The biogeochemistry and bioremediation of uranium and other priority radionuclides

被引:350
作者
Newsome, Laura [1 ]
Morris, Katherine
Lloyd, Jonathan R.
机构
[1] Univ Manchester, Sch Earth Atmospher & Environm Sci, Res Ctr Radwaste & Decommissioning, Manchester M13 9PL, Lancs, England
关键词
Biostimulation; Microorganisms; Metal reduction; Electron transport; In situ; Nuclear; MICROBIAL COMMUNITY STRUCTURE; SULFATE-REDUCING BACTERIA; IN-SITU BIOREMEDIATION; C-TYPE CYTOCHROMES; X-RAY-ABSORPTION; EXTRACELLULAR ELECTRON-TRANSFER; ENZYMATICALLY-MEDIATED GROWTH; DISSIMILATORY IRON REDUCTION; HIGHLY CONTAMINATED AQUIFER; HEAVY-METAL ACCUMULATION;
D O I
10.1016/j.chemgeo.2013.10.034
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Microbial metabolism has the potential to alter the solubility of a broad range of priority radionuclides, including uranium, other actinides and fission products. Of notable interest has been the biostimulation of anaerobic microbial communities to remove redox-sensitive radionuclides such as uranium U(VI) from contaminated groundwaters at nuclear sites. Particularly promising are bioreduction processes, whereby bacteria enzymatically reduce aqueous U(VI) to insoluble U(IV) coupled to oxidation of an organic electron donor; and uranium phosphate biomineralisation, in which bacterial phosphatase activity cleaves organophosphates, liberating inorganic phosphate that precipitates with aqueous U(VI) as uranyl phosphate minerals. Here we review the mechanisms of uranium bioreduction and phosphate biomineralisation and their suitability to facilitate long-term precipitation of uranium from groundwater, with particular focus on in situ trials at the US Department of Energy field sites. Redox interactions of other priority radionuclides (technetium, neptunium, plutonium, americium, iodine, strontium and caesium) are also reviewed. (C) 2013 The Authors. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 184
页数:21
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