过氧二硫酸盐
光化学
催化作用
可见光谱
降级(电信)
电子顺磁共振
化学
激进的
离解(化学)
污染物
材料科学
有机化学
光电子学
物理
计算机科学
电信
核磁共振
作者
Yinghao Wen,Ching‐Hua Huang,Daniel C. Ashley,Dan Meyerstein,Dionysios D. Dionysiou,Virender K. Sharma,Xingmao Ma
标识
DOI:10.1021/acs.est.1c06696
摘要
Activation of peroxydisulfate (PDS, S2O82-) via various catalysts to degrade pollutants in water has been extensively investigated. However, catalyst-free activation of PDS by visible light has been largely ignored. This paper reports effective visible light activation of PDS without any additional catalyst, leading to the degradation of a wide range of organic compounds of high environmental and human health concerns. Importantly, the formation of reactive species is distinctively different in the PDS visible light system with and without pollutants [e.g., atrazine (ATZ)]. In addition to SO4•- generated via S2O82- dissociation under visible light irradiation, O2•- and 1O2 are also produced in both systems. However, in the absence of ATZ, H2O2 and O2•- are key intermediates and precursors for 1O2, whereas in the presence of ATZ, a different pathway was followed to produce O2•- and 1O2. Both radical and nonradical processes contribute to the degradation of ATZ in the PDS visible light system. The active role of 1O2 in the degradation of ATZ besides SO4•- is manifested by the enhanced degradation of contaminants and electron paramagnetic resonance spectroscopy measurements in D2O.
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