NO313837B1 - FremgangsmÕte for fremstilling av fargekonsentrater og trykkfarge fremstilt ved fremgangsmÕten - Google Patents
FremgangsmÕte for fremstilling av fargekonsentrater og trykkfarge fremstilt ved fremgangsmÕten Download PDFInfo
- Publication number
- NO313837B1 NO313837B1 NO19964867A NO964867A NO313837B1 NO 313837 B1 NO313837 B1 NO 313837B1 NO 19964867 A NO19964867 A NO 19964867A NO 964867 A NO964867 A NO 964867A NO 313837 B1 NO313837 B1 NO 313837B1
- Authority
- NO
- Norway
- Prior art keywords
- metal phthalocyanine
- color
- extruder
- concentrate
- phthalocyanine
- Prior art date
Links
- 239000012141 concentrate Substances 0.000 title claims description 62
- 238000000034 method Methods 0.000 title claims description 33
- 239000000976 ink Substances 0.000 title description 41
- 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 claims description 44
- 229910052751 metal Inorganic materials 0.000 claims description 38
- 239000002184 metal Substances 0.000 claims description 38
- 229920005989 resin Polymers 0.000 claims description 38
- 239000011347 resin Substances 0.000 claims description 38
- 239000007788 liquid Substances 0.000 claims description 26
- 238000000227 grinding Methods 0.000 claims description 17
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical group [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 claims description 17
- 239000000049 pigment Substances 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 238000002156 mixing Methods 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 238000004898 kneading Methods 0.000 claims description 8
- 239000011230 binding agent Substances 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 26
- 239000000463 material Substances 0.000 description 15
- 229960000541 cetyl alcohol Drugs 0.000 description 13
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 13
- 239000006185 dispersion Substances 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 238000010422 painting Methods 0.000 description 8
- 230000019612 pigmentation Effects 0.000 description 8
- -1 aliphatic alcohols Chemical class 0.000 description 6
- 229920000180 alkyd Polymers 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 101001012040 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) Immunomodulating metalloprotease Proteins 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000009775 high-speed stirring Methods 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008431 aliphatic amides Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- WDEQGLDWZMIMJM-UHFFFAOYSA-N benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate Chemical compound OCC1CC(O)CN1C(=O)OCC1=CC=CC=C1 WDEQGLDWZMIMJM-UHFFFAOYSA-N 0.000 description 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000009500 colour coating Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- IPHJYJHJDIGARM-UHFFFAOYSA-M copper phthalocyaninesulfonic acid, dioctadecyldimethylammonium salt Chemical compound [Cu+2].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.C=1C(S(=O)(=O)[O-])=CC=C(C(=NC2=NC(C3=CC=CC=C32)=N2)[N-]3)C=1C3=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 IPHJYJHJDIGARM-UHFFFAOYSA-M 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 239000013067 intermediate product 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
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-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
- 150000002576 ketones Chemical class 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
- C09D11/037—Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
-
- 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
- C09B67/0014—Influencing the physical properties by treatment with a liquid, e.g. solvents
- C09B67/0016—Influencing the physical properties by treatment with a liquid, e.g. solvents of phthalocyanines
-
- 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
- C09B67/0022—Wet grinding of pigments
- C09B67/0023—Wet grinding of pigments of phthalocyanines
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9523387.0A GB9523387D0 (en) | 1995-11-16 | 1995-11-16 | Production process |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO964867D0 NO964867D0 (no) | 1996-11-15 |
| NO964867L NO964867L (no) | 1997-05-20 |
| NO313837B1 true NO313837B1 (no) | 2002-12-09 |
Family
ID=10783938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19964867A NO313837B1 (no) | 1995-11-16 | 1996-11-15 | FremgangsmÕte for fremstilling av fargekonsentrater og trykkfarge fremstilt ved fremgangsmÕten |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US5964929A (de) |
| EP (1) | EP0774494B2 (de) |
| JP (1) | JP3802165B2 (de) |
| KR (1) | KR100459355B1 (de) |
| CN (1) | CN1088080C (de) |
| AU (1) | AU716273B2 (de) |
| BR (1) | BR9605576A (de) |
| CA (1) | CA2190327A1 (de) |
| CZ (1) | CZ291206B6 (de) |
| DE (1) | DE69613195T3 (de) |
| DK (1) | DK0774494T4 (de) |
| ES (1) | ES2158251T5 (de) |
| GB (1) | GB9523387D0 (de) |
| IL (1) | IL119626A (de) |
| NO (1) | NO313837B1 (de) |
| SG (1) | SG43442A1 (de) |
| ZA (1) | ZA969603B (de) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3139396B2 (ja) * | 1996-02-05 | 2001-02-26 | 東洋インキ製造株式会社 | 印刷インキの製造方法 |
| GB9709762D0 (en) * | 1997-05-15 | 1997-07-09 | Ciba Geigy Ag | Production process |
| US6056814A (en) * | 1997-12-08 | 2000-05-02 | Toyo Ink Mfg. Co., Ltd. | Pigment composition and aqueous pigment dispersion prepared therefrom |
| GB9808169D0 (en) | 1998-04-20 | 1998-06-17 | Ciba Sc Holding Ag | Production process |
| US6379451B1 (en) | 1999-04-05 | 2002-04-30 | Toyo Ink Mfg. Co., Ltd. | Pigment composition and aqueous pigment dispersion product using the same |
| DE19927835A1 (de) * | 1999-06-18 | 2000-12-21 | Clariant Gmbh | Verwendung von verbesserten Cyanpigmenten in elektrophotographischen Tonern und Entwicklern, Pulverlacken und Ink-Jet-Tinten |
| US6410619B2 (en) | 1999-11-22 | 2002-06-25 | Bayer Corporation | Method for conditioning organic pigments |
| US6379450B1 (en) † | 2000-03-08 | 2002-04-30 | Sun Chemical Corporation | Process for producing β-phase copper phthalocyanine pigment |
| US6530989B1 (en) | 2001-12-28 | 2003-03-11 | Sun Chemical Corporation | Methods for production of organic pigments for printing inks |
| WO2005123844A1 (de) * | 2004-06-16 | 2005-12-29 | Colour Ltd. | Verfahren zur herstellung von beta-kupferphthalocyanin-blaupigmenten und deren verwendung |
| US7550041B2 (en) * | 2004-11-01 | 2009-06-23 | Ciba Specialty Chemicals Corporation | Highly concentrated flowable pigment composition and process for its manufacture |
| EP1888692A2 (de) * | 2005-05-02 | 2008-02-20 | Ciba Specialty Chemicals Holding, Inc. | Verfahren zur herstellung einer neuen pigmentierten zusammensetzung zur verwendung für offset-tinten |
| CN101309985B (zh) | 2005-11-16 | 2011-10-12 | 精工爱普生株式会社 | 品红墨液组合物、墨盒、使用其的记录系统以及记录物 |
| JP5664834B1 (ja) * | 2013-07-31 | 2015-02-04 | Dic株式会社 | フタロシアニン顔料組成物の製造方法 |
| DE102016120102A1 (de) * | 2016-10-21 | 2018-04-26 | Epple Druckfarben Ag | Druckfarbe oder Drucklack |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1149898A (en) * | 1965-09-17 | 1969-04-23 | Ici Ltd | Manufacture of pigment compositions |
| BE785654A (fr) * | 1971-06-30 | 1973-01-02 | Basf Ag | Procede de fabrication de pigments en pate pour encres d'imprimerie et peintures |
| JPS5647436A (en) * | 1979-09-28 | 1981-04-30 | Toyo Soda Mfg Co Ltd | Preparation of concentrated pigment dispersion |
| US4371643A (en) † | 1980-07-31 | 1983-02-01 | American Cyanamid Co. | Particle size reduction of pigments by non-salt milling |
