JPH05160302A - Resin composition for sealing semiconductor - Google Patents

Resin composition for sealing semiconductor

Info

Publication number
JPH05160302A
JPH05160302A JP34808391A JP34808391A JPH05160302A JP H05160302 A JPH05160302 A JP H05160302A JP 34808391 A JP34808391 A JP 34808391A JP 34808391 A JP34808391 A JP 34808391A JP H05160302 A JPH05160302 A JP H05160302A
Authority
JP
Japan
Prior art keywords
curing agent
silica
epoxy resin
filling
low water
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.)
Withdrawn
Application number
JP34808391A
Other languages
Japanese (ja)
Inventor
Yasuo Uchimiya
康夫 内宮
Hirotoshi Manako
裕俊 真名子
Shigeaki Tauchi
茂顕 田内
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.)
Nippon Steel Chemical and Materials Co Ltd
Original Assignee
Nippon Steel Chemical 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 Nippon Steel Chemical Co Ltd filed Critical Nippon Steel Chemical Co Ltd
Priority to JP34808391A priority Critical patent/JPH05160302A/en
Publication of JPH05160302A publication Critical patent/JPH05160302A/en
Withdrawn legal-status Critical Current

Links

Landscapes

  • Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)

Abstract

PURPOSE:To improve solder heat resistance, low stress, low water absorptive property, and adhesion by adding silica for filling in high density to epoxy resin, using a low water absorptive curing agent. CONSTITUTION:This is composed at a ratio of 300-2000 pts.wt. for silica for filling and 20-100 pts.wt. for curing agent to 100 pts.wt. for epoxy resin. As the epoxy resin, 0-cresol novolak type epoxy resin is used. For the silica for filling, the globular silica 10mum or more in grain diameter and smashed silica 10mum or less in grain diameter are used in combination. The globular silica 10mum in grain diameter is in a range of 20-80% of the all silica for filling. A low water absorptive curing agent expressed by the formula is used as the curing agent. Moreover, as the curing agent, it can be used by mixing phenol novolak resin in itself. At this time, for the curing agent expressed by the formula, 30wt.% or more out of all the quantity of the curing agent is added. Hereby, cracks can be prevented by improving low stress and low water absorption.

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、はんだ耐熱性に優れ
た、低粘度、低吸水、低応力で成形性に優れた半導体封
止用樹脂組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition for semiconductor encapsulation which has excellent solder heat resistance, low viscosity, low water absorption, low stress and excellent moldability.

【0002】[0002]

【従来の技術】近年、半導体装置の高集積化が急速に進
められており、素子サイズの大型化と配線幅の微細化が
著しく進展している。これは、信頼性の他界、優れた性
能を有する封止用樹脂の開発によるところが大きい。
2. Description of the Related Art In recent years, high integration of semiconductor devices has been rapidly advanced, and the size of elements and the miniaturization of wiring width have been remarkably advanced. This is largely due to the development of a sealing resin having excellent performance as well as reliability.

【0003】一方、プリント基板えの部品実装において
は、高密度実装、作業合理化のため、挿入型パッケージ
であるDIPパッケージから、表面実装型パッケージで
あるSOPパッケージに変化してきた。
On the other hand, in mounting components on a printed circuit board, a DIP package which is an insertion type package has been changed to a SOP package which is a surface mounting type package for high density mounting and streamlining of work.

【0004】また、近年ではより高密度実装化のため、
表面実装素子第一世代であるSOP、QFPパッケージ
から、薄型化が進められたTSOP、TQFPパッケー
ジに移行しつつある。パッケージの薄型化にともない、
チップ上面の樹脂厚が非常に薄くなってきている。この
ため、実装時における加熱による樹脂部分のクラック
が、より深刻な問題となっている。
Further, in recent years, for higher density mounting,
The SOP and QFP packages, which are the first generation of surface mount devices, are being moved to TSOP and TQFP packages, which have been made thinner. With the thinner package,
The resin thickness on the top surface of the chip is becoming very thin. For this reason, cracking of the resin portion due to heating during mounting has become a more serious problem.

