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Removal of Phosphate by Ivory Coast Shale in a Homogeneous Reactor and Under Hydrodynamic Conditions: Influence of Soluble Species

Published online by Cambridge University Press:  01 January 2024

D. E. Kpannieu*
Affiliation:
Laboratoire de Chimie Physique et Microbiologie pour l’Environnement - LCPME UMR 7564 CNRS, Universiteé de Lorraine, 405 rue de Vandoeuvre, 54600 Villers-le`s-Nancy (France) Laboratoire d’Environnement et Biologie Aquatique, Universiteé Nangui Abrogoua, 02 BP 801, Abidjan 02 Côte d’Ivoire
C. Ruby
Affiliation:
Laboratoire de Chimie Physique et Microbiologie pour l’Environnement - LCPME UMR 7564 CNRS, Universiteé de Lorraine, 405 rue de Vandoeuvre, 54600 Villers-le`s-Nancy (France)
L. Coulibaly
Affiliation:
Laboratoire d’Environnement et Biologie Aquatique, Universiteé Nangui Abrogoua, 02 BP 801, Abidjan 02 Côte d’Ivoire
M. Abdelmoula
Affiliation:
Laboratoire de Chimie Physique et Microbiologie pour l’Environnement - LCPME UMR 7564 CNRS, Universiteé de Lorraine, 405 rue de Vandoeuvre, 54600 Villers-le`s-Nancy (France)
M. Mallet
Affiliation:
Laboratoire de Chimie Physique et Microbiologie pour l’Environnement - LCPME UMR 7564 CNRS, Universiteé de Lorraine, 405 rue de Vandoeuvre, 54600 Villers-le`s-Nancy (France)
*
*E-mail address of corresponding author: [email protected]
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Abstract

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Developing low cost and effective phosphate adsorbents is crucial to prevent eutrophication of natural waters. Here, phosphate removal by a natural and abundant shale from the Ivory Coast was investigated in both batch and column experiments with special attention devoted to understand the adsorption process. Batch experiments were carried out to assess the influence of initial phosphate concentration, sorbent dosage, contact time, and pH on phosphate removal. The phosphate removal efficiency increased with increased shale dosage while phosphate uptake decreased. Aqueous Ca, Mg, Al, and Fe species concentrations decreased in the presence of phosphate. Additionally, phosphate uptake strongly decreased with pH increases in the range 2–11, but then increased at pH 12. The kinetics were well described using a pseudo-second order model, and Langmuir adsorption isotherms were used for the equilibrium surface reactions. Adsorption to nanoparticles of goethite was hypothesized to be the major phosphate removal mechanism in the pH range 4–10. Column experiments with a flow rate of 1 mL min−1 and an initial phosphate concentration of 25 mg L−1 showed a breakthrough point at a V/Vp value of ~17, where Vis the volume of phosphate solution added to the column and Vp is the pore volume. A V/Vp value of ~17 corresponded to a phosphate uptake of 0.17 mg/g, which was in agreement with the batch experiments. Column experiments revealed a strong correlation between the aqueous concentrations of Ca, Mg, Al, and Fe species and phosphate removal and, thus, suggest that phosphate removal by the shale occurred by aqueous dissolution/precipitation.

Type
Article
Copyright
Copyright © Clay Minerals Society 2018

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