KR960010307B1 - Epoxy resin composition for encapsulating semiconductor element - Google Patents

Epoxy resin composition for encapsulating semiconductor element Download PDF

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KR960010307B1
KR960010307B1 KR1019910021872A KR910021872A KR960010307B1 KR 960010307 B1 KR960010307 B1 KR 960010307B1 KR 1019910021872 A KR1019910021872 A KR 1019910021872A KR 910021872 A KR910021872 A KR 910021872A KR 960010307 B1 KR960010307 B1 KR 960010307B1
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epoxy resin
resin composition
semiconductor element
sealing
present
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KR1019910021872A
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KR930010117A (en
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김환건
이병원
이지윤
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제일모직 주식회사
이대원
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Priority to KR1019910021872A priority Critical patent/KR960010307B1/en
Priority to JP4278866A priority patent/JPH0794535B2/en
Priority to US07/964,457 priority patent/US5254605A/en
Publication of KR930010117A publication Critical patent/KR930010117A/en
Priority to KR1019960010884A priority patent/KR0172663B1/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • C08L63/04Epoxynovolacs

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  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)
  • Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)

Abstract

The resin composition comprises epoxy resin of cresol nobolak type, curing agent, curing accelerator, plasticizer, inorganic filler and 0.1-20wt.% high functional epoxy resin of formula(I) with respect to the total resin composition. In formula, R1 and R2 is (CH2)nCH3 or H2; n is 0 or over 1.

Description

반도체 소자 밀봉용 에폭시수지 조성물Epoxy Resin Composition for Semiconductor Device Sealing

본 발명은 반도체의 대용량화 및 패키지의 소형, 박형화에 따라 반도체 소자 밀봉용 수지 조성물에 요구되는 저응력화, 고내열화, 고내습성화를 실현한 반도체 소자 밀봉용 에폭시수지 조성물에 관한 것이다.BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an epoxy resin composition for semiconductor element encapsulation that realizes low stress, high heat resistance, and high moisture resistance required for a semiconductor element encapsulation resin composition in accordance with a large capacity of a semiconductor, a small size, and a thin package.

IC와 LSI 패키지는 전기, 전자부품 및 세트가 소형, 박형화됨에 따라 매우 급속하게 다양화되고 있다. 특히 칩의 크기는 점점 커짐에 불구하고 패키지는 점점 박형화, 소형화되고 높은 핀수를 가지는 패키지는 변화하고 있다. 실장방식도 표면실장 방식으로 변화되고 있으며, 최근에는 두께 1mm 정도의 TSOJ(Thin Small Out-line J-Bend Package)가 등장, 실현되고 있다. 이것은 SOJ(Small Out-line J-Bend Package)/QFP(Quad Flat Package)와 TAB(Tape Automated Bonding) 방식 사이의 중간단계 형태로서 향후 기억소자 분야의 주된 형태로 사용될 전망이다. 이러한 패키지의 변화에 대응하여 반도체 소자 밀봉용 수지 조성물도 또한 종래의 기술보다 더 엄격한 저응력화, 고내열화 및 고내습성화를 동시에 요구하고 있다.IC and LSI packages are rapidly diversifying as electrical, electronic components and sets become smaller and thinner. In particular, although chips are getting larger, packages are getting thinner, smaller, and have higher pin counts. The mounting method is also being changed to the surface mounting method, and recently, a TSOJ (Thin Small Out-line J-Bend Package) having a thickness of about 1 mm has been introduced and realized. This is an intermediate step between SOJ (Small Out-line J-Bend Package) / QFP (Quad Flat Package) and Tape Automated Bonding (TAB). In response to such a package change, the resin composition for semiconductor element sealing also demands more stringent lower stress, higher heat resistance, and higher moisture resistance than the prior art.

종래의 저응력화 기술로서는 내부응력을 감소시키기 위해 변성 실리콘 오일이나 CTBN과 같은 가소성부여제를 첨가하는 방법과(일본 공개특허 소63-230725, 62-7723, 62-106920, 62-260817) 충진제의 양을 증가시켜 열팽창계수를 낮추는 방법(일본 공개특허 소62-106920) 등이 알려져 있으나 상기의 방법들은 각각 내열성의 저하와 성형성 및 제조시의 설비의 마모 등 제조상의 심각한 문제를 야기시키고 있다. 한편, 내열성을 향상시키기 위해서는 다기능 에폭시수지의 사용(일본 공개특허 소62-7723, 소62-7913)과 내열성이 우수한 비스말레이미드의 사용(일본 공개특허 소54-142298, 소58-215452) 등이 알려져 있으나 이 기술 역시 유리전이온도 상승에 따른 내습성의 저하가 큰 문제로 대두되고 있다.Conventional low-stressing techniques include the addition of plasticizing agents such as modified silicone oil or CTBN to reduce internal stress and fillers (JP-A-63-230725, 62-7723, 62-106920, 62-260817). Although a method of lowering the coefficient of thermal expansion by increasing the amount thereof is known (Japanese Patent Laid-Open No. 62-106920), the above methods cause serious manufacturing problems such as deterioration of heat resistance, moldability, and wear of equipment during manufacturing, respectively. . On the other hand, in order to improve the heat resistance, the use of multifunctional epoxy resins (Japanese Patent Laid-Open Nos. 62-7723, 62-2913) and the use of bismaleimide excellent in heat resistance (Japanese Laid-Open Patent Nos. Although it is known that this technology is also a problem that is lowered moisture resistance due to the glass transition temperature rise.

따라서 본 발명은 내습성, 내열성 및 저응력화 부여가 가능한 고기능 에폭시수지를 사용함으로써 초박형 고집적 IC 밀봉에 적합한 수지 조성물을 제공하는데 그 목적이 있다.Accordingly, an object of the present invention is to provide a resin composition suitable for ultra-thin highly integrated IC sealing by using a high-performance epoxy resin capable of imparting moisture resistance, heat resistance and low stress.

즉, 본 발명은 크레졸노블락형 에폭시수지와 페놀노블락형 경화제, 경화촉진제, 무기충진제 등을 함유하는 반도체 소자 밀봉용 에폭시수지 조성물에 있어서, 상기 크레졸노블락형 에폭시수지에 하기 일반식(I)로 표시되는 고기능 에폭시수지가 함유되어 있는 것을 그 특징으로 한다.That is, the present invention is a epoxy resin composition for sealing a semiconductor device containing a cresol noblock type epoxy resin, a phenol noblock type curing agent, a curing accelerator, an inorganic filler, and the like, wherein the cresol noblock type epoxy resin is represented by the following general formula (I): It is characterized by containing a high-performance epoxy resin.

(여기에서, R1, R2는 H 또는 (CH2)nCH3기이고, n은 0 또는 1 이상의 정수이다.)(Wherein R 1 , R 2 are H or (CH 2 ) n CH 3 groups and n is 0 or an integer of 1 or more.)

본 발명의 상기 일반식(I)의 고기능성 에폭시수지는 예를 들면 다음과 같은 경로로 합성할 수 있다. 즉, 드롭핑펀넬(dropping funnel)과 리플럭스 콘덴사(reflux condenser)를 장치한 라운드보텀플라스크에 하기 구조식(II)의 에폭시수지(일본화학 제품)와 비극성 유기용매(CCl4, C2H4Cl2)를 ;The high functional epoxy resin of the general formula (I) of the present invention can be synthesized by the following route, for example. That is, a round bottom flask equipped with a dropping funnel and a reflux condenser is an epoxy resin (Japanese Chemical) and a nonpolar organic solvent (CCl 4 , C 2 H 4) Cl 2 );

넣고, 교환하여 녹이고 에폭시수지에 대해 0.1~1중량%의 벤조일피록사이드(Aldrich사 제품)를 촉매로 넣고 충분히 교반하면서 NBS(1-bromo-2,5-Pyrrolidinedion : Aldrich사 제품)를 한방울씩 적하하여 넣은 후 2~6시간 리플럭스한다.Dissolve by adding, replacing, and dissolving 0.1-1% by weight of benzoylpyoxide (Aldrich) as a catalyst to the epoxy resin and dropping NBS (1-bromo-2,5-Pyrrolidinedion: manufactured by Aldrich) dropwise while stirring sufficiently. After reflux, reflux for 2-6 hours.

