KR101130881B1 - 경화성 수지 조성물, 이를 이용한 화상표시장치 및 화상표시장치의 제조방법 - Google Patents
경화성 수지 조성물, 이를 이용한 화상표시장치 및 화상표시장치의 제조방법 Download PDFInfo
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- KR101130881B1 KR101130881B1 KR1020080114517A KR20080114517A KR101130881B1 KR 101130881 B1 KR101130881 B1 KR 101130881B1 KR 1020080114517 A KR1020080114517 A KR 1020080114517A KR 20080114517 A KR20080114517 A KR 20080114517A KR 101130881 B1 KR101130881 B1 KR 101130881B1
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- KR
- South Korea
- Prior art keywords
- meth
- acrylate
- curable resin
- resin composition
- acrylate oligomer
- Prior art date
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- 239000011342 resin composition Substances 0.000 title claims abstract description 70
- 238000004519 manufacturing process Methods 0.000 title abstract description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 247
- 239000000758 substrate Substances 0.000 claims abstract description 86
- 238000000034 method Methods 0.000 claims abstract description 35
- 239000000049 pigment Substances 0.000 claims abstract description 23
- 238000005530 etching Methods 0.000 claims abstract description 22
- 239000003086 colorant Substances 0.000 claims abstract description 20
- 239000000178 monomer Substances 0.000 claims abstract description 16
- 238000007789 sealing Methods 0.000 claims abstract description 16
- 230000008569 process Effects 0.000 claims abstract description 15
- 239000010802 sludge Substances 0.000 claims abstract description 11
- 238000001179 sorption measurement Methods 0.000 claims abstract description 8
- -1 acryl Chemical group 0.000 claims description 58
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 34
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 33
- 125000003003 spiro group Chemical group 0.000 claims description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 239000004593 Epoxy Substances 0.000 claims description 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- 239000004973 liquid crystal related substance Substances 0.000 claims description 14
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 13
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 239000000565 sealant Substances 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 11
- 150000008064 anhydrides Chemical group 0.000 claims description 8
- 238000002845 discoloration Methods 0.000 claims description 8
- FAQVDANXTSFXGA-UHFFFAOYSA-N 2,3-dihydro-1h-benzo[g]indole Chemical compound C1=CC=CC2=C(NCC3)C3=CC=C21 FAQVDANXTSFXGA-UHFFFAOYSA-N 0.000 claims description 6
- 239000000975 dye Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 3
- VFUGUWZYXGNQHR-UHFFFAOYSA-N 2h-1,2-benzoxazine;2,3-dihydro-1h-indole Chemical compound C1=CC=C2NCCC2=C1.C1=CC=C2C=CNOC2=C1 VFUGUWZYXGNQHR-UHFFFAOYSA-N 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- 229910052727 yttrium Inorganic materials 0.000 claims description 3
- WCQAZRJBAWCCMZ-UHFFFAOYSA-N 2,3-dihydro-1h-indole;2h-pyran Chemical compound C1OC=CC=C1.C1=CC=C2NCCC2=C1 WCQAZRJBAWCCMZ-UHFFFAOYSA-N 0.000 claims description 2
- UJKRMSUGENCHEY-UHFFFAOYSA-N 2,3-dihydro-1h-indole;2h-pyrano[3,2-b]quinoline Chemical compound C1=CC=C2NCCC2=C1.C1=CC=C2N=C(C=CCO3)C3=CC2=C1 UJKRMSUGENCHEY-UHFFFAOYSA-N 0.000 claims description 2
- RFPBBTGDNJHSRB-UHFFFAOYSA-N 2,3-dihydro-1h-indole;2h-pyrido[2,3-h][1,2]benzoxazine Chemical compound C1=CC=C2NCCC2=C1.C1=CC2=NC=CC=C2C2=C1C=CNO2 RFPBBTGDNJHSRB-UHFFFAOYSA-N 0.000 claims description 2
