DE60002564T2 - Verfahren zur herstellung von farbpigmenten - Google Patents
Verfahren zur herstellung von farbpigmenten Download PDFInfo
- Publication number
- DE60002564T2 DE60002564T2 DE60002564T DE60002564T DE60002564T2 DE 60002564 T2 DE60002564 T2 DE 60002564T2 DE 60002564 T DE60002564 T DE 60002564T DE 60002564 T DE60002564 T DE 60002564T DE 60002564 T2 DE60002564 T2 DE 60002564T2
- Authority
- DE
- Germany
- Prior art keywords
- pigment
- group
- mixing
- modified color
- modified
- 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.)
- Expired - Lifetime
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- 238000000034 method Methods 0.000 claims abstract description 96
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- 238000006243 chemical reaction Methods 0.000 claims abstract description 13
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 8
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- 230000015572 biosynthetic process Effects 0.000 claims description 2
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- 125000000962 organic group Chemical group 0.000 abstract description 19
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- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 34
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- 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 7
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- 238000012545 processing Methods 0.000 description 5
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
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- 150000001409 amidines Chemical class 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
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- 150000001875 compounds Chemical class 0.000 description 4
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- 239000000178 monomer Substances 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
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- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000003973 alkyl amines Chemical class 0.000 description 3
- 125000005210 alkyl ammonium group Chemical group 0.000 description 3
- 150000001414 amino alcohols Chemical class 0.000 description 3
- 150000004982 aromatic amines Chemical class 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
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- 235000019239 indanthrene blue RS Nutrition 0.000 description 3
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- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 2
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 2
- JFGQHAHJWJBOPD-UHFFFAOYSA-N 3-hydroxy-n-phenylnaphthalene-2-carboxamide Chemical compound OC1=CC2=CC=CC=C2C=C1C(=O)NC1=CC=CC=C1 JFGQHAHJWJBOPD-UHFFFAOYSA-N 0.000 description 2
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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- 229920002873 Polyethylenimine Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
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- 150000007513 acids Chemical class 0.000 description 2
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- 230000032683 aging Effects 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- MYONAGGJKCJOBT-UHFFFAOYSA-N benzimidazol-2-one Chemical compound C1=CC=CC2=NC(=O)N=C21 MYONAGGJKCJOBT-UHFFFAOYSA-N 0.000 description 2
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- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 2
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- VBCJJAZGEJSVTL-UHFFFAOYSA-N (Z)-18-methylnonadec-9-en-1-amine Chemical compound CC(CCCCCCCC=C/CCCCCCCCN)C VBCJJAZGEJSVTL-UHFFFAOYSA-N 0.000 description 1
