Efficient peroxymonosulfate activation by magnetic CoFe2O4 nanoparticle immobilized on biochar toward sulfamethoxazole degradation: Performance, mechanism and pathway

生物炭 催化作用 降级(电信) 电子顺磁共振 化学 纳米颗粒 化学工程 过氧二硫酸盐 光化学 核化学 热解 有机化学 工程类 物理 电信 核磁共振 计算机科学
作者
Minghui Xiong,Ya Sun,Bo Chai,Guozhi Fan,Guangsen Song
出处
期刊:Applied Surface Science [Elsevier]
卷期号:615: 156398-156398 被引量:13
标识
DOI:10.1016/j.apsusc.2023.156398
摘要

Utilizing biomass waste to create highly efficient biochar-based catalysts has drawn intensively interest since it adheres to the idea of waste recycling in environmental conservation. Herein, CoFe2O4 nanoparticles immobilized on biochar (BC) derived from rape straw were synthesized and applied in degrading sulfamethoxazole (SMX) by activating peroxymonosulfate (PMS). Experimental results indicated that the 30 wt% CoFe2O4/BC composite catalyst had the best catalytic activity with the SMX degradation efficiency of 93% within 20 min, which was probably the fact that BC as a carrier not only effectively inhibited the agglomeration of CoFe2O4 nanoparticles and increased the active sites, but also could simultaneously participate in the catalytic degradation reaction as an activator of PMS. In addition, cycle experiments illustrated that the as-prepared catalyst possessed the excellent stability, and the magnetic property measurements implied that they were convenient for separation and recovery. According to quenching experiments, electron paramagnetic resonance (EPR) and electrochemical studies, both radical and non-radical process participated into degrading SMX, where the generated SO4·-, ·OH and O2·- as the major radical active species while 1O2 and direct electron transfer were responsible for the non-radical route. Besides, using high-performance liquid chromatography-mass spectrometry (HPLC-MS) analysis, a potential SMX degradation pathway was suggested. The present CoFe2O4/BC composite would be a promising PMS activation catalyst for environmental remediation.
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