JP2000281869A - Epoxy resin composition and semiconductor device - Google Patents

Epoxy resin composition and semiconductor device

Info

Publication number
JP2000281869A
JP2000281869A JP8783699A JP8783699A JP2000281869A JP 2000281869 A JP2000281869 A JP 2000281869A JP 8783699 A JP8783699 A JP 8783699A JP 8783699 A JP8783699 A JP 8783699A JP 2000281869 A JP2000281869 A JP 2000281869A
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
weight
storage characteristics
semiconductor device
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
JP8783699A
Other languages
Japanese (ja)
Inventor
Masakatsu Maeda
将克 前田
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 JP8783699A priority Critical patent/JP2000281869A/en
Publication of JP2000281869A publication Critical patent/JP2000281869A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain an epoxy resin composition for sealing a semiconductor excellent in storage characteristics at high temperatures and further balance between the storage characteristics at the high temperatures with flame retardance. SOLUTION: The characteristic of this epoxy resin composition is to comprise (A) an epoxy resin, (B) a phenol resin, (C) a zeolite having 3-20 Å pore diameter and 0.1-0.4 cm3/g pore volume in an amount of 0.1-5 wt.% in the whole epoxy resin composition, (D) bismuth oxide in an amount of 0.1-5 wt.% based on the whole epoxy resin composition, (E) a bromine compound, (F) an inorganic filler and (G) a curing accelerator as essential components and further to have 0.1-1.5 wt.% content of bromine in the bromine compound.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、高温保管特性と難
燃性とのバランスに優れた半導体封止用エポキシ樹脂組
成物、及びこれを用いて半導体素子を封止してなる半導
体装置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 encapsulating a semiconductor having an excellent balance between high-temperature storage characteristics and flame retardancy, and a semiconductor device obtained by encapsulating a semiconductor element using the same. It is.

【0002】[0002]

【従来の技術】近年、IC、LSI等の半導体素子の封
止には、エポキシ樹脂組成物を用いた低圧封入法が一般
に用いられている。この樹脂組成物には難燃性が要求さ
れており、難燃性の付与のため、通常、臭素化合物と酸
化アンチモンとが配合されている。しかしながら、この
樹脂組成物で封止された半導体装置を高温下に保管した
場合、これらの難燃剤成分から熱分解した臭素化物が遊
離し、半導体素子の接合部の信頼性を損なうことが知ら
れている。ここで言う信頼性とは、この樹脂組成物で封
止された半導体装置を高温下(例えば185℃等)に放
置した後の半導体素子の接合部(ボンディングパッド
部)の信頼性のことである(以下、高温保管特性とい
う)。この高温保管特性を改善する手法としては、五酸
化二アンチモンを使用する方法(特開昭55−1469
50号公報)や、酸化アンチモンと有機ホスフィンとを
組み合わせる方法(特開昭61−53321号公報)等
が検討されているが、最近の半導体装置に対する高温保
管特性の要求水準には到達していないのが現状である。
2. Description of the Related Art In recent years, a low-pressure encapsulation method using an epoxy resin composition has been generally used for sealing semiconductor elements such as ICs and LSIs. This resin composition is required to have flame retardancy, and usually contains a bromine compound and antimony oxide for imparting flame retardancy. However, when a semiconductor device sealed with this resin composition is stored at a high temperature, it is known that brominated products thermally decomposed from these flame retardant components are liberated, which impairs the reliability of the junction of the semiconductor element. ing. The term “reliability” as used herein refers to the reliability of a bonding portion (bonding pad portion) of a semiconductor element after the semiconductor device sealed with the resin composition is left at a high temperature (for example, 185 ° C.). (Hereinafter referred to as high-temperature storage characteristics). As a method for improving the high-temperature storage characteristics, a method using diantimony pentoxide (JP-A-55-1469) is used.
No. 50) and a method of combining antimony oxide with an organic phosphine (Japanese Patent Application Laid-Open No. 61-53321) have been studied, but have not yet reached the required level of high-temperature storage characteristics for recent semiconductor devices. is the current situation.

【0003】[0003]

【発明が解決しようとする課題】本発明は、高温保管特
性と難燃性とのバランスに優れた半導体封止用エポキシ
樹脂組成物、及びこれを用いて半導体素子を封止してな
る半導体装置を提供するものである。
SUMMARY OF THE INVENTION The present invention relates to an epoxy resin composition for semiconductor encapsulation having an excellent balance between high-temperature storage characteristics and flame retardancy, and a semiconductor device using the same to encapsulate a semiconductor element. Is provided.

