JPH06100658A - Epoxy resin composition - Google Patents

Epoxy resin composition

Info

Publication number
JPH06100658A
JPH06100658A JP25094892A JP25094892A JPH06100658A JP H06100658 A JPH06100658 A JP H06100658A JP 25094892 A JP25094892 A JP 25094892A JP 25094892 A JP25094892 A JP 25094892A JP H06100658 A JPH06100658 A JP H06100658A
Authority
JP
Japan
Prior art keywords
epoxy resin
curing agent
resin composition
formula
solder
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
JP25094892A
Other languages
Japanese (ja)
Other versions
JP3235798B2 (en
Inventor
Naoki Mogi
直樹 茂木
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
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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP25094892A priority Critical patent/JP3235798B2/en
Publication of JPH06100658A publication Critical patent/JPH06100658A/en
Application granted granted Critical
Publication of JP3235798B2 publication Critical patent/JP3235798B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001Technical content checked by a classifier
    • H01L2924/0002Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Abstract

PURPOSE:To obtain a semiconductor-sealing epoxy resin composition excellent in soldering cracking resistance and humidity resistance by mixing a specified epoxy resin with a cresol resin curing agent and then with an inorganic filler and a cure accelerator. CONSTITUTION:An epoxy resin component comprising 30-100wt.%, based on the total epoxy resin content, epoxy resin of formula I wherein R1 to R8 are each H, halogen or alkyl (e.g. 3,3',5,5'-tetramethyl-4,4'-dihydroxybiphenyl glycidyl ether) is mixed with 30-100wt.%, based on the total curing agent content, cresol resin curing agent of formula II. The obtained resin composition is further mixed with an inorganic filler (e.g. fused silica powder) and a cure accelerator (e.g. 2-methylimidazole) as essential components and a flame retardant, a colorant, etc., as optional components to produce a semiconductor-sealing epoxy resin composition.

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 resistance to solder stress in surface mounting semiconductor devices.

【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O−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
で硬化させたエポキシ樹脂が用いられている。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QFP,SOP,SOJ,TS
OP,TQFP,PLCCに変わってきている。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
るのに適した、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。これらの問題を解決するためにエポ
キシ樹脂として下記式(1)で示されるエポキシ樹脂の
使用(特開昭64−65116号公報)が
2. Description of the Related Art Conventionally, electronic parts such as diodes, transistors and integrated circuits have been sealed with a thermosetting resin. Especially in integrated circuits, O-cresol novolac epoxy resin which is excellent in heat resistance and moisture resistance is used as a novolak. An epoxy resin cured with a type phenolic resin is used. However, in recent years, as the integration of integrated circuits has become higher and higher, the chips have become larger and smaller, and the packages are small and thin QFPs, SOPs, SOJs, TSs that are surface-mounted from the conventional DIP type.
It has changed to OP, TQFP, PLCC. That is, a large chip is enclosed in a small and thin package, and problems such as cracks caused by stress and deterioration of moisture resistance due to these cracks have been greatly highlighted. In particular, when exposed to a high temperature of 200 ° C. or more in the soldering process, moisture resistance is deteriorated due to cracking of the package and peeling of the resin and the chip. It has been desired to develop a highly reliable encapsulating resin composition suitable for encapsulating these large chips. In order to solve these problems, the use of an epoxy resin represented by the following formula (1) as an epoxy resin (Japanese Patent Laid-Open No. 64-65116) has been proposed.

【0003】[0003]

【化3】 [Chemical 3]

【0004】検討されてきた。式(1)で示されるエポ
キシ樹脂の使用によりレジン系の低粘度化が図られ、従
って溶融シリカ粉末を更に多く配合することにより組成
物の成形後の低熱膨張化及び低吸水化より耐半田ストレ
ス性の向上が図られた。ただし、溶融シリカ粉末を多く
配合することによる弾性率の増加も一方の弊害であり、
更なる耐半田ストレス性の向上が必要である。
It has been studied. By using the epoxy resin represented by the formula (1), it is possible to reduce the viscosity of the resin system. Therefore, by adding a larger amount of fused silica powder, it is possible to reduce the thermal expansion coefficient and the water absorption after molding the composition, and thus the solder stress resistance can be improved. The sexuality was improved. However, increasing the elastic modulus by blending a large amount of fused silica powder is one of the harmful effects,
Further improvement in solder stress resistance is required.

