JPS61190961A - Semiconductor device - Google Patents

Semiconductor device

Info

Publication number
JPS61190961A
JPS61190961A JP60031741A JP3174185A JPS61190961A JP S61190961 A JPS61190961 A JP S61190961A JP 60031741 A JP60031741 A JP 60031741A JP 3174185 A JP3174185 A JP 3174185A JP S61190961 A JPS61190961 A JP S61190961A
Authority
JP
Japan
Prior art keywords
epoxy resin
sphericity
amorphous silica
silica powder
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.)
Granted
Application number
JP60031741A
Other languages
Japanese (ja)
Other versions
JP2593843B2 (en
Inventor
Kazuo Iko
伊香 和夫
Saburo Omori
大森 三郎
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.)
Nitto Denko Corp
Original Assignee
Nitto Electric Industrial 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 Nitto Electric Industrial Co Ltd filed Critical Nitto Electric Industrial Co Ltd
Priority to JP60031741A priority Critical patent/JP2593843B2/en
Publication of JPS61190961A publication Critical patent/JPS61190961A/en
Application granted granted Critical
Publication of JP2593843B2 publication Critical patent/JP2593843B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00Details of semiconductor or other solid state devices
    • H01L23/28Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
    • H01L23/29Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
    • H01L23/293Organic, e.g. plastic
    • H01L23/295Organic, e.g. plastic containing a filler
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001Technical content checked by a classifier
    • H01L2924/0002Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Abstract

PURPOSE:To prevent the formation of cracks in a passivation layer by sealing a semiconductor element by using an epoxy resin composition containing epoxy resin, a phenolic novolak group curing agent and amorphous silica powder having specific sphericity. CONSTITUTION:A semiconductor element is sealed by using an epoxy resin composition containing epoxy resin, a phenolic novolak group curing agent, one molecule thereof has two or more of hydroxyl groups, and amorphous silica powder having the Wadel's sphericity, preferably, sphericity of 0.7-1.0. Epoxy resin having epoxy equivalent of 175-250 and the softening point of 60-130 deg.C can particularly be employed preferably as the epoxy resin. Novolak type epoxy resin is preferable as the form of the epoxy resin. The phenolic novolak group curing agent having the softening point of 60-120 deg.C can specially be used preferably as the curing agent. It means that a particle is close to a true sphere with an approach to 1.0 of the Wadel's sphericity. Sphericity of less than 0.5 results in the formation of a number of sharp projecting pieces, and is undesirable.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はIC,LSIなどのいわゆる半導体装置に関し
、その目的はエポキシ樹脂組成物を用いてトランスファ
ー成型法で半導体素子を封止して半導体装置を製造する
際に半導体装置のパシベーション層にクランク等が入り
その結果半導体装置の不良品が発生しやすかった欠点を
解消することができる半導体装置の提供にある。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to so-called semiconductor devices such as ICs and LSIs, and its purpose is to manufacture semiconductor devices by sealing semiconductor elements using an epoxy resin composition using a transfer molding method. An object of the present invention is to provide a semiconductor device that can eliminate the drawback that cranks or the like enter the passivation layer of the semiconductor device during manufacturing, resulting in easy production of defective semiconductor devices.

[従来技術] (発明の背景) 従来、一般にIC,LSIなどの半導体装置は、トラン
スファー成形等の手法で樹脂封止して製造されるもので
あるが、このトランスファー成型で半導体装置を製造す
る際無機材料からなる素子と封止材料との熱膨張係数の
差が大きいため、成形時もしくは成形後の急激な温度変
化を受けると樹脂封止内部にひずみを生じて、半導体素
子のパッシベーション層にクランクが入るという問題が
あった。
[Prior Art] (Background of the Invention) Conventionally, semiconductor devices such as ICs and LSIs are generally manufactured by resin sealing using methods such as transfer molding. Because there is a large difference in the coefficient of thermal expansion between the element made of inorganic material and the encapsulating material, sudden temperature changes during or after molding can cause strain inside the resin encapsulation, causing cracks in the passivation layer of the semiconductor element. There was a problem with entering.

このように半導体素子のパッシベーション層にクランク
が入った半導体装置は、耐湿性に劣るため電気的緒特性
が劣化し信頼性の低い不良品となった。
Semiconductor devices in which the passivation layer of the semiconductor element is cranked in this manner have poor moisture resistance, resulting in deteriorated electrical characteristics and become unreliable defective products.

