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ES239126A1 - New colouration process for cellulosic textiles - Google Patents

New colouration process for cellulosic textiles

Info

Publication number
ES239126A1
ES239126A1 ES0239126A ES239126A ES239126A1 ES 239126 A1 ES239126 A1 ES 239126A1 ES 0239126 A ES0239126 A ES 0239126A ES 239126 A ES239126 A ES 239126A ES 239126 A1 ES239126 A1 ES 239126A1
Authority
ES
Spain
Prior art keywords
dyestuff
dyestuffs
printing
group
sodium
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
ES0239126A
Other languages
Spanish (es)
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of ES239126A1 publication Critical patent/ES239126A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/523Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl amido or hydroxyalkyl amino sulfonyl group, a quaternised or non-quaternised amino alkyl sulfonyl amido group, or a substituted alkyl amino sulfonyl group, or a halogen alkyl sulfonyl amido or halogen alkyl amino sulfonyl group or a vinyl sulfonylamido or a substituted vinyl sulfonamido group
    • C09B62/537Porphines; Azaporphines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Cellulosic textile materials are dyed or printed by applying a dyestuff, e.g. an azo, nitro, anthraquinone or phthalocyanine dyestuff, which contains at least one solubilizing group, such as a sulphonic acid group, and at least one -SO2R group, in which R represents a beta-chloroethylamino or a beta-bromoethylamino radical, and also applying before, together with or after the dyestuff, an acidbinding agent such as a caustic alkali, sodium carbonate or bicarbonate, trisodium phosphate, sodium metasilicate or hydrated magnesium oxide. The dyestuff solutions or pastes may contain the usual adjuvants such as sodium chloride, sodium sulphate, urea, sodium alginate, cellulose ethers, starch, locust bean gum or a water-in-oil or oil-in-water emulsion. The dyestuff and/or acid-binding agent solutions may be applied at temperatup to the bolres in. When the dyestuff and the acid-binding agent are applied in succession a drying operation may be applied between the two treatments. Fixation of the dyestuff may be effected by drying alone, or by heating or, in the case of printing, by steaming. In the case of printing, other dyestuffs such as leuco esters of vat dyestuffs and dyestuffs obtained by reacting colouring matters containing halogenomethyl groups with tertiary amines or thioureas may be printed alongside. Numerous examples of dyeing and printing (including one of discharge printing with a reducing discharge) are given. The dyestuffs may be obtained by treating an azo, nitro, anthraquinone or phthalocyanine dye containing a plurality of sulphonchloride groups with b -chloro-(or bromo-) ethylamine. Nitro dyestuffs may also be obtained by reacting an o-chlornitrobenzene carrying a b -chlorethylsulphonamide group with a primary aromatic amine carrying a solubilizing group, such as 4-aminoanisole-3-sulphonic acid. Azo dyestuffs may also be made by diazotizing primary amines containing -SO2R groups, such as m-aminobenzenesulphon-b -chloro-(or bromo-) ethylamide or aniline 3 : 5-di-(sulphon-b -chlorethylamide), with various coupling components, many of which are specified.
ES0239126A 1956-12-14 1957-12-14 New colouration process for cellulosic textiles Expired ES239126A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3819756A GB823098A (en) 1956-12-14 1956-12-14 New colouration process for cellulosic textiles

Publications (1)

Publication Number Publication Date
ES239126A1 true ES239126A1 (en) 1958-06-01

Family

ID=10401884

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0239126A Expired ES239126A1 (en) 1956-12-14 1957-12-14 New colouration process for cellulosic textiles

Country Status (3)

Country Link
DE (1) DE1231203B (en)
ES (1) ES239126A1 (en)
GB (1) GB823098A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR976047A (en) * 1942-03-26 1951-03-13 Ig Farbenindustrie Ag Process for fixing organic substances, soluble in water, on supports and making them insoluble

Also Published As

Publication number Publication date
GB823098A (en) 1959-11-04
DE1231203B (en) 1966-12-29

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