In situ investigation on Co-phase evolution and its performance for Fischer–Tropsch synthesis over Nb-promoted cobalt catalysts
Nb-promoted cobalt catalysts were prepared by the incipient wetness impregnation method and characterized by ex / in situ XRD, in situ DRIFTS, N 2 physisorption, TEM, EDS-mapping, H 2 -TPR, CO/H 2 -TPD, and XPS. Their performance was investigated in a fixed bed reactor for Fischer–Tropsch synthesis...
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Veröffentlicht in: | Catalysis science & technology 2017, Vol.7 (23), p.5530-5539 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Nb-promoted cobalt catalysts were prepared by the incipient wetness impregnation method and characterized by
ex
/
in situ
XRD,
in situ
DRIFTS, N
2
physisorption, TEM, EDS-mapping, H
2
-TPR, CO/H
2
-TPD, and XPS. Their performance was investigated in a fixed bed reactor for Fischer–Tropsch synthesis (FTS). As regards the sample texture, niobium oxide (NbO
x
) can obviously reduce the BET surface area and pore volume, and promote the formation of uniform cobalt particles with a smaller size. The presence of NbO
x
complexes can weaken the metal–support interaction, while it also makes Co
3
O
4
species easily reducible to metallic cobalt and favours the formation of a hexagonal close-packed cobalt phase, as confirmed by the results of H
2
-TPR and
ex
/
in situ
XRD. What's more, NbO
x
can enhance the adsorption stability and the amount of CO adsorbed under approximately actual FTS reaction conditions, as verified by the results of CO-TPD. In addition, NbO
x
complexes can be considered as weak electron donors, as confirmed by the results of XPS, leading to a higher concentration of surface carbon species. According to the performance results, the selectivity to C
5
+
products increased to 89.3% from 85.6% and the CO conversion was significantly increased to 94.1% from 70.7% with the increase of Nb loading to 1.57 wt% from zero. It is found that highly selective production of heavy hydrocarbons can be achieved at a higher activity level over Nb-promoted cobalt catalysts. |
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ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/C7CY01325F |