JP5534457B2 - 粘着剤組成物、これを含む保護フィルム及び偏光板並びに液晶表示装置 - Google Patents
粘着剤組成物、これを含む保護フィルム及び偏光板並びに液晶表示装置 Download PDFInfo
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- JP5534457B2 JP5534457B2 JP2010542181A JP2010542181A JP5534457B2 JP 5534457 B2 JP5534457 B2 JP 5534457B2 JP 2010542181 A JP2010542181 A JP 2010542181A JP 2010542181 A JP2010542181 A JP 2010542181A JP 5534457 B2 JP5534457 B2 JP 5534457B2
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- meth
- acrylate
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- 239000000203 mixture Substances 0.000 title claims description 48
- 230000001681 protective effect Effects 0.000 title claims description 23
- 239000000853 adhesive Substances 0.000 title claims description 18
- 230000001070 adhesive effect Effects 0.000 title claims description 18
- 239000004973 liquid crystal related substance Substances 0.000 title claims description 17
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 53
- 239000000178 monomer Substances 0.000 claims description 50
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 42
- 229910052751 metal Inorganic materials 0.000 claims description 32
- 239000002184 metal Substances 0.000 claims description 32
- 229920006243 acrylic copolymer Polymers 0.000 claims description 31
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 29
- -1 n-octyl Chemical group 0.000 claims description 27
- 150000003839 salts Chemical class 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 125000000524 functional group Chemical group 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 15
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 14
- 239000012790 adhesive layer Substances 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 10
- 239000000758 substrate Substances 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 8
- 210000002858 crystal cell Anatomy 0.000 claims description 5
- 239000004593 Epoxy Substances 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 239000013522 chelant Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 150000001450 anions Chemical class 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000012948 isocyanate Substances 0.000 claims description 3
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 239000011777 magnesium Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- 229910020366 ClO 4 Inorganic materials 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 229910052788 barium Inorganic materials 0.000 claims description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052792 caesium Inorganic materials 0.000 claims description 2