- QDEJGQKJMKXYLM-UHFFFAOYSA-N 2h-pyrido[2,3-h][1,2]benzoxazine Chemical compound C1=CC2=NC=CC=C2C2=C1C=CNO2 QDEJGQKJMKXYLM-UHFFFAOYSA-N 0.000 claims description 2
- VCMLCMCXCRBSQO-UHFFFAOYSA-N 3h-benzo[f]chromene Chemical compound C1=CC=CC2=C(C=CCO3)C3=CC=C21 VCMLCMCXCRBSQO-UHFFFAOYSA-N 0.000 claims description 2
- HEDFZCGDROAIPW-UHFFFAOYSA-N 3h-benzo[f]chromene;2,3-dihydro-1h-benzo[g]indole Chemical compound C1=CC=CC2=C(NCC3)C3=CC=C21.C1=CC=CC2=C(C=CCO3)C3=CC=C21 HEDFZCGDROAIPW-UHFFFAOYSA-N 0.000 claims description 2
- KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- UEOGLANRPZAEAC-UHFFFAOYSA-N indeno-naphthopyran Chemical compound O1C=CC=C2C3=C4C=C(C=CC=C5)C5=C4C=CC3=CC=C21 UEOGLANRPZAEAC-UHFFFAOYSA-N 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- ZLLLODBXLDFWER-UHFFFAOYSA-N 2h-chromene;2,3-dihydro-1h-indole Chemical compound C1=CC=C2NCCC2=C1.C1=CC=C2C=CCOC2=C1 ZLLLODBXLDFWER-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 26
- 238000001723 curing Methods 0.000 description 18
- 125000002843 carboxylic acid group Chemical group 0.000 description 17
- 239000011521 glass Substances 0.000 description 14
- 239000001294 propane Substances 0.000 description 13
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 12
- 239000012948 isocyanate Substances 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 150000002513 isocyanates Chemical class 0.000 description 7
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 7
- 230000035515 penetration Effects 0.000 description 7
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 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 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229920001451 polypropylene glycol Polymers 0.000 description 5
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 4
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- 239000004305 biphenyl Substances 0.000 description 4
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 3
- PXKLMJQFEQBVLD-UHFFFAOYSA-N Bisphenol F Natural products C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- LPAGFVYQRIESJQ-UHFFFAOYSA-N indoline Chemical compound C1=CC=C2NCCC2=C1 LPAGFVYQRIESJQ-UHFFFAOYSA-N 0.000 description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 3
- 229940014800 succinic anhydride Drugs 0.000 description 3
- 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 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 description 2
- LAQYHRQFABOIFD-UHFFFAOYSA-N 2-methoxyhydroquinone Chemical compound COC1=CC(O)=CC=C1O LAQYHRQFABOIFD-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- NQVQBIMDDKDYAO-UHFFFAOYSA-N 8-methoxy-1',3',3'-trimethylspiro[chromene-2,2'-indole] Chemical compound CN1C2=CC=CC=C2C(C)(C)C11C=CC(C=CC=C2OC)=C2O1 NQVQBIMDDKDYAO-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-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
- BHELIUBJHYAEDK-OAIUPTLZSA-N Aspoxicillin Chemical compound C1([C@H](C(=O)N[C@@H]2C(N3[C@H](C(C)(C)S[C@@H]32)C(O)=O)=O)NC(=O)[C@H](N)CC(=O)NC)=CC=C(O)C=C1 BHELIUBJHYAEDK-OAIUPTLZSA-N 0.000 description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 238000003848 UV Light-Curing Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 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
- 150000001562 benzopyrans Chemical class 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 description 2
