JPH02237139A - Electronic-component sealed and molded body - Google Patents
Electronic-component sealed and molded bodyInfo
- Publication number
- JPH02237139A JPH02237139A JP5618589A JP5618589A JPH02237139A JP H02237139 A JPH02237139 A JP H02237139A JP 5618589 A JP5618589 A JP 5618589A JP 5618589 A JP5618589 A JP 5618589A JP H02237139 A JPH02237139 A JP H02237139A
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- electronic component
- sealed
- pas
- silicone rubber
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000011342 resin composition Substances 0.000 claims abstract description 42
- 239000004945 silicone rubber Substances 0.000 claims abstract description 27
- 229920002379 silicone rubber Polymers 0.000 claims abstract description 13
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims abstract description 8
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000005538 encapsulation Methods 0.000 claims description 23
- 239000012765 fibrous filler Substances 0.000 claims description 10
- 229920000412 polyarylene Polymers 0.000 claims description 7
- 238000007789 sealing Methods 0.000 abstract description 19
- 238000000034 method Methods 0.000 abstract description 17
- 229920002631 room-temperature vulcanizate silicone Polymers 0.000 abstract description 17
- 229910000679 solder Inorganic materials 0.000 abstract description 6
- 239000007788 liquid Substances 0.000 abstract description 3
- 238000011049 filling Methods 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract 1
- 238000010008 shearing Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 description 18
- 238000000465 moulding Methods 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 238000005476 soldering Methods 0.000 description 11
- 239000011324 bead Substances 0.000 description 10
- 239000000155 melt Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 229920003002 synthetic resin Polymers 0.000 description 8
- 239000000057 synthetic resin Substances 0.000 description 8
- 239000003365 glass fiber Substances 0.000 description 7
- 229920001296 polysiloxane Polymers 0.000 description 7
- 239000000806 elastomer Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- XWUCFAJNVTZRLE-UHFFFAOYSA-N 7-thiabicyclo[2.2.1]hepta-1,3,5-triene Chemical compound C1=C(S2)C=CC2=C1 XWUCFAJNVTZRLE-UHFFFAOYSA-N 0.000 description 5
- 238000006482 condensation reaction Methods 0.000 description 5
- -1 copper Chemical class 0.000 description 5
- 238000006073 displacement reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000011256 inorganic filler Substances 0.000 description 4
- 229910003475 inorganic filler Inorganic materials 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000004734 Polyphenylene sulfide Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003990 capacitor Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000010292 electrical insulation Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229920000069 polyphenylene sulfide Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- SOHCOYTZIXDCCO-UHFFFAOYSA-N 6-thiabicyclo[3.1.1]hepta-1(7),2,4-triene Chemical group C=1C2=CC=CC=1S2 SOHCOYTZIXDCCO-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-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
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 241000719149 Caranx crysos Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- KZTYYGOKRVBIMI-UHFFFAOYSA-N S-phenyl benzenesulfonothioate Natural products C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 229910052977 alkali metal sulfide Inorganic materials 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
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Natural products C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical group C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 239000011521 glass 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
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 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
- 238000004898 kneading Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 1
- 229960002261 magnesium phosphate Drugs 0.000 description 1
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006124 polyolefin elastomer Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 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
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
- H01L23/293—Organic, e.g. plastic
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
Landscapes
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Details Of Resistors (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、耐湿性および半田耐熱性に優れた電子部品封
止成形物に関し、さらに詳しくは、ポリアリーレンスル
フィド(以下、rPAsJと略記)樹脂組成物で封止成
形してなる電子部品封止成形物であって、封止成形後に
、PAS樹脂組成物とリードフレーム等金属部との界面
が特定の室温硬化型シリコーンゴムでシール(充填)さ
れていることにより、チップ工法での実装時における高
温環境に耐え、かつ、高耐湿性を有する電子部品封正成
形物に関するものである.
【従来の技術〕
電子部品、例えば、コンデンサー ダイオード、トラン
ジスター rc,LsI等は電気絶縁性の保持、外部雰
囲気による特性変化の防止に加え、生産性やコストの有
利さ等の目的で、合成樹脂封止を施すことが広く行なわ
れている。Detailed Description of the Invention [Industrial Application Field] The present invention relates to an electronic component encapsulation molded product having excellent moisture resistance and soldering heat resistance, and more specifically, polyarylene sulfide (hereinafter abbreviated as rPAsJ) resin. An electronic component encapsulation molded product formed by encapsulation molding with a composition, in which the interface between the PAS resin composition and a metal part such as a lead frame is sealed (filled) with a specific room temperature curing silicone rubber after encapsulation molding. This relates to an electronic component encapsulation molded product that can withstand the high temperature environment during mounting using the chip method and has high moisture resistance. [Prior art] Electronic components, such as capacitor diodes, transistors rc, LSI, etc., are sealed with synthetic resin for the purpose of maintaining electrical insulation and preventing changes in characteristics due to external atmosphere, as well as for productivity and cost advantages. It is widely practiced to prevent
従来、封止用の合成樹脂としては、エボキシ樹脂やシリ
コーン樹脂等の熱硬化性樹脂が用いられているが、熱硬
化に艮時間を要し成形サイクルが長いこと、硬化の進行
を防ぐための樹脂の保存方法が容易でないこと、スブル
ーランナーの再利用ができないこと等の欠陥が指摘され
ている。Conventionally, thermosetting resins such as epoxy resins and silicone resins have been used as synthetic resins for sealing, but they require time to thermoset and have long molding cycles, and there are Deficiencies have been pointed out, including the difficulty in preserving the resin and the inability to reuse the blue runner.
そこで、近年、耐熱性、難燃性、電気的特性などに優れ
た熱可塑性樹脂であるPAS樹脂、特にその代表的な樹
脂であるポリフエニレンスルフィド(以下、rPPSJ
と略記)を主体とする樹脂組成物を電子部品封止用樹脂
として用いることが提案されている(例えば、特公昭5
6−9014号、特開昭57−21844号、特開昭5
7−40557号、特開昭59−20910号、特開昭
59−209 1 1号、特公昭60−40188号、
特開昭62−66351号、特開昭62−197451
号、特開昭63−146963号、特開昭63−219
145号)。Therefore, in recent years, PAS resin, a thermoplastic resin with excellent heat resistance, flame retardance, and electrical properties, has been developed, and in particular, its representative resin, polyphenylene sulfide (rPPSJ), has been developed.
