Kinetics of copper desorption from soils as affected by different organic ligands

Abstract

Desorption of Cu and low molecular weight dissolved organics are the primary factors that impact fate and transport of Cu in soils. To improve predictions of the toxicity and threat from Cu contaminated soil, it is critical that time-dependent desorption behavior be understood. In this paper, the effect of organic ligands citrate, malate, and succinate on the kinetics of Cu desorption from contaminated soils varying widely in soil characteristics was investigated at 250 C and the soils used were referred to as clay, calcareous and sandy soils. The amount of Cu released by the used organic ligands varied greatly with physicochemical properties of the soils. The rate of Cu release by different extractants was in the order citric > malic > succinic, which was consistent with the stability constants of Cu complexes with these ligands. The modified Freundlich and the Elovich and Parabolic diffusion models were used to describe dsorption of Cu2+ from the three studied soils as affected by the organic ligands. All of the models fit the data well with correlation coefficients ranging from 0.83 to 1.00 (P < 0.01). Each Model has a set of assumptions for the different physical and chemical properties of the systems to which they are being applied. The uses of these equations yield different magnitudes for the calculated variable, but the relationships between the soil + organic ligands and their effect (i.e., increase or decrease) on these variables are the same. Such information is critical, since Cu is used in a variety of industrial and manufacturing processes and is one of the most common contaminants found at hazardous waste sites.

Authors and Affiliations

E. A. Elkhatib, A. M. Mahdy, M. E. Saleh, N. H. Barakat

Keywords

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  • EP ID EP133995
  • DOI -
  • Views 87
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How To Cite

E. A. Elkhatib, A. M. Mahdy, M. E. Saleh, N. H. Barakat (2007). Kinetics of copper desorption from soils as affected by different organic ligands. International Journal of Environmental Science and Technology, 4(3), 331-338. https://europub.co.uk./articles/-A-133995