JP3359445B2 - Resin composition - Google Patents

Resin composition

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Publication number
JP3359445B2
JP3359445B2 JP32004894A JP32004894A JP3359445B2 JP 3359445 B2 JP3359445 B2 JP 3359445B2 JP 32004894 A JP32004894 A JP 32004894A JP 32004894 A JP32004894 A JP 32004894A JP 3359445 B2 JP3359445 B2 JP 3359445B2
Authority
JP
Japan
Prior art keywords
weight
curing agent
epoxy resin
resin composition
formula
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
JP32004894A
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Japanese (ja)
Other versions
JPH08176278A (en
Inventor
浩規 大須賀
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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Application filed by Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP32004894A priority Critical patent/JP3359445B2/en
Publication of JPH08176278A publication Critical patent/JPH08176278A/en
Application granted granted Critical
Publication of JP3359445B2 publication Critical patent/JP3359445B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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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
実装化における半田耐熱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 having excellent solder heat 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
ルノボラック型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、かつパッケージには従来の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、TSOP、SOJ、QFP、TQFP等
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。
2. Description of the Related Art Conventionally, electronic components such as diodes, transistors, and integrated circuits have been sealed with a thermosetting resin. In particular, in an integrated circuit, an ortho-cresol novolak type epoxy resin having excellent heat resistance and moisture resistance is used. An epoxy resin composition cured with a mold phenol resin is used. However, in recent years, the chip has been gradually increased in size with the increase in the degree of integration of integrated circuits, and the package has changed from a conventional DIP type to a small, thin flat package surface-mounted, SOP, TSOP, SOJ, QFP, TQFP, etc. Is coming. That is, a large chip is sealed 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.

【0003】これらの問題を解決するために半田付け時
の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62−11585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62−136860号公
報)等の手法で対応しているが、樹脂強度が低下するた
めに、半田付け工程での熱ストレスに対して、かえって
樹脂クラックを発生するのが常であった。一方、半田付
け時の耐熱ストレス性、つまり半田耐熱性に優れた半導
体封止用エポキシ樹脂組成物を得るために、樹脂系とし
てビフェニル型エポキシ樹脂の使用(特開昭64−65
116号公報)等が検討されてきたがビフェニル型エポ
シキ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、半田耐熱性の向上、特にクラック発生
が低減するが250℃以上の高温では半田耐熱性が不十
分であり、信頼性の優れた半導体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。
In order to solve these problems, addition of thermoplastic oligomers (Japanese Patent Laid-Open No. 62-15849) and addition of various silicone compounds (Japanese Patent Laid-Open No. 62-15849) have been proposed for the purpose of reducing thermal shock during soldering. No. 11585, 62-
116654, 62-128162) and silicone modification (Japanese Patent Application Laid-Open No. 62-136860). However, since the resin strength is reduced, heat stress in the soldering process is reduced. On the other hand, resin cracks usually occurred. 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 heat resistance, a biphenyl-type epoxy resin is used as a resin system (Japanese Patent Laid-Open No. 64-65).
No. 116) has been studied, but by using a biphenyl type epoxy resin, the adhesion to the lead frame and low water absorption are improved, and the solder heat resistance is improved, especially the occurrence of cracks is reduced. However, the solder heat resistance was insufficient, and it was not possible to obtain a highly reliable epoxy resin composition for semiconductor encapsulation.

【0004】[0004]

【発明が解決しようとする課題】本発明は、この様な問
題点に対して、フェノール樹脂硬化剤として式(1)で
示される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。
SUMMARY OF THE INVENTION The present invention solves such a problem by using a phenol resin curing agent represented by the formula (1) as a phenol resin curing agent so that a semiconductor package at the time of mounting on a substrate is manufactured. It is an object of the present invention to provide an epoxy resin composition for semiconductor encapsulation with significantly improved soldering stress resistance.