It has been proposed to use a resin composition mainly consisting of
No. 6-9014, JP-A-57-21844, JP-A-5
7-40557, JP-A-59-20910, JP-A-59-209-11, JP-A-60-40188,
JP-A-62-66351, JP-A-62-197451
No., JP-A-63-146963, JP-A-63-219
No. 145).
しかしながら、PAS樹脂組成物で封止を行なった場合
、PASは電子部品のリードフレームあるいはリードワ
イヤー(ボンディングワイヤー)との密着性に劣るため
、高湿度雰囲気下に置いた場合、封止用樹脂とリードフ
レーム等との界面から容易に水分が侵入し、電気絶縁性
の低下や、リードフレームやワイヤーの腐食等を引き起
こし、電子部品の電気的特性を低下させるという欠点を
有している。However, when sealing is performed with a PAS resin composition, PAS has poor adhesion to the lead frame or lead wire (bonding wire) of electronic components, so if it is placed in a high humidity atmosphere, the sealing resin will not adhere properly. It has the disadvantage that moisture easily enters from the interface with the lead frame, etc., causing a decrease in electrical insulation, corrosion of the lead frame and wires, and deteriorating the electrical characteristics of electronic components.
また、樹脂封止による電子部品は、封止すべき素子の熱
膨張等による変形に追随して変形できるようにし、半田
浴槽に浸漬した時などに外装ひび割れを起こさないこと
が要求される。Further, electronic components sealed with resin are required to be able to deform following the deformation due to thermal expansion of the element to be sealed, and to not cause exterior cracks when immersed in a solder bath.
さらに、封止用樹脂組成物は成形時に高粘度であると素
子「ずれ」やボンデイングワイヤーの外れを起こしやす
《、低粘度であることが要求される。Furthermore, the encapsulating resin composition is required to have a low viscosity, since high viscosity during molding tends to cause elements to "slip" and bonding wires to come off.
最近、電子部品なPPS樹脂で封止したのち、電子部品
のリードフレーム等とPPS樹脂との界面部に低粘度の
接着剤を充填することにより耐湿特性などを改善する方
法が提案されているが(特開昭62−120036号)
、具体的に提示されている接着剤はいずれも酸性物質で
あるため、銅などの金属を腐食するおそれがあり、また
、接着膜が硬く、熱膨張によるひび割れが発生するおそ
れがある。Recently, a method has been proposed to improve moisture resistance by sealing electronic parts with PPS resin and then filling the interface between the lead frame, etc. of the electronic parts and the PPS resin with a low-viscosity adhesive. (Unexamined Japanese Patent Publication No. 62-120036)
Since the adhesives specifically proposed are all acidic substances, there is a risk of corroding metals such as copper, and the adhesive film is hard, so there is a risk of cracking due to thermal expansion.
このように電子部品封止成形物は耐湿性、半田耐熱性お
よび成形加工性に優れていることが要求されるが、これ
までのPAS樹脂組成物による電子部品封止成形物では
、これらの点についての改善効果が未だ不充分であり、
実用化する上での解決すべき課題となっている。As described above, electronic component encapsulation molded products are required to have excellent moisture resistance, solder heat resistance, and moldability, but conventional electronic component encapsulation molded products made from PAS resin compositions do not meet these requirements. The improvement effect is still insufficient,
This is an issue that must be resolved before it can be put into practical use.
本発明の目的は、封止用樹脂としてPAS樹脂組成物を
用い、耐湿性および半田耐熱性に優れた電子部品封止成
形物を得ることにある。An object of the present invention is to use a PAS resin composition as a sealing resin to obtain an electronic component sealing molded product having excellent moisture resistance and soldering heat resistance.
また、本発明の目的は、低粘度で高流動性のPAS樹脂
組成物を用い、成形加工性、耐湿性および半田耐熱性に
優れた電子部品封止成形物を得ることにある。Another object of the present invention is to use a PAS resin composition with low viscosity and high fluidity to obtain an electronic component encapsulation molded product having excellent moldability, moisture resistance, and soldering heat resistance.
本発明者等は、従来技術の有する問題を解決すべ《鋭意
研究した結果、PAS樹脂組成物で封止された電子部品
のリードフレームおよび/またはリードワイヤーと該封
止樹脂組成物との界面を硬化前粘度0.1〜800ポイ
ズ(25℃)の脱アルコール型の1液形室温硬化型シリ
コーンゴムでシールすることにより、界面部の間隙が封
鎖され、耐湿性および半田耐熱性に優れた電子部品封土
成形物の得られることを見出した。In order to solve the problems of the prior art, the present inventors have conducted extensive research and found that the interface between the lead frame and/or lead wire of an electronic component encapsulated with a PAS resin composition and the encapsulation resin composition has been determined. By sealing with dealcoholized, one-component, room-temperature-curing silicone rubber with a viscosity of 0.1 to 800 poise (25°C) before curing, the gap at the interface is sealed, making it an electronic material with excellent moisture resistance and soldering heat resistance. It has been found that a component fief molded product can be obtained.
また、PAS樹脂組成物として、繊維状充填材を配合し
、高温で可撓性のあるPAS樹脂組成物を用いると、加
工性、耐湿性および半田耐熱性に優れた電子部品封止成
形物の得られることを見出した。In addition, when a PAS resin composition containing a fibrous filler and being flexible at high temperatures is used, it is possible to create electronic component encapsulation moldings with excellent processability, moisture resistance, and soldering heat resistance. I found out what I can get.
本発明は、これらの知見に基づいて完成するに至ったも
のである。The present invention has been completed based on these findings.
