4.7 Article

Sorption fractionation of bacterial extracellular polymeric substances (EPS) on mineral surfaces and associated effects on phenanthrene sorption to EPS-mineral complexes

Journal

CHEMOSPHERE
Volume 263, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2020.128264

Keywords

Phenanthrene; Mineral surfaces; Extracellular polymeric substances; Fractionation; Preferential sorption

Funding

  1. National Natural Science Foundation of China [21777002, 21920102002, 41991331]
  2. National Key Research and Development Program of China [2019YFC1804200]

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Microbial EPS are an important source of labile component in natural organic matter, and their sorption behavior to mineral surfaces can significantly affect the sorption of hydrophobic organic contaminants. The type and surface properties of minerals, as well as the biological source of EPS, play key roles in sorption fractionation of EPS on minerals and ultimately impact the sorption affinity of apolar HOCs to EPS-mineral complexes.EPS-mineral complexes exhibited larger sorption coefficients than pristine EPS, indicating that sorptive interactions were facilitated by sorbed EPS on mineral surfaces.
Microbial extracellular polymeric substances (EPS) represent an important source of labile component in natural organic matter (NOM) pool. However, the sorption behavior of EPS to mineral surfaces and associated effects on sorption of hydrophobic organic contaminants (HOCs) are not well understood. Here, we systematically investigated the fractionation of EPS extracted from two different microbial sources (Gram-positive B. subtilis and Gram-negative E. coli) during sorption to montmorillonite, kaolinite, and goethite using collective characterization methods (SEM, electrophoretic mobility, FTIR, H-1 NMR, UV-vis, fluorescence, and size exclusion chromatography). The peptide-like substances and acidic components with high aromaticity in B. subtilis EPS were more preferentially sorbed than those fractions in E. coli EPS by the three minerals, especially by goethite. Additionally, goethite sorbed more negatively charged and lower molecular weight fractions compared to montmorillonite. The presorption of EPS (1.68-3.79% organic carbon) on the three minerals increased the sorption distribution coefficient (K-d) of phenanthrene (a model apolar HOC) by 2.83-5.29 times, depending on the EPS-mineral complex. All the six examined EPS-mineral complexes exhibited approximately one order of magnitude larger organic carbon (OC)-normalized sorption coefficient (K-OC) than the two pristine EPS, indicating that the sorptive interactions were pronouncedly facilitated by the sorbed EPS on mineral surfaces. Thus, the type and surface property of minerals as well as the biological source of EPS are key determinants of sorption fractionation of EPS on minerals and in turn affect sorption affinity of apolar HOCs to EPS-mineral complexes. (C) 2020 Elsevier Ltd. All rights reserved.

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