Degradation mechanisms and toxicity determination of bisphenol A by FeOx-activated peroxydisulfate under ultraviolet light.

Abstract

Ultraviolet light (UV)-assisted advanced oxidation processes (AOPs) are commonly used to degrade organic contaminants. However, this reaction system's extensive comprehension of the degradation mechanisms and toxicity assessment remains inadequate. This study focuses on investigating the degradation mechanisms and pathways of bisphenol A (BPA), generation of reactive oxygen species (ROS), and toxicity of degradation intermediates in UV/PDS/ferrous composites (FeO_x) systems. The degradation rate of BPA gradually increased from the initial 11.92% to 100% within 120 min. Sulfate radicals (${\mathrm{SO}}_4^{.-}$), hydroxyl radicals (^.OH), superoxide anions ($O_2^{.-}$), and singlet oxygen (¹O₂) were the primary factors in the photocatalytic degradation of BPA in the UV/PDS/FeO_x systems. The main reactions of BPA in this system were deduced to be β-bond cleavage, hydroxyl substitution reaction, hydrogen bond cleavage, and oxidation reaction. A trend of decreasing toxicity for the degradation intermediates of BPA was observed according to the toxicity investigations. The efficient degradation of BPA in UV/PDS/FeO_x systems provided theoretical data for AOPs, which will improve the understanding of organic contaminants by FeO_x in natural industry wastewater.