- GUYIZQZWDFCUTA-UHFFFAOYSA-N (pentadecachlorophthalocyaninato(2-))-copper Chemical compound [Cu+2].N1=C([N-]2)C3=C(Cl)C(Cl)=C(Cl)C(Cl)=C3C2=NC(C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C22)=NC2=NC(C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C22)=NC2=NC2=C(C(Cl)=C(C(Cl)=C3)Cl)C3=C1[N-]2 GUYIZQZWDFCUTA-UHFFFAOYSA-N 0.000 description 1
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
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- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
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- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-O dicyclohexylazanium Chemical compound C1CCCCC1[NH2+]C1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-O 0.000 description 1
- ZFAKTZXUUNBLEB-UHFFFAOYSA-N dicyclohexylazanium;nitrite Chemical compound [O-]N=O.C1CCCCC1[NH2+]C1CCCCC1 ZFAKTZXUUNBLEB-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- VPWFPZBFBFHIIL-UHFFFAOYSA-L disodium 4-[(4-methyl-2-sulfophenyl)diazenyl]-3-oxidonaphthalene-2-carboxylate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1N=NC1=C(O)C(C([O-])=O)=CC2=CC=CC=C12 VPWFPZBFBFHIIL-UHFFFAOYSA-L 0.000 description 1
- FBELJLCOAHMRJK-UHFFFAOYSA-L disodium;2,2-bis(2-ethylhexyl)-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCC(CC)CC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CC(CC)CCCC FBELJLCOAHMRJK-UHFFFAOYSA-L 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-O dodecylazanium Chemical compound CCCCCCCCCCCC[NH3+] JRBPAEWTRLWTQC-UHFFFAOYSA-O 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000001056 green pigment Substances 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical class CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
- OWFXIOWLTKNBAP-UHFFFAOYSA-N isoamyl nitrite Chemical compound CC(C)CCON=O OWFXIOWLTKNBAP-UHFFFAOYSA-N 0.000 description 1
- 238000010902 jet-milling Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- IDNHOWMYUQKKTI-UHFFFAOYSA-M lithium nitrite Chemical compound [Li+].[O-]N=O IDNHOWMYUQKKTI-UHFFFAOYSA-M 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000010303 mechanochemical reaction Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 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
- 239000012466 permeate Substances 0.000 description 1
- 150000002979 perylenes Chemical class 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 229940110337 pigment blue 1 Drugs 0.000 description 1
- CLYVDMAATCIVBF-UHFFFAOYSA-N pigment red 224 Chemical compound C=12C3=CC=C(C(OC4=O)=O)C2=C4C=CC=1C1=CC=C2C(=O)OC(=O)C4=CC=C3C1=C42 CLYVDMAATCIVBF-UHFFFAOYSA-N 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
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000010289 potassium nitrite Nutrition 0.000 description 1
- 239000004304 potassium nitrite Substances 0.000 description 1
- 238000000746 purification Methods 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
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 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
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- WPPDXAHGCGPUPK-UHFFFAOYSA-N red 2 Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=2C=3C4=CC=C5C6=CC=C7C8=C(C=9C=CC=CC=9)C9=CC=CC=C9C(C=9C=CC=CC=9)=C8C8=CC=C(C6=C87)C(C=35)=CC=2)C4=C1C1=CC=CC=C1 WPPDXAHGCGPUPK-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 229940043230 sarcosine Drugs 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- IJRHDFLHUATAOS-DPMBMXLASA-M sodium ricinoleate Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O IJRHDFLHUATAOS-DPMBMXLASA-M 0.000 description 1
