JPH02209949A - Epoxy resin composition and cured product for semiconductor encapsulation - Google Patents
Epoxy resin composition and cured product for semiconductor encapsulationInfo
- Publication number
- JPH02209949A JPH02209949A JP1030813A JP3081389A JPH02209949A JP H02209949 A JPH02209949 A JP H02209949A JP 1030813 A JP1030813 A JP 1030813A JP 3081389 A JP3081389 A JP 3081389A JP H02209949 A JPH02209949 A JP H02209949A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- resin composition
- filler
- cured product
- spherical silica
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Abstract
Description
【発明の詳細な説明】
1呈上夏■且分見
本発明は、膨張係数が低い硬化物を与える上、流動性が
高く、未充填やワイヤー流れ等の成形不良が少ない成形
性に優れた半導体封止用エポキシ樹脂組成物及びその硬
化物に関する。[Detailed Description of the Invention] 1 Presentation Summer ■ and Minute Sample The present invention provides a semiconductor that provides a cured product with a low expansion coefficient, has high fluidity, and has excellent moldability with few molding defects such as unfilling and wire flow. The present invention relates to an epoxy resin composition for sealing and a cured product thereof.
来の び が しよ と る
従来、半導体封止用として使用するエポキシ樹脂組成物
としては、エポキシ樹脂に硬化剤としてフェノール樹脂
等、無機充填剤としてシリカ等を配合したものが一般的
である。このようなエポキシ樹脂組成物は、例えばフェ
ノール樹脂組成物等の他の熱硬化性樹脂組成物に比較し
て、溶融時の粘度が低く流動性に富んでいるため、LS
IやIC,トランジスター等の微細なパターンやワイヤ
ーの損傷を抑えて耐湿性を向上させるのに有効で、この
ため半導体封止用として好適に使用されている。Conventionally, epoxy resin compositions used for semiconductor encapsulation have generally been made by blending epoxy resin with phenol resin or the like as a hardening agent and silica or the like as an inorganic filler. Such epoxy resin compositions have low viscosity when melted and high fluidity compared to other thermosetting resin compositions such as phenolic resin compositions, so they are suitable for LS.
It is effective in suppressing damage to fine patterns and wires of I, IC, transistors, etc. and improving moisture resistance, and is therefore suitably used for semiconductor encapsulation.
また、最近の動向として、シリコンチップの大型化や配
線幅の微細化に伴い、半導体封止材の膨張係数をシリコ
ンチップのそれに近づけることが要望されており、この
ためエポキシ樹脂組成物への充填剤配合量を増やしてそ
の硬化物の膨張係数を低くすることが行なわれている。In addition, as recent trends have shown that silicon chips have become larger and wiring widths have become finer, there has been a demand for semiconductor encapsulants to have an expansion coefficient closer to that of silicon chips. The expansion coefficient of the cured product is lowered by increasing the amount of the agent blended.
しかしながら、その一方で、パッケージの大型化や多ビ
ン化が進んでいることがら封止材の高流動化も望まれて
いるが、一般に充填剤を増量すればする程エポキシ樹脂
組成物の流動性は悪くなり、成形時に未充填やワイヤー
流れが発生し易く、成形性が低下して、得られる硬化物
の耐湿性が劣ると言った問題があった。従って、低膨張
係数の硬化物を与え、かつ高い流動性を有し、成形性に
優れた半導体封止用エポキシ樹脂組成物の開発が望まれ
ていた。However, on the other hand, as packages are becoming larger and the number of bottles is increasing, it is desired that the sealing material has higher fluidity, but generally speaking, the greater the amount of filler, the higher the fluidity of the epoxy resin composition. There were problems in that the molding properties were poor, unfilling and wire flow were likely to occur during molding, moldability was reduced, and the moisture resistance of the obtained cured product was poor. Therefore, it has been desired to develop an epoxy resin composition for semiconductor encapsulation that provides a cured product with a low coefficient of expansion, has high fluidity, and has excellent moldability.
本発明は、上記事情に鑑みなされたもので、膨張係数が
低い硬化物を与える上、流動性が高く。The present invention was developed in view of the above circumstances, and provides a cured product with a low expansion coefficient and high fluidity.
成形時に未充填やワイヤー流れ等の成形不良がほとんど
発生しない成形性に優れた半導体封止用エポキシ樹脂組
成物及びその硬化物を提供することを目的とする。An object of the present invention is to provide an epoxy resin composition for semiconductor encapsulation that has excellent moldability and hardly causes molding defects such as unfilling or wire flow during molding, and a cured product thereof.
