ES265332A1 - Procedimiento para obtener preparados de pigmentos - Google Patents

Procedimiento para obtener preparados de pigmentos

Info

Publication number: ES265332A1
Authority: ES; Spain
Prior art keywords: radical; dyes; resins; grinding; aliphatic
Prior art date: 1960-03-04
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

Application number

ES0265332A

Other languages

English (en)

Spanish (es)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Sandoz AG

Original Assignee

Sandoz AG

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.)

1960-03-04

Filing date

1961-03-02

Publication date

1961-09-01

1961-03-02 Application filed by Sandoz AG filed Critical Sandoz AG

1961-09-01 Publication of ES265332A1 publication Critical patent/ES265332A1/es

Status Expired legal-status Critical Current

Links

239000000049 pigment Substances 0.000 title abstract 13
238000002360 preparation method Methods 0.000 title abstract 11
238000000034 method Methods 0.000 title 1
-1 hydrocarbon radical Chemical class 0.000 abstract 23
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 12
238000000227 grinding Methods 0.000 abstract 12
125000001931 aliphatic group Chemical group 0.000 abstract 8
239000002270 dispersing agent Substances 0.000 abstract 8
150000002170 ethers Chemical class 0.000 abstract 8
150000003254 radicals Chemical group 0.000 abstract 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 7
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 6
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 6
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 abstract 6
229910052751 metal Inorganic materials 0.000 abstract 6
239000002184 metal Substances 0.000 abstract 6
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 4
239000004215 Carbon black (E152) Substances 0.000 abstract 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 4
241000551547 Dione <red algae> Species 0.000 abstract 4
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 abstract 4
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 abstract 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 4
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 4
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 abstract 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 4
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 4
239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 abstract 4
239000000654 additive Substances 0.000 abstract 4
125000002877 alkyl aryl group Chemical group 0.000 abstract 4
150000005840 aryl radicals Chemical class 0.000 abstract 4
239000000987 azo dye Substances 0.000 abstract 4
239000000981 basic dye Substances 0.000 abstract 4
125000004432 carbon atom Chemical group C* 0.000 abstract 4
150000001768 cations Chemical class 0.000 abstract 4
239000003795 chemical substances by application Substances 0.000 abstract 4
150000001875 compounds Chemical class 0.000 abstract 4
239000007859 condensation product Substances 0.000 abstract 4
125000004122 cyclic group Chemical group 0.000 abstract 4
229960001760 dimethyl sulfoxide Drugs 0.000 abstract 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 abstract 4
150000002148 esters Chemical class 0.000 abstract 4
150000002191 fatty alcohols Chemical class 0.000 abstract 4
229930195733 hydrocarbon Natural products 0.000 abstract 4
229910052739 hydrogen Inorganic materials 0.000 abstract 4
239000001257 hydrogen Substances 0.000 abstract 4
150000002596 lactones Chemical class 0.000 abstract 4
239000007788 liquid Substances 0.000 abstract 4
238000003801 milling Methods 0.000 abstract 4
239000000203 mixture Substances 0.000 abstract 4
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 abstract 4
239000001006 nitroso dye Substances 0.000 abstract 4
FVDOBFPYBSDRKH-UHFFFAOYSA-N perylene-3,4,9,10-tetracarboxylic acid Chemical compound C=12C3=CC=C(C(O)=O)C2=C(C(O)=O)C=CC=1C1=CC=C(C(O)=O)C2=C1C3=CC=C2C(=O)O FVDOBFPYBSDRKH-UHFFFAOYSA-N 0.000 abstract 4
239000010695 polyglycol Substances 0.000 abstract 4
229920000151 polyglycol Polymers 0.000 abstract 4
229910052700 potassium Inorganic materials 0.000 abstract 4
