Vanadium oxide-supported copper ferrite nanoparticles: A reusable and highly efficient catalyst for rhodamine B degradation via activation of peroxymonosulfate

被引:10
作者
Salami, Rasoul [1 ]
Amini, Mojtaba [1 ,2 ]
Bagherzadeh, Mojtaba [3 ]
Chae, Keun Hwa [4 ]
机构
[1] Univ Maragheh, Dept Chem, Fac Sci, Maragheh, Iran
[2] Univ Tabriz, Dept Inorgan Chem, Fac Chem, Tabriz, Iran
[3] Sharif Univ Technol, Chem Dept, Tehran, Iran
[4] Korea Inst Sci & Technol, Adv Anal Ctr, Seoul, South Korea
基金
美国国家科学基金会;
关键词
copper ferrite; peroxymonosulfate; rhodamine B degradation; SO4; radicals; vanadium oxides; REDUCED GRAPHENE OXIDE; RATE CONSTANTS; BISPHENOL-A; PHOTOCATALYTIC DEGRADATION; HYDROXYL RADICALS; CUFE2O4; NANOPARTICLES; ORGANIC CONTAMINANTS; ADVANCED OXIDATION; MN NANOPARTICLES; MFE2O4; M;
D O I
10.1002/aoc.6367
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A magnetic vanadium oxide nanoparticles supported on spinel copper ferrite (CuFe2O4-VOx) are prepared, characterized, and examined for the peroxymonosulfate (PMS) activation to degrade Rhodamine B (RhB) in water solution. Interestingly, the results show that despite the inability of mixture of copper ferrite and vanadium oxides nanoparticles to the effective RhB decomposition, the prepared catalyst exhibits an excellent catalytic ability toward RhB oxidation. The influence of vital parameters, such as temperature, PMS concentration, catalyst loading, and initial pH are discussed comprehensively. The kinetic studies demonstrate that the pseudo-first-order model is well fitted for RhB degradation in CuFe2O4-VOx/PMS system and the activation energy is estimated at 19.60 kJ mol(-1). Furthermore, it is found out that the concentration of leached metal ions in solution is negligible and PMS activation is done mainly on the surface of the catalyst. A probable mechanism of PMS activation over RhB degradation is proposed based on the results of free radical quenching studies and X-ray photoelectron spectroscopy (XPS) analysis. Radical quenching experiments using various scavengers suggest SO4 center dot- as a main reactive species in the degradation.
引用
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页数:12
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