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Influence of redox mediators and salinity level on the (bio)transformation of Direct Blue 71: kinetics aspects
The rate-limiting step of azo dye decolorization was elucidated by exploring the microbial reduction of a model quinone and the chemical decolorization by previously reduced quinone at different salinity conditions (2–8%). Microbial experiments were performed in batch with a marine consortium. The d...
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Published in: | Journal of environmental management 2016-12, Vol.183, p.84-89 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The rate-limiting step of azo dye decolorization was elucidated by exploring the microbial reduction of a model quinone and the chemical decolorization by previously reduced quinone at different salinity conditions (2–8%). Microbial experiments were performed in batch with a marine consortium. The decolorization of Direct Blue 71 (DB71) by the marine consortium at 2% salinity, mediated with anthraquinone-2,6-disulfonate (AQDS), showed the highest rate of decolorization as compared with those obtained with riboflavin, and two samples of humic acids. Moreover, the incubations at different salinity conditions (0–8%) performed with AQDS showed that the highest rate of decolorization of DB71 by the marine consortium occurred at 2% and 4% salinity. In addition, the highest microbial reduction rate of AQDS occurred in incubations at 0%, 2%, and 4% of salinity. The chemical reduction of DB71 by reduced AQDS occurred in two stages and proceeded faster at 4% and 6% salinity. The results indicate that the rate-limiting step during azo decolorization was the microbial reduction of AQDS.
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•A marine consortium uses humic substances as redox mediators for azo dye treatment.•Azo dye reduction was evaluated at different salt conditions using redox mediators.•The rate limiting step of azo dye reduction is the microbial reduction of AQDS. |
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ISSN: | 0301-4797 1095-8630 |
DOI: | 10.1016/j.jenvman.2016.08.044 |