JP2005314568A - Epoxy resin composition for semiconductor sealing and semiconductor device - Google Patents

Epoxy resin composition for semiconductor sealing and semiconductor device Download PDF

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JP2005314568A
JP2005314568A JP2004134758A JP2004134758A JP2005314568A JP 2005314568 A JP2005314568 A JP 2005314568A JP 2004134758 A JP2004134758 A JP 2004134758A JP 2004134758 A JP2004134758 A JP 2004134758A JP 2005314568 A JP2005314568 A JP 2005314568A
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epoxy resin
resin composition
semiconductor
sealing
hexagonal
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Keiichi Sakumichi
慶一 作道
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Sumitomo Bakelite Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an epoxy resin composition for semiconductor sealing that has low dielectric constant and excellent moldability. <P>SOLUTION: This epoxy resin composition for semiconductor sealing comprises, as essential components, (A) epoxy resin, (B) phenol resin, (C) hardening accelerator, (D) an inorganic filler including crushed or spherical hexagonal BN as essential components. Preferably, the hexagonal BN is crushed or spherical in the epoxy resin composition for semiconductor sealing. The semiconductor devices are produced by sealing the device with these semiconductor-sealing epoxy resin compositions. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、半導体封止用エポキシ樹脂組成物、及びこれを用いた半導体装置に関するものである。   The present invention relates to an epoxy resin composition for semiconductor encapsulation and a semiconductor device using the same.

IC、LSI、トランジスター等の半導体素子の封止には金属缶、セラミック、エポキシ樹脂組成物等が用いられている。中でもエポキシ樹脂組成物のトランスファー成形は、低コスト且つ大量生産に適しており広く用いられている。また、信頼性の点でもエポキシ樹脂や硬化剤であるフェノール樹脂の改良により、耐湿性の向上や、半田リフローへの対応などが図られてきた。
しかし、近年の電子機器の高速化により、エポキシ樹脂組成物に新たな対応が求められている。つまり電子機器の高速化に伴う、半導体装置が扱う周波数の高周波化への対応である。半導体装置が扱う周波数は年々上昇しており、例えば情報処理分野ではCPUの扱う動作周波数が既に1GHzを越え、更に年々上昇している。情報通信分野では、携帯電話や無線LAN等で既に2.4GHz、5GHz、更に数10GHz等での高周波を利用した通信が実施されようとしており、そこに組み込まれる半導体装置には高周波対応が求められている。
Metal cans, ceramics, epoxy resin compositions, and the like are used for sealing semiconductor elements such as ICs, LSIs, and transistors. Among them, transfer molding of an epoxy resin composition is suitable for low cost and mass production and is widely used. In terms of reliability, improvement of moisture resistance and solder reflow have been achieved by improving epoxy resins and phenolic resins as curing agents.
However, with the recent increase in speed of electronic devices, new measures are required for epoxy resin compositions. In other words, this corresponds to the increase in the frequency handled by the semiconductor device as the speed of electronic equipment increases. The frequency handled by the semiconductor device is increasing year by year. For example, in the information processing field, the operating frequency handled by the CPU has already exceeded 1 GHz and further increased year by year. In the field of information communication, communication using high frequencies at 2.4 GHz, 5 GHz, and several tens of GHz has already been carried out in mobile phones and wireless LANs, and semiconductor devices incorporated therein are required to support high frequencies. ing.

高周波を扱う半導体装置に用いるエポキシ樹脂組成物の誘電率が高い問題に対して、これまでも種々の方策が提案されてきた。誘電率の低いシアネートレジン(例えば、特許文献1、特許文献2参照。)、或いはエポキシでもOH当量、及びエポキシ当量を上げることで、低誘電率を図ったものが提案されてきた(例えば、特許文献3参照。)。しかし、シアネートレジンは成形性、特に硬化性が悪いため、生産性が著しく低下する。同様に水酸基当量、エポキシ当量を上げたレジンでも当量を上げるに従ってやはり成形性が著しく低下するという問題点があり、十分な対応が取られていない。更に離型性と低誘電率を両立する技術として中空無機充填材の使用が提案されているが(例えば、特許文献4参照。)、中空フィラーは殻破壊が発生するため中空フィラーを用いたエポキシ樹脂組成物には製造中に殻破壊による誘電率の上昇が発生し充分な低誘電率化できない。   Various measures have been proposed so far for the problem that the epoxy resin composition used in a semiconductor device handling high frequency has a high dielectric constant. A cyanate resin having a low dielectric constant (see, for example, Patent Document 1 and Patent Document 2), or an epoxy having a low dielectric constant by increasing the OH equivalent and the epoxy equivalent has been proposed (for example, patents). Reference 3). However, since cyanate resin has poor moldability, particularly curability, productivity is significantly reduced. Similarly, even with a resin having a higher hydroxyl equivalent and epoxy equivalent, there is a problem that the moldability is significantly lowered as the equivalent is increased, and sufficient measures have not been taken. Furthermore, the use of hollow inorganic fillers has been proposed as a technique for achieving both releasability and low dielectric constant (see, for example, Patent Document 4). However, since hollow shells cause shell fracture, epoxy using hollow fillers is used. In the resin composition, the dielectric constant increases due to shell destruction during production, and the dielectric constant cannot be sufficiently reduced.

