JPH09176279A - Epoxy resin composition - Google Patents

Epoxy resin composition

Info

Publication number
JPH09176279A
JPH09176279A JP34158395A JP34158395A JPH09176279A JP H09176279 A JPH09176279 A JP H09176279A JP 34158395 A JP34158395 A JP 34158395A JP 34158395 A JP34158395 A JP 34158395A JP H09176279 A JPH09176279 A JP H09176279A
Authority
JP
Japan
Prior art keywords
epoxy resin
thermoplastic polymer
resin
curing
resin composition
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.)
Withdrawn
Application number
JP34158395A
Other languages
Japanese (ja)
Inventor
Hiromoto Nikaido
広基 二階堂
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 JP34158395A priority Critical patent/JPH09176279A/en
Publication of JPH09176279A publication Critical patent/JPH09176279A/en
Withdrawn legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain a semiconductor-sealing epoxy resin compsn. having a good shelf stability at around ordinary temp. (20 deg.C) and a soldering cracking resistance by incorporating thereinto a specific amt. of an inorg. filler and setting the glass transition temp. thereof prior to curing in a specific range. SOLUTION: This resin compsn. comprises as the indispensable components an epoxy resin, a phenolic resin curing agent, a curing accelerator, an inorg. filler, and a thermoplastic polymer, provided that it contains 80-90wt.% inorg. filler and has a grass transition temp. of 20 to 50 deg.C before curing of the whole resin compsn. The thermoplastic polymer to be used is desirably compatible with the epoxy resin or the phenolic resin curing agent, and desirably has its own grass transition temp. of 90 to 250 deg.C. Pref. examples of the thermoplastic polymer include polyarylates, polycarbonates, and polymethyl methacryalte.

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】本発明は常温保管性に優れた
半導体封止用エポキシ樹脂組成物に関するものである。
TECHNICAL FIELD The present invention relates to an epoxy resin composition for semiconductor encapsulation, which is excellent in storability at room temperature.

【0002】[0002]

【従来の技術】従来、ダイオ−ド、トランジスタ、集積
回路等の電子部品を 熱硬化性樹脂で封止しているが、
特に集積回路では耐熱性、耐湿性に優れたオルソクレゾ
−ルノボラック型エポキシ樹脂をフェノ−ルノボラック
樹脂で硬化させ、充填材として溶融シリカ、結晶シリカ
等の無機充填材を配合したエポキシ樹脂組成物が用いら
れている。ところが近年、集積回路の高集積化に伴いチ
ップがますます大型化し、かつパッケ−ジは従来のDI
Pタイプから表面実装化された小型、薄型のQFP、S
OP、SOJ、TSOP、TQFP、PLCCに変わっ
てきている。これらの表面実装化に伴い半導体封止用エ
ポキシ樹脂も耐半田クラック性の要求が高まり、低粘度
エポキシ樹脂を用いたフィラー高充填材料が主流になっ
ている。しかし、フィラー高充填化の為にエポキシ樹
脂、フェノール樹脂共に増々低粘度化している。その為
に封止樹脂組成物の保存性が低下している。従って、フ
ィラー高充填手法による耐半田クラック性が良好で、且
つ保存性が良好な半導体封止用エポキシ樹脂組成物の開
発が望まれている。
2. Description of the Related Art Conventionally, electronic parts such as diodes, transistors and integrated circuits are sealed with thermosetting resin.
Particularly in integrated circuits, an epoxy resin composition in which an ortho-cresol novolac type epoxy resin having excellent heat resistance and moisture resistance is cured with a phenol novolac resin, and fused silica as a filler or an inorganic filler such as crystalline silica is used is used. ing. However, in recent years, the chips have become larger and larger due to the high integration of integrated circuits, and the package has a conventional DI.
Small and thin QFP, S surface mounted from P type
OP, SOJ, TSOP, TQFP, PLCC have been changed. The demand for solder crack resistance of epoxy resins for semiconductor encapsulation has increased with the surface mounting, and filler-filled materials using low-viscosity epoxy resins have become the mainstream. However, both the epoxy resin and the phenol resin are becoming less viscous due to higher filling of the filler. Therefore, the preservability of the encapsulating resin composition is lowered. Therefore, it is desired to develop an epoxy resin composition for semiconductor encapsulation, which has good solder crack resistance by a high filler filling method and good storage stability.

