JPH07188515A - Resin composition for semiconductor sealing - Google Patents

Resin composition for semiconductor sealing

Info

Publication number
JPH07188515A
JPH07188515A JP32942093A JP32942093A JPH07188515A JP H07188515 A JPH07188515 A JP H07188515A JP 32942093 A JP32942093 A JP 32942093A JP 32942093 A JP32942093 A JP 32942093A JP H07188515 A JPH07188515 A JP H07188515A
Authority
JP
Japan
Prior art keywords
resin
resin composition
weight
resole
parts
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
JP32942093A
Other languages
Japanese (ja)
Inventor
Akihiro Hirata
明広 平田
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 JP32942093A priority Critical patent/JPH07188515A/en
Publication of JPH07188515A publication Critical patent/JPH07188515A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)

Abstract

PURPOSE:To obtain a resin composition for semiconductor sealing, having excellent storage stability at normal temperature and excellent flame-retardancy in spite of the absence of flame-retardant and exhibiting excellent moldability, soldering heat-resistance and reliability in humid atmosphere by compounding a specific resol resin and a phenolic novolak resin at a specific total amount. CONSTITUTION:This resin composition contains (A) a resol resin of formula (l is 0 or 2; m and p each is 0 or <=10; n is 0 or <=4; m+p is <=15), (B) a phenolic novolak resin, (C) a cure accelerator (e.g. 1,8-diazabicycloundecene) and (D) an inorganic filler (e.g. spherical fused silica) as essential components. The sum of the components A and B in the total resin composition is 15-35wt.% and the weight ratio of A/(A+B) is preferably 0.5-0.9.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は常温保管性、成形性、半
田耐熱性、耐湿信頼性、難燃性に優れた半導体封止用樹
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 a resin composition for semiconductor encapsulation which is excellent in room temperature storage property, moldability, solder heat resistance, moisture resistance reliability and flame retardancy.

【0002】[0002]

【従来の技術】トランジスター、コンデンサー、ダイオ
ード、IC、LSI等の半導体封止用樹脂組成物の樹脂
成分としては、エポキシ樹脂とフェノール樹脂硬化剤の
組み合わせが成形性、信頼性、低コスト、量産性に適し
た樹脂として採用されている。しかし、近年の電子機器
の小型化、軽量化、高性能化の市場動向の中で、特に民
生用は低価格化を前提にされる用途も多くなってきてお
り、半導体封止材料への要求は益々厳しいものとなって
きている。このため、従来の封止材料では解決できない
問題点もでてきている。
2. Description of the Related Art As a resin component of a resin composition for encapsulating semiconductors such as transistors, capacitors, diodes, ICs, LSIs, a combination of an epoxy resin and a phenol resin curing agent is moldable, reliable, low cost and mass producible. Adopted as a resin suitable for. However, in the recent market trend of miniaturization, weight reduction, and high performance of electronic devices, there are many applications for which the price is low, especially for consumer products, and the demand for semiconductor encapsulation materials is increasing. Is becoming more and more severe. Therefore, there are problems that cannot be solved by the conventional sealing material.