特開平6−306168号公報(第2〜9頁)JP-A-6-306168 (pages 2-9) 特開2001−339130号公報(第2〜26頁)JP 2001-339130 A (pages 2 to 26) 特開2001−72743号公報(第2〜9頁)JP 2001-72743 A (pages 2 to 9) 特開2001−354754号広報(第2〜12頁)JP 2001-354754 A (Publication 2-12)

本発明は、従来の上述のような問題点を解決するためになされたもので、その目的とするところは低誘電率で成形性も良好な半導体封止用エポキシ樹脂組成物、及びこれを用いた半導体装置を提供するものである。   The present invention has been made to solve the conventional problems as described above, and an object of the present invention is to provide an epoxy resin composition for semiconductor encapsulation having a low dielectric constant and good moldability, and the use thereof. A semiconductor device is provided.

本発明は、
[1](A)エポキシ樹脂、(B)フェノール樹脂、(C)硬化促進剤、及び(D)六方晶チッカホウ素を含む無機充填材を必須成分とすることを特徴とする半導体封止用エポキシ樹脂組成物、
[2]前記六方晶チッカホウ素が破砕状又は球状である第[1]項記載の半導体封止用エポキシ樹脂組成物、
[3]該エポキシ樹脂組成物の硬化物の誘電率が1.5以上、3.0以下である第[1]又は[2]項記載の半導体封止用エポキシ樹脂組成物、
[4]第[1]又は[3]項のいずれかに記載の半導体封止用エポキシ樹脂組成物を用いて封止してなることを特徴とする半導体装置、
である。
The present invention
[1] An epoxy for semiconductor encapsulation, comprising (A) an epoxy resin, (B) a phenol resin, (C) a curing accelerator, and (D) an inorganic filler containing hexagonal ticker boron as an essential component. Resin composition,
[2] The epoxy resin composition for semiconductor encapsulation according to item [1], wherein the hexagonal ticker boron is crushed or spherical.
[3] The epoxy resin composition for semiconductor encapsulation according to [1] or [2], wherein the cured product of the epoxy resin composition has a dielectric constant of 1.5 or more and 3.0 or less,
[4] A semiconductor device characterized by being sealed using the epoxy resin composition for semiconductor sealing according to any one of [1] or [3],
It is.

本発明に従うと、低誘電率で且つ成形性も良好な半導体封止用エポキシ樹脂組成物を得ることができる。   According to the present invention, an epoxy resin composition for semiconductor encapsulation having a low dielectric constant and good moldability can be obtained.

本発明は、エポキシ樹脂、フェノール樹脂、硬化促進剤、及び六方晶チッカホウ素を含む無機充填材を必須成分とするエポキキシ樹脂組成物であることにより、低誘電率で且つ、成形性も良好な半導体封止用エポキシ樹脂組成物が得られるものである。更に硬化物の誘電率が3.0以下と低いため1GHz以上の高周波を扱うデバイスにおいてその素子の特性を十分発揮できるものである。
以下、本発明について詳細に説明する。
The present invention is an epoxy resin composition comprising an inorganic filler containing an epoxy resin, a phenol resin, a curing accelerator, and a hexagonal ticker boron as an essential component, thereby providing a semiconductor having a low dielectric constant and good moldability. An epoxy resin composition for sealing is obtained. Furthermore, since the dielectric constant of the cured product is as low as 3.0 or less, the characteristics of the element can be sufficiently exhibited in a device that handles a high frequency of 1 GHz or more.
Hereinafter, the present invention will be described in detail.