課 を するための び
本発明者は、上記目的を達成するため鋭意検討を重ねた
結果、エポキシ樹脂と硬化剤と充填剤とを含有してなる
エポキシ樹脂組成物において、充填剤として、平均粒径
が5〜35Mで比表面積が1.4rr?/g以下である
球状シリカを好ましくはかかる球状シリカの含有量が充
填剤全体の50重量%以上となるように配合し、かつ粒
径754以上の粒子の含有量を充填剤全体の1重量%以
下とした充填剤を用いた場合、硬化物の膨張係数を低く
するために充填剤配合量を増やしても組成物の流動性が
低下せず、成形時に未充填やワイヤー流れなどの成形不
良が発生することもほとんどなく、耐湿性の良好な硬化
物が得られること、それ故、低膨張係数の硬化物を与え
ると共に、高い流動性を有し、成形性に優れた半導体封
止用エポキシ樹脂組成物が得られることを知見し、本発
明をなすに至った。In order to achieve the above object, the inventor of the present invention has made extensive studies and found that, in an epoxy resin composition containing an epoxy resin, a curing agent, and a filler, the average particle size is The diameter is 5-35M and the specific surface area is 1.4rr? /g or less is preferably blended so that the content of such spherical silica is 50% by weight or more of the total filler, and the content of particles with a particle size of 754 or more is 1% by weight of the total filler. When the following fillers are used, the fluidity of the composition does not decrease even if the filler content is increased to lower the expansion coefficient of the cured product, and molding defects such as unfilled and wire flow occur during molding. An epoxy resin for semiconductor encapsulation that hardly generates moisture and can provide a cured product with good moisture resistance.Therefore, it provides a cured product with a low expansion coefficient, has high fluidity, and has excellent moldability. It was discovered that a composition can be obtained, and the present invention was completed.
従って1本発明は、エポキシ樹脂と硬化剤と充填剤とを
含有してなるエポキシ樹脂組成物において、充填剤とし
て平均粒径が5〜35声で比表面積が1.4rr?/g
以下である球状シリカを含有すると共に、粒径75P以
上の粒子の含有量が充填剤全体の1重量%以下である充
填剤を使用したことを特徴とする半導体封止用エポキシ
樹脂組成物及びこれを硬化することにより得られる硬化
物を提供する。Accordingly, the present invention provides an epoxy resin composition containing an epoxy resin, a curing agent, and a filler, in which the filler has an average particle size of 5 to 35 mm and a specific surface area of 1.4 rr. /g
An epoxy resin composition for semiconductor encapsulation characterized in that it contains the following spherical silica and uses a filler in which the content of particles with a particle size of 75P or more is 1% by weight or less of the entire filler, and the same: A cured product obtained by curing is provided.
以下、本発明につき更に詳述する。The present invention will be explained in more detail below.
本発明のエポキシ樹脂組成物は、上述したようにエポキ
シ樹脂と硬化剤と充填剤とを主成分として含有する。As described above, the epoxy resin composition of the present invention contains an epoxy resin, a curing agent, and a filler as main components.
ここで、エポキシ樹脂としては、従来から知られている
種々のものを使用することができ、例えばエポキシ化オ
ルソクレゾールノボラック樹脂。Here, as the epoxy resin, various conventionally known ones can be used, such as epoxidized orthocresol novolak resin.
エポキシ化フェノールノボラック樹脂、脂環式エポ掃シ
樹脂、エポキシ化ビスフェノール樹脂、@換又は非置換
のトリフエノールアルカン型エポキシ樹脂や、これらに
ハロゲン原子を導入したエポキシ樹脂等を挙げることが
できる。なお、これらエポキシ樹脂は、その使用に当た
って必ずしも1種類のみの使用に限定されるものではな
く、2種類又はそれ以上を混合して配合してもよい。Examples include epoxidized phenol novolac resins, alicyclic epoxy scavenging resins, epoxidized bisphenol resins, @-substituted or unsubstituted triphenol alkane type epoxy resins, and epoxy resins in which halogen atoms are introduced therein. Note that these epoxy resins are not necessarily limited to the use of only one type, and two or more types may be mixed and blended.
