JPH07118366A - Epoxy resin composition - Google Patents

Epoxy resin composition

Info

Publication number
JPH07118366A
JPH07118366A JP26618893A JP26618893A JPH07118366A JP H07118366 A JPH07118366 A JP H07118366A JP 26618893 A JP26618893 A JP 26618893A JP 26618893 A JP26618893 A JP 26618893A JP H07118366 A JPH07118366 A JP H07118366A
Authority
JP
Japan
Prior art keywords
epoxy resin
formula
weight
curing agent
total
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
JP26618893A
Other languages
Japanese (ja)
Inventor
Hiroshi Fujita
浩史 藤田
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.)
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 JP26618893A priority Critical patent/JPH07118366A/en
Publication of JPH07118366A publication Critical patent/JPH07118366A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain an epoxy resin composition which can give a cured molding reduced in thermal expansion and water absorptivity, improved in adhesion to a lead frame and a semiconductor chip and reduced in stress in the molding by mixing an inorganic filler with a specified epoxy resin, a curing agent and a cure accelerator. CONSTITUTION:The composition is prepared by mixing 85-92wt.%, based on the total epoxy resin composition, inorganic filler (e.g. spherical silica powder or a mixture of a fused silica powder with a spherical silica powder) with an epoxy resin mixture in which the total amount of the epoxy resin of formula I (wherein Rs, which may be the same or different from each other, are each an atom or a group selected from among H, halogen or alkyl) is at least 80wt.% based on the total epoxy resin weight, and in which the weight ratio, formula I/formula II (wherein R1 to R5, which may be the same or different from each other, are each an atom or a group selected from among H, halogen and alkyl) is 2/8 to 8/2, a curing agent in which the amount of the phenolic resin of formula III (wherein n=1-6) is at least 20wt.% based on the total phenolic resin curing agent, and a cure accelerator for accelerating the curing reaction of the epoxy group with the hydroxyl group and optionally additives, and melt-kneading the resulting mixture.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は半導体デバイスの表面実
装化における耐半田ストレス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。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an epoxy resin composition for semiconductor encapsulation which is excellent in resistance to solder stress in surface mounting semiconductor devices.

【0002】[0002]

【従来の技術】従来、ダイオード、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ー
ルノボラックエポキシ樹脂をフェノールノボラック樹脂
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
がだんだん大型化し、かつパッケージは従来のDIPタ
イプから、表面実装化された小型、薄型のQFP、SO
P、SOJ、TSOP、TQFP、PLCCに変わって
きている。即ち大型チップを小型で薄いパッケージに封
入することになり、熱応力によりクラックが発生し、こ
れらのクラックによる耐湿性の低下等の問題が大きくク
ローズアップされている。特に半田付けの工程において
急激に200℃以上の高温にさらされることにより、パ
ッケージの割れや樹脂とチップの剥離により耐湿性が劣
化してしまうといった問題点がでてきている。従って、
これらの大型チップを封止するのに適した信頼性の高い
半導体封止用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 have been sealed with a thermosetting resin. Especially in integrated circuits, orthocresol novolac epoxy resin, which is excellent in heat resistance and moisture resistance, is replaced with phenol novolac. An epoxy resin composition which is cured with a resin and contains an inorganic filler such as fused silica or crystalline silica as a filler is used. However, in recent years, as the integration of integrated circuits has increased, the size of chips has gradually increased, and the package has changed from the conventional DIP type to surface-mounted small and thin QFP and SO.
It has changed to P, SOJ, TSOP, TQFP, PLCC. That is, a large chip is enclosed in a small and thin package, and cracks are generated due to thermal stress, and problems such as deterioration of moisture resistance due to these cracks are greatly highlighted. In particular, when exposed to a high temperature of 200 ° C. or higher in the soldering process, moisture resistance is deteriorated due to cracking of the package and peeling of the chip from the resin. Therefore,
It is desired to develop a highly reliable resin composition for semiconductor encapsulation suitable for encapsulating these large chips.

