4.8 Article

Hexavalent Chromium Generation within Naturally Structured Soils and Sediments

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 51, Issue 4, Pages 2058-2067

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.6b04039

Keywords

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Funding

  1. National Science Foundation [DGE-114747]
  2. US Department of Energy (DOE) Office of Science, Office of Biological and Environmental Research (BER), through the SLAC National Accelerator Laboratory scientific focus area (SEA) [DE-AC02-76SF00515]

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Chromium(VI) produced from the oxidation of indigenous Cr(III) minerals is increasingly being recognized as a threat to groundwater quality. A critical determinant of Cr(VI) generation within soils and sediments is the necessary interaction of two low-solubility phases Cr(III) silicates or (hydr)oxides and Mn(III/IV) oxides that lead to its production. Here we investigate the potential for Cr(III) oxidation by Mn oxides within fixed solid matrices common to soils and sediments. Artificial aggregates were constructed from Cr(OH)(3)(-) and Cr0.25Fe0.75(OH)(3)-coated quartz grains and either mixed with synthetic birnessite or inoculated with the Mn(II)-oxidizing bacterium Leptothrix cholodnii. In aggregates simulating low organic carbon environments, we observe Cr(VI) concentrations within advecting solutes at levels more than twenty-times the California drinking water standard. Chromium(VI) production is highly dependent on Crmineral solubility; increasing Fe-substitution (x = 0 to x = 0.75) decreases the solubility of the solid and concomitantly decreases total Cr(VI) generation by 37%. In environments with high organic carbon, reducing conditions within aggregate cores (microbially) generate sufficient Fe(II) to suppress Cr(VI) efflux. Our results illustrate Cr(VI) generation from reaction with Mn oxides within structured media simulating soils and sediments and provide insight into how fluctuating hydrologic and redox conditions impact coupled processes controlling Cr and Mn cycling.

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