また、硬化剤は特に制限されるものではなく、使用する
エポキシ樹脂に応じて適宜選定することができ1例えば
アミン系硬化剤、酸無水物系硬化剤、フェノールノボラ
ック型硬化剤等が挙げられるが、中でもフェノールノボ
ラック型硬化剤が組成物の成形性、耐湿性の面でより望
ましく、好適に使用できる。なお、フェノールノボラッ
ク型硬化剤としては、具体的にフェノールノボラック樹
脂、クレゾールノボラック樹脂等が例示される。Further, the curing agent is not particularly limited and can be appropriately selected depending on the epoxy resin used. Examples include amine curing agents, acid anhydride curing agents, phenol novolak type curing agents, etc. Among these, phenol novolak type curing agents are more desirable in terms of moldability and moisture resistance of the composition, and can be suitably used. Note that specific examples of the phenol novolac type curing agent include phenol novolak resin, cresol novolak resin, and the like.
硬化剤の配合量は通常使用される量とすることができ、
フェノールノボラック型硬化剤を用いた場合、好ましく
はエポキシ樹脂中のエポキシ基と硬化剤中のOH基との
比がモル比で1:0.5〜1:1.5となるように配合
する。The amount of curing agent blended can be the amount normally used,
When a phenol novolac type curing agent is used, it is preferably blended so that the molar ratio of epoxy groups in the epoxy resin to OH groups in the curing agent is 1:0.5 to 1:1.5.
なお、本発明では、エポキシ樹脂と硬化剤との反応を促
進させる目的で各種硬化促進剤、例えばイミダゾール類
、三級アミン類、ホスフィン系化合物、シクロアミジン
化合物などを併用することが望ましい。In the present invention, it is desirable to use various curing accelerators, such as imidazoles, tertiary amines, phosphine compounds, and cycloamidine compounds, in order to accelerate the reaction between the epoxy resin and the curing agent.
また更に、本発明では硬化物の応力を低下させる目的で
組成物中にシリコーン系ポリマーを配合してもよい。シ
リコーン系ポリマーを添加すると、硬化物の熱衝撃テス
トにおけるパッケージクラブりの発生を著しく少なくす
ることが可能である。Furthermore, in the present invention, a silicone polymer may be blended into the composition for the purpose of reducing stress in the cured product. By adding a silicone polymer, it is possible to significantly reduce the occurrence of package scrubbing in a thermal shock test of a cured product.
シリコーン系ポリマーとしては、例えばエポキシ基、ア
ミノ基、カルボキシル基、水酸基、ヒドロシリル基、ビ
ニル基等を有するシリコーンオイル。Examples of silicone-based polymers include silicone oils having epoxy groups, amino groups, carboxyl groups, hydroxyl groups, hydrosilyl groups, vinyl groups, and the like.
シリコーンレジン、シリコーンゴムなどやこれらシリコ
ーンポリマーと有機重合体1例えば置換又は非置換のフ
ェノールノボラック樹脂、エポキシ化フェノールノボラ
ック樹脂などとの共重合体を挙げることができる。Examples include silicone resins, silicone rubbers, and copolymers of these silicone polymers and organic polymers 1, such as substituted or unsubstituted phenol novolak resins, epoxidized phenol novolak resins, and the like.
なおごシリコーン系ポリマーの添加量は特に限定されな
いが、通常エポキシ樹脂と硬化剤との合計使用量100
部(重量部、以下同様)に対し1〜50部とすることが
好ましい。The amount of silicone polymer added is not particularly limited, but usually the total amount of epoxy resin and curing agent used is 100
The amount is preferably 1 to 50 parts (parts by weight, hereinafter the same).
次いで、本発明で用いられる充填剤としては、充填剤全
体における粒径75.以上の粒子の含有量が1%(重量
%、以下同じ)以下、好ましくは0.5%以下であって
、かつ特定の球状シリカを含有するものである。Next, as the filler used in the present invention, the particle size of the entire filler is 75. The content of the above particles is 1% (weight %, same hereinafter) or less, preferably 0.5% or less, and contains a specific spherical silica.
ここで、球状シリカとしては粒径75Im以上の粒子が
球状シリカ全体の2%以下、好ましくは1%以下であり
、平均粒径が5〜35.、好ましくは8〜32戸である
と共に、比表面積が1.4ポ/g以下、好ましくは1r
rf/g以下であるものを使用する。Here, as for the spherical silica, particles having a particle size of 75 Im or more account for 2% or less, preferably 1% or less of the total spherical silica, and the average particle size is 5-35. , preferably 8 to 32 units, and a specific surface area of 1.4 po/g or less, preferably 1r
Use one with rf/g or less.
