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GB190423193A - Manufacture of Blue and Violet to Black Dyestuffs by Oxidation on the Fibre. - Google Patents

Manufacture of Blue and Violet to Black Dyestuffs by Oxidation on the Fibre.

Info

Publication number
GB190423193A
GB190423193A GB190423193DA GB190423193A GB 190423193 A GB190423193 A GB 190423193A GB 190423193D A GB190423193D A GB 190423193DA GB 190423193 A GB190423193 A GB 190423193A
Authority
GB
United Kingdom
Prior art keywords
blue
black
fibre
violet
amidodiphenylamine
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
Inventor
Oliver Imray
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Application granted granted Critical
Publication of GB190423193A publication Critical patent/GB190423193A/en
Expired legal-status Critical Current

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Abstract

23,193. Imray, O., [Farbwerke vorm. Meister, Lucius, & Br³ning]. Oct.. 27. Dyeing.-Fabrics of vegetable or animal fibres, such as cotton, silk, wool, and mixed fabrics, are dyed blue and violet to black shades, fast to soap, soda, acid, and light, by oxidizing p-amidodiphenylamine or its derivatives, on the fibre, together with hydroxy- and amino-aryl compounds and their ethers, such as phenols, naphthols, or their ethers, oxycarboxylic acids or their esters, o-amidophenol ethers, primary, secondary, and tertiary m-amidophenols, alkylated and alphylated m-phenylenediamines or naphthylamines, or the like, a large number of examples being given. For the p-amidodiphenylamine may be substituted p-amidomethyldiphenylamine, p-amidophenyltolylamine, p-amidop-oxy-diphenylamine, and p-diamido- and symmetrical dimethyl-p-diamido-diphenylamines and other analogous or homologous derivatives. To prepare the dyes, the two components to be oxidized are dissolved together or separately and stirred with a thickener, such as acid starch or tragacanth, for printing or padding respectively, and the oxidizing- agents added, the chlorates in the presence or absence of oxygen carriers being specially suitable. Acid salts, such as aluminium chloride, which do not attack the fibre, may be used to start the oxidation, free mineral acids being unnecessary. After the material to be dyed has been printed or padded with the mixture, it is dried and the colour developed, and simultaneously fixed, by prolonged aÙration in a warm place or by steaming, after which it is washed and soaped. The components may be successively applied and then oxidized jointly. Most dyes so produced are fast without a mordant. Those with strong basic groups, such as a dialkylamine group, may be fixed with tannin, and those with an o-carboxyl or o-hydroxyl group may be fixed with a chromium mordant. For example, a colour for printing blue-black contains p-amidodiphenylamine, m-oxydiphenylamine, acetic and lactic acids, acid starch thickening, aluminium and cerous chlorides, alcohol, and water. A greenish-blue is obtained when the second component is m-oxydiethylaniline, tannin being added, and ceric chloride and glycerine replacing the cerous chloride and alcohol, respectively. Tannin colours may be passed through an antimony bath. A chromium-blue is given by a mixture containing ceric chloride and chromium acetate with methyl gallate as the second component. p-Amidodiphenylamine also gives with : #-naphthol, blue ; diethyl-m-amidophenol, greenish-blue ; resorcin, indigo-blue ; m-oxydiphenylamine, copper chloride replacing the cerium salt, blue-black ; o-anisidine, o-phenetidine, or m-amido-p-tolylphenylamine, violet; thioaniline, black. p-Amido-p-oxydiphenylamine with m-amido-p-tolylphenylamine gives violet. Resists may be obtained by printing with reducing-agents, such as potassium sulphite, hydrosulphite, or tin salts, and may be tinted as usual with reduction-resisting dyes. The process may be combined with that for producing an oxidation or steam black on the fibre which does not turn green, the black being thus shaded.
GB190423193D 1904-10-27 1904-10-27 Manufacture of Blue and Violet to Black Dyestuffs by Oxidation on the Fibre. Expired GB190423193A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB190423193T 1904-10-27

Publications (1)

Publication Number Publication Date
GB190423193A true GB190423193A (en) 1905-10-26

Family

ID=32432612

Family Applications (1)

Application Number Title Priority Date Filing Date
GB190423193D Expired GB190423193A (en) 1904-10-27 1904-10-27 Manufacture of Blue and Violet to Black Dyestuffs by Oxidation on the Fibre.

Country Status (1)

Country Link
GB (1) GB190423193A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3253878A (en) * 1966-05-31 Processes for dyeing and padding of hydrophobic materials
US3254934A (en) * 1963-10-09 1966-06-07 Bayer Ag Process for the coloring of hydrophobic materials
US3254936A (en) * 1966-06-07 Dyeing hydrophobic textiles with an azomethine of an aromatic amine and a quinone, n-haloquinoneimine or a cyclohexeneone
US3634013A (en) * 1968-05-30 1972-01-11 Therachemie Chem Therapeut Aqueous coupled hydrazono hair-dyeing composition and process
US3658455A (en) * 1968-06-14 1972-04-25 Oreal Dyeing hair with aqueous solution of phenyl-toluyl-or pyridyl amino base compound and benzimidazole coupler

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3253878A (en) * 1966-05-31 Processes for dyeing and padding of hydrophobic materials
US3254936A (en) * 1966-06-07 Dyeing hydrophobic textiles with an azomethine of an aromatic amine and a quinone, n-haloquinoneimine or a cyclohexeneone
US3254934A (en) * 1963-10-09 1966-06-07 Bayer Ag Process for the coloring of hydrophobic materials
US3634013A (en) * 1968-05-30 1972-01-11 Therachemie Chem Therapeut Aqueous coupled hydrazono hair-dyeing composition and process
US3658455A (en) * 1968-06-14 1972-04-25 Oreal Dyeing hair with aqueous solution of phenyl-toluyl-or pyridyl amino base compound and benzimidazole coupler

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