Time-resolved XANES studies on used silica supported cobalt catalysts

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Abstract

In order to investigate the phases of used Co/SiO 2 catalysts, one of the most commonly used catalysts for Fischer-Tropsch synthesis, time-resolved X-ray absorption near edge structure (TR-XANES) technique was introduced. The catalysts were prepared by incipient wetness impregnation method with %Co loading of 15% and 20% and used for Fischer-Tropsch synthesis at the reaction temperature of 190°C and the pressure of 10 and 20 bar, called 15%Co/Aerosil_wi_used_10_bar, 15%Co/Aerosil_wi_used_20_bar, and 20%Co/Aerosil_wi_used_20_bar. TR-XANES showed the edge energy of 7721 eV for all used catalysts and by looking at the feature of their spectra, the results implied that the major phase was CoO. To further investigate their ability of being oxidized at elevated temperatures, the catalysts were oxidized by heating from ambient to 450°C with the heating rate of 8°C/min at the pressure of 1 bar with the O 2:N 2 flow rate of 70:30 ml/min. Once reaching 450°C, the temperature was held at 450°C for 90 min before cooling down to room temperature. During heating, holding, and cooling, the catalyst properties were measured by TR-XANES. When all catalysts heating up from 300 to 400°C, the edge energy of 15%Co/Aerosil_wi_used_10_bar, 15%Co/Aerosil_wi_used_20_bar, and 20%Co/Aerosil_wi_used_20_bar at 7719, 7717, and 7718 eV, respectively, showed the main phase of CoO mixed with Co 3O 4. There were no significant changes in phase while holding the temperature at 450°C. Once cooling from 450°C to room temperature, the edge energy of 15%Co/Aerosil_wi_used_10_bar at 7724 eV showed the main Co 3O 4 phase, the ones of 15%Co/Aerosil_wi_used_20_bar and 20%Co/Aerosil_wi_used_20_bar at 7717 and 7718 eV showed the mixed phase of Co 3O 4 and CoO. All results would be confirmed by further studies on temperature programmed oxidation (TPO).

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Chotiwan, S., Kityakarn, S., Poo-arporn, Y., & Viravathana, P. (2012). Time-resolved XANES studies on used silica supported cobalt catalysts. Engineering Journal, 16(3), 115–121. https://doi.org/10.4186/ej.2012.16.3.115

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