JP5428158B2 - Double-sided adhesive tape - Google Patents
Double-sided adhesive tape Download PDFInfo
- Publication number
- JP5428158B2 JP5428158B2 JP2007336083A JP2007336083A JP5428158B2 JP 5428158 B2 JP5428158 B2 JP 5428158B2 JP 2007336083 A JP2007336083 A JP 2007336083A JP 2007336083 A JP2007336083 A JP 2007336083A JP 5428158 B2 JP5428158 B2 JP 5428158B2
- Authority
- JP
- Japan
- Prior art keywords
- sensitive adhesive
- double
- pressure
- adhesive tape
- sided
- 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.)
- Active
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- 239000002390 adhesive tape Substances 0.000 title claims description 34
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 126
- 239000010410 layer Substances 0.000 claims description 54
- 239000000203 mixture Substances 0.000 claims description 31
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 21
- 238000003860 storage Methods 0.000 claims description 12
- 238000007639 printing Methods 0.000 claims description 9
- 238000002834 transmittance Methods 0.000 claims description 5
- 238000007598 dipping method Methods 0.000 claims description 4
- 238000001228 spectrum Methods 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 description 29
- 229920002799 BoPET Polymers 0.000 description 26
- 239000000178 monomer Substances 0.000 description 25
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 23
- 229920000642 polymer Polymers 0.000 description 21
- 230000001070 adhesive effect Effects 0.000 description 18
- 239000000853 adhesive Substances 0.000 description 17
- 239000000126 substance Substances 0.000 description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 15
- 229940114077 acrylic acid Drugs 0.000 description 15
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 239000011521 glass Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 12
- 229940048053 acrylate Drugs 0.000 description 12
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 11
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 11
- 239000003505 polymerization initiator Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- 239000012948 isocyanate Substances 0.000 description 10
- 150000002513 isocyanates Chemical class 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 238000005034 decoration Methods 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- -1 polyethylene terephthalate Polymers 0.000 description 8
- 229920002635 polyurethane Polymers 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 239000012790 adhesive layer Substances 0.000 description 7
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 7
- 239000006260 foam Substances 0.000 description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 5
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- 239000013032 Hydrocarbon resin Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 229920006270 hydrocarbon resin Polymers 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 229930195734 saturated hydrocarbon Natural products 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 244000028419 Styrax benzoin Species 0.000 description 3
- 235000000126 Styrax benzoin Nutrition 0.000 description 3
- 235000008411 Sumatra benzointree Nutrition 0.000 description 3
- 229960002130 benzoin Drugs 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 235000019382 gum benzoic Nutrition 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 235000007586 terpenes Nutrition 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
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- 238000009863 impact test Methods 0.000 description 2
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- 238000004519 manufacturing process Methods 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000003578 releasing effect Effects 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- VMHYWKBKHMYRNF-UHFFFAOYSA-N (2-chlorophenyl)-phenylmethanone Chemical compound ClC1=CC=CC=C1C(=O)C1=CC=CC=C1 VMHYWKBKHMYRNF-UHFFFAOYSA-N 0.000 description 1
- HUDYANRNMZDQGA-UHFFFAOYSA-N 1-[4-(dimethylamino)phenyl]ethanone Chemical compound CN(C)C1=CC=C(C(C)=O)C=C1 HUDYANRNMZDQGA-UHFFFAOYSA-N 0.000 description 1
- LMAUULKNZLEMGN-UHFFFAOYSA-N 1-ethyl-3,5-dimethylbenzene Chemical compound CCC1=CC(C)=CC(C)=C1 LMAUULKNZLEMGN-UHFFFAOYSA-N 0.000 description 1
- GPDFVOVLOXMSBT-UHFFFAOYSA-N 1-propan-2-yloxybutane Chemical compound CCCCOC(C)C GPDFVOVLOXMSBT-UHFFFAOYSA-N 0.000 description 1
- ZHKJHQBOAJQXQR-UHFFFAOYSA-N 1H-azirine Chemical compound N1C=C1 ZHKJHQBOAJQXQR-UHFFFAOYSA-N 0.000 description 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
- LZHUBCULTHIFNO-UHFFFAOYSA-N 2,4-dihydroxy-1,5-bis[4-(2-hydroxyethoxy)phenyl]-2,4-dimethylpentan-3-one Chemical compound C=1C=C(OCCO)C=CC=1CC(C)(O)C(=O)C(O)(C)CC1=CC=C(OCCO)C=C1 LZHUBCULTHIFNO-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 1
- SHJXSYJQBXYBGA-UHFFFAOYSA-N 2-cyclohexyl-2-hydroxy-1-phenylethanone Chemical compound C=1C=CC=CC=1C(=O)C(O)C1CCCCC1 SHJXSYJQBXYBGA-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
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 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
- YRNDGUSDBCARGC-UHFFFAOYSA-N 2-methoxyacetophenone Chemical compound COCC(=O)C1=CC=CC=C1 YRNDGUSDBCARGC-UHFFFAOYSA-N 0.000 description 1
- MYISVPVWAQRUTL-UHFFFAOYSA-N 2-methylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3SC2=C1 MYISVPVWAQRUTL-UHFFFAOYSA-N 0.000 description 1
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 1
- OKISUZLXOYGIFP-UHFFFAOYSA-N 4,4'-dichlorobenzophenone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1=CC=C(Cl)C=C1 OKISUZLXOYGIFP-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- NQSLZEHVGKWKAY-UHFFFAOYSA-N 6-methylheptyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C(C)=C NQSLZEHVGKWKAY-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- XFZOHDFQOOTHRH-UHFFFAOYSA-N 7-methyloctyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C(C)=C XFZOHDFQOOTHRH-UHFFFAOYSA-N 0.000 description 1
- CUXGDKOCSSIRKK-UHFFFAOYSA-N 7-methyloctyl prop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C=C CUXGDKOCSSIRKK-UHFFFAOYSA-N 0.000 description 1
- COCLLEMEIJQBAG-UHFFFAOYSA-N 8-methylnonyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C(C)=C COCLLEMEIJQBAG-UHFFFAOYSA-N 0.000 description 1
- LVGFPWDANALGOY-UHFFFAOYSA-N 8-methylnonyl prop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C=C LVGFPWDANALGOY-UHFFFAOYSA-N 0.000 description 1
- YYVYAPXYZVYDHN-UHFFFAOYSA-N 9,10-phenanthroquinone Chemical compound C1=CC=C2C(=O)C(=O)C3=CC=CC=C3C2=C1 YYVYAPXYZVYDHN-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- HLJYBXJFKDDIBI-UHFFFAOYSA-N O=[PH2]C(=O)C1=CC=CC=C1 Chemical compound O=[PH2]C(=O)C1=CC=CC=C1 HLJYBXJFKDDIBI-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- FKIRSCKRJJUCNI-UHFFFAOYSA-N ethyl 7-bromo-1h-indole-2-carboxylate Chemical compound C1=CC(Br)=C2NC(C(=O)OCC)=CC2=C1 FKIRSCKRJJUCNI-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
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- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
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- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
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- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Images
Landscapes
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
本発明は、装飾部が設けられた透明パネルを画像表示装置表面に貼付固定する両面粘着テープに関する。 The present invention relates to a double-sided pressure-sensitive adhesive tape for sticking and fixing a transparent panel provided with a decorative portion to the surface of an image display device.
LCDモジュール(液晶表示装置)をはじめとする表示素子は、ワープロやパソコンを始めとする広範な分野で用いられている。特に電子手帳、携帯電話、携帯オーディオプレイヤー等においては、近年益々小型化や薄型化が進み、更に動画再生機能等への対応から高精細化の要求も高い。 Display elements such as LCD modules (liquid crystal display devices) are used in a wide range of fields including word processors and personal computers. In particular, electronic notebooks, cellular phones, portable audio players, and the like are becoming increasingly smaller and thinner in recent years, and there is a high demand for higher definition due to the compatibility with moving image playback functions and the like.
このような小型電子機器の画像表示部の構成の一例として、LCDモジュールと画像表示パネルとを額縁状の両面テープにより固定した画像表示装置が使用されている(例えば、特許文献1参照)。しかし、当該構成の画像表示装置は、LCDモジュールと画像表示パネルとの間に空気層による空隙を有するため、当該空気層による反射率の低下が避けられないものであった。 As an example of the configuration of the image display unit of such a small electronic device, an image display device in which an LCD module and an image display panel are fixed with a frame-like double-sided tape is used (for example, see Patent Document 1). However, since the image display device having the above configuration has a gap due to the air layer between the LCD module and the image display panel, a decrease in reflectance due to the air layer is inevitable.
上記のような空隙を有さない構成の液晶表示装置として、表示素子ユニットと保護パネルとの間を全面接着する構成のものが検討されている。当該構成においては、表示素子ユニットと保護パネルとの接着に、液状の接着剤(例えば、特許文献2参照)が適用されることが多い。しかし、各種部品を組み立てる工程中に、液状接着剤の塗付や硬化の工程を有すると製造工程が煩雑であり、製造コストの増加を引き起こす。このため、上記構成のような表示素子ユニットと保護パネルとを容易に固定できる粘着テープが要請されている。 As a liquid crystal display device having a structure having no gap as described above, a structure in which a display element unit and a protective panel are entirely bonded has been studied. In such a configuration, a liquid adhesive (for example, see Patent Document 2) is often applied to the adhesion between the display element unit and the protective panel. However, in the process of assembling various parts, if a liquid adhesive coating or curing process is included, the manufacturing process is complicated, which causes an increase in manufacturing cost. Therefore, there is a demand for an adhesive tape that can easily fix the display element unit and the protection panel as described above.
LCDモジュール等の小型電子機器の部品を固定する粘着テープとしては、例えば、タッチパネルの分野では、軽量化及び割れ防止等の安全面から、導電性ポリエチレンテレフタレートフィルム(PETフィルム)と補強材であるポリカーボネートとを全面で固定するための、無色透明で耐剥がれ性と耐発泡性に優れた両面粘着テープが提案されている(特許文献3参照)。 For example, in the field of touch panels, a conductive polyethylene terephthalate film (PET film) and a polycarbonate, which is a reinforcing material, are used as adhesive tapes for fixing components of small electronic devices such as LCD modules, for safety reasons such as weight reduction and crack prevention. A double-sided pressure-sensitive adhesive tape that is colorless and transparent and has excellent peeling resistance and foam resistance has been proposed (see Patent Document 3).
