Novel hollow microspheres of hierarchical zinc-aluminum layered double hydroxides and their enhanced adsorption capacity for phosphate in water

被引:211
作者
Zhou, Jiabin [1 ,2 ]
Yang, Siliang [2 ]
Yu, Jiaguo [1 ]
Shu, Zhan [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Hubei, Peoples R China
[2] Wuhan Univ Technol, Sch Resources & Environm Engn, Wuhan 430070, Hubei, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Zn-Al LDHs; Hierarchical porous structures; Hollow microspheres; Phosphate; Adsorption isotherm; Kinetics; MACRO-/MESOPOROUS TITANIA; TEMPLATE-FREE FABRICATION; PHOSPHORUS REMOVAL; PHOTOCATALYTIC ACTIVITY; AQUEOUS-SOLUTION; ACTIVATED CARBON; FURNACE SLAG; WASTE-WATER; FLY-ASH; IRON;
D O I
10.1016/j.jhazmat.2011.06.013
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hollow microspheres of hierarchical Zn-Al layered double hydroxides (LDHs) were synthesized by a simple hydrothermal method using urea as precipitating agent. The morphology and microstructure of the as-prepared samples were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), nitrogen adsorption-desorption isotherms and fourier transform infrared (FTIR) spectroscopy. It was found that the morphology of hierarchical Zn-Al LDHs can be tuned from irregular platelets to hollow microspheres by simply varying concentrations of urea. The effects of initial phosphate concentration and contact time on phosphate adsorption using various Zn-Al LDHs and their calcined products (LDOs) were investigated from batch tests. Our results indicate that the equilibrium adsorption data were best fitted by Langmuir isothermal model, with the maximum adsorption capacity of 54.1-232 mg/g: adsorption kinetics follows the pseudo-second-order kinetic equation and intra-particle diffusion model. In addition, Zn-Al LDOs are shown to be effective adsorbents for removing phosphate from aqueous solutions due to their hierarchical porous structures and high specific surface areas. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1114 / 1121
页数:8
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