JPH1060228A - Epoxy resin composition for semiconductor sealing - Google Patents
Epoxy resin composition for semiconductor sealingInfo
- Publication number
- JPH1060228A JPH1060228A JP22523796A JP22523796A JPH1060228A JP H1060228 A JPH1060228 A JP H1060228A JP 22523796 A JP22523796 A JP 22523796A JP 22523796 A JP22523796 A JP 22523796A JP H1060228 A JPH1060228 A JP H1060228A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- silicone oil
- resin composition
- resin
- weight
- 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.)
- Withdrawn
Links
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 30
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 30
- 239000000203 mixture Substances 0.000 title claims abstract description 10
- 239000004065 semiconductor Substances 0.000 title claims description 15
- 238000007789 sealing Methods 0.000 title description 3
- 229920002545 silicone oil Polymers 0.000 claims abstract description 34
- 239000011342 resin composition Substances 0.000 claims abstract description 16
- 239000005011 phenolic resin Substances 0.000 claims abstract description 14
- 239000011256 inorganic filler Substances 0.000 claims abstract description 10
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 10
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 9
- 238000005538 encapsulation Methods 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 15
- -1 curing promoter Substances 0.000 abstract description 8
- 239000000843 powder Substances 0.000 abstract description 7
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract description 4
- 229920001568 phenolic resin Polymers 0.000 abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 3
- 229930185605 Bisphenol Natural products 0.000 abstract description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract description 2
- 239000005350 fused silica glass Substances 0.000 abstract description 2
- 238000005476 soldering Methods 0.000 abstract description 2
- 229910000679 solder Inorganic materials 0.000 description 15
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 238000013329 compounding Methods 0.000 description 6
- 239000012778 molding material Substances 0.000 description 6
- 238000000465 moulding Methods 0.000 description 6
- 229920003986 novolac Polymers 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 125000003700 epoxy group Chemical group 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- USFPINLPPFWTJW-UHFFFAOYSA-N tetraphenylphosphonium Chemical compound C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 USFPINLPPFWTJW-UHFFFAOYSA-N 0.000 description 3
- CQOZJDNCADWEKH-UHFFFAOYSA-N 2-[3,3-bis(2-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC=CC=C1CCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O CQOZJDNCADWEKH-UHFFFAOYSA-N 0.000 description 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 125000003396 thiol group Chemical class [H]S* 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- 239000011800 void material Substances 0.000 description 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 229910002026 crystalline silica Inorganic materials 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000005007 epoxy-phenolic resin Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、内部及び外部ボイ
ドが少なく、かつ耐半田クラック性、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 has few internal and external voids, and is excellent in solder crack resistance and moisture resistance reliability.
【0002】[0002]
【従来の技術】IC本体を機械的、化学的作用から保護
するために、エポキシ樹脂系半導体封止用樹脂組成物が
開発、生産されてきた。ICに必要な特性を満足させる
ために、半導体封止用樹脂組成物には各種の性能が要求
されている。近年の要求項目としては、耐半田クラック
特性の向上がある。耐半田クラック特性を向上させるた
めに半導体封止用樹脂組成物の吸水率を低減する必要が
あるが、そのためには無機充填材の配合量を従来以上に
増加させる必要がある。配合量が多すぎると、封止用樹
脂に均一に分散できず、成形時にボイドが多発するとい
う現象が生じる。発生するボイドを低減するために、粘
度が高い樹脂を用いたり、無機充填材の粒度分布を変更
するなど、各種の手法が試みられた。ボイドの低減に効
果のあるものとして、ポリエチレンオキサイドとポリプ
ロピレンオキサイドのブロックコポリマーをシリコーン
主鎖にグラフト又はブロック共重合させた構造のシリコ
ーンオイルの添加が挙げられる(特公平2−36148
号公報)。しかし、この手法は現在の表面実装材に適用
した場合、ボイド低減効果が十分には発現しなかった。
更に、これらのシリコーンオイルの添加によって、耐半
田クラック性の低下、特に各種金属との密着性が低下す
ることも問題であった。2. Description of the Related Art Epoxy resin-based resin compositions for semiconductor encapsulation have been developed and manufactured to protect IC bodies from mechanical and chemical actions. In order to satisfy the characteristics required for ICs, various properties are required for the resin composition for semiconductor encapsulation. A recent requirement is an improvement in solder crack resistance. Although it is necessary to reduce the water absorption of the resin composition for semiconductor encapsulation in order to improve the solder crack resistance, it is necessary to increase the compounding amount of the inorganic filler more than before. If the compounding amount is too large, it cannot be uniformly dispersed in the sealing resin, and a phenomenon that voids frequently occur during molding occurs. In order to reduce the generated voids, various techniques such as using a resin having a high viscosity or changing the particle size distribution of the inorganic filler have been tried. An example of an effective method for reducing voids is the addition of silicone oil having a structure in which a block copolymer of polyethylene oxide and polypropylene oxide is grafted or block-copolymerized onto a silicone main chain (Japanese Patent Publication No. 2-36148).