【0005】[0005]

【発明が解決しようとする課題】本発明はこの様な問題
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、弾性率の低下による応力低下を達成せし
めるために硬化剤して式(2)で示されるクレゾール樹
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。
In the present invention, the epoxy resin represented by the formula (1) is used as the epoxy resin to solve the above problems, and the epoxy resin is used as a curing agent in order to achieve a stress reduction due to a decrease in elastic modulus. An object of the present invention is to provide a semiconductor encapsulating epoxy resin composition in which the solder stress resistance of a semiconductor package during mounting on a substrate is remarkably improved by using the cresol resin curing agent represented by the formula (2).

【0006】[0006]

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

【0007】[0007]

【化4】 [Chemical 4]

【0008】を総エポキシ樹脂に対して30〜100重
量%含むエポキシ樹脂、(B)下記式(2)で示される
クレゾール樹脂硬化剤
An epoxy resin containing 30 to 100% by weight of the total epoxy resin, (B) a cresol resin curing agent represented by the following formula (2)

【0009】[0009]

【化5】 [Chemical 5]

【0010】を総硬化剤に対して30〜100重量%含
む硬化剤、(C)無機充填材および(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あ
る。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。
An epoxy resin composition for encapsulating a semiconductor, which comprises, as essential components, a curing agent containing 30 to 100% by weight of the total curing agent, (C) an inorganic filler, and (D) a curing accelerator. It has excellent solder stress resistance as compared with conventional epoxy resin compositions.

【0011】式(1)の構造で示されるビフェニル型エ
ポキシ樹脂は1分子中に2つのエポキシ基を有する2官
能性エポキシ樹脂で、従来の多官能性エポキシ樹脂に比
べ溶融粘度が低くトランスファー成形時の流動性に優れ
る。従って組成物の溶融シリカ粉末を多く配合すること
ができ、低熱膨張化及び低吸水化が図られ、耐半田スト
レス性に優れるエポキシ樹脂組成物を得ることができ
る。このビフェニル型エポキシ樹脂の使用量はこれを調
節することにより耐半田ストレス性を最大限に引き出す
ことができる。耐半田ストレス性の効果を出すためには
式(1)で示されるビフェニル型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50重量%以
上使用するのが望ましい。30重量%未満だと低熱膨張
化及び低吸水性が得られず耐半田ストレス性が不充分で
ある。更に式中のR1〜R4はメチル基、R5〜R8は水素
原子が好ましい。
The biphenyl type epoxy resin represented by the structure of the formula (1) is a bifunctional epoxy resin having two epoxy groups in one molecule and has a low melt viscosity as compared with the conventional polyfunctional epoxy resin and is used in transfer molding. Has excellent fluidity. Therefore, a large amount of fused silica powder of the composition can be blended, low thermal expansion and low water absorption can be achieved, and an epoxy resin composition having excellent solder stress resistance can be obtained. By adjusting the amount of the biphenyl type epoxy resin used, solder stress resistance can be maximized. In order to obtain the effect of resistance to solder stress, it is desirable to use the biphenyl type epoxy resin represented by the formula (1) in an amount of 30% by weight or more, preferably 50% by weight or more based on the total amount of epoxy resin. If it is less than 30% by weight, low thermal expansion and low water absorption cannot be obtained, and solder stress resistance is insufficient. Further, in the formula, R 1 to R 4 are preferably methyl groups, and R 5 to R 8 are preferably hydrogen atoms.

【0012】式(1)で示されるビフェニル型エポキシ
樹脂以外に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及びオリゴ
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、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、トリアジン核
含有エポキシ樹脂等のことをいう。
When another epoxy resin is used in combination with the biphenyl type epoxy resin represented by the formula (1), the epoxy resin to be used means all polymers and oligomers having an epoxy group. For example, bisphenol type epoxy resin, cresol novolac type epoxy resin, phenol novolac type epoxy resin, triphenol methane type epoxy resin, trifunctional epoxy resin such as alkyl modified triphenol methane type epoxy resin, triazine nucleus-containing epoxy resin, etc. Say.

