Anthraquinone compounds as redox mediators for enhanced continuous-flow anaerobic biotransformation of reactive dyes under hypersaline conditions

Authors
Lee, Young H.Bottomley, Lawrence A.Pavlostathis, Spyros G.
Issue Date
2011-09
Publisher
TAYLOR & FRANCIS INC
Citation
DESALINATION AND WATER TREATMENT, v.33, no.1-3, pp.68 - 76
Abstract
The effect of anthraquinone disulfonate (AQDS) on the decolorization of the azo dye Reactive Red 198 (RR198) and the anthraquinone dye Reactive Blue 4 (RB4), as well as the effect of RB4 on the decolorization of RR198, both AQDS and RB4 serving as redox mediators, was assessed. An anaerobic, continuous-flow, fluidized-bed bioreactor with an immobilized halotolerant mixed culture was used in this study. All tests were performed at a reactor temperature of 35 degrees C, a hydraulic retention time of 6.1 h, pH 7.2 +/- 0.1, with glucose used as the carbon and electron source. AQDS at relatively low influent concentrations (10-150 mu M) enhanced the extent of RR198 reduction, but had a negligible effect on the biodecolorization of RB4. At an equal concentration of 50 mu M, RB4 and AQDS had a similar enhancing effect on the biodecolorization of the azo dye RR198. Therefore, anthraquinone dyes can serve as redox mediators in mixed, spent textile dyebaths potentially leading to enhanced reductive biodecolorization rate and extent of other types of dyes (i.e., azo dyes).
Keywords
OXIDATION-REDUCTION CONDITIONS; AZO DYES; METHANOGENIC CONDITIONS; BIOLOGICAL DECOLORIZATION; THERMOPHILIC 55-DEGREES-C; MESOPHILIC 30-DEGREES-C; TEXTILE WASTEWATERS; BIODECOLORIZATION; TRANSFORMATION; TOXICITY; OXIDATION-REDUCTION CONDITIONS; AZO DYES; METHANOGENIC CONDITIONS; BIOLOGICAL DECOLORIZATION; THERMOPHILIC 55-DEGREES-C; MESOPHILIC 30-DEGREES-C; TEXTILE WASTEWATERS; BIODECOLORIZATION; TRANSFORMATION; TOXICITY; Textile dyes; Decolorization; Redox mediators; Fluidized-bed bioreactor; Salt
ISSN
1944-3994
URI
https://pubs.kist.re.kr/handle/201004/130016
DOI
10.5004/dwt.2011.2619
Appears in Collections:
KIST Article > 2011
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