【0003】[0003]

【発明が解決しようとする課題】本発明は、これらの問
題点に対して、無機充填材を80〜90重量%含み、硬
化前のガラス転移温度が20〜35℃になるようにする
ことにより、常温(20℃)付近での保存性が良好な耐
半田クラック半導体封止用エポキシ樹脂組成物を提供す
るところにある。
SUMMARY OF THE INVENTION The present invention addresses these problems by including an inorganic filler in an amount of 80 to 90% by weight so that the glass transition temperature before curing is 20 to 35 ° C. Another object of the present invention is to provide a solder crack resistant epoxy resin composition for semiconductor encapsulation, which has good storage stability at around room temperature (20 ° C.).

【0004】[0004]

【課題を解決するための手段】本発明は、エポキシ樹
脂、フェノール樹脂硬化剤、硬化促進剤、無機充填材、
及び熱可塑性ポリマーを必須成分とし、無機充填材を8
0〜90重量%含み、全樹脂組成物の硬化前のガラス転
移温度が20℃〜50℃であることを特徴とするエポキ
シ樹脂組成物であり、好ましくは熱可塑性ポリマーが、
エポキシ樹脂もしくはフェノール樹脂硬化剤に相溶し、
ガラス転移温度が、90〜250℃である半導体封止用
エポキシ樹脂組成物である。
The present invention provides an epoxy resin, a phenol resin curing agent, a curing accelerator, an inorganic filler,
And a thermoplastic polymer as an essential component, and an inorganic filler 8
An epoxy resin composition comprising 0 to 90% by weight and having a glass transition temperature of 20 ° C. to 50 ° C. before curing of all resin compositions, preferably a thermoplastic polymer,
Compatible with epoxy resin or phenol resin curing agent,
It is an epoxy resin composition for semiconductor encapsulation having a glass transition temperature of 90 to 250 ° C.

【0005】上記特性を有していれば、常温付近での保
管が長くなり、流動性が低下することなく成形できる。
硬化前のガラス転移温度が20℃未満だと保管性が低下
し、長時間常温で放置すると未充填や金線流れ等の成形
不良が生じてしまう。又、50℃を越えると流動性、耐
半田クラック性が低下する。ガラス転移温度は、TAイ
ンスツルメント社製 示差走査熱量計(2910MDS
C)で測定範囲:−20〜130℃、昇温速度:5℃/
min、振幅:±1.0、乾燥窒素気流中で測定する。
If it has the above-mentioned characteristics, it can be stored for a long time at around room temperature and can be molded without lowering the fluidity.
If the glass transition temperature before curing is less than 20 ° C., the storability is deteriorated, and if the glass transition temperature is left at room temperature for a long time, molding defects such as unfilling and gold wire flow occur. On the other hand, if the temperature exceeds 50 ° C., the fluidity and the solder crack resistance deteriorate. The glass transition temperature is a differential scanning calorimeter (2910MDS) manufactured by TA Instruments.
C) measuring range: -20 to 130 ° C, heating rate: 5 ° C /
min, amplitude: ± 1.0, measured in a stream of dry nitrogen.

【0006】[0006]

【発明の実施の形態】本発明に用いるエポキシ樹脂とは
エポキシ基を有するモノマー、オリゴマー、ポリマー全
般を言う。例えば、ビフェニル型エポキシ化合物、ビス
フェノール型エポキシ化合物、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化合物、アルキル変性
トリフェノールメタン型エポキシ化合物及びトリアジン
核含有エポキシ樹脂等を挙げることができる。
BEST MODE FOR CARRYING OUT THE INVENTION The epoxy resin used in the present invention refers to all monomers, oligomers and polymers having an epoxy group. For example, biphenyl type epoxy compound, bisphenol type epoxy compound, phenol novolac type epoxy resin, cresol novolac type epoxy resin,
Examples thereof include triphenol methane type epoxy compounds, alkyl-modified triphenol methane type epoxy compounds, and triazine nucleus-containing epoxy resins.

