JP3004463B2 - Epoxy resin composition - Google Patents

Epoxy resin composition

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Publication number
JP3004463B2
JP3004463B2 JP4106933A JP10693392A JP3004463B2 JP 3004463 B2 JP3004463 B2 JP 3004463B2 JP 4106933 A JP4106933 A JP 4106933A JP 10693392 A JP10693392 A JP 10693392A JP 3004463 B2 JP3004463 B2 JP 3004463B2
Authority
JP
Japan
Prior art keywords
epoxy resin
weight
solder
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 - Lifetime
Application number
JP4106933A
Other languages
Japanese (ja)
Other versions
JPH05299537A (en
Inventor
賢至 鮫島
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
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Filing date
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  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)
  • Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、半導体デバイスの表面
実装化における耐半田ストレス性に優れた半導体封止用
エポキシ樹脂組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an epoxy resin composition for semiconductor encapsulation which is excellent in soldering stress resistance in surface mounting of a semiconductor device.

【0002】[0002]

【従来の技術】従来、ダイオード、トランジスタ、集積
回路等の電子部品を熱硬化性樹脂で封止しているが、特
に集積回路では耐熱性、耐湿性に優れたオルソクレゾー
ルノボラックエポキシ樹脂をノボラック型フェノール樹
脂で硬化させるエポキシ樹脂組成物が用いられている。
ところが近年、集積回路の高集積化に伴いチップがだん
だん大型化し、かつパッケージは従来のDIPタイプか
ら表面実装化された小型、薄型のフラットパッケージ、
SOP,SOJ,PLCCに変わってきている。
2. Description of the Related Art Conventionally, electronic components such as diodes, transistors, and integrated circuits are sealed with a thermosetting resin. In particular, in an integrated circuit, ortho-cresol novolak epoxy resin having excellent heat resistance and moisture resistance is made of a novolak type. An epoxy resin composition cured with a phenol resin is used.
However, in recent years, chips have become larger and larger as integrated circuits have become more highly integrated, and packages have become smaller and thinner flat packages that are surface-mounted from conventional DIP types.
It is changing to SOP, SOJ, PLCC.

【0003】即ち大型チップを小型で薄いパッケージに
封入することになり、応力によりクラック発生、これら
のクラックによる耐湿性の低下等の問題が大きくクロー
ズアップされてきている。特に半田付けの工程において
急激に200℃以上の高温にさらされることによりパッ
ケージの割れや樹脂とチップの剥離により耐湿性が劣化
してしまうといった問題点がでてきている。これらの大
型チップを封止するに適した、信頼性の高い封止用樹脂
組成物の開発が望まれてきている。
That is, a large chip is enclosed in a small and thin package, and cracks are generated due to stress, and problems such as a decrease in moisture resistance due to the cracks have been greatly highlighted. In particular, there has been a problem in that abrupt exposure to a high temperature of 200 ° C. or more in a soldering process causes a crack in a package and a peeling of a resin and a chip to deteriorate moisture resistance. Development of a highly reliable sealing resin composition suitable for sealing these large chips has been desired.

【0004】これらの問題点を解決するために、半田付
け時に熱衝撃を緩和する目的で、熱可塑性オリゴマーの
添加(特開昭62−115849号公報)や各種シリコ
ーン化合物の添加(特開昭62−115850号公報、
62−116654号公報、62−128162号公
報)、更にはシリコーン変性(特開昭62−13686
0号公報)等の手法で対処しているが、いずれも半田付
け時にパッケージにクラックが生じてしまい、信頼性の
高い封止用エポキシ樹脂組成物を得るまでには至らなか
った。
[0004] In order to solve these problems, addition of thermoplastic oligomers (Japanese Patent Application Laid-Open No. 62-15849) and addition of various silicone compounds (Japanese Patent Application Laid-Open No. JP-115850,
62-116654 and 62-128162) and further modified with silicone (Japanese Patent Application Laid-Open No. 62-13686).
No. 0), however, cracks occurred in the package during soldering, and none of these methods resulted in obtaining a highly reliable sealing epoxy resin composition.

