JP2011074338A - Phenol resin, epoxy resin, and epoxy resin cured product - Google Patents
Phenol resin, epoxy resin, and epoxy resin cured product Download PDFInfo
- Publication number
- JP2011074338A JP2011074338A JP2009230271A JP2009230271A JP2011074338A JP 2011074338 A JP2011074338 A JP 2011074338A JP 2009230271 A JP2009230271 A JP 2009230271A JP 2009230271 A JP2009230271 A JP 2009230271A JP 2011074338 A JP2011074338 A JP 2011074338A
- Authority
- JP
- Japan
- Prior art keywords
- phenol resin
- epoxy resin
- phenol
- resin
- hydrogen atom
- 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
- 239000005011 phenolic resin Substances 0.000 title claims abstract description 129
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 94
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 93
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 47
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000004305 biphenyl Substances 0.000 claims abstract description 29
- 235000010290 biphenyl Nutrition 0.000 claims abstract description 29
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 21
- -1 biphenyl compound Chemical class 0.000 claims abstract description 20
- 238000002441 X-ray diffraction Methods 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims description 40
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 229920001568 phenolic resin Polymers 0.000 claims description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
- 239000004065 semiconductor Substances 0.000 claims description 16
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 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 claims description 7
- 229920003986 novolac Polymers 0.000 claims description 7
- 238000007789 sealing Methods 0.000 claims description 7
- 238000006482 condensation reaction Methods 0.000 claims description 6
- 238000005538 encapsulation Methods 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 150000002989 phenols Chemical class 0.000 abstract description 12
- 239000007787 solid Substances 0.000 abstract description 5
- 238000006735 epoxidation reaction Methods 0.000 abstract description 3
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 28
- 238000000034 method Methods 0.000 description 23
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229920006336 epoxy molding compound Polymers 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000013078 crystal Substances 0.000 description 7
- 239000011521 glass Substances 0.000 description 7
- 239000003566 sealing material Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000002425 crystallisation Methods 0.000 description 6
- 230000008025 crystallization Effects 0.000 description 6
- 239000011256 inorganic filler Substances 0.000 description 6
- 229910003475 inorganic filler Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000000243 solution 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
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 125000004849 alkoxymethyl group Chemical group 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 229910001873 dinitrogen Inorganic materials 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 239000008098 formaldehyde solution Substances 0.000 description 5
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 230000009477 glass transition Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000012778 molding material Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- SFHGONLFTNHXDX-UHFFFAOYSA-N [4-[4-(hydroxymethyl)phenyl]phenyl]methanol Chemical group C1=CC(CO)=CC=C1C1=CC=C(CO)C=C1 SFHGONLFTNHXDX-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003377 acid catalyst Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000008393 encapsulating agent Substances 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000002648 laminated material Substances 0.000 description 3
- 239000004579 marble Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000001721 transfer moulding Methods 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- INZDTEICWPZYJM-UHFFFAOYSA-N 1-(chloromethyl)-4-[4-(chloromethyl)phenyl]benzene Chemical group C1=CC(CCl)=CC=C1C1=CC=C(CCl)C=C1 INZDTEICWPZYJM-UHFFFAOYSA-N 0.000 description 2
- MODAACUAXYPNJH-UHFFFAOYSA-N 1-(methoxymethyl)-4-[4-(methoxymethyl)phenyl]benzene Chemical group C1=CC(COC)=CC=C1C1=CC=C(COC)C=C1 MODAACUAXYPNJH-UHFFFAOYSA-N 0.000 description 2
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-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
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-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
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000011230 binding agent Substances 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
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- 229910002026 crystalline silica Inorganic materials 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- IXQGCWUGDFDQMF-UHFFFAOYSA-N o-Hydroxyethylbenzene Natural products CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- 238000005476 soldering Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- USFPINLPPFWTJW-UHFFFAOYSA-N tetraphenylphosphonium Chemical class C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 USFPINLPPFWTJW-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- UQWJRHXJJRTQCX-UHFFFAOYSA-N 1-(ethoxymethyl)-4-[4-(ethoxymethyl)phenyl]benzene Chemical group C1=CC(COCC)=CC=C1C1=CC=C(COCC)C=C1 UQWJRHXJJRTQCX-UHFFFAOYSA-N 0.000 description 1
- UIMJANTUJQGSEX-UHFFFAOYSA-N 2,2'-biphenyldimethanol Chemical group OCC1=CC=CC=C1C1=CC=CC=C1CO UIMJANTUJQGSEX-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- ABMULKFGWTYIIK-UHFFFAOYSA-N 2-hexylphenol Chemical compound CCCCCCC1=CC=CC=C1O ABMULKFGWTYIIK-UHFFFAOYSA-N 0.000 description 1
- LCHYEKKJCUJAKN-UHFFFAOYSA-N 2-propylphenol Chemical compound CCCC1=CC=CC=C1O LCHYEKKJCUJAKN-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- MCUFTLAXJMCWPZ-UHFFFAOYSA-N 3-butyl-2-methylphenol Chemical compound CCCCC1=CC=CC(O)=C1C MCUFTLAXJMCWPZ-UHFFFAOYSA-N 0.000 description 1
- 101100426973 Caenorhabditis elegans ttr-3 gene Proteins 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
- QEYKYHBKQHGNPQ-UHFFFAOYSA-N [4-[2-(hydroxymethyl)phenyl]phenyl]methanol Chemical group C1=CC(CO)=CC=C1C1=CC=CC=C1CO QEYKYHBKQHGNPQ-UHFFFAOYSA-N 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
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001638 boron Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 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
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical class OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
- 229940008406 diethyl sulfate Drugs 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- BTZNPZMHENLISZ-UHFFFAOYSA-N fluoromethanesulfonic acid Chemical compound OS(=O)(=O)CF BTZNPZMHENLISZ-UHFFFAOYSA-N 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Images
Landscapes
- Phenolic Resins Or Amino Resins (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Abstract
Description
本発明は、取り扱い性、保存時の安定性に優れ、かつ、機械的強度、耐熱性及び耐湿性に優れた硬化物を与える新規フェノール樹脂に関する。また、電気・電子部品の封止材料、成形材料、注型材料、積層材料、複合材料、接着剤及び粉体塗料等の用途に有用である、本発明のフェノール樹脂又は該フェノール樹脂をエポキシ化したエポキシ樹脂を含有してなる硬化性エポキシ樹脂組成物及びその硬化体に関する。 The present invention relates to a novel phenol resin that provides a cured product that is excellent in handleability and stability during storage, and excellent in mechanical strength, heat resistance, and moisture resistance. In addition, the phenolic resin of the present invention or the phenolic resin is epoxidized which is useful for applications such as sealing materials, molding materials, casting materials, laminated materials, composite materials, adhesives and powder coatings for electrical and electronic parts. The present invention relates to a curable epoxy resin composition containing the prepared epoxy resin and a cured product thereof.
フェノール樹脂は種々のエポキシ剤で硬化させることにより、機械的性質、耐湿性、電気的性質などに優れた硬化物を与えるので電気・電子部品の封止材料、成形材料、注型材料、積層材料、複合材料、接着剤及び粉体塗料等などの幅広い分野に利用されている（特許文献１、特許文献２参照）。
しかしながら、技術の進歩に伴い、フェノール樹脂の高性能化に対する要求が高まってきており、従来のフェノール樹脂ではその要求に対応できなくなってきた。例えば、電気・電子用途の分野においては封止材料の小型化、薄型化技術の進展に伴い、低粘度のフェノール樹脂が望まれているが、これは小型化した部品内部の狭い空隙にも十分に樹脂を送り込ませる必要があるためである。
Phenolic resins are cured with various epoxy agents to give cured products with excellent mechanical properties, moisture resistance, electrical properties, etc., so sealing materials for electrical and electronic parts, molding materials, casting materials, laminate materials It is used in a wide range of fields such as composite materials, adhesives and powder coatings (see Patent Document 1 and Patent Document 2).
However, with the advancement of technology, there is an increasing demand for higher performance of phenolic resins, and conventional phenolic resins cannot meet the demands. For example, in the field of electrical and electronic applications, low-viscosity phenolic resins are desired along with advances in miniaturization and thinning technology for sealing materials. This is sufficient for narrow gaps inside miniaturized parts. This is because it is necessary to feed the resin into the.
半導体の封止方法としては、経済性、生産性、物性のバランスからエポキシ樹脂による樹脂封止が一般的に使用されており、中でもオルソクレゾールノボラック型エポキシ樹脂とフェノールノボラック硬化剤とシリカなどの無機充填材とからなる樹脂封止が広く使用されてきた。しかし近年、ＬＳＩチップの大型化、パッケージの薄型化／小型化、実装方式の変更などに伴い、封止材に対する要求性能が大きく変わってきており、従来のエポキシ樹脂封止材料では、耐湿性、耐熱性、信頼性などの点で充分な対応が難しくなってきている。例えば、半田付け時の熱処理時に、吸湿水分の急激な気化膨張に伴うパッケージのクラックや剥離の発生が問題になっている。とくに最近では鉛フリー半田が多用されるようになり、この問題は一層厳しくなってきている。また難燃剤として使用されてきた臭素化合物やアンチモン化合物などが、環境問題からその使用が見直されている。 As a semiconductor sealing method, resin sealing with an epoxy resin is generally used from the balance of economical efficiency, productivity, and physical properties. Among them, an ortho-cresol novolac type epoxy resin, a phenol novolac curing agent, and inorganic such as silica are used. Resin sealing consisting of fillers has been widely used. However, in recent years, the required performance for sealing materials has changed greatly with the increase in size of LSI chips, thinning / miniaturization of packages, changes in mounting methods, etc. With conventional epoxy resin sealing materials, moisture resistance, Sufficient measures are becoming difficult in terms of heat resistance and reliability. For example, during heat treatment during soldering, the occurrence of cracks and peeling of the package due to rapid vaporization and expansion of moisture absorption moisture has become a problem. In particular, recently, lead-free solder has been frequently used, and this problem has become more severe. In addition, bromine compounds and antimony compounds that have been used as flame retardants have been reviewed for environmental reasons.