【0007】本発明で用いる硬化剤としては、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、パラキシリレン変
性フェノール樹脂、テルペン変性フェノール樹脂、トリ
フェノールメタン化合物等が挙げられ、特にフェノール
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、パラキシリレン変性フェノール樹脂、メタキシリ
レン変性フェノール樹脂、テルペン変性フェノール樹脂
及びこれらの混合物が好ましい。また、これらの硬化剤
の配合量としてはエポキシ化合物のエポキシ基数と硬化
剤の水酸基数を合わせるように配合することが好まし
い。
Examples of the curing agent used in the present invention include phenol novolac resin, cresol novolac resin, dicyclopentadiene modified phenol resin, paraxylylene modified phenol resin, terpene modified phenol resin and triphenol methane compound, and particularly phenol novolac resin. Preferred are dicyclopentadiene modified phenolic resin, paraxylylene modified phenolic resin, metaxylylene modified phenolic resin, terpene modified phenolic resin, and mixtures thereof. Moreover, it is preferable to mix these curing agents so that the number of epoxy groups of the epoxy compound and the number of hydroxyl groups of the curing agent are matched.

【0008】本発明に用いる硬化促進剤はエポキシ基と
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されているものを広く使用すること
ができる。例えば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、ジメチルベンジルアミンや2
−メチルイミダゾール等が挙げられ、単独でも混合して
用いてもよい。
The curing accelerator used in the present invention may be any one as long as it accelerates the curing reaction between the epoxy group and the hydroxyl group, and those generally used for sealing materials can be widely used. For example, 1,8-diazabicycloundecene,
Triphenylphosphine, dimethylbenzylamine and 2
-Methylimidazole, etc. may be mentioned, and they may be used alone or in combination.

【0009】本発明に用いる無機充填材は一般に封止材
料に使用されているものを広く使用することができる。
例えば、球状溶融シリカ粉末、破砕溶融シリカ粉末、結
晶シリカ粉末、2次凝集シリカ粉末、多孔質シリカ粉
末、アルミナ等が挙げられる。全樹脂組成物中の配合量
は80〜90重量%が望ましく、80重量%未満だと半
田クラック性が低下し、90重量%を越えると流動性が
低下し、成形不良が生じる。
As the inorganic filler used in the present invention, those generally used for the sealing material can be widely used.
Examples thereof include spherical fused silica powder, crushed fused silica powder, crystalline silica powder, secondary agglomerated silica powder, porous silica powder and alumina. The content in the entire resin composition is preferably 80 to 90% by weight, and if it is less than 80% by weight, the solder cracking property is deteriorated, and if it exceeds 90% by weight, the fluidity is deteriorated and molding failure occurs.

