过硫酸盐
双金属片
催化作用
化学
X射线光电子能谱
无机化学
激进的
羟基自由基
光化学
核化学
化学工程
有机化学
工程类
作者
Yifei Zhang,Jia Wei,Luyi Xing,Jiamei Li,Mengdie Xu,Guoping Pan,Jun Li
标识
DOI:10.1016/j.seppur.2021.120124
摘要
Metal organic frameworks (MOFs) have been widely concerned by researchers as catalytic materials. In this work, nitrogen doped Fe, Co bimetallic MOF named FeCo/N-MOF was prepared by “one-pot” hydrothermal method as a catalyst for activating persulfate to degrade tetracycline. The hexagonal spindle crystals morphology and porous structure were observed on the FeCo/N-MOF. The X-ray photoelectron spectroscopy (XPS) showed that Fe(III) and Co(II) were the main active sites and the presence of pyrrole N was positive to the catalysis. The different conditions of catalyst dosage, pH and persulfate concentration were discussed to further understand the mechanism of FeCo/N-MOF on tetracycline (TC) degradation. The results revealed that about 99% of tetracycline was degraded in 150 min when FeCo/N-MOF was 0.4 g/L and persulfate was 5 mmol/L in a wide range of pH from 3 to 9. Moreover, the reaction stoichiometric efficiency of persulfate was 6.13%. There were radicals and non-radical pathways in the process of TC degradation and the superoxide radical was the main active substances. This study suggested that FeCo/N-MOF was of great potential in persulfate activation for water purification, which also provided a platform for MOF-derived catalysts in the field of advanced oxidation.
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