【0003】[0003]

【発明が解決しようとする課題】本発明は、この様な問
題に対して、無機充填材を総エポキシ樹脂組成物中に8
5〜92重量%含むことにより、成形物の低熱膨張化及
び低吸水化を図り、エポキシ樹脂として式(1)、式
(2)で示されるエポキシ樹脂及び硬化剤として式
(3)で示される硬化剤を所定量配合することにより、
低吸水化、リードフレーム及び半導体チップとの接着性
の向上、成形物の高温時における低弾性率化による低応
力化により、基板実装時における半導体パッケージの耐
半田ストレス性を著しく向上させた半導体封止用エポキ
シ樹脂組成物を提供するものである。
The present invention addresses the above problems by adding an inorganic filler to the total epoxy resin composition in an amount of 8%.
By including 5 to 92% by weight, low thermal expansion and low water absorption of the molded product are achieved, and the epoxy resin represented by the formula (1) and the formula (2) and the curing agent are represented by the formula (3). By blending a specified amount of curing agent,
A semiconductor encapsulation that significantly improves the solder stress resistance of the semiconductor package when mounted on a board by reducing the water absorption, improving the adhesion to the lead frame and semiconductor chip, and reducing the stress by lowering the elastic modulus of the molded product at high temperatures. An epoxy resin composition for stopping is provided.

【0004】[0004]

【課題を解決するための手段】本発明は、(A)総エポ
キシ樹脂組成物中の85〜92重量%が無機充填材で、
(B)総エポキシ樹脂量中の式(1)で示されるエポキ
シ樹脂と式(2)で示されるエポキシ樹脂の合計量が8
0重量%以上で、かつその重量比が式(1)/式(2)
=2/8〜8/2であるエポキシ樹脂、
According to the present invention, 85 to 92% by weight of the total epoxy resin composition (A) is an inorganic filler,
The total amount of the epoxy resin represented by the formula (1) and the epoxy resin represented by the formula (2) in the total amount of the epoxy resin (B) is 8
0% by weight or more, and the weight ratio is the formula (1) / the formula (2)
= 2/8 to 8/2 epoxy resin,

【0005】[0005]

【化4】 [Chemical 4]

【0006】[0006]

【化5】 [Chemical 5]

【0007】(C)総フェノール樹脂硬化剤量中の式
(3)で示されるフェノール樹脂が20重量%以上であ
る硬化剤 及び
(C) A curing agent containing 20% by weight or more of the phenol resin represented by the formula (3) in the total amount of the phenol resin curing agent, and

【0008】[0008]

【化6】 [Chemical 6]

【0009】(D)硬化促進剤を必須成分とする半導体
封止用エポキシ樹脂組成物で、従来の樹脂組成物に比べ
優れた耐半田クラック性を有するものである。
(D) An epoxy resin composition for semiconductor encapsulation containing a curing accelerator as an essential component, which has excellent solder crack resistance as compared with conventional resin compositions.

【0010】本発明で用いる無機充填材としては、溶融
シリカ粉末、球状シリカ粉末、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、特に球状シリカ粉末、及び溶融シリカ粉末と球状シ
リカ粉末との混合物が好ましい。また無機充填材の配合
量としては、耐半田クラック性と成形性及び流動性のバ
ランスから総エポキシ樹脂組成物中に85〜92重量
%、更に望ましくは87〜90重量%であることが好ま
しい。無機充填材量が85重量%未満だと低熱膨張化、
低吸水化が得られず耐半田クラック性が不充分である。
また、無機充填材量が92重量%を越えると高粘度化に
よる半導体パッケージ中のダイパッド、金線ワイヤーの
ずれ等の不都合が生じる。
Examples of the inorganic filler used in the present invention include fused silica powder, spherical silica powder, crystalline silica powder, secondary agglomerated silica powder, porous silica powder, alumina and the like. In particular, spherical silica powder and fused silica powder. A mixture of powder and spherical silica powder is preferred. Further, the blending amount of the inorganic filler is preferably 85 to 92% by weight, and more preferably 87 to 90% by weight in the total epoxy resin composition in view of the balance between solder crack resistance, moldability and fluidity. If the amount of inorganic filler is less than 85% by weight, low thermal expansion,
Low water absorption cannot be obtained and solder crack resistance is insufficient.
Further, if the amount of the inorganic filler exceeds 92% by weight, there is a problem such as displacement of the die pad and the gold wire in the semiconductor package due to the high viscosity.

