4.6 Article

On the support dependency of the CO2 methanation - decoupling size and support effects

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CATALYSIS SCIENCE & TECHNOLOGY
卷 11, 期 12, 页码 4098-4114

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cy00399b

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  1. DFG research training group 1860 MIMENIMA

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The influence of support basicity on Ru-catalyzed CO2 methanation was investigated, with different types of basic surface sites on the support playing a significant role in catalytic behavior. Basic supports can contribute to catalytic turnover by opening new pathways or promoting existing ones, depending on the type, density, and strength of basic sites available, which varies with temperature.
The influence of the support basicity, according to the Lewis and Bronsted definition, was investigated for the Ru catalyzed CO2 methanation in the temperature range from 200 degrees C to 400 degrees C. Due to the structure-sensitivity of the reaction, a novel building block approach was used to ensure a constant Ru particle size, while varying the support material. In this way, differences in the catalytic behaviour could be directly related to support effects. Eight oxides - the rare earth metal oxides Gd2O3, Sm2O3 and Y2O3 (REOs) as well as TiO2, ZrO2, Al2O3, MgO and SiO2 as a non-basic oxide - were chosen to cover different types and combinations of basic surface sites on the support, such as Bronsted basic hydroxyl groups, Lewis basic oxygen atoms and oxygen vacancies. Above 310 degrees C, the REO supported catalysts showed the highest methane formation rates. The consumption of carbonate species formed upon CO2 adsorption on all three types of basic sites indicated their catalytic involvement in the high temperature regime. Below 310 degrees C, TiO2 and - to a lesser extent - ZrO2 excelled the other supports. For ZrO2 the enhanced performance could be related to the sole presence of Lewis basic oxygen vacancies, acting as additional CO2 adsorption and activation sites on the support. On contrary, in case of TiO2 they seemed not to be directly but only indirectly involved by facilitating the conversion on the Ru particles on the basis of a favourable electronic metal-support interaction. The inferior catalytic results obtained with the other supports were in accord with the absence of basic sites or a spectator role of the carbonates formed - except for Al2O3 which stood out probably due to Bronsted basic OH-groups formed under reaction conditions. Overall, the study reveals that basic supports can noticeably contribute to the catalytic turnover by opening new support-related pathways in addition to the Ru-related pathway evidenced in all cases and/or by promoting the latter. Their impact is dependent on the type, density and strength of basic sites available and varies with temperature.

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