JP2002145985A - Liquid sealing resin composition - Google Patents

Liquid sealing resin composition

Info

Publication number
JP2002145985A
JP2002145985A JP2000342861A JP2000342861A JP2002145985A JP 2002145985 A JP2002145985 A JP 2002145985A JP 2000342861 A JP2000342861 A JP 2000342861A JP 2000342861 A JP2000342861 A JP 2000342861A JP 2002145985 A JP2002145985 A JP 2002145985A
Authority
JP
Japan
Prior art keywords
epoxy resin
liquid sealing
resin composition
resin
sealing 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.)
Pending
Application number
JP2000342861A
Other languages
Japanese (ja)
Inventor
Mieko Kikuchi
美恵子 菊池
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.)
Kyocera Chemical Corp
Original Assignee
Toshiba Chemical Corp
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 Toshiba Chemical Corp filed Critical Toshiba Chemical Corp
Priority to JP2000342861A priority Critical patent/JP2002145985A/en
Publication of JP2002145985A publication Critical patent/JP2002145985A/en
Pending legal-status Critical Current

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

Abstract

PROBLEM TO BE SOLVED: To provide a liquid sealing resin composition which gives a cured product having a low glass transition point and a low elastic modulus, can reduce the warpage of the cured product, and is suitable for the liquid sealing of semiconductors. SOLUTION: This liquid sealing resin composition is characterized by containing as essential components (A) an epoxy resin containing an alkyl type bifunctional epoxy resin, a such as 1,6-hexanediol diglycidyl ether, (B) a curing agent such as a novolak phenolic resin, (C) a curing accelerator, and (D) a filler. The alkyl type bifuncitonal epoxy resin is preferably added in an amount of 5 to 40 wt.% in (A) the epoxy resin.

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、半導体などの液状
封止に好適に使用される一液性の液状封止用樹脂組成物
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a one-part liquid sealing resin composition suitably used for liquid sealing of semiconductors and the like.

【0002】[0002]

【従来の技術】近年、半導体パッケージを封止、実装す
る形態は軽薄短小化傾向にある。それに伴い、パッケー
ジの携帯は、QFP、SOP等からさらに小さくするた
めにBGAやCSPが開発された。BGAはトランスフ
ァー成形されるQFP、SOPと異なり片面封止である
ためパッケージの反りが発生しやすい。パッケージが反
ってしまうと実装信頼性に劣る問題がある。また、最近
検討されているMAP(マトリックスアレイパッケー
ジ)といわれる、多数のチップを一括封止し、後で切断
するという成形方法では、パッケージの反りがさらに厳
しくなる。
2. Description of the Related Art In recent years, the form of sealing and mounting a semiconductor package has been tending to be light and thin. Accordingly, BGA and CSP have been developed in order to further reduce the size of the package from QFP and SOP. Unlike QFPs and SOPs which are transfer-molded, BGAs have single-sided sealing, so that package warpage is likely to occur. If the package warps, there is a problem that mounting reliability is inferior. Further, in a molding method called MAP (matrix array package), which is recently studied, in which a large number of chips are collectively sealed and cut later, the package warpage becomes more severe.

【0003】[0003]

【発明が解決しようとする課題】本発明は、上記の事情
に鑑みてなされたもので、樹脂のガラス転移点を低くす
ることにより樹脂の加熱硬化後の冷却過程における内部
応力を低下させ、反り量の小さい半導体パッケージを与
える液状封止用樹脂組成物を提供するものである。
SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and reduces the internal stress in the cooling process after heat-curing of a resin by lowering the glass transition point of the resin. An object of the present invention is to provide a liquid encapsulating resin composition that provides a small amount of semiconductor package.

【0004】[0004]

【課題を解決するための手段】本発明者は、上記の目的
を達成しようと鋭意研究を進めた結果、エポキシ樹脂に
アルキル型2官能エポキシ樹脂を任意の割合で混合した
ものを用いることにより、上記の目的を達成できること
を見いだし、本発明を完成したもである。
Means for Solving the Problems As a result of diligent research aimed at achieving the above object, the present inventor has found that by using an epoxy resin mixed with an alkyl-type bifunctional epoxy resin at an arbitrary ratio, The inventors have found that the above objects can be achieved, and have completed the present invention.