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 239000011575 calcium Substances 0.000 claims description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000010408 film Substances 0.000 description 59
- 238000000034 method Methods 0.000 description 17
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- 230000003068 static effect Effects 0.000 description 11
- 230000005611 electricity Effects 0.000 description 9
- 230000002209 hydrophobic effect Effects 0.000 description 9
- 239000010410 layer Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 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 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000006087 Silane Coupling Agent Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 229910021645 metal ion Inorganic materials 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 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 4
- 229920002284 Cellulose triacetate Polymers 0.000 description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 3
- 239000002738 chelating agent Substances 0.000 description 3
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004695 Polyether sulfone Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000010724 Wisteria floribunda Nutrition 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- FFBZKUHRIXKOSY-UHFFFAOYSA-N aziridine-1-carboxamide Chemical compound NC(=O)N1CC1 FFBZKUHRIXKOSY-UHFFFAOYSA-N 0.000 description 2
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 239000002346 layers by function Substances 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920006393 polyether sulfone Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-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
- OZDGMOYKSFPLSE-UHFFFAOYSA-N 2-Methylaziridine Chemical compound CC1CN1 OZDGMOYKSFPLSE-UHFFFAOYSA-N 0.000 description 1
- COORVRSSRBIIFJ-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]-1-methoxyethanol;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(O)COCCOCCO COORVRSSRBIIFJ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- JYSWMLAADBQAQX-UHFFFAOYSA-N 2-prop-2-enoyloxyacetic acid Chemical compound OC(=O)COC(=O)C=C JYSWMLAADBQAQX-UHFFFAOYSA-N 0.000 description 1
- YAHLUTXNMRWKSM-UHFFFAOYSA-N 2-prop-2-enoyloxybutanoic acid Chemical compound CCC(C(O)=O)OC(=O)C=C YAHLUTXNMRWKSM-UHFFFAOYSA-N 0.000 description 1
- CUTWSDAQYCQTGD-UHFFFAOYSA-N 2-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)C(C)OC(=O)C=C CUTWSDAQYCQTGD-UHFFFAOYSA-N 0.000 description 1
- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-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
- URDOJQUSEUXVRP-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C(C)=C URDOJQUSEUXVRP-UHFFFAOYSA-N 0.000 description 1
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- NVGBPTNZLWRQSY-UWVGGRQHSA-N Lys-Lys Chemical class NCCCC[C@H](N)C(=O)N[C@H](C(O)=O)CCCCN NVGBPTNZLWRQSY-UWVGGRQHSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- IIGAAOXXRKTFAM-UHFFFAOYSA-N N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C Chemical compound N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C IIGAAOXXRKTFAM-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- FYAMXEPQQLNQDM-UHFFFAOYSA-N Tris(1-aziridinyl)phosphine oxide Chemical compound C1CN1P(N1CC1)(=O)N1CC1 FYAMXEPQQLNQDM-UHFFFAOYSA-N 0.000 description 1
- AVTLBBWTUPQRAY-BUHFOSPRSA-N V-59 Substances CCC(C)(C#N)\N=N\C(C)(CC)C#N AVTLBBWTUPQRAY-BUHFOSPRSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- KYIKRXIYLAGAKQ-UHFFFAOYSA-N abcn Chemical compound C1CCCCC1(C#N)N=NC1(C#N)CCCCC1 KYIKRXIYLAGAKQ-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
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Description
(a)金属塩をキレート化することができる官能基を有する単量体と、疎水性単量体とを含有するアクリル系共重合体、および
(b)金属塩を含む。
基材と、
上記基材の一面または両面に形成され、本発明による粘着剤組成物の硬化物を含有する粘着層とを含む。
偏光フィルムまたは偏光素子と、
上記偏光フィルムまたは偏光素子の一面または両面に形成され、本発明による粘着剤組成物の硬化物を含有する粘着層とを含む。
(a)アクリル系共重合体
本発明に使用するアクリル系共重合体は、この技術分野において通常粘着剤として使用されるものであれば特に限定されず、例えば、
(i)アルキレンオキシド基を有する(メタ)アクリル酸エステル系単量体0.8乃至5重量部と、
(ii)疎水性単量体3乃至18重量部と
を含むものを使用することができる。
(iv)架橋性官能基含有単量体0.1重量部乃至10重量部と、をさらに含むことができる。
本発明において使用される金属塩には、アクリル系共重合体に含まれる単量体によってキレート化され得る金属陽イオン及び/または陰イオンが含まれる。上記金属塩は、溶媒またはキレート化可能な官能基を含む共重合体と混合すると、金属イオンが塩化ら解離されやすい化合物であることが好ましく、また、上記金属イオンは、イオン半径が小さく、解離エネルギーが小さいことが好ましい。
上記のような成分よりなる本発明のアクリル系粘着剤組成物は、必要に応じて多官能性架橋剤をさらに含むことができる。多官能性架橋剤は、アクリル系共重合体に含まれる架橋性官能基と反応することによって、粘着剤の凝集力を高める作用をする。
上記のような成分よりなる本発明の粘着剤組成物は、必要に応じてシラン系カップリング剤および/または粘着性付与樹脂をさらに含むことができる。
ゲル含量(%)=B/A×100
偏光フィルムまたは偏光素子と、
上記偏光フィルムまたは偏光素子の一面または両面に形成され、本発明による粘着剤組成物の硬化物を含有する粘着層と、を含む偏光板を提供する。
窒素ガスを流し、温度調節が容易になるように冷却装置を設置した1Lの反応器に2−エチルヘキシルアクリレート(EHA)90重量部、ラウリルアクリレート5重量部、メトキシトリエチレングリコールアクリレート2重量部及び2−ヒドロキシエチルアクリレート(HEA)3重量部を含む単量体混合物及び溶剤として酢酸エチル(EAc)100重量部を投入した。次に、酸素除去のために、窒素ガスを60分間パージ(purging)した後、温度を70℃に維持した。その後、混合物を均一にした後、反応開始剤として2、2’−アゾビス(2−メチルブチロニトリル)(Wako、V−59)0.1重量部を投入し、6時間反応させた。反応の後、得られた生成物を酢酸エチルで希釈することによって、固形分含量が44%であり、重量平均分子量が58万であり、分子量分布が7.0のアクリル系共重合体を製造した。