なお、充填剤中に粒径75pm以上の粗粒子が1%より
多く存在すると、硬化物のチップ表面へのダメージが大
きくなり、耐湿性に支障をきたす。It should be noted that if more than 1% of coarse particles with a particle size of 75 pm or more are present in the filler, the damage to the chip surface of the cured product will be increased and the moisture resistance will be impaired.
また、球状シリカの平均粒径が5−より小さいと、硬化
物のヒートサイクル時の耐クラツク性が悪くなる。一方
、平均粒径が35−を越えると成形時にワイヤーの流れ
を引き起こす、更に、比表面積が1.4m/gより大き
い球状シリカを用いると。Furthermore, if the average particle size of the spherical silica is smaller than 5-5, the crack resistance of the cured product during heat cycling will be poor. On the other hand, if the average particle size exceeds 35 mm, wire flow occurs during molding, and furthermore, if spherical silica with a specific surface area larger than 1.4 m/g is used.
組成物の流動性が著しく低下する。The fluidity of the composition is significantly reduced.
上記球状シリカは、天然の石英を溶融して得たり、ある
いは精製したクロロシラン、アルコキシシランを加水分
解や熱溶融して得る方法、ゾル−ゲル法などの種々の方
法で得ることができる。The spherical silica can be obtained by various methods, such as by melting natural quartz, by hydrolyzing or thermally melting purified chlorosilane or alkoxysilane, or by a sol-gel method.
また1本発明では充填剤として上記の特定の球状シリカ
のみを単独で配合してもよいが、上記球状シリカと共に
目的とする組成物の低膨張係数、高流動性を損なわない
範囲で破砕溶融シリカ、比表面積が1 rrr/ gよ
り大きい球状シリカ、ヒユームドシリカ等のその他の無
機質充填剤を併用することができる。この場合、上記球
状シリカの配合割合は全充填剤量の50%以上となるよ
うに配合することが好ましく、配合量が50%に満たな
いと組成物の流動性が低下し、成形性が悪くなる場合が
ある。In addition, in the present invention, only the above-mentioned specific spherical silica may be blended alone as a filler, but crushed fused silica may be used together with the above-mentioned spherical silica to the extent that the low expansion coefficient and high fluidity of the target composition are not impaired. , other inorganic fillers such as spherical silica and fumed silica having a specific surface area of more than 1 rrr/g can be used in combination. In this case, it is preferable that the blending ratio of the spherical silica is 50% or more of the total filler amount; if the blending amount is less than 50%, the fluidity of the composition will decrease and the moldability will be poor. It may happen.
なお、無機質充填剤は、その使用に際して予めシランカ
ップリング剤で表面処理した後に使用すると、より一層
耐湿性の高い硬化物を与える組成物を得ることができる
。Note that if the inorganic filler is used after being subjected to surface treatment with a silane coupling agent before use, a composition that provides a cured product with even higher moisture resistance can be obtained.
更に、充填剤の配合量は、エポキシ樹脂と硬化剤との合
計量100部に対して250〜700部、特に350〜
500部とすることが好ましい。Furthermore, the blending amount of the filler is 250 to 700 parts, particularly 350 to 700 parts, based on 100 parts of the total amount of the epoxy resin and curing agent.
Preferably, the amount is 500 parts.
本発明の組成物には、更に必要により各種の添加材を添
加することができ、例えばカルナバワックス等のワック
ス類、ステアリン酸等の脂肪酸やその金属塩などの離型
剤(中でも接着性、離型性の面からカルナバワックスが
好適に用いられる)。Various additives can be further added to the composition of the present invention, if necessary. Carnauba wax is preferably used from the viewpoint of moldability).
有機ゴム系等の可撓性付与剤、カーボンブラック。Flexibility imparting agents such as organic rubber, carbon black.
コバルトブルー、ベンガラ等の顔料、酸化アンチモン、
ハロゲン化合物等の難燃化剤2表面処理剤(Y−グリシ
ドキシプロビルトリメトキシシラン等)、エポキシシラ
ン、ビニルシラン、はう素化合物、アルキルチタネート
等のカップリング剤、老化防止剤、その他の添加剤の1
種又は2種以上を配合することができる。Pigments such as cobalt blue and red iron, antimony oxide,
Flame retardants such as halogen compounds 2 Surface treatment agents (Y-glycidoxyprobyltrimethoxysilane, etc.), coupling agents such as epoxysilane, vinyl silane, boromine compounds, alkyl titanates, anti-aging agents, etc. Additive 1
A species or two or more species can be blended.
