JPH04256345A - Semiconductor device - Google Patents
Semiconductor deviceInfo
- Publication number
- JPH04256345A JPH04256345A JP6087691A JP6087691A JPH04256345A JP H04256345 A JPH04256345 A JP H04256345A JP 6087691 A JP6087691 A JP 6087691A JP 6087691 A JP6087691 A JP 6087691A JP H04256345 A JPH04256345 A JP H04256345A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- semiconductor device
- organic polymer
- molding material
- parts
- 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
- 239000004065 semiconductor Substances 0.000 title claims abstract description 13
- 239000003822 epoxy resin Substances 0.000 claims abstract description 16
- 239000012778 molding material Substances 0.000 claims abstract description 16
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 16
- 229920000620 organic polymer Polymers 0.000 claims abstract description 15
- 239000011256 inorganic filler Substances 0.000 claims abstract description 7
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 7
- 125000003700 epoxy group Chemical group 0.000 claims abstract description 4
- 238000007789 sealing Methods 0.000 abstract description 9
- 230000035939 shock Effects 0.000 abstract description 4
- 230000010354 integration Effects 0.000 abstract description 2
- 239000002775 capsule Substances 0.000 description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 15
- 239000000839 emulsion Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- -1 triphenylphosphine tetraphenylborate Chemical compound 0.000 description 9
- 239000000843 powder Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 7
- 239000005350 fused silica glass Substances 0.000 description 6
- 230000035882 stress Effects 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 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 4
- 229910010272 inorganic material Inorganic materials 0.000 description 4
- 239000011147 inorganic material Substances 0.000 description 4
- 229920003986 novolac Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 2
- 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 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 229910000410 antimony oxide Inorganic materials 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 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 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000011162 core material Substances 0.000 description 2
- 239000011258 core-shell material Substances 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 125000005372 silanol group Chemical group 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 238000003786 synthesis reaction 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
- 229920002554 vinyl polymer Polymers 0.000 description 2
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- WORVYYDNYUXZBS-UHFFFAOYSA-N 2,4,6-tris(dimethylamino)-3-methylphenol Chemical compound CN(C)C1=CC(N(C)C)=C(O)C(N(C)C)=C1C WORVYYDNYUXZBS-UHFFFAOYSA-N 0.000 description 1
- FWWXYLGCHHIKNY-UHFFFAOYSA-N 2-ethoxyethyl prop-2-enoate Chemical compound CCOCCOC(=O)C=C FWWXYLGCHHIKNY-UHFFFAOYSA-N 0.000 description 1
- LLEASVZEQBICSN-UHFFFAOYSA-N 2-undecyl-1h-imidazole Chemical compound CCCCCCCCCCCC1=NC=CN1 LLEASVZEQBICSN-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- KBQVDAIIQCXKPI-UHFFFAOYSA-N 3-trimethoxysilylpropyl prop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C=C KBQVDAIIQCXKPI-UHFFFAOYSA-N 0.000 description 1
- BESKSSIEODQWBP-UHFFFAOYSA-N 3-tris(trimethylsilyloxy)silylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C BESKSSIEODQWBP-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241001483078 Phyto Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- WOXXJEVNDJOOLV-UHFFFAOYSA-N ethenyl-tris(2-methoxyethoxy)silane Chemical compound COCCO[Si](OCCOC)(OCCOC)C=C WOXXJEVNDJOOLV-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 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
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 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
【産業上の利用分野】本発明は集積度が高く或いは小型
薄型であっても優れた信頼性を有している半導体装置に
関するものであり、電子工業を始めとして各種産業で利
用されるものである。[Industrial Application Field] The present invention relates to a semiconductor device that has excellent reliability even if it is highly integrated or small and thin, and is used in various industries including the electronic industry. be.
【0002】0002
【従来技術】半導体封止用成形材料に用いられるエポキ
シ樹脂について、その低応力化が種々検討されており、
それらの中では弾性率の小さい有機重合体、特にゴム質
の添加、或いは熱膨張率の低い無機質、特に溶融シリカ
粉の配合を行う方法が主体である。[Prior Art] Various efforts have been made to reduce the stress of epoxy resins used as molding materials for semiconductor encapsulation.
