JPS62209126A - Epoxy resin composition for sealing semiconductor device - Google Patents

Epoxy resin composition for sealing semiconductor device

Info

Publication number
JPS62209126A
JPS62209126A JP5143486A JP5143486A JPS62209126A JP S62209126 A JPS62209126 A JP S62209126A JP 5143486 A JP5143486 A JP 5143486A JP 5143486 A JP5143486 A JP 5143486A JP S62209126 A JPS62209126 A JP S62209126A
Authority
JP
Japan
Prior art keywords
parts
epoxy resin
epoxy
resin
weight
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
JP5143486A
Other languages
Japanese (ja)
Inventor
Akira Yoshizumi
善積 章
Hisashi Hirai
久之 平井
Shinetsu Fujieda
新悦 藤枝
Takeshi Uchida
健 内田
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.)
Toshiba Corp
Original Assignee
Toshiba Corp
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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP5143486A priority Critical patent/JPS62209126A/en
Publication of JPS62209126A publication Critical patent/JPS62209126A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)

Abstract

PURPOSE:The titled composition capable of providing a cured material having improved thermal shock resistance, containing an epoxy resin, a novolak phenolic resin, silica powder, a dimethyl-siloxane oil and a surface active agent in a specific ratio. CONSTITUTION:The aimed composition consisting of (A) 100pts.wt. epoxy resin (preferably containing at least two epoxy groups in one molecule), (B) 30-70pts. wt. novolak type phenolic resin (preferably one having 80-100 deg.C softening point and 100-110 OH equivalents) as a curing agent, (C) 300-550pts.wt. silica powder (preferably one having 5-30mu average particle diameter) as a filler, (D) 0.2-20pts.wt. dimethylsiloxane oil (preferably one having 50,000-500,000cps at 20 deg.C) and (E) 0.2-20pts.wt., preferably 1-10pts.wt. fluorine type and/or silicone type surface active agent.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は半導体装置封止用エポキシ樹脂組成物に関し、
更に詳しくは、優れた耐熱衝撃性を有する硬化物を与え
る半導体装置封止用エポキシ樹脂組成物に関する。
[Detailed Description of the Invention] [Technical Field of the Invention] The present invention relates to an epoxy resin composition for encapsulating semiconductor devices,
More specifically, the present invention relates to an epoxy resin composition for encapsulating semiconductor devices that provides a cured product having excellent thermal shock resistance.

〔発明の技術的背最とその問題点〕[Technical background of the invention and its problems]

近年、半導体装置の封止に関する分野においては、半導
体パッケージの4内化に伴い、寅だな間dが生じてきて
いる。薄肉化したフラットパッケージをJfj、仮に実
装する際1通常のDIPと異なり。
In recent years, in the field of encapsulation of semiconductor devices, a gap has been occurring due to the shift to four-pack semiconductor packages. When mounting a thinner flat package with JFJ, 1Unlike normal DIP.

樹脂パッケージ側から高温半田(たとえば260℃)処
理を行つ。そのため従来の樹脂では熱衝撃により、樹脂
フラッグが生じたり、その後の加速耐湿テスト(PUT
)に耐えられない。
High-temperature soldering (for example, 260° C.) is performed from the resin package side. Therefore, with conventional resins, resin flags may occur due to thermal shock, and subsequent accelerated moisture resistance tests (PUT
) can't stand it.

そこでこのような問題の対策としては、フレーム設計と
榴脂濶から改善が行なわれているが、十分な対東法は見
出されていない。たとえば、樹脂1−からの対策として
は、樹脂のガラス転移12,1度を下げて、半田にさら
された際の熱衝撃を樹脂の柔軟化で吸収しようとする試
みなどがあるが、一方で、ワイヤーオープン等の別の不
良が多発するという間租が生じるため好ましくない・ 〔発明の目的〕 本発明の目的は、上シした欠点の解消または上記対策項
目の光足を可能にし、優れた耐熱:衝毫注を有する硬化
物を与える半導体4Aa封止用エポキシ樹脂@成物を機
供することにある。
Therefore, as a countermeasure for such problems, improvements have been made from the frame design and the structure, but no sufficient countermeasures have been found. For example, as a countermeasure for resin 1-, there are attempts to lower the glass transition of the resin by 12.1 degrees and soften the resin to absorb the thermal shock when exposed to solder. This is undesirable because other defects such as open wires occur frequently. Heat resistance: The objective is to provide an epoxy resin composition for semiconductor 4Aa sealing that provides a cured product with impact resistance.