No.). However, when this method was applied to current surface mount materials, the effect of reducing voids was not sufficiently exhibited.
Further, the addition of these silicone oils also has a problem that the solder crack resistance is reduced, particularly the adhesion to various metals is reduced.
【0003】[0003]
【発明が解決しようとする課題】本発明は、上記の欠点
を解決するために鋭意研究をした結果、成形時の流動中
の樹脂が不均一である場合、流動先端は非常に不均一と
なり空隙ができ易く、ボイドが多発することに注目し、
内部、外部ボイドの発生を少なくすることの可能な半導
体封止用樹脂組成物の開発を目的とするものであり、同
時に、各種金属成分との密着性を向上させることによ
り、耐半田クラック性に優れた半導体封止用エポキシ樹
脂組成物を提供するものである。As a result of intensive studies to solve the above-mentioned drawbacks, the present invention has found that when the resin flowing during molding is non-uniform, the leading edge of the flow becomes very non-uniform and voids are generated. Noting that voids occur frequently,
The purpose is to develop a resin composition for semiconductor encapsulation that can reduce the occurrence of internal and external voids.At the same time, by improving the adhesion to various metal components, solder crack resistance is improved. An object of the present invention is to provide an excellent epoxy resin composition for semiconductor encapsulation.
【0004】[0004]
【課題を解決するための手段】本発明は、エポキシ樹
脂、フェノール樹脂硬化剤、硬化促進剤、無機充填材、
及び下記式で示されるシリコーンオイルからなり、全樹
脂組成物中のシリコーンオイルの量が0.02〜4重量
%であることを特徴とする半導体封止用エポキシ樹脂組
成物である。The present invention provides an epoxy resin, a phenol resin curing agent, a curing accelerator, an inorganic filler,
And a silicone oil represented by the following formula, wherein the amount of the silicone oil in the total resin composition is 0.02 to 4% by weight.
【化2】 Embedded image
【0005】[0005]
【発明の実施の形態】以下に各成分について説明する。
本発明で用いられるエポキシ樹脂は、分子中に2個以上
のエポキシ基を有するものならば特に限定するものでは
ないが、好ましいものとしては、例えば、オルソクレゾ
ールノボラック型エポキシ樹脂、フェノールノボラック
型エポキシ樹脂、ビスフェノール型エポキシ樹脂、ビフ
ェニル型エポキシ樹脂、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、スチルベン型エポキシ樹脂、ジシクロペンタジエ
ン型エポキシ樹脂、イミド変性エポキシ樹脂、更にこれ
らのシリコーン変性物等が挙げられ、これらは単独でも
混合して用いても差し支えない。エポキシ当量や軟化点
に関しても特に限定するものではない。BEST MODE FOR CARRYING OUT THE INVENTION Each component will be described below.
The epoxy resin used in the present invention is not particularly limited as long as it has two or more epoxy groups in a molecule, and is preferably, for example, an orthocresol novolak type epoxy resin, a phenol novolak type epoxy resin. , Bisphenol type epoxy resin, biphenyl type epoxy resin, triphenol methane type epoxy resin, alkyl modified triphenol methane type epoxy resin, stilbene type epoxy resin, dicyclopentadiene type epoxy resin, imide modified epoxy resin, and silicone modified products thereof And these may be used alone or as a mixture. The epoxy equivalent and the softening point are not particularly limited.
