JPH05166974A - Epoxy resin composition - Google Patents
Epoxy resin compositionInfo
- Publication number
- JPH05166974A JPH05166974A JP32927791A JP32927791A JPH05166974A JP H05166974 A JPH05166974 A JP H05166974A JP 32927791 A JP32927791 A JP 32927791A JP 32927791 A JP32927791 A JP 32927791A JP H05166974 A JPH05166974 A JP H05166974A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- resin composition
- weight
- formula
- hardening agent
- 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
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 37
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 37
- 239000000203 mixture Substances 0.000 title claims abstract description 18
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 19
- 239000005011 phenolic resin Substances 0.000 claims abstract description 14
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 239000011256 inorganic filler Substances 0.000 claims abstract description 6
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 6
- 239000004843 novolac epoxy resin Substances 0.000 claims abstract description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 5
- 125000004429 atom Chemical group 0.000 claims abstract description 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 150000002367 halogens Chemical class 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 claims description 18
- 238000005538 encapsulation Methods 0.000 claims description 6
- 239000004065 semiconductor Substances 0.000 claims description 6
- 238000005476 soldering Methods 0.000 abstract description 10
- 238000010521 absorption reaction Methods 0.000 abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
- 239000011342 resin composition Substances 0.000 abstract description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 229920001568 phenolic resin Polymers 0.000 abstract description 3
- 230000002542 deteriorative effect Effects 0.000 abstract description 2
- 239000004615 ingredient Substances 0.000 abstract 2
- 229950011260 betanaphthol Drugs 0.000 abstract 1
- 229910000679 solder Inorganic materials 0.000 description 26
- 238000012360 testing method Methods 0.000 description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 17
- 229920003986 novolac Polymers 0.000 description 11
- 239000000843 powder Substances 0.000 description 11
- 239000012778 molding material Substances 0.000 description 10
- 230000035882 stress Effects 0.000 description 9
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 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 6
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000005350 fused silica glass Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 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 3
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- -1 dicyclopentadiene modified phenol Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 2
- CQOZJDNCADWEKH-UHFFFAOYSA-N 2-[3,3-bis(2-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC=CC=C1CCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O CQOZJDNCADWEKH-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000003566 sealing material 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
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 description 1
- XYXBMCIMPXOBLB-UHFFFAOYSA-N 3,4,5-tris(dimethylamino)-2-methylphenol Chemical compound CN(C)C1=CC(O)=C(C)C(N(C)C)=C1N(C)C XYXBMCIMPXOBLB-UHFFFAOYSA-N 0.000 description 1
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000006243 chemical reaction 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
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 229910002026 crystalline silica Inorganic materials 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 230000008642 heat stress Effects 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-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
- WXAZIUYTQHYBFW-UHFFFAOYSA-N tris(4-methylphenyl)phosphane Chemical compound C1=CC(C)=CC=C1P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 WXAZIUYTQHYBFW-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Abstract
Description
ãïŒïŒïŒïŒã[0001]
ãç£æ¥äžã®å©çšåéãæ¬çºæã¯ãèåç°ã¹ãã¬ã¹æ§ã«åª
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ããBACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an epoxy resin composition for semiconductor encapsulation which is excellent in solder stress resistance.
ãïŒïŒïŒïŒã[0002]
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è¡ããŠããã2. Description of the Related Art Most highly integrated IC devices are encapsulated by a resin encapsulation method using an epoxy resin encapsulating material which is excellent in reliability, cost and mass productivity. As the epoxy resin encapsulating material, a resin composition composed of an orthocresol novolac epoxy resin and a novolac type phenol resin, which are excellent in heat resistance, moisture resistance and moldability, is used. However, with the recent high integration and multi-functionalization,
Highly integrated IC packages have a strong tendency to be smaller and thinner due to the larger size of devices and the rationalization of mounting. Compared to the conventional DIP type, small and thin SOJs, SOPs, and QFs are used.
P and TSOP type surface mount packages are rapidly shifting.
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ãŸããŠãããThis means that, unlike the conventional DIP type, the package itself is exposed to a high temperature of 215 to 260 ° C. at the time of soldering, and the surface mount type package in which a large chip is enclosed in a small and thin package exerts a large stress. This causes cracking of the package resin and peeling of the chip interface, which is a fatal problem in the reliability of the IC package. A highly reliable encapsulating resin composition suitable for encapsulating these surface mount packages is desired.
