JPS58179214A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPS58179214A
JPS58179214A JP6151482A JP6151482A JPS58179214A JP S58179214 A JPS58179214 A JP S58179214A JP 6151482 A JP6151482 A JP 6151482A JP 6151482 A JP6151482 A JP 6151482A JP S58179214 A JPS58179214 A JP S58179214A
Authority
JP
Japan
Prior art keywords
unsaturated polyester
parts
resin composition
resin
acid
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
JP6151482A
Other languages
Japanese (ja)
Other versions
JPH0151488B2 (en
Inventor
Hisashi Nishigaki
寿 西垣
Akira Uchiyama
明 内山
Yuji Aimono
四十物 雄次
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.)
Resonac Corp
Original Assignee
Hitachi Chemical 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP6151482A priority Critical patent/JPS58179214A/en
Publication of JPS58179214A publication Critical patent/JPS58179214A/en
Publication of JPH0151488B2 publication Critical patent/JPH0151488B2/ja
Granted legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Organic Insulating Materials (AREA)

Abstract

PURPOSE:A resin composition, containing an unsaturated polyester resin, and a compound having a specific structure respectively in a specific proportion, and capable of preventing the noise in transformers of power sources, and improving the drying property and curability of a resin to be in contact with the copper surface and appearance of cured varnishes at the same time. CONSTITUTION:A resin composition obtained by incorporating 100pts.wt. unsaturated polyester resin, e.g. prepared by reacting an acidic component such as maleic acid with an alcoholic component such as propylene glycol, if necessary reacting the resultant product with a modifying component such as linseed oil, and dissolving the reaction product in a crosslinking monomer such as styrene, with 5-30pts.wt. compound expressed by the formula (R1 is 2-6C alkylene or 4-6C alkyleneheteroakylene; R2 is H or methyl), e.g. prepared by esterifying an adduct of dicyclopentadiene with a glycol with acrylic acid, etc. A curing accelerator and if necessary a polymerization inhibitor are added thereto to give the aimed cured article. USE:Impregnating coils of electrical apparatuses, etc.

Description

【発明の詳細な説明】 不飽和ポリエステル樹脂は電気的8機械的。[Detailed description of the invention] Unsaturated polyester resin is electrically 8 mechanically.

熱的特性9作業性1価格的にバランスがとれているため
、FRP積層板をはじめ多用途に使用されており、電気
絶縁用としても、特性9作業性に優れている九めコイル
含浸用、注型用などに多く使用されている。
Thermal properties 9 Workability 1 Well-balanced in terms of price, it is used for a variety of purposes including FRP laminates, and can also be used for electrical insulation. It is often used for casting.

本発明は通電時に放電灯安定器、小形電源トランスなど
の電気機器のコイル含浸用等に使用される樹脂組成物V
C@するものであり、密着性及び防振効果の優れた樹脂
組成物を提供するものである。
The present invention relates to a resin composition V used for impregnating coils of electrical equipment such as discharge lamp ballasts and small power transformers when energized.
C@, and provides a resin composition with excellent adhesion and anti-vibration effects.

放電灯安定器、小形電源トランスなどの電気*aにおい
ては1通電時に磁歪や磁気力による鉄心の振動及び電磁
力によるコイルの振動に起因して騒音が発生する。この
騒音を防止するため、鉄心及びコイルとの密着性に優れ
た不飽和ポリエステル樹脂で含浸処理されているが、E
型トランスの場合1例えばコアサイズが80〜120■
などのようなやや大型な電源トランスでは騒音が大龜く
なる。
In electricity*a such as discharge lamp ballasts and small power transformers, noise is generated due to the vibration of the iron core due to magnetostriction and magnetic force and the vibration of the coil due to electromagnetic force when electricity is applied once. In order to prevent this noise, the iron core and coil are impregnated with an unsaturated polyester resin that has excellent adhesion to the coil.
In the case of a type transformer 1.For example, the core size is 80~120■
A rather large power transformer, such as a power transformer, produces a lot of noise.

