JPS6079083A - Adhesive tape - Google Patents
Adhesive tapeInfo
- Publication number
- JPS6079083A JPS6079083A JP18755883A JP18755883A JPS6079083A JP S6079083 A JPS6079083 A JP S6079083A JP 18755883 A JP18755883 A JP 18755883A JP 18755883 A JP18755883 A JP 18755883A JP S6079083 A JPS6079083 A JP S6079083A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- tape
- adhesive
- adhesive tape
- parts
- 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
- 239000002390 adhesive tape Substances 0.000 title claims abstract description 24
- 239000003822 epoxy resin Substances 0.000 claims abstract description 14
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 14
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims abstract description 10
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 9
- 229920005989 resin Polymers 0.000 claims abstract description 7
- 239000011347 resin Substances 0.000 claims abstract description 7
- 238000001035 drying Methods 0.000 claims abstract description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- 239000003960 organic solvent Substances 0.000 claims description 6
- 239000011342 resin composition Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 abstract description 14
- 230000001070 adhesive effect Effects 0.000 abstract description 14
- 239000000203 mixture Substances 0.000 abstract description 8
- 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 abstract description 3
- 229930003836 cresol Natural products 0.000 abstract description 3
- 239000007787 solid Substances 0.000 abstract description 3
- RIAHASMJDOMQER-UHFFFAOYSA-N 5-ethyl-2-methyl-1h-imidazole Chemical compound CCC1=CN=C(C)N1 RIAHASMJDOMQER-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004848 polyfunctional curative Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 1
- 238000004804 winding Methods 0.000 description 15
- 239000004020 conductor Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 7
- 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 6
- 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 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000004760 aramid Substances 0.000 description 4
- 229920003235 aromatic polyamide Polymers 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- FVCSARBUZVPSQF-UHFFFAOYSA-N 5-(2,4-dioxooxolan-3-yl)-7-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C(C(OC2=O)=O)C2C(C)=CC1C1C(=O)COC1=O FVCSARBUZVPSQF-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- JDVIRCVIXCMTPU-UHFFFAOYSA-N ethanamine;trifluoroborane Chemical compound CCN.FB(F)F JDVIRCVIXCMTPU-UHFFFAOYSA-N 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- LTVUCOSIZFEASK-MPXCPUAZSA-N (3ar,4s,7r,7as)-3a-methyl-3a,4,7,7a-tetrahydro-4,7-methano-2-benzofuran-1,3-dione Chemical compound C([C@H]1C=C2)[C@H]2[C@H]2[C@]1(C)C(=O)OC2=O LTVUCOSIZFEASK-MPXCPUAZSA-N 0.000 description 1
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- VVHFXJOCUKBZFS-UHFFFAOYSA-N 2-(chloromethyl)-2-methyloxirane Chemical compound ClCC1(C)CO1 VVHFXJOCUKBZFS-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- BDEDPKFUFGCVCJ-UHFFFAOYSA-N 3,6-dihydroxy-8,8-dimethyl-1-oxo-3,4,7,9-tetrahydrocyclopenta[h]isochromene-5-carbaldehyde Chemical compound O=C1OC(O)CC(C(C=O)=C2O)=C1C1=C2CC(C)(C)C1 BDEDPKFUFGCVCJ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000784 Nomex Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000008430 aromatic amides Chemical class 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- FLBJFXNAEMSXGL-UHFFFAOYSA-N het anhydride Chemical compound O=C1OC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl FLBJFXNAEMSXGL-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- ZTAAALGPDJSKAL-UHFFFAOYSA-N n-methylmethanamine;trifluoroborane Chemical compound CNC.FB(F)F ZTAAALGPDJSKAL-UHFFFAOYSA-N 0.000 description 1
- 239000004763 nomex Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Insulating Bodies (AREA)
Abstract
Description
【発明の詳細な説明】 する。[Detailed description of the invention] do.
従来、発電機用の絶縁電線としては主として導体にガラ
ス糸を巻回したガラス巻線などが使用されてきている。Conventionally, as insulated wires for generators, glass winding wires in which a glass thread is wound around a conductor have mainly been used.