当該両面粘着テープは、特定の粘着剤層により優れた耐剥がれ性や耐発泡性を有するものである。しかし、近年の小型電子機器の保護パネル、特に携帯電話の保護パネルにおいては、各種文字や図柄の装飾が表面から視認されるように、裏面側の画像表示部以外の額縁部に印刷層等による装飾層が設けられる場合が多い。透明パネルと画像表示装置との貼り合わせに、従来の部品固定用粘着テープを適用すると、透明パネルの装飾部の段差により、画像表示部と透明パネルの装飾部以外の部分との間に気泡が発生し、加熱加圧処理後でも気泡が残ってしまう問題があった。
したがって、本発明が解決しようとする課題は、装飾部が設けられた透明パネルと画像表示装置表面とを好適に固定でき、装飾部による段差を有する透明パネルと平坦な画像表示装置表面との貼り合わせの際に段差部分において生じる気泡の発生を抑え、また経時での発泡を抑制でき、さらに耐落下衝撃性にも優れた両面粘着テープを提供することにある。 Therefore, the problem to be solved by the present invention is that the transparent panel provided with the decorative portion and the surface of the image display device can be suitably fixed, and the transparent panel having a step due to the decorative portion is bonded to the flat surface of the image display device. An object of the present invention is to provide a double-sided pressure-sensitive adhesive tape that can suppress the generation of bubbles at the step portion during the bonding, suppress the foaming with the passage of time, and has excellent drop impact resistance.
本発明においては、両面粘着テープの粘着剤層を、低温域に損失正接ピークを有し、かつ高温域における損失正接及び貯蔵弾性率を特定範囲となる粘弾性特性とすることで、部材貼り合わせ時に粘着剤層の流動性が高く、かつ衝撃発生時の振動吸収性のよい両面粘着テープとできる。これにより、本発明の両面粘着テープは、段差を有する部材を固定する際や、貼付後の経時においても視認される気泡の発生を抑制でき、また、落下衝撃時にも部材間の剥がれが生じにくい。 In the present invention, the pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape has a loss tangent peak in the low temperature range, and has a loss tangent and storage elastic modulus in the high temperature range within a specific range, thereby bonding the members together. Sometimes, the pressure-sensitive adhesive layer has a high fluidity and can be a double-sided pressure-sensitive adhesive tape with good vibration absorption when an impact occurs. As a result, the double-sided pressure-sensitive adhesive tape of the present invention can suppress the generation of air bubbles that are visible even when fixing a member having a step or after aging, and is less likely to peel off even during a drop impact. .
すなわち本発明は、装飾部が設けられた透明パネルを画像表示装置表面に貼付固定するための両面粘着テープであって、炭素数1〜12の(メタ)アクリル酸アルキルエステルを主成分とする光硬化型粘着剤組成物を硬化してなる粘着剤層からなり、前記粘着剤層の周波数1Hzでの動的粘弾性スペクトルの70℃の損失正接が0.43〜0.98であり、70℃の貯蔵弾性率が0.8×104〜3.4×104Paであり、前記粘着層が、−40〜−10℃の温度領域に損失正接の極大値を有してなり、前記粘着剤層の厚さが100〜250μmであることを特徴とする両面粘着テープを提供するものである。 That is, the present invention is a double-sided pressure-sensitive adhesive tape for sticking and fixing a transparent panel provided with a decorative portion to the surface of an image display device, and is a light mainly composed of (meth) acrylic acid alkyl ester having 1 to 12 carbon atoms. It consists of a pressure-sensitive adhesive layer obtained by curing a curable pressure-sensitive adhesive composition, and the loss tangent at 70 ° C. of the dynamic viscoelastic spectrum at a frequency of 1 Hz of the pressure-sensitive adhesive layer is 0.43 to 0.98. The storage elastic modulus is 0.8 × 10 4 to 3.4 × 10 4 Pa, and the adhesive layer has a maximum value of loss tangent in a temperature range of −40 to −10 ° C. The present invention provides a double-sided pressure-sensitive adhesive tape characterized in that the thickness of the agent layer is 100 to 250 μm.
本発明の両面粘着テープは、高温条件下において粘着剤層の損失正接が高く、貯蔵弾性率が低く、両面粘着テープの厚さが100〜250μmであるため、装飾部を有する部材の固定において混入する気泡のエア抜け性に優れて、また経時での発泡を抑制可能である。
また、この両面粘着テープは、粘着剤層が−40〜−10℃の温度領域に損失正接の極大値を有するため、耐落下衝撃性に優れている。
The double-sided pressure-sensitive adhesive tape of the present invention has a high loss tangent of the pressure-sensitive adhesive layer under a high temperature condition, a low storage elastic modulus, and a thickness of the double-sided pressure-sensitive adhesive tape is 100 to 250 μm. It is excellent in air bleedability of bubbles to be generated, and foaming over time can be suppressed.
Further, this double-sided pressure-sensitive adhesive tape has excellent drop impact resistance because the pressure-sensitive adhesive layer has a maximum value of loss tangent in a temperature range of −40 to −10 ° C.
本発明の両面粘着テープは、装飾部が設けられた透明パネルを画像表示装置表面に貼付固定する両面粘着テープであり、炭素数1〜12の(メタ)アクリル酸アルキルエステルを主成分とする光硬化型粘着剤組成物を硬化した硬化物からなる粘着剤層から形成され、その総厚さが100〜250μmの両面粘着テープである。当該両面粘着テープの粘着剤層は、周波数1Hzでの動的粘弾性スペクトルの70℃の損失正接が0.43〜0.98、70℃の貯蔵弾性率が0.8×104〜3.4×104Paであり、−40〜−10℃の温度領域に損失正接の極大値を有する。 The double-sided pressure-sensitive adhesive tape of the present invention is a double-sided pressure-sensitive adhesive tape for sticking and fixing a transparent panel provided with a decorative part to the surface of an image display device, and is a light mainly composed of (meth) acrylic acid alkyl ester having 1 to 12 carbon atoms. It is a double-sided pressure-sensitive adhesive tape formed from a pressure-sensitive adhesive layer made of a cured product obtained by curing a curable pressure-sensitive adhesive composition and having a total thickness of 100 to 250 μm. The pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape has a loss tangent at 70 ° C. of the dynamic viscoelastic spectrum at a frequency of 1 Hz of 0.43 to 0.98, and a storage elastic modulus at 70 ° C. of 0.8 × 10 4 to 3. 4 × 10 4 Pa, and has a maximum value of loss tangent in a temperature range of −40 to −10 ° C.
[光硬化型粘着剤組成物]
本発明に使用する光硬化型粘着剤組成物は、炭素数1〜12の(メタ)アクリル酸アルキルエステルを主成分とする。当該光硬化型粘着剤組成物を使用することで、両面粘着テープの厚さを好適な範囲に調整しやすい。また、当該炭素数1〜12の(メタ)アクリル酸アルキルエステルを主成分とすることで、部材間の固定における必要な接着力を付与できる。
なお、本明細書においてはアクリル酸及びメタクリル酸を総称して(メタ)アクリル酸と標記し、これらの誘導体についても同様に表記する。
[Photocurable adhesive composition]
The photocurable pressure-sensitive adhesive composition used in the present invention contains a C1-C12 (meth) acrylic acid alkyl ester as a main component. By using the said photocurable adhesive composition, it is easy to adjust the thickness of a double-sided adhesive tape to a suitable range. Moreover, the adhesive force required in the fixation between members can be provided by making the said C1-C12 (meth) acrylic-acid alkylester into a main component.
In the present specification, acrylic acid and methacrylic acid are collectively referred to as (meth) acrylic acid, and these derivatives are also represented in the same manner.
炭素数が1〜12のアルキル側鎖を有する(メタ)アクリル酸アルキルエステルとしては、具体的には、メチルアクリレート、エチルアクリレート、n−プロピルアクリレート、イソプロピルアクリレート、n−ブチルアクリレート、sec−ブチルアクリレート、t−ブチルアクリレート、n−ヘキシルアクリレート、シクロヘキシルアクリレート、n−オクチルアクリレート、イソオクチルアクリレート、2−エチルヘキシルアクリレート、イソノニルアクリレート、イソデシルアクリレート、ラウリルアクリレート、メチルメタクリレート、エチルメタクリレート、n−プロピルメタクリレート、イソプロピルメタクリレート、n−ブチルメタクリレート、sec−ブチルメタクリレート、t−ブチルメタクリレート、n−ヘキシルメタクリレート、シクロヘキシルメタクリレート、n−オクチルメタクリレート、イソオクチルメタクリレート、2−エチルヘキシルメタクリレート、イソノニルメタクリレート、イソデシルメタクリレート、ラウリルメタクリレート等が挙げられる。 Specific examples of the (meth) acrylic acid alkyl ester having an alkyl side chain having 1 to 12 carbon atoms include methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, and sec-butyl acrylate. , T-butyl acrylate, n-hexyl acrylate, cyclohexyl acrylate, n-octyl acrylate, isooctyl acrylate, 2-ethylhexyl acrylate, isononyl acrylate, isodecyl acrylate, lauryl acrylate, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, Isopropyl methacrylate, n-butyl methacrylate, sec-butyl methacrylate, t-butyl methacrylate, n-hexylme Acrylate, cyclohexyl methacrylate, n- octyl methacrylate, isooctyl methacrylate, 2-ethylhexyl methacrylate, isononyl methacrylate, isodecyl methacrylate, lauryl methacrylate and the like.
そのなかでも、炭素数が4〜9のアルキル側鎖を有するメタアクリル酸アルキルエステル又は炭素数が4〜9のアルキル側鎖を有するアクリル酸アルキルエステルが好ましく、炭素数が4〜9のアルキル側鎖を有するアクリル酸アルキルエステルがより好ましい。当該範囲の炭素数のアルキル側鎖を有する(メタ)アクリル酸アルキルエステルを使用することで、得られる粘着テープに好適な柔軟性を付与でき、段差追従性の向上に有用である。 Among them, a methacrylic acid alkyl ester having an alkyl side chain having 4 to 9 carbon atoms or an acrylic acid alkyl ester having an alkyl side chain having 4 to 9 carbon atoms is preferable, and the alkyl side having 4 to 9 carbon atoms is preferred. More preferred are alkyl acrylates having a chain. By using a (meth) acrylic acid alkyl ester having an alkyl side chain with a carbon number within the range, suitable flexibility can be imparted to the resulting adhesive tape, which is useful for improving the step following ability.
光硬化型粘着剤組成物中の上記(メタ)アクリル酸アルキルエステルの含有量は、当該組成物に含まれる光硬化性化合物の総量に対し、50〜85質量%とすることが好ましく、60〜85質量%とすることがより好ましい。当該範囲の光硬化型粘着剤組成物中の上記(メタ)アクリル酸アルキルエステルの含有量にすることで、接着力の向上に優位である。 It is preferable that content of the said (meth) acrylic-acid alkylester in a photocurable adhesive composition shall be 50-85 mass% with respect to the total amount of the photocurable compound contained in the said composition, 60- It is more preferable to set it as 85 mass%. By making the content of the above (meth) acrylic acid alkyl ester in the photocurable pressure-sensitive adhesive composition in this range, it is advantageous in improving the adhesive force.
