Comparative evaluation of metoprolol degradation by UV/chlorine and UV/H2O2 processes

The degradation of metoprolol (MTP), a beta-blocker commonly used for cardiovascular diseases, by UV/chlorine and UV/H2O2 processes'was comparatively evaluated. MTP direct photolysis at 254 nm could be neglected, but remarkable MTP degradation was observed in both the UV/chlorine and UV/H2O2 systems. Compared with UV/H2O2, UV/chlorine has a more pronounced MTP degradation efficiency. In addition to primary radicals (center dot OH and Cl center dot), secondary radicals (ClO center dot and Cl-2(center dot-)) played a pivotal role in degrading MTP by UV/chlorine process. The relative contributions of hydroxyl radicals (center dot OH) and reactive chlorine species (RCS) in the UV/chlorine system varied at different solution pH values (i.e., the contribution of RCS increased from 57.7% to 75.1% as the pH increased from 6 to 8). The degradation rate rose as the oxidant dosage increased in the UV/chlorine and UV/H2O2 processes. The presence of slightly affected MTP degradation in both processes, while the existence of HCO3 and HA inhibited MTP degradation to different extents in both processes. In terms of the overall cost of electrical energy, UV/chlorine is more cost efficient than UV/H2O2. The degradation products during the two processes were identified and compared, and the degradation pathways were proposed accordingly. Compared with the direct chlorination of MTP, pre-oxidation with UV/chlorine and UV/H2O2 significantly enhanced the formation of commonly known DBPs. Therefore, when using UV/chlorine and UV/H2O2 in real waters to remove organic pollutants, the possible risk of enhanced DBP formation resulting from the degradation of certain pollutants during post-chlorination should be carefully considered. (C) 2019 Elsevier Ltd. All reserved.