激进的
单线态氧
针铁矿
化学
光化学
氧气
密度泛函理论
反应速率常数
四环素
电子顺磁共振
催化作用
单重态
动力学
物理化学
生物化学
计算化学
有机化学
核磁共振
激发态
吸附
核物理学
物理
抗生素
量子力学
作者
Xuguang Li,Le Wang,Yanxiu Guo,Wen Song,Yanfei Li,Liangguo Yan
标识
DOI:10.1016/j.cej.2022.138104
摘要
MoS2-based materials have recently attracted much attention in advanced oxidation processes based on peroxymonosulfate (PMS). Herein, a series of goethite-MoS2 hybrids (G-MoS2) with dual sites (Fe and Mo) were applied as PMS activators to remove tetracycline (TC). The pseudo-first-order rate constant for TC degradation in 0.1G-MoS2/PMS system was 3.25 times that in MoS2/PMS system. Electron paramagnetic resonance spectra and density functional theory calculation demonstrated that PMS was more likely to be adsorbed and activated on the surface of 0.1G-MoS2 compared with pristine MoS2. Moreover, the total contributions of •OH and 1O2 were over 95% for TC removal in both MoS2/PMS and 0.1G-MoS2/PMS systems. However, the contribution of •OH (66.72%) was enhanced, and that of 1O2 (32.17%) was weakened in 0.1G-MoS2/PMS system compared with those in MoS2/PMS system. This work could provide new strategies to construct high-efficiency PMS catalysts and further understand the role of main reactive species in catalyst/PMS system.
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