JP2000273285A - Epoxy resin composition and semiconductor device - Google Patents

Epoxy resin composition and semiconductor device

Info

Publication number
JP2000273285A
JP2000273285A JP11079545A JP7954599A JP2000273285A JP 2000273285 A JP2000273285 A JP 2000273285A JP 11079545 A JP11079545 A JP 11079545A JP 7954599 A JP7954599 A JP 7954599A JP 2000273285 A JP2000273285 A JP 2000273285A
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
semiconductor device
semiconductor
silane coupling
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
JP11079545A
Other languages
Japanese (ja)
Inventor
Takashi Yagisawa
隆 八木澤
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 JP11079545A priority Critical patent/JP2000273285A/en
Publication of JP2000273285A publication Critical patent/JP2000273285A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/44Structure, shape, material or disposition of the wire connectors prior to the connecting process
    • H01L2224/45Structure, shape, material or disposition of the wire connectors prior to the connecting process of an individual wire connector
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/44Structure, shape, material or disposition of the wire connectors prior to the connecting process
    • H01L2224/45Structure, shape, material or disposition of the wire connectors prior to the connecting process of an individual wire connector
    • H01L2224/45001Core members of the connector
    • H01L2224/4501Shape
    • H01L2224/45012Cross-sectional shape
    • H01L2224/45015Cross-sectional shape being circular
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/44Structure, shape, material or disposition of the wire connectors prior to the connecting process
    • H01L2224/45Structure, shape, material or disposition of the wire connectors prior to the connecting process of an individual wire connector
    • H01L2224/45001Core members of the connector
    • H01L2224/45099Material
    • H01L2224/451Material with a principal constituent of the material being a metal or a metalloid, e.g. boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), tellurium (Te) and polonium (Po), and alloys thereof
    • H01L2224/45138Material with a principal constituent of the material being a metal or a metalloid, e.g. boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), tellurium (Te) and polonium (Po), and alloys thereof the principal constituent melting at a temperature of greater than or equal to 950°C and less than 1550°C
    • H01L2224/45144Gold (Au) as principal constituent

Abstract

PROBLEM TO BE SOLVED: To obtain an epoxy resin composition for semiconductor sealing use excellent in releasability, flowability, soldering resistance, and reliability. SOLUTION: This composition essentially comprises an epoxy resin, a phenolic resin curing agent, a curing promoter, an inorganic filler, an amino group- bearing silane coupling agent, and oxidized paraffin 5-80 in acid value.

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、吸湿後の
耐半田性等の信頼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 which is excellent in moldability, soldering resistance after moisture absorption, and the like, and a semiconductor device using the same.

【0002】[0002]

【従来の技術】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、半導体の高集積化が年々進
み、又半導体装置の表面実装化が促進されるなかで、半
導体封止材料への要求は益々厳しいものとなってきてい
る。特に半導体装置の表面実装化が一般的になってきて
いる現状では、吸湿した半導体装置が半田処理時に高温
にさらされ、気化した水蒸気の爆発的応力によりパッケ
ージにクラックが発生したり、あるいは半導体素子やリ
ードフレームと半導体封止材料との界面に剥離が発生す
ることにより、電気的信頼性を大きく損なう不良が生
じ、これらの不良の防止、即ち耐半田特性の向上が大き
な課題となっている。この耐半田特性の向上のために、
半導体封止材料は無機質充填材を多量に配合することに
より、半導体装置の低吸湿化、低熱膨張化、高強度化を
図ってきている。このため、エポキシ樹脂としては低粘
度型のものや、常温では結晶性であるが融点を越えると
極めて低粘性を示す結晶性エポキシ樹脂を使用して、無
機質充填材の配合量の増加に伴うエポキシ樹脂組成物の
成形時の流動性の低下を防止する手法が一般的にとられ
ている。
2. Description of the Related Art In recent years, in the market trend of miniaturization, weight reduction and high performance of electronic equipment, semiconductor integration is progressing year by year, and surface mounting of semiconductor devices is promoted. Demands on materials are becoming more and more severe. In particular, in the current situation where surface mounting of semiconductor devices is becoming common, a semiconductor device that has absorbed moisture is exposed to high temperatures during soldering, and cracks occur in the package due to the explosive stress of vaporized water vapor, or semiconductor devices may be damaged. And the occurrence of peeling at the interface between the lead frame and the semiconductor encapsulating material causes defects that greatly impair electrical reliability. Prevention of these defects, that is, improvement of solder resistance, has become a major issue. To improve the solder resistance,
The semiconductor encapsulating material has been trying to reduce the moisture absorption, lower the thermal expansion, and increase the strength of the semiconductor device by blending a large amount of an inorganic filler. For this reason, low-viscosity epoxy resins and crystalline epoxy resins that are crystalline at room temperature but exhibit extremely low viscosity above the melting point are used. A method for preventing a decrease in fluidity during molding of a resin composition is generally adopted.

