樹脂、熱硬化ポリアミドイミド樹脂、熱
硬化ポリイミド樹脂を主成分とするものが使用できる。The insulating film used in the present invention is not limited in any way, and any commonly used insulating film can be used. For example, polyvinyl formal resin,
The main components are thermosetting polyurethane resin, thermosetting acrylic resin, epoxy resin, thermosetting polyester resin, thermosetting polyesterimide resin, thermosetting polyesteramideimide resin, aromatic polyamide resin, thermosetting polyamideimide resin, and thermosetting polyimide resin. You can use whatever you want.
【0018】これらの絶縁皮膜上に、前述の融着塗料を
発泡剤が分解しない焼き付け条件で塗布焼き付けするこ
とにより、本発明の自己融着性絶縁電線が得られる。The self-bonding insulated wire of the present invention can be obtained by applying and baking the above-mentioned fusing paint onto these insulating coatings under baking conditions that do not decompose the foaming agent.
【0019】得られた自己融着絶縁電線を所定のコイル
状に捲き、通電加熱あるいは熱風乾燥で融着層が発泡す
る。その際、加熱温度は150℃前後の低温でも発泡が
生じる。The obtained self-fusing insulated wire is wound into a predetermined coil shape, and the fusing layer is foamed by heating with electricity or drying with hot air. At that time, foaming occurs even when the heating temperature is as low as around 150°C.
【0020】[0020]
【実施例】以下実施例に基ずき本発明を詳細に説明する
。EXAMPLES The present invention will be explained in detail based on the following examples.
【0021】〔比較例1〕フェニキシ樹脂(YP−50
:東都化成)をNM2Pに25%になるように溶解しさ
らにA.D.C.AビニホールAC3M(永和化成工業
)を10PHR添加しディゾルバーで混合攪拌し融着塗
料とした。3.0mmφの銅線に周知の方法により炉長
3mの横炉でポリエステルイミドワニス(アイソミッド
40:日触スケネクタディー)を塗布焼き付けし膜厚2
1ミクロンの1種エステルイミド線を作成した。さらに
、前述の融着塗料を炉温250℃で塗布焼き付けし8ミ
クロンの融着層を形成し自己融着性絶縁電線を作成した
。得られた自己融着性絶縁電線からヘリカルコイルを作
成し所定の温度の恒温槽に5分間放置し発泡する温度を
調べた。その結果及び、自己融着性絶縁電線の電線作成
時の外観を表1に示す。[Comparative Example 1] Phenoxy resin (YP-50
: Toto Kasei) was dissolved in NM2P to a concentration of 25%, and further A. D. C. 10 PHR of A-vinihole AC3M (Eiwa Kasei Kogyo) was added and mixed and stirred with a dissolver to obtain a fusion coating. A polyester imide varnish (Isomid 40: Nippon Schenectady) was coated and baked on a 3.0 mmφ copper wire using a well-known method in a horizontal furnace with a furnace length of 3 m to a film thickness of 2.
A 1 micron type 1 esterimide wire was created. Further, the above-mentioned fusing paint was applied and baked at an oven temperature of 250° C. to form a fusing layer of 8 microns, thereby producing a self-fusing insulated wire. A helical coil was made from the obtained self-bonding insulated wire and left in a constant temperature bath at a predetermined temperature for 5 minutes, and the temperature at which foaming occurred was examined. Table 1 shows the results and the appearance of the self-bonding insulated wire when it was made.
【0022】〔実施例1〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し2PHR添加し他は比較
例1と同様に行った。[Example 1] The same procedure as in Comparative Example 1 was carried out except that zinc white was added as a foaming aid to the fusion coating of Comparative Example 1 in an amount of 2 PHR relative to the foaming agent.
【0023】〔実施例2〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し5PHR添加し他は比較
例1と同様に行った。[Example 2] The same procedure as in Comparative Example 1 was carried out except that 5 PHR of zinc white was added as a foaming aid to the fusing paint of Comparative Example 1 based on the foaming agent.
【0024】〔実施例3〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し50PHR添加し他は比
較例1と同様に行った。[Example 3] The same procedure as in Comparative Example 1 was carried out except that 50 PHR of zinc white was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.
【0025】〔実施例4〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し100PHR添加し他は
比較例1と同様に行った。[Example 4] The same procedure as in Comparative Example 1 was carried out except that 100 PHR of zinc white was added as a foaming aid to the fusing paint of Comparative Example 1 based on the foaming agent.
【0026】〔実施例5〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し200PHR添加し他は
比較例1と同様に行った。[Example 5] The same procedure as in Comparative Example 1 was carried out except that 200 PHR of zinc white was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.
【0027】〔実施例6〕比較例1の融着塗料に発泡助
剤としてBZを発泡剤に対し50PHR添加し他は比較
例1と同様に行った。[Example 6] The same procedure as in Comparative Example 1 was carried out except that 50 PHR of BZ was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.
【0028】〔実施例7〕比較例1の融着塗料に発泡助
剤としてTLBを発泡剤に対し100PHR添加し他は
比較例1と同様に行った。[Example 7] The same procedure as in Comparative Example 1 was carried out except that 100 PHR of TLB was added as a foaming aid to the fusion coating of Comparative Example 1 based on the foaming agent.
【0029】〔実施例8〕比較例1の融着塗料に発泡助
剤として亜鉛華を発泡剤に対し300PHR添加し他は
比較例1と同様に行った。[Example 8] The same procedure as in Comparative Example 1 was carried out except that 300 PHR of zinc white was added to the foaming agent as a foaming aid to the adhesive coating of Comparative Example 1.
