GB933687A - Process for colouring organic products with pigment dyestuffs - Google Patents
Process for colouring organic products with pigment dyestuffsInfo
- Publication number
- GB933687A GB933687A GB4650161A GB4650161A GB933687A GB 933687 A GB933687 A GB 933687A GB 4650161 A GB4650161 A GB 4650161A GB 4650161 A GB4650161 A GB 4650161A GB 933687 A GB933687 A GB 933687A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aqueous
- pigment
- water
- milled
- mixed
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/20—Carboxylic acid amides
-
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/36—Dyes with acylated amino groups
- C09B1/42—Dyes with acylated amino groups the acyl groups being residues of an aromatic carboxylic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Viscose rayon, cellulose esters, nitrocellulose, urea- or melamine-formaldehyde resins, epoxy resins, polyurethane resins, alkyd resins, vinyl chloride polymers and copolymers, polyvinyl acetals, polyethylene, polypropylene, polystyrene, and mixed polymers thereof with polyesters of unsaturated dicarboxylic acids and dihydric alcohols, polyacrylates and acrylate copolymers and polyacrylonitrile are coloured yellow by incorporating the pigment:- <FORM:0933687/IV(a)/1> In examples, the above pigment is (1) milled with dioctyl phthalate and mixed with polyvinyl chloride, dioctyl phthalate, cadmium stearate and titanium dioxide; (2) milled with a nitrocellulose lacquer and titanium dioxide; (3) kneaded with acetyl cellulose, sodium chloride and diacetone alcohol and added to a spinning mass comprising acetyl cellulose and acetone; (4) milled with an alkyd-melamine stoving enamel and titanium dioxide to yield a lacquer, and (5) milled with sodium 1:11-dinaphthylmethane-2:21-disulphonic acid and water and added to a viscose rayon spinning mass. Specification 658,722 is referred to.ALSO:1:5-di(ortho-fluorobenzoylamino)-anthraquinone is obtained in finely-divided form, for example having an average particle size of not more than 3m or 1m , by milling dry or watermoist if desired in the presence of an organic solvent and/or a salt in a ball or roller mill or in kneading apparatus. In examples, (6), cotton is dyed yellow in an aqueous dye-bath containing a mixed-polymer latex of isobutyl acrylate, acrylonitrile and acrylic acid, an aqueous emulsion of methyl-melamine-allyl ether, turkey red oil and soya bean fatty acid, a water-soluble methyl ether of a urea-formaldehyde condensation product, formic acid and a preparation comprising the above pigment milled with aqueous sodium 1:11-dinaphthylmethane-2:21disulphonate, and the dyeing is hardened by heating; (7), natural or regenerated cellulose fabric is printed yellow with a paste made by mixing an aqueous paste, obtained by milling the above pigment with an ethylene oxide-di-tertiary-butyl-p-cresol and water, with an oil-in-water emulsion of petroleum hydrocarbons, a styrene-butadiene mixed polymerisate emulsion, a solution forming a separate inner phase and consisting of a water-insoluble melamine-formaldehyde primary condensation product modified with n-butenol and n-butanol, a solution forming the outer phase and consisting of an ion-free emulsifying agent and water, and aqueous ammonium nitrate; (9), chrome grain leather is dyed using a pigment dispersion obtained by mixing with aqueous casein solution, sodium sulphoricinoleate and egg albumin a pigment paste diluted with a wash-emulsion and casein solution and made by milling the above pigment with aqueous casein solution and a dispersing agent; and (10), bleached cellulose paper pulp containing a zinc sulphide or titanium dioxide filler is mixed with the above pigment and fixed with aluminium sulphate. Specifications 658,722 and 822,504 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH15061A CH402805A (en) | 1961-01-06 | 1961-01-06 | Process for mass coloring organic products with pigments |
Publications (1)
Publication Number | Publication Date |
---|---|
GB933687A true GB933687A (en) | 1963-08-08 |
Family
ID=4180382
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4650161A Expired GB933687A (en) | 1961-01-06 | 1961-12-28 | Process for colouring organic products with pigment dyestuffs |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE612333A (en) |
CH (1) | CH402805A (en) |
GB (1) | GB933687A (en) |
-
0
- BE BE612333D patent/BE612333A/xx unknown
-
1961
- 1961-01-06 CH CH15061A patent/CH402805A/en unknown
- 1961-12-28 GB GB4650161A patent/GB933687A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
CH402805A (en) | 1965-11-30 |
BE612333A (en) |
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