ãïŒïŒïŒïŒããããã®åé¡ã解決ããããã«åç°ä»ãæ
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å°äœå°æ¢çšãšããã·æš¹èçµæç©ãåŸããŸã§ã«ã¯è³ããªã
ã£ããIn order to alleviate the thermal shock during soldering in order to solve these problems, addition of a thermoplastic oligomer (JP-A-62-115849) and addition of various silicone compounds (JP-A-62-158). No. 115850, 62
-116654, 62-128162),
Furthermore, methods such as silicone modification (Japanese Patent Laid-Open No. 62-136860) are used, but in all cases cracks occur in the package during soldering, and a highly reliable epoxy resin composition for semiconductor encapsulation is obtained. It didn't reach.
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åç°ã¹ãã¬ã¹æ§ãäžååã§ãããOn the other hand, in order to obtain a semiconductor encapsulating epoxy resin composition having excellent heat stress resistance during soldering, that is, solder stress resistance, use of a biphenyl type epoxy resin as a resin system (Japanese Patent Laid-Open No. 64-65116). Gazette) has been studied, but the use of a biphenyl type epoxy resin improves the adhesion to the lead frame and the low water absorption, improves the solder stress resistance, and particularly reduces the occurrence of cracks.
Since the heat resistance is poor, the solder stress resistance is insufficient especially at a high temperature of 250 ° C. or higher.
ãïŒïŒïŒïŒã[0006]
ãçºæã解決ããããšãã課é¡ãæ¬çºæã¯ãæåœ¢æ§ãã
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ã®ã§ãããSUMMARY OF THE INVENTION The present invention provides an epoxy resin composition for semiconductor encapsulation which is excellent in solder heat resistance during soldering without deteriorating moldability and reliability.
ãïŒïŒïŒïŒã[0007]
ã課é¡ã解決ããããã®ææ®µãæ¬çºæã¯ïŒïŒ¡ïŒäžèšåŒ
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å«ããšããã·æš¹èãThe present invention comprises (A) a co-condensed novolak epoxy resin of orthocresol and β-naphthol represented by the following formula (1) in a total epoxy resin amount of 3: 1.
Epoxy resin containing 0 to 100% by weight,
ãïŒïŒïŒïŒã[0008]
ãåïŒã ïŒïœïŒïŒãïŒïŒ[Chemical 3] (N = 1 to 6)
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ã硬åå€ã(B) A curing agent containing a phenol resin curing agent represented by the following formula (2) in an amount of 30 to 100% by weight based on the total amount of the curing agent,
ãïŒïŒïŒïŒã[0010]
ãåïŒã [Chemical 4]
ãïŒïŒïŒïŒãïŒåŒäžã®ïŒ²1 ã2 ã¯æ°ŽçŽ ãããã²ã³ãäœ
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ç±æ§ãæãããã®ã§ããã(Wherein R 1 and R 2 are the same or different atoms or groups selected from hydrogen, halogen and lower alkyl groups, n = 1 to 6) (C) inorganic filler and (D) curing An epoxy resin composition for semiconductor encapsulation containing an accelerator as an essential component,
It has extremely excellent solder heat resistance as compared with conventional epoxy resin compositions.
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æå€§éã«åŒãåºãããšãã§ãããThe co-condensed novolak epoxy resin of orthocresol and β-naphthol used in the present invention is an epoxidized novolak resin obtained by co-condensing orthocresol and β-naphthol from formaldehyde, and β-naphthol at the time of the co-condensation thereof. The amount is preferably 50% by weight or more, and the compound mainly has the structure of formula (1). Further, n is 1 to 6, and if it exceeds 6, the fluidity at the time of molding is poor. Formula (1) has the characteristics of excellent low water absorption, a small linear expansion coefficient of the resin, and excellent releasability at the time of molding, and shows good results for solder heat resistance during soldering. By adjusting the amounts of the orthocresol and β-naphthol co-condensed novolac epoxy resin to be used, solder heat resistance can be maximized.
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ã®ããšããããIn order to obtain the effect of solder heat resistance, orthocresol and β-naphthol co-condensed novolac epoxy resin are contained in an amount of 30% by weight or more, preferably 60% by weight or more of the total amount of epoxy resin.
It is desirable to use more than weight%. If it is less than 30% by weight, low water absorption and low linear expansion coefficient cannot be sufficiently obtained, and solder heat resistance is insufficient. When orthocresol and an epoxy resin other than the β-naphthol co-condensed novolac epoxy resin are used in combination, the epoxy resin to be used refers to all polymers having an epoxy group. For example, bisphenol type epoxy resin, cresol novolac type epoxy resin, biphenyl type epoxy resin, phenol novolac type epoxy resin and triphenol methane type epoxy resin, alkyl modified triphenol methane type epoxy resin, etc.