【0011】式(1)の分子構造で示されるエポキシ樹
脂は、ジシクロペンタジエンとフェノールを付加反応に
より重合させたフェノール樹脂をグリシジルエーテル化
することによって得られるもので、従来のオルソクレゾ
ールノボラックエポキシ樹脂に比べ、非常に低吸水であ
り、ガラス転移温度を越えた高温時の弾性率が低く、リ
ードフレーム等の金属類との接着性に優れる。従って表
面実装の半田付け時における熱ストレスを低減させるこ
とができ、耐半田クラック性に優れるエポキシ樹脂組成
物を得ることができる。nの値は0〜6で、かつこれら
の混合物であり、6を越えると流動性が低下し、成形性
が悪くなる。式(2)の構造で示されるビフェニル型エ
ポキシ樹脂は1分子中に2個のエポキシ基を有する2官
能性エポキシ樹脂で、従来のオルソクレゾールノボラッ
クエポキシ樹脂に比べ溶融粘度が低く、トランスファー
成形時の流動性に優れる。従って組成物中に溶融シリカ
粉末を多く配合することができ、低熱膨張化及び低吸水
化が図られ、耐半田ストレス性に優れるエポキシ樹脂組
成物を得ることができる。エポキシ樹脂の使用量はこれ
を調節することにより耐半田クラック性を最大限に引き
出すことが出来る。式(1)と式(2)で示されるエポ
キシ樹脂の合計量が総エポキシ樹脂量中に80重量%以
上、望ましくは90重量%以上の使用が好ましい。80
重量%未満では、低吸水性、接着性が十分に得られず、
耐半田クラック性が不十分である。次に、式(1)と式
(2)で示されるエポキシ樹脂は重量比で式(1)/式
(2)=2/8〜8/2で、好ましくは式(1)/式
(2)=3/7〜7/3である。式(1)の比率が20
重量%未満であると、式(1)の利点である低吸水性、
低弾性、高接着性が十分に得られず、また式(1)の比
率が80重量%を越えると式(2)の利点である低粘度
性が得られずトランスファー成形時の流動性に悪影響を
与える。式(1)、式(2)で示されるエポキシ樹脂以
外に他のものを併用する場合、用いるエポキシ樹脂はエ
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、ナフタレン型エポキシ化合物、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が挙げられる。
The epoxy resin represented by the molecular structure of the formula (1) is obtained by glycidyl etherification of a phenol resin obtained by polymerizing dicyclopentadiene and phenol by an addition reaction, and is a conventional orthocresol novolak epoxy resin. Compared with, it has a very low water absorption, has a low elastic modulus at high temperatures exceeding the glass transition temperature, and has excellent adhesiveness to metals such as lead frames. Therefore, the thermal stress at the time of soldering of surface mounting can be reduced, and the epoxy resin composition excellent in solder crack resistance can be obtained. The value of n is 0 to 6 and it is a mixture thereof, and if it exceeds 6, the fluidity is lowered and the moldability is deteriorated. The biphenyl type epoxy resin represented by the structure of the formula (2) is a bifunctional epoxy resin having two epoxy groups in one molecule, has a lower melt viscosity than the conventional orthocresol novolac epoxy resin, and is excellent in transfer molding. Excellent fluidity. Therefore, a large amount of fused silica powder can be blended in the composition, low thermal expansion and low water absorption can be achieved, and an epoxy resin composition excellent in solder stress resistance can be obtained. By adjusting the amount of epoxy resin used, solder crack resistance can be maximized. The total amount of the epoxy resins represented by the formulas (1) and (2) is preferably 80% by weight or more, more preferably 90% by weight or more based on the total amount of the epoxy resin. 80
If it is less than wt%, low water absorption and adhesiveness cannot be obtained sufficiently,
Solder crack resistance is insufficient. Next, the epoxy resins represented by the formulas (1) and (2) have a weight ratio of formula (1) / formula (2) = 2/8 to 8/2, preferably formula (1) / formula (2). ) = 3/7 to 7/3. The ratio of formula (1) is 20
When it is less than wt%, low water absorption, which is an advantage of the formula (1),
Low elasticity and high adhesiveness are not sufficiently obtained, and when the ratio of the formula (1) exceeds 80% by weight, the low viscosity which is the advantage of the formula (2) cannot be obtained and the flowability during transfer molding is adversely affected. give. When the other epoxy resin is used in combination with the epoxy resin represented by the formula (1) or (2), the epoxy resin to be used is a monomer, an oligomer or a polymer having an epoxy group in general. For example, naphthalene 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.

