Sequential Process Combination of Photocatalytic Oxidation and Dark Reduction for the Removal of Organic Pollutants and Cr(VI) using Ag/TiO2

作者：Yeoseon Choi, Min Seok Koo, Alok D. Bokare, Donghyo Kim, Detlef W. Bahnemann, Wonyong Choi · 发表于：Environmental Science & Technology · 年份：2017 · DOI：10.1021/acs.est.6b06303 · 被引用次数：219 · 研究领域：Advanced Photocatalysis Techniques、TiO2 Photocatalysis and Solar Cells、Advanced Nanomaterials in Catalysis

We investigated a sequential photocatalysis-dark reaction, wherein organic pollutants were degraded on Ag/TiO 2 under UV irradiation and the dark reduction of hexavalent chromium (Cr(VI)) was subsequently followed. The photocatalytic oxidation of 4-chlorophenol (4-CP), a test organic substrate, induced the generation of degradation intermediates and the storage of electrons in Ag/TiO 2 which were then utilized for reducing Cr(VI) in the postirradiation period. The dark reduction efficiency of Cr(VI) was much higher with Ag/TiO 2 (87%), compared with bare TiO 2 (27%) and Pt/TiO 2 (22%). The Cr(VI) removal by Ag/TiO 2 (87%) was contributed by adsorption (31%), chemical reduction by intermediates of 4-CP degradation (26%), and reduction by electrons stored in Ag (30%). When formic acid, humic acid or ethanol was used as an alternative organic substrate, the electron storage effect was also observed. The postirradiation removal of Cr(VI) on Ag/TiO 2 continued for hours, which is consistent with the observation that a residual potential persisted on the Ag/TiO 2 electrode in the dark whereas little residual potential was observed on bare TiO 2 and Pt/TiO 2 electrodes. The stored electrons in Ag/TiO 2 and their transfer to Cr(VI) were also indicated by the UV–visible absorption spectral change. Moreover, the electrons stored in the preirradiated Ag/TiO 2 reacted with O 2 with showing a sign of low-level OH radical generation in the dark period.