【0006】本発明で用いられるフェノール樹脂硬化剤
は、分子中に水酸基を有するものならば特に限定するも
のではないが、好ましいものとしては、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、ジシ
クロペンタジエン変性フェノール樹脂、パラキシリレン
変性フェノール樹脂、トリフェノールメタン型フェノー
ル樹脂、テルペン変性フェノール樹脂、イミド変性フェ
ノール樹脂、更にこれらのシリコーン変性物等が挙げら
れ、これらは単独でも混合して用いても差し支えない。
更に水酸基当量や軟化点に関しても特に限定するもので
はない。全樹脂組成物中のエポキシ樹脂とフェノール樹
脂の合計量は5〜35重量%が好ましい。5重量%未満
だと成形時の流動性が劣り、35重量%を越えると耐半
田クラック性が劣る。[0006] The phenolic resin curing agent used in the present invention is not particularly limited as long as it has a hydroxyl group in the molecule. Preferred examples thereof include phenol novolak resin, cresol novolak resin, and dicyclopentadiene-modified resin. Examples thereof include phenol resins, paraxylylene-modified phenol resins, triphenolmethane-type phenol resins, terpene-modified phenol resins, imide-modified phenol resins, and silicone-modified products thereof. These may be used alone or in combination.
Further, the hydroxyl equivalent and the softening point are not particularly limited. The total amount of the epoxy resin and the phenol resin in the entire resin composition is preferably from 5 to 35% by weight. If it is less than 5% by weight, the fluidity during molding is poor, and if it exceeds 35% by weight, the solder crack resistance is poor.
【0007】本発明に用いられる硬化促進剤は、エポキ
シ基と水酸基の硬化反応を促進させるものならばよく、
一般に半導体封止用樹脂組成物に使用されているものを
広く利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、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、ベンジルジメチルアミン、2−メチルイ
ミダゾール、テトラフェニルホスフォニウム・テトラ安
息酸ボレート、テトラフェニルホスフォニウム・テトラ
ナフトエ酸ボレート等が挙げられ、単独でも混合して用
いても差し支えない。全樹脂組成物中の硬化促進剤量
は、0.01〜1重量%が好ましい。0.01重量%未
満だと硬化不充分で、1重量%を越えると硬化が速すぎ
て充分な流動性が得られない。The curing accelerator used in the present invention may be any as long as it promotes a curing reaction between an epoxy group and a hydroxyl group.
What is generally used for the resin composition for semiconductor encapsulation can be widely used. For example, 1,8-diazabicyclo (5,4,0) undecene-7, triphenylphosphine, tetraphenylphosphonium / tetraphenylborate, benzyldimethylamine, 2-methylimidazole, tetraphenylphosphonium / tetrabenzoic acid Borates, tetraphenylphosphonium / tetranaphthoic acid borate, and the like can be mentioned, and they may be used alone or as a mixture. The amount of the curing accelerator in the entire resin composition is preferably from 0.01 to 1% by weight. If it is less than 0.01% by weight, curing is insufficient, and if it exceeds 1% by weight, curing is too fast to obtain sufficient fluidity.
【0008】本発明で用いられる無機充填材としては、
溶融シリカ粉末、球状シリカ粉末、結晶シリカ粉末、2
次凝集シリカ粉末、アルミナ等が挙げられ、特に半導体
封止用樹脂組成物の流動性の向上の点から、球状シリカ
粉末が望ましい。球状シリカ粉末の形状は、流動性改善
のために、粒子自体の形状は限りなく真球状であること
が望ましく、更に粒度分布がブロードで有ることが望ま
しい。全樹脂組成物中の無機充填材量は、65〜93重
量%が好ましい。65未満だと耐半田性が劣り、93重
量%を越えると充分な流動性がが得られない。The inorganic filler used in the present invention includes:
Fused silica powder, spherical silica powder, crystalline silica powder, 2
Sub-agglomerated silica powder, alumina and the like are mentioned, and in particular, spherical silica powder is desirable from the viewpoint of improving the fluidity of the resin composition for semiconductor encapsulation. Regarding the shape of the spherical silica powder, in order to improve the fluidity, it is desirable that the shape of the particles themselves be infinitely spherical and that the particle size distribution be broad. The amount of the inorganic filler in the entire resin composition is preferably from 65 to 93% by weight. If it is less than 65, the solder resistance is poor, and if it exceeds 93% by weight, sufficient fluidity cannot be obtained.
