JP3093051B2 - Epoxy resin composition - Google Patents

Epoxy resin composition

Info

Publication number
JP3093051B2
JP3093051B2 JP25600692A JP25600692A JP3093051B2 JP 3093051 B2 JP3093051 B2 JP 3093051B2 JP 25600692 A JP25600692 A JP 25600692A JP 25600692 A JP25600692 A JP 25600692A JP 3093051 B2 JP3093051 B2 JP 3093051B2
Authority
JP
Japan
Prior art keywords
epoxy resin
weight
solder
test
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
JP25600692A
Other languages
Japanese (ja)
Other versions
JPH06112368A (en
Inventor
浩史 藤田
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 JP25600692A priority Critical patent/JP3093051B2/en
Priority to EP93107683A priority patent/EP0589143B1/en
Priority to DE69307442T priority patent/DE69307442T2/en
Priority to SG9502396A priority patent/SG87725A1/en
Priority to MYPI93000905A priority patent/MY109105A/en
Priority to KR1019930009377A priority patent/KR100215537B1/en
Publication of JPH06112368A publication Critical patent/JPH06112368A/en
Priority to US08/287,592 priority patent/US5578660A/en
Application granted granted Critical
Publication of JP3093051B2 publication Critical patent/JP3093051B2/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

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、薄型のフラットパッケージ、SOP,
SOJ,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
に半田づ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。
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, an O-cresol novolak epoxy resin having excellent heat resistance and moisture resistance is made of novolak. An epoxy resin cured with a mold phenol resin is used. However, in recent years, chips have become larger and larger with the increase in the degree of integration of integrated circuits, and packages have become smaller and thinner flat packages that are surface-mounted from conventional DIP types.
It is changing to SOJ and PLCC. 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 is a problem that the package is cracked due to rapid exposure to a high temperature of 200 ° C. or more in the soldering process, and the moisture resistance is deteriorated due to the separation of the resin and the chip. 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)が検討されてきた。
In order to solve these problems, use of an epoxy resin represented by the following formula (1) as an epoxy resin (Japanese Patent Laid-Open No. 64-65116) has been studied.

【0004】[0004]

【化3】 Embedded image

【0005】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により、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。
[0005] The use of the epoxy resin represented by the formula (1) lowers the viscosity of the resin system. Therefore, by blending a larger amount of fused silica powder, the composition has low thermal expansion and low water absorption after molding. In addition, improvement in solder stress resistance was achieved. However, an increase in the modulus of elasticity due to the incorporation of a large amount of the fused silica powder is another adverse effect, and it is necessary to further improve the solder stress resistance.

【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
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、成形品の弾性率、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
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 to reduce the elastic modulus, water absorption and thermal expansion coefficient of a molded product. Another object of the present invention is to provide an epoxy resin composition for semiconductor encapsulation in which the use of a curing agent represented by the formula (2) as a curing agent has significantly improved the solder stress resistance of a semiconductor package during mounting on a substrate.

【0004】[0004]

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

【0005】[0005]

【化4】 Embedded image

【0006】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
るナフトール樹脂硬化剤
[0006] 30 to 100 with respect to the total epoxy resin amount
(B) a naphthol resin curing agent represented by the following formula (2):

【0007】[0007]

【化5】 Embedded image

【0008】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。
[0008] 30 to 100% by weight based on the total amount of the curing agent
It is an epoxy resin composition for semiconductor encapsulation which contains a hardener containing (C) an inorganic filler and (D) a hardening accelerator as essential components.

【0009】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
が出来、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。
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 lower melt viscosity than conventional polyfunctional epoxy resins during transfer molding. Excellent fluidity. Therefore, a large amount of the fused silica powder of the composition can be blended, an epoxy resin composition having low thermal expansion and low water absorption, and having excellent solder stress resistance can be obtained.

