WO1996034303A1 - Materiau permettant de realiser un film protecteur filtrant les couleurs et film protecteur filtrant ainsi les couleurs - Google Patents
Materiau permettant de realiser un film protecteur filtrant les couleurs et film protecteur filtrant ainsi les couleurs Download PDFInfo
- Publication number
- WO1996034303A1 WO1996034303A1 PCT/JP1996/001117 JP9601117W WO9634303A1 WO 1996034303 A1 WO1996034303 A1 WO 1996034303A1 JP 9601117 W JP9601117 W JP 9601117W WO 9634303 A1 WO9634303 A1 WO 9634303A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- color filter
- protective film
- epoxy resin
- forming
- color
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims abstract description 39
- 239000003822 epoxy resin Substances 0.000 claims abstract description 62
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 62
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 19
- 230000002378 acidificating effect Effects 0.000 claims abstract description 12
- 230000001681 protective effect Effects 0.000 claims description 64
- 229920005989 resin Polymers 0.000 claims description 18
- 239000011347 resin Substances 0.000 claims description 18
- 150000001735 carboxylic acids Chemical class 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 230000001588 bifunctional effect Effects 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims description 2
- 150000008442 polyphenolic compounds Chemical class 0.000 claims 2
- 235000013824 polyphenols Nutrition 0.000 claims 2
- OCNZHGHKKQOQCZ-CLFAGFIQSA-N [(z)-octadec-9-enoyl] (z)-octadec-9-enoate Chemical class CCCCCCCC\C=C/CCCCCCCC(=O)OC(=O)CCCCCCC\C=C/CCCCCCCC OCNZHGHKKQOQCZ-CLFAGFIQSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229920002050 silicone resin Polymers 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 13
- 239000002253 acid Substances 0.000 abstract description 10
- 239000002904 solvent Substances 0.000 abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000003513 alkali Substances 0.000 abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- -1 3, 4-Epoxy cyclohexyl methyl Chemical group 0.000 description 24
- 239000011248 coating agent Substances 0.000 description 21
- 238000000576 coating method Methods 0.000 description 21
- 239000000203 mixture Substances 0.000 description 21
- 238000001723 curing Methods 0.000 description 19
- 238000000034 method Methods 0.000 description 16
- 239000011521 glass Substances 0.000 description 11
- 239000000758 substrate Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 9
- 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 8
- 238000010438 heat treatment Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000004973 liquid crystal related substance Substances 0.000 description 7
- 239000004593 Epoxy Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000006087 Silane Coupling Agent Substances 0.000 description 5
- 239000000976 ink Substances 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000002518 antifoaming agent Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000013007 heat curing Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- DJKGDNKYTKCJKD-BPOCMEKLSA-N (1s,4r,5s,6r)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene-5,6-dicarboxylic acid Chemical compound ClC1=C(Cl)[C@]2(Cl)[C@H](C(=O)O)[C@H](C(O)=O)[C@@]1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-BPOCMEKLSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 239000009719 polyimide resin Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- 238000007740 vapor deposition 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
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-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-OLQVQODUSA-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
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 208000023514 Barrett esophagus Diseases 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 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
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000004844 aliphatic epoxy resin Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- ZCILODAAHLISPY-UHFFFAOYSA-N biphenyl ether Natural products C1=C(CC=C)C(O)=CC(OC=2C(=CC(CC=C)=CC=2)O)=C1 ZCILODAAHLISPY-UHFFFAOYSA-N 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- 239000004842 bisphenol F epoxy resin Substances 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Substances FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 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
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000010485 coping Effects 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000005262 ferroelectric liquid crystals (FLCs) Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 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
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- RPDJEKMSFIRVII-UHFFFAOYSA-N oxomethylidenehydrazine Chemical compound NN=C=O RPDJEKMSFIRVII-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 1
- UJJLJRQIPMGXEZ-UHFFFAOYSA-N tetrahydro-2-furoic acid Chemical compound OC(=O)C1CCCO1 UJJLJRQIPMGXEZ-UHFFFAOYSA-N 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/24—Di-epoxy compounds carbocyclic
-
- G02B1/105—
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/14—Protective coatings, e.g. hard coatings
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/201—Filters in the form of arrays
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
- G02F1/133509—Filters, e.g. light shielding masks
- G02F1/133514—Colour filters
- G02F1/133519—Overcoatings
Definitions
- the present invention relates to a color filter protective film forming material suitable for forming a color filter protective film of a liquid crystal display element, and a color filter formed using the same. -Filters Regarding protective films. Background technology
- the steps of the color filter are made flat, and after the color filter is made, In this process, a protective film is provided on the surface to protect the color filter against heat treatment and chemical treatment under high temperature. Yes.