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- PODOEQVNFJSWIK-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethoxyphenyl)methanone Chemical compound COC1=CC(OC)=CC(OC)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 PODOEQVNFJSWIK-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000001072 heteroaryl group Chemical group 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- QQYNRBAAQFZCLF-FBXFSONDSA-N (3ar,4s,7r,7as)-rel-3a,4,7,7a-tetrahydro-4,7-epoxyisobenzofuran-1,3-dione Chemical compound O1[C@@H]2[C@@H]3C(=O)OC(=O)[C@@H]3[C@H]1C=C2 QQYNRBAAQFZCLF-FBXFSONDSA-N 0.000 description 1
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- MUTGBJKUEZFXGO-WDSKDSINSA-N (3as,7as)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@H]21 MUTGBJKUEZFXGO-WDSKDSINSA-N 0.000 description 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 1
- IVSZLXZYQVIEFR-UHFFFAOYSA-N 1,3-Dimethylbenzene Natural products CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 1
- DLYGWHUJQCJNSR-UHFFFAOYSA-N 1,3-bis[4-[2-[4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenoxy]propan-2-ol Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC(O)COC(C=C1)=CC=C1C(C)(C)C(C=C1)=CC=C1OCC1CO1 DLYGWHUJQCJNSR-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- ATOUXIOKEJWULN-UHFFFAOYSA-N 1,6-diisocyanato-2,2,4-trimethylhexane Chemical compound O=C=NCCC(C)CC(C)(C)CN=C=O ATOUXIOKEJWULN-UHFFFAOYSA-N 0.000 description 1
- QGLRLXLDMZCFBP-UHFFFAOYSA-N 1,6-diisocyanato-2,4,4-trimethylhexane Chemical compound O=C=NCC(C)CC(C)(C)CCN=C=O QGLRLXLDMZCFBP-UHFFFAOYSA-N 0.000 description 1
- KYSSIYAMBDPPMZ-UHFFFAOYSA-N 1-[3-[2-[4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenoxy]-3-[4-[2-[4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenoxy]propan-2-ol Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC(O)COC(C=1)=CC=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 KYSSIYAMBDPPMZ-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 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
- MFGALGYVFGDXIX-UHFFFAOYSA-N 2,3-Dimethylmaleic anhydride Chemical compound CC1=C(C)C(=O)OC1=O MFGALGYVFGDXIX-UHFFFAOYSA-N 0.000 description 1
- ITHGKFNFXCDUDC-UHFFFAOYSA-N 2,3-dihydro-1h-benzo[g]indole;2h-pyrido[2,3-h][1,2]benzoxazine Chemical compound C1=CC=CC2=C(NCC3)C3=CC=C21.C1=CC2=NC=CC=C2C2=C1C=CNO2 ITHGKFNFXCDUDC-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- WMYINDVYGQKYMI-UHFFFAOYSA-N 2-[2,2-bis(hydroxymethyl)butoxymethyl]-2-ethylpropane-1,3-diol Chemical compound CCC(CO)(CO)COCC(CC)(CO)CO WMYINDVYGQKYMI-UHFFFAOYSA-N 0.000 description 1
- ZJRAAAWYHORFHN-UHFFFAOYSA-N 2-[[2,6-dibromo-4-[2-[3,5-dibromo-4-(oxiran-2-ylmethoxy)phenyl]propan-2-yl]phenoxy]methyl]oxirane Chemical compound C=1C(Br)=C(OCC2OC2)C(Br)=CC=1C(C)(C)C(C=C1Br)=CC(Br)=C1OCC1CO1 ZJRAAAWYHORFHN-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
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- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
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- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
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- C—CHEMISTRY; METALLURGY
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
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- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
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- C08F220/325—Esters containing oxygen in addition to the carboxy oxygen containing epoxy radicals containing glycidyl radical, e.g. glycidyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
- C08F220/343—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate in the form of urethane links
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
