JP3450260B2 - Epoxy resin composition and coil casting - Google Patents

Epoxy resin composition and coil casting

Info

Publication number
JP3450260B2
JP3450260B2 JP2000079197A JP2000079197A JP3450260B2 JP 3450260 B2 JP3450260 B2 JP 3450260B2 JP 2000079197 A JP2000079197 A JP 2000079197A JP 2000079197 A JP2000079197 A JP 2000079197A JP 3450260 B2 JP3450260 B2 JP 3450260B2
Authority
JP
Japan
Prior art keywords
epoxy resin
weight
casting
resin composition
curing agent
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.)
Expired - Fee Related
Application number
JP2000079197A
Other languages
Japanese (ja)
Other versions
JP2001048958A (en
Inventor
愼二 土屋
好造 渡辺
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.)
Kyocera Chemical Corp
Original Assignee
Kyocera Chemical 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 Kyocera Chemical Corp filed Critical Kyocera Chemical Corp
Priority to JP2000079197A priority Critical patent/JP3450260B2/en
Publication of JP2001048958A publication Critical patent/JP2001048958A/en
Application granted granted Critical
Publication of JP3450260B2 publication Critical patent/JP3450260B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

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、耐熱性、成形性、
耐クラック性に優れたエポキシ樹脂組成物および当該エ
ポキシ樹脂組成物を注型してなるコイル注型物に関す
る。
TECHNICAL FIELD The present invention relates to heat resistance, moldability,
The present invention relates to an epoxy resin composition having excellent crack resistance and a coil casting product obtained by casting the epoxy resin composition.

【0002】[0002]

【従来の技術】従来、コイル等の電気・電子部品は、外
部雰囲気や機械的衝撃から保護するため、エポキシ樹脂
で注型、封止したり、エポキシ樹脂を含浸、塗布して硬
化することが行われてきた。
2. Description of the Related Art Conventionally, electric and electronic parts such as coils have been cast or sealed with an epoxy resin or impregnated and coated with an epoxy resin to be cured in order to protect them from an external atmosphere and mechanical shock. Has been done.

【0003】近年、コイル注型物等にかかる特性、すな
わち耐熱性、成形性、耐クラック性等の信頼性のみなら
ず、コスト低減等の生産性の向上要求から、速硬化性の
エポキシ樹脂組成物が求められるようになってきた。
In recent years, not only the characteristics related to coil castings, that is, reliability such as heat resistance, moldability, and crack resistance, but also improvement in productivity such as cost reduction are demanded. Things have come to be demanded.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、組成物
中の硬化促進剤の増量や種類の変更は、信頼性の低下を
招いたり、樹脂のポットライフを著しく低下させるばか
りでなく、現行の成形、注型方法の大幅な変更をも必要
とすることもあり、現行のプロセスを最大限に維持しな
がら、エポキシ樹脂組成物のみを速硬化することは難し
かった。
However, increasing the amount or changing the type of the curing accelerator in the composition not only leads to a decrease in reliability and the pot life of the resin, but also the current molding, It may be necessary to make a drastic change in the casting method, and it has been difficult to quickly cure only the epoxy resin composition while maximizing the current process.

【0005】本発明の目的は、上記の事情に鑑みてなさ
れたもので、耐熱性、成形性に優れ、コイル注型等に好
適な速硬化性を有するエポキシ樹脂組成物とコイル注型
物を提供しようとするものである。
The object of the present invention was made in view of the above circumstances, and provides an epoxy resin composition and a coil casting product which are excellent in heat resistance and moldability and have a rapid curing property suitable for coil casting and the like. It is the one we are trying to provide.

【0006】[0006]

【課題を解決するための手段】本発明者は、上記目的を
達成しようと鋭意研究を進めた結果、特定の酸無水物硬
化剤を用いることによって、上記目的を達成できること
を見いだし、本発明を完成したものである。
As a result of intensive studies aimed at achieving the above object, the present inventor has found that the above object can be achieved by using a specific acid anhydride curing agent, and It has been completed.