〔発明のg要〕[Key points of invention]

本発明者らは、少1脂封止型の半導体装置の信・項性を
改嵜丁べく鋭意研究を重ねた結果、樹脂組成物の成分と
してジメチルシロキサンオイルとフッ素系及び/又はシ
リコーン系界面活性剤とを併用することにより、その組
成物が優れた耐熱衝撃性を有する硬化物を与えることを
見い出し1本発明を完成するに到った。
As a result of intensive research aimed at improving the reliability and properties of low-fat encapsulated semiconductor devices, the present inventors discovered that dimethylsiloxane oil and fluorine-based and/or silicone-based interfaces were used as components of the resin composition. The present invention was completed based on the discovery that the composition can provide a cured product having excellent thermal shock resistance when used in combination with an activator.

すなわち、本発明の半導体装置封止用エポキシ樹脂組成
物は、 a)エポキシ樹脂       100重量部b)ノボ
ラック型フェノール樹脂。
That is, the epoxy resin composition for encapsulating a semiconductor device of the present invention includes: a) 100 parts by weight of an epoxy resin; b) a novolac type phenol resin.

30〜70重量部 C)シリカ粉末     300〜550′!量部d)
ジメチルシロキサ/オイル0.2〜20重量部e)フッ
素系及び/又は、シリコーン系界面活性剤      
  0.2〜20重量部からなることを特徴とするもの
である。
30-70 parts by weight C) Silica powder 300-550'! Volume part d)
Dimethylsiloxa/oil 0.2-20 parts by weight e) Fluorine-based and/or silicone-based surfactant
It is characterized by comprising 0.2 to 20 parts by weight.

本発明に係る組成物中の一成分であるエポキシ樹脂(a
)は1分子中にエポキシ基を少なくとも2個有するもの
であればいかなるものであってもよく。
Epoxy resin (a) which is one component in the composition according to the present invention
) may be of any type as long as it has at least two epoxy groups in one molecule.

例えば、ビスフェノールA基エポキシ樹脂、ノボラック
型エポキシ樹脂、脂環型エポキシ樹脂、グリシジルエス
テル型エポキシ樹脂が挙げられる。
Examples include bisphenol A-based epoxy resins, novolak-type epoxy resins, alicyclic-type epoxy resins, and glycidyl ester-type epoxy resins.

また、これらを適宜に組み合わせて用いても良い。Moreover, you may use these in combination suitably.

これらのエポキシ樹脂の具体例としては、l!30CN
−1028(日本化薬〔株〕、軟化点74℃、エポキシ
当量215)、ESCN−195XL(住友化学(株)
、軟化点71℃、エポキシ当量198)、ECN−12
73(チバガイギー社、軟化点り3℃、エポキシ当11
230)EPPN−201(日本化薬(火、軟化点65
℃、エポキシ当量181)、エピコート1001 (シ
ェル化学、軟化点70℃、エポキシ当!1t475)、
チッソノックス201(チッソc力、粘度1800 c
ps(25°C)、エポキシ当2154)、チッソノッ
クス289(チッソ0株)粘度870cps(25℃)
、エポキシ当121q)などが挙げられる。上記エポキ
シ樹脂の中でも軟化点60〜100℃を有するものが好
ましく、特に好ましくは70〜85℃を有するものであ
る。また、エポキシ当1−100〜300 を有するも
のが好ましく、特に好ましくは175〜220を有する
ものである。
Specific examples of these epoxy resins include l! 30CN
-1028 (Nippon Kayaku Co., Ltd., softening point 74°C, epoxy equivalent 215), ESCN-195XL (Sumitomo Chemical Co., Ltd.)
, softening point 71°C, epoxy equivalent weight 198), ECN-12
73 (Ciba Geigy, softening point 3℃, epoxy 11
230) EPPN-201 (Nippon Kayaku (Tue, Softening Point 65
℃, epoxy equivalent 181), Epicote 1001 (Shell Chemical, softening point 70℃, epoxy equivalent! 1t475),
Chisson Knox 201 (Chisso c force, viscosity 1800 c
ps (25°C), epoxy 2154), Chissonox 289 (Chisso 0 stock) viscosity 870cps (25°C)
, epoxy 121q), etc. Among the above epoxy resins, those having a softening point of 60 to 100°C are preferred, and those having a softening point of 70 to 85°C are particularly preferred. Moreover, those having an epoxy weight of 1-100 to 300 are preferable, and those having an epoxy weight of 1-175 to 220 are particularly preferable.

