JPH07173255A - Epoxy resin composition - Google Patents

Epoxy resin composition

Info

Publication number
JPH07173255A
JPH07173255A JP31870593A JP31870593A JPH07173255A JP H07173255 A JPH07173255 A JP H07173255A JP 31870593 A JP31870593 A JP 31870593A JP 31870593 A JP31870593 A JP 31870593A JP H07173255 A JPH07173255 A JP H07173255A
Authority
JP
Japan
Prior art keywords
epoxy resin
curing agent
formula
resin
resin composition
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.)
Pending
Application number
JP31870593A
Other languages
Japanese (ja)
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 JP31870593A priority Critical patent/JPH07173255A/en
Publication of JPH07173255A publication Critical patent/JPH07173255A/en
Pending 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)

Abstract

PURPOSE:To obtain an epoxy resin composition excellent in soldering crack resistance and humidity resistance after soldering by mixing a specified epoxy resin with a specified curing agent, an inorganic filler and a cure accelerator. CONSTITUTION:This resin composition is used for semiconductor sealing and essentially consists of an epoxy resin (A) containing 30-100wt.%, based on the total weight of the epoxy resin, epoxy resin represented by formula I (wherein R is H, halogen or alkyl; and n is 0-20), a phenolic resin curing agent (B) containing 30-100wt.%, based on the total weight of the phenolic resin curing agent, phenolic resin curing agent of formula II (wherein R and n are each as defined above), an inorganic filler (C), and a cure accelerator (D). By using a combination of resin A with curing agent B, this composition can give a cured product markedly excellent in cracking resistance under thermal stress resulting from a rapid temperature change in the soldering step and having good humidity resistance, and therefore being desirable for sealing, coating insulation or the like of electronic or electrical components.

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、耐湿性に優れたオルソクレゾー
ルノボラック型エポキシ樹脂をフェノールノボラック樹
脂で硬化させ、充填材として溶融シリカ、結晶シリカ等
の無機充填材を配合した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QFP、SO
P、SOJ、TSOP、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、熱応力によりクラックが発生し、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。従って、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半
導体封止用樹脂組成物の開発が望まれている。
2. Description of the Related Art Conventionally, electronic parts such as diodes, transistors, and integrated circuits have been sealed with thermosetting resin. Particularly in integrated circuits, orthocresol novolac type epoxy resin excellent in heat resistance and moisture resistance is used as a phenol resin. An epoxy resin composition is used which is hardened with a novolac resin and mixed with an inorganic filler such as fused silica or crystalline silica as a filler. However, in recent years, as the integration of integrated circuits has increased, the size of the chips has gradually increased, and the package is the conventional DIP.
Small and thin type QFP and SO
It has changed to P, SOJ, TSOP, TQFP, PLCC. That is, a large chip is enclosed in a small and thin package, and cracks are generated due to thermal stress, and problems such as deterioration of moisture resistance due to these cracks are greatly highlighted. In particular, in the soldering process, when exposed to a high temperature of 200 ° C. or more, the moisture resistance is deteriorated due to cracking of the package and peeling of the resin and the chip. Therefore, development of a highly reliable resin composition for semiconductor encapsulation suitable for encapsulating these large chips is desired.

【0003】[0003]

【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、フェノール樹脂硬化剤として式
(2)で示されるフェノール樹脂硬化剤を用いることに
より、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 addresses the above problems by using an epoxy resin represented by the formula (1) as an epoxy resin and a phenol resin represented by the formula (2) as a phenol resin curing agent. Another object of the present invention is to provide an epoxy resin composition for semiconductor encapsulation, in which the solder stress resistance of a semiconductor package during mounting is remarkably improved by using a curing agent.

