单线态氧
化学
光催化
罗丹明B
光化学
亚甲蓝
反应速率常数
催化作用
氢氧化物
猝灭(荧光)
矿化(土壤科学)
降级(电信)
煤
氧气
无机化学
有机化学
动力学
氮气
荧光
物理
电信
量子力学
计算机科学
作者
Hongjun Fang,Jie Ding,Xinzhen Feng,Weijie Ji,Chak-Tong Au
标识
DOI:10.1016/j.jwpe.2022.103372
摘要
Novel Mo/Mo2C/CoAl-LDH (CoAl layered double hydroxide) photocatalysts were fabricated through a hydrothermal route and applied for efficient PMS activation and typical pollutants (tetracycline/TC, ciprofloxacin/CIP, methylene blue/MB, congo red/CR and rhodamine B/RhB) degradation. Specifically, tetracycline removal efficiency of 99 % (TC, 20 mg/L) with a TOC mineralization efficiency of 65 % was achieved by the Mo/Mo2C/CoAl-LDH/PMS/Vis system within 4 min-reaction, and the obtained reaction rate constant was 5.5 and 41.5 times greater than that of CoAl-LDH/PMS/Vis and Mo/Mo2C/PMS/Vis system, respectively. The exceptional performance over this joint system was mainly attributed to the synergism of the MoCo dual active components and the involved photocatalysis. The quenching/ESR investigations clearly demonstrated that all of the generated species contributed to TC degradation, and among them the singlet oxygen showed the greatest impact. The toxicity assessment suggested that most of degraded intermediates become more eco-friendly to the environment. Moreover, the involved reaction mechanism and degradation pathways of TC were proposed and discussed in detail. This work provides a promising strategy for PMS activation and environmental purification through an integrated photo-chemical catalysis.
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