特に封止用樹脂材料としてエポキシ樹脂組成物を使用す
る場合には通常150〜185℃の高温で成形を行うた
め、成形後常温まで冷却される間に半導体素子に比べて
熱膨張係数の大きい封止用樹脂が相対的に熱収縮し、そ
の結果、この様な封止用樹脂で封止された半導体素子(
特にこの半導体素子を保護するパッシベーション層にク
ラ1.り等の損傷を与え延いては半導体素子)に損傷を
与え半導体装置の不良品の発生の原因となっていた。
In particular, when an epoxy resin composition is used as a resin material for sealing, molding is usually carried out at a high temperature of 150 to 185°C. The encapsulating resin undergoes relative heat shrinkage, and as a result, the semiconductor element encapsulated with such encapsulating resin (
In particular, the passivation layer that protects this semiconductor element has a cracker. This causes damage such as damage to semiconductor devices, which in turn causes damage to semiconductor devices, resulting in the production of defective semiconductor devices.

(従来の技術) 従来、上記欠点を解消する為に即ち封止用エポキシ樹脂
組成物の熱膨張係数を低下させる目的で、更にこの目的
に加え一般の成形材料樹脂と同様に価格低減の目的や材
料樹脂にチキソトロピー性を付与して成形作業を向上さ
せる目的で、適宜の無機質充填剤を含有させた封止用エ
ポキシ樹脂組成物が半導体装置の封正に用いられている
(Prior art) Conventionally, in order to eliminate the above-mentioned drawbacks, that is, to lower the coefficient of thermal expansion of the epoxy resin composition for sealing, in addition to this purpose, it has been used for the purpose of reducing the price as well as for general molding material resins. Epoxy resin compositions for sealing containing appropriate inorganic fillers are used for sealing semiconductor devices in order to improve molding operations by imparting thixotropy to the resin material.

この様な目的で用いる封止用エポキシ樹脂組成物に配合
する無機充填剤としては、半導体装置の封止作業時にお
ける優れた成形作業性を付与できしかも無機充填剤中に
半導体素子に対して悪影響を与える不純物が少ないとい
う少なくとも二つの条件を充たすことが必要である。
The inorganic filler added to the encapsulating epoxy resin composition used for this purpose can provide excellent molding workability during the encapsulation work of semiconductor devices, but the inorganic filler does not have any harmful effects on the semiconductor element. It is necessary to satisfy at least two conditions that there are few impurities that give .

従来から、この条件に舎致するものとして無定形シリカ
粉末が代表的なものとして存在し、通常この粉末が封止
用エポキシ樹脂組成物に配合する無機充填剤として汎用
されている。
Conventionally, amorphous silica powder has been a typical material that satisfies this condition, and this powder is commonly used as an inorganic filler to be added to an epoxy resin composition for sealing.

(従来技術の欠点) ところが、成るほど封止用エポキシ樹脂組成物中に無定
形シリカ粉末等の無機質充填剤を添加すると封止用エポ
キシ樹脂組成物の熱膨張係数がその添加量に比例して小
さくなる効果が得られる、反面無定形シリカ粉末の配合
量が非常に多くなると無定形シリカ粉末本来の特徴であ
る良好な成形作業性を損ねることとなるともに封止用エ
ポキシ樹脂組成物の弾性率が高くなるという問題があっ
た。
(Disadvantages of the prior art) However, when an inorganic filler such as amorphous silica powder is added to an epoxy resin composition for sealing, the coefficient of thermal expansion of the epoxy resin composition for sealing becomes proportional to the amount added. On the other hand, if the amount of amorphous silica powder is too large, it will impair the good molding workability that is the original characteristic of amorphous silica powder, and the elastic modulus of the epoxy resin composition for sealing will decrease. There was a problem that the amount of

この問題は封止用エポキシ樹脂組成物の弾性率が高くな
ると、応力ひずみは熱膨張係数と弾性率との積に比例す
るものであるため、無定形シリカ粉末の添加量を多くし
て封止用エポキシ樹脂組成物熱膨張係数を小さくできた
としても結果的には応力ひずみの低下につながらない原
因となるものであった。
This problem can be solved by increasing the amount of amorphous silica powder added as the elastic modulus of the epoxy resin composition for sealing increases, since the stress strain is proportional to the product of the coefficient of thermal expansion and the modulus of elasticity. Even if the coefficient of thermal expansion of the epoxy resin composition could be reduced, it would not result in a reduction in stress strain.