- the performance required of such a color filter protective film is not only heat resistance and chemical resistance, but also the color filter type. Adhesion with glass substrates and the like, flatness, high hardness and the like are mentioned.
- the heat resistance when a transparent electrode such as ITO (indium tin oxide) is formed on the protective film by the sputtering method, the protective film is formed. Of 200 ° C or more, or 250 ° C when baking the liquid crystal alignment film on ITO, and 270 ° C when coping with ferroelectric liquid crystal. Is required, and it is required to be stable under these temperature conditions.
- resins for forming such a protective film at present, acrylate resins, melamine resins, and polyimide resins (Japanese Patent Application Laid-Open No. No. 63371), epoxy resin (Japanese Patent Application Laid-Open No. Hei 4-170421), and the like.
- Cryogenic resin has low heat resistance, low hardness and insufficient hardness, and unreacted light and thermal polymerization initiator are likely to evaporate as little as IT0 spatter with high vacuum. In other words, this evaporated substance contaminates the surface of the protective film, and also reduces the physical properties such as adhesion of ITO.o
- the melamine resin has a three-dimensional network structure, has good heat resistance, and is unlikely to generate wrinkles and cracks during I ⁇ 0 sputtering.
- poor wettability with glass substrates and color filters, poor coatability, and consequent loss of flatness of the formed protective film There is a problem.
- Polyimide resin is also said to be excellent in heat resistance, but inferior in transparency and inevitable in image quality.
- Epoxy resin on the other hand, has good adhesion to glass substrates and provides a protective film with excellent transparency and chemical resistance, but tends to repel during coating, resulting in poor coatability. And consequently flatness And it is difficult to balance heat resistance. Therefore, it has been proposed to solve this fundamental problem of poor applicability by using a high molecular weight polymer as a base resin, but it is still cured to form a protective film. After formation, the flatness between pixels of the color filter is inferior, and the flatness as a protective film of the color filter cannot be sufficiently solved.
- the epoxy resin composition Japanese Patent Publication No. 7-911365
- the cured coating film have a high heat distortion temperature, and have heat resistance, moisture resistance, hardness, plating resistance, and chemical resistance.
- a solder resist ink composition having excellent electrical insulation properties and the like JP-A-4-345673 has been proposed.
- Japanese Patent Application Laid-Open No. 6-192394 discloses a low-shrinkage epoxy resin composition. It is intended for use as an adhesive.
- the present invention has been made in view of such a viewpoint, and an object of the present invention is to provide a material for forming a color filter protective film having excellent flatness. Another object of the present invention is to provide a resin composition.
- Another object of the present invention is to use an epoxy resin composition, which is a material for forming a color filter protective film having such flatness, to provide heat resistance. It is also excellent in terms of transparency, hardness, adhesion, chemical resistance (acid resistance, alkali resistance, solvent resistance), water resistance, etc., and provides a high quality liquid crystal display device. To provide a color filter protective film that can be removed
- the present invention provides: (A) the following general formula (1) (Wherein, R and R 2 represent a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, and n represents a number of 0 to 20). And a material for forming a color filter protective film.
- the present invention provides a material for forming a color filter and a protective film, comprising (A) the epoxy resin of the general formula (1) and (C) an acidic curing agent. .
- the present invention provides (A) an epoxy resin represented by the general formula (1) and (B) an epoxy resin other than the epoxy resin (A), wherein the epoxy resin is bifunctional or more.
- the present invention provides a color filter-protective film formed by applying and curing such a material for forming a color filter protective film, or a color filter-protective film.
- a color filter provided with such a color filter protective film.
- the divalent alcohol component (diol component) present in the above-mentioned general formula (1), which is the component A, generally has the following general formula (2)
- the geological components such as those derived from geoles represented by the formula (1) are dependent on the geoles used as raw materials.