しかしながらスペース7アクター、絶縁耐圧などの点か
ら、芳香族ポリアミド紙製テープや芳香族ボリアミド紙
を基材の一部として含むテープ、マイカ會チtr4p者
寺混抄紙などの片面に接着剤を塗布した接着性テープを
導体に縦添したテープ巻線が検討されている。However, from the viewpoint of Space 7 Actor and dielectric strength, adhesives were applied to one side of aromatic polyamide paper tapes, tapes containing aromatic polyamide paper as part of the base material, mica paper mixed paper, etc. Tape winding in which adhesive tape is attached vertically to a conductor is being considered.
前記のごときテープ巻線は、ガラス巻線と比較して、絶
縁層の厚さ当りの破壊電圧が高く、コイルとしたばあい
コイルをコンパクトにすることができる。また接着性テ
ープを縦添するため、接着性テープを横巻するよりも接
着性テープ材料の消費量を少なくすることができる。し
かしながら、このようなテープ巻線を製造するばあい、
予熱した導体にAステージ接着剤を塗布した直後に絶縁
テープをそわせるか、またはあらかじめ接着剤を塗布乾
燥させBステージ化したテープの接着剤塗布面をそわせ
たのち加熱圧着し、該テープで導体周囲を包みこむので
あるが、接着剤の硬化速度が遅いと加熱圧着後、テープ
と導体間またはテープとテープ間でテープのはがれが生
ずることがある。このような問題を防止するためには、
ヒータ温度を上昇させたり、ヒータを長くしたり、線速
度を遅くするなどの方法があるが、いずれも生産効率、
作業性などの面で悪影響が生ずる。The tape winding described above has a higher breakdown voltage per insulating layer thickness than a glass winding, and when used as a coil, the coil can be made compact. Furthermore, since the adhesive tape is applied vertically, the amount of adhesive tape material consumed can be reduced compared to when the adhesive tape is wound horizontally. However, when manufacturing such a tape winding,
Immediately after applying the A-stage adhesive to the preheated conductor, remove the insulating tape, or apply the adhesive in advance and dry it, then align the adhesive-coated surface of the B-stage tape, then heat and press it. The adhesive wraps around the conductor, but if the curing speed of the adhesive is slow, the tape may peel off between the tape and the conductor or between the tapes after heat-pressing. To prevent such problems,
There are methods such as increasing the heater temperature, lengthening the heater, and slowing down the linear speed, but all of these methods reduce production efficiency and
This will have an adverse effect on workability, etc.
本発明者らは、Bステージ接着剤をテープ片面に塗布し
た接着性テープを導体に縦添してなるテープ巻線の製造
時における前記問題点を解消し、高速でBステージ接着
剤を塗布した接着性テープを導体に接着させ、しかも可
撓性の良好なテープ巻線をうるため鋭意研究を重ねた結
果、エポキシ樹脂とブチラール樹脂とが40/60〜6
0/40 (重量比、以下同様)の範囲で混合されてな
る樹脂100部(重量部、以下同様)、一般式:
%式%
(式中、nは10〜11の整数を表わす)で示される構
成単位からなるポリアミド樹脂40〜200部□および
硬化剤からなる樹脂組成物の有機溶剤溶液をテープに塗
布、乾燥してなる接着性テープを用いることにより、前
記問題点を解消しうろことを見出し、本発明を完成した
。The present inventors have solved the above-mentioned problems in manufacturing a tape winding in which an adhesive tape with a B-stage adhesive applied to one side of the tape is attached vertically to a conductor, and has applied the B-stage adhesive at high speed. As a result of extensive research in order to bond adhesive tape to conductors and obtain a tape winding with good flexibility, we found that epoxy resin and butyral resin were 40/60~6.
100 parts (parts by weight, same below) of resin mixed in the range of 0/40 (weight ratio, same below), general formula: % formula % (wherein n represents an integer from 10 to 11) The above-mentioned problems can be solved by using an adhesive tape obtained by coating a tape with an organic solvent solution of a resin composition consisting of 40 to 200 parts of a polyamide resin consisting of structural units of The present invention has been completed.