このため吸湿性が低く、半田付け温度における弾性率が低い、接着性に優れたフェノール樹脂や硬化剤の開発が望まれている。併せて、燃えにくく難燃性に優れたフェノール樹脂やエポキシ樹脂の開発が望まれている。 For this reason, it is desired to develop a phenol resin or a curing agent having a low hygroscopic property, a low elastic modulus at a soldering temperature, and an excellent adhesive property. In addition, development of phenolic resins and epoxy resins that are difficult to burn and excellent in flame retardancy is desired.
このような要望を満足する硬化剤として、４，４’−ビスメチルビフェニル化合物とフェノール化合物とから誘導されるビフェニル骨格を有するフェノール系重合体が注目されている（例えば特許文献１〜３参照）。ところが半導体封止材などの製造時の混練ロールやニーダーの温度は１２０℃以下であり、これ以上の高い温度では、混練中にエポキシ樹脂と硬化剤の反応による粘度増加などの問題が起こるため、封止材の製造が困難となる。そのため、この用途に用いられる硬化剤やエポキシ樹脂は、その軟化点が１００℃以下、好ましくは８０℃以下のものが望ましい。また半導体封止材に配合することが必須の無機フィラーを多量に配合しても、成形時の溶融粘度を低く維持するためには、硬化剤やエポキシ樹脂の成形温度域での溶融粘度が低いことが望まれている。 As a curing agent satisfying such a demand, a phenol polymer having a biphenyl skeleton derived from a 4,4′-bismethylbiphenyl compound and a phenol compound has attracted attention (see, for example, Patent Documents 1 to 3). . However, the temperature of the kneading roll and kneader at the time of production of the semiconductor encapsulant and the like is 120 ° C. or lower, and at higher temperatures, problems such as an increase in viscosity due to the reaction between the epoxy resin and the curing agent occur during the kneading, It becomes difficult to manufacture the sealing material. Therefore, it is desirable that the curing agent or epoxy resin used for this purpose has a softening point of 100 ° C. or lower, preferably 80 ° C. or lower. In order to keep the melt viscosity at the time of molding low even if a large amount of inorganic filler essential to be blended in the semiconductor encapsulant is blended, the melt viscosity in the molding temperature range of the curing agent or epoxy resin is low. It is hoped that.
しかしながら上記文献記載のビフェニル骨格を有するフェノール系重合体は、溶融粘度を低下させるために平均分子量を小さくしていくと、融点（軟化点）の低下がおこり、取り扱い性、保管時の安定性に問題があった。
すなわちこのような分子量を小さくする手法では、低溶融粘度とこれらフェノール樹脂としての払い出し、計量、移送等の取り扱い性（ハンドリング）、保管時の安定性（樹脂がブロッキングしにくい）、エポキシ樹脂組成物、EMC（Ｅｐｏｘｙ Ｍｏｌｄｅｒｉｎｇ Ｃｏｍｐｏｕｎｄ）の計量、移送等のハンドリング、保管時の安定性（組成物がブロッキングしにくい）、およびエポキシ樹脂組成物、EMC（Ｅｐｏｘｙ Ｍｏｌｄｅｒｉｎｇ Ｃｏｍｐｏｕｎｄ）製造工程でのフェノール樹脂の移送、計量、粉砕等のハンドリング性を両立させることができなかった。
However, the phenolic polymer having a biphenyl skeleton described in the above document has a lower melting point (softening point) when the average molecular weight is decreased in order to lower the melt viscosity. There was a problem.
In other words, such a method for reducing the molecular weight has a low melt viscosity, handling as a phenolic resin, handling properties such as weighing and transporting (handling), stability during storage (resin is difficult to block), epoxy resin composition , EMC (Epoxy Molding Compound) weighing, handling such as transfer, storage stability (composition is difficult to block), and epoxy resin composition, transfer of phenolic resin in EMC (Epoxy Molding Compound) manufacturing process, Handling properties such as weighing and crushing could not be made compatible.
そこで本発明者らは、低溶融粘度とフェノール樹脂としての取り扱い性（ハンドリング）、エポキシ樹脂組成物の取り扱い性（ハンドリング）、およびエポキシ樹脂組成物の作成時の取り扱い性（ハンドリング）、保存時の安定性を両立させ、しかも成形硬化性、低吸水性のフェノール系重合体を得るべく検討を行った。
その結果、ＣｕＫα線により測定したＸ回折パターンにおいて回折角２θが１７〜１９°の範囲に結晶性化合物であることを示す最大強度ピークを有するフェノール樹脂とすることによって、このような性能を充足するものを得ることが可能であることを見出すに至った。
Therefore, the present inventors have a low melt viscosity and handling property as a phenol resin (handling), handling property of an epoxy resin composition (handling), handling property when preparing an epoxy resin composition (handling), and storage property. Studies were conducted to obtain a phenolic polymer having both stability and molding curability and low water absorption.
As a result, the phenol resin having the maximum intensity peak indicating that the diffraction angle 2θ is a crystalline compound in the range of 17 to 19 ° in the X diffraction pattern measured by CuKα ray satisfies such performance. I came to find that I can get things.
本発明は、上記課題を解決するためになされたものであり、具体的には、以下の構成を有する。
（１） 下記一般式（１）〜（３）で表される３種類の繰り返し単位からなるフェノール樹脂とし、ＣｕＫα線により測定したＸ線回折パターンにおいて、回折角２θが１７．０°〜１９．０°の範囲に鋭い（半値幅１．０以下）最大強度ピークを有するフェノール樹脂である。
（２） 式（１）中のＲが水素原子である前記（１）に記載のフェノール樹脂である。
（３） 下記一般式（４）で表されるフェノール類と、下記一般式（５）で表されるビフェニル化合物と、ホルムアルデヒドとを縮合反応させて得られる前記（１）又は（２）に記載のフェノール樹脂の製造方法である。
（４） フレーク状または、マーブル状である上記一般式（４）で表されるフェノール類と、上記一般式（５）で表されるビフェニル化合物と、ホルムアルデヒドとを縮合反応させて得られるフェノール樹脂。
（５） 下記一般式（４）で表されるフェノール類と、下記一般式（５）で表されるビフェニル化合物と、ホルムアルデヒドとを縮合反応させて得られるフェノール樹脂とし、ＣｕＫα線により測定したＸ線回折パターンにおいて、回折角２θが１７．０°〜１９．０°の範囲に半値幅１．０以下の最大強度ピークを有するフェノール樹脂である。
（６） ペレット状である前記（１），（２），（４）又は（５）のいずれか一つに記載のフェノール樹脂である。
（７） 前記（１），（２），（４）又は（５）のいずれか一つに記載のフェノール樹脂と、エピハロヒドリンとを反応させて得られるエポキシ樹脂である。
（８） 前記（１），（２），（４）又は（５）のいずれか一つに記載のフェノール樹脂と、エポキシ樹脂とを含有するエポキシ樹脂組成物である。
（９） 前記（７）に記載のエポキシ樹脂と、硬化剤とを含有するエポキシ樹脂組成物である。
（１０） 半導体封止用に用いられる前記（８）又は（９）に記載のエポキシ樹脂組成物である。
（１１） 前記（８）又は（９）に記載のエポキシ樹脂組成物を硬化してなるエポキシ樹脂硬化物である。
（１２） 前記（８）又は（９）に記載のエポキシ樹脂組成物を用いて半導体素子を封止してなる半導体装置である。
The present invention has been made to solve the above problems, and specifically has the following configuration.
(1) In an X-ray diffraction pattern measured with CuKα rays, the diffraction angle 2θ is 17.0 ° to 19. 19. The phenol resin is composed of three types of repeating units represented by the following general formulas (1) to (3). It is a phenol resin having a sharp maximum peak at half maximum (1.0 or less half-value width) in the range of 0 °.
(2) The phenol resin according to (1), wherein R in formula (1) is a hydrogen atom.
(3) Described in the above (1) or (2) obtained by subjecting a phenol represented by the following general formula (4), a biphenyl compound represented by the following general formula (5), and formaldehyde to a condensation reaction It is a manufacturing method of this phenol resin.
(4) Phenol resin obtained by condensation reaction of phenols represented by the above general formula (4), flakes or marbles, the biphenyl compound represented by the above general formula (5), and formaldehyde .
(5) X measured by CuKα ray as a phenol resin obtained by condensation reaction of a phenol represented by the following general formula (4), a biphenyl compound represented by the following general formula (5), and formaldehyde In the line diffraction pattern, the phenol resin has a maximum intensity peak with a half-value width of 1.0 or less in a diffraction angle 2θ of 17.0 ° to 19.0 °.
(6) The phenol resin according to any one of (1), (2), (4), and (5), which is in a pellet form.
(7) An epoxy resin obtained by reacting the phenol resin according to any one of (1), (2), (4) and (5) with epihalohydrin.
(8) An epoxy resin composition comprising the phenol resin according to any one of (1), (2), (4) and (5) and an epoxy resin.
(9) An epoxy resin composition comprising the epoxy resin according to (7) and a curing agent.
(10) The epoxy resin composition according to (8) or (9), which is used for semiconductor encapsulation.
(11) An epoxy resin cured product obtained by curing the epoxy resin composition according to (8) or (9).
(12) A semiconductor device obtained by sealing a semiconductor element using the epoxy resin composition according to (8) or (9).
本発明によれば、成形材、各種バインダー、コーティング材、積層材などに有用な、低軟化点、低溶融粘度のフェノール樹脂を提供することができる。特に本発明のフェノール樹脂は、フレークト状またはマーブル状である場合に、フレークト状またはマーブル状同士のブロッキングが抑制される。また、エポキシ樹脂硬化剤として有用であり、とりわけ半導体封止用として用いた場合に、低吸水性、熱時低弾性率、高接着性で、難燃性に優れたエポキシ樹脂組成物を形成することができる。 ADVANTAGE OF THE INVENTION According to this invention, the low softening point and the low melt viscosity phenol resin useful for a molding material, various binders, a coating material, a laminated material, etc. can be provided. In particular, when the phenol resin of the present invention is in the form of a fract or a marble, blocking between the fract or the marble is suppressed. Also useful as an epoxy resin curing agent, especially when used for semiconductor encapsulation, it forms an epoxy resin composition with low water absorption, low thermal modulus, high adhesion and excellent flame retardancy. be able to.
