Characterization of uranium redox state in organic-rich Eocene sediments. (March 2018)
- Record Type:
- Journal Article
- Title:
- Characterization of uranium redox state in organic-rich Eocene sediments. (March 2018)
- Main Title:
- Characterization of uranium redox state in organic-rich Eocene sediments
- Authors:
- Cumberland, Susan A.
Etschmann, Barbara
Brugger, Joël
Douglas, Grant
Evans, Katy
Fisher, Louise
Kappen, Peter
Moreau, John W. - Abstract:
- Abstract: The presence of organic matter (OM) has a profound impact on uranium (U) redox cycling, either limiting or promoting the mobility of U via binding, reduction, or complexation. To understand the interactions between OM and U, we characterised U oxidation state and speciation in nine OM-rich sediment cores (18 samples), plus a lignite sample from the Mulga Rock polymetallic deposit in Western Australia. Uranium was unevenly dispersed within the analysed samples with 84% of the total U occurring in samples containing >21 wt % OM. Analyses of U speciation, including x-ray absorption spectroscopy and bicarbonate extractions, revealed that U existed predominately (∼71%) as U(VI), despite the low pH (4.5) and nominally reducing conditions within the sediments. Furthermore, low extractability by water, but high extractability by a bi-carbonate solution, indicated a strong association of U with particulate OM. The unexpectedly high proportion of U(VI) relative to U(IV) within the OM-rich sediments implies that OM itself does not readily reduce U, and the reduction of U is not a requirement for immobilizing uranium in OM-rich deposits. The fact that OM can play a significant role in limiting the mobility and reduction of U(VI) in sediments is important for both U-mining and remediation. Highlights: 84% of U in Mulga Rock OM-bearing sediments occurred within the OM-richest samples (>21% TOC; 9 of 18 samples). 71% of U was present in the U(VI) oxidation state. HigherAbstract: The presence of organic matter (OM) has a profound impact on uranium (U) redox cycling, either limiting or promoting the mobility of U via binding, reduction, or complexation. To understand the interactions between OM and U, we characterised U oxidation state and speciation in nine OM-rich sediment cores (18 samples), plus a lignite sample from the Mulga Rock polymetallic deposit in Western Australia. Uranium was unevenly dispersed within the analysed samples with 84% of the total U occurring in samples containing >21 wt % OM. Analyses of U speciation, including x-ray absorption spectroscopy and bicarbonate extractions, revealed that U existed predominately (∼71%) as U(VI), despite the low pH (4.5) and nominally reducing conditions within the sediments. Furthermore, low extractability by water, but high extractability by a bi-carbonate solution, indicated a strong association of U with particulate OM. The unexpectedly high proportion of U(VI) relative to U(IV) within the OM-rich sediments implies that OM itself does not readily reduce U, and the reduction of U is not a requirement for immobilizing uranium in OM-rich deposits. The fact that OM can play a significant role in limiting the mobility and reduction of U(VI) in sediments is important for both U-mining and remediation. Highlights: 84% of U in Mulga Rock OM-bearing sediments occurred within the OM-richest samples (>21% TOC; 9 of 18 samples). 71% of U was present in the U(VI) oxidation state. Higher proportions of U occur as U(VI) in mature OM-rich sediments than previously thought. OM strongly complexes U(VI), limiting its mobility and reactivity. U reduction processes are not ubiquitous within OM-rich sediments. … (more)
- Is Part Of:
- Chemosphere. Volume 194(2018)
- Journal:
- Chemosphere
- Issue:
- Volume 194(2018)
- Issue Display:
- Volume 194, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 194
- Issue:
- 2018
- Issue Sort Value:
- 2018-0194-2018-0000
- Page Start:
- 602
- Page End:
- 613
- Publication Date:
- 2018-03
- Subjects:
- Mulga Rock -- Uranium -- Mobility -- Organic matter -- Oxidation state -- X-ray absorption spectroscopy
Pollution -- Periodicals
Pollution -- Physiological effect -- Periodicals
Environmental sciences -- Periodicals
Atmospheric chemistry -- Periodicals
551.511 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00456535/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.chemosphere.2017.12.012 ↗
- Languages:
- English
- ISSNs:
- 0045-6535
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.280000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5516.xml