Adsorption kinetics, capacity and mechanism of arsenate and phosphate on a bifunctional TiO2-Fe2O3 bi-composite

被引:112
作者
D'Arcy, Mitch [1 ]
Weiss, Dominik [1 ]
Bluck, Michael [2 ]
Vilar, Ramon [3 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Earth Sci & Engn, London SW7 5PD, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Mech Engn, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
关键词
Adsorption; Arsenate; Phosphate; Iron titanium oxide; Langmuir; Freundlich; Dubinin-Radushkevich; Adsorption kinetics; Pseudo-second order rate law; REMOVAL; SURFACE; ARSENITE; SB(III); AS(III); OXIDE;
D O I
10.1016/j.jcis.2011.08.023
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
Mixed oxide TiO2-Fe2O3 bi-composites have been recognised as efficient and economical sorbents with great promise for arsenic removal from groundwater. In this study, we use a fast, simple and inexpensive synthesis method for this type of bi-composite and assess its adsorption performance. The kinetics of arsenate and phosphate adsorption onto the bi-composite are determined, demonstrating rapid and stable uptake of both oxy-anions over several days and with improved performance compared to the widely used TiO2 sorbent. A modified pseudo-second order rate equation is introduced, which allows the adsorption kinetics to be modelled as two simultaneous, parallel reaction pathways with separate kinetic parameters. This equation reproduces the experimental observations accurately across a wide range of timescales from minutes to days. Our experimental data agrees with previous interpretations of the adsorption mechanism including the formation of mono-dentate and bi-dentate inner-sphere surface complexes. The arsenate and phosphate uptake capacities of the bi-composite are reported. Equilibrium studies were conducted between pH 5 and 9 and interpreted within the Langmuir, Freundlich and Dubinin-Radushkevich isotherm models. (C) 2011 Elsevier Inc. All rights reserved.
引用
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页码:205 / 212
页数:8
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