Pb(II) removal of Fe3O4@SiO2–NH2 core–shell nanomaterials prepared via a controllable sol–gel process
Pb(II) removal of Fe3O4@SiO2–NH2 core–shell nanomaterials prepared via a controllable sol–gel process
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DOI:
10.1016/j.cej.2012.11.043
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发表时间:
2013-01
影响因子:
15.1
通讯作者:
Jian-Ming Zhang;S. Zhai;Shi Li;Zuoyi Xiao;Yu Song;Qing-da An;Ge Tian
中科院分区:
文献类型:
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作者:
Jian-Ming Zhang;S. Zhai;Shi Li;Zuoyi Xiao;Yu Song;Qing-da An;Ge Tian
Contamination of natural water with heavy metals (especially lead ions) is a problem of major concern and thus great demand of effective adsorbents for removal of toxic ions is increasing. Due to the task-specific properties of amino groups, core–shell nanostructures of Fe3O4@SiO2–NH2have been extensively investigated as advanced adsorbents; however, most studies on surface modification of Fe3O4@SiO2substances were of environmentally inefficient grafting methods. Herein, we demonstrated that mono-dispersed and spherical Fe3O4@SiO2–NH2nanomaterials can be facilely prepared by co-condensation of TEOS with APTMS employing a green sol–gel process. The as-prepared Fe3O4@SiO2–NH2magnetic nanoparticles (MNPs) prepared under optimum conditions possessing uniform core–shell structure (∼200nm in diameter), relatively high loading of amino-functionality (∼5.45wt%), easy recovery by external magnet and effective removal of Pb(II) (qm=243.9mg/g, 25°C). The adsorption was shown to be effective and a higher temperature was more favorable for the adsorption. The adsorption equilibrium data obeyed the Langmuir model and the kinetic data were well fitted to the pseudo-second-order model. Thermodynamic studies revealed the feasibility and endothermic nature of the system. These results demonstrated that the sol–gel produced Fe3O4@SiO2–NH2, due to its easy synthesis and recovery and eco-friendliness, can be a potential adsorbent for Pb(II) removal.