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Reactions between bacterial exopolymers and goethite: A combined macroscopic and spectroscopic investigation

Authors :
Fang, Linchuan
Cao, Yuanyuan
Huang, Qiaoyun
Walker, Sharon L.
Cai, Peng
Source :
Water Research. Nov2012, Vol. 46 Issue 17, p5613-5620. 8p.
Publication Year :
2012

Abstract

Abstract: The adsorption to goethite of extracellular polymeric substances (EPS) isolated from Pseudomonas putida was investigated using batch adsorption experiments, electrophoretic mobility (EM) measurements, Fourier transform infrared (FTIR) spectroscopy, isothermal titration calorimetry (ITC) and X-ray absorption fine structure (XAFS) spectroscopy. The adsorption of EPS decreased the point of zero charge of goethite from 7.6 to 3.2, suggesting the formation of negatively charged inner-sphere surface complexes. The adsorption isotherms of EPS on goethite conformed to the Langmuir equation. The adsorption energy constant (K) of EPS on goethite was in the sequence of EPS phosphate-containing moieties > nitrogen-containing moieties > carbon-containing moieties, indicating those containing phosphate were the most strongly adsorbed. FTIR showed ligand exchange of phosphate groups of EPS with surface hydroxyls on goethite. Extended X-ray absorption fine structure (EXAFS) and X-ray absorption near edge structure (XANES) spectroscopy results further demonstrated phosphate groups of EPS can form monodentate inner-sphere complexes at lower pH 3.0, while form bidentate inner-sphere complexes at higher pH 9.0. The oxidation state of iron in goethite was not changed after the reaction with EPS at different pH values. The information obtained in this study is of fundamental significance for the understanding of the interaction mechanisms between bacteria and minerals in soil and aquatic environments. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00431354
Volume :
46
Issue :
17
Database :
Academic Search Index
Journal :
Water Research
Publication Type :
Academic Journal
Accession number :
79804090
Full Text :
https://doi.org/10.1016/j.watres.2012.07.046