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CO-free hydrogen production over Au/CeO2–Fe2O3 catalysts: Part 1. Impact of the support composition on the performance for the preferential CO oxidation reaction

Authors :
Maela Manzoli
Joan Papavasiliou
Flora Boccuzzi
K. Tenchev
Floriana Vindigni
George Avgouropoulos
T. Tabakova
Theophilos Ioannides
Source :
Applied Catalysis B: Environmental. 101:256-265
Publication Year :
2011
Publisher :
Elsevier BV, 2011.

Abstract

Ce–Fe mixed oxides were prepared by urea gelation coprecipitation method and used as supports of gold catalysts. The impact of the support composition on the catalytic performance for the preferential CO oxidation (PROX) was studied by varying the Ce/(Ce + Fe) ratio. A deep characterization study by different tools such as XRD, HRTEM, TPR and FTIR spectroscopy was undertaken in order to correlate the structural characteristics of the catalysts and the gold oxidation state and dispersion with the catalytic properties. The results revealed that the variation of the support composition led to significant differences in the gold particles size (in the range 1–25 nm), which affected strongly the CO oxidation activity of Au/CeO2–Fe2O3 catalysts under PROX conditions. The following activity order was observed: Au/CeO2 ≈ Au/Ce50Fe50 > Au/Ce75Fe25 > Au/Ce25Fe75 > Au/Fe2O3. The support with composition 50 wt.% CeO2–50 wt.% Fe2O3 appeared beneficial not only for nucleation and growth of highly dispersed gold particles (1–1.8 nm), but also for activation of oxygen and its mobility. Moreover, the presence of Fe2O3 in the supports composition improved the resistance towards deactivation by CO2. The CeO2–Fe2O3 supports comprised different amount of two phases: cubic CeO2-like solid solution and hematite. The analysis of the characterization data suggested that the solid solution formation probably proceeded via a dopant interstitial compensation mechanism.

Details

ISSN :
09263373
Volume :
101
Database :
OpenAIRE
Journal :
Applied Catalysis B: Environmental
Accession number :
edsair.doi.dedup.....b988433b51ad94b1ae534da6ccba2757
Full Text :
https://doi.org/10.1016/j.apcatb.2010.10.016