KR101487555B1 - 프탈로시아닌 안료를 포함하는 착색 조성물, 그것을 포함하는 잉크젯 잉크, 및 컬러 필터 기판 - Google Patents
프탈로시아닌 안료를 포함하는 착색 조성물, 그것을 포함하는 잉크젯 잉크, 및 컬러 필터 기판 Download PDFInfo
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- KR101487555B1 KR101487555B1 KR20080087110A KR20080087110A KR101487555B1 KR 101487555 B1 KR101487555 B1 KR 101487555B1 KR 20080087110 A KR20080087110 A KR 20080087110A KR 20080087110 A KR20080087110 A KR 20080087110A KR 101487555 B1 KR101487555 B1 KR 101487555B1
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- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- RMIODHQZRUFFFF-UHFFFAOYSA-N methoxyacetic acid Chemical compound COCC(O)=O RMIODHQZRUFFFF-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 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
- 230000004048 modification Effects 0.000 description 1
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- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- UPHWVVKYDQHTCF-UHFFFAOYSA-N octadecylazanium;acetate Chemical class CC(O)=O.CCCCCCCCCCCCCCCCCCN UPHWVVKYDQHTCF-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 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
- 239000003208 petroleum Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 229940067265 pigment yellow 138 Drugs 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 229960000380 propiolactone Drugs 0.000 description 1
- LLBIOIRWAYBCKK-UHFFFAOYSA-N pyranthrene-8,16-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1C=C4C=C5 LLBIOIRWAYBCKK-UHFFFAOYSA-N 0.000 description 1
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical group [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 1
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
- C09B69/108—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds containing a phthalocyanine dye
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/322—Pigment inks
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/324—Inkjet printing inks characterised by colouring agents containing carbon black
- C09D11/326—Inkjet printing inks characterised by colouring agents containing carbon black characterised by the pigment dispersant
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/36—Inkjet printing inks based on non-aqueous solvents
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mathematical Physics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Optical Filters (AREA)
- Ink Jet (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JPJP-P-2007-00241387 | 2007-09-18 | ||
JP2007241387 | 2007-09-18 |
Publications (2)
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KR20090029643A KR20090029643A (ko) | 2009-03-23 |
KR101487555B1 true KR101487555B1 (ko) | 2015-01-29 |
Family
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KR20080087110A Active KR101487555B1 (ko) | 2007-09-18 | 2008-09-04 | 프탈로시아닌 안료를 포함하는 착색 조성물, 그것을 포함하는 잉크젯 잉크, 및 컬러 필터 기판 |
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JP (2) | JP4631949B2 (enrdf_load_stackoverflow) |
KR (1) | KR101487555B1 (enrdf_load_stackoverflow) |
TW (1) | TWI443155B (enrdf_load_stackoverflow) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5534140B2 (ja) * | 2008-09-12 | 2014-06-25 | Jsr株式会社 | 着色感放射線性組成物、カラーフィルタおよびカラー液晶表示素子 |
JP2010139538A (ja) * | 2008-12-09 | 2010-06-24 | Toppan Printing Co Ltd | カラーフィルタ用インクジェットインク組成物、カラーフィルタの製造方法、カラーフィルタおよび表示装置 |
WO2010140519A1 (ja) * | 2009-06-05 | 2010-12-09 | 大日精化工業株式会社 | 緑色顔料、その製造方法、それを含んでなる着色剤およびそれを用いた着色方法 |
JP5577647B2 (ja) * | 2009-08-11 | 2014-08-27 | 東洋インキScホールディングス株式会社 | カラーフィルタ用着色組成物、及びカラーフィルタ |
JP5607906B2 (ja) * | 2009-09-09 | 2014-10-15 | 理想科学工業株式会社 | 油性インクジェットインク |
JP5623818B2 (ja) | 2009-09-18 | 2014-11-12 | 富士フイルム株式会社 | 着色硬化性組成物、カラーフィルタ、及びカラーフィルタの製造方法 |
CN103080240B (zh) | 2010-11-24 | 2016-04-13 | M技术株式会社 | 固溶体颜料纳米粒子及控制了固溶比的固溶体颜料纳米粒子的制造方法 |
