Highly active and stable supported iron Fischer-Tropsch catalysts: Effects of support properties and SiO2 stabilizer on catalyst performance

Display Omitted * Effects of support properties on catalyst activity and stability were investigated. * A support with large pore volume accommodates higher Fe loading without pore blocking. * Fewer OH groups lead to higher extent of reduction and higher activity. * SiO2 stabilization inhibits deact...

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Veröffentlicht in:Journal of catalysis 2014-11, Vol.319, p.220-231
Hauptverfasser: KEYVANLOO, Kamyar, HECKER, William C, WOODFIELD, Brian F, BARTHOLOMEW, Calvin H
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Sprache:eng
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Zusammenfassung:Display Omitted * Effects of support properties on catalyst activity and stability were investigated. * A support with large pore volume accommodates higher Fe loading without pore blocking. * Fewer OH groups lead to higher extent of reduction and higher activity. * SiO2 stabilization inhibits deactivation by sintering and increases activity. * SiO2 was found to be a more effective hydrothermal stabilizer than La2O3. The effects of support properties including pore size, hydroxyl group concentration, and support stabilizer were investigated for six alumina-supported FeCuK Fischer-Tropsch catalysts containing 20% or 40% iron. Catalysts were supported on one of four aluminas stabilized with La2O3 or SiO2. A large pore support was found to accommodate 40% Fe without pore blockage. Catalyst activity was found to increase with increasing support pore size, lower OH group concentrations, and higher extents of reduction. SiO2 was found to be a more effective hydrothermal stabilizer than La2O3 as it suppresses the high-temperature transformation of [GREEK SMALL LETTER GAMMA]-Al2O3 to α-Al2O3 up to 1200°C allowing SiO2-stabilized catalysts to be dehydroxylated at higher temperatures. SiO2 stabilization also inhibits deactivation by sintering and increases activity, possibly due to surface silicate groups. Indeed, the activity of Fe/Si-Al2O3 continues to increase after 700h on stream, while the Fe/La-Al2O3 catalysts lose activity over the same time period.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2014.08.015