摘要：Nanocrystalline iowaite, a Mg/Fe-based layered double hydroxide (LDH) intercalated with chloride, was synthesized to evaluate its performance for arsenic removal from water and to investigate the contributing dearsenication mechanisms. It is characterized by fast arsenic sorption rates and has a much higher arsenic uptake capacity than other LDHs that are commonly used for water dearsenication. The surface adsorption of the solution arsenic onto the iowaite samples and the anion exchange of the arsenic in solution with chloride, which is originally in the iowaite interlayers, are the primary mechanisms for the uptake of arsenic by iowaite. In addition to the Coulombic attraction between arsenate/arsenite and positively charged layers of iowaite, the inner-sphere complexation of arsenic with Fe (instead of Mg) in the iowaite layers is responsible for the formation of more stable and stronger arsenic bonds, as indicated by both XPS and EXAFS analyses. Specifically, bidentate-binuclear and monodentate-mononuclear As-Fe complexes were detected in the arsenate removal experiments, whereas bidentate-mononuclear, bidentate-binuclear, and monodentate-mononuclear As-Fe complexes were present for the arsenite-treated iowaite samples. This study shows that nanocrystalline iowaite is a promising, low-cost material for arsenic removal from natural arsenic-rich waters or contaminated high-arsenic waters.
