Article ID Journal Published Year Pages File Type
42968 Applied Catalysis A: General 2009 9 Pages PDF
Abstract

Alumina supported cobalt catalysts were prepared by atomic layer deposition (ALD) of cobalt acetylacetonate precursors (Co(acac)2 and Co(acac)3). The main modes of interaction between the acetylacetonate precursors and the support were found to be the exchange reaction between the alumina OH-groups and the acac-ligands of the precursor and dissociative adsorption on coordinatively unsaturated Al3+ sites. The amount of precursor that could adsorb on the support was determined by steric hindrance. Samples were prepared using 1–5 reaction cycles, i.e. subsequent precursor addition (Co(acac)2) and calcination, resulting in catalysts containing ca. 3–10 wt.% Co. Samples were also prepared where the last calcination step was omitted, i.e. uncalcined catalysts. Calcination at 450 °C decreased the reducibility of the Co(acac)2/Al2O3 catalysts due to formation of a cobalt oxide phase strongly interacting with the support and aluminate type surface species. The reducibility increased with metal loading on both calcined and uncalcined catalysts; however the reducibility of the calcined catalysts remained lower than of the uncalcined ones. The dispersion was found to be lower on the calcined catalysts. The cobalt particle sizes on the calcined samples was ca. 8 nm and on the uncalcined 4–5 nm, for cobalt loadings of ca. 6–10 wt.%. Catalytic activity was tested by gas phase hydrogenation of toluene in temperature programmed mode (30–150 °C).

Graphical abstractAlumina supported cobalt catalysts were prepared by atomic layer deposition of cobalt acetylacetonate precursors. The interaction between cobalt species and the alumina support was studied. Calcination decreased the reducibility of the Co/Al2O3 catalysts due to formation of a cobalt oxide phase strongly interacting with the support and probably aluminate type surface species. The dispersion was also found to decrease due to calcination. The catalytic activity for toluene hydrogenation correlated with the cobalt surface area.Figure optionsDownload full-size imageDownload as PowerPoint slide

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Physical Sciences and Engineering Chemical Engineering Catalysis
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