【0005】一方、半田付け時の耐熱ストレス性、つま
り耐半田ストレス性に優れた半導体封止用エポキシ樹脂
組成物を得る為に、樹脂系としてビフェニル型エポキシ
樹脂の使用(特開昭64−65116号公報)等が検討
されてきたが、ビフェニル型エポキシ樹脂の使用によ
り、リードフレームとの密着性及び、低吸水性が向上
し、耐半田ストレス性の向上、特にクラック発生が低減
するが、250℃以上の高温では、まだ耐半田ストレス
性が不十分である。
On the other hand, in order to obtain an epoxy resin composition for semiconductor encapsulation having excellent heat stress resistance during soldering, that is, excellent solder stress resistance, a biphenyl type epoxy resin is used as a resin system (Japanese Patent Application Laid-Open No. 64-65116). Although the use of a biphenyl-type epoxy resin improves the adhesion to the lead frame and low water absorption, the solder stress resistance is improved, and crack generation is particularly reduced. At a high temperature of at least ℃, the solder stress resistance is still insufficient.

【0006】[0006]

【発明が解決しようとする課題】本発明はこのような問
題に対してエポキシ樹脂として式(1)で示されるエポ
キシ樹脂を用い、成形品の吸水量、熱膨張係数を低下せ
しめるために、硬化剤として式(2)で示されるαナフ
トールとパラクレゾールの共縮合ノボラック型フェノー
ル樹脂硬化剤を用いることにより、基板実装時における
半導体パッケージの耐半田ストレス性を著しく向上させ
た半導体封止用エポキシ樹脂組成物を提供するところに
ある。
The present invention solves such a problem by using an epoxy resin represented by the formula (1) as an epoxy resin and curing the molded product in order to lower the water absorption and the coefficient of thermal expansion of the molded product. Epoxy resin for semiconductor encapsulation that has significantly improved the soldering stress resistance of a semiconductor package when mounted on a substrate by using a co-condensed novolak-type phenolic resin curing agent of α-naphthol and paracresol represented by the formula (2) as an agent It is an object to provide a composition.

【0007】[0007]

【課題を解決するための手段】即ち本発明は(A)下記
式(1)で示されるエポキシ樹脂
That is, the present invention provides (A) an epoxy resin represented by the following formula (1):

【0008】[0008]

【化3】 Embedded image

【0009】(n=1〜6)を総エポキシ樹脂量に対し
て30〜100重量%含むエポキシ樹脂、 (B)下記式(2)で示されるフェノール樹脂硬化剤
An epoxy resin containing (n = 1 to 6) in an amount of 30 to 100% by weight based on the total amount of the epoxy resin; (B) a phenol resin curing agent represented by the following formula (2):

【0010】[0010]

【化4】 Embedded image

【0011】(n=1〜6)を総硬化剤量に対して30
〜100重量%含む硬化剤、 (C)無機充填材及び (D)硬化促進剤 を必須成分とする半導体封止用エポキシ樹脂組成物で、
従来のエポキシ樹脂組成物に比べ、優れた耐半田ストレ
ス性を有するものである。
(N = 1 to 6) is calculated as 30 to the total amount of the curing agent.
An epoxy resin composition for encapsulating a semiconductor comprising, as essential components, a curing agent containing (C) an inorganic filler and (D) a curing accelerator.
It has excellent solder stress resistance as compared with a conventional epoxy resin composition.

