Environ. Sci. Technol., 38 (7), 2067 -2074, 2004. 10.1021/es0348703 S0013-936X(03)04870-3
Web Release Date: February 25, 2004

Copyright © 2004 American Chemical Society

Uranium Immobilization by Sulfate-Reducing Biofilms

Haluk Beyenal, Rajesh K. Sani, Brent M. Peyton, Alice C. Dohnalkova, James E. Amonette, and Zbigniew Lewandowski*

Center for Biofilm Engineering and Department of Civil Engineering, Montana State University, Bozeman, Montana 59717-3980, Department of Chemical Engineering, Center for Multiphase Environmental Research, Washington State University, Dana Hall Room 118, Pullman, Washington 99164-2710, and Fundamental Science Directorate, Pacific Northwest National Laboratory, P.O. Box 999, K8-96, 3335 Q Avenue, Richland, Washington 99352

Received for review August 5, 2003

Revised manuscript received January 14, 2004

Accepted January 16, 2004

Abstract:

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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