【0012】式(3)で示されるフェノール樹脂硬化剤
は、フェノールとP−キシリレングリコールジメチルエ
ーテルの重縮合物であり、低吸水性及び可撓性に優れる
特徴を有する。特に半田付け時の高温時の可撓性に優れ
ており、250〜260℃での半田付け時の半田耐熱性
に著しい効果をもたらす。このフェノールとP−キシリ
レングリコールジメチルエーテルの重縮合フェノール樹
脂硬化剤の使用量は、これを調整することにより半田耐
熱性を最大限に引き出すことができる。半田耐熱性の効
果を引き出すには式(3)で示されるフェノール樹脂硬
化剤を総硬化剤の20重量%以上、望ましく30重量%
以上の使用が好ましい。20重量%未満では可撓性が不
充分となり、半田付け時の半田耐熱性が充分に得られな
い。nの値は1〜6で、かつこれらの混合物であり、6
を越えると流動性が低下し、成形性が悪くなる。式
(3)で示されるフェノール樹脂硬化剤以外に他のもの
を併用する場合、用いるものとしては主にフェノール性
水酸基を有するポリマー全般をいう。例えば、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、ジシクロペンタジ
エン変性フェノール樹脂とフェノールノボラック及びク
レゾールノボラック樹脂との共重合物、ナフタレン変性
フェノール樹脂等を用いることができる。また、これら
の硬化剤の配合量としては、エポキシ樹脂のエポキシ基
数と硬化剤の水酸基数の割合は、0.8〜1.2で、望
ましく当量が好ましい。
The phenol resin curing agent represented by the formula (3) is a polycondensation product of phenol and P-xylylene glycol dimethyl ether, and has characteristics of low water absorption and excellent flexibility. In particular, it is excellent in flexibility at high temperature during soldering, and has a remarkable effect on solder heat resistance during soldering at 250 to 260 ° C. By adjusting the amount of the phenol and P-xylylene glycol dimethyl ether polycondensation phenol resin curing agent used, solder heat resistance can be maximized. In order to bring out the effect of solder heat resistance, the phenol resin curing agent represented by the formula (3) is contained in an amount of 20% by weight or more, preferably 30% by weight of the total curing agent.
The above uses are preferred. If it is less than 20% by weight, the flexibility becomes insufficient and the solder heat resistance during soldering cannot be sufficiently obtained. The value of n is 1 to 6 and is a mixture of these,
If it exceeds, the fluidity is lowered and the moldability is deteriorated. When used in combination with other than the phenol resin curing agent represented by the formula (3), it mainly refers to all polymers having a phenolic hydroxyl group. For example, phenol novolac resin, cresol novolac resin, dicyclopentadiene modified phenol resin, copolymer of dicyclopentadiene modified phenol resin and phenol novolac or cresol novolac resin, naphthalene modified phenol resin and the like can be used. As the compounding amount of these curing agents, the ratio of the number of epoxy groups in the epoxy resin to the number of hydroxyl groups in the curing agent is 0.8 to 1.2, and preferably an equivalent amount.