【0010】本発明に用いる熱可塑性ポリマーは、エポ
キシ樹脂もしくはフェノール樹脂硬化剤に相溶するもの
であればよく、熱可塑性ポリマー自体のガラス転移温度
は90〜250℃であることが望ましい。ガラス転移温
度が90℃未満であると熱可塑性ポリマーの使用割合が
増え、流動性が低下し、又、250℃を越えると熱可塑
性ポリマーにより増粘し、流動性が低下して好ましくな
い。尚、熱可塑性ポリマーのガラス転移温度の測定は、
セイコー電子社製 示差走査熱量計(DSC220)
で、測定範囲:0〜300℃、昇温速度:10℃/mi
n、乾燥窒素気流中で測定する。更に、熱可塑性ポリマ
ーはエポキシ樹脂、フェノール樹脂硬化剤もしくはその
混合物に予め溶融混合して使用した方が望ましい。尚、
ここで示す相溶性とは、一般的に用いられるエポキシ樹
脂もしくはフェノール樹脂硬化剤が溶融する温度70℃
〜140℃において熱可塑性ポリマーとエポキシ樹脂も
しくはフェノール樹脂硬化剤が均一な透明になることを
示すものである。熱可塑性ポリマーとして好ましいもの
はポリアリレート、ポリカーボネート、ポリメチルメタ
クリレート等が挙げられる。
The thermoplastic polymer used in the present invention may be one compatible with an epoxy resin or phenol resin curing agent, and the glass transition temperature of the thermoplastic polymer itself is preferably 90 to 250 ° C. If the glass transition temperature is lower than 90 ° C, the proportion of the thermoplastic polymer used increases and the fluidity decreases, and if it exceeds 250 ° C, the thermoplastic polymer thickens and the fluidity decreases, which is not preferable. Incidentally, the measurement of the glass transition temperature of the thermoplastic polymer,
Seiko Electronics Differential Scanning Calorimeter (DSC220)
And measurement range: 0 to 300 ° C., heating rate: 10 ° C./mi
n, measured in a stream of dry nitrogen. Further, it is desirable that the thermoplastic polymer is melt-mixed in advance with an epoxy resin, a phenol resin curing agent or a mixture thereof before use. still,
The compatibility shown here means a temperature of 70 ° C. at which a generally used epoxy resin or phenol resin curing agent melts.
It shows that the thermoplastic polymer and the epoxy resin or phenol resin curing agent become uniformly transparent at ˜140 ° C. Preferred examples of the thermoplastic polymer include polyarylate, polycarbonate, polymethylmethacrylate and the like.

【0011】本発明のエポキシ樹脂組成物はエポキシ樹
脂、硬化剤、無機充填材、硬化促進剤及び熱可塑性ポリ
マー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、ブロム化エポキシ樹脂、三酸化アン
チモン、ヘキサブロム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がな
い。また、本発明の封止用エポキシ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、硬化剤、硬化促
進剤、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。これらの成形材料は電気部品あるいは電子部品で
あるトランジスタ、集積回路等の被覆、絶縁、封止等に
適用することができる。
The epoxy resin composition of the present invention contains an epoxy resin, a curing agent, an inorganic filler, a curing accelerator and a thermoplastic polymer as essential components, but other than this, a silane coupling agent, a brominated epoxy may be added if necessary. Resins, antimony trioxide, flame retardants such as hexabromobenzene, colorants such as carbon black and red iron oxide, mold release agents such as natural wax and synthetic wax, and various additives such as low stress additives such as silicone oil and rubber. There is no problem in properly blending. Further, in order to produce the encapsulating epoxy resin composition of the present invention as a molding material, after the epoxy resin, the curing agent, the curing accelerator, the 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. These molding materials can be applied to coating, insulation, sealing, etc. of transistors, integrated circuits, etc., which are electric or electronic parts.

【0012】[0012]