【0004】[0004]

【課題を解決するための手段】本発明は、(A)エポキ
シ樹脂、(B)フェノール樹脂、(C)全エポキシ樹脂
組成物中に0.1〜5重量%の細孔径3〜20オングス
トローム、空孔容積0.1〜0.4cm3/gのゼオラ
イト、(D)全エポキシ樹脂組成物中に0.1〜5重量
%の酸化ビスマス、(E)臭素化合物、(F)無機充填
材、及び(G)硬化促進剤を必須成分とし、臭素化合物
中の臭素量が0.1〜1.5重量%であることを特徴と
するエポキシ樹脂組成物、及びこれを用いて半導体素子
を封止してなる半導体装置である。
The present invention provides (A) an epoxy resin, (B) a phenolic resin, and (C) 0.1 to 5% by weight of the total epoxy resin composition having a pore size of 3 to 20 Å. A zeolite having a pore volume of 0.1 to 0.4 cm 3 / g, (D) 0.1 to 5% by weight of bismuth oxide in the total epoxy resin composition, (E) a bromine compound, (F) an inorganic filler, And (G) an epoxy resin composition comprising a curing accelerator as an essential component and a bromine content in the bromine compound of 0.1 to 1.5% by weight, and encapsulating a semiconductor element using the epoxy resin composition. Semiconductor device.

【0005】[0005]

【発明の実施の形態】本発明に用いるエポキシ樹脂は、
分子中にエポキシ基を有するものであれば特に限定しな
いが、例えば、オルソ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、トリフェ
ノールメタン型エポキシ樹脂、ビスフェノール型エポキ
シ樹脂、ビフェニル型エポキシ樹脂、スチルベン型エポ
キシ樹脂、ジシクロペンタジエン変性フェノール型エポ
キシ樹脂、ナフタレン型エポキシ樹脂等が挙げられ、こ
れらは単独でも混合して用いてもよい。樹脂組成物の硬
化性のためには、エポキシ当量は150〜300が望ま
しい。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The epoxy resin used in the present invention is:
There is no particular limitation as long as it has an epoxy group in the molecule, for example, orthocresol novolak type epoxy resin, phenol novolak type epoxy resin, triphenolmethane type epoxy resin, bisphenol type epoxy resin, biphenyl type epoxy resin, stilbene type An epoxy resin, a dicyclopentadiene-modified phenol type epoxy resin, a naphthalene type epoxy resin and the like can be mentioned, and these may be used alone or in combination. For the curability of the resin composition, the epoxy equivalent is desirably 150 to 300.

【0006】本発明に用いるフェノール樹脂は、分子中
にフェノール性水酸基を有するのもであれば特に限定し
ないが、例えば、フェノールノボラック樹脂、フェノー
ルアラルキル樹脂、テルペン変性フェノール樹脂、ジシ
クロペンタジエン変性フェノール樹脂、トリフェノール
メタン型樹脂等が挙げられ、これらは単独でも混合して
用いてもよい。樹脂組成物の硬化性のためには、水酸基
当量は80〜250が望ましい。
The phenolic resin used in the present invention is not particularly limited as long as it has a phenolic hydroxyl group in the molecule. Examples thereof include a phenol novolak resin, a phenol aralkyl resin, a terpene-modified phenol resin, and a dicyclopentadiene-modified phenol resin. And triphenolmethane type resins, and these may be used alone or in combination. For the curability of the resin composition, the hydroxyl equivalent is preferably from 80 to 250.