【0013】本発明に使用される硬化促進剤は、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良
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単独もしくは2種類
以上混合して用いられる。本発明のエポキシ樹脂組成物
は無機充填材、エポキシ樹脂、硬化剤及び硬化促進剤を
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 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, 2-methylimidazole and the like are used alone or in combination of two or more. The epoxy resin composition of the present invention contains an inorganic filler, an epoxy resin, a curing agent and a curing accelerator as essential components, but in addition to this, a silane coupling agent, a brominated epoxy resin, antimony trioxide, and hexa may be added if necessary. Flame retardants such as brombenzene, 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 may be appropriately blended. There is no.
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.

【0014】以下、本発明を実施例で具体的説明する。 実施例1 式(4)で示されるエポキシ樹脂(軟化点65℃、エポキシ当量250g/e q) 3.4重量部The present invention will be specifically described below with reference to examples. Example 1 3.4 parts by weight of an epoxy resin represented by the formula (4) (softening point: 65 ° C., epoxy equivalent: 250 g / eq)

【0015】[0015]

【化7】 (nの値は0から2を示す混合物であり、その重量割合
はn=0が1に対してn=1が0.4、n=2が0.2
5である)
[Chemical 7] (The value of n is a mixture showing 0 to 2, and the weight ratio thereof is 1 for n = 0 and 0.4 for n = 1 and 0.2 for n = 2.
5)

【0016】 式(5)で示されるエポキシ樹脂(融点110℃、エポキシ当量190g/e q) 3.4重量部3.4 parts by weight of the epoxy resin represented by the formula (5) (melting point: 110 ° C., epoxy equivalent: 190 g / eq)

【0017】[0017]

【化8】 [Chemical 8]

【0018】 式(6)で示されるフェノール樹脂硬化剤(軟化点80℃、水酸基当量170 g/eq) 2.1重量部2.1 parts by weight of a phenol resin curing agent represented by the formula (6) (softening point 80 ° C., hydroxyl group equivalent 170 g / eq)

【0019】[0019]

【化9】 (nの値は1から3を示す混合物であり、その重量割合
はn=1が1に対してn=2が3、n=3が1である)
[Chemical 9] (The value of n is a mixture showing 1 to 3, and the weight ratio is 1 for n = 1 and 3 for n = 2 and 1 for n = 3)

【0020】 フェノールノボラック樹脂硬化剤(軟化点105℃、水酸基当量100g/e q) 2.1重量部 溶融シリカ粉末(平均粒径10μm、比表面積2.0m2/g) 88重量部 トリフェニルホスフィン 0.2重量部 カーボンブラック 0.3重量部 カルナバワックス 0.5重量部 をミキサーで常温で混合し、70〜100℃で2軸ロー
ルにより混練し、冷却後粉砕して成形材料とした。粉砕
して得られた成形材料を175℃、70kg/cm2
120秒の条件でスパイラルフローを測定した。更に得
られた成形材料をタブレット化し、低圧トランスファー
成形機にて175℃、70kg/cm2、120秒の条件
で半田クラック性試験用として6×6mmのチップを5
2pQFPに封止し、また半田耐湿性試験用として3×
6mmのチップを16pSOPに封止した。封止したテ
スト用素子について下記の半田クラック性試験及び半田
耐湿性試験を行った。評価結果を表1に示す。
Phenol novolac resin curing agent (softening point 105 ° C., hydroxyl group equivalent 100 g / eq) 2.1 parts by weight fused silica powder (average particle size 10 μm, specific surface area 2.0 m 2 / g) 88 parts by weight triphenylphosphine 0.2 parts by weight carbon black 0.3 parts by weight Carnauba wax 0.5 parts by weight were mixed in a mixer at room temperature, kneaded at 70 to 100 ° C. with a biaxial roll, cooled and pulverized to obtain a molding material. The molding material obtained by crushing was 175 ° C., 70 kg / cm 2 ,
The spiral flow was measured under the condition of 120 seconds. Further, the obtained molding material was tabletted, and a 6 × 6 mm chip was tested for solder cracking test under the conditions of 175 ° C., 70 kg / cm 2 , 120 seconds with a low-pressure transfer molding machine.
Sealed in 2pQFP and 3x for solder moisture resistance test
A 6 mm chip was encapsulated in 16 pSOP. The following solder cracking property test and solder moisture resistance test were conducted on the sealed test element. The evaluation results are shown in Table 1.

