Innovation of BiOBr/BiOI@Bi5O7I Ternary Heterojunction for Catalytic Degradation of Sodium P-Perfluorous Nonenoxybenzenesulfonate

Author:

Xu Tao1,Liu Yang1ORCID,You Tie-Qing1,Bao Jia1ORCID

Affiliation:

1. School of Environmental and Chemical Engineering, Shenyang University of Technology, Shenyang 110870, China

Abstract

As an alternative for perfluorooctane sulfonic acid (PFOS), sodium p-perfluorononyloxybenzene sulfonate (OBS) has been widely used in petroleum, fire-fighting materials, and other industries. In order to efficiently and economically remove OBS contaminations from water bodies, in this study, a ternary heterojunction was constructed by coupling BiOBr and BiOI@Bi5O7I for improving the redox capacity and carrier separation ability of the material and investigating the effect of the doping ratios of BiOBr and BiOI@ Bi5O7I on the performance of the catalysts. Furthermore, the effects on the degradation of OBS were also explored by adjusting different catalyst doping ratios, OBS concentrations, catalyst amounts, and pH values. It was observed that when the concentration of OBS was 50 mg/L, the amount of catalyst used was 0.5 g/L, and the pH was not changed. The application of BiOBr/BiOI@ Bi5O7I consisting of 25% BiOBr and 75% BiOI@ Bi5O7I showed excellent stability and adsorption degradation performance for OBS, and almost all of the OBS in the aqueous solution could be removed. The removal rate of OBS by BiOBr/BiOI@ Bi5O7I was more than 20% higher than that of OBS by BiOI@Bi5O7I and BiOBr when the OBS concentration was 100 mg/L. In addition, the reaction rate constants of BiOBr/BiOI@ Bi5O7I were 2.4 and 10.8 times higher than those of BiOI@ Bi5O7I and BiOBr, respectively. Therefore, the BiOBr/BiOI@ Bi5O7I ternary heterojunction can be a novel type of heterojunction for the efficient degradation of OBS in water bodies.

Funder

National Natural Science Foundation of China

Applied Basic Research Plan of Liaoning Province

Science and Technology Joint Foundation of Liaoning Province

Publisher

MDPI AG

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