Multi-scale investigation of uranium attenuation by arsenic at an abandoned uranium mine, South Terras

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作者
Claire L. Corkhill
Daniel E. Crean
Daniel J. Bailey
Carmen Makepeace
Martin C. Stennett
Ryan Tappero
Daniel Grolimund
Neil C. Hyatt
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[1] The University of Sheffield,Department of Materials Science and Engineering, NucleUS Immobilisation Science Laboratory
[2] Atomic Weapons Establishment plc,Photon Sciences Directorate
[3] Brookhaven National Laboratory,Swiss Light Source
[4] Paul Scherrer Institute,undefined
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Detailed mineralogical analysis of soils from the UK’s historical uranium mine, South Terras, was performed to elucidate the mechanisms of uranium degradation and migration in the 86 years since abandonment. Soils were sampled from the surface (0–2 cm) and near-surface (25 cm) in two distinct areas of ore processing activities. Bulk soil analysis revealed the presence of high concentrations of uranium (<1690 p.p.m.), arsenic (1830 p.p.m.) and beryllium (~250 p.p.m.), suggesting pedogenic weathering of the country rock and ore extraction processes to be the mechanisms of uranium ore degradation. Micro-focus XRF analysis indicated the association of uranium with arsenic, phosphate and copper; µ-XRD data confirmed the presence of the uranyl-arsenate minerals metazeunerite (Cu(UO2)2(AsO4)2·8H2O) and metatorbernite (Cu(UO2)2(PO4)2·8H2O) to be ubiquitous. Our data are consistent with the solid solution of these two uranyl-mica minerals, not previously observed at uranium-contaminated sites. Crystallites of uranyl-mica minerals were observed to coat particles of jarosite and muscovite, suggesting that the mobility of uranium from degraded ores is attenuated by co-precipitation with arsenic and phosphate, which was not previously considered at this site.
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