JP5858347B2 - 粘着剤組成物およびそれを用いた粘着フィルム - Google Patents
粘着剤組成物およびそれを用いた粘着フィルム Download PDFInfo
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- JP5858347B2 JP5858347B2 JP2014020236A JP2014020236A JP5858347B2 JP 5858347 B2 JP5858347 B2 JP 5858347B2 JP 2014020236 A JP2014020236 A JP 2014020236A JP 2014020236 A JP2014020236 A JP 2014020236A JP 5858347 B2 JP5858347 B2 JP 5858347B2
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- pressure
- sensitive adhesive
- adhesive composition
- resin
- acrylic resin
- Prior art date
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- 239000000853 adhesive Substances 0.000 title claims description 64
- 230000001070 adhesive effect Effects 0.000 title claims description 64
- 239000000203 mixture Substances 0.000 title claims description 58
- 239000002313 adhesive film Substances 0.000 title description 2
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 104
- 229920005989 resin Polymers 0.000 claims description 58
- 239000011347 resin Substances 0.000 claims description 58
- -1 polyethylene acrylate Polymers 0.000 claims description 53
- 229920000178 Acrylic resin Polymers 0.000 claims description 50
- 239000004925 Acrylic resin Substances 0.000 claims description 50
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 26
- 239000003431 cross linking reagent Substances 0.000 claims description 26
- 239000010410 layer Substances 0.000 claims description 26
- 239000000758 substrate Substances 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 20
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 16
- 230000009477 glass transition Effects 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 12
- 238000001723 curing Methods 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 238000004132 cross linking Methods 0.000 claims description 7
- 239000004593 Epoxy Substances 0.000 claims description 6
- 239000012948 isocyanate Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000000016 photochemical curing Methods 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 229920000728 polyester Polymers 0.000 claims description 4
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 claims description 3
- 239000000178 monomer Substances 0.000 description 24
- 238000000576 coating method Methods 0.000 description 17
- 239000011248 coating agent Substances 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- 206010040844 Skin exfoliation Diseases 0.000 description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 11
- 230000001681 protective effect Effects 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 7
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 7
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229920006243 acrylic copolymer Polymers 0.000 description 6
