JP5971498B2 - 偏光板 - Google Patents
偏光板 Download PDFInfo
- Publication number
- JP5971498B2 JP5971498B2 JP2014525946A JP2014525946A JP5971498B2 JP 5971498 B2 JP5971498 B2 JP 5971498B2 JP 2014525946 A JP2014525946 A JP 2014525946A JP 2014525946 A JP2014525946 A JP 2014525946A JP 5971498 B2 JP5971498 B2 JP 5971498B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive layer
- polarizing plate
- pressure
- sensitive adhesive
- weight
- 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.)
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 127
- 150000001875 compounds Chemical class 0.000 claims description 120
- 239000000203 mixture Substances 0.000 claims description 98
- 239000010410 layer Substances 0.000 claims description 93
- 239000000178 monomer Substances 0.000 claims description 77
- 239000004593 Epoxy Substances 0.000 claims description 75
- 230000001070 adhesive effect Effects 0.000 claims description 72
- 239000000853 adhesive Substances 0.000 claims description 70
- 239000012790 adhesive layer Substances 0.000 claims description 44
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 37
- 125000002723 alicyclic group Chemical group 0.000 claims description 29
- 239000011521 glass Substances 0.000 claims description 25
- 229920000058 polyacrylate Polymers 0.000 claims description 24
- 230000001681 protective effect Effects 0.000 claims description 24
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 22
- 239000004973 liquid crystal related substance Substances 0.000 claims description 20
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 18
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 18
- 239000003431 cross linking reagent Substances 0.000 claims description 17
- 230000002209 hydrophobic effect Effects 0.000 claims description 9
- 239000003513 alkali Substances 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000011159 matrix material Substances 0.000 claims description 4
- 239000006096 absorbing agent Substances 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 239000004695 Polyether sulfone Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 230000005684 electric field Effects 0.000 claims description 2
- 229920006289 polycarbonate film Polymers 0.000 claims description 2
- 229920006267 polyester film Polymers 0.000 claims description 2
- 229920006393 polyether sulfone Polymers 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 106
- -1 for example Chemical class 0.000 description 74
- 239000000126 substance Substances 0.000 description 62
- 125000004432 carbon atom Chemical group C* 0.000 description 49
- 125000000217 alkyl group Chemical group 0.000 description 36
- 238000001723 curing Methods 0.000 description 35
- 238000000034 method Methods 0.000 description 28
- 238000006243 chemical reaction Methods 0.000 description 27
- 239000001257 hydrogen Substances 0.000 description 25
- 229910052739 hydrogen Inorganic materials 0.000 description 25
- 239000003999 initiator Substances 0.000 description 23
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 20
- 239000011247 coating layer Substances 0.000 description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 17
- 125000000524 functional group Chemical group 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 16
