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JP2003292730A - Epoxy resin composition and semiconductor device - Google Patents

Epoxy resin composition and semiconductor device

Info

Publication number
JP2003292730A
JP2003292730A JP2002097547A JP2002097547A JP2003292730A JP 2003292730 A JP2003292730 A JP 2003292730A JP 2002097547 A JP2002097547 A JP 2002097547A JP 2002097547 A JP2002097547 A JP 2002097547A JP 2003292730 A JP2003292730 A JP 2003292730A
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
semiconductor device
compound
semiconductor
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
JP2002097547A
Other languages
Japanese (ja)
Inventor
Hidetoshi Seki
秀俊 関
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 JP2002097547A priority Critical patent/JP2003292730A/en
Publication of JP2003292730A publication Critical patent/JP2003292730A/en
Pending legal-status Critical Current

Links

Classifications

    • 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

Landscapes

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

Abstract

(57)【要約】 【課題】 ワイヤーボンディング時などに酸化されたリ
ードフレームに対しても吸水後の半田処理時の半導体装
置での剥離が少なく、クラックが少ない耐半田性に優れ
た特性を有する半導体封止用エポキシ樹脂組成物及び半
導体装置を提供すること。 【解決手段】 (A)エポキシ樹脂、(B)フェノール
樹脂、(C)硬化促進剤、(D)無機充填材及び(E)
還元作用を有する化合物を必須成分とすることを特徴と
する半導体封止用エポキシ樹脂組成物。
(57) [Problem] To be excellent in soldering resistance with little peeling in a semiconductor device during soldering after water absorption even with respect to a lead frame oxidized at the time of wire bonding and the like, with few cracks and excellent solder resistance. To provide an epoxy resin composition for semiconductor encapsulation and a semiconductor device. SOLUTION: (A) Epoxy resin, (B) phenolic resin, (C) curing accelerator, (D) inorganic filler and (E)
An epoxy resin composition for semiconductor encapsulation, comprising a compound having a reducing action as an essential component.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、成形性に優れた半
導体封止用エポキシ樹脂組成物及びこれを用いた半導体
装置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 having excellent moldability and a semiconductor device using the same.

【0002】[0002]

【従来の技術】IC、LSI等の半導体素子の封止方法
としてエポキシ樹脂組成物のトランスファー成形が低コ
スト、大量生産に適しており、採用されて久しく、信頼
性の点でもエポキシ樹脂や硬化剤であるフェノール樹脂
の改良により特性の向上が図られてきた。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にお
いて、半導体素子の高集積化も年々進み、また、半導体
装置の表面実装化が促進されるなかで、半導体封止用エ
ポキシ樹脂組成物への要求は益々厳しいものとなってき
ている。このため、従来からのエポキシ樹脂組成物では
解決できない問題点も出てきている。その最大の問題点
は、表面実装の採用により半導体装置が半田浸漬或いは
半田リフロー工程で急激に200℃以上の高温にさらさ
れ、吸水した水分が爆発的に気化する際の応力によっ
て、半導体素子、リードフレーム、インナーリード上の
各種メッキされた各接合部分とエポキシ樹脂組成物の硬
化物の界面で剥離が生じたり、半導体装置にクラックが
発生し、信頼性が著しく低下する現象である。
2. Description of the Related Art Transfer molding of an epoxy resin composition is suitable for encapsulating semiconductor elements such as ICs and LSIs at low cost and is suitable for mass production. It has been adopted for a long time, and the epoxy resin and curing agent are also reliable. The properties have been improved by improving the phenol resin. However, in recent market trends of miniaturization, weight reduction, and high performance of electronic equipment, semiconductor elements are becoming highly integrated year by year, and the surface mounting of semiconductor devices is being promoted. The demand for epoxy resin compositions is becoming more and more severe. Therefore, there are some problems that cannot be solved by conventional epoxy resin compositions. The biggest problem is that the semiconductor device is rapidly exposed to a high temperature of 200 ° C. or higher in the solder dipping or solder reflow process due to the use of the surface mounting, and the stress caused when the absorbed water explosively vaporizes the semiconductor element, This is a phenomenon in which peeling occurs at the interface between various plated joints on the lead frame or inner lead and the cured product of the epoxy resin composition, or cracks occur in the semiconductor device, resulting in a marked decrease in reliability.

【0003】半田処理による信頼性低下を改善するため
に、エポキシ樹脂組成物中の無機充填材の充填量を増加
させることで低吸水化、高強度化、低熱膨張化を達成し
耐半田性を向上させるとともに、低溶融粘度の樹脂成分
を使用して、成形時に低粘度で高流動性を維持させる手
法が一般的となりつつある。一方、半田処理時の信頼性
において、エポキシ樹脂組成物の硬化物と半導体装置内
部に存在する半導体素子やリードフレーム等の部材との
界面の接着性は非常に重要になってきている。この界面
の接着力が弱いと、半田処理後に部材との界面で剥離が
生じ、更にはこの剥離に起因し半導体装置にクラックが
発生すが、リードフレームとエポキシ樹脂組成物の硬化
物との界面の接着力の低下の一つの要因としてワイヤー
ボンディング時などにおけるリードフレームの酸化が上
げられる。
In order to improve the reliability deterioration due to the soldering treatment, the amount of the inorganic filler in the epoxy resin composition is increased to achieve low water absorption, high strength and low thermal expansion, thereby improving the solder resistance. It is becoming common to use a resin component having a low melt viscosity to improve the fluidity and maintain a low viscosity and a high fluidity during molding. On the other hand, in terms of reliability during soldering, the adhesiveness at the interface between a cured product of an epoxy resin composition and a member such as a semiconductor element or a lead frame existing inside a semiconductor device has become very important. If the adhesive strength at this interface is weak, peeling occurs at the interface with the member after soldering, and further cracking occurs in the semiconductor device due to this peeling, but at the interface between the lead frame and the cured product of the epoxy resin composition. Oxidation of the lead frame at the time of wire bonding is one of the causes of the decrease in the adhesive strength of the.

【0004】[0004]

【発明が解決しようとする課題】本発明は、ワイヤーボ
ンディング時などに酸化されたリードフレームに対して
も吸水後の半田処理時の半導体装置での剥離が少なく、
クラックが少ない耐半田性に優れた特性を有する半導体
封止用エポキシ樹脂組成物及び半導体装置を提供するも
のである。
DISCLOSURE OF THE INVENTION The present invention provides less peeling in a semiconductor device during a soldering process after absorbing water even for a lead frame that is oxidized during wire bonding.
The present invention provides an epoxy resin composition for semiconductor encapsulation and a semiconductor device which have few cracks and excellent solder resistance.

【0005】[0005]

【課題を解決するための手段】本発明は、[1](A)
エポキシ樹脂、(B)フェノール樹脂、(C)硬化促進
剤、(D)無機充填材及び(E)還元作用を有する化合
物を必須成分と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](E)還元作用を有する化合物
が芳香族ヒドロキシ化合物であり、該化合物を一種類あ
るいは二種類以上併用して用いる第[1]項記載の半導
体封止用エポキシ樹脂組成物、[3]第[1]、及び
[2]項記載のエポキシ樹脂組成物を用いて半導体素子
を封止してなることを特徴とする半導体装置、である。
The present invention provides [1] (A)
An epoxy resin composition for semiconductor encapsulation, which comprises an epoxy resin, (B) a phenol resin, (C) a curing accelerator, (D) an inorganic filler and (E) a compound having a reducing action as essential components, [2] The epoxy resin composition for semiconductor encapsulation according to the item [1], wherein the compound (E) having a reducing action is an aromatic hydroxy compound and the compound is used alone or in combination of two or more. ] A semiconductor device comprising a semiconductor element encapsulated with the epoxy resin composition according to the items [1] and [2].

【0006】[0006]

【発明実施の形態】本発明で用いられるエポキシ樹脂
は、分子内にエポキシ基を有するモノマー、オリゴマ
ー、ポリマーであり、例えばビスフェノールA型エポキ
シ樹脂、フェノールノボラック型エポキシ樹脂、オルソ
クレゾールノボラック型エポキシ樹脂、ナフトールノボ
ラック型エポキシ樹脂、フェノールアラルキル型エポキ
シ樹脂、ジシクロペンタジエン変性フェノール型エポキ
シ樹脂、ビフェニル型エポキシ樹脂、スチルベン型エポ
キシ樹脂、トリフェノールメタン型エポキシ樹脂、アル
キル変性トリフェノールメタン型エポキシ樹脂、及びト
リアジン核含有エポキシ樹脂等が挙げられ、これらは単
独でも混合して用いてもよい。これらのエポキシ樹脂の
中では、一般式(1)で示されるエポキシ樹脂が、硬化
物の架橋点間距離が長くなるため半田リフロー温度での
弾性率が低い特長を有し、このため発生する応力が低く
密着性にも優れるため、耐半田リフロー性が良好であり
好ましい。
BEST MODE FOR CARRYING OUT THE INVENTION The epoxy resin used in the present invention is a monomer, oligomer or polymer having an epoxy group in the molecule, and examples thereof include bisphenol A type epoxy resin, phenol novolac type epoxy resin, orthocresol novolac type epoxy resin, Naphthol novolac type epoxy resin, phenol aralkyl type epoxy resin, dicyclopentadiene modified phenol type epoxy resin, biphenyl type epoxy resin, stilbene type epoxy resin, triphenolmethane type epoxy resin, alkyl modified triphenolmethane type epoxy resin, and triazine nucleus Examples thereof include epoxy resins, and these may be used alone or in combination. Among these epoxy resins, the epoxy resin represented by the general formula (1) has a feature that the elastic modulus at the solder reflow temperature is low because the distance between the cross-linking points of the cured product becomes long, and the stress generated by this Is low and the adhesion is excellent, so that the solder reflow resistance is good, which is preferable.

【化1】 (pは平均値で1〜5の整数)[Chemical 1] (P is an average value and is an integer of 1 to 5)

【0007】本発明で用いられるフェノール樹脂は、分
子内にフェノール性水酸基を有するモノマー、オリゴマ
ー、ポリマーであり、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、フェノールアラルキル
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、トリフェ
ノールメタン等が挙げられ、これらは単独でも混合して
用いてもよい。これらのフェノール樹脂の中では、一般
式(2)で示されるエポキシ樹脂が、硬化物の架橋点間
距離が長くなるため半田リフロー温度での弾性率が低い
特長を有し、このため発生する応力が低く密着性にも優
れるため、耐半田リフロー性が良好であり好ましい。
The phenol resin used in the present invention is a monomer, oligomer or polymer having a phenolic hydroxyl group in the molecule, and examples thereof include phenol novolac resin, cresol novolac resin, phenol aralkyl resin, terpene modified phenol resin and dicyclopentadiene modified resin. Phenol resin, bisphenol A, triphenol methane and the like can be mentioned, and these may be used alone or in combination. Among these phenolic resins, the epoxy resin represented by the general formula (2) has a characteristic that the elastic modulus at the solder reflow temperature is low because the distance between the cross-linking points of the cured product becomes long, and the stress generated by this Is low and the adhesion is excellent, so that the solder reflow resistance is good, which is preferable.

【化2】 (pは平均値で1〜5の整数)[Chemical 2] (P is an average value and is an integer of 1 to 5)

【0008】本発明に用いられる硬化促進剤としては、
エポキシ基とフェノール性水酸基との硬化反応を促進さ
せるものであればよく、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(5,4,0)ウンデセン−7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、トリフェニルホスフィン等の有機リン系化合物等
が挙げられ、これらは単独でも混合して用いてもよい。
As the curing accelerator used in the present invention,
Any material that accelerates the curing reaction between the epoxy group and the phenolic hydroxyl group may be used, and those generally used for sealing materials may be widely used. Examples thereof include amine compounds such as 1,8-diazabicyclo (5,4,0) undecene-7, imidazole compounds such as 2-methylimidazole, and organic phosphorus compounds such as triphenylphosphine. These may be used alone or as a mixture. You may use it.