- IWZMRTOJHVIXKV-UHFFFAOYSA-M sodium;2-octyldodecanoate Chemical compound [Na+].CCCCCCCCCCC(C([O-])=O)CCCCCCCC IWZMRTOJHVIXKV-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 125000000626 sulfinic acid group Chemical group 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 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
- 238000012360 testing method Methods 0.000 description 1
- 229920006029 tetra-polymer Polymers 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- WAGFXJQAIZNSEQ-UHFFFAOYSA-M tetraphenylphosphonium chloride Chemical compound [Cl-].C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 WAGFXJQAIZNSEQ-UHFFFAOYSA-M 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- HHIMNFJHTNVXBJ-UHFFFAOYSA-L zinc;dinitrite Chemical compound [Zn+2].[O-]N=O.[O-]N=O HHIMNFJHTNVXBJ-UHFFFAOYSA-L 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
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0001—Post-treatment of organic pigments or dyes
- C09B67/0004—Coated particulate pigments or dyes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- 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
- C09C1/14—Compounds of lead
- C09C1/20—Lead chromate
-
- 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
- C09C1/36—Compounds of titanium
- C09C1/3607—Titanium dioxide
- C09C1/3669—Treatment with low-molecular organic compounds
-
- 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
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/50—Agglomerated particles
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/51—Particles with a specific particle size distribution
-
- 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
-
- 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
- C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/10—Solid density
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/12—Surface area
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/80—Compositional purity
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Nanotechnology (AREA)
- General Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Composite Materials (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Compounds Of Unknown Constitution (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12294199P | 1999-03-05 | 1999-03-05 | |
| US122941P | 1999-03-05 | ||
| PCT/US2000/005742 WO2000052102A1 (en) | 1999-03-05 | 2000-03-03 | Process for preparing colored pigments |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60002564D1 DE60002564D1 (de) | 2003-06-12 |
| DE60002564T2 true DE60002564T2 (de) | 2004-04-08 |
Family
ID=22405791
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60002564T Expired - Lifetime DE60002564T2 (de) | 1999-03-05 | 2000-03-03 | Verfahren zur herstellung von farbpigmenten |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6398858B1 (enExample) |
| EP (1) | EP1157069B1 (enExample) |
| JP (1) | JP4704571B2 (enExample) |
| AT (1) | ATE239769T1 (enExample) |
| AU (1) | AU3725000A (enExample) |
| DE (1) | DE60002564T2 (enExample) |
| DK (1) | DK1157069T3 (enExample) |
| ES (1) | ES2193059T3 (enExample) |
| PT (1) | PT1157069E (enExample) |
| WO (1) | WO2000052102A1 (enExample) |
Families Citing this family (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7002728B2 (en) | 1997-08-28 | 2006-02-21 | E Ink Corporation | Electrophoretic particles, and processes for the production thereof |
| US7247379B2 (en) | 1997-08-28 | 2007-07-24 | E Ink Corporation | Electrophoretic particles, and processes for the production thereof |
| JP2001055531A (ja) * | 1999-06-09 | 2001-02-27 | Seiko Epson Corp | 水性インク組成物 |