【0004】[0004]

【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、
The present invention provides (A) an epoxy resin containing 30 to 100% by weight of an epoxy resin represented by the following formula (1) with respect to the total amount of epoxy resin:

【0005】[0005]

【化3】 (式中のRは水素、ハロゲン類、アルキル基の中から選
択される同一もしくは異なる原子または基、n=0〜2
0)
[Chemical 3] (R in the formula is the same or different atom or group selected from hydrogen, halogens and alkyl groups, n = 0 to 2
0)

【0006】(B)下記式(2)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、
(B) The phenol resin curing agent represented by the following formula (2) is added in an amount of 30 to 30 with respect to the total amount of the phenol resin curing agent.
Phenolic resin curing agent containing 100% by weight,

【0007】[0007]

【化4】 (式中のRは水素、ハロゲン類、アルキル基の中から選
択される同一もしくは異なる原子または基、n=0〜2
0)
[Chemical 4] (R in the formula is the same or different atom or group selected from hydrogen, halogens and alkyl groups, n = 0 to 2
0)

【0008】(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、従
来のエポキシ樹脂組成物に比べ優れた信頼性として耐半
田クラック性と半田処理後の耐湿性を有するものであ
る。
An epoxy resin composition for semiconductor encapsulation containing (C) an inorganic filler and (D) a curing accelerator as essential components, and solder crack resistance and solder treatment which are superior in reliability as compared with conventional epoxy resin compositions. The latter has moisture resistance.

【0009】式(1)の分子構造で示されるエポキシ樹
脂は、パラキシレンとフェノールをフリーデル・クラフ
ツ・アルキル反応により重合し、エピクロルヒドリンで
グリシジルエーテル化することによって得られる。従来
のクレゾールノボラックエポキシ樹脂に比べ、硬化物の
ゴム領域での弾性率が低く、低吸湿性、リードフレーム
(42アロイ、銅合金)等の金属類との接着性に優れ
る。このエポキシ樹脂の使用量はこれを調節することに
より、耐半田クラック性を最大限に引き出すことができ
る。耐半田クラック性の効果を引き出すためには式
(1)で示されるエポキシ樹脂を総エポキシ樹脂量に対
して30重量%以上、好ましくは50重量%以上の使用
が望ましい。30重量%未満だと目標とした耐半田クラ
ック性が不充分である。更に式中のRは水素原子が好ま
しい。式中のnは0〜20であるが、20を越えると流
動性が悪化する。式(1)で示されるエポキシ樹脂以外
の他のエポキシ樹脂を併用する場合、エポキシ基を2個
以上有する化合物あるいはポリマー全般を言う。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。
The epoxy resin represented by the molecular structure of the formula (1) is obtained by polymerizing paraxylene and phenol by Friedel-Crafts-alkyl reaction and glycidyl etherification with epichlorohydrin. Compared with the conventional cresol novolac epoxy resin, the elastic modulus of the cured product in the rubber region is low, the moisture absorption is low, and the adhesiveness to metals such as lead frame (42 alloy, copper alloy) is excellent. By adjusting the amount of the epoxy resin used, solder crack resistance can be maximized. In order to bring out the effect of solder crack resistance, it is desirable to use the 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, the target solder crack resistance is insufficient. Further, R in the formula is preferably a hydrogen atom. In the formula, n is 0 to 20, but if it exceeds 20, fluidity deteriorates. When an epoxy resin other than the epoxy resin represented by the formula (1) is used in combination, it means a compound or polymer having two or more epoxy groups in general. For example, biphenyl type epoxy compound, bisphenol type epoxy compound, phenol novolac type epoxy resin,
It refers to cresol novolac type epoxy resin, triphenol methane type epoxy compound, alkyl modified triphenol methane type epoxy compound and the like.

