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Synthesis of magnetic CoFe2O4/ordered mesoporous carbon nanocomposites and application in Fenton-like oxidation of rhodamine B
Authors:Deng  Jing  Chen  Yi-Jing  Lu  Yu-An  Ma  Xiao-Yan  Feng  Shan-Fang  Gao  Naiyun  Li  Jun
Institution:1.College of Civil Engineering and Architecture, Zhejiang University, Hangzhou, 310058, China
;2.College of Civil Engineering and Architecture, Zhejiang University of Technology, Hangzhou, 310014, China
;3.College of Environmental Science & Engineering, State Key Laboratory of Pollution Control & Resources Reuse, Key Laboratory of Yangtze Water Environment, Ministry of Education, Shanghai, 200092, China
;4.College of Environment, Zhejiang University of Technology, 18 Chaowang Road, Xiacheng District, Hangzhou, 310014, China
;
Abstract:

CoFe2O4/ordered mesoporous carbon (OMC) nanocomposites were synthesized and tested as heterogeneous peroxymonosulfate (PMS) activator for the removal of rhodamine B. Characterization confirmed that CoFe2O4 nanoparticles were tightly bonded to OMC, and the hybrid catalyst possessed high surface area, pore volume, and superparamagnetism. Oxidation experiments demonstrated that CoFe2O4/OMC nanocomposites displayed favorable catalytic activity in PMS solution and rhodamine B degradation could be well described by pseudo-first-order kinetic model. Sulfate radicals (SO4 ?·) were verified as the primary reactive species which was responsible for the decomposition of rhodamine B. The optimum loading ratio of CoFe2O4 and OMC was determined to be 5:1. Under optimum operational condition (catalyst dosage 0.05 g/L, PMS concentration 1.5 mM, pH 7.0, and 25 °C), CoFe2O4/OMC-activated peroxymonosulfate system could achieve almost complete decolorization of 100 mg/L rhodamine B within 60 min. The enhanced catalytic activity of CoFe2O4/OMC nanocomposites compared to that of CoFe2O4 nanoparticles could be attributable to the increased adsorption capacity and accelerated redox cycles between Co(III)/Co(II) and Fe(III)/Fe(II).

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