Effect of co-solutes on the products and solubility of uranium(VI) precipitated with phosphate

•Chernikovite forms instead of uranyl orthophosphate in the absence of cations.•Na+/Ca2 + in the presence of PO43 − reduced uranium solubility by more than 100 times.•Na+ resulted in formation of sodium autunite particles smaller than 0.22 μm.•Ca2 + resulted in U(VI) uptake through adsorption and/or incorporation onto Ca-PO4.

Uranyl phosphate solids are often found with uranium ores, and their low solubility makes them promising target phases for in situ remediation of uranium-contaminated subsurface environments. The products and solubility of uranium(VI) precipitated with phosphate can be affected by the pH, dissolved inorganic carbon (DIC) concentration, and co-solute composition (e.g. Na+/Ca2 +) of the groundwater. Batch experiments were performed to study the effect of these parameters on the products and extent of uranium precipitation induced by phosphate addition. In the absence of co-solute cations, chernikovite [H3O(UO2)(PO4)·3H2O] precipitated despite uranyl orthophosphate [(UO2)3(PO4)2·4H2O] being thermodynamically more favorable under certain conditions. As determined using powder X-ray diffraction, electron microscopy, and laser induced fluorescence spectroscopy, the presence of Na+ or Ca2 + as a co-solute led to the precipitation of sodium autunite ([Na2(UO2)2(PO4)2] and autunite [Ca(UO2)2(PO4)2]), which are structurally similar to chernikovite. In the presence of sodium, the dissolved U(VI) concentrations were generally in agreement with equilibrium predictions of sodium autunite solubility. However, in the calcium-containing systems, the observed concentrations were below the predicted solubility of autunite, suggesting the possibility of uranium adsorption to or incorporation in a calcium phosphate precipitate in addition to the precipitation of autunite.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide