Adsorption of lead(II) and copper(II) on activated carbon by complexation with surface functional groups

被引:91
|
作者
Pesavento, M
Profumo, A
Alberti, G
Conti, F
机构
[1] Univ Pavia, Dipartimento Chim Gen, I-27100 Pavia, Italy
[2] Univ Pavia, Dipartimento Ingn Idraul & Ambientale, I-27100 Pavia, Italy
关键词
activated carbon; lead(II); copper(II); adsorption on activated carbon;
D O I
10.1016/S0003-2670(02)01597-0
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The adsorption of lead(II) and copper(II) on an activated carbon (Filtrasorb 300, Chemviron) was characterized assuming that it takes place by formation of complexes with functional groups, present in the activated carbon. Their concentration and conditional adsorption coefficients were determined for each metal by titration of the carbon in suspension in aqueous phase, at constant acidity, with the metal itself For each titration point, the concentration of the metal in the solution phase after equilibration was determined, and the data were processed by the Ruzic linearization method, to obtain the concentration of the active sites involved in the sorption, and the conditional constant. The effect of the pH was also examined, in the range 4-6, obtaining that the adsorption increases at increasing pH. The protonation and adsorption constants were determined from the conditional adsorption coefficients obtained at the different acidities. The concentration of the active sites is 0.023 and 0.042 mmol g(-1), and the protonation constants are 1.0 x 10(6) and 4.6 x 10(4) M-1 for Pb(II) and Cu(II). The corresponding adsorption constants are respectively 1.4 x 10(5) and 6.3 x 10(3) M-1. All the parameters are affected by a large uncertainty, probably due to the heterogeneity of the active groups in the activated carbon. Even if so, these parameters make it possible a good prediction of the adsorption in a wide range of conditions. Other sorption mechanism can be set up at different conditions, in particular at different pH, as it has been demonstrated in the case of copper(II). (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:171 / 180
页数:10
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