【0003】ところが、低粘度エポキシ樹脂や結晶性エ
ポキシ樹脂は一般的に低分子量化合物であり、このため
成形時に加熱により3次元化して得られる架橋構造の架
橋密度が低いものである。従って、成形後に機械的強度
や弾性率が低い成形品となるため、金型からの離型時に
成形品が金型に付着したり、あるいは成形品の割れ・欠
けが発生するなど離型性に劣るという欠点を有する。離
型性を向上させるためには、離型剤を多量に配合するこ
とが対策として挙げられる、一方、多量の離型剤が成形
時に半導体装置内部に存在する半導体素子やそれを搭載
するリードフレームと樹脂組成物の硬化物との界面に移
行するため、これら界面の接着性を著しく損なう結果に
なる。このことにより、半導体装置を吸湿後半田処理す
るとこれら界面で剥離が発生したり、その剥離に起因す
るパッケージクラックが発生する不良が起こることにな
る。このため、成形時の離型性と耐半田特性に優れる樹
脂組成物の開発が望まれていた。
However, low-viscosity epoxy resins and crystalline epoxy resins are generally low-molecular-weight compounds, and therefore have a low cross-linking density in a cross-linked structure obtained by heating to three-dimensionality during molding. Therefore, since the molded product has low mechanical strength and elastic modulus after molding, the molded product adheres to the mold at the time of release from the mold, or the molded product has cracking or chipping. It has the disadvantage of being inferior. To improve the releasability, mixing a large amount of a release agent is mentioned as a countermeasure. On the other hand, a large amount of the release agent is present inside the semiconductor device at the time of molding, and a semiconductor element and a lead frame on which the semiconductor element is mounted. To the interface between the resin and the cured product of the resin composition, resulting in a significant loss of adhesion at these interfaces. As a result, when the semiconductor device is subjected to the soldering process after the moisture absorption, the interface may be peeled off, or the package may be cracked due to the peeling. For this reason, development of a resin composition having excellent releasability and solder resistance during molding has been desired.

【0004】[0004]

【発明が解決しようとする課題】本発明は、成形時の離
型性に優れると共に半導体装置の耐半田性に優れた半導
エポキシ樹脂組成物、及びこれを用いた半導体装置を提
供するものである。
SUMMARY OF THE INVENTION The present invention provides a semiconductor epoxy resin composition which is excellent in mold releasability at the time of molding and is excellent in solder resistance of a semiconductor device, and a semiconductor device using the same. is there.

【0005】[0005]

【課題を解決するための手段】本発明は、(A)エポキ
シ樹脂、(B)フェノール樹脂、(C)硬化促進剤、
(D)無機質充填材、(E)シランカップリング剤、特
に好ましくはアミノ基を有するシランカップリング剤
及び(F)酸価が5〜80の酸化パラフィンを必須成分
とする半導体封止用エポキシ樹脂組成物である。
The present invention provides (A) an epoxy resin, (B) a phenolic resin, (C) a curing accelerator,
(D) an inorganic filler, (E) a silane coupling agent, particularly preferably a silane coupling agent having an amino group
And (F) an epoxy resin composition for semiconductor encapsulation containing paraffin oxide having an acid value of 5 to 80 as an essential component.

【0006】[0006]