【0005】はんだ付け工程におけるクラック発生は、
後硬化させてから実装工程までの間にパッケージダイパ
ット裏面に剥離が発生し、ここにたまった水分がはんだ
付け加熱時に爆発的に水蒸気化、膨張することに起因す
るといわれており、その対策として後硬化してのち、完
全に乾燥し、防湿梱包させて出荷する方法が採られてい
る。
The occurrence of cracks in the soldering process is
It is said that peeling occurs on the back surface of the package die pad between the post-curing and the mounting process, and the accumulated water vaporizes and expands explosively during soldering heating. A method is adopted in which after post-curing, the product is completely dried, moisture-proof packed and shipped.

【0006】封止用樹脂の改良も検討されてきた。例え
ば封止用樹脂にゴム成分を配合し、内部応力を低下させ
る方法、充填剤を高充填し線膨張係数を低下させる方法
などがある(特開昭63−189421号公報、特開昭
63−16445号公報)。充填剤表面をカップリング
剤で処理し、樹脂と充填剤の界面の密着性を向上させ、
強度を上げる方法が提案されている(特開昭61−22
1222号公報)。
Improvements in sealing resins have also been investigated. For example, there is a method in which a rubber component is mixed with a sealing resin to reduce the internal stress, a method in which a filler is highly filled to reduce the linear expansion coefficient (JP-A-63-189421, JP-A-63-63421). 16445 publication). The surface of the filler is treated with a coupling agent to improve the adhesiveness at the interface between the resin and the filler.
A method of increasing the strength has been proposed (Japanese Patent Laid-Open No. 61-22).
1222).

【0007】[0007]

【発明が解決しようとする課題】上記従来方法におい
て、防湿梱包する方法は製品の取扱作業が煩雑となり、
製造コストが上昇する。
In the above-mentioned conventional method, the moisture-proof packaging method requires complicated product handling,
Manufacturing cost rises.

【0008】また、各種方法で改良された封止用樹脂
も、それぞれ少しずつ効果をあげてきているが、実装技
術の進歩に伴う、より高度なはんだ耐熱要求に応えるに
は充分でない。例えばゴム成分の添加による低応力化
は、表面実装第2世代であるTSOP、TQFPパッケ
ージにはなお不十分であり、ゴム成分を配合することは
曲げ強度の低下を招き、はんだ耐熱性が低下する。充填
剤を高充填する方法では、破砕シリカを用いた場合には
流動性の低下を招き、成形が困難になり、球状シリカの
使用は強度低下を招くといった欠点がある。また、充填
剤表面をカップリング剤で処理することによる効果も要
求に応えるには充分でない。
Further, the encapsulating resins improved by various methods have been gradually effective, but they are not sufficient to meet the higher soldering heat resistance requirements accompanying the progress of mounting technology. For example, lowering the stress by adding a rubber component is still insufficient for the surface mounting second generation TSOP and TQFP packages, and compounding a rubber component causes a decrease in bending strength and a decrease in solder heat resistance. .. The method of highly filling the filler has a drawback that when crushed silica is used, the fluidity is reduced, molding becomes difficult, and the use of spherical silica causes a reduction in strength. Further, the effect of treating the surface of the filler with the coupling agent is not sufficient to meet the demand.

【0009】本発明の目的は、上記問題点を解決し、は
んだ耐熱性に優れ、低応力、低吸水で密着性、成形性に
優れた半導体封止用樹脂組成物を提供することにある。
An object of the present invention is to solve the above problems and provide a resin composition for semiconductor encapsulation which has excellent solder heat resistance, low stress, low water absorption, and excellent adhesion and moldability.

【0010】[0010]

【課題を解決するための手段】本発明者らは上記問題点
を解決するために鋭意研究を行った結果、低吸水性硬化
剤を使用し、充填用シリカを高密度に充填させることに
より、上記問題点を解決できるという知見に基づき本発
明を完成するに至った。
Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that a low water-absorption curing agent is used and the filling silica is filled at a high density. The present invention has been completed based on the finding that the above problems can be solved.