【0005】[0005]

【課題を解決するための手段】本発明は、(A)エポキ
シ基を2個以上有する芳香族化合物、(B)式(1)で
示されるフェノール樹脂硬化剤を総フェノール樹脂硬化
剤量に対して30〜100重量%含むフェノール樹脂硬
化剤、
The present invention provides (A) an aromatic compound having two or more epoxy groups, and (B) a phenolic resin curing agent represented by the formula (1) based on the total amount of the phenolic resin curing agent. Phenolic resin curing agent containing 30 to 100% by weight,

【0006】[0006]

【化2】 (l、mは1以上の整数、nは0又は1以上の整数で、
l+m+n=1〜20、l+m+nに対するl+mの割
合が30重量%以上、lのl+m+nに対する割合が7
0重量%未満、Rは水素、ハロゲン、アルキル基から選
択される同一又は異なる原子又は基)
Embedded image (L and m are integers of 1 or more, n is 0 or an integer of 1 or more,
l + m + n = 1 to 20, l + m divided by l + m + n
30% by weight or more, and the ratio of l to l + m + n is 7
Less than 0% by weight, R is the same or different atom or group selected from hydrogen, halogen, and alkyl group)

【0007】(C)無機充填材及び(D)硬化促進剤か
らなる半導体封止用エポキシ樹脂組成物であり、従来の
エポキシ樹脂組成物に比べ、優れた信頼性として半田耐
熱性と半田処理後の耐湿性を有するものである。
[0007] An epoxy resin composition for semiconductor encapsulation comprising (C) an inorganic filler and (D) a curing accelerator. Compared with the conventional epoxy resin composition, the epoxy resin composition has excellent reliability such as solder heat resistance and after solder treatment. It has the moisture resistance.

【0008】本発明で用いるエポキシ基を2個以上有す
る芳香族化合物とは、例えば、ビフェニル型エポキシ化
合物、ビスフェノール型エポキシ化合物、フェノールノ
ボラック型エポキシ樹脂、クレゾールノボラック型エポ
キシ樹脂、トリフェノールメタン型エポキシ化合物、ア
ルキル変性トリフェノールメタン型エポキシ化合物等の
ことを言う。特にエポキシ樹脂組成物としての無機充填
材量を80〜90重量%と設定する場合、3,3′,
5,5′−テトラメチルビフェニルジグリシジルエーテ
ルやビスフェノール型エポキシ化合物等の比較的低分子
のものを用いた方が溶融粘度の設定上好ましい。
The aromatic compound having two or more epoxy groups used in the present invention includes, for example, a biphenyl type epoxy compound, a bisphenol type epoxy compound, a phenol novolak type epoxy resin, a cresol novolak type epoxy resin, and a triphenol methane type epoxy compound. And alkyl-modified triphenol methane type epoxy compounds. Particularly, when the amount of the inorganic filler as the epoxy resin composition is set to 80 to 90% by weight, 3, 3 ',
It is more preferable to use a relatively low molecular weight compound such as 5,5'-tetramethylbiphenyldiglycidyl ether and bisphenol type epoxy compound in terms of setting the melt viscosity.

【0009】式(1)の分子構造で示されるフェノール
樹脂硬化剤は、オルソキシレン及び/又はメタキシレ
ン、オルソキシレン及び/又はメタキシレン及びパラキ
レンと、フェノール類とをフリーデル・クラフツ反応に
より重合させることにより得られる樹脂硬化剤で、従来
のフェノールノボラック樹脂と比較し、ゴム領域におけ
る高湿時の弾性率が低く、低吸湿性、リードフレーム及
び半導体素子との接着性に優れている。又、最近半田耐
熱性に優れているとして用いられる式(2)に示される
パラキシリレン変性フェノール樹脂硬化剤に替えて、式
(1)のフェノール樹脂硬化剤を用いることにより、
The phenolic resin curing agent represented by the molecular structure of the formula (1) is obtained by polymerizing ortho-xylene and / or meta-xylene, ortho-xylene and / or meta-xylene and para-alkylene with a phenol by a Friedel-Crafts reaction. It is a resin curing agent obtained by this method, and has a lower elastic modulus at high humidity in a rubber region than a conventional phenol novolak resin, low moisture absorption, and excellent adhesion to a lead frame and a semiconductor element. Further, by using a phenolic resin curing agent of the formula (1) instead of the paraxylylene-modified phenolic resin curing agent represented by the formula (2) which is recently used as having excellent solder heat resistance,

【0010】[0010]

