JPH08220324A - Production of color filter - Google Patents
Production of color filterInfo
- Publication number
- JPH08220324A JPH08220324A JP2669295A JP2669295A JPH08220324A JP H08220324 A JPH08220324 A JP H08220324A JP 2669295 A JP2669295 A JP 2669295A JP 2669295 A JP2669295 A JP 2669295A JP H08220324 A JPH08220324 A JP H08220324A
- Authority
- JP
- Japan
- Prior art keywords
- photosensitive resin
- resin layer
- base film
- film
- colored photosensitive
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 26
- 229920005989 resin Polymers 0.000 claims abstract description 89
- 239000011347 resin Substances 0.000 claims abstract description 89
- 239000000758 substrate Substances 0.000 claims abstract description 56
- 238000000034 method Methods 0.000 claims abstract description 29
- 239000003086 colorant Substances 0.000 claims abstract description 19
- 238000010438 heat treatment Methods 0.000 claims description 31
- 239000000853 adhesive Substances 0.000 claims description 12
- 230000001070 adhesive effect Effects 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 19
- -1 polyethylene terephthalate Polymers 0.000 description 16
- 230000007704 transition Effects 0.000 description 12
- 239000000049 pigment Substances 0.000 description 11
- 229920000139 polyethylene terephthalate Polymers 0.000 description 11
- 239000005020 polyethylene terephthalate Substances 0.000 description 11
- 238000010030 laminating Methods 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 230000001681 protective effect Effects 0.000 description 8
- 239000011342 resin composition Substances 0.000 description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 230000003746 surface roughness Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- 239000004640 Melamine resin Substances 0.000 description 3
- 238000000149 argon plasma sintering Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 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 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
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 206010034972 Photosensitivity reaction Diseases 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000036211 photosensitivity Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
- LMGYOBQJBQAZKC-UHFFFAOYSA-N 1-(2-ethylphenyl)-2-hydroxy-2-phenylethanone Chemical compound CCC1=CC=CC=C1C(=O)C(O)C1=CC=CC=C1 LMGYOBQJBQAZKC-UHFFFAOYSA-N 0.000 description 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- MDKSQNHUHMMKPP-UHFFFAOYSA-N 2,5-bis(4-methoxyphenyl)-4-phenyl-1h-imidazole Chemical class C1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC(OC)=CC=2)N1 MDKSQNHUHMMKPP-UHFFFAOYSA-N 0.000 description 1
- CTWRMVAKUSJNBK-UHFFFAOYSA-N 2-(2,4-dimethoxyphenyl)-4,5-diphenyl-1h-imidazole Chemical class COC1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 CTWRMVAKUSJNBK-UHFFFAOYSA-N 0.000 description 1
- NSWNXQGJAPQOID-UHFFFAOYSA-N 2-(2-chlorophenyl)-4,5-diphenyl-1h-imidazole Chemical class ClC1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 NSWNXQGJAPQOID-UHFFFAOYSA-N 0.000 description 1
- UIHRWPYOTGCOJP-UHFFFAOYSA-N 2-(2-fluorophenyl)-4,5-diphenyl-1h-imidazole Chemical class FC1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 UIHRWPYOTGCOJP-UHFFFAOYSA-N 0.000 description 1
- SNFCQJAJPFWBDJ-UHFFFAOYSA-N 2-(4-methoxyphenyl)-4,5-diphenyl-1h-imidazole Chemical class C1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 SNFCQJAJPFWBDJ-UHFFFAOYSA-N 0.000 description 1
- GZYZPHPDKCTFFH-UHFFFAOYSA-N 2-(4-methylsulfanylphenyl)-4,5-diphenyl-1h-imidazole Chemical class C1=CC(SC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 GZYZPHPDKCTFFH-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-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
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 1
- VZMLJEYQUZKERO-UHFFFAOYSA-N 2-hydroxy-1-(2-methylphenyl)-2-phenylethanone Chemical compound CC1=CC=CC=C1C(=O)C(O)C1=CC=CC=C1 VZMLJEYQUZKERO-UHFFFAOYSA-N 0.000 description 1
- NLGDWWCZQDIASO-UHFFFAOYSA-N 2-hydroxy-1-(7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-yl)-2-phenylethanone Chemical compound OC(C(=O)c1cccc2Oc12)c1ccccc1 NLGDWWCZQDIASO-UHFFFAOYSA-N 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
- BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 1
- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- YYVYAPXYZVYDHN-UHFFFAOYSA-N 9,10-phenanthroquinone Chemical compound C1=CC=C2C(=O)C(=O)C3=CC=CC=C3C2=C1 YYVYAPXYZVYDHN-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- XXOHYUTZQHIVGK-UHFFFAOYSA-N ClC1=C(C=CC=C1)C=1NC(C(N1)(C1=CC=CC=C1)C1=CC(=CC=C1)OC)(C1=CC=CC=C1)C1=CC(=CC=C1)OC Chemical class ClC1=C(C=CC=C1)C=1NC(C(N1)(C1=CC=CC=C1)C1=CC(=CC=C1)OC)(C1=CC=CC=C1)C1=CC(=CC=C1)OC XXOHYUTZQHIVGK-UHFFFAOYSA-N 0.000 description 1
- 229920003270 Cymel® Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- ARNIZPSLPHFDED-UHFFFAOYSA-N [4-(dimethylamino)phenyl]-(4-methoxyphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 ARNIZPSLPHFDED-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000008365 aromatic ketones Chemical class 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 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
- QDVNNDYBCWZVTI-UHFFFAOYSA-N bis[4-(ethylamino)phenyl]methanone Chemical compound C1=CC(NCC)=CC=C1C(=O)C1=CC=C(NCC)C=C1 QDVNNDYBCWZVTI-UHFFFAOYSA-N 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000005674 electromagnetic induction Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- JZMPIUODFXBXSC-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical class OC(=O)C=C.OC(=O)C=C.CCOC(N)=O JZMPIUODFXBXSC-UHFFFAOYSA-N 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000001056 green pigment Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229940086559 methyl benzoin Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- 239000001053 orange pigment Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229940059574 pentaerithrityl Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Optical Filters (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、カラーフイルタの製造
法に関する。FIELD OF THE INVENTION The present invention relates to a method for manufacturing a color filter.
【0002】[0002]
【従来の技術】カラーフイルタは、ガラス等の光学的に
透明な基板の表面に、2種以上の色相を異にする極めて
微細なストライプ状又はモザイク状のパターンを、一定
の間隔を開けて平行又は交差して並べた物である。これ
らのパターンは、色相を所定の順序に所定の間隔をおい
て整然と配置し、厚さムラの少ない均一な層とする必要
があり、スクリーン印刷法、フォトリソグラフィ法、染
色法等のカラーフイルタの製造法が提案されている。2. Description of the Related Art A color filter is an extremely transparent stripe-like or mosaic-like pattern having two or more different hues, which are parallel to each other on a surface of an optically transparent substrate such as glass. Or, they are crossed and arranged. These patterns must be arranged in order in a predetermined order with hues at a predetermined interval, and it is necessary to form a uniform layer with little thickness unevenness, and the color filters of the screen printing method, the photolithography method, the dyeing method, etc. Manufacturing methods have been proposed.
【0003】また、ベースフイルム及び感光性樹脂層を
有する感光性フイルムを使用した、多色の微細なストラ
イプ状又はモザイク状のパターンを簡単に高精度で形成
できるカラーフイルタの製造法が知られている。感光性
フイルムは公知であり、特公昭45−25231号公報
等に開示されている。There is also known a method for producing a color filter, which uses a base film and a photosensitive film having a photosensitive resin layer and can easily form a multi-color fine stripe-shaped or mosaic-shaped pattern with high accuracy. There is. Photosensitive films are known and disclosed in Japanese Patent Publication No. 45-25231.
【0004】感光性フイルムを用いてカラーフイルタを
作成する方法としては、一色に着色された感光性樹脂組
成物をベースフイルムに塗布乾燥した感光性フイルムの
感光性樹脂層を、透明な基板の上に転写して、所定のパ
ターンマスクを介して露光、現像してパターンを形成す
る方法(特開昭61−99102号公報、特開平3−1
60454号公報、特開平3−111802号公報、特
開平2−151805号公報、特開平4−212161
号公報、特開平4−301602号公報、特開平5−2
107号公報等)が知られている。As a method for preparing a color filter using a photosensitive film, a photosensitive resin composition of a photosensitive film obtained by applying a photosensitive resin composition colored in one color to a base film and drying the photosensitive resin composition on a transparent substrate is used. And then exposed to light through a predetermined pattern mask and developed to form a pattern (JP-A-61-99102 and JP-A-3-1).
No. 60454, No. 3-111802, No. 2-151805, No. 4-212161.
Japanese Patent Application Laid-Open No. 4-301602, Japanese Patent Application Laid-Open No. 5-2
No. 107, etc.) is known.
