Adsorption of uranium(VI) on amorphous ferric oxyhydroxide at high concentrations of dissolved carbon(IV) and sulfur(VI)

Abstract

Amorphous ferric oxyhydroxide is being used to treat groundwater contaminated with uranium(VI); the compound also has potential for use as a component in in situ chemical barriers. To quantitatively evaluate its effectiveness in such applications, adsorption of uranium(VI) onto amorphous ferric oxyhydroxide was experimentally investigated under a wide range of uranium(VI) (8.40·10 −7−2.10·10 −3 mol L −1; 0.2–500 mg L −1), sulfur(VI) (0–0.07 mol L −1; 0–2240 mg L −1) and carbon(IV) (0–0.0195 mol L −1; 0–234 mg L −1) concentrations, and pH-values (4–9.6). The adsorption behavior of uranium(VI) (uranyl ion and its complexes) is similar to that of other cations; it exhibits a sharp rise in the extent of adsorption with increasing pH. Interactions among uranyl complexes and surface sites are interpreted using a site complexation model. Although the model does not incorporate electrostatics and includes only a single type of adsorption site, it provides a reasonable match to measured adsorption and proton exchange data. The simplicity of the model and the resulting reduction in computational demand allow its efficient incorporation into coupled reaction-transport models.