| WO2001025340A1 (en) * | 1999-10-01 | 2001-04-12 | Cabot Corporation | Modified pigments having steric and amphiphilic groups |
| JP4851040B2 (ja) * | 1999-10-28 | 2012-01-11 | キャボット コーポレイション | インクジェット用インク、インク、および着色顔料を含有するその他の組成物 |
| CN100386390C (zh) | 1999-10-28 | 2008-05-07 | 卡伯特公司 | 喷墨油墨、油墨以及含着色颜料的其它组合物 |
| EP1252237B1 (en) | 2000-01-07 | 2006-08-09 | Cabot Corporation | Polymers and other groups attached to pigments and subsequent reactions |
| KR100831782B1 (ko) | 2000-07-06 | 2008-05-27 | 캐보트 코포레이션 | 개질된 안료 생성물을 포함하는 인쇄판 |
| EP1307513B1 (en) | 2000-07-06 | 2009-01-21 | Cabot Corporation | Modified pigment products, dispersions thereof, and compositions comprising the same |
| DE60111480T2 (de) * | 2000-12-12 | 2005-11-24 | Konica Corp. | Flüssige Pigmentdispersionen zum Tintenstrahldrucken |
| US7230750B2 (en) | 2001-05-15 | 2007-06-12 | E Ink Corporation | Electrophoretic media and processes for the production thereof |
| US6645287B2 (en) | 2001-04-27 | 2003-11-11 | Cabot Corporation | Coating compositions comprising high t-area carbon products |
| US6712894B2 (en) | 2001-05-09 | 2004-03-30 | Cabot Corporation | Method of producing secure images using inks comprising modified pigment particles |
| JP4188091B2 (ja) | 2001-05-15 | 2008-11-26 | イー インク コーポレイション | 電気泳動粒子 |
| EP1387868A1 (en) | 2001-05-18 | 2004-02-11 | Ciba SC Holding AG | Surface-treated organic pigments |
| JP2005501159A (ja) | 2001-08-23 | 2005-01-13 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 安定化した有機顔料粒子を製造する方法、およびそのための装置 |
| US6641656B2 (en) | 2001-10-17 | 2003-11-04 | Cabot Corporation | Dispersions comprising modified pigments |
| JP2006503114A (ja) * | 2002-01-07 | 2006-01-26 | キャボット コーポレイション | 改質ピグメント生成物およびそれを含むブラックマトリクス |
| US7001934B2 (en) | 2002-01-24 | 2006-02-21 | Cabot Coroporation | Inkjet ink systems comprising a gelling agent |
| US7173078B2 (en) | 2002-04-12 | 2007-02-06 | Cabot Corporation | Process for preparing modified pigments |
| US6699319B2 (en) | 2002-05-06 | 2004-03-02 | Cabot Corporation | Process for preparing modified pigments |
| US6833026B2 (en) | 2002-05-10 | 2004-12-21 | Cabot Corporation | Modified pigments and process for preparing modified pigments |
| JP4855923B2 (ja) * | 2003-01-17 | 2012-01-18 | キャボット コーポレイション | 水性有色顔料分散液を製造する方法及びインクジェット用組成物 |
| US6936097B2 (en) * | 2003-04-16 | 2005-08-30 | Cabot Corporation | Modified organic colorants and dispersions, and methods for their preparation |
| US6942724B2 (en) * | 2003-04-16 | 2005-09-13 | Cabot Corporation | Modified organic colorants and dispersions, and methods for their preparation |
| US8492456B2 (en) * | 2004-02-09 | 2013-07-23 | Hewlett-Packard Development Company, L.P. | Ink compositions for ink-jet printing |
| US20050256225A1 (en) * | 2004-05-11 | 2005-11-17 | Viola Michael S | Aqueous inkjet ink compositions comprising comb-branched copolymers |
| US7347892B2 (en) * | 2004-08-13 | 2008-03-25 | Xerox Corporation | Phase change inks containing modified pigment particles |
| KR101341262B1 (ko) | 2004-10-15 | 2013-12-13 | 캐보트 코포레이션 | 높은 저항률 조성물 |
| EP1833932B1 (en) * | 2004-12-17 | 2012-01-18 | Cabot Corporation | Method of preparing oxidized modified pigments and inkjet ink compositions comprising the same |
| US7115164B2 (en) * | 2005-02-28 | 2006-10-03 | Sun Chemical Corporation | Preparation of yellow pigments |
| MX2007011788A (es) * | 2005-03-24 | 2007-11-16 | Cabot Corp | Fluoroquinolonoquinolonas y composiciones de tintas de inyeccion de tinta que comprenden las mismas. |
| DE102005028742B3 (de) * | 2005-06-21 | 2006-09-21 | Siemens Audiologische Technik Gmbh | Hörhilfegerät mit Mitteln zur Rückkopplungskompensation und Verfahren zur Rückkopplungsunterdrückung |
| CN101291996B (zh) * | 2005-08-31 | 2012-10-03 | 卡伯特公司 | 制备改性颜料的方法 |
| US8268064B2 (en) * | 2005-09-30 | 2012-09-18 | Hewlett-Packard Development Company, L.P. | Ink-jet inks and ink sets exhibiting reduced bleed, wicking, and/or halo effect and associated methods |
| US7691197B2 (en) | 2005-10-21 | 2010-04-06 | Cabot Corporation | Method of preparing yellow pigments |
| JP5057261B2 (ja) * | 2005-10-25 | 2012-10-24 | 東海カーボン株式会社 | カーボンブラック水性分散体及びその製造方法 |
| EP1951819B2 (en) | 2005-10-31 | 2019-02-27 | Cabot Corporation | Modified colorants and inkjet ink compositions comprising modified colorants |
| US7381257B2 (en) * | 2006-02-15 | 2008-06-03 | Canon Kabushiki Kaisha | Aqueous ink, ink-jet recording method, ink cartridge, recording unit and ink jet recording apparatus |
| US7749957B2 (en) | 2006-04-06 | 2010-07-06 | E.I. Du Pont De Nemours And Company | Clay-binding peptides and methods of use |
| US8021471B2 (en) * | 2006-08-28 | 2011-09-20 | Cabot Corporation | Modified colorants with aliphatic poly-acid groups |
| US8163075B2 (en) | 2006-10-31 | 2012-04-24 | Sensient Colors Llc | Inks comprising modified pigments and methods for making and using the same |
| BRPI0807978A2 (pt) * | 2007-02-27 | 2014-06-10 | Cabot Corp | Composições de tinta de impressora a jato de tinta compreendendo múltiplos pigmentos modificados |
| US7799121B2 (en) * | 2007-04-20 | 2010-09-21 | E.I. Du Pont De Nemours And Company | Inkjet ink |
| US7771523B2 (en) * | 2007-04-20 | 2010-08-10 | E.I. Du Pont De Nemours And Company | Ink jet ink |
| US20090020035A1 (en) * | 2007-04-20 | 2009-01-22 | Christian Jackson | Inkjet ink |
| CN101855302B (zh) | 2007-08-23 | 2014-10-01 | 森馨颜色公司 | 自分散颜料及制造和使用该自分散颜料的方法 |
| US20100288163A1 (en) * | 2007-12-18 | 2010-11-18 | E.I Du Pont De Nemours And Company | Aqueous inkjet ink comprising a bleed control agent |
| CN101978000A (zh) * | 2008-01-25 | 2011-02-16 | 卡伯特公司 | 制备改性有色颜料的方法 |
| US8562122B2 (en) * | 2008-01-25 | 2013-10-22 | E I Du Pont De Nemours And Company | Ink jet inks having improved corrosion resistance for use in ink jet print heads comprising nickel or nickel alloys |
| US20100081740A1 (en) * | 2008-09-29 | 2010-04-01 | Christian Jackson | Aqueous inkjet ink comprising self-dispersing pigment |
| US8398762B2 (en) | 2009-03-24 | 2013-03-19 | E I Du Pont De Nemours And Company | Pigmented inkjet ink comprising a bleed control agent |
| US8481678B2 (en) | 2009-03-30 | 2013-07-09 | E I Du Pont De Nemours And Company | Peptide-based tooth whitening reagents |
| BRPI1014677A2 (pt) * | 2009-03-30 | 2016-04-12 | Du Pont | sistemas baseados em peptídeos para distribuição de agentes cosméticos |
| JP2012523479A (ja) | 2009-04-07 | 2012-10-04 | センシエント カラーズ エルエルシー | 自己分散性粒子並びにその製造方法及び使用方法 |
| ES2438465B2 (es) | 2010-09-03 | 2016-04-05 | Cabot Corporation | Cargas modificadas y compuestos elastoméricos que comprenden los mismos. |
| JP5872565B2 (ja) | 2010-10-15 | 2016-03-01 | キャボット コーポレイションＣａｂｏｔ Ｃｏｒｐｏｒａｔｉｏｎ | 表面改質有機黒色顔料、表面改質カーボンブラック、それを用いた顔料混合物、ならびに低誘電性黒色分散体、コーティング、フィルム、ブラックマトリックス、およびそれを被覆した装置 |
| US8331014B2 (en) | 2010-11-02 | 2012-12-11 | Hewlett-Packard Development Company, L.P. | Pigment-based inks |
| KR101939419B1 (ko) | 2010-12-30 | 2019-01-16 | 바스프 에스이 | 표면-개질된 안료 제제 |
| US9175150B2 (en) | 2012-03-02 | 2015-11-03 | Cabot Corporation | Modified carbon blacks having low PAH amounts and elastomers containing the same |
| KR101696529B1 (ko) | 2012-03-02 | 2017-01-13 | 캐보트 코포레이션 | 개질된 충전제 및 관능화 엘라스토머를 함유하는 엘라스토머 복합재 |
| US20140162064A1 (en) | 2012-07-13 | 2014-06-12 | Cabot Corporation | High structure carbon blacks |