本発明に用いるエポキシ樹脂はとくに限定さレス、りと
エバビスフェノールAとエビクロルヒドリンメから合成
されるエピコート1001、エピコート1004、エピ
コート1007、エピコート1009 (以下、ンエル
化学社製)などやビスフェノールAとβ−メチルエピク
ロルヒドリンとから合成されるエピクロン1010、エ
ピクロン6010(以上、大日本インキ化学工業11な
どのビスフェノールA型エポキシ樹脂、このほかビスフ
ェノールy型エポキシ樹脂、ノボラック型エポキシ樹脂
などがあげられる。The epoxy resins used in the present invention are not particularly limited, and include Epikot 1001, Epicoat 1004, Epicoat 1007, and Epicoat 1009 (hereinafter, manufactured by Neru Kagaku Co., Ltd.) synthesized from Les, Ritoeva bisphenol A and shrimp chlorohydrin, and bisphenol A. Examples include bisphenol A type epoxy resins such as Epiclon 1010 and Epiclon 6010 (both manufactured by Dainippon Ink Chemical Industry Co., Ltd. 11) synthesized from β-methylepichlorohydrin, bisphenol Y type epoxy resins, novolak type epoxy resins, etc.
本発明に用いるブチラール樹脂はとくに限定されるもの
ではなく、たとえばデンカブチラール$2000−L、
デンカブチラール#60叩−1、デンカブチラール#4
000−2 (以下、電気化学工業■製)などがあげら
れる。The butyral resin used in the present invention is not particularly limited, and examples include Denka Butyral $2000-L,
Denka Butyral #60 Hit-1, Denka Butyral #4
000-2 (hereinafter, manufactured by Denki Kagaku Kogyo ■), etc.
前記エポキシ樹脂とブチラール樹脂との混合割合は40
AO〜60/40、好ましくは45755〜55A5で
ある。該エポキシ樹脂の割合が前記範囲より小さくなる
とコイル巻後150°0〜200°aで加熱すると、テ
ープ間でハガレが生じやすくなり、前記範囲より大きく
なるとテープ間、テープ導体間の接着速度が遅くなり、
製造速度が低下し、いずれも好ましくない。The mixing ratio of the epoxy resin and butyral resin is 40
AO to 60/40, preferably 45755 to 55A5. If the proportion of the epoxy resin is smaller than the above range, peeling will easily occur between the tapes when heated at 150°0 to 200°a after coil winding, and if it is larger than the above range, the adhesion speed between tapes and tape conductors will be slow. Become,
The production speed decreases, which is not preferable.
本発明に用いる一般式:
(式中、nは前記と同じ)で示される構成単位からなる
ポリアミド樹脂としては、たとえばリルサン社製のNy
lon 11 、Nylon 12のようなアルキレン
基の長いポリアミド樹脂があげられる。前記構成単位中
のnは10〜11の整数であり、nが10未満になると
、ポリアミド樹脂の融点が高くなり、接着性がわるくな
り1nが11をこえると工業的に入手できなくなる。As the polyamide resin composed of the structural unit represented by the general formula: (wherein n is the same as above) used in the present invention, for example, Ny
Examples include polyamide resins with long alkylene groups such as lon 11 and nylon 12. n in the structural unit is an integer of 10 to 11; when n is less than 10, the melting point of the polyamide resin becomes high and the adhesiveness deteriorates, and when 1n exceeds 11, it becomes impossible to obtain it industrially.
