TW200303902A - Treated pigment, use thereof, and compound for treating pigment - Google Patents
Treated pigment, use thereof, and compound for treating pigment Download PDFInfo
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- TW200303902A TW200303902A TW92105056A TW92105056A TW200303902A TW 200303902 A TW200303902 A TW 200303902A TW 92105056 A TW92105056 A TW 92105056A TW 92105056 A TW92105056 A TW 92105056A TW 200303902 A TW200303902 A TW 200303902A
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- compound
- pigment
- chain
- side chain
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- 239000000049 pigment Substances 0.000 title claims abstract description 175
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- 229920000570 polyether Polymers 0.000 claims abstract description 64
- 125000000524 functional group Chemical group 0.000 claims abstract description 58
- 239000006229 carbon black Substances 0.000 claims abstract description 54
- 239000012860 organic pigment Substances 0.000 claims abstract description 27
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- 125000003277 amino group Chemical group 0.000 claims description 11
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- 210000004556 brain Anatomy 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
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- BTMVHUNTONAYDX-UHFFFAOYSA-N butyl propionate Chemical compound CCCCOC(=O)CC BTMVHUNTONAYDX-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
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- 238000007796 conventional method Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate group Chemical group [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- TWXWPPKDQOWNSX-UHFFFAOYSA-N dicyclohexylmethanone Chemical compound C1CCCCC1C(=O)C1CCCCC1 TWXWPPKDQOWNSX-UHFFFAOYSA-N 0.000 description 1
- UBPGILLNMDGSDS-UHFFFAOYSA-N diethylene glycol diacetate Chemical compound CC(=O)OCCOCCOC(C)=O UBPGILLNMDGSDS-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
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- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- OYCRCCBMNOLTOD-UHFFFAOYSA-N ethene prop-2-enoic acid Chemical compound C=C.C=C.C=C.C=C.OC(=O)C=C.OC(=O)C=C OYCRCCBMNOLTOD-UHFFFAOYSA-N 0.000 description 1
- XTEBISFIAYHLQY-UHFFFAOYSA-N ethene;2-(2-hydroxyethoxy)ethanol Chemical compound C=C.OCCOCCO XTEBISFIAYHLQY-UHFFFAOYSA-N 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- CKSRFHWWBKRUKA-UHFFFAOYSA-N ethyl 2-ethoxyacetate Chemical compound CCOCC(=O)OCC CKSRFHWWBKRUKA-UHFFFAOYSA-N 0.000 description 1
- WUDNUHPRLBTKOJ-UHFFFAOYSA-N ethyl isocyanate Chemical compound CCN=C=O WUDNUHPRLBTKOJ-UHFFFAOYSA-N 0.000 description 1
- 229940117360 ethyl pyruvate Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- 229940119545 isobornyl methacrylate Drugs 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 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
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002596 lactones Chemical group 0.000 description 1
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 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
