JP5530470B2 - 偏光板用接着剤 - Google Patents
偏光板用接着剤 Download PDFInfo
- Publication number
- JP5530470B2 JP5530470B2 JP2012053615A JP2012053615A JP5530470B2 JP 5530470 B2 JP5530470 B2 JP 5530470B2 JP 2012053615 A JP2012053615 A JP 2012053615A JP 2012053615 A JP2012053615 A JP 2012053615A JP 5530470 B2 JP5530470 B2 JP 5530470B2
- Authority
- JP
- Japan
- Prior art keywords
- mass
- parts
- polymerizable monomer
- meth
- adhesive composition
- 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
Links
- 239000000853 adhesive Substances 0.000 title claims description 74
- 230000001070 adhesive effect Effects 0.000 title claims description 72
- 239000000178 monomer Substances 0.000 claims description 72
- -1 methacryloyl group Chemical group 0.000 claims description 53
- 239000000203 mixture Substances 0.000 claims description 53
- 125000002091 cationic group Chemical group 0.000 claims description 36
- 230000001681 protective effect Effects 0.000 claims description 36
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims description 21
- 239000007870 radical polymerization initiator Substances 0.000 claims description 16
- 238000010538 cationic polymerization reaction Methods 0.000 claims description 13
- 239000003504 photosensitizing agent Substances 0.000 claims description 12
- 239000003505 polymerization initiator Substances 0.000 claims description 12
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical group C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 7
- 125000003700 epoxy group Chemical group 0.000 claims description 7
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims description 5
- 125000003566 oxetanyl group Chemical group 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 claims description 3
- 150000008065 acid anhydrides Chemical class 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 41
- 150000003254 radicals Chemical class 0.000 description 30
- 238000012360 testing method Methods 0.000 description 30
- 229920005989 resin Polymers 0.000 description 27
- 239000011347 resin Substances 0.000 description 27
- 150000001875 compounds Chemical class 0.000 description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 17
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 230000005764 inhibitory process Effects 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 12
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 11
- 239000000126 substance Substances 0.000 description 10
- 239000004372 Polyvinyl alcohol Substances 0.000 description 9
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 9
- 229920002451 polyvinyl alcohol Polymers 0.000 description 9
- 229920002284 Cellulose triacetate Polymers 0.000 description 8
- 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 8
- 238000003851 corona treatment Methods 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 8
- 230000000670 limiting effect Effects 0.000 description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 7
- 230000035939 shock Effects 0.000 description 7
- 102100033806 Alpha-protein kinase 3 Human genes 0.000 description 6
- 101710082399 Alpha-protein kinase 3 Proteins 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 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 6
- 208000028659 discharge Diseases 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 5
- 239000012790 adhesive layer Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- 238000004043 dyeing Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229910052740 iodine Inorganic materials 0.000 description 5
- 239000011630 iodine Substances 0.000 description 5
- 239000004973 liquid crystal related substance Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 5
- 229910052753 mercury Inorganic materials 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000002834 transmittance Methods 0.000 description 5
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 4
- 229920002799 BoPET Polymers 0.000 description 4
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 4
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 4
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 3
- RBHIUNHSNSQJNG-UHFFFAOYSA-N 6-methyl-3-(2-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane Chemical compound C1CC2(C)OC2CC1C1(C)CO1 RBHIUNHSNSQJNG-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- 150000004056 anthraquinones Chemical class 0.000 description 3