여기에서 수득된 하기 구조식(III)의 Br 치환 에폭시수지를 잘 건조된 디에틸에테르 또는 THF(tetrahydrofuran)에 녹이고 마그네슘을 넣어 다 녹은 것을 확인한 후 O-메틸하이드록실아민(CH3ONH2: Aldrich사 제품)을 넣고 따뜻한 상태에서 4~8시간 교반 반응시킨다.Br-substituted epoxy resin of the following structural formula (III) obtained in this was dissolved in well-dried diethyl ether or THF (tetrahydrofuran), and after checking that magnesium was dissolved, O-methylhydroxylamine (CH 3 ONH 2 : Aldrich) Product) and the reaction is stirred for 4-8 hours in a warm state.

이렇게 하여 얻은 아민 그룹이 치환된 하기 구조식(IV)의 에폭시수지를 하기 구조식(V)의 말레이미드(미스비시유화 제품)와 함께 ;Epoxy resin of the following structural formula (IV) substituted with the amine group obtained in this way with the maleimide (product of the Mitsubishi emulsification product) of the following structural formula (V);

(여기에서 R1, R2에 대한 기의 정의는 상기 일반식(I)과 같다.)(Herein, the definition of the group for R 1 , R 2 is the same as the general formula (I).)

DMF에 녹여 리플럭스시키며 수시간 반응시켜 최종적으로 본 발명의 일반식(I)의 고기능성 에폭시수지를 수득하게 된다.It is dissolved in DMF, refluxed and reacted for several hours to finally obtain a high functional epoxy resin of general formula (I) of the present invention.

본 발명의 반도체 소자 밀봉용 에폭시수지 조성물을 보다 상세히 언급하면, 올소-크레졸노블락형 에폭시수지와 상기 일반식(I)의 고기능 에폭시수지를 혼합한 에폭시수지 성분을 기본으로 하고, 페놀노블락형 경화제, 그리고 유기 포스핀계 화합물인 트라이페닐포스핀을 경화촉진제로 첨가하였으며, 또한 충진제로서는 고순도 용융실리카를, 개질제로는 에폭시변성 실리콘오일을 첨가하며, 기타 이형제, 착색제, 그리고 유기 및 무기난연제 등을 첨가하여 조성된다.When referring to the epoxy resin composition for sealing a semiconductor device of the present invention in more detail, based on the epoxy resin component mixed with an olso-cresol noblock type epoxy resin and the high-performance epoxy resin of the general formula (I), a phenol noblock type curing agent, In addition, triphenylphosphine, an organic phosphine compound, was added as a curing accelerator, and high purity molten silica was added as a filler, epoxy modified silicone oil was added as a modifier, other mold release agents, colorants, and organic and inorganic flame retardants were added. It is created.

이와 같이 본 발명의 수지 조성물의 바람직한 조성예를 정리하면 다음과 같다.Thus, the preferable composition example of the resin composition of this invention is summarized as follows.