| US4427810A (en) * | 1981-05-04 | 1984-01-24 | Inmont Corporation | Continuous method of producing aqueous phthalocyanine pigment dispersions |
| US4371642A (en) * | 1981-07-07 | 1983-02-01 | E. I. Du Pont De Nemours And Company | Process for preparing polyolefin resin extended pigments |
| US4478968A (en) * | 1983-04-06 | 1984-10-23 | Ciba-Geigy Corporation | Manufacture of resin extended pigments |
| JPS6053566A (ja) * | 1983-09-02 | 1985-03-27 | Hodogaya Chem Co Ltd | 染料濃厚溶液 |
| US4522654A (en) * | 1983-12-23 | 1985-06-11 | Inmont Corporation | Continuous method of producing phthalocyanine pigment dispersions in organic solvent |
| US4709021A (en) * | 1985-11-06 | 1987-11-24 | Basf Corporation | Copper phthalocyanine pigments |
| NL8701075A (nl) * | 1987-05-07 | 1988-12-01 | O & R Inktchemie | Werkwijze voor het bereiden van een halffabrikaat ten gebruike voor de bereiding van drukinkt alsmede drukinkt verkregen onder toepassing van dat halffabrikaat. |
| DE3824054A1 (de) * | 1988-07-15 | 1990-01-18 | Basf Ag | Verfahren zur ueberfuehrung von rohkupferphthalocyaninen in eine pigmentform |
| DE3911476A1 (de) * | 1989-04-08 | 1990-10-11 | Basf Ag | Verfahren zur herstellung von fuer pastoese druckfarben geeignetem kupferphthalocyanin |
| US5175282A (en) * | 1989-07-11 | 1992-12-29 | Basf Aktiengesellschaft | Preparation of copper phthalocyanine pigments of the beta-modification |
| GB9326374D0 (en) | 1993-12-23 | 1994-02-23 | Zeneca Ltd | Process |
-
1995
- 1995-11-16 GB GBGB9523387.0A patent/GB9523387D0/en active Pending
-
1996
- 1996-11-05 EP EP96308021A patent/EP0774494B2/de not_active Expired - Lifetime
- 1996-11-05 DK DK96308021T patent/DK0774494T4/da active
- 1996-11-05 ES ES96308021T patent/ES2158251T5/es not_active Expired - Lifetime
- 1996-11-05 DE DE69613195T patent/DE69613195T3/de not_active Expired - Lifetime
- 1996-11-12 AU AU71741/96A patent/AU716273B2/en not_active Ceased
- 1996-11-13 US US08/748,299 patent/US5964929A/en not_active Expired - Lifetime
- 1996-11-14 BR BR9605576A patent/BR9605576A/pt not_active IP Right Cessation
- 1996-11-14 CZ CZ19963361A patent/CZ291206B6/cs not_active IP Right Cessation
- 1996-11-14 CA CA002190327A patent/CA2190327A1/en not_active Abandoned
- 1996-11-15 NO NO19964867A patent/NO313837B1/no unknown
- 1996-11-15 SG SG1996011133A patent/SG43442A1/en unknown
- 1996-11-15 JP JP30340796A patent/JP3802165B2/ja not_active Expired - Fee Related
- 1996-11-15 CN CN96123385A patent/CN1088080C/zh not_active Expired - Fee Related
- 1996-11-15 KR KR1019960054491A patent/KR100459355B1/ko not_active IP Right Cessation
- 1996-11-15 ZA ZA969603A patent/ZA969603B/xx unknown
- 1996-11-17 IL IL11962696A patent/IL119626A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPH09188845A (ja) | 1997-07-22 |
| ZA969603B (en) | 1997-05-16 |
| JP3802165B2 (ja) | 2006-07-26 |
| KR100459355B1 (ko) | 2005-05-16 |
| AU7174196A (en) | 1997-05-22 |
| US5964929A (en) | 1999-10-12 |
| DE69613195D1 (de) | 2001-07-12 |
| DE69613195T3 (de) | 2005-03-10 |
| EP0774494A1 (de) | 1997-05-21 |
| ES2158251T5 (es) | 2005-04-01 |
| CN1088080C (zh) | 2002-07-24 |
| IL119626A0 (en) | 1997-02-18 |
| GB9523387D0 (en) | 1996-01-17 |
| CZ291206B6 (cs) | 2003-01-15 |
| NO964867L (no) | 1997-05-20 |
| CA2190327A1 (en) | 1997-05-17 |
| EP0774494B2 (de) | 2004-09-22 |
| KR970027239A (ko) | 1997-06-24 |
| ES2158251T3 (es) | 2001-09-01 |
| NO964867D0 (no) | 1996-11-15 |
| AU716273B2 (en) | 2000-02-24 |
| EP0774494B1 (de) | 2001-06-06 |
| CN1161359A (zh) | 1997-10-08 |
| DK0774494T3 (da) | 2001-09-10 |
| DK0774494T4 (da) | 2004-10-11 |
| DE69613195T2 (de) | 2001-12-20 |
| SG43442A1 (en) | 1997-10-17 |
| IL119626A (en) | 2003-11-23 |
| BR9605576A (pt) | 1998-08-18 |
| CZ336196A3 (cs) | 1998-05-13 |
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