Study of the synthesis of CeO2 nanoparticles for their use in CO preferential oxidation (COPrOx)

•Ceria nanoparticles were synthesized by a simple, easy to scale-up method.•The effect of EG and TMAH on particle and crystallite size was studied.•Complete elimination of nitrates and organic matter could be achieved at 500°C.•The activity of ceria nanoparticles in COPrOx depends on calcination tem...

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Published in:Chemical engineering journal (Lausanne, Switzerland : 1996) Vol. 223; pp. 507 - 515
Main Authors: Peiretti, Leonardo F., Tiscornia, Inés S., Miró, Eduardo E.
Format: Journal Article
Language:English
Published: Elsevier B.V 01-05-2013
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Summary:•Ceria nanoparticles were synthesized by a simple, easy to scale-up method.•The effect of EG and TMAH on particle and crystallite size was studied.•Complete elimination of nitrates and organic matter could be achieved at 500°C.•The activity of ceria nanoparticles in COPrOx depends on calcination temperature.•Samples pretreated at 500°C presented high conversions at the lowest temperature. CeO2 nanoparticles were synthesized by the controlled precipitation method from a Ce(NO3)3 solution. To this end, two additives were used alternatively: ethylene glycol (EG) and tetramethylammonium hydroxide (TMAH). Their function was to reduce the particle size obtained after the synthesis. After precipitation and drying, nitrate and organic residuals must be removed, and the method employed for this step could affect the structure and size of the particles. This is an important issue for achieving contaminant-free measurements in catalytic tests. In order to optimize the residuals removing process, a thorough study of the species present and/or eliminated was carried out. Our findings show that a calcination temperature of at least 500°C is necessary in order to accomplish the complete removal of solvent and precursors such as NO3-. Among the catalysts studied, the one prepared with EG showed the best activity for CO preferential oxidation. In order to study the effect of the residuals upon the catalytic activity, samples prepared using EG were calcined at different temperatures and tested for the COPrOx reaction. CO conversions for all the samples were between 80% and 93% at different temperatures. The best activity was obtained with the sample calcined at 500°C, which is in agreement with the minimum temperature necessary for the total elimination of residuals.
Bibliography:http://dx.doi.org/10.1016/j.cej.2013.02.121
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ISSN:1385-8947
1873-3212
DOI:10.1016/j.cej.2013.02.121