【0013】式(2)の分子構造で示される硬化剤はオ
ルソクレゾールとシクロヘキサンを用い、縮合反応によ
り得た2官能硬化剤である。この使用は従来のフェノー
ルノボラック樹脂硬化剤等の使用と比べると半田処理温
度近辺での弾性率の低下とリードフレーム及び半導体チ
ップとの密着力を向上せしめ、また低吸水化を得ること
ができる。従って半田付時の熱衝撃に対し発生応力の低
下とそれに伴なう半導体チップ及びリードフレーム等と
の剥離不良の防止に有効である。この様なクレゾール樹
脂硬化剤の使用量はこれを調節することにより、耐半田
ストレス性を最大限に引き出すことができる。耐半田ス
トレス性の効果を引き出すためには式(2)で示される
クレゾール樹脂硬化剤を総硬化剤量に対して30重量%
以上、更に好ましくは50重量%以上使用するのが望ま
しい。使用が30重量%未満だと低弾性、低吸水性等及
びリードフレーム、半導体チップとの密着力が不充分で
耐半田ストレス性の向上が望めない。
The curing agent represented by the molecular structure of formula (2) is a bifunctional curing agent obtained by a condensation reaction using orthocresol and cyclohexane. Compared with the use of a conventional phenol novolac resin curing agent, this use can lower the elastic modulus near the soldering temperature, improve the adhesion to the lead frame and the semiconductor chip, and achieve low water absorption. Therefore, it is effective in reducing the generated stress due to thermal shock during soldering and preventing the defective peeling from the semiconductor chip, the lead frame and the like due to it. By adjusting the amount of such a cresol resin curing agent used, solder stress resistance can be maximized. In order to bring out the effect of solder stress resistance, the cresol resin curing agent represented by the formula (2) is used in an amount of 30% by weight based on the total amount of the curing agent.
More preferably, 50% by weight or more is used. If the amount used is less than 30% by weight, low elasticity, low water absorption and the like, and insufficient adhesion to the lead frame and semiconductor chip, it cannot be expected to improve solder stress resistance.

【0014】式(2)で示されるクレゾール樹脂硬化剤
以外に他のものを併用する場合、用いるものとは主にフ
ェノール性水酸基を有するポリマー及びオリゴマー全般
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、ジシクロペンタジエン変性フェノール樹脂とフェ
ノールノボラック及びクレゾールノボラック樹脂との共
重合物、パラキシレン変性フェノール樹脂、トリフェノ
ールメタン樹脂、フェノール及びクレゾールとサリチル
アルデヒドとの縮合物等を用いることができる。
When using other than the cresol resin curing agent represented by the formula (2) in combination, what is used mainly means polymers and oligomers having a phenolic hydroxyl group in general. For example, phenol novolac resin, cresol novolac resin, dicyclopentadiene modified phenol resin, copolymer of dicyclopentadiene modified phenol resin with phenol novolac and cresol novolac resin, paraxylene modified phenol resin, triphenol methane resin, phenol and cresol A condensate with salicylaldehyde or the like can be used.

【0015】本発明で用いる無機充填材としては、溶融
シリカ粉末、球状シリカ粉末、結晶シリカ粉末、2次凝
集シリカ粉末、多孔質シリカ粉末、2次凝集シリカ粉末
または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組成物量に対して70〜9
0重量%が好ましい。
As the inorganic filler used in the present invention, fused silica powder, spherical silica powder, crystalline silica powder, secondary agglomerated silica powder, porous silica powder, secondary agglomerated silica powder or silica obtained by pulverizing porous silica powder is used. Examples thereof include powder and alumina, and fused silica powder, spherical silica powder, and a mixture of fused silica powder and spherical silica powder are particularly preferable. In addition, the compounding amount of the inorganic filler is 70 to 9 relative to the total amount of the composition in view of the balance between solder stress resistance and moldability.
0% by weight is preferred.