【0005】即ち、本発明は、(A)アルキル型2官能
エポキシ樹脂を含むエポキシ樹脂、(B)硬化剤 (C)硬化促進剤および(D)充填剤を必須成分とする
ことを特徴とする一液性の液状封止用樹脂組成物であ
る。
That is, the present invention is characterized in that (A) an epoxy resin containing an alkyl-type bifunctional epoxy resin, (B) a curing agent, (C) a curing accelerator and (D) a filler are essential components. It is a one-part liquid sealing resin composition.

【0006】以下、本発明を詳細に説明する。Hereinafter, the present invention will be described in detail.

【0007】本発明に用いる(A)エポキシ樹脂に含ま
れるアルキル型2官能エポキシ樹脂は、アルカンジオー
ルジグリシジルエーテルであるエポキシ樹脂で、例え
ば、1,6−ヘキサンジオールジグリシジルエーテル、
ネオペンタンジオールジグリシジルエーテル、(ポリ)
エチレングリコールジグリシジルエーテル、(ポリ)プ
ロピレングリコールジグリシジルエーテル等が挙げられ
る。
The alkyl type bifunctional epoxy resin contained in the epoxy resin (A) used in the present invention is an epoxy resin which is an alkanediol diglycidyl ether, for example, 1,6-hexanediol diglycidyl ether,
Neopentanediol diglycidyl ether, (poly)
Examples include ethylene glycol diglycidyl ether and (poly) propylene glycol diglycidyl ether.

【0008】これらアルキル型2官能エポキシ樹脂の配
合割合は、(A)エポキシ樹脂中に5〜40重量%の割
合で混合することが好ましい。アルキル型2官能エポキ
シ樹脂の割合が5重量%未満であると、内部応力の低減
効果が小さく、40重量%を超えると、樹脂の硬化速度
が著しく遅くなって、好ましくない。
The mixing ratio of these alkyl-type bifunctional epoxy resins is preferably 5 to 40% by weight in the epoxy resin (A). When the proportion of the alkyl-type bifunctional epoxy resin is less than 5% by weight, the effect of reducing the internal stress is small, and when it exceeds 40% by weight, the curing speed of the resin becomes extremely slow, which is not preferable.

【0009】本発明に用いる(A)エポキシ樹脂におけ
るアルキル型2官能エポキシ樹脂以外のエポキシ樹脂と
しては、1分子中に2個以上のエポキシ基を有する、硬
化可能な液状エポキシ樹脂であればよく、例えば、ビス
フェノールA型エポキシ樹脂、ビスフェノールF型エポ
キシ樹脂、ビスフェノールAD型エポキシ樹脂、ノボラ
ック型エポキシ樹脂、グリシジルエステル型エポキシ樹
脂、脂環式エポキシ樹脂等の液状のものが好ましく、こ
れらのエポキシ樹脂は、単独又は2種以上混合して使用
することができる。
The epoxy resin other than the alkyl type bifunctional epoxy resin in the epoxy resin (A) used in the present invention may be a curable liquid epoxy resin having two or more epoxy groups in one molecule. For example, bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol AD type epoxy resin, novolak type epoxy resin, glycidyl ester type epoxy resin, alicyclic epoxy resin and the like are preferable, and these epoxy resins are preferably They can be used alone or in combination of two or more.

【0010】また、上記のエポキシ樹脂の他に、含複素
環エポキシ樹脂、水添型ビスフェノールA型エポキシ樹
脂、脂肪族エポキシ樹脂、芳香族、脂肪族もしくは脂環
式のカルボン酸とエピクロルヒドリンとの反応によって
得られるエポキシ樹脂、スピロ環含有エポキシ樹脂等を
適宜併用しても差支えない。
In addition to the above-mentioned epoxy resins, a reaction between a heterocyclic epoxy resin, a hydrogenated bisphenol A type epoxy resin, an aliphatic epoxy resin, an aromatic, aliphatic or alicyclic carboxylic acid and epichlorohydrin. The epoxy resin, spiro ring-containing epoxy resin and the like obtained by the above method may be used in combination as appropriate.

