Stability of cerium-modified γ-alumina catalyst support in supercritical water
Supercritical water is emerging as a promising medium to carry out a variety of catalytic reactions. However the support material can undergo transformation in the hydrothermal environment, as shown in the figure below. In this work the stability of a common support material γ-Al 2O 3 is examined at...
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Veröffentlicht in: | Applied catalysis. A, General General, 2010-06, Vol.381 (1), p.177-182 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Supercritical water is emerging as a promising medium to carry out a variety of catalytic reactions. However the support material can undergo transformation in the hydrothermal environment, as shown in the figure below. In this work the stability of a common support material γ-Al
2O
3 is examined at 500–700
°C and 246
bar.
Supercritical water (above 374.1
°C and 220.6
bar) is emerging as a promising medium to carry out a variety of catalytic reactions, including reforming to produce hydrogen. However, when using a heterogeneous catalyst the support material can undergo transformations in the hydrothermal environment. In this work the stability of γ-Al
2O
3 modified with 1–10
wt% Ce in supercritical water is examined, specifically in the temperature range of 500–700
°C at 246
bar. Transformations of the γ-phase were slowed but not prevented. Based on X-ray analysis, the transformation of γ-Al
2O
3 proceeded through the κ phase toward the stable α phase. Reduced cerium species were seen to be oxidized in the supercritical water environment, and low Ce-loading supports maintained the highest BET surface areas. The stabilization was greatest at 700
°C, where Ce-modified aluminas retained significantly higher specific surface areas than unmodified alumina. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2010.04.006 |