【0011】すなわち本発明は、(a)エポキシ樹脂1
00重量部、(b)充填用シリカ300〜2000重量
部、(c)下記一般式(1)
That is, the present invention relates to (a) epoxy resin 1
00 parts by weight, (b) 300 to 2000 parts by weight of silica for filling, (c) the following general formula (1)

【化2】 で表される硬化剤20〜100重量部を必須の成分とす
ることを特徴とする半導体封止用樹脂組成物である。
[Chemical 2] The resin composition for semiconductor encapsulation is characterized by containing 20 to 100 parts by weight of a curing agent represented by

【0012】低吸水性硬化剤を使用し、充填用シリカを
高充填することて、流動性を維持した上で線膨張率を低
下させ、さらに低粘度で低応力、低吸水で密着性に優
れ、耐はんだ性に優れた硬化物とすることができる。
By using a low water-absorbing curing agent and highly filling silica for filling, the linear expansion coefficient is lowered while maintaining the fluidity, and the viscosity is low, the stress is low, and the water absorption is excellent. A cured product having excellent solder resistance can be obtained.

【0013】本発明で使用するエポキシ樹脂としては、
o−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、ビスフェノールA型エポキ
シ樹脂、ビスフェノールF型エポキシ樹脂、ビフェニル
型エポキシ樹脂など公知のものが使用できる。
The epoxy resin used in the present invention includes:
Known compounds such as o-cresol novolac type epoxy resin, phenol novolac type epoxy resin, bisphenol A type epoxy resin, bisphenol F type epoxy resin, and biphenyl type epoxy resin can be used.

【0014】本発明による効果を最大限に引き出すため
には、粒径10μm以上の球状シリカと粒径10μm以
下の破砕シリカを併用することが好ましく、このときシ
リカの総量が、エポキシ樹脂100重量部に対して50
0重量部以上添加することが好ましい。また、粒径10
μm以上の球状シリカは、全充填用シリカの20〜80
%の範囲が好ましい。この範囲より少ないと流動性が低
下し、また、この範囲より多いと強度低下が起こり所望
の効果が得られない。
In order to maximize the effects of the present invention, it is preferable to use spherical silica having a particle size of 10 μm or more and crushed silica having a particle size of 10 μm or less, and the total amount of silica is 100 parts by weight of the epoxy resin. Against 50
It is preferable to add 0 part by weight or more. Also, the particle size 10
Spherical silica with a size of μm or more is 20 to 80 of the total filling silica.
% Range is preferred. If it is less than this range, the fluidity is lowered, and if it is more than this range, the strength is lowered and the desired effect cannot be obtained.

【0015】硬化剤としては、下記一般式(1)As the curing agent, the following general formula (1)

【化3】 で表される硬化剤を全量使用することが好ましいが、他
の硬化物と混合使用することもできる。他の硬化剤とし
ては、フェノールノボラック樹脂、酸無水物など公知の
ものが使用できる。この際上記一般式(1)で示す硬化
剤は、硬化剤の全量の30重量%以上添加することが好
ましい。これ以下では、吸水特性が悪化し、はんだ耐熱
性が低下する。また、エポキシ樹脂100重量部に対し
て、硬化剤は30〜80重量部、望ましくはエポキシ当
量とフェノール性水酸基当量の比率を1:0.8〜1.
2である。フェノール性水酸基当量の割合がこの範囲以
下であると、硬化性、強度、吸水特性が悪化し、はんだ
耐熱性が低下する。
[Chemical 3] It is preferable to use the entire amount of the curing agent represented by, but it is also possible to use it in combination with other cured products. As other curing agents, known ones such as phenol novolac resin and acid anhydride can be used. At this time, the curing agent represented by the general formula (1) is preferably added in an amount of 30% by weight or more based on the total amount of the curing agent. Below this, the water absorption characteristics deteriorate and the solder heat resistance decreases. Further, the curing agent is 30 to 80 parts by weight with respect to 100 parts by weight of the epoxy resin, and preferably the ratio of the epoxy equivalent and the phenolic hydroxyl group equivalent is 1: 0.8 to 1.
It is 2. When the ratio of the phenolic hydroxyl group equivalent is less than this range, curability, strength and water absorption properties are deteriorated and solder heat resistance is reduced.

