JPH1139946A - Injection resin composition for insulation of electric apparatus - Google Patents

Injection resin composition for insulation of electric apparatus

Info

Publication number
JPH1139946A
JPH1139946A JP18952297A JP18952297A JPH1139946A JP H1139946 A JPH1139946 A JP H1139946A JP 18952297 A JP18952297 A JP 18952297A JP 18952297 A JP18952297 A JP 18952297A JP H1139946 A JPH1139946 A JP H1139946A
Authority
JP
Japan
Prior art keywords
resin
resin composition
epoxy resin
epoxy
equivalent
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
Application number
JP18952297A
Other languages
Japanese (ja)
Inventor
Takehiro Hamamura
武広 浜村
Katsushi Takano
克史 高野
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.)
Meidensha Corp
Meidensha Electric Manufacturing Co Ltd
Original Assignee
Meidensha Corp
Meidensha Electric Manufacturing Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Meidensha Corp, Meidensha Electric Manufacturing Co Ltd filed Critical Meidensha Corp
Priority to JP18952297A priority Critical patent/JPH1139946A/en
Publication of JPH1139946A publication Critical patent/JPH1139946A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Organic Insulating Materials (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide an injection resin composition for insulation of electric apparatus which has excellent characteristics as injection resin and good workability. SOLUTION: This resin composition for electric insulation consists of bisphenol epoxy resin as a main component and a curing agent and the main component is produced by mixing epoxy resin with 250 epoxy equivalent and epoxy resin with 400 epoxy equivalent at 80:20 ratio and the main component and the curing agent are mixed at 1:0.9 equivalent ratio and moreover, a silane coupling agent is added to silica as a filler.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は電気機器絶縁用注型
樹脂組成物及びエポキシ樹脂注型品に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cast resin composition for insulating electrical equipment and an epoxy resin cast product.

【0002】[0002]

【従来の技術】従来より、高電圧機器の絶縁材料及び構
造材料として、エポキシ樹脂をマトリックスとした高分
子複合硬化物、いわゆるモールド注型品が広く用いられ
ている。また、近年の社会の高度化、集中化に伴い、機
器の大容量・小型・高信頼性化が強く要求されており、
モールド注型品においても、静止機器最高使用温度10
5℃以上でも材料の物性が安定なガラス転移温度(以下
「Tg」という)115℃以上の耐熱性エポキシ注型品
を使用する傾向が強まってきている。
2. Description of the Related Art Hitherto, as an insulating material and a structural material for high-voltage equipment, a polymer composite cured product using an epoxy resin as a matrix, that is, a so-called molded product has been widely used. In addition, with the recent sophistication and concentration of society, large capacity, small size and high reliability of equipment are strongly demanded.
Even for mold cast products, the maximum operating temperature of stationary equipment is 10
There is an increasing tendency to use heat-resistant epoxy cast products having a glass transition temperature (hereinafter referred to as “Tg”) of 115 ° C. or higher, in which the physical properties of the material are stable even at 5 ° C. or higher.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、従来技
術によるTg=115℃以上の耐熱性エポキシ樹脂は、
硬く脆いため、得られた注型品が割れやすいという問題
がある。この結果、鉄導体を用いた耐クラック性試験結
果が−30℃以下を保持するために、作業性の悪い固形
エポキシ樹脂を使用したり、充填剤を多量に充填する必
要がある。この結果、粘度が著しく増粘し、作業可能時
間(ポットライフ)が短くなるために、作業性が大変悪
く工業的に非常に問題がある。
However, the heat-resistant epoxy resin having a Tg of 115 ° C. or higher according to the prior art,
Since it is hard and brittle, there is a problem that the obtained cast product is easily broken. As a result, it is necessary to use a solid epoxy resin having poor workability or to fill a large amount of a filler in order to maintain a crack resistance test result of −30 ° C. or lower using an iron conductor. As a result, the viscosity is remarkably increased, and the operable time (pot life) is shortened.