本発明に使用する光硬化型粘着剤組成物においては、上記(メタ)アクリル酸アルキルエステル以外のモノマーとして、極性基を有するモノマーを併用することが好ましい。極性基を有するモノマーとしては、ヒドロキシル基を含有するモノマーやカルボキシル基を含有するモノマー、窒素原子を含有するモノマー等が挙げられる。なかでも、ヒドロキシ基を含有するモノマーまたはカルボキシル基を含有するモノマーを使用することが好ましい。また、ヒドロキシ基を含有するモノマーとカルボキシル基を含有するモノマーとを併用することも好ましい。ヒドロキシ基を含有するモノマー、及びカルボキシル基を含有するモノマーは、粘着剤層の凝集力を向上でき、剥離時の糊残りを低減しやすくなる。 In the photocurable pressure-sensitive adhesive composition used in the present invention, it is preferable to use a monomer having a polar group in combination as a monomer other than the (meth) acrylic acid alkyl ester. Examples of the monomer having a polar group include a monomer containing a hydroxyl group, a monomer containing a carboxyl group, and a monomer containing a nitrogen atom. Among these, it is preferable to use a monomer containing a hydroxy group or a monomer containing a carboxyl group. Moreover, it is also preferable to use together the monomer containing a hydroxyl group, and the monomer containing a carboxyl group. A monomer containing a hydroxy group and a monomer containing a carboxyl group can improve the cohesive strength of the pressure-sensitive adhesive layer, and easily reduce adhesive residue at the time of peeling.
ヒドロキシル基を含有するモノマーとしては、2−ヒドロキシエチル(メタ)アクリレート、4−ヒドロキシブチル(メタ)アクリレート、6−ヒドロキシヘキシル(メタ)アクリレート、ヒドロキシプロピル(メタ)アクリレート、カプロラクトン変性(メタ)アクリレート、ポリエチレングリコールモノ(メタ)アクリレート、ポリプロピレングリコール(メタ)アクリレート等が挙げられる。 Examples of the monomer containing a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, hydroxypropyl (meth) acrylate, caprolactone-modified (meth) acrylate, Examples include polyethylene glycol mono (meth) acrylate and polypropylene glycol (meth) acrylate.
ヒドロキシル基を含有するモノマーを使用する場合には、光硬化型粘着剤組成物中のヒドロキシル基を含有するモノマーの含有量は、当該組成物に含まれる光硬化性化合物の総量に対し、0.01〜1.0質量%とすることが好ましく、0.01〜0.8質量%とすることがより好ましい。上記のヒドロキシル基を含有するモノマーの含有量にすることで、粘着剤層の凝集力を調整しやすくなる。 When the monomer containing a hydroxyl group is used, the content of the monomer containing a hydroxyl group in the photocurable pressure-sensitive adhesive composition is 0. 0 relative to the total amount of the photocurable compound contained in the composition. It is preferable to set it as 01-1.0 mass%, and it is more preferable to set it as 0.01-0.8 mass%. By adjusting the content of the monomer containing the hydroxyl group, the cohesive force of the pressure-sensitive adhesive layer can be easily adjusted.
カルボキシル基を含有するモノマーとしては、アクリル酸、メタクリル酸、イタコン酸、マレイン酸、クロトン酸、アクリル酸ダイマー、エチレンオキサイド変性コハク酸アクリレート等が挙げられる。 Examples of the monomer containing a carboxyl group include acrylic acid, methacrylic acid, itaconic acid, maleic acid, crotonic acid, acrylic acid dimer, and ethylene oxide-modified succinic acrylate.
カルボキシル基を含有するモノマーを使用する場合には、光硬化型粘着剤組成物中のカルボキシル基を含有するモノマーの含有量は、当該組成物に含まれる光硬化性化合物の総量に対し、0.1〜8.0質量%とすることが好ましく、0.5〜7.0質量%とすることがより好ましく、1.0〜6.0質量%とすることがさらに好ましい。上記のカルボキシル基を含有するモノマーの含有量にすることで、粘着剤層の凝集力を調整しやすくなる。 When the monomer containing a carboxyl group is used, the content of the monomer containing a carboxyl group in the photocurable pressure-sensitive adhesive composition is 0. 0 relative to the total amount of the photocurable compound contained in the composition. It is preferable to set it as 1-8.0 mass%, It is more preferable to set it as 0.5-7.0 mass%, It is further more preferable to set it as 1.0-6.0 mass%. It becomes easy to adjust the cohesion force of an adhesive layer by making it content of the monomer containing said carboxyl group.
また、光硬化型粘着剤組成物中には、得られる粘着剤層の凝集力を上げるために、架橋剤を含有することが好ましい。 In addition, the photocurable pressure-sensitive adhesive composition preferably contains a crosslinking agent in order to increase the cohesive strength of the resulting pressure-sensitive adhesive layer.
使用する架橋剤としては、イソシアネート系架橋剤、エポキシ系架橋剤、キレート系架橋剤、アジリン系架橋剤、多官能アクリレート系等が挙げられる。その中でも、(メタ)アクリル系共重合体との反応性に富むイソシアネート系架橋剤、または、光照射で架橋可能な多官能アクリレート系架橋剤が好ましい。 Examples of the crosslinking agent used include isocyanate crosslinking agents, epoxy crosslinking agents, chelating crosslinking agents, azirine crosslinking agents, and polyfunctional acrylates. Among them, an isocyanate-based crosslinking agent rich in reactivity with the (meth) acrylic copolymer or a polyfunctional acrylate-based crosslinking agent that can be crosslinked by light irradiation is preferable.
架橋剤を添加する際の光硬化型粘着剤組成物中の架橋剤の配合量は、0.1〜5質量部が好ましく、0.1〜3質量部がより好ましく、0.1〜1.5質量部がさらに好ましい。当該範囲の架橋剤の含有量にすることで、粘着剤層のゲル分率を好適な範囲に調整しやすい。 0.1-5 mass parts is preferable, as for the compounding quantity of the crosslinking agent in the photocurable adhesive composition at the time of adding a crosslinking agent, 0.1-3 mass parts is more preferable, and 0.1-1. 5 parts by mass is more preferable. By setting the content of the crosslinking agent in this range, it is easy to adjust the gel fraction of the pressure-sensitive adhesive layer to a suitable range.
また、粘着剤層の分子量を好適な範囲に調整する手段として、各種添加剤を添加する方法が挙げられる。各種添加剤としては、光重合阻害の少ない水添ロジンエステル、水添テルペンフェノール、極性脂肪族飽和炭化水素樹脂、アクリル共重合体等が挙げられる。その中でも、無色透明な極性脂肪族飽和炭化水素樹脂や水添テルペンフェノールが好ましい。 Moreover, the method of adding various additives is mentioned as a means to adjust the molecular weight of an adhesive layer to a suitable range. Examples of the various additives include hydrogenated rosin esters, hydrogenated terpene phenols, polar aliphatic saturated hydrocarbon resins, and acrylic copolymers with little photopolymerization inhibition. Among these, a colorless and transparent polar aliphatic saturated hydrocarbon resin and hydrogenated terpene phenol are preferable.
光硬化型粘着剤組成物中の添加剤の配合量は、5〜40質量部が好ましく、5〜30質量部がより好ましく、5〜20質量部がさらに好ましい。当該範囲の添加剤の含有量にすることで、粘着剤層の分子量を好適な範囲に調整しやすい。 5-40 mass parts is preferable, as for the compounding quantity of the additive in a photocurable adhesive composition, 5-30 mass parts is more preferable, and 5-20 mass parts is further more preferable. By setting the content of the additive in this range, it is easy to adjust the molecular weight of the pressure-sensitive adhesive layer to a suitable range.
また、粘着剤には、必要に応じて性能を阻害しない範囲で酸化防止剤、充填剤、顔料、増粘剤等を添加しても良い。 Moreover, you may add antioxidant, a filler, a pigment, a thickener, etc. to the adhesive in the range which does not inhibit performance as needed.
本発明に使用する光硬化型組成物中には、前記(メタ)アクリル酸アルキルエステルを事前に重合した(メタ)アクリル酸アルキルエステルポリマーを含有することも好ましい。当該ポリマーを光硬化型組成物中に含有させることにより、粘着塗液を塗工に好適な粘度に調整しやすい。 The photocurable composition used in the present invention preferably contains a (meth) acrylic acid alkyl ester polymer obtained by previously polymerizing the (meth) acrylic acid alkyl ester. By containing the polymer in the photocurable composition, it is easy to adjust the adhesive coating liquid to a viscosity suitable for coating.
当該ポリマーの質量平均分子量(Mw)は10万〜200万であることが好ましく、質量平均分子量(Mw)が15万〜150万であることがより好ましい。当該範囲のポリマーの配合量にすることで、両面粘着テープに高温高湿条件下での粘着特性、特に高温高湿条件下での耐発泡性および耐剥がれ性を付与しやすくなる。 The mass average molecular weight (Mw) of the polymer is preferably 100,000 to 2,000,000, and more preferably 150,000 to 1,500,000. By setting the blending amount of the polymer in this range, the double-sided pressure-sensitive adhesive tape can be easily imparted with pressure-sensitive adhesive properties under high-temperature and high-humidity conditions, in particular, foam resistance and peeling resistance under high-temperature and high-humidity conditions.
また、当該ポリマーの含有量は、光硬化型組成物中に含有する(メタ)アクリル酸アルキルエステルに対して、5〜40質量部が好ましく、10〜30質量部がより好ましい。当該範囲のポリマーの含有量にすることで、粘着塗液を塗工に好適な粘度に調整しやすい。 Moreover, 5-40 mass parts is preferable with respect to the (meth) acrylic-acid alkylester contained in a photocurable composition, and, as for content of the said polymer, 10-30 mass parts is more preferable. By setting the content of the polymer in this range, it is easy to adjust the pressure-sensitive adhesive coating liquid to a viscosity suitable for coating.