この(at酸成分は、好ましくは、エポキシ樹脂100
重′看部に対して、30重量部までの難燃エポキシ樹脂
を加えることで、構成される。
This (at acid component is preferably an epoxy resin 100%
It is constructed by adding up to 30 parts by weight of a flame retardant epoxy resin to the heavy part.

本発明に係るノボラック型フェノール樹脂(b)は(a
)K分のエポキシ樹脂の硬化剤として作用するものでち
り1例えば、フェノールノボラック樹脂。
The novolac type phenolic resin (b) according to the present invention is (a
) Dust 1 that acts as a hardening agent for epoxy resins with K content, for example, phenol novolac resins.

ブレゾールノボラック樹脂などのフェノール性水鐵基を
2個以上有するものが挙げられる。具体例としてはB几
M−558(昭和ユニオン合成化学(株)、軟化点97
℃、Q H当合約104ン、BR,M−557(昭和ユ
ニオン合成化学(a)、軟化点86℃、OH当聞約10
4)などがある。前記ノボラック型フェノール樹脂の中
でも、軟化点60〜120℃を有するものが好ましく、
特に好ましくは80〜1oo℃を有するものであり、水
酸基当量100〜150を有するものが好ましく、特に
好゛ましくは100〜110 を有するものである。
Examples include those having two or more phenolic hydrogen groups such as bresol novolak resin. A specific example is B-M-558 (Showa Union Synthetic Chemical Co., Ltd., softening point 97).
°C, QH current approximately 104 m, BR, M-557 (Showa Union Synthetic Chemical (a), softening point 86°C, OH current approximately 10
4) etc. Among the novolac type phenolic resins, those having a softening point of 60 to 120°C are preferred,
Particularly preferred are those having a temperature of 80 to 100°C, and those having a hydroxyl equivalent of 100 to 150, particularly preferably 100 to 110.

又、このフェノール樹脂の添加量は、30〜70重量部
が好ましいその理由は30ii部以下では十分な強度が
得られず、一方70i量都以上だと耐湿性が劣化するか
らである。
The amount of the phenol resin added is preferably 30 to 70 parts by weight, because if it is less than 30 parts, sufficient strength cannot be obtained, while if it is more than 70 parts, the moisture resistance will deteriorate.

この発明の(c)成分としての充填剤べ、封と材料の線
膨張係数を小さくして封止樹脂と素子や11−ドフレー
ムなどとのはくり現壕を防止し、その結果として半導体
デバイスの耐湿性を向上させるためのものである。
The filler as component (c) of this invention reduces the linear expansion coefficient of the sealing material to prevent peeling of the sealing resin and the element or frame, and as a result, the semiconductor device This is to improve the moisture resistance of.

具体例としてに、破砕状1球状などの形状を持つ溶融シ
リカ粉末や結晶性シリカ粉が便用できる。
As a specific example, fused silica powder or crystalline silica powder having a shape such as a crushed spherical shape can be conveniently used.

粉末の平均粒径としては5〜30μmが好ましい。The average particle size of the powder is preferably 5 to 30 μm.

又、充填債としては300〜550重量部が好ましい、
その理由は、300重針部以下では、熱膨張係数が大き
くなりワイヤーオープンによる不良が生じやすい。一方
550市締部以上では、成形時の粘度が高くなり成形性
が悪くなる。
In addition, the filling bond is preferably 300 to 550 parts by weight.
The reason is that below 300 needles, the coefficient of thermal expansion becomes large and defects due to wire open tend to occur. On the other hand, if it is above 550 degrees, the viscosity during molding becomes high and moldability deteriorates.

不発明に係るシリコーンオイルfdlは。Silicone oil fdl according to the invention.