TWI422631B (zh) * | 2011-06-30 | 2014-01-11 | Everlight Chem Ind Corp | 黑色樹脂組成物、黑色矩陣及遮光層 |
JP5734913B2 (ja) * | 2011-08-31 | 2015-06-17 | 富士フイルム株式会社 | 感放射線性組成物、パターン形成方法、カラーフィルタ及びその製造方法、並びに、固体撮像素子 |
JP5277469B1 (ja) * | 2012-07-25 | 2013-08-28 | 東洋インキScホールディングス株式会社 | π型フタロシアニン顔料、該π型フタロシアニン顔料の製造方法および該π型フタロシアニン顔料を用いた着色組成物 |
JP2016126154A (ja) * | 2014-12-26 | 2016-07-11 | 花王株式会社 | カラーフィルター用顔料分散体 |
KR102279575B1 (ko) * | 2015-03-26 | 2021-07-20 | 동우 화인켐 주식회사 | 착색 감광성 수지 조성물, 컬러 필터 및 이를 구비한 화상 표시 장치 |
CN106019838A (zh) * | 2015-03-30 | 2016-10-12 | 住友化学株式会社 | 着色感光性树脂组合物 |
KR101998931B1 (ko) * | 2016-12-30 | 2019-07-11 | 한국생산기술연구원 | 개질된 프탈로시아닌계 안료 및 이를 포함하는 승화 전사잉크 조성물 |
JP7560970B2 (ja) | 2019-07-31 | 2024-10-03 | 住友化学株式会社 | 着色硬化性樹脂組成物 |
CN113174017B (zh) * | 2021-03-23 | 2023-12-22 | 黄山万丽美油墨科技有限公司 | 一种陶瓷釉料用水性分散剂及其制备方法与应用 |
JP2023019164A (ja) | 2021-07-28 | 2023-02-09 | 山陽色素株式会社 | 顔料分散体及び塗膜形成用組成物 |
JP2025117384A (ja) * | 2024-01-30 | 2025-08-12 | 関西ペイント株式会社 | 塗料組成物 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003192947A (ja) * | 2001-12-26 | 2003-07-09 | Dainippon Ink & Chem Inc | カラーフィルター用インクジェットインキ組成物及びカラーフィルター |
KR20060025102A (ko) * | 2004-09-15 | 2006-03-20 | 삼성전자주식회사 | 잉크 조성물 및 상기 잉크 조성물을 포함하는 컬러 필터 |
JP2006284691A (ja) | 2005-03-31 | 2006-10-19 | Dainippon Ink & Chem Inc | カラーフィルター用緑色顔料組成物およびそれを緑色画素部に含有してなるカラーフィルター |
JP2007231248A (ja) * | 2006-02-01 | 2007-09-13 | Daicel Chem Ind Ltd | 顔料分散液 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ187714A (en) * | 1977-07-15 | 1980-09-12 | Ici Ltd | Dispersing agent reaction product of a polyalkylene imine and a polyester |
JP3718915B2 (ja) * | 1995-10-16 | 2005-11-24 | 味の素株式会社 | 顔料分散剤 |
CN1238443C (zh) * | 2000-04-17 | 2006-01-25 | 松下电器产业株式会社 | 显示板用油墨和使用该油墨的等离子显示板的制造方法 |
JP2003161828A (ja) * | 2001-09-17 | 2003-06-06 | Dainippon Ink & Chem Inc | 顔料分散組成物、顔料分散レジスト、およびカラーフィルター |
JP2003192948A (ja) * | 2001-12-26 | 2003-07-09 | Dainippon Ink & Chem Inc | カラーフィルター用インクジェットインキ組成物、カラーフィルターおよびその製造方法 |
JP2004339332A (ja) * | 2003-05-14 | 2004-12-02 | Nof Corp | 熱硬化性インク、カラーフィルターの製造方法、カラーフィルター及び表示パネル |
JP5335175B2 (ja) * | 2004-09-15 | 2013-11-06 | 三星ディスプレイ株式會社 | インク組成物及び前記インク組成物を含むカラーフィルター |
JP4900555B2 (ja) * | 2005-04-20 | 2012-03-21 | Jsr株式会社 | 顔料分散組成物、インクジェット方式カラーフィルタ用(感放射線性)樹脂組成物、カラーフィルタ、および液晶表示装置 |
JP4333682B2 (ja) * | 2006-01-27 | 2009-09-16 | 東洋インキ製造株式会社 | カラーフィルタ用着色組成物およびそれを用いたカラーフィルタ |
JP4983029B2 (ja) * | 2006-02-03 | 2012-07-25 | 東洋インキScホールディングス株式会社 | 着色組成物 |
JP2007231122A (ja) * | 2006-02-28 | 2007-09-13 | Canon Inc | 液体組成物の製造方法、液体付与形成方法および液体付与装置 |
JP5136406B2 (ja) * | 2006-03-07 | 2013-02-06 | コニカミノルタIj株式会社 | 非水系インクジェットインク及びインクジェット記録方法 |
JP5320760B2 (ja) * | 2007-07-27 | 2013-10-23 | 三菱化学株式会社 | カラーフィルタ用着色組成物、カラーフィルタ、及び液晶表示装置 |
-
2008
- 2008-08-28 JP JP2008220563A patent/JP4631949B2/ja active Active
- 2008-09-02 TW TW97133548A patent/TWI443155B/zh active
- 2008-09-04 KR KR20080087110A patent/KR101487555B1/ko active Active
-
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- 2010-04-19 JP JP2010095954A patent/JP5408020B2/ja active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003192947A (ja) * | 2001-12-26 | 2003-07-09 | Dainippon Ink & Chem Inc | カラーフィルター用インクジェットインキ組成物及びカラーフィルター |
KR20060025102A (ko) * | 2004-09-15 | 2006-03-20 | 삼성전자주식회사 | 잉크 조성물 및 상기 잉크 조성물을 포함하는 컬러 필터 |
JP2006284691A (ja) | 2005-03-31 | 2006-10-19 | Dainippon Ink & Chem Inc | カラーフィルター用緑色顔料組成物およびそれを緑色画素部に含有してなるカラーフィルター |
JP2007231248A (ja) * | 2006-02-01 | 2007-09-13 | Daicel Chem Ind Ltd | 顔料分散液 |
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JP2010254996A (ja) | 2010-11-11 |
JP5408020B2 (ja) | 2014-02-05 |
JP4631949B2 (ja) | 2011-02-16 |
JP2009091551A (ja) | 2009-04-30 |
TW200920801A (en) | 2009-05-16 |
KR20090029643A (ko) | 2009-03-23 |
TWI443155B (zh) | 2014-07-01 |
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