See S. Robinson, The History of Dyed Textiles (1970); H. Zollinger, Color Chemistry: Syntheses, Properties, and Applications of Organic Dyes and Pigments (1987); D. R. Waring and G. Hallas, ed., The Chemistry and Application of Dyes (1989).
Any of a class of intensely coloured complex organic compounds used to colour textiles, leather, paper, and other materials. Dyes known to the ancients came from plants such as indigo and madder (see madder family) or from the shells of mollusks; today most dyes are made from coal tar and petrochemicals. The chemical structure of dyes is relatively easy to modify, so many new colours and types of dyes have been synthesized. Dye molecules are deposited from solution onto materials in such a way that they cannot be removed by the original solvent. Fibre-reactive dyes form a covalent bond with the fibre. Other dyes require prior application of a mordant, an inorganic material that causes the dye to precipitate as an insoluble salt. Another technique is vat dyeing, in which a soluble colourless compound is absorbed by the fibres, then oxidized (see oxidation-reduction) to the insoluble coloured compound, making it remarkably resistant to the fading effects of washing, light, and chemicals. Seealso azo dye.
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Any of a large class of synthetic organic compounds, dyes containing two nitrogen atoms joined by a double bond (see bonding, covalent bond) in the form singlehorzbondNdoublehorzbondNsinglehorzbond as part of their molecular structure. More than half the dyes in commercial use are azo dyes. They are usually classed according to the fibres for which they are useful or the methods by which they are applied; direct dyes are absorbed from solution by the fibres, but others require a second solution (a mordant) or a second step before the colour is fast.
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