【0010】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60
重量%以上の使用が望ましい。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
水素原子が好ましい。
By adjusting the amount of the biphenyl type epoxy resin used, the solder stress resistance can be maximized. In order to obtain the effect of resistance to soldering stress, the biphenyl type epoxy resin represented by the formula (1) is used in an amount of 30% by weight or more, preferably 60% by weight of the total epoxy resin amount.
It is desirable to use not less than weight%. If it is less than 30% by weight, low thermal expansion and low water absorption cannot be obtained, and the solder stress resistance is insufficient. Further, in the formula, R 1 to R 4 are preferably a methyl group, and R 5 to R 8 are preferably a hydrogen atom.

【0011】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
ポキシ樹脂として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、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 addition to the biphenyl type epoxy resin represented by the formula (1), the epoxy resin used generally refers to any polymer having an epoxy group. For example, trifunctional epoxy resins such as bisphenol type epoxy resin, cresol novolak type epoxy resin, phenol novolak type epoxy resin, triphenolmethane type epoxy resin, alkyl-modified triphenolmethane type epoxy resin, and epoxy resin containing triazine nucleus. Say.

【0012】式(2)の分子構造で示される硬化剤を用
いることにより、従来のフェノールノボラック樹脂硬化
剤等に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、低熱膨張化及び低吸水化を得ることが出来る。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
なう半導体チップ等との剥離不良の防止に有効である。
By using the curing agent represented by the molecular structure of the formula (2), compared with the conventional phenol novolak resin curing agent, the elastic modulus decreases near the soldering temperature and the adhesion to the lead frame and the semiconductor chip. By improving the force, it is possible to obtain low thermal expansion and low water absorption. Therefore, it is effective for preventing a reduction in stress generated due to a thermal shock at the time of soldering and a peeling defect with a semiconductor chip or the like accompanying the reduction.

【0013】式(2)の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%以上の使用が望ま
しい。使用量が30重量%未満だと低吸水性、低弾性等
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。更に式中のnの
値は1から6の範囲であることが望ましく、nの値が6
を越えると、トランスファー成形時での流動性が低下
し、成形性が劣化する傾向がある。
By adjusting the amount of the curing agent of the formula (2), the solder stress resistance can be maximized. In order to bring out the effect of resistance to solder stress, it is desirable to use the curing agent represented by the formula (2) in an amount of 30% by weight or more, more preferably 50% by weight or more based on the total amount of the curing agent. If the amount used is less than 30% by weight, low water absorption, low elasticity, etc., and insufficient adhesion to the lead frame and semiconductor chip cannot be expected to improve solder stress resistance. Further, the value of n in the formula is desirably in the range of 1 to 6, and the value of n is 6
If it exceeds, the fluidity during transfer molding tends to decrease, and moldability tends to deteriorate.

【0014】式(2)で示される硬化剤以外に他の硬化
剤を併用する場合、用いるもの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、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等を用いることが出来る。
When other curing agents other than the curing agent represented by the formula (2) are used in combination, those used generally refer to all polymers having a phenolic hydroxyl group. For example, phenol novolak resins, cresol novolak resins, dicyclopentadiene-modified phenol resins, copolymers of dicyclopentadiene-modified phenol resins with phenol novolak and cresol novolak resins, and para-xylene-modified phenol resins 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。
The inorganic filler used in the present invention includes fused silica powder, spherical silica powder, crystalline silica powder, secondary aggregated silica powder, porous silica powder, secondary aggregated silica powder or silica obtained by pulverizing porous silica powder. Examples thereof include powder, alumina, and the like, and particularly preferred are fused silica powder, spherical silica powder, and a mixture of fused silica powder and spherical silica powder. The amount of the inorganic filler is 70 to 9 with respect to the total amount of the composition in consideration 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(2M
Z)等が単独もしくは2種類以上混合して用いられる。
The curing accelerator used in the present invention may be any one which promotes the reaction between an epoxy group and a hydroxyl group, and those generally used for sealing materials can be widely used. Zabicycloundecene (DBU),
Triphenylphosphine (TPP), dimethylbenzylamine (BDMA) and 2-methylimidazole (2M
Z) and the like are used alone or in combination of two or more.

【0017】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 epoxy resin composition for encapsulation of the present invention comprises an epoxy resin, a curing agent, an inorganic filler and a curing accelerator as essential components. In addition to this, a silane coupling agent and a brominated epoxy resin may be used if necessary. And various additives such as flame retardants such as 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 it is appropriately blended.