【0005】感光性フイルムは、良好なパターンを得る
ために、その追従性を向上させることが必要である。感
光性フイルムの追従性を向上させる方法としては、例え
ば、基板に段差があっても、その基板を正確に微細加工
できることを特徴とする三層レジスト法(J.Vac.Sci.Te
chnol.,16巻1620頁 1968年発行等)、現像前で露光後に
感光性レジスト層を50〜150℃、30〜60秒の条
件で加熱して、UV光が充分に当たらない下層部分の反
応を促進させるアフタベーク法(特開平3−19659
6号公報等)等が挙げられる。また、顔料分散フォトポ
リマーを用いたカラーフイルタで、光開始剤のラジカル
により誘起したモノマーラジカルの発生とその重合連鎖
反応を促進し、スピンナーを用いて感光性レジスト層を
塗布し、溶剤除去のためにプリベーク(例えば、85℃
で5分間)を行うプリベーク法(J.Photopolym.Sci.Tec
hnol.,Vol.2,No.2,1989年 244頁〜248頁)等が挙げられ
る。In order to obtain a good pattern, the photosensitive film needs to improve its followability. As a method of improving the followability of the photosensitive film, for example, even if there is a step on the substrate, the three-layer resist method (J.Vac.Sci.Te
chnol., 16: 1620, published in 1968, etc.), the photosensitive resist layer is heated before development and after exposure at 50 to 150 ° C. for 30 to 60 seconds to cause reaction of the lower layer portion which is not sufficiently exposed to UV light. After-bake method for promoting heat treatment (Japanese Patent Application Laid-Open No. 3-19659)
No. 6, etc.) and the like. In addition, in a color filter using a pigment-dispersed photopolymer, the generation of monomer radicals induced by the radicals of the photoinitiator and its polymerization chain reaction are promoted, and a photosensitive resist layer is applied using a spinner to remove the solvent. Pre-bake (eg, 85 ℃
Prebaking method (J.Photopolym.Sci.Tec)
hnol., Vol.2, No.2, 1989, pp. 244-248).
【0006】従来のカラーフイルタの製造法(例えば、
染色法、顔料分散液状レジスト法、印刷法、ロールコー
タ法、顔料分散フイルムレジスト法等)では、二色目以
降の層を形成する際に、既に形成された着色層上の二色
目以降の着色層と前記基板上に直接接触する着色層との
間に段差が生ずる。この段差は、最大で1.0μmを超
え、この上に直接ITOをスパッタリングするとITO
の断線や液晶を挾む電極間の距離が不均一になり、良好
なカラーデスプレイが得られないために、一般には、保
護膜又はオーバコート膜と称する2〜5μmの膜を形成
し、表面を均一化することが行われている。フイルム法
では、この段差は既に形成された着色層の厚さ(1〜5
μm)により決まり、この段差があるために新着色層が
下地(透明ガラス)に接触しにくく、また、接着圧力が
不充分であることにより、新着色層が下地に密着せず、
ベースフイルムを剥離すると、ベースフイルムとともに
剥離されて、下地に新着色層が付着しない部分が発生
し、そのまま、露光現像すると、新着色層が存在しない
部分を露光する等の不都合が生じ、所望のカラーフイル
タが得られない欠点がある。また、二色目以降の画素上
では、一色目の画素上に乗っていた着色感光性樹脂層の
一部が流れ込んできて、二色目では、一色目の画素に近
い端が持ち上がり、画素表面が斜めになる(J状、n状
の断面となる)。三色目の画素上では、両隣の画素から
の着色感光性樹脂層の流れ込みがあるため画素の両端が
持ち上がる(M状の断面となる)。図2にJ状、n状及
びM状の画素の断面の模式図を示す。J状やM状の持ち
上がりがあると、三色の画素の表面の不均一を招き、所
望の平坦性が得られず、持ち上がった端が対極と接触し
て、画素不良を生じ、色ムラを発生させる等の欠点があ
った。基板を加熱後、前記の感光性フイルムの保護フイ
ルムを剥がしながら、着色感光性樹脂層を基板と接着さ
せて加圧ロールを通す(ラミネートする)だけでは、フ
イルム追随性は改善できない。Conventional color filter manufacturing methods (eg,
Dyeing method, pigment-dispersed liquid resist method, printing method, roll coater method, pigment-dispersed film resist method, etc.), when forming the layer of the second color or later, the colored layer of the second color or later on the already formed color layer. A step is formed between the colored layer and the colored layer that is in direct contact with the substrate. This step exceeds 1.0 μm at maximum, and if ITO is directly sputtered on this step, the ITO
Since the wire breakage and the distance between the electrodes sandwiching the liquid crystal become non-uniform and a good color display cannot be obtained, a film of 2 to 5 μm generally called a protective film or an overcoat film is formed, and the surface is covered. It is being made uniform. In the film method, this step is the thickness of the already formed colored layer (1-5
μm), and this step makes it difficult for the new colored layer to come into contact with the base (transparent glass), and because the adhesive pressure is insufficient, the new colored layer does not adhere to the base,
When the base film is peeled off, a part where the new color layer is not adhered is peeled off along with the base film, and when exposed and developed as it is, disadvantages such as exposure of a part where the new color layer does not exist are generated, and the desired There is a drawback that a color filter cannot be obtained. In addition, on the pixels of the second and subsequent colors, part of the colored photosensitive resin layer that had been on the pixels of the first color flows in, and in the second color, the edge close to the pixels of the first color is lifted and the pixel surface is slanted. (J-shaped, n-shaped cross section). On the pixel of the third color, the colored photosensitive resin layer flows in from the adjacent pixels on both sides, so that both ends of the pixel are lifted (it becomes an M-shaped cross section). FIG. 2 shows a schematic view of a cross section of J-shaped, n-shaped, and M-shaped pixels. If there is a J-shaped or M-shaped lifting, the unevenness of the surface of the three-color pixels is not obtained, the desired flatness cannot be obtained, and the lifted edge comes into contact with the counter electrode, resulting in pixel failure and uneven color. There was a defect such as causing it. The film followability cannot be improved only by adhering the colored photosensitive resin layer to the substrate and passing it through a pressure roll (laminating) while peeling off the protective film of the photosensitive film after heating the substrate.
【0007】[0007]
【発明が解決しようとする課題】本発明は、前記の従来
の技術の問題を解消し、感光性フィルムのベースフィル
ムの剥離がスムーズで、追随性、作業性よく基板上に均
一な厚さの高精度の段差、追随性不良のない、画素の欠
落のない多色の微細パターンの形成された優れた耐熱性
を有するカラーフイルタの製造法を提供するものであ
る。DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned problems of the prior art and allows the base film of the photosensitive film to be peeled off smoothly, with good followability and workability, and with a uniform thickness on the substrate. It is intended to provide a method of manufacturing a color filter having high heat resistance, in which a multi-color fine pattern having no steps with high precision, no defect in followability, and lack of pixels is formed.
【0008】[0008]
【課題を解決するための手段】本発明は、透明基板上
に、ベースフイルムと一色に着色された感光性樹脂層と
からなる感光性フイルムを、(1)着色された感光性樹
脂層が前記基板に面するように貼り合わせる工程、
(2)パターン状に露光する工程及び(3)現像工程を
含む工程を繰り返して多色パターンを形成させるカラー
フイルタの製造法であって、二色目以降の着色された感
光性樹脂層が前記基板に面するように、画素間に空間を
形成して貼り合わせる工程を行い、前記(1)と(3)
の工程の間に、加熱により二色目以降の感光性樹脂層を
ベースフイルムから画素間空間へ移行させる移行工程及
びベースフイルムを剥離する剥離工程を行うカラーフイ
ルタの製造法において、ベースフイルムを剥離する剥離
工程を、ベースフイルムと着色感光性樹脂層の密着力よ
り着色感光性樹脂層と前置画素との密着力のほうが大き
く、ベースフイルムと着色感光性樹脂層の密着力より着
色感光性樹脂層の破断応力の方が大きい温度範囲で行う
ことを特徴とするカラーフイルタの製造法に関する。According to the present invention, there is provided a photosensitive film comprising a base film and a photosensitive resin layer colored in one color on a transparent substrate, wherein (1) the colored photosensitive resin layer is A step of bonding so as to face the substrate,
A method for manufacturing a color filter, wherein a multi-color pattern is formed by repeating a step of (2) exposing in a pattern and a step of (3) a developing step, wherein the second and subsequent colored photosensitive resin layers are formed on the substrate. To form a space between the pixels so that they face each other.
In the manufacturing method of the color filter, the base film is peeled off during the step of performing a transfer step of moving the photosensitive resin layer of the second and subsequent colors from the base film to the inter-pixel space by heating and a peeling step of peeling the base film. In the peeling process, the adhesive force between the colored photosensitive resin layer and the front pixel is greater than the adhesive force between the base film and the colored photosensitive resin layer, and the colored photosensitive resin layer is stronger than the adhesive force between the base film and the colored photosensitive resin layer. The present invention relates to a method for manufacturing a color filter, which is characterized in that it is carried out in a temperature range in which the breaking stress is higher.
【0009】以下、本発明を詳細に説明する。二色目以
降のカラーフイルタの画素の表面を平坦化するために前
記(1)と(3)の工程の間で、加熱により二色目以降
の感光性樹脂層をベースフイルムから基板表面上の空間
に移行する移行工程の態様についてさらに詳細に図1を
用いて説明する。図1は本発明の製造法を示す感光性フ
イルム及びカラーフイルタの断面図であり、ベースフイ
ルム1がPET(ポリエチレンテレフタレートフイル
ム)で、着色感光性樹脂層は赤(R)、緑(G)の順に
形成していく場合を例にとって説明する。The present invention will be described in detail below. In order to flatten the surface of the pixels of the color filters of the second and subsequent colors, the photosensitive resin layer of the second and subsequent colors is heated from the base film to a space on the substrate surface by heating between the steps (1) and (3). The aspect of the transition step of transition will be described in more detail with reference to FIG. FIG. 1 is a sectional view of a photosensitive film and a color filter showing a production method of the present invention. The base film 1 is PET (polyethylene terephthalate film), and the colored photosensitive resin layers are red (R) and green (G). An example will be described in which the layers are formed in order.
【0010】(a)は、ベースフイルム1(PET(ポ
リエチレンテレフタレートフイルム))と着色感光性樹
脂層(緑)2からなる感光性フイルムの着色感光性樹脂
層(緑)2と前置画素(赤)3が整然と配列されている
透明基板4が面している状態を示す。(b)は、感光性
フイルムの着色感光性樹脂層(緑)2と前置画素(赤)
3が整然と配列されている透明基板4との画素間に、空
間5を形成した貼り合わせを示している。着色感光性樹
脂層(緑)2は、前置画素(赤)3及び透明基板4に追
随している必要はなく、完全に平坦なままで、前置画素
(赤)3表面に接触していることが好ましい。(b)で
は、着色感光性樹脂層(緑)2が前置画素(赤)3に密
着した様子を示したものであり、空間5と表示してある
部分は、着色感光性樹脂層(緑)2も前置画素(赤)3
も存在していない部分である。(A) is a colored photosensitive resin layer (green) 2 of a photosensitive film comprising a base film 1 (PET (polyethylene terephthalate film)) and a colored photosensitive resin layer (green) 2 and a front pixel (red). ) 3 shows a state in which the transparent substrate 4 in which the elements are arranged in order is facing. (B) is a colored photosensitive resin layer (green) 2 and a front pixel (red) of the photosensitive film.
3 shows the bonding in which the space 5 is formed between the pixels of the transparent substrate 4 and the transparent substrate 4 arranged in an orderly manner. The colored photosensitive resin layer (green) 2 does not need to follow the front pixel (red) 3 and the transparent substrate 4, but remains completely flat and contacts the front pixel (red) 3 surface. Is preferred. (B) shows a state in which the colored photosensitive resin layer (green) 2 is in close contact with the front pixel (red) 3, and the portion indicated as space 5 is the colored photosensitive resin layer (green). ) 2 is also a front pixel (red) 3
Is a part that does not exist.
【0011】(c)は、本発明の移行工程後の状態を示
す図であり、移行工程は、上記の(1)〜(3)の工程
の間に行われ、着色感光性樹脂層(緑)2と空間5を置
換する工程であり、着色感光性樹脂層(緑)2の空間5
部分への移行は、加熱により行う。(b)の状態で貼り
合わせ直後は、着色感光性樹脂層(緑)2はベースフイ
ルム1に密着しているが、加熱により、流動性が増大
し、重力によって透明基板4表面上の空間5内に移行を
始める。着色感光性樹脂層(緑)2は、ベースフイルム
1よりも透明基板4に対する密着力が大きく、着色感光
性樹脂層(緑)2の接触角がPET(ポリエチレンテレ
フタレート)の接触角よりも透明基板4に対して大きい
ので、前置画素(赤)3の壁を伝って流れ落ちる場合、
ベースフイルム1面で液滴を作って増大し、透明基板4
と接触した後、透明基板4上に広がって移行を完了す
る。(C) is a diagram showing a state after the transfer step of the present invention, wherein the transfer step is performed between the steps (1) to (3) described above, and the colored photosensitive resin layer (green) ) 2 for replacing the space 5 with the space 5 of the colored photosensitive resin layer (green) 2
The transfer to the part is performed by heating. Immediately after bonding in the state of (b), the colored photosensitive resin layer (green) 2 is in close contact with the base film 1, but the fluidity is increased by heating, and the space 5 on the surface of the transparent substrate 4 is increased by gravity. The transition begins within. The colored photosensitive resin layer (green) 2 has a larger adhesion to the transparent substrate 4 than the base film 1, and the contact angle of the colored photosensitive resin layer (green) 2 is more transparent than the contact angle of PET (polyethylene terephthalate). Since it is larger than 4, when it flows down the wall of the front pixel (red) 3,
A transparent film is formed on the transparent surface of the base film 1 by increasing the number of droplets formed on one surface.
After contacting with, it spreads on the transparent substrate 4 to complete the transition.
【0012】移行工程が完了すると、着色感光性樹脂層
(緑)2は、透明基板4表面上の空間5に移行を完了
し、その表面上に空間が出現し、着色感光性樹脂層
(緑)2と空間5が入れ変る。このとき、着色感光性樹
脂層(緑)2は、その表面張力によって均一化している
ので、表面の平坦性は優れたものであり、現像後の画素
は一色目とほとんど同一の断面形状を持つ。以上に、一
色目が赤、二色目が緑の場合を例として説明したが、色
の順序はこれに限定されず、どのような色順序も可能で
ある。When the transfer process is completed, the colored photosensitive resin layer (green) 2 completes the transfer to the space 5 on the surface of the transparent substrate 4 and a space appears on the surface, and the colored photosensitive resin layer (green) is formed. ) 2 and space 5 interchange. At this time, since the colored photosensitive resin layer (green) 2 is made uniform by its surface tension, the surface flatness is excellent, and the pixel after development has a cross-sectional shape almost the same as that of the first color. . Although the case where the first color is red and the second color is green has been described above as an example, the order of colors is not limited to this, and any color order is possible.
【0013】移行工程における加熱は、室温以上で、着
色感光性樹脂層が熱硬化反応を開始する温度以下で行
い、低温では長時間、高温では短時間で移行は完了し、
移行した着色感光性樹脂層表面は高度の平坦性を有す
る。加熱には、熱板加熱、オーブン加熱、超音波加熱、
赤外線加熱、電磁誘導加熱、摩擦熱加熱等があるが、こ
れらに制限されない。本発明における移行工程は、上記
の(1)〜(3)の間で行われるが、(2)の露光工程
の前でも後でもよく、露光工程の前と後の二回実施して
もよく、また、露光工程において行うことも可能であ
る。移行工程は、上記ではベースフイルムが存在する状
態での移行工程を説明したがベースフイルムの剥離後に
前記移行工程を実施することもできる。すなわち、ベー
スフイルムの存在が無くても、着色感光性樹脂層の画素
間の空間への移動は可能で、基板表面に最終的に密着さ
せることができる。The heating in the transfer step is carried out at room temperature or above and below the temperature at which the colored photosensitive resin layer starts the thermosetting reaction, and the transfer is completed at a low temperature for a long time and at a high temperature for a short time.
The surface of the transferred colored photosensitive resin layer has a high degree of flatness. For heating, hot plate heating, oven heating, ultrasonic heating,
There are, but not limited to, infrared heating, electromagnetic induction heating, frictional heating, and the like. The transition step in the present invention is performed between the above (1) to (3), but may be performed before or after the exposure step of (2), or may be performed twice before and after the exposure step. It is also possible to perform it in the exposure step. As the transfer step, the transfer step in the state where the base film exists has been described above, but the transfer step may be performed after the base film is peeled off. That is, even without the presence of the base film, the colored photosensitive resin layer can be moved to the space between the pixels and can be finally brought into close contact with the substrate surface.
【0014】ベースフイルムを剥離する剥離工程は上記
の(1)〜(3)の間で行うことができ、移行工程の前
でも後でも良く露光工程の前でも後でも良い。剥離工程
後移行工程を行う例として図3に示す。The peeling step for peeling the base film can be carried out between the above steps (1) to (3) and may be carried out before or after the transferring step, or before or after the exposing step. FIG. 3 shows an example of performing the transfer step after the peeling step.
【0015】ベースフイルムの剥離をスムーズに行うた
めには、ベースフイルムと着色感光性樹脂層の密着力
(A)、着色感光性樹脂層と前置画素との密着力(B)
及び着色感光性樹脂層の破断応力(C)とすると、(A)
<(C)で(A)<(B)の時に着色感光性樹脂層はベースフ
イルムからスムーズに剥離され前置画素の表面に密着す
る。(C)は着色感光性樹脂層の材質に依存し、着色感
光性樹脂層の貯蔵弾性率が高いほど大きな値を示す。
(C)の値は温度に逆比例するので低温では大きく高温
では小さくなる。移行工程は着色感光性樹脂層が表面張
力により基板表面に密着する現象であるから、(C)の
値は小さいほどよく着色感光性樹脂層が溶融軟化するま
で高温に保つことが好ましい。本発明においては、ベー
スフイルムの剥離をスムーズに行なう点からベースフイ
ルムを剥離する剥離工程は、ベースフイルムと着色感光
性樹脂層の密着力より着色感光性樹脂層と前置画素との
密着力のほうが大きく、前記ベースフイルムと前記着色
感光性樹脂層の密着力より着色感光性樹脂層の破断応力
の方が大きい温度範囲で行うことが必要である。前記温
度範囲は、−10〜30℃とすることが好ましい。この
温度範囲が、−10℃未満及び30℃を超えると、ベー
スフイルムに着色感光性樹脂が残存する傾向がある。ま
た、剥離工程におけるベースフイルムの剥離速度は、ベ
ースフイルムの剥離をスムーズに行なう点から、1〜2
0m/秒とすることが好ましい。この剥離速度が、1m
/秒未満及び20m/秒を超えると、ベースフイルムに
着色感光性樹脂が残存する傾向がある。本発明において
は、前記(1)と(3)の工程の間に、加熱により二色
目以降の感光性樹脂層をベースフイルムから画素間空間
へ移行させる移行工程を行った後ベースフイルムを剥離
する剥離工程を行うことが好ましい。In order to smoothly peel off the base film, the adhesive force (A) between the base film and the colored photosensitive resin layer and the adhesive force (B) between the colored photosensitive resin layer and the front pixel.