- 239000012965 benzophenone Substances 0.000 description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 239000012461 cellulose resin Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- SKYXLDSRLNRAPS-UHFFFAOYSA-N 1,2,4-trifluoro-5-methoxybenzene Chemical compound COC1=CC(F)=C(F)C=C1F SKYXLDSRLNRAPS-UHFFFAOYSA-N 0.000 description 2
- CYIGRWUIQAVBFG-UHFFFAOYSA-N 1,2-bis(2-ethenoxyethoxy)ethane Chemical compound C=COCCOCCOCCOC=C CYIGRWUIQAVBFG-UHFFFAOYSA-N 0.000 description 2
- XUVKSPPGPPFPQN-UHFFFAOYSA-N 10-Methyl-9(10H)-acridone Chemical compound C1=CC=C2N(C)C3=CC=CC=C3C(=O)C2=C1 XUVKSPPGPPFPQN-UHFFFAOYSA-N 0.000 description 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-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
- LJWZDTGRJUXOCE-UHFFFAOYSA-N 2-(2-ethylhexyl)oxetane Chemical compound CCCCC(CC)CC1CCO1 LJWZDTGRJUXOCE-UHFFFAOYSA-N 0.000 description 2
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 description 2
- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 description 2
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- XAYDWGMOPRHLEP-UHFFFAOYSA-N 6-ethenyl-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCCC2OC21C=C XAYDWGMOPRHLEP-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 229920001747 Cellulose diacetate Polymers 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 208000034189 Sclerosis Diseases 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- 150000008062 acetophenones Chemical class 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 150000002366 halogen compounds Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 229940077844 iodine / potassium iodide Drugs 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- 125000006839 xylylene group Chemical group 0.000 description 2
- 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 1
- VLTYTTRXESKBKI-UHFFFAOYSA-N (2,4-dichlorophenyl)-phenylmethanone Chemical compound ClC1=CC(Cl)=CC=C1C(=O)C1=CC=CC=C1 VLTYTTRXESKBKI-UHFFFAOYSA-N 0.000 description 1
- UNMJLQGKEDTEKJ-UHFFFAOYSA-N (3-ethyloxetan-3-yl)methanol Chemical compound CCC1(CO)COC1 UNMJLQGKEDTEKJ-UHFFFAOYSA-N 0.000 description 1
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- JWTGRKUQJXIWCV-UHFFFAOYSA-N 1,2,3-trihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(O)C(O)CO JWTGRKUQJXIWCV-UHFFFAOYSA-N 0.000 description 1
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- QWQFVUQPHUKAMY-UHFFFAOYSA-N 1,2-diphenyl-2-propoxyethanone Chemical compound C=1C=CC=CC=1C(OCCC)C(=O)C1=CC=CC=C1 QWQFVUQPHUKAMY-UHFFFAOYSA-N 0.000 description 1
- DQNSRQYYCSXZDF-UHFFFAOYSA-N 1,4-bis(ethenoxymethyl)cyclohexane Chemical compound C=COCC1CCC(COC=C)CC1 DQNSRQYYCSXZDF-UHFFFAOYSA-N 0.000 description 1
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-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
- SAMJGBVVQUEMGC-UHFFFAOYSA-N 1-ethenoxy-2-(2-ethenoxyethoxy)ethane Chemical compound C=COCCOCCOC=C SAMJGBVVQUEMGC-UHFFFAOYSA-N 0.000 description 1
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 description 1
- QFDDZIRGHKFRMR-UHFFFAOYSA-N 10-butylacridin-9-one Chemical compound C1=CC=C2N(CCCC)C3=CC=CC=C3C(=O)C2=C1 QFDDZIRGHKFRMR-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
- IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 description 1
- RNIPJYFZGXJSDD-UHFFFAOYSA-N 2,4,5-triphenyl-1h-imidazole Chemical class C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 RNIPJYFZGXJSDD-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- WVXLLHWEQSZBLW-UHFFFAOYSA-N 2-(4-acetyl-2-methoxyphenoxy)acetic acid Chemical compound COC1=CC(C(C)=O)=CC=C1OCC(O)=O WVXLLHWEQSZBLW-UHFFFAOYSA-N 0.000 description 1
- SFRDXVJWXWOTEW-UHFFFAOYSA-N 2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)CO SFRDXVJWXWOTEW-UHFFFAOYSA-N 0.000 description 1
- FPKCTSIVDAWGFA-UHFFFAOYSA-N 2-chloroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3C(=O)C2=C1 FPKCTSIVDAWGFA-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-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
- 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
- CBECDWUDYQOTSW-UHFFFAOYSA-N 2-ethylbut-3-enal Chemical compound CCC(C=C)C=O CBECDWUDYQOTSW-UHFFFAOYSA-N 0.000 description 1
- GDHROTCPZLVPJT-UHFFFAOYSA-N 2-ethyloxetane Chemical compound CCC1CCO1 GDHROTCPZLVPJT-UHFFFAOYSA-N 0.000 description 1
- QPXVRLXJHPTCPW-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-(4-propan-2-ylphenyl)propan-1-one Chemical compound CC(C)C1=CC=C(C(=O)C(C)(C)O)C=C1 QPXVRLXJHPTCPW-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- 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
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 1
- NJWGQARXZDRHCD-UHFFFAOYSA-N 2-methylanthraquinone Chemical class C1=CC=C2C(=O)C3=CC(C)=CC=C3C(=O)C2=C1 NJWGQARXZDRHCD-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- WGKYSFRFMQHMOF-UHFFFAOYSA-N 3-bromo-5-methylpyridine-2-carbonitrile Chemical compound CC1=CN=C(C#N)C(Br)=C1 WGKYSFRFMQHMOF-UHFFFAOYSA-N 0.000 description 1
- CXJAFLQWMOMYOW-UHFFFAOYSA-N 3-chlorofuran-2,5-dione Chemical compound ClC1=CC(=O)OC1=O CXJAFLQWMOMYOW-UHFFFAOYSA-N 0.000 description 1
- BIDWUUDRRVHZLQ-UHFFFAOYSA-N 3-ethyl-3-(2-ethylhexoxymethyl)oxetane Chemical compound CCCCC(CC)COCC1(CC)COC1 BIDWUUDRRVHZLQ-UHFFFAOYSA-N 0.000 description 1
- FNYWFRSQRHGKJT-UHFFFAOYSA-N 3-ethyl-3-[(3-ethyloxetan-3-yl)methoxymethyl]oxetane Chemical compound C1OCC1(CC)COCC1(CC)COC1 FNYWFRSQRHGKJT-UHFFFAOYSA-N 0.000 description 1
- FHFOJGCIXOUQMZ-UHFFFAOYSA-N 3-ethyl-3-[[3-[(3-ethyloxetan-3-yl)methoxy]phenoxy]methyl]oxetane Chemical compound C=1C=CC(OCC2(CC)COC2)=CC=1OCC1(CC)COC1 FHFOJGCIXOUQMZ-UHFFFAOYSA-N 0.000 description 1
- AXGOOCLYBPQWNG-UHFFFAOYSA-N 3-ethylfuran-2,5-dione Chemical compound CCC1=CC(=O)OC1=O AXGOOCLYBPQWNG-UHFFFAOYSA-N 0.000 description 1
- FMEYPAIIOVKZRA-UHFFFAOYSA-N 3-ethylideneoxolane-2,5-dione Chemical compound CC=C1CC(=O)OC1=O FMEYPAIIOVKZRA-UHFFFAOYSA-N 0.000 description 1
- CGRJJOYCFCCGPX-UHFFFAOYSA-N 3-ethyloxetane Chemical compound CCC1COC1 CGRJJOYCFCCGPX-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- XSTITJMSUGCZDH-UHFFFAOYSA-N 4-(4-hydroxy-2,6-dimethylphenyl)-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1C1=C(C)C=C(O)C=C1C XSTITJMSUGCZDH-UHFFFAOYSA-N 0.000 description 1
- DGUJJOYLOCXENZ-UHFFFAOYSA-N 4-[2-[4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenol Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C1=CC=C(O)C=C1 DGUJJOYLOCXENZ-UHFFFAOYSA-N 0.000 description 1
- UGVRJVHOJNYEHR-UHFFFAOYSA-N 4-chlorobenzophenone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1=CC=CC=C1 UGVRJVHOJNYEHR-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 1
- YHTLGFCVBKENTE-UHFFFAOYSA-N 4-methyloxan-2-one Chemical compound CC1CCOC(=O)C1 YHTLGFCVBKENTE-UHFFFAOYSA-N 0.000 description 1
- IKVYHNPVKUNCJM-UHFFFAOYSA-N 4-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(C(C)C)=CC=C2 IKVYHNPVKUNCJM-UHFFFAOYSA-N 0.000 description 1
- OECTYKWYRCHAKR-UHFFFAOYSA-N 4-vinylcyclohexene dioxide Chemical compound C1OC1C1CC2OC2CC1 OECTYKWYRCHAKR-UHFFFAOYSA-N 0.000 description 1
- YXALYBMHAYZKAP-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCC1CC2OC2CC1 YXALYBMHAYZKAP-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-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
- 229930185605 Bisphenol Natural products 0.000 description 1
- DQXLKPYPPWESQM-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)C1=C(C(=O)OC)C=CC=C1.C(C1=CC=CC=C1)(=O)C1=CC=CC=C1 Chemical class C(C1=CC=CC=C1)(=O)C1=C(C(=O)OC)C=CC=C1.C(C1=CC=CC=C1)(=O)C1=CC=CC=C1 DQXLKPYPPWESQM-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- UAKWLVYMKBWHMX-UHFFFAOYSA-N SU4312 Chemical compound C1=CC(N(C)C)=CC=C1C=C1C2=CC=CC=C2NC1=O UAKWLVYMKBWHMX-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 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
- 125000004036 acetal group Chemical group 0.000 description 1
- FZEYVTFCMJSGMP-UHFFFAOYSA-N acridone Chemical class C1=CC=C2C(=O)C3=CC=CC=C3NC2=C1 FZEYVTFCMJSGMP-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- RRFQCEWDBIZSDW-UHFFFAOYSA-N benzenediazonium fluoro(dioxido)borane Chemical compound [O-]B([O-])F.[O-]B([O-])F.[O-]B([O-])F.[O-]B([O-])F.[O-]B([O-])F.[O-]B([O-])F.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1.N#[N+]C1=CC=CC=C1 RRFQCEWDBIZSDW-UHFFFAOYSA-N 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- GLROGUSVUGSGPO-UHFFFAOYSA-N bis(3-methyl-7-oxabicyclo[4.1.0]heptan-4-yl) hexanedioate Chemical compound C1C2OC2CC(C)C1OC(=O)CCCCC(=O)OC1CC2OC2CC1C GLROGUSVUGSGPO-UHFFFAOYSA-N 0.000 description 1