| KR102001887B1 (ko) * | 2012-08-28 | 2019-07-19 | 엘지디스플레이 주식회사 | 전기변색입자 및 이를 포함하는 표시장치 |
| JP2016516105A (ja) | 2013-03-05 | 2016-06-02 | キャボット コーポレイションＣａｂｏｔ Ｃｏｒｐｏｒａｔｉｏｎ | 水性の顔料分散液 |
| US20140267515A1 (en) | 2013-03-12 | 2014-09-18 | Cabot Corporation | Aqueous dispersions comprising nanocrystalline cellulose, and compositions for commercial inkjet printing |
| CN105051073A (zh) | 2013-03-14 | 2015-11-11 | 卡博特公司 | 核-壳聚合物材料 |
| CA2910229C (en) | 2013-04-25 | 2019-11-26 | Nissan Motor Co., Ltd. | Catalyst and electrode catalyst layer, membrane electrode assembly, and fuel cell using the catalyst |
| WO2014175097A1 (ja) | 2013-04-25 | 2014-10-30 | 日産自動車株式会社 | 触媒およびその製造方法ならびに当該触媒を用いる電極触媒層 |
| US9920209B2 (en) | 2014-10-14 | 2018-03-20 | Cabot Corporation | Aqueous inkjet ink compositions |
| CN107210447B (zh) | 2014-10-29 | 2019-08-23 | 日产自动车株式会社 | 燃料电池用电极催化剂层、其制造方法以及使用该催化剂层的膜电极接合体及燃料电池 |
| EP3250651B1 (en) | 2015-01-30 | 2019-08-28 | Hewlett-Packard Development Company, L.P. | Aqueous pigment co-dispersions |
| WO2016187059A1 (en) | 2015-05-15 | 2016-11-24 | Cabot Corporation | Amphoteric polymers and use in inkjet ink compositions |
| JP6869241B2 (ja) | 2015-11-18 | 2021-05-12 | キャボット コーポレイションＣａｂｏｔ Ｃｏｒｐｏｒａｔｉｏｎ | インクジェットインク組成物 |
| JP6860330B2 (ja) * | 2015-12-28 | 2021-04-14 | キヤノン株式会社 | 自己分散顔料の製造方法、インクの製造方法、及びインクジェット記録方法 |
| GB2592298B (en) | 2016-10-31 | 2022-09-28 | Cabot Corp | Polymers for inkjet ink compositions |
| US10954402B2 (en) | 2017-09-07 | 2021-03-23 | Cabot Corporation | Inkjet ink compositions |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56147865A (en) | 1980-04-17 | 1981-11-17 | Canon Inc | Preparation of recording solution |
| JPS5721466A (en) | 1980-07-14 | 1982-02-04 | Canon Inc | Recording fluid |
| JPS57179251A (en) * | 1981-04-28 | 1982-11-04 | Tone Sangyo Kk | Novel powder composition and its preparation |
| JPS6039705B2 (ja) | 1983-02-21 | 1985-09-07 | 学校法人近畿大学 | 無機粉体を核とする有機顔料の製造法 |
| JPS6448875A (en) | 1987-08-18 | 1989-02-23 | Mitsubishi Pencil Co | Stabilized pigment ink composition and its preparation |
| US5026427A (en) | 1988-10-12 | 1991-06-25 | E. I. Dupont De Nemours And Company | Process for making pigmented ink jet inks |
| US5281261A (en) | 1990-08-31 | 1994-01-25 | Xerox Corporation | Ink compositions containing modified pigment particles |
| EP0677556A3 (en) | 1994-04-15 | 1997-02-26 | Toyo Ink Mfg Co | Coated pigment and coloring composition. |
| US5418277A (en) | 1994-04-26 | 1995-05-23 | E. I. Du Pont De Nemours And Company | Aqueous ink jet inks containing fluorinated polymers |
| JP3405817B2 (ja) | 1994-06-20 | 2003-05-12 | オリヱント化学工業株式会社 | 水性顔料インキ及びその製造方法 |
| IL116378A (en) | 1994-12-15 | 2003-05-29 | Cabot Corp | Non-aqueous coating or ink composition with improved optical properties containing modified carbon product and method of preparation of the composition |
| US5571311A (en) | 1994-12-15 | 1996-11-05 | Cabot Corporation | Ink jet ink formulations containing carbon black products |
| IL116377A (en) * | 1994-12-15 | 2003-05-29 | Cabot Corp | Reaction of carbon black with diazonium salts, resultant carbon black products and their uses |
| US5554739A (en) | 1994-12-15 | 1996-09-10 | Cabot Corporation | Process for preparing carbon materials with diazonium salts and resultant carbon products |
| IL116379A (en) | 1994-12-15 | 2003-12-10 | Cabot Corp | Aqueous inks and coatings containing modified carbon products |
| IL116376A (en) | 1994-12-15 | 2001-03-19 | Cabot Corp | Aqueous ink jet ink compositions containing modified carbon products |
