A vat dye is a type of dye that can be dyed after reduction. They are insoluble in water. The molecule contains two or more carbonyl groups. Under the action of the alkali solution of the powder, the carbonyl group is reduced to a hydroxyl group to dissolve the dye in the alkali solution, so that the dye has an affinity for the cellulose and dyes the fiber, and then passes through the air or the oxidant. Oxidation, and then restored to the original insoluble dye fixed to the fiber. The vat dyes are classified into an anthraquinone dye and an anthraquinone dye according to the structure, among which the anthraquinone dyes are various. The vat dye is the most fast of all dyes, and the chromatogram is complete and the color is bright, which is second only to the basic dye. It can be used for dyeing and printing cotton, linen and viscose. A strong base must be used for the reduction of the vat dye, which is not suitable for the dyeing of protein fibers such as wool and silk, and the leveling property is poor. Therefore, the leuco body of some vat dyes is made into a stable water-soluble sulfate and dyed in water, and then hydrolyzed by dilute acid and reoxidized to a vat to fix on the fiber. Such dye is called soluble reduction. dye. Soluble vat dyes do not use strong alkali in the process, can dye wool, silk and other protein fibers, and the leveling is good, but the price is more expensive, and can only be used to dye medium or light color, difficult to dye dark. The vat dye has a long history. The Han Ma Tomb Ma Wang piled out the linen fabric and dyed with the plant vat dye indigo. Indigo, which is present in the form of a glycoside in plants, is leached with water and can be obtained by fermentation, hydrolysis, and oxidation. From 1870 to 1883, Bayer (AVBayer) analyzed the structure of indigo and synthesized it. In 1890, K. Heumann proposed the industrial production method. In 1897, BASF produced the first indigo dyes. In 1901, BeneBohn developed the important blue quinone vat dye linketone-indanthrene. Later, sulfur sulfonium and reduced green XBN were synthesized. By the 1930s, the basic color of these pigments was complete, and it became a commonly used dye in modern printing and dyeing factories. The vat dyes have various fastnesses. After the successful development of reactive dyes, although some of them are replaced by this dye, it is still a very important dye variety for printing and dyeing cellulose fiber textiles. The vat dye can also be used for vinylon dyeing. Some vat dyes are used as disperse dyes for dyeing polyester fibers.
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Amino compound
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Oxy-containing amino compound
Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts thereof
Acyclic monoamines, polyamines and their derivatives and salts
Amide compound
Sulfonic acid amino compound
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Alcohols, phenols, phenolic compounds and derivatives
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2-cycloalcohol
Halogenated, sulfonated, nitrated or nitrosated derivatives of alcohols
Extremely halogenated, sulfonated, nitrated or nitrosated derivatives of phenols
Phenol and its halogenated, sulfonated, nitrated or nitrosated derivatives
Acyclic alcohol
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Nitrogen-containing compound
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Nitrile compound
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Organic derivative of hydrazine or hydrazine
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Terpenoid
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Ether compounds and their derivatives
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Ether, ether alcohol
Halogenation, sulfonation, nitration or nitrosation of ethers, ether alcohols, ether phenols
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Aldehyde
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Carboxylic compounds and derivatives
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Cyclic carboxylic acid
Halogenation, sulfonation, nitration or nitrosation of carboxylic acids
Halogenation, sulfonation, nitration or nitration of carboxylic anhydrides
Carboxylic acid halide
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Salt of carboxylic acid ester and its derivatives
Acyclic carboxylic acid
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Hydrocarbon compounds and their derivatives
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Aromatic hydrocarbon
Cyclic hydrocarbon
Hydrocarbon sulfonate
Hydrocarbon halide
Hydrocarbon nitrite
Acyclic hydrocarbon
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Ketone compound
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Alkyl ureas and their derivatives and salts
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Inorganic acid ester
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Heterocyclic compound
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Diazo, azo or azo compound
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Organosilicon compound
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Organometallic compound
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Organic palladium
Organic germanium, cobalt, strontium, barium, gallium, germanium, germanium, germanium, germanium, etc.
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Organotin
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Organotin
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Organic
Organic germanium, mercury, silver, platinum, etc.
Organic germanium, antimony, bismuth, tungsten, antimony, bismuth, lead, vanadium, molybdenum, chromium, antimony, etc.
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Organic sulfur compound
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Organic phosphine compound
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Organometallic salt
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Organic fluorine compound
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Fluorobenzoic acid series
Fluorobenzonitrile series
Fluorobenzaldehyde series
Fluorobenzyl alcohol series
Fluoroanisole series
Fluoroaniline series
Fluorophenylacetic acid series
Fluorophenol series
Fluorobenzoic acid series
Fluoronitrobenzene series
Fluoropyridine series
Potassium fluoroborate series
Fluorobenzyl alcohol series
Fluorotoluene series
Fluorine red series
Fluoroethane series
Fluoropropane series