本発明に用いるエポキシ樹脂は、1分子内にエポキシ基を2個以上有するモノマー、オリゴマー、ポリマー全般であり、その分子量、分子構造は特に限定するものではない。例えば、ビフェニル型エポキシ樹脂、ビスフェノール型エポキシ樹脂、スチルベン型エポキシ樹脂、フェノールノボラック型エポキシ樹脂、クレゾ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、アルキル変性トリフェノールメタン型エポキシ樹脂、トリアジン核含有エポキシ樹脂、ジシクロペンタジエン変性フェノール型エポキシ樹脂、フェノールアラルキル型エポキシ樹脂(フェニレン骨格、ビフェニレン骨格等を有する)等を用いることができる。
また、これらのエポキシ樹脂は単独でも2種類以上混合して用いても良い。
Epoxy resins used in the present invention are monomers, oligomers, and polymers in general having two or more epoxy groups in one molecule, and the molecular weight and molecular structure are not particularly limited. For example, biphenyl type epoxy resin, bisphenol type epoxy resin, stilbene type epoxy resin, phenol novolac type epoxy resin, cresol novolac type epoxy resin, triphenolmethane type epoxy resin, alkyl-modified triphenolmethane type epoxy resin, triazine nucleus-containing epoxy resin Dicyclopentadiene-modified phenol type epoxy resin, phenol aralkyl type epoxy resin (having a phenylene skeleton, a biphenylene skeleton, or the like) can be used.
These epoxy resins may be used alone or in combination of two or more.

本発明に用いるフェノール樹脂は、1分子内にフェノール性水酸基を2個以上有するモノマー、オリゴマー、ポリマー全般であり、その分子量、分子構造を特に限定するものではない。例えば、フェノールノボラック樹脂、クレゾールノボラック樹脂、ジシクロペンタジエン変性フェノール樹脂、テルペン変性フェノール樹脂、トリフェノールメタン型樹脂、フェノールアラルキル樹脂(フェニレン骨格、ビフェニレン骨格等を有する)等が挙げられ、これらは単独でも混合して用いても差し支えない。   The phenol resin used in the present invention is a monomer, oligomer or polymer in general having two or more phenolic hydroxyl groups in one molecule, and its molecular weight and molecular structure are not particularly limited. For example, phenol novolac resin, cresol novolak resin, dicyclopentadiene modified phenol resin, terpene modified phenol resin, triphenolmethane type resin, phenol aralkyl resin (having phenylene skeleton, biphenylene skeleton, etc.) and the like can be mentioned. A mixture may be used.

エポキシ樹脂とフェノール樹脂の含有量は、全エポキシ樹脂のエポキシ基数と全フェノール樹脂のフェノール性水酸基数の比が0.8〜1.3であることが好ましく、この範囲を外れると、エポキシ樹脂組成物の硬化性の低下、或いは硬化物のガラス転移温度の低下、耐湿信頼性の低下等が生じる可能性がある。   The content of the epoxy resin and the phenol resin is preferably such that the ratio of the number of epoxy groups in the total epoxy resin and the number of phenolic hydroxyl groups in the total phenol resin is 0.8 to 1.3. There is a possibility that the curability of the product is lowered, the glass transition temperature of the cured product is lowered, and the moisture resistance reliability is lowered.

本発明に用いる硬化促進剤としては、エポキシ基とフェノール性水酸基との硬化反応を促進させるものであればよく、一般に封止材料に使用するものを使用することができる。例えば、1,8−ジアザビシクロ(5,4,0)ウンデセン−7等のジアザビシクロアルケン及びその誘導体、トリフェニルホスフィン等の有機ホスフィン類、2−メチルイミダゾール等のイミダゾール化合物、テトラフェニルホスホニウム・テトラフェニルボレート等のテトラ置換ホスホニウム・テトラ置換ボレート、ベンゾキノンをアダクトしたトリフェニルホスフィン等が挙げられ、これらは単独でも混合して用いても差し支えない。   As a hardening accelerator used for this invention, what is necessary is just to accelerate | stimulate the hardening reaction of an epoxy group and a phenolic hydroxyl group, and what is generally used for a sealing material can be used. For example, diazabicycloalkenes such as 1,8-diazabicyclo (5,4,0) undecene-7 and derivatives thereof, organic phosphines such as triphenylphosphine, imidazole compounds such as 2-methylimidazole, tetraphenylphosphonium tetra Examples thereof include tetra-substituted phosphonium / tetra-substituted borates such as phenyl borate, and triphenylphosphine adducted with benzoquinone, and these may be used alone or in combination.