【0018】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、
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、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,
After the inorganic filler, the curing accelerator, and other additives are sufficiently and uniformly mixed by a mixer or the like, the mixture is further melt-kneaded by 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.

【0019】以下本発明を実施例にて具体的に説明す
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110℃、エ
ポキシ当量190) 6.8重量部
Hereinafter, the present invention will be described specifically with reference to Examples. Example 1 The following composition: 6.8 parts by weight of an epoxy resin represented by the formula (3) (softening point: 110 ° C., epoxy equivalent: 190)

【0020】[0020]

【化6】 Embedded image

【0021】 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 0) 4.5重量部 式(4)で示される硬化剤(軟化点114℃、水酸基当量216) 5.3重量部Orthocresol novolak epoxy resin (softening point: 65 ° C., epoxy equivalent: 200) 4.5 parts by weight Curing agent represented by formula (4) (softening point: 114 ° C., hydroxyl equivalent: 216) 5.3 parts by weight

【0022】[0022]

【化7】 Embedded image

【0023】(n=1が1に対し、n=2が0.2、n
=3以上が0.1) フェノールノボラック樹脂硬化剤(軟化点90℃、水酸基当量104) 3.4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5
2p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。
(N = 1 is 1 while n = 2 is 0.2, n
= 3 or more 0.1) Phenol novolak resin curing agent (softening point 90 ° C, hydroxyl equivalent 104) 3.4 parts by weight Fused silica powder 78.8 parts by weight Triphenylphosphine 0.2 part by weight Carbon black 0.5 part by weight 0.5 part by weight of carnauba wax 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 was tableted, and a 6 × 6 mm chip was used for a solder crack test at 175 ° C., 70 kg / cm 2 and 120 seconds by a low-pressure transfer molding machine.
Sealed in 2p package, and 3 for solder moisture resistance test
A 6 mm chip was sealed in a 16 pSOP package. The sealed test element was subjected to the following solder crack test and solder moisture resistance test.

【0024】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。
Solder crack test: The sealed test element was subjected to 48 hours and 72 hours under an environment of 85 ° C. and 85% RH.
After the treatment, it was immersed in a solder bath at 260 ° C. for 10 seconds, and external cracks were observed with a microscope. Solder moisture resistance test: Sealed test element was tested at 85 ° C for 8
After being treated for 72 hours in an environment of 5% RH, and then immersed in a solder bath at 260 ° C. for 10 seconds, a pressure cooker test (125 ° C., 100% RH) was performed to measure open circuit failure. Table 1 shows the test results.

【0025】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 Compounded according to the formulation shown in Table 1, and a molding material was obtained in the same manner as in Example 1. A sealed molded product for a test was obtained from this molding material, 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.

【0026】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 1-4 Compounded according to the recipe in Table 1,
A molding material was obtained in the same manner as in Example 1. A sealed molded product for a test was obtained from this molding material, 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.

【0027】実施例6 下記組成物 式(3)で示されるエポキシ樹脂(軟化点110℃、エポキシ当量190) 3.8重量部 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 0) 8.6重量部 式(5)で示される硬化剤(軟化点109℃、水酸基当量200) 2.3重量部Example 6 The following composition: Epoxy resin represented by formula (3) (softening point: 110 ° C., epoxy equivalent: 190) 3.8 parts by weight ortho-cresol novolak epoxy resin (softening point: 65 ° C., epoxy equivalent: 200) 8 2.6 parts by weight 2.3 parts by weight of a curing agent represented by the formula (5) (softening point 109 ° C., hydroxyl equivalent 200)

【0028】[0028]