0.1・ の化合物であればいかなるものであってもよく、具体的
にはTSF−451−IM(東芝(禦、粘度(2(JC
)約10000cpS)、TSF−451−10M(東
芝シリコーン+m s枯反(20°C)約IQOOOO
cps)、TSF−451−50M(東芝シリコーン■
、粘度(20℃)約5oooo。
Any compound with a viscosity of 0.1.
) approx. 10,000 cpS), TSF-451-10M (Toshiba silicone + m s deadback (20°C) approx. IQOOOO
cps), TSF-451-50M (Toshiba Silicone ■
, viscosity (20°C) approximately 5oooo.

cps )、5H−200−5000(東しシリコーン
fi@、粘度(20℃)約5000cps)などがあげ
られる。
cps), 5H-200-5000 (Toshi Silicone fi@, viscosity (20°C) approximately 5000 cps), and the like.

ただシリコーンオイルの中でも、粘度(20℃)500
〜1000000cpsを有するものが好ましく、特に
好ましくは500tlO〜500000cpsをMする
ものである。
However, among silicone oils, the viscosity (20℃) is 500.
It is preferable to have an M of 1,000,000 cps, and particularly preferably 500 to 500,000 cps.

この(d)成分の配合割合に、a常、0.2〜20i量
部で、好ましくは1〜10菖を部である。この配合割合
が0.2貞降部未満の場合には耐熱衝撃性の改良効果が
十分でな(,20車+i部を超える場合には硬化物の表
面がシリコーンオイルの浮キ出しで汚れ好ましくない。
The blending ratio of component (d) is usually 0.2 to 20 parts, preferably 1 to 10 parts. If this blending ratio is less than 0.2 parts, the effect of improving thermal shock resistance will not be sufficient (if it exceeds 20 parts + i parts, the surface of the cured product will become dirty due to silicone oil embossment). do not have.

本発明方法に用いるfe)フッ素系界面活性剤としては
1例えば、非イオン−性界面活性剤FC−430゜FC
−431,FC−176(商品名、いずれも注文スリー
エム■社製)など、また、シリコーン系界面活性剤とし
ては1例えば非イオン性界面活性剤5H−3746,5
t(−3749,5F−8421,5F−8410(商
品名、いずれも東しシリコーン■辻製)のようなグリコ
ール変性シリコーン系界面活性剤などがあげられる。
fe) Fluorine surfactants used in the method of the present invention include 1, for example, the nonionic surfactant FC-430°FC.
-431, FC-176 (trade name, both manufactured by 3M Corporation), etc. Silicone surfactants include 1, for example, nonionic surfactants 5H-3746, 5
Examples include glycol-modified silicone surfactants such as t(-3749, 5F-8421, 5F-8410 (trade names, all manufactured by Toshi Silicone Tsuji).

このfe)成分の配合割合は1通常、0.2〜20厘量
部で、好ましくはl−10Wt部である。この配合“割
合が0.2上置部未満の場合には、耐熱衝撃性能の改良
硬化が十分でな(2部mt部を超える場合には樹脂の底
形性が劣化して好ましくない。
The blending ratio of this component (fe) is usually 0.2 to 20 parts by weight, preferably 1-10 parts by weight. If this blending ratio is less than 0.2 parts, the improved curing of thermal shock resistance will not be sufficient (if it exceeds 2 parts mt, the bottom shape of the resin will deteriorate, which is not preferred).

つぎに1本発明の半導体樹脂封止用エポキシ樹脂組成物
の製造方法について述べる。
Next, a method for manufacturing the epoxy resin composition for semiconductor resin encapsulation of the present invention will be described.

本発明の組成物は、上記した各成分を、加熱ロールによ
る溶融混線、ニーダ−による溶融混線。
The composition of the present invention is prepared by melting and mixing the above-mentioned components using a heated roll and a kneader.

押出機による溶融混線、微扮砕後の特殊混合機による混
合及びこれらの各方法の適宜な組合せによって容易に製
造することができる。
It can be easily produced by melt blending using an extruder, mixing using a special mixer after fine crushing, or an appropriate combination of these methods.

なお1本発明の組成物は、必要に応じて、イミダゾール
もしくはその誘導体、再三級アミン系誘導体、ホスフィ
ン誘導体、シクロアミジン誘導体などの硬化促進剤; 高級脂肪酸、ワックス類などの離型剤;エポキシシラン
、ビニルシラン、アミノシラン、ボラン系化合物、アル
コキシチタネート系化合物、アルミキレート系化合物な
どのカップリング剤;アンチ七ン、リン化合物、臭素や
塩素を含む公知の難燃化剤が配合されてもよい。
Note that the composition of the present invention may optionally contain a curing accelerator such as imidazole or its derivative, a tertiary amine derivative, a phosphine derivative, a cycloamidine derivative; a mold release agent such as a higher fatty acid or wax; and an epoxy. Coupling agents such as silanes, vinylsilanes, aminosilanes, borane compounds, alkoxytitanate compounds, and aluminum chelate compounds; known flame retardants containing anti-sulfur compounds, phosphorus compounds, bromine, and chlorine may be blended.