本発明に用いる硬化剤としては、エポキシ樹脂の硬化剤
として通常使用される硬化剤、たとえばエチルメチルイ
ミダゾールまたは2−メチルイミダゾールなどのイミダ
ゾール系硬化剤、ジエチレントリアミン、トリエチレン
テトラミン、ジアジ/ジフェニルメタンなどのアミン系
硬化剤、三フッ化ホウ素−モノエチルアミン、三フッ化
ホウ素−モツメチルアミン、三フッ化ホウ)ジメチルア
ミンなどのアミン錯塩系硬化剤、無水へキサヒドロフタ
ル酸、無水メチルナジック酸、無水クロレンド酸などの
酸無水物系硬化剤などが使用されうる。The curing agent used in the present invention includes curing agents commonly used as curing agents for epoxy resins, such as imidazole curing agents such as ethylmethylimidazole or 2-methylimidazole, and amines such as diethylenetriamine, triethylenetetramine, and diazi/diphenylmethane. Amine complex curing agents such as boron trifluoride-monoethylamine, boron trifluoride-motumethylamine, boron trifluoride dimethylamine, hexahydrophthalic anhydride, methylnadic anhydride, chlorendic anhydride An acid anhydride curing agent such as an acid may be used.
エポキシ樹脂とブチラール樹脂との混合物100部に対
するどリアミド樹脂の配合量は40〜200部、好まし
くは100〜200部である。該配合量が40部未満に
なると、コイル巻後iso 0o〜2oooOで加熱す
ると、テープ間でハガレが生じゃすくなり、200部を
こえると成形時、テープ間、テープ導体間の接着速度が
遅くなり、製造速度が低下し、好ましくない。The amount of doryamide resin blended is 40 to 200 parts, preferably 100 to 200 parts, per 100 parts of the mixture of epoxy resin and butyral resin. If the blending amount is less than 40 parts, peeling tends to occur between the tapes when heated at ISO 0 to 2oooO after coil winding, and if it exceeds 200 parts, the adhesion speed between tapes and tape conductors during molding is slow. This decreases the manufacturing speed, which is undesirable.
エポキシ樹脂とブチラール樹脂との混合物100部に対
する硬化剤の配合源はイミダゾール、7tン、アミン錯
体系硬化剤のはあい0.2〜10部、酸無水物系硬化剤
のばあい20〜50部の範囲で添加すればよい。The source of the curing agent for 100 parts of the mixture of epoxy resin and butyral resin is imidazole, 7 tons, 0.2 to 10 parts of the amine complex curing agent, and 20 to 50 parts of the acid anhydride curing agent. It may be added within this range.
前記樹脂組成物に必要に応じて他の成分を添加してもよ
い。添加されうる他の成分としては、たとえばフェノー
ル樹脂、メラミン樹脂などがあげられ、該組成物100
部に対しする添加量としては10部以下、好ましくは5
部以下である。Other components may be added to the resin composition as necessary. Other components that may be added include, for example, phenol resin, melamine resin, etc., and the composition 100
The amount added per part is 10 parts or less, preferably 5 parts.
below.
エポキシ樹脂、ブチラール樹脂、ポリアミド樹脂、硬化
剤および必要に応じて加えられる他の成分の調製方法と
してはとくに制限はないが、加熱混合させる工程が必要
な方法を採用するばあいには、この工程が終了したのち
硬化剤を加えることが好ましい。前記組成物は、有機溶
剤溶液の状態でテープに塗布され、乾燥され、本発明の
接着性テープが製造されるため、有機溶剤に溶解し、溶
液として調製することが製造効率、製造された接着性テ
ープの性能などの点から好ましい。There are no particular restrictions on the method for preparing the epoxy resin, butyral resin, polyamide resin, curing agent, and other components added as necessary. However, if a method that requires heating and mixing is adopted, this step It is preferable to add a curing agent after the completion of the curing process. The composition is applied to the tape in the form of an organic solvent solution and dried to produce the adhesive tape of the present invention. Therefore, dissolving the composition in an organic solvent and preparing it as a solution increases the production efficiency and the produced adhesive. This is preferable from the viewpoint of the performance of the adhesive tape.