【0009】本発明に用いられるシリコーンオイルは、
本発明における技術上の重要なポイントであるので詳細
に説明する。通常、シリコーンオイルはポリジメチルシ
ロキサンをその基本骨格としているが、本発明に用いら
れるシリコーンオイルはこれとは異なり、主鎖のSiO
単位のR(フェニル、フェネチル、エポキシ、メルカプ
ト、アルコキシ)が結合しており、従来のポリジメチル
シロキサンとは著しく異なる特性を有している。従来の
ポリジメチルシロキサンの場合、シリコーンオイル分子
はαヘリックス状態、即ち螺旋状態で熱的に安定してい
るので、シリコーンオイル分子は表面にメチル基を有し
ており、疎水性で表面張力の小さい構造を有している。
しかし本発明に用いられるシリコーンオイルは、SiO
単位のうち80モル%以上にメチル基以外の官能基のR
が結合しているために、オイル分子は螺旋構造が取れ
ず、分子の表面にはメチル基以外のRやSiOが露出し
た状態になる。その為に本発明に用いられるシリコーン
オイルは、シリコーンオイルの特徴である疎水性を有し
ている上に、SiO単位による親水性を有し、更に官能
基Rのためにエポキシ樹脂及び各種金属に対する親和性
や反応性を有しているという大きな特徴がある。The silicone oil used in the present invention comprises:
Since this is an important technical point in the present invention, it will be described in detail. Normally, silicone oil has polydimethylsiloxane as its basic skeleton, but the silicone oil used in the present invention is different from this, and the main chain SiO
The unit R (phenyl, phenethyl, epoxy, mercapto, alkoxy) is bonded, and has characteristics significantly different from those of conventional polydimethylsiloxane. In the case of conventional polydimethylsiloxane, since silicone oil molecules are thermally stable in an α-helix state, that is, a helical state, the silicone oil molecules have a methyl group on the surface and are hydrophobic and have low surface tension. It has a structure.
However, the silicone oil used in the present invention is SiO 2
80% by mole or more of the functional groups other than the methyl group
Are bonded to each other, the oil molecule cannot take a helical structure, and R and SiO other than the methyl group are exposed on the surface of the molecule. Therefore, the silicone oil used in the present invention has not only the hydrophobicity characteristic of the silicone oil, but also the hydrophilicity of the SiO unit, and further has a functional group R for epoxy resin and various metals. There is a great feature that it has affinity and reactivity.
【0010】本発明のシリコーンオイルは、親水、疎水
の両方を有した両親媒性のため、界面活性効果を有し、
無機充填材と樹脂を均一分散できるので、成形時のボイ
ドが低減できる。各種金属に対する親和性が有るため
に、ICパッケージ内部で各種金属(42合金、銅、A
g,Au)と良好に密着し、耐半田クラック特性が向上
する。The silicone oil of the present invention has both hydrophilic and hydrophobic amphipathic properties and therefore has a surfactant effect.
Since the inorganic filler and the resin can be uniformly dispersed, voids during molding can be reduced. Due to its affinity for various metals, various metals (42 alloy, copper, A
g, Au), and the solder crack resistance is improved.
【0011】本発明に用いられるシリコーンオイル中の
官能基Rは、フェニル基、フェネチル基、エポキシ基、
脂環式エポキシ基、メルカプト基、アルコキシ基のいず
れかである。これら官能基は、同一でも、異なっていて
もよい。nは2〜300である。2未満では粘度が低す
ぎて揮発しやすく成形品のボイドの数が増える。300
を越えると封止用樹脂との相溶性が低下し、ボイドの低
減と耐半田クラック性の向上の両方の効果が発現しな
い。また、mは、0以上である。ただし、m/(m+
n)は0.2以下である必要がある。m=0、即ちジメ
チルシロキサンユニットは存在しなくても問題ない。更
に、m/(m+n)が0.2を越えると、従来のポリジ
メチルシロキサンの特徴がでてきて基材に対する密着力
の低下のため耐半田クラック性が低下するので好ましく
ない。The functional group R in the silicone oil used in the present invention is a phenyl group, a phenethyl group, an epoxy group,
An alicyclic epoxy group, a mercapto group, or an alkoxy group. These functional groups may be the same or different. n is 2 to 300. If it is less than 2, the viscosity is too low and it tends to volatilize, and the number of voids in the molded product increases. 300
If the ratio exceeds the range, the compatibility with the sealing resin is reduced, and both effects of reducing voids and improving solder crack resistance are not exhibited. M is 0 or more. However, m / (m +
n) needs to be 0.2 or less. There is no problem if m = 0, that is, no dimethylsiloxane unit is present. Further, if m / (m + n) exceeds 0.2, the characteristics of the conventional polydimethylsiloxane appear, and the solder cracking resistance decreases due to a decrease in the adhesion to the substrate, which is not preferable.
