ZA200302309B - Phthalic acid imides as synergists for improving the properties of aqueous pigment preparations. - Google Patents

Phthalic acid imides as synergists for improving the properties of aqueous pigment preparations. Download PDF

Info

Publication number: ZA200302309B
Authority: ZA; South Africa
Prior art keywords: pigment; preparation; weight; pigment preparation; synergist
Prior art date: 2000-10-26

Application number

ZA200302309A

Other languages

English (en)

Inventor

Martin Alexander Winter

Andreas Harz

Hans-Joachim Metz

Original Assignee

Clariant Gmbh

Priority date (The priority date 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 date listed.)

2000-10-26

Filing date

2003-03-25

Publication date

2003-10-02

2003-03-25 Application filed by Clariant Gmbh filed Critical Clariant Gmbh

2003-10-02 Publication of ZA200302309B publication Critical patent/ZA200302309B/en

Links

239000000049 pigment Substances 0.000 title claims description 157
238000002360 preparation method Methods 0.000 title claims description 132
-1 Phthalic acid imides Chemical class 0.000 title claims description 27
XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
239000002966 varnish Substances 0.000 claims description 18
238000000227 grinding Methods 0.000 claims description 17
239000000976 ink Substances 0.000 claims description 15
239000000654 additive Substances 0.000 claims description 14
150000001412 amines Chemical class 0.000 claims description 12
150000002191 fatty alcohols Chemical class 0.000 claims description 11
238000004519 manufacturing process Methods 0.000 claims description 9
239000003086 colorant Substances 0.000 claims description 8
239000000463 material Substances 0.000 claims description 8
239000004094 surface-active agent Substances 0.000 claims description 8
238000004040 coloring Methods 0.000 claims description 7
235000014113 dietary fatty acids Nutrition 0.000 claims description 7
229930195729 fatty acid Natural products 0.000 claims description 7
239000000194 fatty acid Substances 0.000 claims description 7
150000004665 fatty acids Chemical class 0.000 claims description 7
239000012860 organic pigment Substances 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000011248 coating agent Substances 0.000 claims description 6
238000000576 coating method Methods 0.000 claims description 6
150000003949 imides Chemical class 0.000 claims description 6
239000000843 powder Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
239000001023 inorganic pigment Substances 0.000 claims description 5
239000003973 paint Substances 0.000 claims description 5
239000000047 product Substances 0.000 claims description 5
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 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
125000000129 anionic group Chemical group 0.000 claims description 4
125000004093 cyano group Chemical group *C#N 0.000 claims description 4
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 4
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
239000004033 plastic Substances 0.000 claims description 4
229920003023 plastic Polymers 0.000 claims description 4
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 4
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims description 4
230000000996 additive effect Effects 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
239000003945 anionic surfactant Substances 0.000 claims description 3
PGEHNUUBUQTUJB-UHFFFAOYSA-N anthanthrone Chemical compound C1=CC=C2C(=O)C3=CC=C4C=CC=C5C(=O)C6=CC=C1C2=C6C3=C54 PGEHNUUBUQTUJB-UHFFFAOYSA-N 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
230000015572 biosynthetic process Effects 0.000 claims description 3
125000002091 cationic group Chemical group 0.000 claims description 3
239000003093 cationic surfactant Substances 0.000 claims description 3
239000007859 condensation product Substances 0.000 claims description 3
PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
239000002736 nonionic surfactant Substances 0.000 claims description 3
125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 3
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 3
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 3
229940124530 sulfonamide Drugs 0.000 claims description 3
150000003456 sulfonamides Chemical class 0.000 claims description 3
WLXGQMVCYPUOLM-UHFFFAOYSA-N 1-hydroxyethanesulfonic acid Chemical compound CC(O)S(O)(=O)=O WLXGQMVCYPUOLM-UHFFFAOYSA-N 0.000 claims description 2
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 2
AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 claims description 2
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 2
235000000177 Indigofera tinctoria Nutrition 0.000 claims description 2
229910019142 PO4 Inorganic materials 0.000 claims description 2
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 claims description 2
150000008051 alkyl sulfates Chemical class 0.000 claims description 2
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims description 2
150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
MYONAGGJKCJOBT-UHFFFAOYSA-N benzimidazol-2-one Chemical compound C1=CC=CC2=NC(=O)N=C21 MYONAGGJKCJOBT-UHFFFAOYSA-N 0.000 claims description 2
SUMDYPCJJOFFON-UHFFFAOYSA-N beta-hydroxyethanesulfonic acid Natural products OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
239000006229 carbon black Substances 0.000 claims description 2
150000003857 carboxamides Chemical class 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
239000004359 castor oil Substances 0.000 claims description 2
235000019438 castor oil Nutrition 0.000 claims description 2
150000001768 cations Chemical class 0.000 claims description 2
238000009833 condensation Methods 0.000 claims description 2
230000005494 condensation Effects 0.000 claims description 2
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
150000002148 esters Chemical class 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims description 2
229940097275 indigo Drugs 0.000 claims description 2
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 2
PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 claims description 2
GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 claims description 2
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 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
235000021317 phosphate Nutrition 0.000 claims description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
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 claims description 2
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 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
238000003786 synthesis reaction Methods 0.000 claims description 2
229960003080 taurine Drugs 0.000 claims description 2
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 2
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 claims description 2
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 claims description 2
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
239000006185 dispersion Substances 0.000 description 42
238000012360 testing method Methods 0.000 description 26
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 18
238000003860 storage Methods 0.000 description 16
239000000203 mixture Substances 0.000 description 14
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
238000003756 stirring Methods 0.000 description 11
230000000694 effects Effects 0.000 description 10
229910052799 carbon Inorganic materials 0.000 description 9
238000005189 flocculation Methods 0.000 description 9
230000016615 flocculation Effects 0.000 description 9
239000004615 ingredient Substances 0.000 description 9
239000003755 preservative agent Substances 0.000 description 9
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230000002335 preservative effect Effects 0.000 description 8
238000010348 incorporation Methods 0.000 description 7
239000007787 solid Substances 0.000 description 7
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LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 6
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 6
QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
239000012530 fluid Substances 0.000 description 5
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230000000052 comparative effect Effects 0.000 description 4
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238000000034 method Methods 0.000 description 4
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150000008442 polyphenolic compounds Chemical class 0.000 description 4
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REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 3
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HVWGGPRWKSHASF-UHFFFAOYSA-N Sulfuric acid, monooctadecyl ester Chemical compound CCCCCCCCCCCCCCCCCCOS(O)(=O)=O HVWGGPRWKSHASF-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000011324 bead Substances 0.000 description 2
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150000001991 dicarboxylic acids Chemical class 0.000 description 2
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 2
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238000004043 dyeing Methods 0.000 description 2
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230000002708 enhancing effect Effects 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
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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 2
238000010438 heat treatment Methods 0.000 description 2
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150000002431 hydrogen Chemical class 0.000 description 2
150000004668 long chain fatty acids Chemical class 0.000 description 2
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NJVOHKFLBKQLIZ-UHFFFAOYSA-N (2-ethenylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C=C NJVOHKFLBKQLIZ-UHFFFAOYSA-N 0.000 description 1
125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical class CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 1
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SJIQTGOBEGYKSI-UHFFFAOYSA-N 2-[(1,3-dioxoisoindol-2-yl)methyl]-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1CC1=CC=C(NC=2C(=CC3=C(C(C4=CC=CC=C4N3)=O)C=2)C2=O)C2=C1 SJIQTGOBEGYKSI-UHFFFAOYSA-N 0.000 description 1
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MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
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UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
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229910052759 nickel Inorganic materials 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000002918 oxazolines Chemical class 0.000 description 1
SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
239000000123 paper Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
238000001935 peptisation Methods 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
230000000485 pigmenting effect Effects 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002492 poly(sulfone) Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000001054 red pigment Substances 0.000 description 1
239000005060 rubber Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000013049 sediment Substances 0.000 description 1
238000010008 shearing Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000010186 staining Methods 0.000 description 1
239000011115 styrene butadiene Substances 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
239000004034 viscosity adjusting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical class [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- 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
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0084—Dispersions of dyes
- 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
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/008—Preparations of disperse dyes or solvent dyes
- 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
- C09B67/006—Preparation of organic pigments
- C09B67/0066—Aqueous dispersions of pigments containing only dispersing agents
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/08—Treatment with low-molecular-weight non-polymer organic compounds
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Dispersion Chemistry (AREA)
Paints Or Removers (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

ZA200302309A 2000-10-26 2003-03-25 Phthalic acid imides as synergists for improving the properties of aqueous pigment preparations. ZA200302309B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2000153119 DE10053119A1 (de)	2000-10-26	2000-10-26	Phthalsäureimide als Synergisten zur Verbesserung der Eigenschaften wässriger Pigmentpräparationen

Publications (1)

Publication Number	Publication Date
ZA200302309B true ZA200302309B (en)	2003-10-02

Family

ID=7661147

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200302309A ZA200302309B (en)	2000-10-26	2003-03-25	Phthalic acid imides as synergists for improving the properties of aqueous pigment preparations.

