Concomittant Zn-Cd and Pb retention in a carbonated fluvio-glacial deposit under both static and dynamic conditions

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01/11/2007

Titre de la revue : Chemosphere Volume : 69 N° : 9 Pagination : 1499-1508 Date de publication : 01/11/2007

Type de document > *Article de revue
Mots clés publication scientifique > calcaire , depôt fluvio-glacial , métaux lourds , modélisation , PHREEQC , SEM , transfert
Unité de recherche > IRSN/DEI/SECRE/LRE
Auteurs > DELOLME Cécile , FEVRIER Laureline , GALVEZ-CLOUTIER R. , LASSABATERE Laurent , SPADINI Lorenzo , WINIARSKI Thierry

The chemical and physical process involved in the retention of 10-2 M Zn, Pb and Cd in a calcareous medium were studied under dynamic (column) and static (batchs) conditions. Retention in columns decreased in order Pb>>Cd=Zn. In the batch experiments, the same order was observed for a contact time of less than 40 h and over, Pb>>Cd>Zn. Stronger Pb retention is in accordance with the lower solubility of Pb carbonates. However, the equality of retained Zn and Cd does not fit the solubility constants of carbonated solids. SEM analysis revealed that heavy metals and carbonated particles are associated. Pb precipitated as individualized Zn-Cd-Ca-free carbonated crystallites. All the heavy metals were also found to be associated with calcareous particles, without any change in their porosity, pointing to a surface/lattice diffusion-controlled substitution process. Zn and Cd were always found in concomitancy, through Pb fixed separately at the particle circumferences. The Phreeqc 2.12 interactive code was used to model experimental data on the following basis: flow fractionation in the columns, precipitation of Pb as cerrusite linked to kinetically controlled calcite dissolution, and heavy metal sorption onto proton exchanging sites (presumably surface complexation onto a calcite surface). This model simulates exchanges of metals with surface protons, pH buffering and the prevention of early Zn and Cd precipitation. Both modeling and SEM analysis show a probable significant decrease of calcite dissolution along with its contamination with metals.

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