【0030】[0030]
【表1】[Table 1]
【0031】[0031]
【発明の効果】以上に示したように、本発明の自己融着
性絶縁電線を用いると融着層を150℃前後の低温で発
泡させることができるという利点を有している。As described above, the use of the self-bonding insulated wire of the present invention has the advantage that the fusion layer can be foamed at a low temperature of around 150°C.
【図1】本発明の自己融着性絶縁電線の断面図である。FIG. 1 is a sectional view of a self-bonding insulated wire of the present invention.
1 導体 2 絶縁皮膜 3 自己融着層 1 Conductor 2 Insulating film 3 Self-adhesive layer
Claims (3)
と発泡助剤を含有する融着層を形成させたことを特徴と
する自己融着性絶縁電線。1. A self-bonding insulated wire characterized in that a welding layer containing a foaming agent and a foaming aid is formed on a metal conductor via an insulating layer.
量部から200重量部である請求項1に記載の自己融着
性絶縁電線。2. The self-fusing insulated wire according to claim 1, wherein the amount of the foaming aid added is from 5 parts by weight to 200 parts by weight based on the foaming agent.
を用い捲線加工した後、融着層を発泡させたことを特徴
としたコイル。3. A coil characterized in that the self-fusing insulated wire according to claim 1 is wound, and then the fusing layer is foamed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP00976891A JP3151836B2 (en) | 1991-01-30 | 1991-01-30 | Self-fusing insulated wire and coil using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP00976891A JP3151836B2 (en) | 1991-01-30 | 1991-01-30 | Self-fusing insulated wire and coil using the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04245110A true JPH04245110A (en) | 1992-09-01 |
JP3151836B2 JP3151836B2 (en) | 2001-04-03 |
Family
ID=11729448
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP00976891A Expired - Fee Related JP3151836B2 (en) | 1991-01-30 | 1991-01-30 | Self-fusing insulated wire and coil using the same |
Country Status (1)
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JP (1) | JP3151836B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0706300A3 (en) * | 1994-10-03 | 1998-11-18 | Star Micronics Co., Ltd. | Electroacoustic transducer and electronic equipment using the same |
WO2002099821A1 (en) * | 2001-06-01 | 2002-12-12 | The Furukawa Electric Co., Ltd. | Multilayer insulated wire and transformer using the same |
JP2006252852A (en) * | 2005-03-09 | 2006-09-21 | Matsushita Electric Ind Co Ltd | Insulated wire |
JP2009070722A (en) * | 2007-09-14 | 2009-04-02 | Fujifilm Corp | Composition for insulating film formation and electronic device |
JP4776048B2 (en) * | 1997-10-24 | 2011-09-21 | 古河電気工業株式会社 | Multilayer insulated wire and transformer using the same |
WO2016017648A1 (en) * | 2014-08-01 | 2016-02-04 | 住友電気工業株式会社 | Self-bonding insulated wire and wire for coil |
JP2016035836A (en) * | 2014-08-01 | 2016-03-17 | 住友電気工業株式会社 | Self-fusion insulated wire and wire for coil |
JP2016081563A (en) * | 2014-10-09 | 2016-05-16 | 住友電気工業株式会社 | Self-fusible insulated electric wire, electric wire for coil and winding wire bundle |
JP2016126903A (en) * | 2014-12-26 | 2016-07-11 | 住友電気工業株式会社 | Insulated wire |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63159748U (en) * | 1987-04-09 | 1988-10-19 | ||
JPH0250654U (en) * | 1989-08-31 | 1990-04-09 | ||
JPH0257046U (en) * | 1988-10-18 | 1990-04-25 |
-
1991
- 1991-01-30 JP JP00976891A patent/JP3151836B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63159748U (en) * | 1987-04-09 | 1988-10-19 | ||
JPH0257046U (en) * | 1988-10-18 | 1990-04-25 | ||
JPH0250654U (en) * | 1989-08-31 | 1990-04-09 |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0706300A3 (en) * | 1994-10-03 | 1998-11-18 | Star Micronics Co., Ltd. | Electroacoustic transducer and electronic equipment using the same |
JP4776048B2 (en) * | 1997-10-24 | 2011-09-21 | 古河電気工業株式会社 | Multilayer insulated wire and transformer using the same |
WO2002099821A1 (en) * | 2001-06-01 | 2002-12-12 | The Furukawa Electric Co., Ltd. | Multilayer insulated wire and transformer using the same |
US7087843B2 (en) | 2001-06-01 | 2006-08-08 | The Furukawa Electric Co. Ltd. | Multilayer insulated wire and transformer using the same |
JP2006252852A (en) * | 2005-03-09 | 2006-09-21 | Matsushita Electric Ind Co Ltd | Insulated wire |
JP2009070722A (en) * | 2007-09-14 | 2009-04-02 | Fujifilm Corp | Composition for insulating film formation and electronic device |
WO2016017648A1 (en) * | 2014-08-01 | 2016-02-04 | 住友電気工業株式会社 | Self-bonding insulated wire and wire for coil |
JP2016035836A (en) * | 2014-08-01 | 2016-03-17 | 住友電気工業株式会社 | Self-fusion insulated wire and wire for coil |
CN106575549A (en) * | 2014-08-01 | 2017-04-19 | 住友电气工业株式会社 | Self-bonding insulated wire and wire for coil |
CN110164605A (en) * | 2014-08-01 | 2019-08-23 | 住友电气工业株式会社 | Self-bonding insulated wire, coil electric wire and electromagnetism harness |
JP2016081563A (en) * | 2014-10-09 | 2016-05-16 | 住友電気工業株式会社 | Self-fusible insulated electric wire, electric wire for coil and winding wire bundle |
JP2016126903A (en) * | 2014-12-26 | 2016-07-11 | 住友電気工業株式会社 | Insulated wire |
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