GB466846A - Process for producing dyeings and printings - Google Patents

Process for producing dyeings and printings

Info

Publication number
GB466846A
GB466846A GB33172/35A GB3317235A GB466846A GB 466846 A GB466846 A GB 466846A GB 33172/35 A GB33172/35 A GB 33172/35A GB 3317235 A GB3317235 A GB 3317235A GB 466846 A GB466846 A GB 466846A
Authority
GB
United Kingdom
Prior art keywords
acid
dried
rinsed
compound
diazotized
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
GB33172/35A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB466846A publication Critical patent/GB466846A/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
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/02General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes
    • D06P1/12General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes prepared in situ
    • D06P1/127General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes prepared in situ using a stabilised diazo component, e.g. diazoamino, anti-diazotate or nitrosamine R-N=N-OK, diazosulfonate, hydrazinesulfonate, R-N=N-N-CN

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Abstract

Azo dyes, forming on the material; printing; regenerated celluloses, dyeing.--In producing upon the fibre azo dyestuffs insoluble in water, the material is first treated with a solution of an acid, acid compound or compound yielding acid by hydrolytic or thermal dissociation, there is then applied a mixture of a substantive coupling component with a diazoamino compound soluble in water, in which the group imparting solubility is in the radicle of the stabilizer which does not take part in the formation of the dyestuff, and the dyestuff is then developed by steaming. Specified acids and acid compounds are sulphuric, phosphoric, lactic, tartaric, glycollic and oxalic acids and acid salts, e.g. sodium bisulphate, and specified compounds yielding acid are the sulphates and chlorides of magnesium, zinc and aluminium, ammonium salts of organic acids, esters, e.g. diethyl tartrate, succinate and malonate, ethyl laevulinate and hippurate, dibutyl diglycollate, esters of phosphoric and boric acids, amides, e.g. a -chlorisovalerianamide, malonamide and oxamide, and alkali salts of certain inorganic or organic acids, e.g. potassium fluorosulphonate, sodium 1 - acetoxyethane - 2 - sulphonate, sodium bromacetate and the sodium salt of oxalic acid methyl ester. Specified coupling components are naphthols, arylamides of 2 : 3-oxynaphthoic acid, of 2 : 3-oxyanthracenecarboxylic acid, of oxyphenanthrenecarboxylic acids and of o-oxycarbazole-, o-oxybenzocarbazole- and o-oxynaphthocarbazole-carboxylic acids, pyrazolones, arylamides of acetoacetic, benzoylacetic and terephthaloyl diacetic acids and di(acetoacetyl)-benzidine or -tolidine. The diazoamino compounds may be, for example, those described in Specification 320,324, 329,353, [both in Class 2 (iii)], 427,803, 429,618, 433,878, or 443,222. The following examples are specified: (1) a fabric of unloaded natural silk is impregnated with dilute sulphuric acid, dried, printed with an aqueous composition containing caustic soda, tragacanth thickening, the diazoamino compound from diazotized 5-chloro-2-methyl-1-aminobenzeneand 4-sulpho-2-aminobenzoic acid, and the 2<1>-toluidide of 2 : 3-oxynaphthoic acid, again dried, steamed, rinsed and soaped at the boil to obtain a full yellowish red print; (2) unloaded silk is impregnated with dilute ammonium sulphate solution, dried, printed in adjacent parts with aqueous compositions containing (a) caustic soda, tragacanth thickening, the diazoamino compound from diazotized 5-chloro-2-methoxy-1-aminobenzene and sarcosine, and the 4<1>-chloranilideof 2 : 3-oxycarbazolecarboxylic acid, (b) thiodiglycol, British gum, gum arabic, sodium chlorate, acetic acid, green chromium acetate, the chromium complex compound of the dyestuff from nitrated diazotized 1 : 2 aminonaphthol-4-sulphonic acid and b -naphthol and the chromium complex compound of the dyestuff, 