GB224925A - Improvements in or relating to the dyeing or coloring of products made with cellulose acetate - Google Patents
Improvements in or relating to the dyeing or coloring of products made with cellulose acetateInfo
- Publication number
- GB224925A GB224925A GB1344523A GB1344523A GB224925A GB 224925 A GB224925 A GB 224925A GB 1344523 A GB1344523 A GB 1344523A GB 1344523 A GB1344523 A GB 1344523A GB 224925 A GB224925 A GB 224925A
- Authority
- GB
- United Kingdom
- Prior art keywords
- azo
- solution
- sulphonic
- acids
- naphthol
- 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/34—Material containing ester groups
- D06P3/40—Cellulose acetate
- D06P3/42—Cellulose acetate using dispersed dyestuffs
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Abstract
Insoluble or difficulty-soluble dyes or amino bases of the types described in Specification 219,349, for dyeing cellulose acetate goods are dispersed by means of carbocyclic compounds containing salt-forming groups, or salts of these bodies, or mixtures thereof with the dispersing-agents described in the above-mentioned Specification. Suitable carbocyclic compounds are naphthenic acids, naphthene sulphonic acids, or other carboxylic or sulphonic acids of the cycloparaffins, phenol, sulphonic, or carboxylic acids, phenol sulphonic acids, or other derivatives of the benzene, naphthalene, or anthracene series. According to examples:-m-Nitrobenzene-azo-diphenylamine is heated and stirred with naphthenic acid, water or soap solution is added, and the mixture made slightly alkaline with caustic soda and boiled; 1-methyl-amino-4-p-tolylaminoanthraquinone is dispersed similarly with naphthenic acid and soap solution; benzene-azo-benzene-azo-b -naphthol is heated and stirred with p-cresol and sodium sulphoricinoleate and diluted with sodium oleate solution; p-methoxybenzene-azo-b -naphthol is heated and stirred with 1-naphthol-4-sulphonic acid sodium sulphoricinoleate and diluted with sodium oleate solution containing caustic soda.ALSO:Insoluble or difficultly-soluble dyes or amino bases of the types described in Specification 219,349, for dyeing cellulose acetate goods are dispersed by means of carbocyclic compounds containing salt-forming groups, or salts of these bodies, or mixtures thereof with the dispersing-agents described in the above-mentioned Specification. Suitable carbocyclic compounds are naphthenic acids, naphthene sulphonic acids, or other carboxylic or sulphonic acids of the cycloparaffins, phenols, sulphonic or carboxylic acids, phenol sulphonic acids, or other derivatives of the benzene, naphthalene, or anthracene series. According to examples:-m-nitrobenzene-azo-diphenylamine is heated and stirred with naphthenic acid, water or soap solution is added, and the mixture made slightly alkaline with caustic soda and boiled; the resulting solution dyes cellulose acetate yellow; a similar dispersion of 1-methylamino-4-p-tolylaminoanthraquinone with naphthenic acid and soap solution gives a sky-blue shade; a red shade is obtained with the solution prepared by heating and stirring benzene-azo-benzene-azo-b -naphthol with p-cresol and sodium sulphoricinoleate and diluting with sodium oleate solution; an orange shade is obtained with the solution prepared by heating and stirring p-methoxybenzene-azo-b -naphthol with 1-naphthol-4-sulphonic acid and sodium sulphoricinoleate and diluting with sodium oleate solution containing caustic soda.ALSO:The dyeing or colouring of cellulose acetate goods (yarns, threads, filaments, fabrics, films, &c.) is effected by means of insoluble or difficultly-soluble dyes which have been stabilized by pretreatment with carbocyclic compounds containing salt-forming groups, or salts of these bodies, or mixtures thereof with the solubilizing-agents described in Specification 219,349. The procedure is similar to that of the above-mentioned Specification, and may be applied to the types of dyes mentioned therein for dyeing, printing, or stencilling the goods, to amino bases used in forming azo dyes on the material, for dyeing mixed goods containing cellulose acetate in uniform or contrasting shades, &c. Suitable carbocyclic compounds are naphthenic acids, naphthene sulphonic acids, or other carboxylic or sulphonic acids of the cyclo paraffins, phenols, sulphonic or carboxylic