【0021】半田クラック性試験:封止したテスト用素
子を85℃、85%RHの環境下で48時間及び72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。 半田耐湿性試験:封止しテスト用素子を85℃、85%
RHの環境下で72時間処理し、その後260℃の半田
槽に10秒間浸漬後、プレッシャークッカー試験(12
5℃、100%RH)を行い、回路のオープン不良を測
定した。 実施例2〜10 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。実施例10に用いたオルソクレゾールノボ
ラックエポキシ樹脂(EOCNという)の軟化点は65
℃、エポキシ当量200g/eqである。この成形材料
で試験用の封止した成形品を得、この成形品を用いて実
施例1と同様に半田クラック性試験及び半田耐湿性試験
を行った。評価結果を表1に示す。
Solder cracking property test: The sealed test element was treated in an environment of 85 ° C. and 85% RH for 48 hours and 72 hours, then immersed in a solder bath at 260 ° C. for 10 seconds, and external cracks were observed with a microscope. did. Solder moisture resistance test: Sealed test element at 85 ℃, 85%
It is treated for 72 hours in an environment of RH and then immersed in a solder bath at 260 ° C for 10 seconds, and then subjected to a pressure cooker test (12
5 ° C., 100% RH) was performed to measure the open defect of the circuit. Examples 2 to 10 Compounding was performed according to the formulation shown in Table 1, and molding materials were obtained in the same manner as in Example 1. The ortho-cresol novolak epoxy resin (referred to as EOCN) used in Example 10 has a softening point of 65.
C., epoxy equivalent is 200 g / eq. Using this molding material, a sealed molded product for testing was obtained, and a solder cracking resistance test and a solder moisture resistance test were conducted in the same manner as in Example 1 using this molded product. The evaluation results are shown in Table 1.

【0022】比較例1〜6 表2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。この成形材料で試験用の封止した成形品を
得、この成形品を用いて実施例1と同様に半田クラック
性試験及び半田耐湿性試験を行った。評価結果を表2に
示す。
Comparative Examples 1 to 6 Compounding was carried out according to the formulation shown in Table 2, and molding materials were obtained in the same manner as in Example 1. Using this molding material, a sealed molded product for testing was obtained, and a solder cracking resistance test and a solder moisture resistance test were conducted in the same manner as in Example 1 using this molded product. The evaluation results are shown in Table 2.

【0023】[0023]

【表1】 [Table 1]

【0024】[0024]

【表2】 [Table 2]

【0025】[0025]

【発明の効果】本発明に従うと従来技術では得ることが
できなかった耐半田ストレス性を有するエポキシ樹脂組
成物を得ることができるので、半田付け工程による急激
な温度変化による熱ストレスを受けた時の耐クラック性
に非常に優れ、更に耐湿性が良好なことから電子、電気
部品の封止用、被覆用、絶縁用等に用いた場合、特に表
面実装パッケージに搭載された高集積大型チップICに
おいて信頼性が非常に必要とする製品につい好適であ
る。
According to the present invention, it is possible to obtain an epoxy resin composition having a solder stress resistance which could not be obtained by the prior art. Therefore, when the epoxy resin composition is subjected to thermal stress due to a rapid temperature change due to the soldering process. Has very good crack resistance and good moisture resistance, so when used for encapsulation, coating, insulation, etc. of electronic and electrical parts, especially highly integrated large chip IC mounted in surface mount package It is suitable for products that require high reliability.

