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In a reactive dye, a chromophore (an atom or group whose presence is responsible for the colour of a compound) contains a substituent that reacts with the substrate. Reactive dyes have good fastness properties owing to the covalent bonding that occurs during dyeing. Reactive dyeing is the most important method for coloring cellulose fibers.
Reactive blue 4 61205 anthraquinone 13324-20-4: BODIPY: Dipyrrometheneboron difluoride 138026-71-8: Brazilin/Brazilein: Natural red 24 75280 natural 474-07-7: Brilliant Black BN: Food Black 1 28440 diazo 2519-30-4: Brilliant blue FCF: Erioglaucine FD&C Blue No. 1 Acid blue 9 Food blue 2 42090 triarylethlamine 3844-45-9: Brilliant cresyl blue ...
If the vinyl sulfone group is introduced via a primary or secondary aliphatic amine, this is performed again by condensation with a halotriazine compound. An example is 2-[2-(2-chlorethylsulfonyl)ethoxy]ethanamine used in bifunctional reactive dyes in combination with a monofluoro or monochlorotriazine hook. [3]
Examples of acid dye are Alizarine Pure Blue B, Acid red 88, etc. Basic dyes are water-soluble cationic dyes that are mainly applied to acrylic fibers, but find some use for wool and silk. Usually acetic acid is added to the dye bath to help the uptake of the dye onto the fiber. Basic dyes are also used in the coloration of paper.
reactive dye Reactive dyes are a class of synthetic dyes that first appeared commercially in 1956, after their invention in 1954 by Rattee and Stephens at the Imperial Chemical Industries Dyestuffs Division site in the United Kingdom. Reactive dyes are used primarily to dye natural fibers and cellulose fibers such as rayon. [39] resist dyeing
Also called direct dyes, substantive dyes are employed for cellulose-based textiles, which includes cotton. The dyes bind to the textile by non-electrostatic forces. In another classification, azo dyes can be classified according to the number of azo groups. Trypan blue is an example of a direct dye, used for cotton.
These dyes, which are chemically similar to vat dyes, are developed by light instead of being applied in an oxygen-free bath and being developed in the fabric by exposure to oxygen. Inkodyes are true dyes, not fabric paints. A dye itself attaches to the fabric; fabric paint includes a glue-like binder, which imparts a stiffer feeling to the fabric.
With amines, one or more chloride is displaced. The remaining chlorides are reactive, and this theme is the basis of the large field of reactive dyes. Cyanuric chloride assists in the amidation of carboxylic acids. [3] The 1,2,4-triazines can react with electron-rich dienophiles in an inverse electron demand Diels-Alder reaction. This forms a ...