【0007】本発明に用いるゼオライトは、吸着剤とし
て用いられるものであれば特に限定しないが、天然物よ
りも、不純物の少ない合成物の方がより好ましい。又、
特性としては、細孔径3〜20オングストローム、空孔
容積0.1〜0.4cm3/gのものが好ましい。細孔
径が3オングストローム未満だと、モレキュラーシーブ
による吸着分子数の低下を招き、高温保管特性に必要な
吸着特性の効果が減少し、20オングストロームを越え
ると、細孔内に分子を保持しておくことができず、高温
保管特性に効果がないので好ましくない。又、空孔容積
が0.1未満だと高温保管特性に必要な吸着効果が少な
く、0.4cm3/gを越えると流動性の低下を招くお
それがあるので好ましくない。ゼオライトの配合量とし
ては、全樹脂組成物中に0.1〜5重量%が好ましい。
0.1重量%未満だと高温保管特性に対する効果が少な
く、5重量%を越えると封止材料特性として必要不可欠
な難燃性が満足されず、又、流動性が低下するので好ま
しくない。
[0007] The zeolite used in the present invention is not particularly limited as long as it is used as an adsorbent, but a synthetic product having less impurities is more preferable than a natural product. or,
As the characteristics, those having a pore diameter of 3 to 20 angstroms and a pore volume of 0.1 to 0.4 cm 3 / g are preferable. If the pore diameter is less than 3 angstroms, the number of adsorbed molecules is reduced by molecular sieves, and the effect of the adsorption properties required for high-temperature storage characteristics is reduced. This is not preferable because it has no effect on the high-temperature storage characteristics. On the other hand, if the pore volume is less than 0.1, the adsorbing effect required for high-temperature storage characteristics is small, and if it exceeds 0.4 cm 3 / g, the fluidity may decrease, which is not preferable. The blending amount of zeolite is preferably 0.1 to 5% by weight in the whole resin composition.
If it is less than 0.1% by weight, the effect on high-temperature storage characteristics is small, and if it exceeds 5% by weight, flame retardancy, which is indispensable as a sealing material characteristic, is not satisfied, and fluidity is undesirably reduced.

【0008】本発明に用いる酸化ビスマスは、硝酸ヒド
ロ塩である。これをゼオライトと併用することにより、
難燃剤として添加する臭素化合物に由来する臭素量を減
少できるので、高温保管特性と難燃性とのバランスが取
りやすくなり、更に高温保管特性も向上する。酸化ビス
マスの配合量としては、全エポキシ樹脂組成物中に0.
1〜5重量%が好ましい。0.1重量%未満だと高温保
管特性に影響を及ぼすイオン性不純物の吸着が不十分で
高温保管特性に対する効果が低く、5重量%を越えると
硬化性が低下するので好ましくない。
The bismuth oxide used in the present invention is a nitric acid hydrosalt. By using this with zeolite,
Since the amount of bromine derived from the bromine compound added as a flame retardant can be reduced, the balance between high-temperature storage characteristics and flame retardancy is easily achieved, and the high-temperature storage characteristics are further improved. The amount of bismuth oxide to be added is 0.1% in all epoxy resin compositions.
1-5% by weight is preferred. If the amount is less than 0.1% by weight, the adsorption of ionic impurities affecting the high-temperature storage characteristics is insufficient, and the effect on the high-temperature storage characteristics is low.

【0009】本発明に用いる臭素化合物としては、例え
ば、臭素化フェノールノボラック型エポキシ樹脂、臭素
化ビスフェノールA型エポキシ樹脂等が挙げられ、これ
らは単独でも混合して用いてもよい。臭素化エポキシ樹
脂の配合量としては、全樹脂組成物中に臭素量として
0.1〜1.5重量%で、より好ましいのは0.1〜
1.2重量%である。エポキシ当量としては、200〜
450がより好ましい。
As the bromine compound used in the present invention, for example, brominated phenol novolak type epoxy resin, brominated bisphenol A type epoxy resin and the like can be mentioned, and these may be used alone or in combination. The amount of the brominated epoxy resin is from 0.1 to 1.5% by weight, more preferably from 0.1 to 1.5% by weight, based on the total resin composition.
1.2% by weight. Epoxy equivalent, 200 ~
450 is more preferred.

【0010】本発明に用いる無機充填材の種類は特に制
限はなく、一般に封止材料に用いられているものを使用
することができる。例えば、溶融破砕シリカ粉末、溶融
球状シリカ粉末、結晶シリカ粉末、アルミナ、チタンホ
ワイト、水酸化アルミニウム、タルク、クレー、ガラス
繊維等が挙げられる。
[0010] The kind of the inorganic filler used in the present invention is not particularly limited, and those generally used for a sealing material can be used. For example, fused silica powder, fused spherical silica powder, crystalline silica powder, alumina, titanium white, aluminum hydroxide, talc, clay, glass fiber and the like can be mentioned.

【0011】本発明に用いる硬化促進剤は、エポキシ樹
脂とフェノール樹脂の反応を促進できるものであれば特
に限定しないが、例えば、1,8−ジアザビシクロ
(5,4,0)ウンデセン−7、トリブチルアミン等の
アミン化合物、トリフェニルホスフィン、テトラフェニ
ルホスフォニウム・テトラフェニルボレート塩等の有機
リン系化合物、2−メチルイミダゾール等のイミダゾー
ル化合物等が挙げられ、これらは単独でも混合して用い
てもよい。
The curing accelerator used in the present invention is not particularly limited as long as it can promote the reaction between the epoxy resin and the phenol resin. For example, 1,8-diazabicyclo (5,4,0) undecene-7, Amine compounds such as butylamine, organic phosphorus compounds such as triphenylphosphine, tetraphenylphosphonium / tetraphenylborate, imidazole compounds such as 2-methylimidazole, and the like. Good.

【0012】本発明の樹脂組成物は、(A)〜(G)成
分の他、必要に応じて臭素化合物以外の難燃剤、シラン
カップリング剤、着色剤、天然ワックスや合成ワックス
等の離型剤、シリコーンオイル等の低応力成分等の種々
の添加剤を適宜添加して使用しても差し支えない。本発
明の樹脂組成物は、(A)〜(G)成分、及びその他の
添加剤等をミキサーを用いて常温混合し、ロール、押出
機等の混練機で混練し、冷却後粉砕して得られる。本発
明の樹脂組成物を用いて、半導体素子等の電子部品を封
止し、半導体装置を製造するには、トランスファーモー
ルド、コンプレッションモールド、インジェクションモ
ールド等の成形方法で硬化成形すればよい。
The resin composition of the present invention comprises, in addition to the components (A) to (G), a mold release agent such as a flame retardant other than a bromine compound, a silane coupling agent, a coloring agent, a natural wax or a synthetic wax, if necessary. Various additives such as low-stress components such as silicone oil and silicone oil may be appropriately added and used. The resin composition of the present invention is obtained by mixing components (A) to (G) and other additives at room temperature using a mixer, kneading with a kneading machine such as a roll or an extruder, cooling, and pulverizing. Can be In order to manufacture a semiconductor device by encapsulating an electronic component such as a semiconductor element using the resin composition of the present invention, it is sufficient to cure and mold by a molding method such as a transfer mold, a compression mold, and an injection mold.

【0013】[0013]

【実施例】以下に、実施例を挙げて説明するが、本発明
はこれらの実施例によりなんら限定されるものではな
い。配合割合は重量部とする。先ず、実施例及び比較例
で用いた原料を示す。 エポキシ樹脂A(住友化学工業(株)・製ESCN−1
95LA、軟化点65℃、エポキシ当量200) フェノール樹脂(フェノールノボラック樹脂、軟化点9
0℃、水酸基当量104) X型ゼオライト(東ソー(株)・製ゼオラムF−9、平
均細孔径10オングストローム、空孔容積0.27cm
3/g) 酸化ビスマス(東亜合成(株)・製IXE−500S) 臭素化エポキシ樹脂(大日本インキ化学工業(株)・製
エピクロン153、軟化点70℃、エポキシ当量40
0、臭素含有率48重量%) 溶融球状シリカ(平均粒径30μm、比表面積1.4m
2/g) 硬化促進剤(1,8−ジアザビシクロ(5,4,0)ウ
ンデセン−7、以下DBUという) 三酸化アンチモン シランカップリング剤 カーボンブラック カルナバワックス
EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited to these examples. The mixing ratio is by weight. First, raw materials used in Examples and Comparative Examples will be described. Epoxy resin A (ESCN-1 manufactured by Sumitomo Chemical Co., Ltd.)
95LA, softening point 65 ° C, epoxy equivalent 200) phenolic resin (phenol novolak resin, softening point 9)
X-type zeolite (Zeolam F-9 manufactured by Tosoh Corporation, average pore diameter 10 Å, pore volume 0.27 cm)
3 / g) Bismuth oxide (IXE-500S, manufactured by Toagosei Co., Ltd.) Brominated epoxy resin (Epiclon 153, manufactured by Dainippon Ink and Chemicals, Inc., softening point 70 ° C., epoxy equivalent 40)
0, bromine content: 48% by weight) fused spherical silica (average particle size: 30 μm, specific surface area: 1.4 m)
2 / g) Curing accelerator (1,8-diazabicyclo (5,4,0) undecene-7, hereinafter referred to as DBU) Antimony trioxide Silane coupling agent Carbon black Carnauba wax

