期刊
CHINESE CHEMICAL LETTERS
卷 29, 期 6, 页码 887-891出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2017.11.029
关键词
Core-shell; Magnetic nanoparticle; Dithiocarbamate; Adsorption; Heavy metals removal
资金
- National Natural Science Foundation of China [21671026]
- Science and Technology Key Project of Hunan Province [2015SK20823]
- Scientific Research Key Fund of Hunan Provincial Education Department [15A001]
- Foundation of Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation [2017CL06]
A novel magnetic nanoparticles-based dithiocarbamate absorbent (Fe3O4@SiO2-DTC) with core-shell structure was synthesized under mild conditions and used in aqueous solution Ni2+ and Cu2+ ions treatment. The structure, morphology and magnetic properties of the adsorbent were characterized by Xray diffraction (XRD), Fourier transformed infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and vibrating sample magnetometer (VSM). Fe3O4@SiO2-DTC exhibited a typical superparamagnetic with a saturation magnetization value of 52.7 emu/g, which could be rapidly separated from aqueous solution under external magnetic field. We investigated the effects of solution pH, adsorption time, and the initial concentration of heavy metal ions on the adsorption of Ni2+ and Cu2+ The adsorption equilibrium times of Nit' and Cu2+ on Fe3O4@SiO2-DTC were reached at 15 min and 90 min, respectively. The adsorption kinetic data were fitted to the pseudo second-order model, and the adsorption data were consistent with the Frenudlich isotherm model. When the initial concentration of heavy metal ions was 250 mg/L, the maximum adsorption capacity of Ni2+ and Cu2+ at room temperature was 235.23 mg/g and 230.49 mg/g, respectively. In addition, we discussed the plausible adsorption mechanism. The results indicated that the adsorption was mainly dominated by chelation. (C) 2017 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
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