And the breaking stress (C) of the colored photosensitive resin layer, (A)
When (A) <(B) in <(C), the colored photosensitive resin layer is smoothly peeled off from the base film and adheres to the surface of the front pixel. (C) depends on the material of the colored photosensitive resin layer, and shows a larger value as the storage elastic modulus of the colored photosensitive resin layer is higher.
Since the value of (C) is inversely proportional to temperature, it becomes large at low temperatures and small at high temperatures. Since the transition step is a phenomenon in which the colored photosensitive resin layer adheres to the substrate surface due to surface tension, the smaller the value of (C), the better the temperature is preferably maintained until the colored photosensitive resin layer melts and softens. In the present invention, the peeling step of peeling the base film from the viewpoint of smoothly peeling the base film, the adhesion of the colored photosensitive resin layer and the front pixel is more than the adhesion of the base film and the colored photosensitive resin layer. It is necessary to carry out in a temperature range in which the breaking stress of the colored photosensitive resin layer is larger than the adhesive force between the base film and the colored photosensitive resin layer. The temperature range is preferably −10 to 30 ° C. If this temperature range is lower than -10 ° C or higher than 30 ° C, the colored photosensitive resin tends to remain on the base film. In addition, the peeling speed of the base film in the peeling step is from 1 to 2 from the viewpoint of smoothly peeling the base film.
It is preferably 0 m / sec. This peeling speed is 1 m
If it is less than / sec and exceeds 20 m / sec, the colored photosensitive resin tends to remain on the base film. In the present invention, between the steps (1) and (3), the base film is peeled off after performing a transfer step of transferring the photosensitive resin layers of the second and subsequent colors from the base film to the inter-pixel space by heating. It is preferable to perform a peeling step.
【0016】(d)は、着色感光性樹脂層(緑)2露光
後に現像した後のカラーフイルタの画素の断面の形状を
示す。なお、ベースフイルムの剥離は、露光工程後現像
工程前又は露光工程前に行われる。(D) shows the shape of the cross section of the pixel of the color filter after the development of the colored photosensitive resin layer (green) 2 after exposure. The base film is peeled off after the exposure step and before the development step or before the exposure step.
【0017】本発明に用いられる感光性フイルムは、透
明なベースフイルム、例えば、ポリエチレンテレフタレ
ート等のフイルム上に、一色に着色された感光性樹脂組
成物を塗布し、乾燥させて一色に着色された感光性樹脂
層を形成させたものである。この着色感光性樹脂層は未
硬化であり、柔軟で、粘着性を有するため、この上にさ
らにポリエチレンフイルム等の保護フイルムを貼り合わ
せて、外部からの損傷、異物の付着等を防止することが
望ましい。感光性フイルムに形成された着色感光性樹脂
層は、保護フイルムを剥がしながら透明基板上に貼り合
わされ、また、前記着色感光性樹脂層表面のベースフイ
ルムは、所定パターンのネガマスクを通じて露光した後
に除去される。The photosensitive film used in the present invention is formed by coating a transparent base film, for example, a film of polyethylene terephthalate or the like, with a photosensitive resin composition colored in one color, and drying it to color the film in one color. A photosensitive resin layer is formed. Since this colored photosensitive resin layer is uncured, flexible and adhesive, a protective film such as a polyethylene film may be further laminated on the colored photosensitive resin layer to prevent external damage or adhesion of foreign matter. desirable. The colored photosensitive resin layer formed on the photosensitive film is attached on a transparent substrate while peeling off the protective film, and the base film on the surface of the colored photosensitive resin layer is removed after exposure through a negative mask having a predetermined pattern. It
【0018】一色に着色された感光性樹脂組成物は、エ
チレン性不飽和化合物(a)、カルボキシル基含有フイ
ルム性付与ポリマー(b)、光重合開始剤(c)及び顔
料又は染料(d)は含有することが好ましく、この感光
性樹脂組成物を用いた感光性フイルムの感光性樹脂組成
物層の厚さは、0.5〜15μmであることが好まし
い。The photosensitive resin composition colored in one color contains the ethylenically unsaturated compound (a), the carboxyl group-containing film-forming polymer (b), the photopolymerization initiator (c) and the pigment or dye (d). It is preferable to contain the photosensitive resin composition, and the thickness of the photosensitive resin composition layer of the photosensitive film using this photosensitive resin composition is preferably 0.5 to 15 μm.
【0019】エチレン性不飽和化合物(a)としては、
例えば、多価アルコールにα,β−不飽和カルボン酸を
付加して得られる化合物(トリメチロールプロパンジ
(メタ)アクリレート(メタアクリレート又はアクリレ
ートを意味する。以下同じ)、トリメチロールプロパン
トリ(メタ)アクリレート、テトラメチロールメタント
リ(メタ)アクリレート、ジペンタエリスリトールペン
タ(メタ)アクリレート、ジペンタエリスリトールヘキ
サ(メタ)アクリレート等)、グリシジル基含有化合物
にα,β−不飽和カルボン酸を付加して得られる化合物
(トリメチロールプロパントリグリシジルエーテルトリ
アクリレート、ビスフェノールAジグリシジルエーテル
ジ(メタ)アクリレート等)、多価カルボン酸(無水フ
タル酸等)と水酸基及びエチレン性不飽和基を有する化
合物(β−ヒドロキシエチル(メタ)アクリレート等)
とのエステル化物、(メタ)アクリル酸(メタアクリル
酸又はアクリル酸を意味する、以下同じ)のアルキルエ
ステル((メタ)アクリル酸メチル、(メタ)アクリル
酸エチル、(メタ)アクリル酸ブチル、(メタ)アクリ
ル酸2−エチルヘキシル等)、トリメチルヘキサメチレ
ンジイソシアナートと2価アルコールと2価の(メタ)
アクリル酸モノエステルとを反応させて得られるウレタ
ンジアクリレート化合物などが挙げられる。これらの化
合物は単独で又は2種以上を組み合わせて使用される。
(a)成分の配合量は、(a)成分と(b)成分の総量
を100重量部として90〜50重量部とすることが好
ましい。As the ethylenically unsaturated compound (a),
For example, a compound obtained by adding an α, β-unsaturated carboxylic acid to a polyhydric alcohol (trimethylolpropane di (meth) acrylate (means methacrylate or acrylate; hereinafter the same), trimethylolpropane tri (meth)) Acrylate, tetramethylolmethane tri (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa (meth) acrylate, etc., obtained by adding α, β-unsaturated carboxylic acid to a glycidyl group-containing compound Compounds (trimethylolpropane triglycidyl ether triacrylate, bisphenol A diglycidyl ether di (meth) acrylate, etc.), polyvalent carboxylic acids (phthalic anhydride, etc.) and compounds having a hydroxyl group and an ethylenically unsaturated group (β-hydroxy ether Chill (meth) acrylate etc.)
And an ester of (meth) acrylic acid (meaning methacrylic acid or acrylic acid, the same applies hereinafter) (methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, ( (Meth) acrylic acid 2-ethylhexyl), trimethylhexamethylene diisocyanate, dihydric alcohol and divalent (meth)
Examples thereof include urethane diacrylate compounds obtained by reacting with acrylic acid monoester. These compounds are used alone or in combination of two or more.
The blending amount of the component (a) is preferably 90 to 50 parts by weight based on 100 parts by weight of the total amount of the components (a) and (b).
【0020】カルボキシル基含有フイルム性付与ポリマ
ー(b)としては、例えば、(メタ)アクリル酸アルキ
ルエステルと(メタ)アクリル酸との共重合体、(メ
タ)アクリル酸アルキルエステルと(メタ)アクリル酸
とこれらと共重合し得るビニルモノマーとの共重合体等
が挙げられる。(メタ)アクリル酸アルキルエステルと
しては、例えば(メタ)アクリル酸メチル、(メタ)ア
クリル酸エチル、(メタ)アクリル酸ブチル、(メタ)
アクリル酸2−エチルヘキシル等が挙げられる。また、
(メタ)アクリル酸アルキルエステル、(メタ)アクリ
ル酸及びこれらと共重合し得るビニルモノマーとして
は、(メタ)アクリル酸ジメチルエチル、(メタ)アク
リル酸テトラヒドロフルフリル、(メタ)アクリル酸ジ
エチル、2,2,2−トリフルオロエチル(メタ)アク
リレート、2,2,3,3−テトラフルオロプロピル
(メタ)アクリレート、アクリルアミド、ジアセトンア
クリルアミド、スチレン、ビニルトルエン等が挙げられ
る。(b)成分には、テレフタル酸、イソフタル酸、セ
バシン酸等を用いたポリエステル、ブタジエンとアクリ
ロニトリルとの共重合体、セルロースアセテート、セル
ロースアセテートブチレート、メチルセルロース、エチ
ルセルロース等を添加することができる。(b)成分の
使用によって、塗膜性や硬化物の膜特性が向上し、その
配合量は、(a)成分と(b)成分の総量を100重量
部として10〜50重量部とすることが好ましい。この
配合量が10重量部未満では、エチレン性不飽和化合物
が多くなるため光感度が低下する傾向があり、50重量
部を超えると、光硬化物が脆くなる傾向がある。また、
(b)成分の重量平均分子量は、前記塗膜性や膜強度の
点から10,000以上とすることが好ましい。Examples of the carboxyl group-containing film-forming polymer (b) include copolymers of (meth) acrylic acid alkyl ester and (meth) acrylic acid, (meth) acrylic acid alkyl ester and (meth) acrylic acid. And a vinyl monomer copolymerizable therewith. Examples of alkyl (meth) acrylates include methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, and (meth) acrylate.