【0012】式(1)で示されるエポキシ樹脂は、パラ
クレゾールとαナフトールの共縮合ノボラックエポキシ
樹脂であり、低吸水性に優れ、かつ線膨張係数が小さい
という特徴を有し、半田付け時の半田耐熱性に良好な結
果を示す。このパラクレゾールとαナフトールの共縮合
ノボラックエポキシ樹脂の使用量は、これを調節するこ
とにより半田耐熱性を最大限に引き出すことができる。
半田耐熱性の効果を出すためには、パラクレゾールとα
ナフトールの共縮合ノボラックエポキシ樹脂を総エポキ
シ樹脂量の30重量%以上、好ましくは60重量%以上
の使用が望ましい。30重量%未満では低吸水性、低線
膨張係数が十分に得られず、半田耐熱性が不十分であ
る。nの値は1〜6であり、6を超えると流動性が低下
し、成形性が悪くなる。パラクレゾールとαナフトール
共縮合ノボラックエポキシ樹脂以外の他のエポキシ樹脂
を併用する場合、用いるエポキシ樹脂とは、エポキシ基
を有するポリマー全般をいう。例えばビスフェノール型
エポキシ樹脂、クレゾールノボラック型エポキシ樹脂、
ビフェニル型エポキシ樹脂、フェノールノボラック型エ
ポキシ樹脂、及びトリフェノールメタン型エポキシ樹
脂、アルキル変性トリフェノールメタン型エポキシ樹脂
等の3官能型エポキシ樹脂、トリアジン環含有エポキシ
樹脂等のことをいう。
The epoxy resin represented by the formula (1) is a co-condensed novolak epoxy resin of paracresol and α-naphthol, and is characterized by low water absorption and a small coefficient of linear expansion. It shows good results in solder heat resistance. By adjusting the amount of the co-condensed novolak epoxy resin of paracresol and α-naphthol, the solder heat resistance can be maximized by adjusting the amount.
In order to achieve solder heat resistance, paracresol and α
It is desirable to use 30% by weight or more, preferably 60% by weight or more of the copolycondensed novolak epoxy resin of naphthol based on the total amount of the epoxy resin. If it is less than 30% by weight, low water absorption and low linear expansion coefficient cannot be sufficiently obtained, and solder heat resistance is insufficient. The value of n is from 1 to 6, and when it exceeds 6, the fluidity is reduced and the moldability is deteriorated. When an epoxy resin other than the para-cresol and α-naphthol co-condensed novolak epoxy resin is used in combination, the epoxy resin used generally refers to any polymer having an epoxy group. For example, bisphenol type epoxy resin, cresol novolak type epoxy resin,
It refers to a trifunctional epoxy resin such as a biphenyl epoxy resin, a phenol novolak epoxy resin, a triphenolmethane epoxy resin, an alkyl-modified triphenolmethane epoxy resin, and a triazine ring-containing epoxy resin.

【0013】式(2)で示される硬化剤はパラクレゾー
ルとのαナフトールの共縮合ノボラックフェノール樹脂
であり低吸水性に優れ線膨張係数が小さいという特徴を
有し、半田付け時の半田耐熱性に良好な結果を示す。半
田耐熱性の効果をだすためには、式(2)で示されるフ
ェノール樹脂を総フェノール樹脂量の30重量%以上、
好ましくは60重量%以上の使用が望ましい。30重量
%未満では可撓性が不十分となり、半田付け時の半田耐
熱性が十分に得られない。nの値は1〜6であり、6を
超えると流動性が低下し、成形性が悪くなる。式(2)
で示されるフェノール樹脂硬化剤以外の併用する他の硬
化剤としては、主にフェノール性水酸基を有するポリマ
ー全般をいう。例えば、フェノールノボラック樹脂、ク
レゾールノボラック樹脂、ジシクロペンタジエン変性フ
ェノール樹脂等を用いることができる。
The curing agent represented by the formula (2) is a co-condensed novolak phenol resin of α-naphthol with paracresol, has a characteristic of low water absorption and a small linear expansion coefficient, and has a solder heat resistance at the time of soldering. Shows good results. In order to obtain the effect of solder heat resistance, the phenolic resin represented by the formula (2) should be used in an amount of 30% by weight or more based on the total amount of the phenolic resin.
Preferably, 60% by weight or more is used. If the amount is less than 30% by weight, the flexibility becomes insufficient and the soldering heat resistance at the time of soldering cannot be sufficiently obtained. The value of n is from 1 to 6, and when it exceeds 6, the fluidity is reduced and the moldability is deteriorated. Equation (2)
The other curing agents to be used in combination other than the phenolic resin curing agent represented by the general formula (1) generally refer to all polymers having a phenolic hydroxyl group. For example, a phenol novolak resin, a cresol novolak resin, a dicyclopentadiene-modified phenol resin, or the like can be used.