- Specific examples of the geoles include, for example, 9, 9-vis (4-hydroxyfenyl) phenolic, 9, 9 —Bis (3—Methyl 1—4—Hydroxy) 2 9 9 9 (2) It is possible to include phenol
- the method for producing the epoxy resin represented by the general formula (1) of the component A is the same as the method for synthesizing a general epoxy resin.
- the polyols are heated and dissolved together with an appropriate amount of epichlorohydrin to polymerize.
- the average number of repetitions n is in the range of 0 to 20, preferably 0 to 2, and when the n force exceeds 20, the resin becomes The melt viscosity and the viscosity as a solution become so high that it becomes difficult to handle.
- Doepoxy resin (trade name: ESF-300, manufactured by Nippon Steel Chemical Co., Ltd.) can be mentioned.
- the material for forming a color filter protective film of the present invention is an epoxy resin composition containing the epoxy resin (A component) represented by the general formula (1).
- the other essential component in the composition is an epoxy resin curing agent, and any known curing agent can be used, and the amount of the curing agent can be reduced. Within the known range Good.
- a better color filter can be obtained by including other epoxy resins and a specific acidic curing agent. It can be used as a material for forming a protective film. That is, the epoxy resin (A component) of the general formula (1) may be added to the epoxy resin other than the epoxy resin of the A component (component B) or acid hardened. An agent (component C) is blended. Examples of the components B and C include the following.
- the epoxy resin as the component B of the present invention may be any epoxy resin other than the epoxy resin as the component A, and may be a bifunctional or more functional epoxy resin.
- aromatic epoxy resins are preferably used from the viewpoint of maintaining the heat resistance, which is a characteristic of the A-component epoxy resin.
- an alicyclic epoxy resin such as bisphenol A-type epoxy resin, bisphenol F-type epoxy resin, and vinyl resin.
- Polypropylene resin, aliphatic epoxy resin, etc. can also be mixed. These may be mixed with oligomeric units during the formation of the grissile ether, but there is no problem in the performance of the material.
- the epoxy resin of the B component has a viewpoint of improving flatness and, at least, preferably on a color filter. Melts below the curing temperature after application Or a liquid at room temperature.
- Specific examples of such a B component epoxy resin include liquid bisphenol A epoxy resins and bisphenol F epoxy resins. Pox resin, 3,4—Epoxy cyclohexyl methacrylate 1,3,41 Epoxy mouth hexyl carboxylate and the like.
- the amount of the component is not more than 400 parts by weight based on 100 parts by weight of the component A epoxy resin. It is. If the amount exceeds 400 parts by weight, the inherent properties of the epoxy resin of the component A will deteriorate, and as a result, heat resistance, water resistance and flatness will be impaired.
- the acidic curing agent for the epoxy resin which is the component c specifically, polyvalent carboxylic acids composed of polyvalent carboxylic acid and its acid anhydride, Examples include polyvalent phenols having a phenolic hydroxyl group.
- polyvalent carboxylic acids that can be used as the component C include, for example, polycarboxylic acids such as itaconic acid, Succinic acid, phthalanoic acid, tetrahydrofuranoic acid, hexahydrophthalic acid, methylendmethylentetrahydrophthalanoic acid, Chlorendic acid, trimellitic acid, etc.
- polycarboxylic acids such as itaconic acid, Succinic acid, phthalanoic acid, tetrahydrofuranoic acid, hexahydrophthalic acid, methylendmethylentetrahydrophthalanoic acid, Chlorendic acid, trimellitic acid, etc.
- Aromatic polycarboxylic anhydrides such as dianhydride and biphenyl ether tetracarboxylic dianhydride can be mentioned.
- polyvalent phenols examples include, for example, phenol phenolic resin and cresol phenolic resin. And other various aromatic bisphenol compounds.
- the curing agent for the epoxy resin may be, for example, disocyanide, an imidazole compound, a triazine derivative, a perylene compound, or an aromatic amine compound.
- disocyanide an imidazole compound
- a triazine derivative a perylene compound
- aromatic amine compound an aromatic amine compound
- the amount of the acidic curing agent, which is the component C, is less than 1 part by weight, the curing will be insufficient, and the chemical resistance and hardness will be inferior. ⁇ The cause of the decrease in Become.
