JP2000212401A - Epoxy resin composition and semiconductor device - Google Patents

Epoxy resin composition and semiconductor device

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Publication number
JP2000212401A
JP2000212401A JP11020473A JP2047399A JP2000212401A JP 2000212401 A JP2000212401 A JP 2000212401A JP 11020473 A JP11020473 A JP 11020473A JP 2047399 A JP2047399 A JP 2047399A JP 2000212401 A JP2000212401 A JP 2000212401A
Authority
JP
Japan
Prior art keywords
resin composition
epoxy resin
weight
formula
resin
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.)
Granted
Application number
JP11020473A
Other languages
Japanese (ja)
Other versions
JP3478380B2 (en
Inventor
Masayuki Ikeda
雅之 池田
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 JP02047399A priority Critical patent/JP3478380B2/en
Publication of JP2000212401A publication Critical patent/JP2000212401A/en
Application granted granted Critical
Publication of JP3478380B2 publication Critical patent/JP3478380B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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

Abstract

PROBLEM TO BE SOLVED: To provide a semiconductor epoxy resin composition which causes no delamination from the semiconductor element during molding and has excellent moisture-resistance reliability, in the case where an island minimizing frame such as a window-pad frame is used. SOLUTION: The composition comprises, as essential ingredients, a dicyclopentadiene-modified epoxy resin, a phenolic resin, a curing accelerator, an inorganic filler, and silane coupling agents of formulae I, II and III, the ratio (a)/(b) of the number (a) of epoxy groups in the total epoxy resin to the number (b) of phenolic hydroxy groups in the total phenolic resin being 1.10-1.20, the content of the inorganic filler being 80-90 wt.% in the total resin composition, the content of the whole silane coupling agents being 0.3-1.3 wt.% in the total resin composition, the weight ratio I/(II+III) of the compounds of formulae I, II and III being 0.5-3.0.

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、耐湿信頼
性に優れた半導体封止用エポキシ樹脂組成物、及びこれ
を用いて半導体素子を封止してなる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 excellent in moldability and humidity resistance, and to a semiconductor device obtained by encapsulating a semiconductor element 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(以下、樹脂組成物とい
う)のトランスファー成形による方法が、低コスト、大
量生産に適した方法として採用され、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、その向上が図られてきた。しかし、近年、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
体の多様化も年々進み、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、従来の樹脂組成物
では解決できない問題点も出てきている。一つには、半
導体パッケージの多様化に伴い、パッケージ中に占める
樹脂組成物の硬化物の厚みが、それぞれのパッケージに
おいて著しく異なってきているということである。例え
ば、1mm厚のTSOPの場合等、半導体素子上面に形
成される樹脂組成物の硬化物の厚みは0.2〜0.3m
m程度となる。一方、4mm厚のSOJ等の厚型パッケ
ージの場合では、半導体素子上面に形成される樹脂組成
物の硬化物の厚みは1mm以上にもなる。そのため、成
形性、及び耐湿信頼性、耐熱信頼性に差が生じることは
明らかである。このため、様々な添加剤を加え、樹脂組
成物とリードフレームや半導体素子との密着性の向上を
図ってきたが、そのいずれにおいても、完全な解決策と
はならず、更に改良が望まれている。二番目の問題点と
して、リードフレームの形状、特に半導体素子と接着さ
れるアイランドの形状が変わってきたという点である。
例えば、ウインドウ・パッドフレーム等がこれに相当す
る。ウインドウ・パッドフレームは、耐湿信頼性、耐熱
信頼性の向上を目的として開発されたものであるが、こ
れを使用することで、封止する際の樹脂組成物と半導体
素子裏面との密着性不良に起因する半導体素子裏面の剥
離の問題が生じてきた。このため、密着性の向上を目指
して様々な改良が進められてきたが、そのいずれにおい
ても、完全な解決策とはならず、更に改良が望まれてい
る。
2. Description of the Related Art As a method for encapsulating semiconductor elements such as ICs and LSIs, a method by transfer molding of an epoxy resin composition (hereinafter referred to as a resin composition) has been adopted as a method suitable for low cost and mass production. In terms of reliability, improvements have been made by improving epoxy resins and phenol resins as curing agents. However, in recent years, semiconductors have been diversified year by year in the market trend of miniaturization, weight reduction, and high performance of electronic devices, and demands for resin compositions have become increasingly severe. For this reason, a problem which cannot be solved by the conventional resin composition has come out. One is that, with the diversification of semiconductor packages, the thickness of the cured product of the resin composition occupying the packages has been significantly different in each package. For example, in the case of a TSOP having a thickness of 1 mm, the thickness of the cured product of the resin composition formed on the upper surface of the semiconductor element is 0.2 to 0.3 m.
m. On the other hand, in the case of a thick package such as a 4 mm-thick SOJ, the cured product of the resin composition formed on the upper surface of the semiconductor element has a thickness of 1 mm or more. Therefore, it is clear that there is a difference between the moldability, the moisture resistance reliability, and the heat resistance reliability. For this reason, various additives have been added to improve the adhesion between the resin composition and the lead frame or the semiconductor element. However, none of them has been a complete solution, and further improvement is desired. ing. A second problem is that the shape of the lead frame, especially the shape of the island bonded to the semiconductor element, has changed.
For example, a window / pad frame corresponds to this. The window / pad frame was developed for the purpose of improving the humidity resistance and the heat resistance. However, by using this, the poor adhesion between the resin composition and the back surface of the semiconductor element when sealing is used. The problem of peeling of the back surface of the semiconductor element resulting from the above has arisen. For this reason, various improvements have been made with the aim of improving the adhesion, but none of them is a complete solution, and further improvements are desired.

