Acid black dyes

Acid amide herbicides Acid anhydrides Acid azine dyes Acid-base catalysis Acid-base chemistry Acid Black [1064-48-8]... 

Naphthalenediol. This diol is prepared by the alkah fusion of 2-hydroxynaphthalene-6-sulfonic acid (Schaffer acid) at 290—295°C. Schaffer acid is usually produced by sulfonation of 2-naphthol with the addition of sodium sulfate at 85—105°C. This acid is also used as a coupling component in the production of a2o dyes such as Acid Black 26. 2,6-Naphthalenediol is used as a component in the manufacture of aromatic polyesters which, as is also tme of the corresponding amides, display Hquid crystal characteristics (52). 

Tendering Effects. CeUulosic materials dyed with sulfur black have been known to suffer degradation by acid tendering when stored under moist warm conditions. This effect may result from the Hberation of small quantities of sulfuric acid which occurs when some of the polysulfide links of the sulfur dye are mptured. A buffer, such as sodium acetate, or a dilute alkaH in the final rinse, especially after oxidation in acidic conditions, may prevent this occurrence. Copper salts should never be used with sulfur black dyes because they cataly2e sulfuric acid generation. Few instances of tendering with sulfur dyes other than black occur and the problem is largely confined to cotton. 

Minor uses of vanadium chemicals are preparation of vanadium metal from refined pentoxide or vanadium tetrachloride Hquid-phase organic oxidation reactions, eg, production of aniline black dyes for textile use and printing inks color modifiers in mercury-vapor lamps vanadyl fatty acids as driers in paints and varnish and ammonium or sodium vanadates as corrosion inhibitors in flue-gas scmbbers. 

Dyes in these classes are generally basic dyes ie, the chiomophoie is cationic. Some stmctures have been sulfonated to acid dyes, eg, the Nigrosine, (Cl Solvent Black 5 Cl 50415), (8) to Cl Acid Black 2 [8005-03-6] (Cl 50420) (9). 

Calcocid Blue Black Ex [1064-48-8] (28) (Cl Acid Black 1 Cl 20470) is an unsymmetrical primary disazo dye with bihmctional coupling component (H-acid). 

Another class of metal complex dyes is derived from the formazan stmcture. These dyes are appHed to wool and nylon from a neutral or weakly acidic dyebath analogous to the 2 1 premetallized OjO -dihydroxyazo complexes. The bluish-gray dye Cl Acid Black 180 [11103-91-6] (61) (Cl 13710) is a 2 1 cobalt complex of the formazan type. 

Acid Black 63 [32517-36-5] (Cl 12195) is a typical premera11i2ed dye. The commercial product contains some of the 1 2 chelate shown. 

Acid—mordant dyes have characteristics similar to those of acid dyes which have a relatively low molecular weight, anionic substituents, and an affinity to polyamide fibers and mordant dyes. In general, brilliant shades caimot be obtained by acid—mordant dyes because they are used as their chromium mordant by treatment with dichromate in the course of the dyeing procedure. However, because of their excellent fastness for light and wet treatment, they are predominandy used to dye wool in heavy shades (navy blue, brown, and black). In terms of chemical constitution, most of the acid—mordant dyes are azo dyes some are triphenyhnethane dyes and very few anthraquinone dyes are used in this area. Cl Mordant Black 13 [1324-21 -6] (183) (Cl 63615) is one of the few examples of currentiy produced anthraquinone acid—mordant dyes. It is prepared by condensation of purpurin with aniline in the presence of boric acid, followed by sulfonation and finally by conversion to the sodium salt (146,147). 

Copper and chromium are used for complexing a number of dyes such as the coppered direct and reactive dyes for cotton and metaUi2ed and neutral metal complex acid dyes for nylon, wool, etc. Examples are Direct Blue 218 [28407-37-6] (Cl 24401) (317), Reactive Violet 2 [8063-57-8] (Cl 18157) (318), and Acid Black 52 [5610-64-0] (Cl 15711) (319). 

Ferrous gluconate is a black dye. It is composed of iron bound to two molecules of gluconic acid, which is the acid form of glucose. 

Various methods have been used for the reoxidation of vat leuco dyeings atmospheric skying, hypochlorite, chlorite and acidified dichromate are now rarely employed. Atmospheric oxidation can be difficult to control and thus uneven with some dyes it is also too slow, particularly for continuous methods. Sodium hypochlorite is used only for those few black dyes that tend to become dark green when oxidised with peroxide obviously hypochlorite should be avoided with the many chlorine-sensitive dyes. Similarly sodium chlorite, acidified to below pH 5 with acetic acid, can only be used with certain dyes, although with these it certainly gives rapid oxidation. Dye selectivity is also a drawback with... 

There have also been attempts to obtain a black phthalocyanine dye for ink jet printing. Thus, a patent47 from Nippon Kayaku describes reacting the amino phthalocyanine (59) with acrylic or methacrylic acid to produce the black dyes (60). 

