JPH06184272A - Epoxy resin composition - Google Patents

Epoxy resin composition

Info

Publication number
JPH06184272A
JPH06184272A JP4338992A JP33899292A JPH06184272A JP H06184272 A JPH06184272 A JP H06184272A JP 4338992 A JP4338992 A JP 4338992A JP 33899292 A JP33899292 A JP 33899292A JP H06184272 A JPH06184272 A JP H06184272A
Authority
JP
Japan
Prior art keywords
epoxy resin
resin
epoxy
resin composition
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.)
Pending
Application number
JP4338992A
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 JP4338992A priority Critical patent/JPH06184272A/en
Publication of JPH06184272A publication Critical patent/JPH06184272A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide a resin composition containing a specified epoxy resin, a specific phenol resin curing agent, a specified inorganic filler and a specific curing promoter as the essential components, excellent in solder stress resistance, solder cracking resistance, heat resistance and moisture resistance and suitable for semiconductor sealing, etc. CONSTITUTION:This resin composition consists of (A) an epoxy resin containing an epoxy compound of the formula (R1 to R4 are each H, a halogen or an alkyl) in an amount of 10 to 100wt.% based on the total amount of the epoxy resin, (B) a phenol resin curing agent such as a phenolic novolak resin, (C) preferably 70 to 90wt.% inorganic filler such as fused silica powder and (D) a curing promoter such as diazabicycloundecene as the essential 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
ルノボラックエポキシ樹脂をフェノールノボラック樹脂
で硬化させ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,SOP,SO
J,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 a thermosetting resin. Especially in integrated circuits, orthocresol novolac epoxy resin, which has excellent heat resistance and moisture resistance, is used as phenol novolac. An epoxy resin composition cured with a resin is used. However, in recent years, as the integration of integrated circuits has increased, the size of the chips has gradually increased, and the package is a small and thin QFP, SOP, SO that is surface-mounted from the conventional DIP type.
It has changed to J, TSOP, TQFP, PLCC. That is, a large chip is enclosed in a small and thin package, cracks are generated by thermal stress, and problems such as deterioration of moisture resistance due to these cracks are 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. Therefore, development of a highly reliable resin composition for semiconductor encapsulation suitable for encapsulating these large chips is 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(2)で示されるエポキシ化合物の使用
(特開昭64−65116号公報)が
In order to solve these problems, the use of an epoxy compound represented by the following formula (2) as an epoxy resin (Japanese Patent Laid-Open No. 64-65116) has been proposed.

【0004】[0004]

【化2】 (式中のR1 〜R8 は水素、ハロゲン、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)
[Chemical 2] (In the formula, R 1 to R 8 are the same or different atoms or groups selected from hydrogen, halogen and alkyl groups)

【0005】検討されてきた。式(2)で示されるエポ
キシ化合物の使用によりレジン系の低粘度化が図られ、
従って溶融シリカ等の無機充填材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が図
られ、耐半田ストレス性の向上が得られている。ただ
し、このエポキシ化合物を用いても無機充填材を多く配
合することに対して限界が有り、更に耐半田ストレス性
の向上を図るために、無機充填材を多く配合できるよう
な樹脂系を用いる必要がある。
It has been studied. By using the epoxy compound represented by the formula (2), the viscosity of the resin system is reduced,
Therefore, by adding a larger amount of an inorganic filler such as fused silica, low thermal expansion and low water absorption can be achieved after the composition is molded, and solder stress resistance can be improved. However, even if this epoxy compound is used, there is a limit to blending a large amount of inorganic filler, and it is necessary to use a resin system capable of blending a large amount of inorganic filler in order to improve solder stress resistance. There is.