【0016】本発明に使用される硬化促進剤はエポキシ
基と水酸基との反応を促進するものであればよく、一般
に封止用材料に使用されているものを広く使用すること
ができ、例えばジアザビシクロウンデセン(DBU)、
トリフェニルホスフィン(TPP)、ジメチルベンジル
アミン(BDMA)や2メチルイミダゾール(2MZ)
等が単独もしくは2種類以上混合して用いられる。本発
明の封止用エポキシ樹脂組成物はエポキシ樹脂、硬化
剤、無機充填材及び硬化促進剤を必須成分とするが、こ
れ以外に必要に応じてシランカップリング剤、ブロム化
エポキシ樹脂、三酸化アンチモン、ヘキサブロムベンゼ
ン等の難燃剤、カーボンブラック、ベンガラ等の着色
剤、天然ワックス、合成ワックス等の離型剤及びシリコ
ーンオイル、ゴム等の低応力添加剤等の種々の添加剤を
適宜配合しても差し支えがない。
The curing accelerator used in the present invention may be any one as long as it accelerates the reaction between the epoxy group and the hydroxyl group, and those generally used for sealing materials can be widely used. Zabicyclo undecene (DBU),
Triphenylphosphine (TPP), dimethylbenzylamine (BDMA) and 2-methylimidazole (2MZ)
Etc. are used alone or in combination of two or more. The encapsulating epoxy resin composition of the present invention contains an epoxy resin, a curing agent, an inorganic filler, and a curing accelerator as essential components, but other than this, a silane coupling agent, a brominated epoxy resin, and trioxide may be added if necessary. Flame retardants such as antimony and hexabromobenzene, colorants such as carbon black and red iron oxide, mold release agents such as natural wax and synthetic wax, and various additives such as low-stress additives such as silicone oil and rubber. But there is no problem.

【0017】又、本発明の封止用エポキシ樹脂組成物を
成形材料として製造するには、エポキシ樹脂、硬化剤、
硬化促進剤、充填剤、その他の添加剤をミキサー等によ
って十分に均一に混合した後、さらに熱ロール又はニー
ダー等で溶融混練し、冷却後粉砕して成形材料とするこ
とができる。これらの成形材料は電子部品あるいは電気
部品の封止、被覆、絶縁等に適用することができる。
In order to produce the encapsulating epoxy resin composition of the present invention as a molding material, an epoxy resin, a curing agent,
A curing accelerator, a filler, and other additives are sufficiently and uniformly mixed with a mixer or the like, and then the mixture is melt-kneaded with a hot roll or a kneader, cooled, and then pulverized to obtain a molding material. These molding materials can be applied to sealing, coating, insulating, etc. of electronic parts or electric parts.

【0018】[0018]

【実施例】以下本発明を実施例で具体的に説明する。 実施例1 式(3)で示されるエポキシ樹脂(軟化点110℃、エポキシ当量190g/ eq) 9.3重量部EXAMPLES The present invention will be specifically described below with reference to examples. Example 1 9.3 parts by weight of an epoxy resin represented by the formula (3) (softening point 110 ° C., epoxy equivalent 190 g / eq)

【0019】[0019]

【化6】 [Chemical 6]

【0020】 オルソクレゾールノボラックエポキシ樹脂(軟化点65℃、エポキシ当量20 0g/eq) 2.3重量部 式(2)で示されるクレゾール樹脂硬化剤(軟化点203℃、水酸基当量14 8g/eq) 6.7重量部 フェノールノボラック樹脂硬化剤(軟化点90℃、水酸基当量105g/eq ) 1.7重量部 溶融シリカ粉末 78.8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 0.5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、冷却後粉砕した成形材料とした。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パッケージに封止し、又半田耐湿性試験用として
3×6mmのチップを16pSOPパッケージに封止し
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。 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℃で、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
(125℃、100%RH)を行い回路のオープン不良
を測定した。試験結果を表1に示す。
Ortho-cresol novolac epoxy resin (softening point 65 ° C., epoxy equivalent 200 g / eq) 2.3 parts by weight Cresol resin curing agent represented by the formula (2) (softening point 203 ° C., hydroxyl equivalent 148 g / eq) 6.7 parts by weight Phenol novolac resin curing agent (softening point 90 ° C., hydroxyl equivalent 105 g / eq) 1.7 parts by weight fused silica powder 78.8 parts by weight triphenylphosphine 0.2 parts by weight carbon black 0.5 parts by weight 0.5 part by weight of carnauba wax was mixed at room temperature with a mixer, kneaded with a twin-screw roll at 70 to 100 ° C., cooled, and ground to obtain a molding material. The obtained molding material is made into a tablet, and a 6 × 6 mm chip is sealed in a 52p package for a solder crack test under the conditions of 175 ° C., 70 kg / cm 2 and 120 seconds with a low-pressure transfer molding machine, and solder moisture resistance. A 3 × 6 mm chip was encapsulated in a 16 pSOP package for a sex test. The following solder crack test and solder moisture resistance test were performed on the sealed test element. Solder crack test: sealed test element at 85 ° C, 8
After 48 hours and 72 hours of treatment in an environment of 5% RH, the pieces were immersed in a solder bath at 260 ° C. for 10 seconds, and then external cracks were observed with a microscope. Solder moisture resistance test: Sealed test element at 85 ° C for 8
After 72 hours of treatment in an environment of 5% RH, and after dipping in a solder bath at 260 ° C. for 10 seconds, a pressure cooker test (125 ° C., 100% RH) was performed to measure the open circuit failure. The test results are shown in Table 1.