【発明の実施の形態】本発明に用いられるエポキシ樹脂
は、1分子中に2個以上のエポキシ基を有するモノマ
ー、オリゴマー、ポリマー全般を指し、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、トリフェノ
ールメタン型エポキシ樹脂、ジシクロペンタジエン変性
フェノール型エポキシ樹脂、フェノールアラルキル型エ
ポキシ樹脂、テルペ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、ハイドロキノン型エポキシ
樹脂、スチルベン型エポキシ樹脂、ビスフェノールF型
エポキシ樹脂等が挙げられるが、これらに限定されるも
のではない。又、これらのエポキシ樹脂は単独でも混合
して用いてもよい。半導体装置の耐半田特性を向上する
ことを目的に樹脂組成物中の無機質充填材の配合量を増
大させ、得られた樹脂組成物の硬化物の低吸湿化、低熱
膨張化、高強度化を達成させる場合には、エポキシ樹脂
として、常温で結晶性を示し、融点を越えると極めて低
粘度の液状となる結晶性エポキシ樹脂を用いることが特
に好ましい。
BEST MODE FOR CARRYING OUT THE INVENTION The epoxy resin used in the present invention refers to all monomers, oligomers and polymers having two or more epoxy groups in one molecule, such as bisphenol A type epoxy resin and phenol novolak type epoxy resin. , Ortho-cresol novolak type epoxy resin, naphthol novolak type epoxy resin, triphenol methane type epoxy resin, dicyclopentadiene modified phenol type epoxy resin, phenol aralkyl type epoxy resin, terpene modified phenol type epoxy resin,
Examples include, but are not limited to, biphenyl-type epoxy resins, hydroquinone-type epoxy resins, stilbene-type epoxy resins, and bisphenol-F-type epoxy resins. These epoxy resins may be used alone or as a mixture. In order to improve the solder resistance of the semiconductor device, the amount of the inorganic filler in the resin composition is increased to reduce the moisture absorption, lower the thermal expansion, and increase the strength of the cured product of the obtained resin composition. In order to achieve this, it is particularly preferable to use, as the epoxy resin, a crystalline epoxy resin which exhibits crystallinity at normal temperature and becomes a liquid having an extremely low viscosity when the melting point is exceeded.

【0007】本発明で用いられるフェノール樹脂として
は、1分子中に2個以上のフェノール性水酸基を有する
モノマー、オリゴマー、ポリマー全般を指し、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、ナ
フトールノボラック樹脂、トリフェノールメタン型樹
脂、ビスフェノール化合物等が挙げられるが、これらに
限定されるものではない。又、これらのフェノール樹脂
は単独でも混合して用いてもよい。
The phenolic resin used in the present invention refers to all monomers, oligomers and polymers having two or more phenolic hydroxyl groups in one molecule.
Phenol novolak resin, cresol novolak resin, phenol aralkyl resin, terpene-modified phenol resin, dicyclopentadiene-modified phenol resin, naphthol novolak resin, triphenolmethane-type resin, bisphenol compound, and the like, but are not limited thereto. . Further, these phenol resins may be used alone or in combination.

【0008】本発明で用いられる硬化促進剤としては、
前記エポキシ樹脂とフェノール樹脂との架橋反応の触媒
となり得るものを指し、具体例としては、トリブチルア
ミン、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、トリフェニルホスフィン、
テトラフェニルホスホニウム・テトラフェニルボレート
塩等の有機リン系化合物、2−メチルイミダゾール等の
イミダゾール化合物等が挙げられるが、これらに限定さ
れるものではない。又、これらの硬化促進剤は単独でも
混合して用いてもよい。
The curing accelerator used in the present invention includes:
A substance that can serve as a catalyst for a crosslinking reaction between the epoxy resin and the phenol resin. Specific examples include amine compounds such as tributylamine and 1,8-diazabicyclo (5,4,0) undecene-7, and triphenylphosphine. ,
Examples include organic phosphorus compounds such as tetraphenylphosphonium / tetraphenylborate salts, and imidazole compounds such as 2-methylimidazole, but are not limited thereto. These curing accelerators may be used alone or as a mixture.

【0009】本発明で用いられる無機質充填材として
は、例えば、溶融シリカ、結晶シリカ、アルミナ、窒化
珪素、窒化アルミ等が挙げられる。無機質充填材の配合
量を特に大きくする場合は、溶融シリカを用いるのが一
般的である。溶融シリカは、破砕状、球状のいずれでも
使用可能であるが、溶融シリカの配合量を高め、且つ成
形材料の溶融粘度の上昇を抑えるためには、球状のもの
を主に用いる方が好ましい。更に球状シリカの配合量を
高めるためには、球状シリカの粒度分布がより広くなる
ように調整することが望ましい。
The inorganic filler used in the present invention includes, for example, fused silica, crystalline silica, alumina, silicon nitride, aluminum nitride and the like. When the amount of the inorganic filler is particularly large, it is common to use fused silica. Fused silica can be used in either crushed or spherical form. However, in order to increase the blending amount of the fused silica and suppress an increase in the melt viscosity of the molding material, it is preferable to mainly use a spherical form. In order to further increase the blending amount of the spherical silica, it is desirable to adjust the particle size distribution of the spherical silica to be wider.