【0003】[0003]

【発明が解決しようとする課題】本発明は、特にウイン
ドウ・パッドフレーム等のアイランド細小化フレームを
使用した場合における成形性、半導体素子裏面との密着
性、及び耐湿信頼性に優れた半導体封止用エポキシ樹脂
組成物、及びこれを用いて半導体素子を封止してなる半
導体装置を提供するものである。
SUMMARY OF THE INVENTION The present invention relates to a semiconductor encapsulation having excellent moldability, adhesion to the back surface of a semiconductor element, and excellent moisture resistance reliability, particularly when an island miniaturized frame such as a window / pad frame is used. The present invention provides an epoxy resin composition for use and a semiconductor device obtained by sealing a semiconductor element using the same.

【0004】[0004]

【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、及び(E)式(E−1)、式(E
−2)、及び式(E−3)のシランカップリング剤を必
須成分とし、全エポキシ樹脂のエポキシ基数(a)と全
フェノール樹脂のフェノール性水酸基数(b)との比
(a)/(b)が1.10〜1.20であり、且つ、無
機質充填材の含有量が全樹脂組成物中に80〜90重量
%であり、且つ、全シランカップリング剤の含有量が全
樹脂組成物中に0.3〜1.3重量%であり、且つ、式
(E−1)、式(E−2)、及び式(E−3)の化合物
の重量比(E−1)/{(E−2)+(E−3)}が、
0.5〜3.0であることを特徴とし、特に好ましいエ
ポキシ樹脂が式(1)のジシクロペンタジエン変性エポ
キシ樹脂である半導体封止用エポキシ樹脂組成物、及び
これを用いて半導体素子を封止してなる半導体装置であ
る。 H2NCH2CH2CH2Si(OCH2CH33 (E−1)
The present invention provides (A) an epoxy resin, (B) a phenolic resin, (C) a curing accelerator,
(D) an inorganic filler, and (E) Formula (E-1), Formula (E)
-2) and the silane coupling agent of the formula (E-3) as an essential component, and the ratio (a) / () of the number of epoxy groups (a) of all epoxy resins to the number of phenolic hydroxyl groups (b) of all phenol resins. b) is 1.10 to 1.20, the content of the inorganic filler is 80 to 90% by weight in the whole resin composition, and the content of the whole silane coupling agent is the whole resin composition. 0.3 to 1.3% by weight in the product, and the weight ratio (E-1) / {of the compounds of the formulas (E-1), (E-2) and (E-3). (E-2) + (E-3)} is
0.5 to 3.0, wherein a particularly preferred epoxy resin is a dicyclopentadiene-modified epoxy resin of the formula (1), and an epoxy resin composition for semiconductor encapsulation, and a semiconductor element is encapsulated using the same. The semiconductor device is stopped. H 2 NCH 2 CH 2 CH 2 Si (OCH 2 CH 3 ) 3 (E-1)

