JPH0827252A - Epoxy resin composition and semiconductor sealing device - Google Patents
Epoxy resin composition and semiconductor sealing deviceInfo
- Publication number
- JPH0827252A JPH0827252A JP18677894A JP18677894A JPH0827252A JP H0827252 A JPH0827252 A JP H0827252A JP 18677894 A JP18677894 A JP 18677894A JP 18677894 A JP18677894 A JP 18677894A JP H0827252 A JPH0827252 A JP H0827252A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- resin composition
- silicon nitride
- nitride powder
- 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
Links
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 33
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 33
- 239000004065 semiconductor Substances 0.000 title claims abstract description 31
- 239000000203 mixture Substances 0.000 title claims abstract description 16
- 238000007789 sealing Methods 0.000 title abstract description 7
- 239000000843 powder Substances 0.000 claims abstract description 20
- 229910052581 Si3N4 Inorganic materials 0.000 claims abstract description 18
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 15
- 239000011342 resin composition Substances 0.000 claims abstract description 13
- 150000007530 organic bases Chemical class 0.000 claims abstract description 12
- 239000002245 particle Substances 0.000 claims abstract description 11
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000005011 phenolic resin Substances 0.000 claims abstract description 9
- 235000010290 biphenyl Nutrition 0.000 claims abstract description 5
- 239000004305 biphenyl Substances 0.000 claims abstract description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- 238000005538 encapsulation Methods 0.000 claims description 13
- 125000003700 epoxy group Chemical group 0.000 claims description 8
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims 1
- 229920001568 phenolic resin Polymers 0.000 claims 1
- 229910000679 solder Inorganic materials 0.000 abstract description 13
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004593 Epoxy Substances 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- 239000012778 molding material Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 238000010521 absorption reaction Methods 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- 239000011256 inorganic filler Substances 0.000 description 4
- 229910003475 inorganic filler Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 239000005350 fused silica glass Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000001721 transfer moulding Methods 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
- 239000001993 wax Substances 0.000 description 2
- 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
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- -1 cyclic organic bases Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000007429 general method Methods 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
- 230000017525 heat dissipation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000010680 novolac-type phenolic resin Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000005480 straight-chain fatty acid group Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
Landscapes
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、耐湿性、半田耐熱性、
成形性及び熱伝導性に優れたエポキシ樹脂組成物および
半導体封止装置に関する。The present invention relates to moisture resistance, solder heat resistance,
The present invention relates to an epoxy resin composition excellent in moldability and thermal conductivity and a semiconductor encapsulation device.
【0002】[0002]
【従来の技術】近年、半導体集積回路の分野において、
高集積化、高信頼性化の技術開発と同時に半導体装置の
実装工程の自動化が推進されている。例えばフラットパ
ッケージ型の半導体装置を回路基板に取り付ける場合
に、従来、リードピン毎に半田付けを行っていたが、最
近では半田浸漬方式や半田リフロー方式が採用されてい
る。2. Description of the Related Art In recent years, in the field of semiconductor integrated circuits,
At the same time as technology development for high integration and high reliability, automation of the mounting process of semiconductor devices is being promoted. For example, when mounting a flat package type semiconductor device on a circuit board, conventionally, soldering is performed for each lead pin, but recently, a solder dipping method or a solder reflow method has been adopted.
【0003】[0003]
【発明が解決しようとする課題】従来の半導体装置、す
なわちノボラック型エポキシ樹脂等のエポキシ樹脂、ノ
ボラック型フェノール樹脂および無機充填剤からなる樹
脂組成物によって封止した半導体装置は、装置全体の半
田浴浸漬を行うと耐湿性が低下するという欠点があっ
た。特に吸湿した半導体装置を浸漬すると、封止樹脂と
半導体チップ、あるいは封止樹脂とリードフレームとの
間の剥がれや、内部樹脂クラックが生じて著しい耐湿性
劣化を起こし、電極の腐蝕による断線や水分によるリー
ク電流を生じ、その結果、半導体装置は、長期間の信頼
性を保証することができないという欠点があった。A conventional semiconductor device, that is, a semiconductor device sealed with a resin composition comprising an epoxy resin such as a novolac type epoxy resin, a novolac type phenolic resin and an inorganic filler is a solder bath for the entire device. There is a drawback in that the moisture resistance is lowered by the immersion. In particular, when a semiconductor device that has absorbed moisture is dipped, peeling between the encapsulating resin and the semiconductor chip, or the encapsulating resin and the lead frame, and internal resin cracking cause significant deterioration in moisture resistance, causing disconnection and moisture due to electrode corrosion. As a result, there is a drawback that a semiconductor device cannot guarantee long-term reliability.
