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负载于碳毡上的稳定且可循环使用的FeC@CN催化剂用于高效活化过一硫酸盐。

Stable and recyclable FeC@CN catalyst supported on carbon felt for efficient activation of peroxymonosulfate.

作者信息

Guo Chuanyi, Chen Chaofa, Lu Jiaying, Fu Du, Yuan Cheng-Zong, Wu Xi-Lin, Hui Kwun Nam, Chen Jianrong

机构信息

College of Geography and Environmental Science, Zhejiang Normal University, Jinhua 321004, China.

Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau SAR, China.

出版信息

J Colloid Interface Sci. 2021 Oct;599:219-226. doi: 10.1016/j.jcis.2021.04.092. Epub 2021 Apr 20.

Abstract

Stable and recyclable catalysts are crucial to the peroxymonosulfate (PMS) based advanced oxidation process (AOPs) for wastewater treatment. Herein, nitrogen-rich carbon wrapped FeC (FeC@CN) on carbon felt (CF) substrate was synthesized by using Prussian blue (PB) loaded CF as the precursors. The obtained FeC@CN/CF catalyst was applied for degradation of bisphenol A (BPA) via the heterogeneous catalytic activation of PMS. Results showed that ~91.7%, 95.2%, 98.1% and 99.1% of BPA (20 mg/L) were eliminated in the FeC@CN/CF + PMS system within 4, 10, 20 and 30 min, respectively. The fast degradation kinetics is attributed to the production of abundant reactive species (OH, SO and O) in the FeC@CN/CF + PMS system, as demonstrated by the electron paramagnetic resonance spectroscopy and quench experiments. The FeC@CN/CF catalyst was stable and can be easily recycled by using an external magnet. The results indicated that the nanoconfined FeC endowed FeC@CN/CF with high stability and magnetic property and enabled the efficient electron transfer for PMS activation. This study provides a cost-effective approach for the fabrication of stable and recyclable FeC@CN/CF catalyst, and shed a new light on the rational design of multifunctional catalyst for advanced water remediation.

摘要

稳定且可循环使用的催化剂对于基于过一硫酸盐(PMS)的高级氧化工艺(AOPs)处理废水至关重要。在此,以负载普鲁士蓝(PB)的碳毡(CF)为前驱体,合成了碳毡(CF)基底上富氮碳包裹的FeC(FeC@CN)。将所得的FeC@CN/CF催化剂用于通过PMS的非均相催化活化降解双酚A(BPA)。结果表明,在FeC@CN/CF + PMS体系中,4、10、20和30分钟内分别去除了约91.7%、95.2%、98.1%和99.1%的BPA(20 mg/L)。电子顺磁共振光谱和猝灭实验表明,快速降解动力学归因于FeC@CN/CF + PMS体系中产生了大量的活性物种(OH、SO和O)。FeC@CN/CF催化剂稳定,可通过外部磁铁轻松回收。结果表明,纳米限域的FeC赋予FeC@CN/CF高稳定性和磁性,并实现了PMS活化的高效电子转移。本研究为制备稳定且可循环使用的FeC@CN/CF催化剂提供了一种经济有效的方法,并为高级水修复多功能催化剂的合理设计提供了新的思路。

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