Degradation of Organic Micropollutants in UV/NH2Cl Advanced Oxidation Process

Monochloramine (NH2Cl) can be irradiated by UV to create an advanced oxidation condition (i.e., UV/NH2Cl) for the elimination of organic micropollutants (OMPs) from source water. However, information in retrospective studies was scarce on how UV/NH2Cl performance would be affected by the water matrix and OMP molecular structures. In this study, the degradation of five representative OMPs, including triclosan, carbamazepine, sulfamethoxazole, estradiol (E2), and ethinylestradiol (EE2), was examined in different water matrices. All OMPs were rapidly removed by UV/NH2Cl but exhibited different degradation mechanisms. Although center dot OH, center dot Cl, and direct photolysis mainly contributed to the overall degradation of OMPs in buffered nanopure water, the contribution of reactive nitrogen species (RNS) generated from the photolysis of NH2Cl was not negligible in the degradation of E2 and EE2. A phenolic group was identified as the moiety reactive toward RNS. Based on quantitative analysis of the impact on OMP degradation from cosolutes (including Cl-, HCO3-, NOM) as well as pH and NH2Cl doses, we developed a kinetic model for the prediction of OMP degradation in complex water matrices. In environmental water matrices, the performance and radical contributions in UV/NH2Cl and UV/H2O2 systems were taken into comparison, which showed faster degradation of OMPs and a more significant contribution of CO(3)( )(center dot-)in the UV/NH2Cl process.