【0003】1番目の問題としては、半導体パッケージ
の表面実装の採用によりパッケージが半田浸漬、あるい
はリフロー工程で急激に200℃以上の高温にさらさ
れ、このためにパッケージが割れたり、チップと封止樹
脂との界面剥離が生じて耐湿性が低下したりするという
半田耐熱性の問題が挙げられる。この半田耐熱性の向上
に関しては、耐熱エポキシ樹脂の使用、半田浸漬時の応
力低減やリードフレーム、チップとの接着性向上のため
の可撓性樹脂の使用、接着性付与成分の添加、熱膨張係
数を小さくするための無機質充填材の配合量の増量、あ
るいはシリカ表面のシランカップリング剤の処理条件の
改良等数多くの提案がなされてきている。しかし、根本
的な欠点としてエポキシ樹脂は耐熱性が低く、200℃
以上の環境では急激に物理的耐久性が低下してしまい、
熱応力に耐え得る強度を保つことは不可能である。この
耐熱性の低下を改良しなければ、上記諸提案の効果を充
分に得ることはできない。特殊な骨格構造のエポキシ樹
脂を用いることにより、特性のかなりの改善が達成され
つつあるものの、高価格となり、自ずと用途が高付加価
値製品用のみに限定されてしまっている。2番目の問題
としては、総合的生産コストの上昇である。特殊な原材
料を用いることで原材料価格は上昇せざるを得ず、また
保管条件にも極低温保管等非常に厳しい条件を要する場
合が多い。3番目の問題としては、環境衛生面からのブ
ロム化エポキシ、アンチモン等の存在であり、エポキシ
樹脂は生来的にこれら難燃剤を配合しなければ使用に耐
えうる難燃性を有することはできない。
The first problem is that the surface mounting of a semiconductor package causes the package to be rapidly exposed to a high temperature of 200 ° C. or higher during solder dipping or a reflow process, which may cause the package to crack or seal the chip and the chip. There is a problem of solder heat resistance that interface separation from the resin occurs and moisture resistance decreases. Regarding the improvement of solder heat resistance, use of heat-resistant epoxy resin, use of flexible resin for stress reduction during solder immersion and improvement of adhesion to lead frames and chips, addition of adhesion-imparting components, thermal expansion Many proposals have been made such as increasing the amount of the inorganic filler compounded to reduce the coefficient or improving the treatment conditions of the silane coupling agent on the silica surface. However, the fundamental drawback is that epoxy resin has low heat resistance,
In the above environment, the physical durability suddenly decreases,
It is impossible to maintain the strength that can withstand thermal stress. The effects of the above proposals cannot be sufficiently obtained unless the reduction in heat resistance is improved. Although the use of an epoxy resin having a special skeleton structure has achieved a considerable improvement in characteristics, the price is high and the application is naturally limited to high value-added products. The second problem is the increase in total production cost. The use of special raw materials inevitably raises the price of raw materials, and storage conditions often require very strict conditions such as cryogenic storage. The third problem is the presence of brominated epoxies, antimony, etc. from the viewpoint of environmental hygiene. Epoxy resins cannot inherently have flame retardancy that can be used without blending these flame retardants.

【0004】[0004]

【発明が解決しようとする課題】半導体封止用樹脂組成
物の耐熱性、常温保管性、難燃性につき種々の検討を行
った結果、上記特性には封止樹脂組成物中の樹脂成分の
寄与が非常に大きいことを明らかにし、この樹脂成分を
レゾール樹脂にすることで、飛躍的に特性が向上するこ
とを見いだした。即ち本発明は半導体封止用樹脂組成物
の常温保管性、半導体パッケージの表面実装化における
半田処理工程後の信頼性維持のための耐熱性、及びブロ
ム化エポキシやアンチモン等の難燃剤を添加することな
く、優れた難燃性を有することのいずれをも達成するこ
とができる半導体封止用樹脂組成物を提供するものであ
る。
As a result of various studies on the heat resistance, room temperature storability, and flame retardancy of the resin composition for semiconductor encapsulation, the above characteristics show that the resin component in the encapsulating resin composition has It was clarified that the contribution was very large, and it was found that the characteristics were dramatically improved by using this resin component as a resole resin. That is, the present invention adds a room temperature storability of a resin composition for semiconductor encapsulation, heat resistance for maintaining reliability after a soldering process in surface mounting of a semiconductor package, and a flame retardant such as brominated epoxy or antimony. It is intended to provide a resin composition for semiconductor encapsulation, which can achieve both of excellent flame retardancy without any of the above.

