GB2186099A - Method for the manufacture of a color filter - Google Patents
Method for the manufacture of a color filter Download PDFInfo
- Publication number
- GB2186099A GB2186099A GB08602258A GB8602258A GB2186099A GB 2186099 A GB2186099 A GB 2186099A GB 08602258 A GB08602258 A GB 08602258A GB 8602258 A GB8602258 A GB 8602258A GB 2186099 A GB2186099 A GB 2186099A
- Authority
- GB
- United Kingdom
- Prior art keywords
- photopolymer
- pattern
- colored
- color
- manufacture
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 239000003086 colorant Substances 0.000 claims abstract description 34
- 235000019646 color tone Nutrition 0.000 claims abstract description 25
- 239000000758 substrate Substances 0.000 claims abstract description 23
- 238000011161 development Methods 0.000 claims abstract description 5
- 239000002904 solvent Substances 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 50
- 229920005989 resin Polymers 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 21
- -1 azide compounds Chemical class 0.000 claims description 13
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 9
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 9
- 229920001477 hydrophilic polymer Polymers 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 5
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 4
- 239000003999 initiator Substances 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- WTQZSMDDRMKJRI-UHFFFAOYSA-N 4-diazoniophenolate Chemical class [O-]C1=CC=C([N+]#N)C=C1 WTQZSMDDRMKJRI-UHFFFAOYSA-N 0.000 claims description 3
- 239000004677 Nylon Substances 0.000 claims description 3
- 239000003638 chemical reducing agent Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 229920001778 nylon Polymers 0.000 claims description 3
- CMWKITSNTDAEDT-UHFFFAOYSA-N 2-nitrobenzaldehyde Chemical group [O-][N+](=O)C1=CC=CC=C1C=O CMWKITSNTDAEDT-UHFFFAOYSA-N 0.000 claims description 2
- 150000003926 acrylamides Chemical class 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 239000003431 cross linking reagent Substances 0.000 claims description 2
- 239000012954 diazonium Substances 0.000 claims description 2
- 150000001989 diazonium salts Chemical class 0.000 claims description 2
- 239000011964 heteropoly acid Substances 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 35
- 239000010408 film Substances 0.000 description 25
- 239000000975 dye Substances 0.000 description 17
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- 239000000049 pigment Substances 0.000 description 11
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- 235000019322 gelatine Nutrition 0.000 description 10
- 235000011852 gelatine desserts Nutrition 0.000 description 10
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- 238000001035 drying Methods 0.000 description 8
- 238000004043 dyeing Methods 0.000 description 8
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- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000002835 absorbance Methods 0.000 description 3
- 239000001045 blue dye Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- UEUDBBQFZIMOQJ-UHFFFAOYSA-K ferric ammonium oxalate Chemical compound [NH4+].[NH4+].[NH4+].[Fe+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O UEUDBBQFZIMOQJ-UHFFFAOYSA-K 0.000 description 3
- 239000001046 green dye Substances 0.000 description 3
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920002689 polyvinyl acetate Polymers 0.000 description 3
- 239000011118 polyvinyl acetate Substances 0.000 description 3
- 239000001044 red dye Substances 0.000 description 3
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 3
- UCTWMZQNUQWSLP-VIFPVBQESA-N (R)-adrenaline Chemical compound CNC[C@H](O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-VIFPVBQESA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- CUARLQDWYSRQDF-UHFFFAOYSA-N 5-Nitroacenaphthene Chemical compound C1CC2=CC=CC3=C2C1=CC=C3[N+](=O)[O-] CUARLQDWYSRQDF-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- FRHBOQMZUOWXQL-UHFFFAOYSA-L ammonium ferric citrate Chemical compound [NH4+].[Fe+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O FRHBOQMZUOWXQL-UHFFFAOYSA-L 0.000 description 2
- NUVKLMFCVGVDFG-IWZZCOQPSA-K azanium (2R,3R)-2,3-dihydroxybutanedioate iron(3+) Chemical compound [NH4+].[Fe+3].O[C@H]([C@@H](O)C([O-])=O)C([O-])=O.O[C@H]([C@@H](O)C([O-])=O)C([O-])=O NUVKLMFCVGVDFG-IWZZCOQPSA-K 0.000 description 2
- HNBQFKZSMFFZQY-UHFFFAOYSA-L chembl1559341 Chemical compound [Na+].[Na+].C1=CC(C)=CC=C1S(=O)(=O)OC1=CC=C(N=NC=2C(=CC(=CC=2)C=2C=C(C)C(N=NC=3C4=C(C=C(C=C4C=CC=3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=2)C)C=C1 HNBQFKZSMFFZQY-UHFFFAOYSA-L 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- ZRYQXQUPWQNYSX-UHFFFAOYSA-L disodium;5-[(3-methyl-5-oxo-1-phenyl-4h-pyrazol-4-yl)diazenyl]-2-[4-[(3-methyl-5-oxo-1-phenyl-4h-pyrazol-4-yl)diazenyl]-2-sulfonatophenyl]benzenesulfonate Chemical compound [Na+].[Na+].CC1=NN(C=2C=CC=CC=2)C(=O)C1N=NC(C=C1S([O-])(=O)=O)=CC=C1C(C(=C1)S([O-])(=O)=O)=CC=C1N=NC(C1=O)C(C)=NN1C1=CC=CC=C1 ZRYQXQUPWQNYSX-UHFFFAOYSA-L 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 2
- 239000004313 iron ammonium citrate Substances 0.000 description 2
- 235000000011 iron ammonium citrate Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
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- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