実際、無定形シリカ粉末が多量に配合されている封止用
エポキシ樹脂組成物で封止された半導体装置には、結局
パッシベーション層にクラック等が入りやすく不良品と
なり易いという欠点が存在した。
In fact, semiconductor devices encapsulated with encapsulating epoxy resin compositions containing a large amount of amorphous silica powder have the disadvantage that they tend to end up with cracks in the passivation layer, resulting in defective products.

(発明が解決しようとする問題点) この発明者らは、前記従来の事情に照らし無定形シリカ
粉末を添加することにより封止用エポキシ樹脂組成物の
熱膨張係数を低下させ半導体素子との間の熱膨張係数の
差を小さくするとともに無定形シリカ粉末の配合量を増
大させても良好な成形作業性を損ねることなく且つ弾性
率が高くならない封止層エポキシ樹脂組成物について鋭
意研究した結果この発明に到達したものである。
(Problems to be Solved by the Invention) In light of the above-mentioned conventional circumstances, the inventors have proposed that by adding amorphous silica powder, the coefficient of thermal expansion of the epoxy resin composition for sealing can be lowered and the relationship between the composition and the semiconductor element can be reduced. As a result of intensive research on an epoxy resin composition for a sealing layer that does not impair good molding workability and do not increase its elastic modulus even when the difference in thermal expansion coefficient is reduced and the amount of amorphous silica powder blended is increased, this result was obtained. This invention has been achieved.

(解決手段) 即ちこの発明はエポキシ樹脂と1分子中に2(固以上の
水酸基を有するフェノールノボラック系硬化剤とワーデ
ルの球形度で0.5〜1.0の球形度を持つ無定形シリ
カ粉条を含む封止用エポキシ樹脂組成物を用いて半導体
素子が封止されてなることを特徴とする半導体装置を提
供することにより、エポキシ樹脂組成物を用いてトラン
スファー成型法で半導体素子を封止して半導体装置を製
造しても半導体装置のパシベーション層にクランク等が
入りその結果半導体装置の不良品が発生しやすかった欠
点を解消することができる半導体装置を提供せんとする
にある。
(Solution Means) That is, the present invention consists of an epoxy resin, a phenol novolac curing agent having 2 (hard or more) hydroxyl groups in one molecule, and an amorphous silica powder having a Wardell sphericity of 0.5 to 1.0. By providing a semiconductor device characterized in that a semiconductor element is sealed using an epoxy resin composition for sealing containing It is an object of the present invention to provide a semiconductor device which can eliminate the drawback that cranks or the like enter the passivation layer of the semiconductor device even when the semiconductor device is manufactured using the same method, and as a result, the semiconductor device tends to be defective.

(発明の構成) この発明において使用されるエポキシ樹脂としては、−
分子中に2個以上のエポキシ基を有する化合物であって
エピクロルヒドリンとビスフェノールAや各種ノボラッ
ク類とから合成される樹脂であればすべてよく、例えば
脂環式のエポキシ樹脂あるいは難燃機能を付与するため
に臭素や塩素のようなハロゲン原子を導入したエポキシ
樹脂などをも例示することができる。
(Structure of the Invention) The epoxy resin used in this invention is -
Any compound having two or more epoxy groups in the molecule and a resin synthesized from epichlorohydrin, bisphenol A, or various novolaks may be used, such as an alicyclic epoxy resin or a resin that imparts a flame retardant function. Examples include epoxy resins into which halogen atoms such as bromine or chlorine are introduced.

この様なエポキシ樹脂のうちこの発明においては、エポ
キシ当量175〜250で軟化点60〜130℃のエポ
キシ樹脂が特に好適に使用できる。
Among such epoxy resins, epoxy resins having an epoxy equivalent of 175 to 250 and a softening point of 60 to 130° C. can be particularly preferably used in the present invention.

またエポキシ樹脂の形態としてはフェノールノボラック
エポキシ樹脂やタレゾールノボラックエポキシ樹脂の如
きノボラック型エポキシ樹脂が好通である。
As for the form of the epoxy resin, novolac type epoxy resins such as phenol novolac epoxy resin and Talesol novolac epoxy resin are preferred.