【化3】 Embedded image

【0011】エポキシ樹脂組成物としてはゴム領域にお
ける高温時の強度が高く、半田耐熱性に優れるエポキシ
樹脂組成物を得ることができる。式(1)で示されるフ
ェノール樹脂硬化剤の使用量は、これを調整することに
より、半田耐熱性を最大限に引きだすことができる。半
田耐熱性の効果をだすためには、式(1)で示されるフ
ェノール樹脂硬化剤を総フェノール樹脂硬化剤量の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%未満では、低吸水性、密着性が充分
に得られず、半田耐熱性が不十分である。又、式(1)
の構造式中のl、mは1以上の整数、nは0又は1以上
の整数で、l+m+n=1〜20を満たすものである。
l+m+nに対するl+mの割合は、半田耐熱性の効果
をだすために30重量%以上の変性割合が好ましい。
又、l部の特徴は、m部と比較し、高温時の弾性率が低
く半田耐熱性に優れているが、欠点として硬化性がやや
劣り、成形性が低下する傾向がある。従って、lのl+
m+nに対する割合は、70重量%未満が好ましい。
又、l+m+nが20を超えると流動性が低下し、成形
性が悪くなる。更に式(1)の構造式中のRは、撥水性
の点からは大きな置換基が好ましいが、フェノール性水
酸基の反応性を阻害するため、水素原子が最適である。
式(1)で示されるフェノール樹脂硬化剤以外に他のフ
ェノール樹脂硬化剤を併用する場合、フェノール性水酸
基を有するモノマー、オリゴマー、ポリマー全般を言
う。例えば、フェノールノボラック樹脂、クレゾールノ
ボラック樹脂等が挙げられる。
As the epoxy resin composition, an epoxy resin composition having high strength in a rubber region at a high temperature and excellent in solder heat resistance can be obtained. By adjusting the amount of the phenol resin curing agent represented by the formula (1), the solder heat resistance can be maximized by adjusting the amount. In order to obtain the effect of solder heat resistance, the phenol resin curing agent represented by the formula (1) should be used in an amount of 30 times the total phenol resin curing agent amount.
It is desirable to use at least 50% by weight, preferably at least 50% by weight. If the amount is less than 30% by weight, low water absorption and adhesion cannot be sufficiently obtained, and solder heat resistance is insufficient. Equation (1)
In the structural formulas, l and m are integers of 1 or more, n is 0 or an integer of 1 or more, and satisfy l + m + n = 1 to 20.
The ratio of l + m to l + m + n is preferably a modification ratio of 30% by weight or more in order to obtain the effect of solder heat resistance.
The characteristic of the l part is that the elastic modulus at high temperature is low and the soldering heat resistance is excellent as compared with the m part, but as a disadvantage, the curability is slightly inferior and the moldability tends to be reduced. Therefore, l + l +
The ratio to m + n is preferably less than 70% by weight.
On the other hand, when l + m + n exceeds 20, the fluidity is reduced and the moldability is deteriorated. Further, R in the structural formula of the formula (1) is preferably a large substituent from the viewpoint of water repellency, but is preferably a hydrogen atom because it inhibits the reactivity of the phenolic hydroxyl group.
When a phenol resin curing agent other than the phenol resin curing agent represented by the formula (1) is used in combination, it refers to all monomers, oligomers and polymers having a phenolic hydroxyl group. For example, a phenol novolak resin, a cresol novolak resin and the like can be mentioned.

【0012】本発明で用いる無機充填材としては、溶融
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次凝集シリカ粉末又は多孔質シリカ
粉末を粉砕したシリカ粉末、アルミナ等が挙げられ、熱
膨張率、耐水性、不純物等の点から溶融シリカ粉末が好
ましい。又、無機充填材の配合量は、半田耐熱性、流動
性の点から、全樹脂組成物中の70〜95重量%が好ま
しい。70重量%未満だと吸水性が増大し、半田耐熱性
が悪くなる。また95重量%を超えると流動性が低下し
成形性が悪くなる。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1,8−ジアザビシク
ロウンデセン、トリフェニルホスフィン、ベンジルジメ
チルアミンや2−メチルイミダゾール等が挙げられ、こ
れらは単独もしくは混合して用いてもよい。
The inorganic filler used in the present invention includes fused silica powder, crystalline silica powder, secondary aggregated silica powder, porous silica powder, silica powder obtained by pulverizing secondary aggregated silica powder or porous silica powder, alumina and the like. And fused silica powder is preferred from the viewpoints of thermal expansion coefficient, water resistance, impurities and the like. The amount of the inorganic filler is preferably from 70 to 95% by weight based on the total resin composition in view of solder heat resistance and fluidity. If it is less than 70% by weight, the water absorption increases and the solder heat resistance deteriorates. On the other hand, if it exceeds 95% by weight, the fluidity decreases and the moldability deteriorates. The curing accelerator used in the present invention may be any one that promotes the reaction between an epoxy group and a phenolic hydroxyl group, and those generally used as a sealing material can be widely used. -Diazabicycloundecene, triphenylphosphine, benzyldimethylamine, 2-methylimidazole and the like, and these may be used alone or as a mixture.

