Electro-adsorption and reduction of Uranium(VI) by Fe3O4@COFs electrode with enhanced removal performance

吸附 朗缪尔吸附模型 化学 选择性 废水 电极 核化学 材料科学 冶金 废物管理 有机化学 催化作用 物理化学 工程类
作者
Sen Yang,Zhouyi Ye,Xiaoya Cheng,Yuchun Wang,Zitong Luan,Wen‐Jun Li,Baowei Hu
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:474: 145598-145598 被引量:74
标识
DOI:10.1016/j.cej.2023.145598
摘要

Electro-adsorption is a promising technology for the removal of radionuclides, the development of electrodes is the key to achieve efficient separation. Herein, Fe3O4@COFs composites were obtained via one-step preparation strategy, and then loaded onto carbon felts to achieve efficient uranium(VI) electro-adsorption and reduction. The morphological and chemical structures of the prepared Fe3O4@COFs composites were confirmed by multiple analysis techniques. The results of adsorption experiments indicated that the adsorption equilibrium can be reached in half an hour at the potential of 1.2 V and 298.15 K. And the adsorption data for uranium(VI) is well consistent with pseudo-second-order kinetics model and Langmuir isotherm model with the maximum uptake capacity of 492.6 mg/g. Meanwhile, the functionalized electrode revealed good selectivity for uranium against other competing ions according to the calculated distribution coefficient Kd (3.24 × 104 mL/g). The simulated uranium-containing wastewater experiment results indicated the vast potential of Fe3O4@COFs electrodes for uranium(VI) removal from wastewaters. XPS studies confirmed that part of the hexavalent uranium(VI) is reduced to tetravalent uranium(IV) by Fe2+ in Fe3O4@COFs composites besides being bound by carboxyl ligands. This work can be extended to efficiently remove other charged pollutants by rational ligands design.
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