- the combination of the above-mentioned components A, B and C is effective in any combination as long as the compatibility is not hindered during the preparation of the composition, and is appropriately selected according to the application.
- the epoxy resin composition as the material of the present invention When used as a coating agent, it should be diluted with a solvent for the purpose of viscosity adjustment and the like. I can do it.
- Solvents used for this purpose are not particularly limited as long as they dissolve these A, B, and C components and do not react with these components. Instead, various solvents can be used. For example, ketones such as methylethylenoketone, methylenzoisobutylenoketone, etc., methylonecellonelone, methylonecellonelone, etc. Cellophanes such as butanol, cellulose, cellulose acetate, etc., ethylene glycol, etc., polyethylene, ethylene, etc. Ethers such as glycol jets, polyethylenes, etc., ethers such as polyesters, abbactylactones, etc. Lactones and the like.
- the epoxy resin composition may further include a curing accelerator, a filler for improving reliability and moisture resistance, and a repellent for enhancing flatness during coating, if necessary. It is possible to mix additives such as anti-foaming agents, anti-foaming agents to eliminate air bubbles that are expected to occur during application and vibration, and silane coupling agents to improve adhesion. Wear.
- Examples of the curing accelerator include amide compounds, imidazole compounds, and 1,8-diazabicyclo (5,4,0) diamine.
- the filler examples include glass filler, silica, mica, and alumina.
- an antifoaming agent and a leveling agent are used. Examples thereof include a silicon-based compound, a fluorine-based compound, and an acrylic-based compound, and these can be added as appropriate according to the purpose. .
- a silane coupling agent is very effective in improving the adhesion, and a functional silane coupling agent is particularly preferred.
- the functional silane coupling agents include vinyl, methacryloyl, hydroxyl, amino, isocyanate, and epoxy groups. Those having a reactive substituent such as a xyl group are desirable.
- the material for forming a color filter protective film of the present invention comprises the above-mentioned component A, component B, and component C for the purpose, use, and production process of the color filter. Taking into account the conditions (coating method, temperature, etc.), mix them within the above mixing ratio, and further dilute with a solvent as necessary, and then use a curing accelerator, filler, leveling agent It is prepared as a material for forming a protective film by adding an antifoaming agent, a silane coupling agent and the like.
- the color filter of the present invention prepared in this manner.
- the material for forming the protective film is applied to the surface of the color filter, and is cured by heating to form the protective film for the color filter. And can be done.
- the method of applying the material of the present invention to the surface of a color filter may be a solution dipping method, a spray method, a roller-coating machine or a runner. Any method, such as using one DOCOMO or one spinner, can be used.
- the color filter to be applied may be glass or transparent film (for example, polycarbonate, polyethylene terephthalate, poly terephthalate).
- a color filter in which a colored and cured film is laminated on a substrate made of glass, etc., and a substrate made of glass / transparent film.
- a transparent electrode made of ITO, metal, or the like is deposited on the electrode, and a patterned color fin- olator or the like can be used.
- a color filter formed by any known method such as an electrodeposition method, a dyeing method, a pigment dispersion method, and a printing method as a method for forming a colored film. Can also be used.
- a lattice black matrix is formed by using a resin black or a chromium vapor deposition film as a medium for forming a color filter. Red, blue and green, and one ink on the entire surface of the glass substrate using a spinner, lone recorder, etc., and apply the paint And evaporate the solvent.
- a photomask that has formed the desired pattern Perform contact exposure using an ultra-high pressure mercury lamp, develop the unexposed area with an alkaline developer such as 1% sodium carbonate aqueous solution, and then wash with water. Then, the coating is post-cured at an appropriate temperature, for example, 200 ° C., and the coating is completely dried to form the first color filter pixels.
- the first color filter using ink having one of the remaining two colors and one of the pigments, follow the same procedure as above to form the first color filter.
- a pixel of a second color reflector is formed adjacent to the pixel.
- the ink having the remaining one-color pigment is used, and similarly, the pixels of the third color filter are formed, and the three primary color filters, the color filter, and the like are formed. To obtain pixels.
- the color filter protective film forming material of the present invention may be applied to the surface of the color filter thus formed by any method, for example, spin coating, dicing. Coat with a coating method such as coating or bar coating.