本発明に用いる無機充填材としては、破砕状、球状の六方晶チッカホウ素を必須成分として用いる。IC等電子部品の封止用に用いられる樹脂組成物には、一般に破砕状、又は球状のシリカを用いる。一方、六方晶チッカホウ素はその結晶性により通常鱗片状の形状をとるが、鱗片状では樹脂組成物中の含有量を上げることが出来ず十分な低誘電化の効果を得ることが出来ない。破砕状又は球状の六方晶チッカホウ素は鱗片状の粉末を破砕状又は球状に賦形後、加熱、溶射により得ることができるが、製造法はこれに限る物ではない。六方晶チッカホウ素の含有量としては、樹脂組成物に対して35〜90重量%、望ましくは60〜90重量%以上用いる必要がある。六方晶チッカホウ素の含有量が下限値を下回ると十分な低誘電化の効果が得られす、上限値を上回ると流動性が大幅に低下し成形性に問題が発生する。六方晶チッカホウ素をシランカップリング剤等により表面処理をしてもかまわない。表面処理の方法としては、単独に処理した物を用いても或いは他の配合原料との混合時に処理してもかまわない。   As the inorganic filler used in the present invention, crushed and spherical hexagonal ticker boron is used as an essential component. In general, crushed or spherical silica is used for a resin composition used for sealing an electronic component such as an IC. On the other hand, hexagonal ticker boron usually takes a scaly shape due to its crystallinity, but in the scaly state, the content in the resin composition cannot be increased, and a sufficient effect of reducing the dielectric cannot be obtained. The crushed or spherical hexagonal ticker boron can be obtained by forming a flaky powder into a crushed or spherical shape, followed by heating and thermal spraying, but the production method is not limited thereto. The content of hexagonal ticker boron is 35 to 90% by weight, preferably 60 to 90% by weight or more based on the resin composition. If the content of hexagonal ticker boron is less than the lower limit, a sufficient effect of lowering the dielectric can be obtained. If the content exceeds the upper limit, the fluidity is greatly lowered and a problem occurs in moldability. Hexagonal ticker boron may be surface-treated with a silane coupling agent or the like. As a method for the surface treatment, a single treated product may be used or it may be treated at the time of mixing with other compounding raw materials.

また、六方晶チッカホウ素以外に、他種の無機充填材を併用しても差し支えない。併用する無機充填材としては、誘電率の大幅な上昇が無い範囲で一般に半導体封止用エポキシ樹脂組成物に使用されているものを用いることができる。例えば、球状溶融シリカ、破砕状溶融シリカ、結晶シリカ、タルク、アルミナ、窒化珪素等が挙げられ、最も好適に使用されるものとしては、誘電率の低い球状溶融シリカ、破砕状溶融シリカである。これらの無機充填剤は、単独でも混合して用いても差し支えない。また、これらがカップリング剤により表面処理されていてもかまわない。   Further, other types of inorganic fillers may be used in combination with hexagonal ticker boron. As the inorganic filler to be used in combination, those which are generally used in epoxy resin compositions for semiconductor encapsulation can be used as long as there is no significant increase in dielectric constant. For example, spherical fused silica, crushed fused silica, crystalline silica, talc, alumina, silicon nitride and the like can be mentioned, and most preferably used are spherical fused silica and crushed fused silica having a low dielectric constant. These inorganic fillers may be used alone or in combination. Moreover, these may be surface-treated with a coupling agent.

