Peer-Reviewed Journal Details
Mandatory Fields
Albadarin, AB,Yang, ZY,Mangwandi, C,Glocheux, Y,Walker, G,Ahmad, MNM
2014
July
Chemical Engineering Research & Design
Experimental design and batch experiments for optimization of Cr(VI) removal from aqueous solutions by hydrous cerium oxide nanoparticles
Published
()
Optional Fields
Chromium Adsorption isotherm Nanoparticles Optimization Hydrous cerium oxide Desorption HEXAVALENT CHROMIUM ADSORPTION FLUORIDE WATER VI SEPARATION MECHANISM ADSORBENT ZEOLITE LIQUID
92
1354
1362
Hydrous cerium oxide (HCO) was synthesized by intercalation of solutions of cerium(III) nitrate and sodium hydroxide and evaluated as an adsorbent for the removal of hexavalent chromium from aqueous solutions. Simple batch experiments and a 2(5) factorial experimental design were employed to screen the variables affecting Cr(VI) removal efficiency. The effects of the process variables; solution pH, initial Cr(VI) concentration, temperature, adsorbent dose and ionic strength were examined. Using the experimental results, a linear mathematical model representing the influence of the different variables and their interactions was obtained. Analysis of variance (ANOVA) demonstrated that Cr(VI) adsorption significantly increases with decreased solution pH, initial concentration and amount of adsorbent used (dose), but slightly decreased with an increase in temperature and ionic strength. The optimization study indicates 99% as the maximum removal at pH 2, 20 degrees C, 1.923 mM of metal concentration and a sorbent dose of 4 g/dm(3). At these optimal conditions, Langmuir, Freundlich and Redlich-Peterson isotherm models were obtained. The maximum adsorption capacity of Cr(VI) adsorbed by HCO was 0.828 mmol/g, calculated by the Langmuir isotherm model. Desorption of chromium indicated that the HCO adsorbent can be regenerated using NaOH solution 0.1 M (up to 85%). The adsorption interactions between the surface sites of HCO and the Cr(VI) ions were found to be a combined effect of both anion exchange and surface complexation with the formation of an inner-sphere complex. Crown Copyright (C) 2013 Published by Elsevier B.V. on behalf of The Institution of Chemical Engineers. All rights reserved.
10.1016/j.cherd.2013.10.015
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