▎ 摘　　要

Due to its unique properties, the potential application of graphene oxide (GO) in treating environmental pollution has attracted wide attention. In this study, the UV-light catalyzed photoreduction of Cr(VI) by GO was assessed as well as its adsorption toward Cr(VI), and FTIR and XPS techniques were adopted to reveal the underlying mechanisms. The surfaces of GO were negatively charged across the pH range examined. Therefore, the increase in pH resulted in the decrease in Cr(VI) adsorption due to the enhancement in repulsion between Cr(VI) and GO surfaces. The kinetic studies showed that the Cr(VI) adsorption proceeded quickly during the 0-24h stage, followed by a slow process until to the end of reaction (96h). Additionally, the kinetic data could be properly described with the pseudo-first-order rate equation (R-2=0.9754). With the UV-light irradiation, Cr(VI) reduction in the presence of 0.5gL(-1) GO was observed with the concentration of Cr(VI) decreased from 0.1mM to zero within 12h at pH3.0, while which would be suppressed as the pH increased. The addition of EDTA could enhance the photocatalytic Cr(VI) reduction due to the consumption of the photogenerated holes (h(+)), leaving more Cr(III) species present in solution. The generation of h(+) was further confirmed by the complete photodegradation of 4-CP during 48h. Moreover, the changes in FTIR and XPS spectrum of GO before and after reaction indicated the oxidization of epoxy and hydroxyl groups by holes or reduction by electrons was involved in the photoreaction. The photoreduction of Cr(VI) could was also observed in an oxisol with the existence of GO, with the disappearance of 0.1mM of aqueous Cr(VI) at pH4.40 after 36h. The results above could enhance our understanding on the essence of photoreactivity of GO, and indicated that the potential release of GO into soil environments would be helpful to eliminate the risk posed by Cr(VI) through the UV-light irradiated photocatalytic reduction.