Process for dyeing synthetic polyamide materials with fibre-reactive anthraquinone dyes
AssigneeCiba-Geigy Corporation
InventorsJames B. Bowles, Marshall White, Jr., Alois Puentener, Jean-Marie Adam, Peter Loew
Life of this patent
Estimating the term…
Abstract
Process for preparing ozone-fast dyeings on synthetic polyamide fibre materials from aqueous liquor with anthraquinone dyes which comprises using at least one anthraquinone dye which contains one or two fibre-reactive groups and one or two sulfo groups. The process according to the invention is suitable for dyeing synthetic polyamide materials producing with the monosulfoanthraquinone or disulfoanthraquinone dyes which contain one or two fibre-reactive groups level dyeings having good fastness properties, in particular good ozone fastness.
Claims20
A continuous process for preparing ozone-fast dyeings on synthetic polyamide fiber material from aqueous liquor with anthraquinone dyes which comprises applying to said fiber material from said liquor at least one anthraquinone dye of the formula ##STR44## in which G.sub.1, G.sub.2, G.sub.4 and G.sub.5 are each hydrogen and G.sub.3 is a .alpha.,.beta.-dibromopropionylamino, or in which G.sub.1, G.sub.3, G.sub.4 and G.sub.5 are each hydrogen and G.sub.2 is vinylsulfonyl, chloroacetylamino, 2-methoxy-4-fluoro-s-triazinylamino or 2-ethylamino-4-fluoro-s-triazinylamino, or in which G.sub.1 is methyl, G.sub.2 is 2,6-difluoro-5-chloropyrimidinylamino, G.sub.3 and G.sub.5 are both hydrogen and G.sub.4 is sulfo, or in which G.sub.1 is methoxy, G.sub.2, G.sub.3 and G.sub.5 are each hydrogen and G.sub.4 is .beta.-sulfatoethylsulfonyl, or in which G.sub.1, G.sub.3 and G.sub.5 are each methyl, G.sub.2 is hydrogen or --CH(COOH)--NH--CO--CHBr--CH.sub.2 Br and G.sub.4 is .alpha.,.beta.-dibromopropionylaminomethyl or --CH(COOH)--NH--CO--CHBr--CH.sub.2 Br, or in which G.sub.1, G.sub.3 and G.sub.5 are each methyl, G.sub.2 is .alpha.,.beta.-dibromopropionylamino and G.sub.4 is sulfo, or in which G.sub.1 is sulfo, G.sub.2, G.sub.4 and G.sub.5 are each hydrogen and G.sub.3 is .alpha.-dibromoacryloylamino.
A continuous process for preparing ozone-fast dyeings on synthetic polyamide fiber material from aqueous liquor with anthraquinone dyes which comprises applying to said fiber material from said liquor at least one anthraquinone dye of the formula ##STR45## in which A.sub.1 is isopropyl, A.sub.2 is hydrogen and A.sub.3 X is a 4-phenoxyphenyl radical which is substituted in the phenoxy radical by sulfo and acryloylaminomethyl, or in which A.sub.2 is hydrogen and each of A.sub.1 X and A.sub.3 X is a 4-alpha-bromoacryloylamino-3-sulfophenyl radical or a phenyl-sec.-butyl radical which is substituted in the phenyl ring by sulfo and chloroacetylaminomethyl.
A process for preparing ozone-fast dyeings on synthetic polyamide fiber material from aqueous liquor with mixtures of two anthraquinone dyes which comprises applying said two dyes to said fiber material from said liquor, each dye independently to the other corresponding to one of the formulae ##STR46## in which X is a chloroacetyl, bromoacetyl, acryloyl, alpha,beta-dichloro-propionyl, alpha,beta-dibromopropionyl, alpha-bromoacryloyl or alpha-chloroacryloyl radical which is bonded via --NH--, ##STR47## or --CH.sub.2 --NH--, or is a radical of the formulae ##STR48## in which R.sub.5 is C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylmercapto or a radical of the formula ##STR49## where R.sub.6 and R.sub.7, independently of each other, are each hydrogen, C.sub.1 -C.sub.6 -alkyl or substituted or unsubstituted phenyl or naphthyl, or is a vinylsulfonyl, .beta.-sulfatoethylsulfonyl, .beta.-acetoxyethylsulfonyl, .beta.-chloroethylsulfonyl or .beta.-(.beta.-sulfatoethylsulfonyl)-propionylaminomethyl radical and the phenyl ring L.sub.1 is unsubstituted or monosubstituted, disubstituted, trisubstituted or tetrasubstituted by C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or phenoxy, or ##STR50## in which A.sub.4 is a C.sub.1 -C.sub.6 -alkyl or C.sub.5 -C.sub.7 -cycloalkyl radical, X is as defined above and the phenyl ring L.sub.2 is unsubstituted or monosubstituted, disubstituted or trisubstituted or by C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, phenoxy or C.sub.1 -C.sub.4 -alkylphenoxy, or ##STR51## in which A.sub.4 is as defined under the formula (3), X is as defined above and the phenyl ring L.sub.3 is unsubstituted, or monosubstituted or disubstituted by C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy, or ##STR52## in which X is as defined above.
Dependencies are inferred from the claim text.