〔発明の実施例〕[Embodiments of the invention]

以下において、実施例及び比較例を掲げ1本発明を更に
詳しく説明する。
Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.

なお、実施列及び比較例中、「都」μ全て「直皺部」を
示す。
In the Examples and Comparative Examples, "Miyako" μ all indicate "straight wrinkles".

実施例1 オルトクレゾールノボラック型エポキシ樹脂(軟化点7
6℃、当1206)1009.臭素化フェノールノボラ
ッグ型エポキシ樹脂(某素言M1130%、軟化点87
℃、エポキシ当量27o)15都、フェノールノボラッ
ク樹脂(軟化点95℃、水酸基当量104 ) 50部
、光填剤として浴融シリカ粉(平均粒径18μm)42
0部、ジメチルシロキサンオイルとしてTSF−451
−1部M(東芝シリp−ン■)3s、フッ素系界面活a
剤FC−430(注文スリーエム■)1.5都、さらに
硬1ヒ促進剤としてトルフェニルホスフィン1.5綿、
雌型剤としてカルナバワックス1fIs、着色剤として
カーボン粉末1.8部、#!燃助剤として三酸化アンチ
モン粉末15部アンチモン粉末1糸 中でエポキシシラン系カップリング剤で処理したのち,
ジメチルシロキサンオイルとフッ素系界面活性剤を加え
て混合し、最後に残余の材料を加えて混線用の配合物と
した。
Example 1 Orthocresol novolac type epoxy resin (softening point 7
6℃, 1206) 1009. Brominated phenol novolag type epoxy resin (certain raw material M1130%, softening point 87
50 parts of phenol novolak resin (softening point 95°C, hydroxyl equivalent 104), bath-fused silica powder (average particle size 18 μm) as optical filler 42
0 parts, TSF-451 as dimethylsiloxane oil
-1 part M (Toshiba silicon ■) 3s, fluorine-based surfactant a
agent FC-430 (Order 3M ■) 1.5 ml, and as a hardening accelerator, tolphenylphosphine 1.5 ml,
1 fIs of carnauba wax as a female mold agent, 1.8 parts of carbon powder as a coloring agent, #! After treating 15 parts of antimony trioxide powder as a combustion aid in one thread of antimony powder with an epoxy silane coupling agent,
Dimethylsiloxane oil and fluorosurfactant were added and mixed, and finally the remaining materials were added to form a mixture for crosstalk.

そののち、70〜100℃の二軸ロールで混練し。After that, it is kneaded with twin screw rolls at 70 to 100°C.

得られた混練物を冷却・粉砕し、タブレット化して本発
明の半導体装置封止用エポキシ棟脂組成物を得た。
The obtained kneaded product was cooled, crushed, and tableted to obtain an epoxy ridge resin composition for encapsulating a semiconductor device of the present invention.

得られた組成物を用いて、低圧トランスファー成形機(
東亜精機50トンプレス)により、175℃、80 k
g/cm” 、  120秒の条件で、耐熱1#濯性試
、験用に3mmX3mmの大きさのテスト素子を2mm
厚さの24ビンフラツトパツケージに封止した。
Using the obtained composition, a low pressure transfer molding machine (
Toa Seiki 50 ton press), 175℃, 80k
g/cm”, 120 seconds, heat resistance 1# washing property test, test element of size 3mm x 3mm was 2mm
It was sealed in a 24-bottle flat package.

得られた試料素子について耐熱衝撃性を又機械特性(曲
げ弾性率1曲げ強さ)及び熱特注(ガラス転移点、熱膨
張係数)を評価するために成形品モールドし、後述する
各試験を実施した。
The obtained sample element was molded into a molded product to evaluate thermal shock resistance, mechanical properties (flexural modulus 1 bending strength), and thermal customization (glass transition point, coefficient of thermal expansion), and various tests described below were conducted. did.

