Abstract

The batch experiments of photocatalytic oxidation-reduction of bromate and ibuprofen (IBP) by graphene oxide (GO) and TiO2 heterostructure doped with F (FGT) particles were conducted. The performance and mechanism of synergistic removal of bromate and IBP by FGT were discussed. The results show that a demonstrable synergistic effect and excellent removal rate of bromate and IBP by FGT were exhibited. When pH is 5.2 and the dosage of FGT is 0.1 g/L, the reaction rate constants of bromate and IBP increased from 0.0584 min-1 and 0.4188 min-1 to 0.1353 min-1 and 0.4504 min-1, respectively, compared with the degradation of bromate or IBP alone. The reaction of photocatalytic synergistic degradation is appropriately fitted through Langmuir-Hinshelwood first-order kinetics. The mechanism of synergistic removal of bromate and IBP by FGT was discussed. And electrons (e-), hydroxyl radical (⋅OH), and superoxide radical (⋅O2-) are the main active species. The electrons play a main role in the bromate reduction, and bromine is the only reduction product, while the oxidation of IBP is the result of ⋅OH and ⋅O2-, and ⋅OH plays a key role. The recombination of electrons and holes is inhibited by simultaneous consumption of bromate and IBP, which makes full use of the redox properties of FGT and plays a synergistic role in the removal of pollutants. The results indicate that photocatalytic oxidation-reduction by FGT is a promising, efficient, and environmental-friendly method for synchronous removal of combined pollution in water.

Highlights

  • With the development of industry and agriculture, the complex characteristics of water pollution are becoming more and more prominent

  • Due to its advantages of high efficiency, good photochemical stability, nontoxicity, and low cost, TiO2 photocatalysis has been proved to be one of the most promising environmentalfriendly technologies for the decomposition of environmental pollutants, and it has been widely studied in water treatment and air pollution control [1,2,3]

  • The photocatalytic activity of TiO2 is limited by band gap and the recombination of photogenerated electronhole pairs

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Summary

Introduction

With the development of industry and agriculture, the complex characteristics of water pollution are becoming more and more prominent. Due to its advantages of high efficiency, good photochemical stability, nontoxicity, and low cost, TiO2 photocatalysis has been proved to be one of the most promising environmentalfriendly technologies for the decomposition of environmental pollutants, and it has been widely studied in water treatment and air pollution control [1,2,3]. The performance of TiO2 photocatalysts can be obviously enhanced through appropriate modification, and co-doped TiO2 usually exhibits better results of pollutants removal than singly doped TiO2 [4, 5]. A photocatalyst of graphene oxide (GO) and TiO2 heterostructure doped with F (FGT) was synthesized, which exhibited a commendable reduction performance of bromate [6]. Over 90% of 100 μg/L bromate could be removed with a

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