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- 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
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Abstract
Description
성분 |
실시예 | 비교예1 | |||||||||||||
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | |||
(메타)아크릴레이트올리고머 | EB600 | 36 | 35 | 24 | 75 | 22 | 35 | 94 | |||||||
합성예1 | 17 | 30 | 47 | 85 | 25 | 30 | 34 | 34 | |||||||
합성예2 | 14 | 15 | 46 | 75 | 21 | 26 | 40 | 25 | |||||||
FA401 | 10 | 15 | 70 | 20 | |||||||||||
자외선 경화형 단량체 |
(a) | 20 | 8 | 18 | 10 | 12 | |||||||||
(b) | 25 | 26 | 20 | 18 | 5 | 9 | 23 | 3 | 3 | 3 | 23 | ||||
(c) | 8 | 2 | 72 | ||||||||||||
착색제 | 2 | 3 | 3 | 3 | 2 | 2 | 2 | 2 | 1 | 2 | 1 | 1 | 1 | 1 | |
변색안료 | 1 | 2 | 3 | 3 | 2 | 2 | 2 | 2 | 2 | 2 | 1 | 1 | 1 | 2 | |
광개시제 | 5 | 4 | 4 | 4 | 3 | 3 | 3 | 3 | 3 | 3 | 1 | 1 | 1 | 2 |
점도(cps) | 접착력(N/㎠) | 내화학성 | 경화전후시인성 | 빛샘 정도 | |
실시예 1 | 1700 | 20 | ○ | ○ | ○ |
실시예 2 | 1800 | 25 | △ | ○ | ○ |
실시예 3 | 800 | 40 | ○ | ○ | ○ |
실시예 4 | 1300 | 22 | ○ | ○ | ○ |
실시예 5 | 2000 | 17 | △ | ○ | ○ |
실시예 6 | 1200 | 50 | ○ | ○ | ○ |
실시예 7 | 1500 | 15 | ○ | ○ | ○ |
실시예 8 | 1950 | 17 | ○ | ○ | ○ |
실시예 9 | 1800 | 18 | ○ | ○ | ○ |
실시예 10 | 1000 | 20 | ○ | △ | ○ |
실시예 11 | 900 | 30 | △ | X | ○ |
실시예 12 | 7700 | 25 | ○ | X | ○ |
실시예 13 | 8700 | 5 | X | X | ○ |
비교예 1 | 1900 | 1 | X | X | △ |
Claims (29)
- 화상표시장치의 경량화를 위한 기판 식각 공정시 식각액으로부터 내부 액정 영역을 보호하고 슬러지의 흡착을 방지하기 위한 것으로서, (메타)아크릴레이트 올리고머, 자외선 경화형 (메타)아크릴레이트 단량체, 광개시제 및 착색제를 포함하고,상기 (메타)아크릴레이트 올리고머가 에폭시 (메타)아크릴레이트 올리고머(a1), 우레탄 (메타)아크릴레이트 올리고머(a2), 산변성 (메타)아크릴레이트 올리고머(a3), 에테르 (메타)아크릴레이트 올리고머(a4)로 이루어진 군으로부터 선택된 적어도 1종을 포함하고,상기 에폭시 (메타)아크릴레이트 올리고머(a1)는 하기 화학식 1로 표현되는 에폭시 (메타)아크릴레이트이고,[화학식 1](화학식 1에서 R은 수소 또는 메틸이고, X는 O이고, Y는 하기 화학식 2로 표현되며, n은 2이다.)[화학식 2](화학식 2에서 Q는 -C(CH3)2-, -CH2-, -C(O)-, -S(O)-, -S-, -O- 또는 -S(O)2-이고, A는 하이드록시 치환된 C1-C 6 알킬렌이며, L은 각각 독립적으로 1 내지 10의 정수이고, m은 각각 독립적으로 0 내지 4의 정수이며, a는 1 내지 3의 정수이다.)상기 우레탄 (메타)아크릴레이트 올리고머(a2)는 하기 화학식 4로 표현되는 우레탄 (메타)아크릴레이트이고,[화학식 4](상기 식에서, Y는 1~10개의 (메타)아크릴레이트 관능기를 포함하는 탄소수 7~80개의 지방족 또는 방향족 탄화수소이고, R는 탄소수 1~15개의 지방족 또는 방향족 탄화수소이다)상기 산변성 (메타)아크릴레이트 올리고머(a3)는 무수물기를 갖는 화합물과 분자내 1개 이상의 히드록시기를 갖는 (메타)아크릴레이트를 반응하여 제조된 분자내 적어도 하나의 카르복시기를 갖는 산변성 (메타)아크릴레이트이고,상기 에테르 (메타)아크릴레이트 올리고머(a4)는 하기 화학식 5로 표현되는 에테르 (메타)아크릴레이트이고,[화학식 5](상기 화학식 5에서, R1은 에틸렌기 또는 이소프로필렌기이고, R2는 수소원자 또는 메틸기이며, Y는 탄소수 1~10개의 지방족 탄화수소이고, n은 1 내지 100인 정수이다)상기 자외선 경화형 (메타)아크릴레이트 단량체는 분자내 1개 이상의 에틸렌성 불포화기를 갖는 지방족 또는 방향족 (메타)아크릴레이트인 것을 특징으로 하는 경화성 수지 조성물.
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- 제 1항에 있어서,상기 자외선 경화형 (메타)아크릴레이트 단량체는 25℃에서 점도 1 내지 10000cps인 것을 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 (메타)아크릴레이트 올리고머는 경화성 수지 조성물 총 100중량부에 대하여 1 내지 90중량부 포함되는 것을 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 (메타)아크릴레이트 올리고머가 우레탄 (메타)아크릴레이트 올리고머(a2) 및 산변성 (메타)아크릴레이트 올리고머(a3)를 포함하는 것을 특징으로 하는 경화성 수지 조성물.
- 제 13항에 있어서,상기 우레탄 (메타)아크릴레이트 올리고머(a2) 및 산변성 (메타)아크릴레이트 올리고머(a3)는 경화성 수지 조성물 총 100중량부에 대하여 각각 0.1 내지 89.9중량부 및 0.1 내지 89.9중량부 포함되는 것을 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 (메타)아크릴레이트 올리고머가 에폭시 (메타)아크릴레이트 올리고머(a1)와 우레탄 (메타)아크릴레이트 올리고머(a2) 및 산변성 (메타)아크릴레이트 올리고머(a3)를 포함하는 것을 특징으로 하는 경화성 수지 조성물.
- 제 15항에 있어서,상기 에폭시 (메타)아크릴레이트 올리고머(a1)와 우레탄 (메타)아크릴레이트 올리고머(a2) 및 산변성 (메타)아크릴레이트 올리고머(a3)는 경화성 수지 조성물 총 100중량에 대하여 각각 0.1 내지 89.8중량부, 0.1 내지 89.8중량부 및 0.1 내지 89.8중량부 포함되는 것을 것을 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 (메타)아크릴레이트 올리고머가 우레탄 (메타)아크릴레이트 올리고머(a1), 산변성 (메타)아크릴레이트 올리고머(a3) 및 에테르 (메타)아크릴레이트 올리고머(a4)를 포함하는 것을 특징으로 하는 경화성 수지 조성물.