Country Status (11)

Country	Link
US (1)	US6821335B2 (zh)
EP (1)	EP1332183B1 (zh)
JP (1)	JP4925387B2 (zh)
KR (1)	KR100757788B1 (zh)
CN (1)	CN1195805C (zh)
BR (1)	BR0114857B1 (zh)
DE (2)	DE10053119A1 (zh)
ES (1)	ES2223945T3 (zh)
MX (1)	MXPA03003679A (zh)
WO (1)	WO2002034840A1 (zh)
ZA (1)	ZA200302309B (zh)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10053119A1 (de)	2000-10-26	2002-05-08	Clariant Gmbh	Phthalsäureimide als Synergisten zur Verbesserung der Eigenschaften wässriger Pigmentpräparationen
US8530569B2 (en) *	2003-12-05	2013-09-10	Sun Chemical Corporation	Polymeric dispersants and dispersions containing same
DE102004010282A1 (de) *	2004-03-03	2005-09-22	Clariant Gmbh	Violettes Farbmittel für Color Filter, Ink Jet Tinten, elektrophotographische Toner und Entwickler und e-inks
US7300511B2 (en)	2005-07-01	2007-11-27	Sun Chemical Corporation	Low viscosity, highly pigmented oil based dispersions exhibiting a low relative interfacial tension drop
TWI351422B (en) *	2006-04-28	2011-11-01	Toyo Ink Mfg Co	Thiazineindigo pigment dispersant, and pigment com
DE102008003829A1 (de)	2008-01-10	2009-07-16	Clariant International Ltd.	Verwendung von hydrophoben, lösungsmittelbasierenden Pigmentpräparationen in elektronischen Displays
JP5268410B2 (ja) *	2008-04-11	2013-08-21	富士フイルム株式会社	顔料分散組成物、顔料分散組成物の製造方法、着色重合性組成物、カラーフィルタ、及びカラーフィルタの製造方法
US7776147B1 (en) *	2009-01-27	2010-08-17	Xerox Corporation	Pigmented phase change inks with dispersant and synergist
US7780774B2 (en) *	2009-01-27	2010-08-24	Xerox Corporation	Method of making a pigmented phase change ink with dispersant and synergist
DE102012000230A1 (de)	2012-01-10	2013-07-11	Clariant International Ltd.	Alkoxylate und Amine enthaltende anorganische Pigmentdispersionen
DE102012009239A1 (de)	2012-05-09	2013-11-14	Clariant International Ltd.	Fettsäureethanolamidethoxylate und Amine enthaltende anorganische Pigmentdispersionen
EP2802632A1 (de)	2012-01-13	2014-11-19	Clariant Finance (BVI) Limited	Fettsäureethanolamidethoxylate und amine enthaltende anorganische pigmentdispersionen
US8616693B1 (en) *	2012-11-30	2013-12-31	Xerox Corporation	Phase change ink comprising colorants derived from plants and insects
CN103965094B (zh) *	2013-01-31	2016-07-06	江苏道博化工有限公司	N-甲基-4-氨基-5-溴-邻苯二甲酰亚胺的合成方法

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Publication number	Priority date	Publication date	Assignee	Title
GB1104939A (en) *	1964-06-10	1968-03-06	Laporte Titanium Ltd	Improvements in and relating to the treatment of pigments
DE2342293A1 (de) *	1973-08-22	1975-04-24	Bayer Ag	Druck- und faerbeverfahren
US4478968A (en)	1983-04-06	1984-10-23	Ciba-Geigy Corporation	Manufacture of resin extended pigments
DE3811983A1 (de) *	1988-04-11	1989-10-19	Siemens Ag	Anordnung zum betrieb einer symmetrischen hochfrequenz-antenne
US4992204A (en)	1989-08-22	1991-02-12	Miliken Research Corporation	Irradiation detection and identification method and compositions useful therein
DE4317651A1 (de)	1993-05-27	1994-12-01	Hoechst Ag	Substituierte Bernsteinsäureimide
DE4325247A1 (de)	1993-07-28	1995-02-02	Basf Ag	Pigmentzubereitungen mit Perylenderivaten als Dispergiermitteln
US5560770A (en)	1993-10-26	1996-10-01	Seiko Epson Corporation	Ink composition for ink jet recording
DE19703549C1 (de)	1997-01-31	1999-03-04	Clariant Gmbh	Verfahren zur Herstellung von Diacylimiden
US6039769A (en) *	1998-12-15	2000-03-21	Bayer Corporation	Process for the preparation of highly chromatic perylene pigments
DE10053119A1 (de)	2000-10-26	2002-05-08	Clariant Gmbh	Phthalsäureimide als Synergisten zur Verbesserung der Eigenschaften wässriger Pigmentpräparationen