2-chloro-4-toluidine --> 1-(5<1>-sulpho2<1>-salicylsulphonyl) phenyl-3-methyl-5-pyrazoline, again dried, steamed, rinsed and soaped at 40 DEG C. to obtain a brown and black print; (3) unloaded natural silk is impregnated with a dilute solution of diethyl tartrate, dried, printed in adjacent parts with aqueous compositions containing (a) denatured alcohol, caustic soda, tragacanth thickening, the diazoamino compound from diazotized 5-chloro-2-methyl-1-aminobenzene and 4-sulpho-2-amino benzoic acid, and di-(acetoacetyl)-tolidine, (b) potassium carbonate, sodium formaldehydesulphoxylate, tragacanth thickening and the vat dyestuff from 4-methyl-5-chloro-7-methoxyisatin and 5 : 7-dichloro-oxythionaphthene, again dried, steamed, rinsed, oxidized with hydrogen peroxide, again rinsed and soaped to obtain a yellow and blue print; (4) a viscose cr<\>zepe fabric is impregnated with a dilute solution of diethyl tartrate, dried, printed with an aqueous composition containing caustic soda, tragacanth thickening, the diazoamino compound from diazotized 2 : 5-dichloraniline and 5-sulpho-2-methylaminobenzoic acid, and the 2<1>-anisidide of 2 : 3-oxynaphthoic acid, steamed, rinsed and soaped at the boil to obtain a vivid yellowish red print; (5) a viscose fabric is impregnated with a dilute solution of diethyl tartrate, dried, printed in adjacent parts with aqueous compositions containing (a) urea, caustic soda, tragacanth thickening, the diazoamino compound from diazotized 1 - amino - 4 - benzoylamino - 2 : 5-dimethoxybenzene and methyltaurine, and the anilide of 2 : 3-oxynaphthoic acid, (b) thiodiglycol, starch-tragacanth thickening, acetic acid, violet chromium acetate and Galloviridine GA, steamed, chalked, malted, rinsed and soaped to obtain a navy blue and bright green print; (6) a viscose cr<\>zepe is impregnated with a dilute solution of diethyl tartrate, padded with an aqueous composition containing ethyl alcohol, caustic soda, tragacanth thickening, the diazoamino compound from diazotized 5-chloro-2-methoxy-1-aminobenzene and sarcosine, and the 4<1>-chloranilide of 2 : 3-oxycarbazolecarboxylic acid, dried, printed in adjacent parts with aqueous compositions containing potassium carbonate, sodium formaldehydesulphoxylate, tragacanth thickening and (a) the vat dyestuff obtainable by condensing 1-aminoanthraquinone with isophthalic acid (80 per cent) and terephthalic acid (20 per cent), glycerol and anthraflavine, (b) the stable leuco compound of 6 : 6<1>-diethoxythioindigo (cf. Specifications 334,920, [Class 2 (iii)], and 352,283), steamed, rinsed, oxidized with sodium perborate and acetic acid, again rinsed and soaped at the boil to obtain a yellow and orange print on a dark brown ground; (7) a wool muslin fabric is impregnated with a dilute solution of diethyl tartrate, dried, printed with an aqueous composition as in (3) (a) above, steamed, rinsed and soaped at 80 DEG C. to obtain an intense yellow print; (8) a wool-viscose mixed fabric is impregnated with a dilute solution of diethyl tartrate, dried, printed with an aqueous composition containing caustic soda, tragacanth thickening, the diazoamino compound from diazotized 4-chloro-2-methyl-1-aminobenzene and 4-sulpho-2-aminobenzoic acid, and the 2<1>-methyl-4<1>-methoxyanilide of 2 : 3-oxynaphthoic acid, steamed, rinsed and soaped hot to obtain a full bluish red print. 5 - Sulpho - 2 - methylaminobenzoic acid is obtained by condensing 5-sulpho-2-chlorobenzoic acid with methylamine.
GB33172/35A 1934-11-29 1935-11-29 Process for producing dyeings and printings Expired GB466846A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE466846X 1934-11-29

Publications (1)

Publication Number Publication Date
GB466846A true GB466846A (en) 1937-05-31

Family

ID=6540610

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33172/35A Expired GB466846A (en) 1934-11-29 1935-11-29 Process for producing dyeings and printings

Country Status (1)

Country Link
GB (1) GB466846A (en)

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