【0010】本発明で用いられるシランカップリング剤
としては、γ−グリシドキシプロピルトリメトキシシラ
ン、β−(3,4エポキシシクロヘキシル)エチルトリ
メトキシシラン、γ−メルカプトプロピルトリメトキシ
シラン、ビニルトリメトキシシラン、γ−(メタクリロ
キシプロピル)トリメトキシシランなどの化合物の他、
γ−アミノプロピルトリエトキシシラン、N−β(アミ
ノエチル)γ−アミノプロピルトリメトキシシラン、N
−フェニル−γ−アミノプロピルトリメトキシシランな
どのアミノ基を有するシランカップリング剤は硬化物の
機械的強度に優れると共に、半導体素子やリードフレー
ムとエポキシ樹脂組成物の硬化物との界面接着力も向上
する特徴を有する。このため吸湿後の半田処理や温度サ
イクル試験での耐半田性に優れておることから、特に好
ましい。
The silane coupling agents used in the present invention include γ-glycidoxypropyltrimethoxysilane, β- (3,4 epoxycyclohexyl) ethyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, vinyltrimethoxysilane In addition to compounds such as silane and γ- (methacryloxypropyl) trimethoxysilane,
γ-aminopropyltriethoxysilane, N-β (aminoethyl) γ-aminopropyltrimethoxysilane, N
-A silane coupling agent having an amino group, such as phenyl-γ-aminopropyltrimethoxysilane, has excellent mechanical strength of the cured product, and also has an improved interfacial adhesive force between the semiconductor device or lead frame and the cured product of the epoxy resin composition. It has the following characteristics. For this reason, it is particularly preferable because it has excellent soldering resistance in a soldering process after moisture absorption and a temperature cycle test.

【0011】本発明で用いられる酸価が5〜80の酸化
パラフィンワックスは、パラフィンワックスを空気酸化
あるいは酸付加することなどにより酸化物としたものの
総称であり、酸化されることにより、カルボキシル基が
導入される。原料のパラフィンワックスは、天然ワック
スである石油ワックスを減圧蒸留した留出油あるいは残
査油を分離精製したもので、通常炭素数は20〜60、
分子量は300〜900程度である。一般に半導体封止
用エポキシ樹脂組成物に用いられる離型剤としては、カ
ルナバワックス、モンタン酸エステル類、ステアリン酸
及びその金属塩、ポリエチレン、酸化ポリエチレンなど
の酸化ポリオレフィンなどが代表的である。しかし、低
粘度エポキシ樹脂や結晶性エポキシ樹脂などを使用した
エポキシ樹脂組成物では、従来の離型剤を使用しても成
形時の離型性が不十分である。特にアミノ基を有するシ
ランカップリング剤を使用する場合は、このシランカッ
プリング剤の良好な接着性のために離型性が更に劣る。
一方、酸価が5〜80の酸化パラフィンを用いると、少
量の添加で金型との離型性が良好となる。特にアミノ基
を有するシランカップリング剤を用いても、離型性が良
好な特徴がある。更に、類似の構造の酸化ポリエチレン
等の酸化ポリオレフィン化合物とは異なって、酸化パラ
フィンの場合は添加によりエポキシ樹脂組成物の成形温
度での溶融粘度が著しく低減するため、成形時の流動性
に優れる特徴がある。酸化パラフィンの酸価は、定法に
より水酸化カリウム溶液で中和滴定することにより求め
ることができる。単位は、mgKOH/gで表される。
The oxidized paraffin wax having an acid value of 5 to 80 used in the present invention is a general term for an oxide obtained by, for example, oxidation of paraffin wax by air or addition of an acid. be introduced. The paraffin wax as the raw material is obtained by separating and purifying a distillate oil or a residual oil obtained by distilling a petroleum wax which is a natural wax under reduced pressure, and usually has 20 to 60 carbon atoms.
The molecular weight is about 300-900. In general, examples of the release agent used in the epoxy resin composition for semiconductor encapsulation include carnauba wax, montanic acid esters, stearic acid and metal salts thereof, and polyolefin oxide such as polyethylene and polyethylene oxide. However, an epoxy resin composition using a low-viscosity epoxy resin, a crystalline epoxy resin, or the like has insufficient mold releasability during molding even when a conventional mold release agent is used. In particular, when a silane coupling agent having an amino group is used, the releasability is further deteriorated due to the good adhesion of the silane coupling agent.
On the other hand, when an oxidized paraffin having an acid value of 5 to 80 is used, the releasability from a mold can be improved with a small amount of addition. In particular, even when a silane coupling agent having an amino group is used, there is a characteristic that the releasability is good. Furthermore, unlike oxidized polyolefin compounds such as oxidized polyethylene having a similar structure, the addition of paraffin oxide significantly reduces the melt viscosity at the molding temperature of the epoxy resin composition by addition, thereby providing excellent fluidity during molding. There is. The acid value of oxidized paraffin can be determined by neutralization titration with a potassium hydroxide solution by a conventional method. The unit is expressed in mgKOH / g.

【0012】本発明に用いる酸化パラフィンワックスの
酸価は、5〜80の範囲である。酸価が5未満では、樹
脂との相溶性が低く、成形時に成形品表面や金型にブリ
ードし易いため、連続で成形した場合に成形品表面や金
型表面を汚染してしまう。更に、半導体素子やリードフ
レームとエポキシ樹脂組成物の硬化物との界面の接着性
も低下させてしまい、その結果耐半田性に劣る。一方、
酸価が80を越えると樹脂との相溶性が良好になり過ぎ
て、エポキシ樹脂との反応が起こりやすくなり、成形時
の粘度が増大し、流動性が低下するため、金型内充填時
に半導体素子に結線されている金線の変形を起こし易
い。特に、シランカップリング剤としてアミノシランを
用いる場合は、酸化パラフィンとアミノ基との反応がよ
り起こり易いため、酸価は80以下が好ましい。本発明
の酸価が5〜80の酸化パラフィンの特性を損なわない
範囲で、前記した他の離型剤と併用しても可能である。
The acid value of the oxidized paraffin wax used in the present invention is in the range of 5-80. If the acid value is less than 5, the compatibility with the resin is low, and bleeding easily occurs on the surface of the molded product or the mold during molding, so that the surface of the molded product or the surface of the mold is contaminated when molded continuously. Furthermore, the adhesiveness at the interface between the semiconductor element or the lead frame and the cured product of the epoxy resin composition is also reduced, and as a result, the solder resistance is poor. on the other hand,
If the acid value exceeds 80, the compatibility with the resin becomes too good, the reaction with the epoxy resin is likely to occur, the viscosity at the time of molding increases, and the fluidity decreases. The gold wire connected to the element is easily deformed. In particular, when aminosilane is used as the silane coupling agent, the acid value is preferably 80 or less because the reaction between the paraffin oxide and the amino group is more likely to occur. As long as the properties of the oxidized paraffin of the present invention having an acid value of 5 to 80 are not impaired, it can be used in combination with the above-mentioned other release agent.

【0013】本発明のエポキシ樹脂組成物は、(A)〜
(F)成分を必須成分とするが、必要に応じて臭素化エ
ポキシ樹脂、三酸化アンチモン等の難燃剤、カーボンブ
ラック等の着色剤、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等を適宜配合してもよ
い。本発明のエポキシ樹脂組成物は、(A)〜(F)成
分、及びその他の添加剤等を混合後、加熱ニーダや熱ロ
ールを用いて加熱混練し、続いて冷却粉砕して得られ
る。この樹脂組成物は一般的には粉末状、又はタブレッ
トとして使用される。本発明のエポキシ樹脂組成物を用
いて、半導体等の素子を封止し、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従来からの成形方
法で硬化成形すればよい。
The epoxy resin composition of the present invention comprises (A)
The component (F) is an essential component, but if necessary, a brominated epoxy resin, a flame retardant such as antimony trioxide, a coloring agent such as carbon black, a low stress additive such as silicone oil, silicone rubber, and synthetic rubber. May be appropriately compounded. The epoxy resin composition of the present invention is obtained by mixing the components (A) to (F), other additives, and the like, kneading with heat using a heating kneader or a hot roll, and then cooling and pulverizing. This resin composition is generally used in powder form or as a tablet. In order to manufacture a semiconductor device by encapsulating an element such as a semiconductor using the epoxy resin composition of the present invention, it is sufficient to cure and mold by a conventional molding method such as transfer molding, compression molding, injection molding and the like.

