JP3305097B2 - Epoxy resin composition - Google Patents

Epoxy resin composition

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Publication number
JP3305097B2
JP3305097B2 JP03254794A JP3254794A JP3305097B2 JP 3305097 B2 JP3305097 B2 JP 3305097B2 JP 03254794 A JP03254794 A JP 03254794A JP 3254794 A JP3254794 A JP 3254794A JP 3305097 B2 JP3305097 B2 JP 3305097B2
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
test
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.)
Expired - Lifetime
Application number
JP03254794A
Other languages
Japanese (ja)
Other versions
JPH07238141A (en
Inventor
広基 二階堂
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
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Filing date
Publication date
Application filed by Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP03254794A priority Critical patent/JP3305097B2/en
Publication of JPH07238141A publication Critical patent/JPH07238141A/en
Application granted granted Critical
Publication of JP3305097B2 publication Critical patent/JP3305097B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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 soldering stress in surface mounting of 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 components such as diodes, transistors, and integrated circuits are sealed with a thermosetting resin. In particular, in an integrated circuit, an ortho-cresol novolac type epoxy resin having excellent heat resistance and moisture resistance is replaced with phenol. An epoxy resin composition cured with a novolak resin and blended with an inorganic filler such as fused silica or crystalline silica as a filler is used. However, in recent years, the chip has been gradually increased in size with the increase in the integration degree of the integrated circuit, and the package has been changed to the conventional DIP.
Small and thin QFP, SO surface mounted from type
P, SOJ, TSOP, TQFP, PLCC have been changed. That is, a large chip is sealed in a small and thin package, and cracks are generated due to thermal stress. Problems such as a decrease in moisture resistance due to these cracks are greatly highlighted. In particular, there has been a problem in that the device is suddenly exposed to a high temperature of 200 ° C. or more in the soldering process, and the moisture resistance is deteriorated due to cracking of the package or separation of the resin and the chip. Therefore,
The development of a highly reliable resin composition for semiconductor encapsulation suitable for encapsulating these large chips has been 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
ポキシ樹脂を用いることにより、リードフレーム及び半
導体チップとの接着性の向上、成形物の高温時における
低弾性率化による低応力化により、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 an epoxy resin represented by the formula (1) as an epoxy resin to improve adhesion to a lead frame and a semiconductor chip. An object of the present invention is to provide an epoxy resin composition for semiconductor encapsulation in which a molded article has a low stress due to a low elastic modulus at a high temperature, thereby significantly improving the solder stress resistance of a semiconductor package when mounted on a substrate.

【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
The present invention relates to (A) an epoxy resin represented by the following formula (1):

【0005】[0005]

【化2】 (式中のRは水素、ハロゲン、炭素数1〜10のアルキ
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)
Embedded image (R in the formula is the same or different atom or group selected from hydrogen, halogen, and an alkyl group having 1 to 10 carbon atoms)

【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)フェノール樹脂硬化
剤、(C)無機充填材、(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。
[0006] 30 to 100 with respect to the total amount of epoxy resin
It is an epoxy resin composition for semiconductor encapsulation containing, as essential components, an epoxy resin containing by weight, (B) a phenol resin curing agent, (C) an inorganic filler, and (D) a curing accelerator. In comparison, it has solder crack resistance and moisture resistance after soldering as excellent reliability.

【0007】式(1)の分子構造で示されるエポキシ樹
脂は、メタキシレンとフェノール類をフリーデル・クラ
フツ・アルキル化反応により重合させたフェノール樹脂
をグリシジルエーテル化することによって得られるエポ
キシ樹脂で、従来のオルソクレゾールノボラック型エポ
キシ樹脂に比べ、硬化物はガラス転移温度を越えた高温
時での弾性率が低く、リードフレーム等の金属類との接
着性に優れる。従って表面実装の半田付け時における熱
ストレスを低減させることができ、耐半田クラック性に
優れるエポキシ樹脂組成物を得ることができる。式
(1)中のRは水素、ハロゲン、炭素数1〜10のアル
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
は基であるが、これらの内で好ましいのは、水素原子で
ある。また炭素数が10を超えるアルキル基を選択する
場合、硬化性が低下する傾向にある。nは0〜20であ
るが、20を越えると流動性が劣る。好ましいnは0〜
10である。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%未満だと高温時の低弾性率
化及び接着性が得られず耐半田クラック性が不充分であ
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、用いるエポキシ樹脂とはエポキ
シ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、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及びトリアジン核含有
エポキシ樹脂等のことを言う。
The epoxy resin represented by the molecular structure of formula (1) is an epoxy resin obtained by glycidyl etherification of a phenol resin obtained by polymerizing meta-xylene and phenols by a Friedel-Crafts alkylation reaction. Compared with the conventional orthocresol novolak epoxy resin, the cured product has a low elastic modulus at a high temperature exceeding the glass transition temperature and has excellent adhesion to metals such as a lead frame. Therefore, it is possible to reduce the thermal stress at the time of surface mounting soldering, and to obtain an epoxy resin composition having excellent solder crack resistance. R in the formula (1) is the same or different atom or group selected from hydrogen, halogen, and an alkyl group having 1 to 10 carbon atoms, and among them, a hydrogen atom is preferable. When an alkyl group having more than 10 carbon atoms is selected, the curability tends to decrease. n is from 0 to 20, but when it exceeds 20, the fluidity is poor. Preferred n is 0
It is 10. By adjusting the amount of the epoxy resin used, solder crack resistance can be maximized. In order to obtain 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 the epoxy resin. If it is less than 30% by weight, a low elastic modulus at high temperature and adhesiveness cannot be obtained, and solder crack resistance is insufficient. When an epoxy resin other than the epoxy resin represented by the formula (1) is used in combination, the epoxy resin used refers to all monomers, oligomers and polymers having an epoxy group. For example, a biphenyl-type epoxy compound, a bisphenol-type epoxy compound, a phenol novolak-type epoxy resin, a cresol novolak-type epoxy resin, a triphenolmethane-type epoxy compound, an alkyl-modified triphenolmethane-type epoxy compound, and a triazine nucleus-containing epoxy resin. .