【0004】また、無機充填剤を高充填することによ
り、樹脂分の割合を少なくし、樹脂組成物の低吸湿化を
図ることができるが、無機質充填剤の高充填化に伴い流
動性が著しく損なわれるばかりでなく、樹脂等の有機分
と無機質充填剤との界面が多くなるため、内部樹脂クラ
ックがその界面を伝って外部樹脂クラックへと進行する
という欠点があった。Further, by highly filling the inorganic filler, the proportion of the resin component can be reduced and the moisture absorption of the resin composition can be reduced. However, the fluidity is remarkably increased as the inorganic filler is highly filled. Not only is it damaged, but the interface between the organic components such as the resin and the inorganic filler is increased, so that the internal resin crack propagates through the interface and progresses to the external resin crack.
【0005】さらに、高集積化に伴う半導体素子の発熱
量の増大により、パッケージ構造ばかりでなく、封止材
料においても熱伝導率のよい材料が求められつつある。
窒化珪素粉末は、溶融シリカ粉末に比べて熱伝導率が高
いため、これを充填剤として用いた場合、高い熱伝導率
が期待できるが、高充填化した際に良好な流動性が得ら
れないという欠点があった。Further, due to the increase in the amount of heat generated by the semiconductor element due to high integration, a material having a high thermal conductivity is being demanded not only for the package structure but also for the sealing material.
Since silicon nitride powder has higher thermal conductivity than fused silica powder, when it is used as a filler, high thermal conductivity can be expected, but good fluidity cannot be obtained when highly filled. There was a drawback.
【0006】本発明は、上記の欠点を解消するためにな
されたもので、吸湿の影響が少なく、特に半田浴浸漬後
の耐湿性、半田耐熱性、成形性、流動性、熱伝導性に優
れ、封止樹脂と半導体チップあるいは封止樹脂とリード
フレームとの間の剥がれや、内部樹脂クラックの発生が
なく、また電極の腐蝕による断線や水分によるリーク電
流の発生や金型摩耗もなく、長期信頼性を保証できるエ
ポキシ樹脂組成物および半導体封止装置を提供しようと
するものである。The present invention has been made in order to solve the above-mentioned drawbacks and is less affected by moisture absorption, and particularly excellent in moisture resistance after solder bath immersion, solder heat resistance, moldability, fluidity and thermal conductivity. No peeling between the encapsulation resin and the semiconductor chip or the encapsulation resin and the lead frame, no internal resin cracks, no wire breakage due to electrode corrosion, no leakage current due to moisture, and no die wear, and long-term It is intended to provide an epoxy resin composition and a semiconductor encapsulation device that can guarantee reliability.
【0007】[0007]
【課題を解決するための手段】本発明者らは、上記の目
的を達成しようと鋭意研究を重ねた結果、特定のエポキ
シ樹脂、特定のシランカップリング剤および窒化珪素粉
末を用いることによって、耐湿性、半田耐熱性、成形
性、熱伝導性に優れた樹脂組成物が得られることを見い
だし、本発明を完成したものである。As a result of intensive studies aimed at achieving the above object, the present inventors have found that moisture resistance is improved by using a specific epoxy resin, a specific silane coupling agent and a silicon nitride powder. It was found that a resin composition excellent in heat resistance, solder heat resistance, moldability, and thermal conductivity can be obtained, and the present invention has been completed.
