Abstract
Abstract
A series of precious metal catalysts (M/titanium dioxide [TiO2], M = Ru, Rh, Pd, Ag, Ir, Pt, or Au) were prepared by a light deposition method, and for the first time, synergistic effects of photocatalytic degradation of phenol (20 mg/L) under UV irradiation (365 nm) by M/TiO2 with electron capture agent hydrogen peroxide (H2O2) have been investigated. Results showed that H2O2 plays a great synergistic role on M/TiO2, and the photocatalytic activity of M/TiO2 is closely related to its work function. Ag loading greatly enhanced activity of TiO2 due to the normal reduction mechanism and the “activated” mechanism between H2O2 and Ag nanoparticles. Under the optimum conditions of Ag loading at 0.5 wt.%, Ag/TiO2 concentration at 0.1 g/L, H2O2 concentration at 50 mmol/L, and pH value of the reaction solution at 5, the phenol can be degraded by 65% within 3 h, which is 45% more than that in the TiO2 photocatalytic system. Kinetics of the degradation of phenol can be characterized as pseudo-first order. Such synergistic photocatalytic degradation by precious metal supported TiO2 with H2O2 provides a new approach for the degradation of refractory pollutants in waste water.
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