Arsenic and iron speciation in uranium mine tailings using X-ray absorption spectroscopy

2013 ◽  
Vol 28 ◽  
pp. 11-18 ◽  
Author(s):  
Joseph Essilfie-Dughan ◽  
M. Jim Hendry ◽  
Jeff Warner ◽  
Tom Kotzer
2011 ◽  
Vol 45 (2) ◽  
pp. 455-460 ◽  
Author(s):  
Joseph Essilfie-Dughan ◽  
Ingrid J. Pickering ◽  
M. Jim Hendry ◽  
Graham N. George ◽  
Tom Kotzer

Atmosphere ◽  
2020 ◽  
Vol 11 (7) ◽  
pp. 735
Author(s):  
Chiara Petroselli ◽  
Beatrice Moroni ◽  
Stefano Crocchianti ◽  
Roberta Selvaggi ◽  
Francesco Soggia ◽  
...  

In this work, we applied X-ray Absorption Spectroscopy (XAS) and selective leaching experiments for investigating iron speciation in different dust advections collected on different unwashed quartz fiber filters. XAS analysis evidenced a predominance of Fe(III) in 6-fold coordination for Saharan dust and a trend towards Fe(II) and 4-fold coordination in the order: Saharan dust, mixed Saharan, and non-Saharan aerosol samples. The role of the sampling substrate was evaluated explicitly, including in the analysis a set of blank filters. We were able to pinpoint the possible contribution to the overall XAS spectrum of the residual Fe on quartz as the concentration decrease towards the blank value. In particular, the filter substrate showed a negligible effect on the structural trend mentioned above. Furthermore, selective leaching experiments evidenced a predominance of the residual fraction on Fe speciation and indicated the lowest Fe concentrations for which the blank contribution is <20% are 1 μ g for the first three steps of the procedure (releasing the acid-labile, reducible and oxidizable phases, respectively) and 10 μ g for the last step (dissolving the insoluble residuals).


1998 ◽  
Vol 83 (5-6) ◽  
pp. 553-568 ◽  
Author(s):  
Andrea L. Foster ◽  
Gordon E. Brown ◽  
Tracy N. Tingle ◽  
George A. Parks

2008 ◽  
Vol 35 (5) ◽  
pp. 1317-1328 ◽  
Author(s):  
K.M. Wetherall ◽  
R.M. Moss ◽  
A.M. Jones ◽  
A.D. Smith ◽  
T. Skinner ◽  
...  

2014 ◽  
Vol 11 (1) ◽  
pp. 18 ◽  
Author(s):  
Lyndsay D. Troyer ◽  
James J. Stone ◽  
Thomas Borch

Environmental context Uranium and arsenic, two elements of human health concern, are commonly found at sites of uranium mining, but little is known about processes influencing their environmental behaviour. Here we focus on understanding the chemical and physical processes controlling uranium and arsenic transport at an abandoned uranium mine. We find that the use of sedimentation ponds limits the mobility of uranium; however, pond conditions at our site resulted in arsenic mobilisation. Our findings will help optimise restoration strategies for mine tailings. Abstract Although As can occur in U ore at concentrations up to 10wt-%, the fate and transport of both U and As at U mine tailings have not been previously investigated at a watershed scale. The major objective of this study was to determine primary chemical and physical processes contributing to transport of both U and As to a down gradient watershed at an abandoned U mine site in South Dakota. Uranium is primarily transported by erosion at the site, based on decreasing concentrations in sediment with distance from the tailings. Sequential extractions and U X-ray absorption near-edge fine structure (XANES) fitting indicate that U is immobilised in a near-source sedimentation pond both by prevention of sediment transport and by reduction of UVI to UIV. In contrast to U, subsequent release of As to the watershed takes place from the pond partially due to reductive dissolution of Fe oxy(hydr)oxides. However, As is immobilised by adsorption to clays and Fe oxy(hydr)oxides in oxic zones and by formation of As–sulfide mineral phases in anoxic zones down gradient, indicated by sequential extractions and As XANES fitting. This study indicates that As should be considered during restoration of uranium mine sites in order to prevent transport.


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