【0012】本発明で使用するシリコーンオイルの添加
量は特には限定しないが、全樹脂組成物100重量%中
の0.02〜4重量%が好ましい。0.02重量%未満
ではシリコーンオイルの効果がなく、成形品のボイドが
低減しない。4重量%を越えると、成形品の機械的強度
が低下して耐半田性が低下する。更に本発明で使用する
シリコーンオイルは、他のシリコーンオイルと併用して
も問題ない。但し併用するシリコーンオイルは、全シリ
コーンオイル中30%重量以下好ましい。30重量%を
越えると、耐半田クラック性やボイド特性が低減する。The amount of the silicone oil used in the present invention is not particularly limited, but is preferably 0.02 to 4% by weight based on 100% by weight of the whole resin composition. If the amount is less than 0.02% by weight, the effect of the silicone oil is not obtained, and the voids of the molded product are not reduced. If it exceeds 4% by weight, the mechanical strength of the molded product is reduced, and the solder resistance is reduced. Further, the silicone oil used in the present invention can be used in combination with another silicone oil without any problem. However, the silicone oil used in combination is preferably 30% by weight or less of the total silicone oil. If it exceeds 30% by weight, solder crack resistance and void characteristics are reduced.
【0013】本発明の半導体封止用樹脂組成物には、必
要に応じてカーボンブラック等の着色剤、ブロム化エポ
キシ樹脂、三酸化アンチモン等の難燃剤、γ−グリシド
キシプロピルトリメトキシシラン等のカップリング剤、
ゴム等の低応力成分、カルナバワックス等のワックス成
分を添加することができる。本発明の半導体封止用樹脂
組成物は、エポキシ樹脂、フェノール樹脂硬化剤、硬化
促進剤、シリコーンオイル、無機充填材、その他添加剤
をミキサーにて常温混合し、ロール、押し出し機等の混
練機にて混練し、冷却後粉砕し成形材料とする。The resin composition for encapsulating a semiconductor of the present invention may contain, if necessary, a coloring agent such as carbon black, a brominated epoxy resin, a flame retardant such as antimony trioxide, γ-glycidoxypropyltrimethoxysilane and the like. Coupling agent,
Low stress components such as rubber and wax components such as carnauba wax can be added. The resin composition for encapsulating a semiconductor of the present invention comprises an epoxy resin, a phenol resin curing agent, a curing accelerator, a silicone oil, an inorganic filler, and other additives mixed at room temperature with a mixer, and a kneader such as a roll or an extruder. , And after cooling, pulverized to obtain a molding material.
【0014】以下本発明を実施例にて具体的に説明す
る。 《実施例1》 下記組成物 ビフェニル型エポキシ樹脂(E−1) 10.5重量部 フエノールノボラック樹脂(H−1) 7.3重量部 球状シリカ(平均粒径15μm) 80.0重量部 1,8-ジアザビシクロ(5,4,0)ウンデセン-7 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 0.2重量部 臭素化フェノールノボラック型エポキシ樹脂 0.5重量部 三酸化アンチモン 0.4重量部 γ−グリシドキシトリメトキシシラン 0.2重量部 シリコーンオイル(S−1) 0.5重量部 を、ミキサーにて常温混合し、100℃で二軸ロールに
て混練し、冷却後粉砕し成形材料とし、得られた材料を
ドライエアーで乾燥させて材料化を完了させた。成形材
料のボイドの有無、耐半田クラック性の評価を行った。
その結果を表1に示す。Hereinafter, the present invention will be described specifically with reference to Examples. << Example 1 >> The following composition Biphenyl type epoxy resin (E-1) 10.5 parts by weight Phenol novolak resin (H-1) 7.3 parts by weight Spherical silica (average particle diameter 15 μm) 80.0 parts by weight 1, 8-diazabicyclo (5,4,0) undecene-7 0.2 parts by weight Carbon black 0.2 parts by weight Carnauba wax 0.2 parts by weight Brominated phenol novolak epoxy resin 0.5 parts by weight Antimony trioxide 0.4 Parts by weight γ-glycidoxytrimethoxysilane 0.2 parts by weight Silicone oil (S-1) 0.5 parts by weight was mixed at room temperature with a mixer, kneaded at 100 ° C. with a biaxial roll, cooled and ground. The resulting material was dried with dry air to complete the materialization. The presence or absence of voids in the molding material and the solder crack resistance were evaluated.
