化学
激进的
催化作用
电子顺磁共振
羟基自由基
光化学
核化学
氧气
活性氧
无机化学
环境化学
降级(电信)
有机化学
物理
电信
生物化学
核磁共振
计算机科学
作者
Chaoqun Tan,Qing‐Long Xu,Tianyu Sheng,Xinxin Cui,Zhiren Wu,Haiying Gao,He Li
标识
DOI:10.1016/j.jhazmat.2020.123084
摘要
Iron oxychloride (FeOCl) is utilized as a activator of peroxymonosulfate (PMS) for the degradation of paracetamol (APAP) and phenacetin (PNCT) in response to the water pollution by persistent pharmaceuticals. The degradation process was well fitted with a pseudo-first order kinetic pattern, and the excellent catalytic performance towards APAP (100 % removal) and PNCT (86.5 % removal) was obtained in the presence of 0.2 g/L FeOCl and 2.0 mM PMS at pH 7.0 in 30 min. In-situ electron spin resonance (ESR) and scavenging tests revealed the generation of a series of ROS (·OH, SO4−, O2−, 1O2), which was highly dependent on pH. Besides, the non-radical pathways process involved 1O2 was dominant in APAP oxidation, while both ·OH and 1O2 are significant in PNCT removal. Furthermore, the formation of disinfection by-products (DBPs) during post-chlorination showed neglectable increment at neutral and alkaline condition with FeOCl/PMS pre-oxidation, and the calculated cytotoxicity would experience a continuous deterioration with pH increase. These results displayed high efficiency of FeOCl/PMS system in micropollutants degradation and a relatively comprehensive activation process of PMS, which may promote practical application in environmental remediation.
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