【0014】本発明で用いる無機質充填材としては、溶
融シリカ粉末、球状シリカ粉末、結晶シリカ粉末、二次
凝集シリカ粉末、多孔質シリカ粉末を粉砕したシリカ粉
末、アルミナ等が挙げられ、特に溶融シリカ粉末、球状
シリカ粉末及び溶融シリカ粉末と球状シリカ粉末との混
合物が好ましい。また無機質充填材の配合量としては、
耐半田ストレス性と成形性のバランスから、総樹脂組成
物に対して70〜90重量%が望ましい。
Examples of the inorganic filler used in the present invention include fused silica powder, spherical silica powder, crystalline silica powder, secondary agglomerated silica powder, silica powder obtained by pulverizing porous silica powder, and alumina. Powders, spherical silica powders and mixtures of fused silica powder and spherical silica powder are preferred. In addition, as the compounding amount of the inorganic filler,
From the balance between solder stress resistance and moldability, 70 to 90% by weight based on the total resin composition is desirable.

【0015】更に本発明に用いる硬化促進剤はエポキシ
基とフェノール性水酸基の反応を促進するものであれば
良く、一般に封止材料に使用されているものを広く使用
することができる。例えばトリフェニルホスフィン、ト
リブチルホスフィン、トリ(4−メチルフェニル)ホス
フィン等の有機ホスフィン化合物、トリブチルアルミ
ン、トリエチルアミン、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、1,8−ジアザビ
シクロ[5,4,0]−7−ウンデセン等の3級アミ
ン、2−メチルイミダゾール、2−フェニルイミダゾー
ル、2−エチル−4−メチルイイミダゾール等のイミダ
ゾール化合物等が挙げられる。これらを単独で用いて
も、あるいはその2種以上の併用も可能である。
Further, the curing accelerator used in the present invention may be any one which promotes the reaction between an epoxy group and a phenolic hydroxyl group, and those generally used for a sealing material can be widely used. For example, organic phosphine compounds such as triphenylphosphine, tributylphosphine and tri (4-methylphenyl) phosphine, tributylaluminum, triethylamine, benzyldimethylamine, trisdimethylaminomethylphenol, 1,8-diazabicyclo [5,4,0]- Examples include tertiary amines such as 7-undecene, and imidazole compounds such as 2-methylimidazole, 2-phenylimidazole and 2-ethyl-4-methylimidazole. These can be used alone or in combination of two or more.

【0016】本発明の組成物は前述のもの以外、必要に
応じてカーボンブラック等の着色剤、カルナバワック
ス、合成ワックス等の離型剤、ブロム化エポキシ樹脂、
三酸化アンチモン等の難燃剤、γ−グリシドキシプロピ
ルトリメトキシシラン等のカップリング剤、シリコーン
オイル、ゴム等の低応力成分を添加することができる。
本発明のエポキシ樹脂組成物はエポキシ樹脂、硬化剤、
無機質充填材、硬化促進剤、その他の添加剤をミキサー
等で均一に混合した後、ロール、押し出し機等の一般混
練装置により熱溶融混練し、冷却、粉砕することにより
成形材料とすることができる。
The composition of the present invention may further comprise a coloring agent such as carbon black, a release agent such as carnauba wax or synthetic wax, a brominated epoxy resin, etc., if necessary.
Flame retardants such as antimony trioxide, coupling agents such as γ-glycidoxypropyltrimethoxysilane, and low-stress components such as silicone oil and rubber can be added.
The epoxy resin composition of the present invention is an epoxy resin, a curing agent,
After uniformly mixing the inorganic filler, the curing accelerator, and other additives with a mixer or the like, the mixture is hot-melt-kneaded with a general kneading device such as a roll or an extruder, and then cooled and pulverized to form a molding material. .

