Facile synthesis of Ag-Co bimetallic nanoparticles decorated Fe3O4@EDTA nanocomposites and their enhanced catalytic activity

双金属片 催化作用 X射线光电子能谱 材料科学 纳米颗粒 纳米复合材料 螯合作用 还原剂 动力学 核化学 金属 化学工程 水溶液中的金属离子 纳米技术 化学 冶金 有机化学 物理 量子力学 工程类
作者
Yan Xing,Xiaohui Bai,Ya Zhang,G. Y. Hu,Liguo Gao,Pengcheng Qi,Xiangrong Ma,Xu‐Chun Gao,Muhuo Yu,Min Bai
出处
期刊:Journal of Magnetism and Magnetic Materials [Elsevier BV]
卷期号:579: 170857-170857 被引量:1
标识
DOI:10.1016/j.jmmm.2023.170857
摘要

In this study, firstly, bimetallic Ag-Co nanoparticles with rich catalytic sites decorated on Fe3O4 magnetic carriers through metal ion chelating agent EDTA (Ag-Co@EDTA@Fe3O4 NPs) were fabricated by co-reducing agent in-situ deposition method for the first time. The synthesized nanocomposites were characterized by various techniques, including UV–vis, XRD, TEM, EDX, XPS and VSM. Secondly, the catalytic reduction performance of Ag-Co@EDTA@Fe3O4 NPs was analyzed for 2-nitrophenol in the presence of NaBH4 at 25 ℃. Results showed that the k of Ag-Co@EDTA@Fe3O4 NPs was 10.9 and 2.7 times higher than that of Co@EDTA@Fe3O4 and Ag@EDTA@Fe3O4 NPs, respectively, which considered to obey the first-order kinetics equation, proving the strong synergistic effect between Ag and Co nanoparticles. Furthermore, the significantly enhanced catalytic activity of Ag-Co@EDTA@Fe3O4 NPs was discussed. Plenty of Ag NPs were successfully anchored on Fe3O4@EDTA supports maybe the crucial factor, and the doped Co provided much more active sites in the catalytic process. Finally, the degradation efficiency of Ag-Co@EDTA@Fe3O4 NPs still remained above 95% after 5 cycles. Importantly, there was no significant difference between the fresh catalyst and after cycling for 5 times, observed by TEM and SEM. Meanwhile, the change of hydrodynamic diameter of the used Ag-Co@EDTA@Fe3O4 NPs over cycle number was measured around 230 nm which increased unobviously, making it a promising candidate for wastewater treatment in industries.
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