| Literature DB >> 20060217 |
Xiang Cheng1, Xinrui Huang, Xingzu Wang, Dezhi Sun.
Abstract
The influence of calcination of Zn-Al layered double hydroxides (LDHs) on their phosphate adsorption capacity was studied in order to improve phosphorus removal from an excess sludge liquor. Powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), thermogravimetry-differential scanning calorimetry (TG-DSC) and nitrogen adsorption-desorption were employed to characterize the raw Zn-Al and the calcined products. The results reveal that the Zn-Al LDHs evolved to a phase of mixed metal oxides with the calcination temperature increasing to 300 degrees C and finally to spinel ZnAl(2)O(4) at 600 degrees C. When the Zn-Al was calcined at 300 degrees C, the interlayer carbonate ions were removed and the greatest BET surface area of 81.20 m(2)/g was achieved. The tested phosphate adsorption capacities of the raw and calcined Zn-Al were closely related to the evolution of physicochemical properties of the LDHs during the calcination. The Zn-Al-300 (Zn-Al LDHs calcined at 300 degrees C) exhibited the highest P uptake of 41.26 mg P/g in 24h. The phosphate adsorption by the raw Zn-Al and the Zn-Al-300 both follows a pseudo-second-order kinetic model; the adsorption isotherms show a good fit with a Langmuir-type equation. Copyright (c) 2009 Elsevier B.V. All rights reserved.Entities:
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Year: 2009 PMID: 20060217 DOI: 10.1016/j.jhazmat.2009.12.063
Source DB: PubMed Journal: J Hazard Mater ISSN: 0304-3894 Impact factor: 10.588