크레졸노블락형 에폭시수지0.1-20중량%Cresol noblock type epoxy resin 0.1-20% by weight

고기능 에폭시수지0.1-20중량%High Performance Epoxy Resin 0.1-20% by weight

경화제1.0-10.0중량%Curing agent 1.0-10.0 wt%

경화촉진제0.1-1.0중량%Curing accelerator 0.1-1.0 wt%

커플링제0.5-2.0중량%Coupling agent 0.5-2.0 wt%

착색제0.1-0.5중량%0.1-0.5% by weight of colorant

충진제65.0-85.0중량%Filler 65.0-85.0 wt%

이형제0.1-1.0중량%Release agent 0.1-1.0 wt%

유기난연제1.0-5.0중량%Organic flame retardant 1.0-5.0 wt%

무기난연제0.5-3.0중량%Inorganic flame retardant 0.5-3.0 wt%

가소성부여제0.5-5.0중량%Plasticizer 0.5-5.0 wt%

본 발명의 수지 조성물은 상기와 같은 조성으로 하는 것이 가장 좋은데, 본 발명에서 사용하는 에폭시수지로서는 내열성이 우수한 올소크레졸노블락형 수지를 사용하며, 특히 에폭시 당량이 190-220이고, 불순물 함량이 10ppm 이하인 고순도 에폭시수지이어야 한다. 또한, 경화제로는 페놀노블락형 수지를 사용하는데, 연화점이 80-100℃이어야 하고, 하이드록실 당량이 100-120이며, 역시 불순물의 함량이 10ppm 이하인 수지를 사용해야 한다.The resin composition of the present invention is best to have the composition as described above, as the epoxy resin used in the present invention is used an allocresol noblock type resin excellent in heat resistance, in particular epoxy equivalent of 190-220, impurity content of 10ppm or less It should be a high purity epoxy resin. In addition, a phenol noblock type resin is used as a curing agent, and a softening point of 80-100 ° C., a hydroxyl equivalent weight of 100-120, and a resin having an impurity content of 10 ppm or less should be used.

한편, 본 발명에서 특징적으로 사용되는 일반식(I)의 고기능성 에폭시로서는 이미드-에폭시로서 전체 수지 조성물에 대해 0.1-20.0중량%, 좋기로는 1.0-10.0중량%로 사용하는 것이 좋다.On the other hand, as a high functional epoxy of the general formula (I) used characteristically in this invention, it is good to use it as an imide-epoxy at 0.1-20.0 weight% with respect to the whole resin composition, Preferably it is 1.0-10.0 weight%.

만일 그 사용량이 0.1중량% 미만이면 내열효과 및 내습효과가 없으며, 20중량%가 넘게 되면 레진블리드 및 금형오염 등의 현상이 나타나 성형성이 저하되고 겔화시간 및 후경화시의 조건에 많은 문제를 야기시킨다.If the amount used is less than 0.1% by weight, there is no heat and moisture resistance. If the amount is more than 20% by weight, resin bleed and mold contamination may occur, resulting in poor moldability and many problems in gelation time and post-curing conditions. Cause.

그리고, 본 발명에서 사용하는 충진제로서는 고순도 용융 실리카를 사용하며, 입자 크기가 10㎛-30㎛ 범위의 것을 사용하는 것이 좋다. 또한, 경화촉진제로는 통상 아민류, 이미다졸 유도체 및 유기포스핀계 화합물이 사용되고 있는데, 본 발명에서는 유기포스핀계 화합물로서 트레페닐포스핀이, 이미다졸 유도체로서는 2-메틸이미다졸, 2-메틸-4-에틸이미다졸 등을 사용하는 것이 바람직하다.As the filler used in the present invention, high purity fused silica is used, and a particle size of 10 μm to 30 μm may be preferably used. In addition, amines, imidazole derivatives, and organophosphine compounds are generally used as curing accelerators. In the present invention, trephenylphosphine is used as the organic phosphine compound, and 2-methylimidazole, 2-methyl- is used as the imidazole derivative. Preference is given to using 4-ethylimidazole or the like.

본 발명에서 무기충진제의 표면처리에 사용하는 커플링제로서는 실란계 커플링제가 사용되는데, 특히 감마-글리시독시프로필트리메톡시실란을 사용하는 것이 가장 좋다. 또한 가소성부여제로서는 통상적으로 실리콘 고무나 에폭시변성 실리콘오일을 사용하는데, 반도체의 고집적화에 따라 상용성을 증가시키기 위해서 본 발명에 사용된 가소성부여제는 페놀노블락수지와 에폭시변성 실리콘오일의 어덕트를 사용하였다.In the present invention, as the coupling agent used for the surface treatment of the inorganic filler, a silane coupling agent is used, and in particular, gamma-glycidoxypropyltrimethoxysilane is most preferably used. In addition, as a plasticizer, silicone rubber or epoxy modified silicone oil is generally used. In order to increase compatibility with high integration of a semiconductor, the plasticizer used in the present invention is an adduct of phenol nobloc resin and epoxy modified silicone oil. Used.

그외의 이형제로서는 카르나우바왁스나 몬탄왁스를 0.1-1.0중량%로, 착색제로는 카본블랙 0.1-0.5중량%를 각각 사용하며, 유기난연제는 브롬화에폭시수지를, 무기난연제로는 삼산화안티몬을 사용하였다.Other release agents use carnauba wax or montan wax at 0.1-1.0% by weight, and carbon black 0.1-0.5% by weight, and organic flame retardant is brominated epoxy resin and inorganic flame retardant antimony trioxide. It was.