【0008】即ち、本発明は、(A)次の一般式で示さ
れるビフェニル型エポキシ樹脂、That is, the present invention provides (A) a biphenyl type epoxy resin represented by the following general formula,
【0009】[0009]
【化5】 (B)フェノール樹脂、(C)有機塩基を極微量添加し
た、次の一般式で示されるエポキシ基を有するシランカ
ップリング剤、Embedded image (B) a phenol resin, (C) an silane coupling agent having an epoxy group represented by the following general formula, to which an organic base is added in a very small amount,
【0010】[0010]
【化6】R1 −Cn H2n−Si (OR2 )3 (但し、式中R1 はエポキシ基を有する原子団を、R2
はメチル基又はエチル基を、n は0 又は1 以上の整数を
それぞれ表す) (D)最大粒径が100 μm 以下の窒化珪素粉末および
(E)硬化促進剤を必須成分とし、全体の樹脂組成物に
対して前記(D)の窒化珪素粉末を25〜90重量%の割合
で含有してなることを特徴とするエポキシ樹脂組成物で
ある。また、このエポキシ樹脂組成物の硬化物によっ
て、半導体チップが封止されてなることを特徴とする半
導体封止装置である。Embedded image R 1 —C n H 2n —Si (OR 2 ) 3 (wherein R 1 is an atomic group having an epoxy group, R 2
Represents a methyl group or an ethyl group, and n represents an integer of 0 or 1 or more.) (D) A silicon nitride powder having a maximum particle size of 100 μm or less and (E) a curing accelerator are essential components, and the entire resin composition An epoxy resin composition comprising the above-mentioned (D) silicon nitride powder in a proportion of 25 to 90% by weight with respect to the product. A semiconductor encapsulation device is obtained by encapsulating a semiconductor chip with a cured product of this epoxy resin composition.
【0011】以下、本発明を詳細に説明する。The present invention will be described in detail below.
【0012】本発明に用いる(A)エポキシ樹脂は、前
記の一般式化5で示されるビフェニル型エポキシ樹脂が
使用される。また、このエポキシ樹脂には、ノボラック
系エポキシ樹脂、エピビス系エポキシ樹脂、その他の公
知のエポキシ樹脂を併用することができる。As the epoxy resin (A) used in the present invention, the biphenyl type epoxy resin represented by the above general formula 5 is used. In addition, a novolac-based epoxy resin, an epibis-based epoxy resin, and other known epoxy resins can be used in combination with this epoxy resin.
【0013】本発明に用いる(B)フェノール樹脂とし
ては、前記(A)のエポキシ樹脂のエポキシ基と反応し
得るフェノール性水酸基を分子中に2 個以上有するもの
であれば特に制限するものではない。具体的な化合物と
して例えばThe (B) phenol resin used in the present invention is not particularly limited as long as it has at least two phenolic hydroxyl groups in the molecule capable of reacting with the epoxy groups of the epoxy resin (A). . As a specific compound, for example,
【0014】[0014]
【化7】 (但し、n は0 又は1 以上の整数を表す)[Chemical 7] (However, n represents 0 or an integer of 1 or more)
【0015】[0015]
【化8】 (但し、n は0 又は1 以上の整数を表す)Embedded image (However, n represents 0 or an integer of 1 or more)
【0016】[0016]
【化9】 (但し、n は0 又は1 以上の整数を表す)[Chemical 9] (However, n represents 0 or an integer of 1 or more)
【0017】[0017]
【化10】 (但し、n は0 又は1 以上の整数を表す)[Chemical 10] (However, n represents 0 or an integer of 1 or more)
【0018】[0018]
【化11】 (但し、n は0 又は1 以上の整数を表す)等が挙げら
れ、これらは単独又は混合して使用することができる。[Chemical 11] (However, n represents 0 or an integer greater than or equal to 1) etc., These can be used individually or in mixture.
【0019】本発明に用いる(C)有機塩基を極微量添
加した、エポキシ基を有するシランカップリング剤とし
ては、前記の一般式化6で示されるものが使用される。
具体的なものとして、例えば、As the silane coupling agent having an epoxy group, to which an extremely small amount of the organic base (C) is added, which is used in the present invention, the one represented by the above general formula 6 is used.
As a concrete example, for example,
【0020】[0020]
【化12】 [Chemical 12]
【0021】[0021]
【化13】 等が挙げられ、これらは単独又は混合して使用すること
ができる。[Chemical 13] Etc., and these can be used alone or in combination.