【0004】[0004]

【課題を解決するための手段】上記課題を解決する本発
明の電気絶縁用樹脂組成物は、ビスフェノール型エポキ
シ樹脂からなる主剤と、硬化剤とからなる電気絶縁用樹
脂組成物であって、主剤がエポキシ当量250のエポキ
シ樹脂とエポキシ当量400のエポキシ樹脂とを80:
20の割合で配合してなり、該主剤と硬化剤とを当量比
が1:0.9の範囲で混合し、充填材としてシリカにシラ
ンカップリング剤を添加してなることを特徴とする。
The electric insulating resin composition of the present invention for solving the above-mentioned problems is an electric insulating resin composition comprising a main agent comprising a bisphenol type epoxy resin and a curing agent, wherein the main agent comprises Is an epoxy resin having an epoxy equivalent of 250 and an epoxy resin having an epoxy equivalent of 400:
20. The main agent and the curing agent are mixed in an equivalent ratio of 1: 0.9, and a silane coupling agent is added to silica as a filler.

【0005】上記電気絶縁用樹脂組成物において、上記
充填剤のシリカの粒径が10〜15μmであることを特
徴とする。
[0005] The resin composition for electrical insulation is characterized in that the filler silica has a particle size of 10 to 15 µm.

【0006】本発明のエポキシ樹脂注型品は、上記電気
絶縁用樹脂組成物を用いてなることを特徴とする。
The epoxy resin cast product of the present invention is characterized by using the above-mentioned resin composition for electrical insulation.

【0007】[0007]

【発明の実施の形態】以下、本発明の実施の形態を説明
する。
Embodiments of the present invention will be described below.

【0008】本発明の電気絶縁用樹脂組成物は、エポキ
シ当量250のエポキシ樹脂とエポキシ当量400のエ
ポキシ樹脂とを80:20の割合で配合してなる主剤
と、硬化剤とからなり、該主剤と硬化剤とを当量比が
1:0.95〜0.9の範囲で混合し、充填材としてシリカ
シランカップリング剤を添加してなるものである。ここ
で、上記ビスフェノール型エポキシ樹脂とは、例えばエ
ポキシ当量250の「エピコート834」(商品名;油
化シェル社製)、エポキシ当量400の「YL−642
5B」(商品名;油化シェル社製)、エポキシ当量40
0の「CT−200」(商品名;チバガイギー社製)等
を挙げることができるが、本発明はこれに限定されるも
のではない。
[0008] The resin composition for electrical insulation of the present invention comprises a main agent obtained by mixing an epoxy resin having an epoxy equivalent of 250 and an epoxy resin having an epoxy equivalent of 400 in a ratio of 80:20, and a curing agent. And a curing agent in an equivalent ratio of 1: 0.95 to 0.9, and a silica silane coupling agent as a filler. Here, the above-mentioned bisphenol-type epoxy resin is, for example, “Epicoat 834” (trade name, manufactured by Yuka Shell Co., Ltd.) having an epoxy equivalent of 250, and “YL-642” having an epoxy equivalent of 400.
5B "(trade name; manufactured by Yuka Shell Co., Ltd.), epoxy equivalent 40
0 "CT-200" (trade name; manufactured by Ciba Geigy), but the present invention is not limited thereto.

【0009】上記エポキシ樹脂の配合としては、例えば
エポキシ当量が250のビスフェノール型エポキシ樹脂
とエポキシ当量が400のビスフェノール型エポキシ樹
脂とが、80:20で混合したものを主剤とするのが、
好ましい。
The epoxy resin is mixed with a bisphenol-type epoxy resin having an epoxy equivalent of 250 and a bisphenol-type epoxy resin having an epoxy equivalent of 400 at a ratio of 80:20.
preferable.

