GB848236A - Textile dyeing process - Google Patents

Textile dyeing process

Info

Publication number
GB848236A
GB848236A GB3114457A GB3114457A GB848236A GB 848236 A GB848236 A GB 848236A GB 3114457 A GB3114457 A GB 3114457A GB 3114457 A GB3114457 A GB 3114457A GB 848236 A GB848236 A GB 848236A
Authority
GB
United Kingdom
Prior art keywords
thiophenol
phenol
amine
dispersion
halogeno
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
GB3114457A
Inventor
Harry Rose Hadfield
Walter Percival Mills
Ronald Herbert Ricketts
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 GB3114457A priority Critical patent/GB848236A/en
Publication of GB848236A publication Critical patent/GB848236A/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
    • D06P1/38General 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 reactive dyes

Landscapes

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

Abstract

Synthetic polymeric textile materials, such as polyamide, polyester, polyacrylonitrile, insolubilised polyvinyl alcohol, cellulose acetate and cellulose triacetate textiles, are dyed by applying an amine, phenol or thiophenol and simultaneously, previously or subsequently also applying a water-insoluble reactive dyestuff which contains a halogen atom or other group which is capable of reacting with the amine, phenol or thiophenol. Specified amines, phenols, and thiophenols which are applied from aqueous solution or dispersion are 2-hydroxydiphenyl, p-phenylenediamine, hexamethylenediamine, benzylamine, 4 : 41-diaminodiphenylmethane, ethylene diamine, 2-mercaptobenzthiazole, dianisidine, benzidine, tetraethylene pentamine, 4 : 41-di-aminobenzophenone, 2 : 7-diaminonaphthalene, 1 : 5-diphenyl biguanidine, 4 : 41-diaminodiphenylsulphone, cyclohexylamine, 6-aminoindazole, 5 : 6-diaminoindazole, 4 : 41-dichloro -2-aminodiphenyloxide, 3:31-diaminodiphenyl urea, 3 : 31-diaminobenzophenone, 4 : 41-diaminodibenzyl, pyridine, N-(p-aminobenzenesulphon) -N-methylglucosamine, 1-acetamido -3- diethylaminopropan -2- ol, 3- aminobenz-n-butylamide, N : N1-di-(p-aminobenzoyl) ethylenediamine, b -phenylacetamido-ethylamine and 11-amino -1- caprylamido -3 : 6 : 9-triazaundecane. Suitable reactive dyestuffs which are applied from aqueous dispersion are insoluble azo, anthraquinone, nitro or phthalocyanine dyes containing as reactive groups mono- or di-halogeno -striazinyl-, mono- or di-halogenopyrimidinyl-, g -halogeno -b - hydroxypropylamino-, b -halogenoethylsulphamyl-, b -halogenoethoxy, b -halogenothioethane-, g -halogeno -b -hydroxypropylsulphamyl-, chloracetylamino-, vinylsulphonyl- and epoxypropylgroups and numerous examples are given. When an aqueous solution or dispersion of the amine, phenol or thiophenol is applied after the dyestuff, then an alkali, e.g., sodium carbonate, is preferably added to the solution or dispersion. The aqueous dispersions of the dyestuff and of the amine, phenol or thiophenol may be applied at temperatures up to 100 DEG C., or above, under pressure.
GB3114457A 1957-10-04 1957-10-04 Textile dyeing process Expired GB848236A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3114457A GB848236A (en) 1957-10-04 1957-10-04 Textile dyeing process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3114457A GB848236A (en) 1957-10-04 1957-10-04 Textile dyeing process

Publications (1)

Publication Number Publication Date
GB848236A true GB848236A (en) 1960-09-14

Family

ID=10318671

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3114457A Expired GB848236A (en) 1957-10-04 1957-10-04 Textile dyeing process

Country Status (1)

Country Link
GB (1) GB848236A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117005056A (en) * 2023-08-22 2023-11-07 江苏新视界先进功能纤维创新中心有限公司 Polymer coloring method, spinning color paste, spinning solution and colored fiber

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117005056A (en) * 2023-08-22 2023-11-07 江苏新视界先进功能纤维创新中心有限公司 Polymer coloring method, spinning color paste, spinning solution and colored fiber

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