【化8】 Embedded image

【0029】(nの値は、1から4を示す混合物であり
その重量割合はn=1が1に対してn=2が0.2、n
=3以上が0.1である。) フェノールノボラック樹脂硬化剤(軟化点90℃、水酸基当量104) 5.3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 を常温混合し、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た。得られた成形材料
を実施例1と同様にテスト用サンプルを作製し、試験を
行った。試験結果を表2に示す。
(The value of n is a mixture of 1 to 4, and the weight ratio is 0.2 for n = 2 for 1 for n = 1, n for 2
= 3 or more is 0.1. ) Phenol novolak resin curing agent (softening point 90 ° C., hydroxyl equivalent 104) 5.3 parts by weight Fused silica powder 78.8 parts by weight Triphenylphosphine 0.2 parts by weight Carbon black 0.5 parts by weight Carnauba wax 0.5 parts by weight The mixture was mixed at room temperature, kneaded at 70 to 100 ° C. with a biaxial roll, cooled, and pulverized to obtain a molding material. A test sample was prepared from the obtained molding material in the same manner as in Example 1, and a test was performed. Table 2 shows the test results.

【0030】実施例7〜10 表2の処方に従って配合し、実施例6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6と同様に半田クラック
試験及び半田耐湿試験を行った。試験結果を表2に示
す。
Examples 7 to 10 Compounded according to the formulation shown in Table 2 to obtain a molding material in the same manner as in Example 6. A sealed molded product for a test was obtained from this molding material, and a solder crack test and a solder moisture resistance test were performed using this molded product in the same manner as in Example 6. Table 2 shows the test results.

【0031】比較例5〜7 表2の処方に従って配合し、実施例6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6と同様に半田クラック
試験及び半田耐湿試験を行った。試験結果を表2に示
す。
Comparative Examples 5 to 7 Compounded according to the formulation shown in Table 2 and obtained in the same manner as in Example 6. A sealed molded product for a test was obtained from this molding material, and a solder crack test and a solder moisture resistance test were performed using this molded product in the same manner as in Example 6. Table 2 shows the test results.

【0032】[0032]

【表1】 [Table 1]

【0033】[0033]

【表2】 [Table 2]

【0034】[0034]

【発明の効果】本発明による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
おいて非常に信頼性を必要とする製品について好適であ
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. When used for encapsulation, coating, insulation, etc. of electronic and electrical components, especially for highly integrated large chip ICs mounted on surface mount packages because of their excellent crack resistance and excellent moisture resistance It is suitable for products that require extremely high reliability.

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】 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)で示されるナフトール樹脂硬化剤 【化2】 を総硬化剤量に対して30〜100重量%含む硬化剤、 (C)無機充填剤及び (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): (B) a naphthol resin curing agent represented by the following formula (2): (C) an inorganic filler and (D) an epoxy resin composition for semiconductor encapsulation comprising, as essential components, (C) an inorganic filler and (D) a curing accelerator.
JP25600692A 1992-09-21 1992-09-25 Epoxy resin composition Expired - Fee Related JP3093051B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP25600692A JP3093051B2 (en) 1992-09-25 1992-09-25 Epoxy resin composition
DE69307442T DE69307442T2 (en) 1992-09-21 1993-05-11 Epoxy resin composition based on the diglycidyl ether of biphenyldiol
SG9502396A SG87725A1 (en) 1992-09-21 1993-05-11 Epoxy resin composition
EP93107683A EP0589143B1 (en) 1992-09-21 1993-05-11 Epoxy resin composition based on diglycidylether of biphenyldiol
MYPI93000905A MY109105A (en) 1992-09-21 1993-05-15 Epoxy resin composition
KR1019930009377A KR100215537B1 (en) 1992-09-21 1993-05-27 Epoxy resin composition
US08/287,592 US5578660A (en) 1992-09-21 1994-08-08 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25600692A JP3093051B2 (en) 1992-09-25 1992-09-25 Epoxy resin composition

Publications (2)

Publication Number Publication Date
JPH06112368A JPH06112368A (en) 1994-04-22
JP3093051B2 true JP3093051B2 (en) 2000-10-03

Family

ID=17286600

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25600692A Expired - Fee Related JP3093051B2 (en) 1992-09-21 1992-09-25 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JP3093051B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW452584B (en) 1997-10-03 2001-09-01 Hitachi Chemical Co Ltd Epoxy resin composition and semiconductor devices using it as encapsulant

Also Published As

Publication number Publication date
JPH06112368A (en) 1994-04-22

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