【0022】このシランカップリング剤には極微量の有
機塩基を添加処理することが重要である。有機塩基で処
理することによって加水分解性を高めることができる。
ここで添加処理する有機塩基としては、ジメチルアミ
ン、ジエチルアミン、ピリジン、キノリン、ピペリジン
等の環状有機塩基を挙げることができ、これらは単独又
は2 種以上混合して使用することができる。有機塩基の
添加配合量は、シランカップリング剤に対して0.0005〜
0.05重量%の範囲内で使用することが望ましい。この配
合量が0.0005重量%未満ではシランカップリング剤の加
水分解を十分に促進することができず、また、0.05重量
%を超えると耐湿信頼性が低下して好ましくない。It is important to add a very small amount of organic base to the silane coupling agent. The hydrolyzability can be increased by treating with an organic base.
Examples of the organic base to be added here include cyclic organic bases such as dimethylamine, diethylamine, pyridine, quinoline and piperidine, and these can be used alone or in combination of two or more. The addition amount of the organic base is 0.0005 to the silane coupling agent.
It is desirable to use within the range of 0.05% by weight. If the content is less than 0.0005% by weight, the hydrolysis of the silane coupling agent cannot be sufficiently promoted, and if it exceeds 0.05% by weight, the moisture resistance reliability decreases, which is not preferable.
【0023】本発明に用いる(D)窒化珪素粉末として
は、不純物濃度が低く最大粒径が100 μm 以下ものが好
ましく使用される。また、充填剤を高充填化するため
に、不純物濃度が低く最大粒径が100 μm 以下の溶融シ
リカ粉末を併用することができる。これらの充填剤は、
平均粒径30μm 以下であることが望ましい。平均粒径が
30μm を超えると耐湿性および成形性が劣り好ましくな
い。窒化珪素粉末の配合割合は、全体の樹脂組成物に対
して25〜90重量%含有するように配合することが好まし
い。その割合が25重量%未満では樹脂組成物の吸湿性が
高く、半田浸漬後の耐湿性に劣り、また90重量%を超え
ると極端に流動性が悪くなり、成形性に劣り好ましくな
い。これらの窒化珪素粉末に、シランカップリング剤に
有機塩基を添加し、直ちにヘンシェルミキサー、スーパ
ーミキサー等で処理を行うと均一に表面処理ができ、そ
の効果が十分に発揮できる。The (D) silicon nitride powder used in the present invention preferably has a low impurity concentration and a maximum particle size of 100 μm or less. Further, in order to make the filler highly filled, a fused silica powder having a low impurity concentration and a maximum particle size of 100 μm or less can be used together. These fillers are
The average particle size is preferably 30 μm or less. Average particle size is
If it exceeds 30 μm, the moisture resistance and the moldability are deteriorated, which is not preferable. The silicon nitride powder is preferably blended in such an amount that it is contained in an amount of 25 to 90% by weight based on the total resin composition. When the proportion is less than 25% by weight, the hygroscopicity of the resin composition is high and the moisture resistance after solder immersion is poor, and when it exceeds 90% by weight, the fluidity is extremely deteriorated and the moldability is poor, which is not preferable. By adding an organic base to a silane coupling agent to these silicon nitride powders and immediately treating them with a Henschel mixer, a super mixer or the like, the surface can be uniformly treated and the effect can be sufficiently exhibited.
【0024】本発明に用いる(E)硬化促進剤として
は、リン系硬化促進剤、イミダゾール系硬化促進剤、D
BU系硬化促進剤その他の硬化促進剤等を広く使用する
ことができる。これらは単独又は2 種以上併用すること
ができる。硬化促進剤の配合割合は、全体の樹脂組成物
に対して0.01〜5 重量%含有するように配合することが
望ましい。その割合が0.01重量%未満では樹脂組成物の
ゲルタイムが長く、硬化特性も悪くなり、また、5 重量
%を超えると極端に流動性が悪くなって成形性に劣り、
さらに電気特性も悪くなり耐湿性に劣り好ましくない。As the curing accelerator (E) used in the present invention, a phosphorus curing accelerator, an imidazole curing accelerator, and D
A wide range of BU-based curing accelerators and other curing accelerators can be used. These can be used alone or in combination of two or more kinds. It is desirable that the curing accelerator is blended in an amount of 0.01 to 5% by weight based on the total resin composition. If the proportion is less than 0.01% by weight, the gel time of the resin composition will be long and the curing characteristics will be poor, and if it exceeds 5% by weight, the fluidity will be extremely poor and the moldability will be poor.
