Competitive and cooperative effects of chloride on palladium(II) adsorption to iron (oxyhydr)oxides: Implications for mobility during weathering

Abstract

In surface and near-surface weathering environments, the mobilization and partial loss of palladium (Pd) under oxidizing and weakly acidic conditions has been attributed to aqueous chloride complexation. However, prior work has also observed that a portion of Pd is retained by iron (oxyhydr)oxides in the weathering zone. The effect chloride has on the relative amount of Pd mobilization versus retention by iron (oxyhydr)oxides is currently unclear. We studied the effect of chloride complexation on Pd(II) adsorption to two iron (oxyhydr)oxides, hematite and 2-line ferrihydrite, at pH 4. Increasing chloride concentration suppresses Pd adsorption for both hematite and ferrihydrite, which display similar binding affinities under the conditions studied. Thermodynamic modeling of aqueous Pd speciation indicates that greater suppression of binding to iron (oxyhydr)oxides should occur than is observed because of the strength of Pd-Cl complexation, implying that additional interactions at the mineral surface are counteracting this effect. While increasing dissolved chloride concentration does not measurably impact mineral surface charging, extended X-ray absorption fine structure (EXAFS) spectra indicate that ternary Pd-Cl surface complexes form on both hematite and ferrihydrite. The number of Cl ligands in the surface species increase at greater chloride concentration. A mixture of bidentate and monodentate surface species are indicated by the EXAFS spectra, although the fitting uncertainties precludes determining whether these vary in relative abundance with chloride concentration. In order to offset the effect of strong aqueous Pd-Cl complexation and align with our EXAFS results, a surface complexation model developed for Pd adsorption to hematite involves a mixture of three ternary surface complexes containing 1, 2, and 3 chloride ligands. Our results show that Pd is mobilized as a chloride complex in platinum-group element-rich weathering zones. Porewater chloride concentrations are thus a dominant control on Pd retention by iron (oxyhydr)oxides in these weakly acidic environments.