【0009】本発明に用いられる無機充填材の種類につ
いては特に限定されないが、一般に封止材料に用いられ
ているものを使用することができる。例えば溶融破砕シ
リカ、溶融球状シリカ、結晶シリカ、2次凝集シリカ、
アルミナ、チタンホワイト、水酸化アルミニウム等が挙
げられ、特に溶融球状シリカが好ましい。形状は限りな
く真球状であることが好ましく、また粒子の大きさの異
なるものを混合することにより充填量を多くすることが
できる。無機充填材の配合量としては、全エポキシ樹脂
組成物中に65〜94重量%が好ましく、より好ましく
は75〜92重量%である。下限値を下回ると、無機充
填材による補強効果が十分に発現せず、かつ吸水要因で
ある樹脂成分の配合量が多くなるので、エポキシ樹脂組
成物の硬化物の吸水量が増大してしまうため、半田処理
時に半導体装置にクラックが発生しやすくなるおそれが
ある。上限値を越えるとエポキシ樹脂組成物の流動性が
低下し、成形時に充填不良やチップシフト、パッドシフ
ト、ワイヤースイープが発生しやすくなるおそれがあ
る。
The kind of the inorganic filler used in the present invention is not particularly limited, but those generally used for the sealing material can be used. For example, fused crushed silica, fused spherical silica, crystalline silica, secondary agglomerated silica,
Alumina, titanium white, aluminum hydroxide and the like can be mentioned, and fused spherical silica is particularly preferable. It is preferable that the shape is infinitely spherical, and the filling amount can be increased by mixing particles having different particle sizes. The content of the inorganic filler in the total epoxy resin composition is preferably 65 to 94% by weight, more preferably 75 to 92% by weight. If it is less than the lower limit, the reinforcing effect by the inorganic filler is not sufficiently expressed, and the amount of the resin component that is a water absorption factor increases, so that the water absorption of the cured product of the epoxy resin composition increases. However, cracks may easily occur in the semiconductor device during soldering. If the upper limit is exceeded, the fluidity of the epoxy resin composition will decrease, and filling defects, chip shifts, pad shifts, and wire sweeps may occur during molding.

【0010】本発明に用いる還元作用を有する化合物
は、ヒドロキシベンゼン、ヒドロキノン、カテコール、
ピロガロール、ヒドロキシヒドロキノン、o−アミノフ
ェノール等の芳香族ヒドロキシ化合物であり、該化合物
を一種類あるいは二種類以上併用して用いることが好ま
しい。これらの還元剤はリードフレーム等の金属の表面
の酸化物を還元することができるため、これらの還元剤
をエポキシ樹脂組成物に添加することでリードフレーム
とエポキシ樹脂組成物間の接着強度を向上させることが
できる。還元作用を有する化合物の配合量としては、全
エポキシ樹脂組成物中に0.005〜3重量%が好まし
く、0.01〜1重量%がより好ましい。下限値を下回
ると添加効果が薄いので好ましくない。また、上限値を
超えると未反応の還元作用を有する化合物が界面に残り
密着を疎外するので好ましくない。また、これらの還元
作用を有する化合物は予めエポキシ樹脂やフェノール樹
脂の全部又は一部に加熱混合しても良い。
The compound having a reducing action used in the present invention is hydroxybenzene, hydroquinone, catechol,
It is an aromatic hydroxy compound such as pyrogallol, hydroxyhydroquinone and o-aminophenol, and it is preferable to use one kind or a combination of two or more kinds of these compounds. Since these reducing agents can reduce the oxide on the surface of the metal such as the lead frame, the addition of these reducing agents to the epoxy resin composition improves the adhesive strength between the lead frame and the epoxy resin composition. Can be made. The compounding amount of the compound having a reducing action is preferably 0.005 to 3% by weight, and more preferably 0.01 to 1% by weight in the total epoxy resin composition. If it is less than the lower limit, the effect of addition is weak, which is not preferable. On the other hand, if the amount exceeds the upper limit, unreacted compound having a reducing action remains at the interface and alienates the adhesion, which is not preferable. Further, these compounds having a reducing action may be preliminarily heated and mixed with all or part of the epoxy resin or the phenol resin.