acids, phenol sulphonic acids or other derivatives of the benzene, naphthalene, or anthracene series. According to examples: - m-Nitrobenzene-azo-diphenylamine is heated and stirred with naphthenic acid, water or soap solution is added, and the solution made slightly alkaline with caustic soda and boiled; the resulting solution dyes cellulose acetate yellow; a similar dispersion of 1-methylamino-4-p-tolylaminoanthraquinone with naphthenic acid and soap solution gives a sky-blue shade; a red shade is obtained with the solution prepared by heating and stirring benzene-azo-benzene-azo-b -naphthol with p-cresol and sodium sulphoricinoleate and diluting with sodium oleate solution; an orange shade is obtained with the solution prepared by heating and stirring p-methoxybenzene-azo-b -naphthol with 1-naphthol-4-sulphonic acid and sodium sulphoricinoleate and diluting with sodium oleate solution containing caustic soda.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1344523A GB224925A (en) | 1923-05-22 | 1923-05-22 | Improvements in or relating to the dyeing or coloring of products made with cellulose acetate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1344523A GB224925A (en) | 1923-05-22 | 1923-05-22 | Improvements in or relating to the dyeing or coloring of products made with cellulose acetate |
Publications (1)
Publication Number | Publication Date |
---|---|
GB224925A true GB224925A (en) | 1924-11-24 |
Family
ID=10023110
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1344523A Expired GB224925A (en) | 1923-05-22 | 1923-05-22 | Improvements in or relating to the dyeing or coloring of products made with cellulose acetate |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB224925A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2610182A (en) * | 1949-06-22 | 1952-09-09 | Standard Oil Dev Co | Hydrocarbon thiophosphoric acid salts of thialdine and certain homologues |
US3506991A (en) * | 1964-07-01 | 1970-04-21 | Celanese Corp | Dye receptive fibers and method of preparing same |
-
1923
- 1923-05-22 GB GB1344523A patent/GB224925A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2610182A (en) * | 1949-06-22 | 1952-09-09 | Standard Oil Dev Co | Hydrocarbon thiophosphoric acid salts of thialdine and certain homologues |
US3506991A (en) * | 1964-07-01 | 1970-04-21 | Celanese Corp | Dye receptive fibers and method of preparing same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB224925A (en) | Improvements in or relating to the dyeing or coloring of products made with cellulose acetate | |
GB361362A (en) | Improvements in or relating to the colouration of materials | |
US3265460A (en) | Dyeing of synthetic fibers | |
US2734793A (en) | Method of preparing water-dispersible | |
US1534019A (en) | Dyeing acetyl cellulose or fabrics containing the same and new products for use therein | |
US3642424A (en) | Process for dyeing textile material of mixtures of polyester and cellulose fibers | |
GB352956A (en) | Process for the manufacture of substantive dyeing disazo dyestuffs containing copper | |
US1723271A (en) | Treatment of cellulose derivatives | |
GB285096A (en) | Manufacture of new dyestuffs | |
US1883351A (en) | Treatment of cellulose derivatives | |
US3623831A (en) | Process for dyeing textile material of mixtures of polyester and cellulose fibres | |
US1694414A (en) | Dyeing, printing, or stenciling of cellulose acetate | |
US1886412A (en) | Dyeing and printing process | |
US2957745A (en) | Dyeing and printing of synthetic high polymeric polyesters | |
US1840572A (en) | Treatment of cellulose derivatives | |
GB775885A (en) | Dyestuff preparations and dyeing or printing processes using them | |
US2008966A (en) | Process and composition for applying and fixing dyestuff | |
US2112276A (en) | Coloration of textile materials | |
SU39773A1 (en) | The method of obtaining stable forms of diazocompounds and their application | |
US1892280A (en) | Production of colored compositions | |
US1716721A (en) | Treatment of cellulose derivatives | |
US1928648A (en) | Method of making dispersions of insoluble compounds | |
DE438323C (en) | Dye preparation for dyeing cellulose acetate or fibrous materials containing it | |
GB669028A (en) | Improvements in coloured fluorescent artificial textile materials | |
MATSUZ et al. | Reactive Dyes Containing-SO2NHCH2CH2Cl Group. II |