- 제 17항에 있어서,상기 우레탄 (메타)아크릴레이트 올리고머(a1), 산변성 (메타)아크릴레이트 올리고머(a3) 및 에테르 (메타)아크릴레이트 올리고머(a4)는 경화성 수지 조성물 총 100중량부에 대하여 각각 0.1 내지 89.8중량부, 0.1 내지 89.8중량부 및 0.1 내지 89.8중량부 포함되는 것을 것을 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 착색제는 착색입자, 염료 또는 안료에서 선택된 것을 특징으로 하는 경화성 수지 조성물.
- 제 19항에 있어서,상기 착색제는 분말상을 사용하거나, 용매에 분산 또는 용해 되어 있는 것을 사용함을 특징으로하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 경화성 수지 조성물은 변색 안료를 더 포함하는 것을 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 경화성 수지 조성물은 경화 전후에 색이 변하는 것을 특징으로 하는 경화성 수지 조성물.
- 제 21항에 있어서,상기 변색안료는 경화성 수지 조성물 총 100중량부에 대하여 0.1 내지 20중량부 포함하는 것을 특징으로 하는 경화성 수지 조성물.
- 제 21항에 있어서,상기 변색 안료는 자외선 또는 열을 조사할 경우 변색 되는 것으로써 나프토피란, 벤조피란, 페난트로피란, 인데노나프토피란, 스피로(벤조인돌린)나프토피란, 스피로(인돌린)벤조피란, 스피로(인돌린)나프토피란, 스피로(인돌린)퀴노피란, 스 피로(인돌린)피란, 스피로(인돌린)나프록사진, 스피로(인돌린)피리도벤즈옥사진, 스피로(벤조인돌린)피리도벤즈옥사진, 스피로(벤조인돌린)나프록사진, 스피로(인돌린)벤즈옥사진, 크로멘, 유기-금속 디티조네이트, 펄자이드 및 펄지미드등으로 이루어진 군으로부터 선택된 적어도 1종을 포함하는 것을 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 경화성 수지 조성물은 총 조성물 100 중량부에 대하여 상기 자외선 경화형 (메타)아크릴레이트 단량체 5 내지 80중량부, 광개시제 0.1 내지 10 중량부 및 착색제 0.1 내지 20 중량부 포함하는 것으로 특징으로 하는 경화성 수지 조성물.
- 제 1항에 있어서,상기 경화성 수지 조성물은 점도가 25℃에서 1 내지 500000cps인 것을 특징으로 하는 경화성 수지 조성물.
- 청구항 1에 있어서,상기 화상표시장치가 액정표시장치(Liquid Crystal Display Device; LCD), 유기발광표시장치(Organic Light Emitting Display Device; OLED), 플라즈마 표시장치(Plasma Display Device; PDP)에서 선택된 것임을 특징으로 하는 경화성 수지 조성물.
- 접합된 상부 기판 및 하부 기판을 포함하는 화상표시장치에 있어서,상기 접합된 상기 상부 기판 및 하부 기판이 외곽 실링제 조성물에 의해 밀봉되며, 상기 외곽 실링제 조성물이 제 1항 및 제 11항 내지 제27항 중 어느 한 항의 경화성 수지 조성물인 것을 특징으로 하는 화상표시장치.
- (i) 상부 기판과 하부 기판을 실란트로 접합하는 단계;(ii) 상기 접합된 두 기판의 가장자리를 제1항 및 제 11항 내지 제27항 중 어느 한 항의 경화성 수지조성물로 실링한 후 경화시키는 단계; 및(iii) 상부 기판, 하부 기판을 식각하는 단계를 포함하는 것을 특징으로 하는 화상표시장치의 제조 방법.
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KR101382038B1 (ko) * | 2012-05-31 | 2014-04-04 | 주식회사 소포스 | 자외선 경화접착방식을 이용한 가전제품용 유리판넬의 제조방법 및 가전제품용 유리판넬 |
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KR102448198B1 (ko) * | 2020-11-09 | 2022-09-29 | 솔루스첨단소재 주식회사 | 배리어 실란트 조성물 및 이를 이용한 표시패널의 제조방법 |
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KR102594277B1 (ko) * | 2021-12-02 | 2023-10-26 | 주식회사 한솔케미칼 | 안료를 포함하는 저경도 자외선 경화형 수지조성물 |
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