【0014】[0014]

【実施例】 実施例1 3,3’,5,5’ーテトラメチルビフェノールジグリシジルエーテルを主成 分とするエポキシ樹脂(油化シェルエポキシ(株)・製、YX4000H、融点 105℃、エポキシ当量195;以下ビフェニルエポキシ樹脂という) 7.9重量部 フェノールアラルキル樹脂(三井化学(株)・製 XL225−LL、軟化点 75℃、水酸基当量175;以下フェノールアラルキル樹脂という) 7.1重量部 球状溶融シリカ 84.0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 γ−アミノプロピルトリメトキシシラン 0.3重量部 酸化パラフィンA(酸価15、軟化温度85℃) 0.2重量部 カーボンブラック 0.3重量部 をミキサーを用いて混合した後、表面温度が90℃と2
5℃の2軸ロールを用いて20回混練し、得られた混練
物シートを冷却後粉砕して、エポキシ樹脂組成物とし
た。得られたエポキシ樹脂組成物の特性を以下の方法で
評価した。結果を表1に示す。
EXAMPLES Example 1 Epoxy resin containing 3,3 ′, 5,5′-tetramethylbiphenol diglycidyl ether as a main component (YX4000H, manufactured by Yuka Shell Epoxy Co., Ltd., melting point 105 ° C., epoxy equivalent) 195; hereinafter referred to as biphenyl epoxy resin) 7.9 parts by weight Phenol aralkyl resin (manufactured by Mitsui Chemicals, Inc., XL225-LL, softening point 75 ° C., hydroxyl equivalent 175; hereinafter referred to as phenol aralkyl resin) 7.1 parts by weight Spherical melting Silica 84.0 parts by weight 1,8-diazabicyclo (5,4,0) undecene-7 (hereinafter referred to as DBU) 0.2 part by weight γ-aminopropyltrimethoxysilane 0.3 part by weight Paraffin oxide A (acid value) 15, softening temperature 85 ° C) 0.2 parts by weight of carbon black 0.3 parts by weight were mixed using a mixer, and then mixed. 90 ℃ and 2
The mixture was kneaded 20 times using a biaxial roll at 5 ° C., and the obtained kneaded material sheet was cooled and pulverized to obtain an epoxy resin composition. The properties of the obtained epoxy resin composition were evaluated by the following methods. Table 1 shows the results.

【0015】評価方法 スパイラルフロー:EMMI−I−66に準じたスパイ
ラルフロー測定用の金型を用いて、金型温度175℃、
注入圧力70kg/cm2、硬化時間2分で測定した。 熱時強度:240℃での曲げ強さをJIS−K6911
に準じて測定した。単位はkgf/mm2。 金線変形量:144pQFPパッケージ(パッケージサ
イズ20×20×1.4mm、チップサイズ9×9m
m、金線:25μm径、リードフレーム:銅)を金型温
度175℃、成形圧力75kgf/cm2、2分間で成
形した。得られたパッケージを軟X線透視装置で観察
し、金線の変形率を(流れ量)/(金線長)で表した
(単位%)。 耐半田性:金線変形量を測定した144pQFPパッケ
ージを、175℃、8時間で後硬化させた。得られた半
導体パッケージを85℃、相対湿度85%の環境下で7
2時間及び168時間放置し、その後240℃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、
クラック数((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。 離型性:金線変形量を測定した144pQFPのパッケ
ージを10回連続で成形した。この10回の成形で、離
型時に金型に付着したり、成形品に割れ・欠けが発生し
た回数が5回以上を×、1〜4回を△、発生なしを○で
表した。
Evaluation method Spiral flow: Using a mold for spiral flow measurement in accordance with EMMI-I-66, a mold temperature of 175 ° C.
The measurement was performed at an injection pressure of 70 kg / cm 2 and a curing time of 2 minutes. Heat strength: Flexural strength at 240 ° C. is determined according to JIS-K6911.
It measured according to. The unit is kgf / mm 2 . Gold wire deformation: 144pQFP package (package size 20 × 20 × 1.4mm, chip size 9 × 9m
m, gold wire: 25 μm diameter, lead frame: copper) were molded at a mold temperature of 175 ° C. and a molding pressure of 75 kgf / cm 2 for 2 minutes. The obtained package was observed with a soft X-ray fluoroscope, and the deformation rate of the gold wire was represented by (flow amount) / (gold wire length) (unit%). Solder resistance: The 144pQFP package whose gold wire deformation was measured was post-cured at 175 ° C. for 8 hours. The obtained semiconductor package is placed in an environment of 85 ° C. and 85% relative humidity for 7 minutes.
It was left for 2 hours and 168 hours, and then immersed in a 240 ° C. solder bath for 10 seconds. Observe external cracks with a microscope,
The number of cracks ((the number of packages in which cracks occurred) / (the number of all packages) × 100) was expressed in%. Releasability: A package of 144 pQFP whose gold wire deformation was measured was molded 10 times in a row. In these 10 moldings, the number of times of adhesion to the mold at the time of release from the mold and the occurrence of cracks / chips in the molded product was 5 or more times, Δ was 1 to 4 times, and 発 生 was not generated.