- ZLSMCQSGRWNEGX-UHFFFAOYSA-N bis(4-aminophenyl)methanone Chemical compound C1=CC(N)=CC=C1C(=O)C1=CC=C(N)C=C1 ZLSMCQSGRWNEGX-UHFFFAOYSA-N 0.000 description 1
- UUJZSXVOPPFFOT-UHFFFAOYSA-N bis(4-methylphenyl)-(9-oxo-7-propan-2-ylthioxanthen-2-yl)sulfanium Chemical compound C1=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=CC=C1[S+](C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 UUJZSXVOPPFFOT-UHFFFAOYSA-N 0.000 description 1
- VYHBFRJRBHMIQZ-UHFFFAOYSA-N bis[4-(diethylamino)phenyl]methanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1 VYHBFRJRBHMIQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002981 blocking agent Substances 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
- 229930006711 bornane-2,3-dione Natural products 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 150000004775 coumarins Chemical class 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical group 0.000 description 1
- 150000004294 cyclic thioethers 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
- XOSYHSRXLVMOBA-UHFFFAOYSA-N cyclopenta-1,3-diene;phenol Chemical compound C1C=CC=C1.C1C=CC=C1.OC1=CC=CC=C1 XOSYHSRXLVMOBA-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 1
- WAZPATOMLZGRAY-UHFFFAOYSA-K diphenyl-(4-phenylsulfanylphenyl)sulfanium phosphate Chemical compound [O-]P([O-])([O-])=O.S(c1ccccc1)c1ccc(cc1)[S+](c1ccccc1)c1ccccc1.S(c1ccccc1)c1ccc(cc1)[S+](c1ccccc1)c1ccccc1.S(c1ccccc1)c1ccc(cc1)[S+](c1ccccc1)c1ccccc1 WAZPATOMLZGRAY-UHFFFAOYSA-K 0.000 description 1
- OZLBDYMWFAHSOQ-UHFFFAOYSA-N diphenyliodanium Chemical compound C=1C=CC=CC=1[I+]C1=CC=CC=C1 OZLBDYMWFAHSOQ-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 150000002019 disulfides 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
- 238000001035 drying Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- WGXGKXTZIQFQFO-CMDGGOBGSA-N ethenyl (e)-3-phenylprop-2-enoate Chemical compound C=COC(=O)\C=C\C1=CC=CC=C1 WGXGKXTZIQFQFO-CMDGGOBGSA-N 0.000 description 1
- YCUBDDIKWLELPD-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=C YCUBDDIKWLELPD-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- MDQRDWAGHRLBPA-UHFFFAOYSA-N fluoroamine Chemical class FN MDQRDWAGHRLBPA-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910021432 inorganic complex Inorganic materials 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000000686 lactone group Chemical group 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- FSPSELPMWGWDRY-UHFFFAOYSA-N m-Methylacetophenone Chemical compound CC(=O)C1=CC=CC(C)=C1 FSPSELPMWGWDRY-UHFFFAOYSA-N 0.000 description 1
- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- UUORTJUPDJJXST-UHFFFAOYSA-N n-(2-hydroxyethyl)prop-2-enamide Chemical compound OCCNC(=O)C=C UUORTJUPDJJXST-UHFFFAOYSA-N 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
- JTHNLKXLWOXOQK-UHFFFAOYSA-N n-propyl vinyl ketone Natural products CCCC(=O)C=C JTHNLKXLWOXOQK-UHFFFAOYSA-N 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N p-hydroxyphenylamine Natural products NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 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
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- XBFJAVXCNXDMBH-UHFFFAOYSA-N tetracyclo[6.2.1.1(3,6).0(2,7)]dodec-4-ene Chemical compound C1C(C23)C=CC1C3C1CC2CC1 XBFJAVXCNXDMBH-UHFFFAOYSA-N 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical class C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical compound CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- MKOBNHWWZPEDQJ-UHFFFAOYSA-N trifluoro(methanidylsulfonyl)methane Chemical compound [CH2-]S(=O)(=O)C(F)(F)F MKOBNHWWZPEDQJ-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- WLOQLWBIJZDHET-UHFFFAOYSA-N triphenylsulfonium Chemical compound C1=CC=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 WLOQLWBIJZDHET-UHFFFAOYSA-N 0.000 description 1
- 239000012953 triphenylsulfonium Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229960000834 vinyl ether Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/14—Protective coatings, e.g. hard coatings
-
- 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
-
