JPH021184B2 - - Google Patents
Info
- Publication number
- JPH021184B2 JPH021184B2 JP13274782A JP13274782A JPH021184B2 JP H021184 B2 JPH021184 B2 JP H021184B2 JP 13274782 A JP13274782 A JP 13274782A JP 13274782 A JP13274782 A JP 13274782A JP H021184 B2 JPH021184 B2 JP H021184B2
- Authority
- JP
- Japan
- Prior art keywords
- silica
- particle size
- average particle
- filler
- less
- 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
Links
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 85
- 239000000377 silicon dioxide Substances 0.000 claims description 36
- 239000002245 particle Substances 0.000 claims description 20
- 239000000945 filler Substances 0.000 claims description 14
- 239000003822 epoxy resin Substances 0.000 claims description 12
- 229920000647 polyepoxide Polymers 0.000 claims description 12
- 238000005538 encapsulation Methods 0.000 claims description 9
- 239000005350 fused silica glass Substances 0.000 claims description 9
- 239000011342 resin composition Substances 0.000 claims description 9
- 239000004065 semiconductor Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 5
- 229910002026 crystalline silica Inorganic materials 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 238000010298 pulverizing process Methods 0.000 claims 1
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
Landscapes
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Description
[発明の技術分野]
本発明は成形時のバリが少なく、耐クラツク性
の良好な半導体封止用樹脂組成物に関する。
[発明の技術的背景とその問題点]
従来より半導体封止用に使用するエポキシ樹脂
組成物としては、エポキシ樹脂にフエノール樹
脂、酸無水物、アミン等の硬化剤を配合し、さら
に充填剤としてシリカやクレー等を配合したもの
が知られている。
このようなエポキシ樹脂組成物は、従来の、例
えばフエノール樹脂組成物等の一般的な熱硬化性
樹脂組成物に比較して、溶融時の粘度が極めて低
くて流動性がよいため、ICやトランジスタの微
細なパターンやワイヤの損傷を最少限に抑えるの
に有効であり、また耐湿性を初めとする諸特性が
良好であるという利点がある。
しかしながらこの良好な流動性のために封止成
形時にICやトランジスタのリード端子となるリ
ードフレームの部分に樹脂バリが付着し易く、後
のめつき工程に支障をきたし、またバリ取りの工
程を設けなければならないという欠点があつた。
また、最近ではパツケージ形状がより小形化、
薄形化する傾向にあり、成形時の樹脂バリが極め
て少ない材料が要求されているとともに、使用条
件がより厳しいものであつてもそれに適合する、
より信頼性の高い材料が必要となつてきている。
このバリ対策として、リードフレーム側に種々の
バリ止めのための加工を施したり、原料樹脂の粘
度を調整したり、充填剤への処理方法を種々検討
する等の方法が採用されてきたが、それぞれ耐湿
性、耐クラツク性との調和がとれていない等の欠
点があつた。
[発明の目的]
本発明者らはこのような欠点を解消すべく鋭意
研究を進めた結果、充填剤として用いるシリカの
結晶性と溶融性並びにその平均粒径とを調整する
ことにより耐湿性、耐クラツチ性および成形性の
優れたバランスのよい半導体封止用樹脂組成物が
得られることを見出した。
本発明はこのような知見に基づいてなされたも
ので、耐湿性、耐クラツチ性および成形性に優れ
た半導体封止用樹脂組成物を提供することを目的
とする。
[発明の概要]
すなわち本発明のエポキシ樹脂組成物は、エポ
キシ樹脂と充填剤とを主成分とする半導体封止用
樹脂組成物において、充填剤が平均粒径25〜35μ
(最大粒径80μ以下)の溶融シリカ(シリカAと
平均粒径10〜20μの溶融シリカ(シリカB)と平
均粒径5μ以下の結晶性シリカ(シリカC)とか
らなり、シリカAとシリカBの比率が4:1〜
3:2でシリカCの割合が充填剤中15〜30vol%
を占めるものであることを特徴とするものであ
る。
本発明に使用するエポキシ樹脂としては、特に
制限されるものではないが、ビスフエノール型エ
ポキシ樹脂、ノボラツク型エポキシ樹脂等があげ
られ、これらは酸無水物、フエノール樹脂、各種
アミン類およびこれらの混合物を硬化剤として用
いる。またエポキシ樹脂に他の熱硬化性樹脂を混