The immobilization of the white rot fungus F. trogii in Na-ALG beads allowed the decolorization of the dye Acid Black 52 in a stirred tank reactor operated in batch [55]. Three enzymes, laccase, MnP, LiP, secreted by fungus were reported during decolorization process. Results showed that laccase enzyme activity increased with increasing alginate concentration from 0 to 4%. Cell growth at immobilized cultivation was maintained more stably than suspended cultivation. Total amount of removed dye was reported to be 469 mg/L for immobilized cultures and 440 mg/L for suspended cultures. 

Continuous culture of immobilized P. chrysosporium on PuF was studied for decolorization of 4 different azo dyes [57]. Acid Black 1, Basic Blue 41, Reactive Black 5, and Reactive Orange 16 (R016) were effectively decolorized depending on the dye concentration. 

Bacterial cells of Oenococcus oeni incubated for 48 h with three azo dyes (Fast red, Fast orange, and Methanil yellow) gave rise to decolorization due to adsorption, from 68% with Fast red to 30% with Fast orange and Methanil yellow [41]. Ozdemir et al. [44] observed a 93.9% decolorization of Acid Black 210 within 24 h by Vibrio harveyi TEMS1, a bioluminescent bacterium isolated from coastal seawater in Turkey. After extraction in methanol of biomass, the major part of the decolorized dye was recovered, indicating that decolorization was mainly due to... 

An inverse relation between the efficiency of decolorization and the dye concentration has frequently been observed. This fact can be ascribed to several factors, the main of which can be considered the toxicity of the dyes at higher concentrations [41, 45, 51-53]. With Reactive Red 3B-A, concentrations from 100 to 2,000 ppm were tested with C. bifermentans [5]. At concentrations less than 200 ppm, 90% decolorization within 12 h was observed, while at very high dye concentration (>1,000 ppm), the decolorization rate decreased. Khalid et al. [54] observed an inverse relationship between the velocity of the decolorization reaction and the dye concentrations between 100 and 500 mg L 1 azo dye (Reactive Black 5, Direct Red 81, Acid Red 88, and Disperse Orange 3) by Shewanella putrefaciens. A decrease in decolorization percentage at a Acid Black 210 initial concentration growing from 100 to 400 ppm was also observed with V. harveyi, but the decrease was low [44]. 

Mordant dyes are notoriously troublesome from the viewpoint of colour matching because the hue of the chromium complex usually differs greatly from that of the unmetallised parent dye (section 5.4.1). If other metal ions are present in the treatment bath or on the fibre during chroming, the colour obtained is likely to differ from that of the pure chromium complex. Certain important chrome dyes, including Cl Mordant Black 11 (3.29) and Black 17 (3.30), are particularly sensitive to traces of iron or copper. The hue of the black dyeings obtained is redder in the presence of copper and browner with iron contamination. The fastness to light and wet treatments may also prove inferior under these conditions. Even certain 1 2 metal-complex acid dyes show similar effects in the presence of these impurities,... 

The same naphthylazo-2-naphthol ligand grouping is present in the 1 1 complex Cl Acid Black 52 (5.53 M = Cr) and its symmetrical 1 2 analogue Black 172 (5.54 M = Cr), which are both widely used in the dyeing of wool. The corresponding 1 1 and 1 2 complexes of trivalent iron (M = Fe) have been synthesised and their properties compared with the... 

Cl Sulphur Black 1, which is produced from the relatively simple intermediate 2,4-dinitrophenol and aqueous sodium polysulphide. A similar product (Cl Sulphur Black 2) is obtained from a mixture of 2,4-dinitrophenol and either picric acid (6.148 X = N02) or picramic acid (6.148 X = NH2). A black dye possessing superior fastness to chlorine when on the fibre (Cl Sulphur Black 11) can be made from the naphthalene intermediate 6.149 by heating it in a solution of sodium polysulphide in butanol. An equivalent reaction using the carbazole intermediate 6.150 gives rise to the reddish blue Cl Vat Blue 43 (Hydron blue). This important compound, which also possesses superior fastness properties, is classified as a sulphurised vat dye because it is normally applied from an alkaline sodium dithionite bath. Interestingly, inclusion of copper(II) sulphate in the sulphurisation of intermediate 6.150 leads to the formation of the bluish black Cl Sulphur Black 4. 

Kinetic studies in sediment/water systems with Direct Red 2, Acid Black 92, Acid Red 4, Acid Red 18, and Direct Yellow 1 lead to linear and biphasic plots of dye loss over time. For all but Direct Yellow I, dye loss was usually preceded by a lag or adaptation phase. Acid Black 92 and Direct Red 2 were transformed completely in less than 24 and 48 hours, respectively, but Acid Yellow 151 and Direct Yellow 1 showed half-lives of greater than 2 years. The rapid initial drop in concentration of all dyes observed, with the exception of Acid Red 18, was presumed to be due to sorption. Tests to determine the effect of pH on... 

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