Furthermore, the electrical characteristics are poor and the moisture resistance is poor, which is not preferable.
【0025】本発明のエポキシ樹脂組成物は、前述した
特定のエポキシ樹脂、フェノール樹脂、有機基を微量配
合した特定のシランカップリング剤、窒化珪素粉末およ
び硬化促進剤を必須成分とするが、本発明の目的に反し
ない限度において、また必要に応じて、例えば天然ワッ
クス類、合成ワックス類、直鎖脂肪酸の金属塩、酸アミ
ド類、エステル類、パラフィン類等の離型剤、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、ゴ
ム系やシリコーン系の低応力付与剤等を適宜添加配合す
ることができる。The epoxy resin composition of the present invention contains the above-mentioned specific epoxy resin, phenol resin, specific silane coupling agent containing a small amount of an organic group, silicon nitride powder and a curing accelerator as essential components. Release agents such as natural waxes, synthetic waxes, metal salts of straight-chain fatty acids, acid amides, esters, paraffins, antimony trioxide, etc., as long as they do not violate the object of the invention and as necessary. The flame retardant, the colorant such as carbon black, the rubber-based or silicone-based low stress imparting agent, and the like can be appropriately added and blended.
【0026】本発明のエポキシ樹脂組成物を成形材料と
して調製する場合の一般的方法は、前述した特定のエポ
キシ樹脂、フェノール樹脂、特定のシランカップリング
剤、窒化珪素粉末および硬化促進剤その他の成分を配合
し、ミキサー等によって十分均一に混合した後、さらに
熱ロールによる溶融混合処理またはニーダ等による混合
処理を行い、次いで冷却固化させ適当な大きさに粉砕し
て成形材料とすることができる。こうして得られた成形
材料は、半導体装置をはじめとする電子部品或いは電気
部品の封止・被覆・絶縁等に適用すれば優れた特性と信
頼性を付与させることができる。The general method for preparing the epoxy resin composition of the present invention as a molding material is as follows: the specific epoxy resin, the phenol resin, the specific silane coupling agent, the silicon nitride powder, the curing accelerator and other components. Can be mixed and sufficiently homogenously mixed with a mixer or the like, and further subjected to melt mixing treatment with a hot roll or mixing treatment with a kneader or the like, and then cooled and solidified to be pulverized to an appropriate size to obtain a molding material. When the molding material thus obtained is applied to sealing, coating, insulation, etc. of electronic parts or electric parts such as semiconductor devices, excellent properties and reliability can be imparted.
【0027】また、本発明の半導体封止装置は、上述の
成形材料を用いて半導体チップを封止することにより容
易に製造することができる。封止を行う半導体チップと
しては、例えば集積回路、大規模集積回路、トランジス
タ、サイリスタ、ダイオード等で特に限定されるもので
はない。封止の最も一般的な方法としては、低圧トラン
スファー成形法があるが、射出成形、圧縮成形、注形等
による封止も可能である。成形材料で封止後加熱して硬
化させ、最終的にはこの硬化物によって封止された半導
体封止装置が得られる。加熱による硬化は、175 ℃以上
に加熱して硬化させることが望ましい。The semiconductor encapsulation device of the present invention can be easily manufactured by encapsulating a semiconductor chip using the above molding material. The semiconductor chip to be sealed is not particularly limited to, for example, an integrated circuit, a large scale integrated circuit, a transistor, a thyristor, a diode and the like. The most common method of sealing is a low-pressure transfer molding method, but sealing by injection molding, compression molding, casting or the like is also possible. After sealing with a molding material, it is heated and cured, and finally a semiconductor sealing device sealed with this cured product is obtained. For curing by heating, it is desirable to heat and cure at 175 ° C or higher.
