Enhanced activity of vanadia supported on microporous titania for the selective catalytic reduction of NO with NH 3 : Effect of promoters
Vanadium oxide-based catalysts are considered a promising catalyst for selective catalytic reduction (SCR) of NO with NH , which is an effective NO removal technology. As environmental issues have garnered more attention, however, improvements to vanadium-based SCR catalysts are strongly required. I...
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Published in: | Chemosphere (Oxford) Vol. 275; p. 130105 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
01-07-2021
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Subjects: | |
Online Access: | Get full text |
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Summary: | Vanadium oxide-based catalysts are considered a promising catalyst for selective catalytic reduction (SCR) of NO with NH
, which is an effective NO
removal technology. As environmental issues have garnered more attention, however, improvements to vanadium-based SCR catalysts are strongly required. In a previous study, we found that vanadium oxide on microporous titania as a support (V/MPTiO
) has certain advantages, such as improved thermal stability and more suppressed N
O formation, over the use of conventional nanoparticle titania (DT-51) as a support. In this study, widely used promoters, such as W, Sb, and Mo, were added to V/MPTiO
to investigate whether they have promoting effects on V/MPTiO
as well. Among these promoters added catalysts, the W and Mo were found to have significant promoting effects on the enhancement of deNO
activities at low temperatures, while the addition of Sb to V/MPTiO
tended to have a negative effect on the SCR activity. Based on the characterizations, including laser Raman, H
-temperature programmed reduction (H
-TPR), and in situ diffuse reflectance infrared Fourier transform (in situ DRIFT) analysis, we found that the addition of W and Mo increased the degree of polymerization in V/MPTiO
, which generated more reactive vanadia species. Hence, such changes, resulting from the addition of W and Mo promoters to V/MPTiO
, yielded enhanced catalytic activity at low temperatures. |
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ISSN: | 1879-1298 |