【0008】本発明で用いるフェノール樹脂硬化剤は、
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、パラキ
シリレ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、パラキシリレ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 phenolic resin curing agent used in the present invention comprises:
Phenol novolak resin, cresol novolak resin, dicyclopentadiene-modified phenol resin, paraxylylene-modified phenol resin, terpene-modified phenol resin, triphenolmethane compound, etc. ,
Terpene-modified phenolic resins and mixtures thereof are preferred. The amount of these curing agents is preferably such that the number of epoxy groups in the epoxy compound and the number of hydroxyl groups in the curing agent match.

【0009】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、ジメチルベンジルアミン
や2−メチルイミダゾール等を単独もしくは2種類以上
混合して用いられる。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。80重量%未満だと耐半田クラック性が不都合であ
る。また90重量%を越えると流動性が不十分である。
The curing accelerator used in the present invention may be any as long as it promotes a curing reaction between an epoxy group and a hydroxyl group.
What is generally used for a sealing material can be widely used. For example, 1,8-diazabicycloundecene, triphenylphosphine, dimethylbenzylamine, 2-methylimidazole, or the like is used alone or in combination of two or more. 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, particularly spherical silica powder, and fused silica powder and spherical silica powder. Mixtures with silica powder are preferred. The amount of the inorganic filler is preferably 80 to 90% by weight based on the total amount of the epoxy resin composition from the viewpoint of solder crack resistance. If it is less than 80% by weight, the solder crack resistance is disadvantageous. If it exceeds 90% by weight, the fluidity is insufficient.

【0010】本発明の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。
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、フェノール樹脂硬化
剤、硬化促進剤、無機充填材、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 epoxy resin composition of the present invention comprises an epoxy resin, a phenolic resin curing agent, an inorganic filler and a curing accelerator as essential components. In addition to this, if necessary, a silane coupling agent, a brominated epoxy resin, 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 are appropriately used. It is safe to mix.
In addition, in order to manufacture the epoxy resin composition for encapsulation of the present invention as a molding material, epoxy resin, phenol resin curing agent, curing accelerator, inorganic filler, and other additives are sufficiently and uniformly mixed by a mixer or the like. After that, the mixture is further melt-kneaded with a hot roll or a kneader, cooled and pulverized to obtain a sealing material. These molding materials are used for coating electric or electronic components such as transistors and integrated circuits,
It can be applied to insulation, sealing, and the like.

【0011】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(2)で示されるエポキシ樹脂(軟化点50℃、エポキシ当量240g/e q) 7.6重量部Hereinafter, the present invention will be described specifically with reference to Examples. Example 1 The following composition: 7.6 parts by weight of an epoxy resin represented by the formula (2) (softening point: 50 ° C., epoxy equivalent: 240 g / eq)

【0012】[0012]

【化3】 (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0.7、n=2が0.4
5、n=3が0.35である。)
Embedded image (The value of n is a mixture showing 0 to 3, and the weight ratio is 0.7 for n = 1, 0.7 for n = 1, and 0.4 for n = 2.
5, n = 3 is 0.35. )

【0013】 オルソクレゾールノボラック型エポキシ樹脂(軟化点58℃、エポキシ当量2 00g/eq) 1.9重量部 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 ) 4.3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16pSOP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。
Orthocresol novolak type epoxy resin (softening point 58 ° C., epoxy equivalent 200 g / eq) 1.9 parts by weight Phenol novolak resin curing agent (softening point 65 ° C., hydroxyl equivalent 105 g / eq) 4.3 parts by weight Melting Silica powder (average particle size 10 μm, specific surface area 2.0 m 2 / g) 35 parts by weight Spherical silica powder (average particle size 30 μm, specific surface area 2.5 m 2 / g) 50 parts by weight Triphenylphosphine 0.2 part by weight Carbon 0.5 parts by weight of black 0.5 parts 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 molding material obtained by the pulverization is tabletted, and is 175 ° C., 70 kg / cm 2 , 120 with a low-pressure transfer molding machine.
Under the condition of seconds, a chip of 6 × 6 mm was sealed in 52 pQFP for a solder crack test, and a chip of 3 × 6 mm was sealed in 16 pSOP for a solder moisture resistance test. The sealed test element was subjected to the following solder crack test and solder moisture resistance test.

