Solar light induced removal of arsenic from contaminated groundwater: the interplay of solar energy and chemical variables

Abstract The removal of arsenic by solar oxidation in individual units (SORAS) is currently being explored as a possible economic and simple technology to treat groundwater in Bangladesh and India. Hydroarsenicism affects also large regions of America, especially Argentina, Chile, Mexico and Peru. In this paper, the efficiency of arsenic removal by solar oxidation coupled with precipitation of iron (hydr)oxide, was assessed under various experimental conditions, both on samples of synthetic water and of groundwater of the province of Tucuman (Argentina). The results demonstrate that the underlying chemistry is very complex, and the efficiency is affected often in unpredictable ways by changes in the chemical matrix, or by changes in the operative conditions. Oxides generated from ferrous salts are more efficient than solids formed by hydrolysis of Fe(III); alkalinity contents (bicarbonate) is also important to permit the adequate precipitation. Addition of small amounts of citric acid (lemon juice) is beneficial, but at larger concentrations the effect is negative, probably because of interference in the formation of the solid. The effect of solar irradiation is variable, depending on the other experimental conditions. Although it is possible to remove As partially without solar irradiation under certain special conditions, a procedure versatile enough to cope with waters of different compositions must be based in the use of solar energy. Light plays the role of accelerating the oxidation of As(III) to As(V), and also affects the nature of the solid and, hence, its sorptive properties. The rationale of the effect of light is therefore appreciably more complex than in the case of heterogeneous photocatalysis with TiO 2 .