DE2606831C3 - Pigmentzubereitungen für Lackbindemittel - Google Patents
Pigmentzubereitungen für LackbindemittelInfo
- Publication number
- DE2606831C3 DE2606831C3 DE2606831A DE2606831A DE2606831C3 DE 2606831 C3 DE2606831 C3 DE 2606831C3 DE 2606831 A DE2606831 A DE 2606831A DE 2606831 A DE2606831 A DE 2606831A DE 2606831 C3 DE2606831 C3 DE 2606831C3
- Authority
- DE
- Germany
- Prior art keywords
- pigment preparations
- binders
- wetting agent
- paint
- paint binders
- 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
Links
- 239000000049 pigment Substances 0.000 title claims description 26
- 239000011230 binding agent Substances 0.000 title claims description 20
- 239000003973 paint Substances 0.000 title claims description 18
- 238000002360 preparation method Methods 0.000 title claims description 13
- 239000000080 wetting agent Substances 0.000 claims description 16
- 238000004070 electrodeposition Methods 0.000 claims description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 10
- 229920000647 polyepoxide Polymers 0.000 claims description 9
- 239000003822 epoxy resin Substances 0.000 claims description 8
- 239000007859 condensation product Substances 0.000 claims description 7
- 239000000654 additive Substances 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000002091 cationic group Chemical group 0.000 description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 238000006266 etherification reaction Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000004922 lacquer Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical class C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- OGNVQLDIPUXYDH-ZPKKHLQPSA-N (2R,3R,4S)-3-(2-methylpropanoylamino)-4-(4-phenyltriazol-1-yl)-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid Chemical compound CC(C)C(=O)N[C@H]1[C@H]([C@H](O)[C@H](O)CO)OC(C(O)=O)=C[C@@H]1N1N=NC(C=2C=CC=CC=2)=C1 OGNVQLDIPUXYDH-ZPKKHLQPSA-N 0.000 description 1
- UUGLSEIATNSHRI-UHFFFAOYSA-N 1,3,4,6-tetrakis(hydroxymethyl)-3a,6a-dihydroimidazo[4,5-d]imidazole-2,5-dione Chemical compound OCN1C(=O)N(CO)C2C1N(CO)C(=O)N2CO UUGLSEIATNSHRI-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- -1 aliphatic alcohols Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- IWLBIFVMPLUHLK-UHFFFAOYSA-N azane;formaldehyde Chemical class N.O=C IWLBIFVMPLUHLK-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- VPVSTMAPERLKKM-UHFFFAOYSA-N glycoluril Chemical compound N1C(=O)NC2NC(=O)NC21 VPVSTMAPERLKKM-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 229960004592 isopropanol Drugs 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052914 metal silicate Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005690 transetherification reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C09D17/002—Pigment pastes, e.g. for mixing in paints in organic medium
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/45—Anti-settling agents
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2606831A DE2606831C3 (de) | 1976-02-20 | 1976-02-20 | Pigmentzubereitungen für Lackbindemittel |
| US05/764,196 US4137213A (en) | 1976-02-20 | 1977-01-31 | Pigment formulations for use in surface-coating binders |
| FR7703779A FR2341633A1 (fr) | 1976-02-20 | 1977-02-10 | Produits pigmentaires pour liants de peintures |
| AT110677A AT355162B (de) | 1976-02-20 | 1977-02-18 | Pigmentzubereitung fuer lacke |
| JP1726477A JPS52102346A (en) | 1976-02-20 | 1977-02-21 | Pigment preparation for varnish binding agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2606831A DE2606831C3 (de) | 1976-02-20 | 1976-02-20 | Pigmentzubereitungen für Lackbindemittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2606831A1 DE2606831A1 (de) | 1977-08-25 |
| DE2606831B2 DE2606831B2 (de) | 1979-02-15 |
| DE2606831C3 true DE2606831C3 (de) | 1979-10-11 |
Family
ID=5970393
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2606831A Expired DE2606831C3 (de) | 1976-02-20 | 1976-02-20 | Pigmentzubereitungen für Lackbindemittel |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4137213A (https=) |
| JP (1) | JPS52102346A (https=) |
| AT (1) | AT355162B (https=) |
| DE (1) | DE2606831C3 (https=) |
| FR (1) | FR2341633A1 (https=) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4336116A (en) | 1979-10-20 | 1982-06-22 | Basf Aktiengesellschaft | Polyadducts containing unsaturated amide groups and their use in coatings |
| US4340455A (en) | 1980-07-16 | 1982-07-20 | Basf Aktiengesellschaft | Polyadduct/polycondensate containing basic nitrogen groups, and its use |
| US4427514A (en) | 1981-06-19 | 1984-01-24 | Basf Aktiengesellschaft | Polyadduct/polycondensate which contains basic nitrogen groups, and its use |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4374965A (en) * | 1978-08-31 | 1983-02-22 | Ford Motor Company | Alkaline resistant organic coatings for corrosion susceptible substrates II |
| US4374213A (en) * | 1978-08-31 | 1983-02-15 | Ford Motor Company | Alkaline resistant organic coatings for corrosion susceptible substrates III |
| DE2914297C2 (de) * | 1979-04-09 | 1981-10-01 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Polyadditionsprodukten aus Ammoniak und Epoxidverbindungen und ihre Verwendung |
| US4284729A (en) * | 1980-03-31 | 1981-08-18 | Milliken Research Corporation | Process for coloring thermosetting resins |
| DE3018715A1 (de) * | 1980-05-16 | 1981-11-26 | Basf Ag, 6700 Ludwigshafen | Pigmentzubereitungen fuer lacke |
| JPS61246273A (ja) * | 1985-04-25 | 1986-11-01 | Dainippon Ink & Chem Inc | 顔料ベ−スト |
| DE4111036C2 (de) * | 1991-04-05 | 1997-05-07 | Kluthe Gmbh Chem Werke | Universalfarbpaste |
| US5180835A (en) * | 1991-06-25 | 1993-01-19 | American Cyanamid Company | Process for the preparation of monomeric tetramethoxymethylglycoloril |
| DE4445200A1 (de) * | 1994-12-17 | 1996-06-20 | Herberts Gmbh | Wäßrige Überzugsmittel und deren Verwendung bei Verfahren zur Einschicht- und Mehrschichtlackierung |
| BR112022011789A2 (pt) | 2019-12-20 | 2022-08-30 | Ppg Ind Ohio Inc | Composição de revestimento eletrodepositável incluindo um pigmento de filossilicato e um agente de dispersão |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2824850A (en) * | 1951-12-21 | 1958-02-25 | Ciba Ltd | Reaction product of a compound capable of reacting with hydroxyl groups, with an etherification product of a polyglycidyl ether |
| BE536397A (https=) * | 1954-08-24 | |||
| DE1052026B (de) * | 1957-03-25 | 1959-03-05 | Rheinpreussen Ag | Hochbestaendige Lacke |
| US3145207A (en) * | 1960-09-12 | 1964-08-18 | American Cyanamid Co | Process for preparing epoxy alkyloxymethylamino-s-triazines |
| NL134015C (https=) * | 1966-02-21 | |||
| FR1551536A (https=) * | 1967-01-19 | 1968-12-27 | ||
| US3651169A (en) * | 1970-09-08 | 1972-03-21 | Dow Chemical Co | Epoxy resin amine or amidealdehyde and organic ester of phosphoric acid or organic sulfonic acid |
-
1976
- 1976-02-20 DE DE2606831A patent/DE2606831C3/de not_active Expired
-
1977
- 1977-01-31 US US05/764,196 patent/US4137213A/en not_active Expired - Lifetime
- 1977-02-10 FR FR7703779A patent/FR2341633A1/fr active Granted
- 1977-02-18 AT AT110677A patent/AT355162B/de not_active IP Right Cessation
- 1977-02-21 JP JP1726477A patent/JPS52102346A/ja active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4336116A (en) | 1979-10-20 | 1982-06-22 | Basf Aktiengesellschaft | Polyadducts containing unsaturated amide groups and their use in coatings |
| US4340455A (en) | 1980-07-16 | 1982-07-20 | Basf Aktiengesellschaft | Polyadduct/polycondensate containing basic nitrogen groups, and its use |
| US4427514A (en) | 1981-06-19 | 1984-01-24 | Basf Aktiengesellschaft | Polyadduct/polycondensate which contains basic nitrogen groups, and its use |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2341633B1 (https=) | 1979-08-24 |
| ATA110677A (de) | 1979-07-15 |
| US4137213A (en) | 1979-01-30 |
| DE2606831B2 (de) | 1979-02-15 |
| FR2341633A1 (fr) | 1977-09-16 |
| JPS52102346A (en) | 1977-08-27 |
| AT355162B (de) | 1980-02-25 |
| DE2606831A1 (de) | 1977-08-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8330 | Complete disclaimer |