【0014】 実施例1 エポキシ樹脂A 95重量部 フェノールノボラック樹脂 45重量部 ゼオラムF−9 15重量部 IXE−500S 2重量部 臭素化エポキシ樹脂 20重量部 溶融球状シリカ 800重量部 DBU 4重量部 三酸化アンチモン 24重量部 シランカップリング剤 20重量部 カーボンブラック 6重量部 カルナバワックス 6重量部 をミキサーで混合後、100℃で二軸ロールを用いて混
練し、冷却混合後粉砕し、樹脂組成物とした。得られた
樹脂組成物を以下の方法で評価した。結果を表1に示
す。
Example 1 Epoxy resin A 95 parts by weight Phenol novolak resin 45 parts by weight Zeolam F-9 15 parts by weight IX-500S 2 parts by weight Brominated epoxy resin 20 parts by weight Fused spherical silica 800 parts by weight DBU 4 parts by weight Trioxide 24 parts by weight of antimony 20 parts by weight of a silane coupling agent 6 parts by weight of carbon black 6 parts by weight of carnauba wax were mixed by a mixer, kneaded at 100 ° C. using a biaxial roll, cooled, mixed and pulverized to obtain a resin composition. . The obtained resin composition was evaluated by the following method. Table 1 shows the results.

【0015】評価方法 スパイラルフロー:EMMI−I−66に準じたスパイ
ラルフロー測定用の金型を用い、金型温度175℃、注
入圧力70kg/cm2、硬化時間2分で測定した。単
位はcm。 難燃性:UL−94に準拠し、テストピース厚1/8i
nchで測定した。 高温保管特性:低圧トランスファー成形機を用いて、金
型温度175℃、圧力70kg/cm2、硬化時間2分
で16pDIP(パッケージ幅300mils)を成形
し、175℃、8時間のポストキュアを行い、10個の
パッケージを得た。得られたパッケージを185℃に保
管し、常温でパッケージの配線の電気抵抗値を調べた。
500時間まで試験し、初期抵抗値の1.2倍以上の抵
抗値を示したものを不良と判定した。不良の生じたパッ
ケージがn個であるとき、n/10と表示した。 硬化性(ショア硬度D):低圧トランスファー成形機を
用いて、金型温度175℃、圧力70kg/cm2で作
成した試験片を型開後10秒経過した時の硬度を測定す
る。
Evaluation method Spiral flow: Measurement was performed using a mold for measuring spiral flow according to EMMI-I-66 at a mold temperature of 175 ° C., an injection pressure of 70 kg / cm 2 , and a curing time of 2 minutes. The unit is cm. Flame retardancy: conforms to UL-94, test piece thickness 1 / 8i
It was measured by nch. High-temperature storage characteristics: Using a low-pressure transfer molding machine, a 16 pDIP (package width 300 mils) was molded at a mold temperature of 175 ° C., a pressure of 70 kg / cm 2 , and a curing time of 2 minutes, and was post-cured at 175 ° C. for 8 hours. Ten packages were obtained. The obtained package was stored at 185 ° C., and the electrical resistance of the package wiring was examined at room temperature.
Tests were performed for up to 500 hours, and those showing a resistance value of 1.2 times or more the initial resistance value were determined to be defective. When the number of defective packages was n, it was indicated as n / 10. Curability (Shore hardness D): Using a low-pressure transfer molding machine, a test piece prepared at a mold temperature of 175 ° C. and a pressure of 70 kg / cm 2 is measured for hardness 10 seconds after the mold is opened.

【0016】実施例2〜5 表1の配合に従い、実施例1と同様にして樹脂組成物を
得、実施例1と同様にして評価した。結果を表1に示
す。 比較例1〜6 表2の配合に従い、実施例1と同様にして樹脂組成物を
得、実施例1と同様にして評価した。結果を表2に示
す。
Examples 2 to 5 According to the composition shown in Table 1, a resin composition was obtained in the same manner as in Example 1, and evaluated in the same manner as in Example 1. Table 1 shows the results. Comparative Examples 1 to 6 According to the formulation in Table 2, a resin composition was obtained in the same manner as in Example 1, and evaluated in the same manner as in Example 1. Table 2 shows the results.