───────────────────────────────────────────────────── 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 H01L 23/29 23/31 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location H01L 23/29 23/31

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (A)総エポキシ樹脂組成物中の85〜
92重量%が無機充填材で、(B)総エポキシ樹脂量中
の式(1)で示されるエポキシ樹脂と式(2)で示され
るエポキシ樹脂の合計量が80重量%以上で、かつその
重量比が式(1)/式(2)=2/8〜8/2であるエ
ポキシ樹脂、 【化1】 【化2】 (C)総フェノール樹脂硬化剤量中の式(3)で示され
るフェノール樹脂が20重量%以上である硬化剤 及び 【化3】 (D)硬化促進剤を必須成分とする半導体封止用エポキ
シ樹脂組成物。
1. A total of 85 to 85 of (A) the total epoxy resin composition.
92% by weight is an inorganic filler, the total amount of the epoxy resin represented by the formula (1) and the epoxy resin represented by the formula (2) in the total amount of the epoxy resin (B) is 80% by weight or more, and the weight thereof is An epoxy resin having a ratio of formula (1) / formula (2) = 2/8 to 8/2, [Chemical 2] (C) a curing agent containing 20% by weight or more of the phenol resin represented by the formula (3) in the total amount of the phenol resin curing agent; (D) An epoxy resin composition for semiconductor encapsulation containing a curing accelerator as an essential component.
JP26618893A 1993-10-25 1993-10-25 Epoxy resin composition Pending JPH07118366A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26618893A JPH07118366A (en) 1993-10-25 1993-10-25 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26618893A JPH07118366A (en) 1993-10-25 1993-10-25 Epoxy resin composition

Publications (1)

Publication Number Publication Date
JPH07118366A true JPH07118366A (en) 1995-05-09

Family

ID=17427480

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26618893A Pending JPH07118366A (en) 1993-10-25 1993-10-25 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JPH07118366A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001234035A (en) * 2000-02-24 2001-08-28 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
JP2002053642A (en) * 2000-08-09 2002-02-19 Nitto Denko Corp Epoxy resin composition for semiconductor sealing and semiconductor device produced by using the composition
JP2003012761A (en) * 2001-06-27 2003-01-15 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
WO2003037954A1 (en) * 2001-11-02 2003-05-08 Nippon Petrochemicals Co.,Ltd. Phenolic resin, epoxy resin, process for producing the same, and resin composition for semiconductor encapsulation material
JP2010144016A (en) * 2008-12-17 2010-07-01 Nitto Denko Corp Epoxy resin composition for sealing optical semiconductor element, and optical semiconductor device using the same
CN114644810A (en) * 2020-12-18 2022-06-21 衡所华威电子有限公司 High-temperature fast-curing low-stress epoxy resin composition and preparation method thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001234035A (en) * 2000-02-24 2001-08-28 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
JP2002053642A (en) * 2000-08-09 2002-02-19 Nitto Denko Corp Epoxy resin composition for semiconductor sealing and semiconductor device produced by using the composition
JP2003012761A (en) * 2001-06-27 2003-01-15 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
WO2003037954A1 (en) * 2001-11-02 2003-05-08 Nippon Petrochemicals Co.,Ltd. Phenolic resin, epoxy resin, process for producing the same, and resin composition for semiconductor encapsulation material
JP2010144016A (en) * 2008-12-17 2010-07-01 Nitto Denko Corp Epoxy resin composition for sealing optical semiconductor element, and optical semiconductor device using the same
CN114644810A (en) * 2020-12-18 2022-06-21 衡所华威电子有限公司 High-temperature fast-curing low-stress epoxy resin composition and preparation method thereof
CN114644810B (en) * 2020-12-18 2024-03-01 衡所华威电子有限公司 High-temperature fast-curing low-stress epoxy resin composition and preparation method thereof

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