なお樹脂成形品はすべて175℃x4Hの後硬化を実施
している。耐熱衝撃性試験−得られた試料素子20個を
用い260℃X 10 secの半田浸漬を行なったの
ち、7IO速耐湿テスト(PCT、25気圧、127℃
)を行ない、不良発生をチェックした。
All resin molded products were post-cured at 175°C for 4 hours. Thermal Shock Resistance Test - After performing solder immersion at 260°C for 10 seconds using 20 sample elements obtained, a 7IO rapid moisture resistance test (PCT, 25 atm, 127°C) was performed.
) to check for defects.

曲げ弾性率はJISK−6911に鵡じて測定した。The flexural modulus was measured in accordance with JISK-6911.

曲げ強さはJISK−6911に準じて測定した。Bending strength was measured according to JISK-6911.

ガラス転移点は真空理工製の熱1を張計を用い。The glass transition point was measured using a heat 1 tension meter manufactured by Shinku Riko.

熱膨張カーブの変曲点より求めた。It was determined from the inflection point of the thermal expansion curve.

熱膨張係数は真空理工製熱J膨張計を用いてi!II定
した。
The coefficient of thermal expansion was measured using a thermal J dilatometer manufactured by Shinku Riko. II was determined.

実施例2 実施例1のジメチルシロキサンオイル81都、フッ素系
界面活性剤を3.5部に代えた以外は、実施例1と同様
にして本発明の組成物を傅た。
Example 2 A composition of the present invention was prepared in the same manner as in Example 1, except that 81 parts of the dimethylsiloxane oil and 3.5 parts of the fluorine-based surfactant were used in Example 1.

実施例3 実施例1のフッ素系界面活性剤をシリコーン系界面活性
剤8F−8421(東しシリコーン■投)とした以外は
実施例1と同様にして本発明の組成物を得た。
Example 3 A composition of the present invention was obtained in the same manner as in Example 1, except that the fluorine-based surfactant in Example 1 was replaced with silicone-based surfactant 8F-8421 (Toshi Silicone ■).

実施例4 実施例1のジメチルシロキサンオイル(TsF−451
−10M)を低粘度のTSF−451−IMに代えた以
外は実施例1と同様にして本発明の1組成物を得た。
Example 4 Dimethylsiloxane oil (TsF-451) of Example 1
A composition of the present invention was obtained in the same manner as in Example 1, except that TSF-451-IM, which had a low viscosity, was used instead of TSF-451-IM.

比較例1 実施例1のジメチルシロキサンオイルとフッ素系界面活
性剤を用いずフィラーの充填量を一足にするため1m融
シリカ粉を424.5部にした以外は、実施例1と同様
にして比較用の組成物を得た。
Comparative Example 1 Comparison was made in the same manner as in Example 1, except that the dimethylsiloxane oil and fluorine-based surfactant of Example 1 were not used, and 1 m fused silica powder was changed to 424.5 parts in order to increase the amount of filler. A composition was obtained.

比較例2 実施例1のフッ素系界面活注剤1.5部を用いずに、ジ
メチルシロキサンオイルを4.5部に変更した以外は、
実施例1と同様にして比較用の組成物を得た。
Comparative Example 2 Except for changing the dimethylsiloxane oil to 4.5 parts without using 1.5 parts of the fluorosurfactant in Example 1,
A comparative composition was obtained in the same manner as in Example 1.

比ei列3 実施例1のジメチルシロキサンオイル3.0ii用いず
にフッ素系界面活性剤を4.5部に変更した以外は、実
施例1と同様にして比較用の組成物を得た。
Ratio ei column 3 A comparative composition was obtained in the same manner as in Example 1, except that the dimethylsiloxane oil 3.0ii of Example 1 was not used and the fluorosurfactant was changed to 4.5 parts.

以上の組成物を用いて実施例1と同様のテストを実施し
た。評価結果を表に示す。以下余白〔発明の効果〕 以上に詳述した通り1本発明の半導体装置封止用エポキ
シ樹脂組成物に、その硬化吻が憂れた耐湿性及び耐熱S
s性を有するものであり、−東横度の半導体装【直等の
用途における実用的価匝は惚めて犬と言える。
A test similar to that in Example 1 was conducted using the above composition. The evaluation results are shown in the table. The following margins [Effects of the Invention] As detailed above, the epoxy resin composition for encapsulating semiconductor devices of the present invention has excellent moisture resistance and heat resistance S
It has s-characteristics, and its practical value in applications such as direct use of semiconductor devices can be said to be excellent.

