In 2O 3/Al 2O 3 Catalysts for NO x Reduction in Lean Condition
The lean NO x performance and catalytic properties of In 2O 3/Al 2O 3 catalysts were investigated. High lean NO x activity was observed when propene was used as a reductant in the presence of 9% O 2 and 7% H 2O at a space velocity of 30,000 h −1. The optimum lean NO x activity of In 2O 3/Al 2O 3 cat...
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Veröffentlicht in: | Journal of catalysis 2002, Vol.210 (1), p.97-105 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The lean NO
x
performance and catalytic properties of In
2O
3/Al
2O
3 catalysts were investigated. High lean NO
x
activity was observed when propene was used as a reductant in the presence of 9% O
2 and 7% H
2O at a space velocity of 30,000 h
−1. The optimum lean NO
x
activity of In
2O
3/Al
2O
3 catalysts was observed at a loading of 2.5 wt% indium on γ-Al
2O
3 which was prepared by a sol–gel technique (230 m
2/g). When propane was used as a reductant, the In
2O
3/Al
2O
3 catalyst did not promote NO
x
reduction compared to the alumina substrate. X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and temperature-programmed reduction (TPR) have been used to characterize a series of In
2O
3/Al
2O
3 catalysts to increase understanding of the surface structure of indium oxide species on the alumina support. The XRD data indicated that crystalline In
2O
3 was present at In
2O
3 loadings >5 wt% and the quantity of the crystalline phase increased as a function of indium loading. XPS results suggested that indium oxide existed as a well-dispersed phase up to 10 wt% indium. The well-dispersed or reducible indium oxide species below 400°C in TPR experiments were assigned as the sites which activate propene to oxygenated hydrocarbons such as acetaldehyde and acrolein. Alumina sites readily utilize the oxygenated hydrocarbons to reduce NO
x
. A bifunction mechanism was proposed to explain high NO
x
reduction over In
2O
3/Al
2O
3 catalysts. |
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ISSN: | 0021-9517 1090-2694 |
DOI: | 10.1006/jcat.2002.3667 |