共重合体の成分及び組成を下記表1に示したように変更したことを除いて、上記製造例1と同じ方法でアクリル系共重合体を製造した。
製造例1で製造したアクリル系共重合体100重量部に対して、架橋剤としてヘキサメチレンジイソシアネートのプレポリマー(HDI)5.0重量部及び金属塩としてリチウムトリフルオロメタンスルホンイミド(LiN(CF3SO2)2)0.1重量部を投入し、適正の濃度に希釈して均一に混合した後、厚さ38μmの2軸延伸ポリエチレンテレフタレートフィルムの一面にコーティングし、乾燥させて、厚さ20μmの均一な粘着層を製造した。次に、こうして得られたポリエチレンテレフタレートフィルムの一面にコーティングした粘着層に、離型フィルムをラミネートし、十分な熟成のために23℃の温度および55%の湿度の条件で4日間保管した。その後、上記のように製造された保護フィルムを適当なサイズに切断し、偏光板のトリアセチルセルロース(TACフィルム、日本国富士フィルム社)面及び眩しさ防止フィルム(AG TAC、日本国DNP社)面に各々付着し、評価に使用した。
粘着剤組成物の組成を下記表2に示したように変更したことを除いて、実施例1と同じ方法でサンプルを製造した。
実施例1乃至5及び比較例1及び2で製造した粘着層をトリアセチルセルロース(TAC、富士フィルム社製造)面及び眩しさ防止層(AG、日本国DNP社製造)面にJIS Z 0.27に基づいて2kgのローラーで付着させた後、23℃の温度および65%の相対湿度の条件で24時間保管した。次に、180゜の剥離角度、0.3m/min(低速)及び30m/min(高速)の剥離速度で剥離力を測定した。
実施例1乃至5及び比較例1及び2で製造した保護フィルムを付着させた偏光板を各々25cm×22cm(横×縦)のサイズに切断して試料を準備し、これを23℃の温度および50%の相対湿度の条件で24時間保管した。その後、保護フィルムを40m/minの速度で剥離する際に、偏光板の表面から1cmの高さで静電圧測定器STATRION−M2を使用して、偏光板表面で発生する静電圧を測定した。
保護フィルムを付着させた偏光板を、50℃のオーブン内で10日間保管した後、23℃の温度および65%の相対湿度の条件で24時間保管した。次に、上記と同一の条件で低速、高速剥離力及び剥離帯電圧を測定し、耐久性評価を実施した。
Claims (14)
- (a)アクリル系共重合体100重量部に対して、80重量部乃至95重量部の炭素数1乃至9のアルキル基を有するアルキル(メタ)アクリレート;0.8重量部乃至5重量部の金属塩をキレート化することができる官能基を有する単量体;および、1重量部乃至18重量部の炭素数10以上のアルキル基を有する(メタ)アクリル酸エステル系単量体を含有するアクリル系共重合体;および
(b)金属塩
を含む粘着剤組成物であって、
前記金属塩をキレート化することができる官能基を有する単量体が、アルキレンオキシド基を有する(メタ)アクリル酸エステル系単量体である、粘着剤組成物。 - 前記金属塩をキレート化することができる官能基を有する単量体が、アルコキシジアルキレングリコール(メタ)アクリル酸エステル、アルコキシトリアルキレングリコール(メタ)アクリル酸エステル、アルコキシポリアルキレングリコール(メタ)アクリル酸エステル、フェノキシジアルキレングリコール(メタ)アクリル酸エステル、フェノキシトリアルキレングリコール(メタ)アクリル酸エステル、及びフェノキシポリアルキレングリコール(メタ)アクリル酸エステルからなる群から選択される1つ以上である、請求項1に記載の粘着剤組成物。
- 前記炭素数10以上のアルキル基を有する(メタ)アクリル酸エステル系単量体が、イソボルニル(メタ)アクリレート、ラウリル(メタ)アクリレート、及びトリデシル(メタ)アクリレートからなる群から選択される1つ以上である、請求項1に記載の粘着剤組成物。
- 前記アクリル系共重合体が、アクリル系共重合体100重量部に対して、
架橋性官能基含有単量体0.1重量部乃至10重量部
をさらに含む、請求項1に記載の粘着剤組成物。 - 前記炭素数1乃至9のアルキル基を有するアルキル(メタ)アクリレートが、メチル(メタ)アクリレート、エチル(メタ)アクリレート、n−プロピル(メタ)アクリレート、イソプロピル(メタ)アクリレート、n−ブチル(メタ)アクリレート、t−ブチル(メタ)アクリレート、sec−ブチル(メタ)アクリレート、ペンチル(メタ)アクリレート、n−オクチル(メタ)アクリレート、及び2−エチルヘキシル(メタ)アクリレートからなる群から選択される1つ以上である、請求項1に記載の粘着剤組成物。
- 前記架橋性官能基含有単量体が、ヒドロキシル基含有単量体、カルボキシル基含有単量
体、または窒素含有単量体である、請求項5に記載の粘着剤組成物。 - 前記金属塩が、
リチウム、ナトリウム、カリウム、マグネシウム、カルシウム、バリウム、及びセシウムからなる群から選択される1つ以上の金属の陽イオンと、
Cl−、Br−、I−、BF4 −、PF6 −、AsF−、ClO4 −、NO2 −、CO3 −、N(CF3SO2)2 −、N(CF3CO)2 −、N(C2F5SO2)2 −、N(C2F5CO)2 −、N(C4F9SO2)2 −、C(CF3SO2)3 −、及びCF3SO3 −からなる群から選択される1つ以上の陰イオンと
を含む請求項1に記載の粘着剤組成物。 - 前記金属塩が、アクリル系共重合体100重量部に対して0.001重量部乃至10重量部の量で含まれる、請求項1に記載の粘着剤組成物。
- 前記アクリル系共重合体100重量部に対して、0.1重量部乃至10重量部の多官能性架橋剤がさらに含まれる、請求項1に記載の粘着剤組成物。
- 前記多官能性架橋剤が、イソシアネート系化合物、エポキシ系化合物、アジリジン系化合物、及び金属キレート系化合物からなる群から選択される1つ以上である請求項10に記載の粘着剤組成物。