【0028】[0028]
【作用】本発明のエポキシ樹脂組成物および半導体封止
装置は、特定のエポキシ樹脂、フェノール樹脂、有機塩
基を極微量添加した特定のシランカップリング剤、窒化
珪素粉末および硬化促進剤を用いることによって、その
効果が得られるものである。即ち、微量の有機塩基がシ
ランカップリング剤の加水分解を促進させ、樹脂等の有
機分と無機分との反応性を高め、最大粒径100 μm 以下
の窒化珪素と特定のエポキシ樹脂を用いることによっ
て、流動性を損なわずに高充填化でき、有機分と無機分
との界面強度が上がり、樹脂組成物の吸水性を低減し、
成形性、流動性が向上し、半田浸漬、半田リフロー後の
樹脂クラックの発生がなくなり、良好な熱伝導性を示
し、耐湿性劣化が少なくなるものである。The epoxy resin composition and the semiconductor encapsulation device of the present invention are obtained by using a specific epoxy resin, a phenol resin, a specific silane coupling agent containing a trace amount of an organic base, a silicon nitride powder and a curing accelerator. , The effect is obtained. That is, a small amount of organic base accelerates the hydrolysis of the silane coupling agent, enhances the reactivity between organic components such as resin and inorganic components, and uses silicon nitride with a maximum particle size of 100 μm or less and a specific epoxy resin. By the above, high filling can be achieved without impairing fluidity, the interface strength between the organic content and the inorganic content is increased, and the water absorption of the resin composition is reduced
Moldability and fluidity are improved, resin cracks are not generated after solder immersion and solder reflow, good thermal conductivity is exhibited, and moisture resistance deterioration is reduced.
【0029】[0029]
【実施例】次に本発明を実施例によって説明するが、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「%」とは「重
量%」を意味する。EXAMPLES Next, the present invention will be described with reference to examples, but the present invention is not limited to these examples. In the following examples and comparative examples, “%” means “% by weight”.
【0030】実施例1 窒化珪素粉末(最大粒径100 μm 以下)77%、微細な溶
融球状シリカ粉末(平均粒径0.5 μm )10%をヘンシェ
ルミキサーに入れ、攪拌しながら前述した化12のシラ
ンカップリング剤0.4 %、ジエチルアミン4 ×10-4%を
加えて表面処理をした。Example 1 77% of silicon nitride powder (maximum particle size of 100 μm or less) and 10% of fine fused spherical silica powder (average particle size of 0.5 μm) were put into a Henschel mixer, and the silane of the above chemical formula 12 was stirred while stirring. Surface treatment was performed by adding 0.4% of a coupling agent and 4 × 10 −4 % of diethylamine.
【0031】次に前述した化5のビフェニル型エポキシ
樹脂5.0 %、テトラブロモビスフェノールA型エポキシ
樹脂1.0 %、前述した化7のフェノールノボラック樹脂
1.2%、前述した化8のフェノールアラルキル樹脂2.5
%、トリフェニルホスフィン0.2 %、カルナバワックス
類0.4 %、カーボンブラック0.3 %、三酸化アンチモン
2.0 %を常温で混合し、さらに90〜100 ℃で混練冷却し
た後、粉砕して成形材料を製造した。Next, 5.0% of the biphenyl type epoxy resin of the above chemical formula 5, 1.0% of tetrabromobisphenol A type epoxy resin, and the phenol novolac resin of the above chemical formula 7
1.2%, the above-mentioned phenol aralkyl resin of chemical formula 2.5
%, Triphenylphosphine 0.2%, carnauba wax 0.4%, carbon black 0.3%, antimony trioxide
2.0% was mixed at room temperature, further kneaded and cooled at 90 to 100 ° C., and then pulverized to produce a molding material.
【0032】実施例2〜3 表1に示した組成で実施例1と同様にして成形材料を製
造した。Examples 2 to 3 Molding materials having the compositions shown in Table 1 were produced in the same manner as in Example 1.
【0033】比較例1〜3 表1に示した組成で実施例1と同様にして成形材料を製
造した。Comparative Examples 1 to 3 Molding materials having the compositions shown in Table 1 were produced in the same manner as in Example 1.