本発明に使用する光硬化型組成物に使用する光重合開始剤は、特に限定するものではないが、アセトフェノン、メトキシアセトフェノン、2,2−ジエトキシアセトフェノン、p−ジメチルアミノアセトフェノン、2,2−ジメトキシ−2−フェニルアセトフェノン、α−ヒドロキシ−α,α’−ジメチルアセトフェノン、2−ヒドロキシ−2−シクロヘキシルアセトフェノン、2−メチル−1[4−(メチルチオ)フェニル]−2−モンフォリノプロパノン−1等のアセトフェノン類、ベンゾイン、ベンゾインメチルエーテル、ベンゾインエチルエーテル、ベンゾインイソプロピルブチルエーテル等のベンゾインエーテル類、ベンゾフェノン、2−クロロベンゾフェノン、p,p’−ジクロロベンゾフェノン,N,N’−テトラメチル−4,4’−ジアミノベンゾフェノン、4−(2−ヒドロキシエトキシ)フェニル(2−ヒドロキシ−2−プロピル)ケトン等のケトン類、チオキサンソン、2−クロロチオキサンソン、2−メチルチオキサンソン等のチオキサンソン類、ビスアシルホスフィンオキサイド、ベンゾイルホスフィンオキサイド等のホスフィン酸化物、ベンジルジメチルケタール等のケタール類、カンファン−2,3−ジオン、フェナントレンキノン等のキノン類などを挙げることができる。 The photopolymerization initiator used in the photocurable composition used in the present invention is not particularly limited, but acetophenone, methoxyacetophenone, 2,2-diethoxyacetophenone, p-dimethylaminoacetophenone, 2,2- Dimethoxy-2-phenylacetophenone, α-hydroxy-α, α′-dimethylacetophenone, 2-hydroxy-2-cyclohexylacetophenone, 2-methyl-1 [4- (methylthio) phenyl] -2-monforinopropanone- 1, acetophenones, benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin ethers such as benzoin isopropyl butyl ether, benzophenone, 2-chlorobenzophenone, p, p'-dichlorobenzophenone, N, N'-tetramethyl-4, '-Diaminobenzophenone, ketones such as 4- (2-hydroxyethoxy) phenyl (2-hydroxy-2-propyl) ketone, thioxanthones such as thioxanthone, 2-chlorothioxanthone, 2-methylthioxanthone, bisacyl Examples include phosphine oxides such as phosphine oxide and benzoylphosphine oxide, ketals such as benzyldimethyl ketal, and quinones such as camphane-2,3-dione and phenanthrenequinone.
光重合開始剤の配合量は、0.01〜5質量部が好ましく、0.1〜3質量部がより好ましい。当該範囲の光重合開始剤の含有量にすることで、残留モノマーを少なく、また効率的に両面粘着テープを調整しやすい。 0.01-5 mass parts is preferable and, as for the compounding quantity of a photoinitiator, 0.1-3 mass parts is more preferable. By setting the content of the photopolymerization initiator in this range, it is easy to adjust the double-sided pressure-sensitive adhesive tape with little residual monomer.
光硬化型粘着剤組成物を硬化する方法として、紫外線照射法や電子線照射法が挙げられる。好適な範囲に本発明の両面粘着テープの粘着剤層の質量平均分子量を調整しやすい点から、紫外線照射法が好ましい。 Examples of a method for curing the photocurable pressure-sensitive adhesive composition include an ultraviolet irradiation method and an electron beam irradiation method. From the viewpoint of easily adjusting the mass average molecular weight of the pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape of the present invention within a suitable range, the ultraviolet irradiation method is preferable.
[粘着剤層]
本発明の両面粘着テープの粘着剤層は、上記光硬化性組成物を硬化して得られる粘着剤層である。本発明においては、当該粘着剤層の動的粘弾性スペクトルの70℃の損失正接(tanδ)が0.43〜0.98であり、70℃の貯蔵弾性率が0.8×104〜3.4×104Paである。損失正接及び貯蔵弾性率が当該範囲の粘着剤層を有することにより、本発明の両面粘着テープは、加熱加圧処理時の粘着剤層の流動性が高く、透明パネルに設けられた装飾部による段差によって生じる気泡の抜け性に優れる。さらに、加熱加圧処理時において流動性が上がることで、粘着剤層と被着体との密着性が向上して、経時での発泡の抑制に優れる。これら粘弾性特性の調整は、粘着剤層の質量平均分子量やゲル分率等の調整により好適に調整できる。
[Adhesive layer]
The pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape of the present invention is a pressure-sensitive adhesive layer obtained by curing the photocurable composition. In the present invention, the loss tangent (tan δ) at 70 ° C. of the dynamic viscoelastic spectrum of the pressure-sensitive adhesive layer is 0.43 to 0.98, and the storage elastic modulus at 70 ° C. is 0.8 × 10 4 to 3. 4 × 10 4 Pa. By having a pressure-sensitive adhesive layer with a loss tangent and storage elastic modulus in the above range, the double-sided pressure-sensitive adhesive tape of the present invention has high fluidity of the pressure-sensitive adhesive layer during heating and pressurizing treatment, and is due to the decorative part provided on the transparent panel. Excellent ability to remove bubbles generated by steps. Furthermore, the fluidity is improved during the heat and pressure treatment, whereby the adhesion between the pressure-sensitive adhesive layer and the adherend is improved and the foaming over time is excellently suppressed. Adjustment of these viscoelastic characteristics can be suitably adjusted by adjusting the mass average molecular weight, gel fraction, and the like of the pressure-sensitive adhesive layer.
本発明の両面粘着テープの粘着剤層の70℃における損失正接は、好ましくは0.45〜0.75、さらに好ましくは0.5〜0.70である。損失正接が上記の範囲内にあると、装飾部が設けられた透明パネルを画像表示装置表面に貼付固定した後の加熱加圧処理時の粘着剤層の流動性に優れるため、透明パネルと画像表示装置表面との貼り合わせの際に段差部分において生じる気泡の抜け性を向上できる。 The loss tangent at 70 ° C. of the pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape of the present invention is preferably 0.45 to 0.75, more preferably 0.5 to 0.70. If the loss tangent is in the above range, the transparent panel and the image are excellent because the adhesive layer has excellent fluidity during the heat and pressure treatment after the transparent panel provided with the decoration is pasted and fixed to the surface of the image display device. It is possible to improve the detachability of bubbles generated at the stepped portion when bonded to the display device surface.
また、70℃における貯蔵弾性率は、好ましくは1.2×104〜3.4×104Pa、さらに好ましくは1.5×104〜3.1×104Paである。貯蔵弾性率が上記範囲内にあると、装飾部が設けられた透明パネルを画像表示装置表面に貼付固定した後の加熱加圧処理時に、粘着剤の弾性が低くなり、透明パネルに設けられた装飾部の段差によって粘着剤層と被着体との密着が困難な箇所への密着性を向上できる。 The storage elastic modulus at 70 ° C. is preferably 1.2 × 10 4 to 3.4 × 10 4 Pa, and more preferably 1.5 × 10 4 to 3.1 × 10 4 Pa. When the storage elastic modulus is within the above range, the elasticity of the pressure-sensitive adhesive is lowered during the heat and pressure treatment after the transparent panel provided with the decorative portion is pasted and fixed on the surface of the image display device, and is provided on the transparent panel. The adhesiveness to the location where adhesion between the pressure-sensitive adhesive layer and the adherend is difficult can be improved by the step of the decorative portion.
本発明における粘着剤層の動的粘弾性は、粘弾性試験機(レオメトリックス社製、商品名:アレス2KSTD)を用いて、同試験機の測定部である平行円盤の間に試験片を挟み込み、周波数1Hzでの貯蔵弾性率(G’)と損失弾性率(G”)を測定し、損失正接はtanδ=(G”)/(G’)で表される式により算出される。試験片は厚み0.5〜2.5mmの粘着剤を単独で平行円盤の間に挟んで行う。 The dynamic viscoelasticity of the pressure-sensitive adhesive layer in the present invention is obtained by sandwiching a test piece between parallel disks, which are measuring parts of the tester, using a viscoelasticity tester (manufactured by Rheometrics, trade name: Ares 2KSTD). Then, the storage elastic modulus (G ′) and the loss elastic modulus (G ″) at a frequency of 1 Hz are measured, and the loss tangent is calculated by an expression represented by tan δ = (G ″) / (G ′). The test piece is obtained by sandwiching an adhesive having a thickness of 0.5 to 2.5 mm between parallel disks.
[両面粘着テープ]
本発明の両面粘着テープは、上記粘着剤層からなる粘着テープであり、中芯基材を有さない両面粘着テープである。両面粘着テープは、単層の粘着剤層からなるものであっても、複数の粘着剤層が積層されたものであってもよい。
[Double-sided adhesive tape]
The double-sided pressure-sensitive adhesive tape of the present invention is a pressure-sensitive adhesive tape comprising the above-mentioned pressure-sensitive adhesive layer, and is a double-sided pressure-sensitive adhesive tape having no core substrate. The double-sided pressure-sensitive adhesive tape may be a single-layer pressure-sensitive adhesive layer or may be a laminate of a plurality of pressure-sensitive adhesive layers.
本発明の両面粘着テープの厚みは、100〜250μm、好ましくは、125〜225μm、さらに好ましくは150〜200μmである。両面粘着テープの厚みを当該範囲とすることで、落下時等に生じる衝撃を吸収しやすくなり、また、透明パネルに設けられる装飾部により生じる段差に追従しやすくなる。両面粘着テープの厚みが100μm未満になると、粘着剤層の応力緩和性が低下し、透明パネルに設けられる装飾部により生じる段差の追従が困難になり、両面粘着テープの厚みが250μmを超えると、小型携帯電子機器の薄型化が困難になる。 The thickness of the double-sided pressure-sensitive adhesive tape of the present invention is 100 to 250 μm, preferably 125 to 225 μm, more preferably 150 to 200 μm. By setting the thickness of the double-sided pressure-sensitive adhesive tape within the above range, it becomes easy to absorb an impact generated when dropping or the like, and it is easy to follow a step generated by a decorative portion provided on the transparent panel. When the thickness of the double-sided pressure-sensitive adhesive tape is less than 100 μm, the stress relaxation property of the pressure-sensitive adhesive layer is lowered, and it becomes difficult to follow the step caused by the decorative portion provided on the transparent panel. It becomes difficult to reduce the thickness of small portable electronic devices.
本発明の両面粘着テープは、トルエン中に24時間浸漬した際の下式で表されるゲル分率が、30〜70%であることが好ましく、30〜60%であるのがより好ましく、30〜50%が最も好ましい。粘着剤層のゲル分率が上記の範囲内だと、粘着剤層の70℃における損失正接および貯蔵弾性率を好適な範囲に調整しやすく、且つ粘着剤層の凝集力を向上させやすくなる。
ゲル分率=[(両面粘着テープのトルエン浸漬後質量)/(両面粘着テープのトルエン浸漬前質量)]×100
In the double-sided pressure-sensitive adhesive tape of the present invention, the gel fraction represented by the following formula when immersed in toluene for 24 hours is preferably 30 to 70%, more preferably 30 to 60%, 30 ~ 50% is most preferred. When the gel fraction of the pressure-sensitive adhesive layer is within the above range, it is easy to adjust the loss tangent and storage elastic modulus at 70 ° C. of the pressure-sensitive adhesive layer to suitable ranges and to improve the cohesive force of the pressure-sensitive adhesive layer.
Gel fraction = [(mass after dipping toluene in double-sided pressure-sensitive adhesive tape) / (mass before dipping toluene in double-sided pressure-sensitive adhesive tape)] × 100
本発明の両面粘着テープにおける粘着剤層の質量平均分子量(Mw)は30万〜150万であることが好ましく、30万〜130万がより好ましく、30万〜100万がさらに好ましい。本発明の両面粘着テープにおける粘着剤層の質量平均分子量Mwが上記範囲内だと、好適な範囲に粘着剤層の70℃における損失正接および貯蔵弾性率を調整できる。 The mass average molecular weight (Mw) of the pressure-sensitive adhesive layer in the double-sided pressure-sensitive adhesive tape of the present invention is preferably 300,000 to 1,500,000, more preferably 300,000 to 1,300,000, and further preferably 300,000 to 1,000,000. When the mass average molecular weight Mw of the pressure-sensitive adhesive layer in the double-sided pressure-sensitive adhesive tape of the present invention is within the above range, the loss tangent and storage elastic modulus at 70 ° C. of the pressure-sensitive adhesive layer can be adjusted to a suitable range.
なお、本発明では、本発明の両面粘着テープにおける粘着剤層の質量平均分子量(Mw)は、ゲルパーミエーションクロマトグラフ(GPC)により測定することができる。より具体的には、GPC測定装置として、東ソー株式会社製「SC8020」を用いて、ポリスチレン換算値により、次のGPC測定条件で測定して求めることができる。
(GPCの測定条件)
サンプル濃度:0.5重量%(テトラヒドロフラン溶液)
サンプル注入量:100μL
溶離液:テトラヒドロフラン(THF)
流速:1.0mL/min
カラム温度(測定温度):40℃
カラム:東ソー株式会社製「TSKgel GMHHR−H」
検出器:示差屈折
In the present invention, the mass average molecular weight (Mw) of the pressure-sensitive adhesive layer in the double-sided pressure-sensitive adhesive tape of the present invention can be measured by gel permeation chromatography (GPC). More specifically, as a GPC measurement device, “SC8020” manufactured by Tosoh Corporation can be used to measure and obtain the following GPC measurement conditions based on polystyrene conversion values.
(GPC measurement conditions)
Sample concentration: 0.5% by weight (tetrahydrofuran solution)
Sample injection volume: 100 μL
Eluent: Tetrahydrofuran (THF)
Flow rate: 1.0 mL / min
Column temperature (measurement temperature): 40 ° C
Column: “TSKgel GMHHR-H” manufactured by Tosoh Corporation
Detector: Differential refraction
本発明の両面粘着テープは、画像表示装置に使用する点から、高い透明性を有していることが好ましい。 The double-sided pressure-sensitive adhesive tape of the present invention preferably has high transparency from the viewpoint of use in an image display device.
本発明の両面粘着テープの可視光波長領域における全光線透過率(JIS K 7361)は、85%以上が好ましく、90%以上がより好ましく、95%以上がさらに好ましい。全光線透過率が上記の範囲内だと、両面粘着テープは高い透明性を有しており、表示画面の高精細化が可能となる。 The total light transmittance (JIS K 7361) in the visible light wavelength region of the double-sided pressure-sensitive adhesive tape of the present invention is preferably 85% or more, more preferably 90% or more, and further preferably 95% or more. When the total light transmittance is within the above range, the double-sided pressure-sensitive adhesive tape has high transparency, and high definition of the display screen is possible.
また、本発明の両面粘着テープのヘイズ(JIS K 7136)は、2.0以下が好ましく、1.5%以下がより好ましく、1.0%以下がさらに好ましい。ヘイズが上記の範囲内だと、両面粘着テープは高い透明性を有しており、表示画面の高精細化が可能となる。 Further, the haze (JIS K 7136) of the double-sided pressure-sensitive adhesive tape of the present invention is preferably 2.0 or less, more preferably 1.5% or less, and further preferably 1.0% or less. When the haze is within the above range, the double-sided pressure-sensitive adhesive tape has high transparency, and high definition of the display screen is possible.
本発明の両面粘着テープの接着力(JIS−Z0237(2000))は、ガラス板に対して、5N/20mm以上であると部品間の固定に好適であり、5〜20N/20mmが好ましく、7〜20N/20mmがより好ましく、10〜20N/20mmがさらに好ましい。本発明の両面粘着テープの接着力が上記の範囲内だと、透明パネルの粘着剤層からの剥がれを抑制できる。 The adhesive strength (JIS-Z0237 (2000)) of the double-sided pressure-sensitive adhesive tape of the present invention is suitable for fixing between parts when it is 5 N / 20 mm or more with respect to the glass plate, preferably 5 to 20 N / 20 mm, 7 -20N / 20mm is more preferable, and 10-20N / 20mm is more preferable. When the adhesive force of the double-sided pressure-sensitive adhesive tape of the present invention is within the above range, peeling from the pressure-sensitive adhesive layer of the transparent panel can be suppressed.
[両面粘着テープ作成]
光硬化型粘着剤組成物は、例えば、離型処理したポリエチレンテレフタレート(PET)フィルムに塗工し、離型処理したPETフィルムでラミネートして、紫外線照射を行い、上記光硬化型粘着剤組成物を硬化して両面粘着テープを作成できる。なお、紫外線照射は、残留モノマーを少なくすることが可能で、好適な範囲に本発明の両面粘着テープの質量平均分子量を調整可能な低エネルギー量紫外線ランプで行うことが好ましい。
[Create double-sided adhesive tape]
The photocurable pressure-sensitive adhesive composition is, for example, coated on a release-treated polyethylene terephthalate (PET) film, laminated with the release-treated PET film, and irradiated with ultraviolet rays, and the above-mentioned photocurable pressure-sensitive adhesive composition. Can be cured to create a double-sided adhesive tape. In addition, it is preferable to perform ultraviolet irradiation with the low energy amount ultraviolet lamp which can reduce a residual monomer and can adjust the mass mean molecular weight of the double-sided adhesive tape of this invention in the suitable range.
紫外線照射強度は0.3〜2.0mW/cm2が好ましく、0.3〜1.5mW/cm2がより好ましく、0.3〜1.2mW/cm2がさらに好ましい。上記の範囲内だと、残留モノマーが少なく、また効率的に両面粘着テープを調整できる。0.3mW/cm2未満だと、照射強度不足で多大な紫外線照射時間が必要で、生産性が著しく低下するからである。2.0mW/cm2を超えると、照射強度が強く、残留モノマーが多くなり、粘着性能が著しく低下するからである。 Ultraviolet irradiation intensity is preferably 0.3~2.0mW / cm 2, more preferably 0.3~1.5mW / cm 2, more preferably 0.3~1.2mW / cm 2. Within the above range, the residual monomer is small and the double-sided pressure-sensitive adhesive tape can be adjusted efficiently. If it is less than 0.3 mW / cm 2 , the irradiation intensity is insufficient and a lot of ultraviolet irradiation time is required, and the productivity is remarkably lowered. This is because if it exceeds 2.0 mW / cm 2 , the irradiation intensity is high, the residual monomer is increased, and the adhesive performance is significantly reduced.
また、紫外線積算光量は100〜500mJ/cm2が好ましく、100〜400mJ/cm2がより好ましく、100〜300mJ/cm2がさらに好ましい。上記の範囲だと、光重合開始剤を消費して、残留モノマーが少なく、また効率的に両面粘着テープを調整できる。 The ultraviolet cumulative amount of light is preferably from 100 to 500 mJ / cm 2, more preferably 100 to 400 mJ / cm 2, more preferably 100~300mJ / cm 2. Within the above range, the photopolymerization initiator is consumed, the residual monomer is small, and the double-sided adhesive tape can be adjusted efficiently.
[使用態様]
本発明の両面粘着テープは、装飾部が設けられた透明パネルを画像表示装置表面に貼付固定する際に好適に使用できる。具体的な実施態様としては、例えば、図1に示したような画像表示パネルがある。図1において、1は透明パネル、2は透明パネルに付着した装飾部、3は両面粘着テープ、4は画像表示装置である。
[Usage]
The double-sided pressure-sensitive adhesive tape of the present invention can be suitably used when sticking and fixing a transparent panel provided with a decorative portion on the surface of an image display device. As a specific embodiment, for example, there is an image display panel as shown in FIG. In FIG. 1, 1 is a transparent panel, 2 is a decorative part attached to the transparent panel, 3 is a double-sided adhesive tape, and 4 is an image display device.
透明パネルは、特に制限されないが、(メタ)アクリル樹脂、ポリカーボネート樹脂、ガラス等からなる透明パネルを好適に使用できる。より透明性の高いガラスパネルが好ましい。 The transparent panel is not particularly limited, but a transparent panel made of (meth) acrylic resin, polycarbonate resin, glass or the like can be suitably used. A glass panel with higher transparency is preferred.
透明パネルの厚さは、100μm〜3.0mmのものが好ましく、250μm〜2.0mmのものがより好ましく、500μm〜1.0mmのものがさらに好ましい。透明パネルの厚さが上記の範囲内だと、透明パネルの強度を保持しつつ、小型電子端末への適用時に薄型化が可能となる。 The thickness of the transparent panel is preferably 100 μm to 3.0 mm, more preferably 250 μm to 2.0 mm, and even more preferably 500 μm to 1.0 mm. When the thickness of the transparent panel is within the above range, it is possible to reduce the thickness when applied to a small electronic terminal while maintaining the strength of the transparent panel.
透明パネルに設けられる装飾部は、携帯電子端末の画面表示部の周囲に視認される文字や図形、あるいはこれらの背面に設けられる黒色や白色の下地などがある。これら装飾部は、透明パネルへの印刷により設けることが容易であるため好ましい。印刷方法や印刷インキ等は特に制限されず、シルク印刷、パッド印刷等の通常使用される印刷方法や印刷インキを使用できる。 The decorative part provided on the transparent panel includes characters and figures visually recognized around the screen display part of the portable electronic terminal, or a black or white background provided on the back of these. These decorative portions are preferable because they can be easily provided by printing on a transparent panel. The printing method and printing ink are not particularly limited, and a commonly used printing method such as silk printing or pad printing or printing ink can be used.
本発明の両面粘着テープを使用する際の透明パネルに設けられる装飾部の厚さは、5〜30μmが好ましく、5〜25μmがより好ましく、5〜20μmがさらに好ましい。透明パネルに設けられる装飾部の厚さが上記の範囲内だと本発明の両面粘着テープの段差追従性が特に好適であり、薄型の電子端末への適用時にも気泡の発生抑制等の効果を好適に発現できる。また、装飾部は複数の装飾部が積層されていてもよく、積層される装飾部の大きさや形状が異なっていてもよい。装飾部が複数積層される場合には、当該積層された装飾部の最大厚さが上記範囲内であると、本発明の効果を奏しやすくなる。 5-30 micrometers is preferable, as for the thickness of the decoration part provided in the transparent panel at the time of using the double-sided adhesive tape of this invention, 5-25 micrometers is more preferable, and 5-20 micrometers is more preferable. When the thickness of the decorative portion provided on the transparent panel is within the above range, the step following property of the double-sided pressure-sensitive adhesive tape of the present invention is particularly suitable, and the effect of suppressing the generation of bubbles is also effective when applied to a thin electronic terminal. It can be suitably expressed. Moreover, the decoration part may be laminated | stacked by the some decoration part, and the magnitude | size and shape of the decoration part laminated | stacked may differ. In the case where a plurality of decorative portions are stacked, the effects of the present invention are easily achieved when the maximum thickness of the stacked decorative portions is within the above range.
画像表示装置としては、特に限定されるものではないが、例えば、小型電子端末等の画像表示に使用されるLCDモジュールや有機ELモジュール等が挙げられる。本発明の両面粘着テープは携帯電子機器の薄型化が可能なため、バックライトにより厚くなりやすいLCDモジュールに使用することが好ましい。このようなLCDモジュールにおいては、透明パネルと両面粘着テープにより貼り合わされる表面に偏光フィルムが設けられていることが多い。本発明の両面粘着テープは、貼り合わせる一方の部材表面が、当該偏光フィルム表面のような平坦な表面であると、他方の段差を有する部材の段差追従に優れるため画像表示装置の両面粘着テープと貼り合わされる表面が段差を有さない構成に好適に適用できる。また、当該画像表示装置表面が段差を有する場合であっても、両面粘着テープの厚さ等を好適に調整することで、当該画像表示装置表面の段差に対しても好適に追従できる。 Although it does not specifically limit as an image display apparatus, For example, the LCD module, organic EL module, etc. which are used for image displays, such as a small electronic terminal, are mentioned. Since the double-sided pressure-sensitive adhesive tape of the present invention can reduce the thickness of a portable electronic device, it is preferably used for an LCD module that tends to be thickened by a backlight. In such an LCD module, a polarizing film is often provided on the surface to be bonded with the transparent panel and the double-sided adhesive tape. The double-sided pressure-sensitive adhesive tape of the present invention is excellent in the step following of a member having the other step when the surface of one member to be bonded is a flat surface such as the surface of the polarizing film. It can be suitably applied to a configuration in which the surfaces to be bonded do not have a step. Further, even when the surface of the image display device has a step, the thickness of the double-sided pressure-sensitive adhesive tape can be suitably adjusted to appropriately follow the step on the surface of the image display device.
[パネル固定方法]
透明パネルと画像表示装置との固定に際しては、透明パネルの装飾部の段差により混入した気泡を装置外部へ抜くために加熱加圧処理を行うことが好ましい。
[Panel fixing method]
When fixing the transparent panel and the image display device, it is preferable to perform a heating and pressurizing process in order to remove bubbles mixed in due to the step of the decorative portion of the transparent panel.
上記の加熱加圧処理を行う温度の条件は、40〜85℃が好ましく、50〜80℃がより好ましく、60〜80℃がさらに好ましい。上記の加熱加圧処理を行う温度が上記の範囲内だと、本発明の両面粘着テープの粘着剤層の流動性が高まり、効率的に混入した気泡を装置外部へ抜きやすいからである。 40-85 degreeC is preferable, as for the conditions of the temperature which performs said heat pressurization process, 50-80 degreeC is more preferable, and 60-80 degreeC is further more preferable. This is because when the temperature at which the heat and pressure treatment is performed is within the above range, the fluidity of the pressure-sensitive adhesive layer of the double-sided pressure-sensitive adhesive tape of the present invention is enhanced, and it is easy to efficiently remove mixed bubbles to the outside of the apparatus.
上記の加熱加圧処理を行う圧力の条件は、3〜5気圧が好ましく、4〜5気圧がより好ましく、4.5〜5気圧がさらに好ましい。上記の加熱加圧処理を行う圧力が上記の範囲内だと、粘着剤層が透明パネルおよび画像表示装置と密着しやすいからである。 The pressure condition for performing the heating and pressing treatment is preferably 3 to 5 atm, more preferably 4 to 5 atm, and further preferably 4.5 to 5 atm. This is because the pressure-sensitive adhesive layer easily adheres to the transparent panel and the image display device when the pressure for performing the heating and pressurizing treatment is within the above range.
上記の加熱加圧処理を行う時間の条件は、10〜50分が好ましく、10〜40分がより好ましく、10分〜30分がさらに好ましい。上記の加熱加圧処理を行う時間が上記の範囲内だと、粘着剤層と透明パネルおよび画像表示装置との固定を効率的に実施できるからである。 10-50 minutes are preferable, as for the conditions of the time which performs said heat pressurization process, 10-40 minutes are more preferable, and 10 minutes-30 minutes are further more preferable. This is because when the time for performing the heating and pressing treatment is within the above range, the pressure-sensitive adhesive layer, the transparent panel, and the image display device can be efficiently fixed.
以下に本発明を実施例により具体的に説明する。なお、実施例における「部」との表記は、いずれも「質量部」を表す。 Hereinafter, the present invention will be described specifically by way of examples. In addition, the description of "part" in an Example all represents "mass part".
[実施例1]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」1.2部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)0.5部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射した。その後、40℃で2日間静置し、厚さ175μmの両面粘着テープを得た。
[Example 1]
70 parts of 2-ethylhexyl acrylate, 4.5 parts of acrylic acid, 0.1 part of 4-hydroxybutyl acrylate, 25 parts of a polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, Ciba Specialty as a polymerization initiator Add 1.2 parts of “DAROCUR1173” manufactured by Chemical Co., Ltd. and 0.5 parts of “Coronate L-75” manufactured by Nippon Polyurethane Co., Ltd. (isocyanate-based cross-linking agent, solid content: 75%) as a cross-linking agent. After defoaming, coating was performed on a PET film having a thickness of 75 μm after the release treatment so that the thickness after drying was 175 μm, and then laminated with a PET film having a thickness of 25 μm after being subjected to a release treatment. Irradiation was performed using a “chemical lamp FL20SBL” manufactured by Toshiba Corporation for 5 minutes. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 175 micrometers.
[実施例2]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」0.3部、架橋剤として新中村化学工業社製「APG700」(アクリレート系架橋剤、固形分75%)0.3部、添加剤として荒川化学社製「KR1840」(極性脂肪族飽和炭化水素樹脂)20部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、10分間紫外線を照射して厚さ175μmの両面粘着テープを得た。
[Example 2]
70 parts of 2-ethylhexyl acrylate, 4.5 parts of acrylic acid, 0.1 part of 4-hydroxybutyl acrylate, 25 parts of a polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, Ciba Specialty as a polymerization initiator Chemical "DAROCUR1173" 0.3 parts, Shin-Nakamura Chemical Co., Ltd. "APG700" (acrylate-based crosslinking agent, solid content 75%) 0.3 parts, additive Arakawa Chemical "KR1840" ( Polar aliphatic saturated hydrocarbon resin) 20 parts added, stirred for 15 minutes, degassed under vacuum conditions, and then dried on a 75 μm thick PET film to a thickness of 175 μm after drying After being coated in this way, it is laminated with a 25 μm thick PET film that has been subjected to mold release treatment, and UV irradiation is made by Toshiba Chemical Using the pump FL20SBL ", to obtain a double-sided adhesive tape having a thickness of 175μm was irradiated for 10 minutes ultraviolet rays.
[実施例3]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」0.3部、添加剤としてヤスハラケミカル社製「UH115」(テルペンフェノール)20部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、10分間紫外線を照射して厚さ175μmの両面粘着テープを得た。
[Example 3]
70 parts of 2-ethylhexyl acrylate, 4.5 parts of acrylic acid, 0.1 part of 4-hydroxybutyl acrylate, 25 parts of a polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, Ciba Specialty as a polymerization initiator After adding 0.3 parts of “DAROCUR1173” manufactured by Chemical Co., Ltd. and 20 parts of “UH115” (terpene phenol) manufactured by Yashara Chemical Co., Ltd. as an additive, the mixture was stirred for 15 minutes, defoamed under vacuum conditions, and then subjected to mold release treatment. After coating on a 75 μm thick PET film to a thickness of 175 μm after drying, it is laminated with a 25 μm thick PET film that has been subjected to mold release treatment, and UV irradiation is performed by “Chemical Lamp FL20SBL” manufactured by Toshiba Corporation. Used, and irradiated with ultraviolet rays for 10 minutes to obtain a double-sided adhesive tape having a thickness of 175 μm.
[実施例4]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」1.2部、架橋剤として新中村化学工業社製「APG700」(アクリレート系架橋剤、固形分75%)0.3部、添加剤として荒川化学社製「KR1840」(極性脂肪族飽和炭化水素樹脂)10部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、10分間紫外線を照射して厚さ175μmの両面粘着テープを得た。
[Example 4]
70 parts of 2-ethylhexyl acrylate, 4.5 parts of acrylic acid, 0.1 part of 4-hydroxybutyl acrylate, 25 parts of a polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, Ciba Specialty as a polymerization initiator 1.2 parts of “DAROCUR1173” manufactured by Chemical Co., Ltd. “APG700” manufactured by Shin-Nakamura Chemical Co., Ltd. (acrylate crosslinker, solid content 75%) as a cross-linking agent, and “KR1840” manufactured by Arakawa Chemical Co., Ltd. as an additive ( Polar aliphatic saturated hydrocarbon resin) 10 parts added, stirred for 15 minutes, degassed under vacuum conditions, and then dried on a 75 μm thick PET film to a thickness of 175 μm after drying After being coated in this way, it is laminated with a 25 μm thick PET film that has been subjected to mold release treatment, and UV irradiation is made by Toshiba Chemical Using the pump FL20SBL ", to obtain a double-sided adhesive tape having a thickness of 175μm was irradiated for 10 minutes ultraviolet rays.
[実施例5]
ブチルアクリレート37部、2−エチルヘキシルアクリレート25部、アクリル酸1部、4−ヒドロキシブチルアクリレート0.1部、ブチルアクリレート/2―エチルヘキシルアクリレート=3/1の組成で、質量平均分子量106万のポリマーを16部、シクロヘキシルメタクリレートを主成分とした、質量平均分子量5000のポリマーを17部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」0.3部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)0.5部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射した。その後、40℃で2日間静置し、厚さ175μmの両面粘着テープを得た。
[Example 5]
A polymer having a weight average molecular weight of 1.06 million with a composition of 37 parts butyl acrylate, 25 parts 2-ethylhexyl acrylate, 1 part acrylic acid, 0.1 part 4-hydroxybutyl acrylate, butyl acrylate / 2-ethylhexyl acrylate = 3/1. 16 parts, 17 parts of a polymer having a weight average molecular weight of 5000 based on cyclohexyl methacrylate, 0.3 parts of “DAROCUR1173” manufactured by Ciba Specialty Chemicals as a polymerization initiator, and “Coronate L-75” manufactured by Nippon Polyurethane as a crosslinking agent “(Isocyanate-based crosslinking agent, solid content: 75%) 0.5 part was added, stirred for 15 minutes, degassed under vacuum conditions, and then dried on a 75 μm-thick PET film. 25 μm thick after the mold release treatment after coating to a thickness of 175 μm And laminated with a PET film, ultraviolet irradiation using a "chemical lamp FL20SBL" manufactured by Toshiba Corporation, was irradiated for 5 minutes ultraviolet rays. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 175 micrometers.
[比較例1]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」0.3部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)1.5部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射した。その後、40℃で2日間静置し、厚さ175μmの両面粘着テープを得た。
[Comparative Example 1]
70 parts of 2-ethylhexyl acrylate, 4.5 parts of acrylic acid, 0.1 part of 4-hydroxybutyl acrylate, 25 parts of a polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, Ciba Specialty as a polymerization initiator Add 0.3 parts of “DAROCUR1173” manufactured by Chemical Co., Ltd. and 1.5 parts of “Coronate L-75” manufactured by Nippon Polyurethane Co., Ltd. (isocyanate-based crosslinking agent, solid content: 75%) as a cross-linking agent. After defoaming under conditions, it was coated on a 75 μm-thick PET film that had been subjected to mold release treatment, and then dried to a thickness of 175 μm, and then laminated with a 25 μm-thick PET film that had been mold-released. For the ultraviolet irradiation, “Chemical Lamp FL20SBL” manufactured by Toshiba was used, and ultraviolet irradiation was performed for 5 minutes. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 175 micrometers.
[比較例2]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」0.3部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)0.1部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射した。その後、40℃で2日間静置し、厚さ175μmの両面粘着テープを得た。
[Comparative Example 2]
70 parts of 2-ethylhexyl acrylate, 4.5 parts of acrylic acid, 0.1 part of 4-hydroxybutyl acrylate, 25 parts of a polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, Ciba Specialty as a polymerization initiator Add 0.3 part of “DAROCUR1173” manufactured by Chemical Co., Ltd. and 0.1 part of “Coronate L-75” (isocyanate-based cross-linking agent, solid content: 75%) manufactured by Nippon Polyurethane Co., Ltd. as a cross-linking agent. After defoaming under conditions, it was coated on a 75 μm-thick PET film that had been subjected to mold release treatment, and then dried to a thickness of 175 μm, and then laminated with a 25 μm-thick PET film that had been mold-released. For the ultraviolet irradiation, “Chemical Lamp FL20SBL” manufactured by Toshiba was used, and ultraviolet irradiation was performed for 5 minutes. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 175 micrometers.
[比較例3]
ブチルアクリレート37部、2−エチルヘキシルアクリレート25部、アクリル酸1部、4−ヒドロキシブチルアクリレート0.1部、ブチルアクリレート/2―エチルヘキシルアクリレート=3/1の組成で、質量平均分子量106万のポリマーを16部、シクロヘキシルメタクリレートを主成分とした、質量平均分子量5000のポリマーを17部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」0.3部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)1.5部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射した。その後、40℃で2日間静置し、厚さ175μmの両面粘着テープを得た。
[Comparative Example 3]
A polymer having a weight average molecular weight of 1.06 million with a composition of 37 parts butyl acrylate, 25 parts 2-ethylhexyl acrylate, 1 part acrylic acid, 0.1 part 4-hydroxybutyl acrylate, butyl acrylate / 2-ethylhexyl acrylate = 3/1. 16 parts, 17 parts of a polymer having a weight average molecular weight of 5000 based on cyclohexyl methacrylate, 0.3 parts of “DAROCUR1173” manufactured by Ciba Specialty Chemicals as a polymerization initiator, and “Coronate L-75” manufactured by Nippon Polyurethane as a crosslinking agent “(Isocyanate-based crosslinking agent, solid content: 75%) 1.5 parts added, stirred for 15 minutes, degassed under vacuum conditions, and then dried on a 75 μm-thick PET film after release treatment 25 μm thick after the mold release treatment after coating to a thickness of 175 μm And laminated with a PET film, ultraviolet irradiation using a "chemical lamp FL20SBL" manufactured by Toshiba Corporation, was irradiated for 5 minutes ultraviolet rays. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 175 micrometers.
[比較例4]
ブチルアクリレート45部、2−エチルヘキシルアクリレート15部、アクリル酸3部、4−ヒドロキシブチルアクリレート0.1部、ブチルアクリレート/2―エチルヘキシルアクリレート=3/1の組成で、質量平均分子量106万のポリマーを18部、シクロヘキシルメタクリレートを主成分とした、質量平均分子量5000のポリマーを19部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」0.3部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)1.5部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射して両面粘着テープをした。その後、40℃で2日間静置し、厚さ175μmの両面粘着テープを得た。
[Comparative Example 4]
A polymer having a mass average molecular weight of 1.06 million with a composition of 45 parts butyl acrylate, 15 parts 2-ethylhexyl acrylate, 3 parts acrylic acid, 0.1 part 4-hydroxybutyl acrylate, butyl acrylate / 2-ethylhexyl acrylate = 3/1. 18 parts, 19 parts of a polymer having a weight average molecular weight of 5000 based on cyclohexyl methacrylate, 0.3 parts of “DAROCUR1173” manufactured by Ciba Specialty Chemicals as a polymerization initiator, and “Coronate L-75” manufactured by Nippon Polyurethane as a crosslinking agent “(Isocyanate-based crosslinking agent, solid content: 75%) 1.5 parts added, stirred for 15 minutes, degassed under vacuum conditions, and then dried on a 75 μm-thick PET film after release treatment 25 μm thick after the mold release treatment after coating to a thickness of 175 μm It was laminated with a PET film, ultraviolet irradiation using the "chemical lamp FL20SBL" manufactured by Toshiba Corporation, and a double-sided adhesive tape was irradiated with 5 minutes UV. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 175 micrometers.
[比較例5]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」1.2部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)0.5部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射した。その後、40℃で2日間静置し、厚さ125μmの両面粘着テープを得た。
[Comparative Example 5]
70 parts of 2-ethylhexyl acrylate, 4.5 parts of acrylic acid, 0.1 part of 4-hydroxybutyl acrylate, 25 parts of a polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, Ciba Specialty as a polymerization initiator Add 1.2 parts of “DAROCUR1173” manufactured by Chemical Co., Ltd. and 0.5 part of “Coronate L-75” (isocyanate-based cross-linking agent, solid content: 75%) manufactured by Nippon Polyurethane Co., Ltd. as a cross-linking agent. After defoaming under conditions, it was coated on a 75 μm-thick PET film that had been subjected to mold release treatment, and then dried to a thickness of 175 μm, and then laminated with a 25 μm-thick PET film that had been mold-released. For the ultraviolet irradiation, “Chemical Lamp FL20SBL” manufactured by Toshiba was used, and ultraviolet irradiation was performed for 5 minutes. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 125 micrometers.
[比較例6]
2−エチルヘキシルアクリレート70部、アクリル酸4.5部、4−ヒドロキシブチルアクリレート0.1部、2―エチルヘキシルアクリレートを主成分とした質量平均分子量76万のポリマーを25部、シクロヘキシルメタクリレート/アクリル酸 = 97/3の組成で、質量平均分子量6600のポリマーを20部、重合開始剤としてチバスペシャリティケミカル社製「DAROCUR1173」1.2部、架橋剤として日本ポリウレタン社製「コロナートL−75」(イソシアネート系架橋剤、固形分75%)0.5部添加して、15分攪拌した後、真空条件下で脱泡した後、離型処理した厚さ75μmのPETフィルム上に、乾燥後厚さが175μmになるように塗工した後、離型処理した厚さ25μmのPETフィルムでラミネートして、紫外線照射は東芝社製「ケミカルランプFL20SBL」を使用し、5分間紫外線を照射した。その後、40℃で2日間静置し、厚さ175μmの両面粘着テープを得た。
[Comparative Example 6]
70 parts 2-ethylhexyl acrylate, 4.5 parts acrylic acid, 0.1 part 4-hydroxybutyl acrylate, 25 parts polymer having a weight average molecular weight of 760,000 based on 2-ethylhexyl acrylate, cyclohexyl methacrylate / acrylic acid = 20 parts of a polymer having a mass average molecular weight of 6600 with a composition of 97/3, 1.2 parts of “DAROCUR1173” manufactured by Ciba Specialty Chemicals as a polymerization initiator, and “Coronate L-75” (isocyanate type) manufactured by Nippon Polyurethane as a crosslinking agent After adding 0.5 parts (crosslinking agent, solid content: 75%), stirring for 15 minutes, defoaming under vacuum conditions, and release on a 75 μm thick PET film, the thickness after drying is 175 μm. And coated with a 25μm thick PET film after release. Te, ultraviolet irradiation using a "chemical lamp FL20SBL" manufactured by Toshiba Corporation, was irradiated for 5 minutes ultraviolet rays. Then, it left still at 40 degreeC for 2 days, and obtained the double-sided adhesive tape of thickness 175 micrometers.
(両面粘着テープの評価)
実施例1〜5、比較例1〜6で作成した両面テープについて以下の評価を行い、得られた結果を表1〜2に示した。
(Evaluation of double-sided adhesive tape)
The following evaluation was performed about the double-sided tape created in Examples 1-5 and Comparative Examples 1-6, and the obtained result was shown to Tables 1-2.
(1)粘着剤層の動的粘弾性測定
熟成済みの粘着剤層を、約2mm厚にまで重ね合わせ試験片とした。ティ・エイ・インスツルメントジャパン社製粘弾性試験機(アレス2kSTD)に、直径7.9mmのパラレルプレートを装着し、この試験片を圧縮荷重40〜60gで挟み込んだ。周波数1Hzで、−60〜100℃の温度範囲を測定し、損失正接(tanδ)の極大値(M 1 )を示す温度を測定した。
(1) Measurement of dynamic viscoelasticity of pressure-sensitive adhesive layer Aged pressure-sensitive adhesive layer was laminated to a thickness of about 2 mm to obtain a test piece. A parallel plate having a diameter of 7.9 mm was attached to a viscoelasticity testing machine (ARES 2kSTD) manufactured by T.A. Instruments Japan, and the test piece was sandwiched with a compression load of 40 to 60 g. A temperature range of −60 to 100 ° C. was measured at a frequency of 1 Hz, and a temperature showing a maximum value (M 1) of loss tangent (tan δ) was measured.