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【表2】 [Table 2]

【0019】[0019]

【発明の効果】本発明に従うと、高温保管特性に優れ、
且つ高温保管特性と難燃性とのバランスに極めて優れた
半導体装置を得ることができる。
According to the present invention, excellent high-temperature storage characteristics are obtained.
In addition, a semiconductor device having an extremely excellent balance between high-temperature storage characteristics and flame retardancy can be obtained.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C08K 3/34 C08K 3/34 H01L 23/29 H01L 23/30 R 23/31 Fターム(参考) 4J002 CC04X CC06X CC07X CD04W CD05W CD06W CD07W CD12Y DE097 DE138 DE148 DJ006 DJ018 DJ038 DJ048 DL008 EU119 EU139 EW019 EW179 FA048 FA096 FD159 GQ05 4J036 AA01 AD01 AD07 AD08 AF06 AF08 DA02 DC05 DC41 DC46 DD07 FA03 FA05 FB07 GA04 JA07 KA05 4M109 AA01 BA01 CA21 EA02 EB03 EB04 EB06 EB08 EB09 EB12 EB13 EB18 EB19 EC20 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C08K 3/34 C08K 3/34 H01L 23/29 H01L 23/30 R 23/31 F-term (Reference) 4J002 CC04X CC06X CC07X CD04W CD05W CD06W CD07W CD12Y DE097 DE138 DE148 DJ006 DJ018 DJ038 DJ048 DL008 EU119 EU139 EW019 EW179 FA048 FA096 FD159 GQ05 4J036 AA01 AD01 AD07 AD08 AF06 AF08 DA02 DC05 DC41 DC46 DD07 FA03 FA07 AE03 BA04 EB09 EB12 EB13 EB18 EB19 EC20

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 (A)エポキシ樹脂、(B)フェノール
樹脂、(C)全エポキシ樹脂組成物中に0.1〜5重量
%の細孔径3〜20オングストローム、空孔容積0.1
〜0.4cm3/gのゼオライト、(D)全エポキシ樹
脂組成物中に0.1〜5重量%の酸化ビスマス、(E)
臭素化合物、(F)無機充填材、及び(G)硬化促進剤
を必須成分とし、臭素化合物中の臭素量が0.1〜1.
5重量%であることを特徴とするエポキシ樹脂組成物、
及びこれを用いて半導体素子を封止してなる半導体装
置。
1. An epoxy resin, (B) a phenolic resin, and (C) 0.1 to 5% by weight of a total epoxy resin composition having a pore diameter of 3 to 20 Å and a pore volume of 0.1.
~0.4cm 3 / g of zeolite, (D) 0.1 to 5 wt.% Of bismuth oxide in the total epoxy resin composition, (E)
A bromine compound, (F) an inorganic filler, and (G) a curing accelerator are essential components, and the amount of bromine in the bromine compound is 0.1 to 1.
5% by weight of an epoxy resin composition,
And a semiconductor device in which a semiconductor element is sealed using the same.
【請求項2】 請求項1記載の半導体封止用エポキシ樹
脂組成物を用いて半導体素子を封止してなることを特徴
とする半導体装置。
2. A semiconductor device comprising a semiconductor element encapsulated with the epoxy resin composition for semiconductor encapsulation according to claim 1.
JP8783699A 1999-03-30 1999-03-30 Epoxy resin composition and semiconductor device Pending JP2000281869A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8783699A JP2000281869A (en) 1999-03-30 1999-03-30 Epoxy resin composition and semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8783699A JP2000281869A (en) 1999-03-30 1999-03-30 Epoxy resin composition and semiconductor device

Publications (1)

Publication Number Publication Date
JP2000281869A true JP2000281869A (en) 2000-10-10

Family

ID=13926019

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8783699A Pending JP2000281869A (en) 1999-03-30 1999-03-30 Epoxy resin composition and semiconductor device

Country Status (1)

Country Link
JP (1) JP2000281869A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002338932A (en) * 2001-05-14 2002-11-27 Sony Chem Corp Adhesive
JP2006274186A (en) * 2005-03-30 2006-10-12 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
US8315031B2 (en) 2007-10-12 2012-11-20 Panasonic Corporation Case mold type capacitor

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002338932A (en) * 2001-05-14 2002-11-27 Sony Chem Corp Adhesive
JP2006274186A (en) * 2005-03-30 2006-10-12 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
US8315031B2 (en) 2007-10-12 2012-11-20 Panasonic Corporation Case mold type capacitor

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