- a pre-bake treatment is performed if a solvent evaporation and drying step is required.
- the heat treatment conditions at that time are usually 80 to 150 and 1 to 30 minutes.
- Post bake treatment for curing the epoxy resin is usually performed by heat treatment at 100 to 250 ° C for 10 to 120 minutes.
- the surface of the color filter has the desired heat resistance, transparency, adhesion, surface hardness, flatness, water resistance, chemical resistance
- a color filter protective film having excellent properties and the like is formed, and a power filter provided with the color filter protective film of the present invention is obtained.
- a transparent electrode such as ITO is deposited on this surface, and if necessary, the electrode is etched to form a pattern, and further an alignment film is formed. It is used as a color filter in liquid crystal display panels.
- the material for forming a color filter protective film of the present invention can be suitably used as a coating material, and is particularly suitable for a liquid crystal display device or a photographing device.
- a material for a color filter protective film used in the device and as a color filter protective film formed using the same, furthermore, Useful for the preparation of color filters with a color filter protective film such as
- FIG. 1 is an explanatory sectional view of a power filter provided with a color filter protective film of the present invention.
- a component, B component and C component, and if necessary, an additive and an organic solvent are mixed to form a color filter protective film having the composition (mass part) shown in Table 1 respectively.
- An epoxy resin composition was prepared.
- the obtained cured films of Examples and Comparative Examples were evaluated for adhesion to a substrate, heat-resistant transparency, hardness, and flatness.
- the film cured by heating at 200 ° C. for 60 minutes was placed in an oven at 250 ° C. for 3 hours, and the state of the obtained coating film was evaluated.
- the same glass plate coated with the coating film was used as a reference, and the absorption spectrum at a wavelength of 400 to 800 nm after the heat resistance test was measured.
- the ranking of the evaluation is as follows.
- ⁇ 90% or more in all areas without any abnormal appearance of the coating film.
- the hardness of the coating film heated at 200 ° C for 60 minutes was measured according to the test method of JIS-K540. In the measurement, when a load of 1 kg was applied using a pencil hardness tester, the highest hardness value at which the coating film was not scratched was indicated.
- a glass substrate 1 washed with a neutral detergent, water, isopropyl alcohol, and a nozzle was used as the transparent substrate.
- a black deposition film (0.1 m or less in thickness) 2a is formed by applying a chromium vapor deposition film on the A red pixel (R), a green pixel (G), and a blue pixel (B) are formed using the three types of inks of green, blue, and blue to form a color pixel. , 'Turn.
- the baking was performed at 80 ° C for 5 minutes, and the development was performed using a 0.4% by weight aqueous solution of sodium carbonate.
- the application order was such that pixels 2b were formed at predetermined positions in the order of red (R) -green (G) -blue (B).
- the film thickness of each pixel 2b is about 1.5 / zm, and the film thickness (1.5m) of each pixel 2b is almost the same as the step D before application. was measured.
- the color filter-protective film forming material of each of the examples and the comparative examples is applied on the color filter patterns thus formed. And heat-cured to form a 2 m-thick rough-finoleter protective film 2c, and remove the step d remaining on the surface of the color filter protective film 2c. It was measured.
- an ITO transparent electrode layer 2d is formed on the formed color filter protective film 2c by a sputtering method, and the ITO transparent electrode layer 2d is formed on the ITO transparent electrode layer 2d.
- An alignment film 2 e was formed to form a color finalizer 2.
- composition (parts by weight) 1 2 3 4
- Example Comparative Example Composition (parts by weight) 5 6 1 2
- Bisphenol A type epoxy resin epoxy equivalent: 190, Yuka Shell Epoxy Co., Ltd.
- the epoxy resin composition of Comparative Example 1 uses the epoxy resin of the general formula (1), which is the component A, as a bisphenol A type epoxy resin.
- the composition was the same as that of Example 2 except that the composition was changed, and the epoxy resin composition of Comparative Example 2 was further obtained by adding the B component to an alicyclic ester type epoxy resin. Although they were replaced, all of them were inferior in adhesion, heat resistance and flatness as compared with the examples.
- the material for forming a color filter protective film of the present invention has excellent coatability, and the color filter protective film formed by using the material has heat resistance, Excellent in adhesion, surface hardness, water resistance, flatness, etc.
