JPS58214225A - Method of producing resin coated electric device - Google Patents

Method of producing resin coated electric device

Info

Publication number
JPS58214225A
JPS58214225A JP9872482A JP9872482A JPS58214225A JP S58214225 A JPS58214225 A JP S58214225A JP 9872482 A JP9872482 A JP 9872482A JP 9872482 A JP9872482 A JP 9872482A JP S58214225 A JPS58214225 A JP S58214225A
Authority
JP
Japan
Prior art keywords
epoxy resin
parts
resin
curing
mold
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
Application number
JP9872482A
Other languages
Japanese (ja)
Other versions
JPH0221086B2 (en
Inventor
野上 文夫
土橋 勝
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP9872482A priority Critical patent/JPS58214225A/en
Publication of JPS58214225A publication Critical patent/JPS58214225A/en
Publication of JPH0221086B2 publication Critical patent/JPH0221086B2/ja
Granted legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は屋外で使用する碍子1ブツシング、変成器)変
流器、変圧器などの導体や巻線の周囲を、特殊なエポキ
シ樹脂で被覆して耐候性1耐トラツキング性にすぐれた
電気装置を製造する方法に関する。
Detailed Description of the Invention The present invention provides weather resistance and tracking resistance by coating the conductors and windings of insulators used outdoors, transformers, current transformers, transformers, etc. with a special epoxy resin. The present invention relates to a method of manufacturing an electrical device with excellent performance.

一般(こ屋外用のエポキシ樹脂として脂環式ジグリシジ
ルエステル型エポキシ樹脂が耐候性、耐トラツキング性
にすぐれるので用いられている。屋外で使用される導体
や巻線の周囲を樹脂で被覆して電気装置とするばあいに
おいても同様である。
Generally, alicyclic diglycidyl ester type epoxy resin is used as an epoxy resin for outdoor use because it has excellent weather resistance and tracking resistance. The same applies to electrical equipment.

この屋外電気装置用として用いるばあいには、脂環式ジ
グリシジルエステル型エホ゛キシ樹脂は脂環式酸無水物
や充填剤とともに用いられている。
When used for outdoor electrical equipment, alicyclic diglycidyl ester type epoxy resins are used together with alicyclic acid anhydrides and fillers.

しかしながら、従来の被覆樹脂である脂環式ジグリシジ
ルエステル型エポキシ樹脂と脂環式酸無水物との混合物
は高温において急激に反応速度が大きくなるためえられ
る硬化物の、硬化収縮が大きくなり1また高温において
は僅かの温度差で敏感に反応速度が興なるためえられる
硬化物の硬化度に部分的な差が生じ、その結果樹脂層に
割れやヒケあるいはボイドが生じたり、樹脂部と導体部
や巻線部との間に剥れが生じ、電気装置の電気的特性に
悪影響をおよぼす欠点があった。
However, the reaction rate of conventional coating resins, which are mixtures of alicyclic diglycidyl ester type epoxy resins and alicyclic acid anhydrides, increases rapidly at high temperatures, resulting in large curing shrinkage of the resulting cured product. In addition, at high temperatures, the reaction rate is sensitive to slight temperature differences, so there are local differences in the degree of hardening of the cured product, which can result in cracks, sink marks, or voids in the resin layer, and damage to the resin and conductor. This has the disadvantage that peeling occurs between the parts and the winding parts, which adversely affects the electrical characteristics of the electrical device.

このため、硬化反応を低温で行なわせる方法も従来採ら
れていた。しかし、この低温法も硬化処理に長時間髪す
ること、低温では完全に硬化しないので低温で硬化させ
たのちさらに高温で硬化させる2段階の硬化工程を必要
とすること1そのため作業性、生産性が低下すること、
樹脂と充填剤との混合物が流動状態で長時間存続するた
めその間に充填剤が沈降してえられる硬化物の充填剤含
有率に高低差が生じること、この充填剤含有率の高低差
に基づいて熱膨張率に差が生じ電気装置の割れを発生さ
せる原因となること、ことに電気装置における表面での
充填剤含有率の不均一性は屋外での日光、雨、汚損物に
よって起る表面の荒れにおいてその荒れ状態が不均一化
することを促進すること、表面の荒れ状態が不均一であ
ると表面電界の集中を招き易くなりトラッキング、局部
的エロージョンの集中を招いてしばしば沿面閃絡の模因
となることなどの欠点があった。
For this reason, a method of performing the curing reaction at a low temperature has conventionally been adopted. However, this low-temperature method also requires a long period of time for curing, and since it is not completely cured at low temperatures, it requires a two-step curing process of curing at low temperatures and then curing at higher temperatures.1 This reduces workability and productivity. decrease,
Because the mixture of resin and filler remains in a fluid state for a long time, the filler settles during that time, resulting in a difference in filler content in the cured product.Based on this difference in filler content. Differences in the coefficient of thermal expansion can cause cracks in electrical equipment, and in particular unevenness in the filler content on the surface of electrical equipment is caused by outdoor exposure to sunlight, rain, and dirt. To promote unevenness in the roughness of the surface, uneven surface roughness tends to cause concentration of the surface electric field, leading to tracking, localized concentration of erosion, and often creeping flash. There were drawbacks such as being a cause of death.

本発明の目的は前述の欠点を解消することにある。すな
わち、高温での硬化反応を穏和なものとして割れ、ヒケ
、剥れ、ボイド、充填剤の沈降のない均一な被覆樹脂層
を形成させ為耐候性、耐トラツキング性にすぐれた樹脂
被覆電気装置の製造法を提供するものである。
The aim of the invention is to eliminate the above-mentioned drawbacks. In other words, the curing reaction at high temperatures is mild, and a uniform coating resin layer is formed without cracking, sink marks, peeling, voids, or filler sedimentation, resulting in a resin-coated electrical device with excellent weather resistance and tracking resistance. It provides a manufacturing method.

本発明は(A)脂環式ジグリシジルエステル型エポキシ
樹脂A該エポキシ樹脂100部(重量部、以下同様)あ
たり10〜60部のジグリシジル水添ビスフェノールA
1脂環式酸無水物、石英粉末、シランカップリング剤お
よび促進剤からなる混合物を、(B)あらかじめ加熱反
応させてエポキシ当量が初期値の1.1〜1.4倍、1
00〜120°Cにおける粘度が10〜50ボイズの樹
脂混合物とし、(C)これを導体あるいは巻線がセット
された金型内に注入して100〜140°Oで加熱硬化
させて樹脂被覆電気装置を製造することを特徴とする。
(A) Alicyclic diglycidyl ester type epoxy resin
1. A mixture consisting of an alicyclic acid anhydride, quartz powder, a silane coupling agent, and an accelerator is (B) heated and reacted in advance so that the epoxy equivalent is 1.1 to 1.4 times the initial value, 1
A resin mixture with a viscosity of 10 to 50 voids at 00 to 120°C is prepared, and (C) this is injected into a mold in which a conductor or winding is set and heated and cured at 100 to 140°C to form a resin-coated electrical It is characterized by manufacturing a device.

本発明で用いるジグリシジル水添ビスフェノールAの化
学構造は次式で表わされる。
The chemical structure of diglycidyl hydrogenated bisphenol A used in the present invention is represented by the following formula.

ジグリシジル水添ビスフェノールAは本発明において脂
環式ジグリシジル型エポキシ樹脂100部に対し10〜
60部用いられる。その使用量が10部未満であると硬
化反応を穏和にすることができないし、他方30部を超
えると硬化反応時間が長くなって生産性が低下し、充填
剤の沈降が生じて不均一な被覆樹脂層となり好ましくな
い。
In the present invention, diglycidyl hydrogenated bisphenol A is used in an amount of 10 to 100 parts per 100 parts of alicyclic diglycidyl type epoxy resin.
60 copies are used. If the amount used is less than 10 parts, the curing reaction cannot be moderated, while if it exceeds 30 parts, the curing reaction time becomes longer, productivity decreases, and sedimentation of the filler occurs, resulting in non-uniformity. It becomes a coating resin layer, which is not preferable.