なお1本発明のエポキシ樹脂組成物は、その製造に際し
、上述した成分の所定量を均一に撹拌、混合し、予め7
0〜95℃に加熱しであるニーダ−、ロール、エクスト
ルーダーなどで混線、冷却し、粉砕するなどの方法で得
ることができるが、特にミキシングロール、押出機を用
いた溶融混合法が好適に採用される。ここで、成分の配
合順序に特に制限はない。In addition, 1. When producing the epoxy resin composition of the present invention, predetermined amounts of the above-mentioned components are uniformly stirred and mixed, and the epoxy resin composition is prepared in advance for 7
It can be obtained by heating it to 0 to 95°C, mixing it with a kneader, roll, extruder, etc., cooling it, and pulverizing it, but a melt mixing method using a mixing roll or extruder is particularly preferred. Adopted. Here, there is no particular restriction on the order of blending the components.
上述したように、本発明のエポキシ樹脂組成物はIC,
LSI、 トランジスタ、サイリスタ、ダイオード等の
半導体装置の封止用に使用するものであり、プリント回
路板の製造などにも有効に使用できる。As mentioned above, the epoxy resin composition of the present invention includes IC,
It is used for sealing semiconductor devices such as LSIs, transistors, thyristors, and diodes, and can also be effectively used for manufacturing printed circuit boards.
ここで、半導体装置の封止を行なう場合は、従来より採
用されている成形法、例えばトランスファ成形、インジ
ェクション成形、注型法などを採用して行なうことがで
きる。この場合、エポキシ樹脂組成物の成形温度は15
0〜180℃、ポストキュアーは150〜180℃で2
〜16時間行なうことができる。Here, when sealing the semiconductor device, a conventional molding method such as transfer molding, injection molding, casting method, etc. can be used. In this case, the molding temperature of the epoxy resin composition is 15
0 to 180℃, post cure at 150 to 180℃
It can be carried out for ~16 hours.
11匹羞果 本発明の半導体封止用エポキシ樹脂組成物は。11 people are ashamed The epoxy resin composition for semiconductor encapsulation of the present invention is as follows.
流動性が高く、成形時に未充填やワイヤー流れなどがほ
んど発生しない優れた成形性を有するもので、膨張係数
が低くかつ耐湿特性が良好な硬化物を与える。従って、
IC,LSI、 トランジスタ等の半導体の封止材とし
て微細なパターンやワイヤーの損傷を抑えて耐湿性を向
上させるなどのために有効に使用できる。It has high fluidity and excellent moldability with almost no unfilling or wire flow during molding, and provides a cured product with a low coefficient of expansion and good moisture resistance. Therefore,
It can be effectively used as a sealing material for semiconductors such as ICs, LSIs, and transistors to prevent damage to fine patterns and wires and improve moisture resistance.
以下、実施例と比較例を示し、本発明を具体的に説明す
るが、本発明は下記実施例に制限されるものではない。EXAMPLES Hereinafter, the present invention will be specifically explained by showing examples and comparative examples, but the present invention is not limited to the following examples.
なお、以下の例において部はいずれも重量部を示す。In addition, in the following examples, all parts indicate parts by weight.
〔実施例1〜4.比較例1〜5〕
エポキシ当量200.軟化点65℃のエポキシ化クレゾ
ールノボラック樹脂58部、エポキシ当量280の臭素
化エポキシ化フェノールノボラック樹脂6部、フェノー
ル当量11o、軟化点80℃のフェノールノボラック樹
脂36部、トリフェニルホスフィン0.7部、三酸化ア
ンチモン10部、カルナバワックス1.5部、γ−グリ
シドキシプロビルトリメトキシシラン1.6部、カーボ
ン1部を混合したベースに、γ−グリシドキシプロビル
トリメトキシシラン0.6%で表面処理した第1表に示
すシリカを第2表に示す量で配合し、80℃のミキシン
グロールで5分間溶融混合した後、シート状で取り出し
、これを冷却し粉砕して組成物を得た。[Examples 1 to 4. Comparative Examples 1 to 5] Epoxy equivalent: 200. 58 parts of epoxidized cresol novolak resin with a softening point of 65°C, 6 parts of brominated epoxidized phenol novolak resin with an epoxy equivalent of 280, 36 parts of a phenol novolak resin with a phenol equivalent of 11o and a softening point of 80°C, 0.7 part of triphenylphosphine, A base containing 10 parts of antimony trioxide, 1.5 parts of carnauba wax, 1.6 parts of γ-glycidoxypropyltrimethoxysilane, and 1 part of carbon is mixed with 0.6 parts of γ-glycidoxypropyltrimethoxysilane. % surface-treated silica shown in Table 1 was blended in the amount shown in Table 2, melted and mixed on a mixing roll at 80°C for 5 minutes, taken out in the form of a sheet, cooled and pulverized to form a composition. Obtained.