一般に、騒音を防止する丸めには機器の構造によっても
異なるが不飽和ポリエステル樹脂を可とり化して振動を
防止し九り、Toるいは固着力を大きくして、振動の発
生そのものを防止している。不飽和ポリエステル樹脂を
可とり化する丸めには一般に樹脂組成を植物油で変性し
喪リ、酸成分、fルコール成分に可とり件のある材料を
使用することが行なわれているがこの場合には樹脂全町
とり化できても電気機器に使用されている鋼表面に接す
る部分の硬化性を箸しく阻害し走り、また、硬化物がし
わを発生したり光沢を失うなど外観をそこなうことが多
い。
In general, rounding to prevent noise is done by making unsaturated polyester resin flexible to prevent vibrations, or by increasing the adhesion force to prevent vibrations from occurring at all, although this varies depending on the structure of the equipment. There is. Generally, when rounding unsaturated polyester resin to make it lubricant, the resin composition is modified with vegetable oil and a material that is lubricated with alcohol, acid components, and alcohol components is used. Even if it is possible to completely cure the resin, it will seriously inhibit the hardening of the parts that come into contact with the steel surfaces used in electrical equipment, and the cured product will often wrinkle or lose its luster, resulting in poor appearance. .

本発明者らは検討の結果、不飽和ポリエステル樹脂に特
定の化合物f混合することKよりトランスの騒音防止、
銅表面に接する樹脂の乾燥性、硬化性及びフェス硬化物
の外観を同時に向Fできることを見出した。
As a result of our studies, the present inventors have found that mixing a specific compound f with unsaturated polyester resin can prevent transformer noise.
We have discovered that it is possible to simultaneously improve the drying properties and curability of the resin in contact with the copper surface, as well as the appearance of the cured face.

本発明は不飽和ポリエステル樹@10(l置部及び次式
(1)で示される化合物5〜30重量部を含有してなる
一脂組成物に関する。
The present invention relates to a monolipid composition comprising an unsaturated polyester resin @10 parts and 5 to 30 parts by weight of a compound represented by the following formula (1).

OR鵞 ただし、R+は炭素数2〜6のアルキレン基又は炭fi
84〜6のアルキレンヘテロアルキレン基。
OR: However, R+ is an alkylene group having 2 to 6 carbon atoms or carbon
84-6 alkyleneheteroalkylene group.

Rzは水素又はメチル基である。Rz is hydrogen or a methyl group.

本発明の不飽和ポリエステル樹脂としては。As the unsaturated polyester resin of the present invention.

以下のような酸成分、アルコール成分、必要に応じて変
性成分を反応させ、架橋性単量体に溶解し友ものが用い
られる。
The following acid components, alcohol components, and if necessary modifying components are reacted to dissolve the crosslinkable monomer and used.

酸成分としてはマレイン酸、無水マレイン酸。The acid components are maleic acid and maleic anhydride.

フマル酸などの不飽和酸、フタル酸、無水フタル酸、イ
ソフタル酸、テレフタル酸、テトラヒドロフタル酸、無
水テトラヒドロフタル酸、へ+サヒドロフタル酸、無水
へキサヒドロフタル酸、アジピン酸、セパチン酸などの
飽和酸、大豆油、アマニ油、トール油などから得られる
脂肪酸等が用いられる。
Unsaturated acids such as fumaric acid, phthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid, tetrahydrophthalic acid, tetrahydrophthalic anhydride, saturated acids such as hexahydrophthalic anhydride, adipic acid, cepatic acid, etc. Fatty acids obtained from acids, soybean oil, linseed oil, tall oil, etc. are used.

アルコール成分としては、プロピレングリコール、エチ
レングリコール、ジプロピレングリコール、ジエチレン
グリコール、1.3−ブタンジオール、ネオペンチルグ
リコール、1.6−ヘキサンジオール、グリセリン、ト
リメチロールプロパン、ペンタエリスリトールなどが用
いられる。さらに必要に応じて変性成分として、アマニ
油、大豆油、トール油、脱水ヒマシ油、ヤ/油、シンク
ロペンタジェン、シクロベンタジ工7などが用いられる
As the alcohol component, propylene glycol, ethylene glycol, dipropylene glycol, diethylene glycol, 1,3-butanediol, neopentyl glycol, 1,6-hexanediol, glycerin, trimethylolpropane, pentaerythritol, etc. are used. Furthermore, as a modification component, linseed oil, soybean oil, tall oil, dehydrated castor oil, coconut oil, synchlopentadiene, cyclobentadiene, etc. may be used as necessary.

