Degradation of ciprofloxacin using UV-based advanced removal processes: Comparison of persulfate-based advanced oxidation and sulfite-based advanced reduction processes

亚硫酸盐 过硫酸盐 化学 高级氧化法 降级(电信) 硫化物 连二亚硫酸钠 光化学 核化学 无机化学 催化作用 有机化学 电信 计算机科学
作者
Hannah Milh,Xingyue Yu,Deirdre Cabooter,Raf Dewil
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:764: 144510-144510 被引量:119
标识
DOI:10.1016/j.scitotenv.2020.144510
摘要

In this study, the degradation of ciprofloxacin (CIP) in wastewater was investigated using UV-based sulfate radical advanced oxidation processes (SR-AOP) and UV-based advanced reduction processes (ARP). More specifically, a comparison of the UV-based persulfate advanced oxidation process (the UV/PS process) and the UV-based sulfite advanced reduction process (the UV/sulfite process) was made. Considering the UV-based SR-AOPs, the UV/PS process was much more efficient than the UV-based peroxymonosulfate advanced oxidation process (the UV/PMS process), with pseudo first order reaction rate constants (kobs) of 0.752 and 0.145 min−1, respectively. For the UV-based ARPs, the UV/sulfite process was the most efficient, compared to the UV/sulfide and the UV/dithionite process (kobs of 0.269, 0.0157 and 0.0329 min−1, respectively). The optimal process parameters for both the UV/PS and the UV/sulfite process were determined and the contribution of the produced reactive species were identified. For the UV/PS process, maximal CIP degradation was found at pH 8, and both OH and SO4− were responsible for CIP degradation. For the UV/sulfite process, H and eaq− were responsible for CIP degradation, with eaq− being the predominant radical at pH 8.5. Although CIP degradation was much faster for the UV/PS process, the UV/sulfite process was determined to be much more efficient in the defluorination of CIP.
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