【0016】実施例2〜5、比較例1〜5 実施例1を基本配合とし、離型剤及びシランカップリン
グ剤の種類を変えて、実施例1と同様にしてエポキシ樹
脂組成物を得、実施例1と同様にして評価した。実施
例、比較例に用いた酸化パラフィン、酸化ポリエチレン
の特性は、以下の通りである。 酸価(mgKOH/g) 軟化点(℃) 酸化バラフィンB 72 88 酸化バラフィンC 8 102 酸化バラフィンD 94 97 酸化バラフィンE 4 86 酸化ポリエチレン 17 105 配合処方及び結果を表1、表2に示す。
Examples 2 to 5, Comparative Examples 1 to 5 An epoxy resin composition was obtained in the same manner as in Example 1 except that the composition of Example 1 was used as a basic compound and the types of the release agent and the silane coupling agent were changed. Evaluation was performed in the same manner as in Example 1. The properties of the oxidized paraffin and polyethylene oxide used in Examples and Comparative Examples are as follows. Acid value (mg KOH / g) Softening point (° C.) Oxidized paraffin B 72 88 Oxidized paraffin C 8 102 Oxidized paraffin D 94 97 Oxidized paraffin E 4 86 Oxidized polyethylene 17 105 Formulations and results are shown in Tables 1 and 2.

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【表2】 [Table 2]

【0019】[0019]

【発明の効果】本発明エポキシ樹脂組成物は、離型性、
流動性に優れるため、連続成形性や金線変形等が発生せ
ず成形性に優れたものであり、又これで封止された半導
体装置は耐半田性に優れるものである。
The epoxy resin composition of the present invention has a releasability,
Because of its excellent fluidity, continuous moldability and gold wire deformation do not occur, so that the moldability is excellent, and the semiconductor device sealed with this is excellent in solder resistance.

───────────────────────────────────────────────────── 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 23/29 H01L 23/30 R 23/31 Fターム(参考) 4J002 AE033 CC03X CC04X CC05X CC06X CD01W CD02W CD03W CD05W CD06W CD07W CE00X DE147 DF017 DJ007 DJ017 EN026 EU096 EU106 EW016 EX038 EX068 EX078 EX088 EY016 FD017 FD156 FD160 GQ05 4J036 AA01 AB01 AB07 AC01 AC02 AD01 AD07 AD08 AE05 AF06 AF08 AF19 AJ02 AJ05 AJ08 AJ14 DA05 DC05 DC41 DD07 DD09 FA02 FA04 FA05 FA13 FB07 FB18 JA07 4M109 AA01 BA01 CA21 EA02 EB03 EB04 EB06 EB07 EB08 EB09 EB12 EB19 EC01 EC03 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification code FI Theme coat ゛ (Reference) H01L 23/29 H01L 23/30 R 23/31 F term (Reference) 4J002 AE033 CC03X CC04X CC05X CC06X CD01W CD02W CD03W CD05W CD06W CD07W CE00X DE147 DF017 DJ007 DJ017 EN026 EU096 EU106 EW016 EX038 EX068 EX078 EX088 EY016 FD017 FD156 FD160 GQ05 4J036 AA01 AB01 AB07 AC01 AC02 AD01 AD07 AD08 AE05 AF06 AF08 AF19 AJ02 AJ05 FA07 DD07 FA04 AA01 BA01 CA21 EA02 EB03 EB04 EB06 EB07 EB08 EB09 EB12 EB19 EC01 EC03