239000011591 potassium Substances 0.000 abstract 4
229910052708 sodium Inorganic materials 0.000 abstract 4
239000011734 sodium Substances 0.000 abstract 4
239000000126 substance Substances 0.000 abstract 4
BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 abstract 4
125000002889 tridecyl 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])[H] 0.000 abstract 4
JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 abstract 4
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 3
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 abstract 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
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 abstract 3
150000004056 anthraquinones Chemical class 0.000 abstract 3
229910052980 cadmium sulfide Inorganic materials 0.000 abstract 3
CJOBVZJTOIVNNF-UHFFFAOYSA-N cadmium sulfide Chemical compound [Cd]=S CJOBVZJTOIVNNF-UHFFFAOYSA-N 0.000 abstract 3
229910000019 calcium carbonate Inorganic materials 0.000 abstract 3
239000006229 carbon black Substances 0.000 abstract 3
229910052804 chromium Inorganic materials 0.000 abstract 3
239000011651 chromium Substances 0.000 abstract 3
239000000975 dye Substances 0.000 abstract 3
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
229910052742 iron Inorganic materials 0.000 abstract 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 3
239000011133 lead Substances 0.000 abstract 3
229910052748 manganese Inorganic materials 0.000 abstract 3
239000011572 manganese Substances 0.000 abstract 3
239000003973 paint Substances 0.000 abstract 3
LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 abstract 3
229910052814 silicon oxide Inorganic materials 0.000 abstract 3
239000005018 casein Substances 0.000 abstract 2
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 2
235000021240 caseins Nutrition 0.000 abstract 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
150000005125 dioxazines Chemical class 0.000 abstract 2
229920001971 elastomer Polymers 0.000 abstract 2
239000000025 natural resin Substances 0.000 abstract 2
239000003921 oil Substances 0.000 abstract 2
235000019198 oils Nutrition 0.000 abstract 2
229920005989 resin Polymers 0.000 abstract 2
239000011347 resin Substances 0.000 abstract 2
239000005060 rubber Substances 0.000 abstract 2
229920003002 synthetic resin Polymers 0.000 abstract 2
239000000057 synthetic resin Substances 0.000 abstract 2
239000004408 titanium dioxide Substances 0.000 abstract 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
229920000877 Melamine resin Polymers 0.000 abstract 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
239000002174 Styrene-butadiene Substances 0.000 abstract 1
229920001807 Urea-formaldehyde Polymers 0.000 abstract 1
229920000180 alkyd Polymers 0.000 abstract 1
239000001000 anthraquinone dye Substances 0.000 abstract 1
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 abstract 1
239000003822 epoxy resin Substances 0.000 abstract 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 abstract 1
239000005011 phenolic resin Substances 0.000 abstract 1
229920000058 polyacrylate Polymers 0.000 abstract 1
229920000647 polyepoxide Polymers 0.000 abstract 1
229920000642 polymer Polymers 0.000 abstract 1
229920000193 polymethacrylate Polymers 0.000 abstract 1
229920005749 polyurethane resin Polymers 0.000 abstract 1
229920002689 polyvinyl acetate Polymers 0.000 abstract 1
239000011118 polyvinyl acetate Substances 0.000 abstract 1
239000011115 styrene butadiene Substances 0.000 abstract 1
229920003048 styrene butadiene rubber Polymers 0.000 abstract 1
229920006337 unsaturated polyester resin Polymers 0.000 abstract 1
235000015112 vegetable and seed oil Nutrition 0.000 abstract 1
239000008158 vegetable oil Substances 0.000 abstract 1
229920002554 vinyl polymer Polymers 0.000 abstract 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
- 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
- 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
- C09B67/0085—Non common dispersing agents
- C09B67/0086—Non common dispersing agents anionic dispersing agents