【0010】上記硬化剤としては、酸無水物である4−
メチルテトラヒドロ無水フタル酸(例えば、「HN−2
200」商品名、新日本理化社製、酸無水物当量=16
6:実施例1−1)、3−メチルテトラヒドロ無水フタ
ル酸(例えば、「MT−500」商品名、新日本理化社
製、酸無水物当量=166:実施例1−2)、ヘキサヒ
ドロ無水フタル酸(例えば、「HHPA」商品名、新日
本理化社製、酸無水物当量=154:実施例1−3)等
を挙げることができるが、本発明はこれに限定されるも
のではない。
The curing agent is an acid anhydride, 4-
Methyltetrahydrophthalic anhydride (for example, “HN-2
200 ", manufactured by Shin Nippon Rika Co., Ltd., acid anhydride equivalent = 16
6: Example 1-1), 3-methyltetrahydrophthalic anhydride (for example, “MT-500” trade name, manufactured by Shin Nippon Rika Co., Ltd., acid anhydride equivalent = 166: Example 1-2), hexahydrophthalic anhydride Acids (for example, “HHPA” trade name, manufactured by Shin Nippon Rika Co., Ltd., acid anhydride equivalent = 154: Examples 1-3), and the like, but the present invention is not limited thereto.

【0011】上記硬化促進剤としては、三級アミンを挙
げることができるが、本発明はこれに限定されるもので
はない。
As the curing accelerator, a tertiary amine can be mentioned, but the present invention is not limited to this.

【0012】本発明のエポキシ樹脂注型品は、上記配合
の電気絶縁用樹脂組成物に充填材を加えて所定の形状で
加熱硬化してなるものである。
The epoxy resin cast product of the present invention is obtained by adding a filler to the above-mentioned resin composition for electrical insulation and heating and curing the resin composition in a predetermined shape.

【0013】上記充填材としては、平均粒径10〜15
μmのシリカを挙げることができ、シランカップリング
剤を所定量配合してなるものである。そして、主剤と硬
化剤・硬化促進剤を当量比1:0.9で混合し、これに4
2〜46容量%の上記充填材を添加し均一になるまで混
合し、所定条件で加熱硬化処理をすることで、樹脂注型
品を得る。
[0013] As the filler, an average particle diameter of 10 to 15 is used.
μm of silica can be used, and a predetermined amount of a silane coupling agent is blended. Then, the main agent and the curing agent / curing accelerator are mixed at an equivalent ratio of 1: 0.9, and
2 to 46% by volume of the above filler is added, mixed until uniform, and heat-cured under predetermined conditions to obtain a resin cast product.

【0014】[0014]

【実施例】以下、本発明の効果を示す実施例を説明す
る。
Embodiments of the present invention will be described below.