【0005】[0005]

【課題を解決するための手段】本発明は、式(1)のレ
ゾール樹脂、フェノールノボラック樹脂、硬化促進剤、
無機質充填材を必須成分とするレゾール樹脂組成物にお
いて、全樹脂組成物中のレゾール樹脂とフェノールノボ
ラック樹脂の合計量が15〜35重量%であり、特にそ
の重量比がレゾール樹脂/(レゾール樹脂+フェノール
ノボラック樹脂)=0.5〜0.9である半導体封止用
樹脂組成物である。
The present invention provides a resole resin of the formula (1), a phenol novolac resin, a curing accelerator,
In a resole resin composition containing an inorganic filler as an essential component, the total amount of resole resin and phenol novolac resin in the total resin composition is 15 to 35% by weight, and particularly the weight ratio is resole resin / (resole resin + It is a resin composition for semiconductor encapsulation in which (phenol novolac resin) = 0.5 to 0.9.

【0006】[0006]

【化1】 ( 但し、lは0または2以下の正数、m、pは0また
は10以下の正数、nは0または4以下の正数、かつm
+pは15以下の正数を表す。)
[Chemical 1] (However, l is a positive number of 0 or 2 or less, m or p is a positive number of 0 or 10 or less, n is a positive number of 0 or 4 and m
+ P represents a positive number of 15 or less. )

【0007】以下に本発明を詳細に説明する。本発明に
用いられる式(1)で示されるレゾール樹脂はフェノー
ル性水酸基とメチロール基、ジメチレンエーテル基等を
有するモノマー、オリゴマー、ポリマー及びこれら混合
物全般をいう。平均構造としてlが2を越えると硬化樹
脂の架橋密度が低下してガラス転移温度が低下しまい、
m、pが10を越え、またはm+pが15を越えると樹
脂が高粘度化して流動性や充填性が低下し、低圧成形が
困難になる。本発明に用いるフェノールノボラック樹脂
はフェノール性水酸基を有するモノマー、オリゴマー、
ポリマー及びこれら混合物全般をいい、具体的には、フ
ェノールノボラック樹脂、パラキシリレン変性フェノー
ル樹脂、テルペン変性フェノール樹脂、ジシクロペンタ
ジエン変性フェノール樹脂、ビスフェノールA、あるい
はトリフェノールメタンとアルデヒド化合物との縮合物
等が挙げられるが、本発明はこれらに限定されるもので
はない。また、これらのフェノールノボラック樹脂は単
独でも混合して用いても差し支えない。
The present invention will be described in detail below. The resol resin represented by the formula (1) used in the present invention refers to a monomer, an oligomer, a polymer having a phenolic hydroxyl group and a methylol group, a dimethylene ether group and the like, and mixtures thereof in general. When 1 exceeds 2 as the average structure, the cross-linking density of the cured resin is lowered and the glass transition temperature is lowered,
If m and p exceed 10, or m + p exceeds 15, the resin becomes highly viscous and the flowability and filling property are deteriorated, making low-pressure molding difficult. The phenol novolac resin used in the present invention is a monomer having a phenolic hydroxyl group, an oligomer,
Polymers and mixtures thereof in general, specifically, phenol novolac resin, paraxylylene-modified phenol resin, terpene-modified phenol resin, dicyclopentadiene-modified phenol resin, bisphenol A, or a condensate of triphenolmethane and an aldehyde compound, etc. However, the present invention is not limited thereto. Further, these phenol novolac resins may be used alone or as a mixture.