この発明において使用するこの様なエポキシ樹脂の硬化
剤としては、フェノールノボラックやタレゾールノボラ
ンクなどの1分子中に2個以上(通常の上限値は15程
度)の水酸基を有するフェノールノボラック系硬化剤が
用いられる。
The curing agent for such an epoxy resin used in this invention is a phenol novolac curing agent having two or more hydroxyl groups in one molecule (the normal upper limit is about 15), such as phenol novolak and Talesol Novolanc. is used.

この発明においてエポキシ樹脂の硬化剤としてフェノー
ルノボラックやタレゾールノボランクなどの1分子中に
2個以上の水酸基を有するフェノールノボラック系硬化
剤に限定する理由は、エポキシ樹脂の硬化剤としてしら
れている他のアミン系硬化剤や酸無水物系硬化剤では、
例えば上記アミン系硬化剤は毒性やライフが短くなるな
どの一般的な欠点があり、また酸無水物系硬化剤は成形
性に問題が生じやすく封止材料としての実用性にやや欠
けるきらいがありいずれも好ましくないからである。
The reason why the curing agent for epoxy resins in this invention is limited to phenol novolak-based curing agents having two or more hydroxyl groups in one molecule, such as phenol novolak and Talesol novolanc, is because they are known as curing agents for epoxy resins. With other amine curing agents and acid anhydride curing agents,
For example, the above-mentioned amine-based curing agents have general drawbacks such as toxicity and short life, and acid anhydride-based curing agents tend to have problems with moldability and are somewhat lacking in practicality as sealing materials. This is because both are undesirable.

この様な1分子中に2個以上の水酸基を有するフェノー
ルノボラック系硬化剤のうちこの発明においては、軟化
点60〜120℃のフェノールノボラック系硬化剤が特
に好適に使用できる。
Among such phenol novolac curing agents having two or more hydroxyl groups in one molecule, phenol novolak curing agents having a softening point of 60 to 120° C. can be particularly preferably used in the present invention.

この発明において使用するワーデルの球形度で0.5〜
1.0の球形度を持つ無定形シリカとは、熔融固化した
インゴット状の無定形シリカを機械粉砕し、得られた機
械粉砕物のうちワーデルの球形度で0.5〜1.0この
ましくは0.7〜1.0の球形度を持つ球形の無定形シ
リカのことをいう。
The Wardell sphericity used in this invention is 0.5 to
Amorphous silica with a sphericity of 1.0 is defined as a sphericity of 0.5 to 1.0 in terms of Wardell's sphericity of the mechanically pulverized product obtained by mechanically pulverizing melted and solidified ingot-like amorphous silica. It refers to spherical amorphous silica with a sphericity of 0.7 to 1.0.

ここでワーデルの球形度(化学工学便覧、丸善株式会社
発行参照)とは、粒子の球形度を、(粒子の投影面積に
等しい円の直径)/(粒子の投影像に外接する最小円の
直径)で測る指数で、この指数が1.0に近い程真球体
に近い粒子であることを意味する。
Here, Wardell's sphericity (see Chemical Engineering Handbook, published by Maruzen Co., Ltd.) means the sphericity of a particle as follows: (diameter of a circle equal to the projected area of the particle)/(diameter of the smallest circle circumscribing the projected image of the particle) ), and the closer this index is to 1.0, the closer the particle is to a perfect sphere.

この発明において使用する無定形シリカの形状をワーデ
ルの球形度で0.5〜1.0の球形度に限定する理由は
、球形度が0.5未満の場合は無定形シリカ粉末が異形
状で鋭利な突片を持つことが多く望ましくないからであ
る。
The reason why the shape of the amorphous silica used in this invention is limited to a Wardell sphericity of 0.5 to 1.0 is that if the sphericity is less than 0.5, the amorphous silica powder has an irregular shape. This is because they often have sharp protrusions, which is undesirable.

従って、この発明においては球形度が0.7以上無定形
シリカを使用するのがより望ましい。
Therefore, in the present invention, it is more desirable to use amorphous silica having a sphericity of 0.7 or more.