Functional epoxy resin, triazine nucleus-containing epoxy resin and the like.
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åã§ãããThe phenol resin curing agent represented by the formula (2) is a modification of para-xylene in the skeleton. In the formula, n is 1 to 6, and R 1 and R 2 are the same or different atoms or groups selected from hydrogen, halogen and lower alkyl groups. Among these, when n exceeds 6, the fluidity during molding is poor. The lower alkyl group has 1 to 4 carbon atoms, and when it exceeds 4, the fluidity at the time of molding becomes poor. Each of R 1 and R 2 is preferably a hydrogen atom. It features low elastic modulus above glass transition temperature and low internal stress during soldering.
Further, since it has characteristics such as excellent adhesion to the chip and the lead frame and low water absorption, it shows good results in resistance to solder stress. The amount of the phenol resin curing agent used is preferably 30% by weight or more, more preferably 60% by weight or more, based on the total amount of the curing agent.
If it is less than 30% by weight, the adhesion to the lead frame and the low water absorption will not be improved, and the solder stress resistance will be insufficient.
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ããŒã«æš¹èçãçšããããšãã§ãããWhen another phenol resin curing agent is used in combination with the phenol resin curing agent represented by the formula (2), the phenol resin curing agent used means all polymers having a phenolic hydroxyl group. For example, generally, phenol novolac resin, cresol novolac resin, dicyclopentadiene modified phenol resin, co-condensation product of dicyclopentadiene modified phenol resin and phenol novolac or cresol novolac resin, paraxylene modified phenol resin and the like can be used.
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å«ãŸãããã®ãæãŸãããExamples of the inorganic filler used in the present invention include fused silica powder, spherical silica powder, crystalline silica powder, secondary agglomerated silica powder, silica powder obtained by crushing porous silica powder, alumina, etc., and particularly fused silica. Powders, spherical silica powders and mixtures of fused silica powders and spherical silica powders are preferred. In addition, as the compounding amount of the inorganic filler,
From the standpoint of balance between solder stress resistance and moldability, it is desirable that the total resin composition contains 70 to 90% by weight.
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ããFurther, the curing accelerator used in the present invention may be any one as long as it accelerates the reaction between the epoxy group and the hydroxyl group, and those generally used for the sealing material can be widely used. For example, organic phosphine compounds such as triphenylphosphine (TPP), tributylphosphine, tri (4-methylphenyl) phosphine, tributylamine,
Third such as triethylamine, benzyldimethylamine, trisdimethylaminomethylphenol, 1,8-diazabicyclo [5,4,0] -7-undecene (DBU)
Examples thereof include imidazole compounds such as secondary amine, 2-methylimidazole, 2-phenylimidazole and 2-ethyl-4-methylimidazole. These may be used alone or in combination of two or more.
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ããIn addition to the above, the composition of the present invention may optionally contain a coloring agent such as carbon black, a release agent such as carnauba wax and synthetic wax, a flame retardant such as brominated epoxy and antimony trioxide, and γ-. A coupling agent such as glycidoxypropyltrimethoxysilane and a rubber component such as silicone rubber and polybutadiene can be added.
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æ°éšåã®å°æ¢ã被èŠãçµ¶çžçã«é©çšããããšãã§ãããTo produce the encapsulating epoxy resin composition of the present invention as a molding material, an epoxy resin, a curing agent,
A curing accelerator, a filler, and other additives are sufficiently and uniformly mixed with a mixer or the like, and then melt-kneaded with a hot roll, a kneader, or the like, cooled, and then pulverized to obtain a molding material. These molding materials can be applied to sealing, coating, insulating, etc. of electronic parts or electric parts.
ãïŒïŒïŒïŒã[0020]
ã宿œäŸãä»¥äžæ¬çºæã宿œäŸã§å ·äœçã«èª¬æãããEXAMPLES The present invention will be specifically described below with reference to examples.
