JPH07161879A - Resin composition for sealing semiconductor - Google Patents
Resin composition for sealing semiconductorInfo
- Publication number
- JPH07161879A JPH07161879A JP5308392A JP30839293A JPH07161879A JP H07161879 A JPH07161879 A JP H07161879A JP 5308392 A JP5308392 A JP 5308392A JP 30839293 A JP30839293 A JP 30839293A JP H07161879 A JPH07161879 A JP H07161879A
- Authority
- JP
- Japan
- Prior art keywords
- inorganic filler
- resin
- resin composition
- molding
- weight
- 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
Links
- 239000004065 semiconductor Substances 0.000 title claims abstract description 20
- 239000011342 resin composition Substances 0.000 title claims abstract description 19
- 238000007789 sealing Methods 0.000 title description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000011256 inorganic filler Substances 0.000 claims abstract description 23
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 23
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 12
- 239000003822 epoxy resin Substances 0.000 claims abstract description 10
- 229920003986 novolac Polymers 0.000 claims abstract description 10
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000002245 particle Substances 0.000 claims description 17
- 238000005538 encapsulation Methods 0.000 claims description 10
- 238000000465 moulding Methods 0.000 abstract description 7
- 229920005989 resin Polymers 0.000 abstract description 7
- 239000011347 resin Substances 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 6
- 230000002349 favourable effect Effects 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 5
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 238000001721 transfer moulding Methods 0.000 description 3
- 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 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229920003261 Durez Polymers 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 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
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910002026 crystalline silica Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 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 1
- 238000010438 heat treatment Methods 0.000 description 1
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は薄肉部の成形性に優れた
高信頼性の半導体封止用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 a highly reliable resin composition for semiconductor encapsulation which is excellent in moldability of a thin portion.
【0002】[0002]
【従来の技術】トランジスター、IC、LSI等の半導
体素子の封止には、エポキシ樹脂のトランスファー成形
による方法が低コスト、大量生産に適した方法として採
用され信頼性の面でもエポキシ樹脂の日進月歩の改良に
より十分使用に耐えるレベルにある。一方エレクトロニ
クス製品の軽薄短小化の流れの中で半導体パッケージは
薄型化小型化が年々進み、ICカード、メモリーカー
ド、液晶デバイスに見られる薄型製品へ搭載するため
に、パッケージの厚みが重要な特性となってきた。半導
体パッケージの厚みとして1.0mmから0.5mmの
ものが、今後ますます必要となってきており半導体封止
用樹脂として薄肉部の充填性にすぐれることが必要不可
欠である。例えば0.5mm厚のパッケージの場合、チ
ップが200μm厚、リードフレームが150μm厚と
すると樹脂封止厚は僅か150μm分しかない。従来、
薄肉部の充填性を解決するために最大粒径74μmの球
状シリカを用いる方法があるが、1.0mm以下の薄型
パッケージに対しては十分ではなくなってきた。これは
粒度分布が不適当のためボイド、未充填、ワイヤー流
れ、パッドシフトといった問題が発生していた。2. Description of the Related Art For molding semiconductor elements such as transistors, ICs and LSIs, transfer molding of epoxy resin is adopted as a method suitable for low cost and mass production. It is at a level that can be used sufficiently by improvement. On the other hand, in the trend of lighter, thinner, shorter and smaller electronic products, semiconductor packages are becoming thinner and smaller year by year, and package thickness is an important characteristic for mounting on thin products found in IC cards, memory cards and liquid crystal devices. It's coming. A semiconductor package having a thickness of 1.0 mm to 0.5 mm will be required more and more in the future, and it is indispensable that the resin for semiconductor encapsulation has excellent filling properties in a thin portion. For example, in the case of a 0.5 mm thick package, if the chip is 200 μm thick and the lead frame is 150 μm thick, the resin sealing thickness is only 150 μm. Conventionally,
There is a method of using spherical silica having a maximum particle diameter of 74 μm in order to solve the filling property of the thin portion, but it has become insufficient for a thin package of 1.0 mm or less. Due to the improper particle size distribution, problems such as voids, unfilling, wire flow, and pad shift occurred.
