Neptunium and Uranium Interactions with Environmentally and Industrially Relevant Iron Minerals
Authors:
- Luke T. TownsendLuke T. Townsend
- Kurt F. SmithKSKurt F. Smith
- Ellen H. WinstanleyEWEllen H. Winstanley
- Katherine MorrisKMKatherine Morris
- Olwen StaggOSOlwen Stagg
- J. Frederick W. MosselmansJMJ. Frederick W. Mosselmans
- Francis R. LivensFLFrancis R. Livens
- Liam Abrahamsen-MillsLiam Abrahamsen-Mills
- Richard BlackhamRBRichard Blackham
- Samuel ShawSSSamuel Shaw
Open Access
Abstract
Neptunium (237Np) is an important radionuclide in the nuclear fuel cycle in areas such as effluent treatment and the geodisposal of radioactive waste. Due to neptunium’s redox sensitivity and its tendency to adsorb strongly to mineral phases, such as iron oxides/sulfides, the environmental mobility of Np can be altered significantly by a wide variety of chemical processes. Here, Np interactions with key iron minerals, ferrihydrite (Fe5O8H·4H2O), goethite (α-FeOOH), and mackinawite (FeS), are investigated using X-ray Absorption Spectroscopy (XAS) in order to explore the mobility of neptunyl(V) (Np(V)O2+) moiety in environmental (radioactive waste disposal) and industrial (effluent treatment plant) scenarios. Analysis of the Np LIII-edge X-ray Absorption Near-Edge Structure (XANES) and Extended X-ray Absorption Fine Structure (EXAFS) showed that upon exposure to goethite and ferrihydrite, Np(V) adsorbed to the surface, likely as an inner-sphere complex. Interestingly, analysis showed that only the first two shells (Oax and Oeq) of the EXAFS could be modelled with a high degree of confidence, and there was no clear indication of Fe or carbonate in the fits. When Np(V)O2+ was added to a mackinawite-containing system, Np(V) was reduced to Np(IV) and formed a nanocrystalline Np(IV)O2 solid. An analogous experiment was also performed with U(VI)O22+, and a similar reduction was observed, with U(VI) being reduced to nanocrystalline uraninite (U(IV)O2). These results highlight that Np(V) may undergo a variety of speciation changes in environmental and engineered systems whilst also highlighting the need for multi-technique approaches to speciation determination for actinyl (for example, Np(V)O2+) species.Keywords
Funding Information
- Engineering and Physical Sciences Research Council (EP/R513131/1, EP/T011300/1)
- Science and Technology Facilities Council (ST/N002474/1)
- Diamond Light Source (SP24074-2, SP21441-4, SP13559-5, SP13559-6)
This publication has 68 references indexed in Scilit:
- Abiotic Reductive Immobilization of U(VI) by Biogenic MackinawiteEnvironmental Science & Technology, 2013
- B18: A core XAS spectroscopy beamline for DiamondJournal of Physics: Conference Series, 2009
- I20; the Versatile X-ray Absorption spectroscopy beamline at Diamond Light SourceJournal of Physics: Conference Series, 2009
- Identification of Uranyl Surface Complexes on Ferrihydrite: Advanced EXAFS Data Analysis and CD-MUSIC ModelingEnvironmental Science & Technology, 2009
- Synthesis, Structure, and Magnetism of Np2O5Journal of the American Chemical Society, 2007
- High resolution transmission electron microscopic study of synthetic nanocrystalline mackinawiteEarth and Planetary Science Letters, 2006
- The ferrozine method revisited: Fe(II)/Fe(III) determination in natural watersApplied Geochemistry, 2000
- XANES Spectroelectrochemistry: A New Method for Determining Formal PotentialsAnalytical Chemistry, 1999
- EXAFS Studies of Pentavalent Neptunium Carbonato Complexes. Structural Elucidation of the Principal Constituents of Neptunium in Groundwater EnvironmentsJournal of the American Chemical Society, 1996
- The crystal structure of Liebigite, Ca2UO2(CO3)3 ?11H2OMineralogy and Petrology, 1982