【0008】本発明の最も重要な点は、全樹脂組成物中
に含まれるレゾール樹脂とフェノールノボラック樹脂の
合計量が15〜35重量%であることである。15重量
%未満だと樹脂組成物を半導体封止材料として低圧成型
を実施した際に、高流動性を発揮することが困難であ
り、成型品の充填不良を生じやすくなる。また、35重
量%を越えると、耐クラック性、耐湿信頼性の低下を生
じる。また、レゾール樹脂とフェノールノボラック樹脂
の配合割合を変更することにより、ガラス転移温度、吸
水率、熱時曲げ強度、熱時曲げ弾性率等を自由に調整で
きる。レゾール樹脂/(レゾール樹脂+フェノールノボ
ラック樹脂)の重量比は0.5〜0.9の範囲が好まし
い。0.5未満だと成型時の硬化性が悪化し、ガラス転
移温度が低くなり過ぎ、曲げ強度も低下してしまう。
0.9を越えると硬化収縮率が大きくなるため、大型パ
ッケージや複雑な構造のパッケージでは成型時に反りが
生じ易くなり、更に硬化物の吸水率、曲げ弾性率が高く
なり、また、非常にもろくなってしまう。
The most important point of the present invention is that the total amount of the resole resin and the phenol novolac resin contained in the entire resin composition is 15 to 35% by weight. If it is less than 15% by weight, it is difficult to exhibit high fluidity when low-pressure molding is performed using the resin composition as a semiconductor encapsulating material, and defective filling of molded products is likely to occur. Further, if it exceeds 35% by weight, crack resistance and moisture resistance reliability are deteriorated. Further, by changing the compounding ratio of the resole resin and the phenol novolac resin, it is possible to freely adjust the glass transition temperature, the water absorption rate, the bending strength during heating, the bending elastic modulus during heating, and the like. The weight ratio of resole resin / (resole resin + phenol novolac resin) is preferably in the range of 0.5 to 0.9. If it is less than 0.5, the curability during molding deteriorates, the glass transition temperature becomes too low, and the bending strength also decreases.
When it exceeds 0.9, the curing shrinkage ratio becomes large, so that a large package or a package having a complicated structure is apt to warp during molding, and the water absorption rate and bending elastic modulus of the cured product become high, and it is also very brittle. turn into.

【0009】本発明に用いる硬化促進剤は、レゾール樹
脂の架橋反応の触媒となるものであり、具体的にはヘキ
サミン、アニリン、アンモニア、1,8−ジアザビシク
ロウンデセン等のアミン系化合物、2−メチルイミダゾ
ール等のイミダゾール化合物、p−トルエンスルホン酸
等の酸、水酸化カルシウム、水酸化マグネシウム等のア
ルカリ化合物等が挙げられ、本発明はこれらに限定され
るものではないが、好ましくは1,8−ジアザビシクロ
ウンデセン、2−メチルイミダゾール等のイミダゾール
化合物が用いられる。また、これらの硬化促進剤は単独
であっても、混合して用いても差し支えない。本発明に
用いる無機質充填材は、半導体封止用エポキシ樹脂組成
物に用いられるものと同じもので、平均粒径10〜20
μm、最大粒径70〜150μmの溶融シリカ粉末、結
晶シリカ粉末、アルミナ、窒化珪素等が挙げられる。こ
れら無機質充填材の配合量は成形性と信頼性とのバラン
スから全樹脂組成物中に65〜85重量%含有すること
が好ましい。特に充填材量の多い配合では、球状の溶融
シリカを用いるのが一般的である。
The curing accelerator used in the present invention serves as a catalyst for the cross-linking reaction of the resole resin, and specifically includes amine compounds such as hexamine, aniline, ammonia, and 1,8-diazabicycloundecene. Examples thereof include imidazole compounds such as 2-methylimidazole, acids such as p-toluenesulfonic acid, alkali compounds such as calcium hydroxide and magnesium hydroxide, and the present invention is not limited thereto, but preferably 1 An imidazole compound such as, 8-diazabicycloundecene or 2-methylimidazole is used. Further, these curing accelerators may be used alone or as a mixture. The inorganic filler used in the present invention is the same as that used in the epoxy resin composition for semiconductor encapsulation and has an average particle size of 10 to 20.
Examples include fused silica powder having a particle size of 70 μm and a maximum particle size of 70 to 150 μm, crystalline silica powder, alumina, silicon nitride and the like. The blending amount of these inorganic fillers is preferably 65 to 85% by weight in the entire resin composition from the viewpoint of balance between moldability and reliability. Particularly in the case of a compound having a large amount of filler, spherical fused silica is generally used.