【0005】[0005]

【化3】 HSCH2CH2CH2Si(OCH33 (E−3)Embedded image HSCH 2 CH 2 CH 2 Si (OCH 3 ) 3 (E-3)

【0006】[0006]

【化4】 (式中、n=0〜10)Embedded image (Where n = 0 to 10)

【0007】[0007]

【発明の実施の形態】本発明で用いるエポキシ樹脂は、
1分子内にエポキシ基を2個以上有するモノマー、オリ
ゴマー、及びポリマー全般を言う。例えば、含臭素エポ
キシ樹脂、ビフェニル型エポキシ樹脂、ビスフェノール
型エポキシ樹脂、スチルベン型エポキシ樹脂、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、環状脂肪族エポキシ樹脂、グリシジルエ
ステル系エポキシ樹脂、グリシジルアミン系エポキシ樹
脂、複素環式エポキシ樹脂、3官能型エポキシ樹脂、ト
リスヒドロキシフェニルメタン型エポキシ樹脂等が挙げ
られる。これらのエポキシ樹脂は、分子量、融点又は軟
化点、水酸基当量等に制限なく使用することができる
が、エポキシ樹脂中の塩素含有量は低いことが好まし
い。これらは単独でも混合して用いても良い。これらの
内では、特に式(A−1)で示されるジシクロペンタジ
エン変性エポキシ樹脂が好ましい。このエポキシ樹脂
は、ノボラック型エポキシ樹脂等に比べて、反応起点が
多く、より高い密着性が得られ、又、ビフェニル型エポ
キシ樹脂等の結晶性エポキシ樹脂と比べても、密着性は
同等で、且つ粘度が低いため、無機質充填材の含有量を
増加させることができ、硬化性が向上する。更にn=1
〜2のものが好ましい。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The epoxy resin used in the present invention is:
It refers to all monomers, oligomers, and polymers having two or more epoxy groups in one molecule. For example, brominated epoxy resin, biphenyl type epoxy resin, bisphenol type epoxy resin, stilbene type epoxy resin, phenol novolak type epoxy resin, cresol novolak type epoxy resin, cycloaliphatic epoxy resin, glycidyl ester type epoxy resin, glycidyl amine type epoxy resin Resins, heterocyclic epoxy resins, trifunctional epoxy resins, trishydroxyphenylmethane type epoxy resins, and the like. These epoxy resins can be used without any limitation on the molecular weight, melting point or softening point, hydroxyl equivalent, etc., but the chlorine content in the epoxy resin is preferably low. These may be used alone or as a mixture. Among them, a dicyclopentadiene-modified epoxy resin represented by the formula (A-1) is particularly preferable. This epoxy resin has a larger number of reaction starting points and higher adhesion than a novolak epoxy resin or the like, and has the same adhesion as a crystalline epoxy resin such as a biphenyl epoxy resin. In addition, since the viscosity is low, the content of the inorganic filler can be increased, and the curability is improved. Furthermore, n = 1
~ 2 are preferred.

【0008】本発明で用いるフェノール樹脂は、1分子
内にフェノール性水酸基を2個以上有するモノマー、オ
リゴマー、及びポリマー全般を言う。フェノール樹脂に
は特に制限はなく、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、ナフト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等
が挙げられる。これらのフェノール樹脂は、分子量、軟
化点、水酸基当量等に制限なく用いることができるが、
フェノール樹脂中の塩素含有量は極力低いことが好まし
い。これらは単独でも混合して用いても良い。全エポキ
シ樹脂のエポキシ基数(a)と全フェノール樹脂のフェ
ノール性水酸基数(b)との比(a)/(b)は、1.
10〜1.20が好ましい。1.10未満だと、樹脂組
成物と半導体素子裏面の剥離が生じるおそれがある。
1.20を越えると、金型との離型性が悪くなり、ひい
ては成形性に問題が生じるので好ましくない。
[0008] 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. The phenol resin is not particularly limited, and examples thereof include phenol novolak resin, cresol novolak resin, phenol aralkyl resin, naphthol aralkyl resin, terpene-modified phenol resin, and dicyclopentadiene-modified phenol resin. These phenolic resins can be used without limitation on molecular weight, softening point, hydroxyl equivalent, etc.
It is preferable that the chlorine content in the phenol resin is as low as possible. These may be used alone or as a mixture. The ratio (a) / (b) of the number of epoxy groups (a) of all epoxy resins to the number of phenolic hydroxyl groups (b) of all phenol resins is 1.
10-1.20 is preferred. If it is less than 1.10, the resin composition and the back surface of the semiconductor element may peel off.
When the ratio exceeds 1.20, the releasability from the mold is deteriorated, and the moldability is disadvantageously increased.