得られた組成物につき、以下の諸試験を行なった。The following tests were conducted on the obtained composition.
結果を第2表に併記する。The results are also listed in Table 2.
(イ)スパイラルフロー EMMI規格に準じた金型を使用して175℃。(b) Spiral flow 175℃ using a mold that complies with EMMI standards.
70kgf/fflの条件で測定した。Measurement was performed under the condition of 70 kgf/ffl.
(ロ)膨張係数
175℃、2分で成形し、180℃、4時間ポストキュ
アした5X5X5閤の試験片を用い、アグネ(真空理工
社製)を用いて昇温スピード5℃/厘1nで測定した。(b) Expansion coefficient: Measured using a 5X5X5 test piece formed at 175℃ for 2 minutes and post-cured at 180℃ for 4 hours, using Agne (manufactured by Shinku Riko Co., Ltd.) at a heating rate of 5℃/1n. did.
(ハ)充填不良
64PIN600■ilのDIPのフレームを用い、1
75℃、 70kgf/cj、プレヒート温度85℃で
成形し、組成物の充填性を測定した。この場合、0.5
部以上の未充填があるものを不良とした。(c) Using a DIP frame with 64 PINs and 600 ■ ill filling, 1
The composition was molded at 75°C, 70kgf/cj, and a preheat temperature of 85°C, and the fillability of the composition was measured. In this case, 0.5
Items with more than 100% unfilled were considered defective.
(ニ)ワイヤー流れ
14x20x2.7 (厚さ)鵬の100PINフラツ
トパツケージのフレームを用い、175℃。(d) Wire flow: 14 x 20 x 2.7 (Thickness) Using a frame of Peng's 100 PIN flat package, 175°C.
70kgf/d、プレヒート温度85℃で成形した時の
金線の流れを軟X線で測定し、金線流れの状況を観察し
た。その結果、流れの良い場合は0、やや悪い場合はΔ
、悪い場合は×と判定した。The flow of the gold wire during molding at 70 kgf/d and a preheat temperature of 85° C. was measured using soft X-rays, and the state of the flow of the gold wire was observed. As a result, when the flow is good, it is 0, and when it is slightly bad, it is Δ
, if it was bad, it was judged as ×.
(ホ)耐湿性
最小線幅1.5部m、チップサイズ45−のテストチッ
プを用い、14PIN DIP型半導体装置を用いて評
価した。175℃、2分で成形し、180℃、4時間ポ
ストキュアーし、260℃の半田浴に10秒間浸漬し、
次いで130”Cのプレッシャークンカーに1000時
間放置した後のアルミニウム配線の断線不良率を測定し
た。(e) Moisture resistance Evaluation was performed using a 14-PIN DIP type semiconductor device using a test chip with a minimum line width of 1.5 parts m and a chip size of 45 mm. Molded at 175°C for 2 minutes, post-cured at 180°C for 4 hours, immersed in a 260°C solder bath for 10 seconds,
Next, the disconnection defect rate of the aluminum wiring was measured after being left in a pressure gunker at 130''C for 1000 hours.
第2表の結果より、本発明に係る球状シリカを充填剤と
して配合したエポキシ樹脂組成物(実施例1〜4)は、
硬化物の膨張係数が小さい上、成形時の充填不良やワイ
ヤー流れがほとんどなく、成形性に優れ、耐湿性の良好
な硬化物を与えることが確認された。これらに対し、粒
径75.以上の粒子含有率や平均粒径、比表面積が本発
明範囲外のシリカを配合した組成物(比較例1〜5)は
、成形時の充填不良やワイヤー流れが生じ、硬化物の耐
湿性も悪いものであった。From the results in Table 2, the epoxy resin compositions (Examples 1 to 4) containing spherical silica according to the present invention as a filler are as follows:
It was confirmed that the cured product has a small expansion coefficient, almost no filling defects or wire flow during molding, and provides a cured product with excellent moldability and good moisture resistance. On the other hand, the particle size is 75. Compositions containing silica whose particle content, average particle diameter, and specific surface area are outside the range of the present invention (Comparative Examples 1 to 5) cause poor filling and wire flow during molding, and the moisture resistance of the cured product also deteriorates. It was bad.