合することもできる。
本発明においては硬化促進剤として通常用いら
れる、例えばイミダゾール、第3級アミンを用い
ることができる。
本発明に使用する充填剤としては、平均粒径25
〜35μ(最大粒径80μ以下)の溶融シリカ(シリカ
A)と平均粒径10〜20μの溶融シリカ(シリカ
B)と平均粒径5μ以下の結晶性シリカ(シリカ
C)とを混合して使用する。シリカAとシリカB
の比率4:1〜3:2が適しており、シリカAが
この比率より大きいと粘度が低すぎるために樹脂
バリが多くなり耐クラツク性も悪くなる
また、シリカAがこの比率より小さいと封止材
料として粘度が高くなりすぎて特にフラツトパツ
ケージのようなゲートの隣接距離が小さいものに
使用する場合は、ワイヤ流れが多く信頼性を落す
ので好ましくない。
シリカAとシリカBの比率が上述の範囲にある
場合にのみパツケージ形状の小形化、薄形化に伴
うゲート寸法の縮少傾向による流れの促進と、高
集積化に伴うピン数の増加のためのリードフレー
ムの合理化による材料の流れ過ぎを防止すること
ができる。特にシリカBとして、湿式粉砕法によ
る溶融シリカを使用した場合には、同じ平均粒径
のものでも粒子のかどが取れたいわば球に近い多
面体になつている通常の乾式粉砕物とは異なり、
配合量を増大しても比較的粘度が低くなるという
利点がある。
本発明においてシリカCの配合割合は充填剤中
15〜30vol%を占める量が適しており、その理由
は、15vol%末満では樹脂バリが多くなり形成以
後の工程が多くなつて実用上好ましくないためで
あり、30vol%を越えると耐クラツク性が悪くな
り、クラツクの発生率が増大の傾向を示すことに
よる。
本発明においてはエポキシ樹脂、充填剤および
硬化剤、硬化促進剤をロール等により混練し、混
練後冷却して粉砕し使用に供される。
[発明の実施例]
次に本発明の実施例について説明する。
実施例 1
クレゾールノボラツク型エポキシ樹脂(エポキ
シ当量215、軟化点70℃)100重量部、フエノール
ノボラツク樹脂(軟化点85℃)50重量部、2メチ
ルイミダゾール1.2重量部、カルナウバワツクス
2.5重量部、充填剤としてシリカを表1の割合で
配合したものを合計量で380重量部とを約90℃の
ロール混練機で充分混練した後冷却して粉砕し、
4mmφ以下の成形材料を得た。
得られた成形材料について溶融粘度、ワイヤ流
れ、スパイラルフロー長、樹脂バリ長さ、耐クラ
ツク性を試験した。得られた結果を同表中に示
す。
なお表中の比較例の1〜3はシリカCの比率が
本発明の範囲外のものであり、比較例の4は平均
粒径が30μであるが、最大粒径が80μ以上のもの
を5%含む溶融シリカ(シリカD)を使用した例
であり、比較例の5と6はシリカBを配合しない
例である。
[Technical Field of the Invention] The present invention relates to a resin composition for semiconductor encapsulation that has less burrs during molding and has good crack resistance. [Technical background of the invention and its problems] Conventionally, epoxy resin compositions used for semiconductor encapsulation have been made by blending epoxy resin with a curing agent such as a phenol resin, an acid anhydride, or an amine, and then adding a filler as a filler. Products containing silica, clay, etc. are known. Such epoxy resin compositions have extremely low viscosity and good fluidity when melted compared to conventional thermosetting resin compositions such as phenolic resin compositions, so they are used in ICs and transistors. It is effective in minimizing damage to fine patterns and wires, and has the advantage of having good moisture resistance and other properties. However, due to this good fluidity, resin burrs tend to adhere to the parts of the lead frame that serve as lead terminals for ICs and transistors during sealing molding, which interferes with the subsequent plating process and requires a deburring process. There was a drawback that it had to be done. In addition, recently the package shape has become smaller,
The trend is for materials to become thinner, and there is a need for materials with extremely low resin burrs during molding, as well as materials that can meet even more severe usage conditions.