【0016】本発明においては、エポキシ樹脂の硬化剤
の他に硬化促進剤を配合することができる。硬化促進剤
としては公知のものが使用できるが、好適な硬化促進剤
としては、例えばトリフェニルフォスフィン、イミダゾ
ール、1,8−ジアザビシクロ〔5,4,0〕ウンデセ
ン−1などがある。添加量は用いる硬化促進剤により異
なり、例えばトリフェニルフォスフィンでは、エポキシ
樹脂100重量部に対して0.2〜5重量部の範囲が好
ましい。
In the present invention, a curing accelerator can be blended in addition to the epoxy resin curing agent. Known curing accelerators can be used, and suitable curing accelerators include, for example, triphenylphosphine, imidazole, 1,8-diazabicyclo [5,4,0] undecene-1 and the like. The addition amount varies depending on the curing accelerator used, and for example, in the case of triphenylphosphine, the range is preferably 0.2 to 5 parts by weight with respect to 100 parts by weight of the epoxy resin.

【0017】また本発明の半導体封止用樹脂組成物に
は、必要に応じてOPワックス、カルバナワックスなど
の離型剤、γ−グリトキシプロピルトリメトキシシラン
などのカップリング剤、カーボンブラックなどの着色
剤、三酸化アンチモンなどの難燃剤を添加することもで
きる。
In the resin composition for semiconductor encapsulation of the present invention, if necessary, a release agent such as OP wax and carnauba wax, a coupling agent such as γ-glyoxypropyltrimethoxysilane, carbon black and the like. It is also possible to add a colorant, a flame retardant such as antimony trioxide.

【0018】本発明の半導体封止用樹脂組成物は、従来
公知の方法にしたがって混合、混練され、粉砕されたの
ち、加熱成形することによって半導体素子を封止した半
導体装置とすることができる。
The resin composition for semiconductor encapsulation of the present invention is mixed, kneaded, pulverized, and then heat-molded according to a conventionally known method to obtain a semiconductor device in which a semiconductor element is encapsulated.

【0019】[0019]

【実施例】以下に本発明の実施例を示し、本発明をさら
に詳しく説明する。 実施例1 o−クレゾールノボラック型エポキシ樹脂(YDCN−
702、東都化成社製;以下エポキシ樹脂Aとする)、
下記式(2)
EXAMPLES The present invention will be described in more detail below by showing Examples of the present invention. Example 1 o-cresol novolac type epoxy resin (YDCN-
702, manufactured by Tohto Kasei Co., Ltd .; hereinafter referred to as epoxy resin A),
Formula (2) below

【化4】 で表される硬化剤(以下硬化剤Aとする)、平均粒径2
1μmの球状溶融シリカ粉末、平均粒径6μmの破砕溶
融シリカ粉末、硬化促進剤(トリフェニルフォスフィ
ン)、その他の添加剤を表1に示す割合で混合したの
ち、ミキシングロールを用い、110℃で4分混練し、
冷却後粉砕し、封止用樹脂組成物を調製した。これらの
封止用樹脂組成物を用いて、スパイラルフローを測定し
た。また、同じ封止用樹脂組成物を用いて試験片を作成
し、曲げ強度、曲げ弾性率を測定した。さらに、84p
inICを成形し、ポストキュア後、85℃、85%の
高温恒湿機中で吸湿を24時間、48時間及び72時間
行った後、吸水率を測定し、超音波探傷装置でダイパッ
ト裏面の剥離を観察した後、260℃のはんだ浴に10
秒間浸漬させ、パッケージのクラックを観察した。これ
らの結果を表1に示す。
[Chemical 4] Curing agent represented by (hereinafter referred to as curing agent A), average particle size 2
After mixing 1 μm spherical fused silica powder, crushed fused silica powder having an average particle size of 6 μm, a curing accelerator (triphenylphosphine), and other additives in the proportions shown in Table 1, using a mixing roll at 110 ° C. Knead for 4 minutes,
After cooling, the mixture was pulverized to prepare a sealing resin composition. The spiral flow was measured using these sealing resin compositions. A test piece was prepared using the same sealing resin composition, and the bending strength and bending elastic modulus were measured. Furthermore, 84p
After molding inIC and post-curing, moisture absorption was performed for 24 hours, 48 hours and 72 hours in a high temperature and humidity chamber at 85 ° C and 85%, and then the water absorption rate was measured, and the back surface of the die pad was peeled off with an ultrasonic flaw detector. After observing the
It was immersed for 2 seconds, and the crack of the package was observed. The results are shown in Table 1.