【0011】本発明のエポキシ樹脂組成物は、(A)〜
(D)成分の他、必要に応じて臭素化エポキシ樹脂、酸
化アンチモン、リン化合物、水酸化マグネシウム、水酸
化アルミニウム、硼酸化合物等の難燃剤類、酸化ビスマ
ス水和物等の無機イオン交換体、γ−グリシドキシプロ
ピルトリメトキシシランやγ−アミノプロピルトリエト
キシシラン等のカップリング剤、カーボンブラック、ベ
ンガラ等の着色剤、シリコーンオイル、シリコーンゴム
等の低応力化成分、天然ワックス、合成ワックス、高級
脂肪酸及びその金属塩類もしくはパラフィン等の離型剤
等の各種添加剤を配合することもできる。
The epoxy resin composition of the present invention comprises (A)-
In addition to the component (D), if necessary, brominated epoxy resin, antimony oxide, phosphorus compound, flame retardants such as magnesium hydroxide, aluminum hydroxide and boric acid compound, inorganic ion exchanger such as bismuth oxide hydrate, Coupling agents such as γ-glycidoxypropyltrimethoxysilane and γ-aminopropyltriethoxysilane, colorants such as carbon black and red iron oxide, low stress components such as silicone oil and silicone rubber, natural wax, synthetic wax, Various additives such as a higher fatty acid and a metal salt thereof or a release agent such as paraffin may be blended.

【0012】本発明のエポキシ樹脂組成物は、(A)〜
(D)成分及びその他の添加剤等をミキサー等を用いて
常温混合し、ロール、ニーダー、押し出し機等の混錬機
で溶融混錬し、冷却後粉砕する一般的な方法で得られ
る。本発明のエポキシ樹脂組成物を用いて、半導体素子
等の電子部品を封止し、半導体装置を製造するには、ト
ランスファーモールド、コンプレッションモールド、イ
ンジェクションモールド等の成形方法で成形硬化すれば
よい。
The epoxy resin composition of the present invention comprises (A)-
It can be obtained by a general method in which the component (D) and other additives are mixed at room temperature using a mixer or the like, melt-kneaded with a kneader such as a roll, kneader, or extruder, cooled, and then pulverized. In order to manufacture a semiconductor device by sealing an electronic component such as a semiconductor element using the epoxy resin composition of the present invention, molding and curing may be performed by a molding method such as a transfer mold, a compression mold or an injection mold.

【0013】[0013]

【実施例】以下、本発明を実施例で具体的に説明する。 実施例1 式(3)を主成分とするエポキシ樹脂(ジャパンエポキシレジン(株)製、Y X−4000、エポキシ当量195、融点105℃) 6.2重量部EXAMPLES The present invention will be specifically described below with reference to examples.   Example 1   Epoxy resin containing formula (3) as a main component (manufactured by Japan Epoxy Resin Co., Ltd., Y X-4000, epoxy equivalent 195, melting point 105 ° C)                                                             6.2 parts by weight

【化3】 [Chemical 3]

【0014】 式(4)のフェノール樹脂(三井化学(株)製、XLC−LL、水酸基当量1 74、軟化点75℃) 5.7重量部[0014]   Formula (4) phenol resin (Mitsui Chemicals, Inc., XLC-LL, hydroxyl equivalent 1 74, softening point 75 ° C) 5.7 parts by weight

【化4】 [Chemical 4]

【0015】 ヒドロキシベンゼン 0.1重量部 γ−グリシジルプロピルトリメトキシシラン 0.3重量部 溶融球状シリカ(平均粒径30μm) 87.0重量部 1,8−ジアザビシクロ(5,4,0)ウンデセン−7(以下、DBUという ) 0.2重量部 カーボンブラック 0.2重量部 カルナバワックス 0.3重量部 上記の全成分をミキサーを用いて混合した後、表面温度
が90℃と45℃の2本ロールを用いて混練し、冷却後
粉砕してエポキシ樹脂組成物を得た。得られたエポキシ
樹脂組成物を以下の方法で評価した。
Hydroxybenzene 0.1 part by weight γ-glycidylpropyltrimethoxysilane 0.3 part by weight Fused spherical silica (average particle size 30 μm) 87.0 parts by weight 1,8-diazabicyclo (5,4,0) undecene- 7 (hereinafter referred to as DBU) 0.2 parts by weight carbon black 0.2 parts by weight carnauba wax 0.3 parts by weight After mixing all of the above components using a mixer, two surface temperatures of 90 ° C. and 45 ° C. The mixture was kneaded using a roll, cooled, and then pulverized to obtain an epoxy resin composition. The obtained epoxy resin composition was evaluated by the following methods.