【0006】[0006]

【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
エポキシ化合物を用いることにより、レジン系の低粘度
化を達成せしめ、リードフレーム及び半導体チップとの
濡れ性の増加により接着性の向上を図り、また更に多く
の無機充填材を配合することにより、硬化物の低熱膨張
化及び低吸水化を図ることにより、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 addresses these problems by using an epoxy compound represented by the formula (1) as an epoxy resin to achieve a low viscosity of a resin system and to obtain a lead. The adhesiveness is improved by increasing the wettability with the frame and the semiconductor chip, and by adding more inorganic fillers, it is possible to achieve low thermal expansion and low water absorption of the cured product. It is an object of the present invention to provide an epoxy resin composition for semiconductor encapsulation in which the solder stress resistance of the semiconductor package is remarkably improved.

【0007】[0007]

【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、エポキシ基を有する化合物として下記式(1)
で示される分子構造のハイドロキノンジグリシジルエー
テルを、
The epoxy resin composition of the present invention has the following formula (1) as a compound having an epoxy group.
Hydroquinone diglycidyl ether of the molecular structure shown by

【0008】[0008]

【化3】 (式中のR1 〜R4 は、水素、ハロゲン、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)
[Chemical 3] (Wherein R 1 to R 4 are the same or different atoms or groups selected from hydrogen, halogen and alkyl groups)

【0009】総エポキシ樹脂に対して10〜100重量
%含むエポキシ樹脂を用いることを特徴とし、過去のエ
ポキシ樹脂組成物に比べ優れた流動性と耐半田クラック
性を有するものである。
It is characterized by using an epoxy resin in an amount of 10 to 100% by weight with respect to the total epoxy resin, and has excellent fluidity and solder crack resistance as compared with past epoxy resin compositions.

【0010】式(1)の分子構造で示されるハイドロキ
ノンジグリシジルエーテルは、ハイドロキノン類をグリ
シジルエーテル化することによって得られる1分子中に
2個のエポキシ基を有する2官能性モノマーで、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。従って組成物中の無機充
填材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。このハイドロキノンジグリシ
ジルエーテル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
るハイドロキノンジグリシジルエーテルを総エポキシ樹
脂化合物量の10重量%以上、好ましくは30重量%以
上の使用が望ましい。10重量%未満だと流動性及びリ
ードフレーム、半導体チップとの接着性、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。
更に式中のR1 〜R4 は水素原子が好ましい。
The hydroquinone diglycidyl ether represented by the molecular structure of the formula (1) is a bifunctional monomer having two epoxy groups in one molecule obtained by glycidyl etherification of hydroquinones, and is a conventional polyfunctional monomer. It has a lower melt viscosity than functional epoxy resin and has excellent fluidity during transfer molding. Therefore, a large amount of the inorganic filler in the composition can be blended, low thermal expansion and low water absorption can be achieved, and an epoxy resin composition excellent in solder crack resistance can be obtained. By adjusting the amount of the hydroquinone diglycidyl ether used, solder crack resistance can be maximized. In order to bring out the effect of solder crack resistance, it is desirable to use the hydroquinone diglycidyl ether represented by the formula (1) in an amount of 10% by weight or more, preferably 30% by weight or more based on the total amount of epoxy resin compounds. If it is less than 10% by weight, fluidity, adhesion to lead frames and semiconductor chips, low thermal expansion,
Low water absorption cannot be obtained and solder crack resistance is insufficient.
Further, R 1 to R 4 in the formula are preferably hydrogen atoms.

【0011】式(1)で示されるハイドロキノンジグリ
シジルエーテル以外に他のエポキシ化合物を併用する場
合、用いるエポキシ樹脂としてはエポキシ基を有するモ
ノマー、オリゴマー、ポリマー全般をいう。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
のことをいう。
When another epoxy compound is used in combination with the hydroquinone diglycidyl ether represented by the formula (1), the epoxy resin to be used includes all monomers, oligomers and polymers having an epoxy group. For example, a biphenyl type epoxy compound, a bisphenol type epoxy compound, a phenol novolac type epoxy resin, a cresol novolac type epoxy resin, a triphenol methane type epoxy compound, an alkyl modified triphenol methane type epoxy compound, a triazine nucleus-containing epoxy resin, etc. .