【0010】本発明の樹脂組成物は、式(1)のレゾー
ル樹脂、硬化促進剤、及び無機質充填材を必須成分とす
るが、これ以外にも必要に応じて、シランカップリング
剤に代表される各種カップリング剤、カーボンブラック
に代表される着色剤、天然ワックス及び合成ワックス等
の離型剤、シリコーンオイル、シリコーンゴム、合成ゴ
ム等の低応力添加剤を適宜配合しても差し支えない。成
形材料化するに際しては、加熱ニーダーや熱ロールによ
り全組成物を加熱混練し、続いて冷却、粉砕することで
目的とする半導体封止用エポキシ樹脂組成物が得られ
る。
The resin composition of the present invention contains the resol resin of the formula (1), a curing accelerator, and an inorganic filler as essential components, but in addition to this, if necessary, a silane coupling agent is representative. Various coupling agents such as carbon black, colorants typified by carbon black, release agents such as natural wax and synthetic wax, and low stress additives such as silicone oil, silicone rubber, and synthetic rubber may be appropriately mixed. When forming a molding material, the desired composition for epoxy resin for semiconductor encapsulation is obtained by heating and kneading the entire composition with a heating kneader or a heating roll, followed by cooling and pulverizing.

【0011】以下本発明を実施例で具体的に説明する。 実施例1 式(1)で示されるレゾール樹脂(但し、平均構造としてl=1.1、m=3 .2、n=1.5、p=2.2、以下レゾール樹脂1という) 11.00重量部 フェノールノボラック樹脂(軟化点85℃、水酸基当量104) 5.10重量部 1,8−ジアザビシクロウンデセン 0.15重量部 溶融シリカ粉末 81.55重量部 γーアミノプロピルトリエトキシシラン 0.50重量部 カルナバワックス 0.50重量部 カーボンブラック 0.30重量部 上記配合でレゾール樹脂組成物を製造するにあたって、
全配合原料をミキサーにより混合した後、バレル温度1
00℃で、ニーダー、ロール等で加熱混練し、更に冷却
後粉砕して、封止材料とした。
The present invention will be specifically described below with reference to examples. Example 1 Resol resin represented by the formula (1) (provided that the average structure is l = 1.1, m = 3.2, n = 1.5, p = 2.2, hereinafter referred to as resole resin 1) 11. 00 parts by weight Phenol novolac resin (softening point 85 ° C., hydroxyl equivalent 104) 5.10 parts by weight 1,8-diazabicycloundecene 0.15 parts by weight fused silica powder 81.55 parts by weight γ-aminopropyltriethoxysilane 0.50 parts by weight Carnauba wax 0.50 parts by weight Carbon black 0.30 parts by weight In producing the resol resin composition with the above-mentioned composition,
After mixing all blended ingredients with a mixer, barrel temperature 1
The mixture was heated and kneaded with a kneader or a roll at 00 ° C., further cooled and pulverized to obtain a sealing material.

