Increased Formation of Halomethanes During Chlorination of Chloramphenicol in Drinking Water by UV Irradiation, Persulfate Oxidation, and Combined UV/Persulfate Pre-Treatments
Ultraviolet/persulfate (UV/PS) has been widely used to generate sulfate radicals for degradation of water organic pollutants in previous studies. However, its impacts on disinfection byproduct formation during post-chlorination of degraded compounds is unclear. The objective of this study was to evaluate the impacts of UV irradiation, PS oxidation, and the combined UV/PS advanced oxidation process (AOP) pre-treatments on halomethane formation during the following chlorination of chloramphenicol (CAP), a model antibiotic commonly found in wastewater-impacted water. Results showed that CAP could be transformed to more trichloromethane (TCM) than monochloromethane (MCM) and dichloromethane (DCM) in the presence of excess chlorine. UV photolysis, PS oxidation and UV/PS AOP all directly decomposed CAP to produce halomethanes (HMs) before post-chlorination. Moreover, UV and UV/PS pre-treatments both enhanced the formation of all the HMs in the subsequent chlorination. PS pre-oxidation decreased the TCM formation during post-chlorination, but increased the yields of MCM, DCM and total HMs. UV pre-irradiation significantly increased the bromide utilization of HMs, whereas UV/PS pre-oxidation decreased the bromine incorporation and utilization of HMs from the chlorination of CAP in a low-bromide water. UV irradiation, PS oxidation, and UV/PS AOP can inactivate pathogens and degrade organic pollutants, but this benefit should be weighed against a potential risk of the increased halomethane formation from degraded organic pollutants with and without post-chlorination.
MSU Digital Commons Citation
Chu, Wen Hai; Tengfei, Chu; Erdeng, Du; Deng, Yang; Yingqing, Guo; and Naiyun, Gao, "Increased Formation of Halomethanes During Chlorination of Chloramphenicol in Drinking Water by UV Irradiation, Persulfate Oxidation, and Combined UV/Persulfate Pre-Treatments" (2016). Department of Earth and Environmental Studies Faculty Scholarship and Creative Works. 360.