- 239000012790 adhesive layer Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 6
- 229940095095 2-hydroxyethyl acrylate Drugs 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 5
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 5
- 238000011109 contamination Methods 0.000 description 5
- 125000004386 diacrylate group Chemical group 0.000 description 5
- 229920001296 polysiloxane Polymers 0.000 description 5
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000011889 copper foil Substances 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 4
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000001588 bifunctional effect Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000007667 floating Methods 0.000 description 3
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920001721 polyimide Polymers 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 3
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 2
- WTYYGFLRBWMFRY-UHFFFAOYSA-N 2-[6-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COCCCCCCOCC1CO1 WTYYGFLRBWMFRY-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 2
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 2
- GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-UHFFFAOYSA-N 0.000 description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 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
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 238000007756 gravure coating Methods 0.000 description 2
- 230000005865 ionizing radiation Effects 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 229920003223 poly(pyromellitimide-1,4-diphenyl ether) Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- 238000005476 soldering Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- SZCWBURCISJFEZ-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)COC(=O)C(C)(C)CO SZCWBURCISJFEZ-UHFFFAOYSA-N 0.000 description 1
- JMMVHMOAIMOMOF-UHFFFAOYSA-N (4-prop-2-enoyloxyphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=C(OC(=O)C=C)C=C1 JMMVHMOAIMOMOF-UHFFFAOYSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 1
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 description 1
- WACRZVHHXDZWRU-UHFFFAOYSA-N 1,3-dioxolane;prop-2-enoic acid Chemical compound C1COCO1.OC(=O)C=C WACRZVHHXDZWRU-UHFFFAOYSA-N 0.000 description 1
- OHLKMGYGBHFODF-UHFFFAOYSA-N 1,4-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=C(CN=C=O)C=C1 OHLKMGYGBHFODF-UHFFFAOYSA-N 0.000 description 1
- DKBHJZFJCDOGOY-UHFFFAOYSA-N 1,4-diisocyanato-2-methylbenzene Chemical compound CC1=CC(N=C=O)=CC=C1N=C=O DKBHJZFJCDOGOY-UHFFFAOYSA-N 0.000 description 1
- FWWWRCRHNMOYQY-UHFFFAOYSA-N 1,5-diisocyanato-2,4-dimethylbenzene Chemical compound CC1=CC(C)=C(N=C=O)C=C1N=C=O FWWWRCRHNMOYQY-UHFFFAOYSA-N 0.000 description 1