- the color filter protective film forming material and the color filter protective film of the present invention provide a high-quality and highly reliable power color filter.
- Liquid crystal display, liquid crystal display, color fax, power line image sensor, etc. It is extremely useful for the production of
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Optical Filters (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53235496A JP3909349B2 (ja) | 1995-04-27 | 1996-04-24 | カラーフィルター保護膜形成用材料及びカラーフィルター保護膜 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10422695 | 1995-04-27 | ||
JP7/104226 | 1995-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996034303A1 true WO1996034303A1 (fr) | 1996-10-31 |
Family
ID=14375056
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1996/001117 WO1996034303A1 (fr) | 1995-04-27 | 1996-04-24 | Materiau permettant de realiser un film protecteur filtrant les couleurs et film protecteur filtrant ainsi les couleurs |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP3909349B2 (ja) |
KR (1) | KR100417605B1 (ja) |
WO (1) | WO1996034303A1 (ja) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000009914A (ja) * | 1998-06-18 | 2000-01-14 | Toray Ind Inc | カラーフィルター用熱硬化性樹脂溶液組成物、カラーフィルター、および液晶表示装置 |
JP2000103937A (ja) * | 1998-09-29 | 2000-04-11 | Jsr Corp | 熱硬化性樹脂組成物 |
JP2002179993A (ja) * | 2000-12-14 | 2002-06-26 | Nippon Steel Chem Co Ltd | カラーフィルター保護膜用組成物及びカラーフィルターの製造方法 |
JP2002194272A (ja) * | 2000-12-26 | 2002-07-10 | Nippon Steel Chem Co Ltd | カラーフィルター保護膜用組成物及び保護膜 |
WO2008087890A1 (ja) * | 2007-01-15 | 2008-07-24 | Taiyo Ink Mfg. Co., Ltd. | 熱硬化性樹脂組成物 |
JP2008274000A (ja) * | 2007-04-06 | 2008-11-13 | Osaka Gas Co Ltd | 熱硬化性樹脂組成物およびその硬化物 |
WO2008153000A1 (ja) * | 2007-06-11 | 2008-12-18 | Mitsubishi Chemical Corporation | カラーフィルタ用感光性着色樹脂組成物、カラーフィルタ、液晶表示装置及び有機elディスプレイ |
EP3352003A1 (en) * | 2017-01-19 | 2018-07-25 | Samsung Display Co., Ltd. | Display device |
KR20190080774A (ko) | 2017-12-28 | 2019-07-08 | 닛테츠 케미컬 앤드 머티리얼 가부시키가이샤 | 열 경화성 조성물, 경화막 및 표시 장치 |
KR20210040795A (ko) | 2019-10-04 | 2021-04-14 | 닛테츠 케미컬 앤드 머티리얼 가부시키가이샤 | 실록산 수지를 함유하는 경화성 수지 조성물, 및 그 경화막, 실록산 수지의 제조 방법 |
CN113176681A (zh) * | 2021-04-06 | 2021-07-27 | Tcl华星光电技术有限公司 | 显示面板及其制备方法、显示模组 |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001077628A (ja) * | 1999-09-01 | 2001-03-23 | Alps Electric Co Ltd | 水晶発振回路 |
KR100550938B1 (ko) * | 1999-12-28 | 2006-02-13 | 제일모직주식회사 | 광중합성 감광 수지 조성물 |
KR100655064B1 (ko) * | 2005-05-27 | 2006-12-06 | 제일모직주식회사 | 반사방지성을 갖는 하드마스크 조성물 |
KR100671116B1 (ko) * | 2005-07-28 | 2007-01-17 | 제일모직주식회사 | 반사방지성을 갖는 하드마스크 조성물 |
KR100671117B1 (ko) * | 2005-07-28 | 2007-01-17 | 제일모직주식회사 | 반사방지성을 갖는 하드마스크 조성물 |
KR100699179B1 (ko) * | 2005-12-27 | 2007-03-23 | 제일모직주식회사 | 카도계화합물로 표면처리된 카본블랙 및 이를 이용한 블랙매트릭스용 카본블랙 분산액 조성물 |
KR101344792B1 (ko) | 2010-12-17 | 2013-12-24 | 제일모직주식회사 | 하드마스크 조성물, 이를 사용한 패턴 형성 방법 및 상기 패턴을 포함하는 반도체 집적회로 디바이스 |
JP6117547B2 (ja) * | 2012-12-21 | 2017-04-19 | 新日鉄住金化学株式会社 | 熱硬化性組成物、硬化膜及びカラーフィルター |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0273823A (ja) * | 1988-09-09 | 1990-03-13 | Nippon Steel Chem Co Ltd | 半導体封止用エポキシ樹脂組成物 |
JPH05148410A (ja) * | 1991-11-26 | 1993-06-15 | Shin Etsu Chem Co Ltd | 熱硬化性樹脂組成物及び半導体装置 |
JPH05148411A (ja) * | 1991-11-26 | 1993-06-15 | Shin Etsu Chem Co Ltd | 熱硬化性樹脂組成物及び半導体装置 |
JPH06192394A (ja) * | 1992-12-25 | 1994-07-12 | Nippon Steel Corp | 低収縮性熱硬化性樹脂組成物とそれを用いた接着剤 |
JPH073122A (ja) * | 1993-06-17 | 1995-01-06 | Nippon Steel Chem Co Ltd | 熱硬化性樹脂組成物、その硬化物及びカラーフィルター材料 |
-
1996
- 1996-04-24 JP JP53235496A patent/JP3909349B2/ja not_active Expired - Fee Related
- 1996-04-24 KR KR1019970707628A patent/KR100417605B1/ko not_active Expired - Lifetime
- 1996-04-24 WO PCT/JP1996/001117 patent/WO1996034303A1/ja active IP Right Grant
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0273823A (ja) * | 1988-09-09 | 1990-03-13 | Nippon Steel Chem Co Ltd | 半導体封止用エポキシ樹脂組成物 |
JPH05148410A (ja) * | 1991-11-26 | 1993-06-15 | Shin Etsu Chem Co Ltd | 熱硬化性樹脂組成物及び半導体装置 |
JPH05148411A (ja) * | 1991-11-26 | 1993-06-15 | Shin Etsu Chem Co Ltd | 熱硬化性樹脂組成物及び半導体装置 |
JPH06192394A (ja) * | 1992-12-25 | 1994-07-12 | Nippon Steel Corp | 低収縮性熱硬化性樹脂組成物とそれを用いた接着剤 |
JPH073122A (ja) * | 1993-06-17 | 1995-01-06 | Nippon Steel Chem Co Ltd | 熱硬化性樹脂組成物、その硬化物及びカラーフィルター材料 |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000009914A (ja) * | 1998-06-18 | 2000-01-14 | Toray Ind Inc | カラーフィルター用熱硬化性樹脂溶液組成物、カラーフィルター、および液晶表示装置 |
JP2000103937A (ja) * | 1998-09-29 | 2000-04-11 | Jsr Corp | 熱硬化性樹脂組成物 |
JP2002179993A (ja) * | 2000-12-14 | 2002-06-26 | Nippon Steel Chem Co Ltd | カラーフィルター保護膜用組成物及びカラーフィルターの製造方法 |
JP2002194272A (ja) * | 2000-12-26 | 2002-07-10 | Nippon Steel Chem Co Ltd | カラーフィルター保護膜用組成物及び保護膜 |
WO2008087890A1 (ja) * | 2007-01-15 | 2008-07-24 | Taiyo Ink Mfg. Co., Ltd. | 熱硬化性樹脂組成物 |
JP2008274000A (ja) * | 2007-04-06 | 2008-11-13 | Osaka Gas Co Ltd | 熱硬化性樹脂組成物およびその硬化物 |
WO2008153000A1 (ja) * | 2007-06-11 | 2008-12-18 | Mitsubishi Chemical Corporation | カラーフィルタ用感光性着色樹脂組成物、カラーフィルタ、液晶表示装置及び有機elディスプレイ |
EP3352003A1 (en) * | 2017-01-19 | 2018-07-25 | Samsung Display Co., Ltd. | Display device |