に記の式+11で示される化合物は、ジシクロペンタジ
ェンとグリコールとの付加物をアクリル酸又はメタクリ
ル酸でエステル化して得られる。
The compound represented by formula +11 is obtained by esterifying an adduct of dicyclopentadiene and glycol with acrylic acid or methacrylic acid.

アルキレノヘテロアルキレン基には酸素又は伏縫原子が
含まれる。
The alkylenoheteroalkylene group contains oxygen or a binding atom.

y +)コールとしては、エチレングリコール。y +) The alcohol is ethylene glycol.

プロピレングリコール、1.3−ブタンジオール。Propylene glycol, 1,3-butanediol.

1.6−ヘキサンジオール、ネオペンチルグリコール、
ジエチレングリコール、ジプロピレングリコールなどが
使用できる。式(11で示される化合物の製造法は、ま
ず、ジシクロペンタジェノとグリコールをほぼ等モルで
、酸性触媒下で100〜120℃、3〜7時間反応し、
シンクロペンタジェンにグリコールを付加させる。つい
で、この付加物の末端OH基にアクリル酸又はメタクリ
ル酸を酸性触媒を用いて70〜120℃で2〜5時間エ
ステル化反応させ、得られた反応物をアルカリ成分で中
和し、その後水洗し。
1.6-hexanediol, neopentyl glycol,
Diethylene glycol, dipropylene glycol, etc. can be used. The method for producing the compound represented by formula (11) is to first react dicyclopentageno and glycol in approximately equimolar amounts at 100 to 120°C for 3 to 7 hours under an acidic catalyst,
Glycol is added to synclopentagene. Next, the terminal OH group of this adduct is subjected to an esterification reaction with acrylic acid or methacrylic acid at 70 to 120°C for 2 to 5 hours using an acidic catalyst, and the resulting reaction product is neutralized with an alkaline component, and then washed with water. death.

アルカリ分、水分を減圧蒸留して製造される。Manufactured by vacuum distillation of alkaline content and water.

式(11で示きれる化合物の使用1は、不飽和ポリエス
テルを架橋性単量体に溶解した不飽和ポリエステル樹1
11100重量部に対して5〜30重量部とされ、5重
量部未満では通電時の振動防止の効果が小さく、30重
1部を越えると樹脂の硬化物の表面にしわを生じるよう
Kなり。
Use 1 of the compound represented by formula (11) is an unsaturated polyester tree 1 in which an unsaturated polyester is dissolved in a crosslinkable monomer.
The amount is 5 to 30 parts by weight relative to 11,100 parts by weight, and if it is less than 5 parts by weight, the effect of preventing vibration during energization will be small, and if it exceeds 30 parts by weight, wrinkles will appear on the surface of the cured resin.

且つ硬化物が硬くなりすぎるため電気機4に付属してい
る塩化ビニルリード線が低温で屈曲された場合、塩化ビ
ニル被覆が容1.にクラックを生じやすくなるので好ま
しくない。
In addition, if the vinyl chloride lead wire attached to the electric machine 4 is bent at a low temperature because the cured product becomes too hard, the vinyl chloride coating will become hard. This is not preferable because it tends to cause cracks.

不飽和ポリエステル樹脂に用いられる架橋性単量体とし
てはスチンン又はその誘導体、−官能のアクリル酸エス
テル又はメタクリル酸ニスデル、各種アリルエステル、
各種アリルエーテルなどが使用でき、その使用量は樹脂
組成物100重量部に対して30〜7011量部の範囲
が好ましい。
Examples of crosslinkable monomers used in the unsaturated polyester resin include stinne or its derivatives, -functional acrylic esters or Nisder methacrylates, various allyl esters,
Various allyl ethers can be used, and the amount used is preferably in the range of 30 to 7011 parts by weight per 100 parts by weight of the resin composition.