【0014】評価方法 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、半田耐湿性平均寿命(時間)で表した。試験結
果を表1に示す。 実施例2,3 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1,2 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3 実施例1の式(2)のエポキシ樹脂に変えて、下記式
(3)のエポキシ樹脂(軟化点55℃、エポキシ当量2
45g/eq)を用いた以外は、表1の配合で同様にし
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。
Evaluation method Solder crack test: A sealed test element was heated at 85 ° C. for 8 hours.
The treatment was performed for 24 hours, 48 hours, 72 hours, and 120 hours in an environment of 5% RH, 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 environment for 72 hours, and then immersed in a solder bath at 260 ° C. for 10 seconds, followed by a pressure cooker test (1
(25 ° C., 100% RH), the open defect of the circuit was measured, and the result was represented by the average life (hour) of the solder moisture resistance. Table 1 shows the test results. Examples 2 and 3 The components were blended 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. Comparative Examples 1 and 2 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. Comparative Example 3 Instead of the epoxy resin of the formula (2) in Example 1, an epoxy resin of the following formula (3) (softening point 55 ° C., epoxy equivalent 2
Except for using 45 g / eq), a molding material was obtained in the same manner as in the formulation of Table 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.

【0015】[0015]

【化4】 (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0.8、n=2が0.4
5、n=3が0.4である。)
Embedded image (The value of n is a mixture showing 0 to 3, and the weight ratio of n = 0 to 1 is 0.8 for n = 1 and 0.4 for n = 2.
5, n = 3 is 0.4. )

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【発明の効果】本発明によると、耐半田クラック性、耐
湿性に優れており、また成形性も良好であるため表面実
装のできる樹脂封止半導体パッケージの実現を可能とす
る。
According to the present invention, it is possible to realize a resin-sealed semiconductor package which is excellent in solder crack resistance and moisture resistance and has good moldability and can be surface-mounted.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI H01L 23/31 (56)参考文献 特開 平3−258829(JP,A) 特開 平5−222156(JP,A) 特開 平5−97967(JP,A) 特開 平5−97966(JP,A) 特開 平3−14819(JP,A) 特開 昭60−112813(JP,A) 特開 平5−194708(JP,A) 特開 平7−196568(JP,A) (58)調査した分野(Int.Cl.7,DB名) C08G 59/20 - 59/32 C08G 59/62 C08L 63/00 - 63/04 H01L 23/29 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI H01L 23/31 (56) References JP-A-3-258829 (JP, A) JP-A-5-222156 (JP, A) JP-A-5-99767 (JP, A) JP-A-5-97966 (JP, A) JP-A-3-14819 (JP, A) JP-A-60-112813 (JP, A) JP-A-5-194708 ( JP, A) JP-A-7-196568 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C08G 59/20-59/32 C08G 59/62 C08L 63/00-63 / 04 H01L 23/29

Claims (2)

(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】 (式中のRは水素、ハロゲン、炭素数1〜10のアルキ
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)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)フェノール樹脂硬化剤、(C)
無機充填材、(D)硬化促進剤を必須成分とすることを
特徴とする半導体封止用エポキシ樹脂組成物。
(A) an epoxy resin represented by the following formula (1): (R in the formula is the same or different atom or group selected from hydrogen, halogen, and alkyl group having 1 to 10 carbon atoms) epoxy resin containing 30 to 100% by weight based on the total epoxy resin amount, (B ) Phenolic resin curing agent, (C)
An epoxy resin composition for semiconductor encapsulation, comprising an inorganic filler and (D) a curing accelerator as essential components.
【請求項2】 式(1)のRが水素である請求項1記載
の半導体封止用エポキシ樹脂組成物。
2. The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein R in the formula (1) is hydrogen.
JP03254794A 1994-03-02 1994-03-02 Epoxy resin composition Expired - Lifetime JP3305097B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03254794A JP3305097B2 (en) 1994-03-02 1994-03-02 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03254794A JP3305097B2 (en) 1994-03-02 1994-03-02 Epoxy resin composition

Publications (2)

Publication Number Publication Date
JPH07238141A JPH07238141A (en) 1995-09-12
JP3305097B2 true JP3305097B2 (en) 2002-07-22

Family

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Family Applications (1)

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Country Status (1)

Country Link
JP (1) JP3305097B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3349963B2 (en) * 1998-10-21 2002-11-25 日本電気株式会社 Flame-retardant epoxy resin composition and semiconductor device using the same

Also Published As

Publication number Publication date
JPH07238141A (en) 1995-09-12

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