- 基材と、
上記基材の一面または両面に形成され、請求項1乃至11のいずれか一項に記載の粘着剤組成物を含有する粘着層と
を含む保護フィルム。 - 偏光フィルムまたは偏光素子と、
上記偏光フィルムまたは偏光素子の一面または両面に形成され、請求項1乃至11のいずれか一項に記載の粘着剤組成物を含有する粘着層と
を含む偏光板。 - 請求項12に記載の保護フィルムを付着させた偏光板が液晶セルの一面または両面に接合された液晶パネルを含む、液晶表示装置。
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PCT/KR2009/000178 WO2009091171A2 (en) | 2008-01-14 | 2009-01-13 | Pressure-sensitive adhesive composition, protective film, polarizer and liquid crystal display comprising the same |
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Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101061939B1 (ko) * | 2007-12-12 | 2011-09-05 | 주식회사 엘지화학 | 편광판용 아크릴계 점착제 조성물 |
CN102666767A (zh) * | 2009-12-18 | 2012-09-12 | 3M创新有限公司 | 用于低表面能基材的压敏粘合剂 |
CN102884148B (zh) | 2010-02-26 | 2015-07-08 | Lg化学株式会社 | 粘合剂组合物 |
WO2011115224A1 (ja) * | 2010-03-18 | 2011-09-22 | 積水化学工業株式会社 | 光学部材用粘着剤組成物及び光学部材用粘着テープ |
KR101362879B1 (ko) * | 2010-12-31 | 2014-02-14 | 제일모직주식회사 | 편광판용 점착제 조성물 |
JP5588361B2 (ja) * | 2011-01-06 | 2014-09-10 | 日東電工株式会社 | 表面保護シート |
CN103703095B (zh) | 2011-03-23 | 2016-06-01 | Lg化学株式会社 | 压敏粘合剂组合物 |
KR101541578B1 (ko) | 2011-03-23 | 2015-08-03 | 주식회사 엘지화학 | 점착제 조성물 |
CN103459537B (zh) * | 2011-03-28 | 2015-09-30 | 日本电石工业株式会社 | 粘合剂组合物及光学构件用薄膜 |
JP2012247574A (ja) * | 2011-05-26 | 2012-12-13 | Nitto Denko Corp | 粘着型偏光板および画像表示装置 |
WO2013095064A1 (ko) * | 2011-12-21 | 2013-06-27 | 주식회사 엘지화학 | 점착제 조성물 |
JP5834325B2 (ja) * | 2011-12-22 | 2015-12-16 | 東洋インキScホールディングス株式会社 | 感圧式接着剤組成物、及びそれを用いてなる感圧式接着剤フィルム |
JP2013186808A (ja) * | 2012-03-09 | 2013-09-19 | Lintec Corp | タッチパネル部材貼付用粘着剤、タッチパネル部材貼付用粘着シート、及びタッチパネル装置 |
JP6125789B2 (ja) * | 2012-10-04 | 2017-05-10 | 日本カーバイド工業株式会社 | 粘着剤組成物、粘着シート及び光学用積層シート |
EP2719735A1 (en) * | 2012-10-12 | 2014-04-16 | Celanese Emulsions GmbH | Adhesive compositions |
JP6283355B2 (ja) * | 2013-04-11 | 2018-02-21 | 綜研化学株式会社 | 積層体 |
JP6132219B2 (ja) * | 2013-06-19 | 2017-05-24 | エルジー・ケム・リミテッド | 粘着剤組成物 |
US10066133B2 (en) | 2013-06-19 | 2018-09-04 | Lg Chem, Ltd. | Pressure-sensitive adhesive composition |
CN105189580B (zh) * | 2013-07-19 | 2017-04-19 | Lg化学株式会社 | 具有优异粘合性能的丙烯酸系乳液树脂及其制备方法 |
WO2015022825A1 (ja) * | 2013-08-12 | 2015-02-19 | 日本合成化学工業株式会社 | 接着剤組成物、偏光板用接着剤組成物、偏光板用接着剤、およびそれを用いてなる偏光板 |
PL3023470T3 (pl) * | 2013-08-16 | 2020-11-16 | Lg Chem, Ltd. | Kompozycja adhezyjna |
DE102013217785A1 (de) * | 2013-09-05 | 2015-03-05 | Tesa Se | Verwendung von Haftklebebändern für optische Anwendungen |
CN104845563A (zh) * | 2014-02-17 | 2015-08-19 | 上海精涂新材料技术有限公司 | 一种防静电保护膜用胶水 |