本発明においては、不飽和ポリエステル、架橋性単量体
及び式illで示される化合物の混合法には1%に制限
はない。
In the present invention, the mixing method of the unsaturated polyester, the crosslinkable monomer, and the compound represented by the formula ill is not limited to 1%.

本発明になる樹脂組成物の硬化剤としてベンゾイルパー
オキサイド、アセチルパーオキサイドなどのアシルパー
オキサイド、ターシャリブチルパーオキサイド、キュメ
ンヒドロバーオ中サイドなどのヒドロパーオキサイド、
メチルエチルケトンパーオキサイド、シクロヘキサノン
パーオキ11イドなどのケトンパーオキサイド。
As curing agents for the resin composition of the present invention, acyl peroxides such as benzoyl peroxide and acetyl peroxide, hydroperoxides such as tert-butyl peroxide, and cumene hydroblast;
Ketone peroxides such as methyl ethyl ketone peroxide and cyclohexanone peroxide 11ide.

ジターンヤリブチルパーオキサイド、ジクミルパーオキ
サイド、ターシャリブチルパーオキサイドなどのジアル
キルパーオキサイド、ターシャリブチルパーオキシアセ
テートなどのオキシパーオキサイド等が使用でき、使用
量は一般的に、樹脂組成物100重蓋部に対して0.5
〜5改量部、好ましくは1〜3重量部である。さらに必
要に応じて硬化促進剤としてナフテン酸またはオクテン
酸のコバルト、マンガン、鉄、鉛などの金xiが使用で
き、その使用量は樹脂組成物100重1部に対して0.
1〜5重量部の範囲が好ましい。
Dialkyl peroxides such as ditanyabutyl peroxide, dicumyl peroxide, tertiary butyl peroxide, oxyperoxides such as tertiary butyl peroxy acetate, etc. can be used, and the amount used is generally 100% of the resin composition. 0.5 for heavy lid part
~5 parts by weight, preferably 1 to 3 parts by weight. Further, if necessary, gold xi such as cobalt, manganese, iron, lead, etc. of naphthenic acid or octenoic acid can be used as a curing accelerator, and the amount used is 0.000% per 1 part by weight of the resin composition.
A range of 1 to 5 parts by weight is preferred.

また、必要に応じて重合禁止剤として、・・イドロキノ
ン、ノ、2ラターシャリプチルカテコール。
In addition, if necessary, as a polymerization inhibitor, .

ピロガロールなどのキノン類、その他一般的に使用され
ているものが使用でき、その使用量は樹脂組成物100
重量部に対して0〜0.1重量部の範囲が好ましい。
Quinones such as pyrogallol and other commonly used ones can be used, and the amount used is 100% of the resin composition.
The range of 0 to 0.1 parts by weight is preferred.

以下に実施例、比較例を示す。部とあるのけ重量部であ
る。
Examples and comparative examples are shown below. Parts are parts by weight.

実施例 1、不飽和ポリエステル樹11wAの製造大豆油脂肪酸
35部、m水テトラヒドロフタル酸10部、無水マレイ
ン酸15部、ジプロピレングリコール20部、ジエチレ
ングリコール20部、ハイドロキノン0.024’fl
Seセ宇劃−210℃で10時間加加熱台し、酸価20
.5の不飽和ポリエステルを合成し友。不飽和ポリエス
テル50部にスチレン50部を攪拌溶解し。
Example 1, Production of unsaturated polyester tree 11 wA Soybean oil fatty acid 35 parts, m-water tetrahydrophthalic acid 10 parts, maleic anhydride 15 parts, dipropylene glycol 20 parts, diethylene glycol 20 parts, hydroquinone 0.024'fl
Heat for 10 hours at -210°C, acid value 20
.. Synthesized unsaturated polyester of 5. 50 parts of styrene was dissolved in 50 parts of unsaturated polyester with stirring.

不飽和ポリエステル樹脂入を製造した。An unsaturated polyester resin was produced.