【0010】式(2)で示されるフェノール樹脂硬化剤
は、パラキシレンとフェノールをエポキシ樹脂と同様に
フリーデル、クラフツ、アルキル化反応により重合させ
ることによって得られる。従来のフェノールノボラック
樹脂に比べ、硬化物のゴム領域での弾性率が低く、低吸
湿性、リードフレーム(42アロイ、銅合金)等の金属
類との接着性に優れている。このフェノール樹脂硬化剤
の使用量はこれを調節することにより耐半田クラック性
を最大限に引き出すことができる。耐半田クラック性の
効果を引き出すためには式(2)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重
量%以上、好ましくは50重量%以上の使用が望まし
い。30重量%未満だと目標とした耐半田クラック性が
不充分である。更に式中のRは水素原子が好ましい。式
中のnは0〜20であるが、20を越えると流動性が悪
化する。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、ジシ
クロペンタジエン変性フェノール樹脂、テルペン変性フ
ェノール樹脂、トリフェノールメタン化合物等が挙げら
れ、特にフェノ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、テルペン変性フェノール樹脂
及びこれらの混合物が好ましい。また、これらの硬化剤
の配合量としてはエポキシ化合物のエポキシ基数と硬化
剤の水酸基数を合わせるように配合することが好まし
い。
The phenol resin curing agent represented by the formula (2) can be obtained by polymerizing paraxylene and phenol by Friedel, crafts and alkylation reaction in the same manner as the epoxy resin. Compared with the conventional phenol novolac resin, the elastic modulus of the cured product in the rubber region is low, the moisture absorption is low, and the adhesion to metals such as lead frame (42 alloy, copper alloy) is excellent. By adjusting the amount of the phenol resin curing agent used, solder crack resistance can be maximized. In order to bring out the effect of solder crack resistance, it is desirable to use the phenol resin curing agent represented by the formula (2) in an amount of 30% by weight or more, preferably 50% by weight or more based on the total amount of the phenol resin curing agent. If it is less than 30% by weight, the target solder crack resistance is insufficient. Further, R in the formula is preferably a hydrogen atom. In the formula, n is 0 to 20, but if it exceeds 20, fluidity deteriorates. When other phenol resin curing agent is used in combination with the phenol resin curing agent represented by the formula (1), it means all polymers having a phenolic hydroxyl group. For example, phenol novolac resin, cresol novolac resin, dicyclopentadiene modified phenol resin, terpene modified phenol resin, triphenol methane compound and the like can be mentioned, in particular phenol novolac resin, dicyclopentadiene modified phenol resin, terpene modified phenol resin and mixtures thereof. Is preferred. Moreover, it is preferable to mix these curing agents so that the number of epoxy groups of the epoxy compound and the number of hydroxyl groups of the curing agent are matched.

【0011】以上述べた様に、従来、式(2)で示され
るパラキシリレン構造を有する樹脂は、フェノール樹脂
硬化剤としてのみしか用いられなかったのに対して、こ
れをグリシジルエーテル化し、エポキシ樹脂として用い
ることにより、フェノール樹脂硬化剤だけでなくエポキ
シ樹脂中にもパラキシリレン構造を導入することにより
全ての樹脂中にパラキシリレン構造を導入するところで
ある。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、アルミナ等が挙げられ、特
に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、耐半田クラック性から総エポキシ樹脂組成物量に対
して80〜90重量%が好ましい。無機充填材量が80
重量%未満だと低熱膨張化、低吸水化が得られず耐半田
クラック性が不充分である。また、無機充填材量が90
重量%を越えると高粘度化による半導体パッケージ中の
ダイパッド、金線ワイヤーのずれ等の不都合が生じる。
As described above, conventionally, the resin having the paraxylylene structure represented by the formula (2) has been used only as a curing agent for a phenol resin, but it has been converted into a glycidyl ether to obtain an epoxy resin. By using the paraxylylene structure not only in the phenol resin curing agent but also in the epoxy resin, the paraxylylene structure is introduced into all the resins. Examples of the inorganic filler used in the present invention include fused silica powder, spherical silica powder, crystalline silica powder, secondary agglomerated silica powder, porous silica powder, alumina, and the like. In particular, spherical silica powder and fused silica powder and spherical silica are used. Mixtures with powders are preferred. The amount of the inorganic filler compounded is preferably 80 to 90% by weight based on the total amount of the epoxy resin composition in view of resistance to solder cracking. The amount of inorganic filler is 80
If it is less than wt%, low thermal expansion and low water absorption cannot be obtained and solder crack resistance is insufficient. In addition, the amount of inorganic filler is 90
If it exceeds 5% by weight, problems such as displacement of the die pad and the gold wire in the semiconductor package due to high viscosity may occur.