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- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- MKBNNYRMBCFUSH-UHFFFAOYSA-J sodium;iron(3+);oxalate Chemical compound [Na+].[Fe+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O MKBNNYRMBCFUSH-UHFFFAOYSA-J 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- JKPFLEXJIAZDAZ-UHFFFAOYSA-N (4-ethenylphenyl) 3-phenylprop-2-enoate Chemical compound C1=CC(C=C)=CC=C1OC(=O)C=CC1=CC=CC=C1 JKPFLEXJIAZDAZ-UHFFFAOYSA-N 0.000 description 1
- CCHRVFZBKRIKIX-UHFFFAOYSA-N 1-nitro-3-(3-nitrophenyl)benzene Chemical compound [O-][N+](=O)C1=CC=CC(C=2C=C(C=CC=2)[N+]([O-])=O)=C1 CCHRVFZBKRIKIX-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- YBKWKURHPIBUEM-UHFFFAOYSA-N 2-methyl-n-[6-(2-methylprop-2-enoylamino)hexyl]prop-2-enamide Chemical compound CC(=C)C(=O)NCCCCCCNC(=O)C(C)=C YBKWKURHPIBUEM-UHFFFAOYSA-N 0.000 description 1
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
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- 239000004793 Polystyrene Substances 0.000 description 1
- ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
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- SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
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- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- LHMRXAIRPKSGDE-UHFFFAOYSA-N benzo[a]anthracene-7,12-dione Chemical compound C1=CC2=CC=CC=C2C2=C1C(=O)C1=CC=CC=C1C2=O LHMRXAIRPKSGDE-UHFFFAOYSA-N 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical class C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- TXTCTCUXLQYGLA-UHFFFAOYSA-L calcium;prop-2-enoate Chemical compound [Ca+2].[O-]C(=O)C=C.[O-]C(=O)C=C TXTCTCUXLQYGLA-UHFFFAOYSA-L 0.000 description 1
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- 229910044991 metal oxide Inorganic materials 0.000 description 1
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- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
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- 238000007127 saponification reaction Methods 0.000 description 1
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
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- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0216—Coatings
- H01L31/02161—Coatings for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/02162—Coatings for devices characterised by at least one potential jump barrier or surface barrier for filtering or shielding light, e.g. multicolour filters for photodetectors
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Electromagnetism (AREA)
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Optical Filters (AREA)
Abstract
A method for the manufacture of a color filter comprising a pattern composed of a plurality on minute areas different in color tones on the surface of transparent substrate. A photopolymer layer, which contains one coloring agent and which was coated on a support and dried, is transferred to the surface of a transparent substrate wherein the colored photopolymer layer aforementioned is exposed to light through the mask with a fixed pattern and is treated with a solvent which has different solubilities between exposed area and unexposed area to form the pattern and, for the colored photopolymer layers with other color tones, the procedure of the order aforementioned is conducted and repeated a required number of times. In a further embodiment a photopolymer layer which contains a coloring agent of one color tone is coated on the support and dried, wherein the colored photopolymer layer aforementioned is exposed to light through a fixed pattern mask and the pattern is formed on the support through the development and a process wherein the pattern is transferred to the surface of transparent substrate and, for the photopolymer layers which contain coloring agents of other color tones, the procedure of the order aforementioned is conducted and repeated a required number of times.
Description
SPECIFICATION
Method for the manufacture of a color filter
The present invention relates to a method for the manufacture of an optical color filter which is used for color television cameras etc. and is generally called a stripe filter.
In more detail, the invention relates to the method for the formation of high-quality stripe filter for which the procedure is relatively simple and the mass production is possible without the necessity for high-level and troublesome techniques.
The stripe filter has a structure wherein, on the surface of optically transparent substrates such as glass, minute band stripes with two or not less than three kinds of different color tones are provided in parallel, or intersecting each other.
The width of these stripes is several ,um in case if fine ones and, in addition, the stripes are necessary for color tones to be arranged neatly in a fixed order. For this reason, in spite of various proposals having been made hitherto with regard to the method of manufacturing the stripe filter, no method of forming inexpensive and high-quality stripe filter which is simple in practice and makes mass production possible has yet been realized.
For example, by the use of the screen printing method, it is possible to form a stripe filter which is low in price. But, it is impossible to make the film thin and there is a problem regarding the uniformity of film, too. Further, because of the limitation of size of pattern achieved by means of screen printing, the formation of minute patterns i.e. as fine as several item, is difficult.