Among these, the main methods include adding an organic polymer with a low elastic modulus, especially a rubbery substance, or adding an inorganic material with a low coefficient of thermal expansion, especially a fused silica powder.
【0003】0003
【発明が解決しようとする課題】しかしながら、ゴム質
、特に耐熱性の大きい、高分子量のエラストマー性重合
体を成形材料中に均一に分散することは困難であり、又
溶融シリカ粉を多量配合すると熱膨張率は低下するけれ
ども成形性が著しく低下し限界が見られる。[Problems to be Solved by the Invention] However, it is difficult to uniformly disperse a rubbery material, especially a high molecular weight elastomeric polymer with high heat resistance, in a molding material, and if a large amount of fused silica powder is mixed. Although the coefficient of thermal expansion decreases, the moldability significantly decreases and a limit can be seen.
【0004】0004
【課題を解決するための手段】本発明は1分子中にエポ
キシ基を2個以上含むエポキシ樹脂(以下エポキシ樹脂
と略称する。)100重量部に対して(1)無機質ゾル
を用いた被覆が施された有機重合体(有機重合体を内包
するカプセル体とも言いうるものであり以下カプセル体
と略称する。)1〜100重量部及び(2)無機充填剤
100〜800重量部を含む成形材料により封止されて
いることを特徴とする半導体装置を提供せんとするもの
である。[Means for Solving the Problems] The present invention provides that (1) a coating using an inorganic sol is applied to 100 parts by weight of an epoxy resin containing two or more epoxy groups in one molecule (hereinafter abbreviated as epoxy resin); A molding material containing 1 to 100 parts by weight of the applied organic polymer (which can also be called a capsule body containing the organic polymer and hereinafter abbreviated as the capsule body) and (2) 100 to 800 parts by weight of an inorganic filler. It is an object of the present invention to provide a semiconductor device characterized in that it is sealed by.
【0005】本発明で強調されるべき技術要素は次の点
である。The technical elements to be emphasized in the present invention are as follows.
【0006】○エポキシ樹脂
成形材料中に樹脂成分として含まれるエポキシ樹脂は1
分子中にエポキシ基を2個以上含むならば、特に限定さ
れたものではなくクレゾールノボラック型、フェノール
ノボラック型或いはビスフェノールA型等の従来より、
半導体装置の封止用成形材料として用いられている各種
エポキシ樹脂を使用可能であるが、融点が室温以上であ
るものが好ましい。○ The epoxy resin contained as a resin component in the epoxy resin molding material is 1
As long as the molecule contains two or more epoxy groups, there are no particular limitations, and conventional methods such as cresol novolak type, phenol novolak type, or bisphenol A type, etc.
Various epoxy resins used as molding materials for sealing semiconductor devices can be used, but those having a melting point of room temperature or higher are preferred.
【0007】ノポラック型の場合はエポキシ当量160
〜250、軟化点50〜130℃のものが好ましい。[0007] In the case of noporac type, the epoxy equivalent is 160
~250°C and a softening point of 50~130°C are preferred.
【0008】エポキシ樹脂の硬化剤としては酸無水物、
フェノール類、ポリアミド類を始め公知の硬化剤を用い
ることが出来るが、水酸基当量70〜150のフェノー
ル或いはクレゾールノボラック樹脂が好ましい。さらに
硬化促進剤としては2,4,6−トリジメチルアミノメ
チルフェノール、2−メチルイミダゾール、2−ウンデ
シルイミダゾール、トリフェニルホスフィン、或いはト
リフェニルホスフィンテトラフェニルボレート等が挙げ
られる。[0008] As curing agents for epoxy resins, acid anhydrides,
Known curing agents such as phenols and polyamides can be used, but phenol or cresol novolak resins having a hydroxyl equivalent of 70 to 150 are preferred. Furthermore, examples of the curing accelerator include 2,4,6-tridimethylaminomethylphenol, 2-methylimidazole, 2-undecylimidazole, triphenylphosphine, and triphenylphosphine tetraphenylborate.