この発明において、球形度が0.5以下の異形状で鋭利
な突片を持つ無定形シリカ粉末が好ましく無い理由は1
.この鋭利な突片を持つ無定形シリカ粉末が封止用エポ
キシ樹脂組成物に配合されるとこの様な封止用エポキシ
樹脂組成物で封止された半導体装置は、封止用エポキシ
樹脂組成物の熱収縮時等に半導体素子を保護するパッシ
ベーション層が無定形シリカ粉末の鋭利な突片で損傷さ
れ、この現象が無定形シリカ粉末を配合して熱膨張係数
を小さくした封止樹脂を使用して半導体装置を製造した
場合であってもパッシベーション層が損傷される原因で
あるというこの発明者らの実験的知得に基づくものであ
る。
In this invention, there are 1 reasons why amorphous silica powder having irregularly shaped and sharp protrusions with a sphericity of 0.5 or less is not preferable.
.. When this amorphous silica powder having sharp protrusions is blended into an epoxy resin composition for sealing, a semiconductor device encapsulated with such an epoxy resin composition for sealing can be manufactured using an epoxy resin composition for sealing. The passivation layer that protects semiconductor elements is damaged by sharp protrusions of amorphous silica powder during thermal contraction of semiconductor devices. This is based on the inventors' experimental findings that the passivation layer is the cause of damage even when a semiconductor device is manufactured using the same method.

この発明においてこの様な球形度を持つ無定形シリカ粉
末を全組成分中50〜85重量%の範囲に抑えて配合す
るのが好ましいが、その理由は無定形シリカ粉末の配合
量が50重量%に満たないときは封止用エポキシ樹脂組
成物にチキソトロピー物性を付与しにくく従って作業性
に支障をきたすとともに価格低減にも問題がありさらに
応力ひずみの低下効果も不充分となるから好ましく無い
からである。
In this invention, it is preferable to blend the amorphous silica powder having such sphericity within the range of 50 to 85% by weight in the total composition. If it is less than this, it is difficult to impart thixotropic physical properties to the epoxy resin composition for sealing, which impairs workability and reduces costs, and furthermore, the effect of reducing stress and strain becomes insufficient, which is undesirable. be.

一方、無定形シリカ粉末の配合量が85重量2を超える
割合で配合すると、成形作業性にやはり問題が生じ被膜
形性能も低下し、結局何れの場合も好ましく無いからで
ある。
On the other hand, if the amount of amorphous silica powder exceeds 85% by weight, problems will arise in molding workability and the film-forming performance will also deteriorate, which is undesirable in either case.

尚、この発明において使用する前記の如き球形度を持つ
無定形シリカ粉末の粒径としては、粒径が149μ以下
のものが望ましく、より好ましくは平均粒径16μ程度
とするのが良い。
The particle size of the amorphous silica powder having the above-mentioned sphericity used in this invention is preferably 149 μm or less, more preferably an average particle size of about 16 μm.

この理由は、粒径が149 μより大きくなると封止エ
ポキシ樹脂組成物をもちいて半導体装置を封止する成形
時の充填性が損なわれるからである。
The reason for this is that if the particle size is larger than 149 μm, the filling properties during molding for sealing a semiconductor device using the sealing epoxy resin composition will be impaired.

この発明に係る半導体装置で使用する封止エポキシ樹脂
組成物は、上述のエポキシ樹脂、硬化剤および無定形シ
リカ粉末に加え、通常公知の内部離型剤および硬化促進
剤を配合させることができる。
In addition to the above-mentioned epoxy resin, curing agent, and amorphous silica powder, the encapsulating epoxy resin composition used in the semiconductor device according to the present invention can contain a commonly known internal mold release agent and curing accelerator.

内部離型剤としてはステアリン酸、バルミチン酸などの
長鎖カルボン酸、ステアリン酸亜鉛、ステアリン酸カル
シウムなどの長鎖カルボン酸の金属塩、カルナバワック
ス、モンタンワックスなどのワックス類が挙げられる。
Examples of the internal mold release agent include long chain carboxylic acids such as stearic acid and balmitic acid, metal salts of long chain carboxylic acids such as zinc stearate and calcium stearate, and waxes such as carnauba wax and montan wax.

又、この発明においては硬化促進剤として前記硬化剤と
ともに各種イミダゾール類や三級アミン類、フェノール
類、有機金属化合物或いは三弗化ホウ素化合物のような
触媒的硬化剤等を併用しても良い。
In addition, in the present invention, various imidazoles, tertiary amines, phenols, organometallic compounds, catalytic curing agents such as boron trifluoride compounds, etc. may be used in combination with the curing agent as a curing accelerator.