There is a growing need for more reliable materials.
To counter this burr, methods have been adopted such as applying various burr-preventing treatments to the lead frame side, adjusting the viscosity of the raw resin, and considering various methods of processing the filler. Each had drawbacks such as a lack of harmony with moisture resistance and crack resistance. [Purpose of the Invention] The present inventors have carried out intensive research in order to eliminate such drawbacks, and as a result, by adjusting the crystallinity and meltability of silica used as a filler, as well as its average particle size, moisture resistance, It has been found that a well-balanced resin composition for semiconductor encapsulation with excellent clutch resistance and moldability can be obtained. The present invention was made based on such knowledge, and an object of the present invention is to provide a resin composition for semiconductor encapsulation that has excellent moisture resistance, clutch resistance, and moldability. [Summary of the Invention] That is, the epoxy resin composition of the present invention is a semiconductor encapsulation resin composition containing an epoxy resin and a filler as main components, in which the filler has an average particle size of 25 to 35 μm.
Consisting of fused silica (silica A) with a maximum particle size of 80 μm or less, fused silica (silica B) with an average particle size of 10 to 20 μm, and crystalline silica (silica C) with an average particle size of 5 μm or less, silica A and silica B The ratio is 4:1~
3:2, the ratio of silica C is 15 to 30 vol% in the filler
It is characterized by the fact that it occupies the Epoxy resins used in the present invention include, but are not particularly limited to, bisphenol type epoxy resins, novolak type epoxy resins, etc. These include acid anhydrides, phenolic resins, various amines, and mixtures thereof. is used as a hardening agent. It is also possible to mix other thermosetting resins with the epoxy resin. In the present invention, commonly used curing accelerators such as imidazole and tertiary amine can be used. The filler used in the present invention has an average particle size of 25
Used by mixing fused silica (Silica A) with ~35μ (maximum particle size 80μ or less), fused silica (Silica B) with average particle size 10-20μ, and crystalline silica (Silica C) with average particle size 5μ or less do. Silica A and Silica B
A ratio of 4:1 to 3:2 is suitable; if silica A is larger than this ratio, the viscosity will be too low, resulting in more resin burrs and poor crack resistance.If silica A is smaller than this ratio, sealing This is not preferable as the viscosity becomes too high as a stopper material, especially when used in a flat package where the distance between adjacent gates is small, as it causes a lot of wire flow and reduces reliability. Only when the ratio of silica A and silica B is within the above range, flow is promoted due to the tendency of gate dimensions to decrease as the package shape becomes smaller and thinner, and the number of pins increases due to higher integration. By streamlining the lead frame, excessive flow of material can be prevented. In particular, when fused silica produced by wet milling is used as silica B, unlike ordinary dry milled silica, which has the same average particle size, the edges of the particles are removed and the particles become polyhedrons that are close to spheres.