【0017】[0017]

【実施例】以下本発明を実施例で説明する。 実施例1 式(1)で示されるエポキシ樹脂 (n=1が40重量%、n=2が60重量%の混合物、 エポキシ当量230、軟化点65℃) 4.5重量部 オルソクレゾールノボラックエポキシ樹脂 (エポキシ当量200、軟化点62℃) 10.5重量部 式(2)で示されるフェノール樹脂硬化剤 (n=3が70重量%、n=4が30重量%の混合物、 OH当量140、軟化点106℃) 2.5重量部 フェノールノボラック樹脂(OH当量105、軟化点90℃)5.8重量部 溶融シリカ粉末 75重量部 トリフェニルホスフィン 0.2重量部 カーボンブラック 0.3重量部 カルナバワックス 0.5重量部 をミキサーで常温で混合し、70〜100℃で2軸ロー
ルにより混練し、冷却後粉砕して成形材料とした。得ら
れた成形材料をタブレット化し、低圧トランスファー成
形機にて175℃、70kg/cm2 、120秒の条件で半
田クラック試験用として6×6mmのチップを52pパッ
ケージに封入し、また半田耐湿試験用として3×6mmの
チップを16pSOPパッケージに封入した。封止した
テスト用素子について下記の半田クラック試験及び半田
耐湿性試験を行った。試験結果を表1に示す。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below with reference to embodiments. Example 1 Epoxy resin represented by the formula (1) (a mixture in which n = 1 is 40% by weight and n = 2 is 60% by weight, epoxy equivalent 230, softening point 65 ° C.) 4.5 parts by weight ortho-cresol novolak epoxy resin (Epoxy equivalent: 200, softening point: 62 ° C.) 10.5 parts by weight A phenolic resin curing agent represented by the formula (2) (a mixture of 70% by weight for n = 3 and 30% by weight for n = 4, OH equivalent of 140, softening) 2.5 parts by weight Phenol novolak resin (OH equivalent 105, softening point 90 ° C.) 5.8 parts by weight Fused silica powder 75 parts by weight Triphenylphosphine 0.2 parts by weight Carbon black 0.3 parts by weight Carnauba wax 0.5 part by weight was mixed at room temperature with a mixer, kneaded at 70 to 100 ° C. with a biaxial roll, cooled and pulverized to obtain a molding material. The obtained molding material is tableted, and a 6 × 6 mm chip is sealed in a 52p package for a solder crack test at 175 ° C., 70 kg / cm 2 for 120 seconds using a low pressure transfer molding machine, and for a solder moisture resistance test. A 3 × 6 mm chip was sealed in a 16pSOP package. The sealed test element was subjected to the following solder crack test and solder moisture resistance test. Table 1 shows the test results.

【0018】 半田クラック試験:封止したテスト用素子を85℃、8
5%RHの環境下で48Hr及び72Hr処理し、その
後260℃の半田槽に10秒間浸漬後、顕微鏡で外部ク
ラックを観察した。 半田耐湿性試験 :封止したテスト用素子を85℃、8
5%RHの環境下で72Hr処理しその後260℃の半
田槽に10秒間浸漬後、プレッシャークッカー試験(1
25℃、100%RH)を行い、回路のオープン不良を
測定した。
Solder crack test: The sealed test element was heated at 85 ° C. for 8
48 hours and 72 hours of treatment were performed in an environment of 5% RH, and then immersed in a solder bath at 260 ° C. for 10 seconds, and external cracks were observed with a microscope. Solder moisture resistance test: 85 ° C, 8
After treating for 72 hours in an environment of 5% RH, and then immersing in a solder bath at 260 ° C. for 10 seconds, a pressure cooker test (1
(25 ° C., 100% RH), and the open failure of the circuit was measured.

【0019】実施例2〜5 表1の処方に従って配合し、実施例1と同様にして成形
材料を得た。この成形材料でテスト用素子を封止した成
形品を得、この成形品を用いて実施例1と同様に半田ク
ラック試験及び半田耐湿性試験を行った。試験結果を表
1に示す。
Examples 2 to 5 Compounded according to the formulation shown in Table 1, and a molding material was obtained in the same manner as in Example 1. A molded product in which a test element was sealed with this molding material was obtained, and a solder crack test and a solder moisture resistance test were performed using this molded product in the same manner as in Example 1. Table 1 shows the test results.