【0016】評価方法 スパイラルフロー:EMMI−1−66に準じたスパイ
ラルフロー測定用金型を用いて、金型温度175℃、注
入圧力6.9MPa、硬化時間120秒で測定した。 熱時強度:低圧トランスファー成形機を用いて、金型温
度175℃、注入圧力9.8MPa、硬化時間120秒
で、試験片(長さ80mm、幅10mm、厚さ4mm)
を成形し、175℃、8時間で後硬化させたのち、26
0℃での曲げ強さをJIS K 6911に準じて測定
した。単位はN/mm2。 密着性:低圧トランスファー成形機を用いて、金型温度
175℃、注入圧力9.8MPa、硬化時間120秒
で、エポキシ樹脂組成物を、厚さは150μの被着体上
に成形物(2×2×2mm)が密着するように一体成形
し、図1に示すように矢印の方向へ力を加えて、せん断
強度を測定した。測定温度は260℃、単位はMPa。
被着体は銅素材に銅のフラッシュメッキを施したもの、
更にこの銅フラッシュメッキを施したものを260℃の
熱板上で20秒加熱しワイヤーボンディング後と同程度
の酸化状態にしたもの及び銅素材に銅のフラッシュメッ
キを施した上に更に銀メッキを施したものの3種類を用
いた。 耐半田性:低圧トランスファー成形機を用いて、金型温
度175℃、注入圧力8.3MPa、硬化時間120秒
で、160ピンLQFP(パッケージサイズは24×2
4mm、厚み1.4mm、シリコンチップサイズは7.
0×7.0mm、リードフレームは銅素材に銅のフラッ
シュメッキを施したものと銅素材に銅のフラッシュメッ
キを施したものを260℃の熱板上で20秒加熱しワイ
ヤーボンディング後と同程度の酸化状態にしたものの二
種類)を成形し、175℃、8時間で後硬化させた。得
られたパッケージ10ケを85℃、相対湿度60%の環
境下で168時間加湿処理したもの及び85℃、相対湿
度85%の環境下、72時間加湿処理したものをそれぞ
れ、260℃の半田槽に10秒間浸漬した。顕微鏡で外
部クラックを観察し、クラック発生率[(クラック発生
率)=(クラック発生パッケージ数)/(全パッケージ
数)×100]を%で表示した。また、チップとエポキ
シ樹脂組成物の硬化物との剥離面積の割合を超音波探傷
装置を用いて測定し、剥離率[(剥離率)=(剥離面
積)/(チップ面積)×100]を%で表示した。
Evaluation method Spiral flow: A spiral flow measuring mold according to EMMI-1-66 was used, and the mold temperature was 175 ° C., the injection pressure was 6.9 MPa, and the curing time was 120 seconds. Heat strength: Using a low pressure transfer molding machine, a mold temperature of 175 ° C., an injection pressure of 9.8 MPa, a curing time of 120 seconds, and a test piece (length 80 mm, width 10 mm, thickness 4 mm).
And after post-curing at 175 ° C. for 8 hours, 26
The bending strength at 0 ° C was measured according to JIS K 6911. The unit is N / mm 2 . Adhesion: Using a low-pressure transfer molding machine, a mold temperature of 175 ° C., an injection pressure of 9.8 MPa, a curing time of 120 seconds, an epoxy resin composition, and a molded article (2 × (2 × 2 mm) was integrally molded so as to be in close contact, and a force was applied in the direction of the arrow as shown in FIG. 1 to measure the shear strength. The measurement temperature is 260 ° C, and the unit is MPa.
The adherend is a copper material plated with copper flash,
Furthermore, this copper flash-plated product was heated on a hot plate at 260 ° C for 20 seconds to be in the same oxidation state as that after wire bonding, and the copper material was flash-plated with copper and then silver-plated. Three types of the applied ones were used. Solder resistance: Using a low-pressure transfer molding machine, mold temperature 175 ° C., injection pressure 8.3 MPa, curing time 120 seconds, 160-pin LQFP (package size 24 × 2
4 mm, thickness 1.4 mm, silicon chip size is 7.
0x7.0mm, the lead frame is the same as that after wire bonding after heating the copper material with copper flash plating and the copper material with copper flash plating on a hot plate at 260 ° C for 20 seconds. (2 types of those in the oxidized state) were molded and post-cured at 175 ° C. for 8 hours. The resulting 10 packages were humidified in an environment of 85 ° C. and 60% relative humidity for 168 hours, and in a environment of 85 ° C. and 85% relative humidity for 72 hours in a solder bath at 260 ° C. It was soaked for 10 seconds. External cracks were observed with a microscope, and the crack occurrence rate [(crack occurrence rate) = (number of cracked packages) / (total number of packages) × 100] was expressed in%. Further, the ratio of the peeled area between the chip and the cured product of the epoxy resin composition was measured using an ultrasonic flaw detector, and the peeled rate [(peeled rate) = (peeled area) / (chip area) × 100] was calculated as%. Displayed in.

