Mechanistic investigation and modeling of Cd immobilization by iron (hydr)oxide-humic acid coprecipitates

A molecular-scale understanding of aqueous metal adsorption onto humic acid-iron (hydr)oxide coprecipitates, and our ability to model these interactions, are lacking. Here, the molecular-scale mechanisms for Cd binding onto iron (hydr)oxide-humic acid (HA) composites were probed using X-ray absorption fine structure (XAFS) spectroscopy and surface complexation modeling (SCM). The immobilization of Cd in (hydr)oxide precipitation systems occurs predominantly through adsorption onto the freshly-formed (hydr)oxide nanoparticles, and SCM calculations suggest a specific surface area of 2400 m(2)/g available for Cd. The solution and XAFS measurements indicate that HA promotes the precipitation of both Fe clusters and Fe-Cd associations mainly through ligand exchange reactions. Site masking reactions result in a dramatic blockage of functional sites on HA and similar to 45% migration of the adsorbed Cd to iron (hydr)oxide binding sites at high HA:Fe mass ratios. A composite model that accounts for both site masking between Fe ions and HA and the increase of Fe hydroxyl sites simulate the distribution of Cd in the composites reasonably well. Overall, this study demonstrates that the Fe clusters play an overriding role for heavy metal stabilization in coprecipitation systems, while HA promotes the immobilization of Cd by facilitating the flocculation and dispersion of Fe clusters.

Automated summary

This study investigates the binding mechanisms of Cd onto iron oxide-humic acid composites, revealing that Cd is mainly immobilized onto freshly-formed oxide nanoparticles and that humic acid promotes the precipitation of Fe clusters through ligand exchange reactions. Site masking reactions result in the migration of adsorbed Cd to iron oxide binding sites.