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Enhanced removal of oxytetracycline from aquatic solution using MnOx@Fe3O4bimetallic nanoparticle coated powdered activated carbon: synergism of adsorption and chemical autocatalytic oxidation processesElectronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3en00465a

Authors :
Zhou, Jiahui
Wang, Shu
Source :
Environmental Science: Nano; 2023, Vol. 10 Issue: 11 p3171-3183, 13p
Publication Year :
2023

Abstract

MnOx@Fe3O4bimetallic nanoparticle coated powdered activated carbon (MnOx@Fe3O4-PAC) was successfully synthesized by a two-step chemical co-precipitation method. A comprehensive analysis of MnOx@Fe3O4-PAC's surface profile, crystal structure, and element composition was conducted to investigate its structural characteristics and oxytetracycline (OTC) removal mechanism. It was observed that MnOx@Fe3O4bimetallic nanoparticles were distributed on surfaces, pores, and channels of PAC. The removal efficiency of OTC reached its optimum (76.8%, OTC0= 100 mg L−1) at pH 3. Inorganic ions and humic acid (HA) had a limited impact on the adsorption process of OTC on MnOx@Fe3O4-PAC. The Freundlich isotherm and Elovich kinetic models could accurately describe the adsorption process of OTC on MnOx@Fe3O4-PAC. According to thermodynamic analysis, the adsorption process was dominated by chemisorption/surface complexation, which was a spontaneous endothermic reaction (ΔH= 51.62 kJ mol−1). The magnetically separable MnOx@Fe3O4-PAC had superior adsorption and oxidation capabilities for OTC removal from aqueous solution, and provided an alternative to PAC in the treatment of antibiotic wastewater. Furthermore, the self-catalytic reaction extended the service life of MnOx@Fe3O4-PAC without the additional use of oxidants, which made MnOx@Fe3O4-PAC a green, efficient, and recyclable composite for potentially practical applications.

Details

Language :
English
ISSN :
20518153 and 20518161
Volume :
10
Issue :
11
Database :
Supplemental Index
Journal :
Environmental Science: Nano
Publication Type :
Periodical
Accession number :
ejs64444992
Full Text :
https://doi.org/10.1039/d3en00465a