本発明のエポキシ樹脂組成物は、エポキシ樹脂、フェノール硬化剤、硬化促進剤、六方晶チッカホウ素を含む無機充填材を必須成分とするが、更にこれ以外に、カーボンブラック等の着色剤、天然ワックス、合成ワックス等の離型剤、ゴム等の低応力添加剤、臭素化エポキシ樹脂や三酸化アンチモン、水酸化アルミニウム等の難燃剤等、種々の添加剤を適宜配合しても差し支えない。
本発明は高周波デバイスの特性を充分引き出すため硬化物の誘電率は1.5以上、3.0以下、望ましくは1.9以上、2.5以下である。3.0を越えると殆どのデバイスでノイズ低減の効果が充分でなく、3.0〜2.5では一部のデバイスのみに充分の効果を発現する。
The epoxy resin composition of the present invention comprises an inorganic filler containing an epoxy resin, a phenol curing agent, a curing accelerator and hexagonal ticker boron, but in addition to this, a colorant such as carbon black, a natural wax, and the like. Various additives such as a release agent such as synthetic wax, a low stress additive such as rubber, a flame retardant such as brominated epoxy resin, antimony trioxide, and aluminum hydroxide may be appropriately blended.
In the present invention, the dielectric constant of the cured product is 1.5 or more and 3.0 or less, preferably 1.9 or more and 2.5 or less, in order to bring out the characteristics of the high frequency device sufficiently. When 3.0 is exceeded, the noise reduction effect is not sufficient for most devices, and when 3.0 to 2.5, a sufficient effect is exhibited only for some devices.

また、本発明のエポキシ樹脂組成物は、ミキサー等を用いて原料を充分に均一に混合した後、更に熱ロール又はニーダー等の混練機で溶融混練し、冷却、粉砕しパウダー状にする。更に得られたパウダーを加圧してタブレット化する。
本発明のエポキシ樹脂組成物を用いて、半導体素子等の各種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従来からの成形方法で硬化成形すればよい。
In addition, the epoxy resin composition of the present invention is sufficiently homogeneously mixed using a mixer or the like, and then melt-kneaded with a kneader such as a hot roll or a kneader, cooled and pulverized to form a powder. Furthermore, the obtained powder is pressurized and tableted.
The epoxy resin composition of the present invention is used to encapsulate various electronic components such as semiconductor elements, and to manufacture semiconductor devices by conventional molding methods such as transfer molding, compression molding, and injection molding. do it.

以下に本発明の実施例を示すが、本発明はこれらに限定されるものではない。配合割合は重量部とする。
実施例1
クレゾールノボラックエポキシ樹脂[エポキシ当量200g/eq、軟化点75℃]
41.5重量部
フェノールノボラック樹脂A[水酸基当量104g/eq、軟化点120℃]
21.6重量部
2−メチルイミダゾール(以下、2Mzという) 0.4重量部
破砕状六方晶チッカホウ素[平均粒径35μm、最大粒径212μm]
35.0重量部
シランカップリング剤(γ-グリシジルトリメトキシシラン) 0.4重量部
カルナバワックス 0.8重量部
カーボンブラック 0.3重量部
をミキサーにて混合し後、熱ロールを用いて、95℃で8分間混練して冷却後粉砕し、エポキシ樹脂組成物を得た。得られたエポキシ樹脂組成物を、以下の方法で評価した。結果を表1に示す。
Examples of the present invention are shown below, but the present invention is not limited thereto. The blending ratio is parts by weight.
Example 1
Cresol novolac epoxy resin [epoxy equivalent 200 g / eq, softening point 75 ° C.]
41.5 parts by weight Phenol novolac resin A [hydroxyl equivalent: 104 g / eq, softening point: 120 ° C.]
21.6 parts by weight 2-methylimidazole (hereinafter referred to as 2Mz) 0.4 parts by weight Crushed hexagonal ticker boron [average particle size 35 μm, maximum particle size 212 μm]
35.0 parts by weight Silane coupling agent (γ-glycidyltrimethoxysilane) 0.4 part by weight Carnauba wax 0.8 part by weight Carbon black 0.3 part by weight was mixed with a mixer, and then using a hot roll. The mixture was kneaded at 95 ° C. for 8 minutes, cooled and pulverized to obtain an epoxy resin composition. The obtained epoxy resin composition was evaluated by the following methods. The results are shown in Table 1.

評価方法
スパイラルフロー:EMMI−1−66に準じたスパイラルフロー測定用金型を用いて、金型温度175℃、圧力6.9MPa、硬化時間120秒で測定した。単位はcm。
誘電率:低圧トランスファー成形機を用いて、成形温度175℃、圧力9.8MPa、硬化時間180秒で50φ−3mmのテストピースを成形した。テストピースは175℃/4hrにてポストキュアー後、横川ヒューレットパッカード株式会社製Qメータmodel4342Aにて誘電率を測定した。測定周波数は1MHz。
Evaluation method Spiral flow: Using a mold for spiral flow measurement according to EMMI-1-66, measurement was performed at a mold temperature of 175 ° C., a pressure of 6.9 MPa, and a curing time of 120 seconds. The unit is cm.
Dielectric constant: Using a low-pressure transfer molding machine, a test piece of 50φ-3 mm was molded at a molding temperature of 175 ° C., a pressure of 9.8 MPa, and a curing time of 180 seconds. The test piece was post-cured at 175 ° C./4 hr, and the dielectric constant was measured with a Q meter model 4342A manufactured by Yokogawa Hewlett-Packard Co., Ltd. The measurement frequency is 1 MHz.

