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
Link To Document :
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