【0009】本発明で用いる硬化促進剤としては、例え
ば、トリブチルアミン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フォニウム・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、1,8−ジアザ
ビシクロ(5,4,0)ウンデセン−7等が挙げられる
が、これらに限定されるものではない。これらは単独で
も混合して用いても良い。
Examples of the curing accelerator used in the present invention include amine compounds such as tributylamine, organic phosphorus compounds such as triphenylphosphine and tetraphenylphosphonium tetraphenylborate, and 2-methylimidazole and the like. Examples thereof include, but are not limited to, an imidazole compound and 1,8-diazabicyclo (5,4,0) undecene-7. These may be used alone or as a mixture.

【0010】本発明で用いる無機質充填材には、特に制
限はなく、公知の無機質充填材を使用することができ
る。このような無機質充填材としては、例えば、アルミ
ナ、溶融シリカ、球状シリカ、結晶シリカ、2次凝集シ
リカ等が挙げられる。流動性の向上という点から、特に
溶融球状シリカが好ましい。溶融球状シリカの粒子の形
状としては、流動性の向上のために限りなく真球状であ
り、且つ粒度分布がブロードであることが望ましい。無
機質充填材の含有量としては、全樹脂組成物中に80〜
90重量%が好ましい。80重量%未満だと、無機質充
填材による補強効果が十分に発揮できないおそれがあ
り、90重量%以上を越えると樹脂組成物の流動性が低
下し、成形時に充填不良等が生じるおそれがある。
[0010] The inorganic filler used in the present invention is not particularly limited, and a known inorganic filler can be used. Examples of such an inorganic filler include alumina, fused silica, spherical silica, crystalline silica, and secondary aggregated silica. From the viewpoint of improving fluidity, fused spherical silica is particularly preferred. As the shape of the fused spherical silica particles, it is desirable that the particles be infinitely spherical and have a broad particle size distribution in order to improve fluidity. The content of the inorganic filler in the total resin composition is 80 to
90% by weight is preferred. If it is less than 80% by weight, the reinforcing effect of the inorganic filler may not be sufficiently exerted, and if it is more than 90% by weight, the fluidity of the resin composition may be reduced, and poor filling may occur during molding.

【0011】本発明で使用するシランカップリング剤
は、式(E−1)のγ−アミノプロピルトリエトキシシ
ラン、式(E−2)のγ−グリシドキシプロピルトリメ
トキシシラン、及び式(E−3)のγ−メルカプトプロ
ピルトリメトキシシランである。これらの重量比として
は、(E−1)/{(E−2)+(E−3)}が0.5
〜3.0であることが好ましい。0.5〜3.0の範囲
を外れると、樹脂組成物と半導体素子裏面の剥離が生じ
るおそれがある。3種類のシランカップリング剤の内、
1種類でも欠けると密着性が低下するので好ましくな
い。3種類のシランカップリング剤の各々の添加量とし
ては、全樹脂組成物中に0.1重量%以上が好ましい。
又、本発明の式(E−1)〜式(E−3)のシランカッ
プリング剤の特性を損なわない範囲で、2−(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等
の他のシランカップリング剤を併用してもよい。全シラ
ンカップリング剤の合計重量としては、全樹脂組成物中
に0.3〜1.3重量%が好ましい。0.3重量%未満
だと、樹脂組成物と半導体素子裏面の剥離が生じるおそ
れがあり、1.3重量%を越えると、成形時の離型性が
悪くなるおそれがある。
The silane coupling agent used in the present invention comprises γ-aminopropyltriethoxysilane of the formula (E-1), γ-glycidoxypropyltrimethoxysilane of the formula (E-2), and -3) γ-mercaptopropyltrimethoxysilane. (E-1) / {(E-2) + (E-3)} is 0.5
It is preferably from 3.0 to 3.0. If the ratio is out of the range of 0.5 to 3.0, the resin composition and the back surface of the semiconductor element may be separated. Of the three types of silane coupling agents,
It is not preferable that even one kind is missing because the adhesiveness is reduced. The addition amount of each of the three types of silane coupling agents is preferably 0.1% by weight or more in the entire resin composition.
Further, within the range not impairing the properties of the silane coupling agents of formulas (E-1) to (E-3) of the present invention, 2- (3,4-
Other silane coupling agents such as epoxycyclohexyl) ethyltrimethoxysilane may be used in combination. The total weight of all the silane coupling agents is preferably 0.3 to 1.3% by weight in the whole resin composition. If it is less than 0.3% by weight, the resin composition may peel off from the back surface of the semiconductor element. If it exceeds 1.3% by weight, the releasability at the time of molding may be deteriorated.