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)無機質充填材、(E)
シランカップリング剤、及び(F)酸価が5〜80の酸
化パラフィンを必須成分とする半導体封止用エポキシ樹
脂組成物。
(A) an epoxy resin, (B) a phenolic resin, (C) a curing accelerator, (D) an inorganic filler, (E)
An epoxy resin composition for semiconductor encapsulation comprising a silane coupling agent and (F) paraffin oxide having an acid value of 5 to 80 as essential components.
【請求項2】 シランカップリング剤が、アミノ基を有
するシランカップリング剤である請求項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 silane coupling agent is a silane coupling agent having an amino group.
【請求項3】 請求項1、又は2記載の半導体封止用エ
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 comprising a semiconductor element encapsulated with the epoxy resin composition for semiconductor encapsulation according to claim 1 or 2.
JP11079545A 1999-03-24 1999-03-24 Epoxy resin composition and semiconductor device Pending JP2000273285A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11079545A JP2000273285A (en) 1999-03-24 1999-03-24 Epoxy resin composition and semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11079545A JP2000273285A (en) 1999-03-24 1999-03-24 Epoxy resin composition and semiconductor device

Publications (1)

Publication Number Publication Date
JP2000273285A true JP2000273285A (en) 2000-10-03

Family

ID=13692978

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11079545A Pending JP2000273285A (en) 1999-03-24 1999-03-24 Epoxy resin composition and semiconductor device

Country Status (1)

Country Link
JP (1) JP2000273285A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003096164A (en) * 2001-07-16 2003-04-03 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
WO2006080297A1 (en) * 2005-01-28 2006-08-03 Sumitomo Bakelite Co., Ltd. Epoxy resin composition for semiconductor encapsulation and semiconductor device
WO2009112329A1 (en) * 2008-03-11 2009-09-17 Evonik Degussa Gmbh Post-crosslinking wax and method for producing the same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003096164A (en) * 2001-07-16 2003-04-03 Sumitomo Bakelite Co Ltd Epoxy resin composition and semiconductor device
WO2006080297A1 (en) * 2005-01-28 2006-08-03 Sumitomo Bakelite Co., Ltd. Epoxy resin composition for semiconductor encapsulation and semiconductor device
KR101090608B1 (en) 2005-01-28 2011-12-08 스미토모 베이클라이트 가부시키가이샤 Epoxy resin composition for encapsulating semiconductor chip and semiconductor device
JP5205964B2 (en) * 2005-01-28 2013-06-05 住友ベークライト株式会社 Epoxy resin composition for semiconductor encapsulation and semiconductor device
WO2009112329A1 (en) * 2008-03-11 2009-09-17 Evonik Degussa Gmbh Post-crosslinking wax and method for producing the same

Similar Documents

Publication Publication Date Title
WO2006049156A1 (en) Epoxy resin composition and semiconductor device
JP4692885B2 (en) Epoxy resin composition and semiconductor device
JPH05148411A (en) Thermosetting resin composition and semiconductor device
JP4250987B2 (en) Epoxy resin composition and semiconductor device
JP2002012742A (en) Epoxy resin composition and semiconductor device
JPH0597969A (en) Thermosetting resin composition and semiconductor device
JP2002220434A (en) Epoxy resin composition and semiconductor device
JP2000281751A (en) Epoxy resin composition and semiconductor device
JP2000273280A (en) Epoxy resin composition and semiconductor device
JP4332972B2 (en) Epoxy resin composition and semiconductor device
JP2000273285A (en) Epoxy resin composition and semiconductor device
JP2003105059A (en) Epoxy resin composition and semiconductor device
JP2000273277A (en) Epoxy resin composition and semiconductor device
JP5098125B2 (en) Epoxy resin composition and semiconductor device
JP2002241581A (en) Epoxy resin composition and semiconductor device
JP2003292730A (en) Epoxy resin composition and semiconductor device
JP2005281584A (en) Epoxy resin composition and semiconductor device
JP2002080694A (en) Epoxy resin composition and semiconductor device
JP4608736B2 (en) Method for producing epoxy resin composition for semiconductor encapsulation
JP5055778B2 (en) Epoxy resin composition, epoxy resin molding material and semiconductor device
JP2862777B2 (en) Epoxy resin composition
JP2000273154A (en) Epoxy resin composition and semiconductor device
JP2009256475A (en) Epoxy resin composition for sealing semiconductor and semiconductor device using the same
JP4379972B2 (en) Epoxy resin composition and semiconductor device
JP2001240724A (en) Epoxy resin composition and semiconductor device

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20051128

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20080528

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20080610

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20081014