A facile heterogeneous system for persulfate activation by CuFe2O4 under LED light irradiation

被引:11
|
作者
Zhong, Xin [1 ]
Ye, Xiao-Yu [1 ]
Wu, Di [1 ]
Zhang, Kai-Xin [1 ]
Huang, Wei [1 ]
机构
[1] Beijing Normal Univ, Dept Environm Sci & Engn, Zhuhai 519000, Peoples R China
关键词
NANOSCALED MAGNETIC CUFE2O4; EFFICIENT DEGRADATION; AQUEOUS-SOLUTION; BISPHENOL-A; 2,4-DICHLOROPHENOXYACETIC ACID; PHOTOCATALYTIC DEGRADATION; CATALYTIC DEGRADATION; PEROXYMONOSULFATE PMS; ADVANCED OXIDATION; HYDROXYL RADICALS;
D O I
10.1039/c9ra05574f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, the removal performance for rhodamine B (RB) by persulfate (PS) activated by the CuFe2O4 catalyst in a heterogeneous catalytic system under LED light irradiation was investigated. The effect of vital experimental factors, including initial solution pH, CuFe2O4 dosage, PS concentration, co-existing anion and initial RB concentration on the removal of RB was systematically studied. The removal of RB was in accordance with the pseudo first-order reaction kinetics. Over 96% of 20 mg L-1 RB was removed in 60 min using 0.5 g L-1 CuFe2O4 catalyst and 0.2 mM PS at neutral pH. In addition, free radical quenching experiments and electron spin resonance (EPR) experiments were performed, which demonstrated the dominant role of sulfate radical, photogenerated holes and superoxide radical in the CuFe2O4/PS/LED system. The morphology and physicochemical properties of the catalyst were characterized by XRD, SEM-EDS, TEM, N-2 adsorption-desorption isotherm, UV-vis DRS, and XPS measurements. Moreover, 18.23% and 38.79% total organic carbon (TOC) removal efficiency was reached in 30 min and 60 min, respectively. The catalyst revealed good performance during the reusability experiments with limited iron and copper leaching. Eventually, the major intermediates in the reaction were detected by GC/MS, and the possible photocatalytic pathway for the degradation of RB in the CuFe2O4/PS/LED system was proposed. The results suggest that the CuFe2O4/PS/LED system has good application for further wastewater treatment.
引用
收藏
页码:32328 / 32337
页数:10
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