【0009】○カプセル体
本発明で使用するカプセル体は無機ゾル用いた被覆が施
された有機重合体を内包するカプセル体であり、通常の
有機重合体微粉末とは異なった構造及び性質を有するも
のである。例えば高温度下においても粘着性を示さず、
又、有機溶融中においても膨潤し難く単一の微細粒子形
態を維持することが出来る。従ってこのカプセル体は種
々のエポキシ樹脂中に於いて容易に単一の微細粒子形態
を維持していわゆる「海−島構造」をとることが出来る
為、高度の熱応力の吸収或いは緩和作用を発揮する。さ
らにこのカプセル体は無機質で被覆されている為、耐熱
性が本質的に優れている。又粒子径が0.5〜50μの
とき内部応力の緩和機能が高められ、且つ成形材料の成
形性も良好の為、好ましい。Capsule body The capsule body used in the present invention is a capsule body containing an organic polymer coated with an inorganic sol, and has a structure and properties different from that of ordinary organic polymer fine powder. It is something. For example, it does not show stickiness even under high temperatures,
Furthermore, even during organic melting, it is difficult to swell and can maintain a single fine particle morphology. Therefore, this capsule body can easily maintain a single fine particle morphology in various epoxy resins and take a so-called "sea-island structure", so it exhibits a high degree of thermal stress absorption or relaxation effect. do. Furthermore, since this capsule body is coated with an inorganic material, it has essentially excellent heat resistance. Further, when the particle size is 0.5 to 50 μm, the internal stress relaxation function is enhanced and the moldability of the molding material is also good, so it is preferable.
【0010】以上の効果は内包される有機重合体として
特にTgの低い重合体、さらにはゴム状重合体を用いる
とき内部応力の緩和機能が大きい。カプセル体の使用量
はエポキシ樹脂100重量部に対して1〜100重量部
が必要である。1重量部を満たさないとき緩和機能が発
揮されず、他方100重量部を越えるとき成形材料の成
形性が不良となり各々不適当である。[0010] The above-mentioned effects have a great function of alleviating internal stress when a polymer having a particularly low Tg or a rubber-like polymer is used as the encapsulated organic polymer. The amount of the capsule to be used is 1 to 100 parts by weight per 100 parts by weight of the epoxy resin. If the amount is less than 1 part by weight, the relaxation function will not be exhibited, and if it exceeds 100 parts by weight, the moldability of the molding material will be poor, which is inappropriate.
【0011】○カプセル体の製造方法
有機重合体を無機質ゾルを用いて無機質の被覆を施す、
即ち本発明でいうカプセル化方法としては粉床法、帯電
粉砕法或いは複合エマルジョン法等が知られており、此
等の方法より得られたカプセル体をも本発明に用いるこ
とが出来るが、次の合成法が特に工業的に優位であり、
本発明に好適に使用される。○Production method of capsule body An organic polymer is coated with an inorganic substance using an inorganic sol.
That is, as the encapsulation method referred to in the present invention, the powder bed method, electrostatic pulverization method, composite emulsion method, etc. are known, and capsule bodies obtained by these methods can also be used in the present invention, but the following The synthesis method is particularly industrially advantageous,
Suitably used in the present invention.
【0012】即ち、表面にシラノール基を結合する有機
重合体エマルジョンを合成し、これに無機質ゾルを吸着
させ、得られたエマルジョン混合物を有機高分子水溶液
中でスラリー状になし、以後脱水して微粉末状カプセル
体を得る方法である。That is, an organic polymer emulsion with silanol groups bonded to its surface is synthesized, an inorganic sol is adsorbed onto this emulsion, the resulting emulsion mixture is made into a slurry in an organic polymer aqueous solution, and then dehydrated to form a fine powder. This is a method for obtaining powdered capsules.
【0013】このようにして皮膜が形成される無機質は
シリカ、アルミナ、酸化チタン、酸化鉄、酸化アンチモ
ン、酸化金属或いはジルコニア等の金属酸化物のゾルか
ら由来されるものであり、カプセル体中2〜50重量%
含まれることが本発明にとって好ましい。The inorganic material on which the film is formed in this manner is derived from a sol of silica, alumina, titanium oxide, iron oxide, antimony oxide, metal oxide, or metal oxide such as zirconia, and is ~50% by weight
It is preferred for the present invention that it be included.