【0011】本発明に用いる(B)硬化剤としては、前
記した(A)エポキシ樹脂と反応し、硬化可能なもので
あれば、いかなるものでも使用でき、例えば、メチルヘ
キサヒドロフタル酸無水物、ノボラック型フェノール樹
脂、無水フタル酸誘導体等が挙げられる。これらは硬化
を阻害しない範囲において単独又は2種以上混合して使
用することができる。
As the curing agent (B) used in the present invention, any curing agent capable of reacting with the above-mentioned (A) epoxy resin and curing can be used, for example, methylhexahydrophthalic anhydride, Novolak-type phenol resins, phthalic anhydride derivatives, and the like. These can be used alone or as a mixture of two or more as long as curing is not inhibited.

【0012】本発明に用いる(C)硬化促進剤として
は、1−ベンジル−2−フェニルイミダゾール、2−ヘ
プタデシルイミダゾール、2−フェニル−4,5−ジヒ
ドロキシイミダゾール、2−フェニル−4−メチル−5
−ヒドロキシメチルイミダゾール、2,4−ジアミノ−
6−[2−メチルイミダゾリル−(1)]−エチル−s
−トリアジン、1−シアノエチル−2−ウンデシルイミ
ダゾール、2−エチル−4−メチルイミダゾール、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、トリス−
(2,6−ジメトキシフェニル)ホスフィン等のホスフ
ィン系化合物等が挙げられる。
The (C) curing accelerator used in the present invention includes 1-benzyl-2-phenylimidazole, 2-heptadecylimidazole, 2-phenyl-4,5-dihydroxyimidazole, 2-phenyl-4-methyl- 5
-Hydroxymethylimidazole, 2,4-diamino-
6- [2-methylimidazolyl- (1)]-ethyl-s
-Triazine, 1-cyanoethyl-2-undecylimidazole, 2-ethyl-4-methylimidazole, 1,
Amine compounds such as 8-diazabicyclo [5,4,0] undecene-7, triphenylphosphine, tris-
And phosphine-based compounds such as (2,6-dimethoxyphenyl) phosphine.

【0013】本発明に用いる(E)充填剤としては、溶
融シリカ、粉砕シリカ、タルク、炭酸カルシウム、水酸
化アルミニウム等が挙げられるが、近年の半導体封止用
途では、平均粒径20μm以下の溶融シリカが望まし
く、これらを単独又は2種以上任意の量を組み合わせ混
合して使用することができる。
As the filler (E) used in the present invention, fused silica, pulverized silica, talc, calcium carbonate, aluminum hydroxide and the like can be mentioned. Silica is desirable, and these can be used alone or as a mixture of two or more kinds in an arbitrary amount.

【0014】本発明の液状封止用樹脂組成物には、上述
したアルキル型2官能エポキシ樹脂を含むエポキシ樹
脂、硬化剤、硬化促進剤および充填剤を必須成分とする
が、本発明の目的に反しない範囲において、難燃剤、カ
ップリング剤、消泡剤、顔料、染料、その他成分を適宜
添加配合することができる。
The liquid sealing resin composition of the present invention comprises, as essential components, an epoxy resin containing the above-mentioned alkyl type bifunctional epoxy resin, a curing agent, a curing accelerator and a filler. A flame retardant, a coupling agent, an antifoaming agent, a pigment, a dye, and other components can be appropriately added and blended within a range that does not impair.

【0015】本発明の液状封止用樹脂組成物は、常法に
従い、上述した各成分を十分混合した後、更に三本ロー
ルにより混練処理を行い、その後、万能混合器などによ
り真空混合処理して、容易に製造することができる。
The resin composition for liquid encapsulation of the present invention is prepared by thoroughly mixing the above-mentioned components, kneading with a three-roll mill, and vacuum-mixing with a universal mixer or the like according to a conventional method. And can be easily manufactured.

【0016】[0016]

【作用】本発明の液状封止用樹脂組成物は、上述したア
ルキル型2官能エポキシ樹脂を含むエポキシ樹脂、硬化
剤、硬化促進剤および充填剤を必須成分として使用する
ことによって、従来使用されている汎用の樹脂組成物に
比べて、反り量の小さい液状封止用樹脂組成物の提供が
可能となった。
The liquid encapsulating resin composition of the present invention can be used conventionally by using an epoxy resin containing the above-mentioned alkyl-type bifunctional epoxy resin, a curing agent, a curing accelerator and a filler as essential components. It has become possible to provide a liquid sealing resin composition having a smaller amount of warpage than a general-purpose resin composition.