【0013】本発明の封止用エポキシ樹脂組成物はエポ
キシ樹脂、フェノール樹脂硬化剤、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。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、フェノール樹脂
硬化剤、無機充填材、硬化促進剤、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、更に熱ロー
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
るは電気部品の封止、被覆、絶縁等に適用することがで
きる。
The epoxy resin composition for encapsulation of the present invention comprises an epoxy resin, a phenolic resin curing agent, an inorganic filler and a curing accelerator as essential components. Various additions such as flame retardants such as epoxy resin, antimony trioxide and hexabromobenzene, coloring agents such as carbon black and red iron oxide, release agents such as natural wax and synthetic wax, and low stress additives such as silicone oil and rubber There is no problem if an agent is appropriately compounded. In addition, in order to manufacture the epoxy resin composition for sealing of the present invention as a molding material, epoxy resin, phenol resin curing agent, inorganic filler, curing accelerator, and other additives are sufficiently and uniformly mixed by a mixer or the like. Thereafter, the mixture is further melt-kneaded with a hot roll or a kneader, cooled, and pulverized to obtain a molding material. These molding materials can be applied to sealing, coating, insulating and the like of electronic parts or electric parts.

【0014】以下本発明を実施例で具体的に説明する。 実施例1 式(3)で示される芳香族化合物(3,3′,5,5′
−テトラメチルビフェニルジグリシジルエーテル)(融
点102℃、エポキシ当量192g/eq)8.0重量
Hereinafter, the present invention will be described specifically with reference to Examples. Example 1 An aromatic compound represented by the formula (3) (3,3 ', 5,5'
-Tetramethylbiphenyldiglycidyl ether) (melting point: 102 ° C, epoxy equivalent: 192 g / eq) 8.0 parts by weight

【0015】[0015]

【化4】 Embedded image

【0016】式(4)で示されるフェノール樹脂硬化剤
(軟化点70℃、水酸基当量170)
2.2重
量部
A phenol resin curing agent represented by the formula (4) (softening point 70 ° C., hydroxyl equivalent 170)
2.2 parts by weight

【0017】[0017]

【化5】 (l=1、m=1、n=3の混合物)Embedded image (Mixture of l = 1, m = 1, n = 3)

【0018】 式(2)で示されるフェノール樹脂硬化剤(軟化点65℃、水酸基当量170 )(n=0が1に対し、n=1が0.6、n=2が0.3の重量割合の混合物) 4.8重量部 溶融シリカ粉末(平均粒径14μm) 84.0重量部 トリフェニルホスフィン 0.2重量部 カルナバワックス 0.5重量部 カーボンブラック 0.3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、冷却後粉砕し成形材料とし、これをタ
ブレット化して半導体封止用エポキシ樹脂組成物を得
た。この組成物を低圧トランスファー形成機(成形条
件:175℃、70kg/cm2、120秒)を用い
て、チップサイズ6×6mmの52pQFPを成形し、
得られた成形品を175℃、8時間で後硬化し評価し
た。評価結果を表1に示す。 半田クラック性試験:成形品(チップサイズ6×6m
m、52pQFP)を85℃、85%RHの環境下で2
4時間、48時間、72時間及び120時間処理し、そ
の後260℃の半田槽に10秒浸漬後、顕微鏡で外部ク
ラックを観察した。 半田耐湿性試験:成形品(チップサイズ6×6mm、5
2pQFP)を85℃、85%RHの環境下で72時間
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。
A phenol resin curing agent represented by the formula (2) (softening point: 65 ° C., hydroxyl equivalent: 170) (weight of n = 1 is 0.6, n = 1 is 0.6, and n = 2 is 0.3) 4.8 parts by weight Fused silica powder (average particle size: 14 μm) 84.0 parts by weight Triphenylphosphine 0.2 part by weight Carnauba wax 0.5 part by weight Carbon black 0.3 part by weight at room temperature with a mixer The mixture was mixed, kneaded with a biaxial roll at 70 to 100 ° C., cooled and pulverized to obtain a molding material, which was tabletted to obtain an epoxy resin composition for semiconductor encapsulation. Using a low-pressure transfer forming machine (forming conditions: 175 ° C., 70 kg / cm 2 , 120 seconds), this composition was molded into 52pQFP having a chip size of 6 × 6 mm,
The obtained molded article was post-cured at 175 ° C. for 8 hours and evaluated. Table 1 shows the evaluation results. Solder cracking test: Molded product (chip size 6 × 6m
m, 52pQFP) under an environment of 85 ° C. and 85% RH.
The treatment was carried out for 4, 48, 72 and 120 hours, then immersed in a solder bath at 260 ° C. for 10 seconds, and external cracks were observed with a microscope. Solder moisture resistance test: Molded product (chip size 6 × 6 mm, 5
2pQFP) is treated in an environment of 85 ° C. and 85% RH for 72 hours, then immersed in a solder bath at 260 ° C. for 10 seconds, and then subjected to a pressure cooker test (125 ° C., 100% RH) to measure the open defect of the circuit. did.