CN108333814A (zh) * | 2017-01-19 | 2018-07-27 | 三星显示有限公司 | 显示装置及其制造方法 |
US10962821B2 (en) | 2017-01-19 | 2021-03-30 | Samsung Display Co., Ltd. | Display device and method for manufacturing the same |
CN108333814B (zh) * | 2017-01-19 | 2022-07-19 | 三星显示有限公司 | 显示装置及其制造方法 |
KR20190080774A (ko) | 2017-12-28 | 2019-07-08 | 닛테츠 케미컬 앤드 머티리얼 가부시키가이샤 | 열 경화성 조성물, 경화막 및 표시 장치 |
KR20210040795A (ko) | 2019-10-04 | 2021-04-14 | 닛테츠 케미컬 앤드 머티리얼 가부시키가이샤 | 실록산 수지를 함유하는 경화성 수지 조성물, 및 그 경화막, 실록산 수지의 제조 방법 |
CN113176681A (zh) * | 2021-04-06 | 2021-07-27 | Tcl华星光电技术有限公司 | 显示面板及其制备方法、显示模组 |
CN113176681B (zh) * | 2021-04-06 | 2022-07-12 | Tcl华星光电技术有限公司 | 显示面板及其制备方法、显示模组 |
Also Published As
Publication number | Publication date |
---|---|
KR100417605B1 (ko) | 2004-04-28 |
JP3909349B2 (ja) | 2007-04-25 |
KR19990008104A (ko) | 1999-01-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1996034303A1 (fr) | Materiau permettant de realiser un film protecteur filtrant les couleurs et film protecteur filtrant ainsi les couleurs | |
JP6973461B2 (ja) | 熱硬化性樹脂組成物、硬化膜、硬化膜付き基板および電子部品 | |
TWI446021B (zh) | 保護膜用組成物、彩色濾鏡基板以及液晶顯示元件 | |
JP4569233B2 (ja) | 熱硬化性樹脂組成物及び硬化膜 | |
CN1978519B (zh) | 树脂组合物、彩色滤光片保护膜的形成方法以及彩色滤光片保护膜 | |
TWI401278B (zh) | 熱硬化性聚合物組成物 | |
CN107207702B (zh) | 热固性树脂组合物、固化膜、带固化膜的基板以及电子零件 | |
JPH0764282A (ja) | 熱硬化性樹脂組成物及びその硬化物並びに画像形成材料 | |
CN109071774B (zh) | 热固性树脂组合物、固化膜、带固化膜的基板以及电子零件 | |
JP2016138264A (ja) | 熱硬化性樹脂組成物、硬化膜、硬化膜付き基板および電子部品 | |
KR100186810B1 (ko) | 도막 형성용 재료 | |
JP4410386B2 (ja) | カラーフィルター保護膜用塗工液及びカラーフィルター | |
WO2018190346A1 (ja) | 熱硬化性樹脂組成物、硬化膜、硬化膜付き基板、電子部品およびインクジェット用インク | |
CN103881281B (zh) | 热固性组合物、固化膜及滤色片 | |
JPH038652B2 (ja) | ||
KR102725367B1 (ko) | 열 경화성 조성물, 경화막 및 표시 장치 | |
JPH05173012A (ja) | カラーフィルタ保護膜用樹脂組成物 | |
JP2020173433A (ja) | 感光性樹脂組成物、それを硬化してなる硬化膜、およびその硬化膜を有する表示装置 | |
JPH04170421A (ja) | カラーフイルター保護膜形成用エポキシ樹脂組成物 | |
CN101792568A (zh) | 固化膜 | |
JP2004124005A (ja) | 硬化性樹脂組成物および保護膜 | |
JP2010120977A (ja) | 保護膜形成用硬化性樹脂組成物、保護膜および保護膜の形成方法 | |
JPH11241003A (ja) | カラーフィルター保護膜用樹脂組成物及びこれを用いたカラーフィルター | |
JPH04170503A (ja) | カラーフイルター保護膜形成用エポキシ樹脂組成物 | |
JPH04170504A (ja) | カラーフイルター保護膜形成用エポキシ樹脂組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): CN JP KR US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 1019970707628 Country of ref document: KR |
|
122 | Ep: pct application non-entry in european phase | ||
WWP | Wipo information: published in national office |
Ref document number: 1019970707628 Country of ref document: KR |
|
WWG | Wipo information: grant in national office |
Ref document number: 1019970707628 Country of ref document: KR |