- 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
- 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
- G02B5/3041—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 comprising multiple thin layers, e.g. multilayer stacks
- G02B5/305—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 comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/318—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
-
- G02B1/105—
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
- Y10T428/31515—As intermediate layer
Description
さらに、単官能ラジカル重合性化合物を主として含むラジカル重合性化合物と、(メタ)アクリロイル基を含有しないカチオン重合性化合物を主として含むカチオン重合性化合物とからなる主剤と、光ラジカル重合開始剤と、光カチオン重合開始剤とを含む光硬化性接着剤が知られている(下記特許文献3参照)。特許文献3には、当該接着剤が、保護フィルムと偏光子との接着性のみならず、打ち抜き加工性および耐水性に優れることが記載されている。
(B)カチオン重合性単量体60.9〜20.0質量部と、
(C)不飽和ジカルボン酸無水物0.2〜13質量部と、
ただし、前記(A)、(B)および(C)の合計は100質量部であり、
(D)ラジカル重合開始剤0.5〜5質量部および光増感剤0.1〜5質量部の少なくとも一方と、
(E)カチオン重合開始剤0.5〜5質量部と、
を含む偏光板用接着剤組成物を含む偏光板用接着剤組成物である。
本発明の第一の態様は、(A)ラジカル重合性単量体26.1〜79.8質量部と、(B)カチオン重合性単量体60.9〜20.0質量部と、(C)不飽和ジカルボン酸無水物0.2〜13質量部と、ただし、前記(A)、(B)および(C)の合計は100質量部であり、(D)ラジカル重合開始剤0.5〜5質量部および光増感剤0.1〜5質量部の少なくとも一方と、(E)カチオン重合開始剤0.5〜5質量部と、を含む偏光板用接着剤組成物である。
ラジカル重合性単量体としては、ラジカル重合性を示すものであれば特に制限なく使用できる。典型的には、アリル基、ビニル基、アクリロイル基、メタクリロイル基、マレイミド基、(メタ)アクリルアミド基等を有する単量体を挙げることができ、(メタ)アクリル酸およびその誘導体、スチレンおよびその誘導体、(メタ)アクリロニトリル、(メタ)アクリルアミドおよびその誘導体、マレイミドおよびその誘導体、およびビニルエステル類などが挙げられる。このうち、特にアクリロイル基、メタクリロイル基、ビニル基、およびアリル基を有する単量体が好ましい。これらの単量体は、単独でも、二種以上を用いてもよい。
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、n−ブチル(メタ)アクリレート、イソブチル(メタ)アクリレート、tert−ブチル(メタ)アクリレート、(メタ)アクリレート、シクロヘキシル(メタ)アクリレート、2−エチルヘキシル(メタ)アクリレート、ラウリル(メタ)アクリレート、(メタ)アクリレート、2−メトキシエチル(メタ)アクリレート、(メタ)アクリレート、2−ヒドロキシエチル(メタ)アクリレート、2−ヒドロキシプロピル(メタ)アクリレート、2−ヒドロキシブチル(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、グリセロールモノ(メタ)アクリレート、3−クロロ−2−ヒドロキシプロピル(メタ)アクリレート、2−ヒドロキシ−3−フェノキシプロピル(メタ)アクリレート、エチレングリコールジ(メタ)アクリレート、ジエチレングリコールジ(メタ)アクリレート、トリエチレングリコールジ(メタ)アクリレート、ブチレングリコールジ(メタ)アクリレート、ノナエチレングリコールジ(メタ)アクリレート、ポリプロピレングリコールジ(メタ)アクリレート、ジプロピレングリコールジ(メタ)アクリレート、ネオペンチルグリコールジ(メタ)アクリレート、1,3−ブタンジオールジ(メタ)アクリレート、1,4−ブタンジオールジ(メタ)アクリレート、1.6−ヘキサンジオールジ(メタ)アクリレート、トリメチロールプロパントリ(メタ)アクリレート、ネオペンチルグリコールジ(メタ)アクリレート、ペンタエリスリトールトリ(メタ)アクリレート、トリメチロールメタントリ(メタ)アクリレート、イソボルニル(メタ)アクリレート、N−ビニルピロリドン、アクリロイルモルフォリン、ウレタン(メタ)アクリレート、テトラヒドロフルフリル(メタ)アクリレート、テトラヒドロフルフリルアルコールのモノε−カプロラクトン付加物の(メタ)アクリレート、テトラヒドロフルフリルアルコールのジε−カプロラクトン付加物の(メタ)アクリレート、テトラヒドロフルフリルアルコールのモノβ−メチル−δ−バレロラクトン付加物の(メタ)アクリレート、テトラヒドロフルフリルアルコールのジβ−メチル−δ−バレロラクトン付加物の(メタ)アクリレート、ω−カルボキシ−ポリカプロラクトンモノアクリレート等の(メタ)アクリル酸エステル系化合物;
スチレン、ビニルトルエン、α−メチルスチレン、ジメチルスチレン、クロロスチレン、t−ブチルスチレン、スチレンスルホン酸およびその塩などのスチレン系化合物;
アクリロニトリル、メタクリロニトリル等のニトリル基含有ビニル化合物;
(メタ)アクリルアミド、N−メチル(メタ)アクリルアミド、N−エチル(メタ)アクリルアミド、N−プロピル(メタ)アクリルアミド、N−イソプロピル(メタ)アクリルアミド、N−ブチル(メタ)アクリルアミド、N,N−ジメチル(メタ)アクリルアミド、N,N−ジエチル(メタ)アクリルアミド、N,N−ジメチルアミノプロピル(メタ)アクリルアミド、N−(ヒドロキシエチル)アクリルアミド、N−イソプロピル(メタ)アクリルアミド、N−メチロール(メタ)アクリルアミド、ダイアセトン(メタ)アクリルアミド、N,N−メチレンビス(メタ)アクリルアミド等のアミド基含有ビニル化合物;
酢酸ビニル、プロピオン酸ビニル、ピバリン酸ビニル、安息香酸ビニル、桂皮酸ビニル等のビニルエステル化合物;
マレイミド、N−アルキル置換マレイミド;
1,3−ブタジエン、イソプレン等の共役ジオレフィンなどが挙げられる。
カチオン重合性単量体としては、特に制限はなく、カチオン重合を起こして硬化するものであれば従来公知のカチオン重合性単量体をいずれも使用できる。より具体的には、カチオン重合性単量体としては、エポキシ基、ビニルエーテル基、環状エーテル基、環状アセタール基、環状ラクトン基、または、環状チオエーテル基を有する化合物、スピロオルソエステル化合物等が挙げられる。このうち、特にエポキシ基、オキセタン環、ビニルエーテル基を有する単量体がより好ましい。
本発明で使用し得る不飽和ジカルボン酸無水物としては、上記のように、ラジカル重合性単量体と共重合体を形成することができ、かつ、水によって加水分解され得るものであれば、基本的には制限なく使用できる。
本発明の接着剤組成物は、さらに、ラジカル重合開始剤および光増感剤の少なくとも一方を含む。
カチオン重合開始剤としては、通常光酸発生剤として用いられる化合物を特に制限なく使用できる。具体的には、例えば、芳香族ジアゾニウム塩、芳香族ヨードニウム塩や芳香族スルホニウム塩などのオニウム塩、鉄−アレン錯体などが挙げられる。これらは、単独で使用しても、二種以上を組み合わせて使用してもよい。
本発明の接着剤組成物を製造するには、特に制限はなく、通常は、上記のラジカル重合性単量体、カチオン重合性単量体、不飽和ジカルボン酸無水物、ラジカル重合開始剤、カチオン重合開始剤を混合して接着剤組成物が得られる。粘度調整のために適宜有機溶媒を使用してもよい。混合方法にも特に制限はなく、室温(25℃)で、液体内が均一になるまで十分に攪拌混合すればよい。
本発明の第二の態様によれば、本発明の接着剤組成物を用いて接着した、保護フィルムと、偏光子とを備える偏光板が提供される。本発明の偏光板は、接着剤組成物が水分による硬化阻害を受けないため、高湿度下で製造しても、十分な接着性を示す。
偏光子としては、特に制限はなく、従来公知のものを使用できる。例えば、ポリビニルアルコール系フィルム、部分ホルマール化ポリビニルアルコール系フィルム、エチレン・酢酸ビニル共重合体系部分ケン化フィルム等の親水性高分子フィルムに、ヨウ素や二色性染料等の二色性材料を吸着させて一軸延伸したもの、ポリビニルアルコールの脱水処理物やポリ塩化ビニルの脱塩酸処理物等ポリエン系配向フィルム等が挙げられる。
保護フィルムとしては、透明性、機械的強度、熱安定性、水分遮断性、等方性などに優れる材料が好ましい。例えば、セルロースジアセテートやセルローストリアセテート等のセルロース系樹脂、ポリエチレンテレフタレートやポリエチレンナフタレート等のポリエステル系樹脂、ポリメチルメタクリレート等のアクリル系樹脂、ポリスチレンやアクリロニトリル・スチレン共重合体(AS樹脂)等のスチレン系樹脂、ポリカーボネート系樹脂、ポリエチレン、ポリプロピレン、シクロ系ないしはノルボルネン構造を有するポリオレフィン、エチレン・プロピレン共重合体等のポリオレフィン系樹脂、塩化ビニル系樹脂、ナイロンや芳香族ポリアミド等のアミド系樹脂、イミド系樹脂、スルホン系樹脂、ポリエーテルスルホン系樹脂、ポリエーテルエーテルケトン系樹脂、ポリフェニレンスルフィド系樹脂、ビニルアルコール系樹脂、塩化ビニリデン系樹脂、ビニルブチラール系樹脂、アリレート系樹脂、ポリオキシメチレン系樹脂、エポキシ系樹脂、または前記樹脂のブレンドなどが挙げられる。
(放電量)=(放電電力)÷{(対象物処理速度)×(電極長さ)}
(C)製造方法
偏光板の製造方法としては特に制限はなく、従来公知の方法によって、保護フィルムと偏光子とを、本発明の接着剤組成物を用いて貼り合わせることによって製造し得る。塗布した接着剤組成物は、紫外線照射により接着性を発現して接着層を構成する。
<接着剤組成物の調製>
ラジカル重合性単量体として、4−ヒドロキシブチルアクリレート(日本化成株式会社製)25質量部、アクリル酸テトラヒドロフルフリル(東京化成工業株式会社製)10質量部、アクリル酸イソボルニル(東京化成工業株式会社製)12質量部、ウレタンアクリレート(新中村化学工業株式会社製NKオリゴ(登録商標) U−4HA)3質量部、カチオン重合性単量体として、ビスフェノールAグリシジルエーテル(三菱化学株式会社製エピコート(登録商標)828)47質量部、無水マレイン酸3質量部、ラジカル重合開始剤(BASFジャパン株式会社製IRGACURE(登録商標) 819)1質量部、カチオン重合開始剤として50%−トリアリールスルホニウム塩/プロピレンカーボネート(サンアプロ株式会社製CPI−101A)4質量部を、23℃湿度50%の恒温室内で、目視で均一になるまで撹拌混合し、接着剤組成物を得た。使用した材料およびその配合比は、下記表1−1、表1−2および表2に示すとおりである。
偏光子は、以下の方法で作製した。平均重合度2400、けん化度99.9%の厚み75μmのポリビニルアルコールフィルムを、28℃の温水中に90秒間浸漬し膨潤させ、次いで、ヨウ素/ヨウ化カリウム(重量比2/3)の濃度0.6重量%の水溶液に浸漬し、2.1倍に延伸させながらポリビニルアルコールフィルムを染色した。その後、60℃のホウ酸エステル水溶液中で合計の延伸倍率が5.8倍となるように延伸を行い、水洗、45℃で3分乾燥を行い、偏光子(厚み25μm)を作製した。
実施例2〜7では、下記表1−1、表1−2および表2に示す材料および配合量を用いた以外は、実施例1と同様にして接着剤組成物2〜7を作製した。さらに、得られた各接着剤組成物を用いて、それぞれ、表3に示す保護フィルム1および保護フィルム2を用い、表3に示す環境下で偏光板を貼り合せ紫外線照射を行った以外は、実施例1と同様にして偏光板を完成させた。また、実施例2〜7についても実施例1と同様の試験により評価を行った。
比較例1〜6では、下記表1−1、表1−2および表2に示す材料および配合量を用いた以外は、実施例1と同様にして接着剤組成物8〜13を作製した。さらに、得られた各接着剤組成物を用いて、それぞれ、表4に示す保護フィルム1および保護フィルム2を用い、表4に示す環境下で偏光板を貼り合せ紫外線照射を行った以外は、実施例1と同様にして偏光板を完成させた。また、比較例1〜6についても実施例1と同様の試験により評価を行った。
実施例1〜7、比較例1〜6で得られた接着剤組成物を、上記偏光板の製造方法と同様にして、保護フィルム1および保護フィルム2の代わりにPETフィルムに貼り合わせた。この試料に上記偏光板の製造方法と同様の条件で紫外線を照射し、照射1分後と1日後の表面状態を指で確認した。評価基準は以下の通りとした。
○:指紋がつかない
△:指紋がつく
×:硬化せずに液状のまま。
実施例1〜7、比較例1〜6で作製した偏光板の保護フィルム1もしくは保護フィルム2の一方の面に、図2に示すようにナイフで切れ目(ハーフカット)を入れた。次いで、ハーフカット部が凸側となるように、偏光板の折れが発生するまで変形させた。その後、折れが発生している箇所の保護フィルム1もしくは保護フィルム2の状態を目視で観察した。評価基準は以下の通りとした。
◎:剥離なし
○:0.5mm未満
×:0.5mm以上。
実施例1〜7、比較例1〜6で作製した偏光板を、Thonsom刃で50mm×50mmに裁断し、裁断の際の端部の剥がれの状態を目視で観察した。評価基準は以下の通りとした。
◎:剥がれなし
○:0.5mm未満
×:0.5mm以上。
実施例1〜7、比較例1〜6で作製した偏光板を、Thonsom刃で50mm×50mmに裁断し、60℃の水槽に浸漬し、3時間保持した。その後、水槽から各サンプルを取り出し、水分を拭き取り、温水浸漬によって偏光子の周囲で温水に接する部分からヨウ素が溶け出して、周囲の色が抜けたかどうかを目視で観察した。評価基準は以下の通りとした。
○:変化なし
×:色が抜けた。
実施例1〜7、比較例1〜6で作成した偏光板を、ヘイズメーター(HazeMeter NDH5000W:日本電色工業株式会社製)を用いて透過率およびヘイズを測定した。
実施例1〜7、比較例1〜6で作製した偏光板を、Thonsom刃で50mm×50mmに裁断し、85℃及び60℃95%RH雰囲気下で500時間放置後の様子を観察すると共に、上記光学特性と同様に透過率およびヘイズを測定した。評価基準は以下の通りとした。
○:フィルム端部の剥がれなし、透過率及びヘイズの耐久性試験開始前との差が3%未満
×:フィルム端部の剥がれあり、透過率及びヘイズの耐久性試験開始前との差が3%以上。
実施例1〜7、比較例1〜6で作製した偏光板を、Thonsom刃で50mm×50mmに裁断し、試験片とした。次いで図3(a)に示すように、耐水研磨紙(♯280)で研磨したSUS板に、瞬間接着剤アロンアルファ(登録商標)一般用(東亞合成株式会社製)を用いて前記試験片を貼り合わせ、室温(25℃)で24時間熟成させた。熟成した試験片について熱衝撃試験を行った。
◎:偏光子割れなし
○:0.5mm未満
×:0.5mm以上
Claims (5)
- (A)ラジカル重合性単量体26.1〜79.8質量部と、
(B)カチオン重合性単量体60.9〜20.0質量部と、
(C)不飽和ジカルボン酸無水物0.2〜13質量部と、
ただし、前記(A)、(B)および(C)の合計は100質量部であり、
(D)ラジカル重合開始剤0.5〜5質量部および光増感剤0.1〜5質量部の少なくとも一方と、
(E)カチオン重合開始剤0.5〜5質量部と、
を含む偏光板用接着剤組成物。 - 前記酸無水物が無水マレイン酸および無水イタコン酸の少なくとも一種である請求項1に記載の接着剤組成物。
- 前記ラジカル重合性単量体が45〜55質量部、前記カチオン重合性単量体が55〜45質量部、前記不飽和ジカルボン酸無水物が0.8〜8質量部含まれる請求項1または2に記載の接着剤組成物。
- 前記ラジカル重合性単量体がアクリロイル基、メタクリロイル基、ビニル基、およびアリル基のいずれかを有する単量体であり、前記カチオン重合性単量体が、エポキシ基、オキセタン環およびビニルエーテル基のいずれかを有する単量体である請求項1〜3のいずれか一項に記載の接着材組成物。
- 請求項1〜4のいずれか一項に記載の接着剤組成物を用いて接着した、保護フィルムと、偏光子とを備える偏光板。
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012053615A JP5530470B2 (ja) | 2012-03-09 | 2012-03-09 | 偏光板用接着剤 |
KR20120143970A KR20130103290A (ko) | 2012-03-09 | 2012-12-11 | 편광판용 접착제 조성물 및 이를 이용한 편광판 |
US14/383,753 US9790402B2 (en) | 2012-03-09 | 2013-02-14 | Adhesive composition for polarizer and polarizer using same |
KR1020147023155A KR101676548B1 (ko) | 2012-03-09 | 2013-02-14 | 편광판용 접착제 조성물 및 이를 이용한 편광판 |
CN201380013180.0A CN104169381B (zh) | 2012-03-09 | 2013-02-14 | 用于偏光板的粘合剂组合物以及使用该组合物的偏光板 |
PCT/KR2013/001153 WO2013133539A1 (ko) | 2012-03-09 | 2013-02-14 | 편광판용 접착제 조성물 및 이를 이용한 편광판 |
TW102108247A TWI567151B (zh) | 2012-03-09 | 2013-03-08 | 用於偏光板之黏著劑組成物以及使用該組成物之偏光板 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012053615A JP5530470B2 (ja) | 2012-03-09 | 2012-03-09 | 偏光板用接着剤 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013185133A JP2013185133A (ja) | 2013-09-19 |
JP5530470B2 true JP5530470B2 (ja) | 2014-06-25 |
Family
ID=49116970
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012053615A Active JP5530470B2 (ja) | 2012-03-09 | 2012-03-09 | 偏光板用接着剤 |
Country Status (6)
Country | Link |
---|---|
US (1) | US9790402B2 (ja) |
JP (1) | JP5530470B2 (ja) |
KR (2) | KR20130103290A (ja) |
CN (1) | CN104169381B (ja) |
TW (1) | TWI567151B (ja) |
WO (1) | WO2013133539A1 (ja) |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2014178239A1 (ja) * | 2013-05-02 | 2017-02-23 | Dic株式会社 | 接着剤組成物及び偏光板 |
JP6164609B2 (ja) * | 2013-08-23 | 2017-07-19 | 東亞合成株式会社 | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 |
WO2015046714A1 (ko) * | 2013-09-30 | 2015-04-02 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물 및 이를 포함하는 편광판 |
KR101687874B1 (ko) * | 2013-09-30 | 2016-12-19 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물, 이를 포함하는 편광판 및 광학 부재 |
KR101687872B1 (ko) * | 2013-09-30 | 2016-12-19 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물 및 이를 포함하는 편광판 |
WO2015046818A1 (ko) * | 2013-09-30 | 2015-04-02 | 주식회사 엘지화학 | 편광판 및 이를 포함하는 화상표시장치 |
KR101749792B1 (ko) | 2013-09-30 | 2017-06-22 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물, 이를 포함하는 편광판 및 광학 부재 |
WO2015046817A1 (ko) * | 2013-09-30 | 2015-04-02 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물 및 이를 포함하는 편광판 |
KR101650235B1 (ko) * | 2013-09-30 | 2016-08-22 | 주식회사 엘지화학 | 편광판 |
KR101685257B1 (ko) * | 2013-09-30 | 2016-12-09 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물 및 이를 포함하는 편광판 |
KR101630938B1 (ko) * | 2013-09-30 | 2016-06-15 | 주식회사 엘지화학 | 편광판, 그 제조 방법 및 이를 포함하는 화상표시장치 |
KR101637082B1 (ko) * | 2013-09-30 | 2016-07-06 | 주식회사 엘지화학 | 편광판 및 이를 포함하는 화상표시장치 |
WO2015046819A1 (ko) * | 2013-09-30 | 2015-04-02 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물, 이를 포함하는 편광판 및 광학 부재 |
KR101620164B1 (ko) * | 2013-09-30 | 2016-05-12 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물 및 이를 포함하는 편광판 |
KR101620188B1 (ko) * | 2013-09-30 | 2016-05-12 | 주식회사 엘지화학 | 편광판 및 이를 포함하는 화상표시장치 |
WO2015046814A1 (ko) * | 2013-09-30 | 2015-04-02 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물 및 이를 포함하는 편광판 |
KR101627928B1 (ko) | 2013-09-30 | 2016-06-13 | 주식회사 엘지화학 | 라디칼 경화형 접착제 조성물, 이를 포함하는 편광판 및 광학 부재 |
KR102097484B1 (ko) * | 2013-10-11 | 2020-04-07 | 동우 화인켐 주식회사 | 접착제 조성물 |
JP6265697B2 (ja) | 2013-11-18 | 2018-01-24 | サムスン エスディアイ カンパニー,リミテッドSamsung Sdi Co.,Ltd. | 偏光板用接着剤組成物 |
JP6331367B2 (ja) * | 2013-12-05 | 2018-05-30 | 東洋インキScホールディングス株式会社 | 樹脂組成物、活性エネルギー線重合性接着剤、及び積層体 |
KR101702707B1 (ko) * | 2014-04-30 | 2017-02-07 | 제일모직주식회사 | 편광판용 접착필름, 이를 위한 편광판용 접착제 조성물, 이를 포함하는 편광판 및 이를 포함하는 광학표시장치 |
KR20150145548A (ko) * | 2014-06-20 | 2015-12-30 | 동우 화인켐 주식회사 | 접착제 조성물 및 이를 포함하는 편광판 |
KR101748409B1 (ko) * | 2014-07-30 | 2017-06-16 | 주식회사 엘지화학 | 편광자 보호 필름용 수지 조성물, 편광자 보호 필름, 및 이를 포함하는 편광판 |
JP2016050230A (ja) * | 2014-08-29 | 2016-04-11 | 日東電工株式会社 | 光学用感光性樹脂組成物およびそれを用いた光学材料 |
WO2016052952A1 (ko) * | 2014-09-30 | 2016-04-07 | 주식회사 엘지화학 | 편광판 및 이를 포함하는 디스플레이장치 |
TWI715542B (zh) * | 2014-11-12 | 2021-01-11 | 日商迪睿合股份有限公司 | 光硬化系異向性導電接著劑、連接體之製造方法及電子零件之連接方法 |
US10604659B2 (en) | 2015-06-08 | 2020-03-31 | Dsm Ip Assets B.V. | Liquid, hybrid UV/VIS radiation curable resin compositions for additive fabrication |
EP3294780A4 (en) * | 2015-06-08 | 2018-11-21 | DSM IP Assets B.V. | Liquid, hybrid uv/vis radiation curable resin compositions for additive fabrication |
CN105176412B (zh) * | 2015-08-13 | 2017-12-26 | 京东方科技集团股份有限公司 | 一种封框胶及其固化方法、显示装置 |
EP3341793B1 (en) | 2015-10-01 | 2021-05-26 | DSM IP Assets B.V. | Liquid, hybrid uv/vis radiation curable resin compositions for additive fabrication |
JP6589561B2 (ja) * | 2015-10-30 | 2019-10-16 | 東洋インキScホールディングス株式会社 | 光学用活性エネルギー線重合性接着剤および光学積層体 |
JP2017090522A (ja) | 2015-11-04 | 2017-05-25 | 日東電工株式会社 | 偏光板の製造方法 |
JP6408046B2 (ja) * | 2016-02-17 | 2018-10-17 | 住友化学株式会社 | 光硬化性接着剤、並びにそれを用いた偏光板及び積層光学部材 |
KR102103619B1 (ko) * | 2016-07-29 | 2020-04-22 | 주식회사 엘지화학 | 접착제 조성물, 이를 이용하여 형성된 접착제층을 포함하는 보호필름 및 편광판, 및 이를 포함하는 화상표시장치 |
KR102124232B1 (ko) * | 2016-07-29 | 2020-06-17 | 주식회사 엘지화학 | 접착제 조성물, 이를 이용하여 형성된 접착제층을 포함하는 보호필름 및 편광판, 및 이를 포함하는 화상표시장치 |
JP6862995B2 (ja) * | 2017-03-29 | 2021-04-21 | 東洋インキScホールディングス株式会社 | 活性エネルギー線重合性接着剤および積層体 |
JPWO2018181846A1 (ja) * | 2017-03-31 | 2020-02-13 | 株式会社Adeka | 硬化性組成物、硬化物の製造方法、その硬化物、およびそれを用いた接着剤 |
KR102181860B1 (ko) * | 2017-09-22 | 2020-11-23 | 주식회사 엘지화학 | 접착제 조성물, 이를 이용하여 형성된 접착제층을 포함하는 편광판 |
KR102181849B1 (ko) * | 2017-09-22 | 2020-11-23 | 주식회사 엘지화학 | 접착제 조성물, 이를 이용하여 형성된 접착제층을 포함하는 편광판 |
