Abstract

Phosphoryl functionalized Aluminum silicate (ASP) composite sorbent was synthesized using sol–gel technique and characterized with different techniques. The synthesized sorbent was tested for the sorption of Ni2+ and Cd2+ in aqueous solution at both single- and binary-solute systems under simulated conditions using batch technique. Batch experiments were executed as a function of pH, initial metal ion concentration and temperature. Structural and surface morphology of the synthesized sorbent were determined using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Scanning electron microscopy (SEM). The studied kinetic models suggested that the sorption of Ni2+ and Cd2+ onto ASP was found to follow the pseudo-second order and the Langmuir-Freundlich model was the best model to depict the sorption isotherms. The sorption equilibria of both ions were analyzed using two diverse statistical physics models (homogeneous and heterogeneous monolayer models). A Theoretical scrutiny of statistical physics calculations indicated that Ni2+ and Cd2+ sorption was multi-ionic where two sorption sites were involved but with a diverse contribution degree. The removal nature of Ni2+ and Cd2+ was endothermic and the calculated sorption amounts at saturation implied that Ni2+> Cd2+. Calculated interaction energies indicated the participation of physical forces in the sorption of both ions onto the synthesized sorbent surface and the variation of these sorption energies confirmed that both sorption sites participated in the removal of Ni2+ and Cd2+ but through different interactions type. Ions sorption capacity was increased with the temperature owing to increase in thermal agitation. This study reveals that phosphoryl functionalized aluminum silicate is an efficient sorbent that can be used for the sorption of Ni2+ and Cd2+ from aqueous solutions in both single- and binary -solute systems.

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