【0012】本発明の樹脂組成物は、(A)〜(E)成
分の他、必要に応じて、カーボンブラック等の着色剤、
臭素化エポキシ樹脂、酸化アンチモン、リン化合物等の
難燃剤、シリコーンオイル、シリコーンゴム等の低応力
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、酸化防止剤
等の各種添加剤を配合することができる。本発明の樹脂
組成物は、(A)〜(E)成分、及びその他の添加剤等
をミキサーを用いて常温混合し、ロール、ニーダー、押
出機等の混練機で溶融混練し、冷却後粉砕して得られ
る。本発明の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硬化成形すればよい。
The resin composition of the present invention may further comprise, if necessary, a coloring agent such as carbon black, in addition to the components (A) to (E).
Flame retardants such as brominated epoxy resin, antimony oxide and phosphorus compounds, low stress components such as silicone oil and silicone rubber, release agents such as natural wax, synthetic wax, higher fatty acids and their metal salts or paraffin, antioxidants, etc. Can be blended. The resin composition of the present invention is obtained by mixing the components (A) to (E) and other additives at room temperature using a mixer, melt-kneading the mixture with a kneading machine such as a roll, kneader, extruder, etc., and then pulverizing after cooling. Is obtained. In order to manufacture a semiconductor device by encapsulating an electronic component such as a semiconductor element using the resin composition of the present invention, it is sufficient to cure and mold by a molding method such as a transfer mold, a compression mold, and an injection mold.

【0013】[0013]

【実施例】以下に、実施例を挙げて説明するが、本発明
はこれらの実施例によりなんら限定されるものではな
い。配合割合は重量部とする。 実施例1 式(1)のエポキシ樹脂(大日本インキ化学工業(株)・製HP−7200、 軟化点65℃、エポキシ当量265g/eq) 10.0重量部
EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited to these examples. The mixing ratio is by weight. Example 1 Epoxy resin of formula (1) (HP-7200, manufactured by Dainippon Ink and Chemicals, Inc., softening point 65 ° C., epoxy equivalent 265 g / eq) 10.0 parts by weight