【0012】この材料を用いて、スパイラルフロー、ゲ
ル化時間、ショア硬度D、硬化収縮率、ガラス転移温
度、吸水率、曲げ強度、曲げ弾性率、難燃性の各項目を
測定した。更にクラック数、耐湿信頼性の評価を行っ
た。サンプルの成形は全てトランスファー成形で、金型
温度175℃、硬化120秒にて実施した。後硬化は1
75℃で8時間実施した。 スパイラルフロー:内部がスパイラル状になった金型を
用い、トランスファー成形175℃、実効圧70kgf
/cm2で約120秒硬化した時の金型内で樹脂が流動
した長さ。 ゲル化時間 :175℃の熱板上に成形材料を2g
乗せ、スパチュラを用いて約25mm角の大きさに広げ
て熱板にこすりつけた後、樹脂が硬化して熱板より剥が
れる時間。 ショアD硬度 :トランスファー成形175℃、硬化
120秒、金型オープン10秒後にショアD硬度計で測
定した硬度の測定値。 硬化収縮率 :JIS K 6911に準ずる。 ガラス転移温度 :TMA法により測定。 吸水率 :JIS K 6911に準ずる。 曲げ強度 :JIS K 6911に準ずる。 曲げ弾性率 :JIS K 6911に準ずる。 難燃性 :UL94垂直法。厚さ1.0mmの
試験片を使用。 半田クラック数 :80pQFPパッケージ(パッケー
ジサイズは14×20mm、厚み1.5mm、チップサ
イズは9×9mm)を成形、後硬化後、85℃/85%
RHの環境下で168時間放置し、その後260℃の半
田槽に10秒間浸漬した。顕微鏡でパッケージを観察
し、外部クラック数(クラック発生パッケージ数/全パ
ッケージ数)をクラック数と表現した。 耐湿信頼性 :80pQFPパッケージを成形、後
硬化後、85℃、85%RHの環境下で24時間放置
し、その後260℃の半田槽に10秒間浸漬した。次に
このパッケージに125℃、2.3気圧のPCT処理を
行い、不良率が50%となる迄のPCT処理時間を耐湿
信頼性として表現した。これらの評価結果を表1に示す
Using this material, each item of spiral flow, gelation time, Shore hardness D, cure shrinkage, glass transition temperature, water absorption, bending strength, bending elastic modulus, flame retardancy was measured. Further, the number of cracks and the moisture resistance reliability were evaluated. All samples were molded by transfer molding at a mold temperature of 175 ° C. and curing for 120 seconds. Post cure is 1
It was carried out at 75 ° C for 8 hours. Spiral flow: Using a mold with a spiral inside, transfer molding 175 ° C, effective pressure 70 kgf
The length that the resin has flowed in the mold when cured for about 120 seconds at / cm 2 . Gelation time: 2 g of molding material on a hot plate at 175 ° C
Time to put on, spread with a spatula to a size of about 25 mm square and rub on the hot plate, then the resin cures and peels off from the hot plate. Shore D hardness: Measured value of hardness measured by a Shore D hardness meter after transfer molding at 175 ° C., curing for 120 seconds, and mold opening for 10 seconds. Curing shrinkage ratio: According to JIS K 6911. Glass transition temperature: Measured by TMA method. Water absorption rate: According to JIS K 6911. Bending strength: According to JIS K 6911. Flexural modulus: According to JIS K 6911. Flame retardance: UL94 vertical method. Uses a 1.0 mm thick test piece. Number of solder cracks: 80 pQFP package (package size 14 × 20 mm, thickness 1.5 mm, chip size 9 × 9 mm) is molded and post-cured, 85 ° C./85%
It was left for 168 hours in the environment of RH and then immersed in a solder bath at 260 ° C. for 10 seconds. The packages were observed with a microscope, and the number of external cracks (the number of cracked packages / the total number of packages) was expressed as the number of cracks. Moisture resistance reliability: 80 pQFP package was molded, post-cured, left for 24 hours in an environment of 85 ° C. and 85% RH, and then immersed in a solder bath at 260 ° C. for 10 seconds. Next, this package was subjected to PCT treatment at 125 ° C. and 2.3 atm, and the PCT treatment time until the defect rate became 50% was expressed as moisture resistance reliability. The evaluation results are shown in Table 1.