本発明の一般式（１）、（２）、（３）で表される３種類の繰り返し単位からなるフェノール樹脂において、Ｒは、水素原子、炭素数１〜６のアルキル基または水酸基のいずれかである。Ｒがアルキル基である場合において、炭素数が７以上になると、耐熱性が低下するという問題がある。
また、本発明の一般式（１）、（２）、（３）で表される３種類の繰り返し単位からなるフェノール樹脂は、例えば、フェノール類とビフェニル化合物とホルムアルデヒドとを触媒の存在下又は不存在下で縮合反応させることによって得られる。
In the phenol resin comprising three types of repeating units represented by the general formulas (1), (2), and (3) of the present invention, R is any one of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, and a hydroxyl group. It is. In the case where R is an alkyl group, when the number of carbon atoms is 7 or more, there is a problem that heat resistance is lowered.
In addition, the phenol resin comprising the three types of repeating units represented by the general formulas (1), (2), and (3) of the present invention includes, for example, phenols, biphenyl compounds, and formaldehyde in the presence or absence of a catalyst. It can be obtained by carrying out a condensation reaction in the presence.
前記フェノール類は、一般式（１）及び一般式（４）で記載したとおり、ベンゼン環に水酸基を少なくとも１個有し、Ｒは水素、炭素数６以下のアルキル基または水酸基のいずれかである。
これらのフェノール類は、単独でも２種以上を併用してもよい。
具体的なフェノール類としては、例えばフェノール、クレゾール、エチルフェノール、プロピルフェノール、ブチルフェノール、ヘキシルフェノール、ノニルフェノール、キシレノール、ブチルメチルフェノール等の１価フェノール、カテコール、レゾルシン、ハイドロキノン等の２価フェノールが挙げられる。前記フェノール類の中でも、本発明のフェノール樹脂を用いてエポキシ樹脂硬化物とした際に耐熱性が高く、フェノール樹脂の溶融粘度が低いという観点から、フェノールが好ましい。
As described in the general formulas (1) and (4), the phenols have at least one hydroxyl group on the benzene ring, and R is either hydrogen, an alkyl group having 6 or less carbon atoms, or a hydroxyl group. .
These phenols may be used alone or in combination of two or more.
Specific phenols include, for example, monohydric phenols such as phenol, cresol, ethylphenol, propylphenol, butylphenol, hexylphenol, nonylphenol, xylenol, and butylmethylphenol, and divalent phenols such as catechol, resorcin, and hydroquinone. . Among the phenols, phenol is preferable from the viewpoint of high heat resistance when the epoxy resin cured product is formed using the phenol resin of the present invention and low melt viscosity of the phenol resin.
前記ビフェニル化合物は、一般式（２）及び一般式（５）で記載したとおり、２つの置換基を有するビフェニル化合物であり、Xはハロゲン原子、ヒドロキシル基又は炭素原子数１〜６のアルコキシ基のいずれかである。
具体的には、４，４’−ビス（ハロゲノメチル）ビフェニル、２，４’−ビス（ハロゲノメチル）ビフェニル、２，２’−ビス（ハロゲノメチル）ビフェニル等のビス（ハロゲノメチル）ビフェニル、４，４’−ビス（アルコキシメチル）ビフェニル、２，４’−ビス（アルコキシメチル）ビフェニル、２，２’−ビス（アルコキシメチル）ビフェニル等のビス（アルコキシメチル）ビフェニル、あるいは、４，４’−ビス（ヒドロキシメチル）ビフェニル、２，４’−ビス（ヒドロキシメチル）ビフェニル、２，２’−ビス（ヒドロキシメチル）ビフェニル等のビス（ヒドロキシメチル）ビフェニルが挙げられる。
The biphenyl compound is a biphenyl compound having two substituents as described in the general formula (2) and the general formula (5), and X is a halogen atom, a hydroxyl group, or an alkoxy group having 1 to 6 carbon atoms. Either.
Specifically, bis (halogenomethyl) biphenyl such as 4,4′-bis (halogenomethyl) biphenyl, 2,4′-bis (halogenomethyl) biphenyl, 2,2′-bis (halogenomethyl) biphenyl, 4 , 4′-bis (alkoxymethyl) biphenyl, 2,4′-bis (alkoxymethyl) biphenyl, bis (alkoxymethyl) biphenyl such as 2,2′-bis (alkoxymethyl) biphenyl, or 4,4′- Examples thereof include bis (hydroxymethyl) biphenyl such as bis (hydroxymethyl) biphenyl, 2,4′-bis (hydroxymethyl) biphenyl, and 2,2′-bis (hydroxymethyl) biphenyl.
前記ビフェニル化合物において、Ｘは、反応性の観点から、ハロゲン原子又は炭素数１〜６のアルコキシ基であることが好ましい。
前記ハロゲン原子としては、フッ素、塩素、臭素及び沃素が挙げられるが、取り扱い性及び反応性の観点から塩素が好ましい。
前記アルコキシ基としては、炭素数１〜６個の脂肪族アルコキシが好ましく、取り扱い性及び反応性の観点からメトキシ基およびエトキシ基がより好ましい。
また、ビフェニル化合物の２つの置換基の位置は、特に制限されないが、得られるフェノール樹脂の粘度が低くなる観点から、４位及び４’位であることが好ましい。
前記ビフェニル化合物として、好ましい具体的な化合物としては、４，４’−ビス（クロロメチル）ビフェニル、４，４’−ビス（メトキシメチル）ビフェニル、４，４’−ビス（エトキシメチル）ビフェニル、が挙げられる。
前記ビフェニル化合物は、１種のみを単独出使用してもよいし、複数種を併用してもよい。
In the biphenyl compound, X is preferably a halogen atom or an alkoxy group having 1 to 6 carbon atoms from the viewpoint of reactivity.
Examples of the halogen atom include fluorine, chlorine, bromine and iodine, and chlorine is preferable from the viewpoint of handling and reactivity.
As said alkoxy group, a C1-C6 aliphatic alkoxy is preferable, and a methoxy group and an ethoxy group are more preferable from a handleable and reactive viewpoint.
Further, the positions of the two substituents of the biphenyl compound are not particularly limited, but are preferably the 4-position and the 4′-position from the viewpoint of reducing the viscosity of the obtained phenol resin.
Preferred examples of the biphenyl compound include 4,4′-bis (chloromethyl) biphenyl, 4,4′-bis (methoxymethyl) biphenyl, and 4,4′-bis (ethoxymethyl) biphenyl. Can be mentioned.
The biphenyl compound may be used alone or in combination of two or more.
本発明のフェノール樹脂において、メチレン架橋基を形成する化合物としては、特に制限はないが、ホルムアルデヒドが好適である。前記ホルムアルデヒドは種々の方法で用いることができる。前記ホルムアルデヒドを用いる方法としては、例えば、反応系にホルムアルデヒド水溶液を添加する方法、及びパラホルムアルデヒド、トリオキサン等酸存在下で分解してホルムアルデヒドとなる重合物を反応系に添加する方法などを用いることもできる。
前記ホルムアルデヒドを用いる方法の中でも、ホルムアルデヒド水溶液を反応系に添加する方法が簡便であり好ましい。また、ホルムアルデヒド水溶液としては、市販品の４２％ホルムアルデヒド水溶液をそのまま使用することができる。
In the phenol resin of the present invention, the compound that forms a methylene crosslinking group is not particularly limited, but formaldehyde is preferred. The formaldehyde can be used in various ways. Examples of the method using formaldehyde include a method of adding an aqueous formaldehyde solution to the reaction system, and a method of adding a polymer that is decomposed in the presence of an acid such as paraformaldehyde and trioxane to formaldehyde. it can.
Among the methods using formaldehyde, a method of adding an aqueous formaldehyde solution to the reaction system is simple and preferable. As the formaldehyde aqueous solution, a commercially available 42% formaldehyde aqueous solution can be used as it is.
前記ビフェニル化合物が、ビス（ハロゲノメチル）ビフェニルである場合には、ビス（ハロゲノメチル）ビフェニルの分解によって発生する酸が触媒となる。また、僅かな水を存在させることによって反応を開始させることもでき、反応によって生じるハロゲン化水素によって、さらに反応を進行させることができる。
また、ビフェニル化合物が、ビス（アルコキシメチル）ビフェニルやビス（ヒドロキシメチル）ビフェニルである場合には、酸触媒を添加する必要がある。
前記酸触媒としては、リン酸、硫酸、塩酸、臭化水素酸、弗化水素酸等の無機酸、蓚酸、ベンゼンスルホン酸、トルエンスルホン酸、メタンスルホン酸、フルオロメタンスルホン酸等の有機酸、塩化亜鉛、塩化第２錫、塩化第２鉄、ジエチル硫酸などのフリーデルクラフツ触媒を使うことができる。前記酸触媒は、１種のみを用いてもよいし、複数種を併用してもよい。
本発明のフェノール樹脂を半導体封止材の原料として使う場合には、触媒痕が残らない観点から、塩酸等のハロゲン化水素酸又は蓚酸を触媒とすることが好ましい。
When the biphenyl compound is bis (halogenomethyl) biphenyl, an acid generated by the decomposition of bis (halogenomethyl) biphenyl serves as a catalyst. The reaction can also be initiated by the presence of a small amount of water, and the reaction can be further advanced by the hydrogen halide generated by the reaction.
Further, when the biphenyl compound is bis (alkoxymethyl) biphenyl or bis (hydroxymethyl) biphenyl, it is necessary to add an acid catalyst.
Examples of the acid catalyst include inorganic acids such as phosphoric acid, sulfuric acid, hydrochloric acid, hydrobromic acid, hydrofluoric acid, organic acids such as oxalic acid, benzenesulfonic acid, toluenesulfonic acid, methanesulfonic acid, and fluoromethanesulfonic acid, Friedel-Crafts catalysts such as zinc chloride, stannic chloride, ferric chloride, and diethyl sulfate can be used. The acid catalyst may be used alone or in combination of two or more.
When the phenol resin of the present invention is used as a raw material for a semiconductor encapsulant, it is preferable to use hydrohalic acid such as hydrochloric acid or oxalic acid as a catalyst from the viewpoint of leaving no catalyst traces.
本発明のフェノール樹脂は、一般式（１）、（２）、（３）で表される３種類の繰り返し単位からなるフェノール化合物を主成分として含有する。 The phenol resin of this invention contains the phenolic compound which consists of three types of repeating units represented by General formula (1), (2), (3) as a main component.