【化5】 Embedded image

【0014】 フェノールノボラック樹脂(軟化点80℃、水酸基当量105g/eq) 4.2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 溶融球状シリカ(平均粒径15μm、比表面積4.0m2/g) 100重量部 式(E−1) 0.50重量部 式(E−2) 0.20重量部 式(E−3) 0.30重量部 臭素化エポキシ樹脂(エポキシ当量273g/eq) 2.1重量部 カーボンブラック 0.4重量部 カルナバワックス 0.7重量部 をミキサーで混合し、70〜100℃で混練し、冷却後
粉砕して樹脂組成物を得た。得られた樹脂組成物を以下
の方法で評価した。結果を表1に示す。
Phenol novolak resin (softening point 80 ° C., hydroxyl equivalent 105 g / eq) 4.2 parts by weight 1,8-diazabicyclo (5,4,0) undecene-7 (hereinafter referred to as DBU) 0.2 parts by weight Melting Spherical silica (average particle size 15 μm, specific surface area 4.0 m 2 / g) 100 parts by weight Formula (E-1) 0.50 parts by weight Formula (E-2) 0.20 parts by weight Formula (E-3) 30 parts by weight Brominated epoxy resin (epoxy equivalent: 273 g / eq) 2.1 parts by weight Carbon black 0.4 parts by weight Carnauba wax 0.7 parts by weight is mixed with a mixer, kneaded at 70 to 100 ° C., and cooled and ground. Thus, a resin composition was obtained. The obtained resin composition was evaluated by the following method. 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、金型温度175℃、注
入圧力70kg/cm2、硬化時間2分で測定した。ス
パイラルフローは流動性のパラメータであり、数値が大
きい方が流動性が良好である。単位はcm。 成形後密着性:低圧トランスファー成形機を用いて、金
型温度175℃、圧力75kg/cm2、硬化時間2分
で、9×9mmの半導体素子を9.5×9.9mmのア
イランドを有する80pQFPのウインドウパッドフレ
ームに封止し、175℃、8時間で後硬化を行った。1
8個のパッケージを超音波探査映像装置を用いて、成形
品内部の樹脂組成物の硬化物と半導体素子の密着性につ
いて観察した。 耐湿密着性:低圧トランスファー成形機を用いて、金型
温度175℃、圧力75kg/cm2、硬化時間2分
で、前記の80pQFPを成形し、175℃、8時間で
後硬化を行った。18個のパッケージを85℃、相対湿
度85%の環境下で72時間処理し、超音波探査映像装
置を用いて、成形品内部の樹脂組成物の硬化物と半導体
素子の密着性を観察した。
Evaluation method Spiral flow: Measurement was performed using a mold for measuring spiral flow according to EMMI-I-66 at a mold temperature of 175 ° C., an injection pressure of 70 kg / cm 2 , and a curing time of 2 minutes. Spiral flow is a parameter of fluidity, and the larger the value, the better the fluidity. The unit is cm. Adhesion after molding: using a low-pressure transfer molding machine, a mold temperature of 175 ° C., a pressure of 75 kg / cm 2 , and a curing time of 2 minutes, a 9 × 9 mm semiconductor element having a 9.5 × 9.9 mm island and 80 pQFP. And then post-cured at 175 ° C. for 8 hours. 1
Eight packages were observed for the adhesiveness between the cured product of the resin composition inside the molded article and the semiconductor element by using an ultrasonic probe imager. Moisture resistance: The 80pQFP was molded using a low-pressure transfer molding machine at a mold temperature of 175 ° C, a pressure of 75 kg / cm 2 , and a curing time of 2 minutes, and post-cured at 175 ° C for 8 hours. Eighteen packages were treated in an environment of 85 ° C. and 85% relative humidity for 72 hours, and the adhesion between the cured product of the resin composition inside the molded article and the semiconductor element was observed using an ultrasonic probe.

【0016】実施例2〜10、比較例1〜11 表1、表2の配合に従い、実施例1と同様にして樹脂組
成物を得、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9、10では、オルソク
レゾールノボラック型エポキシ樹脂(軟化点55℃、エ
ポキシ当量196g/eq)を使用した。
Examples 2 to 10 and Comparative Examples 1 to 11 According to the formulations shown in Tables 1 and 2, a resin composition was 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. In Examples 9 and 10, an ortho-cresol novolak type epoxy resin (softening point: 55 ° C., epoxy equivalent: 196 g / eq) was used.

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【表2】 [Table 2]

【0019】[0019]

【発明の効果】本発明に従うと、特にウインドウ・パッ
ドフレーム等のアイランド細小化フレームを使用した場
合において、成形時に半導体素子との剥離がなく、耐湿
信頼性に優れた半導体装置を得ることができる。
According to the present invention, a semiconductor device having excellent moisture resistance reliability can be obtained without peeling from a semiconductor element at the time of molding, particularly when an island miniaturized frame such as a window / pad frame is used. .