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- 125000002947 alkylene group Chemical group 0.000 description 15
- 238000004519 manufacturing process Methods 0.000 description 15
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- 238000011156 evaluation Methods 0.000 description 14
- 230000000704 physical effect Effects 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 12
- 150000001768 cations Chemical class 0.000 description 11
- 238000006116 polymerization reaction Methods 0.000 description 10
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- 239000006097 ultraviolet radiation absorber Substances 0.000 description 10
- 125000003118 aryl group Chemical group 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
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- 238000012360 testing method Methods 0.000 description 8
- 125000001118 alkylidene group Chemical group 0.000 description 7
- 230000005540 biological transmission Effects 0.000 description 7
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- 150000003839 salts Chemical class 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000006087 Silane Coupling Agent Substances 0.000 description 6
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
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- 230000001965 increasing effect Effects 0.000 description 6
- 150000002513 isocyanates Chemical class 0.000 description 6
- 239000002356 single layer Substances 0.000 description 6
- 229920002799 BoPET Polymers 0.000 description 5
- 229920002284 Cellulose triacetate Polymers 0.000 description 5
- 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 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 5
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- 125000003700 epoxy group Chemical group 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
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- 229910052751 metal Inorganic materials 0.000 description 5
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- 238000003860 storage Methods 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 4
- 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-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
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- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001334 alicyclic compounds Chemical class 0.000 description 4
- 239000012964 benzotriazole Substances 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 4
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 230000001976 improved effect Effects 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
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- 229920000139 polyethylene terephthalate 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
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 3
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
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- 235000008411 Sumatra benzointree Nutrition 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
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- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229960002130 benzoin Drugs 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
