GB827570A - Process for the production of dyeings and printings on cellulose fibres - Google Patents

Process for the production of dyeings and printings on cellulose fibres

Info

Publication number
GB827570A
GB827570A GB37935/57A GB3793557A GB827570A GB 827570 A GB827570 A GB 827570A GB 37935/57 A GB37935/57 A GB 37935/57A GB 3793557 A GB3793557 A GB 3793557A GB 827570 A GB827570 A GB 827570A
Authority
GB
United Kingdom
Prior art keywords
acid
sulphofluoride
pyrazolone
naphthol
amino
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
GB37935/57A
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.)
Cassella Farbwerke Mainkur AG
Original Assignee
Cassella Farbwerke Mainkur 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.)
Filing date
Publication date
Application filed by Cassella Farbwerke Mainkur AG filed Critical Cassella Farbwerke Mainkur AG
Publication of GB827570A publication Critical patent/GB827570A/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
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/66Natural or regenerated cellulose using reactive dyes

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Cellulose fibres or textile materials made therefrom are dyed or printed with an aqueous solution or paste of a water-soluble azo, nitro or anthraquinone dye which contains at least one SO2F group, and the dyeing or printing is fixed by steaming. The dyeing or printing may be carried out at an elevated temperature, and dyeing, printing and fixing may be effected in the presence of a weakly alkaline or acid-binding agent. In an example, 1-aminobenzene-3-sulphofluoride is diazotized and coupled with the sodium salt of 1-(41-sulphophenyl)-5-pyrazolone-3 carboxylic acid, mineral acid being partly neutralized, if necessary, by addition of sodium formate or acetate. A yellow water-soluble dyestuff is obtained. Cotton may be dyed or printed with the concentrated aqueous solution and the dyeing, possibly after intermediate drying, may be steamed in the presence of sodium acetate or other acid-binding agent. During steaming the fibres are acylated with the dye, hydrogen fluoride or fluorides being evolved, and a greenish-yellow dyeing is obtained which is fast to wet-processing, has good light-fastness and may be discharged to a pure white. Printing pastes may be made, using conventional thickeners, binding agents and printing auxiliaries. Other diazo components which may be used include 1-aminobenzene-2,3, or 4-sulphofluoride, 1 - aminobenzene - 3 - sulphofluoride - 5 - or 6 - sulphonic acid, 1 amino - benzene-3,5 - disulphofluoride, 1 - amino - 2 - methylbenzene - 5 - sulphofluoride, 1 - amino - 4-methylbenzene - 3 - sulphofluoride, 1 - amino-2,4 - dimethylbenzene - 5 - or 6 - sulphofluoride, 1 - amino - 4 - chlorobenzene - 2 - sulphofluoride, 1 - amino - 2 - chlorobenzene - 5-sulphofluoride, 1 - amino - 2 - methoxybenzene-5 - sulphofluoride and 1 - amino - 4 - methylbenzene - 3 - sulphofluoride - 6 - sulphonic acid. Other specified coupling components are 1-(41-sulphophenyl) - 3 - methyl - 5 - pyrazolone, 1-(31 - sulphophenyl) - 3 - methyl - 5 - pyrazolone, 1 - (21 - carboxy - 41 - sulphophenyl) - 3 - methyl- 5 - pyrazolone, 1 - (31 - carboxyphenyl) - 5-pyrazolone - 3 - carboxylic acid, 1 - (31 - sulpho-amidophenyl) - 5 - pyrazolone - 3 - carboxylic acid, 1 - (41 - sulphophenyl) - 5 - pyrazolone - 3-carboxyli acid amide, 1-(51,71-disulpho-21-naphthyl) - 3 - methyl - 5 - pyrazolone, 1 - (41-81 - disulpho - 21 - naphthyl) - 3 - methyl - 5-pyrazolone, 1 - (21 - chloro - 51 - sulphophenyl)-3 - methyl - 5 - pyrazolone, 2 - naphthylamine-3,6 - disulphonic acid, 2 - naphthylamine - 5,7-disulphonic acid, 1 - naphthol - 3,6 - disulphonic acid, 1 - naphthol - 3,6,8 - trisulphonic acid, 2-naphthol - 6 - sulphonic acid, 2 - naphthol - 6,8-disulphonic acid, 2 - naphthol - 3,6 - disulphonic acid, 1 - chloro - 8 - naphthol - 3,6 - disulphoric acid, 1 - acetylamino - 8 - naphthol - 4,6 - disulphonic acid and 1 - acetylamino - 8 - naphthol-3,6-disulphonic acid. Specification 460,224 is referred to.
GB37935/57A 1956-12-06 1957-12-05 Process for the production of dyeings and printings on cellulose fibres Expired GB827570A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE827570X 1956-12-06

Publications (1)

Publication Number Publication Date
GB827570A true GB827570A (en) 1960-02-10

Family

ID=6748053

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37935/57A Expired GB827570A (en) 1956-12-06 1957-12-05 Process for the production of dyeings and printings on cellulose fibres

Country Status (1)

Country Link
GB (1) GB827570A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3268571A (en) * 1964-04-06 1966-08-23 Minnesota Mining & Mfg Difluoromethyl esters and process for their preparation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3268571A (en) * 1964-04-06 1966-08-23 Minnesota Mining & Mfg Difluoromethyl esters and process for their preparation

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