【0012】本発明で用いる硬化剤としては、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、パラキシレン変性
フェノール樹脂、ナフトール変性フェノール樹脂、フェ
ノール類とベンズアルデヒドあるいはナフチルアルデヒ
ドとの縮合物、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、パラキシレン変性フェノール
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。
As the curing agent used in the present invention, phenol novolac resin, cresol novolac resin, dicyclopentadiene modified phenol resin, paraxylene modified phenol resin, naphthol modified phenol resin, condensate of phenol with benzaldehyde or naphthyl aldehyde, Examples thereof include triphenol methane compounds, and phenol novolac resin, dicyclopentadiene modified phenol resin, paraxylene modified phenol resin and mixtures thereof are particularly preferable. 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.

【0013】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、耐半田クラック性と
成形性及び流動性のバランスから総エポキシ樹脂組成物
量に対して70〜90重量%が好ましい。
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, etc., and particularly fused silica powder, spherical silica powder. , And a mixture of fused silica powder and spherical silica powder are preferred. Further, the blending amount of the inorganic filler is preferably 70 to 90% by weight based on the total amount of the epoxy resin composition in view of balance between solder crack resistance, moldability and fluidity.

【0014】本発明に使用される硬化促進剤はエポキシ
基と水酸基との硬化反応を促進させるもであればよく、
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。例えばジアザビシクロウンデセン(DB
U)、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)等が挙げられ、これらは単独もしくは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 that 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, diazabicycloundecene (DB
U), triphenylphosphine (TPP), dimethylbenzylamine (BDMA), 2-methylimidazole (2MZ) and the like can be mentioned, and these can be used alone or in admixture of two or more.

【0015】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。
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, if necessary,
A variety of flame retardants such as brominated epoxy resin, antimony trioxide, hexabromobenzene, colorants such as carbon black and red iron oxide, mold release agents such as natural wax and synthetic wax, and low stress additives such as silicone oil and rubber. There is no problem even if the above-mentioned additive is properly mixed.

【0016】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。
Further, in order to produce the encapsulating epoxy resin composition of the present invention as a molding material, the epoxy resin, the curing agent, the curing accelerator, the filler, and other additives are sufficiently uniformly mixed with a mixer or the like. After that, the mixture can be further melt-kneaded with a hot roll or a kneader, cooled and pulverized to obtain a sealing material. These molding materials can be applied to coating, insulation, sealing, etc. of transistors, integrated circuits, etc., which are electric or electronic parts.

【0017】以下本発明を実施例で具体的に説明する。The present invention will be specifically described below with reference to examples.

【実施例】【Example】

実施例1 下記組成物 式(3)で示されるエポキシ化合物(融点110℃、エポキシ当量130g/ eq) 9.0重量部 Example 1 The following composition 9.0 parts by weight of an epoxy compound represented by the formula (3) (melting point: 110 ° C., epoxy equivalent: 130 g / eq)

【0018】[0018]

【化4】 [Chemical 4]

【0019】 式(4)で示されるエポキシ化合物(融点110℃、エポキシ当量190g/ eq) 3.0重量部3.0 parts by weight of the epoxy compound represented by the formula (4) (melting point 110 ° C., epoxy equivalent 190 g / eq)

【0020】[0020]

【化5】 [Chemical 5]

【0021】 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 ) 8.8重量部 溶融シリカ粉末 78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、スパイラルフロー用試験金型
を用い、175℃、70kg/cm2 、120秒の条件
でスパイラルフローを測定(EMMI−1−66に準ず
る)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℃、70kg/cm
2 、120秒の条件で半田クラック試験用として6×6
mm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。
Phenol novolac resin curing agent (softening point 90 ° C., hydroxyl group equivalent 105 g / eq) 8.8 parts by weight fused silica powder 78 parts by weight triphenylphosphine 0.2 parts by weight carbon black 0.5 parts by weight carnauba wax 0. 5 parts by weight were mixed with a mixer at room temperature, kneaded with a twin-screw roll at 70 to 100 ° C., cooled and pulverized to obtain a molding material. The molding material obtained by pulverizing was measured for spiral flow (according to EMMI-1-66) under the conditions of 175 ° C., 70 kg / cm 2 , and 120 seconds using a test mold for spiral flow. Further, the obtained molding material is made into a tablet, which is then transferred to a low pressure transfer molding machine at 175 ° C. and 70 kg / cm.
2 6 × 6 for solder crack test under 120 seconds condition
mm chips were encapsulated in 52 pQFP, and 3 × 6 mm chips were encapsulated in 16 pSOP for solder moisture resistance testing. The following solder crack test and solder moisture resistance test were performed on the sealed test element.