2000
- 2000-10-26 DE DE2000153119 patent/DE10053119A1/de not_active Withdrawn
2001
- 2001-10-23 WO PCT/EP2001/012228 patent/WO2002034840A1/de active IP Right Grant
- 2001-10-23 EP EP01988749A patent/EP1332183B1/de not_active Expired - Lifetime
- 2001-10-23 BR BR0114857A patent/BR0114857B1/pt not_active IP Right Cessation
- 2001-10-23 CN CNB01817051XA patent/CN1195805C/zh not_active Expired - Lifetime
- 2001-10-23 DE DE50102632T patent/DE50102632D1/de not_active Expired - Lifetime
- 2001-10-23 MX MXPA03003679A patent/MXPA03003679A/es active IP Right Grant
- 2001-10-23 US US10/415,200 patent/US6821335B2/en not_active Expired - Lifetime
- 2001-10-23 ES ES01988749T patent/ES2223945T3/es not_active Expired - Lifetime
- 2001-10-23 KR KR20037005788A patent/KR100757788B1/ko not_active IP Right Cessation
- 2001-10-23 JP JP2002537819A patent/JP4925387B2/ja not_active Expired - Fee Related
2003
- 2003-03-25 ZA ZA200302309A patent/ZA200302309B/en unknown

Also Published As

Publication number	Publication date
EP1332183A1 (de)	2003-08-06
DE10053119A1 (de)	2002-05-08
EP1332183B1 (de)	2004-06-16
CN1468287A (zh)	2004-01-14
BR0114857B1 (pt)	2012-06-12
ES2223945T3 (es)	2005-03-01
JP2004512416A (ja)	2004-04-22
CN1195805C (zh)	2005-04-06
KR20030048448A (ko)	2003-06-19
WO2002034840A1 (de)	2002-05-02
JP4925387B2 (ja)	2012-04-25
US6821335B2 (en)	2004-11-23
US20040040471A1 (en)	2004-03-04
KR100757788B1 (ko)	2007-09-11
BR0114857A (pt)	2004-01-06
DE50102632D1 (de)	2004-07-22
MXPA03003679A (es)	2003-08-07

Publication	Publication Date	Title
CA2064725C (en)	2000-02-22	New pigment preparations based on perylene compounds
CA2582104C (en)	2014-02-18	Pigment preparations based on py 155
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US20070131144A1 (en)	2007-06-14	Water-based pigment preparations
KR100588884B1 (ko)	2006-06-13	페릴렌 화합물 및 안료 조제물
US6821335B2 (en)	2004-11-23	Phthalic acid imides as synergists for improving the properties of aqueous pigment preparations
US7833343B2 (en)	2010-11-16	Universal stir-in pigments
JP4694559B2 (ja)	2011-06-08	フタロシアニン色素に基づいた色素調製物
JPH05311090A (ja)	1993-11-22	顔料調製物
KR20050085476A (ko)	2005-08-29	프탈로시아닌 안료 제제
KR100740040B1 (ko)	2007-07-16	디케토피롤로피롤 안료 및 염기성 페릴렌 분산제에 기초한안료 제제
CN102272236B (zh)	2013-12-04	易于分散的固体颜料制剂
US7172653B2 (en)	2007-02-06	Solid pigment preparations comprising surface-active additives based on alkoxylated bisphenols
JP2000297224A (ja)	2000-10-24	２種類以上のペリレン化合物を含む顔料調製物
US4217265A (en)	1980-08-12	Pigment preparations
JP2812444B2 (ja)	1998-10-22	顔料調製物
KR101406378B1 (ko)	2014-06-13	색소 유도체, 착색제 및 착색 방법
EP1416018A1 (en)	2004-05-06	Pigment formulations and processes for their preparation