JP2000230110A - Epoxy resin composition and semiconductor device - Google Patents
Epoxy resin composition and semiconductor deviceInfo
- Publication number
- JP2000230110A JP2000230110A JP3553199A JP3553199A JP2000230110A JP 2000230110 A JP2000230110 A JP 2000230110A JP 3553199 A JP3553199 A JP 3553199A JP 3553199 A JP3553199 A JP 3553199A JP 2000230110 A JP2000230110 A JP 2000230110A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- resin composition
- weight
- semiconductor device
- bromine
- 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
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Landscapes
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【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(以下、樹脂組成物とい
う)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55−146950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6
1−53321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レベルには到達
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 (hereinafter, referred to as a 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 technique for improving the high-temperature storage characteristics, a method using diantimony pentoxide (Japanese Patent Application Laid-Open No. 55-146950) and a method using a combination of antimony oxide and organic phosphine (Japanese Patent Application Laid-Open No.
No. 1-53321) is being studied, but at present it has not yet reached the required level of high-temperature storage characteristics for semiconductor devices.
【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のゼオライトを0.1〜5重
量%、(D)全エポキシ樹脂組成物中にハイドロタルサ
イトを0.1〜5重量%、(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全エポキシ樹脂組成物中に0.1〜
1.5重量%であることを特徴とする半導体封止用エポ
キシ樹脂組成物、及びこれを用いて半導体素子を封止し
てなる半導体装置である。According to the present invention, there are provided an epoxy resin (A), a phenolic resin (B), and a total epoxy resin composition (C) having a pore size of 3 to 20 angstroms and a pore volume of 0.1 to 0. 0.1 to 5% by weight of 0.4 cm 3 / g zeolite, (D) 0.1 to 5% by weight of hydrotalcite in the total epoxy resin composition, (E) bromine compound, (F) inorganic filler , And (G) a curing accelerator as an essential component, and the bromine content in the bromine compound is from 0.1 to 0.1 in the total epoxy resin composition.
An epoxy resin composition for semiconductor encapsulation, which is 1.5% by weight, and a semiconductor device obtained by encapsulating a semiconductor element using the same.
【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、及びこれらの変性樹脂等が挙げられ、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. , Triphenolmethane type resins, and modified resins thereof, and these may be used alone or as a mixture. 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出来ず高温保
管特性に効果がないので好ましくない。又、空孔容積が
0.1cm3/g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 molecules adsorbed by the molecular sieve will be reduced, and the effect of the adsorption characteristics required for high-temperature storage characteristics will be 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 cm 3 / g, 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】本発明に用いるハイドロタルサイトは、含
水炭酸アルミニウム・マグネシウムである。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。ハイドロタルサイトの配合量とし
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%未満だと分解した臭素化物の吸着
が不十分で、5重量%を越えると難燃性が低下するので
好ましくない。The hydrotalcite used in the present invention is hydrous aluminum magnesium carbonate. By using this in combination with zeolite, the amount of bromine derived from the bromine compound added as a flame retardant can be reduced, so that the balance between high-temperature storage characteristics and flame retardancy is easily achieved, and the high-temperature storage characteristics are further improved. The blending amount of hydrotalcite is preferably 0.1 to 5% by weight in the total epoxy resin composition. If it is less than 0.1% by weight, adsorption of the decomposed bromide is insufficient, and if it exceeds 5% by weight, the flame retardancy is undesirably reduced.
【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。臭素化合物の配合
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%が望ましく、又、エポキシ当量は200〜
450が望ましい。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 bromine compound is 0.1 to 10 parts per million in the total resin composition.
1.5% by weight is desirable, and the epoxy equivalent is 200 to
450 is preferred.
【0010】本発明に用いる無機充填材の種類には特に
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。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(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) ハイドロタルサイト(協和化学工業(株)・製DHT−
4H) 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%) 無機充填材(溶融球状シリカ、平均粒径30μm、比表
面積1.4m2/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) 三酸化二アンチモン 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 (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) Hydrotalcite (Kyowa Chemical Industry Co., Ltd. DHT-
4H) 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) Inorganic filler (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) diantimony trioxide silane coupling agent carbon black carnauba wax
【0014】 実施例1 エポキシ樹脂 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 10重量部 DHT−4H 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 三酸化二アンチモン 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 95 parts by weight of epoxy resin 45 parts by weight of phenol novolak resin 10 parts by weight of Zeolam F-9 2 parts by weight of DHT-4H 20 parts by weight of brominated epoxy resin 20 parts by weight of fused spherical silica 4 parts by weight of DBU 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。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.
【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, it is possible to obtain a semiconductor device having an excellent balance between high-temperature storage characteristics and flame retardancy.
