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1.
Uranium isotope fractionation during adsorption, (co) precipitation, and biotic reduction
Douglas R. Evans, Bastian R. Georg, Wei Wang, Breda Novotnik, Duc Huy Dang, 2016, izvirni znanstveni članek

Opis: Uranium contamination of surface environments is a problem associated with both U-ore extraction/processing and situations in which groundwater comes into contact with geological formations high in uranium. Apart from the environmental concerns about U contamination, its accumulation and isotope composition have been used in marine sediments as a paleoproxy of the Earth’s oxygenation history. Understanding U isotope geochemistry is then essential either to develop sustainable remediation procedures as well as for use in paleotracer applications. We report on parameters controlling U immobilization and U isotope fractionation by adsorption onto Mn/Fe oxides, precipitation with phosphate, and biotic reduction. The light U isotope (235U) is preferentially adsorbed on Mn/Fe oxides in an oxic system. When adsorbed onto Mn/Fe oxides, dissolved organic carbon and carbonate are the most efficient ligands limiting U binding resulting in slight differences in U isotope composition (δ238U = 0.22 ± 0.06‰) compared to the DOC/DIC-free configuration (δ238U = 0.39 ± 0.04‰). Uranium precipitation with phosphate does not induce isotope fractionation. In contrast, during U biotic reduction, the heavy U isotope (238U) is accumulated in reduced species (δ238U up to −1‰). The different trends of U isotope fractionation in oxic and anoxic environments makes its isotope composition a useful tracer for both environmental and paleogeochemical applications.
Najdeno v: osebi
Ključne besede: Uranium, fractionation, biotic, abiotic, oxides
Objavljeno: 04.10.2019; Ogledov: 145; Prenosov: 0
.pdf Polno besedilo (4,30 MB)

2.
Variations in U concentrations and isotope signatures in two Canadian lakes impacted by U mining: A combination of anthropogenic and biogeochemical processes
Wei Wang, Duc Huy Dang, Breda Novotnik, R. Douglas Evans, Thai T. Phan, 2019, izvirni znanstveni članek

Opis: Temporal and vertical variations in uranium (U) concentrations and U isotope (δ238U, ‰) signatures were examined in sediment cores collected seven times over a one year period, from two lakes in Ontario, Canada, which are contaminated with U by historical mining activities. Bow Lake is holomictic, experiencing seasonal anoxia, while the sediments of meromictic Bentley Lake are permanently anoxic. Average annual peak concentrations of U in Bow Lake subsurface sediments were approximately 300 μg L−1 and 600 μg g−1 in porewater and bulk sediments, respectively. Similar ranges of concentrations (900 μg L−1 and 600 μg g−1, respectively) were observed in Bentley Lake sediments. The exceedingly high levels of U observed in the porewaters of both lakes, as well as the seasonal variability in U levels, challenge the traditional paradigm regarding U chemistry, i.e., that reduced U(IV) should be insoluble under anoxic conditions. The average annual δ238U ‰ values at the sediment-water interface of both lakes were similar (i.e., 0.47 ± 0.09‰ and 0.50 ± 0.16‰, relative to IRMM-184). The deep sediments in both Bentley Lake and Bow Lake record U isotope composition with a typical fractionation of 0.6‰ relative to the surface water, confirming authigenic U accumulation, i.e., negligible contribution of particulate material from the tailings. Also, the δ238U values in porewater have an average offset of ca. −0.1‰ relative to bulk sediments in anoxic zones and are reversed in the oxic sediment layer.
Najdeno v: osebi
Ključne besede: Uranium Isotope composition Uranium tailings Biogeochemical cycling Redox chemistry
Objavljeno: 09.10.2019; Ogledov: 175; Prenosov: 0
.pdf Polno besedilo (3,89 MB)

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