代理人 弁理士   則 近 憲 右 同     竹 花 喜久男Agent Patent Attorney Norihiro Chika Same Bamboo Flower Kikuo

Claims (1)

【特許請求の範囲】 (a)エポキシ樹脂100重量部 (b)ノボラック型フェノール樹脂30〜70重量部(
c)シリカ粉末300〜550重量部 (d)ジメチルシロキサンオイル0.2〜20重量部(
e)フッ素系及び/又はシリコーン系界面活性剤0.2
〜20重量部 からなることを特徴とする半導体装置封止用エポキシ樹
脂組成物。
[Scope of Claims] (a) 100 parts by weight of epoxy resin (b) 30 to 70 parts by weight of novolac type phenolic resin (
c) 300 to 550 parts by weight of silica powder (d) 0.2 to 20 parts by weight of dimethylsiloxane oil (
e) Fluorine and/or silicone surfactant 0.2
An epoxy resin composition for encapsulating a semiconductor device, characterized in that the composition contains 20 parts by weight.
JP5143486A 1986-03-11 1986-03-11 Epoxy resin composition for sealing semiconductor device Pending JPS62209126A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5143486A JPS62209126A (en) 1986-03-11 1986-03-11 Epoxy resin composition for sealing semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5143486A JPS62209126A (en) 1986-03-11 1986-03-11 Epoxy resin composition for sealing semiconductor device

Publications (1)

Publication Number Publication Date
JPS62209126A true JPS62209126A (en) 1987-09-14

Family

ID=12886822

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5143486A Pending JPS62209126A (en) 1986-03-11 1986-03-11 Epoxy resin composition for sealing semiconductor device

Country Status (1)

Country Link
JP (1) JPS62209126A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0299513A (en) * 1988-10-06 1990-04-11 Toray Ind Inc Epoxy based composition
EP0384774A2 (en) * 1989-02-23 1990-08-29 Kabushiki Kaisha Toshiba Semiconductor device encapsulant
EP1149864A1 (en) * 2000-04-28 2001-10-31 STMicroelectronics S.r.l. Polymeric composition for packaging a semiconductor electronic device and packaging obtained therefrom
JP2005206725A (en) * 2004-01-23 2005-08-04 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
KR100642026B1 (en) 2003-09-30 2006-11-02 도오꾜오까고오교 가부시끼가이샤 Positive photoresist composition
US20120193817A1 (en) * 2011-01-31 2012-08-02 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition, die attach method using same, and semiconductor device containing cured product thereof
CN105440558A (en) * 2015-12-10 2016-03-30 无锡普瑞腾传动机械有限公司 Organic silicon sealant for automotive glass

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0299513A (en) * 1988-10-06 1990-04-11 Toray Ind Inc Epoxy based composition
EP0384774A2 (en) * 1989-02-23 1990-08-29 Kabushiki Kaisha Toshiba Semiconductor device encapsulant
US5258426A (en) * 1989-02-23 1993-11-02 Kabushiki Kaisha Toshiba Semiconductor device encapsulant
EP1149864A1 (en) * 2000-04-28 2001-10-31 STMicroelectronics S.r.l. Polymeric composition for packaging a semiconductor electronic device and packaging obtained therefrom
WO2001083604A1 (en) * 2000-04-28 2001-11-08 Stmicroelectronics S.R.L. Polymeric composition for packaging a semiconductor electronic device and packaging obtained therefrom
JP2003531938A (en) * 2000-04-28 2003-10-28 エスティーマイクロエレクトロニクスエス.アール.エル. Polymer composition for package of semiconductor electronic device and package obtained therefrom
KR100642026B1 (en) 2003-09-30 2006-11-02 도오꾜오까고오교 가부시끼가이샤 Positive photoresist composition
JP2005206725A (en) * 2004-01-23 2005-08-04 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
US20120193817A1 (en) * 2011-01-31 2012-08-02 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition, die attach method using same, and semiconductor device containing cured product thereof
US8815400B2 (en) * 2011-01-31 2014-08-26 Shin-Etsu Chemical Co., Ltd. Epoxy resin composition, die attach method using same, and semiconductor device containing cured product thereof
CN105440558A (en) * 2015-12-10 2016-03-30 无锡普瑞腾传动机械有限公司 Organic silicon sealant for automotive glass

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