【0017】実施例2〜12、比較例1〜6 表1、表2の配合に従い、実施例1と同様にしてエポキ
シ樹脂組成物を得て、実施例1と同様にして評価した。
結果を表1、表2に示す。なお、実施例1で用いた以外
の成分について以下に示す。
Examples 2 to 12 and Comparative Examples 1 to 6 According to the formulations shown in Tables 1 and 2, epoxy resin compositions were obtained in the same manner as in Example 1 and evaluated in the same manner as in Example 1.
The results are shown in Tables 1 and 2. The components other than those used in Example 1 are shown below.

【0018】式(1)のエポキシ樹脂(エポキシ当量2
72、軟化点58℃)
An epoxy resin of the formula (1) (epoxy equivalent 2
72, softening point 58 ° C)

【化5】 [Chemical 5]

【0019】オルソクレゾールノボラック型エポキシ樹
脂(エポキシ当量196、軟化点55℃)
Orthocresol novolac type epoxy resin (epoxy equivalent 196, softening point 55 ° C.)

【0020】式(2)のフェノール樹脂(水酸基当量2
00、軟化点65℃)、
Phenolic resin of formula (2) (hydroxyl equivalent 2
00, softening point 65 ° C),

【化6】 [Chemical 6]

【0021】フェノールノボラック樹脂(水酸基当量1
05、軟化点105℃) ヒドロキノン カテコール 溶融混合物A:式(2)のフェノールアラルキル樹脂
5.7重量部を110℃で完全に溶融させた後、還元作
用を有する化合物であるヒドロキシベンゼンを0.1重
量部加えて溶融混合物Aを得た。トリフェニルホスフィ
Phenol novolac resin (hydroxyl equivalent 1
05, softening point 105 ° C.) Hydroquinone catechol molten mixture A: 5.7 parts by weight of the phenol aralkyl resin of the formula (2) was completely melted at 110 ° C., and then hydroxybenzene, a compound having a reducing action, was added to 0.1 wt. A part by weight was added to obtain a molten mixture A. Triphenylphosphine

【0022】[0022]

【表1】 [Table 1]

【0023】[0023]

【表2】 [Table 2]

【0024】[0024]

【発明の効果】本発明のエポキシ樹脂組成物は、ワイヤ
ーボンディング時などに酸化されたリードフレームに対
しても吸水後の半田処理時の半導体装置での剥離が少な
く、クラックが少ない耐半田性に優れた特性を有し、こ
れを用いた半導体装置の信頼性向上に寄与する。
EFFECT OF THE INVENTION The epoxy resin composition of the present invention has less soldering resistance even in a lead frame that is oxidized during wire bonding, and is less likely to peel off in a semiconductor device during soldering treatment after absorbing water and has less cracks. It has excellent characteristics and contributes to improving the reliability of a semiconductor device using the same.

【図面の簡単な説明】[Brief description of drawings]

【図1】 被着体とエポキシ樹脂組成物を一体成形した
せん断強度測定用成形品の断面図。
FIG. 1 is a cross-sectional view of a shear strength measurement molded product in which an adherend and an epoxy resin composition are integrally molded.