【0015】(実施例1) a)主剤の調整 ベースの樹脂として一般的な特性を持つエポキシ当量2
50のビスフェノールA型エポキシ樹脂(例えば、「エ
ピコート834」商品名、油化シェル社製)とエポキシ
当量400のビスフェノールA型エポキシ樹脂(例え
ば、「CT−200」商品名、チバガイギー社製)を8
0:20の一定比率でブレンドした物を用いた。この樹
脂の所定量をステンレスビーカーにとり、100℃で加
熱しながら均一になるまで攪拌した。 b)硬化剤・硬化促進剤の調整 硬化剤は酸無水物である4−メチルテトラヒドロ無水フ
タル酸(例えば、「HN−2200」商品名、日立化成
社製、酸無水物当量=166:実施例1−1)、3−メ
チルテトラヒドロ無水フタル酸(例えば、「MT−50
0」商品名、新日本理化社製、酸無水物当量=154:
実施例1−2)、ヘキサヒドロ無水フタル酸(例えば、
「HHPA」商品名、新日本理化社製、酸無水物当量=
154:実施例1−3)を用い、反応をスムーズに開始
するため三級アミン(例えば、「DMP−30」商品
名、化薬アクゾ社製)を硬化促進剤として少量(0.2重
量%)添加し、均一になるまで攪拌した。 c)充填材 充填材として結晶状態が溶融で平均粒径11μmのシリ
カ(例えば「MCF−4」商品名)にシランカップリン
グ剤(例えば「KBM−403」商品名:信越シリコー
ン社製)を1phr添加し、(a)の主剤と(b)の硬
化剤・硬化促進剤を当量比1:0.9で混合し、均一に
なるまで混合し、100℃−2hr+100℃−15h
rで加熱硬化を行った。上記充填材の添加量は42容量
%とした。得られた樹脂は、下記「表2」に示すよう
に、Tgが115℃以上で且つ耐クラック性の高い耐熱
性注型樹脂であった。
(Example 1) a) Preparation of main agent Epoxy equivalent 2 having general properties as base resin
50 bisphenol A type epoxy resin (for example, “Epicoat 834” trade name, manufactured by Yuka Shell Co., Ltd.) and an epoxy equivalent of 400 bisphenol A type epoxy resin (for example, “CT-200” trade name, manufactured by Ciba Geigy Co., Ltd.)
What was blended at a fixed ratio of 0:20 was used. A predetermined amount of this resin was placed in a stainless beaker and stirred while heating at 100 ° C. until uniform. b) Adjustment of Curing Agent / Curing Accelerator The curing agent was 4-methyltetrahydrophthalic anhydride (for example, “HN-2200” trade name, manufactured by Hitachi Chemical Co., Ltd., acid anhydride equivalent = 166) as an acid anhydride. 1-1), 3-methyltetrahydrophthalic anhydride (for example, “MT-50”)
0 "trade name, manufactured by Shin Nippon Rika Co., Ltd., acid anhydride equivalent = 154:
Example 1-2), hexahydrophthalic anhydride (for example,
"HHPA" brand name, manufactured by Shin Nippon Rika, acid anhydride equivalent =
154: Using Example 1-3), a small amount (0.2% by weight) of a tertiary amine (for example, “DMP-30” (trade name, manufactured by Kayaku Akzo)) as a curing accelerator to start the reaction smoothly ) Was added and stirred until uniform. c) Filler 1 phr of silane coupling agent (for example, “KBM-403” (trade name, manufactured by Shin-Etsu Silicone Co., Ltd.)) is mixed with silica (for example, “MCF-4” (trade name)) having a crystalline state of melting and having an average particle diameter of 11 μm. Then, the main agent of (a) and the curing agent / curing accelerator of (b) are mixed at an equivalent ratio of 1: 0.9, and mixed until uniform, and 100 ° C.-2 hr + 100 ° C.-15 hours
Heat curing was performed at r. The amount of the filler added was 42% by volume. The obtained resin was a heat-resistant cast resin having a Tg of 115 ° C. or higher and a high crack resistance, as shown in Table 2 below.

【0016】(比較例1)比較例としては、ベースの樹
脂として一般的な特性を持つエポキシエポキシ当量40
0のビスフェノールA型エポキシ樹脂(例えば、「CT
−200」商品名、チバガイギー社製)を100とし、
硬化剤として4−メチルテトラヒドロ無水フタル酸(例
えば、「HN−2200」商品名、新日本理化社製、酸
無水物当量=166:実施例1−1と同様のもの)を用
いた以外は、実施例1と同様に操作した。なお、硬化促
進剤は添加しなかった。
(Comparative Example 1) As a comparative example, an epoxy epoxy equivalent of 40 having general characteristics as a base resin was used.
0 bisphenol A type epoxy resin (for example, “CT
−200 ”(trade name, manufactured by Ciba-Geigy) as 100,
Except that 4-methyltetrahydrophthalic anhydride (for example, “HN-2200” (trade name, manufactured by Shin Nippon Rika Co., Ltd., acid anhydride equivalent = 166: the same as in Example 1-1)) was used as a curing agent, The same operation as in Example 1 was performed. Note that no curing accelerator was added.

【0017】(実施例2)上記実施例1において、
「c)充填材」として結晶状態が溶融で平均粒径12μ
mのシリカ(例えば「FX−4」商品名:龍森社製)を
用いた以外は、実施例1と同様に操作した。得られた樹
脂は、下記「表3」に示すように、Tgが115℃以上
で且つ耐クラック性の高い耐熱性注型樹脂であった。
(Embodiment 2) In Embodiment 1 described above,
“C) Filler” has crystalline state of melting and average particle size of 12μ
The same operation as in Example 1 was performed except that m silica (for example, “FX-4” trade name: manufactured by Tatsumori Co., Ltd.) was used. As shown in Table 3 below, the obtained resin was a heat-resistant cast resin having a Tg of 115 ° C. or higher and a high crack resistance.