【0013】実施例2〜6 表1の配合に従い、実施例1と同様にして封止材料を得
た。実施例6のレゾール樹脂は式(1)で示されるレゾ
ール樹脂で、但し、平均構造は、l=0.8、m=4.
5、n=2.1、p=1.8である。これを以下レゾー
ル樹脂2という。評価結果を表1に示す。 比較例1〜5 表2の配合に従い、実施例1と同様にして封止材料を得
た。比較例5のレゾール樹脂は式(1)で示されるレゾ
ール樹脂で、但し、平均構造は、l=1.2、m=1
3.1、n=2.2、p=12.8である。これを以下
レゾール樹脂3という。評価結果を表2に示す。
Examples 2 to 6 According to the formulations shown in Table 1, sealing materials were obtained in the same manner as in Example 1. The resole resin of Example 6 is the resole resin represented by the formula (1), provided that the average structure is l = 0.8, m = 4.
5, n = 2.1 and p = 1.8. Hereinafter, this is referred to as resole resin 2. The evaluation results are shown in Table 1. Comparative Examples 1 to 5 According to the formulations in Table 2, the encapsulating material was obtained in the same manner as in Example 1. The resole resin of Comparative Example 5 is the resole resin represented by the formula (1), provided that the average structure is l = 1.2 and m = 1.
3.1, n = 2.2 and p = 12.8. Hereinafter, this is referred to as a resol resin 3. The evaluation results are shown in Table 2.

【0014】比較例6 O−オルソクレゾールノボラック型エポキシ樹脂(軟化点65℃、エポキシ当 量195) 17.50重量部 フェノールノボラック樹脂硬化剤(軟化点85℃、水酸基当量104) 7.50重量部 1,8−ジアザビシクロウンデセン 0.20重量部 溶融シリカ粉末 73.50重量部 γーアミノプロピルトリエトキシシラン 0.50重量部 カルナバワック 0.50重量部 カーボンブラッ 0.30重量部 実施例1と同様に封止材料を得た。評価結果を表2に示
す。
Comparative Example 6 O-Orthocresol novolac type epoxy resin (softening point 65 ° C., epoxy equivalent 195) 17.50 parts by weight Phenol novolac resin curing agent (softening point 85 ° C., hydroxyl equivalent 104) 7.50 parts by weight 1,8-diazabicycloundecene 0.20 parts by weight fused silica powder 73.50 parts by weight γ-aminopropyltriethoxysilane 0.50 parts by weight Carnaubawak 0.50 parts by weight Carbon black 0.30 parts by weight Examples A sealing material was obtained in the same manner as in 1. The evaluation results are shown in Table 2.

【0015】[0015]

【表1】 [Table 1]

【0016】[0016]

【表2】 [Table 2]

【0017】[0017]

【発明の効果】本発明に従うと、優れた常温保管性を有
し、ブロム化エポキシやアンチモン等の難燃剤を含まな
いにも関わらず難燃性に優れ、良好な成形性、半田耐熱
性、耐湿信頼性を有する半導体封止用樹脂組成物を得る
ことができる。
EFFECTS OF THE INVENTION According to the present invention, it has excellent room temperature storage properties and is excellent in flame retardance despite not containing a flame retardant such as brominated epoxy or antimony, good moldability, solder heat resistance, A resin composition for semiconductor encapsulation having moisture resistance reliability can be obtained.

【手続補正書】[Procedure amendment]

【提出日】平成6年5月12日[Submission date] May 12, 1994

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0014[Correction target item name] 0014

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0014】比較例6 O−オルソクレゾールノボラック型エポキシ樹脂(軟化点65℃、エポキシ当 量195) 17.50重量部 フェノールノボラック樹脂硬化剤(軟化点85℃、水酸基当量104) 7.50重量部 1,8−ジアザビシクロウンデセン 0.20重量部 溶融シリカ粉末 73.50重量部 γーアミノプロピルトリエトキシシラン 0.50重量部 カルナバワックス 0.50重量部 カーボンブラック 0.30重量部 実施例1と同様に封止材料を得た。評価結果を表2に示
す。
Comparative Example 6 O-Orthocresol novolac type epoxy resin (softening point 65 ° C., epoxy equivalent 195) 17.50 parts by weight Phenol novolac resin curing agent (softening point 85 ° C., hydroxyl equivalent 104) 7.50 parts by weight 1,8-diazabicycloundecene 0.20 parts by weight fused silica powder 73.50 parts by weight γ-aminopropyltriethoxysilane 0.50 parts by weight carnauba wax 0.50 parts by weight carbon black 0.30 parts by weight Examples A sealing material was obtained in the same manner as in 1. The evaluation results are shown in Table 2.