2-ethylhexyl acrylate and the like can be mentioned. Also,
Examples of (meth) acrylic acid alkyl ester, (meth) acrylic acid and vinyl monomers copolymerizable therewith include dimethylethyl (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, diethyl (meth) acrylate, and 2 , 2,2-trifluoroethyl (meth) acrylate, 2,2,3,3-tetrafluoropropyl (meth) acrylate, acrylamide, diacetone acrylamide, styrene, vinyltoluene and the like. Polyester using terephthalic acid, isophthalic acid, sebacic acid and the like, copolymer of butadiene and acrylonitrile, cellulose acetate, cellulose acetate butyrate, methyl cellulose, ethyl cellulose and the like can be added to the component (b). By using the component (b), the coating properties and the film properties of the cured product are improved, and the blending amount is 10 to 50 parts by weight based on the total amount of the components (a) and (b) being 100 parts by weight. Is preferred. If the blending amount is less than 10 parts by weight, the ethylenically unsaturated compound is increased, so that the photosensitivity tends to decrease, and if it exceeds 50 parts by weight, the photocured product tends to become brittle. Also,
The weight average molecular weight of the component (b) is preferably 10,000 or more in view of the coating property and film strength.
【0021】光重合開始剤(c)としては、例えば、芳
香族ケトン(ベンゾフェノン、N,N′−テトラメチル
−4,4′−ジアミノベンゾフェノン(ミヒラーのケト
ン)、N,N′−テトラメチル−4,4′−ジアミノベ
ンゾフェノン、4−メトキシ−4′−ジメチルアミノベ
ンゾフェノン、4,4′−ジエチルアミノベンゾフェノ
ン、2−エチルアントラキノン、フェナントレンキノン
等)、ベンゾインエーテル(ベンゾインメチルエーテ
ル、ベンゾインエチルエーテル、ベンゾインフェニルエ
ーテル等)、ベンゾイン(メチルベンゾイン、エチルベ
ンゾイン等)、2,4,5−トリアリールイミダゾール
二量体(2−(o−クロロフェニル)−4,5−ジフェ
ニルイミダゾール二量体、2−(o−クロロフェニル)
−4,5−ジ(m−メトキシフェニル)−4,5−ジフ
ェニルイミダゾール二量体、2−(o−フルオロフェニ
ル)−4,5−ジフェニルイミダゾール二量体、2−
(o−メトキシフェニル)−4,5−ジフェニルイミダ
ゾール二量体、2−(p−メトキシフェニル)−4,5
−ジフェニルイミダゾール二量体、2,4−ジ(p−メ
トキシフェニル)−5−フェニルイミダゾール二量体、
2−(2,4−ジメトキシフェニル)−4,5−ジフェ
ニルイミダゾール二量体、2−(p−メチルメルカプト
フェニル)−4,5−ジフェニルイミダゾール二量体
等)などが用いられる。これらは、単独で又は2種類以
上を組み合わせて使用される。(c)成分の配合量は、
(a)成分と(b)成分の総量100重量部に対して
0.1〜10重量部とすることが好ましい。この配合量
が0.1重量部未満では、光感度が不十分となる傾向が
あり、10重量部を超えると、露光の際に組成物の表面
での光吸収が増大し、内部の光硬化が不十分となる傾向
がある。Examples of the photopolymerization initiator (c) include aromatic ketones (benzophenone, N, N'-tetramethyl-4,4'-diaminobenzophenone (Michler's ketone), N, N'-tetramethyl-). 4,4'-diaminobenzophenone, 4-methoxy-4'-dimethylaminobenzophenone, 4,4'-diethylaminobenzophenone, 2-ethylanthraquinone, phenanthrenequinone, etc., benzoin ether (benzoin methyl ether, benzoin ethyl ether, benzoinphenyl) Ether, etc.), benzoin (methylbenzoin, ethylbenzoin, etc.), 2,4,5-triarylimidazole dimer (2- (o-chlorophenyl) -4,5-diphenylimidazole dimer, 2- (o- Chlorophenyl)
-4,5-Di (m-methoxyphenyl) -4,5-diphenylimidazole dimer, 2- (o-fluorophenyl) -4,5-diphenylimidazole dimer, 2-
(O-Methoxyphenyl) -4,5-diphenylimidazole dimer, 2- (p-methoxyphenyl) -4,5
-Diphenylimidazole dimer, 2,4-di (p-methoxyphenyl) -5-phenylimidazole dimer,
2- (2,4-dimethoxyphenyl) -4,5-diphenylimidazole dimer, 2- (p-methylmercaptophenyl) -4,5-diphenylimidazole dimer and the like) are used. These are used alone or in combination of two or more. The blending amount of the component (c) is
The total amount of the components (a) and (b) is preferably 0.1 to 10 parts by weight based on 100 parts by weight. If the amount is less than 0.1 parts by weight, the photosensitivity tends to be insufficient, and if it exceeds 10 parts by weight, the light absorption on the surface of the composition increases during exposure, and the internal photocuring Tends to be insufficient.
【0022】前記顔料又は染料(d)としては、一般に
知られている着色剤が使用でき、感光性樹脂層、特にエ
チレン性不飽和化合物又はカルボキシル基含有フイルム
性付与ポリマーに対する相溶性、目標とする色相、光透
過性等を考慮して選択される。カラーフイルタに使用で
きる顔料としては、各種の化合物が使用でき、例えば、
硫酸バリウム、酸化亜鉛、硫酸鉛、酸化チタン、ベンガ
ラ、カーボンブラック、グラファイト、酸化クロムなど
の無機顔料、下記の有機顔料(カラーインデックス番
号)などがある。 黄色顔料:C.I.ピグメントイエロー20、24、83、
86、93、109、110、117、125、13
7、138、139、147、148、153、15
4、166、168 オレンジ顔料:C.I.ピグメントオレンジ36、43、5
1、55、59、61 赤色顔料:C.I.ピグメントレッド9、97、122、1
23、149、168、177、180、092、21
5、216、217、220、223、224、22
6、227、228、240、48:1 バイオレット顔料:C.I.ピグメントバイオレット19、
23、29、30、37、40、50 青色顔料:C.I.ピグメントブルー15、15:6、2
2、60、64 緑色顔料:C.I.ピグメントグリーン7、36 黒色顔料:C.I.ピグメントブラック7 (d)の配合量は、(a)と(b)の総量100重量部
に対して1〜50重量部とすることが好ましい。この配
合量が1重量部未満では、着色が不十分となる傾向があ
り、50重量部を超えると、光透過率が低下する傾向が
ある。As the pigment or dye (d), a generally known coloring agent can be used, and compatibility with a photosensitive resin layer, particularly an ethylenically unsaturated compound or a carboxyl group-containing film imparting polymer, is targeted. It is selected in consideration of hue, light transmittance and the like. As the pigment that can be used in the color filter, various compounds can be used, for example,
There are inorganic pigments such as barium sulfate, zinc oxide, lead sulfate, titanium oxide, red iron oxide, carbon black, graphite and chromium oxide, and the following organic pigments (color index numbers). Yellow pigment: CI Pigment Yellow 20, 24, 83,
86, 93, 109, 110, 117, 125, 13
7, 138, 139, 147, 148, 153, 15
4, 166, 168 Orange Pigment: CI Pigment Orange 36, 43, 5
1, 55, 59, 61 Red pigment: CI Pigment Red 9, 97, 122, 1
23, 149, 168, 177, 180, 092, 21
5, 216, 217, 220, 223, 224, 22
6, 227, 228, 240, 48: 1 violet pigment: CI pigment violet 19,
23, 29, 30, 37, 40, 50 Blue Pigment: CI Pigment Blue 15, 15: 6, 2
2, 60, 64 Green pigment: CI Pigment Green 7, 36 Black pigment: CI Pigment Black 7 (d) is blended in an amount of 1 to 50 parts by weight based on 100 parts by weight of the total amount of (a) and (b). Preferably. If the content is less than 1 part by weight, coloring tends to be insufficient, and if it exceeds 50 parts by weight, the light transmittance tends to decrease.
【0023】前記着色感光性樹脂層には、加熱硬化性を
高めるためにカルボキシル基含有フイルム性付与ポリマ
ーのカルボキシル基と熱反応するメラミン樹脂及び/又
はエポキシ樹脂を、(a)成分と(b)成分の総量10
0重量部に対して、1〜20重量部添加し、加熱するこ
とが好ましい。加熱温度は130〜200℃とすること
が好ましく、加熱時間は30〜60分とすることが着色
層の架橋密度向上、耐熱性向上等の点から好ましい。In the colored photosensitive resin layer, a melamine resin and / or an epoxy resin which thermally reacts with a carboxyl group of a carboxyl group-containing film-forming polymer in order to enhance heat-curability, a component (a) and a component (b). Total amount of ingredients 10
It is preferable to add 1 to 20 parts by weight to 0 parts by weight and heat. The heating temperature is preferably 130 to 200 ° C., and the heating time is preferably 30 to 60 minutes from the viewpoint of improving the crosslink density and heat resistance of the colored layer.
【0024】[0024]
【実施例】以下、実施例によって本発明を説明する。 実施例1 (1)着色感光性樹脂層用の塗工液の製造 表1の材料を均一に溶解した溶液200重量部に表2の
いずれかの顔料ペースト135重量部、メラミン樹脂5
重量部及びシランカップリング剤5重量部をそれぞれ添
加し、溶解分散して着色感光性樹脂層用の塗工液を得
た。EXAMPLES The present invention will be described below with reference to examples. Example 1 (1) Production of coating liquid for colored photosensitive resin layer 135 parts by weight of the pigment paste of any one of Table 2 and 200 parts by weight of a solution prepared by uniformly dissolving the materials of Table 1 and 5 of melamine resin
Parts by weight and 5 parts by weight of a silane coupling agent were added and dissolved and dispersed to obtain a coating liquid for a colored photosensitive resin layer.
【0025】[0025]
【表1】 [Table 1]
【0026】[0026]
【表2】 [Table 2]
【0027】メラミン樹脂 サイメル300(三井東圧社製、ヘキサメトキシメチル
メラミンの商品名)シランカップリング剤 KBM503(信越化学社製) 塗工液の調整 塗工液を使用直前に超音波で2.5時間分散して調整し
た。Melamine resin Cymel 300 (trade name of hexamethoxymethyl melamine manufactured by Mitsui Toatsu Co., Ltd.) Silane coupling agent KBM503 (manufactured by Shin-Etsu Chemical Co., Ltd.) Preparation of coating liquid Ultrasonic wave is applied immediately before using the coating liquid. It was dispersed and adjusted for 5 hours.
【0028】(2)感光性フイルムの製造 得られた塗工液を、厚さ6μmのポリエチレンテレフタ
レートフイルム(テイジン社製テトロンフイルムS6)
上に均一な厚さにキスタッチリバース方式の塗工機を用
いて塗布し、100℃の乾燥機で2分間乾燥した。保護
フイルムとして厚さ30μmのポリエチレンフイルムを
貼り合わせて感光性フイルムを得た。乾燥後の感光性樹
脂層の厚さは、赤、青及び緑ともに2.0μmであっ
た。(2) Production of Photosensitive Film The obtained coating solution was applied to a polyethylene terephthalate film having a thickness of 6 μm (Tetron film S6 manufactured by Teijin Ltd.).
It was applied to a uniform thickness using a kiss-touch reverse type coating machine and dried in a dryer at 100 ° C. for 2 minutes. As a protective film, a 30-μm-thick polyethylene film was laminated to obtain a photosensitive film. The thickness of the photosensitive resin layer after drying was 2.0 μm for each of red, blue and green.
【0029】(3)カラーフイルタの製造 (a)基板加熱工程 カラーフイルタ用の下地基板を80℃で10分間加熱し
た。 (b)貼り合わせ工程 前記感光性フイルムの保護フイルムを剥がしながら、着
色感光性樹脂層をロール温度60℃、ロール圧1.0kg
f/cm2、速度2.5m/分で前記カラーフイルタ用の下
地基板上にラミネートした。 (c)露光工程 所定のパターン(通常のストライプ状のパターンで、7
0μm(白)/230μm(黒)で長さ150mmのストライ
プ状)のネガマスクを通して露光機HMW−201B
(3kW、超高圧水銀灯、オーク製作所製)で露光した。 (d)移行工程 二色目と三色目の画素形成時には、加熱を60℃で15
分間行い、空間を介していた着色感光性樹脂層を基板表
面に移行させた。(3) Production of color filter (a) Substrate heating step The base substrate for the color filter was heated at 80 ° C. for 10 minutes. (B) Laminating step While peeling off the protective film of the photosensitive film, the colored photosensitive resin layer is rolled at a temperature of 60 ° C. and a roll pressure of 1.0 kg.
It was laminated on the base substrate for the color filter at f / cm 2 and a speed of 2.5 m / min. (C) Exposure step Predetermined pattern (normal stripe-shaped pattern,
Exposure machine HMW-201B through a negative mask of 0 μm (white) / 230 μm (black) and 150 mm long)
(3 kW, ultra-high pressure mercury lamp, manufactured by Oak Manufacturing Co., Ltd.) was used for exposure. (D) Transition process When forming the second and third color pixels, heating is performed at 60 ° C. for 15
It was carried out for a minute, and the colored photosensitive resin layer that had been through the space was transferred to the substrate surface.
【0030】(e)剥離工程 一色目の赤については室温でポリエチレンテレフタレー
トフイルムを自動剥離装置(自家製試作品、両面テープ
を貼り合わせたロールでポリエチレンテレフタレートフ
イルムを剥離する装置)で剥離した。なお、二色目及び
三色目の青及び緑については下記の剥離条件とした。剥
離温度を−10℃、0℃、10℃、15℃、20℃、2
5℃、30℃、35℃、40℃、60℃、80℃及び1
00℃とし、剥離速度を1m/分、3m/分、5m/
分、0.1m/秒、0.3m/秒、0.5m/秒、0.
7m/秒及び1.0m/秒とした。本実施例における着
色感光性樹脂層のベースフイルムと着色感光性樹脂層の
密着力(A)、着色感光性樹脂層と前置画素との密着力
(B)及び着色感光性樹脂層の破断応力(C)の関係
を、剥離工程によって、ベースフイルムに着色感光性樹
脂層が残る(×)、残らない(○)で判定した。すなわ
ち、(A)<(C)、(A)<(B)のときは○、(A)>(C)、
(A)<(B)のときは×となる。本実施例、以後の実施例
ともにすべて(A)<(B)であった。(A)<(B)であって
も(A)>(C)のときは図1の空間部分に接している着色
感光性樹脂層はベースフイルムに付着し、基板には移行
して来ないことになる。着色感光性樹脂層が完全に基板
に移行したときは、ベースフイルムに付着していないの
で、剥離工程後にはベースフイルムに残らない。逆に、
移行が不十分であると、工程後にもベースフイルムに着
色感光性樹脂が残存し、剥離が不十分となる。緑色の感
光性フィルムの剥離特性として、剥離温度と剥離速度に
よる剥離後の着色感光性樹脂層の密着力を○×評価し、
結果を表3に示した。(E) Peeling Process For the first color red, the polyethylene terephthalate film was peeled at room temperature with an automatic peeling device (home-made prototype, a device for peeling polyethylene terephthalate film with a roll having double-sided tape stuck). The following peeling conditions were applied to the second and third colors, blue and green. Peeling temperature is -10 ° C, 0 ° C, 10 ° C, 15 ° C, 20 ° C, 2
5 ° C, 30 ° C, 35 ° C, 40 ° C, 60 ° C, 80 ° C and 1
The peeling speed is 1 m / min, 3 m / min, 5 m /
Minutes, 0.1 m / sec, 0.3 m / sec, 0.5 m / sec, 0.
It was set to 7 m / sec and 1.0 m / sec. In the present embodiment, the adhesive force (A) between the base film of the colored photosensitive resin layer and the colored photosensitive resin layer, the adhesive force (B) between the colored photosensitive resin layer and the front pixel, and the breaking stress of the colored photosensitive resin layer The relationship of (C) was judged by the peeling process, in which the colored photosensitive resin layer remained (x) and did not remain (◯) on the base film. That is, when (A) <(C), (A) <(B), ○, (A)> (C),
When (A) <(B), it becomes x. In all of the present and subsequent examples, (A) <(B). Even if (A) <(B), when (A)> (C), the colored photosensitive resin layer in contact with the space portion of FIG. 1 adheres to the base film and does not move to the substrate. It will be. When the colored photosensitive resin layer is completely transferred to the substrate, it does not remain on the base film after the peeling process because it is not attached to the base film. vice versa,
If the transfer is insufficient, the colored photosensitive resin remains on the base film even after the process, resulting in insufficient peeling. As the peeling property of the green photosensitive film, the adhesion of the colored photosensitive resin layer after peeling according to the peeling temperature and the peeling speed was evaluated as XX,
The results are shown in Table 3.
【0031】[0031]
【表3】 [Table 3]
【0032】(f)現像工程 上記の剥離工程で評価○の条件で剥離できた着色感光性
樹脂層について現像した。30℃で0.08重量%のN
a2Co3水溶液で15秒スプレー現像をして未露光部を
除去し、現像後水洗し、オーブン加熱乾燥し、着色パタ
ーンを形成した。この(a)から(f)の着色パターン
の形成工程を、赤、青及び緑の順に各色の感光性フイル
ムを用いて繰り返し行った。二色目の青のラミネートの
時にフイルムの送り方向を前置画素の赤のストライプ状
のパターンに直交させてフイルムを送った。得られた青
色の感光性フイルム付きの基板の表面は平坦であり、斜
めに透かしても光の散乱はなく平坦であった。表面の粗
さを測定し、フイルム表面の平坦性を調べたところ、前
置画素による変形は認められなかった。三色目の緑につ
いても同様とし、多色パターンを形成した。この際の露
光量は赤、青及び緑色の感光性樹脂層に対しては50mJ
/cm2とした。使用したマスクのパターンはストライプが
画素ごとに独立した長方形を形成しストライプの長手方
向に隙間を設けたものである。得られた多色パターンに
紫外線照射機(ランプH5600L/2、東芝電材社
製)を用いて3J/cm2で照射した後、150℃で45分
間加熱してカラーフイルタを得た。得られたカラーフイ
ルタは赤、青及び緑色のパターン(ストライプ状のパタ
ーン)が整然と並んでおり、追随性は良好であった。ま
た、画素の段差はなく、画素の断面ではM状もJ状も認
められなかった。(F) Developing Step The colored photosensitive resin layer which could be peeled off under the conditions of evaluation ○ in the above peeling step was developed. 0.08 wt% N at 30 ° C
Spray development was carried out for 15 seconds with an aqueous solution of a 2 Co 3 to remove the unexposed portion, and after development, it was washed with water and dried by heating in an oven to form a colored pattern. The steps of forming the colored patterns (a) to (f) were repeated using a photosensitive film of each color in the order of red, blue and green. When laminating the second color blue, the film was fed with the feeding direction of the film orthogonal to the red stripe pattern of the front pixels. The surface of the obtained substrate with the blue photosensitive film was flat, and even if it was obliquely watermarked, it was flat without light scattering. When the surface roughness was measured and the flatness of the film surface was examined, no deformation due to front pixels was observed. The same was applied to the third color, green, to form a multicolor pattern. The exposure dose at this time is 50 mJ for the red, blue and green photosensitive resin layers.
/ cm 2 . The pattern of the mask used is one in which the stripes form an independent rectangle for each pixel and a gap is provided in the longitudinal direction of the stripes. The resulting multicolor pattern was irradiated at 3 J / cm 2 with an ultraviolet irradiation device (lamp H5600L / 2, manufactured by Toshiba Denshi Co., Ltd.) and then heated at 150 ° C. for 45 minutes to obtain a color filter. The obtained color filter had red, blue and green patterns (striped patterns) arranged in order, and had good followability. Further, there was no step in the pixel, and neither M-shaped nor J-shaped was observed in the cross section of the pixel.
【0033】実施例2 表1の材料を、下記表4の材料に置き換え、二色目及び
三色目の青及び緑については(b)の貼り合わせ工程を
下記とした以外は実施例1と同様に行った。 本実施例の貼り合わせ工程 前記カラーフイルタ用の感光性フイルムの保護フイルム
を剥がしながら、着色感光性樹脂層を前記カラーフイル
タ用の下地基板上に下記条件でラミネートした。 ロール温度 80℃ ロール圧 4.0kgf/cm2 速度 1.5m/分Example 2 The same as Example 1 except that the materials in Table 1 were replaced with the materials in Table 4 below, and for the second and third colors blue and green, the bonding step (b) was as follows. went. Laminating Step of this Example While removing the protective film of the photosensitive film for the color filter, the colored photosensitive resin layer was laminated on the base substrate for the color filter under the following conditions. Roll temperature 80 ℃ Roll pressure 4.0kgf / cm 2 Speed 1.5m / min
【0034】[0034]
【表4】 緑色の感光性フイルムの剥離特性として、剥離温度と剥
離速度による剥離後の着色感光性樹脂層の密着力を○×
評価し、結果を表5に示した。[Table 4] As the peeling property of the green photosensitive film, the adhesion of the colored photosensitive resin layer after peeling depending on the peeling temperature and the peeling speed is ○ ×
The evaluation was performed and the results are shown in Table 5.
【0035】[0035]
【表5】 得られた青色の感光性フイルム付きの基板の表面は平坦
であり、斜めに透かしても光の散乱はなく平坦であっ
た。表面の粗さを測定し、フイルム表面の平坦性を調べ
たところ、前置画素による変形は認められなかった。得
られたカラーフイルタは赤、青及び緑色のパターンが整
然と並んでおり、追随性は良好であった。また、画素の
段差はなく、画素の断面ではM状もJ状も認められなか
った。[Table 5] The surface of the obtained substrate with the blue photosensitive film was flat, and even if it was obliquely watermarked, it was flat without light scattering. When the surface roughness was measured and the flatness of the film surface was examined, no deformation due to front pixels was observed. The color filter thus obtained had red, blue and green patterns arranged in order, and had good followability. Further, there was no step in the pixel, and neither M-shaped nor J-shaped was observed in the cross section of the pixel.
【0036】実施例3 表1の材料を、下記表6の材料に置き換え、二色目及び
三色目の青及び緑については(b)の貼り合わせ工程を
下記とした以外は実施例1と同様に行った。 本実施例の貼り合わせ工程 前記カラーフイルタ用の感光性フイルムの保護フイルム
を剥がしながら、着色感光性樹脂層を前記カラーフイル
タ用の下地基板上に下記条件でラミネートした。 ロール温度 100℃ ロール圧 4.0kgf/cm2 速度 1.0m/分Example 3 The same as Example 1 except that the materials in Table 1 were replaced with the materials in Table 6 below, and for the second and third colors, blue and green, the bonding step (b) was as follows. went. Laminating Step of this Example While removing the protective film of the photosensitive film for the color filter, the colored photosensitive resin layer was laminated on the base substrate for the color filter under the following conditions. Roll temperature 100 ℃ Roll pressure 4.0kgf / cm 2 Speed 1.0m / min
【0037】[0037]
【表6】 緑色の感光性フイルムの剥離特性として、剥離温度と剥
離速度による剥離後の着色感光性樹脂層の密着力を○×
評価し、結果を表7に示した。[Table 6] As the peeling property of the green photosensitive film, the adhesion of the colored photosensitive resin layer after peeling depending on the peeling temperature and the peeling speed is ○ ×
The evaluation was performed and the results are shown in Table 7.
【0038】[0038]
【表7】 得られた青色の感光性フイルム付きの基板の表面及び緑
色の感光性フイルム付きの基板の表面は平坦であり、斜
めに透かしても光の散乱はなく平坦であった。表面の粗
さを測定し、フイルム表面の平坦性を調べたところ、前
置画素による変形は認められなかった。得られたカラー
フイルタは、赤、青及び緑色のパターン(ストライプ状
のパターン)が整然と並んでおり、追随性は良好であっ
た。また、画素の段差はなく、画素の断面ではM状もJ
状も認められなかった。[Table 7] The surface of the obtained substrate with the blue photosensitive film and the surface of the substrate with the green photosensitive film were flat, and even when obliquely perforated, light was not scattered and was flat. When the surface roughness was measured and the flatness of the film surface was examined, no deformation due to front pixels was observed. The obtained color filter had red, blue and green patterns (striped patterns) arranged neatly, and had good followability. In addition, there is no step in the pixel, and the cross section of the pixel has an M shape of J.
No condition was observed.
【0039】実施例4 表1の材料を、下記の表8の材料に置き換えた以外は実
施例1と同様に行った。Example 4 Example 4 was repeated except that the materials in Table 1 were replaced with the materials in Table 8 below.
【表8】 得られた青色の感光性フイルム付きの基板の表面及び緑
色の感光性フイルム付きの基板の表面は平坦であり、斜
めに透かしても光の散乱はなく平坦であった。表面の粗
さを測定し、フイルム表面の平坦性を調べたところ、前
置画素による変形は認められなかった。得られたカラー
フイルタは、赤、青及び緑色のパターン(ストライプ状
のパターン)が整然と並んでおり、追随性は良好であっ
た。また、画素の段差はなく、画素の断面ではM状もJ
状も認められなかった。[Table 8] The surface of the obtained substrate with the blue photosensitive film and the surface of the substrate with the green photosensitive film were flat, and even when obliquely perforated, light was not scattered and was flat. When the surface roughness was measured and the flatness of the film surface was examined, no deformation due to front pixels was observed. The obtained color filter had red, blue and green patterns (striped patterns) arranged neatly, and had good followability. In addition, there is no step in the pixel, and the cross section of the pixel has an M shape of J.
No condition was observed.
【0040】実施例5 二色目及び三色目の青及び緑については下記の(d)剥
離工程とした以外は実施例1と同様に実施した。 (d)剥離工程 ポリエチレンテレフタレートフイルムを剥離する前の基
板の表面の温度は33℃であった。これを10℃の冷水
に浸漬し、10分間保持した。冷水から引き上げてフイ
ルムを剥離したところ、剥離は良好であった。実施例1
と同様に、得られた青色の感光性フイルム付きの基板の
表面及び緑色の感光性フイルム付きの基板の表面は平坦
であり、斜めに透かしても光の散乱はなく平坦であっ
た。表面の粗さを測定し、フイルム表面の平坦性を調べ
たところ、前置画素による変形は認められなかった。得
られたカラーフイルタは、赤、青及び緑色のパターン
(ストライプ状のパターン)が整然と並んでおり、追随
性は良好であった。また、画素の段差はなく、画素の断
面ではM状もJ状も認められなかった。Example 5 The same procedure as in Example 1 was carried out except for the following (d) peeling step for the second and third colors, blue and green. (D) Peeling step The temperature of the surface of the substrate before peeling the polyethylene terephthalate film was 33 ° C. This was immersed in cold water at 10 ° C. and kept for 10 minutes. When the film was pulled up from cold water and peeled off, the peeling was good. Example 1
Similarly to the above, the surface of the obtained substrate with the blue photosensitive film and the surface of the substrate with the green photosensitive film obtained were flat, and even if the light was obliquely reflected, there was no light scattering and the surface was flat. When the surface roughness was measured and the flatness of the film surface was examined, no deformation due to front pixels was observed. The obtained color filter had red, blue and green patterns (striped patterns) arranged neatly, and had good followability. Further, there was no step in the pixel, and neither M-shaped nor J-shaped was observed in the cross section of the pixel.