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- 230000008859 change Effects 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
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- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 3
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- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
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- 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 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
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- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 description 2
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- 239000007983 Tris buffer Substances 0.000 description 2
- GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-UHFFFAOYSA-N 0.000 description 2
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- 150000001491 aromatic compounds Chemical class 0.000 description 2
- FFBZKUHRIXKOSY-UHFFFAOYSA-N aziridine-1-carboxamide Chemical compound NC(=O)N1CC1 FFBZKUHRIXKOSY-UHFFFAOYSA-N 0.000 description 2
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- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
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- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
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- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- WREOTYWODABZMH-DTZQCDIJSA-N [[(2r,3s,4r,5r)-3,4-dihydroxy-5-[2-oxo-4-(2-phenylethoxyamino)pyrimidin-1-yl]oxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]1N(C=C\1)C(=O)NC/1=N\OCCC1=CC=CC=C1 WREOTYWODABZMH-DTZQCDIJSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical group CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 238000003483 aging Methods 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 125000005336 allyloxy group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001555 benzenes Chemical class 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
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- ZNAAXKXXDQLJIX-UHFFFAOYSA-N bis(2-cyclohexyl-3-hydroxyphenyl)methanone Chemical compound C1CCCCC1C=1C(O)=CC=CC=1C(=O)C1=CC=CC(O)=C1C1CCCCC1 ZNAAXKXXDQLJIX-UHFFFAOYSA-N 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- QDVNNDYBCWZVTI-UHFFFAOYSA-N bis[4-(ethylamino)phenyl]methanone Chemical compound C1=CC(NCC)=CC=C1C(=O)C1=CC=C(NCC)C=C1 QDVNNDYBCWZVTI-UHFFFAOYSA-N 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125758 compound 15 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical compound C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- OTARVPUIYXHRRB-UHFFFAOYSA-N diethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](C)(OCC)CCCOCC1CO1 OTARVPUIYXHRRB-UHFFFAOYSA-N 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 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 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- DIIUFWYILXGGIL-UHFFFAOYSA-N ethynylcyclohexane Chemical compound [C]#CC1CCCCC1 DIIUFWYILXGGIL-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
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- 238000001879 gelation Methods 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
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- 230000001939 inductive effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 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
- 238000002156 mixing Methods 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000001421 myristyl 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])C([H])([H])[H] 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 229920003986 novolac Polymers 0.000 description 1
- RNVAPPWJCZTWQL-UHFFFAOYSA-N octadecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 RNVAPPWJCZTWQL-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
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- 229960000969 phenyl salicylate Drugs 0.000 description 1
- LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
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- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000379 polypropylene carbonate Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- QROGIFZRVHSFLM-UHFFFAOYSA-N prop-1-enylbenzene Chemical group CC=CC1=CC=CC=C1 QROGIFZRVHSFLM-UHFFFAOYSA-N 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 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
- 238000012546 transfer Methods 0.000 description 1
- IUCJMVBFZDHPDX-UHFFFAOYSA-N tretamine Chemical compound C1CN1C1=NC(N2CC2)=NC(N2CC2)=N1 IUCJMVBFZDHPDX-UHFFFAOYSA-N 0.000 description 1
- 229950001353 tretamine Drugs 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- 239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
- 238000011077 uniformity evaluation Methods 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
- G02F1/133528—Polarisers
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
- G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/03—Viewing layer characterised by chemical composition
- C09K2323/031—Polarizer or dye
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/05—Bonding or intermediate layer characterised by chemical composition, e.g. sealant or spacer
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F2201/00—Constructional arrangements not provided for in groups G02F1/00 - G02F7/00
- G02F2201/50—Protective arrangements
- G02F2201/503—Arrangements improving the resistance to shock
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Nonlinear Science (AREA)
- Mathematical Physics (AREA)
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Polarising Elements (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
Description
上記エポキシ化合物としては、例えば、陽イオン反応によって架橋または重合されることができるものを使用することができる。
また、上記化学式14で、pは、好ましくは、0または1であることができる。
X2−X1>50gf/25mm
アクリル重合体が上記化学式17の単量体を含む場合、その比率は、20重量部以下であることが好ましい。
ゲル含量(重量%)=B/A×100
窒素ガスが還流され、温度調節が容易になるように冷却装置を設置した1L反応器にn−ブチルアクリレート(n−BA)98重量部及び2−ヒドロキシエチルアクリレート(2−HEA)2重量部を投入した。次いで、反応器に溶剤としてエチルアセテート(EAc;ethyl aceate)180重量部を投入し、酸素除去のために窒素ガスを60分間パージング(purging)した。その後、温度を67℃に維持し、反応開始剤であるAIBN(azobisisobutyronitrile)0.05重量部を投入し、8時間反応させた。反応後に、エチルアセテートで希釈し、固形分の濃度が30重量%であり、重量平均分子量が100万であり、分子量分布が4.9であるアクリル重合体(A)を製造した。
アクリル系単量体として、ヒドロキシエチルアクリレート30重量部、フェノキシエチルアクリレート15重量部及びイソボルニルアクリレート9重量部を配合した混合物にさらにエポキシ化合物として、脂環式エポキシ化合物(7−oxabicyclo[4、1、0]hetan−3−ylmethyl 7−oxa−bicyclo[4、1、0]heptane−3−carboxylate、セロキサイド2021P、ダイセル社製)20重量部及びグリシジルエーテルタイプエポキシ化合物(CHDMDG、1、4−cyclohexane dimethanol diglycidyl ether)20重量部を配合した。次いで、上記混合物にラジカル重合開始剤(CGI 819、(2、6−dimethoxybenzoyl)−(2、4、4−trimethylpentyl)phosphoryl]−(2、6−dimethoxyphenyl)methanone)3重量部及び陽イオン開始剤(IHT−PI 45、50wt% mixed triarylsulfonium hexafluorophosphate salt 50wt% propylene carbonate)3重量部を配合し、25℃での粘度が約10cPである接着剤組成物を製造した。
