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
Links
- 239000000835 fiber Substances 0.000 title abstract 4
- 230000003647 oxidation Effects 0.000 title abstract 3
- 238000007254 oxidation reaction Methods 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 6
- 239000000975 dye Substances 0.000 abstract 3
- 150000002170 ethers Chemical class 0.000 abstract 3
- 239000001648 tannin Substances 0.000 abstract 3
- 235000018553 tannin Nutrition 0.000 abstract 3
- 229920001864 tannin Polymers 0.000 abstract 3
- 241000974482 Aricia saepiolus Species 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N Indigo Chemical compound N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 abstract 2
- 229920002472 Starch Polymers 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- 239000004744 fabric Substances 0.000 abstract 2
- FBSFWRHWHYMIOG-UHFFFAOYSA-N methyl 3,4,5-trihydroxybenzoate Chemical compound COC(=O)C1=CC(O)=C(O)C(O)=C1 FBSFWRHWHYMIOG-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 235000019698 starch Nutrition 0.000 abstract 2
- 239000008107 starch Substances 0.000 abstract 2
- ULHFFAFDSSHFDA-UHFFFAOYSA-N 1-amino-2-ethoxybenzene Chemical compound CCOC1=CC=CC=C1N ULHFFAFDSSHFDA-UHFFFAOYSA-N 0.000 abstract 1
- ICNFHJVPAJKPHW-UHFFFAOYSA-N 4,4'-Thiodianiline Chemical compound C1=CC(N)=CC=C1SC1=CC=C(N)C=C1 ICNFHJVPAJKPHW-UHFFFAOYSA-N 0.000 abstract 1
- 241000416162 Astragalus gummifer Species 0.000 abstract 1
- 150000000703 Cerium Chemical class 0.000 abstract 1
- 229910004664 Cerium(III) chloride Inorganic materials 0.000 abstract 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 abstract 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 229940099408 Oxidizing agent Drugs 0.000 abstract 1
- 239000004285 Potassium sulphite Substances 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- 229920001615 Tragacanth Polymers 0.000 abstract 1
- 235000011054 acetic acid Nutrition 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- -1 aluminium chloride Chemical class 0.000 abstract 1
- 125000005001 aminoaryl group Chemical group 0.000 abstract 1
- 229910052787 antimony Inorganic materials 0.000 abstract 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- VYLVYHXQOHJDJL-UHFFFAOYSA-K cerium trichloride Chemical compound Cl[Ce](Cl)Cl VYLVYHXQOHJDJL-UHFFFAOYSA-K 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 239000011651 chromium Substances 0.000 abstract 1
- WYYQVWLEPYFFLP-UHFFFAOYSA-K chromium(3+);triacetate Chemical compound [Cr+3].CC([O-])=O.CC([O-])=O.CC([O-])=O WYYQVWLEPYFFLP-UHFFFAOYSA-K 0.000 abstract 1
- 239000003086 colorant Substances 0.000 abstract 1
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 abstract 1
- 125000005265 dialkylamine group Chemical group 0.000 abstract 1
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical compound OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 abstract 1
- 238000004043 dyeing Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- 125000005027 hydroxyaryl group Chemical group 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical class CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 abstract 1
- 235000014655 lactic acid Nutrition 0.000 abstract 1
- 150000004988 m-phenylenediamines Chemical class 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- IBKQQKPQRYUGBJ-UHFFFAOYSA-N methyl gallate Natural products CC(=O)C1=CC(O)=C(O)C(O)=C1 IBKQQKPQRYUGBJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 150000004780 naphthols Chemical class 0.000 abstract 1
- 150000005002 naphthylamines Chemical class 0.000 abstract 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 abstract 1
- 239000007800 oxidant agent Substances 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 abstract 1
- 235000019252 potassium sulphite Nutrition 0.000 abstract 1
- 230000002035 prolonged effect Effects 0.000 abstract 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 1
- 229960001755 resorcinol Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000344 soap Substances 0.000 abstract 1
- 238000010025 steaming Methods 0.000 abstract 1
- 230000008719 thickening Effects 0.000 abstract 1
- 239000002562 thickening agent Substances 0.000 abstract 1
- 235000010487 tragacanth Nutrition 0.000 abstract 1
- 239000000196 tragacanth Substances 0.000 abstract 1
- 229940116362 tragacanth Drugs 0.000 abstract 1
- 235000013311 vegetables Nutrition 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 229940124024 weight reducing agent Drugs 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
Landscapes
- Coloring (AREA)
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.
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)
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 |
-
1904
- 1904-10-27 GB GB190423193D patent/GB190423193A/en not_active Expired
Cited By (5)
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 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4149849A (en) | Process for printing and dyeing | |
US2995412A (en) | Process for dyeing and printing of textile materials containing hydroxyl groups | |
GB190423193A (en) | Manufacture of Blue and Violet to Black Dyestuffs by Oxidation on the Fibre. | |
US2146646A (en) | Vat dyestuff printing | |
US2095600A (en) | Process for the production of fast tints on the fiber | |
US2069215A (en) | Printing process and composition therefor | |
US2184495A (en) | Printing assistant | |
DE2837500A1 (en) | METHOD FOR COLORING CELLULOSE-CONTAINING TEXTILE MATERIAL AND NEW DYES | |
US2428836A (en) | Printing of cellulose acetate | |
US4032291A (en) | Phenyl phthalate carriers in dyeing and printing synthetic fibers | |
US3679358A (en) | Process for the dyeing or printing of textile materials made from polymers or copolymers of acrylonitrile | |
US3012843A (en) | Process for the coloration of linear polyester fibres with new azo dyestuffs | |
US4013405A (en) | Aqueous printing pastes for producing transfer printing papers by rotary screen printing | |
US2053274A (en) | Production and use of dyestuffs | |
US3857676A (en) | Process for the printing and continuous fixing of disperse dyestuffs on polyester, cellulose-triacetate, cellulose-2{178 -acetate and mixtures thereof | |
US796715A (en) | Process of dyeing violet to black. | |
US3342542A (en) | Ho o nhx c chax c chjx o oh | |
JPS5714654A (en) | Dyeing of cellulosic fiber | |
US2093402A (en) | Printing and dyeing compositions and processes | |
US2292436A (en) | Dyeing | |
US3043647A (en) | Colouring of polyester fiberes | |
US2205032A (en) | Dye compositions | |
DE1928372B2 (en) | Water-insoluble monoazo dyes, process for their preparation and their use for dyeing and printing | |
US3207569A (en) | Mixture of anthraquinone and azo dyes, dyeing ester type textiles therewith and the dyed textiles from said process | |
US2008966A (en) | Process and composition for applying and fixing dyestuff |