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
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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