前記目的に用いる有機溶剤としては、エポキシ樹脂、ブ
チラール樹脂、ポリアミド樹脂、硬化剤などを溶解する
ものであればとくに限定されるものではなく、たとえば
クレゾール、ナフt、)ルエン、キンレン、セロソルブ
なトカアげられる。しかし、本発明に用いられる芳香族
アミド紙製テープ、芳香族ポリアミド紙を基材の一部と
して含むテープ、マイカ混抄紙などの混抄紙製テープ、
織布製テープ、不織布製テープ、紙テープ、あるいはフ
ィルムとこれらとの組合わせテープなど20〜2009
/m”、好ましくは40〜100g/m のテープへの
塗布しやすさ、乾燥性、接着剤の溶解性などの点からク
レゾール、ナフサなどが好ましい。The organic solvent used for the above purpose is not particularly limited as long as it dissolves epoxy resins, butyral resins, polyamide resins, curing agents, etc., and includes, for example, cresol, napht, )luene, quinolene, and cellosolve. can be lost. However, the aromatic amide paper tape used in the present invention, the tape containing aromatic polyamide paper as part of the base material, the tape made from mixed paper such as mica mixed paper,
Woven fabric tape, non-woven fabric tape, paper tape, or combination tape of film and these, etc. 20-2009
/m'', preferably 40 to 100 g/m 2 Cresol, naphtha, etc. are preferred from the viewpoint of ease of application to tape, drying properties, solubility of adhesive, etc.
前記有機溶剤溶液のテープへの塗布法としては、通常用
いられるスプレー塗布、ロールツーター塗布などの方法
が採用されうる。テープの片面へ該溶液を塗布後、該テ
ープは接着剤が硬化しない程度の条件、たとえば120
°0×15〜60分間のような条件で乾燥され、接着性
テープかえられる。テープへの接着剤の塗布量は固形分
で20〜sop/m2、好ましくは25〜aoy/rn
2である。As a method for applying the organic solvent solution to the tape, commonly used methods such as spray coating and roll-to-roll coating may be employed. After applying the solution to one side of the tape, the tape is heated under conditions such that the adhesive does not harden, e.g.
The adhesive tape is dried under conditions such as 0x15 to 60 minutes and replaced with adhesive tape. The amount of adhesive applied to the tape is 20 to sop/m2 in terms of solid content, preferably 25 to aoy/rn.
It is 2.
つぎに本発明の接着性テープを実施例にもとづき説明す
る。Next, the adhesive tape of the present invention will be explained based on Examples.
実施例1〜6および比較例1〜4
第1表に示す樹脂組成物をクレゾールに溶解させた20
%(重量%、以下同様)溶液を調製し、該溶液を2 n
il Nomex 410 (デュポン社製の芳香族ポ
リアミド紙)にロールツーターにより塗布し、120°
O×20分間加熱乾燥させた片面接着性テープを製造し
た。なお、使用したブチラール樹脂は電気化学工業■製
の$ 5000− K、硬化剤は三フフ化ホウ素モノエ
チルアミンであった。Examples 1 to 6 and Comparative Examples 1 to 4 20 in which the resin compositions shown in Table 1 were dissolved in cresol.
% (wt%, the same applies hereinafter) solution, and the solution was diluted with 2 n
il Nomex 410 (aromatic polyamide paper manufactured by DuPont) with a roll tool and rotated at 120°
A single-sided adhesive tape was produced by heating and drying it for 20 minutes. The butyral resin used was $5000-K manufactured by Denki Kagaku Kogyo ■, and the curing agent was boron trifluoride monoethylamine.
えられた接着性テープには接着剤組成物が固形分で32
9/m”塗布されていた。The resulting adhesive tape contained an adhesive composition with a solid content of 32
9/m” was applied.
該テープを2−0mm X 5.Onmの平角銅線に2
5m/分でそわせたのち、300qO11,2mのヒー
タ中を通過させ、縦添し、テープ巻線をえた。The tape is 2-0mm x 5. Onm rectangular copper wire 2
After being aligned at a rate of 5 m/min, the wire was passed through a 300 qO11, 2 m heater, and was vertically attached to obtain a tape winding.
えられたテープ巻線を用いて下記の方法で、接着性テー
プの接着速さである。早期接着性、絶縁破壊電圧(BD
V)(直線)、加熱後の接着状態、可撓性を測定した。The adhesion speed of the adhesive tape was determined using the obtained tape winding in the following manner. Early adhesion, breakdown voltage (BD
V) (straight line), adhesion state after heating, and flexibility were measured.