【0007】即ち、本発明は、 (A)エポキシ樹脂、 (B)異性体である(a)4−メチルヘキサヒドロ無水
フタル酸と(b)3−メチルヘキサヒドロ無水フタル酸
を主成分とするメチルヘキサヒドロ無水フタル酸中に、
(c)3−メチル−Δ1 −テトラヒドロ無水フタル酸と
(d)3−メチル−Δ2 −テトラヒドロ無水フタル酸の
混合物が0.1重量%以上5重量%未満含まれる酸無水
物硬化剤、 (C)硬化促進剤および (D)無機質充填剤 を必須成分とし、(A)エポキシ樹脂と(D)無機質充
填剤とからなるエポキシ樹脂配合成分と、(B)の酸無
水物硬化剤と(C)硬化促進剤とからなる硬化剤配合成
分とを混合してなり、電気・電子部品(但し、光学用製
品を除く)の注型に適用されることを特徴とするエポキ
シ樹脂組成物である。また、そのエポキシ樹脂組成物を
注型してなることを特徴とするコイル注型物である。
お、ここで光学用製品とは、特開平1−132621号
公報に記載された光学用材料、光学用製品をいう。
That is, the present invention comprises (A) an epoxy resin, (B) isomers (a) 4-methylhexahydrophthalic anhydride and (b) 3-methylhexahydrophthalic anhydride as main components. In methylhexahydrophthalic anhydride,
(C) 3-methyl-Δ 1 -tetrahydrophthalic anhydride and (d) 3-methyl-Δ 2 -tetrahydrophthalic anhydride
An acid anhydride curing agent containing a mixture of 0.1% by weight or more and less than 5% by weight, (C) a curing accelerator and (D) an inorganic filler as essential components, and (A) an epoxy resin and (D) an inorganic filler. And a mixture of an epoxy resin compounding component consisting of (B), an acid anhydride curing agent of (B) and a curing agent compounding component of (C) a curing accelerator .
It is an epoxy resin composition characterized by being applied to casting of products (excluding products) . A coil casting product is obtained by casting the epoxy resin composition. Na
Here, the optical product refers to JP-A-1-132621.
The optical materials and optical products described in the publication.

【0008】以下、本発明を詳細に説明する。The present invention will be described in detail below.

【0009】本発明に用いる(A)エポキシ樹脂として
は、1分子中に2個以上のエポキシ基を有する化合物で
ある限り、分子構造、分子量等に制限されることなく汎
用のものを広く使用することができる。例えば、エポキ
シノボラック型、ビフェニル型等の芳香族系、シクロヘ
キサン誘導体等の脂環族系、さらに次の一般式で示され
るビスフェノールA型のエポキシ樹脂が挙げられる。
As the epoxy resin (A) used in the present invention, as long as it is a compound having two or more epoxy groups in one molecule, general-purpose resins are widely used without being limited by the molecular structure, molecular weight and the like. be able to. For example, an epoxy novolac type, a biphenyl type aromatic type, an alicyclic type cyclohexane derivative or the like, and a bisphenol A type epoxy resin represented by the following general formula can be given.

【0010】[0010]

【化1】 (但し、式中、nは0以上の整数を表す) これらは単独又は2種以上混合して使用することができ
る。
[Chemical 1] (However, in the formula, n represents an integer of 0 or more.) These may be used alone or in combination of two or more.

【0011】本発明に用いる(B)成分の特定硬化剤と
しては、メチルヘキサヒドロ無水フタル酸を主成分とし
てその異性体である次式化2に示す(a)4−メチルヘ
キサヒドロ無水フタル酸と
The specific curing agent of the component (B) used in the present invention is 4-methylhexahydrophthalic anhydride (a) represented by the following formula 2 which is an isomer of methylhexahydrophthalic anhydride as a main component. When

【化2】 次式化3に示す(b)3−メチルヘキサヒドロ無水フタ
ル酸の混合物中に、
[Chemical 2] In a mixture of (b) 3-methylhexahydrophthalic anhydride represented by the following formula 3,