【0018】(実施例3)上記実施例1において、
「c)充填材」として結晶状態が溶融で平均粒径15μ
mのシリカ(例えば「RD−8AL」商品名:龍森社
製)を用いた以外は、実施例1と同様に操作した。得ら
れた樹脂は、下記「表4」に示すように、Tgが115
℃以上で且つ耐クラック性の高い耐熱性注型樹脂であっ
た。
Example 3 In Example 1 described above,
“C) Filler” has crystalline state of melting and average particle size of 15μ
The same operation as in Example 1 was performed except that m silica (for example, “RD-8AL” trade name: manufactured by Tatsumori) was used. The obtained resin had a Tg of 115 as shown in Table 4 below.
It was a heat-resistant cast resin having a temperature of at least ℃ and a high crack resistance.

【0019】(実施例4)上記実施例1において、
「c)充填材」として結晶状態が溶融で平均粒径14μ
mのシリカ(例えば「SS−F1」商品名:イズミテッ
ク社製)を用いた以外は、実施例1と同様に操作した。
得られた樹脂は、下記「表5」に示すように、Tgが1
15℃以上で且つ耐クラック性の高い耐熱性注型樹脂で
あった。
(Embodiment 4) In Embodiment 1 described above,
“C) Filler” has crystalline state of melting and average particle size of 14μ
The same operation as in Example 1 was performed except that m silica (for example, “SS-F1” trade name: manufactured by Izumi Tech Co., Ltd.) was used.
The resulting resin had a Tg of 1 as shown in Table 5 below.
It was a heat-resistant cast resin having a crack resistance of 15 ° C. or higher.

【0020】(実施例5)上記実施例1において、
「c)充填材」として結晶状態が溶融で平均粒径10μ
mのシリカ(例えば「E−1」商品名:龍森社製)を用
いた以外は、実施例1と同様に操作した。得られた樹脂
は、下記「表6」に示すように、Tgが115℃以上で
且つ耐クラック性の高い耐熱性注型樹脂であった。
(Embodiment 5) In Embodiment 1 described above,
“C) Filler” has a crystalline state of melting and an average particle size of 10μ
The same operation as in Example 1 was performed, except that m silica (for example, “E-1” trade name: manufactured by Tatsumori Co., Ltd.) was used. The obtained resin was a heat-resistant cast resin having a Tg of 115 ° C. or higher and a high crack resistance, as shown in Table 6 below.

【0021】(実施例6)上記実施例1において、
「c)充填材」として結晶状態が溶融で平均粒径10μ
mのシリカ(例えば「A−1」商品名:龍森社製)を用
い、充填量を265phrとした以外は、実施例1と同
様に操作した。得られた樹脂は、下記「表7」に示すよ
うに、Tgが115℃以上で且つ耐クラック性の高い耐
熱性注型樹脂であった。
(Embodiment 6) In Embodiment 1 described above,
“C) Filler” has a crystalline state of melting and an average particle size of 10μ
m of silica (for example, “A-1” trade name: manufactured by Tatsumori Co., Ltd.) and the same operation as in Example 1 except that the filling amount was 265 phr. The obtained resin was a heat-resistant cast resin having a Tg of 115 ° C. or higher and high crack resistance, as shown in Table 7 below.

【0022】下記「表1」に試験項目及びその条件を、
「表2」〜「表7」にその結果を示す。
Table 1 below shows the test items and their conditions.
"Table 2" to "Table 7" show the results.

【0023】なお、用いたシリカの粒径分布を図1に示
す。
FIG. 1 shows the particle size distribution of the silica used.