───────────────────────────────────────────────────── 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) C08K 5/544 C08K 5/54 F 5/5435 E 5/548 L H01L 23/29 H01L 23/30 R 23/31 Fターム(参考) 4J002 CC04X CC05X CD02W CD03W CD05W CD06W CD07W CD08W CD12W CD13W CE00X DE147 DJ017 EN026 EU116 EU136 EW016 EW176 EX068 EX078 EX088 FA087 FD017 FD090 FD130 FD14X FD156 FD208 GJ02 GQ01 4J036 AB02 AB07 AD07 AD08 AD11 AD12 AE07 AF06 AF07 AH04 DC05 DC06 DC41 DC46 DD07 DD09 FA03 FA05 FB07 FB08 JA07 4M109 AA01 BA01 CA21 EA02 EA03 EB03 EB04 EB06 EB07 EB08 EB09 EB12 EB13 EB19 EC01 EC09 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C08K 5/544 C08K 5/54 F 5/5435 E 5/548 L H01L 23/29 H01L 23/30 R 23 / 31 F-term (reference) 4J002 CC04X CC05X CD02W CD03W CD05W CD06W CD07W CD08W CD12W CD13W CE00X DE147 DJ017 EN026 EU116 EU136 EW016 EW176 EX068 EX078 EX088 FA087 FD017 FD090 FD130 FD14X FD156 AD01 AD07 AD02 AD01 AD07 AD07 DC06 DC41 DC46 DD07 DD09 FA03 FA05 FB07 FB08 JA07 4M109 AA01 BA01 CA21 EA02 EA03 EB03 EB04 EB06 EB07 EB08 EB09 EB12 EB13 EB19 EC01 EC09

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、及び
(E)式(E−1)、式(E−2)、及び式(E−3)
のシランカップリング剤を必須成分とし、全エポキシ樹
脂のエポキシ基数(a)と全フェノール樹脂のフェノー
ル性水酸基数(b)との比(a)/(b)が1.10〜
1.20であり、且つ、無機質充填材の含有量が全樹脂
組成物中に80〜90重量%であり、且つ、全シランカ
ップリング剤の含有量が全樹脂組成物中に0.3〜1.
3重量%であり、且つ、式(E−1)、式(E−2)、
及び式(E−3)の化合物の重量比(E−1)/{(E
−2)+(E−3)}が、0.5〜3.0であることを
特徴とする半導体封止用エポキシ樹脂組成物。 H2NCH2CH2CH2Si(OCH2CH33 (E−1) 【化1】 HSCH2CH2CH2Si(OCH33 (E−3)
1. An epoxy resin (A), a phenolic resin (B), a curing accelerator (C), an inorganic filler (D), and (E) formulas (E-1), (E-2), Formula (E-3)
And the ratio (a) / (b) of the number of epoxy groups (a) of all epoxy resins to the number of phenolic hydroxyl groups (b) of all phenolic resins is 1.10 to 10%.
1.20, and the content of the inorganic filler is 80 to 90% by weight in the whole resin composition, and the content of the whole silane coupling agent is 0.3 to 0.3% in the whole resin composition. 1.
3% by weight, and formula (E-1), formula (E-2),
And the weight ratio of the compound of the formula (E-3) (E-1) / {(E
-2) + (E-3)} is 0.5 to 3.0, wherein the epoxy resin composition for semiconductor encapsulation is characterized in that: H 2 NCH 2 CH 2 CH 2 Si (OCH 2 CH 3 ) 3 (E-1) HSCH 2 CH 2 CH 2 Si (OCH 3 ) 3 (E-3)
【請求項2】 エポキシ樹脂が、式(1)で示されるジ
シクロペンタジエン変性エポキシ樹脂である請求項1記
載の半導体封止用エポキシ樹脂組成物。 【化2】 (式中、n=0〜10)
2. The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein the epoxy resin is a dicyclopentadiene-modified epoxy resin represented by the formula (1). Embedded image (Where n = 0 to 10)
【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.
JP02047399A 1999-01-28 1999-01-28 Epoxy resin composition and semiconductor device Expired - Fee Related JP3478380B2 (en)

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Country Link
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006193595A (en) * 2005-01-12 2006-07-27 Sumitomo Bakelite Co Ltd Liquid sealing resin composition for underfill, semiconductor apparatus using the same and method for producing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006193595A (en) * 2005-01-12 2006-07-27 Sumitomo Bakelite Co Ltd Liquid sealing resin composition for underfill, semiconductor apparatus using the same and method for producing the same

Also Published As

Publication number Publication date
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