KR102172568B1 (ko) | 2017-09-22 | 2020-11-02 | 주식회사 엘지화학 | 접착제 조성물 및 이를 이용하여 형성된 접착제층을 포함하는 편광판 |
JP2019211799A (ja) * | 2019-09-24 | 2019-12-12 | 日東電工株式会社 | 偏光板の製造方法 |
JP2021073352A (ja) * | 2021-01-29 | 2021-05-13 | Eneos株式会社 | 硬化性組成物およびその硬化物 |
CN113200596A (zh) * | 2021-04-15 | 2021-08-03 | 成都安捷芮环保科技有限公司 | 复合型溶解活化自由基簇水处理剂及其应用 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0321629A (ja) * | 1989-06-19 | 1991-01-30 | Toagosei Chem Ind Co Ltd | 光硬化性樹脂組成物 |
JP3511113B2 (ja) * | 1995-02-14 | 2004-03-29 | 株式会社ブリヂストン | 液晶表示装置用偏光板 |
KR970048905A (ko) * | 1995-12-28 | 1997-07-29 | 서영배 | 공중합성 광개시제를 사용하여 라디칼 중합과 양이온 중합을 동시에 일으키는 광경화성 조성물 |
JP3739211B2 (ja) * | 1998-08-28 | 2006-01-25 | 積水化学工業株式会社 | 光硬化型粘接着シート、光硬化型粘接着シートの製造方法及び接合方法 |
US6777102B2 (en) * | 2001-02-23 | 2004-08-17 | Fuji Photo Film Co., Ltd. | Curable composition and hardcoated article employing same |
US6949297B2 (en) * | 2001-11-02 | 2005-09-27 | 3M Innovative Properties Company | Hybrid adhesives, articles, and methods |
JP2005036077A (ja) | 2003-07-18 | 2005-02-10 | Sumitomo Chemical Co Ltd | 接着性フィルム |
CN1926213B (zh) | 2004-03-03 | 2011-01-26 | 日本化药株式会社 | 偏光元件用水基粘合剂和用其得到的偏振器 |
WO2008001722A1 (fr) * | 2006-06-27 | 2008-01-03 | Nippon Kayaku Kabushiki Kaisha | Composition durcissable par rayons énergétiques actifs à des fins optiques, et résine à indice de réfraction élevé |
JP5046721B2 (ja) * | 2007-04-13 | 2012-10-10 | 大倉工業株式会社 | 活性エネルギー線硬化型接着性組成物、それを用いた偏光板及びその製造方法 |
KR101023839B1 (ko) | 2008-07-24 | 2011-03-22 | 주식회사 엘지화학 | 점착제 조성물, 상기를 포함하는 편광판 및 액정표시장치 |
JP4913787B2 (ja) * | 2008-09-24 | 2012-04-11 | 日東電工株式会社 | 偏光板用接着剤、偏光板、その製造方法、光学フィルムおよび画像表示装置 |
JP5296575B2 (ja) * | 2009-03-06 | 2013-09-25 | 住友化学株式会社 | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 |
TWI493005B (zh) | 2009-07-28 | 2015-07-21 | Toagosei Co Ltd | An active energy ray hardening agent composition for a plastic film or sheet |
JP4561936B1 (ja) * | 2009-09-04 | 2010-10-13 | 東洋インキ製造株式会社 | 偏光板及び偏光板形成用光硬化性接着剤 |
JP5495906B2 (ja) * | 2010-04-06 | 2014-05-21 | 東亞合成株式会社 | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 |
-
2012
- 2012-03-09 JP JP2012053615A patent/JP5530470B2/ja active Active
- 2012-12-11 KR KR20120143970A patent/KR20130103290A/ko not_active Application Discontinuation
-
2013
- 2013-02-14 US US14/383,753 patent/US9790402B2/en active Active
- 2013-02-14 WO PCT/KR2013/001153 patent/WO2013133539A1/ko active Application Filing
- 2013-02-14 KR KR1020147023155A patent/KR101676548B1/ko active IP Right Grant
- 2013-02-14 CN CN201380013180.0A patent/CN104169381B/zh active Active
- 2013-03-08 TW TW102108247A patent/TWI567151B/zh active
Also Published As
Publication number | Publication date |
---|---|
CN104169381A (zh) | 2014-11-26 |
US20150099127A1 (en) | 2015-04-09 |
WO2013133539A1 (ko) | 2013-09-12 |
KR20130103290A (ko) | 2013-09-23 |
TWI567151B (zh) | 2017-01-21 |
KR101676548B1 (ko) | 2016-11-15 |
TW201343844A (zh) | 2013-11-01 |
JP2013185133A (ja) | 2013-09-19 |
CN104169381B (zh) | 2017-06-13 |
KR20140142232A (ko) | 2014-12-11 |
US9790402B2 (en) | 2017-10-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5530470B2 (ja) | 偏光板用接着剤 | |
JP5788841B2 (ja) | 偏光板用接着剤 | |
TWI629329B (zh) | 光硬化性接著劑組成物、偏光板及其製造方法、光學構件、以及液晶顯示裝置 | |
JP6103687B2 (ja) | 偏光板用接着剤組成物 | |
JP6265697B2 (ja) | 偏光板用接着剤組成物 | |
KR20100100695A (ko) | 광경화성 접착제 조성물, 편광판과 그의 제조법, 광학 부재 및 액정 표시 장치 | |
JP6571318B2 (ja) | 偏光板用接着剤およびこれを用いた表示装置 | |
JP6603446B2 (ja) | 偏光板およびこれを用いた表示装置 | |
JP5596207B2 (ja) | 光硬化性接着剤組成物、偏光板とその製造法、光学部材及び液晶表示装置 | |
JPWO2018147247A1 (ja) | 活性エネルギー線硬化性接着剤組成物、偏光板用接着剤組成物、偏光板用接着剤、およびそれを用いた偏光板 | |
KR102158870B1 (ko) | 광학 필름용 접착제, 이를 포함하는 편광판 및 이를 포함하는 화상표시장치 | |
JP6279853B2 (ja) | 偏光板用接着剤組成物 | |
JP6622450B2 (ja) | 偏光板用接着剤およびこれを用いた表示装置 | |
KR20210158303A (ko) | 광학 부재용 경화성 수지 조성물, 그의 경화물, 편광판 및 화상표시장치 | |
JP6273103B2 (ja) | 偏光板用接着剤組成物 | |
JP2022536080A (ja) | ラジカル系接着剤組成物、それを含む偏光板用保護フィルム、それを含む偏光板、及びそれを含む画像表示装置 | |
JP2018059011A (ja) | 活性エネルギー線硬化性接着剤組成物、偏光板用接着剤組成物、偏光板用接着剤、およびそれを用いた偏光板 | |
JP2017076141A (ja) | 偏光フィルムの製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20140326 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20140401 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20140418 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5530470 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |