Catalytic oxidation of NO over Mn–Co–Ce–Ox catalysts: effect of reaction conditions

Catalytic oxidation of NO over Mn–Co–Ce–Ox catalysts: effect of reaction conditions Manganese–cobalt–cerium oxide (Mn–Co–Ce–Ox) catalysts were synthesized by the co-precipitation method and tested for activity in low-temperature catalytic oxidation of NO in the presence of excess O2. With the best Mn–Co–Ce mixed-oxide catalyst, approximately 80 % NO conversion was achieved at 150 °C and a space velocity of 35,000 h−1. The effect of reaction conditions (reaction temperature, volume fractions of NO and O2, gas hourly space velocity (GHSV), and catalyst stability) was investigated. The optimum reaction temperature was 150 °C. Increasing the O2 content above 3 % results in almost no improvement of NO oxidation. This catalyst enables highly effective removal of NO within a wide range of GHSV. Furthermore, the stability of the Me–Co–Ce–Ox catalyst was excellent; no noticeable decrease of NO conversion was observed in 40 h. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Catalytic oxidation of NO over Mn–Co–Ce–Ox catalysts: effect of reaction conditions

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Publisher
Springer Journals
Copyright
Copyright © 2012 by Springer Science+Business Media Dordrecht
Subject
Chemistry; Catalysis; Physical Chemistry; Inorganic Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1007/s11164-012-0953-7
Publisher site
See Article on Publisher Site

Abstract

Manganese–cobalt–cerium oxide (Mn–Co–Ce–Ox) catalysts were synthesized by the co-precipitation method and tested for activity in low-temperature catalytic oxidation of NO in the presence of excess O2. With the best Mn–Co–Ce mixed-oxide catalyst, approximately 80 % NO conversion was achieved at 150 °C and a space velocity of 35,000 h−1. The effect of reaction conditions (reaction temperature, volume fractions of NO and O2, gas hourly space velocity (GHSV), and catalyst stability) was investigated. The optimum reaction temperature was 150 °C. Increasing the O2 content above 3 % results in almost no improvement of NO oxidation. This catalyst enables highly effective removal of NO within a wide range of GHSV. Furthermore, the stability of the Me–Co–Ce–Ox catalyst was excellent; no noticeable decrease of NO conversion was observed in 40 h.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Dec 18, 2012

References

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