【0017】[0017]

【発明の実施の形態】次に、本発明を実施例によって具
体的に説明する。本発明は、これらの実施例によって限
定されるものではない。以下の実施例および比較例にお
いて「部」とは「重量部」を意味する。
Next, the present invention will be specifically described with reference to examples. The present invention is not limited by these examples. In the following Examples and Comparative Examples, “parts” means “parts by weight”.

【0018】実施例1 ビスフェノールF型エポキシ樹脂YL983U(油化シ
ェル社製、商品名)80部、1,6−ヘキサンジオール
ジグリシジルエーテル20部、フェノール樹脂のMEH
8000(明和化成社製、商品名)83部、溶融シリカ
(平均粒径7μm)200部、カップリング剤A−18
7(日本ユニカー社製、商品名)2.0部および硬化促
進剤ノバキュアーHX3941(旭化成工業社製、商品
名)10部を混練し、真空脱気して液状封止用樹脂組成
物を製造した。
Example 1 Bisphenol F type epoxy resin YL983U (trade name, manufactured by Yuka Shell Co., Ltd.) 80 parts, 1,6-hexanediol diglycidyl ether 20 parts, phenol resin MEH
8000 (manufactured by Meiwa Kasei Co., Ltd., 83 parts), fused silica (average particle size: 7 μm) 200 parts, coupling agent A-18
7 (manufactured by Nippon Unicar, trade name) and 10 parts of a curing accelerator Novacure HX3941 (manufactured by Asahi Chemical Industry Co., Ltd.) were kneaded and vacuum degassed to produce a liquid sealing resin composition. .

【0019】実施例2 ビスフェノールF型エポキシ樹脂YL983U(油化シ
ェル社製、商品名)100部、ポリプロピレングリコー
ルジグリシジルエーテル20部、フェノール樹脂のME
H8000(明和化成社製、商品名)83部、溶融シリ
カ(平均粒径7μm)200部、カップリング剤A−1
87(日本ユニカー社製、商品名)2.0部および硬化
促進剤ノバキュアーHX3941(旭化成工業社製、商
品名)10部を混練し、真空脱気して液状封止用樹脂組
成物を製造した。
Example 2 100 parts of bisphenol F type epoxy resin YL983U (trade name, manufactured by Yuka Shell Co., Ltd.), 20 parts of polypropylene glycol diglycidyl ether, ME of phenol resin
83 parts of H8000 (trade name, manufactured by Meiwa Kasei Co., Ltd.), 200 parts of fused silica (average particle size: 7 μm), coupling agent A-1
87 (manufactured by Nippon Unicar Co., Ltd., 2.0 parts) and 10 parts of a hardening accelerator Novacure HX3941 (manufactured by Asahi Kasei Kogyo Co., Ltd.) were kneaded, and vacuum degassed to produce a liquid sealing resin composition. .

【0020】比較例1 ビスフェノールF型エポキシ樹脂YL983U(油化シ
ェル社製、商品名)100部、フェノール樹脂のMEH
8000(明和化成社製、商品名)83部、溶融シリカ
(平均粒径7μm)200部、カップリング剤A−18
7(日本ユニカー社製、商品名)2.0部および硬化促
進剤ノバキュアーHX3941(旭化成工業社製、商品
名)10部を混練し、真空脱気して液状封止用樹脂組成
物を製造した。
Comparative Example 1 100 parts of bisphenol F type epoxy resin YL983U (trade name, manufactured by Yuka Shell Co., Ltd.) and MEH of phenol resin
8000 (manufactured by Meiwa Kasei Co., Ltd., 83 parts), fused silica (average particle size: 7 μm) 200 parts, coupling agent A-18
7 (manufactured by Nippon Unicar, trade name) and 10 parts of a curing accelerator Novacure HX3941 (manufactured by Asahi Chemical Industry Co., Ltd.) were kneaded and vacuum degassed to produce a liquid sealing resin composition. .

