Photocatalyst-coated carbon microtube electrodes: Preparation and characterization of their properties and photocatalytic degradation of methylene blue

Photocatalysis is a potential technology for removing pollutants from water. As the recombination of the photogenerated electron-hole pairs can hinder the photocatalytic efficiency in the treatment of wastewater, the surface of the carrier is usually coated with a semiconductor. In this study, carbon microtube electrode prepared from corncob was coated with either titanium oxide (TiO2) or bismuth phosphate (BiPO4) and then used as a photocatalyst (C-TiO2 or C-BiPO4) to investigate the photodegradation of methylene blue (MB). The two photocatalysts, C-TiO2 and C-BiPO4, were characterized by phase determination, microstructure observation, water contact angle measurement, and base site analysis. The influences of reaction time, stability, MB concentration, initial pH, and center dot OH radicals quenching on the degradation of MB were also evaluated. The degradation of MB by C-TiO2 and C-BiPO4 was mainly dominated by center dot OH radical oxidation. The carbon microtube increased both the mass transfer rate and the photogenerated electron-hole pairs separation rate, thereby increasing the photocatalysis of both C-TiO2 and C-BiPO4 as revealed by an increase in the rate of MB degradation. The rate constants obtained for the degradation of MB by C-TiO2 and C-BiPO4 at 20 degrees C were 9.739 x 10(-7) mM min(-1) and 1.111 x 10(-7) mM min(-1) , respectively. The coating of TiO2 and BiPO4 on the surface of the carbon microtube electrode enhanced their photocatalytic performance, and therefore, C-TiO2 and C-BiPO4 could be developed into a novel material to be used in the photodegradation of dye pollutants. (C) 2020 Elsevier Ltd. All rights reserved.

Automated summary

Photocatalysis using carbon microtube electrodes coated with titanium oxide and bismuth phosphate enhanced the degradation of methylene blue; degradation was mainly driven by hydroxyl radical oxidation; increase in mass transfer rate and separation rate of electron-hole pairs improved photocatalytic efficiency for degradation of pollutants.