【実施例】【Example】

〔実施例1〕下記組成物 ・溶融混合物A 12.8重量部 ・球状溶融シリカ粉末(平均粒径15μm、比表面積1.0m2/cm3) 85.0重量部 ・1,8−ジアザビシクロ(5,4,0)ウンデセン−7(DBU) 0.2重量部 ・カーボンブラック 0.5重量部 ・カルナバワックス 0.5重量部 をミキサ−で常温で混合し、70〜100℃で2軸ロ−
ルにより混練し、冷却後粉砕して成形材料とした。[溶
融混合物A]とは、ビフェニル型エポキシ樹脂(融点9
5℃、エポキシ当量200g/eq)5.1重量部、パ
ラキシリレン変性フェノール樹脂硬化剤A(軟化点65
℃、水酸基当量175g/eq)4.7重量部、ブロム
化エポキシ樹脂(軟化点53℃、エポキシ当量360g
/eq)1.0重量部及びポリアリレート(ガラス転移
温度110℃)3.0重量部を150℃で溶融混合した
ものである。粉砕して得られた成形材料をタブレット化
し、低圧トランスファ−成形機にて175℃、70Kg
/cm2、半田クラック試験用として6×6mmのチッ
プを52pQFPに封止した。得られた成形材料につい
てガラス転移温度の測定及び保管性試験を行った。更
に、封止したテスト用素子について半田クラック試験を
行った。
[Example 1] The following composition-Fused mixture A 12.8 parts by weight-Spherical fused silica powder (average particle size 15 µm, specific surface area 1.0 m 2 / cm 3 ) 85.0 parts by weight-1,8-diazabicyclo ( 5,4,0) Undecene-7 (DBU) 0.2 parts by weight Carbon black 0.5 parts by weight Carnauba wax 0.5 parts by weight are mixed in a mixer at room temperature, and the mixture is biaxially rotated at 70 to 100 ° C. −
Kneading with a mullet, cooling and pulverizing to obtain a molding material. [Melted mixture A] means biphenyl type epoxy resin (melting point 9
5 ° C., epoxy equivalent of 200 g / eq, 5.1 parts by weight, paraxylylene-modified phenol resin curing agent A (softening point 65
° C, hydroxyl equivalent 175 g / eq) 4.7 parts by weight, brominated epoxy resin (softening point 53 ° C, epoxy equivalent 360 g)
/ Eq) 1.0 part by weight and polyarylate (glass transition temperature 110 ° C.) 3.0 parts by weight are melt mixed at 150 ° C. The molding material obtained by crushing is tableted, and is 175 ° C. and 70 Kg by a low pressure transfer molding machine.
/ Cm 2, the 6 × 6 mm of chip as a solder crack test was sealed in 52PQFP. The glass transition temperature was measured and the storability test was performed on the obtained molding material. Further, a solder crack test was conducted on the sealed test element.

【0013】《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金型を用いて、金型温度175℃、
注入圧力70kg/cm2 、硬化時間2分で測定した。 ・保管性試験:25℃で保存した成形材料のスパイラル
フロー流動性について経時変化を測定し、スパイラルフ
ロー残存率=[(ある日数保管した後のスパイラルフロ
ー値)/(保管前のスパイラルフロー値)×100]が
90%になるまでの日数で評価した 。 ・半田クラック試験:封止したテスト用素子を85℃、
85%RHの環境下で120時間及び168時間処理
し、その後260℃の半田槽に10秒間浸漬後顕微鏡で
外部クラックを観察した。
<< Evaluation Method >> Spiral Flow: A mold for measuring spiral flow according to EMMI-I-66 was used, and the mold temperature was 175 ° C.
The measurement was performed at an injection pressure of 70 kg / cm 2 and a curing time of 2 minutes. Storability test: Spiral flow fluidity of a molding material stored at 25 ° C. was measured over time, and spiral flow residual rate = [(spiral flow value after storage for a certain number of days) / (spiral flow value before storage) × 100] was evaluated by the number of days until it reached 90%.・ Solder crack test: sealed test device at 85 ℃,
It was treated in an environment of 85% RH for 120 hours and 168 hours, then immersed in a solder bath at 260 ° C. for 10 seconds, and then external cracks were observed with a microscope.