상기와 같은 본 발명의 조성물을 만들기 위하여 먼저 무기충전제를 커플링제로서 표면처리한 후 나머지 약제를 헨셀믹서나 기타 예비믹서기에서 균일하게 혼합시키고, 니이더 또는 롤밀을 이용하여 90-100℃에서 약 5-20분간 용융혼합시킨 다음 냉각시켜서 분쇄기를 이용하여 분말로 만든다.In order to make the composition of the present invention as described above, the inorganic filler is first surface-treated as a coupling agent, and then the remaining medicament is uniformly mixed in a Henschel mixer or other premixer, using a kneader or a roll mill at about 5 to about 90 ° C. Melt-mix for 20 minutes and then cool to powder using a grinder.

이러한 분말조성물을 이용하여 반도체 소자를 밀봉작업할 시에는 분말상태를 타정기에 넣어 타정한다. 이렇게 하여 제조된 타블렛 형태의 수지 조성물을 고주파 예열기를 이용하여 예열시킨 후 170-180℃에서 90-120초간 트랜스퍼 몰딩 프레스로 성형시키면 반도체 소자를 밀봉시킬 수 있게 된다.When sealing the semiconductor device using the powder composition, the powder is put into a tableting machine and tableted. The resin composition in the tablet form thus prepared is preheated using a high frequency preheater, and then molded in a transfer molding press at 170-180 ° C. for 90-120 seconds to seal the semiconductor device.

상술한 바와 같이 본 발명에 의해 제조한 수지 조성물은 반도체 소자 밀봉용 에폭시수지 조성물을 제조하기 위하여 에폭시수지로서 기존의 크레졸노블락형 에폭시수지에 내열성 및 보습성을 향상시키기 위하여 고기능 에폭시수지를 첨가시켜 줌으로써, 종래에 비하여 높은 유리전이온도를 가지면서 내습성이 향상되어 초박형 고집적반도체 밀봉에 적합한 수지 조성물을 제공할 수가 있는 것이다.As described above, the resin composition prepared according to the present invention is prepared by adding a high-performance epoxy resin to the existing cresol noblock type epoxy resin to improve heat resistance and moisture retention as an epoxy resin in order to prepare an epoxy resin composition for semiconductor element sealing. It is possible to provide a resin composition suitable for sealing an ultra-thin high-integration semiconductor having improved glass transition temperature compared to the conventional one.

이하 본 발명을 실시예에 의거 더욱 상세히 설명하면 다음과 같은 바, 실시예에 의거 본 발명이 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to Examples. However, the present invention is not limited to Examples.

[실시예 1-4]Example 1-4

다음 표-1에 나타낸 조성대로 조성물들을 헨셀믹서에서 균일하게 혼합하여 분말상태의 1차 조성물을 만든다. 그 다음에는 니이더를 이용하여 100℃에서 10분간 혼련시킨 후 냉각 과정을 거친 다음 분쇄하여 에폭시수지 성형재료를 제조하였다. 이렇게 하여 얻어진 에폭시수지 조성물에 대해서 다음과 같은 방법으로 물성을 측정하고 그 결과를 다음 표-2에 나타내었다.The compositions are uniformly mixed in a Henschel mixer according to the compositions shown in Table-1 below to form a powdery primary composition. Then, the mixture was kneaded at 100 ° C. for 10 minutes using a kneader, and then cooled and pulverized to prepare an epoxy resin molding material. The physical properties of the epoxy resin composition thus obtained were measured in the following manner, and the results are shown in Table 2 below.

1) 스피랄 플로우(Spiral Flow) : EMMI 규격에 준해 금형을 제작하여 성형온도 175℃, 성형압력 70kgf/cm2에서 측정.1) Spiral Flow: According to EMMI standard, mold is made and measured at molding temperature of 175 ℃ and molding pressure of 70kgf / cm 2 .

2) 유리전이온도(Tg) : TMA 측정설비를 이용하여 측정.2) Glass Transition Temperature (Tg): Measured using TMA measuring equipment.

3) 탄성율 E(kgf/mm2) : UTM을 사용하여 ASTM D190에 의해 측정.3) Modulus of elasticity E (kgf / mm 2 ): measured by ASTM D190 using UTM.

4) 열팽창계수 α(℃-1) : ASTM D96에 의해 측정.4) Thermal expansion coefficient α (° C -1 ): measured by ASTM D96.

5) 흡습율(%) : 성형품을 121℃ 2기압 수증기중에 48시간 동안 방치한 후 포화흡습율을 측정.5) Moisture absorption rate (%): After leaving the molded product in 121 ℃ 2 atm steam for 48 hours to measure the saturated moisture absorption.

6) 내크랙성 : 성형시킨 칩을 -55℃에서 30분, 150℃에서 30분을 1주기로 한 시험 조건에서 열충격시험을 2,000회 실시하고, 그때의 크랙발생수를 구하여 측정하였다.6) Crack resistance: The molded chip was subjected to 2,000 times of thermal shock tests under test conditions of 30 minutes at -55 ° C and 30 minutes at 150 ° C for 1 cycle.

[비교예][Comparative Example]

다음 표-1의 조성에 따라 상기 실시예 1-4와 동일한 방법으로 실시하고 물성을 측정하여 그 결과를 다음 표-2에 나타내었다.According to the composition of Table-1 and carried out in the same manner as in Example 1-4 and measured the physical properties and the results are shown in the following Table-2.

[표-1]Table-1

[표-2]TABLE 2

*내크랙성에서의 숫치중 분모는 시료수를, 분자는 불량갯수를 나타낸다. * In the crack resistance value, the denominator represents the number of samples and the molecule represents the number of defects.

상기 표-2에서 나타난 결과에서 보듯이 본 발명에 의한 수지 조성물은 비교예에 비해 뒤지지 않는 성형성을 가질 뿐 아니라 비교예보다 우수한 내열특성 및 내습성을 가지고 있어, 그 결과 내크랙성이 현저히 향상된 우수한 반도체 소자 밀봉용 수지 조성물임을 알 수 있다.As shown in the results shown in Table 2, the resin composition according to the present invention not only has a moldability which is inferior to that of the comparative example, but also has excellent heat resistance and moisture resistance than the comparative example, and as a result, the crack resistance is significantly improved. It can be seen that it is an excellent resin composition for sealing semiconductor elements.

Claims (2)

크레졸노블락형 에폭시수지와 경화제, 경화촉진제, 가소성부여제 및 고기능 에폭시를 함유하는 반도체 소자 밀봉용 에폭시수지 조성물에 있어서, 상기 고기능 에폭시수지로서 하기 일반식(I)로 표시되는 에폭시수지를 함유하는 것을 특징으로 하는 반도체 소자 밀봉용 에폭시수지 조성물.In the epoxy resin composition for sealing a semiconductor device containing a cresol noblock type epoxy resin, a curing agent, a curing accelerator, a plasticizer, and a high functional epoxy, the high functional epoxy resin containing an epoxy resin represented by the following general formula (I): Epoxy resin composition for sealing semiconductor elements. (여기에서, R1, R2는 H 또는 (CH2)nCH3기이고, n은 0 또는 1 이상의 정수이다.)(Wherein R 1 , R 2 are H or (CH 2 ) n CH 3 groups and n is 0 or an integer of 1 or more.) 제 1 항에 있어서, 상기 고기능 에폭시수지가 전체 수지 조성물에 대하여 0.1 내지 20.0중량%만큼 함유되어 있는 것을 특징으로 하는 반도체 소자 밀봉용 에폭시수지 조성물.The epoxy resin composition for semiconductor element sealing according to claim 1, wherein the high-performance epoxy resin is contained in an amount of 0.1 to 20.0% by weight based on the total resin composition.
KR1019910021872A 1991-11-30 1991-11-30 Epoxy resin composition for encapsulating semiconductor element KR960010307B1 (en)

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KR1019910021872A KR960010307B1 (en) 1991-11-30 1991-11-30 Epoxy resin composition for encapsulating semiconductor element
JP4278866A JPH0794535B2 (en) 1991-11-30 1992-10-16 Epoxy resin composition for semiconductor device sealing
US07/964,457 US5254605A (en) 1991-11-30 1992-10-21 Imide epoxy resin composition for sealing semiconductor elements
KR1019960010884A KR0172663B1 (en) 1991-11-30 1996-04-08 Method of manufacturing epoxy resin for sealing semiconductor device

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