【0020】表1に示した結果より、本発明の半導体封
止用樹脂組成物は、流動性、強度、密着性、吸水性、は
んだ耐熱性に優れていることがわかる。
From the results shown in Table 1, it can be seen that the resin composition for semiconductor encapsulation of the present invention is excellent in fluidity, strength, adhesion, water absorption and solder heat resistance.

【0021】実施例2 エポキシ樹脂A、下記式(3)Example 2 Epoxy resin A, the following formula (3)

【化5】 で表される硬化剤(以下硬化剤Bとする)、平均粒径2
1μmの球状溶融シリカ粉末、平均粒径6μmの破砕溶
融シリカ粉末、硬化促進剤(トリフェニルフォスフィ
ン)、その他の添加剤を表1に示す割合で混合したの
ち、実施例1と同様にして各物性を測定した。
[Chemical 5] Curing agent represented by (hereinafter referred to as curing agent B), average particle size 2
1 μm spherical fused silica powder, crushed fused silica powder having an average particle size of 6 μm, a curing accelerator (triphenylphosphine), and other additives were mixed in the proportions shown in Table 1 and then mixed in the same manner as in Example 1. The physical properties were measured.

【0022】実施例3 フェノールノボラック型エポキシ樹脂(YDPN−63
8、東都化成社製;以下エポキシ樹脂Bとする)、硬化
剤A、平均粒径21μmの球状溶融シリカ粉末、平均粒
径6μmの破砕溶融シリカ粉末、硬化促進剤(トリフェ
ニルフォスフィン)、その他の添加剤を表2に示す割合
で混合したのち、実施例1と同様にして各物性を測定し
た。
Example 3 Phenol novolac type epoxy resin (YDPN-63
8, manufactured by Toto Kasei Co., Ltd .; hereinafter referred to as epoxy resin B), curing agent A, spherical fused silica powder having an average particle size of 21 μm, crushed fused silica powder having an average particle size of 6 μm, curing accelerator (triphenylphosphine), etc. Each of the additives was mixed in the proportions shown in Table 2, and then the physical properties were measured in the same manner as in Example 1.

【0023】実施例4 エポキシ樹脂B、硬化剤B、平均粒径21μmの球状溶
融シリカ粉末、平均粒径6μmの破砕溶融シリカ粉末、
硬化促進剤(トリフェニルフォスフィン)、その他の添
加剤を表1に示す割合で混合したのち、実施例1と同様
にして各物性を測定した。
Example 4 Epoxy resin B, curing agent B, spherical fused silica powder having an average particle size of 21 μm, crushed fused silica powder having an average particle size of 6 μm,
After curing accelerator (triphenylphosphine) and other additives were mixed in the proportions shown in Table 1, each physical property was measured in the same manner as in Example 1.

【0024】比較例1 エポキシ樹脂A、フェノールノボラック硬化剤(PSF
−4224、群栄化学社製;以下硬化剤Cとする)、平
均粒径21μmの球状溶融シリカ粉末、平均粒径6μm
の破砕溶融シリカ粉末、硬化促進剤(トリフェニルフォ
スフィン)、その他の添加剤を表3に示す割合で混合し
たのち、実施例1と同様にして各物性を測定した。
Comparative Example 1 Epoxy resin A, phenol novolac curing agent (PSF
-4224, manufactured by Gunei Chemical Co., Ltd .; hereinafter referred to as curing agent C), spherical fused silica powder having an average particle size of 21 μm, average particle size of 6 μm
The crushed fused silica powder, the curing accelerator (triphenylphosphine), and the other additives were mixed in the proportions shown in Table 3, and then the physical properties were measured in the same manner as in Example 1.

【0025】比較例2 エポキシ樹脂B、硬化剤C、平均粒径21μmの球状溶
融シリカ粉末、平均粒径6μmの破砕溶融シリカ粉末、
硬化促進剤(トリフェニルフォスフィン)、その他の添
加剤を表3に示す割合で混合したのち、実施例1と同様
にして各物性を測定した。
Comparative Example 2 Epoxy resin B, curing agent C, spherical fused silica powder having an average particle size of 21 μm, crushed fused silica powder having an average particle size of 6 μm,
After curing accelerator (triphenylphosphine) and other additives were mixed in the proportions shown in Table 3, each physical property was measured in the same manner as in Example 1.