この発明においては他の添加剤として、β−(3・4−
エポキシシクロヘキシル)エチルトリメトキシシラン、
r−グリシドキシプロビルトリメトキシシランなどのシ
ランカップリング剤のような充填剤の表面処理剤、酸化
アンチモン、ハロゲン化物、リン化物などの難燃化剤、
各種顔料など従来公知の添加剤を配合してもよい。
In this invention, β-(3・4-
epoxycyclohexyl)ethyltrimethoxysilane,
surface treatment agents for fillers such as silane coupling agents such as r-glycidoxypropyltrimethoxysilane; flame retardants such as antimony oxide, halides, and phosphides;
Conventionally known additives such as various pigments may also be blended.

この発明に係る半導体装置で使用する上記組成からなる
封止エポキシ樹脂組成物を調製するには、常法に準じて
行えばよく、前記の各成分をトライブレンド法および溶
融混合法のいずれかの方法で調製すれば良い。
To prepare the encapsulating epoxy resin composition having the above composition used in the semiconductor device according to the present invention, it may be carried out according to a conventional method. It can be prepared by any method.

この様な封止エポキシ樹脂組成物を使用してこの発明に
係る半導体装置を得るには、トランスファー成形等の公
知方法で半導体素子を封止して調製すれば良い。
In order to obtain a semiconductor device according to the present invention using such a sealing epoxy resin composition, a semiconductor element may be sealed and prepared by a known method such as transfer molding.

(実施例及び試験例) 次にこの発明の実施例及び比較例を記載することにより
、この発明の効果をより一層具体的に説明する。なお以
下において部及び%とあるは、それぞれ、重量部および
重量%を意味する。
(Examples and Test Examples) Next, the effects of the present invention will be explained more specifically by describing Examples and Comparative Examples of the present invention. Note that in the following, parts and % mean parts by weight and % by weight, respectively.

実施例1 タレゾールノボラックエポキシ樹脂(エポキシ当量21
0、軟化点80℃)100部、フェノールノボラック(
軟化点78℃)50部、コーメチルイミダゾール 0.
7部、球状の無定形シリカ粉末(ワーデルの球形度0.
7平均粒径16μ)350部、シランカフプリング剤A
−186(日本ユニカー社製商品名)1.8部、カルナ
バワックス6.0部、カーボンブランク2.0部を80
〜90℃熱ロールにより混練し、冷却粉砕してこの発明
に係る半導体装置で使用するエポキシ樹脂組成物を得た
Example 1 Talesol novolak epoxy resin (epoxy equivalent weight 21
0, softening point 80°C) 100 parts, phenol novolac (
softening point 78°C) 50 parts, comethylimidazole 0.
7 parts, spherical amorphous silica powder (Wardell sphericity 0.
7 average particle size 16μ) 350 parts, silane cuff pulling agent A
-186 (trade name manufactured by Nippon Unicar Co., Ltd.) 1.8 parts, carnauba wax 6.0 parts, carbon blank 2.0 parts at 80 parts
The mixture was kneaded with a heated roll at ~90°C, cooled and pulverized to obtain an epoxy resin composition to be used in the semiconductor device according to the present invention.

実施例2 実施例1に於いて、上記球状の無定形シリカ粉末を42
0部使用した以外は、実施例1と全く同様とした。
Example 2 In Example 1, the spherical amorphous silica powder was
The procedure was exactly the same as in Example 1 except that 0 part was used.

比較例1 実施例1の球状の無定形シリカ粉末の代わりに、無定形
シリカ粉末(ワーデルの球形度0.4  平均粒径12
μ)350部用いた以外は実施例1と全く同様にしてエ
ポキシ樹脂組成物を得た。
Comparative Example 1 Instead of the spherical amorphous silica powder of Example 1, amorphous silica powder (Wardell's sphericity 0.4, average particle size 12
An epoxy resin composition was obtained in exactly the same manner as in Example 1 except that 350 parts of μ) were used.

比較例2 比較例1において無定形シリカ粉末(ワーデルの球形度
0.4平均粒径12μ)420部用いた以外は実施例1
と全く同様にしてエポキシ樹脂組成物を得た。
Comparative Example 2 Example 1 except that 420 parts of amorphous silica powder (Wardell's sphericity 0.4 average particle size 12μ) was used in Comparative Example 1.
An epoxy resin composition was obtained in exactly the same manner.