【0022】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48時間及び72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 treated in an environment of 85 ° C. and 85% RH for 48 hours and 72 hours, and then immersed in a solder bath at 260 ° C. for 10 seconds, and then external cracks were observed with a microscope. did. 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.

【0023】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。
Examples 2 to 6 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.

【0024】比較例1 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 Example 1 A molding material was obtained in the same manner as in Example 1 except that the ingredients were blended according to the formulation shown in Table 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.

【0025】[0025]

【表1】 [Table 1]

【0026】[0026]

【発明の効果】本発明のエポキシ樹脂組成物は、耐半田
クラック性に非常に優れ、かつ耐湿性にも優れている。
The epoxy resin composition of the present invention is extremely excellent in solder crack resistance and moisture resistance.

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
化合物 【化1】 (式中のR1 〜R4 は、水素、ハロゲン、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10〜100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
填材および(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。
1. An epoxy compound represented by the following formula (1): An epoxy resin containing 10 to 100% by weight (wherein R 1 to R 4 in the formula are the same or different atoms or groups selected from hydrogen, halogen and alkyl groups) with respect to the total amount of the epoxy resin, (B). An epoxy resin composition for semiconductor encapsulation, which comprises a phenol resin curing agent, (C) an inorganic filler, and (D) a curing accelerator as essential components.
JP4338992A 1992-12-18 1992-12-18 Epoxy resin composition Pending JPH06184272A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4338992A JPH06184272A (en) 1992-12-18 1992-12-18 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4338992A JPH06184272A (en) 1992-12-18 1992-12-18 Epoxy resin composition

Publications (1)

Publication Number Publication Date
JPH06184272A true JPH06184272A (en) 1994-07-05

Family

ID=18323247

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4338992A Pending JPH06184272A (en) 1992-12-18 1992-12-18 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JPH06184272A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002294036A (en) * 2001-03-29 2002-10-09 Toray Ind Inc Epoxy resin composition for sealing semiconductor and semiconductor devices using the same
JP2005120269A (en) * 2003-10-17 2005-05-12 Shin Etsu Chem Co Ltd Adhesive composition, adhesive film and adhesive tape for dicing/die bond
JP2009173728A (en) * 2008-01-23 2009-08-06 Nippon Steel Chem Co Ltd Epoxy resin composition and cured product
WO2009110424A1 (en) * 2008-03-03 2009-09-11 新日鐵化学株式会社 Modified epoxy resin, epoxy resin compositions and cured articles

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002294036A (en) * 2001-03-29 2002-10-09 Toray Ind Inc Epoxy resin composition for sealing semiconductor and semiconductor devices using the same
JP2005120269A (en) * 2003-10-17 2005-05-12 Shin Etsu Chem Co Ltd Adhesive composition, adhesive film and adhesive tape for dicing/die bond
JP4530125B2 (en) * 2003-10-17 2010-08-25 信越化学工業株式会社 Adhesive composition, adhesive film, and adhesive tape for dicing and die bonding
JP2009173728A (en) * 2008-01-23 2009-08-06 Nippon Steel Chem Co Ltd Epoxy resin composition and cured product
WO2009110424A1 (en) * 2008-03-03 2009-09-11 新日鐵化学株式会社 Modified epoxy resin, epoxy resin compositions and cured articles

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