- ZDQNWDNMNKSMHI-UHFFFAOYSA-N 1-[2-(2-prop-2-enoyloxypropoxy)propoxy]propan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC(C)COC(C)COCC(C)OC(=O)C=C ZDQNWDNMNKSMHI-UHFFFAOYSA-N 0.000 description 1
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
- FDUFQLNPPGRIKX-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CC(C)(CO)CO FDUFQLNPPGRIKX-UHFFFAOYSA-N 0.000 description 1
- CZZVAVMGKRNEAT-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol;3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)CO.OCC(C)(C)C(O)=O CZZVAVMGKRNEAT-UHFFFAOYSA-N 0.000 description 1
- OWPUOLBODXJOKH-UHFFFAOYSA-N 2,3-dihydroxypropyl prop-2-enoate Chemical compound OCC(O)COC(=O)C=C OWPUOLBODXJOKH-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
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- JLZQMKLXOVLQFA-UHFFFAOYSA-N 2-(oxolan-2-ylmethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCC1CCCO1 JLZQMKLXOVLQFA-UHFFFAOYSA-N 0.000 description 1
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 description 1
- FDSUVTROAWLVJA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.OCC(CO)(CO)COCC(CO)(CO)CO FDSUVTROAWLVJA-UHFFFAOYSA-N 0.000 description 1
- VUIWJRYTWUGOOF-UHFFFAOYSA-N 2-ethenoxyethanol Chemical compound OCCOC=C VUIWJRYTWUGOOF-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- NPSJHQMIVNJLNN-UHFFFAOYSA-N 2-ethylhexyl 4-nitrobenzoate Chemical compound CCCCC(CC)COC(=O)C1=CC=C([N+]([O-])=O)C=C1 NPSJHQMIVNJLNN-UHFFFAOYSA-N 0.000 description 1
- 239000004808 2-ethylhexylester Substances 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 1
- AUZRCMMVHXRSGT-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid;prop-2-enamide Chemical compound NC(=O)C=C.CC(C)CS(O)(=O)=O AUZRCMMVHXRSGT-UHFFFAOYSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- ROPDSOYFYJCSTC-UHFFFAOYSA-N 2-phenoxyundecyl prop-2-enoate Chemical compound CCCCCCCCCC(COC(=O)C=C)OC1=CC=CC=C1 ROPDSOYFYJCSTC-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- YYIOIHBNJMVSBH-UHFFFAOYSA-N 2-prop-2-enoyloxynaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=C(OC(=O)C=C)C=CC2=C1 YYIOIHBNJMVSBH-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
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- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
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- B32B7/06—Interconnection of layers permitting easy separation
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- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
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- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
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- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
- C08G18/6225—Polymers of esters of acrylic or methacrylic acid
- C08G18/6229—Polymers of hydroxy groups containing esters of acrylic or methacrylic acid with aliphatic polyalcohols
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8003—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
- C08G18/8006—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32
- C08G18/8009—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203
- C08G18/8022—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen with compounds of C08G18/32 with compounds of C08G18/3203 with polyols having at least three hydroxy groups
- C08G18/8029—Masked aromatic polyisocyanates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L75/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C08L75/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
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Description
前記基材の一方の面に、請求項1〜7のいずれか一項に記載の粘着剤組成物を塗布し、
前記粘着剤組成物を加熱して前記アクリル系樹脂を架橋させ、かつ、前記粘着剤組成物に光照射を行い前記光硬化性樹脂を硬化させることによって、粘着剤層を形成する、
ことを含んでなることを特徴とするものである。
本発明による粘着剤組成物は、アクリル系樹脂と前記アクリル系樹脂を架橋させるための架橋剤と、光硬化性樹脂と、前記光硬化性樹脂を硬化させるための光硬化剤とを必須成分として含む。以下、粘着剤組成物を構成する各成分について説明する。
本発明による粘着剤組成物を構成するアクリル系樹脂は、(メタ)アクリル酸エステルを主成分とするアクリル系樹脂を好適に使用できる。なお、本明細書において、(メタ)アクリル酸とは、アクリル酸および/またはメタクリル酸をいうものとする。(メタ)アクリル酸エステルとしては、メチルエステル、エチルエステル、プロピルエステル、イソプロピルエステル、ブチルエステル、イソブチルエステル、s−ブチルエステル、t−ブチルエステル、ペンチルエステル、イソペンチルエステル、ヘキシルエステル、ヘプチルエステル、オクチルエステル、2−エチルヘキシルエステル、イソオクチルエステル、ノニルエステル、イソノニルエステル、デシルエステル、イソデシルエステル、ウンデシルエステル、ドデシルエステル、トリデシルエステル、テトラデシルエステル、ヘキサデシルエステル、オクタデシルエステル、エイコシルエステル等の炭素数1〜30、特に炭素数1〜18の直鎖状または分岐状のアルキルエステル等の(メタ)アクリル酸アルキルエステル、および、シクロペンチルエステル、シクロヘキシルエステル等(メタ)アクリル酸シクロアルキルエステルを使用することができる。これらアクリル酸エステルは1種または2種以上を含んでいてもよい。
本発明による粘着剤組成物は、上記したアクリル系樹脂を架橋させるための架橋剤が含まれる。架橋剤を添加することにより、接着強度を維持しながらベタつきを改善することができる。架橋剤としては、熱硬化系架橋剤であれば従来公知のものを使用することができ、例えば、多官能エポキシ系化合物やイソシアネート系化合物が挙げられる。
本発明による粘着剤組成物は、上記したアクリル系樹脂および架橋剤に加えて、光硬化性樹脂を含む。ここで、光硬化性樹脂とは、活性光線を照射する前の前駆体または組成物を意味し、活性光線を照射して活性光線硬化性樹脂を硬化させたものを活性光線硬化樹脂というものとする。また、活性光線とは、活性光線硬化性樹脂に対して化学的に作用させて重合を促進せしめる放射線を意味し、具体的には、可視光線、紫外線、X線、電子線、α線、β線、γ線等を意味するものとする。
本発明による粘着シートは、上記した粘着剤組成物を粘着剤層として、その両面を離型シートで挟持したものであってもよく、また、基材と前記基材の一方の面に設けられた粘着剤層とを備えたものであってもよい。また、基材の一方の面に粘着剤層を設けた場合は、粘着剤層の他方の面に離型シートを設けてもよい。粘着剤層は、上記した粘着剤組成物中の光硬化性樹脂を硬化させたものを使用する。
<粘着剤組成物の調製>
モノマー単位として、メチルアクリレート、2−エチルヘキシルアクリレート、アクリル酸、2−ヒドロキシエチルアクリレートをそれぞれ質量基準で50:40:0.5:9.5の割合で含むアクリル系共重合体樹脂(質量平均分子量20万、ガラス転移温度6℃)を用いた。このアクリル系共重合体樹脂の酢酸エチル溶液(固形分35質量%)を100質量部と、架橋剤としてイソシアネート(商品名:コロネートL、日本ポリウレタン社製)を2.4質量部と、光硬化性樹脂として10官能ウレタンアクリレート(商品名:U−10PPA、新中村化学工業社製)を7質量部と、光開始剤(商品名:Irgcure819、BASF社製)を0.21質量部とを、トルエンおよびメチルエチルケトンの混合溶媒(商品名:KT−11,質量比1:1、DICグラフィクス社製)に溶解させ、固形分が25%となるようにディスパーにて回転数500rpmで30分間撹拌した後、常温で気泡がなくなるまで放置することにより粘着剤組成物を得た。
得られた粘着剤組成物を、片面にシリコーン系剥離剤による易剥離処理が施されている厚さ38μmのポリエステルフィルム(商品名:SP−PET−01、三井化学東セロ社製)の易剥離処理面上にアプリケータを用いて全面塗工した後、乾燥オーブンにより100℃で2分間乾燥し、次いで、波長365nmの紫外線を300mJ/cm2で照射することにより光硬化性樹脂を硬化させて、厚さ10μmの粘着層を形成した。形成した粘着層の面に、厚さ25μmのポリイミドフィルム基材(商品名:カプトン100H、東レ・デュポン社製)をラミネートすることにより、粘着シート1を得た。
光硬化性樹脂として、2官能ウレタンアクリレート(商品名:ビームセット502H、荒川化学社製)を7質量部さらに加えた以外は、実施例1と同様にして粘着シート2を得た。
実施例1で使用したアクリル系共重合体樹脂に代えて、アクリロニトリルと(メタ)アクリル酸エステルとを共重合したアクリル系共重合体樹脂(商品名:テイサンレジンSG−700AS、ナガセケムテックス社製)を使用した以外は、実施例1と同様にして粘着シート3を得た。
実施例1で使用した光硬化性樹脂を、ポリエステル系硬化性樹脂であるU−200PA(新中村化学製)に変更した以外は、実施例1と同様にして粘着シート4を得た。
実施例1で使用した光硬化性樹脂を、エポキシ系硬化性樹脂であるA−BPE−10(新中村化学製)に変更した以外は、実施例1と同様にして粘着シート5を得た。
<粘着剤組成物の調製>
粘着剤組成物として、光硬化性樹脂および光硬化剤を配合しなかった以外は実施例1と同様にして調製したものを用いた。
得られた粘着剤組成物を、片面にシリコーン系剥離剤による易剥離処理が施されている厚さ38μmのポリエステルフィルム(商品名:SP−PET−01、三井化学東セロ社製)の易剥離処理面上にアプリケータを用いて全面塗工した後、乾燥オーブンにより100℃で2分間乾燥し、厚さ10μmの粘着層を形成した。形成した粘着層の面に、厚さ25μmのポリイミドフィルム基材(商品名:カプトン100H、東レ・デュポン社製)をラミネートすることにより、粘着シート4を得た。
得られた粘着シートを、25mm×150mmのサイズに切り出し、易剥離処理が施されたポリエステルフィルムを粘着シートから剥離して粘着剤層を露出させ、粘着シートの粘着剤層を、銅箔(商品名:RCF−T58、福田金属箔粉工業社製)に貼合し、2kgのローラーを用いて圧着し、常温常圧(約23℃、約60%RH)環境下に20分間放置した後、引張試験機(型番:RTF−1150H、エー・アンド・デイ社製)を用いてJIS Z 0237に準拠した測定条件(引張速度:300mm/分、剥離距離:150mm、剥離角度:180度)により、粘着シートを銅箔から剥離する際の粘着力を測定した(初期粘着力)。また、粘着シートと銅箔とを貼合し、2kgのローラーを用いて圧着した後、230℃の環境下に60分間放置し、続いて常温常圧環境下に60分間放置した後の粘着力も上記と同様にして測定した(加熱処理後の粘着力)。測定結果は下記の表1に示される通りであった。
Claims (8)
- アクリル系樹脂と、前記アクリル系樹脂を架橋させるための架橋剤と、光硬化性樹脂と、前記光硬化性樹脂を硬化させるための光硬化剤と、を含んでなり、
前記光硬化性樹脂が、エポキシアクリレート、ポリエステルアクリレート、及びポリエチレンアクリレートからなる群より選択される少なくとも1種であり、
前記光硬化性樹脂が、前記アクリル系樹脂に対して5〜60質量%の範囲で含まれてなり、
前記アクリル系樹脂が、(メタ)アクリル酸エステルを主成分とするものであり、ガラス転移温度が−15〜20℃であることを特徴とする、粘着剤組成物。 - 前記アクリル系樹脂の質量平均分子量が5〜100万である、請求項1に記載の粘着剤組成物。
- 前記架橋剤が、熱硬化型エポキシ系化合物または熱硬化型イソシアネート系化合物である、請求項1または2に記載の粘着剤組成物。
- 前記架橋剤が、前記アクリル系樹脂に対して0.5〜20質量%の範囲で含まれてなる、請求項1〜3のいずれか一項に記載の粘着剤組成物。
- 基材と、前記基材の一方の面に設けられた粘着剤層と、を備えてなる粘着シートであって、前記粘着剤層が、請求項1〜4のいずれか一項に記載の粘着剤組成物からなり、前記粘着剤組成物中のアクリル系樹脂が架橋しており、かつ前記光硬化性樹脂が硬化していることを特徴とする、粘着シート。
- 前記粘着剤層の基材側とは反対側の面に、離型シートを備えてなる、請求項5に記載の粘着シート。
- 基材と、前記基材の一方の面に設けられた粘着剤層と、を備えてなる粘着シートを製造する方法であって、
前記基材の一方の面に、請求項1〜4のいずれか一項に記載の粘着剤組成物を塗布し、
前記粘着剤組成物を加熱して前記アクリル系樹脂を架橋させ、かつ、前記粘着剤組成物に光照射を行い前記光硬化性樹脂を硬化させることによって、粘着剤層を形成する、
ことを含んでなることを特徴とする、方法。 - 前記粘着剤組成物を塗布した後、前記加熱および/または光照射を行う前に、前記粘着剤組成物を乾燥させ、次いで、乾燥した前記粘着剤組成物の表面に離型シートを設けて、積層体を形成する、ことを含んでなる、請求項7に記載の方法。
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Family Cites Families (27)
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JP3506519B2 (ja) * | 1995-03-06 | 2004-03-15 | リンテック株式会社 | 粘接着テープおよびその使用方法 |
JP3516384B2 (ja) * | 1998-07-31 | 2004-04-05 | 日本合成化学工業株式会社 | 再剥離型粘着剤組成物 |
JP4823436B2 (ja) | 2001-05-29 | 2011-11-24 | リンテック株式会社 | 紫外線架橋型感圧接着剤組成物、感圧接着剤シート及び感圧接着剤シートの製造方法 |
JP4969744B2 (ja) * | 2001-09-03 | 2012-07-04 | ソマール株式会社 | 粘着組成物及び粘着シート |
JP2005307134A (ja) | 2004-04-19 | 2005-11-04 | Hitachi Kasei Polymer Co Ltd | 部品仮固定用複合体 |
JP5164339B2 (ja) * | 2005-04-28 | 2013-03-21 | 日本合成化学工業株式会社 | 粘着剤層付き光学積層体 |
JP5095926B2 (ja) * | 2005-06-01 | 2012-12-12 | 三菱樹脂株式会社 | 粘着剤及びこれを用いた粘着体 |
WO2007099851A1 (ja) * | 2006-02-28 | 2007-09-07 | Lintec Corporation | 塗膜の保護シート |
JP5560537B2 (ja) | 2007-07-10 | 2014-07-30 | 住友ベークライト株式会社 | 半導体ウエハ加工用粘着テープ |
WO2009066654A1 (ja) * | 2007-11-19 | 2009-05-28 | The Nippon Synthetic Chemical Industry Co., Ltd. | 粘着剤、光学部材用粘着剤、及び粘着剤層付き光学部材 |
JP4318743B1 (ja) * | 2008-10-07 | 2009-08-26 | 昭和高分子株式会社 | 紫外線硬化型再剥離性粘着剤組成物及びこれを用いた粘着シート |
JP5455362B2 (ja) * | 2008-12-25 | 2014-03-26 | チェイル インダストリーズ インコーポレイテッド | 粘着剤組成物およびこれを用いた光学部材 |
WO2010092995A1 (ja) * | 2009-02-16 | 2010-08-19 | 綜研化学株式会社 | 光学部材用放射線硬化型粘着剤組成物および粘着型光学部材 |
CN102482550B (zh) * | 2009-09-01 | 2013-12-18 | 综研化学株式会社 | 用于光学部件的放射线固化型压敏粘合剂组合物及压敏粘合型光学部件 |
KR20110025258A (ko) * | 2009-09-04 | 2011-03-10 | 도레이첨단소재 주식회사 | 도금용 점착시트 |
JP4937327B2 (ja) * | 2009-10-06 | 2012-05-23 | 藤森工業株式会社 | 粘着剤組成物の製造方法、粘着フィルムの製造方法、粘着剤用原料組成物及び粘着フィルム |
KR101194544B1 (ko) * | 2011-01-20 | 2012-10-25 | 도레이첨단소재 주식회사 | 다이 익스포즈드 플립칩 패키지(defcp)의 몰드 언더필 공정용 점착 마스킹 테이프 |
JP2012177084A (ja) * | 2011-01-31 | 2012-09-13 | Dainippon Printing Co Ltd | 耐熱仮着用の粘着剤組成物及び粘着テープ |
JP2012193321A (ja) * | 2011-03-18 | 2012-10-11 | Furukawa Electric Co Ltd:The | 放射線硬化型粘着剤組成物、それを用いたウェハ加工用粘着テープ、放射線硬化型粘着剤組成物の判定方法 |
EP3650512A1 (en) * | 2011-08-03 | 2020-05-13 | LINTEC Corporation | Gas barrier adhesive sheet, method for producing same, electronic member, and optical member |
WO2013061938A1 (ja) * | 2011-10-24 | 2013-05-02 | 王子ホールディングス株式会社 | 粘着シート及びその使用方法並びに積層体 |
JP2013142132A (ja) * | 2012-01-11 | 2013-07-22 | Dainippon Printing Co Ltd | 積層体、この積層体を用いた透明光学部材及びこの積層体を用いた画像表示装置 |
JP6093624B2 (ja) * | 2012-05-24 | 2017-03-08 | 日東電工株式会社 | 光学フィルム用粘着剤層、粘着剤層付光学フィルム、及び、画像表示装置 |
WO2014003056A1 (ja) * | 2012-06-29 | 2014-01-03 | 日立化成株式会社 | 半導体装置の製造方法 |
JP5994445B2 (ja) * | 2012-07-11 | 2016-09-21 | Dic株式会社 | 紫外線硬化型粘着剤用樹脂組成物及び粘着剤 |
TWI586777B (zh) * | 2012-10-24 | 2017-06-11 | Toagosei Co | Production method of active energy ray hardening type adhesive preparation and laminate |
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2014
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2015
- 2015-01-29 WO PCT/JP2015/052562 patent/WO2015119042A1/ja active Application Filing
- 2015-01-29 KR KR1020167019773A patent/KR20160118239A/ko not_active Ceased
- 2015-01-29 CN CN201580004040.6A patent/CN105899633A/zh active Pending
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WO2015119042A1 (ja) | 2015-08-13 |
CN105899633A (zh) | 2016-08-24 |
TWI681026B (zh) | 2020-01-01 |
JP2015147828A (ja) | 2015-08-20 |
TW201534673A (zh) | 2015-09-16 |
KR20160118239A (ko) | 2016-10-11 |
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