ãïŒïŒïŒïŒã宿œäŸïŒ äžèšçµæç© ãªã«ãœã¯ã¬ãŸãŒã«ãšÎ²âããããŒã«ã®å ±çž®åããã©ãã¯ãšããã·æš¹è ïŒïœã¯ïœïŒïŒãïŒïŒééïŒ ãïœïŒïŒãïŒïŒééïŒ ã®æ··åç©ã ãšããã·åœéïŒïŒïŒãè»åç¹ïŒïŒâïŒ ïŒ3.ïŒéééš äžèšåŒïŒïŒïŒã§ç€ºããããã§ããŒã«æš¹è硬åå€ ïŒïœã¯ïœïŒïŒãïŒïŒééïŒ ãïœïŒïŒãïŒïŒééïŒ ã®æ··åç©ã æ°Žé žåºåœéïŒïŒïŒïŒè»åç¹ïŒïŒâïŒ ïŒ0.ïŒéé éšExample 1 The following composition Co-condensed novolak epoxy resin of orthocresol and β-naphthol (n is a mixture of 70% by weight of n = 3 and 30% by weight of n = 4, epoxy equivalent 225, softening point 84 ° C.) ) 13.5 parts by weight Phenolic resin curing agent represented by the following formula (3) (n is a mixture in which n = 2 is 30% by weight and n = 3 is 70% by weight, hydroxyl equivalent 175, softening point 75 ° C.) 10. 5 parts by weight
ãïŒïŒïŒïŒã[0022]
ãåïŒã [Chemical 5]
ãïŒïŒïŒïŒã 溶èã·ãªã«ç²æ« ïŒïŒéééš ããªãã§ãã«ãã¹ãã£ã³ 0.ïŒéééš ã«ãŒãã³ãã©ã㯠0.ïŒéééš ã«ã«ããã¯ãã¯ã¹ 0.ïŒéééš ããããµãŒã§åžžæž©ã§æ··åããïŒïŒãïŒïŒïŒâã§ïŒè»žããŒ
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湿æ§è©Šéšãè¡ã£ãã75 parts by weight of fused silica powder 0.2 parts by weight of triphenylphosphine 0.3 parts by weight of carbon black 0.5 parts by weight of carnauba wax are mixed in a mixer at room temperature and kneaded by a twin-screw roll at 70 to 100 ° C. The obtained molding material was made into a molding material that was crushed after cooling, and the obtained molding material was tabletized and a 6 à 6 mm chip was put in a 52p package for solder crack testing under the conditions of 175 ° C., 70 kg / cm 2 and 120 seconds on a low-pressure transfer molding machine. And a 3 à 6 mm chip for a solder moisture resistance test in a 16 pSOP package. The sealed test element was subjected to the following solder crack test and solder moisture resistance test.
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å®ããã 詊éšçµæã衚ïŒã«ç€ºããSolder crack test: The sealed test element was subjected to an environment of 85 ° C. and 85% RH for 48 hours and 72 hours.
After processing, it was immersed in a solder bath at 260 ° C. for 10 seconds, and external cracks were observed with a microscope. Solder moisture resistance test: sealed test element at 85 ° C, 85
After 72 Hr treatment in an environment of% RH and then dipping in a solder bath at 260 ° C for 10 seconds, a pressure cooker test (12
The circuit was opened at 5 ° C. and 100% RH, and the open circuit failure was measured. The test results are shown in Table 1.
ãïŒïŒïŒïŒã宿œäŸïŒãïŒ è¡šïŒã®åŠæ¹ã«ãããã£ãŠé
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æåœ¢ææãåŸãããã®æåœ¢ææã§ãã¹ãçšçŽ åãå°æ¢ã
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ã衚ïŒã«ç€ºããExamples 2 to 5 Compounding was performed according to the formulation shown in Table 1, and molding materials were obtained in the same manner as in Example 1. A molded product in which a test element was sealed with this molding material was obtained, and a solder crack test and a solder moisture resistance test were conducted using this molded product in the same manner as in Example 1. The test results are shown in Table 1.
ãïŒïŒïŒïŒãæ¯èŒäŸïŒãïŒ è¡šïŒã®åŠæ¹ã«ãããã£ãŠé
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æåœ¢ææãåŸãããã®æåœ¢ææã§ãã¹ãçšçŽ åãå°æ¢ã
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ã衚ïŒã«ç€ºããComparative Examples 1 to 5 Compounding was carried out according to the formulation shown in Table 1, and a molding material was obtained in the same manner as in Example 1. A molded product in which a test element was sealed with this molding material was obtained, and a solder crack test and a solder moisture resistance test were conducted using this molded product in the same manner as in Example 1. The test results are shown in Table 1.
ãïŒïŒïŒïŒã[0027]
ã衚ïŒã [Table 1]
ãïŒïŒïŒïŒã[0028]
ãçºæã®å¹æãèç±æ§ãäœåžæ°Žæ§ã坿æ§ã«åªããæš¹è
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èç±æ§ã«éåžžã«åªããŠãããEFFECT OF THE INVENTION A resin composition having excellent heat resistance, low water absorption and flexibility can be obtained. As a sealing material for highly integrated IC packages to be surface-mounted on a printed circuit board, it has excellent solder heat resistance during soldering.