実施例2〜8、比較例1
表1の配合に従い、実施例1と同様にしてエポキシ樹脂組成物を得て、実施例1と同様にして評価した。結果を表1に示す。
実施例1以外で用いた成分について、以下に示す。
ビフェニルエポキシ樹脂[エポキシ当量195g/eq、融点105℃]
ビスフェノールA型エポキシ樹脂[エポキシ当量195g/eq、融点72℃]
フェノールノボラック樹脂B[水酸基当量105g/eq、軟化点80℃]
フェノールノボラック樹脂C[水酸基当量105g/eq、軟化点63℃]
トリフェニルホスフィン(以下TPPという)
球状六方晶チッカホウ素[平均粒径25μm、最大粒径74μm]
溶融球状シリカ(平均粒径23μm)
Examples 2-8, Comparative Example 1
According to the composition of Table 1, an epoxy resin composition was obtained in the same manner as in Example 1 and evaluated in the same manner as in Example 1. The results are shown in Table 1.
The components used in other than Example 1 are shown below.
Biphenyl epoxy resin [epoxy equivalent 195 g / eq, melting point 105 ° C.]
Bisphenol A type epoxy resin [epoxy equivalent 195 g / eq, melting point 72 ° C.]
Phenol novolac resin B [hydroxyl equivalent 105 g / eq, softening point 80 ° C.]
Phenol novolac resin C [hydroxyl equivalent 105 g / eq, softening point 63 ° C.]
Triphenylphosphine (hereinafter referred to as TPP)
Spherical hexagonal ticker boron [average particle size 25 μm, maximum particle size 74 μm]
Fused spherical silica (average particle size 23μm)

Figure 2005314568
Figure 2005314568

本発明に従うと、低誘電率で且つ成形性も良好な半導体封止用エポキシ樹脂組成物を得ることができるので、1GHz以上の高周波を扱うデバイスに好適である。   According to the present invention, an epoxy resin composition for semiconductor encapsulation having a low dielectric constant and good moldability can be obtained, which is suitable for a device that handles a high frequency of 1 GHz or more.

Claims (4)

(A)エポキシ樹脂、(B)フェノール樹脂、(C)硬化促進剤、及び(D)六方晶チッカホウ素を含む無機充填材を必須成分とすることを特徴とする半導体封止用エポキシ樹脂組成物。 (A) Epoxy resin, (B) Phenolic resin, (C) Curing accelerator, and (D) An inorganic filler containing hexagonal ticker boron as an essential component, and an epoxy resin composition for semiconductor encapsulation . 前記六方晶チッカホウ素が破砕状又は球状である請求項1記載の半導体封止用エポキシ樹脂組成物。 The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein the hexagonal ticker boron is crushed or spherical. 該エポキシ樹脂組成物の硬化物の誘電率が1.5以上、3.0以下である請求項1又は2記載の半導体封止用エポキシ樹脂組成物。 The epoxy resin composition for semiconductor encapsulation according to claim 1 or 2, wherein the cured product of the epoxy resin composition has a dielectric constant of 1.5 or more and 3.0 or less. 請求項1ないし3のいずれかに記載の半導体封止用エポキシ樹脂組成物を用いて封止してなることを特徴とする半導体装置。 4. A semiconductor device, wherein the semiconductor device is sealed using the epoxy resin composition for semiconductor sealing according to claim 1.
JP2004134758A 2004-04-28 2004-04-28 Epoxy resin composition for semiconductor sealing and semiconductor device Pending JP2005314568A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20200038631A (en) * 2018-10-04 2020-04-14 주식회사 엘지화학 An encapsulation composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20200038631A (en) * 2018-10-04 2020-04-14 주식회사 엘지화학 An encapsulation composition
KR102522185B1 (en) * 2018-10-04 2023-04-14 주식회사 엘지화학 An encapsulation composition

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