Abstract

The degradation of methyl orange (MO) and neutral red (NR) was studied by the direct electrooxidation using nitrogen and sulfur co-doped graphene (NSG) supported antimony doped tin oxide (SnO<sub>2</sub>-Sb). Sol-gel and microwave technics were used to prepare the material (Ti/SnO<sub>2</sub>-Sb-NSG). Raman, XRD, FTIR and TGA/DSC analyses help to confirm the coating of titanium substrate with the SnO<sub>2</sub>-Sb-NSG film. Linear sweet voltammetry results show that Ti/SnO<sub>2</sub>-Sb-NSG material possesses high oxygen overvoltage. Three independent variables including electrolysis time, current density and dye concentration on the performance of the anodic oxidation system was modeled using the Box-Behnken Design. The optimum conditions for MO and NR degradation were for current density 18 mA/cm² and 58 mA/cm², electrolysis time 6 h and 6 h and dye concentration 29 mg/L and 82 mg/L, respectively. However, based on these optimums, MO was degraded at 98.71 % while NR was just degraded at 82.7%. Based on the intermediate compounds, the degradation mechanism of MO at the Ti/SnO<sub>2</sub>-Sb-NSG anode was proposed. Ti/SnO<sub>2</sub>-Sb-NSG electrode showed a higher efficient electrocatalytic performance for NR and MO degradation than that of Ti/Sb-SnO<sub>2</sub> or Ti/Sb-SnO<sub>2</sub>-NG electrodes. Furthermore, the lifetime of Ti/SnO<sub>2</sub>-Sb-NSG was about 31.6 h while Ti/SnO<sub>2</sub>-Sb electrode was 9.0 h.

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