With the interference method by multilayer film wherein metal oxide is evaporated in multilayer, the film becomes thick and the manufacturing price is high. Therefore, this is impractical.
Moreover, in a method comprising partial dyeing of a transparent film coating on a substrate to form stripe filter which is then dried and the operation is repeated or partial dyeing of film dyed whole surface with a coloring agent having a fixed spectral characteristic is repeated, the repeating of the formation and the removal of resist dyeing layer or decolorization-preventing layer is necessary resulting in a complicated manufacture of stripe filter. Furthermore, the staining from the sides of band stripes having already been dyed cannot be avoided and the control of dyeing conditions such as selection of dye etc. and the maintenance of accuracy of product are difficult.
With the method for the manufacture accompanying the decoloring treatment, in addition, there has also been a problem that the spectral characteristic of minute band stripes with respective color tones changes with the lapse of time because of the remaining of decoloring agent and decomposed products of dye.
The purpose of the invention is to remove the shortcomings of conventional methods as above.
Accoerding to the invention, first the stripe filter is formed easily in a manner such that, after the photopolymer layer has been coated on a support and dried and having been colored in a fixed color tone is transferred to a substrate to form a stripe filter, the colored photopolymer layer aforementioned is exposed to light through a fixed pattern mask and the colored photopolymer layer is developed with a fixed developing solution to form the pattern, the colored photopolymer layer with another color tone is transferred thereon again, and the process aforementioned is repeated the necessary number of times.
Moreover, secondly, the stripe filter is formed in a way such that, after the photopolymer layer containing a color agent of one color tone was coated on the support and dried and the colored photopolymer layer aforementioned was exposed through a fixed pattern mask to form the pattern on the support by development, the pattern is transferred to the transparent substrate and the supporter film is stripped off and removed, and subse quentiy similar procedure is repeated in sequence for the colored photopolymer layers with other color tones to transfer the colored patterns in sequence on the transparent substrate.
In the invention, known photopolymers, coloring agents, etc. can be utilized effectively and, through the selection of the photopolymer, the formation of minute patterns as fine as several #m is possible. Moreover, since dyeing is unnecessary, the film can be made thin. Furthermore, the coloring agent used for the formation of color images can also be selected from pigments, dyes, etc, in a wide range. Therefore, the most suitable coloring agent can be selected putting fastness, color tone, etc, together.
In the case of a stripe filter used for color television camera, the band stripes with a thickness of about 1 to 2 um and a width of about 10 to 30 /m in red, green and blue colors (the primary colors of light) are arranged in parallel putting the three colors alternately. However, the invention can, of course, be applied to stripe filters other than this, for example, one wherein the order of arrangement differs from this or one wherein number of colors is two or not less than four.
Moreover, the invention is applicable to one wherein colors consist of a plurality of colors for substractive mixing and the band stripes with these color tones are formed crossing each other, or to color filters having patterns other than stripes.
In following, the invention will be explained in more detail.
The photopolymer in the invention is a pho tosensitive material wherein changes such as polymerization, crosslinking, dimerization, decrosslinking, decomposition, rearrangement, etc. are caused through the irradiation of light, and based thereon, changes occur such that the solubility to the solvent is increased or decreased and the like, and indicates one in the class which is also called a photosensitive material for plate-making, photoresist, photosensitive resin, etc. up to this time.
The photopolymers may be of negative type or of positive type. Although negative type photopolymer is used in the first part of the invention, both types of photopolymers can be used in the second part of the invention. This is a significant feature of the latter.
As examples of photopolymer, the following are known, but the invention is not confined to these examples.
Examples of negative type photopolymer:
(1) Compositions consisting of photosensitive ferric salts such as ammonium ferric citrate, ammonium ferric tartrate, ammonium ferric oxalate and sodium ferric oxalate which give ferrous ions through the irradiation of light and hydrophilic polymers such as gelatin, modified gelatin, polyvinyl alcohol, partially saponified polyvinyl acetate, polyacrylic acid and copolymer therewith and polyacrylamide and homologs thereof.
(2) Compositions consisting of hydrophilic polymers such as gelatin, fish glue, arabic gum, polyvinyl alcohol, polyacryl-amide, car boxymethylcellulose, copolymer of vinyl methyl ether with maleic anhydride, etc. and tetrazonium salt of diamino compounds such as benzidine and dianidine or diazo resin condensed p-diazodiphenylamine with paraformaldehyde.
t3) Diazo resins condensed diazo compounds such as p-diazodiphenylamine with paraformaldehyde.
(4) Compositions consisting of azide compounds such as sodium 4, 4'-diazidestilbene-2, 2'-disulfonate and sodium 4-azidebenzalacetone-2-sulfonate and polymers such as polyacrylamide, polyvinylpyrrolidone, gelatin, casein, partially saponified polyvinyl acetate grafted with acrylonitrile, N-alkoxymethylated nylon, etc.