【0021】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。この成形材料で試験用の封止した成形品を
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 Compounding was carried out according to the formulation shown in Table 1, and a molding material was obtained in the same manner as in Example 1. Using this molding material, a molded product sealed for testing was obtained, and a solder crack test and a solder moisture resistance test were carried out in the same manner as in Example 1 using this molded product. The test results are shown in Table 1.

【0022】比較例1〜4 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。この成形材料で試験用の封止した成形品を
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 to 4 Compounding was carried out according to the formulation shown in Table 1, and molding materials were obtained in the same manner as in Example 1. Using this molding material, a molded product sealed for testing was obtained, and a solder crack test and a solder moisture resistance test were carried out in the same manner as in Example 1 using this molded product. The test results are shown in Table 1.

【0023】[0023]

【表1】 [Table 1]

【0024】[0024]

【発明の効果】本発明に従うと従来技術では得ることの
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、半田付け工程による急激
な温度変化による熱ストレスを受けた時の耐クラック性
に非常に優れ、更に耐湿性が良好なことから電子、電気
部品の封止用、被覆用、絶縁用等に用いた場合、特に表
面実装パッケージに搭載された高集積大型チップICに
おいて信頼性が非常に必要とする製品について好適であ
る。
According to the present invention, it is possible to obtain an epoxy resin composition having a solder stress resistance which could not be obtained by the prior art. Therefore, when an epoxy resin composition is subjected to a thermal stress due to a rapid temperature change due to a soldering process. Has very good crack resistance and good moisture resistance, so when used for encapsulation, coating, insulation, etc. of electronic and electrical parts, especially highly integrated large chip IC mounted in surface mount package It is suitable for products for which reliability is highly required.

フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08L 63/00 NJW 8830−4J H01L 23/29 23/31 Continuation of front page (51) Int.Cl. 5 Identification number Office reference number FI technical display location C08L 63/00 NJW 8830-4J H01L 23/29 23/31

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (A)下記式(1)で示されるエポキシ
樹脂 【化1】 を総エポキシ樹脂に対して30〜100重量%含むエポ
キシ樹脂、(B)下記式(2)で示されるクレゾール樹
脂硬化剤 【化2】 を総硬化剤に対して30〜100重量%含む硬化剤、
(C)無機充填材および(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。
1. An epoxy resin represented by the following formula (1): An epoxy resin containing 30 to 100% by weight based on the total epoxy resin, (B) a cresol resin curing agent represented by the following formula (2): A curing agent containing 30 to 100% by weight based on the total curing agent,
An epoxy resin composition for semiconductor encapsulation, which comprises (C) an inorganic filler and (D) a curing accelerator as essential components.
JP25094892A 1992-09-21 1992-09-21 Epoxy resin composition Expired - Fee Related JP3235798B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25094892A JP3235798B2 (en) 1992-09-21 1992-09-21 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25094892A JP3235798B2 (en) 1992-09-21 1992-09-21 Epoxy resin composition

Publications (2)

Publication Number Publication Date
JPH06100658A true JPH06100658A (en) 1994-04-12
JP3235798B2 JP3235798B2 (en) 2001-12-04

Family

ID=17215392

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25094892A Expired - Fee Related JP3235798B2 (en) 1992-09-21 1992-09-21 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JP3235798B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002284961A (en) * 2001-03-22 2002-10-03 Toray Ind Inc Epoxy-based resin composition and semiconductor device using the same
JP2002284856A (en) * 2001-03-26 2002-10-03 Toray Ind Inc Epoxy resin composition and semiconductor device using the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002284961A (en) * 2001-03-22 2002-10-03 Toray Ind Inc Epoxy-based resin composition and semiconductor device using the same
JP2002284856A (en) * 2001-03-26 2002-10-03 Toray Ind Inc Epoxy resin composition and semiconductor device using the same

Also Published As

Publication number Publication date
JP3235798B2 (en) 2001-12-04

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