【化3】 次式化4に示す(c)3−メチル−Δ1 −テトラヒドロ
無水フタル酸と
[Chemical 3] (C) 3-methyl-Δ 1 -tetrahydrophthalic anhydride represented by the following formula 4

【化4】 次式化5に示す(d)3−メチル−Δ2 −テトラヒドロ
無水フタル酸
[Chemical 4] (D) 3-Methyl-Δ 2 -tetrahydrophthalic anhydride represented by the following formula 5

【化5】 を含む酸無水物である また、それらの配合割合は、(a)成分と(b)成分の
主成分混合物中に、(c)成分と(d)成分の合計量が
0.1重量%以上5重量%未満、好ましくは0.1重量
%以上3重量%未満含まれるように配合する。この割合
が、0.1重量%未満では、速硬化性に対する効果が少
なく、5重量%以上であるとガラス転移点の低下が起こ
り、耐熱性が低下するため好ましくない。
[Chemical 5] Further, the compounding ratio of them is such that the total amount of the (c) component and the (d) component is 0.1% by weight or more in the main component mixture of the (a) component and the (b) component. The content is less than 5% by weight, preferably 0.1% by weight or more and less than 3% by weight. If this ratio is less than 0.1% by weight, the effect on the rapid curing property is small, and if it is 5% by weight or more, the glass transition point is lowered and the heat resistance is lowered, which is not preferable.

【0012】本発明に用いる(C)硬化促進剤として
は、(A)のエポキシ樹脂同士、または(A)エポキシ
樹脂と(B)硬化剤との反応を促進するものであれば、
いかなるものであってもよい。具体的には、例えば、2
−エチル−4−メチルイミダゾール、2−フェニルイミ
ダゾール、2−フェニル−4−メチルイミダゾールなど
のイミダゾール類、2−(ジメチルアミノメチル)フェ
ノール、1,8−ジアザ−ビシクロ[5,4,0]ウン
デセン−7、ベンジルジメチルアミン等の3級アミン
類、トリエチルホスフィン、ジフェニルホスフィン、ト
リフェニルホスフィン等が挙げられ、これらは単独又は
2種以上混合して使用することができる。
The (C) curing accelerator used in the present invention may be any one that accelerates the reaction between the epoxy resins of (A) or between the epoxy resin of (A) and the curing agent of (B).
It can be anything. Specifically, for example, 2
-Imidazoles such as ethyl-4-methylimidazole, 2-phenylimidazole, 2-phenyl-4-methylimidazole, 2- (dimethylaminomethyl) phenol, 1,8-diaza-bicyclo [5,4,0] undecene -7, tertiary amines such as benzyldimethylamine, triethylphosphine, diphenylphosphine, triphenylphosphine and the like can be mentioned, and these can be used alone or in admixture of two or more.

【0013】本発明に用いる(D)無機充填剤として
は、一般に使用されているものが広く使用される。具体
的には、例えば、シリカ粉末、アルミナ、三酸化アンチ
モン、タルク、炭酸カルシウム、チタンホワイト、クレ
ー、ベンガル、ガラス繊維、炭素繊維等が挙げられ、特
にシリカ粉末およびアルミナが好ましく用いられる。無
機充填剤の配合割合は、全体の樹脂組成物に対して25
〜95重量%含有するように配合することが好ましい。
その割合が25重量%未満では、樹脂組成物の吸湿性が
高く耐湿性に劣り、95重量%を超えると、極端に流動
性が悪くなり、注型作業性に劣り好ましくない。
As the inorganic filler (D) used in the present invention, generally used ones are widely used. Specific examples include silica powder, alumina, antimony trioxide, talc, calcium carbonate, titanium white, clay, bengal, glass fiber, carbon fiber, and the like, and silica powder and alumina are particularly preferably used. The compounding ratio of the inorganic filler is 25 with respect to the total resin composition.
It is preferable to mix such that the content is from ˜95% by weight.
If the proportion is less than 25% by weight, the resin composition has a high hygroscopicity and is inferior in moisture resistance.