【0019】実施例2〜、比較例1〜3 表1の配合に従い、実施例1と同様に樹脂組成物を得、
実施例1と同様にして評価した
Examples 2 to 5 and Comparative Examples 1 to 3 According to the formulations shown in Table 1, a resin composition was obtained in the same manner as in Example 1.
Evaluation was performed in the same manner as in Example 1 .

【0020】式(5)のフェノール樹脂硬化剤(軟化点
65℃、水酸基当量170)
Phenolic resin curing agent of formula (5) (softening point 65 ° C., hydroxyl equivalent 170)

【化6】 (l=1、m=1の混合物)Embedded image (Mixture of l = 1, m = 1)

【0021】[0021]

【表1】 [Table 1]

【0022】[0022]

【発明の効果】本発明に従うと、半田付け工程における
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、表面実装用パッケージにおいて信頼
性が向上するため工業的価値は絶大である。
According to the present invention, the resistance to cracks when subjected to thermal stress due to a rapid temperature change in the soldering process is very excellent, and the reliability of the surface mounting package is improved, so that the industrial value is enormous. It is.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C08G 59/24 C08G 59/62 C08L 63/02 H01L 23/29 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int. Cl. 7 , DB name) C08G 59/24 C08G 59/62 C08L 63/02 H01L 23/29

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 (A)エポキシ基を2個以上有する芳香
族化合物、(B)式(1)で示されるフェノール樹脂硬
化剤を総フェノール樹脂硬化剤量に対して30〜100
重量%含むフェノール樹脂硬化剤、 【化1】 (l、mは1以上の整数、nは0又は1以上の整数で、
l+m+n=1〜20、l+m+nに対するl+mの割
合が30重量%以上、lのl+m+nに対する割合が7
0重量%未満、Rは水素、ハロゲン、アルキル基から選
択される同一又は異なる原子又は基) (C)無機充填材及び(D)硬化促進剤からなることを
特徴とする半導体封止用エポキシ樹脂組成物。
(A) an aromatic compound having two or more epoxy groups, and (B) a phenolic resin curing agent represented by the formula (1) in an amount of 30 to 100 with respect to the total amount of the phenolic resin curing agent.
Phenol resin curing agent containing 1% by weight (L and m are integers of 1 or more, n is 0 or an integer of 1 or more,
l + m + n = 1 to 20, l + m divided by l + m + n
30% by weight or more, and the ratio of l to l + m + n is 7
Less than 0% by weight, R is the same or different atom or group selected from hydrogen, halogen and alkyl group) (C) an epoxy resin for semiconductor encapsulation comprising an inorganic filler and (D) a curing accelerator Composition.
【請求項2】 芳香族化合物が、3,3′,5,5′−
テトラメチルビフェニルジグリシジルエーテルである請
求項1記載の半導体封止用エポキシ樹脂組成物。
2. The method according to claim 1, wherein the aromatic compound is 3,3 ′, 5,5′-
The epoxy resin composition for semiconductor encapsulation according to claim 1, which is tetramethylbiphenyldiglycidyl ether.
【請求項3】 式(1)中のRが水素である請求項1、
又は請求項2記載の半導体封止用エポキシ樹脂組成物。
3. The method according to claim 1, wherein R in the formula (1) is hydrogen.
Or the epoxy resin composition for semiconductor encapsulation according to claim 2.
JP32004894A 1994-12-22 1994-12-22 Resin composition Expired - Fee Related JP3359445B2 (en)

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JPH08176278A JPH08176278A (en) 1996-07-09
JP3359445B2 true JP3359445B2 (en) 2002-12-24

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JP (1) JP3359445B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG114473A1 (en) * 2000-09-26 2005-09-28 Sumitomo Bakelite Co Epoxy resin composition and semiconductor devices
CN112226041A (en) * 2020-10-12 2021-01-15 江苏华海诚科新材料股份有限公司 High-thermal-conductivity epoxy resin composition and preparation method thereof

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