【0012】本発明に用いる硬化促進剤は、エポキシ基
と水酸基との硬化反応を促進させるものであればよく、
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、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あり、単独でも混合して用
いても差し支えない。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。また、
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
材、その他の添加剤をミキサー等によって充分に均一に
混合した後、更に熱ロールまたはニーダー等で溶融混練
し、冷却後粉砕して封止材料とすることができる。これ
らの成形材料は電気部品あるいは電子部品であるトラン
ジスタ、集積回路等の被覆、絶縁、封止等に適用するこ
とができる。
The curing accelerator used in the present invention may be any one as long as it accelerates the curing reaction between the epoxy group and the hydroxyl group.
What is generally used as a sealing material can be widely used. For example, there are 1,8-diazabicycloundecene, triphenylphosphine, benzyldimethylamine, 2-methylimidazole and the like, which may be used alone or in combination. The 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 in addition to this, a silane coupling agent, a brominated epoxy resin, antimony trioxide, hexa Flame retardants such as brombenzene, 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 may be appropriately blended. There is no. Also,
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 uniformly mixed with a mixer or the like, and then further heated. A sealing material can be obtained by melt-kneading with a roll or a kneader, cooling and pulverizing. These molding materials can be applied to coating, insulation, sealing, etc. of transistors, integrated circuits, etc., which are electric or electronic parts.

【0013】以下本発明を実施例で具体的に説明する。 実施例1 下記組成物 式(3)で示されるエポキシ樹脂(軟化点50℃、エポキシ当量250g/e q) 6.76重量部The present invention will be specifically described below with reference to examples. Example 1 The following composition Epoxy resin represented by the formula (3) (softening point 50 ° C., epoxy equivalent 250 g / eq) 6.76 parts by weight

【0014】[0014]

【化5】 (nの値は0から3を示す混合物であり、その重合割合
はn=0が1に対してn=1が0.70、n=2が0.
45、n=3が0.30である。)
[Chemical 5] (The value of n is a mixture showing 0 to 3, and the polymerization ratio of n = 0 is 1, n = 1 is 0.70, and n = 2 is 0.
45 and n = 3 is 0.30. )

【0015】 オルソクレゾールノボラックエポキシ樹脂(軟化点58℃、エポキシ当量20 0g/eq) 1.69重量部 式(4)で示されるフェノール樹脂硬化剤(軟化点63℃、水酸基当量170 g/eq) 4.28重量部Orthocresol novolac epoxy resin (softening point 58 ° C., epoxy equivalent 200 g / eq) 1.69 parts by weight Phenolic resin curing agent represented by the formula (4) (softening point 63 ° C., hydroxyl equivalent 170 g / eq) 4.28 parts by weight

【0016】[0016]

【化6】 (nの値は0から3を示す混合物であり、その重量割合
はn=0が1に対してn=1が0.60、n=2が0.
42、n=3が0.22である。)
[Chemical 6] (The value of n is a mixture showing 0 to 3, and the weight ratio thereof is 1 for n = 0 and 0.60 for n = 1 and 0.
42 and n = 3 is 0.22. )

【0017】 フェノールノボラック樹脂硬化剤(軟化点65℃、水酸基当量105g/eq ) 1.07重量部 溶融シリカ粉末(平均粒径10μm、比表面積2.0m2/g) 35重量部 球状シリカ粉末(平均粒径30μm、比表面積2.5m2/g) 50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、冷却後粉砕して成形材料とした。粉砕
して得られた成形材料は、EMMI−I−66に準じて
175℃、70kg/cm2、120秒の条件でスパイ
ラルフローを測定した。更に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℃、7
0kg/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52pQFPに封止し、ま
た半田耐湿性試験用として3×6mmのチップを16p
SOP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。
Phenolic novolac resin curing agent (softening point 65 ° C., hydroxyl equivalent 105 g / eq) 1.07 parts by weight fused silica powder (average particle size 10 μm, specific surface area 2.0 m 2 / g) 35 parts by weight spherical silica powder ( Average particle diameter 30 μm, specific surface area 2.5 m 2 / g) 50 parts by weight triphenylphosphine 0.2 parts by weight carbon black 0.5 parts by weight Carnauba wax 0.5 parts by weight are mixed at room temperature with a mixer to give 70 to 100 parts. The mixture was kneaded with a biaxial roll at ℃, cooled and pulverized to obtain a molding material. The molding material obtained by pulverization was measured for spiral flow according to EMMI-I-66 under the conditions of 175 ° C., 70 kg / cm 2 , and 120 seconds. Further, the obtained molding material is tabletized and is treated with a low-pressure transfer molding machine at 175 ° C.
A 6 x 6 mm chip is sealed in 52p QFP for a solder crack test under the conditions of 0 kg / cm 2 and 120 seconds, and a 3 x 6 mm chip is 16p for a solder moisture resistance test.
Sealed to SOP. The following solder crack test and solder moisture resistance test were performed on the sealed test element.

