Particle size effect in the low temperature reforming of methane by carbon dioxide on silica-supported Ni nanoparticles

Particle size does not affect the intrinsic activity of silica-supported nickel nanoparticles in dry reforming at 500°C. [Display omitted] ► Different silica supported nickel catalyst prepared with varying particle size (1.6–7.3nm). ► Neutral silica support favours a very high reduction degree (>...

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Published inJournal of catalysis Vol. 297; pp. 27 - 34
Main Authors Baudouin, David, Rodemerck, Uwe, Krumeich, Frank, Mallmann, Aimery de, Szeto, Kaï C., Ménard, Hervé, Veyre, Laurent, Candy, Jean-Pierre, Webb, Paul B., Thieuleux, Chloé, Copéret, Christophe
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.01.2013
Elsevier
Elsevier BV
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Summary:Particle size does not affect the intrinsic activity of silica-supported nickel nanoparticles in dry reforming at 500°C. [Display omitted] ► Different silica supported nickel catalyst prepared with varying particle size (1.6–7.3nm). ► Neutral silica support favours a very high reduction degree (> 90%) at 500°C. ► Intrinsic Ni/SiO2 performances are independent of nickel particle size in dry reforming at 773K. ► The H2/CO ratio is controlled by the thermodynamic of the fast reverse water gas shift reaction. The influence of nickel particle size in the range of 1.6–7.3nm on catalyst performance in low temperature CO2 reforming of methane reaction has been investigated using well-defined catalysts based on a neutral silica support. XAS and XPS studies indicated a reduction degree greater than 90%. The intrinsic Ni/SiO2 performances were found to be independent of nickel particle size in dry reforming at 773K using a CH4/CO2 ratio of 1.3 at 1atm, both at an early stage and in steady state conditions. The H2/CO ratio was also found to be structure in sensitive but is controlled by thermodynamics through the faster reverse water gas shift reaction.
Bibliography:http://dx.doi.org/10.1016/j.jcat.2012.09.011
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2012.09.011