MXPA04010752A - Composiciones y metodos para impartir reologia mejorada a tintas y pinturas basadas en pigmentos. - Google Patents
Composiciones y metodos para impartir reologia mejorada a tintas y pinturas basadas en pigmentos.Info
- Publication number
- MXPA04010752A MXPA04010752A MXPA04010752A MXPA04010752A MXPA04010752A MX PA04010752 A MXPA04010752 A MX PA04010752A MX PA04010752 A MXPA04010752 A MX PA04010752A MX PA04010752 A MXPA04010752 A MX PA04010752A MX PA04010752 A MXPA04010752 A MX PA04010752A
- Authority
- MX
- Mexico
- Prior art keywords
- pigment
- anionic
- cationic
- dye
- red
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 102
- 239000003973 paint Substances 0.000 title claims abstract description 17
- 238000000034 method Methods 0.000 title claims description 30
- 238000000518 rheometry Methods 0.000 title abstract description 4
- 239000001042 pigment based ink Substances 0.000 title 1
- 239000000049 pigment Substances 0.000 claims abstract description 285
- 239000000975 dye Substances 0.000 claims abstract description 93
- 125000002091 cationic group Chemical group 0.000 claims abstract description 78
- 125000000129 anionic group Chemical group 0.000 claims abstract description 73
- 239000012860 organic pigment Substances 0.000 claims abstract description 41
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 238000007639 printing Methods 0.000 claims abstract description 12
- 239000002253 acid Substances 0.000 claims description 29
- 239000006185 dispersion Substances 0.000 claims description 17
- 239000010802 sludge Substances 0.000 claims description 17
- 239000007864 aqueous solution Substances 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- 239000003945 anionic surfactant Substances 0.000 claims description 11
- 239000003093 cationic surfactant Substances 0.000 claims description 11
- MHOFGBJTSNWTDT-UHFFFAOYSA-M 2-[n-ethyl-4-[(6-methoxy-3-methyl-1,3-benzothiazol-3-ium-2-yl)diazenyl]anilino]ethanol;methyl sulfate Chemical compound COS([O-])(=O)=O.C1=CC(N(CCO)CC)=CC=C1N=NC1=[N+](C)C2=CC=C(OC)C=C2S1 MHOFGBJTSNWTDT-UHFFFAOYSA-M 0.000 claims description 10
- 239000012065 filter cake Substances 0.000 claims description 10
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [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 10
- 239000000126 substance Substances 0.000 claims description 10
- -1 triarylmethane Chemical compound 0.000 claims description 10
- 239000000654 additive Substances 0.000 claims description 9
- 239000001054 red pigment Substances 0.000 claims description 9
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 claims description 8
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 7
- 239000001052 yellow pigment Substances 0.000 claims description 7
- BTLXPCBPYBNQNR-UHFFFAOYSA-N 1-hydroxyanthraquinone Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2O BTLXPCBPYBNQNR-UHFFFAOYSA-N 0.000 claims description 6
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 6
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 6
- 239000008187 granular material Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 5
- 239000000980 acid dye Substances 0.000 claims description 5
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 5
- 150000004056 anthraquinones Chemical class 0.000 claims description 5
- 239000001055 blue pigment Substances 0.000 claims description 5
- 150000004696 coordination complex Chemical class 0.000 claims description 5
- 239000000982 direct dye Substances 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
- 239000000983 mordant dye Substances 0.000 claims description 4
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 claims description 3
- 235000000177 Indigofera tinctoria Nutrition 0.000 claims description 3
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical group [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 3
- MYONAGGJKCJOBT-UHFFFAOYSA-N benzimidazol-2-one Chemical compound C1=CC=CC2=NC(=O)N=C21 MYONAGGJKCJOBT-UHFFFAOYSA-N 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 230000003750 conditioning effect Effects 0.000 claims description 3
- 239000001056 green pigment Substances 0.000 claims description 3
- 229940097275 indigo Drugs 0.000 claims description 3
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 claims description 3
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 claims description 3
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 claims description 3
- OBJNZHVOCNPSCS-UHFFFAOYSA-N naphtho[2,3-f]quinazoline Chemical compound C1=NC=C2C3=CC4=CC=CC=C4C=C3C=CC2=N1 OBJNZHVOCNPSCS-UHFFFAOYSA-N 0.000 claims description 3
- PYUYQYBDJFMFTH-WMMMYUQOSA-N naphthol red Chemical group CCOC1=CC=CC=C1NC(=O)C(C1=O)=CC2=CC=CC=C2\C1=N\NC1=CC=C(C(N)=O)C=C1 PYUYQYBDJFMFTH-WMMMYUQOSA-N 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- AZLXCBPKSXFMET-UHFFFAOYSA-M sodium 4-[(4-sulfophenyl)diazenyl]naphthalen-1-olate Chemical compound [Na+].C12=CC=CC=C2C(O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 AZLXCBPKSXFMET-UHFFFAOYSA-M 0.000 claims description 3
- 238000003786 synthesis reaction Methods 0.000 claims description 3
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 claims description 3
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 claims description 2
- INOIOAWTVPHTCJ-UHFFFAOYSA-N 6-acetamido-4-hydroxy-3-[[4-(2-sulfooxyethylsulfonyl)phenyl]diazenyl]naphthalene-2-sulfonic acid Chemical compound CC(=O)NC1=CC=C2C=C(C(N=NC3=CC=C(C=C3)S(=O)(=O)CCOS(O)(=O)=O)=C(O)C2=C1)S(O)(=O)=O INOIOAWTVPHTCJ-UHFFFAOYSA-N 0.000 claims description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 2
- DGOBMKYRQHEFGQ-UHFFFAOYSA-L acid green 5 Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=CC(=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 DGOBMKYRQHEFGQ-UHFFFAOYSA-L 0.000 claims description 2
- 239000001045 blue dye Substances 0.000 claims description 2
- 238000009472 formulation Methods 0.000 claims description 2
- 239000001046 green dye Substances 0.000 claims description 2
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 claims description 2
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 claims description 2
- 239000001048 orange dye Substances 0.000 claims description 2
- 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 claims description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 2
- 239000001044 red dye Substances 0.000 claims description 2
- 239000008247 solid mixture Substances 0.000 claims description 2
- 150000001449 anionic compounds Chemical class 0.000 claims 3
- 239000007788 liquid Substances 0.000 claims 3
- 238000010422 painting Methods 0.000 claims 3
- 150000001767 cationic compounds Chemical class 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 claims 2
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 claims 1
- JVICFMRAVNKDOE-UHFFFAOYSA-M ethyl violet Chemical compound [Cl-].C1=CC(N(CC)CC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 JVICFMRAVNKDOE-UHFFFAOYSA-M 0.000 claims 1
- FPVGTPBMTFTMRT-NSKUCRDLSA-L fast yellow Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-NSKUCRDLSA-L 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- IPSIPYMEZZPCPY-UHFFFAOYSA-N new fuchsin Chemical compound [Cl-].C1=CC(=[NH2+])C(C)=CC1=C(C=1C=C(C)C(N)=CC=1)C1=CC=C(N)C(C)=C1 IPSIPYMEZZPCPY-UHFFFAOYSA-N 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 238000007591 painting process Methods 0.000 claims 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 claims 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims 1
