Persulfate activation over CoFe2O4/CuS for degradation of Orange II under visible light

被引:12
|
作者
Hao, Yixing [1 ]
Zhu, Fang [1 ]
Cheng, Hao [2 ]
Komarneni, Sridhar [3 ,4 ]
Ma, Jianfeng [1 ]
机构
[1] Changzhou Univ, Sch Environm Sci & Engn, Changzhou 213164, Jiangsu, Peoples R China
[2] Guangxi Univ Sci & Technol, Coll Biol & Chem Engn, Guangxi Key Lab Green Proc Sugar Resources, Liuzhou 545006, Guangxi, Peoples R China
[3] Penn State Univ, Dept Ecosyst Sci & Management, University Pk, PA 16802 USA
[4] Penn State Univ, Mat Res Inst, Mat Res Lab 204, University Pk, PA 16802 USA
关键词
Dye degradation; Optical materials; Persulfate activation; Heterojunction; REMOVAL; OXIDATION; METAL; WATER; PEROXYMONOSULFATE; PHOTOCATALYSTS; NANOCOMPOSITES; NANOPARTICLES; MICROSPHERES; NITRIDE;
D O I
10.1016/j.jpcs.2023.111787
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A magnetic porous composite catalyst has been synthesized from CoFe2O4 and CuS. Its degradation performance towards organic pollutants in a heterogeneous photocatalytic system has been compared with those of the in-dividual photocatalysts and those of individual chemocatalysis systems. Orange II served as a target contaminant. Persulfate and catalyst were combined under visible light conditions to achieve degradation of the organic pollutant, whereupon the degradation efficiency reached up to 97 %. The catalyst has been characterized by X-ray diffraction (XRD) analysis, X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET) analysis, Mott-Schottky analysis, scanning electron microscopy (SEM), and solid-state UV/Vis spectrophotometry. The influences of pH and different catalyst and persulfate loadings in the system have been studied. The results of quenching experiments showed non-radical degradation to be a major pathway, with singlet molecular oxygen (1O2) and photogenerated holes (h+) as the critical reactive species. Besides, the magnetic properties of the catalyst are conducive to its recycling, and it still showed high degradation efficiency after three cycles.
引用
收藏
页数:14
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