(2)ゲル分率測定
熟成後の粘着剤層の組成物をトルエン中に浸漬し、23℃下で24時間放置後に残った不溶分の乾燥後の質量を測定し、元の質量に対する百分率で表した。
(2) Gel fraction measurement The composition of the pressure-sensitive adhesive layer after aging is immersed in toluene, the mass after drying of the insoluble matter remaining after being allowed to stand at 23 ° C. for 24 hours is measured, and is expressed as a percentage of the original mass. expressed.
(3)気泡抜け性
厚さ0.5mm、長さ50mm、幅40mm、窓枠状に厚さ15μm、幅5mmの印刷付きガラス板に、印刷面側から実施例1〜5及び比較例1〜6の各両面粘着テープを貼り付けた後、厚さ0.5mm、長さ50mm、幅40mmのガラス板との貼り合わせを行い、5気圧、70℃、20分の条件で加熱加圧処理を行い固定した後、目視により、気泡の有無を確認した。
気泡抜け性の評価基準は、下記の通りとした。
○:気泡なし。
×:気泡あり。
(3) Air bubble releasing properties Examples 1 to 5 and Comparative Examples 1 to 5 from a printing surface side to a glass plate with printing having a thickness of 0.5 mm, a length of 50 mm, a width of 40 mm, and a window frame shape of a thickness of 15 μm and a width of 5 mm. After pasting each double-sided adhesive tape of No. 6, it is bonded to a glass plate having a thickness of 0.5 mm, a length of 50 mm, and a width of 40 mm, and is heated and pressurized under conditions of 5 atm, 70 ° C. and 20 minutes. After performing and fixing, the presence or absence of bubbles was visually confirmed.
The evaluation criteria for the bubble releasing property were as follows.
○: No bubbles.
X: Air bubbles are present.
また、実施例1及び比較例2の両面粘着テープの気泡の有無を、ハイロックス社製光学顕微鏡「パワースコープ KH−2700」により、50倍の倍率にて観察した。実施例1の観察結果を図2に、比較例2の観察結果を図3に示した。 Moreover, the presence or absence of air bubbles in the double-sided pressure-sensitive adhesive tapes of Example 1 and Comparative Example 2 was observed at a magnification of 50 times with an optical microscope “Powerscope KH-2700” manufactured by Hilox. The observation result of Example 1 is shown in FIG. 2, and the observation result of Comparative Example 2 is shown in FIG.
(4)耐発泡性
各両面粘着テープを厚さ25μm、長さ50mm、幅50mmのポリエチレンテレフタエートフィルム(PETフィルム)にラミネートした後、これを、厚さ2.5mm、長さ50mm、幅50mmのポリメチルメタクリレート板(PMMA板)に貼り付けて、5気圧、70℃、20分の条件で加熱加圧処理を行い固定して、PETフィルム/粘着剤層/PMMA板の層の構成を有するサンプルを調整した。このサンプルを85℃の加熱機に500時間投入することにより、耐発泡性試験を行った。この耐発泡性試験後、目視により、気泡の有無を確認した。
耐発泡性の評価基準は、下記の通りとした。
○:気泡なし。
×:気泡あり。
(4) Foam resistance After laminating each double-sided adhesive tape to a polyethylene terephthalate film (PET film) having a thickness of 25 μm, a length of 50 mm, and a width of 50 mm, this is 2.5 mm thick, 50 mm long, and wide. Affixed to a 50 mm polymethylmethacrylate plate (PMMA plate), fixed by heat and pressure treatment under conditions of 5 atm, 70 ° C., 20 minutes, and the configuration of the PET film / adhesive layer / PMMA plate layer A sample with was prepared. This sample was put in a heater at 85 ° C. for 500 hours to conduct a foam resistance test. After the foam resistance test, the presence or absence of bubbles was confirmed by visual observation.
The evaluation criteria for foam resistance were as follows.
○: No bubbles.
X: Air bubbles are present.
(5)耐落下衝撃性試験(デュポン式耐衝撃試験機)
(i)23℃条件下、厚さ0.5mm、長さ50mm、幅40mmのガラス板に、長さ50mm、幅40mmの各両面粘着テープを貼り付けた。
(ii)厚さ2mm、長さ150mm、幅100mmのPC板に、(i)の両面粘着テープ付きガラス板を貼付し、5気圧、70℃、20分の条件で加熱加圧処理を行った後、23℃下で1時間静置した。
(iii)デュポン衝撃試験機の台座の上に、(ii)で作成した板を、ガラス板が下側になるように静置した。
次に、板の上面から、直径25mm、質量300gのステンレス製の撃芯(先端直径12.7mm)を、高さ10cmの位置から落下させた。板の中心部分に衝撃を加えて、衝撃が加えられている面とは反対側に貼付されているガラス板が、脱落するか否か評価した。脱落しなかった場合は、撃芯の高さを10cmづつ上昇させて、再度衝撃試験を行い、最終的には、脱落するまでの撃芯の高さを測定した。なお、撃芯を50cmの高さから落下させても脱落しない場合は、「50<」と表示した。
(5) Drop impact resistance test (DuPont impact resistance tester)
(I) Double-sided pressure-sensitive adhesive tapes having a length of 50 mm and a width of 40 mm were attached to a glass plate having a thickness of 0.5 mm, a length of 50 mm, and a width of 40 mm under 23 ° C. conditions.
(Ii) A glass plate with a double-sided adhesive tape of (i) was attached to a PC plate having a thickness of 2 mm, a length of 150 mm, and a width of 100 mm, and subjected to heat and pressure treatment at 5 atm, 70 ° C. for 20 minutes. Then, it left still at 23 degreeC for 1 hour.
(Iii) On the pedestal of the DuPont impact tester, the plate prepared in (ii) was allowed to stand so that the glass plate was on the lower side.
Next, a stainless steel strike core (tip diameter: 12.7 mm) having a diameter of 25 mm and a mass of 300 g was dropped from the top surface of the plate from a position having a height of 10 cm. An impact was applied to the central portion of the plate, and it was evaluated whether or not the glass plate attached to the side opposite to the surface to which the impact was applied dropped. When it did not fall off, the height of the hitting core was raised by 10 cm, an impact test was performed again, and finally the hitting height until dropping was measured. In addition, "50 <" was displayed when it did not fall even if it dropped from the height of 50cm.
(6)全光線透過率
両面粘着テープを、厚さ0.5mm、長さ50mm、幅40mmのガラス板に貼り付けた後、これを、厚さ0.5mm、長さ50mm、幅40mmのガラス板と貼り合わせて、5気圧、70℃、20分の条件で加熱加圧処理を行い固定して、ガラス板/粘着剤層/ガラス板の層の構成を有するサンプルを調製した。村上色彩技術研究所社製「HR−100型」を使用して、サンプルのJIS K 7105及びJIS K 7136に基づいて全光線透過率を測定した。
(6) Total light transmittance After a double-sided pressure-sensitive adhesive tape is attached to a glass plate having a thickness of 0.5 mm, a length of 50 mm, and a width of 40 mm, this is formed into a glass having a thickness of 0.5 mm, a length of 50 mm, and a width of 40 mm. A sample having a structure of glass plate / adhesive layer / glass plate was prepared by bonding to a plate and fixing it by heating and pressing under conditions of 5 atm and 70 ° C. for 20 minutes. The total light transmittance was measured based on JIS K 7105 and JIS K 7136 of the sample using “HR-100 Model” manufactured by Murakami Color Research Laboratory.
表1〜2及び図2〜3に示したように、実施例1〜5の本発明の両面粘着テープは、貼り合わせ時の気泡抜け性と、貼り合わせ後の経時の発泡を抑制でき、視認される気泡が見られなかった。また、落下衝撃試験においても部材の脱落が生じず、段差が設けられた部品の固定に好適であることが明らかであった。一方、比較例1〜6の両面粘着テープにおいては、いずれも貼り合わせ時の発泡の抑制が困難であり、比較例1、2、5、6の両面粘着テープでは、経時での気泡の発生も多く確認された。 As shown in Tables 1 and 2 and FIGS. 2 to 3, the double-sided pressure-sensitive adhesive tapes of the present invention of Examples 1 to 5 can suppress the bubble-removability at the time of bonding and foaming with time after bonding, and are visually recognized. No bubbles were seen. Also, in the drop impact test, the member did not fall off, and it was clear that it was suitable for fixing a component provided with a step. On the other hand, in the double-sided pressure-sensitive adhesive tapes of Comparative Examples 1 to 6, it is difficult to suppress foaming at the time of bonding, and in the double-sided pressure-sensitive adhesive tapes of Comparative Examples 1, 2, 5, and 6, the generation of bubbles over time is also difficult. Many were confirmed.
1:透明パネル
2:装飾部
3:両面粘着テープ
4:画像表示装置
1: Transparent panel 2: Decoration part 3: Double-sided adhesive tape 4: Image display device
Claims (5)
炭素数1〜12の(メタ)アクリル酸アルキルエステルを主成分とする光硬化型粘着剤組成物を硬化してなる粘着剤層からなり、
前記粘着剤層の周波数1Hzでの動的粘弾性スペクトルの70℃の損失正接が0.43〜0.98であり、70℃の貯蔵弾性率が0.8×104〜3.4×104Paであり、
前記粘着剤層が、−40〜−10℃の温度領域に損失正接の極大値を有しており、
総厚さが100〜250μmであることを特徴とする両面粘着テープ。 A double-sided pressure-sensitive adhesive tape for sticking and fixing a transparent panel provided with a decorative portion on the surface of an image display device,
It consists of a pressure-sensitive adhesive layer formed by curing a photocurable pressure-sensitive adhesive composition containing a C1-C12 (meth) acrylic acid alkyl ester as a main component,
The loss tangent at 70 ° C. of the dynamic viscoelastic spectrum at a frequency of 1 Hz of the pressure-sensitive adhesive layer is 0.43 to 0.98, and the storage elastic modulus at 70 ° C. is 0.8 × 10 4 to 3.4 × 10. 4 Pa,
The pressure-sensitive adhesive layer has a maximum value of loss tangent in a temperature range of −40 to −10 ° C.,
A double-sided pressure-sensitive adhesive tape having a total thickness of 100 to 250 μm.
ゲル分率=[(両面粘着テープのトルエン浸漬後質量)/(両面粘着テープのトルエン浸漬前質量)]×100 The double-sided pressure-sensitive adhesive tape according to claim 1 or 2, wherein a gel fraction represented by the following formula when the double-sided pressure-sensitive adhesive tape is immersed in toluene for 24 hours is 30 to 70%.
Gel fraction = [(mass after dipping toluene in double-sided pressure-sensitive adhesive tape) / (mass before dipping toluene in double-sided pressure-sensitive adhesive tape)] × 100
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