本発明で用いる脂環式ジグリシジル型エポキシ樹脂とし
ては、たとえばヘキサヒドロフタル酸ジグリシジルエス
テル、テトラヒドロフタル酸ジグリシジルエステル、ヘ
キサヒドロイソフタル酸ジクリシジルエステル、ヘキサ
ヒドロテレフタル酸ジグリシジルエステルを構成単位と
するものなどをあげることができ、また脂環式酸無水物
としては、たとえばヘキサヒドロ無水フタル酸、テトラ
ヒドロ無水フタル酸、3−(4−)メチルテトラ無水フ
タル酸、3−(4−)メチルへキサヒドロ無水7タル酸
などをあげることができる。
The alicyclic diglycidyl type epoxy resin used in the present invention has, for example, hexahydrophthalic acid diglycidyl ester, tetrahydrophthalic acid diglycidyl ester, hexahydroisophthalic acid dicrycidyl ester, hexahydroterephthalic acid diglycidyl ester as a constituent unit. Examples of alicyclic acid anhydrides include hexahydrophthalic anhydride, tetrahydrophthalic anhydride, 3-(4-)methyltetraphthalic anhydride, and 3-(4-)methylhexahydrophthalic anhydride. Examples include 7-talic anhydride.

石英粉末としてはたとえばシリカ、熔融石英などの粉末
が用いられ、シランカップリング剤としてはたとえばβ
−(6,4−エポキシシクロヘキシル)エチルトリメト
キシシラン、γ−グリシドキシプロピルトリメトキシシ
ランなどが用いられる。
As the quartz powder, for example, silica or fused quartz powder is used, and as the silane coupling agent, for example, β
-(6,4-epoxycyclohexyl)ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, etc. are used.

また1促進剤としてはたとえばベンジルジメチルアミン
、トリス(ジメチルアミノメチル)フェノールのような
アミ7類、三フッ化ホウ素エチルアミン錯化合物、トリ
エタノールアミンホウ素酸[,2−エチル−4−エチル
イミダゾール、2−メチルイミダゾールのようなイミダ
ゾール類などが用いられる。
Further, as the first accelerator, for example, benzyldimethylamine, tris(dimethylaminomethyl)phenol, etc., boron trifluoride ethylamine complex compound, triethanolamine boron acid [,2-ethyl-4-ethylimidazole, -Imidazoles such as methylimidazole are used.

本発明においては所望に応じて炭酸カルシウム、酸化7
 ルミニウム、水酸化アルミニウム、タルク、クレーの
ような充填剤、顔料、染料、可塑剤、難燃化剤などを適
量添加してもよい。
In the present invention, calcium carbonate, 7 oxide
Appropriate amounts of fillers such as aluminum, aluminum hydroxide, talc, clay, pigments, dyes, plasticizers, flame retardants, etc. may be added.

以下、実施例および比較例をあげて本発明を具体的に説
明する。
The present invention will be specifically explained below with reference to Examples and Comparative Examples.

実施例1〜3 脂環式ジグリシジルエポキシ樹脂(アラルダイ) OY
 184 、チバガイギー社製) 100部、ジグリシ
ジル水添ビスフェノールA to部(実施例1)、20
部(実施例2)または30部(実施例6)、ヘキサヒド
ロ無水7タル酸100部、シリカ@(平均粒径1.5μ
rn)500部、r−グリシドキシプロビルトリメトキ
シシラン6部およびベンジルジメチルアミン0.5部を
混合し、ついで1時間105°Oで加熱反応させてえた
シリカ粉を除いた樹脂部のエポキシ当量が初期値(55
0)の1.62倍(実施例1)、1.19倍(実施例2
)、1.15倍(実施例6)、105°Oにおける粘度
が22ボイス(実施例1)、15ボイズ(実施例2)、
15ボイス(実施例6)の樹脂混合物を所定の金型内に
注入して160°aで24時間加熱し硬化させ、第1図
に示した被覆樹脂長500mm。
Examples 1-3 Alicyclic diglycidyl epoxy resin (Araldai) OY
184, manufactured by Ciba Geigy) 100 parts, diglycidyl hydrogenated bisphenol A to parts (Example 1), 20
parts (Example 2) or 30 parts (Example 6), 100 parts of hexahydroheptalic anhydride, silica@(average particle size 1.5μ)
rn) 500 parts, r-glycidoxypropyltrimethoxysilane 6 parts and benzyldimethylamine 0.5 part were mixed and then heated and reacted at 105°O for 1 hour to obtain an epoxy resin part from which silica powder was removed. The equivalent weight is the initial value (55
0) 1.62 times (Example 1), 1.19 times (Example 2)
), 1.15 times (Example 6), viscosity at 105 ° O is 22 voices (Example 1), 15 voices (Example 2),
A resin mixture of 15 voices (Example 6) was injected into a predetermined mold and heated at 160° a for 24 hours to cure, resulting in a coated resin length of 500 mm as shown in FIG.