本発明のフェノール樹脂は、重量平均分子量が６００〜１０００であることが好ましく、７５０〜８５０であることがより好ましい。重量平均分子量が低すぎると、本発明のフェノール樹脂を用いてエポキシ樹脂硬化物とした際に、耐熱性が悪くなる傾向がある。また、重量平均分子量が高すぎると、本発明のフェノール樹脂を用いてエポキシ樹脂組成物とした場合に、粘度が高くなる傾向がある。 The phenol resin of the present invention preferably has a weight average molecular weight of 600 to 1000, more preferably 750 to 850. If the weight average molecular weight is too low, the heat resistance tends to deteriorate when an epoxy resin cured product is formed using the phenol resin of the present invention. Moreover, when a weight average molecular weight is too high, when it is set as an epoxy resin composition using the phenol resin of this invention, there exists a tendency for a viscosity to become high.
本発明のフェノール樹脂において、一般式（２）で表される繰り返し単位と、一般式（３）で表される繰り返し単位とのモル比は、８：２〜５：５であることが好ましい。一般式（２）で表される繰り返し単位が少なすぎると、得られるフェノール樹脂やエポキシ樹脂硬化物の難燃性が低くなる場合がある。また、一般式（３）で表される繰り返し単位が少なすぎると、得られるエポキシ樹脂硬化物の耐熱性が低くなる場合がある。 In the phenol resin of the present invention, the molar ratio of the repeating unit represented by the general formula (2) and the repeating unit represented by the general formula (3) is preferably 8: 2 to 5: 5. When there are too few repeating units represented by General formula (2), the flame retardance of the phenol resin obtained or epoxy resin hardened | cured material may become low. Moreover, when there are too few repeating units represented by General formula (3), the heat resistance of the obtained epoxy resin hardened | cured material may become low.
本発明のフェノール樹脂において、フェノール樹脂の軟化点が、６５〜８０℃であることが好ましい。軟化点が低すぎると、フェノール樹脂がブロッキングする場合があり、高すぎると封止材用エポキシ樹脂組成物の製造が困難となる場合がある。 In the phenol resin of the present invention, the softening point of the phenol resin is preferably 65 to 80 ° C. If the softening point is too low, the phenol resin may block, and if it is too high, it may be difficult to produce an epoxy resin composition for a sealing material.
本発明のフェノール樹脂は、Ｘ線回折において、２θ＝１７．０〜１９．０°に鋭い（半値幅１．０以下）最大強度ピークを有する。特に、２θ＝１８．６°付近に、鋭い（半値幅１．０以下）ピークを有するのが好ましい。 The phenol resin of the present invention has a sharp maximum intensity peak at 2θ = 17.0 to 19.0 ° (half-value width of 1.0 or less) in X-ray diffraction. In particular, it is preferable to have a sharp (half-value width of 1.0 or less) peak in the vicinity of 2θ = 18.6 °.
本発明のフェノール樹脂は、結晶化を促進させて得ることが好ましい。フェノール樹脂の結晶化促進方法としては、例えば、高温で溶融状態のフェノール樹脂をバット等に抜き出し自然冷却により固形化する方法、抜き出した後、あらかじめ用意したそのフェノール樹脂の結晶固形物を結晶核として少量添加し結晶化を促進する方法、溶融状態のフェノール樹脂を攪拌したり、振動を与えるなどにより結晶化を促進する方法、ニーダーなどで強い外力を加えながら抜き出す方法、過冷却にならないように温度を管理しながら結晶化を促進させる方法などが上げられ、これらの方法を単独あるいは複数組み合わせて行うことができる。本発明のフェノール樹脂についても上記のような操作を行い、固化することが、生産性の観点から望ましい。 The phenol resin of the present invention is preferably obtained by promoting crystallization. As a method for accelerating the crystallization of a phenol resin, for example, a method of extracting a phenol resin in a molten state at a high temperature into a vat and solidifying by natural cooling, and using the crystal solid of the phenol resin prepared in advance as a crystal nucleus after extraction Add a small amount to promote crystallization, stir the molten phenolic resin, promote crystallization by giving vibration, etc., pull out while applying a strong external force with a kneader, temperature to prevent overcooling The method of promoting crystallization, etc., can be raised while managing the above, and these methods can be carried out singly or in combination. It is desirable from the viewpoint of productivity that the phenol resin of the present invention is solidified by the above-described operation.
本発明のフェノール樹脂は、重合後、必要に応じて未反応モノマーの留去や洗浄を行い、フレーク化又はマーブル化することができる。
工業的には、反応生成物を反応装置内で結晶化させ、この溶融状態のフェノール樹脂をフレーク状、またはマーブル状に取り出す方法等があり、特に指定がなく公知の方法を用いることができる。
また溶融した反応生成物を、スリットフレーカー、オープンフレーカー、造粒機などを通し、ドラムフレーカーや冷却ベルトに連続的に滴下することによって、フレーク状もしくは、マーブル状に工業的に取り出す場合生産性の観点から望ましい。
The phenol resin of the present invention can be flaked or marbled after the polymerization by distilling off unreacted monomers and washing as necessary.
Industrially, there is a method of crystallizing a reaction product in a reaction apparatus and taking out this molten phenol resin in the form of flakes or marbles, and there is no particular designation, and a known method can be used.
In addition, when the molten reaction product is industrially taken out in the form of flakes or marbles by continuously dropping them onto a drum flaker or cooling belt through a slit flaker, open flaker, granulator, etc. Desirable from the viewpoint of productivity.
前記フレーク化又はマーブル化の方法としては、工業化においては、溶融状態又は軟化した状態のフェノール樹脂をドラムフレーカーや冷却ベルトに連続的に滴下し、固化を効率的に行うことができる。また、前記フレーク化又はマーブル化の方法としては、融状態又は軟化した状態のフェノール樹脂を板状に取り出し徐冷した後、破砕する方法や、マーブル状に取り出したフェノール樹脂を徐冷する方法も採用することができる。
具体的には、通常未反応フェノール類の除去はフェノール類の沸点近傍かそれ以上の温度で実施されるため、フェノール類除去直後のフェノール樹脂は溶融状態である。この溶融状態のフェノール樹脂を徐冷させ、固形化させる。
As a method for flaking or marbleizing, in industrialization, a phenol resin in a molten state or a softened state can be continuously dropped onto a drum flaker or a cooling belt, and solidification can be performed efficiently. In addition, as a method of flaking or marbleizing, there is a method of taking out a molten or softened phenol resin in a plate shape and gradually cooling it, then crushing it, or a method of slowly cooling a phenol resin taken out in a marble shape. Can be adopted.
Specifically, since removal of unreacted phenols is usually carried out at a temperature near or higher than the boiling point of the phenols, the phenol resin immediately after removal of the phenols is in a molten state. The molten phenol resin is gradually cooled and solidified.
本発明のフェノール樹脂は、バインダー、コーティング材、積層材、成形材料等の用途に広く使用できるが、特に低溶融粘度で、しかも高ガラス転移温度、低吸湿性、高密着性、耐熱性、速硬化、難燃性を有し、フェノール樹脂としての取り扱い性（ハンドリング）、エポキシ樹脂組成物の取り扱い性（ハンドリング）、およびエポキシ樹脂組成物の作成時の取り扱い性（ハンドリング）が良好であるところから、特に半導体封止用、プリント基板絶縁用などのエポキシ硬化剤に適している。 The phenolic resin of the present invention can be widely used in applications such as binders, coating materials, laminates, molding materials, etc., but it has a particularly low melt viscosity and high glass transition temperature, low hygroscopicity, high adhesion, heat resistance, high speed. Because it has curing and flame retardancy, it is easy to handle as a phenolic resin (handling), easy to handle epoxy resin composition (handling), and easy to handle when creating an epoxy resin composition (handling) In particular, it is suitable for epoxy curing agents for semiconductor sealing and printed circuit board insulation.
［エポキシ樹脂］
本発明のフェノール樹脂を、アルカリ金属水酸化物存在下で、エピハロヒドリンを反応させることによって、エポキシ樹脂を得ることができる。エピハロヒドリンを反応させる際の反応温度としては、４０〜１５０℃が好ましく、５０〜１２０℃がより好ましい。
前記アルカリ金属水酸化物としては、例えば、水酸化ナトリウムや水酸化カリウム等が挙げられる。前記アルカリ金属水酸化物の添加量は、前記フェノール樹脂の水酸基当量に対して、０．８〜１．２倍モルが好ましく、０．９〜１．１倍モルがより好ましい。
前記エピハロヒドリンとしては、例えば、エピクロルヒドリンやα−メチルエピクロルヒドリン、γ−メチルエピクロルヒドリン、エピブロモヒドリン等が挙げられる。前記エピハロヒドリンの添加量は、フェノール樹脂の水酸基当量に対して、２〜２０倍モルが好ましく、２〜１０倍モルがより好ましい。
[Epoxy resin]
An epoxy resin can be obtained by reacting the phenol resin of the present invention with an epihalohydrin in the presence of an alkali metal hydroxide. As reaction temperature at the time of making epihalohydrin react, 40-150 degreeC is preferable and 50-120 degreeC is more preferable.
Examples of the alkali metal hydroxide include sodium hydroxide and potassium hydroxide. The addition amount of the alkali metal hydroxide is preferably 0.8 to 1.2 times mol, more preferably 0.9 to 1.1 times mol, based on the hydroxyl equivalent of the phenol resin.
Examples of the epihalohydrin include epichlorohydrin, α-methylepichlorohydrin, γ-methylepichlorohydrin, epibromohydrin, and the like. The added amount of the epihalohydrin is preferably 2 to 20 times by mole and more preferably 2 to 10 times by mole with respect to the hydroxyl equivalent of the phenol resin.
フェノール樹脂のエポキシ化反応では、必要に応じて、テトラメチルアンモニウムクロライド等の４級アンモニウム塩触媒やメタノール等の非プロトン性極性溶媒など添加することができる。
エポキシ化反応終了後、過剰のエピクロルヒドリンを蒸留除去し、残留物をメチルイソブチルケトン等の有機溶剤に溶解し、ろ過し水洗して無機塩を除去し、次いで有機溶剤を留去することにより、目的とするエポキシ樹脂を得ることができる。
In the epoxidation reaction of a phenol resin, a quaternary ammonium salt catalyst such as tetramethylammonium chloride or an aprotic polar solvent such as methanol can be added as necessary.
