JP2008531762A - 結合したポリマー基を有する改質顔料を含むインクジェットインク - Google Patents
結合したポリマー基を有する改質顔料を含むインクジェットインク Download PDFInfo
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- JP2008531762A JP2008531762A JP2007555258A JP2007555258A JP2008531762A JP 2008531762 A JP2008531762 A JP 2008531762A JP 2007555258 A JP2007555258 A JP 2007555258A JP 2007555258 A JP2007555258 A JP 2007555258A JP 2008531762 A JP2008531762 A JP 2008531762A
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- 239000000049 pigment Substances 0.000 title claims abstract description 330
- 229920000642 polymer Polymers 0.000 title claims abstract description 117
- 239000000203 mixture Substances 0.000 claims abstract description 158
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 43
- 238000000034 method Methods 0.000 claims description 107
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- -1 copper halide Chemical class 0.000 claims description 68
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 49
- 125000004429 atom Chemical group 0.000 claims description 47
- 239000006229 carbon black Substances 0.000 claims description 45
- 239000002245 particle Substances 0.000 claims description 35
- 125000003010 ionic group Chemical group 0.000 claims description 30
- 229910052723 transition metal Inorganic materials 0.000 claims description 29
- 150000003624 transition metals Chemical class 0.000 claims description 29
- 125000000524 functional group Chemical group 0.000 claims description 28
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- 239000003054 catalyst Substances 0.000 claims description 22
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- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 239000003446 ligand Substances 0.000 claims description 17
- 125000000129 anionic group Chemical group 0.000 claims description 16
- 239000010949 copper Substances 0.000 claims description 15
- 125000004185 ester group Chemical group 0.000 claims description 15
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- 125000000217 alkyl group Chemical group 0.000 claims description 12
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- 125000002091 cationic group Chemical group 0.000 claims description 10
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- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- 150000003254 radicals Chemical class 0.000 claims description 6
- 238000012712 reversible addition−fragmentation chain-transfer polymerization Methods 0.000 claims description 6
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 5
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 5
- 125000001188 haloalkyl group Chemical group 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
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- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
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- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 159000000000 sodium salts Chemical class 0.000 claims description 4
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 claims description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 238000007323 disproportionation reaction Methods 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 3
- 229910052703 rhodium Inorganic materials 0.000 claims description 3
- 239000010948 rhodium Substances 0.000 claims description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 claims description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 claims description 3
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 claims description 2
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229920005603 alternating copolymer Polymers 0.000 claims description 2
- 125000000732 arylene group Chemical group 0.000 claims description 2
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- 239000004917 carbon fiber Substances 0.000 claims description 2
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- 229910002804 graphite Inorganic materials 0.000 claims description 2
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- 239000001257 hydrogen Substances 0.000 claims description 2
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- 229920000831 ionic polymer Polymers 0.000 claims description 2
- 125000000468 ketone group Chemical group 0.000 claims description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 2
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 claims description 2
- 239000002687 nonaqueous vehicle Substances 0.000 claims description 2