Table 1 shows the results.
【0015】《評価方法》 ・ボイドの評価:160pQFP(28×28mmの1
60pQFP)を成形温度;175℃、注入時間;15
秒、硬化時間;120秒(注入時間を含む)、予熱時
間;80℃の条件で成形し、成形品の内部ボイドの数を
超音波探傷機により確認した。4パッケージ中の外部お
よび内部のボイド数(0.5mmφ以上のサイズのも
の)を合計し、1パッケージ当たりに換算してボイド数
とする。 ・耐半田クラック性評価:80pQFP(厚さ1.5m
m)を成形し、ポストキュア後、恒温恒室槽中で85℃
/85%で168時間処理する。処理直後、IRリフロ
ー炉によって240℃、10秒の処理を行い、リフロー
処理の後、超音波探傷機を利用してパッケージの内部の
剥離状況を観察する。8パッケージ中に何パッケージに
剥離が発生しているかを評価する。半田後の剥離パッケ
ージ数とする。<< Evaluation Method >> Evaluation of void: 160 pQFP (1 × 28 × 28 mm)
60 pQFP) at molding temperature; 175 ° C., injection time;
Molding was performed under the conditions of seconds, curing time: 120 seconds (including the injection time), preheating time: 80 ° C., and the number of internal voids in the molded product was confirmed by an ultrasonic flaw detector. The number of voids inside and outside of the four packages (one having a size of 0.5 mmφ or more) is summed and converted into the number of voids per package. -Solder crack resistance evaluation: 80pQFP (1.5m thickness)
m), after post-curing, in a constant temperature and constant temperature bath at 85 ° C.
Treat at / 85% for 168 hours. Immediately after the treatment, a treatment is performed at 240 ° C. for 10 seconds using an IR reflow furnace. After the reflow treatment, the peeling state inside the package is observed using an ultrasonic flaw detector. Evaluate how many packages have peeled out of 8 packages. The number of peeled packages after soldering.
【0016】《実施例2〜12》シリコーンオイルの種
類[(S−2)〜(S−12)]を代えた以外は実施例
1と同一の配合割合で成形材料を得、同様に評価した。
その結果を表1に示す。 《実施例13〜15、比較例1〜3》実施例15はシリ
コーンオイル(S−1)とシリコーンオイル(S−1
5)を併用し、実施例13、14及び比較例1〜3はシ
リコーンオイル(S−1)の添加量を代えた以外は、実
施例1と同一の配合割合で成形材料を得、同様に評価し
た。但し、シリコーンオイルを増減した分は球状シリカ
を増減して調節した。その結果を表2に示す。 《実施例16〜20》エポキシ樹脂の種類[(E−1)
〜(E−5)]及びフェノール樹脂硬化剤の種類[(H
−1)〜(H−3)]を使用し、[エポキシ樹脂+フェ
ノール樹脂硬化剤]NO添加量が17.8重量部になる
ようにした以外は実施例1と同一の配合割合で成形材料
を得、同様に評価した。その結果を表2に示す。 《比較例4〜7》本発明で使用するシリコーンオイル以
外のシリコーンオイル[(S−13)〜(S−16)]
を使用した以外は、実施例1と同一の配合割合で成形材
料を得、同様に評価した。その結果を表2に示す。Examples 2 to 12 A molding material was obtained at the same compounding ratio as in Example 1 except that the type of silicone oil [(S-2) to (S-12)] was changed, and evaluated in the same manner. .
Table 1 shows the results. << Examples 13 to 15 and Comparative Examples 1 to 3 >> In Example 15, silicone oil (S-1) and silicone oil (S-1) were used.