7ランジ& 220mmのブッシングを作製した。7 langes & 220mm bushings were made.

比較例1 アラルダイト(OY 184) 100部、ヘキサヒド
ロ無水フタル酸90部、シリカ粉450部、γ−グリシ
ドキシプロピルトリメトキシシラン2.7部およびベン
ジルジメチルアミン0.5部を10500で10分間万
口熱混合したほかは実施例1と同様にしてブッシングを
作製した。
Comparative Example 1 100 parts of Araldite (OY 184), 90 parts of hexahydrophthalic anhydride, 450 parts of silica powder, 2.7 parts of γ-glycidoxypropyltrimethoxysilane and 0.5 parts of benzyldimethylamine were heated at 10500 for 10 minutes. A bushing was produced in the same manner as in Example 1, except that the mixture was mixed by mouth.

比較例2 加熱混合を80°Oで10分間行ない、金型内での加熱
硬化条件をまず80°0で4時間、ついで150’Oで
20時間としたほかは比較例1と同様にしてブッシング
を作製した。
Comparative Example 2 A bushing was prepared in the same manner as in Comparative Example 1, except that heating and mixing was performed at 80°O for 10 minutes, and the heat curing conditions in the mold were first at 80°0 for 4 hours and then at 150°O for 20 hours. was created.

前記の実施例および比較例におけるその金型内での硬化
時に上部であったヒダ部のシリカ粉充填率を測定し、そ
の値と配合量から算出した理論充填率との差を重量%で
表わし、これを沈降量として第1表に示す。
In the above Examples and Comparative Examples, the silica powder filling rate of the upper pleat part during curing in the mold was measured, and the difference between that value and the theoretical filling rate calculated from the blended amount was expressed in weight%. This is shown in Table 1 as the amount of sedimentation.

第   1   表 実施例1〜6でえたブッシングには割れ、ヒケ、ボイド
が認められながったが、比較例1でえたものには硬化後
の金型内においてすでに7ランジの根元で円周方向の割
れが認められたし、比較例2におけるものには割れは認
められないものの金型内で上部となったヒダ部にシリカ
粉充填率の少ない部分が認められ、えられたブッシング
はその表面のシリカ粉充填率が不均一なものであった。
Table 1 No cracks, sink marks, or voids were observed in the bushings obtained in Examples 1 to 6, but in the bushings obtained in Comparative Example 1, the circumference was already broken at the root of the 7 flange in the mold after curing. Cracks in the direction were observed, and although no cracks were observed in the bushing of Comparative Example 2, a portion with a low silica powder filling rate was observed in the folds at the upper part of the mold, and the resulting bushing The silica powder filling rate on the surface was non-uniform.

また、実施例1〜6でえたブッシングはウェザオメータ
を用いて屋外暴露10年間に相当する試験を行なったの
ちにおいても外観性、機械的性質、耐トラツキング性が
低下しないものであり、■EC法によるトラッキング指
数が600 V以上であった。
In addition, the bushings obtained in Examples 1 to 6 did not deteriorate in appearance, mechanical properties, and tracking resistance even after being subjected to a test equivalent to 10 years of outdoor exposure using a weatherometer. The tracking index was 600 V or more.

