Speciation of uranium in sediments before and after in situ biostimulation

被引:98
作者
Kelly, Shelly D. [1 ]
Kemner, Kenneth M. [1 ]
Carley, Jack [2 ]
Criddle, Craig [3 ]
Jardine, Phillip M. [2 ]
Marsh, Terence L. [4 ]
Phillips, Debra [5 ]
Watson, David [2 ]
Wu, Wei-Min [3 ]
机构
[1] Argonne Natl Lab, Biosci Div, Argonne, IL 60439 USA
[2] Oak Ridge Natl Lab, Div Environm Sci, Oak Ridge, TN 37831 USA
[3] Stanford Univ, Dept Civil & Environm Engn, Stanford, CA 94305 USA
[4] Michigan State Univ, E Lansing, MI 48824 USA
[5] Queens Univ Belfast, Environm Engn Res Ctr, Sch Planning Architecture & Civil Engn, Belfast BT9 5AG, Antrim, North Ireland
关键词
D O I
10.1021/es071764i
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The success of sequestration-based remediation strategies will depend on detailed information, including the predominant U species present as sources before biostimulation and the products produced during and after in situ biostimulation. We used X-ray absorption spectroscopy to determine the valence state and chemical speciation of U in sediment samples collected at a variety of depths through the contaminant plume at the Field Research Center at Oak Ridge, TN, before and after approximately 400 days of in situ biostimulation, as well as in duplicate bioreduced sediments after 363 days of resting conditions. The results indicate that U(VI) in subsurface sediments was partially reduced to 10-40% U(IV) during biostimulation. After biostimulation, U was no longer bound to carbon ligands and was adsorbed to Fe/Mn minerals. Reduction of 01) to U(IV) continued in sediment samples stored under anaerobic condition at < 4 degrees C for 12 months, with the fraction of U(IV) in sediments more than doubling and U concentrations in the aqueous phase decreasing from 0.5-0.74 to < 0.1 mu M. A shift of uranyl species from uranyl bound to phosphorus ligands to uranyl bound to carbon ligands and the formation of nanoparticulate uraninite occurred in the sediment samples during storage.
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页码:1558 / 1564
页数:7
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