比較例3 比較例1において無定形シリカ粉末(ワーデルの球形度
0.7平均粒径12μ)700部用いた以外は実施例1
と全く同様にしてエポキシ樹脂組成物を得た。
Comparative Example 3 Example 1 except that 700 parts of amorphous silica powder (Wardell's sphericity 0.7 average particle size 12μ) was used in Comparative Example 1.
An epoxy resin composition was obtained in exactly the same manner.

比較例4 比較例1において無定形シリカ粉末(ワーデルの球形度
0.7平均粒径12μ)150部用いた以外は実施例1
と全く同様にしてエポキシ樹脂組成物を得た。
Comparative Example 4 Example 1 except that 150 parts of amorphous silica powder (Wardell's sphericity 0.7 average particle size 12μ) was used in Comparative Example 1.
An epoxy resin composition was obtained in exactly the same manner.

次に各々のエポキシ樹脂組成物を175℃×3分のトラ
ンスファー成形して得た42ピン旧Pにつき175℃X
5Hrのポストキュアーを行い、−65℃から150℃
まで500回熱衝撃試験を行い、半導体装置のパッシベ
ーションクラックを調べた。
Next, each epoxy resin composition was transfer molded at 175°C for 3 minutes.
Post-cure for 5 hours and heat from -65℃ to 150℃
Thermal shock tests were conducted 500 times to investigate passivation cracks in semiconductor devices.

第1表の数値は試験個数100ケ中の不良品の発生数を
調べた結果である。
The numerical values in Table 1 are the results of investigating the number of defective products out of 100 tested products.

以上の結果から明らかな様に球状の無定形シリカ粉末は
半導体素子のパソシベーションクラノクに効果がある事
がわかる。
As is clear from the above results, it can be seen that spherical amorphous silica powder is effective for passivation of semiconductor devices.

(発明の効果) 以上詳述した如くこの発明に係る半導体装置は、エポキ
シ樹脂と1分子中に2個以上の水酸基を有するフェノー
ルノボラック系硬化剤とワーデルの球形度で0.5〜1
.0の球形度を持つ無定形シリカ粉末を含む封止用エポ
キシ樹脂組成物を用いて半導体素子が封止されてなるこ
とを特徴とする半導体装置であるから、この半導体装置
は製造時に無定形シリカ粉末に起因する優れた成形作業
性が得られるとともに電気特性的に半導体素子に対する
適合性が得られる封止用樹脂で封止できるとともに、か
つ無定形シリカ粉末の封止用エポキシ樹脂組成物への配
合量が大量になってもこの無定形シリカ粉末はワーデル
の球形度で0.5〜1.0の球形度を持つ球形であるか
ら前記両特性を損なうことなく半導体装置のパンシベー
ション層のクラックを顕著に低下できる効果を持つ半導
体装置である。
(Effects of the Invention) As detailed above, the semiconductor device according to the present invention combines an epoxy resin, a phenol novolak curing agent having two or more hydroxyl groups in one molecule, and a Wardell sphericity of 0.5 to 1.
.. Since this semiconductor device is characterized in that a semiconductor element is sealed using an epoxy resin composition for sealing containing amorphous silica powder having a sphericity of 0, this semiconductor device is manufactured using amorphous silica powder during manufacturing. It is possible to seal with a sealing resin that provides excellent molding workability due to the powder and is compatible with semiconductor elements in terms of electrical properties, and it is also possible to use amorphous silica powder in an epoxy resin composition for sealing. This amorphous silica powder has a spherical shape with a Wardell sphericity of 0.5 to 1.0 even when mixed in a large amount, so it can prevent cracks in the pansivation layer of semiconductor devices without impairing both of the above characteristics. This is a semiconductor device that has the effect of significantly reducing the

Claims (1)

【特許請求の範囲】[Claims] (1)エポキシ樹脂と1分子中に2個以上の水酸基を有
するフェノールノボラック系硬化剤とワーデルの球形度
で0.5〜1.0の球形度を持つ無定形シリカ粉末を含
む封止用エポキシ樹脂組成物を用いて半導体素子が封止
されてなることを特徴とする半導体装置。
(1) A sealing epoxy containing an epoxy resin, a phenol novolac curing agent having two or more hydroxyl groups in one molecule, and an amorphous silica powder having a Wardell sphericity of 0.5 to 1.0. A semiconductor device characterized in that a semiconductor element is sealed using a resin composition.
JP60031741A 1985-02-19 1985-02-19 Semiconductor device Expired - Lifetime JP2593843B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60031741A JP2593843B2 (en) 1985-02-19 1985-02-19 Semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60031741A JP2593843B2 (en) 1985-02-19 1985-02-19 Semiconductor device

Publications (2)

Publication Number Publication Date
JPS61190961A true JPS61190961A (en) 1986-08-25
JP2593843B2 JP2593843B2 (en) 1997-03-26

Family

ID=12339456

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60031741A Expired - Lifetime JP2593843B2 (en) 1985-02-19 1985-02-19 Semiconductor device

Country Status (1)

Country Link
JP (1) JP2593843B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63108021A (en) * 1986-10-24 1988-05-12 Hitachi Ltd Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith
JPS63128020A (en) * 1986-11-18 1988-05-31 Hitachi Ltd Epoxy resin composition and resin-sealed type semiconductor device
JPS63160255A (en) * 1986-12-23 1988-07-04 Nitto Electric Ind Co Ltd Semiconductor device
JPH02209949A (en) * 1989-02-09 1990-08-21 Shin Etsu Chem Co Ltd Epoxy resin composition and cured material for sealing of semiconductor
JPH08104730A (en) * 1995-06-20 1996-04-23 Nitto Denko Corp Resin composition for semiconductor sealing

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS583382A (en) * 1981-06-27 1983-01-10 Matsushita Electric Ind Co Ltd Power supply for dc-dc converter
JPS5837939A (en) * 1982-07-24 1983-03-05 Nitto Electric Ind Co Ltd Semiconductor device
JPS58138740A (en) * 1982-02-15 1983-08-17 Denki Kagaku Kogyo Kk Resin composition
JPS58145613A (en) * 1982-02-15 1983-08-30 Denki Kagaku Kogyo Kk Molten silica sphere, its preparation and its device
JPS594630A (en) * 1982-06-30 1984-01-11 Matsushita Electric Works Ltd Resin composition
JPS60210643A (en) * 1983-11-30 1985-10-23 Denki Kagaku Kogyo Kk Filler and its composition
JPS6159758A (en) * 1984-08-30 1986-03-27 Mitsubishi Electric Corp Resin sealed type semiconductor device

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS583382A (en) * 1981-06-27 1983-01-10 Matsushita Electric Ind Co Ltd Power supply for dc-dc converter
JPS58138740A (en) * 1982-02-15 1983-08-17 Denki Kagaku Kogyo Kk Resin composition
JPS58145613A (en) * 1982-02-15 1983-08-30 Denki Kagaku Kogyo Kk Molten silica sphere, its preparation and its device
JPS594630A (en) * 1982-06-30 1984-01-11 Matsushita Electric Works Ltd Resin composition
JPS5837939A (en) * 1982-07-24 1983-03-05 Nitto Electric Ind Co Ltd Semiconductor device
JPS60210643A (en) * 1983-11-30 1985-10-23 Denki Kagaku Kogyo Kk Filler and its composition
JPS6159758A (en) * 1984-08-30 1986-03-27 Mitsubishi Electric Corp Resin sealed type semiconductor device

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63108021A (en) * 1986-10-24 1988-05-12 Hitachi Ltd Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith
JPS63128020A (en) * 1986-11-18 1988-05-31 Hitachi Ltd Epoxy resin composition and resin-sealed type semiconductor device
JPH0554865B2 (en) * 1986-11-18 1993-08-13 Hitachi Ltd
JPH0680863A (en) * 1986-11-18 1994-03-22 Hitachi Ltd Epoxy resin composition
JPS63160255A (en) * 1986-12-23 1988-07-04 Nitto Electric Ind Co Ltd Semiconductor device
JPH02209949A (en) * 1989-02-09 1990-08-21 Shin Etsu Chem Co Ltd Epoxy resin composition and cured material for sealing of semiconductor
JPH08104730A (en) * 1995-06-20 1996-04-23 Nitto Denko Corp Resin composition for semiconductor sealing

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