2 ジシクロペンタオキシエチルアクリレート及びメタ
クリレートの製造 ジノクロペンタジェン132M、エチレングリコール6
2部、パラトルエンスルホン酸O,S部を(財)1コ1
20℃で4時間反応させた後80℃までド温し、さらに
アクリル酸72部と90℃で5時間反応させて得られ九
反応物をアルカリ中和し、水洗しその後アルカリ分、水
分を減圧蒸留してジシクロペンタオキシエチルアクリレ
ートを得た。
2 Production of dicyclopentaoxyethyl acrylate and methacrylate Dinoclopentadiene 132M, ethylene glycol 6
2 parts, 1 part of paratoluenesulfonic acid O, S part (Foundation) 1 part
After reacting at 20°C for 4 hours, the mixture was heated to 80°C, and further reacted with 72 parts of acrylic acid at 90°C for 5 hours. Dicyclopentaoxyethyl acrylate was obtained by distillation.

また、′)/クロベンタオキシエチルメタクリレートハ
、ジシクロペンタジェン132m、エチレンクリコール
62部、パラトルエンスルホン酸08部を1在−kz1
20℃で4時間反応させた後80℃まで下温し、さらに
メタクリル酸86部、パラトルエンスルホン酸08部を
添加友反応′@τアルカリ中和し、水洗しその後アルハ カリ分、水分を減圧蒸留して得た。
In addition, ')/chlorobentaoxyethyl methacrylate, 132 m of dicyclopentadiene, 62 parts of ethylene glycol, and 08 parts of para-toluenesulfonic acid were added to -kz1
After reacting at 20°C for 4 hours, the temperature was lowered to 80°C, and further 86 parts of methacrylic acid and 08 parts of para-toluenesulfonic acid were added to neutralize the alkali, wash with water, and then remove the alkali content and water by vacuum distillation. I got it.

不飽和ポリエステル41N脂Aに、ジシクロペンタオキ
シエチルアクリレート又はジシクロペンタオキシエチル
メタクリレートを表1に示す配合で、8憾ナフテン酸マ
ンガンをtoIi、il化剤としてターシャリブチルパ
ーベンゾエートを1.0m混合し硬化物の轡性癖を測定
した。
Unsaturated polyester 41N resin A was mixed with dicyclopentaoxyethyl acrylate or dicyclopentaoxyethyl methacrylate as shown in Table 1, with manganese naphthenate toIi and 1.0m of tert-butyl perbenzoate as an il-forming agent. The curdling tendency of the mixed and cured product was measured.

その結果を表1に示す。The results are shown in Table 1.

表中において、○は良好、△は実用上問題ないが多少問
題あり、×は問題ありを示す。
In the table, ◯ indicates good results, △ indicates no practical problems but there are some problems, and × indicates problems.

硬化物外INKついては、直径60■の金属シャーレ裏
側に樹脂組成物2?を塗布し、100℃で5時間硬化後
の表面のしわ、光沢外観を観察しえ。
For INK outside the cured product, resin composition 2? After coating and curing at 100°C for 5 hours, observe the wrinkles and glossy appearance of the surface.

金属鋼の乾燥性は鋼板を樹脂組成物に浸漬し。The drying properties of metallic steel are determined by immersing the steel plate in a resin composition.

直ちに取出し、余滴々ド5分後100℃に加熱し、鋼表
面の組成物の乾燥性全指触により測定した。
It was immediately taken out, and after 5 minutes, the steel was heated to 100° C., and the dryness of the composition on the steel surface was measured by touching it with all fingers.

塩化ビニルリード線の低温屈曲性の試験は第1図に示す
ように長さ50麿、直径約2■のUL規格合格品UL−
1015(日立電線株式会社製、塩化ビニルリード、I
)1の4本を直径0、29 wmのエナメル線2でしば
り、これを樹脂組成物に10分間浸漬し、余滴415分
後120℃で3時間硬化させ、その後−10℃の温度の
低温槽に30分放置した後、直ちにその中央部を90度
の角度まで屈曲させ、塩化ビニルリード#に発生1.た
クラックの数を測定した。
The low-temperature flexibility test of vinyl chloride lead wire was conducted using a UL standard-compliant product with a length of 50 mm and a diameter of approximately 2 cm, as shown in Figure 1.
1015 (manufactured by Hitachi Cable Co., Ltd., vinyl chloride lead, I
) 1 were tied together with enameled wire 2 with a diameter of 0.29 wm, and this was immersed in the resin composition for 10 minutes, and after 415 minutes of residual dripping, it was cured at 120°C for 3 hours, and then placed in a low temperature bath at -10°C. After leaving it for 30 minutes, immediately bend the center part to a 90 degree angle to remove the 1. The number of cracks was measured.

余滴415分後に120℃で2時間硬化させ。After 415 minutes of dripping, it was cured at 120°C for 2 hours.

トランスが室温(約20℃)まで冷却してからトランス
の一次入力端に120Vを印加し。
After the transformer cooled to room temperature (approximately 20°C), 120V was applied to the primary input terminal of the transformer.

TRANSFORMER,CHECK、ER,TC−5
522(株式会社、tf副制御ループ製)を用いて騒音
を今 測定した。単位はノ(加速K)で表わされ、数値が大き
い程騒音が大きいことを示す。他の特性は、JIS、C
,2105に準じて測定し九。
TRANSFORMER, CHECK, ER, TC-5
522 (manufactured by TF Sub Control Loop Co., Ltd.) to measure the noise. The unit is expressed in acceleration K, and the larger the value, the louder the noise. Other characteristics are JIS, C
, 2105.9.

実施例から明らかなように、不飽和ポリエステル樹脂、
100重を部に対して式(11で示される化合物を5〜
30重を部添加することにより。
As is clear from the examples, unsaturated polyester resin,
5 to 100 parts of the compound represented by the formula (11)
By adding 30 parts by weight.

不飽和ポリエステル樹脂本来の特性を低下させ1j/ るこへ、フェス硬化物外観(しわ、光沢)の向上及び通
電時のfitの減少が達成され、しかも銅表面の硬化性
も改良される。
By reducing the inherent properties of the unsaturated polyester resin, the appearance of the cured face (wrinkles, gloss) is improved and the fit when energized is reduced, and the hardenability of the copper surface is also improved.

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

第1図は紹施例で行な”りた順化ビニルリード線の低温
屈曲性の試験に用いた試験方を示す略図でめる。 特開昭58−179214 (5)
Figure 1 is a schematic diagram showing the test method used in the test of low temperature flexibility of the conditioned vinyl lead wire conducted in the introductory example. JP-A-58-179214 (5)

Claims (1)

【特許請求の範囲】 1、 不飽和ポリエステル樹IIW100重量部及び次
式(1)で示される化合物5〜30重量部を含有してな
る樹脂組成物。 友だし、R1は炭素数2〜6のアルキレン基又ハ炭素数
4〜6のアルキレンヘテロアルキレン基+ Rxは水素
又はメチル基で6る。
[Scope of Claims] 1. A resin composition comprising 100 parts by weight of an unsaturated polyester resin IIW and 5 to 30 parts by weight of a compound represented by the following formula (1). R1 is an alkylene group having 2 to 6 carbon atoms or an alkyleneheteroalkylene group having 4 to 6 carbon atoms + Rx is hydrogen or a methyl group.
JP6151482A 1982-04-13 1982-04-13 Resin composition Granted JPS58179214A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6151482A JPS58179214A (en) 1982-04-13 1982-04-13 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6151482A JPS58179214A (en) 1982-04-13 1982-04-13 Resin composition

Publications (2)

Publication Number Publication Date
JPS58179214A true JPS58179214A (en) 1983-10-20
JPH0151488B2 JPH0151488B2 (en) 1989-11-02

Family

ID=13173265

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6151482A Granted JPS58179214A (en) 1982-04-13 1982-04-13 Resin composition

Country Status (1)

Country Link
JP (1) JPS58179214A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02135208A (en) * 1988-11-15 1990-05-24 Hitachi Chem Co Ltd Resin composition and concrete composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58108218A (en) * 1981-12-21 1983-06-28 Dainippon Ink & Chem Inc Unsaturated polyester resin composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58108218A (en) * 1981-12-21 1983-06-28 Dainippon Ink & Chem Inc Unsaturated polyester resin composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02135208A (en) * 1988-11-15 1990-05-24 Hitachi Chem Co Ltd Resin composition and concrete composition

Also Published As

Publication number Publication date
JPH0151488B2 (en) 1989-11-02

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