X-ray absorption spectroscopy studies of reactions of technetium, uranium and neptunium with mackinawite |
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Authors: | Livens Francis R Jones Mark J Hynes Amanda J Charnock John M Mosselmans J Fred W Hennig Christoph Steele Helen Collison David Vaughan David J Pattrick Richard A D Reed Wendy A Moyes Lesley N |
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Affiliation: | Centre for Radiochemistry Research, Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, UK. francis.livens@man.ac.uk |
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Abstract: | Technetium, uranium and neptunium may all occur in the environment in more than one oxidation state (IV or VII, IV or VI and IV or V respectively). The surface of mackinawite, the first-formed iron sulfide phase in anoxic conditions, can promote redox changes so a series of laboratory experiments were carried out to explore the interactions of Tc, U and Np with this mineral. The products of reaction were characterised using X-ray absorption spectroscopy. Technetium, added as TcO4(-), is reduced to oxidation state IV and forms a TcS(2)-like species. On oxidation of the mackinawite in air to form goethite, Tc remains in oxidation state IV but in an oxide, rather than a sulfide environment. At low concentrations, uranium forms uranyl surface complexes on oxidised regions of the mackinawite surface but at higher concentrations, the uranium promotes surface oxidation and forms a mixed oxidation state oxide phase. Neptunium is reduced to oxidation IV and forms a surface complex with surface sulfide ions. The remainder of the Np coordination sphere is filled with water molecules or hydroxide ions. |
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