- 230000005588 protonation Effects 0.000 claims description 2
- 229920005604 random copolymer Polymers 0.000 claims description 2
- WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 claims 1
- 239000001055 blue pigment Substances 0.000 claims 1
- 239000001058 brown pigment Substances 0.000 claims 1
- 239000001056 green pigment Substances 0.000 claims 1
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 230000005012 migration Effects 0.000 claims 1
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- 239000001053 orange pigment Substances 0.000 claims 1
- 239000001057 purple pigment Substances 0.000 claims 1
- 239000001054 red pigment Substances 0.000 claims 1
- 239000012463 white pigment Substances 0.000 claims 1
- 239000001052 yellow pigment Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000000976 ink Substances 0.000 description 72
- 239000006185 dispersion Substances 0.000 description 58
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 56
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 40
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 38
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 24
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 150000001721 carbon Chemical class 0.000 description 21
- 239000000047 product Substances 0.000 description 20
- 229910052757 nitrogen Inorganic materials 0.000 description 19
- 239000000243 solution Substances 0.000 description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 18
- 239000000463 material Substances 0.000 description 18
- 239000002253 acid Substances 0.000 description 17
- 239000002270 dispersing agent Substances 0.000 description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 13
- 229920001577 copolymer Polymers 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 11
- 239000012528 membrane Substances 0.000 description 11
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 11
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- 229930195729 fatty acid Natural products 0.000 description 10
- 238000000926 separation method Methods 0.000 description 10
- 241000894007 species Species 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
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- XLYOFNOQVPJJNP-ZSJDYOACSA-N Heavy water Chemical compound [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 7
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 7
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- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
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- 230000000052 comparative effect Effects 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- QJVYRYDARHKQAF-UHFFFAOYSA-N 3,3-dimethyl-2-methylidenebutanoic acid Chemical compound CC(C)(C)C(=C)C(O)=O QJVYRYDARHKQAF-UHFFFAOYSA-N 0.000 description 5
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- 125000000962 organic group Chemical group 0.000 description 5
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
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- 241000721047 Danaus plexippus Species 0.000 description 4
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- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- 125000003158 alcohol group Chemical group 0.000 description 4
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- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 4
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- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
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- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 3
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- CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical compound OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 238000012705 nitroxide-mediated radical polymerization Methods 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical compound C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 3
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- RIBFXMJCUYXJDZ-UHFFFAOYSA-N propanoyl bromide Chemical compound CCC(Br)=O RIBFXMJCUYXJDZ-UHFFFAOYSA-N 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 3
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- 125000000542 sulfonic acid group Chemical group 0.000 description 3
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- 229920003169 water-soluble polymer Polymers 0.000 description 3
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- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 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