After completion of the epoxidation reaction, excess epichlorohydrin is removed by distillation, the residue is dissolved in an organic solvent such as methyl isobutyl ketone, filtered, washed with water to remove inorganic salts, and then the organic solvent is distilled off. An epoxy resin can be obtained.
［エポキシ樹脂組成物］
本発明のフェノール樹脂は、エポキシ樹脂用硬化剤として用いることができる。よって、通常使用されるエポキシ樹脂と本発明のフェノール樹脂との組成物、上述した本発明のフェノール樹脂をエポキシ化したエポキシ樹脂と通常使用されるフェノール樹脂との組成物、上述した本発明のフェノール樹脂をエポキシ化したエポキシ樹脂と本発明のフェノール樹脂との組成物とすることにより、エポキシ樹脂組成物を得ることができる。
このエポキシ樹脂組成物には、硬化促進剤や充填剤等の一般的に使用される添加剤を添加することができる。
[Epoxy resin composition]
The phenol resin of the present invention can be used as a curing agent for epoxy resins. Therefore, a composition of a normally used epoxy resin and the phenol resin of the present invention, a composition of an epoxy resin obtained by epoxidizing the above-described phenol resin of the present invention and a commonly used phenol resin, and the above-described phenol of the present invention An epoxy resin composition can be obtained by using a composition of an epoxy resin obtained by epoxidizing a resin and the phenol resin of the present invention.
Commonly used additives such as curing accelerators and fillers can be added to the epoxy resin composition.
本発明のエポキシ樹脂組成物において、フェノール樹脂とエポキシ樹脂の配合比は、耐熱性、機械的特性などを考慮すると、水酸基／エポキシ基の当量比が０．５〜１．５、とくに０．８〜１．２の範囲にあるようにすることが好ましい。また他の硬化剤と併用する場合にも、水酸基／エポキシ基の当量比が上記割合となるように調節するのが好ましい。
前記硬化促進剤は、硬化特性や諸物性を考慮すると、エポキシ樹脂１００重量部に対して０．１〜５重量部の範囲で使用するのが好ましい。さらに半導体封止用のエポキシ樹脂組成物においては、無機充填剤の種類によっても若干異なるが、はんだ耐熱性、成形性（溶融粘度、流動性）、低応力性、低吸水性などを考慮すると、無機充填剤がエポキシ樹脂組成物全体の６０〜９３重量％を占めるような割合で配合することが好ましい。
In the epoxy resin composition of the present invention, the mixing ratio of the phenol resin and the epoxy resin is such that the equivalent ratio of hydroxyl group / epoxy group is 0.5 to 1.5, particularly 0.8, considering heat resistance, mechanical properties and the like. It is preferable to be in the range of -1.2. Also, when used in combination with other curing agents, it is preferable to adjust the hydroxyl group / epoxy group equivalent ratio to the above ratio.
The curing accelerator is preferably used in the range of 0.1 to 5 parts by weight with respect to 100 parts by weight of the epoxy resin in consideration of curing characteristics and various physical properties. Furthermore, in the epoxy resin composition for semiconductor encapsulation, although slightly different depending on the type of inorganic filler, considering solder heat resistance, moldability (melt viscosity, fluidity), low stress, low water absorption, etc. The inorganic filler is preferably blended in such a proportion that it accounts for 60 to 93% by weight of the entire epoxy resin composition.
エポキシ樹脂組成物を調製する場合の一般的な方法としては、所定の割合の各原料を、例えばミキサーによって充分混合後、熱ロールやニーダーなどによって混練処理を加え、さらに冷却固化後、適当な大きさに粉砕し、必要に応じタブレット化するどの方法を挙げることができる。このようにして得たエポキシ樹脂組成物は、例えば低圧トランスファー成形などにより半導体封止に用いることができる。前記エポキシ樹脂組成物の硬化は、例えば１００〜２５０℃の温度範囲で行なうことができる。 As a general method for preparing an epoxy resin composition, a predetermined proportion of each raw material is sufficiently mixed by, for example, a mixer, kneaded by a hot roll or a kneader, and further cooled and solidified, and then an appropriate size. Any method of crushing and tableting as necessary can be mentioned. The epoxy resin composition thus obtained can be used for semiconductor encapsulation by, for example, low-pressure transfer molding. Curing of the epoxy resin composition can be performed, for example, in a temperature range of 100 to 250 ° C.
［エポキシ樹脂硬化物］
本発明のフェノール樹脂は、エポキシ樹脂用硬化剤として用いることができる。エポキシ樹脂硬化物はフェノール樹脂とエポキシ樹脂及び硬化促進剤を混合し、１００〜２５０℃の温度範囲で硬化させることによりエポキシ樹脂硬化物を得ることができる。
[Hardened epoxy resin]
The phenol resin of the present invention can be used as a curing agent for epoxy resins. The cured epoxy resin can be obtained by mixing a phenol resin, an epoxy resin, and a curing accelerator and curing the mixture in a temperature range of 100 to 250 ° C.
前記エポキシ樹脂としては、例えば、ビスフェノールＡ型エポキシ樹脂、ビスフェノールＦ型エポキシ樹脂、クレゾールノボラック型エポキシ樹脂、フェノールノボラック型エポキシ樹脂、トリフェノールメタン型エポキシ樹脂、ビフェニル型エポキシ樹脂などのグリシジルエーテル型エポキシ樹脂、グリシジルエステル型エポキシ樹脂、グリシジルアミン型エポキシ樹脂、ハロゲン化エポキシ樹脂など、分子中にエポキシ基を二個以上有するエポキシ樹脂などが挙げられる。これらエポキシ樹脂は単独で使用しても、２種類以上を併用してもよい。 Examples of the epoxy resin include glycidyl ether type epoxy resins such as bisphenol A type epoxy resin, bisphenol F type epoxy resin, cresol novolac type epoxy resin, phenol novolac type epoxy resin, triphenolmethane type epoxy resin, and biphenyl type epoxy resin. And glycidyl ester type epoxy resin, glycidyl amine type epoxy resin, halogenated epoxy resin and the like, and epoxy resins having two or more epoxy groups in the molecule. These epoxy resins may be used alone or in combination of two or more.
［硬化促進剤］
硬化促進剤としては、エポキシ樹脂をフェノール系硬化剤で硬化させるための公知の硬化促進剤を用いることが出来る。このような硬化促進剤としては例えば有機ホスフィン化合物およびそのボロン塩、３級アミン、４級アンモニウム塩、イミダゾール類及びそのテトラフェニルボロン塩などを挙げることができるが、この中でも、硬化性や耐湿性の点から、トリフェニルホスフィン及び１，８−ジアザビシクロ［５，４，０］ウンデセン−７（ＤＢＵ）が好ましい。また、より高流動性にするためには、加熱により活性が発現する熱潜在性の硬化促進剤がより好ましく、テトラフェニルホスフォニウム・テトラフェニルボレートなどのテトラフェニルホスフォニウム誘導体が好ましい。
[Curing accelerator]
As a hardening accelerator, the well-known hardening accelerator for hardening an epoxy resin with a phenol type hardening | curing agent can be used. Examples of such curing accelerators include organic phosphine compounds and their boron salts, tertiary amines, quaternary ammonium salts, imidazoles and their tetraphenylboron salts, and among them, curability and moisture resistance. From this point, triphenylphosphine and 1,8-diazabicyclo [5,4,0] undecene-7 (DBU) are preferable. In order to achieve higher fluidity, a heat-latent curing accelerator that exhibits activity by heating is more preferable, and tetraphenylphosphonium derivatives such as tetraphenylphosphonium and tetraphenylborate are preferable.
［その他添加剤］
本発明のエポキシ樹脂組成物には、必要に応じて、無機充填剤、離型剤、着色剤、難燃剤、低応力剤等を、添加または予め反応して用いることができる。特に半導体封止用に使用する場合は、無機充填剤の添加するのが好ましい。
前記無機充填剤としては、例えば、非晶性シリカ、結晶性シリカ、アルミナ、ガラス、珪酸カルシウム、石膏、炭酸カルシウム、マグネサイト、クレー、タルク、マイカ、マグネシア、硫酸バリウムなどを挙げることができるが、とくに非晶性シリカ、結晶性シリカなどが好ましい。これら添加剤の使用量は、従来の半導体封止用エポキシ樹脂組成物における使用量と同様でよい。
[Other additives]
In the epoxy resin composition of the present invention, an inorganic filler, a release agent, a colorant, a flame retardant, a low stress agent, or the like can be added or reacted in advance as necessary. In particular, when used for semiconductor encapsulation, it is preferable to add an inorganic filler.
Examples of the inorganic filler include amorphous silica, crystalline silica, alumina, glass, calcium silicate, gypsum, calcium carbonate, magnesite, clay, talc, mica, magnesia, barium sulfate, and the like. In particular, amorphous silica and crystalline silica are preferred. The usage-amount of these additives may be the same as the usage-amount in the conventional epoxy resin composition for semiconductor sealing.
本発明のフェノール樹脂は適当量のフェノールノボラック樹脂単位を有し、エポキシ樹脂硬化剤として用いた場合、得られるエポキシ樹脂組成物は低粘度で取り扱いやすく、速硬化性を有する。また、前記エポキシ樹脂組成物から得られるエポキシ樹脂硬化物は高いガラス転移温度、低吸湿性、高密着性、耐熱性、難燃性に優れる。 The phenol resin of the present invention has an appropriate amount of a phenol novolak resin unit, and when used as an epoxy resin curing agent, the resulting epoxy resin composition has a low viscosity and is easy to handle and has fast curability. Moreover, the epoxy resin hardened | cured material obtained from the said epoxy resin composition is excellent in a high glass transition temperature, low moisture absorption, high adhesiveness, heat resistance, and a flame retardance.