(5) Compositions consisting of azide compounds such as 4,4'-azide benzalacetone, 4,4'diazidebenzal, methylcyclohexanone, etc. and polymers such as cyclized rubber, synthetic rubber, etc.
(6) Compositions consisting of cinnamic ester of polyvinyl alcohol or allylacrylic ester and sensitizers such as 5-nitroace-naphthene,
1 ,2-benzanthraquinone, etc.
(7) Compositions consisting of polymers of vinyl monomers having photosensitive groups, for example, cinnamic p-vinylphenyl ester or copolymers thereof with other monomers and sensitizers such as 5-nitroacenaphthene.
(8) Compositions consisting of vinyl monomers such as acrylamide, methylenebisacrylamide, acrylic acid, acrylic ester, triethyleneglycol diacrylate, polyethyleneglycol dimethacrylate, trimethylolpropane trimethacrylate, and pentaerythritol tetramethacrylate, cellulose derivatives or polyvinyl alcohol derivatives and photopolymerization initiators.
(9) Compositions consisting of acrylamides such as methylenebisacrylamide and N,N'-hexamethylenbismethacrylamide, alcohol-soluble nylon and photopolymerization initiators.
(10) Compositions consisting of ethylenic unsaturated compounds such as acrylamide, acrylic acid and N,N'-methyleneacryl-amide, photosensitive ferric salts such as ammonium ferric citrate, ammonium ferric tartrate, ammonium ferric oxalate and sodium ferric oxalate, and hydrophilic polymers such as gelatin, modified gelatin, polyvinyl alcohol, partially saponified polyvinyl acetate, polyacrylamide and copolymer therewith and polyacrylamide and nomolog thereof.
(11) Compositions according of ethylenic unsaturated monomers such as acrylamide and acrylic acid, photo-reducible colors such as thionine, riboflavin and methylene blue, reducing agents such as triethanolamine ascorbate, thiourea, sodium ethylenediamine-tetraacetate, etc., hydrophilic polymers such as gelatin, polyvinyl alcohol, polyacrylamide, etc., and, if necessary, crosslinking agents such as calcium acrylate, barium acrylate, N,N'-methylenebisacrylamide, etc.
Examples of positive type photopolymer:
(1) Quinonediazide compounds such as ester of O-naphthoquinonediazidesulfonic acid, sulfonamide, etc. or mixtures of these quinonediazide compounds with alkali-soluble resins such as Novolak phenol resin.
(2) Reaction products of polynuclear anions of heteropolyacid or isopolyacid with diazonium salts.
(3) Compounds having O-nitrobenzaldehyde group such as bis-(3-aldehyde-4-nitrophenyl)- phthalate and 3-aldehyde-4-nitrophenylcarbonate.
(4) Ethylenedioxy-5,5'-resorcinol.
The photosensitive layer consisting of photopolymer as described above is coated on the support and dried by conventional methods after the coloring agents such as pigments, dyes, etc. were incorporated into the solution or dispersion of the photopolymer or, after the solution of photopolymer alone was coated and dried, resin solution incorporated the coloring agent is coated on the photosensitive layer and dried. Further, the photosensitive layer can also be made by coating and drying resin solutions incorporating the coloring agent and by coating the solution of photopolymer thereon.
As the coloring agents used for the formation of the color image of the photopolymer pigments and dyes are used. The pigments may be inorganic pigments, organic pigments, etc used in the form of an aqueous dispersion or solvent dispersion, respectively. As the dyes, various oil-soluble dyes, water-soluble dyes, spirit dyes, disperse dyes, etc. can be used.
In the invention, since conventional pigments and dyes can be used depending on the kind of photopolymer to be used, the constitution of the photosensitive layer or the like, the range of selection of coloring agent becomes wide. This is a significant feature of the invention and the most suitable coloring agent can be selected combining fastness and color tone, etc. Upon the selection of coloring agent, however, it is necessary to select the coloring agent which has compatibility with the photopolymer and the color tone aimed, that is, the color tone corresponding to the three primary colors of light or the substractive mixing an which has also high purity, high transparency, excellent light fastness, etc., of course.
Moreover, the formation of image through exposure and development, can follow conventional methods depending on the photopolymer or the constitution of the photosensitive layer. As the supports, polyvinyl chloride, polyethylene, polypropylene, polystyrene, polyamide, polycarbonate, acetylcellulose, polyester, polyethylene terephthalate, etc. can be mentioned. These are selected taking the adherence to photosensitive layer, the dimensional stability or the like into consideration.
Next, for the purpose of enhancement of transferability, adherence or the like of the colored photopolymer to the substrate to form stripe filter, preliminary undercoat layers such as release layer etc. are provided more effectively on the support of the colored photopolymer. Also, a thin-film pressure-sensitive or thermosensitive layer can be provided on the colored photopolymer layer. Moreover, if a pressure-sensitive or thermosensitive adhesive layer is provided on the substrate to form a stripe filter, firmer adhesion can be obtained.