【0018】半田クラック試験:封止したテスト用素子
を85℃、85%RHの環境下で24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℃、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(1
25℃、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。
Solder crack test: The sealed test element was placed in an environment of 85 ° C. and 85% RH for 24 hours, 48 hours,
It was treated for 72 hours and 120 hours and then 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, 85
% RH for 72 hours, then immersed in a solder bath at 260 ° C for 10 seconds, and then pressure cooker test (1
25 degreeC, 100% RH was performed, and the open defect of the circuit was measured. The test results are shown in Table 1.

【0019】実施例2〜6 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。 比較例1〜4 表2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2に示
す。
Examples 2 to 6 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. Comparative Examples 1 to 4 Compounding was performed according to the formulation shown in Table 2, 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 2.

【0020】[0020]

【表1】 [Table 1]

【0021】[0021]

【表2】 [Table 2]

【0022】[0022]

【発明の効果】本発明に従うと、従来技術で得ることの
できなかった半田付け時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、更に耐湿性が良好のことから、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において、信頼
性が非常に必要とされる製品に好適である。
According to the present invention, it is possible to obtain excellent crack resistance when subjected to thermal stress due to a rapid temperature change in the soldering process, which cannot be obtained by the prior art, and further excellent moisture resistance. Therefore, when it is used for encapsulation, coating, insulation, etc. of electronic and electrical parts, it is suitable for products that require extremely high reliability, especially in highly integrated large-sized chips mounted in surface mount packages. is there.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01L 23/29 23/31 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location 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、 【化1】 (式中のRは水素、ハロゲン類、アルキル基の中から選
択される同一もしくは異なる原子または基、n=0〜2
0) (B)下記式(2)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2】 (式中のRは水素、ハロゲン類、アルキル基の中から選
択される同一もしくは異なる原子または基、n=0〜2
0) (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。
1. An epoxy resin containing (A) an epoxy resin represented by the following formula (1) in an amount of 30 to 100% by weight based on the total amount of epoxy resin: (R in the formula is the same or different atom or group selected from hydrogen, halogens and alkyl groups, n = 0 to 2
0) (B) The phenol resin curing agent represented by the following formula (2) is contained in an amount of 30 to 100% by weight based on the total amount of the phenol resin curing agent.
Phenolic resin curing agent containing, (R in the formula is the same or different atom or group selected from hydrogen, halogens and alkyl groups, n = 0 to 2
0) An epoxy resin composition for semiconductor encapsulation, which comprises (C) an inorganic filler and (D) a curing accelerator as essential components.
JP31870593A 1993-12-17 1993-12-17 Epoxy resin composition Pending JPH07173255A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31870593A JPH07173255A (en) 1993-12-17 1993-12-17 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31870593A JPH07173255A (en) 1993-12-17 1993-12-17 Epoxy resin composition

Publications (1)

Publication Number Publication Date
JPH07173255A true JPH07173255A (en) 1995-07-11

Family

ID=18102077

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31870593A Pending JPH07173255A (en) 1993-12-17 1993-12-17 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JPH07173255A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7431990B2 (en) * 2004-05-27 2008-10-07 Sumitomo Bakelite Co Resin composition for encapsulating semiconductor chip and semiconductor device therewith
JP4639460B2 (en) * 2000-11-08 2011-02-23 住友ベークライト株式会社 Epoxy resin composition and semiconductor device
CN112980138A (en) * 2019-12-17 2021-06-18 衡所华威电子有限公司 Epoxy resin composition for packaging electronic components and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4639460B2 (en) * 2000-11-08 2011-02-23 住友ベークライト株式会社 Epoxy resin composition and semiconductor device
US7431990B2 (en) * 2004-05-27 2008-10-07 Sumitomo Bakelite Co Resin composition for encapsulating semiconductor chip and semiconductor device therewith
CN112980138A (en) * 2019-12-17 2021-06-18 衡所华威电子有限公司 Epoxy resin composition for packaging electronic components and preparation method thereof

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