Kinetic, isotherm and thermodynamic investigations of the adsorption of Ag+ and Cu2+ on vermiculite

被引:57
作者
Dlugosz, Olga [1 ]
Banach, Marcin [1 ]
机构
[1] Cracow Univ Technol, Fac Chem Engn & Technol, Krakow, Poland
关键词
Adsorption; Silver and copper; Thermodynamics; Kinetics; Isotherms; Statistical analysis; AQUEOUS-SOLUTION; CLAY-MINERALS; HEAVY-METALS; MONTMORILLONITE; REMOVAL; DESORPTION; IONS; EQUILIBRIUM; ADSORBENTS; ELEMENTS;
D O I
10.1016/j.molliq.2018.03.041
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
Vermiculite was used as a low-cost adsorbent for the removal of silver and copper ions from aqueous solutions. The raw material and acid- or base-treated adsorbents were characterised by SEM, BET, XRD and FFIR analysis. The effect of the pH and temperature of the solution, dose and average size of adsorbent particles, contact time, stirring rate and initial of metal ions concentration on the adsorption efficiency was studied systematically. The maximum adsorption capacity of vermiculite was determined (for Ag(I) as about 73 mg/g and for Cu(II) 117 mg/g). In this study, the four isotherm models (Langmuir, Freundlich, Temkin and Sips) were employed to correlate experimental adsorption isotherm data, which were obtained by batch tests. The linear and non-linear isotherm models were compared. The pseudo-first-order, pseudo-second-order, and Elovich models were used to describe the kinetic data. The kinetics of adsorption indicates that the process followed pseudo-second order kinetics well, which suggests the chemical character of adsorption. Finally, the thermodynamic parameters (Delta G degrees, Delta H degrees and Delta S degrees) were determined. The parameters indicated that, in the studied temperature range, the adsorption of Ag(I) and Cu(II) by vermiculite had a spontaneous and endothermic nature. Based on all of the results, vermiculite can be evaluated as a potentially cost-effective sorbent for the removal of Ag(I) and Cu(II) from aqueous solutions. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:295 / 309
页数:15
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