5) was used in combination, and in Examples 13 and 14 and Comparative Examples 1 to 3, molding materials were obtained in the same compounding ratio as in Example 1 except that the amount of addition of the silicone oil (S-1) was changed. evaluated. However, the amount by which the silicone oil was increased or decreased was adjusted by increasing or decreasing the spherical silica. Table 2 shows the results. << Examples 16 to 20 >> Types of epoxy resin [(E-1)
~ (E-5)] and the type of phenol resin curing agent [(H
-1) to (H-3)] and [Epoxy resin + phenol resin curing agent] molding material in the same compounding ratio as in Example 1 except that the added amount of NO was 17.8 parts by weight. And evaluated similarly. Table 2 shows the results. << Comparative Examples 4-7 >> Silicone oils other than the silicone oil used in the present invention [(S-13) to (S-16)]
A molding material was obtained at the same compounding ratio as in Example 1 except for using, and the same evaluation was performed. Table 2 shows the results.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】実施例及び比較例で使用したシリコーンオ
イル、エポキシ樹脂及びフェノール樹脂硬化剤の種類は
下記のとおりである。The types of silicone oils, epoxy resins and phenolic resin curing agents used in the examples and comparative examples are as follows.
【化3】 Embedded image
【0020】[0020]
【化4】 Embedded image
【0021】[0021]
【化5】 Embedded image
【0022】[0022]
【化6】 Embedded image
【0023】[0023]
【化7】 Embedded image
【0024】[0024]
【化8】 Embedded image
【0025】[0025]
【化9】 Embedded image
【0026】[0026]
【発明の効果】本発明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することにより、ボイドが
少なく、信頼性が高く、かつ耐半田クラック性に優れた
半導体装置を得ることができる。従って、ドライパック
が不要となり工数削減、コスト削減に大きな効果があ
る。According to the present invention, by encapsulating a semiconductor element using the epoxy resin composition for semiconductor encapsulation of the present invention, it is possible to obtain a semiconductor device having few voids, high reliability, and excellent solder crack resistance. Can be. Therefore, a dry pack is not required, which has a great effect on reduction of man-hours and cost.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C08K 3/00 NKT C08K 3/00 NKT H01L 23/29 H01L 23/30 R 23/31 ──────────────────────────────────────────────────の Continuation of the front page (51) Int.Cl. 6 Identification code Agency reference number FI Technical display location C08K 3/00 NKT C08K 3/00 NKT H01L 23/29 H01L 23/30 R 23/31
Claims (1)
硬化促進剤、無機充填剤、及び下記式で示されるシリコ
ーンオイルからなり、全樹脂組成物中のシリコーンオイ
ルの量が0.02〜4重量%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。 【化1】 An epoxy resin, a phenol resin curing agent,
An epoxy resin for semiconductor encapsulation comprising a curing accelerator, an inorganic filler, and a silicone oil represented by the following formula, wherein the amount of the silicone oil in the total resin composition is 0.02 to 4% by weight. Composition. Embedded image
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22523796A JPH1060228A (en) | 1996-08-27 | 1996-08-27 | Epoxy resin composition for semiconductor sealing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22523796A JPH1060228A (en) | 1996-08-27 | 1996-08-27 | Epoxy resin composition for semiconductor sealing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH1060228A true JPH1060228A (en) | 1998-03-03 |
Family
ID=16826150
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22523796A Withdrawn JPH1060228A (en) | 1996-08-27 | 1996-08-27 | Epoxy resin composition for semiconductor sealing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH1060228A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000128990A (en) * | 1998-10-27 | 2000-05-09 | Degussa Huels Ag | Sulfur-functional polyorganosiloxane, its production, rubber blend containing the same, production of the rubber blend, and molded form made therefrom |
| CN116925122A (en) * | 2023-07-17 | 2023-10-24 | 深圳市首骋新材料科技有限公司 | Organosiloxane monomer, organosiloxane sealant, preparation method thereof, thin film packaging method and flexible semiconductor device |
-
1996
- 1996-08-27 JP JP22523796A patent/JPH1060228A/en not_active Withdrawn
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000128990A (en) * | 1998-10-27 | 2000-05-09 | Degussa Huels Ag | Sulfur-functional polyorganosiloxane, its production, rubber blend containing the same, production of the rubber blend, and molded form made therefrom |
| CN116925122A (en) * | 2023-07-17 | 2023-10-24 | 深圳市首骋新材料科技有限公司 | Organosiloxane monomer, organosiloxane sealant, preparation method thereof, thin film packaging method and flexible semiconductor device |
| CN116925122B (en) * | 2023-07-17 | 2026-02-06 | 深圳市首骋新材料科技有限公司 | Organosiloxane monomer, organosiloxane sealant, preparation method thereof, thin film packaging method and flexible semiconductor device |
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