───────────────────────────────────────────────────── 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) H01L 23/29 C08G 59/62 23/31 H01L 23/30 R // C08G 59/62 (C08L 63/00 101:04) Fターム(参考) 4J002 CC032 CC042 CC062 CC072 CD041 CD051 CD061 CD071 CD123 DE138 DE148 DE287 DJ006 DJ018 DJ038 DJ048 DL008 EN029 EU119 EU139 EW149 EW179 EY019 FA048 FD018 FD133 FD159 FD206 FD207 GQ05 4J032 CA04 CA07 CF03 CG00 4J036 AA01 AC02 AD01 AD07 AD09 AF05 AF06 AF10 AF28 DC05 DC41 DC46 DD07 DD09 FA01 FA02 FA03 FA05 FB07 JA07 4M109 AA01 BA01 CA21 EA02 EA06 EB03 EB04 EB06 EB07 EB08 EB12 EB18 EB19 EC20 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) H01L 23/29 C08G 59/62 23/31 H01L 23/30 R // C08G 59/62 (C08L 63/00 101: 04) F-term (reference) 4J002 CC032 CC042 CC062 CC072 CD041 CD051 CD061 CD071 CD123 DE138 DE148 DE287 DJ006 DJ018 DJ038 DJ048 DL008 EN029 EU119 EU139 EW149 EW179 EY019 FA048 FD018 FD133 FD159 FD206 FD207 GQ05 A0704 AD09 AF05 AF06 AF10 AF28 DC05 DC41 DC46 DD07 DD09 FA01 FA02 FA03 FA05 FB07 JA07 4M109 AA01 BA01 CA21 EA02 EA06 EB03 EB04 EB06 EB07 EB08 EB12 EB18 EB19 EC20
Claims (2)
樹脂、(C)全エポキシ樹脂組成物中に細孔径3〜20
オングストローム、空孔容積0.1〜0.4cm3/g
のゼオライトを0.1〜5重量%、(D)全エポキシ樹
脂組成物中にハイドロタルサイトを0.1〜5重量%、
(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全エポ
キシ樹脂組成物中に0.1〜1.5重量%であることを
特徴とする半導体封止用エポキシ樹脂組成物。1. The composition of (A) an epoxy resin, (B) a phenol resin, and (C) a total epoxy resin composition having a pore diameter of 3 to 20.
Angstrom, pore volume 0.1-0.4 cm 3 / g
0.1 to 5% by weight of zeolite, (D) 0.1 to 5% by weight of hydrotalcite 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 in the total epoxy resin composition. An epoxy resin composition for encapsulating a semiconductor, comprising:
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.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3553199A JP2000230110A (en) | 1999-02-15 | 1999-02-15 | Epoxy resin composition and semiconductor device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3553199A JP2000230110A (en) | 1999-02-15 | 1999-02-15 | Epoxy resin composition and semiconductor device |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000230110A true JP2000230110A (en) | 2000-08-22 |
Family
ID=12444328
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3553199A Pending JP2000230110A (en) | 1999-02-15 | 1999-02-15 | Epoxy resin composition and semiconductor device |
Country Status (1)
Country | Link |
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JP (1) | JP2000230110A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006274186A (en) * | 2005-03-30 | 2006-10-12 | Sumitomo Bakelite Co Ltd | Epoxy resin composition and semiconductor device |
EP2043147A2 (en) | 2007-09-28 | 2009-04-01 | Shin-Etsu Chemical Co., Ltd. | Automotive electric/electronic package |
JP2009073997A (en) * | 2007-09-21 | 2009-04-09 | Panasonic Electric Works Co Ltd | Epoxy resin composition, prepreg using the same, and metal-clad laminated sheet |
US7671160B2 (en) | 2005-02-14 | 2010-03-02 | Shin-Etsu Chemical Co., Ltd. | Curable perfluoropolyether compositions and rubber or gel articles comprising the cured products of the compositions |
US7999016B2 (en) | 2004-08-02 | 2011-08-16 | Shin-Etsu Chemical Co., Ltd. | Semiconductor encapsulating epoxy resin composition and semiconductor device |
US8315031B2 (en) | 2007-10-12 | 2012-11-20 | Panasonic Corporation | Case mold type capacitor |
CN106133055A (en) * | 2014-03-24 | 2016-11-16 | 住友电木株式会社 | Resin composition for sealing and semiconductor device |
-
1999
- 1999-02-15 JP JP3553199A patent/JP2000230110A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7999016B2 (en) | 2004-08-02 | 2011-08-16 | Shin-Etsu Chemical Co., Ltd. | Semiconductor encapsulating epoxy resin composition and semiconductor device |
US7671160B2 (en) | 2005-02-14 | 2010-03-02 | Shin-Etsu Chemical Co., Ltd. | Curable perfluoropolyether compositions and rubber or gel articles comprising the cured products of the compositions |
JP2006274186A (en) * | 2005-03-30 | 2006-10-12 | Sumitomo Bakelite Co Ltd | Epoxy resin composition and semiconductor device |
JP2009073997A (en) * | 2007-09-21 | 2009-04-09 | Panasonic Electric Works Co Ltd | Epoxy resin composition, prepreg using the same, and metal-clad laminated sheet |
EP2043147A2 (en) | 2007-09-28 | 2009-04-01 | Shin-Etsu Chemical Co., Ltd. | Automotive electric/electronic package |
US8315031B2 (en) | 2007-10-12 | 2012-11-20 | Panasonic Corporation | Case mold type capacitor |
CN106133055A (en) * | 2014-03-24 | 2016-11-16 | 住友电木株式会社 | Resin composition for sealing and semiconductor device |
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