Such release layer or adhesive layer should be selected taking the kind of support used, the kind of pohotopolymer, the kind of developing solution, etc. into consideration.
Similarly, also when the pattern formed on the support is transferred to the transparent substrate as in the second part of the invention, preliminary provision of undercoat layers such as release layer, peel layer, etc. on the support is more effective for the improvement in the transferability. Further, in order to enhance the adherence of the pattern after it is transferred to the transparent substrate, a pressure-sensitive or thermosensitive adhesive layer which has excellent adherence to the photosensitive layer and is readily strippable off from the support may be provided on the support. Similarly, the provision of a pressuresensitive or thermosensitive adhesive layer on the transparent substrate is more effective.
As the release agents used for this purpose, polymers, prepolymer and the like with release function, which have been used hitherto for release paper, for example, one or a mixture of not less than two of silicone-based resin, alkyd-based resin, urethane-based resin, polyester-based resin, amino-based resin and phenolic resin can be used. Moreover, the functional groups may be introduced in a side chain or at an end so that these polymers or prepolymers are crosslinked or polymerized through light or radial rays.
As the thermosensitive adhesive agents which are excellent in the adherence with photosensitive layer and strippable off easily from the support, ethylene-vinyl acetate copolymer, vinyl chloride-vinyl propionate copolymer, polyolefinic resin, vinyl chloride-based polymer, ethylene-carboxylic acid ester copolymer, water-soluble polyvinylacetal resin, butyral resin, formal resin, vinylidene chloride-based resin, chlorinated polyolefin, chlorinated ethylene-vinyl acetate copolymer, acrylic resin, rubber-based resin, etc. can be mentioned. These are selected depending on the photosensitive layer used and the kind of support.
Besides, as the adhesive agents applied to the transparent substrate pressure-sensitive or thermosensitive adhesive agents generally known are used and these are not confined particularly.
As the method to transfer the photopolymer layer to glass substrate according to the first part of the invention, a known laminator can be used, and the pressure adhesion, heat-fusing adhesion or the like is utilizable depending on the kind of adhesive agent or pohotopolymer layer aforementioned.
When the pattern formed on the support transferred to the transparent substrate according to the second part of the invention, the film thickness of the stripe filter formed can be made this preferable, if transferred pattern alone. However, the pattern can also be transferred together with the adhesive layer aforementioned which has excellent adherence to the photosensitive layer and is strippable off easily from the support. In this case, it goes without saying that the thickness of the adhesive layer is as thin as possible. For the transfer, laminator is used ordinarily and the pressure sensitive adhesion method or thermosensitive adhesion method is selected properly depending on the kind of photosensitive layer or adhesive layer used as in the first part of the invention.
As described above, in accordance with the invention, photopolymers, coloring agents, release agents, adhesives, etc., all of which have been known hitherto, can be utilized effectively, and, by means of transfer techniques publicly know, high-quality stripe filter for which the procedure is relatively simple can be manufactured, Accordingly, the shortcom ings of various methods known up to this time can be overcome.
Namely, by the use of photopolymer, the formation of the minute pattern as fine as several,um is possible, and, since dyeing etc.
are unnecessary, the film can also be made thin.
Further, according to the invention strict control and the greatest care in the selection and the management of dyeing conditions are not required, but also the greatest problem that, at the time of second and subsequent dyeing, the dye used migrates to the zone having already been dyed previously to stain or to mix and exerts bad influence on the spectral characteristic of the zone thereof is removed. Moreover, in conventional methods conducting partial decolorization, a similar problem has arised through the remaining of decoloring agent consisting of oxidizing agent, reducing agent or the like, but this problem can also be solved by the invention. As described, in accordance with the invention, stable high-quality stripe filter can be manufactured easily without the necessity of high-level and troublesome techniques.
Besides, by selecting the pattern when exposing the colored photopolymer layer, the color filters having various desired patterns such as mosaic etc., as well as stripe can be made.
The following examples further illustrate the invention. Besides, "parts" appearing below mean "parts by weight" in all cases.
Example 1
To an aqueous solution of photopolymer (5% solids) consisting of 10 parts of gelatin (S-778, made by Nippi Co.) and 1 part of potassium dichromate were added dyed having different color tones, respectively, to prepare three kinds of colored compositions.
Red dye in colored composition R:
Suminol Milling Red RS (made by Sumitomo
Chemical)
Green dye in colored composition G:
Equiquantity mixture of Acid Fast Yellow MR (made by Chugai Chemicals) with Sumitomo
Brilliant Blue 5G (made by Sumitomo Chemical)
Blue dye in colored composition B:
Supranol Cyanine 6B (made by Bayer)
Respective dyes were added so as the spectral absorbances of band stripes with a thickness of about 1 zm to become more than 1.5 at respective wavelengths where the absorbance becomes maximum, when made up the stripe filter.
Three kinds of colored compositions thus prepared were coated on the biaxially stretched polyethylene terephthalate film of 75 ,um, respectively, so as the thickness after drying to become about 1 #m and dried.
