Simultaneous adsorption of chlorophenol and heavy metal ions on organophilic bentonite

被引:90
作者
Andini, S
Cioffi, R
Montagnaro, F
Pisciotta, F
Santoro, L
机构
[1] Univ Naples Federico 2, Dipartimento Chim, I-80126 Naples, Italy
[2] Univ Napoli Parthenope, Dipartimento Tecnol, I-80133 Naples, Italy
关键词
organophilic bentonite; adsorption; 2-chlorophenol; heavy metals; quaternary ammonium salts;
D O I
10.1016/j.clay.2005.09.004
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 [物理化学]; 081704 [应用化学];
摘要
Organophilic bentonite obtained by ion exchange with benzyldimethyl octadecylammonium chloride has been used for multiple adsorption of 2-chlorophenol and the metals Pb(2+) and Cd(2+). This is of interest for the stabilization of wastes in which simultaneous organics/heavy metals contamination occurs. In such cases cement-based processes take advantage from the addition of quaternary ammonium salts exchanged bentonite. The results have shown that any of the contaminants is adsorbed according to a multilayer cooperative mechanism. Due to its organophilic nature, exchanged bentonite is able to adsorb 2-chlorophenol to a very high extent (about 0.7 g/g) when the organic is the only solute. On the other hand, each of the two metal ions is adsorbed to a much lesser extent when alone in solution (about 22 and 2.8 mg/g for Ph(2+) and Cd2+, respectively). In the case of simultaneous presence of 2-chlorophenol and Ph(2+) in solution, the adsorption isotherms of both solutes change to monolayer type and the adsorption capacity strongly decreases (about 0.3 g/g for 2-chlorophenol and 0.6 mg/g for Ph(2+)). In the case of the 2-chlorophenol/Cd(2+) systems, the adsorption capacity of about 0.3 g/g for 2-chlorophenol is retained, while Cd(2+) is not adsorbed at all. In all the cases in which the bentonite is in contact with one of the metal ions, it has been checked that no exchange with the ammonium ions takes place. Finally, FT-IR analysis has shown that in all the cases investigated physical adsorption takes place and no new chemical bonds are formed. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:126 / 133
页数:8
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