【0026】[0026]

【発明の効果】本発明の半導体封止用樹脂組成物によれ
ば、流動性を維持した上で、低応力、低吸水ではんだ耐
熱性に優れた硬化物を得ることができるので、これを用
いることにより、クラックの発生しない良好な半導体を
得ることができる。
According to the resin composition for semiconductor encapsulation of the present invention, it is possible to obtain a cured product having low stress, low water absorption and excellent solder heat resistance while maintaining fluidity. By using it, a good semiconductor without cracks can be obtained.

【表1】 [Table 1]

【表2】 [Table 2]

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (a)エポキシ樹脂100重量部、 (b)充填用シリカ300〜2000重量部、 (c)下記一般式(1) 【化1】 で表される硬化剤20〜100重量部を必須の成分とす
ることを特徴とする半導体封止用樹脂組成物。
1. (a) 100 parts by weight of epoxy resin, (b) 300 to 2000 parts by weight of silica for filling, (c) the following general formula (1) A resin composition for semiconductor encapsulation, comprising 20 to 100 parts by weight of a curing agent represented by as an essential component.
JP34808391A 1991-12-04 1991-12-04 Resin composition for sealing semiconductor Withdrawn JPH05160302A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34808391A JPH05160302A (en) 1991-12-04 1991-12-04 Resin composition for sealing semiconductor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34808391A JPH05160302A (en) 1991-12-04 1991-12-04 Resin composition for sealing semiconductor

Publications (1)

Publication Number Publication Date
JPH05160302A true JPH05160302A (en) 1993-06-25

Family

ID=18394632

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34808391A Withdrawn JPH05160302A (en) 1991-12-04 1991-12-04 Resin composition for sealing semiconductor

Country Status (1)

Country Link
JP (1) JPH05160302A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0749996A1 (en) * 1995-01-05 1996-12-27 Toray Industries, Inc. Epoxy resin composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0749996A1 (en) * 1995-01-05 1996-12-27 Toray Industries, Inc. Epoxy resin composition
EP0749996A4 (en) * 1995-01-05 2000-05-03 Toray Industries Epoxy resin composition

Similar Documents

Publication Publication Date Title
JPH07268186A (en) Epoxy resin composition
JPH062799B2 (en) Epoxy resin composition for semiconductor encapsulation
JPH04275325A (en) Resin composition for sealing semiconductor
JPH05160302A (en) Resin composition for sealing semiconductor
JPH1135797A (en) Epoxy resin composition for sealing semiconductor, and semiconductor device
JPH05206331A (en) Resin composition for sealing semiconductor
JP2002080694A (en) Epoxy resin composition and semiconductor device
JP3365065B2 (en) Epoxy resin composition for sealing
JP2003040981A (en) Epoxy resin composition and semiconductor device
JPH05105739A (en) Resin composition for sealing semiconductor
JPH05275572A (en) Semiconductor sealing resin composition
JPH04275324A (en) Resin composition for sealing semiconductor
JP3377911B2 (en) Epoxy resin composition
JPH1135793A (en) Epoxy resin composition and resin-sealed semiconductor device made by using the same
JPH05275571A (en) Semiconductor sealing resin composition
JP3317473B2 (en) Epoxy resin composition
JP2005179585A (en) Epoxy resin composition for use in sealing semiconductor, and semiconductor device
JP2004155841A (en) Sealing resin composition, and semiconductor sealing device
JP3032067B2 (en) Epoxy resin composition
JP3279084B2 (en) Epoxy resin composition for sealing
JP2000103836A (en) Epoxy resin composition and semiconductor device sealed therewith
JPH04275323A (en) Resin composition for sealing semiconductor
JPH04275322A (en) Resin composition for sealing semiconductor
JP2002128991A (en) Epoxy resin composition and semiconductor device
JPH07126490A (en) Epoxy resin composition

Legal Events

Date Code Title Description
A300 Withdrawal of application because of no request for examination

Free format text: JAPANESE INTERMEDIATE CODE: A300

Effective date: 19990311