撹拌装置、コンデンサー、及び窒素ガス導入管を備えたガラス製反応釜に、フェノール３７６ｇ（４モル）、４，４’−ビス（クロロメチル）ビフェニル（以下、４，４’−ＢＣＭＢと略記する。）１５０．７０ｇ（０．６モル）を仕込み１００℃で３時間反応させ、その後４２％ホルムアルデヒド水溶液２８．５７ｇ（０．４モル）を添加し、その後、１００℃で３時間反応させた。その間、生成する塩化水素を除去した。
反応終了後、得られた反応溶液を冷却し、水洗を１回行った。油層を分離し、減圧蒸留により未反応フェノールを留去し、フラスコ内温を100℃まで冷却し、フェノール樹脂の結晶固形物を結晶核として少量添加しそのままの温度で１時間攪拌を行い、結晶化を促進させ、樹脂状物をバットに抜き出し、２５℃にて自然冷却させ、スリットフレーカーによりフレーク化した。これにより１９４ｇのフェノール樹脂を得た。
得られたフェノール樹脂のJIS K ２２０７に基づく環球法軟化点は７５℃であり、１５０℃におけるＩＣＩ粘度は４４mPa・sであり、取扱性は良好であった。得られたフェノール樹脂をＣｕＫα線により測定したＸ線回折パターンにおいて、回折角２θが１７°〜１９°の範囲に結晶性化合物であることを示す最大強度ピークを有するものであった。得られたフェノール樹脂のＸ線回折強度を図１に示す。実施例１のフェノール樹脂は、２θ＝１８．６に半値幅が１．０以下の鋭いピークが検出された。
In a glass reaction kettle equipped with a stirrer, a condenser, and a nitrogen gas inlet tube, 376 g (4 mol) of phenol, 4,4′-bis (chloromethyl) biphenyl (hereinafter, abbreviated as 4,4′-BCMB). ) 150.70 g (0.6 mol) was charged and reacted at 100 ° C. for 3 hours, and then 28.57 g (0.4 mol) of 42% formaldehyde aqueous solution was added, and then reacted at 100 ° C. for 3 hours. Meanwhile, the hydrogen chloride formed was removed.
After completion of the reaction, the obtained reaction solution was cooled and washed once with water. Separate the oil layer, distill off unreacted phenol by distillation under reduced pressure, cool the flask internal temperature to 100 ° C, add a small amount of phenol resin crystal solids as crystal nuclei and stir for 1 hour at the same temperature, The resin was extracted into a vat, allowed to cool naturally at 25 ° C., and flaked with a slit flaker. As a result, 194 g of a phenol resin was obtained.
The obtained phenol resin had a ring-and-ball method softening point based on JIS K 2207 of 75 ° C., an ICI viscosity at 150 ° C. of 44 mPa · s, and handleability was good. In the X-ray diffraction pattern obtained by measuring the obtained phenol resin with CuKα rays, the phenol resin had a maximum intensity peak indicating that the diffraction angle 2θ was a crystalline compound in the range of 17 ° to 19 °. The X-ray diffraction intensity of the obtained phenol resin is shown in FIG. In the phenol resin of Example 1, a sharp peak having a half width of 1.0 or less at 2θ = 18.6 was detected.
撹拌装置、コンデンサー、及び窒素ガス導入管を備えたガラス製反応釜に、フェノール３７６ｇ（４．０モル）、４，４’−ジ（メトキシメチル）ビフェニル（以下、４，４’−ＢＭＭＢと略記する。）１４５．２ｇ（０．６モル）、４２％ホルムアルデヒド水溶液２８．２８ｇ（０．４０モル）、５０％硫酸水溶液０．１４ｇを仕込み、１００℃で３時間反応させた。
その後、反応温度を１２５℃に保ちながら２時間反応させその後１６５℃に昇温し、３時間反応を行った。その間、生成するメタノールを留去した。反応終了後、得られた反応溶液を冷却し、水洗を１回行った。油層を分離し、減圧蒸留により未反応フェノールを留去し、フラスコ内温を130℃まで冷却した。溶融状態のフェノール樹脂に、フェノール樹脂の結晶固形物を結晶核として少量添加し、１３０℃で２時間攪拌を行い、結晶化を促進させ、樹脂状物をバットに抜き出し、２５℃にて自然冷却させ、スリットフレーカーによりフレーク化した。これにより１９６ｇのフェノール樹脂を得た。
得られたフェノール樹脂のJIS K ２２０７に基づく環球法軟化点は、６４℃であり、１５０℃におけるＩＣＩ粘度は４３mPa・sであり、取扱性は良好であった。得られたフェノール樹脂をＣｕＫα線により測定したＸ線回折パターンにおいて、回折角２θが１７°〜１９°の範囲に結晶性化合物であることを示す最大強度ピークを有するものであった。得られたフェノール樹脂のＸ線回折強度を図１に示す。実施例２のフェノール樹脂は、２θ＝１８．６に半値幅が１．０以下の鋭いピークが検出された。
To a glass reaction kettle equipped with a stirrer, a condenser, and a nitrogen gas introduction tube, 376 g (4.0 mol) of phenol, 4,4′-di (methoxymethyl) biphenyl (hereinafter abbreviated as 4,4′-BMMB). 145.2 g (0.6 mol), 28.28 g (0.40 mol) of 42% aqueous formaldehyde solution, and 0.14 g of 50% aqueous sulfuric acid solution were charged and reacted at 100 ° C. for 3 hours.
Thereafter, the reaction was carried out for 2 hours while maintaining the reaction temperature at 125 ° C., then the temperature was raised to 165 ° C. and the reaction was carried out for 3 hours. Meanwhile, the methanol produced was distilled off. After completion of the reaction, the obtained reaction solution was cooled and washed once with water. The oil layer was separated, unreacted phenol was distilled off by distillation under reduced pressure, and the flask internal temperature was cooled to 130 ° C. Add a small amount of phenol resin crystal solids as crystal nuclei to the molten phenol resin, stir at 130 ° C for 2 hours to accelerate crystallization, pull out the resinous material into a vat, and naturally cool at 25 ° C And flaked with a slit flaker. As a result, 196 g of phenol resin was obtained.
The obtained phenol resin had a ring and ball softening point based on JIS K 2207 of 64 ° C., an ICI viscosity at 150 ° C. of 43 mPa · s, and the handleability was good. In the X-ray diffraction pattern obtained by measuring the obtained phenol resin with CuKα rays, the phenol resin had a maximum intensity peak indicating that the diffraction angle 2θ was a crystalline compound in the range of 17 ° to 19 °. The X-ray diffraction intensity of the obtained phenol resin is shown in FIG. In the phenol resin of Example 2, a sharp peak having a half width of 1.0 or less at 2θ = 18.6 was detected.
撹拌装置、コンデンサー、及び窒素ガス導入管を備えたガラス製反応釜に、フェノール３７６ｇ（４モル）、４，４’−ＢＣＭＢ１５０．７０ｇ（０．６モル）を仕込み１００℃で３時間反応させ、その後４２％ホルムアルデヒド水溶液２８．５７ｇ（０．４モル）を添加し、その後、１００℃で３時間反応させた。その間、生成するメタノールを留去した。反応終了後、得られた反応溶液を冷却し、水洗を１回行った。油層を分離し、減圧蒸留により未反応フェノールを留去し溶融状態のフェノール樹脂をバットに抜き出し、ガラス棒で十数回攪拌したのち、２５℃にて自然冷却させた。約２時間後には全体が結晶固化しており、これをスリットフレーカーによりフレーク化することにより２０３ｇのフェノール樹脂を得た。
得られたフェノール樹脂のJIS K ２２０７に基づく環球法軟化点は、６５℃であり、１５０℃におけるＩＣＩ粘度は４４mPa・sであり、取扱性は良好であった。得られたフェノール樹脂をＣｕＫα線により測定したＸ線回折パターンにおいて、回折角２θが１７°〜１９°の範囲に結晶性化合物であることを示す最大強度ピークを有するものであった。得られたフェノール樹脂のＸ線回折強度を図１に示す。実施例３のフェノール樹脂は、２θ＝１８．６に鋭いピークが検出された。
In a glass reaction kettle equipped with a stirrer, a condenser, and a nitrogen gas introduction tube, 376 g (4 mol) of phenol and 150.70 g (0.6 mol) of 4,4′-BCMB were charged and reacted at 100 ° C. for 3 hours. Thereafter, 28.57 g (0.4 mol) of a 42% aqueous formaldehyde solution was added, and then reacted at 100 ° C. for 3 hours. Meanwhile, the methanol produced was distilled off. After completion of the reaction, the obtained reaction solution was cooled and washed once with water. The oil layer was separated, unreacted phenol was distilled off by distillation under reduced pressure, the molten phenol resin was extracted into a vat, stirred for 10 times with a glass rod, and then naturally cooled at 25 ° C. After about 2 hours, the whole crystallized and was flaked with a slit flaker to obtain 203 g of phenol resin.
The obtained phenol resin had a ring and ball softening point based on JIS K 2207 of 65 ° C., an ICI viscosity at 150 ° C. of 44 mPa · s, and handleability was good. In the X-ray diffraction pattern obtained by measuring the obtained phenol resin with CuKα rays, the phenol resin had a maximum intensity peak indicating that the diffraction angle 2θ was a crystalline compound in the range of 17 ° to 19 °. The X-ray diffraction intensity of the obtained phenol resin is shown in FIG. In the phenol resin of Example 3, a sharp peak was detected at 2θ = 18.6.
攪拌装置、及びコンデンサー、及び窒素ガス導入管を備えたガラス製反応容器に、実施例１で得られたフェノールノボラック樹脂１４９．４ｇ（０．９０モル）、エピクロルヒドリン４９９．５ｇ（５．４０モル）、メタノール４６．８８ｇを仕込み、均一に溶解させた。５０℃で固形の９６％水酸化ナトリウム３７．５ｇ（０．９０モル）を９０分かけて分割投入した。その後５０℃で２時間反応させ、７０℃昇温後さらに２時間反応を継続した。反応終了後、過剰のエピクロルヒドリンを減圧下において除去した。
釜残にメチルイソブチルケトンを２４０ｇ投入し溶解させた。２５％水酸化ナトリウム水溶液１４．４０ｇ（０．０９モル）を添加し７０℃で１時間反応させた。反応終了後、水層が中性になるまで水洗処理を５回繰り返した。加熱減圧下メチルイソブチルケトンを留去することで１９１ｇのエポキシ樹脂Bを得た。
得られたエポキシ樹脂の１５０℃におけるＩＣＩ粘度は３４mPa・sであり、エポキシ当量は２３３ｇ／ｅｑ、軟化点は４０℃以下であった。
In a glass reaction vessel equipped with a stirrer, a condenser, and a nitrogen gas introduction tube, 149.4 g (0.90 mol) of phenol novolac resin obtained in Example 1 and 499.5 g (5.40 mol) of epichlorohydrin were obtained. Then, 46.88 g of methanol was charged and dissolved uniformly. At 50 ° C., 37.5 g (0.90 mol) of solid 96% sodium hydroxide was added in portions over 90 minutes. Thereafter, the reaction was carried out at 50 ° C. for 2 hours, and the reaction was continued for another 2 hours after the temperature was raised to 70 ° C. After completion of the reaction, excess epichlorohydrin was removed under reduced pressure.