[課題を解決するための手段〕
すなわち、本発明の要旨は、ポリアリーレンスルフィド
樹脂組成物で封止された電子部品封止成形物であって、
電子部品のリードフレームおよび/またはリードワイヤ
ーと該封止樹脂組成物との界面が、硬化前粘度0.1〜
800ポイズ(25℃)の脱アルコール型の1液形室温
硬化型シリコーンゴムでシールされていることを特徴と
する電子部品封止成形物にある。[Means for Solving the Problems] That is, the gist of the present invention is an electronic component encapsulation molded product encapsulated with a polyarylene sulfide resin composition,
The interface between the lead frame and/or lead wire of the electronic component and the sealing resin composition has a viscosity before curing of 0.1 to
This electronic component encapsulation molded article is characterized in that it is sealed with an 800 poise (25° C.) dealcoholization type one-component room temperature curing silicone rubber.
また、本発明によれば、PAS樹脂組成物として、PA
350〜95重量%と、繊維状充填材5〜50重量%を
含む溶融粘度(310℃、剪断速度104/秒で測定)
40〜300ポイズの樹脂組成物が好適に使用できる.
以下、本発明の各構成要素について詳述する。Further, according to the present invention, as the PAS resin composition, PA
Melt viscosity (measured at 310°C and shear rate of 104/sec) containing 350-95% by weight and 5-50% by weight of fibrous filler.
A resin composition of 40 to 300 poise can be suitably used. Each component of the present invention will be explained in detail below.
(PAS樹脂組成物)
本発明で使用するPAS樹脂組成物は、合成樹脂として
PASを用い、これに物性改良のために各種の繊維状充
填材や無機充填材、!也の合成樹脂、エラストマーなど
を配合した樹脂組成物である。その中でも、半田耐熱性
を向上させるためには、繊維状充填材を配合したものが
好ましい.また、成形加工性を改良するためには、後述
するような溶融粘度を有するPAS樹脂組成物を用いる
ことが好ましい。(PAS resin composition) The PAS resin composition used in the present invention uses PAS as a synthetic resin, and includes various fibrous fillers and inorganic fillers to improve physical properties! It is a resin composition containing synthetic resins, elastomers, etc. Among these, those containing fibrous fillers are preferred in order to improve soldering heat resistance. Moreover, in order to improve moldability, it is preferable to use a PAS resin composition having a melt viscosity as described below.
PAS
本発明で用いるPASは、ボリマーの主構成単位として
p−フエニレンスルフイドの繰り返し単ぱ70重量%以
上、さらに好ましくは90重量%以上含むポリアリーレ
ンスルフイドであり、実質的に線状構造を有するものが
好ましい。PAS The PAS used in the present invention is a polyarylene sulfide containing 70% by weight or more, more preferably 90% by weight or more of repeating p-phenylene sulfide as the main structural unit of the polymer, and is substantially linear. It is preferable to have a structure like that.
実質的に線状構造とは、酸化架橋などによる溶融粘度の
増大処理(キュアー)で得られるような架橋、分枝構造
を有するボリマーではなく、実質的に二官能性モノマー
を主体とするモノマーから得られたボリマーである。A substantially linear structure is not a polymer having a crosslinked or branched structure such as that obtained by curing to increase the melt viscosity by oxidative crosslinking, but a polymer made essentially from monomers mainly consisting of difunctional monomers. This is the obtained polymer.
p−フエニレンスルフイド単位が50重量%以上である
ことに対応して、とのPASは50重量%未溝の他の共
重合単位を含んでいてもよい。このような構成単位とし
ては、m−フエニレンスルフィド単位,ジフェニルスル
フオンスルフイド単位、ジフェニルスルフィド単位、ジ
フエニルエーテルスルフィド単位、2,6−ナフタレン
スルフィド単位等がある。また、p−フエニレンスルフ
ィド繰り返し単位70〜95重量%と、m−フエニレン
スルフイド繰り返し単位5〜30重量%とからなるブロ
ック共重合体も好ましく用いられる。Corresponding to the 50% by weight or more of p-phenylene sulfide units, the PAS may also contain 50% by weight of other copolymerized units. Examples of such structural units include m-phenylene sulfide units, diphenylsulfone sulfide units, diphenyl sulfide units, diphenyl ether sulfide units, and 2,6-naphthalene sulfide units. Also preferably used is a block copolymer consisting of 70 to 95% by weight of p-phenylene sulfide repeating units and 5 to 30% by weight of m-phenylene sulfide repeating units.
本発明で使用するPASは、溶融粘度(310℃、剪断
速度が104/秒で測定)が好ましくは10〜150ポ
イズ、さらに好ましくは20〜130ポイズのボリマー
であること望ましい.溶融粘度が低過ぎると、機械的な
強度が低い封止成形物となり、逆に、高過ぎると、流動
性が悪くなり封止成形が困難となるので、いずれも好ま
しくない。The PAS used in the present invention is preferably a polymer having a melt viscosity (measured at 310°C and a shear rate of 104/sec) of preferably 10 to 150 poise, more preferably 20 to 130 poise. If the melt viscosity is too low, the resulting molded product will have low mechanical strength, while if it is too high, the fluidity will deteriorate and molding will become difficult, so both are not preferred.
このようなPASは、公知の方法で製造することができ
る。例えば、特開昭61−7332号公報に記載されて
いるように、アルカリ金属硫化物とジハロ芳香族化合物
とをN−メチルビロリドンなどの有機アミド溶媒中で水
の存在下に特定の二段階昇温重合する方法により好適に
得ることが出来る.
なお、本発明で使用するPASは、実質的に線状構造を
有するものが加工性や物性上から好ましいが、トリクロ
ルベンゼンなどのボリ八ロベンゼンを少量成分として共
重合させることにより、若干の分枝構造を導入したPA
Sも用いることができる。Such PAS can be manufactured by a known method. For example, as described in JP-A-61-7332, an alkali metal sulfide and a dihaloaromatic compound are heated in a specific two-step heating process in the presence of water in an organic amide solvent such as N-methylpyrrolidone. It can be suitably obtained by a polymerization method. It is preferable that the PAS used in the present invention has a substantially linear structure from the viewpoint of processability and physical properties. PA with structure introduced
S can also be used.
罐1J口L皇且
半田耐熱性を改良するために、繊維状充填材を配合し、
樹脂組成物に可撓性を付与することが好ましい。In order to improve the solder heat resistance, a fibrous filler is added,
It is preferable to impart flexibility to the resin composition.
繊維状充填材としては、例えば、ガラス、チタン酸カリ
ウム、アルミナ、ジルコニア、シリカ、ケイ酸カリウム
、硫酸カルシウム、アラミド等の繊維もしくはウイスカ
ーが使用できる。この中でも特にガラス繊維が物性上、
経済上の観点から好ましい。As the fibrous filler, for example, fibers or whiskers of glass, potassium titanate, alumina, zirconia, silica, potassium silicate, calcium sulfate, aramid, etc. can be used. Among these, glass fiber in particular has physical properties,
Preferable from an economic point of view.
繊維の径は、通常、1.1〜12μm、好ましくは1.
1〜10μmが適当である。繊維径が大きすぎると、素
子ずれやワイヤー変形等を起こすおそれがあり、逆に、
小さすぎると、封止成形時に成形機のスクリューやシリ
ンダーへの粘着が起こって成形加工が困難となるおそれ
があるので、好ましくない。The fiber diameter is usually 1.1 to 12 μm, preferably 1.1 μm to 12 μm.
A suitable thickness is 1 to 10 μm. If the fiber diameter is too large, there is a risk of element displacement or wire deformation;
If it is too small, it is not preferable because it may stick to the screw or cylinder of the molding machine during sealing molding, making molding difficult.
これら繊維状充填材は、単独で、あるいは2種以上組合
せて用いることができる。These fibrous fillers can be used alone or in combination of two or more.
本発明で用いる封止用PAS樹脂組成物として、PAS
50〜95重量%と繊維状充填材5〜50重量%を含み
、かつ、樹脂組成物の溶融粘度(310℃、剪断速度1
04/秒で測定)40〜300ポイズ、好ましくは60
〜250ポイズの樹脂組成物が好ましい。As the PAS resin composition for sealing used in the present invention, PAS
The melt viscosity of the resin composition (310°C, shear rate 1
04/sec) 40 to 300 poise, preferably 60
~250 poise resin compositions are preferred.
繊維状充填材が50重量%超過では、樹脂組成物の溶融
粘度が上昇し、溶融粘度が300ポイズな超えると、素
子ずれ、ワイヤーはずれもしくは変形等を起こし易くな
るので好まし《ない。If the content of the fibrous filler exceeds 50% by weight, the melt viscosity of the resin composition increases, and if the melt viscosity exceeds 300 poise, element displacement, wire dislocation, deformation, etc. are likely to occur, which is not preferred.
一方、5里量%未満では可撓性が不足し、半田耐熱性の
改良効果が少なく、外装割れを生じ易《、かつ、常温で
の曲げ強度が低下し、端子折り曲げ工程での破損の恐れ
があるので好ましくない。また、溶融粘度が40ボイス
未満では、成形時にパリの発生にともなう外観不良を起
こすおそれがあるので好ましくない。On the other hand, if it is less than 5%, the flexibility will be insufficient, the effect of improving soldering heat resistance will be small, and the exterior will be easily cracked (and the bending strength at room temperature will decrease, leading to the risk of breakage during the terminal bending process). I don't like it because there is. Furthermore, if the melt viscosity is less than 40 voices, it is not preferable because there is a risk of poor appearance due to the occurrence of flakes during molding.
本発明で用いる封止用PAS樹脂組成物は、PASおよ
び繊維状充填材の外に、必要に応じて次のような無機充
填材、他の合成樹脂、エラストマー シリコーンオイル
等の耐熱性オイル、顔料、その他各種添加剤を、本発明
の目的を損なわない範囲で添加することができる。In addition to PAS and fibrous fillers, the PAS resin composition for sealing used in the present invention may optionally contain the following inorganic fillers, other synthetic resins, elastomers, heat-resistant oils such as silicone oil, and pigments. , and other various additives may be added within a range that does not impair the purpose of the present invention.
腫1充厘M
本発明で使用できる無機充填材としては、例えば、クル
ク、マイ力、カオリン、クレイ、リン酸マグネシウム、
炭酸マグネシウム、炭酸カルシウム、ケイ酸カルシウム
、硫酸カルシウム、酸化ケイ素、酸化アルミニウム、酸
化マグネシュウム、酸化チタン、酸化クロム、酸化鉄、
酸化銅、酸化亜鉛、フッ化ホウ素、二硫化モリブデン等
の粒状、鱗片状または粉末状の充填材が挙げられる。Inorganic fillers that can be used in the present invention include, for example, curk, mairiki, kaolin, clay, magnesium phosphate,
Magnesium carbonate, calcium carbonate, calcium silicate, calcium sulfate, silicon oxide, aluminum oxide, magnesium oxide, titanium oxide, chromium oxide, iron oxide,
Particulate, scaly, or powdery fillers such as copper oxide, zinc oxide, boron fluoride, and molybdenum disulfide may be used.
これら無機充填材も、それぞれ単独で、あるいは2種以
上組合せて用いることができる。These inorganic fillers can also be used alone or in combination of two or more.
のA およびエラストマ−
本発明の封止用樹脂組成物には、他の合成樹脂およびエ
ラストマーとして、例えば、ポリオレフィン、ポリエス
テル、ボリアミド、ポリイミド、ポリエーテルイミド、
ポリカーボネート、ポリフエニレンエーテル、ボリスル
フォン、ポリエーテルスルフォン、ポリエーテルエーテ
ルケトン、ポリケトンスルフィド、ボリアリーレン、ポ
リアセタール、ボリ四フッ化エチレン、ボリニフッ化エ
チレン、ボリスチレン、ABS樹脂、エボキシ樹脂、シ
リコーン樹脂、フェノール樹脂、ウレタン樹脂等の合成
樹脂、あるいはポリオレフィン系ゴム、フッ素ゴム、シ
リコーンゴム等のエラストマーが使用できる.
これらの合成樹脂およびエラストマーは、それぞれ単独
で、あるいは2種以上を組合わせて使用することができ
る。A and elastomer - The sealing resin composition of the present invention includes other synthetic resins and elastomers such as polyolefin, polyester, polyamide, polyimide, polyetherimide,
Polycarbonate, polyphenylene ether, boris sulfone, polyether sulfone, polyether ether ketone, polyketone sulfide, polyarylene, polyacetal, polytetrafluoroethylene, borifluoroethylene, polystyrene, ABS resin, epoxy resin, silicone resin, phenol resin , synthetic resins such as urethane resin, or elastomers such as polyolefin rubber, fluororubber, silicone rubber, etc. can be used. These synthetic resins and elastomers can be used alone or in combination of two or more.