【0024】[0024]

【表1】 [Table 1]

【0025】[0025]

【表2】 [Table 2]

【0026】[0026]

【表3】 [Table 3]

【0027】[0027]

【表4】 [Table 4]

【0028】[0028]

【表5】 [Table 5]

【0029】[0029]

【表6】 [Table 6]

【0030】[0030]

【表7】 [Table 7]

【0031】「表2」〜「表7」に示すように、本実施
例の組成からなる樹脂は注型用樹脂としての諸特性に優
れ、しかも、Tgが115℃以上で耐熱性が高く、かつ
耐クラック性も鉄ボルトナットで≦−30℃をクリアー
する優れた実力を有していた。また、ポットライフも従
来の10倍程度と長かった。
As shown in Tables 2 to 7, the resin having the composition of this example has excellent properties as a casting resin, and has a high heat resistance at a Tg of 115 ° C. or higher. Also, the steel had excellent ability to clear -30 ° C with iron bolts and nuts in terms of crack resistance. In addition, the pot life was as long as about 10 times the conventional one.

【0032】[0032]

【発明の効果】以上のように、これらの組成からなる樹
脂は注型用樹脂としての諸特性に優れ、しかも、Tgが
115℃以上で耐熱性が高く、かつ耐クラック性も鉄ボ
ルトナットで≦−30℃をクリアーする優れた実力をも
つため、電気機器のコンパクト化、高出力化に伴う絶縁
材料の高耐熱性化に対応できる。また、工業的にもポッ
トライフも長いため量産に対応できる。
As described above, a resin having these compositions is excellent in various properties as a casting resin, and has a high heat resistance at a Tg of 115 ° C. or more, and has a crack resistance of an iron bolt and nut. Since it has an excellent ability to clear ≦ −30 ° C., it can cope with the downsizing of electric devices and the increase in heat resistance of insulating materials accompanying high output. In addition, since the pot life is long industrially, it can be used for mass production.

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

【図1】本実施例で用いたシリカの粒径分布を示す図で
ある。
FIG. 1 is a diagram showing a particle size distribution of silica used in this example.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ビスフェノール型エポキシ樹脂からなる
主剤と、硬化剤とからなる電気絶縁用樹脂組成物であっ
て、 主剤がエポキシ当量250のエポキシ樹脂とエポキシ当
量400のエポキシ樹脂とを80:20の割合で配合し
てなり、該主剤と硬化剤とを当量比が1:0.9の範囲で
混合し、充填材としてシリカにシランカップリング剤を
添加してなることを特徴とする電気絶縁用樹脂組成物。
1. An electrical insulating resin composition comprising a main agent comprising a bisphenol type epoxy resin and a curing agent, wherein the main agents comprise an epoxy resin having an epoxy equivalent of 250 and an epoxy resin having an epoxy equivalent of 400: 20. A mixture of the main agent and the curing agent in an equivalence ratio of 1: 0.9, and adding a silane coupling agent to silica as a filler. Resin composition.
【請求項2】 請求項1において、 上記充填剤のシリカの粒径が10〜15μmであること
を特徴とする電気絶縁用樹脂組成物。
2. The resin composition according to claim 1, wherein the filler has a silica particle diameter of 10 to 15 μm.
【請求項3】 請求項1又は2の電気絶縁用樹脂組成物
を用いてなることを特徴とするエポキシ樹脂注型品。
3. An epoxy resin cast product comprising the resin composition for electrical insulation according to claim 1 or 2.
JP18952297A 1997-07-15 1997-07-15 Injection resin composition for insulation of electric apparatus Pending JPH1139946A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18952297A JPH1139946A (en) 1997-07-15 1997-07-15 Injection resin composition for insulation of electric apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18952297A JPH1139946A (en) 1997-07-15 1997-07-15 Injection resin composition for insulation of electric apparatus

Publications (1)

Publication Number Publication Date
JPH1139946A true JPH1139946A (en) 1999-02-12

Family

ID=16242705

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18952297A Pending JPH1139946A (en) 1997-07-15 1997-07-15 Injection resin composition for insulation of electric apparatus

Country Status (1)

Country Link
JP (1) JPH1139946A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001211589A (en) * 2000-01-28 2001-08-03 Sankyo Seiki Mfg Co Ltd Core insulation structure for motor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001211589A (en) * 2000-01-28 2001-08-03 Sankyo Seiki Mfg Co Ltd Core insulation structure for motor

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