【0014】本発明のエポキシ樹脂組成物には、上述し
たエポキシ樹脂、酸無水物硬化剤、硬化促進剤および無
機充填剤を必須の成分とするが、本発明の目的に反しな
い範囲において、また必要に応じて、例えば脂環式エポ
キシ等の反応性希釈剤およびシランカップリング剤、ま
たは、種々の沈降防止剤、カーボンブラック等の着色剤
等を適宜添加配合することができる。
The epoxy resin composition of the present invention contains the above-mentioned epoxy resin, acid anhydride curing agent, curing accelerator and inorganic filler as essential components, but within the range not deviating from the object of the present invention, If necessary, for example, a reactive diluent such as an alicyclic epoxy and a silane coupling agent, various anti-sedimentation agents, a coloring agent such as carbon black, and the like can be appropriately added and blended.

【0015】本発明のエポキシ樹脂組成物を調製する場
合には、エポキシ樹脂に、無機充填剤、必要に応じて反
応性希釈剤、着色剤、沈降防止剤を配合してなるエポキ
シ樹脂配合成分と酸無水物硬化剤と硬化促進剤とからな
る硬化剤配合成分とを加熱・混練することにより注型材
料とすることができる。
When the epoxy resin composition of the present invention is prepared, an epoxy resin compounding component is prepared by compounding the epoxy resin with an inorganic filler, and if necessary, a reactive diluent, a colorant and an antisettling agent. A casting material can be obtained by heating and kneading the acid anhydride curing agent and the curing agent compounding component consisting of the curing accelerator.

【0016】前述した(B)酸無水物硬化剤と(C)硬
化促進剤とからなる硬化剤配合成分は、前述した(A)
エポキシ樹脂と(D)無機充填剤からなる主剤エポキシ
樹脂配合成分に対して、3〜30重量%の割合で配合す
る。
The above-mentioned curing agent compounding component comprising (B) acid anhydride curing agent and (C) curing accelerator is the above-mentioned (A).
It is blended in a proportion of 3 to 30% by weight with respect to the main component epoxy resin blending component comprising the epoxy resin and the inorganic filler (D).

【0017】こうして得られた注型材料は、コイル注型
をはじめとする電気部品あるいは電子部品の封止、被
覆、絶縁等に適用すれば、優れた特性と信頼性を付与さ
せることができる。注型の一般的な方法としては、真空
注型があるが、特定のエポキシ樹脂、無機充填剤、その
他の成分を配合し、ミキサー等によって十分均一に加熱
混合した樹脂成分と、硬化剤、硬化促進剤およびその他
の成分を配合し、ミキサー等によって十分均一に加熱混
合した樹脂成分との2つの樹脂成分を予め混合してお
き、注型法により封止後加熱して硬化させ、コイル注型
物が得られる。
When the casting material thus obtained is applied to sealing, coating, insulation, etc. of electric parts or electronic parts such as coil casting, excellent properties and reliability can be imparted. As a general method of casting, there is vacuum casting, but a specific epoxy resin, an inorganic filler, and other components are blended, and the resin component is sufficiently evenly heated and mixed by a mixer, etc., a curing agent, and a curing agent. Two resin components, which are a resin component that has been mixed with an accelerator and other components and heated and mixed sufficiently evenly with a mixer, etc., are pre-mixed, and after sealing by a casting method, cured by heating and coil casting. The thing is obtained.

【0018】[0018]

【作用】本発明のエポキシ樹脂組成物は、特定の酸無水
物硬化剤を主剤エポキシ樹脂に対して配合することによ
って、耐熱性、成形性等の信頼性に優れ、コイル注型等
に好適な耐熱性、成形性を有し、速硬化性に優れて生産
性を向上することができるたエポキシ樹脂組成物を提供
できるのである。
The epoxy resin composition of the present invention is excellent in heat resistance, moldability and the like by adding a specific acid anhydride curing agent to the base epoxy resin, and is suitable for coil casting and the like. It is possible to provide an epoxy resin composition that has heat resistance and moldability, is excellent in rapid curing property, and can improve productivity.