KR101866957B1 (ko) * | 2014-04-24 | 2018-06-12 | 동우 화인켐 주식회사 | 대전 방지성 점착제 조성물 및 이를 이용하여 제조되는 편광판 |
KR101816966B1 (ko) * | 2014-08-04 | 2018-01-09 | 주식회사 엘지화학 | 점착제 조성물 |
KR101813764B1 (ko) | 2014-11-28 | 2017-12-29 | 삼성에스디아이 주식회사 | 광학 필름용 점착제 조성물, 점착제층, 광학부재 및 화상표시장치 |
JP6231036B2 (ja) * | 2015-04-03 | 2017-11-15 | 日東電工株式会社 | 偏光フィルム用粘着剤組成物、偏光フィルム用粘着剤層、粘着剤層付偏光フィルム、及び画像表示装置 |
JP7170538B2 (ja) | 2015-12-08 | 2022-11-14 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | 再生可能な材料由来の官能化促進樹脂 |
JP6043445B2 (ja) * | 2016-01-29 | 2016-12-14 | 藤森工業株式会社 | 粘着剤組成物及び表面保護フィルム |
JP6039118B2 (ja) * | 2016-01-29 | 2016-12-07 | 藤森工業株式会社 | 粘着剤組成物及び表面保護フィルム |
JP6431162B2 (ja) * | 2017-11-17 | 2018-11-28 | 藤森工業株式会社 | 粘着剤組成物及び表面保護フィルム |
JP7126796B2 (ja) * | 2018-11-01 | 2022-08-29 | 日東電工株式会社 | 粘着剤層付偏光板 |
KR102139334B1 (ko) | 2018-11-16 | 2020-07-29 | 한국신발피혁연구원 | 실란 개질 아크릴 점착제 조성물 |
MX2023013873A (es) | 2021-05-27 | 2023-12-08 | Agrosustain Sa | Recubrimiento comestible para prevenir el deterioro de los alimentos. |
KR20240093800A (ko) * | 2021-10-25 | 2024-06-24 | 닛토덴코 가부시키가이샤 | 점착제 조성물, 점착제, 점착 시트 및 표면 보호 필름 |
JP7131723B1 (ja) | 2022-01-26 | 2022-09-06 | 東洋インキScホールディングス株式会社 | 粘着剤組成物及び粘着シート |
CN115873169A (zh) * | 2023-01-06 | 2023-03-31 | 中国乐凯集团有限公司 | 丙烯酸酯聚合物、压敏胶粘剂组合物、保护膜和显示器件 |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4871812A (en) * | 1986-11-28 | 1989-10-03 | Minnesota Mining And Manufacturing Company | Moldable medical adhesive |
EP0442983B1 (en) | 1989-08-14 | 1994-04-20 | Avery Dennison Corporation | Emulsion pressure-sensitive adhesive polymers exhibiting excellent room- and low-temperature performance |
JP2955089B2 (ja) | 1991-11-19 | 1999-10-04 | 日東電工株式会社 | 静電気発生の少ない表面保護粘着テープ又はシート |
US5670557A (en) * | 1994-01-28 | 1997-09-23 | Minnesota Mining And Manufacturing Company | Polymerized microemulsion pressure sensitive adhesive compositions and methods of preparing and using same |
JPH08143842A (ja) | 1994-11-18 | 1996-06-04 | Nitto Denko Corp | 再剥離型感圧接着剤とその接着シ―ト類 |
JPH08186658A (ja) | 1994-12-28 | 1996-07-16 | Nec Corp | 情報ターミナル |
JPH08269431A (ja) | 1995-03-31 | 1996-10-15 | Mitsubishi Chem Basf Co Ltd | 粘着剤組成物 |
JP4824154B2 (ja) * | 2000-05-16 | 2011-11-30 | 日東電工株式会社 | 粘着剤及びその粘着剤を用いた光学部材用表面保護フィルム |
JP2001323238A (ja) | 2000-05-16 | 2001-11-22 | Nitto Denko Corp | 光学部材用粘着剤 |
US7169846B2 (en) * | 2001-07-13 | 2007-01-30 | Cytec Surface Specialties, Inc. | Process for improving water-whitening resistance of pressure sensitive adhesives |
