Effective adsorptive removal of Zn2+, Cu2+, and Cr3+ heavy metals from aqueous solutions using silica-based embedded with NiO and MgO nanoparticles
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Published on: June 2, 2022
Saqr Abuhatab1, Amjad El-Qanni2, Hana Al-Qalaq2
1Chemical Engineering Department, An-Najah National University, P.O. Box 7, Nablus, West Bank, Palestine; Department of Chemical and Petroleum Engineering, University of Calgary, Calgary, Alberta, Canada.
Abstract:
In this study, the adsorptive removal of Zn2+, Cu2+, and Cr3+ metal ions from aqueous solutions onto NiO-MgO silica-based nanoparticles (SBNs) has been studied. The effect of several factors such as solution pH, initial concentration, contact time, and coexisting ions on the adsorbed amounts of single Zn2+, Cu2+, and Cr3+ ions have been investigated within an array of batch mode experiments. Interestingly, the adsorption of Cr3+ at high and low concentrations was very fast, and equilibrium was achieved within 2 min compared to Cu2+ and Zn2+ which needed 30 and 60 min to reach equilibrium, respectively. The adsorption equilibrium data fitted very well with the Sips adsorption isotherm model for Cu2+ and Zn2+, and the BET model for Cr3+ ions. The maximum uptake was maintained at 7.23, 13.76, 41.36 (ions per nm2) for Zn2+, Cu2+, and Cr3+, respectively. This equals to 37.69, 69.68, 209.51 (mg adsorbate per g adsorbent), respectively, showing the promising industrial application of those SBNs. Moreover, the adsorption uptake results increase with increasing the pH in the range of 7.0-11.0 for all investigated metal ions. The thermodynamic parameters such as the changes in Gibbs free energy (ΔGo), enthalpy (ΔHo), and entropy (ΔSo) were determined. The adsorption of Zn2+, Cu2+, and Cr3+ was spontaneous, endothermic, and physical for Cu2+ and Cr3+, while exothermic and chemical for Zn2+. The regeneration and reusability studies have proven that the NiO-MgO SBNs can be employed for the adsorptive of these metals repeatedly without impacting the adsorption capacity indicating their sustainability.
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