It has the advantage that the viscosity is relatively low even when the amount of the compound is increased. In the present invention, the blending ratio of silica C in the filler is
An amount of 15 to 30 vol% is suitable.The reason for this is that at less than 15 vol%, resin burrs will increase and the number of steps after formation will increase, which is not practical, and if it exceeds 30 vol%, the crack resistance will deteriorate. This is because the occurrence rate of cracks is increasing. In the present invention, the epoxy resin, filler, curing agent, and curing accelerator are kneaded using a roll or the like, and after kneading, the product is cooled and pulverized for use. [Embodiments of the Invention] Next, embodiments of the present invention will be described. Example 1 100 parts by weight of cresol novolac type epoxy resin (epoxy equivalent 215, softening point 70°C), 50 parts by weight of phenol novolak resin (softening point 85°C), 1.2 parts by weight of 2-methylimidazole, carnauba wax
A total of 380 parts by weight of 2.5 parts by weight and silica as a filler in the proportions shown in Table 1 were sufficiently kneaded in a roll kneader at about 90°C, then cooled and pulverized.
A molding material with a diameter of 4 mm or less was obtained. The obtained molding material was tested for melt viscosity, wire flow, spiral flow length, resin burr length, and crack resistance. The obtained results are shown in the same table. In addition, Comparative Examples 1 to 3 in the table have a silica C ratio outside the range of the present invention, and Comparative Example 4 has an average particle size of 30μ, but those with a maximum particle size of 80μ or more are % of fused silica (silica D), and Comparative Examples 5 and 6 are examples in which silica B is not blended.
【表】
第1表の試験結果からわかるように、平均粒径
5μ以下の結晶性シリカをシリカの全量のうち
30vol%を越えて使用するとスパイラルフロー長
は極めて小さくなると同時に、クラツクの発生率
は極めて大きくなることがわかる。また15vol%
未満ではクラツク発生は少ないがバリが多く、実
使用時には種々の問題が発生する。
また比較例の4〜6のものは、いずれも実施例
に比較して溶融粘度は低いがその割にワイヤ流れ
が大きくなり、バリが長くなることがわかる。
実施例 2
シリカCの配合割合は実施例1のサンプルと同
じように固定し、シリカAとシリカBとの配合割
合のみ表2のように変えて同様にテストした。結
果を同表中に示す。[Table] As can be seen from the test results in Table 1, the average particle size
Crystalline silica with a size of 5 μ or less is included in the total amount of silica.
It can be seen that when more than 30 vol% is used, the spiral flow length becomes extremely small, and at the same time, the crack occurrence rate becomes extremely large. Also 15vol%
If it is less than that, there will be less cracking, but there will be more burrs, and various problems will occur during actual use. It can also be seen that Comparative Examples 4 to 6 all have lower melt viscosities than Examples, but the wire flow becomes larger and the burrs become longer. Example 2 The mixing ratio of silica C was fixed as in the sample of Example 1, and only the mixing ratio of silica A and silica B was changed as shown in Table 2, and tests were conducted in the same manner. The results are shown in the same table.
【表】
第2表から明らかなように、シリカAの配合割
合が大きいと溶融粘度が低くなるがバリが多くな
り、逆にシリカBが多すぎると粘度が高くなりす
ぎ、ワイヤ流れが大きくなりすぎて実用的ではな
い。
[発明の効果]
以上説明したように本発明の半導体封止用樹脂
組成物は、成形し易いうえにバリの発生が少な
く、また耐クラツク性にも優れている。[Table] As is clear from Table 2, if the blending ratio of silica A is high, the melt viscosity will be low, but there will be more burrs, and conversely, if the blending ratio of silica B is too high, the viscosity will become too high and the wire flow will increase. It's too impractical. [Effects of the Invention] As explained above, the resin composition for semiconductor encapsulation of the present invention is easy to mold, generates few burrs, and has excellent crack resistance.
Claims (1)
体封止用樹脂組成物において、充填剤が平均粒径
25〜35μ(最大粒径80μ以下)の溶融シリカ(シリ
カA)と平均粒径10〜20μの溶融シリカ(シリカ
B)と平均粒径5μ以下の結晶性シリカ(シリカ
C)とからなり、シリカAとシリカBの比率が
4:1〜3:2でシリカCの割合が充填剤中15〜
30vol%を占めるものであることを特徴とする半
導体封止用樹脂組成物。 2 シリカBの溶融シリカは湿式粉砕法により得
られるものである特許請求の範囲第1項記載の半
導体封止用樹脂組成物。[Scope of Claims] 1. In a resin composition for semiconductor encapsulation containing an epoxy resin and a filler as main components, the filler has an average particle size of
It consists of fused silica (Silica A) with an average particle size of 25 to 35μ (maximum particle size 80μ or less), fused silica (Silica B) with an average particle size of 10 to 20μ, and crystalline silica (Silica C) with an average particle size of 5μ or less. The ratio of A and silica B is 4:1 to 3:2, and the proportion of silica C is 15 to 15 in the filler.
A resin composition for semiconductor encapsulation, characterized in that it accounts for 30 vol%. 2. The resin composition for semiconductor encapsulation according to claim 1, wherein the fused silica of silica B is obtained by a wet pulverization method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13274782A JPS5922955A (en) | 1982-07-29 | 1982-07-29 | Resin composition for sealing semiconductor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13274782A JPS5922955A (en) | 1982-07-29 | 1982-07-29 | Resin composition for sealing semiconductor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5922955A JPS5922955A (en) | 1984-02-06 |
| JPH021184B2 true JPH021184B2 (en) | 1990-01-10 |
Family
ID=15088633
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13274782A Granted JPS5922955A (en) | 1982-07-29 | 1982-07-29 | Resin composition for sealing semiconductor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5922955A (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS627143A (en) * | 1985-07-04 | 1987-01-14 | Sumitomo Bakelite Co Ltd | Epoxy resin molding material for sealing semiconductor |
| JPS6261350A (en) * | 1985-09-11 | 1987-03-18 | Toshiba Chem Corp | Resin-sealed type semiconductor device |
| JPS62128159A (en) * | 1985-11-29 | 1987-06-10 | Hitachi Ltd | High integration lsi plastic package |
| JPS62149743A (en) * | 1985-12-25 | 1987-07-03 | Sumitomo Bakelite Co Ltd | Epoxy resin molding material for use in sealing semiconductor |
| JPS63160256A (en) * | 1986-12-23 | 1988-07-04 | Nitto Electric Ind Co Ltd | Manufacture of semiconductor device |
| JPS6462362A (en) * | 1987-09-03 | 1989-03-08 | Seitetsu Kagaku Co Ltd | Filler and polymer composition containing same |
| JPH01161065A (en) * | 1987-12-18 | 1989-06-23 | Tokuyama Soda Co Ltd | Silica and its production |
| JPH07103263B2 (en) * | 1988-04-15 | 1995-11-08 | 新日鐵化学株式会社 | Silica for filling sealing resin |
| JPH0645740B2 (en) * | 1989-03-01 | 1994-06-15 | 信越化学工業株式会社 | Epoxy resin composition for semiconductor encapsulation |
| JPH062569B2 (en) * | 1990-12-31 | 1994-01-12 | 住友精化株式会社 | Silica fine powder |
| JPH0726120A (en) * | 1993-09-22 | 1995-01-27 | Nitto Denko Corp | Semiconductor encapsulation equipment |
| JPH08239557A (en) * | 1996-02-15 | 1996-09-17 | Nitto Denko Corp | Semiconductor encapsulation equipment |
| JP2922151B2 (en) * | 1996-02-15 | 1999-07-19 | 日東電工株式会社 | Semiconductor sealing device |
| JP5167567B2 (en) * | 2001-06-27 | 2013-03-21 | 住友ベークライト株式会社 | Epoxy resin composition and semiconductor device |
-
1982
- 1982-07-29 JP JP13274782A patent/JPS5922955A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5922955A (en) | 1984-02-06 |
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