【0003】[0003]
【発明が解決しようとする課題】本発明は、かかる半導
体製品の成形時の充填性を解決するための半導体封止用
樹脂組成物を提供するものである。SUMMARY OF THE INVENTION The present invention provides a resin composition for semiconductor encapsulation for solving the filling property of such a semiconductor product at the time of molding.
【0004】[0004]
【課題を解決するための手段】本発明はエポキシ樹脂、
フェノールノボラック樹脂、硬化促進剤及び無機充填材
を必須成分とする樹脂組成物において、該無機充填材の
最大粒径が45μm以下、平均粒径が7〜30μmで、
全樹脂組成物中の70〜90重量%が無機充填材であ
り、かつ全無機充填材中の50重量%以上が球状シリカ
である半導体封止用樹脂組成物である。The present invention is an epoxy resin,
In a resin composition containing a phenol novolac resin, a curing accelerator, and an inorganic filler as essential components, the maximum particle size of the inorganic filler is 45 μm or less, and the average particle size is 7 to 30 μm.
In the resin composition for semiconductor encapsulation, 70 to 90 wt% of the total resin composition is an inorganic filler, and 50 wt% or more of the total inorganic filler is spherical silica.
【0005】本発明に用いられるエポキシ樹脂は通常の
半導体封止用樹脂組成物に用いられるものならばよく、
例えばクレゾールノボラック型エポキシ、三官能エポキ
シ、ビフェニル型二官能エポキシ、ビスフェノール型エ
ポキシ、臭素化エポキシ等が挙げられるが特に限定する
ものではない。これらのエポキシ樹脂は単独でも混合し
て用いてもよい。硬化剤のフェノールノボラック樹脂
は、通常の半導体封止用樹脂組成物に用いられるものな
らばよく、例えばフェノールノボラック型、クレゾール
ノボラック型、パラキシレン変性型、ジシクロペンタジ
エン型及びこれらの変性樹脂が挙げられるが、特に限定
するものでない。これらは単独または混合して用いても
よい。硬化促進剤はエポキシ基とフェノール性水酸基と
の反応を促進するものであればよく、一般に半導体封止
用樹脂組成物に使用されているものを広く使用すること
ができ、例えばベンジルジメチルアミン等の第3級アミ
ン類、イミダゾール類、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等の有機リン化合物等が
挙げられるが特に限定するものではない。これらは単独
でも混合して用いてもよい。The epoxy resin used in the present invention may be any one used in ordinary semiconductor encapsulating resin compositions,
Examples thereof include cresol novolac type epoxy, trifunctional epoxy, biphenyl type difunctional epoxy, bisphenol type epoxy, brominated epoxy and the like, but are not particularly limited. These epoxy resins may be used alone or in combination. The phenol novolac resin as the curing agent may be any one used in ordinary semiconductor encapsulating resin compositions, and examples thereof include phenol novolac type, cresol novolac type, paraxylene modified type, dicyclopentadiene type and modified resins thereof. However, it is not particularly limited. You may use these individually or in mixture. The curing accelerator may be any as long as it accelerates the reaction between the epoxy group and the phenolic hydroxyl group, and those generally used in the resin composition for semiconductor encapsulation can be widely used, such as benzyldimethylamine. Examples thereof include tertiary amines, imidazoles, organic phosphorus compounds such as 1,8-diazabicycloundecene, and triphenylphosphine, but are not particularly limited. These may be used alone or in combination.