なお、第2図に実施例および比較例でえた樹脂混合物を
金型への注入時に分取し、その加熱混合時における温度
での粘度特性を示した。
In addition, FIG. 2 shows the viscosity characteristics of the resin mixtures obtained in the examples and comparative examples taken at the temperature during heating and mixing, which were separated at the time of injection into the mold.

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

第1図は実施例および比較例で作製したブッシングの断
面図1第2図は樹脂混合物の粘度特性を示すグラフであ
る。 (図面の主要符号) (1):ブツシング (2):被覆樹脂 (3):導 体 代理人  葛  野  信  − (ほか1名)
FIG. 1 is a cross-sectional view of bushings produced in Examples and Comparative Examples. FIG. 2 is a graph showing viscosity characteristics of resin mixtures. (Main symbols on the drawings) (1): Bushing (2): Coating resin (3): Conductor agent Shin Kuzuno - (1 other person)

Claims (1)

【特許請求の範囲】[Claims] (1)導体あるいは巻線がセットされた金型内にエポキ
シ樹脂を注入し、硬化させてエポキシ樹脂で被覆された
電気装置を製造するにあたり、(4)脂環式ジグリシジ
ルエステル型エポキシ樹脂、該エポキシ樹脂100重量
部あたり10〜60重量部のジグリシジル水添ビスフェ
ノールA、脂環式酸無水物、石英粉末、シランカップリ
ング剤および促進剤からなる混合物を− (B)あらかじめ加熱反応させてエポキシ当量が初期値
の1.1〜1.4倍、100〜120°Cにおける粘度
が10〜50ボイズの樹脂混合物とし、 (0)これを金型内に注入して100〜140°Cで加
熱硬化させることを特徴とする樹脂被覆電気装置の製造
法。
(1) When producing an electrical device coated with epoxy resin by injecting epoxy resin into a mold in which a conductor or winding is set and curing it, (4) alicyclic diglycidyl ester type epoxy resin, A mixture consisting of 10 to 60 parts by weight of diglycidyl hydrogenated bisphenol A, alicyclic acid anhydride, quartz powder, a silane coupling agent, and an accelerator per 100 parts by weight of the epoxy resin is heated and reacted in advance to form an epoxy resin. A resin mixture with an equivalent weight of 1.1 to 1.4 times the initial value and a viscosity of 10 to 50 voids at 100 to 120°C, (0) is poured into a mold and heated at 100 to 140°C. A method for producing a resin-coated electrical device characterized by curing.
JP9872482A 1982-06-07 1982-06-07 Method of producing resin coated electric device Granted JPS58214225A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9872482A JPS58214225A (en) 1982-06-07 1982-06-07 Method of producing resin coated electric device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9872482A JPS58214225A (en) 1982-06-07 1982-06-07 Method of producing resin coated electric device

Publications (2)

Publication Number Publication Date
JPS58214225A true JPS58214225A (en) 1983-12-13
JPH0221086B2 JPH0221086B2 (en) 1990-05-11

Family

ID=14227462

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9872482A Granted JPS58214225A (en) 1982-06-07 1982-06-07 Method of producing resin coated electric device

Country Status (1)

Country Link
JP (1) JPS58214225A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06136092A (en) * 1992-10-27 1994-05-17 New Japan Chem Co Ltd Epoxy resin composition
JP2018517018A (en) * 2015-05-19 2018-06-28 ハンツマン・アドヴァンスト・マテリアルズ・ライセンシング・(スイッツランド)・ゲーエムベーハー Curing agent for thermosetting epoxy resin and method for producing insulation system for electrical engineering

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06136092A (en) * 1992-10-27 1994-05-17 New Japan Chem Co Ltd Epoxy resin composition
JP2018517018A (en) * 2015-05-19 2018-06-28 ハンツマン・アドヴァンスト・マテリアルズ・ライセンシング・(スイッツランド)・ゲーエムベーハー Curing agent for thermosetting epoxy resin and method for producing insulation system for electrical engineering

Also Published As

Publication number Publication date
JPH0221086B2 (en) 1990-05-11

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