【0019】[0019]

【発明の実施の形態】次に、本発明を実施例によって具
体的に説明する。本発明は、これらの実施例によって限
定されるものではない。
BEST MODE FOR CARRYING OUT THE INVENTION Next, the present invention will be specifically described with reference to Examples. The invention is not limited by these examples.

【0020】実施例1 エポキシ樹脂(エポキシ当量190)100重量部、溶
融シリカ180重量部、アクリル系消泡剤0.1重量
部、およびシランカップリング剤0.3重量部をミキサ
ーに投入し、60℃で加熱混合してエポキシ樹脂配合成
分とした。別に、4−メチルヘキサヒドロ無水フタル酸
67重量部、3−メチルヘキサヒドロ無水フタル酸17
重量部、3−メチル−Δ1 −テトラヒドロ無水フタル酸
と3−メチル−Δ2 −テトラヒドロ無水フタル酸の5
0:50の混合物0.1重量部、および1−ベンジル−
2−メチルイミダゾール0.4重量部をミキサーに投入
し、60℃で加熱混合して硬化剤配合成分とした。上記
のエポキシ樹脂配合成分と硬化剤配合成分とを混合し、
実施例1のエポキシ樹脂組成物とした。
Example 1 100 parts by weight of an epoxy resin (epoxy equivalent 190), 180 parts by weight of fused silica, 0.1 part by weight of an acrylic defoaming agent, and 0.3 part by weight of a silane coupling agent were charged into a mixer, The mixture was heated and mixed at 60 ° C. to obtain an epoxy resin compounding component. Separately, 67 parts by weight of 4-methylhexahydrophthalic anhydride and 17 parts of 3-methylhexahydrophthalic anhydride
5 parts by weight of 3-methyl-Δ 1 -tetrahydrophthalic anhydride and 3-methyl-Δ 2 -tetrahydrophthalic anhydride
0.1 parts by weight of a 0:50 mixture, and 1-benzyl-
0.4 parts by weight of 2-methylimidazole was charged into a mixer and mixed by heating at 60 ° C. to prepare a curing agent blending component. Mixing the above epoxy resin blending component and curing agent blending component,
The epoxy resin composition of Example 1 was obtained.

【0021】実施例2〜3 表1に示した組成のエポキシ樹脂配合成分と硬化剤配合
成分を、それぞれ60℃で加熱混合した後、エポキシ樹
脂配合成分と硬化剤配合成分を混合し、実施例2〜3の
エポキシ樹脂組成物を得た。
Examples 2 to 3 The epoxy resin compounding component and the curing agent compounding component having the compositions shown in Table 1 were heated and mixed at 60 ° C., respectively, and then the epoxy resin compounding component and the curing agent compounding component were mixed to obtain the examples. A few epoxy resin compositions were obtained.

【0022】比較例1〜3 表2に示した組成のエポキシ樹脂配合成分と硬化剤配合
成分を、実施例と同様に、それぞれ60℃で加熱混合し
た後、エポキシ樹脂配合成分と硬化剤配合成分を混合
し、比較例1〜3のエポキシ樹脂組成物を得た。
Comparative Examples 1 to 3 The epoxy resin compounding components and the curing agent compounding components having the compositions shown in Table 2 were heated and mixed at 60 ° C. in the same manner as in the examples, and then the epoxy resin compounding component and the curing agent compounding component were mixed. Were mixed to obtain the epoxy resin compositions of Comparative Examples 1 to 3.

【0023】実施例1〜3および比較例1〜3によって
製造した、エポキシ樹脂組成物を真空下、60℃の条件
下で試験片作成金型に注形し、100℃で3時間、さら
に130℃で3時間の後硬化をさせた。これらのエポキ
シ樹脂組成物について諸試験を行ったので、その結果を
表3に示したが、本発明の顕著な効果を確認することが
できた。
The epoxy resin compositions prepared in Examples 1 to 3 and Comparative Examples 1 to 3 were cast in a test piece forming mold under vacuum at 60 ° C. for 3 hours at 100 ° C. and then at 130 ° C. It was post-cured at ℃ for 3 hours. Various tests were conducted on these epoxy resin compositions, and the results are shown in Table 3. The remarkable effects of the present invention could be confirmed.