Following this, polyolefinic thermosensitive adhesive agent AC 1000 (made by Mitsubishi
Yuka Fine) was coated on one face of transparent glass plate with a thickness of 2 mm so as the thickness after drying to become 2 film and dried.
After the preparatory processes as these, the face of adhesive layer on transparent glass plate was superposed on the R face of colored composition of film having been coated with colored composition R to adhere with hot roll of 100 C. When stripped off the film, R layer of colored composition was transferred to the glass substrate. Then, placing a mask having light-transmissive areas with a width of 100 ,um at intervals of 200 ,um, ultraviolet rays were irradiated onto the R layer of colored composition on glass substrate to cure the colored composition R at the portions corresponding to light-transmissive areas, and the unexposed areas were dissolved and removed with warm water to form red band stripes.
The film having been coated with colored composition G was superposed on this and the colored composition G was transferred similarly to the red band stripes on glass substrate. Then, moving the position of the mask aforementioned by a frame, ultraviolet rays were irradiated, and the unexposed areas were removed similarly to form an image with red band stripes and green band stripes arranged alternately.
Further, using the film having been coated with colored composition B, the procedure aforementioned was repeated and the stripe filter with red, green and blue band stripes arranged adjacent mutually in the width direction was obtained finally.
Example 2
To an aqueous solution of photopolymer (5% solids) consisting of 10 parts of polyvinyl alcohol (average polymerization degree 1700-2400, saponification degree 98.5+0.5%) and 0.6 parts of sulfonate of condensate of p-diazodiphenylamine with formaldehyde as a curing agent were added following water-dispersed pigments as coloring agents, respectively, to prepare three kinds of colored compositions different in the color tones.
Yellow pigment in colored composition Y:
Aquafine AF Yellow E-2 (made by Dainichi
Seika Co.)
Magenta pigment in colored composition M:
Aquafine AF Red E-3 (made by Dainichi
Seika Co.)
Cyan pigment in colored composition C:
Aquafine AF Blue E-1 (made by Dainichi
Seika Co.)
The addition amount of respective pigments was determined so as the spectral character
istic to become fixed reference as in Example
1.
The procedure was made similar to that in
Example 1, except that uncured areas after the
irradiation of ultraviolet rays were dissolved
and removed with water. Namely, the colored
composition Y was transferred to the transparent glass plate having been coated with
AC 1000 on one face to a thickness of 2 um
and, after exposed with a fixed mask, this
was developed to form yellow band stripes on
the glass plate. Then, using colored compo
sition M and colored composition C, the pro
cedure aforementioned was repeated in se
quence to form the stripe filter having yellow,
magenta and cyan colors.
Example 3
To an aqueous solution of photopolymer (5% solids concentration) consisting of 10
parts of gelatin (S-778, made by Nippi Co.)
and 0.4 parts of ammonium ferric oxalate
were added water-dispersed pigments as co
loring agents, respectively, to prepare colored
compositions R, G and B different in the color
tones.
Red pigment in colored composition R:
Equiquantity mixture of Aquafine AF Yellow
E-2 with Aquafine AF Red E-3.
Green pigment in colored composition G:
Equiquantity mixture of Aquafine AF Yellow
E-2 with Aquafine AF Blue E-1.
Blue pigment in colored composition B:
Equiquantity mixture of Aquafine AF Blue E
1 with Aquafine AF Red E-3
(All pigments are made by Dainichi Seika
Co.)
The procedure was similar to that in
Example 1, except that, in the developing treatment after the irradiation of ultraviolet
rays, the transferred substrate was immersed
into 1Yo aqueous solution of H202 for 1 minute at 18 C to insolubilize the exposed areas suffi
ciently and then immersed into water at 37"C to dissolve and remove the uncured areas.
Example 4
To an aqueous solution of photopolymer
(5% solids) consisting of 10 parts of gelatin
(S-778, made by Nippi Co.) and 1 part of
potassium dichromate were added dyes hav
ing different color tones, respectively, to pre
pare three kinds of colored compositions.
Red dye in colored composition R:
Suminol Milling Red RS (made by Sumitomo
Chemical)
Green dye in colored composition G:
Equiquantity mixture of Acid Fast Yellow MR
(made by Chugai Chemicals) with Sumitomo
Brilliant Blue 5G (made by Sumitomo Chemical)
Blue dye in colored composition B:
Supranol Cyanine 6B (made by Bayer)
Respective dyes were added so as the spectral absorbances of band stripes with a thickness of about 1 llm to become more than 1.5 at respective dominant wavelengths, when made up the stripe filter.
Three kinds of colored compositions thus prepared were coated on the biaxially stretched polyethylene terephthalate film of 75 xm, respectively, so as the thickness after drying to become about 1 ,um and dried.
Following this, polyolefinic thermosensitive adhesive agent AC 1000 (made by Mitsubishi
Yuka Fine) was coated on one face of transparent glass plate with a thickness of 2 mm so as the thickness after drying to become 2 ;#m and dried.