【符号の説明】[Explanation of symbols]

1 成形品 2 被着体 1 molded product 2 Adherend

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) H01L 23/31 Fターム(参考) 4J002 CC04X CC05X CC07X CC12X CD04W CD05W CD06W CD13W CD20W DE137 DE147 DJ017 EJ028 EJ038 EU116 EU206 EW136 FD017 FD156 FD208 GQ05 4J036 AA01 AC02 AC18 AD07 AF06 AF27 AJ07 DB05 DC46 DD07 FA05 FA06 FB07 JA07 4M109 AA01 CA21 EA02 EB18 EC05─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 7 Identification code FI theme code (reference) H01L 23/31 F term (reference) 4J002 CC04X CC05X CC07X CC12X CD04W CD05W CD06W CD13W CD20W DE137 DE147 DJ017 EJ028 EJ038 EU116 EU206 EW136 FD017 FD156 FD208 GQ05 4J036 AA01 AC02 AC18 AD07 AF06 AF27 AJ07 DB05 DC46 DD07 FA05 FA06 FB07 JA07 4M109 AA01 CA21 EA02 EB18 EC05

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 (A)エポキシ樹脂、(B)フェノール
樹脂、(C)硬化促進剤、(D)無機充填材及び(E)
還元作用を有する化合物を必須成分とすることを特徴と
する半導体封止用エポキシ樹脂組成物。
1. (A) Epoxy resin, (B) Phenolic resin, (C) Curing accelerator, (D) Inorganic filler and (E)
An epoxy resin composition for semiconductor encapsulation, which comprises a compound having a reducing action as an essential component.
【請求項2】 (E)還元作用を有する化合物が芳香族
ヒドロキシ化合物であり、該化合物を一種類あるいは二
種類以上併用して用いる請求項1記載の半導体封止用エ
ポキシ樹脂組成物。
2. The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein the compound (E) having a reducing action is an aromatic hydroxy compound, and the compound is used alone or in combination of two or more kinds.
【請求項3】 請求項1、及び2記載のエポキシ樹脂組
成物を用いて半導体素子を封止してなることを特徴とす
る半導体装置。
3. A semiconductor device obtained by encapsulating a semiconductor element with the epoxy resin composition according to claim 1.
JP2002097547A 2002-03-29 2002-03-29 Epoxy resin composition and semiconductor device Pending JP2003292730A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002097547A JP2003292730A (en) 2002-03-29 2002-03-29 Epoxy resin composition and semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002097547A JP2003292730A (en) 2002-03-29 2002-03-29 Epoxy resin composition and semiconductor device

Publications (1)

Publication Number Publication Date
JP2003292730A true JP2003292730A (en) 2003-10-15

Family

ID=29240009

Family Applications (1)

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Country Status (1)

Country Link
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004081078A1 (en) * 2003-03-11 2004-09-23 Sumitomo Bakelite Co. Ltd. Resin composition for sealing semiconductor and semiconductor device using the same
WO2004085511A1 (en) * 2003-03-25 2004-10-07 Sumitomo Bakelite Co., Ltd. Resin composition for sealing semiconductor and semiconductor device using the same
JP2005075869A (en) * 2003-08-29 2005-03-24 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
JP2005089486A (en) * 2003-09-11 2005-04-07 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
JP2005206725A (en) * 2004-01-23 2005-08-04 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
US7291684B2 (en) 2003-03-11 2007-11-06 Sumitomo Bakelite Co., Ltd. Resin composition for encapsulating semiconductor chip and semiconductor device therewith

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004081078A1 (en) * 2003-03-11 2004-09-23 Sumitomo Bakelite Co. Ltd. Resin composition for sealing semiconductor and semiconductor device using the same
US7023098B2 (en) 2003-03-11 2006-04-04 Sumitomo Bakelite Company Resin composition for encapsulating semiconductor chip and semiconductor device therewith
US7291684B2 (en) 2003-03-11 2007-11-06 Sumitomo Bakelite Co., Ltd. Resin composition for encapsulating semiconductor chip and semiconductor device therewith
WO2004085511A1 (en) * 2003-03-25 2004-10-07 Sumitomo Bakelite Co., Ltd. Resin composition for sealing semiconductor and semiconductor device using the same
JP2005075869A (en) * 2003-08-29 2005-03-24 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
JP2005089486A (en) * 2003-09-11 2005-04-07 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
JP2005206725A (en) * 2004-01-23 2005-08-04 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device

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