その結果を第1表に示す。The results are shown in Table 1.
(早期接着性)
線速度25m/分で縦添したときの巻取時に接着したテ
ープ重ね部が開かないものを良、開くものを不良として
判定した。開くものについては線速度を変化させ、開か
ない線速度を測定し、第1表の早期接着性の欄の0内に
記載した。(Early adhesion) When the tape was applied vertically at a linear speed of 25 m/min, the overlapped portion of the tape that did not open during winding was evaluated as good, and the tape that opened was evaluated as poor. For those that opened, the linear speed at which they did not open was measured by changing the linear speed, and the results were recorded in 0 in the early adhesion column of Table 1.
(BDV)
直線状のテープ巻線にアルミ箔を10cmの長さにわた
って巻き、導体とアルミ箔との間にilEを印加し、そ
の耐圧を測定した。(BDV) Aluminum foil was wound around a linear tape winding over a length of 10 cm, and ilE was applied between the conductor and the aluminum foil to measure its withstand voltage.
(加熱後の接着状態ン
(a)直線のばあい:直線状のテープ巻線を2[100
0の恒温槽に6時間放置し、接着性テープがはがれない
ばあいを良、はがれたばあいを不良として判定した。(Adhesion state after heating) (a) In the case of a straight line: A straight tape winding is
The adhesive tape was left in a constant temperature bath for 6 hours, and the case where the adhesive tape did not peel off was judged as good, and the case where it peeled off was judged as poor.
(b)曲げ後のばあい:前もってフラットヮイズに存在
する接着性テープ重ね部分が内側になるように10倍径
(このばあいは2Qmm)の丸棒で180°曲げたのち
、200°O恒温槽に6時間放置し、接着性テープがは
がれないばあいを良、はがれたばあいを不良として判定
した。(b) After bending: After bending 180° with a round rod of 10 times the diameter (in this case, 2Qmm) so that the overlapping part of the adhesive tape that exists in the flat size is on the inside, the adhesive tape is placed in a constant temperature oven at 200°C. The adhesive tape was left to stand for 6 hours, and the case where the adhesive tape did not peel off was judged as good, and the case where it peeled off was judged as poor.
(可撓性)
テープ巻線の7ラツトワイズまたはエツジワイズに丸棒
をあて180°曲げたとき、テープわれが生じない銅線
の厚さまたは巾に対する最小丸棒径を銅線の厚さまたは
巾の倍率として測定した。(Flexibility) When a round bar is applied to the 7-ratwise or edge-wise tape winding and bent 180 degrees, the minimum round bar diameter is the thickness or width of the copper wire that does not cause tape fraying. It was measured as a magnification.
Claims (1)
60〜60/40の範囲で混合されてなる樹脂100重
量部、一般式: (式中、nは10〜11の整数を表わす)で示される構
成単位からなるポリアミド樹脂40〜200重量部およ
び硬化剤からなる樹脂組成物の有機溶剤溶液をテープに
塗布、乾燥してなる接着性テープ。[Claims] 1 The weight ratio of epoxy resin and butyral resin is 40/
100 parts by weight of a resin mixed in the range of 60 to 60/40, 40 to 200 parts by weight of a polyamide resin consisting of structural units represented by the general formula: (wherein n represents an integer of 10 to 11), and cured. An adhesive tape made by coating a tape with an organic solvent solution of a resin composition consisting of an agent and drying it.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18755883A JPS6079083A (en) | 1983-10-06 | 1983-10-06 | Adhesive tape |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18755883A JPS6079083A (en) | 1983-10-06 | 1983-10-06 | Adhesive tape |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6079083A true JPS6079083A (en) | 1985-05-04 |
Family
ID=16208177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18755883A Pending JPS6079083A (en) | 1983-10-06 | 1983-10-06 | Adhesive tape |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6079083A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0397824U (en) * | 1990-01-26 | 1991-10-09 |
-
1983
- 1983-10-06 JP JP18755883A patent/JPS6079083A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0397824U (en) * | 1990-01-26 | 1991-10-09 |
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