【0014】他方内包される有機重合体は表面にシラノ
ール基を表面に有する次のような有機重合体エマルジョ
ンをコアーシェル型エマルジョン重合法から合成するこ
とが出来る。On the other hand, as for the organic polymer to be included, the following organic polymer emulsion having silanol groups on the surface can be synthesized by a core-shell type emulsion polymerization method.
【0015】即ち、予めコアーとする有機重合体エマル
ジョン、例えばポリオレフィン、ポリジエン、不飽和脂
肪族エステル重合体、或いは脂肪酸ビニルの重合体、又
は此等を主成分とする共重合体を含むエマルジョンを合
成する。次に該有機エマルジョン存在下にアクリロニト
リル、メタアクリロニトリル、N−ビニルピロリドン、
或いはN−ビニルカプロラクタムとアクリルオキシ基、
メタアクリルオキシ基或いはビニル基を有するアルコキ
シシランを混合する単量体を共重合させ得られたコアー
シエル型エマルジョンである。尚、アクリルオキシ基、
メタアクリルオキシ基或いはビニル基を有するアルコキ
シシランの具体例としては、γ−アクリルオキシプロピ
ルトリメトキシシラン、γ−メタアクリルオキシプロピ
ルトリメトキシシラン、γ−メタアクリルオキシプロピ
ルトリス(トリメチルシロキシ)シラン、ビニルトリメ
トキシシラン、ビニルトリエトキシシラン、ビニルトリ
ス(メトキシエトキシ)シラン或いはビニルトリクロル
シラン等を挙げることが出来る。That is, an emulsion containing an organic polymer emulsion as a core, such as a polyolefin, a polydiene, an unsaturated aliphatic ester polymer, a fatty acid vinyl polymer, or a copolymer having these as the main component, is synthesized in advance. do. Next, in the presence of the organic emulsion, acrylonitrile, methacrylonitrile, N-vinylpyrrolidone,
Or N-vinylcaprolactam and acryloxy group,
This is a core-shell emulsion obtained by copolymerizing monomers containing alkoxysilanes having methacryloxy groups or vinyl groups. In addition, acryloxy group,
Specific examples of alkoxysilanes having a methacryloxy group or a vinyl group include γ-acryloxypropyltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-methacryloxypropyltris(trimethylsiloxy)silane, vinyl Examples include trimethoxysilane, vinyltriethoxysilane, vinyltris(methoxyethoxy)silane, and vinyltrichlorosilane.
【0016】○無機充填剤
従来知られた種々の0.1〜150μの粒子径をもつ微
粉末状の無機質を用いることが出来るが、電気絶縁性を
阻害しない、溶融シリカ、珪石粉、タルク、アルミナ或
いは炭酸カルシウム等が好ましい。[0016] Inorganic filler Various conventionally known inorganic materials in the form of fine powder with a particle size of 0.1 to 150μ can be used, including fused silica, silica powder, talc, etc., which do not impede electrical insulation properties. Alumina, calcium carbonate, etc. are preferred.
【0017】此等の使用量はエポキシ樹脂100重量部
に対して100〜800重量部でなければならない。The amount used should be 100 to 800 parts by weight per 100 parts by weight of the epoxy resin.
【0018】100重量部を満たさないときは応力の緩
和機能が充分でなく、他方800重量部を越えるとき成
形材料の成形時の溶融粘度が上昇し、成形性を阻害する
為各々不適当である。If the amount is less than 100 parts by weight, the stress relieving function will not be sufficient, and if it exceeds 800 parts by weight, the melt viscosity of the molding material will increase during molding, impeding the moldability, so each is unsuitable. .
【0019】○成形材料を形成させる為の他の配合剤無
機質部分と有機質部分を結合させるカップリング剤とし
て3−グリシドキシプロピルトリメトキシシラン等のシ
ラン系カップリング剤、或いはテトラオクチルビス(ホ
スファイト)チタネート等のチタン系カップリング剤を
離型剤としてカルバナワックス、ステアリン酸及びその
金属塩、モンタン酸或いはエステルワックス等をまた、
難燃性を高める為にホスファゼン化合物、臭系化エポキ
シ樹脂或いは三酸化アンチモン等を顔料としてカーボン
ブラックを配合することが出来る。Other compounding agents for forming the molding material Silane coupling agents such as 3-glycidoxypropyltrimethoxysilane, or tetraoctyl bis(phosphorus Carvana wax, stearic acid and its metal salts, montanic acid or ester wax, etc. can be used as a mold release agent using a titanium-based coupling agent such as phyto) titanate.
In order to improve flame retardancy, carbon black can be blended with a phosphazene compound, a brominated epoxy resin, or antimony trioxide as a pigment.
【0020】○成形方法
エポキシ樹脂、カプセル体及び無機充填剤を含む組成物
を混合し混錬後、粉砕する。次に該組成物を用いてトラ
ンファー成形等で所要の封止部を封止することにより半
導体装置が完成する。Molding method A composition containing an epoxy resin, a capsule and an inorganic filler is mixed and kneaded, and then pulverized. Next, a semiconductor device is completed by sealing required sealing portions using the composition by transfer molding or the like.
【0021】○利用方法
本発明の半導体装置は素子サイズの大型化及びパッケー
ジの小型化又は薄形化に応じ必要とされる超高密度集積
回路の形成に用いられる。○Usage Method The semiconductor device of the present invention is used for forming ultra-high density integrated circuits, which are required in response to increasing element size and miniaturizing or thinning packages.
【0022】[0022]
【作用】半導体装置の封止用成型材料としてエポキシ樹
脂、カプセル体、及び無機充填剤の適性な構成比をもつ
此等の組成物を使用することにより耐熱性及び耐熱衝撃
性を有しており、大きな内部応力緩和機能を付与する。[Action] By using such a composition with an appropriate composition ratio of epoxy resin, capsule body, and inorganic filler as a molding material for encapsulating semiconductor devices, it has heat resistance and thermal shock resistance. , imparts a large internal stress relaxation function.
【0023】[0023]
【実施例】以下本発明の実施例及びこれに対する比較例
を挙げてさらに本発明を詳細に説明するが、本発明は此
等の実施例に限定されるものではない。[Examples] The present invention will be further explained in detail by referring to examples of the present invention and comparative examples thereof, but the present invention is not limited to these examples.
【0024】実施例1〜6、比較例1〜2○カプセル体
の合成
以下の方法でシリカにより被覆されたスチレン−ブタジ
エンゴムを内包するカプセル体を合成した。2L4つ口
フラスコに純水310cc、スチレン−ブタジエンゴム
エマルジョン「トラックスーパー」(固形分45.0重
量%、日本ラテックス化工(株)製)1220gr、ス
チレン98gr、アクリロニトリル42gr、γ−メタ
アクリロキシプロピルトリメトキシシラン8gr及び過
硫酸アンモン0.8grを仕入み窒素を空間部に流しな
がら70℃にてプロペラ型撹拌翼で撹拌下(350rp
m )4時間乳化重合を行った。Examples 1 to 6, Comparative Examples 1 to 2 Synthesis of Capsules Capsules containing styrene-butadiene rubber coated with silica were synthesized by the following method. In a 2L four-necked flask, 310cc of pure water, 1220gr of styrene-butadiene rubber emulsion "Truck Super" (solid content 45.0% by weight, manufactured by Nippon Latex Kako Co., Ltd.), 98gr styrene, 42gr acrylonitrile, γ-methacryloxypropyl tritrile. 8g of methoxysilane and 0.8g of ammonium persulfate were purchased, and while nitrogen was flowing into the space, the temperature was kept at 70°C while stirring with a propeller-type stirring blade (350rpm).
m) Emulsion polymerization was performed for 4 hours.
【0025】得られたエマルジョン(固形分40.5重
量%)720grをシリカゾル「スノーテックスUP」
(固形分20重量%、太さ5〜20mμ、長さ40〜3
00mμの棒状のコロイダルシリカ、日産化学工業(株
)製)160grを混合して「メトローズ90SH40
00」(ヒドロキシプロセルメチルセルロース、高粘度
タイプ、信越化学工業(株)製)0.5重量%の水溶液
3700ccが仕込まれた12L混合槽中に25℃にて
プロペラ型撹拌翼で撹拌下(600rpm )に20分
かけて添加してスラリー状にした。[0025] 720g of the obtained emulsion (solid content 40.5% by weight) was mixed with silica sol "Snowtex UP".
(Solid content 20% by weight, thickness 5-20mμ, length 40-3
00mμ rod-shaped colloidal silica and 160gr manufactured by Nissan Chemical Industries, Ltd. were mixed to make "Metrose 90SH40
00'' (hydroxyprocel methyl cellulose, high viscosity type, manufactured by Shin-Etsu Chemical Co., Ltd.) was placed in a 12 L mixing tank containing 3700 cc of a 0.5% by weight aqueous solution at 25°C under stirring with a propeller type stirring blade (600 rpm). was added over 20 minutes to form a slurry.
【0026】得られたスラリーをロ過及び水洗を繰り返
して固形分9重量%及びPH5.5にして、ディスク型
スプレー乾燥機に通して粒径1〜10μmのブタジエン
共重合体90重量%を芯材とし、シリカ10重量%を皮
膜にもつ微粉末状カプセル体290grを得た。The obtained slurry was repeatedly filtered and washed with water until the solid content was 9% by weight and the pH was 5.5, and then passed through a disk-type spray dryer to remove 90% by weight of a butadiene copolymer with a particle size of 1 to 10 μm. 290 gr of finely powdered capsule bodies having a film containing 10% by weight of silica were obtained.
【0027】○封止用成形材料組成物の調整エポキシ当
量190、軟化点80℃のエポキシ樹脂、100重量部
硬化剤としてフエノール当量130、軟化点80℃のフ
エノールノボラック樹脂50重量部、硬化促進剤として
2−メチルイミダゾール0.5重量部、滑剤としてステ
アリン酸0.5重量部、無機充填剤として粒径3〜12
0μmの球形溶融シリカ及び本例で得られたカプセル体
を表1のように配合後、ミキサーで混合し、更に80〜
90℃の熱ロールにて3分間溶融混合後、冷却粉砕した
。Preparation of the molding material composition for sealing 100 parts by weight of an epoxy resin with an epoxy equivalent of 190 and a softening point of 80°C. 50 parts by weight of a phenol novolac resin with a phenol equivalent of 130 and a softening point of 80°C as a curing agent, and a curing accelerator. 0.5 parts by weight of 2-methylimidazole, 0.5 parts by weight of stearic acid as a lubricant, and particle size 3 to 12 as an inorganic filler.
After blending 0 μm spherical fused silica and the capsules obtained in this example as shown in Table 1, they were mixed in a mixer, and further
After melt-mixing for 3 minutes using a heated roll at 90°C, the mixture was cooled and pulverized.
【0028】○集積回路部品の封止
上記の組成物を用いて18pin DIP(パッケージ
幅8.88mm、素子占有面積率60%)をトランファ
成形(175℃、30kg/cm2 、3分間)で封止
した。これをさらに175℃で4時間後硬化した。○Sealing of integrated circuit components Using the above composition, an 18-pin DIP (package width 8.88 mm, element occupation area ratio 60%) was sealed by transfer molding (175° C., 30 kg/cm2, 3 minutes). did. This was further post-cured at 175° C. for 4 hours.
【0029】○熱衝撃試験
上記の試作した集積回路部品に対して280℃で2分間
及び−196℃で2分間維持させる10サイクル後のク
ラック発生数を観察した結果、表1のようになった。○ Thermal Shock Test The number of cracks generated after 10 cycles of maintaining the above prototype integrated circuit components at 280°C for 2 minutes and -196°C for 2 minutes was as shown in Table 1. .
【0030】[0030]
【表1】[Table 1]
【0031】実施例7〜12、比較例3〜4○カプセル
体の合成
先の合成例に於いて「トマックスーパー」を使用する代
りにブチルアクリレート70重量%、2−エトキシエチ
ルアクリレート29.8重量%及びアリルメタアクリレ
ート0.2重量%よりなるアクリルゴムのエマルジョン
(固形分45.0重量%)1220grを使用し、さら
に「スノーテックスUP」の代りに酸化アンチモンゾル
(A−1510N、固形分1.3重量%、中性水中分散
体、日産化学工業(株)製)246grを使用して、他
の条件は同様にして合成した結果、粒径2〜15μmの
アクリル共重合体90重量%を芯材とし、酸化アンチモ
ン10重量%を皮膜にもつ微粉末300grを得た。Examples 7 to 12, Comparative Examples 3 to 4 ○ In the synthesis example of the capsule body, 70% by weight of butyl acrylate and 29.8% by weight of 2-ethoxyethyl acrylate were used instead of "Tomac Super". % and allyl methacrylate 0.2% by weight (solid content 45.0% by weight). .3% by weight, neutral water dispersion, 246gr (manufactured by Nissan Chemical Industries, Ltd.) was synthesized under the same conditions as above, and as a result, 90% by weight of an acrylic copolymer with a particle size of 2 to 15 μm was synthesized. 300 gr of fine powder was obtained which was used as a core material and had a film containing 10% by weight of antimony oxide.
【0032】○封止用成形材料組成物の調整先の組成物
の調整に於いて(球形溶融シリカの代りに粒径0.5〜
80μmの角形溶融シリカを使用し、又カプセル体とし
て本例で得たものを用い他は同様に表2のように配合後
、以下先の例と同様に評価を行った結果、表2のように
なった。[0032] In the preparation of the composition to which the molding material composition for sealing is prepared (instead of spherical fused silica, particles with a particle size of 0.5 to
Using 80 μm prismatic fused silica and the capsule obtained in this example, the other ingredients were similarly blended as shown in Table 2, and then evaluated in the same manner as in the previous example. Became.
【0033】[0033]
【表2】[Table 2]
【0034】[0034]
【発明の効果】実施例及び比較例にて説明した如く、本
発明の半導体装置はそれに使用された封止用の成形材料
が内部応力緩和機能を著しく発揮する為、耐熱衝撃性が
優れており、集積度が高く或いは小型薄型であっても優
れた信頼性を有しており、本発明は工業的に有益である
ことが判る。[Effects of the Invention] As explained in the Examples and Comparative Examples, the semiconductor device of the present invention has excellent thermal shock resistance because the molding material for sealing used therein exhibits a remarkable internal stress relaxation function. Even if the device has a high degree of integration or is small and thin, it has excellent reliability, and it can be seen that the present invention is industrially useful.
Claims (1)
エポキシ樹脂100重量部に対して無機質ゾルを用いた
被覆が施された有機重合体1〜100重量部、無機充填
剤100〜800重量部を含む成形材料により封止され
ていることを特徴とする半導体装置。Claim 1: 1 to 100 parts by weight of an organic polymer coated with an inorganic sol and 100 to 800 parts by weight of an inorganic filler per 100 parts by weight of an epoxy resin containing two or more epoxy groups in one molecule. 1. A semiconductor device characterized in that the semiconductor device is sealed with a molding material containing a portion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6087691A JPH04256345A (en) | 1991-02-07 | 1991-02-07 | Semiconductor device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6087691A JPH04256345A (en) | 1991-02-07 | 1991-02-07 | Semiconductor device |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04256345A true JPH04256345A (en) | 1992-09-11 |
Family
ID=13155020
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6087691A Pending JPH04256345A (en) | 1991-02-07 | 1991-02-07 | Semiconductor device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04256345A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0634445A1 (en) * | 1993-07-14 | 1995-01-18 | The Dow Chemical Company | Light diffuser composition |
US10876010B2 (en) | 2013-11-13 | 2020-12-29 | Sekisui Kasei Co., Ltd. | Composite particles, method for producing composite particles, and use thereof |
-
1991
- 1991-02-07 JP JP6087691A patent/JPH04256345A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0634445A1 (en) * | 1993-07-14 | 1995-01-18 | The Dow Chemical Company | Light diffuser composition |
US10876010B2 (en) | 2013-11-13 | 2020-12-29 | Sekisui Kasei Co., Ltd. | Composite particles, method for producing composite particles, and use thereof |
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