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0016[Correction target item name] 0016

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0016】[0016]

【表2】 [Table 2]

───────────────────────────────────────────────────── 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 (2)

【特許請求の範囲】[Claims] 【請求項1】 式(1)のレゾール樹脂、フェノールノ
ボラック樹脂、硬化促進剤、無機質充填材を必須成分と
するレゾール樹脂組成物において、全樹脂組成物中のレ
ゾール樹脂とフェノールノボラック樹脂の合計量が15
〜35重量%であることを特徴とする半導体封止用樹脂
組成物。 【化1】 ( 但し、lは0または2以下の正数、m、pは0また
は10以下の正数、nは0または4以下の正数、かつm
+pは15以下の正数を表す。)
1. A resole resin composition comprising a resole resin of the formula (1), a phenol novolac resin, a curing accelerator, and an inorganic filler as essential components, wherein the total amount of the resole resin and the phenol novolac resin in all resin compositions. Is 15
A resin composition for semiconductor encapsulation, characterized in that [Chemical 1] (However, l is a positive number of 0 or 2 or less, m or p is a positive number of 0 or 10 or less, n is a positive number of 0 or 4 and m
+ P represents a positive number of 15 or less. )
【請求項2】 重量比で、レゾール樹脂/(レゾール樹
脂+フェノールノボラック樹脂)=0.5〜0.9であ
る請求項1記載の半導体封止用樹脂組成物。
2. The resin composition for semiconductor encapsulation according to claim 1, wherein a weight ratio of resol resin / (resole resin + phenol novolac resin) = 0.5 to 0.9.
JP32942093A 1993-12-27 1993-12-27 Resin composition for semiconductor sealing Pending JPH07188515A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32942093A JPH07188515A (en) 1993-12-27 1993-12-27 Resin composition for semiconductor sealing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32942093A JPH07188515A (en) 1993-12-27 1993-12-27 Resin composition for semiconductor sealing

Publications (1)

Publication Number Publication Date
JPH07188515A true JPH07188515A (en) 1995-07-25

Family

ID=18221200

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32942093A Pending JPH07188515A (en) 1993-12-27 1993-12-27 Resin composition for semiconductor sealing

Country Status (1)

Country Link
JP (1) JPH07188515A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001008833A1 (en) * 1999-07-31 2001-02-08 Bitrez Ltd Low temperature cure system
JP2005336254A (en) * 2004-05-25 2005-12-08 Hokuetsu Paper Mills Ltd Sheet-like nonflammable molded form
JP2007106814A (en) * 2005-10-12 2007-04-26 Hokuetsu Paper Mills Ltd Sheetlike noncombustible molding
JP2008184490A (en) * 2007-01-26 2008-08-14 Matsushita Electric Works Ltd Phenolic resin molding material and molded article

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001008833A1 (en) * 1999-07-31 2001-02-08 Bitrez Ltd Low temperature cure system
JP2005336254A (en) * 2004-05-25 2005-12-08 Hokuetsu Paper Mills Ltd Sheet-like nonflammable molded form
JP4602698B2 (en) * 2004-05-25 2010-12-22 北越紀州製紙株式会社 Sheet-type non-combustible molding for building materials
JP2007106814A (en) * 2005-10-12 2007-04-26 Hokuetsu Paper Mills Ltd Sheetlike noncombustible molding
JP2008184490A (en) * 2007-01-26 2008-08-14 Matsushita Electric Works Ltd Phenolic resin molding material and molded article

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