DE10221093A1 (de) * | 2002-05-11 | 2003-11-20 | Tesa Ag | Verwendung von Makromonomeren für die Herstellung von Acrylathaftklebemassen |
DE10256511A1 (de) * | 2002-12-04 | 2004-06-24 | Tesa Ag | Haftklebemasse |
US20050142318A1 (en) * | 2003-12-25 | 2005-06-30 | Lintec Corporation | Pressure sensitive adhesive sheet, a multilayer structured article for photorecording media having the sheet and multilayer photorecording medium having the article |
JP5422091B2 (ja) * | 2003-12-26 | 2014-02-19 | 東洋インキScホールディングス株式会社 | 帯電防止アクリル粘着剤 |
JP2005314579A (ja) * | 2004-04-30 | 2005-11-10 | Nitto Denko Corp | 粘着剤組成物、および粘着シート類 |
TWI387629B (zh) * | 2004-07-26 | 2013-03-01 | Nitto Denko Corp | 壓感黏合劑組成物、壓感黏合片及表面保護膜 |
JP4917267B2 (ja) | 2004-09-16 | 2012-04-18 | 日東電工株式会社 | 粘着剤組成物、粘着シート類、および表面保護フィルム |
NL1028411C2 (nl) * | 2005-02-25 | 2006-08-29 | Nat Starch & Chemical B V | Pressure sensitive kleefmiddelsamenstelling alsmede werkwijzen voor het aanbrengen en de bereiding daarvan. |
KR100838973B1 (ko) | 2005-06-08 | 2008-06-17 | 주식회사 엘지화학 | 아크릴계 점착제 조성물 |
KR100784991B1 (ko) * | 2005-06-10 | 2007-12-11 | 주식회사 엘지화학 | 아크릴계 점착제 조성물 |
JP5259940B2 (ja) * | 2005-09-05 | 2013-08-07 | 日東電工株式会社 | 粘着剤組成物、粘着シートおよび表面保護フィルム |
KR100830814B1 (ko) * | 2005-10-14 | 2008-05-20 | 주식회사 엘지화학 | 아크릴계 점착제 조성물 |
US20070092733A1 (en) * | 2005-10-26 | 2007-04-26 | 3M Innovative Properties Company | Concurrently curable hybrid adhesive composition |
KR200430919Y1 (ko) | 2006-08-23 | 2006-11-13 | 주종경 | 진동감지 레일부착식 도유기 |
US8372492B2 (en) * | 2006-12-15 | 2013-02-12 | Nitto Denko Corporation | Pressure-sensitive adhesive optical film and image display |
KR101047925B1 (ko) * | 2007-04-19 | 2011-07-08 | 주식회사 엘지화학 | 아크릴계 점착제 조성물 및 이를 포함하는 편광판 |
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- 2009-01-13 EP EP09702082.0A patent/EP2231807B1/en active Active
- 2009-01-13 CN CN2009801021445A patent/CN101910346B/zh active Active
- 2009-01-13 WO PCT/KR2009/000178 patent/WO2009091171A2/en active Application Filing
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EP2231807A2 (en) | 2010-09-29 |
US10100234B2 (en) | 2018-10-16 |
EP2231807B1 (en) | 2015-02-18 |
WO2009091171A3 (en) | 2009-10-01 |
TWI379875B (en) | 2012-12-21 |
EP2231807A4 (en) | 2011-12-14 |
KR20090078204A (ko) | 2009-07-17 |
CN101910346A (zh) | 2010-12-08 |
WO2009091171A2 (en) | 2009-07-23 |
TW200948917A (en) | 2009-12-01 |
CN101910346B (zh) | 2013-10-02 |
KR101082450B1 (ko) | 2011-11-11 |
US20110187970A1 (en) | 2011-08-04 |
JP2011511853A (ja) | 2011-04-14 |
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