粘着剤層の製造
アクリル重合体(A)100重量部、多官能性架橋剤(TDI系イソシアネート、Coronate L、日本ポリウレタン社製)3重量部、多官能性アクリレート(3官能性ウレタンアクリレート、Aronix M−315、韓国Dong-woo通商製)100重量部、光開始剤(Irg 184、ヒドロキシシクロヘキシルフェニルケトン、スイス国チバスペシャルティケミカルズ製)3重量部、トリアジン系紫外線吸収剤(Tinuvin 400、スイス国チバスペシャルティケミカルズ社製)3重量部及びβ−シアノアセチル基を有するシランカップリング剤(M812、韓国LG化学社製)0.1重量部を固形分の濃度が30重量%になるように溶剤に配合し、粘着剤組成物を製造した。次いで、製造された粘着剤組成物を離型処理されたPET(poly(ethyleneterephthalate))フィルム(厚さ:38μm、MRF−38、三菱社製)の離型処理面に、乾燥後に所定厚さを有するようにコーティングし、110℃のオーブンで3分間乾燥させた。その後、上記乾燥したコーティング層上に離型処理されたPETフィルム(厚さ:38μm、MRF−38、三菱社製)の離型処理面をさらにラミネートし、図3に示された構造の積層体を製造し、高圧水銀ランプを使用して紫外線を照射し、2枚の離型PETフィルム20の間で粘着剤層10を形成した。以下、説明の便宜のために、粘着剤層10で紫外線が照射された側の面を第1表面10Aと言い、その反対面を第2表面10Bと言う。
〈UV照射条件〉
照度:250mW/cm2
光量:300mJ/cm2
ポリビニルアルコール系樹脂フィルムを延伸し、ヨードで染色した後、ホウ酸(boric acid)水溶液で処理して製造された偏光子の一面に保護フィルムとしてアクリルフィルム(フェノキシ樹脂、ポリスチレン及びポリメチルメタクリレートを含む混合物を押出及び延伸して製造されたフィルム)を上記製造された接着剤組成物でラミネートした。次いで、上記ポリビニルアルコール系偏光子において保護フィルムが付着されない面に上記製造された接着剤組成物を使用して上記製造された粘着剤層をラミネートし、偏光板を製造した。具体的には、まず、偏光子に上記接着剤組成物を硬化後に約5μmの厚さを有するように塗布し、その塗布面に上記粘着剤層の第1表面10Aをラミネートした後、下記条件で紫外線を照射して硬化させて、偏光板を製造した。
〈UV照射条件〉
紫外線照射器:高圧水銀ランプ
照射条件:
照度:800mW/cm2
光量:2000mJ/cm2
粘着剤組成物の組成を下記表1のように変更したことを除いて、実施例1と同一の方式で偏光板を製造した。
保護フィルムとして、アクリルフィルムの代わりに、厚さが60μmのTACフィルムを使用し、上記TACフィルムを偏光子に付着する接着剤として保護フィルムの付着に一般的に使用される水系ポリビニルアルコール系接着剤組成物を乾燥後の厚さが0.1μmになるように塗布して使用し、また、上記水系ポリビニルアルコール系接着剤組成物を塗布し、保護フィルムをラミネートした後、80度のオーブンで5分間乾燥した後、上記水系ポリビニルアルコール系接着剤組成物を使用して粘着剤層をラミネートしたことを除いて、実施例1と同一の方式で偏光板を製造した。
1.引張弾性率の評価
本明細書で粘着剤層の引張弾性率は、ASTM D638で規定された方式に従って引張による応力−変形試験法を通じて測定するか、あるいは、直接引張弾性率を測定しにくい場合には、貯蔵弾性率を測定し、下記換算式によって換算して求める。具体的には、実施例または比較例で製造される粘着剤層を含むものとして、図3に示された構造の積層体(離型PETフィルム、粘着剤層及び離型PETフィルムの積層構造)を長さが7cmであり、幅が1cmになるサイズのdog bone typeの試験片に切断し、試験片の両末端を引張実験用ジグで固定した後、引張弾性率を測定する。引張弾性率の測定条件は、下記の通りである。
〈引張弾性率の測定条件〉
測定機器:UTM(Universal Testing Machine)
装備Model:Zwick Roell Z010、Instron社製
測定条件:
Load cell:500N
引張速度:3mm/sec
粘着剤層を15cm×25cm×25μmm(横×縦×厚さ)のサイズに切断し、切断された粘着剤層を5層で積層させる。次いで、積層された粘着剤層を直径が8mmの円形に切断した後、ガラス(glass)を利用して、圧縮した状態で、一晩放置し、各層間の界面での濡れ性(wetting)を向上させることによって、積層時に生じた気泡を除去し、試料を製造する。次いで、試料をパラレルプレート(parallel plate)上に載置し、ギャップ(gap)を調整した後、Normal & Torqueの零点を合わせて、Normal forceの安定化を確認した後、下記条件で貯蔵弾性率を測定し、下記換算式によって引張弾性率を求める。
測定機器:ARES−RDA、TA Instruments Inc. with forced convection oven
測定条件:
geometry:8mm parallel plate
gap:around 1mm
test type:dynamic strain frequency sweep
strain=10.0[%]、temperature:30℃
initial frequency:0.4rad/s、final frequency:100rad/s
E=3G
実施例または比較例で製造された粘着剤層を使用して、実施例1と同一の方式で偏光板を製造し、且つ剥離力を測定しようとする粘着剤層の表面に沿って粘着剤層の方向を変更して偏光板を製造する。すなわち、実施例1で提示された偏光板の製造過程で第1表面の剥離力を測定しようとする場合、第2表面を偏光子側に付着し、第2表面の剥離力を測定しようとする場合、第1表面を偏光子側に付着して偏光板を製造する。その後、偏光板を25mm×100mm(幅×長さ)のサイズに切断し、試験片を製造する。次いで、粘着剤層上に付着された離型PETフィルムを剥離し、粘着剤層の表面をJIS Z 0237の規定によって2kgのローラーを使用して無アルカリガラスに付着する。次いで、粘着剤層が付着された無アルカリガラスをオートクレーブ(50℃、0.5気圧)で約20分間圧着処理し、恒温恒湿条件(23℃、50%相対湿度)で25時間保管する。その後、TA装備(Texture Analyzer、英国ステイブルマイクロシステム社製)を使用して、上記偏光板を無アルカリガラスから300mm/minの剥離速度及び180度の剥離角度で剥離しながら剥離力を測定する。また、再剥離性は、下記基準に基づいて評価する。
〈再剥離性評価基準〉
○:付着1日後に測定した剥離力が800N/25mm以下の場合
△:付着1日後に測定した剥離力が1,000N/25mm以上の場合