240 g of methyl isobutyl ketone was added to the residue and dissolved. A 25% aqueous sodium hydroxide solution (14.40 g, 0.09 mol) was added, and the mixture was reacted at 70 ° C. for 1 hour. After completion of the reaction, the water washing treatment was repeated 5 times until the aqueous layer became neutral. Methyl isobutyl ketone was distilled off under heating and reduced pressure to obtain 191 g of epoxy resin B.
The obtained epoxy resin had an ICI viscosity at 150 ° C. of 34 mPa · s, an epoxy equivalent of 233 g / eq, and a softening point of 40 ° C. or less.
比較例1
撹拌装置、コンデンサー、及び窒素ガス導入管を備えたガラス製反応釜に、フェノール３７６ｇ（４モル）、４，４’−ＢＣＭＢ１５０．７０ｇ（０．６モル）を仕込み１００℃で３時間反応させ、その後４２％ホルムアルデヒド水溶液２８．５７ｇ（０．４モル）を添加し、その後、１００℃で３時間反応させた。その間、生成する塩化水素を除去した。反応終了後、得られた反応溶液を冷却し、水洗を１回行った。油層を分離し、減圧蒸留により未反応フェノールを留去し溶融状態のフェノール樹脂をバットに抜き出し、そのバットを１０℃の水が入った水槽に入れて冷却させた。約３０分後には全体が冷却されており、これをとりだすことにより１９８ｇのフェノール樹脂を得た。
得られたフェノール樹脂のJIS K ２２０７に基づく環球法軟化点は軟化点は５８℃であり、１５０℃におけるＩＣＩ粘度は４４mPa・sであり、軟化点が低く取り扱いに難点があった。得られたフェノール樹脂をＣｕＫα線により測定したＸ線回折パターンにおいて、回折角２θが１７°〜１９°の範囲に結晶性化合物であることを示す最大強度ピークを有さないものであった。得られたフェノール樹脂のＸ線回折強度を図１に示す。比較例１のフェノール樹脂は、２θ＝１９．１に、半値幅７．２の非常にブロードなピークが検出されたのみであった。
Comparative Example 1
In a glass reaction kettle equipped with a stirrer, a condenser, and a nitrogen gas introduction tube, 376 g (4 mol) of phenol and 150.70 g (0.6 mol) of 4,4′-BCMB were charged and reacted at 100 ° C. for 3 hours. Thereafter, 28.57 g (0.4 mol) of a 42% aqueous formaldehyde solution was added, and then reacted at 100 ° C. for 3 hours. Meanwhile, the hydrogen chloride formed was removed. After completion of the reaction, the obtained reaction solution was cooled and washed once with water. The oil layer was separated, unreacted phenol was distilled off by distillation under reduced pressure, the molten phenol resin was extracted into a vat, and the vat was cooled in a water bath containing 10 ° C. water. After about 30 minutes, the whole was cooled, and 198 g of phenol resin was obtained by taking it out.
The obtained phenol resin had a ring-and-ball method softening point based on JIS K 2207 of 58 ° C., an ICI viscosity at 150 ° C. of 44 mPa · s, a low softening point, and a difficulty in handling. In the X-ray diffraction pattern obtained by measuring the obtained phenol resin with CuKα rays, it did not have a maximum intensity peak indicating that the diffraction angle 2θ was a crystalline compound in the range of 17 ° to 19 °. The X-ray diffraction intensity of the obtained phenol resin is shown in FIG. In the phenol resin of Comparative Example 1, only a very broad peak with a half width of 7.2 was detected at 2θ = 19.1.
［ＥＭＣ（Ｅｐｏｘｙ Ｍｏｌｄｅｒｉｎｇ Ｃｏｍｐｏｕｎｄの製造］
表１に示す配合比で、エポキシ樹脂組成物を製造した。実施例１，２，３で得たフェノール樹脂を硬化剤Ａ，Ｂ，Ｃとし、フェノール樹Ｄとして、ＨＦ−３Ｍ（明和化成社製 OH当量１０７ｇ/ｅｑ）、ビフェニルエポキシ樹脂（ジャパン エポキシ レジン社製；ＹＸ−４０００、エポキシ当量１８８ｇ／ｅｑ）をエポキシ樹脂Ａ、溶融シリカ、トリフェニルホスフィン（ＴＰＰ）を表１に示す割合、すなわちフェノール水酸基当量とエポキシ当量比が１：１となるように配合した。これに８３ｗｔ％になるように充填剤を加え、これらを、１００℃〜１１０℃の条件で２軸ニーダで混練後粉砕しＥＭＣ粉体を調整した。
得られたＥＭＣ粉体を用いてタブレットを作成し、スパイラルフロー測定を行った。
また、トランスファー成形機にて試験片を作成し、１８０℃ ８ｈｒのポストキュアをＴＭＡ、曲げ強度、難燃評価用のテストピースを得た。
[EMC (Manufacture of Epoxy Molding Compound)]
The epoxy resin composition was manufactured with the compounding ratio shown in Table 1. The phenol resins obtained in Examples 1, 2, and 3 were used as curing agents A, B, and C, and phenol tree D as HF-3M (OH equivalent 107 g / eq, manufactured by Meiwa Kasei Co., Ltd.) and biphenyl epoxy resin (Japan Epoxy Resin Co., Ltd.). YX-4000, epoxy equivalent 188 g / eq) blended with epoxy resin A, fused silica, and triphenylphosphine (TPP) in the proportions shown in Table 1, that is, the ratio of phenol hydroxyl equivalent to epoxy equivalent is 1: 1. did. The filler was added to 83 wt%, and these were kneaded with a biaxial kneader under conditions of 100 ° C to 110 ° C and pulverized to prepare EMC powder.
A tablet was prepared using the obtained EMC powder, and spiral flow measurement was performed.
Moreover, the test piece was created with the transfer molding machine, and the test piece for TMA, bending strength, and a flame retardance evaluation was obtained for 180 degreeC 8hr postcure.
各種物性の試験方法は次の通りである。これらを表１に示す。
［スパイラルフローの測定］
スパイラルフローは、低圧トランスファー成形機を用いて、ＥＭＭＩ−１−６６に準じたスパイラルフロー測定用金型に、金型温度１７５℃、注入圧力６．８ＭＰａ、保圧時間１２０秒の条件でＥＭＣ組成物を注入し、流動長を測定した。
The test methods for various physical properties are as follows. These are shown in Table 1.
[Measurement of spiral flow]
Spiral flow is performed using a low-pressure transfer molding machine on a spiral flow measurement mold in accordance with EMMI-1-66 under the conditions of a mold temperature of 175 ° C., an injection pressure of 6.8 MPa, and a holding time of 120 seconds. The material was injected and the flow length was measured.
［ガラス転移点（Ｔｇ）の測定］
ガラス転移点は、ＴＭＡ法（Ｔｈｅｒｍａｌ Ｍｅｃｈａｎｉｃａｌ Ａｎａｌｙｓｉｓ、熱機械分析法）（昇温速度５℃／分）を用いて測定した。
［機械強度（曲げ弾性率）の測定］
機械強度（曲げ弾性率）は、ＪＩＳ Ｋ ７１７１に準拠して測定した。
［難燃性の評価］
難燃性は、ＵＬ−９４に準拠して評価した。試験片のサイズは厚さ１ｍｍ×長さ１３５ｍｍ×幅１０ｍｍとした。
［フェノール樹脂の軟化点の測定］
フェノール樹脂の軟化点は、ＪＩＳ Ｋ２２０７に基づく環球法にて測定した。
[Measurement of glass transition point (Tg)]
The glass transition point was measured using the TMA method (Thermal Mechanical Analysis, thermomechanical analysis method) (heating rate 5 ° C./min).
[Measurement of mechanical strength (flexural modulus)]
The mechanical strength (flexural modulus) was measured according to JIS K 7171.
[Evaluation of flame retardancy]
Flame retardancy was evaluated according to UL-94. The size of the test piece was 1 mm thick × 135 mm long × 10 mm wide.
[Measurement of softening point of phenolic resin]
The softening point of the phenol resin was measured by the ring and ball method based on JIS K2207.
［ＩＣＩ粘度の測定］
ＩＣＩコーンプレート粘度計（ＭＯＤＥＬ ＣＶ−１Ｓ ＴＯＡ工業社製）を用いて、フェノール樹脂のＩＣＩ粘度の測定を下記のように行った。
ＩＣＩ粘度計のプレート温度を１５０℃に設定し、試料を所定量、秤量した。その後、プレート部に秤量した樹脂を置き、上部よりコーンで押えつけ、９０ｓｅｃ放置した。前記コーンを回転させて、そのトルク値をＩＣＩ粘度として読み取った。
[Measurement of ICI viscosity]
Using an ICI cone plate viscometer (manufactured by MODEL CV-1S TOA Kogyo Co., Ltd.), the ICI viscosity of the phenol resin was measured as follows.
The plate temperature of the ICI viscometer was set to 150 ° C., and a predetermined amount of the sample was weighed. Thereafter, a weighed resin was placed on the plate portion, pressed from above with a cone, and left for 90 seconds. The cone was rotated and the torque value was read as ICI viscosity.
［取り扱い性（ブロッキング性）評価］
実施例１〜３及び比較例１にて合成したフェノール樹脂をハンマーでフレーク状に粉砕し、このフレーク状フェノール樹脂１００ｇを口径７．５ｃｍ、高さ８．０ｃｍのポリプロピレン製カップに入れ、２７℃で２時間放置した。評価基準を以下に示す。
◎：前記フェノール樹脂をカップから取り出し、前記フェノール樹脂が元のペレット状（フレーク状）に自然に分かれる。
○：前記フェノール樹脂をカップから取り出した段階では一部カップの形状を残すが、手で容易にほぐしてペレット状にすることができる。
△：前記フェノール樹脂をカップから取り出した段階では一部カップの形状を残すが、力を入れれば手でほぐしてフレーク状にすることができる。
×：力を入れて手でほぐそうとしても、カップの形状のままほぐせない。
[Handling (blocking) evaluation]
The phenolic resins synthesized in Examples 1 to 3 and Comparative Example 1 were pulverized into flakes with a hammer, and 100 g of the flaky phenolic resin was placed in a polypropylene cup having a diameter of 7.5 cm and a height of 8.0 cm. And left for 2 hours. The evaluation criteria are shown below.
