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 acetate

Info

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
Application number
GB1344523A
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.)
British Celanese Ltd
Original Assignee
British Cellulose and Chemical Manufacturing Co Ltd
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.)
Filing date
Publication date
Application filed by British Cellulose and Chemical Manufacturing Co Ltd filed Critical British Cellulose and Chemical Manufacturing Co Ltd
Priority to GB1344523A priority Critical patent/GB224925A/en
Publication of GB224925A publication Critical patent/GB224925A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/34Material containing ester groups
    • D06P3/40Cellulose acetate
    • D06P3/42Cellulose 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.
GB1344523A 1923-05-22 1923-05-22 Improvements in or relating to the dyeing or coloring of products made with cellulose acetate Expired GB224925A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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

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