- 239000000976 ink Substances 0.000 abstract description 21
- 239000002002 slurry Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000000047 product Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 238000007792 addition Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 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 4
- 230000000694 effects Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 235000010290 biphenyl Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- SYHRPJPCZWZVSR-UHFFFAOYSA-M n-benzyl-4-[(2,4-dimethyl-1,2,4-triazol-4-ium-3-yl)diazenyl]-n-methylaniline;bromide Chemical compound [Br-].C=1C=C(N=NC2=[N+](C=NN2C)C)C=CC=1N(C)CC1=CC=CC=C1 SYHRPJPCZWZVSR-UHFFFAOYSA-M 0.000 description 3
- 239000000985 reactive dye Substances 0.000 description 3
- 239000006254 rheological additive Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- KWXICGTUELOLSQ-UHFFFAOYSA-N 4-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=C(S(O)(=O)=O)C=C1 KWXICGTUELOLSQ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000005189 flocculation Methods 0.000 description 2
- 230000016615 flocculation Effects 0.000 description 2
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- VVOPUZNLRVJDJQ-UHFFFAOYSA-N phthalocyanine copper Chemical compound [Cu].C12=CC=CC=C2C(N=C2NC(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2N1 VVOPUZNLRVJDJQ-UHFFFAOYSA-N 0.000 description 2
- 230000019612 pigmentation Effects 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 238000010793 Steam injection (oil industry) Methods 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 description 1
- 239000011363 dried mixture Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000019233 fast yellow AB Nutrition 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 description 1
- 125000001905 inorganic group Chemical group 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 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
- 239000001739 pinus spp. Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- VRVDFJOCCWSFLI-UHFFFAOYSA-K trisodium 3-[[4-[(6-anilino-1-hydroxy-3-sulfonatonaphthalen-2-yl)diazenyl]-5-methoxy-2-methylphenyl]diazenyl]naphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].[Na+].COc1cc(N=Nc2cc(c3cccc(c3c2)S([O-])(=O)=O)S([O-])(=O)=O)c(C)cc1N=Nc1c(O)c2ccc(Nc3ccccc3)cc2cc1S([O-])(=O)=O VRVDFJOCCWSFLI-UHFFFAOYSA-K 0.000 description 1
- 229940036248 turpentine Drugs 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
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
-
- 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
-
- 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
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)
- Paints Or Removers (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02405349 | 2002-04-29 | ||
| PCT/EP2003/004259 WO2003093373A1 (en) | 2002-04-29 | 2003-04-24 | Compositions and methods for imparting improved rheology on pigment based inks and paints |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA04010752A true MXPA04010752A (es) | 2005-03-07 |
Family
ID=29286251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA04010752A MXPA04010752A (es) | 2002-04-29 | 2003-04-24 | Composiciones y metodos para impartir reologia mejorada a tintas y pinturas basadas en pigmentos. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7074267B2 (enExample) |
| EP (1) | EP1499683A1 (enExample) |
| JP (1) | JP2005523985A (enExample) |
| KR (1) | KR20050006208A (enExample) |
| CN (1) | CN100343342C (enExample) |
| AU (1) | AU2003224122A1 (enExample) |
| BR (1) | BR0309630A (enExample) |
| CA (1) | CA2483836A1 (enExample) |
| MX (1) | MXPA04010752A (enExample) |
| WO (1) | WO2003093373A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60111480T2 (de) * | 2000-12-12 | 2005-11-24 | Konica Corp. | Flüssige Pigmentdispersionen zum Tintenstrahldrucken |
| CA2544803A1 (en) * | 2003-11-11 | 2005-05-19 | Ciba Specialty Chemicals Holding Inc. | Pigment compositions for oil-based lithographic printing ink systems |
| JP4649291B2 (ja) * | 2005-08-11 | 2011-03-09 | 東洋インキ製造株式会社 | 着色組成物の製造方法、および該方法で製造された着色組成物を用いたカラーフィルタ |
| WO2008134190A2 (en) | 2007-04-24 | 2008-11-06 | Sun Chemical Corporation | Pigments for non-aqueous inks and coatings |
| GB2450975B (en) * | 2007-07-12 | 2010-02-24 | Ciba Holding Inc | Yellow radiation curing inks |
| JP5479343B2 (ja) * | 2007-09-07 | 2014-04-23 | ビーエーエスエフ ソシエタス・ヨーロピア | 電気泳動型移動性有機着色剤を含むカプセル化分散液 |
| US8857963B2 (en) | 2008-04-29 | 2014-10-14 | Hewlett-Packard Development Company, L.P. | Inks and ink sets for improved performance and image quality |
| US8328922B2 (en) * | 2008-12-29 | 2012-12-11 | Pitney Bowes Inc. | Postal blue ink with high reliability |
| US7972425B2 (en) * | 2008-12-29 | 2011-07-05 | Pitney Bowes Inc. | Postal blue ink with improved durability |
| TW201111447A (en) * | 2009-07-14 | 2011-04-01 | Sumitomo Chemical Co | Production method of pigment dispersion solution |
| JP5481647B2 (ja) * | 2009-07-17 | 2014-04-23 | 山陽色素株式会社 | トリアリールメタン系及びローダミン系顔料組成物並びにこれらを用いた顔料分散体 |
| CN102892845A (zh) * | 2010-06-16 | 2013-01-23 | 惠普发展公司，有限责任合伙企业 | 用于邮政印刷的蓝色油墨 |
| CN102250492A (zh) * | 2011-03-11 | 2011-11-23 | 郭长虹 | 多功能染色剂及其配制方法以及本剂对织物染色补色方法 |
| WO2013150622A1 (ja) * | 2012-04-04 | 2013-10-10 | 三菱鉛筆株式会社 | 油性インク組成物 |
| CN104073025A (zh) * | 2013-03-29 | 2014-10-01 | 日本化药株式会社 | 着色分散液、油墨组合物、喷墨记录方法以及着色体 |
| JP2016034994A (ja) * | 2014-08-01 | 2016-03-17 | クラリアント・インターナシヨナル・リミテツド | 彩度と色相が改良されたイエロー着色剤組成物、そのための顔料組成物およびそれらの使用 |
| US10364366B2 (en) * | 2015-09-30 | 2019-07-30 | Brother Kogyo Kabushiki Kaisha | Water-based ink for ink-jet recording and ink cartridge |
| DE102015121562B4 (de) * | 2015-12-10 | 2021-05-06 | Coroplast Fritz Müller Gmbh & Co. Kg | Hochtemperaturbeständiges farbiges, insbesondere orangefarbiges, Klebeband, Verfahren zu seiner Herstellung, Verwendung eines Trägers zu seiner Herstellung sowie Verwendung des Klebebandes zur Herstellung von Kabelbäumen |
| WO2024151604A2 (en) * | 2023-01-13 | 2024-07-18 | Cabot Corporation | Synergists for dimeric pigments |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2012152C3 (de) * | 1970-03-14 | 1974-03-21 | Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt | Verfahren zur Herstellung von Pigmentfarbstoffgemischen aus Disazofarbstoffen und deren Verwendung |
| GB1356253A (en) * | 1970-05-06 | 1974-06-12 | Ciba Geigy Uk Ltd | Azo pigment compositions |
| GB1356254A (en) * | 1970-07-16 | 1974-06-12 | Ciba Geigy Uk Ltd | Pigment compositions |
| US4162348A (en) * | 1973-04-02 | 1979-07-24 | Sumitomo Chemical Company, Limited | Coloring of inorganic substrates and mineral materials |
| JPS5463132A (en) * | 1977-10-31 | 1979-05-21 | Shiseido Co Ltd | Production of red-coloring pigment |
| JPS565552A (en) * | 1979-06-28 | 1981-01-21 | Toyo Ink Mfg Co Ltd | Photoreceptor for electrophotography |
| NZ201300A (en) * | 1981-08-11 | 1985-12-13 | Ici Plc | Pigment:fluidising compositions containing disazo compounds |
| DE3906525A1 (de) * | 1989-03-02 | 1990-09-06 | Basf Ag | Farbmittelmischungen, enthaltend azoverbindungen auf basis von phenyloxdiazolylanilin |
| GB9112155D0 (en) * | 1991-06-06 | 1991-07-24 | Ciba Geigy Ag | Production of pigments |
| DE59206108D1 (de) * | 1991-10-23 | 1996-05-30 | Hoechst Ag | Pigmentzubereitungen |
| EP0648816B1 (de) * | 1993-10-15 | 2000-01-26 | Ciba SC Holding AG | Färben von Leder mit Farbstoffmischungen |
| DE19547800A1 (de) * | 1994-12-23 | 1996-06-27 | Ciba Geigy Ag | Wässrige Drucktinten für den Tintenstrahldruck |
| EP0889934A1 (de) * | 1996-03-26 | 1999-01-13 | Basf Aktiengesellschaft | Stabile farbmittelzusammensetzungen |
| DE69725607T2 (de) * | 1996-12-20 | 2004-08-05 | Ciba Speciality Chemicals Holding Inc. | Polymethin-komplex-farbstoffe und ihre verwendung |
| WO1999061534A1 (en) * | 1998-05-28 | 1999-12-02 | Sun Chemical Corporation | Dye based aqueous pigment dispersions |
| AU6394600A (en) * | 1999-08-09 | 2001-03-05 | Cabot Corporation | Ink compositions having modified pigments with high or low treatment levels |
| US6123758A (en) * | 1999-09-22 | 2000-09-26 | Xerox Corporation | Ink compositions containing undecylenoyl sarcosinate salts |
| US6672717B2 (en) * | 2001-11-13 | 2004-01-06 | Xerox Corporation | Ink jet printing with inks containing cationic-anionic monomer pairs |
-
2003
- 2003-04-24 CA CA002483836A patent/CA2483836A1/en not_active Abandoned
- 2003-04-24 WO PCT/EP2003/004259 patent/WO2003093373A1/en not_active Ceased
- 2003-04-24 EP EP03720522A patent/EP1499683A1/en not_active Withdrawn
- 2003-04-24 BR BR0309630-0A patent/BR0309630A/pt not_active Application Discontinuation
- 2003-04-24 MX MXPA04010752A patent/MXPA04010752A/es not_active Application Discontinuation
- 2003-04-24 JP JP2004501511A patent/JP2005523985A/ja not_active Withdrawn
- 2003-04-24 KR KR10-2004-7017393A patent/KR20050006208A/ko not_active Ceased
- 2003-04-24 AU AU2003224122A patent/AU2003224122A1/en not_active Abandoned
- 2003-04-24 CN CNB038095777A patent/CN100343342C/zh not_active Expired - Fee Related
- 2003-04-24 US US10/512,013 patent/US7074267B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003093373A1 (en) | 2003-11-13 |
| JP2005523985A (ja) | 2005-08-11 |
| CN1649972A (zh) | 2005-08-03 |
| CN100343342C (zh) | 2007-10-17 |
| BR0309630A (pt) | 2005-03-08 |
| EP1499683A1 (en) | 2005-01-26 |
| US20050115464A1 (en) | 2005-06-02 |
| KR20050006208A (ko) | 2005-01-15 |
| AU2003224122A1 (en) | 2003-11-17 |
| US7074267B2 (en) | 2006-07-11 |
| CA2483836A1 (en) | 2003-11-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7074267B2 (en) | Compositions and methods for imparting improved rheology on pigment based inks and paints | |
| US6902613B2 (en) | Preparation and use of nanosize pigment compositions | |
| EP0485441A1 (de) | Neue pigmentzubereitungen auf basis von perylenverbindungen. | |
| JPH05311090A (ja) | 顔料調製物 | |
| US5082498A (en) | Highly concentrated solid pigment formulations | |
| US20050250875A1 (en) | Pigment compositions for oil-based lithographic printing inks | |
| DE69209787T2 (de) | Herstellung von Pigmentzusammensetzungen | |
| EP0770648B1 (en) | Pigment concentrates | |
| EP1031615B1 (en) | Aqueous process for the preparation of linear quinacridones having a reduced particle size | |
| JPS6059264B2 (ja) | フタロシアニン顔料を含有する顔料組成物 | |
| KR20060124779A (ko) | 프탈로시아닌 안료를 기제로 하는 안료 제제 | |
| JP4645865B2 (ja) | 顔料添加剤、顔料組成物及び塗料用樹脂組成物 | |
| JPH0696679B2 (ja) | 有機顔料の顔料化法 | |
| JP2987072B2 (ja) | 顔料組成物 | |
| JPH02102272A (ja) | 顔料の製造方法 | |
| JP5465718B2 (ja) | 色素誘導体、着色剤及び着色方法 | |
| US5779783A (en) | Composition for printing inks | |
| JPH11293139A (ja) | 紅顔料ウエットケーキ組成物および平版インキ | |
| JPH02102273A (ja) | 易分散性顔料の製造方法 | |
| US2774677A (en) | Phthalocyanine lakes | |
| JPS62195053A (ja) | 顔料分散剤 | |
| JPH0645761B2 (ja) | 易分散性顔料の製造方法 | |
| JPH1088016A (ja) | アゾレーキ顔料組成物、その製造方法および顔料分散体 | |
| JPS62153364A (ja) | 平版インキ用粒状着色剤およびこれを用いた顔料濃縮物 | |
| JPH04218576A (ja) | 印刷インキもしくは塗料組成物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |