GB825017A - Textile colouration process - Google Patents

Textile colouration process

Info

Publication number
GB825017A
GB825017A GB3556156A GB3556156A GB825017A GB 825017 A GB825017 A GB 825017A GB 3556156 A GB3556156 A GB 3556156A GB 3556156 A GB3556156 A GB 3556156A GB 825017 A GB825017 A GB 825017A
Authority
GB
United Kingdom
Prior art keywords
triazine
amino
dichloro
phenol
insoluble
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
GB3556156A
Inventor
Water Francis Beech
Donald Arthur Garrett
Harry Rose Hadfield
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
Priority to GB3556156A priority Critical patent/GB825017A/en
Publication of GB825017A publication Critical patent/GB825017A/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
    • D06P1/44General 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 insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/64General 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 insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
    • D06P1/642Compounds containing nitrogen
    • D06P1/6426Heterocyclic compounds

Landscapes

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

Abstract

Water-insoluble compounds containing a mono- or di-halogenated 1:3:5-triazine ring, for use in treating textiles (see Group IV (c)), are obtained by reacting a cyanuric halide such as cyanuric chloride with one or two molecular proportions of a primary or secondary amine, an alcohol, a phenol or a mercaptan which is free from solubilizing groups. Suitable amines, alcohols, phenols and mercaptans are methylamine, diethylamine, b -hydroxyethylamine, aniline, p-diethylaminoaniline, a -naphthylamine, phenol, b -naphthol, p-thiocresol and methanol. By using compounds containing more than one amino, hydroxyl or mercapto group, water-insoluble triazines containing more than one halogenated triazine ring, such as 1:2-bis-(21:41 - dichloro - 11:31:51 - triazinylamino-)-ethane, may be obtained. Alternatively, the compounds may be obtained by reacting equimolecular proportions of an alcohol, primary or secondary amine, phenol or mercaptan with a dihalogenated 1:3:5-triazine containing alkyl or aryl substituents such as 4:6-dichloro-2-phenyl - 1:3:5 - triazine or 4:6 - dichloro - 2 -methyl.-1:3:5-triazine.ALSO:Textile materials of natural protein fibres, such as wool or silk, or of artificial fibres, such as those of cellulose esters (including triacetate) or ethers, polyamides, polyesters, polyacrylonitrile or polyvinyl alcohol are dyed or printed by applying a dyestuff containing a reactive amino group (an amino p group containing a hydrogen atom which is readily replaced by treatment with cyanuric chloride at 20 DEG C. in aqueous medium) and also applying, before, together with or after the dyestuff, an aqueous suspension of a water-insoluble colourless or coloured compound containing a mono- or dihalogenated 1 : 3 : 5-triazine ring. As applied to printing, the printing paste containing the dyestuff and the triazine may also include dispersing agents, ethanol, sodium m-nitrobenzene-sulphonate, urea, thiourea, thiodiglycol and thickeners such as sodium alginate, and the print is fixed by steaming, if desired under pressure. Various soluble and insoluble dyestuffs are specified. Suitable colourless, insoluble triazine derivatives are the condensation products of a cyanuric halide with a primary or secondary amine, an alcohol, a phenol or a mercaptan free from solubilizing groups such as methylamine, diethylamine, b -hydroxyethylamine, aniline, p - diethylaminoaniline, a - naphthylamine, phenol, b -naphthol, p-thiocresol and methanol. Other specified colourless triazine derivatives are 4 : 6 - dichloro - 2 - phenyl - 1 : 3 : 5 - triazine, 4 : 6 - dichloro - 2 - methyl - 1 : 3 : 5 - triazine and 1 : 2 - bis - (21 : 41 - dichloro - 11 : 31 : 51-triazinylamino-) ethane. Specified coloured triazine derivatives are the condensation products of cyanuric halides with aminoazo, aminoanthraquinone and amino nitro diphenylamine compounds such as 4 : 41 - diaminozaobenzene, 4 - amino - 41 - dimethylaminoazobenzene, 2-chloro - 4 - ethanesulphonyl - 41 - N(b - hydroxyethyl) : N(b - aminoethyl) - aminoazobenzene, 2 : 4 - bis - methanesulphonyl - 41 - diethyl-amino - 21 - aminoazobenzene, 41 - amino - 2-nitro - diphenylamine and 1 - (b - aminoethyl) aminoanthraquinone. When the dyestuff or triazine derivative contains metal - complex forming groups, a treatment with a metal-yielding agent may be applied. Numerous examples of dyeing and printing are given.
GB3556156A 1956-11-21 1956-11-21 Textile colouration process Expired GB825017A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3556156A GB825017A (en) 1956-11-21 1956-11-21 Textile colouration process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3556156A GB825017A (en) 1956-11-21 1956-11-21 Textile colouration process

Publications (1)

Publication Number Publication Date
GB825017A true GB825017A (en) 1959-12-09

Family

ID=10379110

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3556156A Expired GB825017A (en) 1956-11-21 1956-11-21 Textile colouration process

Country Status (1)

Country Link
GB (1) GB825017A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3352624A (en) * 1967-11-14 Swf ci
DE2155769A1 (en) * 1971-11-10 1973-05-24 Degussa S-TRIAZINE DERIVATIVES CONTAINING NAPHTHYLAMINOGRAPHS AND USES
WO1999028546A1 (en) * 1997-11-27 1999-06-10 Ciba Specialty Chemicals Holding Inc. Process for dyeing wool-containing fibre materials

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3352624A (en) * 1967-11-14 Swf ci
DE2155769A1 (en) * 1971-11-10 1973-05-24 Degussa S-TRIAZINE DERIVATIVES CONTAINING NAPHTHYLAMINOGRAPHS AND USES
WO1999028546A1 (en) * 1997-11-27 1999-06-10 Ciba Specialty Chemicals Holding Inc. Process for dyeing wool-containing fibre materials

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