【0014】〔実施例2、3〕〔比較例1、2〕 表1の処方に従って配合し、実施例1と同様にして成形
材料を得た。この成形材料でガラス転移温度の測定、保
管性試験及び半田クラック試験を行った。試験結果を表
1に示す。実施例1以外で使用した原材料は下記のとお
りである。 [溶融混合物B]:ビフェニル型エポキシ樹脂(融点9
5℃、エポキシ当量200g/eq)4.5重量部、パ
ラキシリレン変性フェノール樹脂硬化剤B(軟化点75
℃、水酸基当量175g/eq)4.3重量部、ブロム
化エポキシ樹脂(軟化点53℃、エポキシ当量360g
/eq)1.0重量部及びポリアリレート(ガラス転移
温度110℃)2.0重量部を150℃で溶融混合した
ものである。 [溶融混合物C]:ビフェニル型エポキシ樹脂(融点9
5℃、エポキシ当量200g/eq)4.0重量部、パ
ラキシリレン変性フェノール樹脂硬化剤A(軟化点65
℃、水酸基当量175g/eq)3.8重量部、ブロム
化エポキシ樹脂(軟化点53℃、エポキシ当量360g
/eq)1.0重量部及びポリカーボネート(ガラス転
移温度130℃)3.0重量部を150℃で溶融混合し
たものである。 ・ビフェニル型エポキシ樹脂:融点95℃、エポキシ当
量200g/eq ・パラキシリレン変性フェノール樹脂硬化剤A:軟化点
65℃、水酸基当量175g/eq ・ブロム化エポキシ樹脂:軟化点53℃、エポキシ当量
360g/eq
[Examples 2 and 3] [Comparative Examples 1 and 2] Compounding was carried out according to the formulation shown in Table 1, and molding materials were obtained in the same manner as in Example 1. The glass transition temperature was measured, the storability test and the solder crack test were performed on this molding material. Table 1 shows the test results. The raw materials used in other than Example 1 are as follows. [Melted mixture B]: Biphenyl type epoxy resin (melting point 9
5 ° C., epoxy equivalent 200 g / eq) 4.5 parts by weight, paraxylylene-modified phenol resin curing agent B (softening point 75
° C, hydroxyl equivalent 175 g / eq) 4.3 parts by weight, brominated epoxy resin (softening point 53 ° C, epoxy equivalent 360 g)
/ Eq) 1.0 part by weight and polyarylate (glass transition temperature 110 ° C.) 2.0 parts by weight are melt-mixed at 150 ° C. [Melted mixture C]: Biphenyl type epoxy resin (melting point 9
5 ° C., epoxy equivalent 200 g / eq 4.0 parts by weight, paraxylylene-modified phenol resin curing agent A (softening point 65
℃, hydroxyl equivalent 175g / eq 3.8 parts by weight, brominated epoxy resin (softening point 53 ℃, epoxy equivalent 360g
/ Eq) 1.0 part by weight and polycarbonate (glass transition temperature 130 ° C.) 3.0 parts by weight are melt-mixed at 150 ° C. -Biphenyl type epoxy resin: melting point 95 ° C, epoxy equivalent 200g / eq-paraxylylene-modified phenol resin curing agent A: softening point 65 ° C, hydroxyl equivalent 175g / eq-brominated epoxy resin: softening point 53 ° C, epoxy equivalent 360g / eq

【0015】 表 1 実 施 例 比 較 例 1 2 3 1 2 配合(重量部) 溶融混合物A 13.8 溶融混合物B 11.8 溶融混合物C 11.8 ヒ゛フェニル型エホ゜キシ樹脂 5.6 12.3 ハ゜ラキシリレン変性フェノ-ル樹脂A 5.2 10.5 フ゛ロム化エホ゜キシ樹脂 1.0 1.0 球状溶融シリカ 85.0 87.0 87.0 87.0 75.0 DBU 0.2 0.2 0.2 0.2 0.2 カ−ボンブラック 0.5 0.5 0.5 0.5 0.5 カルナバワックス 0.5 0.5 0.5 0.5 0.5 特性 スパイラルフロー(cm) 120 90 100 110 80 ガラス転移温度(℃) 35 35 40 18 20 半田クラック 吸湿120時間 0/8 0/8 0/8 0/8 8/8 吸湿168時間 3/8 0/8 0/8 0/8 8/8 保管性(日) 7 7 10 1 2 Table 1 Example Comparative Example 1 2 3 12 Compounding (parts by weight) Melt mixture A 13.8 Melt mixture B 11.8 Melt mixture C 11.8 Biphenyl type epoxy resin 5.6 12.3 Paraxylylene-modified phenolic resin A 5.2 10.5 Brominated epoxy resin 1.0 1.0 Spherical Fused silica 85.0 87.0 87.0 87.0 75.0 DBU 0.2 0.2 0.2 0.2 0.2 Carbon black 0.5 0.5 0.5 0.5 0.5 Carnauba wax 0.5 0.5 0.5 0.5 0.5 Characteristics Spiral flow (cm) 120 90 100 110 80 Glass transition temperature (° C) 35 35 40 18 20 Solder crack Moisture absorption 120 hours 0/8 0/8 0/8 0/8 8/8 Moisture absorption 168 hours 3/8 0/8 0/8 0/8 8/8 Storability (days) 7 7 10 1 2