【0021】実施例1〜2および比較例1によって製造
した液状封止用樹脂組成物を用いて加熱硬化させた。こ
れらの液状および硬化物特性(粘度、ガラス転移点、弾
性率、反り量)を試験した。また、これらの液状樹脂組
成物を15mm角、厚さ350μmのチップあるいは3
0mm角、厚さ0.4mmのFR−5基板に塗布し、こ
れを加熱硬化(150℃×1hr)させ、冷却後これら
の反り量を測定した。表1にこれらの評価結果をまとめ
た。
The liquid sealing resin compositions prepared in Examples 1 and 2 and Comparative Example 1 were cured by heating. The properties of these liquid and cured products (viscosity, glass transition point, elastic modulus, warpage) were tested. A 15 mm square chip having a thickness of 350 μm or 3 mm
A 0 mm square, 0.4 mm thick FR-5 substrate was applied and cured by heating (150 ° C. × 1 hr). After cooling, the amount of warpage was measured. Table 1 summarizes these evaluation results.

【0022】[0022]

【表1】 表1から、実施例で得られた液状封止用樹脂組成物は、
比較例のそれに比べ、ガラス転移点および弾性率の低い
硬化物が得られ、反り量を低減できることが確認され
た。
[Table 1] From Table 1, the liquid sealing resin composition obtained in the examples,
It was confirmed that a cured product having a lower glass transition point and a lower elastic modulus than that of the comparative example was obtained, and the amount of warpage could be reduced.

【0023】[0023]

【発明の効果】以上の説明および表1から明らかなよう
に、本発明の液状封止用樹脂組成物は、アルキル型2官
能エポキシ樹脂を配合したことにより、反り量の小さい
液状封止用樹脂組成物とすることができた。従って、本
発明の液状封止用樹脂組成物によれば、信頼性の高い半
導体装置を得ることができる。
As apparent from the above description and Table 1, the liquid encapsulating resin composition of the present invention has a small warpage due to the compounding of the alkyl type bifunctional epoxy resin. A composition could be obtained. Therefore, according to the liquid sealing resin composition of the present invention, a highly reliable semiconductor device can be obtained.

フロントページの続き Fターム(参考) 4J002 CC033 CD01X CD05W DE148 DE238 DJ018 DJ048 EL136 EU117 EU137 EU187 EW147 FA088 FD018 FD143 FD146 FD157 GQ05 4J036 AA01 AA05 AB01 AB10 AD08 DB21 DB22 DC40 DC45 DC46 DD07 FA03 FA05 FB08 JA07 4M109 AA01 BA03 CA05 EA03 EB02 EB04 EB13 EC04 Continued on the front page F-term (reference) 4J002 CC033 CD01X CD05W DE148 DE238 DJ018 DJ048 EL136 EU117 EU137 EU187 EW147 FA088 FD018 FD143 FD146 FD157 GQ05 4J036 AA01 AA05 AB01 AB10 AD08 DB21 DB22 DC40 DC45 DC46 DD07 FA03 FA05 FB08 JA03 4 EB04 EB13 EC04

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (A)アルキル型2官能エポキシ樹脂を
含むエポキシ樹脂、 (B)硬化剤 (C)硬化促進剤および (D)充填剤 を必須成分とすることを特徴とする液状封止用樹脂組成
物。
1. A liquid sealing composition comprising (A) an epoxy resin containing an alkyl type bifunctional epoxy resin, (B) a curing agent, (C) a curing accelerator, and (D) a filler as essential components. Resin composition.
JP2000342861A 2000-11-10 2000-11-10 Liquid sealing resin composition Pending JP2002145985A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000342861A JP2002145985A (en) 2000-11-10 2000-11-10 Liquid sealing resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000342861A JP2002145985A (en) 2000-11-10 2000-11-10 Liquid sealing resin composition

Publications (1)

Publication Number Publication Date
JP2002145985A true JP2002145985A (en) 2002-05-22

Family

ID=18817333

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000342861A Pending JP2002145985A (en) 2000-11-10 2000-11-10 Liquid sealing resin composition

Country Status (1)

Country Link
JP (1) JP2002145985A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011157552A (en) * 2009-05-13 2011-08-18 Hitachi Chem Co Ltd Adhesive composition, adhesive sheet for connecting circuit member, and method for producing semiconductor device
TWI404740B (en) * 2005-09-26 2013-08-11 Tokai Carbon Kk Isolation material for fuel cell and manufacturing method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI404740B (en) * 2005-09-26 2013-08-11 Tokai Carbon Kk Isolation material for fuel cell and manufacturing method thereof
JP2011157552A (en) * 2009-05-13 2011-08-18 Hitachi Chem Co Ltd Adhesive composition, adhesive sheet for connecting circuit member, and method for producing semiconductor device

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