【0024】[0024]

【表1】 *:1−ベンジル−2−メチルイミダゾールの配合量は
標準を0.6重量部とするが、3−メチル−Δ1 −テト
ラヒドロ無水フタル酸と3−メチル−Δ2 −テトラヒド
ロ無水フタル酸との混合物が0.1重量部以下のものは
増加し(0.8重量部)、5.0重量部のものでは減少
し(0.4重量部)、ゲルタイムが53分近くになるよ
う調整した。
[Table 1] *: The standard amount of 1-benzyl-2-methylimidazole is 0.6 part by weight, but the amount of 3-methyl-Δ 1 -tetrahydrophthalic anhydride and 3-methyl-Δ 2 -tetrahydrophthalic anhydride is When the mixture was 0.1 parts by weight or less, it increased (0.8 parts by weight), when it was 5.0 parts by weight, it decreased (0.4 parts by weight), and the gel time was adjusted to be close to 53 minutes.

【0025】[0025]

【表2】 *:1−ベンジル−2−メチルイミダゾールの配合量は
標準を0.6重量部とするが、3−メチル−Δ1 −テト
ラヒドロ無水フタル酸と3−メチル−Δ2 −テトラヒド
ロ無水フタル酸との混合物が0.1重量部以下のものは
増加し(0.8重量部)、5.0重量部のものでは減少
し(0.4重量部)、ゲルタイムが53分近くになるよ
う調整した。
[Table 2] *: The standard amount of 1-benzyl-2-methylimidazole is 0.6 part by weight, but the amount of 3-methyl-Δ 1 -tetrahydrophthalic anhydride and 3-methyl-Δ 2 -tetrahydrophthalic anhydride is When the mixture was 0.1 parts by weight or less, it increased (0.8 parts by weight), when it was 5.0 parts by weight, it decreased (0.4 parts by weight), and the gel time was adjusted to be close to 53 minutes.

【0026】[0026]

【表3】 *1:TMA法による、 *2:硬化物外観のボイド等欠陥を目視により観察し
た。
[Table 3] * 1: By TMA method * 2: Defects such as voids in the appearance of the cured product were visually observed.

【0027】[0027]

【発明の効果】以上の説明おび表3の結果から明らかな
ように、3−メチル−Δ1 −テトラヒドロ無水フタル酸
と3−メチル−Δ2 −テトラヒドロ無水フタル酸との混
合物が0.1重量%未満では速硬化性がなく(比較例
1)、5.0重量%を超えるとガラス転移点の低下が起
こる(比較例2、3)。従って、本発明のエポキシ樹脂
組成物は、耐熱性、成形性に優れた速硬化性を有するエ
ポキシ樹脂組成物であり、コイル注型、封止等に好適な
ものである。
As is clear from the above description and the results in Table 3, 0.1% by weight of the mixture of 3-methyl-Δ 1 -tetrahydrophthalic anhydride and 3-methyl-Δ 2 -tetrahydrophthalic anhydride was used. If it is less than%, there is no rapid curing property (Comparative Example 1), and if it exceeds 5.0% by weight, the glass transition point is lowered (Comparative Examples 2 and 3). Therefore, the epoxy resin composition of the present invention is an epoxy resin composition having excellent heat resistance and moldability and having a rapid curing property, and is suitable for coil casting, sealing and the like.