×:付着1日後に測定した剥離力が2,000N/25mm以上の場合
実施例及び比較例で製造された偏光板を90mm×170mm(横×縦)サイズに切断して製造される試験片をそれぞれ実施例及び比較例ごとに2枚ずつ準備した。次いで、用意した2枚の試験片をガラス基板(110mm×190mm×0.7mm=横×縦×厚さ)の両面に各偏光板の光学吸収軸がクロスされるように付着し、サンプルを製造した。上記付着時に加えられた圧力は、約5Kg/cm2であり、気泡または異物が界面に発生しないようにクリーンルーム(Clean room)で作業を行った。その後、耐湿耐久性は、サンプルを60℃の温度及び90%の相対湿度の条件下で1,000時間放置した後、粘着界面での気泡または剥離の発生可否を観察して評価し、耐熱耐久性は、80℃の温度条件の下で1,000時間サンプルを放置した後、粘着界面での気泡または剥離の発生有無を観察して評価した。耐湿熱または耐熱耐久性の測定直前に製造されたサンプルを常温で24時間放置し、評価を進行した。評価条件は、下記の通りである。
〈耐久性評価基準〉
○:気泡及び剥離発生なし
△:気泡及び/または剥離が少し発生
×:気泡及び/または剥離が多量発生
実施例及び比較例で製造された偏光板を90mm×170mm(横×縦)のサイズに切断した試験片をガラス基板(110mm×190mm×0.7mm=横×縦×厚さ)の片面に付着し、サンプルを製造した。付着時に加えられた圧力は、約5Kg/cm2であり、気泡または異物が界面に発生しないようにクリーンルームで作業を行った。次いで、製造されたサンプルを60℃の温度に水に投入し、24時間放置した後、取り出して、気泡または剥離の発生有無を観察し、下記基準に基づいて耐水性を評価した。
〈耐水性評価基準〉
○:気泡及び剥離発生なし
△:気泡及び/または剥離が少し発生
×:気泡及び/または剥離が多量発生
実施例及び比較例で製造した偏光板を22インチLCDモニター(LG Philips LCD社製)の両面に光学吸収軸が互いにクロスされた状態で付着し、恒温恒湿条件(23℃、50%相対湿度)で24時間保管した後、80℃の温度で200時間放置した。その後、暗室でバックライトを利用して上記モニターに光を照射しながら、光透過性の均一性を下記の基準に基づいて評価した。
〈光透過均一性評価基準〉
◎:モニターの4周辺部で光透過性の不均一現象が目視で判断されない場合
○:モニターの4周辺部で光透過性の不均一現象が目視で少し観察される場合
△:モニターの4周辺部で光透過性の不均一現象が目視で多少観察される場合
×:モニターの4周辺部で光透過性の不均一現象が目視で多量観察される場合
アクリル重合体の重量平均分子量及び分子量分布は、GPCを使用して、以下の条件で測定した。検量線の製作には、Agilent systemの標準ポリスチレンを使用して、測定結果を換算した。
〈重量平均分子量測定条件〉
測定器:Agilent GPC(Agilent 1200 series、米国)
カラム:PL Mixed B 2個連結
カラム温度:40℃
溶離液:テトラヒドロフラン
流速:1.0mL/min
濃度:〜2mg/mL(100μL injection)
カール特性は、偏光板の製造過程で130mm×180mm(横(TD(transverse direction)方向)×縦(MD方向))のサイズに切断した保護フィルムと偏光子を接着剤組成物を使用してラミネーションし、紫外線の照射過程または水系ポリビニルアルコール系接着剤が使用された場合には、乾燥過程でTD方向に発生するカールを測定し、下記基準に基づいて評価する。上記で、カールの測定は、図4に示されたような方式で行う。
〈評価基準〉
○:TD方向へのカールが0.5cm未満の場合
△:TD方向へのカールが0.5cm〜2.0cmの場合
×:TD方向へのカールが2.0cmを超過する場合
11 偏光子
10、12 接着剤層
13 粘着剤層
10A 第1表面
10B 第2表面
Claims (17)
- 順次配置された偏光子と;活性エネルギー線硬化型接着剤層と;第1表面及び第2表面を有する単一層の粘着剤層と;を含み、
偏光子の粘着剤層が付着された面の反対面に、接着剤層によって付着された保護フィルムであって、ただし、保護フィルムが接着性を有する場合が除外される、保護フィルムをさらに含み、
粘着剤層が、多官能性架橋剤によって架橋されたアクリル重合体を含む架橋構造、光重合性化合物を含む架橋構造、及び、上記光重合性化合物100重量部に対して0.1重量部〜5重量部の紫外線吸収剤を含み、
上記第1表面の無アルカリガラスに対する剥離力と上記第2表面の無アルカリガラスに対する剥離力の差が下記一般式1を満たし、第1表面の無アルカリガラスに対する剥離力が5gf/25mm〜100gf/25mmであり、第2表面の無アルカリガラスに対する剥離力が100gf/25mm〜1,000gf/25mmであり、
偏光子は、少なくとも一面に上記接着剤層が直接付着されており、上記粘着剤層の第1表面は、上記接着剤層に直接付着されている、偏光板:
[一般式1]
X2−X1>50gf/25mm
上記一般式1で、上記X1は、第1表面の無アルカリガラスに対する剥離力を示し、上記X2は、第2表面の無アルカリガラスに対する剥離力を示す。 - 偏光子は、ポリビニルアルコール系偏光子である、請求項1に記載の偏光板。
- 粘着剤層は、第1表面から第2表面方向に厚さ方向に沿って引張弾性率の勾配が形成されている、請求項1に記載の偏光板。
- 粘着剤層は、25℃での平均引張弾性率が0.1MPa〜500MPaである、請求項3に記載の偏光板。
- 接着剤層は、エポキシ化合物及び/またはアクリル系単量体を含む接着剤組成物を硬化した状態で含む、請求項1に記載の偏光板。
- エポキシ化合物は、脂環式エポキシ化合物及び/またはグリシジルエーテルタイプエポキシ化合物を含む、請求項5に記載の偏光板。
- エポキシ化合物は、重量平均分子量が1000〜5000である、請求項5に記載の偏光板。
- アクリル系単量体は、親水性アクリル系単量体または疎水性アクリル系単量体を含む、請求項5に記載の偏光板。
- 親水性アクリル系単量体は、ヒドロキシ基、カルボキシル基またはアルコキシ基を有する、請求項8に記載の偏光板。
- 接着剤組成物は、反応性オリゴマー1〜40重量部をさらに含む、請求項5に記載の偏光板。
- 接着剤組成物は、無溶剤タイプである、請求項5に記載の偏光板。
- 接着剤組成物は、25℃での粘度が5cps〜1,000cpsである、請求項5に記載の偏光板。
- 保護フィルムは、セルロースフィルム;ポリエステルフィルム;ポリカーボネートフィルム;ポリエーテルスルホンフィルム;アクリルフィルム;またはポリオレフィンフィルムである、請求項1に記載の偏光板。
- 反射防止層、防眩層、位相差板、広視野角補償フィルム及び輝度向上層よりなる群から選択された1つ以上の層をさらに含む、請求項1に記載の偏光板。
- 液晶パネルと;上記液晶パネルの一面または両面に付着されている請求項1に記載の偏光板と;を含む液晶表示装置。
- 上記液晶パネルが前記粘着剤層の前記第2表面に付着されている、請求項15に記載の液晶表示装置。
- 液晶パネルが、パッシブマトリクス方式のパネルと;アクティブマトリクス方式のパネルと;横電界型パネルまたは垂直配向型パネルである、請求項15に記載の液晶表示装置。
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