〔実施例5〜11〕
エポキシ当量198.軟化点60’Cのエポキシ化クレ
ゾールノボラック樹脂100部、エポキシ当量280の
臭素化エポキシ化フェノールノボラック樹脂6部、フェ
ノール当量110.軟化点90℃のフェノールノボラッ
ク樹脂33部、下記式
の化合物60部と下記式
の化合物40部との反応生成物25部、トリフェニルホ
スフィン0.65部、三酸化アンチモン10部、カルナ
バワックス1.2部、γ−グリシドキシプロピルトリメ
トキシシラン1.5部、カーボン1部を混合したベース
に、第3表に示す種類及び量のシリカを配合し、実施例
1と同様に組成物を得た。[Examples 5 to 11] Epoxy equivalent weight 198. 100 parts of an epoxidized cresol novolak resin with a softening point of 60'C, 6 parts of a brominated epoxidized phenol novolac resin with an epoxy equivalent weight of 280, and a phenol equivalent weight of 110. 33 parts of a phenol novolak resin with a softening point of 90°C, 25 parts of a reaction product of 60 parts of a compound of the following formula and 40 parts of a compound of the following formula, 0.65 part of triphenylphosphine, 10 parts of antimony trioxide, 1. A composition was obtained in the same manner as in Example 1 by adding silica of the type and amount shown in Table 3 to a base containing 2 parts of γ-glycidoxypropyltrimethoxysilane and 1 part of carbon. Ta.
組成物の試験結果を第3表に併記する。The test results for the composition are also listed in Table 3.
零シリカ10:平均粒径20yrx、粒径75.以上0
.1重量%、44〜7571117重量%、12−以下
10重量%、比
表面積0.8イ/gの球状シリカ
木本シリカ11;平均粒径0.5−の球状シリカ第3表
の結果より1本発明に係る球状シリカを充填剤全体の5
0%以上配合した組成物は、硬化物が低膨張係数でかつ
充填剤配合量を増やしても成形時に充填不良やワイヤー
流れがほとんど発生せず、優れた成形性を有し、硬化物
の耐湿性も良好であることがわかった。Zero Silica 10: Average particle size 20yrx, particle size 75. More than 0
.. 1% by weight, 44-7571117% by weight, 12-10% by weight or less, specific surface area 0.8 I/g Spherical silica Wooden silica 11; Average particle size 0.5- Spherical silica Based on the results in Table 3, 1 The spherical silica according to the present invention is
Compositions containing 0% or more have a low expansion coefficient, and even if the amount of filler added is increased, there is almost no filling failure or wire flow during molding, and the composition has excellent moldability, and the cured product has excellent moisture resistance. The properties were also found to be good.
出願人 信越化学工業株式会社
代理人 弁理士 小 島 隆 同
学
糸売
補
正
書
(自
発)
6、補正の内容
(1)明細書第18頁第2行目に
1、事件の表示
平成1年特許願第30813号
2、発明の名称
半導体封止用エポキシ樹脂組成物及び硬化物3、補正を
する者
事件との関係
住 所
氏 名Applicant: Shin-Etsu Chemical Co., Ltd. Agent, Patent Attorney: Takashi Kojima Dougaku Itosale Amendment (voluntary) 6. Contents of the amendment (1) 1 on page 18, line 2 of the specification, 1. Indication of the case 1999 patent application No. 30813 2, Title of the invention: Epoxy resin composition and cured product for semiconductor encapsulation 3, Name of person making the amendment Address related to the case
Claims (1)
ポキシ樹脂組成物において、充填剤として、平均粒径が
5〜35μmで比表面積が1.4m^2/g以下である
球状シリカを含有すると共に、粒径75μm以上の粒子
の含有量が充填剤全体の1重量%以下である充填剤を使
用することを特徴とする半導体封止用エポキシ樹脂組成
物。 2、請求項1記載の半導体封止用エポキシ樹脂組成物を
硬化することにより得られる硬化物。[Claims] 1. In an epoxy resin composition containing an epoxy resin, a curing agent, and a filler, the filler has an average particle size of 5 to 35 μm and a specific surface area of 1.4 m^2/g. An epoxy resin composition for semiconductor encapsulation, characterized in that it contains the following spherical silica and uses a filler in which the content of particles with a particle size of 75 μm or more is 1% by weight or less based on the total filler. 2. A cured product obtained by curing the epoxy resin composition for semiconductor encapsulation according to claim 1.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1030813A JPH02209949A (en) | 1989-02-09 | 1989-02-09 | Epoxy resin composition and cured product for semiconductor encapsulation |
| US07/476,700 US5137940A (en) | 1989-02-09 | 1990-02-08 | Semiconductor encapsulating epoxy resin compositions |