(Double-circle): The said phenol resin is taken out from a cup, and the said phenol resin is divided into the original pellet form (flakes form) naturally.
○: At the stage of taking out the phenolic resin from the cup, a part of the cup shape is left, but it can be easily loosened by hand to form a pellet.
Δ: At the stage where the phenol resin is taken out from the cup, a part of the cup shape remains, but if force is applied, it can be loosened by hand to form a flake.
X: Even if it tries to loosen it by hand with force, it does not loosen in the shape of a cup.
［フェノール樹脂のX線回折測定］
株式会社リガク製 TTR-３型 広角Ｘ線回折装置を用いて以下の条件にて、フェノール樹脂のＸ線回折の測定をおこなった。２θ＝１７〜１９°にピークが存在する場合は○、存在しない場合は×とした。
Ｘ線源：CuKα線
管電圧−管電流：50kV−300mA
測定範囲：2-70deg.
ステップ幅：0.02deg.
測定速度：5deg./min.
スリット（発散スリット-受光スリット-散乱スリット）：0.5deg.−0.15mm−0.5deg.
走査速度：５ｄｅｇ／ｍｉｎ
回折線湾曲結晶モノクロメータ
[X-ray diffraction measurement of phenol resin]
Using a TTR-3 type wide-angle X-ray diffractometer manufactured by Rigaku Corporation, the X-ray diffraction of the phenol resin was measured under the following conditions. When a peak was present at 2θ = 17 to 19 °, it was marked as ◯, and when it was not present, it was marked as x.
X-ray source: CuKα tube voltage-tube current: 50 kV-300 mA
Measuring range: 2-70deg.
Step width: 0.02deg.
Measurement speed: 5deg./min.
Slit (divergence slit-light receiving slit-scattering slit): 0.5deg.−0.15mm−0.5deg.
Scanning speed: 5 deg / min
Diffraction line crystal monochromator
Claims (12)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009230271A JP5515583B2 (en) | 2009-10-02 | 2009-10-02 | Phenolic resin, epoxy resin and cured epoxy resin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009230271A JP5515583B2 (en) | 2009-10-02 | 2009-10-02 | Phenolic resin, epoxy resin and cured epoxy resin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011074338A true JP2011074338A (en) | 2011-04-14 |
| JP5515583B2 JP5515583B2 (en) | 2014-06-11 |
Family
ID=44018653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009230271A Active JP5515583B2 (en) | 2009-10-02 | 2009-10-02 | Phenolic resin, epoxy resin and cured epoxy resin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5515583B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117700955A (en) * | 2024-02-06 | 2024-03-15 | 佛山市奥川顺新材料实业有限公司 | Antibacterial PET film material and preparation method thereof |
Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04360663A (en) * | 1991-06-06 | 1992-12-14 | Hayashibara Biochem Lab Inc | Powdery saccharide and production and use thereof |
| JPH06198644A (en) * | 1993-01-08 | 1994-07-19 | Three Bond Co Ltd | Molding method for epoxy resin tablet |
| JPH09324029A (en) * | 1996-06-04 | 1997-12-16 | Sumitomo Chem Co Ltd | Method for forming epoxy resin into particulate article |
| JPH108326A (en) * | 1996-06-27 | 1998-01-13 | Osaka Gas Co Ltd | Phenol resin fiber and phenol resin-based carbon fiber |
| JPH1112445A (en) * | 1997-06-23 | 1999-01-19 | Nippon Kayaku Co Ltd | Marble-like crystalline epoxy compound, epoxy resin composition and cured product thereof |
| JP2004345957A (en) * | 2003-05-09 | 2004-12-09 | Toto Kasei Co Ltd | Method for crystallizing organic oligomer |
| WO2007026553A1 (en) * | 2005-08-31 | 2007-03-08 | Ube Industries, Ltd. | Low softening point phenol novolac resin, method for producing same, and epoxy resin cured product using same |
| WO2007063894A1 (en) * | 2005-11-30 | 2007-06-07 | Nippon Kayaku Kabushiki Kaisha | Phenolic resin, process for production thereof, epoxy resin, and use thereof |
| JP2008156553A (en) * | 2006-12-26 | 2008-07-10 | Ube Ind Ltd | Low-melt-viscosity phenol novolak resin, its preparation method and its use |
| JP2008189708A (en) * | 2007-02-01 | 2008-08-21 | Ube Ind Ltd | Low-melt viscosity phenol novolak resin, method for producing the same and cured product of epoxy resin using the same |
| WO2010087393A1 (en) * | 2009-01-30 | 2010-08-05 | 宇部興産株式会社 | Epoxy resin composition, process for producing the epoxy resin composition, and cured object formed therefrom |
-
2009
- 2009-10-02 JP JP2009230271A patent/JP5515583B2/en active Active
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04360663A (en) * | 1991-06-06 | 1992-12-14 | Hayashibara Biochem Lab Inc | Powdery saccharide and production and use thereof |
| JPH06198644A (en) * | 1993-01-08 | 1994-07-19 | Three Bond Co Ltd | Molding method for epoxy resin tablet |
| JPH09324029A (en) * | 1996-06-04 | 1997-12-16 | Sumitomo Chem Co Ltd | Method for forming epoxy resin into particulate article |
| JPH108326A (en) * | 1996-06-27 | 1998-01-13 | Osaka Gas Co Ltd | Phenol resin fiber and phenol resin-based carbon fiber |
| JPH1112445A (en) * | 1997-06-23 | 1999-01-19 | Nippon Kayaku Co Ltd | Marble-like crystalline epoxy compound, epoxy resin composition and cured product thereof |
| JP2004345957A (en) * | 2003-05-09 | 2004-12-09 | Toto Kasei Co Ltd | Method for crystallizing organic oligomer |
| WO2007026553A1 (en) * | 2005-08-31 | 2007-03-08 | Ube Industries, Ltd. | Low softening point phenol novolac resin, method for producing same, and epoxy resin cured product using same |
| WO2007063894A1 (en) * | 2005-11-30 | 2007-06-07 | Nippon Kayaku Kabushiki Kaisha | Phenolic resin, process for production thereof, epoxy resin, and use thereof |
| JP2008156553A (en) * | 2006-12-26 | 2008-07-10 | Ube Ind Ltd | Low-melt-viscosity phenol novolak resin, its preparation method and its use |
| JP2008189708A (en) * | 2007-02-01 | 2008-08-21 | Ube Ind Ltd | Low-melt viscosity phenol novolak resin, method for producing the same and cured product of epoxy resin using the same |
| WO2010087393A1 (en) * | 2009-01-30 | 2010-08-05 | 宇部興産株式会社 | Epoxy resin composition, process for producing the epoxy resin composition, and cured object formed therefrom |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117700955A (en) * | 2024-02-06 | 2024-03-15 | 佛山市奥川顺新材料实业有限公司 | Antibacterial PET film material and preparation method thereof |
| CN117700955B (en) * | 2024-02-06 | 2024-05-10 | 佛山市奥川顺新材料实业有限公司 | Antibacterial PET film material and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5515583B2 (en) | 2014-06-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5170493B2 (en) | Phenol polymer, its production method and its use | |
| JP5228328B2 (en) | Low melt viscosity phenol novolac resin, process for producing the same, and cured epoxy resin using the same | |
| JP5166610B2 (en) | Epoxy resin, production method thereof, epoxy resin composition and cured product using the same | |
| JP5413488B2 (en) | Phenol novolac resin, method for producing the same, epoxy resin composition and cured product using the same | |
| JPH07292067A (en) | Production of modified epoxy resin, modified epoxy resin and composition of the epoxy resin | |
| TWI438216B (en) | Modified liquid epoxy resin, epoxy resin composition by using modified liquid epoxy resin and cured product thereof | |
| JP5689230B2 (en) | Epoxy resin composition, cured product thereof, semiconductor sealing material, semiconductor device, and epoxy resin | |
| JP4655490B2 (en) | Epoxy resin composition and cured product thereof | |
| JP5476762B2 (en) | Phenol resin, process for producing the resin, epoxy resin composition containing the resin, and cured product thereof | |
| JP5616234B2 (en) | Epoxy resin composition, method for producing the epoxy resin composition, and cured product thereof | |
| JP5734603B2 (en) | Phenolic resin, epoxy resin, production method thereof, epoxy resin composition and cured product | |
| JP5714216B2 (en) | Epoxy resin composition, cured product thereof, epoxy resin, production method thereof, semiconductor sealing material, and semiconductor device | |
| JP5233858B2 (en) | Epoxy resin composition, cured product thereof, and semiconductor device | |
| TWI522385B (en) | An epoxy resin, an epoxy resin composition, and a cured product thereof | |
| JP5515583B2 (en) | Phenolic resin, epoxy resin and cured epoxy resin | |
| JP4493748B2 (en) | Epoxy resin, method for producing the same, epoxy resin composition and cured product thereof | |
| JP3933763B2 (en) | Epoxy resin composition and electronic component | |
| JP4363048B2 (en) | Epoxy resin composition and cured product thereof | |
| JP4667753B2 (en) | Epoxy resin production method, epoxy resin composition and cured product | |
| JP5272963B2 (en) | Epoxy resin and method for producing the same | |
| TW202244099A (en) | Epoxy resin, method for manufacturing the same, epoxy resin composition and cured product using the same | |
| JP2010229203A (en) | Phenolic resin composition, process for producing the resin composition and epoxy resin composition including the resin composition | |
| JP2004043829A (en) | Producing method for epoxy resin solid at ordinary temperature | |
| JP2003277485A (en) | Curing agent for epoxy resin and epoxy resin composition | |
| JP2001261790A (en) | Epoxy resin composition and semiconductor device |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20120404 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130514 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130712 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20131001 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20131127 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20140304 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20140317 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5515583 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |