A geochemical investigation of heterogeneous redox reactions between Fe(II), Fe(III), and uranium
نویسنده
چکیده
Iron (Fe) minerals and ferrous iron (Fe(II)) play an important role in the several natural elemental cycles, including the carbon cycle, nutrient cycles, and the cycling of metals. In this work we have characterized the reactivity structural Fe(II) in several Fe minerals and in natural soil with uranium. We have studied the reactivity of Fe(II) in solution with the Fe oxide goethite conditions relevant to many natural systems. Green rusts are widely recognized as an intermediate phase in the Fe cycle. Here we investigate the reactivity of green rusts containing different structural anions with uranium (U). We have also investigated the effect of aqueous bicarbonate on U sorption and reduction by green rusts. Our findings indicate that green rusts reduce U to U, and that environmentally relevant carbonate concentrations have little effect the rate and extent on this reaction. We have also investigated U reduction by structural Fe(II) in magnetite. Magnetite with varying stoichiometry (x = Fe/Fe) was reacted with U. Results from x-ray absorption spectroscopy indicate that the redox properties of magnetite dictate whether magnetite reduces U. In addition, magnetite reactivity can be “recharged” by electron transfer from aqueous Fe(II). There is little evidence of the reactivity of structural Fe(II) towards U in natural materials. We have characterized a naturally reduced soil and found it contains structural Fe(II) in clay minerals and a possible green rust-like phase. When this soil is exposed to U we find that Fe(II) reduces a portion of the U added. Our work highlights the potential for abiotic reduction of U by Fe(II) in reduced, Fe-rich environments. We have used Fe Mössbauer spectroscopy to study redox reactions of Fe(II) with goethite under biogeochemical conditions relevant to natural systems. When Fe(III) in goethite is substituted with aluminum or anions such as phosphate, silicate, carbonate, and natural organic matter are sorbed onto the surface of goethite, interfacial electron
منابع مشابه
Interactions between magnetite and humic substances: redox reactions and dissolution processes
Humic substances (HS) are redox-active compounds that are ubiquitous in the environment and can serve as electron shuttles during microbial Fe(III) reduction thus reducing a variety of Fe(III) minerals. However, not much is known about redox reactions between HS and the mixed-valent mineral magnetite (Fe3O4) that can potentially lead to changes in Fe(II)/Fe(III) stoichiometry and even dissolve ...
متن کاملFe(II) reduction of pyrolusite (β-MnO2) and secondary mineral evolution
Iron (Fe) and manganese (Mn) are the two most common redox-active elements in the Earth's crust and are well known to influence mineral formation and dissolution, trace metal sequestration, and contaminant transformations in soils and sediments. Here, we characterized the reaction of aqueous Fe(II) with pyrolusite (β-MnO2) using electron microscopy, X-ray diffraction, aqueous Fe and Mn analyses...
متن کاملHeterogeneous reduction of Tc(VII) by Fe(II) at the solid–water interface
Experiments were performed herein to investigate the rates and products of heterogeneous reduction of Tc(VII) by Fe(II) adsorbed to hematite and goethite, and by Fe(II) associated with a dithionite–citrate–bicarbonate (DCB) reduced natural phyllosilicate mixture [structural, ion-exchangeable, and edge-complexed Fe(II)] containing vermiculite, illite, and muscovite. The heterogeneous reduction o...
متن کاملThermodynamic controls on the microbial reduction of iron-bearing nontronite and uranium.
Iron-bearing phyllosilicate minerals help establish the hydrogeological and geochemical conditions of redox transition zones because of their small size, limited hydraulic conductivity, and redox buffering capacity. The bioreduction of soluble U(VI) to sparingly soluble U(IV) can promote the reduction of clay-Fe(III) through valence cycling. The reductive precipitation of U(VI) to uraninite was...
متن کاملBiogeochemical processes in ethanol stimulated uranium-contaminated subsurface sediments.
A laboratory incubation experiment was conducted with uranium-contaminated subsurface sediment to assess the geochemical and microbial community response to ethanol amendment. A classical sequence of terminal electron-accepting processes (TEAPs) was observed in ethanol-amended slurries, with NO3- reduction, Fe(III) reduction, SO4(2-) reduction, and CH4 production proceeding in sequence until al...
متن کامل