Photolysis of sulfamethazine using UV irradiation in an aqueous medium

Although many studies have been focused on the photochemistry of antibiotics, the roles of reactive species in photolysis and the effects of dissolved substances on antibiotic photochemical behavior have been poorly examined. The photolytic behaviors of sulfamethazine (SMN) in pure water were investigated via adding different scavengers to quench the active species. Results showed that decomposition of the triplet-excited state of SMN ((3)SMN*) by direct photolysis was the main path of SMN photolysis in water. Moreover, self-sensitized SMN cannot be ignored during SMN photodegradation. The main photoproducts of SMN were identified by LC-MS/MS, which indicated that SMN could not be mineralized although the photolysis under UV was effective. The effects of Cl(−), NO(3)(−), and fulvic acid (FA) (common substances in natural water) on SMN photolytic behaviors were also studied. The triplet-induced halogenation of SMN increases the ionic strength and reduces the ground state SMN; these are the primary causes of promotion of SMN photolysis by Cl(−). More ˙OH produced in the presence of NO(3)(−) could promote SMN photolysis. Competitive absorption of photons of FA with SMN and ROS scavenged by FA were the main reasons for the inhibition of SMN photolysis. The research findings are helpful for further studies on the environmental risks of ACs in natural waters and promoting the development of AC pollution treatment technology.