ここで各成分を混合する方法は、特に限定されない。通
常広く使用されている方法、例えば、各成分をタンブラ
ー、ブレンダー等の混合機で混合し、押出機などを用い
て溶融混練する方法などを採用すればよい。また、PA
S樹脂組成物を用いて電子部品を封止成形する方法につ
いても特定の方法に限定されない。例えば、射出成形法
等の通常の成形方法が採用できる。The method of mixing each component here is not particularly limited. A commonly used method may be employed, such as a method in which each component is mixed in a mixer such as a tumbler or blender, and then melt-kneaded using an extruder or the like. Also, P.A.
The method for sealing and molding electronic components using the S resin composition is not limited to any particular method. For example, a normal molding method such as an injection molding method can be employed.
(シーリング材)
本発明においては、電子部品封土成形物の外装部(封止
PAS樹脂組成物)とリードフレーム等の封止した電子
部品との界面にシーリング材として、該外装部の樹脂成
分ならびに該金属に対し優れた接着性を示す特定の室温
硬化型シリコーンゴム(以下、rRTVシリコーンゴム
」と略記)を使用する点に最大の特徴を有する。(Sealing material) In the present invention, the resin component of the exterior portion and The most distinctive feature is the use of a specific room temperature curable silicone rubber (hereinafter abbreviated as rRTV silicone rubber) that exhibits excellent adhesion to the metal.
RTVシリコーンゴムとして、脱酢酸縮合反応型、脱オ
キシム縮合反応型、脱アルコール縮合反応型、脱アミン
縮合反応型など多くの種類のものが知られているが、一
般に、作業性ならびに耐湿性や非腐食性等の性能の両面
から、例えば、トーレ・シリコーン■社製の商品名トー
レ・シリコーンSE9 1 55〜SE9158RTV
およびSE9166〜SE9 1 68RTVなどに代
表されるl液形RTVシリコーンゴムであって、シラノ
ールとアルコキシシロキサンとの脱アルコール縮合反応
によるいわゆる脱アルコール(縮合反応)型のものが多
く使用されている。Many types of RTV silicone rubber are known, including deacetic acid condensation reaction type, oxime decondensation reaction type, alcohol dealcoding condensation reaction type, and deamine condensation reaction type, but in general, they are characterized by poor workability, moisture resistance, and non-condensation. In terms of performance such as corrosion resistance, for example, Toray Silicone SE9 1 55 to SE9158RTV manufactured by Toray Silicone Company.
and SE9166 to SE9168RTV, and many of the so-called dealcoholization (condensation reaction) type silicone rubbers produced by a dealcoholization condensation reaction between silanol and alkoxysiloxane are used.
この脱アルコール型の1液形RTVシリコーンゴムとし
ては、上記のほかに、例えば、1・−レ・シリコーン■
社製のSE9 1 00シリーズ、信越化学■社製のK
E48等、および東芝シリコーン■社製のTSE380
等多《の種類が市販されており、硬化反応前は液体であ
る流動タイプと固体である非流動タイプがある。In addition to the above, examples of this dealcoholization type one-component RTV silicone rubber include 1.
SE9 100 series manufactured by Shin-Etsu Chemical, K manufactured by Shin-Etsu Chemical
E48, etc., and TSE380 manufactured by Toshiba Silicone
Many types are commercially available, including a fluid type that is a liquid before the curing reaction and a non-flow type that is a solid.
本発明において使用するRTVシリコーンゴムは、これ
ら脱アルコール型の1液形のものであって、かつ、硬化
反応前の粘度(25℃)が0. 1〜800ポイズ、
好まし《は1〜600ポイズのものであり、特に、この
粘度範囲のものがPAS樹脂組成物で封止された電子部
品成形物に対するシール効果が優れている。The RTV silicone rubber used in the present invention is one-component type of dealcoholization type, and has a viscosity (at 25° C.) of 0.000. 1~800 poise,
Preferably, the viscosity is from 1 to 600 poise, and in particular, those having a viscosity within this range have an excellent sealing effect on molded electronic parts sealed with the PAS resin composition.
粘度が0.1ポイズ未満であると、シーリング材の1液
形RTVシリコーンゴムがリードフレーム等との界面部
から広く拡散しすぎて、シール効率?:充分発揮するの
に必要な厚みの塗膜が得られにくくなる。If the viscosity is less than 0.1 poise, the one-component RTV silicone rubber used as a sealant will diffuse too widely from the interface with the lead frame, etc., resulting in poor sealing efficiency. : It becomes difficult to obtain a coating film of the thickness necessary for sufficient performance.
一方、粘度が800ボイスを越すと、1液形RTVシリ
コーンゴムの流動性が低下し、リードフレーム等との界
面の微細部への浸入が不充分になるとともに、塗膜厚み
の不均一化による耐湿性の低下が生じ、また、塗布作業
性も損われる。On the other hand, when the viscosity exceeds 800 voices, the fluidity of the one-component RTV silicone rubber decreases, and it becomes insufficient to penetrate into the fine parts at the interface with the lead frame, etc., and the coating film thickness becomes uneven. Moisture resistance is reduced and coating workability is also impaired.
このような性状を満たすRTVシリコンゴムシーリング
材として、トーレ・シリコーン側社製SE9 1 56
RTV、SE9 1 57LRTVおよびSE9 1
66RTVなどが、特に好ましく使用できる。これら脱
アルコール型の1液形RTVシリコーンゴムは、金属を
腐食するおそれがなく、電気特性の経時的安定性(封止
効果)に優れているとともに、縮合生成物がアルコール
であるため取扱性においても優れている。As an RTV silicone rubber sealing material that satisfies these properties, SE9 156 manufactured by Toray Silicone Co., Ltd.
RTV, SE9 1 57LRTV and SE9 1
66RTV etc. can be particularly preferably used. These dealcoholized one-component RTV silicone rubbers have no risk of corroding metals, have excellent stability of electrical properties over time (sealing effect), and are easy to handle because the condensation product is alcohol. is also excellent.