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- DSWNRHCOGVRDOE-UHFFFAOYSA-N n,n-dimethylmethanimidamide Chemical compound CN(C)C=N DSWNRHCOGVRDOE-UHFFFAOYSA-N 0.000 description 1
- HNHVTXYLRVGMHD-UHFFFAOYSA-N n-butyl isocyanate Chemical compound CCCCN=C=O HNHVTXYLRVGMHD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- JHRXVSJUASUIAK-UHFFFAOYSA-N oxido-oxo-(3-propyloxiran-2-yl)phosphanium Chemical class P(=O)(=O)C1C(CCC)O1 JHRXVSJUASUIAK-UHFFFAOYSA-N 0.000 description 1
- 101150032584 oxy-4 gene Proteins 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-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
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
- QCCDLTOVEPVEJK-UHFFFAOYSA-N phenylacetone Chemical compound CC(=O)CC1=CC=CC=C1 QCCDLTOVEPVEJK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000005076 polymer ester Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229960003387 progesterone Drugs 0.000 description 1
- 239000000186 progesterone Substances 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- 229960000380 propiolactone Drugs 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000008160 pyridoxine Nutrition 0.000 description 1
- 239000011677 pyridoxine Substances 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229940011671 vitamin b6 Drugs 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
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/10—Treatment with macromolecular organic compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/44—Carbon
- C09C1/48—Carbon black
- C09C1/56—Treatment of carbon black ; Purification
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/44—Carbon
- C09C1/48—Carbon black
- C09C1/56—Treatment of carbon black ; Purification
- C09C1/565—Treatment of carbon black ; Purification comprising an oxidative treatment with oxygen, ozone or oxygenated compounds, e.g. when such treatment occurs in a region of the furnace next to the carbon black generating reaction zone
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002064416 | 2002-03-08 | ||
| JP2002074966 | 2002-03-18 | ||
| JP2002089231 | 2002-03-27 | ||
| JP2002186838 | 2002-06-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200303902A true TW200303902A (en) | 2003-09-16 |
| TWI314945B TWI314945B (enExample) | 2009-09-21 |
Family
ID=27808729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW92105056A TW200303902A (en) | 2002-03-08 | 2003-03-10 | Treated pigment, use thereof, and compound for treating pigment |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7220306B2 (enExample) |
| EP (1) | EP1484366B1 (enExample) |
| JP (1) | JP4247124B2 (enExample) |
| KR (1) | KR100984655B1 (enExample) |
| CN (1) | CN1312232C (enExample) |
| TW (1) | TW200303902A (enExample) |
| WO (1) | WO2003076527A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| EP1535971A4 (en) | 2002-06-25 | 2010-01-20 | Sakata Inx Corp | TREATED PIGMENT, USE THEREOF AND COMPOUND FOR PIGMENT TREATMENT |
| CN1320066C (zh) | 2002-06-26 | 2007-06-06 | 阪田油墨株式会社 | 颜料分散组合物、其用途以及用于颜料处理的化合物 |
| JP4559209B2 (ja) * | 2003-12-24 | 2010-10-06 | サカタインクス株式会社 | カルボジイミド系化合物、顔料分散組成物及びその用途 |
