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Fate of Uranium During Transport Across the Groundwater-Surface Water Interface

Technical Report ·
DOI:https://doi.org/10.2172/1367535· OSTI ID:1367535
 [1];  [2]
  1. Princeton Univ., NJ (United States); Princeton University
  2. Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)
Discharge of contaminated groundwater to surface waters is of concern at many DOE facilities. For example, at F-Area and TNX-Area on the Savannah River Site, contaminated groundwater, including uranium, is already discharging into natural wetlands. It is at this interface where contaminants come into contact with the biosphere. These this research addressed a critical knowledge gap focusing on the geochemistry of uranium (or for that matter, any redox-active contaminant) in wetland systems. Understanding the interactions between hydrological, microbial, and chemical processes will make it possible to provide a more accurate conceptual and quantitative understanding of radionuclide fate and transport under these unique conditions. Understanding these processes will permit better long-term management and the necessary technical justification for invoking Monitored Natural Attenuation of contaminated wetland areas. Specifically, this research did provide new insights on how plant-induced alterations to the sediment biogeochemical processes affect the key uranium reducing microorganisms, the uranium reduction, its spatial distribution, the speciation of the immobilized uranium, and its long-term stability. This was achieved by conducting laboratory mesocosm wetland experiments as well as field measurements at the SRNL. Results have shown that uranium can be immobilized in wetland systems. To a degree some of the soluble U(VI) was reduced to insoluble U(IV), but the majority of the immobilized U was incorporated into iron oxyhydroxides that precipitated onto the root surfaces of wetland plants. This U was immobilized mostly as U(VI). Because it was immobilized in its oxidized form, results showed that dry spells, resulting in the lowering of the water table and the exposure of the U to oxic conditions, did not result in U remobilization.
Research Organization:
Princeton Univ., NJ (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Biological and Environmental Research (BER) (SC-23)
DOE Contract Number:
SC0006847
OSTI ID:
1367535
Report Number(s):
DOE-Princeton--SC0006847
Country of Publication:
United States
Language:
English

References (7)

Unique Organic Matter and Microbial Properties in the Rhizosphere of a Wetland Soil journal April 2016
Iron mineralogy and uranium-binding environment in the rhizosphere of a wetland soil journal November 2016
Uranium fate in wetland mesocosms: Effects of plants at two iron loadings with different pH values journal November 2016
Spectroscopic Evidence of Uranium Immobilization in Acidic Wetlands by Natural Organic Matter and Plant Roots journal February 2015
In situ porewater uranium concentrations in a contaminated wetland: Effect of seasons and sediment depth journal October 2017
Biological reduction of uranium coupled with oxidation of ammonium by Acidimicrobiaceae bacterium A6 under iron reducing conditions journal November 2015
Uranium Immobilization in an Iron-Rich Rhizosphere of a Native Wetland Plant from the Savannah River Site under Reducing Conditions journal July 2014

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