【0020】比較例1〜2 表1の処方に従って配合し、実施例1と同様にして成形
材料を得た。この成形材料でテトス用素子を封止した成
形品を得、この成形品を用いて実施例1と同様に半田ク
ラック試験及び半田耐湿性試験を行った。試験結果を表
1に示す。
Comparative Examples 1-2 Compounds were prepared according to the formulation shown in Table 1 and molding materials were obtained in the same manner as in Example 1. A molded product in which the element for TETOS was sealed with this molding material was obtained, and a solder crack test and a solder moisture resistance test were performed using this molded product in the same manner as in Example 1. Table 1 shows the test results.

【0021】[0021]

【表1】 [Table 1]

【0022】[0022]

【発明の効果】本発明に従うと従来技術では得ることが
できなかった耐半田ストレス性を有するエポキシ樹脂組
成物を得ることができるので、半田付け工程時の耐クラ
ック性に非常に優れ、更に耐湿性が良好なことから表面
実装パッケージに搭載された高集積大型チップICにお
いて好適である。
According to the present invention, an epoxy resin composition having solder stress resistance, which cannot be obtained by the prior art, can be obtained. It is suitable for a highly integrated large chip IC mounted on a surface mount package because of its good performance.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 (A)下記式(1)で示されるエポキシ
樹脂 【化1】 (n=1〜6)を総エポキシ樹脂量に対して30〜10
0重量%含むエポキシ樹脂、 (B)下記式(2)で示されるフェノール樹脂硬化剤 【化2】 (n=1〜6)を総硬化剤量に対して30〜100重量
%含む硬化剤、 (C)無機充填材及び (D)硬化促進剤 を必須成分とする半導体封止用エポキシ樹脂組成物。
(A) an epoxy resin represented by the following formula (1): (N = 1 to 6) is 30 to 10 with respect to the total epoxy resin amount.
An epoxy resin containing 0% by weight; (B) a phenolic resin curing agent represented by the following formula (2): An epoxy resin composition for semiconductor encapsulation comprising, as essential components, a curing agent containing 30 to 100% by weight of (n = 1 to 6) based on the total amount of the curing agent, (C) an inorganic filler and (D) a curing accelerator. .
JP4106933A 1992-04-24 1992-04-24 Epoxy resin composition Expired - Lifetime JP3004463B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4106933A JP3004463B2 (en) 1992-04-24 1992-04-24 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4106933A JP3004463B2 (en) 1992-04-24 1992-04-24 Epoxy resin composition

Publications (2)

Publication Number Publication Date
JPH05299537A JPH05299537A (en) 1993-11-12
JP3004463B2 true JP3004463B2 (en) 2000-01-31

Family

ID=14446206

Family Applications (1)

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JP4106933A Expired - Lifetime JP3004463B2 (en) 1992-04-24 1992-04-24 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JP3004463B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101309822B1 (en) * 2011-05-23 2013-09-23 제일모직주식회사 Epoxy resin composition for encapsulating semiconductor device and semiconductor device encapsulated by using the same
JP2013001807A (en) * 2011-06-16 2013-01-07 Panasonic Corp Resin composition for electronic circuit board material, prepreg and laminated plate
WO2016002241A1 (en) * 2014-06-30 2016-01-07 Dic株式会社 Epoxy resin, curable resin composition, cured product, semiconductor encapsulating material, semiconductor device, prepreg, circuit board, buildup film, buildup substrate, fiber-reinforced composite material and fiber-reinforced molded article
JP2016065250A (en) * 2015-11-25 2016-04-28 パナソニックIpマネジメント株式会社 Prepreg, laminate sheet and metal laminate sheet
JP6078933B2 (en) * 2015-11-25 2017-02-15 パナソニックIpマネジメント株式会社 Resin composition for electronic circuit board material, prepreg, laminate and metal-clad laminate
JP6924292B2 (en) * 2020-01-22 2021-08-25 日本化薬株式会社 Epoxy resin mixture, epoxy resin composition and cured product thereof

Also Published As

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