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 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
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 229920001296 polysiloxane Chemical class 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000013014 purified material Substances 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
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000017709 saponins Nutrition 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 238000005549 size reduction Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 230000006103 sulfonylation Effects 0.000 description 1
- 238000005694 sulfonylation reaction Methods 0.000 description 1
- 150000003463 sulfur Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 229950006389 thiodiglycol Drugs 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-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
- C09D11/322—Pigment inks
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Ink Jet (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65527405P | 2005-02-11 | 2005-02-11 | |
| US70023205P | 2005-07-14 | 2005-07-14 | |
| PCT/US2006/004790 WO2006086660A1 (en) | 2005-02-11 | 2006-02-10 | Inkjet inks comprising modified pigments having attached polymeric groups |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008531762A true JP2008531762A (ja) | 2008-08-14 |
| JP2008531762A5 JP2008531762A5 (enExample) | 2009-04-02 |
Family
ID=36586100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007555258A Pending JP2008531762A (ja) | 2005-02-11 | 2006-02-10 | 結合したポリマー基を有する改質顔料を含むインクジェットインク |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20060211791A1 (enExample) |
| EP (1) | EP1871846A1 (enExample) |
| JP (1) | JP2008531762A (enExample) |
| WO (1) | WO2006086660A1 (enExample) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102011120330A1 (de) | 2010-12-08 | 2012-06-14 | Canon K.K. | Herstellungsverfahren für ein selbst-dispergierendes pigment, selbst-dispergierendes pigment, tintenstrahltinte, tintenkartusche und tintenstrahlaufzeichnungsverfahren |
| JP2013503252A (ja) * | 2009-09-11 | 2013-01-31 | シルバーブルック リサーチ ピーティワイ リミテッド | 表面改質顔料を含む溶媒系インクジェット用インク |
| US8608306B2 (en) | 2009-03-06 | 2013-12-17 | Ricoh Company, Ltd. | Inkjet recording ink, ink cartridge, inkjet recording apparatus, and ink recorded matter |
| WO2016104505A1 (ja) * | 2014-12-24 | 2016-06-30 | 花王株式会社 | 顔料を含有する改質ポリマー粒子の製造方法 |
| JP2017031390A (ja) * | 2015-07-30 | 2017-02-09 | キヤノン株式会社 | 有機顔料、有機顔料の製造方法、トナーの製造方法 |
| JP2023054191A (ja) * | 2019-11-21 | 2023-04-13 | Dic株式会社 | 顔料組成物の製造方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070095250A1 (en) * | 2005-10-28 | 2007-05-03 | Uhlir-Tsang Linda C | Ink Compositions and Methods for Improving Neutrality, Hue Angle and/or Media Independence |
| US20080280031A1 (en) * | 2006-05-16 | 2008-11-13 | Board Of Trustees Of Michigan State University | Conductive coatings produced by monolayer deposition on surfaces |
| US7927416B2 (en) | 2006-10-31 | 2011-04-19 | Sensient Colors Inc. | Modified pigments and methods for making and using the same |
| EP2111430A2 (en) * | 2007-01-24 | 2009-10-28 | Cabot Corporation | Process to form modified pigments |
| WO2009026552A2 (en) | 2007-08-23 | 2009-02-26 | Sensient Colors Inc. | Self-dispersed pigments and methods for making and using the same |
| WO2010061798A1 (ja) * | 2008-11-25 | 2010-06-03 | 花王株式会社 | インクジェット記録用水系インク |
| US9221986B2 (en) | 2009-04-07 | 2015-12-29 | Sensient Colors Llc | Self-dispersing particles and methods for making and using the same |
| US20110063372A1 (en) * | 2009-09-11 | 2011-03-17 | Silverbrook Research Pty Ltd | Method of ejecting solvent-based ink composition comprising acetate solvent |
| US8376541B2 (en) * | 2009-09-11 | 2013-02-19 | Zamtec Ltd | Method of ejecting solvent-based ink composition comprising pyrrolidinone solvent |
| US8110032B2 (en) * | 2009-09-11 | 2012-02-07 | Silverbrook Research Pty Ltd | Solvent-based ink composition for thermal inkjets comprising acetate solvent |
| US20110064920A1 (en) * | 2009-09-11 | 2011-03-17 | Siverbrook Research Pty Ltd. | Solvent-based ink composition for thermal inkjets comprising ketone solvent |
| US20110063373A1 (en) * | 2009-09-11 | 2011-03-17 | Silverbrook Research Pty Ltd | Method of ejecting solvent-based ink composition comprising ether solvent |
| US8080102B2 (en) * | 2009-09-11 | 2011-12-20 | Silverbrook Research Pty Ltd | Solvent-based inkjet inks comprising surface-modified pigments |