フロントページの続き (51)Int.Cl.7 識別記号 FI H01F 5/06 H01F 5/06 27/32 27/32 // B29K 63:00 B29K 63:00 B29L 31:34 B29L 31:34 (56)参考文献 特開 平1−132621(JP,A) 特開 平4−76020(JP,A) 特開 平7−309927(JP,A) 特開 平3−243617(JP,A) (58)調査した分野(Int.Cl.7,DB名) C08G 59/00 - 59/72 B29C 39/10 C08J 5/00 - 5/24 C08L 63/00 - 63/10 H01F 5/06 H01F 27/32 Continuation of front page (51) Int.Cl. 7 Identification code FI H01F 5/06 H01F 5/06 27/32 27/32 // B29K 63:00 B29K 63:00 B29L 31:34 B29L 31:34 (56) References JP-A-1-132621 (JP, A) JP-A-4-76020 (JP, A) JP-A-7-309927 (JP, A) JP-A-3-243617 (JP, A) (58) Survey Fields (Int.Cl. 7 , DB name) C08G 59/00-59/72 B29C 39/10 C08J 5/00-5/24 C08L 63/00-63/10 H01F 5/06 H01F 27/32

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 (A)エポキシ樹脂、(B)異性体であ
る(a)4−メチルヘキサヒドロ無水フタル酸と(b)
3−メチルヘキサヒドロ無水フタル酸を主成分とするメ
チルヘキサヒドロ無水フタル酸中に、(c)3−メチル
−Δ1 −テトラヒドロ無水フタル酸と(d)3−メチル
−Δ2 −テトラヒドロ無水フタル酸の混合物が0.1重
量%以上5重量%未満含まれる酸無水物硬化剤、 (C)硬化促進剤および (D)無機質充填剤 を必須成分とし、(A)エポキシ樹脂と(D)無機質充
填剤とからなるエポキシ樹脂配合成分と、(B)の酸無
水物硬化剤と(C)硬化促進剤とからなる硬化剤配合成
分とを混合してなり、電気・電子部品(但し、光学用製
品を除く)の注型に適用されることを特徴とする注型用
エポキシ樹脂組成物。
1. An epoxy resin (A), an isomer (B) of 4-methylhexahydrophthalic anhydride (b) and an (B) isomer.
(C) 3-methyl-Δ 1 -tetrahydrophthalic anhydride and (d) 3-methyl-Δ 2 -tetrahydrophthalic anhydride in methylhexahydrophthalic anhydride containing 3-methylhexahydrophthalic anhydride as a main component. An acid anhydride curing agent containing 0.1% by weight or more and less than 5% by weight of a mixture of acids, (C) a curing accelerator, and (D) an inorganic filler as essential components, and (A) an epoxy resin and (D) an inorganic substance. an epoxy resin blend component consisting of a filler, an acid anhydride curing agent (B) and (C) Ri greens by mixing the curing agent blend component comprising a curing accelerator, electric and electronic parts (except, optical For
The epoxy resin composition for casting, which is applied to the casting (excluding products) .
【請求項2】 請求項1記載のエポキシ樹脂組成物を注
型してなることを特徴とするコイル注型物。
2. A coil casting product obtained by casting the epoxy resin composition according to claim 1.
JP2000079197A 1999-06-01 2000-03-22 Epoxy resin composition and coil casting Expired - Fee Related JP3450260B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000079197A JP3450260B2 (en) 1999-06-01 2000-03-22 Epoxy resin composition and coil casting

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP11-153485 1999-06-01
JP15348599 1999-06-01
JP2000079197A JP3450260B2 (en) 1999-06-01 2000-03-22 Epoxy resin composition and coil casting

Publications (2)

Publication Number Publication Date
JP2001048958A JP2001048958A (en) 2001-02-20
JP3450260B2 true JP3450260B2 (en) 2003-09-22

Family

ID=26482091

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000079197A Expired - Fee Related JP3450260B2 (en) 1999-06-01 2000-03-22 Epoxy resin composition and coil casting

Country Status (1)

Country Link
JP (1) JP3450260B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5253211B2 (en) * 2009-02-04 2013-07-31 京セラケミカル株式会社 Casting epoxy resin composition, ignition coil and method for producing the same
JP6539017B2 (en) * 2014-01-14 2019-07-03 ソマール株式会社 Two-component epoxy resin composition and method of manufacturing case mold type capacitor

Also Published As

Publication number Publication date
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