| JPH08333542A (ja) * | 1995-06-06 | 1996-12-17 | Brother Ind Ltd | 記録用インク |
| US5679138A (en) | 1995-11-30 | 1997-10-21 | Eastman Kodak Company | Ink jet inks containing nanoparticles of organic pigments |
| US5958999A (en) | 1996-04-05 | 1999-09-28 | Cabot Corporation | Ink compositions and method for generating images produced therefrom |
| JP4697757B2 (ja) | 1996-06-14 | 2011-06-08 | キャボット コーポレイション | 変性された有色顔料類及びそれらを含むインキジェットインキ類 |
| US6069190A (en) | 1996-06-14 | 2000-05-30 | Cabot Corporation | Ink compositions having improved latency |
| US5698016A (en) | 1996-06-14 | 1997-12-16 | Cabot Corporation | Compositions of modified carbon products and amphiphilic ions and methods of using the same |
| US5707432A (en) | 1996-06-14 | 1998-01-13 | Cabot Corporation | Modified carbon products and inks and coatings containing modified carbon products |
| US6110994A (en) | 1996-06-14 | 2000-08-29 | Cabot Corporation | Polymeric products containing modified carbon products and methods of making and using the same |
| US5837045A (en) * | 1996-06-17 | 1998-11-17 | Cabot Corporation | Colored pigment and aqueous compositions containing same |
| US5830265A (en) | 1996-10-31 | 1998-11-03 | Hewlett-Packard Company | Counterion substitution in macromolecular chromophore (MMC) for ink-jet printing including textile, large format and office format printers |
| US5955232A (en) | 1997-07-22 | 1999-09-21 | Cabot Corporation | Toners containing positively chargeable modified pigments |
| US5895522A (en) | 1997-08-12 | 1999-04-20 | Cabot Corporation | Modified carbon products with leaving groups and inks and coatings containing modified carbon products |
| US5985016A (en) | 1997-10-30 | 1999-11-16 | Hewlett-Packard Company | Purification of macromolecular chromophores (MMCs) using membrane processes for ink-jet inks |
| WO1999038921A1 (en) | 1998-01-29 | 1999-08-05 | Cabot Corporation | Processes of purifying a dispersion and making inkjet inks |
| WO1999051690A1 (en) | 1998-04-03 | 1999-10-14 | Cabot Corporation | Modified pigments having improved dispersing properties |
| US6458458B1 (en) | 1998-10-13 | 2002-10-01 | Cabot Corporation | Polymer coated carbon products and other pigments and methods of making same by aqueous media polymerizations or solvent coating methods |
| US6218067B1 (en) | 1998-11-06 | 2001-04-17 | Cabot Corporation | Toners containing chargeable modified pigments |
-
2000
- 2000-03-03 WO PCT/US2000/005742 patent/WO2000052102A1/en not_active Ceased
- 2000-03-03 AT AT00916090T patent/ATE239769T1/de not_active IP Right Cessation
- 2000-03-03 US US09/517,857 patent/US6398858B1/en not_active Expired - Lifetime
- 2000-03-03 AU AU37250/00A patent/AU3725000A/en not_active Abandoned
- 2000-03-03 EP EP00916090A patent/EP1157069B1/en not_active Expired - Lifetime
- 2000-03-03 JP JP2000602719A patent/JP4704571B2/ja not_active Expired - Fee Related
- 2000-03-03 DK DK00916090T patent/DK1157069T3/da active
- 2000-03-03 ES ES00916090T patent/ES2193059T3/es not_active Expired - Lifetime
- 2000-03-03 DE DE60002564T patent/DE60002564T2/de not_active Expired - Lifetime
- 2000-03-03 PT PT00916090T patent/PT1157069E/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE239769T1 (de) | 2003-05-15 |
| JP4704571B2 (ja) | 2011-06-15 |
| AU3725000A (en) | 2000-09-21 |
| ES2193059T3 (es) | 2003-11-01 |
| EP1157069A1 (en) | 2001-11-28 |
| DE60002564D1 (de) | 2003-06-12 |
| WO2000052102A1 (en) | 2000-09-08 |
| EP1157069B1 (en) | 2003-05-07 |
| PT1157069E (pt) | 2003-09-30 |
| US6398858B1 (en) | 2002-06-04 |
| JP2002538260A (ja) | 2002-11-12 |
| DK1157069T3 (da) | 2003-09-01 |
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