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Beyenal, Haluk; Sani, Rajesh K.; Peyton, Brent M.; Dohnalkova, Alice; Amonette, James E.; Lewandowski, Zbigniew
Pacific Northwest National Lab., Richland, WA (United States). Environmental Molecular Sciences Laboratory. Funding organisation: US Department of Energy (United States)2004
Pacific Northwest National Lab., Richland, WA (United States). Environmental Molecular Sciences Laboratory. Funding organisation: US Department of Energy (United States)2004
AbstractAbstract
[en] Hexavalent uranium [U(VI)] was immobilized using biofilms of the sulfate-reducing bacterium (SRB) Desulfovibrio desulfuricans G20. The biofilms were grown in flat-plate continuous-flow reactors using lactate as the electron donor and sulfate as the electron acceptor. U(VI) was continuously fed into the reactor for 32 weeks at a concentration of 126 ?M. During this time, the soluble U(VI) was removed (between 88 and 96% of feed) from solution and immobilized in the biofilms. The dynamics of U immobilization in the sulfate-reducing biofilms were quantified by estimating: (1) microbial activity in the SRB biofilm, defined as the hydrogen sulfide (H2S) production rate and estimated from the H2S concentration profiles measured using microelectrodes across the biofilms; (2) concentration of dissolved U in the solution; and (3) the mass of U precipitated in the biofilm. Results suggest that U was immobilized in the biofilms as a result of two processes: (1) enzymatically and (2) chemically, by reacting with microbially generated H2S. Visual inspection showed that the dissolved sulfide species reacted with U(VI) to produce a black precipitate. Synchrotron-based U L3-edge X-ray absorption near edge structure (XANES) spectroscopy analysis of U precipitated abiotically by sodium sulfide indicated that U(VI) had been reduced to U(IV). Selected-area electron diffraction pattern and crystallographic analysis of transmission electron microscope lattice-fringe images confirmed the structure of precipitated U as being that of uraninite
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Source
PNNL-SA--42569; 4297; 6513; KP1301030; AC--06-76RL01830
Record Type
Journal Article
Journal
Environmental Science and Technology; ISSN 0013-936X; ; v. 38(7); p. 2067-2074
Country of publication
ACTINIDES, BACTERIA, CHALCOGENIDES, CHEMICAL REACTIONS, DECOMPOSITION, ELEMENTS, HYDROGEN COMPOUNDS, MATERIALS, METALS, MICROORGANISMS, MINERALS, OXIDE MINERALS, PHASE TRANSFORMATIONS, RADIOACTIVE MATERIALS, RADIOACTIVE MINERALS, SULFATE-REDUCING BACTERIA, SULFIDES, SULFUR COMPOUNDS, SYNTHESIS, URANIUM MINERALS
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