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Component analysis and heavy metal adsorption ability of extracellular polymeric substances (EPS) from sulfate reducing bacteria
•SRB EPS included carboxyl, thiol/phosphate, amino/hydroxyl functional groups.•Heavy metals had no effect on the type of functional groups of the EPS samples.•Heavy metals increased the concentrations of the surface functional groups.•EPS extracted from the Zn2+-dosed system had a higher binding aff...
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Published in: | Bioresource technology 2015-10, Vol.194, p.399-402 |
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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: | •SRB EPS included carboxyl, thiol/phosphate, amino/hydroxyl functional groups.•Heavy metals had no effect on the type of functional groups of the EPS samples.•Heavy metals increased the concentrations of the surface functional groups.•EPS extracted from the Zn2+-dosed system had a higher binding affinity.•Zn2+ could decrease the toxic effects of Cu2+ and Cd2+ on the SRB.
Extracellular polymeric substances (EPS) play an important role in the treatment of acid mine drainage (AMD) by sulfate-reducing bacteria (SRB). In this paper, Desulfovibrio desulfuricans was used as the test strain to explore the effect of heavy metals on the components and adsorption ability of EPS. Fourier-transform infrared (FTIR) spectroscopy analysis results showed that heavy metals did not influence the type of functional groups of EPS. Potentiometric titration results indicated that the acidic constants (pKa) of the EPS fell into three ranges of 3.5–4.0, 5.9–6.7, and 8.9–9.8. The adsorption site concentrations of the surface functional groups also increased. Adsorption results suggested that EPS had a specific binding affinity for the dosed heavy metal, and that EPS extracted from the Zn2+-dosed system had a higher binding affinity for all heavy metals. Additionally, Zn2+ decreased the inhibitory effects of Cd2+ and Cu2+ on the SRB. |
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ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2015.07.042 |