Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.jcis.2009.03.088
Title: Spectroscopic study of Zn2+ and Co2+ binding to extracellular polymeric substances (EPS) from aerobic granules
Authors: Sun, X.-F.
Wang, S.-G.
Zhang, X.-M.
Paul Chen, J. 
Li, X.-M.
Gao, B.-Y.
Ma, Y.
Keywords: Aerobic granules
Bind
Extracellular polymeric substances (EPS)
Metal ions
XPS analysis
Issue Date: 1-Jul-2009
Citation: Sun, X.-F., Wang, S.-G., Zhang, X.-M., Paul Chen, J., Li, X.-M., Gao, B.-Y., Ma, Y. (2009-07-01). Spectroscopic study of Zn2+ and Co2+ binding to extracellular polymeric substances (EPS) from aerobic granules. Journal of Colloid and Interface Science 335 (1) : 11-17. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jcis.2009.03.088
Abstract: The interacting mechanisms of metallic cations (Zn2+ and Co2+) to active chemical groups on the extracellular polymeric substances (EPS) of the aerobic granules, including loosely bound EPS (LB-EPS) and tightly bound EPS (TB-EPS), were examined by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) spectroscopy. For Zn2+ and Co2+, LB-EPS showed stronger binding properties than TB-EPS and the process of them was described well by the Langmuir isotherm. Compared to the single-metal system, binary-metal addition induced competitive binding between the Zn2+ and Co2+ with reduction of the maximal binding capacity for both EPS. The main chemical groups involved in the interactions between contaminants were apparently alcohol, carboxyl and amino. These groups were part of the EPS structural polymers, namely, polysaccharides, proteins, and hydrocarbon-like products. When biosorption and flocculation occurred at the same time, the LB-EPS were used not only as chelate sorbents but also as flocculants to further enhance their sorption capacity. © 2009 Elsevier Inc. All rights reserved.
Source Title: Journal of Colloid and Interface Science
URI: http://scholarbank.nus.edu.sg/handle/10635/87643
ISSN: 00219797
DOI: 10.1016/j.jcis.2009.03.088
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