Thermodynamics of metal cation binding by a solid soil derived humic acid.: 2.: Binding of Mn(II), Co(NH3)3+6aq and Hg(II)

被引:23
|
作者
Ghabbour, Elham A. [1 ]
Shaker, Medhat
El-Toukhy, Ahmed
Abid, Ismail M.
Davies, Geoffrey
机构
[1] Northeastern Univ, Dept Chem & Biol Chem, Boston, MA 02115 USA
[2] Univ Alexandria, Fac Educ, Dept Chem & Phys, Alexandria, Egypt
[3] Univ Alexandria, Fac Sci, Dept Chem, Alexandria, Egypt
关键词
humic acids; metal cation binding; site capacities; thermodynamics;
D O I
10.1016/j.chemosphere.2005.10.049
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Metal binding is an important function of humic acids (HAs) in soils, sediments and waters. At pH 2.0, Mn(II) and Co(NH3)(6aq)(3+) bind tightly in one step labeled A to a solid humic acid NHA isolated from a New Hampshire soil. Two consecutive steps are observed for Hg(II) binding. All the binding isotherms fit the Langmuir model in the temperature range 10.0-50.0 degrees C. Stoichiometric site capacities indicate predominant binding by charge-neutralizing HA carboxylate groups for Mn(II) and the second step A of Hg(II) binding. The binding affinity order in step A is Co(NH3)L-6(3+) > Hg(II) > Mn(II). Metal binding enthalpy and entropy changes fit the linear correlation found previously for binding of other metal cations by solid HAs. Free energy buffering from cooperative enthalpy and entropy changes and lower enthalpies for metal-HA interactions in solution suggest that desolvation of the cations and HA binding sites as well as HA conformational changes to allow for inner-sphere complexation predominate metal binding by hydrated solid HAs. (c) 2005 Elsevier Ltd. All rights reserved.
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页码:826 / 833
页数:8
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