| US20110063371A1 (en) * | 2009-09-11 | 2011-03-17 | Silverbrook Research Pty Ltd | Method of ejecting solvent-based ink composition comprising ketone solvent |
| KR20120095354A (ko) | 2009-09-30 | 2012-08-28 | 가부시키가이샤 디엔피 파인 케미칼 | 잉크 조성물 |
| US9683113B2 (en) | 2010-08-25 | 2017-06-20 | Hewlett-Packard Development Company, L.P. | Pigment particles containing a vinyl group and encapsulated by a cross-linked polymer |
| US20120053289A1 (en) * | 2010-08-25 | 2012-03-01 | Sivapackia Ganapathiappan | Pigment particles encapsulated by a polymer containing at least one vinyl group |
| US9013781B2 (en) | 2011-04-29 | 2015-04-21 | Hewlett-Packard Development Company, L.P. | Inks including pigments having tri-block copolymer grafts |
| US8435707B2 (en) | 2011-06-16 | 2013-05-07 | Cabot Corporation | Toner additive comprising carbon-silica dual phase particles |
| US9637654B2 (en) | 2011-10-25 | 2017-05-02 | Hewlett-Packard Development Company, L.P. | Ink composition |
| US20140162064A1 (en) | 2012-07-13 | 2014-06-12 | Cabot Corporation | High structure carbon blacks |
| CN105209558A (zh) | 2013-03-13 | 2015-12-30 | 卡博特公司 | 具有拥有组合的低介电常数、高电阻率、和光学密度性质及受控电阻率的填料-聚合物组合物的涂层、用它制成的器件、及其制造方法 |
| WO2017087635A1 (en) | 2015-11-18 | 2017-05-26 | Cabot Corporation | Inkjet ink compositions |
| JP2019038112A (ja) * | 2017-08-22 | 2019-03-14 | 京セラドキュメントソリューションズ株式会社 | 転写捺染用転写紙 |
| WO2019051021A1 (en) | 2017-09-07 | 2019-03-14 | Cabot Corporation | INK COMPOSITIONS FOR INKJET PRINTING |
| CN111621196A (zh) * | 2020-06-28 | 2020-09-04 | 浙江大胜达包装股份有限公司 | 一种耐晒防水的油墨及其制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04234467A (ja) * | 1990-08-31 | 1992-08-24 | Xerox Corp | 修飾顔料粒子を含有するインク組成物 |
| JP2002517765A (ja) * | 1998-06-03 | 2002-06-18 | キャボット コーポレイション | 結合ハロゲン化物を有する粒子、及びその製造法 |
| JP2005015697A (ja) * | 2003-06-27 | 2005-01-20 | Mitsui Chemicals Inc | 水性エマルション組成物の製造方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6153001A (en) * | 1997-12-18 | 2000-11-28 | Fuji Xerox Co., Ltd. | Ink jet recording ink, method for producing the same, and ink jet recording method |
| ATE366781T1 (de) * | 2000-09-27 | 2007-08-15 | Seiko Epson Corp | Tintenset für tintenstrahlaufzeichnungen, verfahren für tintenstrahlaufzeichnungen sowie aufgezeichnetes produkt |
| US6833026B2 (en) * | 2002-05-10 | 2004-12-21 | Cabot Corporation | Modified pigments and process for preparing modified pigments |
| JP2004256737A (ja) * | 2003-02-27 | 2004-09-16 | Konica Minolta Holdings Inc | インクジェット用水性シアンインクとそれを用いたインクジェット用カラーインクセット及び画像形成方法 |
-
2006
- 2006-02-10 WO PCT/US2006/004790 patent/WO2006086660A1/en not_active Ceased
- 2006-02-10 US US11/351,680 patent/US20060211791A1/en not_active Abandoned
- 2006-02-10 EP EP06734773A patent/EP1871846A1/en not_active Withdrawn
- 2006-02-10 JP JP2007555258A patent/JP2008531762A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04234467A (ja) * | 1990-08-31 | 1992-08-24 | Xerox Corp | 修飾顔料粒子を含有するインク組成物 |
| JP2002517765A (ja) * | 1998-06-03 | 2002-06-18 | キャボット コーポレイション | 結合ハロゲン化物を有する粒子、及びその製造法 |
| JP2005015697A (ja) * | 2003-06-27 | 2005-01-20 | Mitsui Chemicals Inc | 水性エマルション組成物の製造方法 |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8608306B2 (en) | 2009-03-06 | 2013-12-17 | Ricoh Company, Ltd. | Inkjet recording ink, ink cartridge, inkjet recording apparatus, and ink recorded matter |
| JP2013503252A (ja) * | 2009-09-11 | 2013-01-31 | シルバーブルック リサーチ ピーティワイ リミテッド | 表面改質顔料を含む溶媒系インクジェット用インク |
| DE102011120330A1 (de) | 2010-12-08 | 2012-06-14 | Canon K.K. | Herstellungsverfahren für ein selbst-dispergierendes pigment, selbst-dispergierendes pigment, tintenstrahltinte, tintenkartusche und tintenstrahlaufzeichnungsverfahren |
| US9260611B2 (en) | 2010-12-08 | 2016-02-16 | Canon Kabushiki Kaisha | Synthesis method for self-dispersible pigment, self-dispersible pigment, ink jet ink, ink cartridge, and ink jet recording method |
| WO2016104505A1 (ja) * | 2014-12-24 | 2016-06-30 | 花王株式会社 | 顔料を含有する改質ポリマー粒子の製造方法 |
| US10421862B2 (en) | 2014-12-24 | 2019-09-24 | Kao Corporation | Process for producing pigment-containing modified polymer particles |
| JP2017031390A (ja) * | 2015-07-30 | 2017-02-09 | キヤノン株式会社 | 有機顔料、有機顔料の製造方法、トナーの製造方法 |
| JP2023054191A (ja) * | 2019-11-21 | 2023-04-13 | Dic株式会社 | 顔料組成物の製造方法 |
| JP7653065B2 (ja) | 2019-11-21 | 2025-03-28 | Dic株式会社 | 顔料組成物の製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1871846A1 (en) | 2008-01-02 |
| WO2006086660A1 (en) | 2006-08-17 |
| US20060211791A1 (en) | 2006-09-21 |
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