| DE4003842A DE4003842C2 (en) | 1989-02-09 | 1990-02-08 | Epoxy resin compositions for encapsulating semiconductors, containing spherical silicon dioxide |
| KR1019900001507A KR950005309B1 (en) | 1989-02-09 | 1990-02-08 | Epoxy resin composition for encapsulating semi-conductors |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1030813A JPH02209949A (en) | 1989-02-09 | 1989-02-09 | Epoxy resin composition and cured product for semiconductor encapsulation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02209949A true JPH02209949A (en) | 1990-08-21 |
Family
ID=12314132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1030813A Pending JPH02209949A (en) | 1989-02-09 | 1989-02-09 | Epoxy resin composition and cured product for semiconductor encapsulation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02209949A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05206333A (en) * | 1992-01-27 | 1993-08-13 | Shin Etsu Chem Co Ltd | Epoxy resin composition for sealing semiconductor and hardened one thereof |
| JPH05267371A (en) * | 1992-03-19 | 1993-10-15 | Hitachi Ltd | Resin-sealed semiconductor device |
| WO1996027900A1 (en) * | 1995-03-07 | 1996-09-12 | Nitto Denko Corporation | Method of production of semiconductor device and sealing pellet used for the method |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61113642A (en) * | 1984-11-09 | 1986-05-31 | Sumitomo Bakelite Co Ltd | Epoxy resin composition for semiconductor sealing use |
| JPS61190961A (en) * | 1985-02-19 | 1986-08-25 | Nitto Electric Ind Co Ltd | Semiconductor device |
| JPS62209128A (en) * | 1986-03-11 | 1987-09-14 | Toshiba Corp | Epoxy resin composition for sealing semiconductor device |
| JPS63108021A (en) * | 1986-10-24 | 1988-05-12 | Hitachi Ltd | Resin-encapsulated semiconductor device |
| JPH01223155A (en) * | 1988-03-01 | 1989-09-06 | Fujitsu Ltd | Epoxy resin composition for semiconductor sealing use |
| JPH02140959A (en) * | 1988-11-22 | 1990-05-30 | Nitto Denko Corp | Semiconductor device |
| JPH02166152A (en) * | 1988-12-20 | 1990-06-26 | Hitachi Chem Co Ltd | Liquid epoxy resin composition for semiconductor sealing |
-
1989
- 1989-02-09 JP JP1030813A patent/JPH02209949A/en active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61113642A (en) * | 1984-11-09 | 1986-05-31 | Sumitomo Bakelite Co Ltd | Epoxy resin composition for semiconductor sealing use |
| JPS61190961A (en) * | 1985-02-19 | 1986-08-25 | Nitto Electric Ind Co Ltd | Semiconductor device |
| JPS62209128A (en) * | 1986-03-11 | 1987-09-14 | Toshiba Corp | Epoxy resin composition for sealing semiconductor device |
| JPS63108021A (en) * | 1986-10-24 | 1988-05-12 | Hitachi Ltd | Resin-encapsulated semiconductor device |
| JPH01223155A (en) * | 1988-03-01 | 1989-09-06 | Fujitsu Ltd | Epoxy resin composition for semiconductor sealing use |
| JPH02140959A (en) * | 1988-11-22 | 1990-05-30 | Nitto Denko Corp | Semiconductor device |
| JPH02166152A (en) * | 1988-12-20 | 1990-06-26 | Hitachi Chem Co Ltd | Liquid epoxy resin composition for semiconductor sealing |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05206333A (en) * | 1992-01-27 | 1993-08-13 | Shin Etsu Chem Co Ltd | Epoxy resin composition for sealing semiconductor and hardened one thereof |
| JPH05267371A (en) * | 1992-03-19 | 1993-10-15 | Hitachi Ltd | Resin-sealed semiconductor device |
| WO1996027900A1 (en) * | 1995-03-07 | 1996-09-12 | Nitto Denko Corporation | Method of production of semiconductor device and sealing pellet used for the method |
| US5976916A (en) * | 1995-03-07 | 1999-11-02 | Nitto Denko Corporation | Method of producing semiconductor device and encapsulating pellet employed therein |
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