【0041】実施例6 実施例1においては、二色目及び三色目の青及び緑では
カラーフイルタの製造を、(a)基板加熱工程、(b)
貼り合わせ工程、(c)露光工程、(d)移行工程、
(e)剥離工程、(f)現像工程の順に行ったが、本実
施例では、基板加熱工程、貼り合わせ工程、露光工程、
剥離工程、移行工程及び現像工程の順に行った。すなわ
ち剥離後に移行工程を行ったところ(図3参照)実施例
1と同様の結果を得た。Example 6 In Example 1, (a) substrate heating step, (b) production of color filters for blue and green of the second and third colors,
Laminating step, (c) exposure step, (d) transition step,
Although (e) peeling step and (f) developing step were performed in this order, in this embodiment, the substrate heating step, the bonding step, the exposure step,
The peeling step, the transferring step and the developing step were performed in this order. That is, when the transfer process was performed after peeling (see FIG. 3), the same results as in Example 1 were obtained.
【0042】実施例7 実施例1においては、二色目及び三色目の青及び緑では
カラーフイルタの製造を、(a)基板加熱工程、(b)
貼り合わせ工程、(c)露光工程、(d)移行工程、
(e)剥離工程、(f)現像工程の順に行ったが、本実
施例では、二色目及び三色目の青及び緑の工程を、基板
加熱工程、貼り合わせ工程、剥離工程、露光工程、移行
工程及び現像工程の順とし、露光工程で露光量を実施例
1の10倍としたところ、実施例1と同様の結果を得
た。Example 7 In Example 1, the production of color filters for the second and third colors, blue and green, was carried out by (a) substrate heating step, (b)
Laminating step, (c) exposure step, (d) transition step,
Although the steps of (e) peeling step and (f) developing step were performed in this order, in the present example, the second and third color blue and green steps were followed by the substrate heating step, the bonding step, the peeling step, the exposure step, and the transfer. When the step and the developing step were performed in this order and the exposure amount in the exposure step was 10 times that in Example 1, the same result as in Example 1 was obtained.
【0043】実施例8 実施例1においては、二色目及び三色目の青及び緑では
カラーフイルタの製造を、(a)基板加熱工程、(b)
貼り合わせ工程、(c)露光工程、(d)移行工程、
(e)剥離工程、(f)現像工程の順に行ったが、本実
施例では、二色目及び三色目の青及び緑の工程を、基板
加熱工程、貼り合わせ工程、移行工程、露光工程、剥離
工程及び現像工程の順としたところ、実施例1と同様の
結果を得た。Example 8 In Example 1, the production of color filters for the second and third colors, blue and green, was carried out by (a) substrate heating step, (b)
Laminating step, (c) exposure step, (d) transition step,
Although the steps of (e) peeling step and (f) developing step were performed in this order, in the present example, the second and third colors of blue and green were changed to the substrate heating step, the bonding step, the transfer step, the exposure step, and the peeling step. When the steps were followed by the developing step, the same results as in Example 1 were obtained.
【0044】実施例9 実施例1においては、二色目及び三色目の青及び緑では
カラーフイルタの製造を、(a)基板加熱工程、(b)
貼り合わせ工程、(c)露光工程、(d)移行工程、
(e)剥離工程、(f)現像工程の順に行ったが、本実
施例では、二色目及び三色目の青及び緑の工程を、基板
加熱工程、貼り合わせ工程、移行工程、剥離工程、露光
工程及び現像工程の順とし、露光工程で露光量を実施例
1の10倍としたところ、実施例1と同様の結果を得
た。Example 9 In Example 1, (a) substrate heating step, (b) production of color filters for blue and green of the second and third colors,
Laminating step, (c) exposure step, (d) transition step,
Although (e) peeling step and (f) developing step were carried out in this order, in the present embodiment, the second and third color blue and green steps are the substrate heating step, the bonding step, the transfer step, the peeling step, and the exposure step. When the step and the developing step were performed in this order and the exposure amount in the exposure step was 10 times that in Example 1, the same result as in Example 1 was obtained.
【0045】実施例10 実施例1においては、二色目及び三色目の青及び緑では
カラーフイルタの製造を、(a)基板加熱工程、(b)
貼り合わせ工程、(c)露光工程、(d)移行工程、
(e)剥離工程、(f)現像工程の順に行ったが、本実
施例では、二色目及び三色目の青及び緑の工程を、基板
加熱工程、貼り合わせ工程、剥離工程、移行工程、露光
工程及び現像工程の順とし、露光工程で露光量を実施例
1の10倍としたところ、実施例1と同様の結果を得
た。Example 10 In Example 1, (a) substrate heating step, (b) production of color filters for blue and green of the second and third colors,
Laminating step, (c) exposure step, (d) transition step,
Although (e) peeling step and (f) developing step were carried out in this order, in the present embodiment, the second and third color blue and green steps are the substrate heating step, the bonding step, the peeling step, the transfer step, and the exposure step. When the step and the developing step were performed in this order and the exposure amount in the exposure step was 10 times that in Example 1, the same result as in Example 1 was obtained.
【0046】[0046]
【発明の効果】本発明の製造法によれば、感光性フイル
ムのベースフィルムの剥離がスムーズで、追随性、作業
性よく基板上に均一な厚さの高精度の多色の段差、白抜
けの欠陥のない微細パターンの形成された優れた耐熱性
を有するカラーフイルタを製造することができる。According to the manufacturing method of the present invention, the base film of the photosensitive film can be peeled off smoothly, and the followability and workability are good, and the high-precision multi-colored steps of uniform thickness and white spots on the substrate are obtained. It is possible to manufacture a color filter having excellent heat resistance with a fine pattern formed without defects.
【図1】本発明の製造法の一例を示す略図である。FIG. 1 is a schematic view showing an example of the production method of the present invention.
【図2】従来のカラーフイルタの画素の断面の模式図で
ある。FIG. 2 is a schematic view of a cross section of a pixel of a conventional color filter.
【図3】本発明の製造法の一例を示す略図である。FIG. 3 is a schematic view showing an example of the production method of the present invention.
1 ベースフイルム 2 着色感光性樹脂層(緑) 3 前置画素(赤) 4 透明基板 5 空間 6 一色目の画素 7 二色目の画素 8 三色目の画素 1 Base Film 2 Colored Photosensitive Resin Layer (Green) 3 Front Pixel (Red) 4 Transparent Substrate 5 Space 6 First Color Pixel 7 Second Color Pixel 8 Third Color Pixel
Claims (1)
着色された感光性樹脂層とからなる感光性フイルムを、
(1)着色された感光性樹脂層が前記基板に面するよう
に貼り合わせる工程、(2)パターン状に露光する工程
及び(3)現像工程を含む工程を繰り返して多色パター
ンを形成させるカラーフイルタの製造法であって、二色
目以降の着色された感光性樹脂層が前記基板に面するよ
うに、画素間に空間を形成して貼り合わせる工程を行
い、前記(1)と(3)の工程の間に、加熱により二色
目以降の感光性樹脂層をベースフイルムから画素間空間
へ移行させる移行工程及びベースフイルムを剥離する剥
離工程を行うカラーフイルタの製造法において、ベース
フイルムを剥離する剥離工程を、ベースフイルムと着色
感光性樹脂層の密着力より着色感光性樹脂層と前置画素
との密着力のほうが大きく、ベースフイルムと着色感光
性樹脂層の密着力より着色感光性樹脂層の破断応力の方
が大きい温度範囲で行うことを特徴とするカラーフイル
タの製造法。1. A photosensitive film comprising a base film and a photosensitive resin layer colored in one color on a transparent substrate,
A color in which a multicolor pattern is formed by repeating steps including (1) a step of attaching a colored photosensitive resin layer so as to face the substrate, (2) a step of exposing in a pattern, and (3) a developing step. A method of manufacturing a filter, which comprises performing a step of forming a space between pixels so that the second and subsequent colored photosensitive resin layers face the substrate, and then bonding them together. In the manufacturing method of the color filter, the base film is peeled off during the step of performing a transfer step of moving the photosensitive resin layer of the second and subsequent colors from the base film to the inter-pixel space by heating and a peeling step of peeling the base film. In the peeling process, the adhesive force between the base film and the colored photosensitive resin layer is larger than the adhesive force between the base film and the colored photosensitive resin layer. Preparation of a color filter, which comprises carrying out in a temperature range larger rupture stress of the colored photosensitive resin layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2669295A JPH08220324A (en) | 1995-02-15 | 1995-02-15 | Production of color filter |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2669295A JPH08220324A (en) | 1995-02-15 | 1995-02-15 | Production of color filter |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH08220324A true JPH08220324A (en) | 1996-08-30 |
Family
ID=12200450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2669295A Pending JPH08220324A (en) | 1995-02-15 | 1995-02-15 | Production of color filter |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH08220324A (en) |
-
1995
- 1995-02-15 JP JP2669295A patent/JPH08220324A/en active Pending
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