After the preparatory processes as these, placing a mask having light-transmissive areas with a width of 100 lIm at intervals of 200 jtm, ultraviolet rays were irradiated onto three colored compositions, respectively, to cure the areas corresponding to these light-transmissive areas, and the unexposed areas were dissolved and removed with warm water to obtain the films formed red, green and blue band stripes, respectively.
Next, the film with red band stripes was contacted closely with the face of adhesive layer on the transparent glass plate aforementioned and passed through two-roll laminator heated to 100"C to adhere. Then, the supporting film was stripped off and the red band stripes were formed on the glass plate. Following this, the film with green band stripes was superposed thereon moving the position of band stripes by a frame and laminated similarly. When stripped the supporting film off, an image with red and green band stripes arranged alternatejy was obtained. Further, the transferring procedure aforementioned was repeated using the film with blue band stripes to obtain stripe filter with red, green and blue band stripes arranged adjacent mutually in the width directio finally.
Example 5
On polypropylene film of 100 /tom, three kinds of colored layers consisting of three kinds of dyes having different color tones and formal resin (Denka Vinylek #30, made by
Denki Kagaku Co.) were coated, respectively, so as the thickness after drying to become 1 ,um and dried. Dyes used were red, green and blue dyes shown in Example 4 and the amount of dyes added was also determined according to Example 4 similarly.
Following this, the photopolymer consisting of alkali-soluble phenol Novolak resin and condensate of 1 ,2-naphthoquinonediazide(2)-5-sulfonyl chloride with alkali-soluble Novolak resin in weight ratio of 2 ~ 1 was coated on respective colored layers so as the thickness after drying to become 0.5 ,um and dried to obtain three kinds of photosensitive films in red, green and blue colors.
Then, on one face of the transparent glass plate with a thickness of 2 mm, polyesterbased adhesive agent (Bostic 7040, made by
Bostic Japan Co.) was coated so as the thickness after drying to become 2 ,um and dried.
After the preparatory processes as these, the formation of band stripes and the transfer to the transparent glass plate were made according to Example 4, except that an aqueous alkaline solution containing 0.4% of sodium hydroxide and 30% of sodium salicylate was used for the development of photosensitive films, to form the stripe filter having red, green and blue colors.
Claims (5)
1. A method for the manufacture of a color filter wherein upon forming a pattern composed of a plurality of minute areas different in color tones on the surface of a transparent substrate, comprising a process wherein a photopolymer layer, which contains one coloring agent and which was coated on a support and dried, is transferred to the surface of the transparent substrate and the colored photopolymer layer is exposed to light through a mask with a fixed pattern and is treated with a solvent which has different solubilities between the exposed area and the unexposed area to form the pattern, and, for the colored photopolymer layers with other tones, the procedure of the order aforementioned is conducted and repeated fixed times; or a process wherein a photopolymer layer which contains a coloring agent of one color tone is coated on the support and dried, wherein the colored photopolymer layer is exposed to light through a fixed pattern mask and the pattern is formed on the support through the development and wherein said pattern is transferred to the surface of transparent substrate, and, for the photopolymer layers which contains coloring agents of other color tones, the procedure of the order aforementioned is conducted and repeated fixed times.
2. A method for the manufacture of a color filter according to claim 1, wherein the colored photopolymer layers consist of three color tones corresponding to three primary colors of light.
3. A method for manufacture of a color filter according to claim 1, wherein the colored photopolymer layers consist of a plurality of primary colors for substractive mixing.
4. A method for the manufacture of a color filter according to any of claims 1 to 3, wherein the photopolymer of negative type is selected from a group of compositions comprising photosensitive ferric salts and hydrophilic polymers, hydrophilic polymers and tetrazonium salt of diamino compounds or diazo resins, diazo resin only, azide compounds and polymers, cinnamic ester of polyvinyl alcohol or allylacrylic ester and sensitizers, polymers or copolymers or vinyl monomers with photosensitive group and sensitizers, vinyl monomers, cellulose-or polyvinyl alcohol derivaties and photopolymerization initiators, acryl-amides, alcoh6l-soluble nylon and photopolymerization initiators, ethylenic unsaturated compounds, photosensitive ferric salts and hydrophilic polymers, and ethylenic unsaturated monomers, photo-reducible colors, reducing agents, hydrophilic polymers and, if necessary, crosslinking agents.
