Environmental Engineering Reference
In-Depth Information
Anthraquinone
Drimarene Blue K
2
RL
Remazol Brilliant Blue R (RBBR)
Reactive Blue 4 (RB4)
Reactive Blue 19 (RB19)
Fig. 1 Chemical structure of anthraquinone and its derivatives
chromophore of reactive dyes. However, anthraquinone dyes are derived from
anthraquinone having a quinoid ring as the chromophore. It may also contain
hydroxyl groups or amino groups in their general structure acting as a chromophore
(Fig.
1
). Anthraquinone dyes are not only resistant to microbial degradation but also
toxic, carcinogenic and mutagenic in nature (Itoh et al.
1996
). During decoloriza-
tion, anthraquinone dyes get converted into a very harmful compound,
i.e.,
benzidine.
Since synthetic dyes are generally very recalcitrant in nature, they can
tbe
removed by conventional wastewater treatments, such as adsorption, photooxida-
tion, coagulation,
'
occulation, photo and chemical degradation. The chemical
methods produce toxic compounds by the cleavage of chromophoric groups present
in the dye which is a major disadvantage associated with this method (Robinson
et al.
2001
). However, the biological treatment is often economical and eco-friendly
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