Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.apcatb.2009.05.010
Title: Effect of hydrothermal treatment and silica on thermal stability and oxygen storage capacity of ceria-zirconia
Authors: Raju, V.
Jaenicke, S. 
Chuah, G.-K. 
Keywords: Ceria-zirconia
Hydrothermal treatment
Oxygen storage capacity
Silica doping
Thermal stability
Issue Date: 7-Sep-2009
Citation: Raju, V., Jaenicke, S., Chuah, G.-K. (2009-09-07). Effect of hydrothermal treatment and silica on thermal stability and oxygen storage capacity of ceria-zirconia. Applied Catalysis B: Environmental 91 (1-2) : 92-100. ScholarBank@NUS Repository. https://doi.org/10.1016/j.apcatb.2009.05.010
Abstract: Hydrothermal digestion of freshly precipitated cerium-zirconium hydroxides was used to synthesize nanocrystalline ceria-zirconia. This simple method produced ceria-zirconia with higher surface area and thermal stability than the untreated oxide. After calcination at 1000 °C, the surface area of the hydrothermally synthesized samples was ∼11-12 m2/g while the untreated Ce0.5Zr0.5O2 had only 4.2 m2/g. The continuous dissolution and reprecipitation of hydroxides during hydrothermal treatment is postulated to a more defect-free structure which is able to withstand loss of surface area when exposed to high temperatures. In addition, these nanocrystalline oxides were more reducible than the untreated oxide. While the addition of silica to ceria-zirconia further increased the surface area and oxygen storage capacity, the oxides suffered severe loss of surface area after calcination to 1000 °C. A silica-rich overlayer was formed which decreased the oxygen storage capacity as compared to silica-free ceria-zirconia. The oxygen storage capacity shows a strong dependence on the surface area for values below 50 m2/g but diffusion of oxygen from the bulk becomes limiting for high surface area ceria-zirconia. © 2009 Elsevier B.V. All rights reserved.
Source Title: Applied Catalysis B: Environmental
URI: http://scholarbank.nus.edu.sg/handle/10635/93648
ISSN: 09263373
DOI: 10.1016/j.apcatb.2009.05.010
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