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Synthesising nanocomposite Co2SnO4@rGO for peroximonosulphate activation in a hybrid ozonation system to effectively degrade cefalexin from wastewater
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This study successfully developed Co2SnO4@rGO nanocomposites at various composite ratios of Co2SnO4 and rGO using the sol-gel method. These nanocomposites were then used as heterogeneous catalysts to activate PMS in the heterogeneous catalytic oxidation of Co2SnO4@rGO/PMS as well as the hybrid ozonation system O3/Co2SnO4@rGO/PMS to degrade cefalexin (CFX). The physical-chemical characteristics of the fabricated catalysts were evaluated through nitrogen adsorption-deadsorption, SEM images, EDS mapping, and XRD. The catalytic activity of the nanocomposite was investigated in a degradation reaction of CFX from an aqueous solution. Besides this, CFX degradation kinetics were determined by fitting experimental data with a first-order model. The results showed that at the composite ratio of 2-Co2SnO4 and 1-rGO for CFX degradation had the highest efficiency reaching 95.07 and 99.07% for Co2SnO4@rGO/PMS and O3/Co2SnO4@rGO/PMS systems, respectively. The degradation of CFX in the O3/Co2SnO4@rGO/PMS system was higher than that of Co2SnO4@rGO/PMS. The results were due to a remarkable increase in SBET in 2-Co2SnO4@1-rGO compared to both Co2SnO4 and rGO, facilitating a catalytic reaction occurring on the catalyst’s surface. Moreover, the coupling between O3 and Co2SnO4@rGO/PMS generated a synergetic effect leading to the generation of more *SO4- and *OH radicals, which enhanced the CFX degradation rate in the hybrid ozonation system. These primary findings illustrated that the nanocomposite catalyst 2-Co2SnO4@1-rGO was feasible for the activation of PMS in hybrid ozonation to effectively degrade antibiotic residues from wastewater.
Ministry of Science and Technology, Vietnam (VMOST)
Title: Synthesising nanocomposite Co2SnO4@rGO for peroximonosulphate activation in a hybrid ozonation system to effectively degrade cefalexin from wastewater
Description:
This study successfully developed Co2SnO4@rGO nanocomposites at various composite ratios of Co2SnO4 and rGO using the sol-gel method.
These nanocomposites were then used as heterogeneous catalysts to activate PMS in the heterogeneous catalytic oxidation of Co2SnO4@rGO/PMS as well as the hybrid ozonation system O3/Co2SnO4@rGO/PMS to degrade cefalexin (CFX).
The physical-chemical characteristics of the fabricated catalysts were evaluated through nitrogen adsorption-deadsorption, SEM images, EDS mapping, and XRD.
The catalytic activity of the nanocomposite was investigated in a degradation reaction of CFX from an aqueous solution.
Besides this, CFX degradation kinetics were determined by fitting experimental data with a first-order model.
The results showed that at the composite ratio of 2-Co2SnO4 and 1-rGO for CFX degradation had the highest efficiency reaching 95.
07 and 99.
07% for Co2SnO4@rGO/PMS and O3/Co2SnO4@rGO/PMS systems, respectively.
The degradation of CFX in the O3/Co2SnO4@rGO/PMS system was higher than that of Co2SnO4@rGO/PMS.
The results were due to a remarkable increase in SBET in 2-Co2SnO4@1-rGO compared to both Co2SnO4 and rGO, facilitating a catalytic reaction occurring on the catalyst’s surface.
Moreover, the coupling between O3 and Co2SnO4@rGO/PMS generated a synergetic effect leading to the generation of more *SO4- and *OH radicals, which enhanced the CFX degradation rate in the hybrid ozonation system.
These primary findings illustrated that the nanocomposite catalyst 2-Co2SnO4@1-rGO was feasible for the activation of PMS in hybrid ozonation to effectively degrade antibiotic residues from wastewater.
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