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The performance of NOx storage-reduction catalyst containing Fe-compound after thermal aging

Authors :
Hirofumi Shinjoh
Kiyoshi Yamazaki
Naoki Takahashi
Masahiro Sugiura
Source :
Applied Catalysis B: Environmental. 53:1-12
Publication Year :
2004
Publisher :
Elsevier BV, 2004.

Abstract

The three-way catalytic performance (TWC performance) and the NO x purification activity through storage-reduction (NSR activity) over a Pt/Ba/(Al 2 O 3 -CeO 2 -Fe 2 O 3 ) catalyst were investigated in comparison with a Pt/Ba/(Al 2 O 3 -CeO 2 ) catalyst. Two kinds of reducing agents, C 3 H 6 and CO, were used for the measurement of the NSR activity. There was no difference in the TWC performance and the NSR activity between these two fresh catalysts. After thermal aging at 1123 K, however, the aged Pt/Ba/(Al 2 O 3 -CeO 2 -Fe 2 O 3 ) catalyst was found to show a higher TWC performance and a higher NSR activity in the case of using CO as a reducing agent than did the aged Pt/Ba/(Al 2 O 3 -CeO 2 ) catalyst, although there was no difference in the NSR activity in the case of using C 3 H 6 as a reducing agent between these two aged catalysts. Oxygen storage-release capacity measurement showed that an Fe-compound on the aged Pt/Ba/(Al 2 O 3 -CeO 2 -Fe 2 O 3 ) catalyst acted to store oxygen more effectively than did CeO 2 . Reaction analysis of a simple binary gas system showed that the Fe-compound weakened the CO self-poisoning for the CO–O 2 reaction and the CO–NO x reaction under reducing conditions, probably by provision of oxygen to the CO from Fe 2 O 3 or/and Fe in a Pt–Fe alloy. The more effective storing of oxygen and the weaker CO self-poisoning for the CO–O 2 reaction and the CO–NO x reaction lead to a higher TWC performance after thermal aging. The weaker CO self-poisoning for the CO–NO x reaction also leads to a greater ability to reduce stored NO x on the catalysts by CO under reducing conditions, causing a higher NSR activity in the case of using CO as a reducing agent after thermal aging.

Details

ISSN :
09263373
Volume :
53
Database :
OpenAIRE
Journal :
Applied Catalysis B: Environmental
Accession number :
edsair.doi...........61aff565c257d8b3f5e8c4013dec0b4c
Full Text :
https://doi.org/10.1016/j.apcatb.2004.04.010