电子顺磁共振
催化作用
化学
矿化(土壤科学)
聚合
降级(电信)
反应速率常数
离子
四环素
核化学
化学工程
铜
动力学
氧化物
有机化学
聚合物
氮气
电信
物理
核磁共振
量子力学
计算机科学
工程类
生物化学
抗生素
作者
Dandan Yang,Peidong Hong,Yi Hu,Yulian Li,Chengming Wang,Junyong He,Bai Sun,Shuguang Zhu,Lingtao Kong,Jinhuai Liu
标识
DOI:10.1016/j.apsusc.2021.149424
摘要
CuO particles encapsulated by an irregular polyhedral carbon framework ([email protected]) were prepared via a one-pot polymerization method. The prepared [email protected] exhibited a highly enhanced performance in the activation of peroxymonosulfate (PMS). Our results indicated that the rate constant of tetracycline (TC) degradation was significantly increased by more than 85%, i.e., from 0.021 to 0.147 min−1, compared with the corresponding value for the bare CuO. TC elimination was completely achieved within 40 min, with the mineralization rate reaching 75.3% in 1 h. In addition, the [email protected]/PMS system exhibited an excellent performance in complex water matrixes containing various inorganic ions. Based on the use of scavengers and spin-trapping electron paramagnetic resonance technology, reactive species including OH, SO4−, and 1O2 were proposed to be the main oxidants of the [email protected]/PMS system, and the possible intermediates were also fully investigated. Moreover, a catalytic cycle involving Cu+/Cu2+/Cu3+ was proposed. It was also demonstrated that the highly stable [email protected] can be easily recycled and reused. The present study therefore embodies the conceptual design of an excellent catalyst with a persistent stability for the activation of PMS, which may serve as a versatile platform for wider environmental applications.
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