5. A method for the manufacture of a color filter according to any of claims 1 to 3, wherein the photopolymer of positive type is selected from a group of compositions comprising quinonediazide compounds or mixtures of these with alkali-soluble resins, reaction products or polynuclear anions of heteropolyacid or isopolyacid with diazonium salts, compounds having O-nitrobenzaldehyde group, and ethylenedioxy-5, 5'-resorcinol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8601226A FR2593611B1 (en) | 1986-01-29 | 1986-01-29 | METHOD FOR MANUFACTURING A COLOR FILTER |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8602258D0 GB8602258D0 (en) | 1986-03-05 |
GB2186099A true GB2186099A (en) | 1987-08-05 |
GB2186099B GB2186099B (en) | 1989-10-25 |
Family
ID=9331596
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB8602258A Expired GB2186099B (en) | 1986-01-29 | 1986-01-30 | Method for the manufacture of a color filter |
Country Status (3)
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DE (1) | DE3602486A1 (en) |
FR (1) | FR2593611B1 (en) |
GB (1) | GB2186099B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0564237A2 (en) * | 1992-03-31 | 1993-10-06 | MITSUI TOATSU CHEMICALS, Inc. | Preparation of color filter and photo-setting resin therefor |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4808501A (en) * | 1985-10-15 | 1989-02-28 | Polaroid Corporation, Patent Dept. | Method for manufacturing an optical filter |
US4877697A (en) * | 1988-05-26 | 1989-10-31 | Hoechst Aktiengesellschaft | Color filter array for liquid crystal display device |
JPH02153353A (en) * | 1988-07-25 | 1990-06-13 | Matsushita Electric Ind Co Ltd | Colored photopolymerization composition and color filter |
DE3837874A1 (en) * | 1988-11-08 | 1990-05-10 | Siemens Ag | Process for the production of grating structures having sections which are mutually offset by half a grating period |
DE3837875A1 (en) * | 1988-11-08 | 1990-05-10 | Siemens Ag | Process for the production of grating structures having sections which are mutually offset by half a grating period |
DE69130701T2 (en) * | 1990-10-29 | 1999-08-26 | Toyo Gosei Kogyo Co. Ltd. | Photosensitive colored resin, colored image, method of manufacturing color filters and method of manufacturing a black matrix |
US5654202A (en) * | 1992-03-24 | 1997-08-05 | Eastman Kodak Company | Stabilization of a patterned planarizing layer for solid state imagers prior to color filter pattern formation |
DE19705909A1 (en) | 1996-08-23 | 1998-08-20 | Inst Physikalische Hochtech Ev | Novel thin films for microsystem technology and microstructuring as well as their use |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2053497A (en) * | 1979-07-09 | 1981-02-04 | Letraset International Ltd | Photosensitive Materials for Making Signs and Labels |
GB2081462A (en) * | 1980-07-03 | 1982-02-17 | Dainippon Screen Mfg | Method of manufacturing multicoloured optical filters |
GB2129952A (en) * | 1982-11-05 | 1984-05-23 | Letraset International Ltd | 'Peel apart' coloured photosensitive materials |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1254475A (en) * | 1968-03-15 | 1971-11-24 | Process Shizai Kabushiki Kaish | A method for transferring colored image and light-sensitive transfer sheets therefor |
US3904411A (en) * | 1971-03-01 | 1975-09-09 | Monsanto Co | Photoimaging and color proofing |
CA1017623A (en) * | 1973-03-09 | 1977-09-20 | American Hoechst Corporation | Overlay proofing system and an abbreviated transfer proofing system |
CA1045872A (en) * | 1974-05-29 | 1979-01-09 | Zafarullah K. Cheema | Surlay proofing method |
JPH0656486B2 (en) * | 1983-07-27 | 1994-07-27 | 日本製紙株式会社 | Method for forming multicolor image and multicolor image forming material for use therein |
US4489153A (en) * | 1983-12-22 | 1984-12-18 | E. I. Du Pont De Nemours And Company | Process for preparing a positive overlay |
-
1986
- 1986-01-28 DE DE19863602486 patent/DE3602486A1/en active Granted
- 1986-01-29 FR FR8601226A patent/FR2593611B1/en not_active Expired - Lifetime
- 1986-01-30 GB GB8602258A patent/GB2186099B/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2053497A (en) * | 1979-07-09 | 1981-02-04 | Letraset International Ltd | Photosensitive Materials for Making Signs and Labels |
GB2081462A (en) * | 1980-07-03 | 1982-02-17 | Dainippon Screen Mfg | Method of manufacturing multicoloured optical filters |
GB2129952A (en) * | 1982-11-05 | 1984-05-23 | Letraset International Ltd | 'Peel apart' coloured photosensitive materials |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0564237A2 (en) * | 1992-03-31 | 1993-10-06 | MITSUI TOATSU CHEMICALS, Inc. | Preparation of color filter and photo-setting resin therefor |
EP0564237A3 (en) * | 1992-03-31 | 1995-09-20 | Mitsui Toatsu Chemicals | Preparation of color filter and photo-setting resin therefor |
US5482804A (en) * | 1992-03-31 | 1996-01-09 | Mitsui Toatsu Chemicals, Incorporated | Resin composition for color filter |
Also Published As
Publication number | Publication date |
---|---|
FR2593611B1 (en) | 1990-04-27 |
FR2593611A1 (en) | 1987-07-31 |
GB8602258D0 (en) | 1986-03-05 |
GB2186099B (en) | 1989-10-25 |
DE3602486A1 (en) | 1987-07-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732E | Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) | ||
PE20 | Patent expired after termination of 20 years |
Effective date: 20060129 |