【0006】本発明で用いられる無機充填材は、全無機
充填材中の50重量%以上が球状シリカであり、残余は
結晶シリカ、溶融シリカ、アルミナの3種類のいづれで
もよく、これらは単独または混合して用いてもよい。無
機充填材の最大粒径は45μm以下で、平均粒径は7〜
30μmが必須であり、最大粒径が45μmを越えると
薄肉部の充填性に劣り、未充填やボイドが発生する。本
発明での最大粒径45μm以下とは、湿式粒度で45μ
m未満が98.0重量%以上、45〜74μmが2.0
重量%以下、74μm以上は0重量%ものと定義する。
湿式粒度とは25gのシリカを500ccの水に均一に
分散させ、均一なメッシュをもった篩上に流し、篩上に
残ったシリカの重量%を測定する方法である。無機充填
材の平均粒径は7〜30μmであり、この範囲から外れ
ると流動性が著しく劣り、スパイラルフローが低下し、
またボイドが発生しやすくなる。全組成物中の無機充填
材の含有量は70〜90重量%であり、70重量%未満
だと樹脂分が多くなり吸湿が高くなるため耐湿信頼性が
劣化する。90重量%を越えると、樹脂分があまりに少
なくなり成形時の流動性が低下する。全無機充填材中の
球状シリカは50重量%以上含むことが必須であり、5
0重量%未満だと成形時の流動性が著しく低下する。In the inorganic filler used in the present invention, 50% by weight or more of the total inorganic filler is spherical silica, and the balance may be any of three kinds of crystalline silica, fused silica and alumina, which may be used alone or. You may mix and use it. The maximum particle size of the inorganic filler is 45 μm or less, and the average particle size is 7 to
30 μm is indispensable, and if the maximum particle size exceeds 45 μm, the filling property of the thin portion is poor and unfilling or voids occur. The maximum particle size of 45 μm or less in the present invention means a wet particle size of 45 μm.
Less than m is 98.0% by weight or more and 45 to 74 μm is 2.0
Weight% or less and 74 μm or more are defined as 0% by weight.
The wet particle size is a method in which 25 g of silica is uniformly dispersed in 500 cc of water, and the silica is allowed to flow on a sieve having a uniform mesh, and the weight% of silica remaining on the sieve is measured. The average particle size of the inorganic filler is 7 to 30 μm, and if it deviates from this range, the fluidity is remarkably inferior and the spiral flow is lowered.
In addition, voids are likely to occur. The content of the inorganic filler in the entire composition is 70 to 90% by weight. If the content is less than 70% by weight, the resin content increases and moisture absorption increases, so that the moisture resistance reliability deteriorates. If it exceeds 90% by weight, the resin content becomes too small and the fluidity at the time of molding is lowered. It is essential that the spherical silica in the total inorganic filler contains 50% by weight or more.
If it is less than 0% by weight, the fluidity at the time of molding remarkably decreases.
【0007】本発明はエポキシ樹脂、フェノールノボラ
ック樹脂、硬化促進剤及び無機充填材を必須成分とする
が、これ以外に必要に応じてシランカップリング剤、三
酸化アンチモン、ヘキサブロモ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
支えない。また、本発明の封止用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、フェノールノボラ
ック樹脂、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。In the present invention, an epoxy resin, a phenol novolac resin, a curing accelerator and an inorganic filler are essential components. In addition to these, a silane coupling agent, antimony trioxide, hexabromobenzene and other flame retardants may be added if necessary. , Carbon black, colorants such as red iron oxide, natural wax,
A release agent such as a synthetic wax and various additives such as a low stress additive such as silicone oil and rubber may be appropriately blended. Further, in order to produce the encapsulating resin composition of the present invention as a molding material, after the epoxy resin, the phenol novolac resin, the curing accelerator, the inorganic filler, and other additives are sufficiently uniformly mixed by a mixer or the like. Further, it can be melt-kneaded with a hot roll or a kneader, cooled, and then pulverized to obtain a sealing material.
【0008】以下本発明を実施例で示す。配合割合は重
量部で示す。 実施例1 ビフェニル型エポキシ樹脂(油化シェル(株)、YX−4000H、エポキシ 当量190、軟化点170℃) 90重量部 臭素化エポキシ樹脂(日本化薬(株)、BREN、エポキシ当量270、軟化 点70℃) 10重量部 フェノールノボラック樹脂(住友デュレズ(株)、PRシリーズ、水酸基当量 104、軟化点80℃) 47重量部 球状シリカA(最大粒径45μ、平均粒径15μ) 500重量部 溶融シリカA(最大粒径30μ、平均粒径5μ) 100重量部 トリフェニルホスフィン(北興化学(株)) 2重量部 γ−グリシドキシプロピルトリメトキシシラン(日本ユニカー(株)、 A−187)(以下エポキシシランという) 4重量部 三酸化アンチモン 10重量部 カルナバワックス 3重量部 カーボンブラック 2重量部 を常温で十分に混合し、次に80〜100℃で二軸熱ロ
ールを用いて混練し冷却後粉砕してタブレット化し半導
体封止用樹脂組成物を得た。この材料をトランスファー
成形機を用いて175℃、注入圧120kg/cm2で
成形し評価用のテストピースを得た。評価結果を表1に
示す。The present invention will be shown below with reference to examples. The blending ratio is shown in parts by weight. Example 1 Biphenyl type epoxy resin (Yuka Kagaku Co., Ltd., YX-4000H, epoxy equivalent 190, softening point 170 ° C.) 90 parts by weight Brominated epoxy resin (Nippon Kayaku Co., Ltd., BREN, epoxy equivalent 270, softening) Point 70 ° C) 10 parts by weight Phenol novolac resin (Sumitomo Durez Co., Ltd., PR series, hydroxyl group equivalent 104, softening point 80 ° C) 47 parts by weight Spherical silica A (maximum particle size 45μ, average particle size 15μ) 500 parts by weight Melt Silica A (maximum particle size 30 μ, average particle size 5 μ) 100 parts by weight Triphenylphosphine (Kitako Chemical Co., Ltd.) 2 parts by weight γ-glycidoxypropyltrimethoxysilane (Nippon Unicar Co., Ltd., A-187) ( Hereinafter referred to as epoxysilane) 4 parts by weight Antimony trioxide 10 parts by weight Carnauba wax 3 parts by weight Carbon black 2 parts by weight The parts were thoroughly mixed at room temperature, then kneaded at 80 to 100 ° C. using a biaxial heating roll, cooled, pulverized and tableted to obtain a resin composition for semiconductor encapsulation. This material was molded using a transfer molding machine at 175 ° C. and an injection pressure of 120 kg / cm 2 to obtain a test piece for evaluation. The evaluation results are shown in Table 1.
【0009】評価方法 スパラルフロー:EMMI法に準ずる。 0.5mm厚パッケージ充填性:模擬素子を入れた52
pQFP(14×14×0.5mm、チップ6×6×
0.23mm、リードフレーム厚0.15mm)で17
5℃にてトランスファー成形し樹脂の充填性を判定。 耐湿信頼性不良率:模擬素子を入れた52pQFP(1
4×14×1.0mm、チップ6×6×0.30mm)
を用い、リフロー処理(85℃、85%RHで、72H
r吸湿処理後、240℃のリフロー処理)後、125
℃、2.3気圧のPCT試験で500Hr処理後のAl
配線不良の発生数で判定。 実施例2 表1の配合により実施例1と同様にして半導体封止用樹
脂組成物を得た。評価結果を表1に示す。 比較例1〜5 表1の配合により実施例1と同様にして半導体封止用樹
脂組成物を得た。評価結果を表1に示す。Evaluation method Sparral flow: According to the EMMI method. Fillability of 0.5 mm thick package: 52 with simulated element
pQFP (14 x 14 x 0.5 mm, chip 6 x 6 x
0.23 mm, lead frame thickness 0.15 mm) 17
Transfer molding is performed at 5 ° C and the filling property of the resin is judged. Moisture resistance reliability failure rate: 52pQFP (1
4 x 14 x 1.0 mm, chip 6 x 6 x 0.30 mm)
Reflow treatment (85 ° C, 85% RH, 72H
After moisture absorption treatment, 240 ° C reflow treatment), then 125
Al after 500hr treatment by PCT test at 2.3 ° C at 2.3 ° C
Judgment is based on the number of wiring defects. Example 2 A resin composition for semiconductor encapsulation was obtained in the same manner as in Example 1 except that the formulation shown in Table 1 was used. The evaluation results are shown in Table 1. Comparative Examples 1 to 5 Using the formulations shown in Table 1, a resin composition for semiconductor encapsulation was obtained in the same manner as in Example 1. The evaluation results are shown in Table 1.
【0010】[0010]
【表1】 [Table 1]
【0011】[0011]
【発明の効果】本発明の半導体封止用樹脂組成物は、薄
肉部の成形性に優れておりパッケージ厚みが0.5〜
1.0mmの薄型パッケージの充填性が良好で、ボイ
ド、未充填、ワイヤー流れおよびパッドシフトの発生が
なく高信頼性の半導体パッケージを得ることができる。The resin composition for semiconductor encapsulation of the present invention is excellent in moldability of the thin portion and has a package thickness of 0.5 to 0.5.
A 1.0 mm thin package has a good filling property, and a highly reliable semiconductor package can be obtained without generation of voids, unfilling, wire flow and pad shift.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C08L 63/00 NLD ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location C08L 63/00 NLD
Claims (1)
脂、硬化促進剤及び無機充填材を必須成分とする樹脂組
成物において、該無機充填材の最大粒径が45μm以
下、平均粒径が7〜30μmで、全樹脂組成物中の70
〜90重量%が無機充填材であり、かつ全無機充填材中
の50重量%以上が球状シリカであることを特徴とする
半導体封止用樹脂組成物。1. A resin composition comprising an epoxy resin, a phenol novolac resin, a curing accelerator, and an inorganic filler as essential components, wherein the inorganic filler has a maximum particle size of 45 μm or less and an average particle size of 7 to 30 μm. 70 in total resin composition
A resin composition for semiconductor encapsulation, characterized in that ˜90 wt% is an inorganic filler, and 50 wt% or more of the total inorganic filler is spherical silica.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5308392A JPH07161879A (en) | 1993-12-08 | 1993-12-08 | Resin composition for sealing semiconductor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5308392A JPH07161879A (en) | 1993-12-08 | 1993-12-08 | Resin composition for sealing semiconductor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07161879A true JPH07161879A (en) | 1995-06-23 |
Family
ID=17980516
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5308392A Pending JPH07161879A (en) | 1993-12-08 | 1993-12-08 | Resin composition for sealing semiconductor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07161879A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000068419A (en) * | 1998-08-19 | 2000-03-03 | Toray Ind Inc | Semiconductor device |
| JP2013183528A (en) * | 2012-03-01 | 2013-09-12 | Sumitomo Bakelite Co Ltd | Rotor and motor car |
| JP2016079344A (en) * | 2014-10-21 | 2016-05-16 | 信越化学工業株式会社 | Thermosetting epoxy resin composition for primary sealing of photocoupler and optical semiconductor device |
-
1993
- 1993-12-08 JP JP5308392A patent/JPH07161879A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000068419A (en) * | 1998-08-19 | 2000-03-03 | Toray Ind Inc | Semiconductor device |
| JP2013183528A (en) * | 2012-03-01 | 2013-09-12 | Sumitomo Bakelite Co Ltd | Rotor and motor car |
| JP2016079344A (en) * | 2014-10-21 | 2016-05-16 | 信越化学工業株式会社 | Thermosetting epoxy resin composition for primary sealing of photocoupler and optical semiconductor device |
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