限制
降级(电信)
催化作用
金属有机骨架
材料科学
金属
化学工程
芯(光纤)
复合材料
化学
物理化学
冶金
计算机科学
机械工程
有机化学
工程类
电信
吸附
作者
Huizhong Wu,Qiong Yi,Xiang Li,Yingxi Wang,Ling Li
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2024-01-01
卷期号:14 (24): 16727-16735
被引量:14
摘要
Low catalytic efficiency and catalyst recovery are the key factors limiting the practical application of advanced oxidation processes. In this work, a core-shell magnetic nanostructure Fe3O4@MIL-101(Fe, Co) was prepared via a simple solvothermal method. The core-shell structure and magnetic recovery performance were characterized by various technologies. The results of dye degradation experiments proved that within 10 minutes, the Fe3O4@MIL-101(Fe, Co)/PMS system can degrade more than 95% of 10 mg per L Rhodamine (RhB) at an initial pH of 7, which possesses higher catalytic activity than the Fe3O4/PMS system and the MIL-101(Fe, Co)/PMS system. The effects of initial solution pH and coexisting anions in water on the degradation of RhB were further discussed. The results showed that Fe3O4@MIL-101(Fe, Co) displayed excellent degradation efficiency in a wide pH range of 3-11 and capability of resisting coexisting anions. It is worth mentioning that after five cycles, the RhB removal rate can still be maintained at over 90% after 10 minutes of reaction. Free radical quenching experiments were further studied, confirming that ˙OH and SO4-˙ were involved in the degradation of RhB, while the dominating active free radical was SO4-˙. The possible reaction mechanism of the RhB degradation process was also inferred.
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