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Dispersion Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Paints Or Removers (AREA)

ES0265332A 1960-03-04 1961-03-02 Procedimiento para obtener preparados de pigmentos Expired ES265332A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH251460A CH387202A (de)	1960-03-04	1960-03-04	Pigmentpräparate

Publications (1)

Publication Number	Publication Date
ES265332A1 true ES265332A1 (es)	1961-09-01

Family

ID=4235491

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0265332A Expired ES265332A1 (es)	1960-03-04	1961-03-02	Procedimiento para obtener preparados de pigmentos

Country Status (4)

Country	Link
CH (1)	CH387202A (de)
DE (1)	DE1211578B (de)
ES (1)	ES265332A1 (de)
GB (1)	GB976084A (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1178546A (en) *	1966-10-12	1970-01-21	Gavaert Agfa N V	Improved Hydrophilic Coating Compositions containing Coating Aids
CH485008A (de) *	1967-11-03	1970-01-31	Geigy Ag J R	Verfahren zur Herstellung farbstarker, transparenter Perylen-Pigmente
DE2244777C3 (de) *	1972-09-13	1975-03-27	Bayer Ag, 5090 Leverkusen	WäBrige Pigmentdispersionen und ihre Verwendung
GB2035384B (en) *	1978-10-16	1982-12-01	Ici Ltd	Stabilised aqueous dyestuff dispersions
JPH0717864B2 (ja) *	1987-02-12	1995-03-01	有限会社三好化成	保湿性粉体および化粧料
JP5586160B2 (ja)	2008-04-02	2014-09-10	関西ペイント株式会社	水性塗料組成物
DE102011010580A1 (de)	2011-02-08	2012-07-12	Clariant International Ltd.	Flüssige, wasserbasierende, universale Pigmentpräparationen

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2745857A (en) *	1952-02-23	1956-05-15	Dow Chemical Co	Glycolic acid ethers of polyoxypropylene compounds and method of preparation
US2809122A (en) *	1954-06-24	1957-10-08	Sherwin Williams Co	Dual purpose tinting base

1960
- 1960-03-04 CH CH251460A patent/CH387202A/de unknown
1961
- 1961-03-02 DE DES72799A patent/DE1211578B/de active Pending
- 1961-03-02 ES ES0265332A patent/ES265332A1/es not_active Expired
- 1961-03-02 GB GB766061A patent/GB976084A/en not_active Expired

Also Published As

Publication number	Publication date
DE1211578B (de)	1966-03-03
CH387202A (de)	1965-01-31
GB976084A (en)	1964-11-25

Publication	Publication Date	Title
GB1402124A (en)	1975-08-13	Aqueous pigment dispersions
ES265332A1 (es)	1961-09-01	Procedimiento para obtener preparados de pigmentos
GB948798A (en)	1964-02-05	Colouring of anodized aluminium
GB1358564A (en)	1974-07-03	Dispersing and stabilizing agents for dyestuffs
GB1518434A (en)	1978-07-19	Disperse dyestuff preparations having safety properties and/or a higher dyestuff yield
DE2759203A1 (de)	1979-07-12	Pigmentdispersionen und ihre verwendung zum pigmentieren hydrophiler und hydrophober medien
GB704687A (en)	1954-02-24	Improvements in liquid detergent compositions
ES344876A1 (es)	1969-01-01	Procedimiento para la preparacion de pigmentos disazoicos.
Ashworth et al.	1958	191. Researches on acetylenic compounds. Part LIX. The synthesis of three polyacetylenic antibiotics
GB1356885A (en)	1974-06-19	Dyeing synthetic hydrophobic fibres with lower alkyl biphenyl carriers
GB1026875A (en)	1966-04-20	Process for increasing the surface area of organic dyestuffs and pigments
EP0356851B1 (de)	1993-12-15	Verfahren zur Herstellung von Lösungen von 1:2-Chromkomplex-Azofarbstoffen
IT1204304B (it)	1989-03-01	Composizione acida per il lavaggio esterno di carrozze ferroviarie e simili
GB1537383A (en)	1978-12-29	Disazo dye derived from a tetrachloro benzidine
GB1025056A (en)	1966-04-06	Mixtures of dyestuffs of the naphthoylene-arylimidazole-peri-dicarboxylic acid series and process for dyeing or printing fibres or foils of polyethylene terephthalates therewith
GB1010570A (en)	1965-11-17	Water soluble phthalocyanine dyestuffs
GB872302A (en)	1961-07-05	Universal tinting paste vehicle and compositions containing same
GB982479A (en)	1965-02-03	New azo dyestuffs
GB1508885A (en)	1978-04-26	Phthalocyanine pigment mixtures
GB978286A (en)	1964-12-23	New dianthrone ethylene derivatives and process of making same
GB1117017A (en)	1968-06-12	Metal complex dyes and their production
GB1509715A (en)	1978-05-04	Phthalocyanine pigment mixtures
DE1932404B2 (de)	1978-05-24	Verbindungen der heterocyclischen Reihe, ihre Herstellung und Verwendung
GB833132A (en)	1960-04-21	Improvements in or relating to blue disperse dyestuffs of the anthraquinone series
GB717766A (en)	1954-11-03	Improvements in or relating to concrete mixtures