次に、これら脱アルコール型の1液形RTVシリコーン
ゴムによるシール法は、特定な方法に限定されるもので
はな《、封止PAS樹脂組成物層と電子部品のリードフ
レーム等との界面に、滴下塗り、刷毛塗りあるいは1液
形RTVシリコーンゴム液中への浸漬塗り等により行う
ことができる。Next, the sealing method using these dealcoholized one-component RTV silicone rubbers is not limited to a specific method. It can be applied by dropping, brushing, or dipping into a one-component RTV silicone rubber solution.
脱アルコール型の1液形RTVシリコーンゴムの硬化は
、通常、室温または数十℃の温度条件下で、数時間〜1
日程度放置すればよい。Dealcoholization type one-component RTV silicone rubber is usually cured at room temperature or at a temperature of several tens of degrees Celsius for several hours to one hour.
You can leave it for about a day.
(電子部品封止成形物)
本発明の電子部品封止成形物は、封止樹脂組成物である
PAS樹脂組成物と電子部品のリードフレーム等との界
面が脱アルコール型の1液形RT■シリコーンゴムで充
填され、シールされているので、封止電子部品が機械的
に保護され、電気絶縁性に優れているとともに、耐湿性
および耐半田耐熱性に優れている.
(以下余白)
〔実施例J
以下に実施例、比較例および合成実験例を挙げて本発明
を具体的に説明するが、本発明はこれら実施例のみに限
定されるものではない。(Electronic component encapsulation molded product) The electronic component encapsulation molded product of the present invention is a one-component RT type in which the interface between the PAS resin composition that is the encapsulation resin composition and the lead frame of the electronic component is dealcoholization type. Filled and sealed with silicone rubber, the sealed electronic components are mechanically protected and have excellent electrical insulation as well as moisture resistance and soldering heat resistance. (The following is a blank space) [Example J The present invention will be specifically described below with reference to Examples, Comparative Examples, and Synthesis Experiment Examples, but the present invention is not limited to these Examples.
[九丘去旦四]
(ポリーp−フェニレンスルフィドの合成)含水硫化ソ
ーダ(水分51.97重量%)373kgおよびN−メ
チルビロリドン(以下、「NMPJと略記”)1070
kgをチタン張りオートクレープに仕込み、約203℃
まで昇温して少量のNMPおよびH.Sを含む水を溜出
させた。[Kukyuu Danshi] (Synthesis of poly p-phenylene sulfide) 373 kg of hydrated sodium sulfide (water content 51.97% by weight) and 1070 kg of N-methylpyrrolidone (hereinafter abbreviated as "NMPJ")
kg into a titanium-lined autoclave and heated to approximately 203℃.
A small amount of NMP and H. Water containing S was distilled out.
次いで、p−ジクロルベンゼン347kgを仕込んだ。Next, 347 kg of p-dichlorobenzene was charged.
220℃で5時間反応させた後に水77kgを追加した
。そして、258℃で3時間重合させた。反応混合物を
目開き0.1mmのスクリーンで篩分してボリマーを分
離し、アセトン洗、水洗して、洗浄ボリマーを得た。After reacting at 220° C. for 5 hours, 77 kg of water was added. Then, polymerization was carried out at 258°C for 3 hours. The reaction mixture was sieved through a screen with an opening of 0.1 mm to separate the polymer, which was then washed with acetone and water to obtain a washed polymer.
この洗浄ボリマーを2%・N84C1水溶液に浸漬し、
40℃で30分間処理した後、水洗し、80℃で減圧し
てポリーp−フェニレンスルフィド(以下、rP P
P SJと略記)を得た。このPPPSの溶融粘度(3
10℃ 剪断速度1047秒)は、100ポイズであっ
た。This washed polymer was immersed in a 2% N84C1 aqueous solution,
After processing at 40°C for 30 minutes, it was washed with water, and vacuumed at 80°C to prepare poly p-phenylene sulfide (hereinafter referred to as rP P
PSJ) was obtained. The melt viscosity of this PPPS (3
The shear rate (1047 seconds) at 10° C. was 100 poise.
[実施例1]
合成実験例で得たPPPS90重量%とガラス繊維(日
本電気硝子社製 ECSO3T−7 1 7DE/P)
10重量%をブレングーを用いて均一にドライブレンド
し、二軸混練押出機にて、シリンダー温度310℃でベ
レット化した。このペレットを用いて、溶融粘度を測定
した。[Example 1] 90% by weight of PPPS obtained in the synthesis experiment example and glass fiber (ECSO3T-7 1 7DE/P manufactured by Nippon Electric Glass Co., Ltd.)
10% by weight was uniformly dry-blended using a blender and pelletized using a twin-screw kneading extruder at a cylinder temperature of 310°C. Melt viscosity was measured using this pellet.
また、シリンダー温度310℃、金型温度150℃の条
件で射出成形してテストビース(形状130xl2.7
X3.2mm)を作成した。In addition, test beads (shape 130xl2.7
X3.2mm) was created.
さらに、このベレットを用いて封止成形機(日本製鋼所
製 JT−4OS)にて、コンデンサー(静電容量1
0 0 n F )を封止成形し、封止成形品の樹脂組
成物とリード間に、脱アルコール型の1液形RTVシリ
コーンゴム(トーレ・シリコーン■社製 SE9 1
57LRTV)を滴下シタ。Furthermore, using this pellet, a capacitor (capacitance 1
0 0 n F) is sealed, and a dealcoholized one-component RTV silicone rubber (manufactured by Toray Silicone SE9 1) is placed between the resin composition of the sealed molded product and the lead.
57LRTV).
滴下後、20℃、湿度50%で20時間放置することに
より、RTVシリコーンゴムな硬化させた。After dropping, the RTV silicone rubber was cured by being left at 20° C. and 50% humidity for 20 hours.
得られた封止電子部品について、次の方法により評価試
験を行なった。Evaluation tests were conducted on the obtained sealed electronic components using the following method.
11l翌工」
く素子ずれ等〉
コンデンサー素子が正常に封止されたものか否か、すな
わち、素子「ずれ」もしくはリードワイヤーの剥離が生
じていないかを判断するために、軟X線透過法により観
察を行なった。素子ずれ等の有無を次の二段階で評価し
た。11L Next Work'' Element displacement, etc.> In order to determine whether the capacitor element is properly sealed, that is, whether there is any element displacement or peeling of the lead wire, a soft X-ray transmission method is used. Observations were made by The presence or absence of element displacement etc. was evaluated in the following two stages.
○:無し、×:有り
〈耐湿性〉
耐湿性は、軟X線透過法による観察にて正常と判断され
た封正電子部品の内5個を高温恒湿槽にてバイアス試験
(85℃×95%・DC−25V)にかけ、500時間
後の静電容量変化値がすべて5%以内に収まっているか
否かの測定を行なった。評価は次の2段階で行なった。○: None, ×: Yes (Moisture resistance) Moisture resistance was determined by conducting a bias test (85°C 95% DC-25V), and it was measured whether all capacitance changes after 500 hours were within 5%. Evaluation was performed in the following two stages.
○:静電容量変化値が5%以内、×:5%超過く半田耐
熱性〉
半田耐熱性は、軟X線透過法による観察にて正常と判断
された封止電子部品の内5個を高温恒湿槽(85℃、8
5%)にて4時間放置処理後、260℃で10秒間半田
槽に浸漬し、外装のひび割れを目視および顕微鏡にて判
定した。評価は次の2段階で行なった。○: Capacitance change value is within 5%, ×: Soldering heat resistance exceeds 5% Soldering heat resistance is determined by measuring 5 of the sealed electronic components judged to be normal by observation using soft X-ray transmission method. High temperature and humidity chamber (85℃, 8
5%) for 4 hours, immersed in a solder bath at 260° C. for 10 seconds, and cracks on the exterior were determined visually and using a microscope. Evaluation was performed in the following two stages.
○:ひび割れ無し、X:ひび割れ有り 測定結果を第1表に示す。○: No cracks, X: With cracks The measurement results are shown in Table 1.
[実施例2]
PPPS70重量%とガラス繊維30重量%をブレンダ
ーを用いて均一にドライブレンドした以外は実施例1と
同様にして、テストビースおよび封止電子部品を成形し
て、同様に評価した。[Example 2] Test beads and sealed electronic components were molded and evaluated in the same manner as in Example 1, except that 70% by weight of PPPS and 30% by weight of glass fiber were uniformly dry blended using a blender. .
[実施例3]
PPP360重量%とガラス繊維30重量%およびチタ
ン酸カリウム繊維(日本チタン工業■製HT−200)
10重量%をブレンダーを用いて均一にドライブレンド
した以外は実施例1と同様にして、テストビースおよび
封止電子部品を成形して、同様に評価した。[Example 3] 360% by weight of PPP, 30% by weight of glass fiber, and potassium titanate fiber (HT-200 manufactured by Nippon Titanium Industry Co., Ltd.)
Test beads and sealed electronic components were molded and evaluated in the same manner as in Example 1, except that 10% by weight was uniformly dry blended using a blender.
[実施例4]
封止成形品の樹脂組成物とリードワイヤー間にRTVシ
リコーンゴム(トーレ・シリコーン■社製 SE9 1
56RTV)を塗布した以外は実施例1と同様にして
、テストビースおよび電子部品を封止成形して、同様に
評価した。[Example 4] RTV silicone rubber (manufactured by Toray Silicone ■ SE9 1) was placed between the resin composition of the encapsulation molded product and the lead wire.
Test beads and electronic components were encapsulated and molded in the same manner as in Example 1, except that 56RTV) was applied, and evaluated in the same manner.
[実施例5]
封止成形品の樹脂組成物とリードワイヤー間にRTVシ
リコーンゴム(トーレ・シリコーン社製SE9 1 6
6RTV)を塗布した以外は実施例1と同様にして、テ
ストビースおよび電子部品を成形して同様に評価した。[Example 5] RTV silicone rubber (SE9 1 6 manufactured by Toray Silicone Co., Ltd.) was placed between the resin composition of the encapsulation molded product and the lead wire.
Test beads and electronic components were molded and evaluated in the same manner as in Example 1, except that 6RTV) was applied.
[実施例6]
pppsso重量%とガラス繊維(日本電気硝子■社製
ECSO3T−717DE)10重量%と溶融シリカ
(電気化学■社製 FS−44シラン処理品)10重量
%をブレンダーを用いて均一にドライブレンドした以外
は実施例1と同様にして、テストビースおよび電子部品
を封止成形して,同様に評価した,
[比較例1]
封止成形品の樹脂組成物とリードワイヤー間へのRTV
シリコーンゴムの滴下を止めた以外は、実施例1と同様
にしてテストビースおよび電子部品を封止成形して、同
様に評価した.
[比較例2]
RTVシリコーンゴムとして粘度(25℃)が900ボ
イスと高粘度のトーレ・シリ.コーン■社製 SE9
1 58RTVを用いた以外は、実施例1と同様にして
テストビースおよび電子部品を封止成形して、同様に評
価した。[Example 6] 10% by weight of pppsso, 10% by weight of glass fiber (ECSO3T-717DE, manufactured by Nippon Electric Glass Co., Ltd.), and 10% by weight of fused silica (FS-44, silane-treated product, manufactured by Denki Kagaku ■ Co., Ltd.) were uniformly mixed using a blender. [Comparative Example 1] Test beads and electronic components were encapsulated and evaluated in the same manner as in Example 1, except that they were dry blended. [Comparative Example 1] RTV
A test bead and an electronic component were sealed and molded in the same manner as in Example 1, except that the dripping of silicone rubber was stopped, and evaluated in the same manner. [Comparative Example 2] Toray Silicone rubber, which has a high viscosity (25° C.) of 900 voices, was used as an RTV silicone rubber. Cone SE9
Test beads and electronic components were sealed and molded in the same manner as in Example 1, except that 158RTV was used, and evaluated in the same manner.
[比較例3コ
PPPS40重量%とガラス繊維60重量%をブレンダ
ーを用いて、均一にドライブレンドしたL:J外は実施
例1と同様にして、テストビースおよび電子部品を封止
成形して、同様に評価した。[Comparative Example 3] 40% by weight of PPPS and 60% by weight of glass fiber were uniformly dry blended using a blender. Test beads and electronic components were encapsulated and molded in the same manner as in Example 1 except for L:J. They were evaluated in the same way.
