Identification of Reactive Oxygen Species and Mechanism on Visible Light-Induced Photosensitized Degradation of Oxytetracycline

Abstract

This study investigated the photolysis and TiO2-assisted photosensitized degradation of oxytetracycline (OTC) under visible light, the active reactive oxygen species (ROS), and the degradation mechanisms in these two reactions. The results show that the deprotonated OTC could be photolyzed more easily under visible light because of the redshift of its absorption spectrum at high pH values. Due to the TiO2-assisted self-photosensitized degradation of OTC, OTC removal in the visible light/TiO2 system was more efficient with the addition of TiO2, as demonstrated when TiO2 was replaced with insulator SiO2. The study's ROS scavenging experiments show that superoxide radical anion (O2•-) ROS was most responsible for the self-sensitized degradation of OTC in both reactions. OTC degradation under the visible light/TiO2 system was enhanced with increasing TiO2 load, while the elimination of total organic carbon (TOC) was very limited after 5 h of visible light irradiation. Based on the eight identified transformation products found, five potential reaction mechanisms, including hydroxylation, quinonization, decarbonylation, de-methylation, and dehydration, were proposed for the photolytic and TiO2-assisted photosensitized degradation mechanisms of OTC under visible light. This study indicates that OTC can degrade under visible light with or without a semiconductor when conditions are suitable.