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Experimental study of mechanisms of fixation and reduction of uranium by sedimentary organic matter under diagenetic or hydrothermal conditions
Authors:S. Nakashima  J.R. Disnar  A. Perruchot  J. Trichet
Affiliation:1. Centre de Recherches sur la Synthése et la Chimie des Minéraux G.I.S. CNRS-BRGM, 1A, rue de la Férollerie, 45045 Orléans Cedex, France and E.R.A. 601 du C.N.R.S.;2. B.R.G.M., Département Gîtes Minéraux, B.P. 6009, 45060 Orléans Cedex, France and E.R.A. 601 du C.N.R.S.;3. Centre de Recherches sur la Synthése et la Chimie des Minéraux G.I.S. CNRS-BRGM, 1A, rue de la Férollerie 45045 Orléans Cedex, France;4. Université d''Orléans, Laboratoire de Géologie Appliquée, 45045 Orléans Cedex, France and E.R.A. 601 du C.N.R.S.
Abstract:Interactions between lignite and soluble uranyl species have been investigated experimentally at different temperatures from 20° to 400°C. Fixation of uranyl species by lignite (45° to 250°C) and their reduction to uraninite (120° to 400°C) were observed. The fixation of uranyl species by lignite results in the formation of stable organo-uranyl compounds. The reduction of uranyl species by lignite results in a stoichiometric liberation of H+ in the solution medium and in a dehydrogenation of lignite. This dehydrogenation can be attributed to two different processes. The first is an oxidation of alcohol functional groups into aldehyde or ketone functions accompanied by a simultaneous reduction of uranyl species. The second is a dehydrogenation of hydrocarbonaceous aliphatic moieties induced by the uranium species. The molecular hydrogen produced during this process is subsequently used for an additional reduction of uranyl species.
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