【0016】[0016]

【発明の効果】本発明の半導体封止用エポキシ樹脂組成
物は、薄型パッケージに対して耐半田クラック性が良好
で、常温(20℃)での保存性が向上した。
EFFECT OF THE INVENTION The epoxy resin composition for semiconductor encapsulation of the present invention has good solder crack resistance for a thin package and has improved storage stability at room temperature (20 ° C.).

───────────────────────────────────────────────────── 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 NJX C08L 63/00 NJX H01L 23/29 H01L 23/30 R 23/31 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display location C08L 63/00 NJX C08L 63/00 NJX H01L 23/29 H01L 23/30 R 23/31

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 エポキシ樹脂、フェノール樹脂硬化剤、
硬化促進剤、無機充填材、及び熱可塑性ポリマーを必須
成分とし、無機充填材を80〜90重量%含み、全樹脂
組成物の硬化前のガラス転移温度が20〜50℃である
ことを特徴とするの半導体封止用エポキシ樹脂組成物。
An epoxy resin, a phenol resin curing agent,
A curing accelerator, an inorganic filler, and a thermoplastic polymer as essential components, containing 80 to 90% by weight of the inorganic filler, and the glass transition temperature of the entire resin composition before curing is 20 to 50 ° C. Epoxy resin composition for semiconductor encapsulation.
【請求項2】 熱可塑性ポリマーが、エポキシ樹脂及び
/又はフェノール樹脂硬化剤に相溶することを特徴とす
る請求項1記載の半導体封止用エポキシ樹脂組成物。
2. The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein the thermoplastic polymer is compatible with an epoxy resin and / or a phenol resin curing agent.
【請求項3】 熱可塑性ポリマーのガラス転移温度が、
90〜250℃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。
3. The glass transition temperature of the thermoplastic polymer is
The epoxy resin composition for semiconductor encapsulation according to claim 1 or 2, which has a temperature of 90 to 250 ° C.
【請求項4】 熱可塑性ポリマーが、ポリアリレート又
はポリカーボネートである請求項1又は3記載の半導体
封止用エポキシ樹脂組成物。
4. The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein the thermoplastic polymer is polyarylate or polycarbonate.
JP34158395A 1995-12-27 1995-12-27 Epoxy resin composition Withdrawn JPH09176279A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34158395A JPH09176279A (en) 1995-12-27 1995-12-27 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34158395A JPH09176279A (en) 1995-12-27 1995-12-27 Epoxy resin composition

Publications (1)

Publication Number Publication Date
JPH09176279A true JPH09176279A (en) 1997-07-08

Family

ID=18347205

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34158395A Withdrawn JPH09176279A (en) 1995-12-27 1995-12-27 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JPH09176279A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100665388B1 (en) * 2005-11-11 2007-01-04 곽봉주 Flexible epoxy resin composites and epoxy copper clad laminates using the same
JP2013203928A (en) * 2012-03-29 2013-10-07 Sumitomo Bakelite Co Ltd Epoxy resin composition for sealing, electronic equipment and method for manufacturing electronic equipment

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100665388B1 (en) * 2005-11-11 2007-01-04 곽봉주 Flexible epoxy resin composites and epoxy copper clad laminates using the same
JP2013203928A (en) * 2012-03-29 2013-10-07 Sumitomo Bakelite Co Ltd Epoxy resin composition for sealing, electronic equipment and method for manufacturing electronic equipment

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