【0034】こうして製造した成形材料を用いて 170℃
に加熱した金型内にトランスファー注入、半導体チップ
を封止し硬化させて半導体封止装置を製造した。これら
の半導体封止装置について、諸試験を行ったのでその結
果を表2に示したが、本発明のエポキシ樹脂組成物およ
び半導体封止装置は、耐湿性、半田耐熱性、成形性、熱
伝導性に優れており、本発明の顕著な効果を確認するこ
とができた。Using the molding material thus produced, 170 ° C.
A semiconductor encapsulation device was manufactured by injecting transfer into a heated mold, encapsulating a semiconductor chip and curing it. Various tests were conducted on these semiconductor encapsulation devices, and the results are shown in Table 2. The epoxy resin composition and the semiconductor encapsulation device of the present invention show moisture resistance, solder heat resistance, moldability, and thermal conductivity. The excellent effect of the present invention could be confirmed.
【0035】[0035]
【表1】 [Table 1]
【0036】[0036]
【表2】 *1 :EMMI−I−66に準じてスパイラルフロー測定した(175 ℃)。 *2 :高化式フロー粘度(175 ℃)。 *3 :175 ℃,80kg/cm2 ,2 分間のトランスファー成形によって得られた成形 品(試験片)をつくり、175 ℃,8 時間の後硬化を行い、JIS−K−6911 に準じて試験した。 *4 :*3 と同様な成形品を作り、175 ℃,8 時間の後硬化を行い、適当な大き さの試験片とし、熱機械分析装置を用いて測定した。 *5 :φ 100mm,厚25mmの成形品を作り、熱伝導率計を用いて測定した。 *6 :5.3 ×5.3mm チップをVQFP80pin (12×12×1.4mm )パッケージ用金 型に納め、成形材料を用いて175 ℃,2 分間トランスファー成形した後、175 ℃ ,8 時間の後硬化を行った。こうして得た半導体封止装置を85℃,85%,48時間 の吸湿処理した後、増加した重量によって計算した。 *7 :*6 のVQFP80pin パッケージの半導体封止装置をエアーリフローマシ ン(Max 240℃)に通し、外部および内部クラックの有無を調査した。 *8 :*6 のVQFP80pin パッケージの成形において充填できなかった。[Table 2] * 1: Spiral flow measurement (175 ° C) according to EMMI-I-66. * 2: Higher flow viscosity (175 ° C). * 3: A molded product (test piece) obtained by transfer molding at 175 ° C, 80 kg / cm 2 for 2 minutes was prepared, post-cured at 175 ° C for 8 hours, and tested according to JIS-K-6911. . * 4: A molded product similar to * 3 was made, post-cured at 175 ° C for 8 hours, and a test piece of appropriate size was measured using a thermomechanical analyzer. * 5: A molded product with a diameter of 100 mm and a thickness of 25 mm was made and measured using a thermal conductivity meter. * 6: A 5.3 x 5.3 mm chip was placed in a VQFP 80-pin (12 x 12 x 1.4 mm) package mold, transfer molded using the molding material for 2 minutes at 175 ° C, and then post-cured at 175 ° C for 8 hours. It was The semiconductor encapsulation device thus obtained was subjected to moisture absorption treatment at 85 ° C, 85% for 48 hours, and then calculated by the increased weight. * 7: The semiconductor encapsulation device of VQFP80pin package of * 6 was passed through an air reflow machine (Max 240 ° C) and examined for external and internal cracks. * 8: Could not be filled in molding the VQFP 80pin package of * 6.
【0037】[0037]
【発明の効果】以上の説明および表2から明らかなよう
に、本発明のエポキシ樹脂組成物および半導体封止装置
は、耐湿性、半田耐熱性、成形性、熱伝導性に優れ、ま
た、薄型パッケージ等の充填性にも優れ、吸湿による影
響が少なく、放熱性が良好でしかも長期間にわたって信
頼性を保証することができる。As is clear from the above description and Table 2, the epoxy resin composition and the semiconductor encapsulating device of the present invention are excellent in moisture resistance, solder heat resistance, moldability and thermal conductivity, and are thin. It is excellent in the filling property of the package and so on, is less affected by moisture absorption, has good heat dissipation, and can guarantee reliability for a long period of time.
───────────────────────────────────────────────────── 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 H01L 23/29 23/31 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location H01L 23/29 23/31
Claims (2)
型エポキシ樹脂、 【化1】 (B)フェノール樹脂、(C)有機塩基を極微量添加し
た、次の一般式で示されるエポキシ基を有するシランカ
ップリング剤、 【化2】R1 −Cn H2n−Si (OR2 )3 (但し、式中R1 はエポキシ基を有する原子団を、R2
はメチル基又はエチル基を、n は0 又は1 以上の整数を
それぞれ表す) (D)最大粒径が100 μm 以下の窒化珪素粉末および
(E)硬化促進剤を必須成分とし、全体の樹脂組成物に
対して前記(D)の窒化珪素粉末を25〜90重量%の割合
で含有してなることを特徴とするエポキシ樹脂組成物。1. (A) a biphenyl type epoxy resin represented by the following general formula: (B) Phenolic resin, (C) Organic base-added silane coupling agent having an epoxy group represented by the following general formula: embedded image R 1 —C n H 2n —Si (OR 2 ) 3 (wherein R 1 is an atomic group having an epoxy group, R 2
Represents a methyl group or an ethyl group, and n represents an integer of 0 or 1 or more.) (D) A silicon nitride powder having a maximum particle size of 100 μm or less and (E) a curing accelerator are essential components, and the entire resin composition An epoxy resin composition comprising 25 to 90% by weight of the silicon nitride powder of (D) with respect to the product.
型エポキシ樹脂、 【化3】 (B)フェノール樹脂、(C)有機塩基を極微量添加し
た、次の一般式で示されるエポキシ基を有するシランカ
ップリング剤、 【化4】R1 −Cn H2n−Si (OR2 )3 (但し、式中R1 はエポキシ基を有する原子団を、R2
はメチル基又はエチル基を、n は0 又は1 以上の整数を
それぞれ表す) (D)最大粒径が100 μm 以下の窒化珪素粉末および
(E)硬化促進剤を必須成分とし、全体の樹脂組成物に
対して前記(D)の窒化珪素粉末を25〜90重量%の割合
で含有したエポキシ樹脂組成物の硬化物によって、半導
体チップが封止されてなることを特徴とする半導体封止
装置。2. A biphenyl-type epoxy resin represented by the following general formula: A silane coupling agent having an epoxy group represented by the following general formula, wherein (B) a phenol resin and (C) an organic base are added in an extremely small amount: embedded image R 1 —C n H 2n —Si (OR 2 ) 3 (wherein R 1 is an atomic group having an epoxy group, R 2
Represents a methyl group or an ethyl group, and n represents an integer of 0 or 1 or more.) (D) A silicon nitride powder having a maximum particle size of 100 μm or less and (E) a curing accelerator are essential components, and the entire resin composition A semiconductor encapsulation device, wherein a semiconductor chip is encapsulated with a cured product of an epoxy resin composition containing 25 to 90% by weight of the silicon nitride powder of (D) with respect to the product.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18677894A JPH0827252A (en) | 1994-07-15 | 1994-07-15 | Epoxy resin composition and semiconductor sealing device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18677894A JPH0827252A (en) | 1994-07-15 | 1994-07-15 | Epoxy resin composition and semiconductor sealing device |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0827252A true JPH0827252A (en) | 1996-01-30 |
Family
ID=16194446
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18677894A Pending JPH0827252A (en) | 1994-07-15 | 1994-07-15 | Epoxy resin composition and semiconductor sealing device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0827252A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100383248B1 (en) * | 2000-12-27 | 2003-05-12 | 제일모직주식회사 | Epoxy resin composition for encapsulating semiconductor device |
| KR100562454B1 (en) * | 1998-07-21 | 2006-03-21 | 신에쓰 가가꾸 고교 가부시끼가이샤 | Epoxy Resin Compositions for Sealing Semiconductor and Semiconductor Devices |
-
1994
- 1994-07-15 JP JP18677894A patent/JPH0827252A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100562454B1 (en) * | 1998-07-21 | 2006-03-21 | 신에쓰 가가꾸 고교 가부시끼가이샤 | Epoxy Resin Compositions for Sealing Semiconductor and Semiconductor Devices |
| KR100383248B1 (en) * | 2000-12-27 | 2003-05-12 | 제일모직주식회사 | Epoxy resin composition for encapsulating semiconductor device |
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