Journal of Ultrafine Grained and Nanostructured  Materials

Journal of Ultrafine Grained and Nanostructured Materials

Improvement of Nanosized CuO-Fe2O3/cordierite System by Li2O-treatment for wastewater treatment

Document Type : Research Paper

Authors
1 Department of Chemistry, College of science and arts, Qassim University, Qassim, Saudi Arabia.
2 Physical Chemistry Department, National Research Centre, Dokki, Cairo, Egypt.
3 Department of Chemistry, Faculty of Education, Ain Shams University, Cairo, Egypt.
Abstract
A mixture of 10 wt% CuO-10 wt% Fe2O3 supported on cordierite were prepared by wet impregnation. The as-prepared solids doped with Li2O (0.75-3 mol %) were calcined at 500-900 ºC. The crystalline phase, morphology, and surface area were investigated by XRD, HR-TEM and N2-adsoprtion-desorption. Moreover, their photocatalytic activities of samples calcined at 700°C on the degradation of phenol were evaluated under UV-irradiation. The catalytic activity of different solids toward H2O2 decomposition was studied. Nano-materials were used to adsorb dyes as Remazole-Red and Congo-Red from aqueous solution. The sorption process was in good agreement of pseudo-second order equation and the Langmuir equation through their adsorption kinetics and isotherms, respectively. The CuO-Fe2O3/ cordierite doped with 0.75% Li2O at 700 ºC adsorbent was found to possess the highest removal efficiency of Remazole-Red and/or Congo-Red dyes and potentially lowering capital and operational costs for \practical applications. The highest removal efficiency of the anionic dyes over 0.75% Li2O at 700 ºC can be discussed by observing the appearance of new active phases as CuO, CuFe2O4 and LiCuO, decreasing the crystallite size of these active phases. 0.75 mol% Li2O has the greatest activity in H2O2 decomposition reached 700 %. This result may be related to the lowest particle size and the highest surface area of this sample, which also produced a large number of electrons donating active sites for H2O2 decomposition.
Keywords

 
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Volume 52, Issue 2
December 2019
Pages 175-187

  • Receive Date 11 June 2019
  • Revise Date 21 October 2019
  • Accept Date 30 October 2019