合成纳米复合材料Co2SnO4@rGO在混合臭氧氧化系统中活化过氧一硫酸盐,有效降解废水中的头孢氨苄

Van Long Nguyen, Minh Thanh Le, Lan Huong Nguyen
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摘要

本研究采用溶胶-凝胶法成功制备了不同比例Co2SnO4和还原氧化石墨烯的Co2SnO4@rGO纳米复合材料。然后将这些纳米复合材料作为非均相催化剂,在Co2SnO4@rGO/PMS的非均相催化氧化中激活PMS,并在O3/Co2SnO4@rGO/PMS的混合臭氧化体系中降解头孢氨苄(CFX)。通过氮吸附-死吸附、扫描电镜、能谱图和x射线衍射(XRD)对催化剂的理化性质进行了评价。研究了该纳米复合材料在水溶液中降解CFX的催化活性。此外,通过一阶模型拟合实验数据,确定了CFX的降解动力学。结果表明,在Co2SnO4@rGO/PMS和O3/Co2SnO4@rGO/PMS体系中,以2-Co2SnO4和1-rGO的复合比例降解CFX的效率最高,分别达到95.07和99.07%。O3/Co2SnO4@rGO/PMS体系对CFX的降解率高于Co2SnO4@rGO/PMS体系。结果是由于与Co2SnO4和rGO相比,2-Co2SnO4@1-rGO中的SBET显著增加,促进了催化剂表面发生的催化反应。此外,O3与Co2SnO4@rGO/PMS之间的耦合产生了协同效应,导致产生更多的*SO4-和*OH自由基,从而提高了混合臭氧化体系中CFX的降解率。这些初步研究结果表明,纳米复合催化剂2-Co2SnO4@1-rGO在混合臭氧氧化中活化PMS以有效降解废水中的抗生素残留物是可行的。
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Synthesising nanocomposite Co2SnO4@rGO for peroximonosulphate activation in a hybrid ozonation system to effectively degrade cefalexin from wastewater
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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