âââââââââââââââââââââââââââââââââââââââââââââââââââââ ããã³ãããŒãžã®ç¶ã (51)Int.Cl.5 èå¥èšå· åºå æŽççªå·  æè¡è¡šç€ºç®æ ïŒïŒïŒ¬ 63/00 ïŒïŒªïŒ³ 8830â4 âââââââââââââââââââââââââââââââââââââââââââââââââââ âââ Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location C08L 63/00 MJS 8830-4J
Claims (1)
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ç·ç¡¬åå€éã«å¯ŸããŠïŒïŒãïŒïŒïŒééïŒ å«ã硬åå€ã ãåïŒã ïŒåŒäžã®ïŒ²1 ã2 ã¯æ°ŽçŽ ãããã²ã³ãäœçŽã¢ã«ãã«åº
ã®äžããéžæãããåäžãããã¯ç°ãªãååãŸãã¯åºã
ïœïŒïŒãïŒïŒ ïŒïŒ£ïŒç¡æ©è³ªå å¡«æåã³ ïŒïŒ€ïŒç¡¬åä¿é²å€ ãå¿ é æåãšããåå°äœå°æ¢çšãšããã·æš¹èçµæç©ã1. An epoxy resin containing (A) an orthocresol and β-naphthol co-condensed novolac epoxy resin represented by the following formula (1) in an amount of 30 to 100% by weight of the total epoxy resin: (N = 1 to 6) (B) A curing agent containing a phenol resin curing agent represented by the following formula (2) in an amount of 30 to 100% by weight based on the total amount of the curing agent: (Wherein R 1 and R 2 are the same or different atoms or groups selected from hydrogen, halogen and lower alkyl groups,
n = 1 to 6) An epoxy resin composition for semiconductor encapsulation, which comprises (C) an inorganic filler and (D) a curing accelerator as essential components.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32927791A JP2963260B2 (en) | 1991-12-13 | 1991-12-13 | Epoxy resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32927791A JP2963260B2 (en) | 1991-12-13 | 1991-12-13 | Epoxy resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05166974A true JPH05166974A (en) | 1993-07-02 |
| JP2963260B2 JP2963260B2 (en) | 1999-10-18 |
Family
ID=18219656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP32927791A Expired - Fee Related JP2963260B2 (en) | 1991-12-13 | 1991-12-13 | Epoxy resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2963260B2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010013406A1 (en) * | 2008-08-01 | 2010-02-04 | äœåããŒã¯ã©ã€ãæ ªåŒäŒç€Ÿ | Resin composition for semiconductor encapsulation and semiconductor device using the same |
| JP2013010903A (en) * | 2011-06-30 | 2013-01-17 | Dic Corp | Epoxy resin, curing resin composition, cured product thereof, semiconductor sealing material, and printed wiring board |
| US8424652B2 (en) | 2007-03-23 | 2013-04-23 | Otis Elevator Company | Electromagnet and elevator door coupler |
| TWI624487B (en) * | 2014-02-21 | 2018-05-21 | Nipponkayaku Kk | Epoxy resin, epoxy resin composition and cured product thereof |
-
1991
- 1991-12-13 JP JP32927791A patent/JP2963260B2/en not_active Expired - Fee Related
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8424652B2 (en) | 2007-03-23 | 2013-04-23 | Otis Elevator Company | Electromagnet and elevator door coupler |
| WO2010013406A1 (en) * | 2008-08-01 | 2010-02-04 | äœåããŒã¯ã©ã€ãæ ªåŒäŒç€Ÿ | Resin composition for semiconductor encapsulation and semiconductor device using the same |
| JPWO2010013406A1 (en) * | 2008-08-01 | 2012-01-05 | äœåããŒã¯ã©ã€ãæ ªåŒäŒç€Ÿ | Semiconductor sealing resin composition and semiconductor device using the same |
| US8552572B2 (en) | 2008-08-01 | 2013-10-08 | Sumitomo Bakelite Co., Ltd. | Resin composition for encapsulating semiconductor and semiconductor device using the same |
| JP2013010903A (en) * | 2011-06-30 | 2013-01-17 | Dic Corp | Epoxy resin, curing resin composition, cured product thereof, semiconductor sealing material, and printed wiring board |
| TWI624487B (en) * | 2014-02-21 | 2018-05-21 | Nipponkayaku Kk | Epoxy resin, epoxy resin composition and cured product thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2963260B2 (en) | 1999-10-18 |
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