| FR2870846B1 (fr) | 2004-05-25 | 2006-08-04 | Sanofi Synthelabo | Derives de tetrahydroisoquinolylsulfonamides, leur preparation et leur utilisation en therapeutique |
| JP4114805B2 (ja) * | 2004-07-06 | 2008-07-09 | サカタインクス株式会社 | 顔料分散組成物、その用途及び顔料処理用化合物 |
| JP2006225431A (ja) * | 2005-02-15 | 2006-08-31 | Sakata Corp | カルボジイミド系化合物及びそれを用いた顔料分散組成物の製造方法 |
| CN101146849B (zh) | 2005-03-24 | 2011-06-15 | 阪田油墨株式会社 | 碳二亚胺类化合物及其用途 |
| CN100561363C (zh) * | 2005-04-28 | 2009-11-18 | 阪田油墨株式会社 | 液体显影剂 |
| CN101203559B (zh) * | 2005-06-21 | 2012-09-12 | 日清纺织株式会社 | 用于基板的填料和用作无机/有机复合基板形成材料的组合物 |
| JP5146649B2 (ja) * | 2005-06-21 | 2013-02-20 | 日清紡ホールディングス株式会社 | 難燃剤および無機−有機複合難燃性組成物 |
| JP4977034B2 (ja) * | 2005-11-28 | 2012-07-18 | サカタインクス株式会社 | 液体現像剤 |
| JP5090338B2 (ja) * | 2006-03-22 | 2012-12-05 | サカタインクス株式会社 | 液体現像剤の製造方法及びその方法によって得られる液体現像剤 |
| ES2563310T3 (es) | 2006-05-31 | 2016-03-14 | The Sherwin-Williams Company | Polímeros dispersantes |
| US9442372B2 (en) * | 2007-09-26 | 2016-09-13 | Fujifilm Corporation | Pigment dispersion composition, photocurable composition and color filter |
| US8722302B2 (en) | 2007-09-28 | 2014-05-13 | Sakata Inx Corp. | Method for producing liquid developer |
| CA2900456C (en) | 2013-02-08 | 2020-09-22 | Sakata Inx Corporation | Liquid developing agent |
| WO2015020128A1 (ja) | 2013-08-07 | 2015-02-12 | サカタインクス株式会社 | 非水性インクジェット用インク組成物及びそれを用いて得られる印刷物 |
| KR101453216B1 (ko) * | 2013-12-09 | 2014-10-22 | 주식회사 엘지생활건강 | 염색제 조성물 |
| WO2015119145A1 (ja) * | 2014-02-04 | 2015-08-13 | サカタインクス株式会社 | 液体現像剤 |
| JP6762134B2 (ja) | 2016-04-28 | 2020-09-30 | サカタインクス株式会社 | 非水性インクジェット用インク組成物 |
| JP6811038B2 (ja) | 2016-06-29 | 2021-01-13 | サカタインクス株式会社 | 非水性インクジェットマゼンタ色インク組成物 |
| JP2018024771A (ja) | 2016-08-10 | 2018-02-15 | サカタインクス株式会社 | 非水性インク組成物 |
| JP6829064B2 (ja) | 2016-12-09 | 2021-02-10 | サカタインクス株式会社 | 非水性インクジェット用インク組成物 |
| CN111095104B (zh) | 2017-09-27 | 2024-01-16 | 三菱化学株式会社 | 感光性着色组合物、固化物、黑色矩阵及图像显示装置 |
| JP6914807B2 (ja) | 2017-10-30 | 2021-08-04 | サカタインクス株式会社 | 黒色着色組成物及びそれを含有する黒色着色レジスト組成物 |
| WO2020057933A1 (en) * | 2018-09-18 | 2020-03-26 | Byk-Chemie Gmbh | An amine functional compound having a urethane group |
| KR20220018968A (ko) | 2019-06-07 | 2022-02-15 | 에스더블유아이엠씨 엘엘씨 | 얇은 코팅을 위한 중합체 조성물 |
| JP7400166B2 (ja) | 2019-10-30 | 2023-12-19 | サカタインクス株式会社 | 非水性インクジェット用インク組成物 |
| JP7400165B2 (ja) | 2019-10-30 | 2023-12-19 | サカタインクス株式会社 | 非水性インクジェット用インク組成物 |
| JP7455637B2 (ja) | 2020-03-31 | 2024-03-26 | サカタインクス株式会社 | 光硬化型インクジェット印刷用インク組成物 |
| JP7506516B2 (ja) | 2020-04-24 | 2024-06-26 | サカタインクス株式会社 | 光硬化型水性インクジェット印刷用インク組成物 |
| US20230312953A1 (en) | 2020-06-24 | 2023-10-05 | Sakata Inx Corporation | Photocurable inkjet printing ink composition |
| CN116137839B (zh) | 2020-07-29 | 2025-02-28 | 阪田油墨股份有限公司 | 活性能量射线固化型喷墨印刷用油墨组合物 |
| EP4190566B1 (en) | 2020-07-29 | 2025-06-11 | Sakata INX Corporation | Actinic ray curable ink composition for inkjet printing |
| CN116137840B (zh) | 2020-07-29 | 2025-02-28 | 阪田油墨股份有限公司 | 活性能量射线固化型喷墨印刷用油墨组合物 |
| JP7354502B2 (ja) | 2020-08-07 | 2023-10-03 | サカタインクス株式会社 | 光硬化型インクジェット印刷用インク組成物 |
| EP3960818A1 (en) | 2020-08-24 | 2022-03-02 | Orion Engineered Carbons Ip Gmbh & Co. Kg | Composite carbon black particles |
| JP7641105B2 (ja) | 2020-10-23 | 2025-03-06 | サカタインクス株式会社 | 光硬化型インクジェット印刷用インク組成物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4049610A (en) * | 1974-01-22 | 1977-09-20 | Bayer Aktiengesellschaft | Pigment preparations |
| US4224212A (en) * | 1977-07-15 | 1980-09-23 | Imperial Chemical Industries Limited | Dispersing agents, dispersions containing these agents and paints and inks made from the dispersions |
| US5371148A (en) * | 1993-06-23 | 1994-12-06 | Union Carbide Chemicals & Plastics Technology Corporation | Reactive polymers having pendant flexible side chains prepared from ethylenically unsaturated carbodiimides |
| US5602264A (en) * | 1994-11-28 | 1997-02-11 | The Regents Of The University Of California | Highly reactive, water soluble carbodiimides, intermediates and derivatives thereof |
| US5908720A (en) * | 1995-10-13 | 1999-06-01 | Tokyo Ohka Kogyo Co., Ltd. | Photosensitive resin composition for forming light shielding films, black matrix formed by the same, and method for the production thereof |
| JP3856402B2 (ja) | 1995-10-13 | 2006-12-13 | 東京応化工業株式会社 | 遮光膜形成用感光性樹脂組成物、該遮光膜形成用感光性樹脂組成物で形成されたブラックマトリックス、及びその製造方法 |
| JP3739214B2 (ja) * | 1998-03-26 | 2006-01-25 | 株式会社神戸製鋼所 | 電子部品用銅合金板 |
| DE19954500A1 (de) * | 1999-11-11 | 2001-05-17 | Basf Ag | Carbodiimide mit Carboxyl- oder Caboxylatgruppen |
| DE10000656A1 (de) * | 2000-01-11 | 2001-07-12 | Basf Ag | Carbodiimide mit Carboxyl- oder Carboxylatgruppen |
| JP4729680B2 (ja) * | 2000-12-18 | 2011-07-20 | Ｄｏｗａメタルテック株式会社 | プレス打ち抜き性に優れた銅基合金 |
| JP4402287B2 (ja) * | 2000-12-27 | 2010-01-20 | サカタインクス株式会社 | 表面処理したカーボンブラック及びそれを含有してなるブラックマトリックス用レジスト組成物 |
| US6718408B2 (en) * | 2001-01-18 | 2004-04-06 | Hewlett-Packard Development Company, L.P. | Interchangeable and configurable input/output module for a computing deviceco |
| JP4117140B2 (ja) * | 2002-03-13 | 2008-07-16 | 日清紡績株式会社 | カルボジイミド含有硬化型反応性粒子、その製造方法及び用途 |
| US8440779B2 (en) * | 2004-11-04 | 2013-05-14 | 3M Innovative Properties Company | Carbodiimide compound and compositions for rendering substrates oil and water repellent |
-
2003
- 2003-03-10 KR KR20047014069A patent/KR100984655B1/ko not_active Expired - Fee Related
- 2003-03-10 JP JP2003574739A patent/JP4247124B2/ja not_active Expired - Fee Related
- 2003-03-10 CN CNB038055422A patent/CN1312232C/zh not_active Expired - Fee Related
- 2003-03-10 TW TW92105056A patent/TW200303902A/zh not_active IP Right Cessation
- 2003-03-10 WO PCT/JP2003/002772 patent/WO2003076527A1/ja not_active Ceased
- 2003-03-10 EP EP20030744030 patent/EP1484366B1/en not_active Expired - Lifetime
- 2003-03-10 US US10/507,012 patent/US7220306B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CN1312232C (zh) | 2007-04-25 |
| JPWO2003076527A1 (ja) | 2005-07-07 |
| US7220306B2 (en) | 2007-05-22 |
| WO2003076527A1 (en) | 2003-09-18 |
| US20050204959A1 (en) | 2005-09-22 |
| CN1639274A (zh) | 2005-07-13 |
| EP1484366A1 (en) | 2004-12-08 |
| KR100984655B1 (ko) | 2010-10-01 |
| EP1484366B1 (en) | 2012-07-25 |
| KR20040111388A (ko) | 2004-12-31 |
| TWI314945B (enExample) | 2009-09-21 |
| JP4247124B2 (ja) | 2009-04-02 |
| EP1484366A4 (en) | 2009-09-30 |
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| MM4A | Annulment or lapse of patent due to non-payment of fees |