MgO coated magnetic Fe3O4@SiO2 nanoparticles with fast and efficient phosphorus removal performance and excellent pH stability

吸附 傅里叶变换红外光谱 介孔材料 水溶液 柠檬酸 核化学 材料科学 纳米颗粒 扫描电子显微镜 化学工程 离子强度 磷酸盐 化学 纳米技术 有机化学 复合材料 催化作用 冶金 工程类
作者
Shuangli Li,Yu Zhang,Sen Qiao,Jiti Zhou
出处
期刊:Chemosphere [Elsevier]
卷期号:307: 135972-135972 被引量:3
标识
DOI:10.1016/j.chemosphere.2022.135972
摘要

A regenerable MgO-coated magnetic Fe3O4@SiO2 (FSM) composite effectively avoided the agglomeration of nano-MgO, which was resoundingly used for efficient and rapid phosphorus removal from aqueous solutions. Based on an initial screening of synthesized FSM with different Mg/citric acid molar ratios in terms of phosphorus adsorption capacity, an FSM composite with a Mg-citric acid molar ratio of 1:1 (FSM-1:1) was determined as the optimal choice. Scanning electron microscope (SEM), Fourier transform infrared (FTIR) and X-ray diffraction (XRD) showed that the prepared Fe3O4 was triumphantly loaded and the nano-MgO nanoparticles were evenly distributed on the surface of magnetic mesoporous silica. N2 adsorption-desorption experiments manifested that FSM-1:1 had a large specific surface area of 124.3 m2/g and the pore size distribution calculated based on the BJH model was centered at 9.36 nm. Furthermore, FSM-1:1 not only exhibited fast adsorption kinetics (60 min) but also had a high maximum theoretical adsorption capacity of 223.6 mg P/g, which was superior to all the other Mg-based adsorbents. Remarkably, due to the coating of MgO, FSM-1:1 exhibited ultra-high stability in the pH range of 3–11, a wider range than many other Mg-modified sorbents. Our adsorbents also showed excellent selectivity for phosphate anions even in the presence of various coexisting anions (e. g. NO3−, Cl− and SO42−) with varying ionic strengths (0.01 and 0.1 M), good recyclability, the removal rate of phosphate still reached 89.0% after three cycles. Electrostatic attraction, Lewis acid-base interaction and the ligand exchange between Mg–OH and phosphate anions were responsible for the phosphate adsorption mechanisms.
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