Adsorption and Stability of Arsenic(III) at the Clay Mineral−Water Interface

Abstract

Adsorption and oxidation reactions of arsenite (As(III)) at the mineral−water interface are two important factors affecting the fate and transport of arsenic in the environ ment. Numerous studies have concluded that As(III) is more soluble and mobile than arsenate (As(V)) in soils, though very little experimental work has demonstrated the differences in reactivity and stability of As(III) and As(V) at the mineral−water interface. In this investigation, As(III) adsorption on kaolinite, illite, montmorillonite, and amorphous aluminum hydroxide (am-Al(OH) 3 ) was studied as a function of pH and ionic strength and was compared with As(V) adsorption. High-performance liquid chromatog raphy−hydride generation atomic absorption spectrophotometry (HPLC−HGAAS) was employed for direct determination of As(III) and As(V). In addition, surface complexation modeling was used to describe As(III) and As(V) adsorption on the four minerals. It was revealed that alkaline solutions (pH > 9) without mineral solids caused homogeneous oxidation of As(III) to As(V). In addition, recovery of adsorbed As from As(III)-treated clay mineral solids showed that oxidation of As(III) to As(V) was enhanced by heterogeneous oxidation on kaolinite and illite surfaces.