[比較例4]
PPPS97重量%とガラス繊維3重量%をブレンダー
を用い、均一にドライブレンドした以外は実施例1と同
様にして、テストビースおよび電子部品を封止成形して
、同様に評価した。[Comparative Example 4] Test beads and electronic components were encapsulated and evaluated in the same manner as in Example 1, except that 97% by weight of PPPS and 3% by weight of glass fiber were uniformly dry blended using a blender. .
【比較例5コ
実施例1で用いたR T VシリコーンゴムのSE−9
157LRTVを四塩化炭素で希釈して、粘度を0.0
5ボイス(25℃)に調整して用いた以外は実施例1と
同様にして、電子部品を封止成形して、同様に評価した
。[Comparative Example 5] R T V silicone rubber used in Example 1 SE-9
Dilute 157LRTV with carbon tetrachloride to reduce the viscosity to 0.0.
Electronic components were sealed and molded in the same manner as in Example 1 except that the temperature was adjusted to 5 voices (25° C.) and evaluated in the same manner.
実施例1〜6および比較例1〜4の結果を一括して第1
表に示す。The results of Examples 1 to 6 and Comparative Examples 1 to 4 were combined into the first
Shown in the table.
(以下余白)
〔発明の効果〕
本発明の電子部品封止成形物は、封止PAS樹脂組成物
と電子部品のリードフレーム等との界面が脱アルコール
型の1液形RTVシリコーンゴムでシールされているた
め、従来品に比べて、耐湿性および耐半田耐熱性等が改
良されている。(The following is a blank space) [Effects of the Invention] In the electronic component encapsulation molded product of the present invention, the interface between the encapsulation PAS resin composition and the lead frame of the electronic component is sealed with a dealcoholized one-component RTV silicone rubber. As a result, moisture resistance, soldering heat resistance, etc. are improved compared to conventional products.
Claims (2)
た電子部品封止成形物であって、電子部品のリードフレ
ームおよび/またはリードワイヤーと該封止樹脂組成物
との界面が、硬化前粘度0.1〜800ポイズ(25℃
)の脱アルコール型の1液形室温硬化型シリコーンゴム
でシールされていることを特徴とする電子部品封止成形
物。(1) An electronic component encapsulation molded product encapsulated with a polyarylene sulfide resin composition, wherein the interface between the lead frame and/or lead wire of the electronic component and the encapsulation resin composition has a viscosity of 0 before curing. .1~800 poise (25℃
1.) An electronic component encapsulation molded article, characterized in that it is sealed with a dealcoholization type one-component room temperature curing silicone rubber.
リーレンスルフィド50〜95重量%と繊維状充填材5
〜50重量%を含む溶融粘度(310℃、剪断速度10
^4/秒で測定)40〜300ポイズの樹脂組成物であ
る請求項1記載の電子部品封止成形物。(2) The polyarylene sulfide resin composition contains 50 to 95% by weight of polyarylene sulfide and 5% by weight of fibrous filler.
Melt viscosity containing ~50% by weight (310°C, shear rate 10
The electronic component encapsulation molded article according to claim 1, which is a resin composition having a poise of 40 to 300 poise (measured at ^4/sec).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1056185A JP2787463B2 (en) | 1989-03-10 | 1989-03-10 | Electronic parts molding |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1056185A JP2787463B2 (en) | 1989-03-10 | 1989-03-10 | Electronic parts molding |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02237139A true JPH02237139A (en) | 1990-09-19 |
JP2787463B2 JP2787463B2 (en) | 1998-08-20 |
Family
ID=13020050
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1056185A Expired - Lifetime JP2787463B2 (en) | 1989-03-10 | 1989-03-10 | Electronic parts molding |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2787463B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997020673A1 (en) * | 1995-12-07 | 1997-06-12 | Matsushita Electric Industrial Co., Ltd. | Process for manufacturing resin-encapsulated electronic product |
US6008681A (en) * | 1998-06-02 | 1999-12-28 | Conexant Systems, Inc. | Method and apparatus for deriving power from a clock signal coupled through a transformer |
JP2009246114A (en) * | 2008-03-31 | 2009-10-22 | Koa Corp | Electronic component and method of forming coating film on electronic component |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5366565A (en) * | 1976-11-26 | 1978-06-14 | Asahi Glass Co Ltd | Method of sealing electronic parts |
JPS62120036A (en) * | 1985-11-20 | 1987-06-01 | Shin Etsu Polymer Co Ltd | Manufacture of resin-sealed electronic component part |
JPS62297356A (en) * | 1986-06-18 | 1987-12-24 | Toshiba Silicone Co Ltd | Room temperature curing polyorganosiloxane composition |
-
1989
- 1989-03-10 JP JP1056185A patent/JP2787463B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5366565A (en) * | 1976-11-26 | 1978-06-14 | Asahi Glass Co Ltd | Method of sealing electronic parts |
JPS62120036A (en) * | 1985-11-20 | 1987-06-01 | Shin Etsu Polymer Co Ltd | Manufacture of resin-sealed electronic component part |
JPS62297356A (en) * | 1986-06-18 | 1987-12-24 | Toshiba Silicone Co Ltd | Room temperature curing polyorganosiloxane composition |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1997020673A1 (en) * | 1995-12-07 | 1997-06-12 | Matsushita Electric Industrial Co., Ltd. | Process for manufacturing resin-encapsulated electronic product |
US6052893A (en) * | 1995-12-07 | 2000-04-25 | Matsushita Electric Industrial Co., Ltd. | Process for manufacturing a resin-encapsulated electronic product |
US6008681A (en) * | 1998-06-02 | 1999-12-28 | Conexant Systems, Inc. | Method and apparatus for deriving power from a clock signal coupled through a transformer |
JP2009246114A (en) * | 2008-03-31 | 2009-10-22 | Koa Corp | Electronic component and method of forming coating film on electronic component |
Also Published As
Publication number | Publication date |
---|---|
JP2787463B2 (en) | 1998-08-20 |
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