Title of article
X-ray absorption spectroscopy studies of reactions of technetium, uranium and neptunium with mackinawite
Author/Authors
Francis R. Livens، نويسنده , , Mark J. Jones، نويسنده , , Amanda J. Hynes، نويسنده , , John M. Charnock، نويسنده , , J. Fred W. Mosselmans، نويسنده , , Christoph Hennig، نويسنده , , Helen Steele، نويسنده , , David Collison، نويسنده , , David J. Vaughan، نويسنده , , Richard A. D. Pattrick، نويسنده , , Wendy A. Reed، نويسنده , , Lesley N. Moyes، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
9
From page
211
To page
219
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 TcS2-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.
Keywords
Technetium , uranium , Neptunium , Sulfides , Spectroscopy
Journal title
Journal of Environmental Radioactivity
Serial Year
2004
Journal title
Journal of Environmental Radioactivity
Record number
706390
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