诺氟沙星
层状结构
光催化
降级(电信)
材料科学
层状双氢氧化物
化学工程
化学
无机化学
冶金
氢氧化物
生物化学
催化作用
抗生素
计算机科学
工程类
电信
环丙沙星
作者
Tao Wu,Xuesong Zhao,Xuesong Zhao
出处
期刊:Catalysts
[MDPI AG]
日期:2024-11-26
卷期号:14 (12): 860-860
被引量:1
标识
DOI:10.3390/catal14120860
摘要
The utilization of the photo catalytic activation of permonosulfate (PMS) for the combined breakdown of pollutants has become a focal point in research. Layered double hydroxides (LDHs) have a unique layered structure which is conducive to the adsorption and diffusion of reactants, and can provide more active sites for photocatalytic reactions. The anions between the layers can be exchanged with a variety of substances so that specific catalytically active species can be introduced as needed. LDHs themselves have certain catalytic activity, which can produce synergistic catalysis between LDHs and the supported photocatalytic active substances, and further improve the degradation effect of antibiotics. In actual wastewater treatment, LDHs as a catalyst carrier have a good application prospect. However, the poor activation effect is attributed to the low separation efficiency of catalyst carriers and insufficient active sites. In this study, a dual active site system consisting of Co and Fe, known as CoFe-LDHs@MoS2, was developed as a catalyst to facilitate the synergistic degradation of norfloxacin (NOF) by PMS under visible light. The findings demonstrate that the material possesses an effective capacity for the synergistic degradation of NOF. A comprehensive investigation was conducted to assess the impact of different catalysts, PMS dosage, degradation systems (Vis, PMS, or Vis PMS), catalyst dosage, NOF concentration, pH, and cycle times on the degradation performance. The active free radicals, degradation pathways, and intermediate toxicity were elucidated through capture experiments, Electron Paramagnetic Resonance Spectrometer (ESR) analysis, a liquid mass spectrometry (LC-MS) toxicity assessment, and theoretical calculations. This research offers a novel approach for designing catalysts with exposed high activity sites for the effective removal of NOF from environmental water.
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