The adsorption characteristics of nitrate on Mg-Fe and Mg-Al layered double hydroxides in a simulated soil solution

被引:101
作者
Halajnia, A. [1 ]
Oustan, S. [1 ]
Najafi, N. [1 ]
Khataee, A. R. [2 ]
Lakzian, A. [3 ]
机构
[1] Univ Tabriz, Fac Agr, Dept Soil Sci, Tabriz 5166416471, Iran
[2] Univ Tabriz, Fac Chem, Dept Appl Chem, Tabriz 5166416471, Iran
[3] Ferdowsi Univ Mashhad, Fac Agr, Dept Soil Sci, Mashhad, Iran
关键词
Layered double hydroxides; Nitrate; Adsorption; Calcinations; Kinetics; Thermodynamic parameters; HYDROTALCITE-LIKE COMPOUND; PHYSICOCHEMICAL CHARACTERIZATION; EXCHANGE PROPERTIES; ION-EXCHANGE; SELECTIVE ADSORBENTS; AQUEOUS-SOLUTION; OXO-ANIONS; REMOVAL; PHOSPHATE; SORPTION;
D O I
10.1016/j.clay.2012.09.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Four types of layered double hydroxides (LDHs) synthesized by coprecipitation method including Mg-Al and Mg-Fe in 3:1 and 4:1 ratios of M2+/M3+ were compared in terms of chemical structure, nitrate adsorption isotherm and kinetics, thermodynamic parameters, anion exchange capacity and nitrate selectivity in the presence of common anions found in soil solutions. Moreover, the influence of calcination on nitrate adsorption was studied. Results showed that the Mg-Al-LDH (4:1) was most effective for the removal of nitrate and its selectivity for nitrate adsorption was remarkable in the presence of phosphate, sulfate and bicarbonate. The nitrate adsorption on Mg-Al-LDH (4:1) followed a pseudo-second order model with rate constant of 0.623 g mmol(-1) min(-1). Furthermore, the kinetic data were described very well with the intraparticle diffusion model with rate constant of 0.046 mmol g(-1) min(-0.5). The nitrate adsorption isotherm of Mg-Al-LDH (4:1) described well with the Freundlich model as indicated by the high values of R-2. The negative values of Delta H-r(0) indicated that the nitrate adsorption on the LDHs was exothermic in nature. Calcination of the LDHs had no significant effect on increasing nitrate adsorption. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 36
页数:9
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