NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells
The catalytic electrochemical reduction of NO with propene was investigated on La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells. The electrodes were infiltrated with BaO and Pt. The cells were catalytically active towards the selective catalytic reduction of NOx with propene, but BaO infiltratio...
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2017-12-01
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doaj-bc4c52ebb753406ba9249bbc3e11ebdc2020-11-25T03:49:22ZengInternational Association of Physical Chemists (IAPC)Journal of Electrochemical Science and Engineering1847-92862017-12-017410.5599/jese.419272NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cellsAnja Zarah Friedberg0Kent Kammer Hansen1Department of Energy Conversion and Storage, Technical University of Denmark, DK-4000 RoskildeDepartment of Energy Conversion and Storage, Technical University of Denmark, DK-4000 RoskildeThe catalytic electrochemical reduction of NO with propene was investigated on La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells. The electrodes were infiltrated with BaO and Pt. The cells were catalytically active towards the selective catalytic reduction of NOx with propene, but BaO infiltration lowered the NO conversion, probably because of active-site blocking on La0.85Sr0.15MnO3+d. Pt infiltration enhanced the reduction of NOx with propene. When a voltage was applied to the cell with BaO infiltrated electrodes, the NO conversion increased in absence and presence of propene in the feed gas and presence of 10 % O2. The addition of propene into the feed gas did not enhance the conversion of NO when the electrodes were infiltrated with BaO. When platinum was co-infiltrated with BaO, the catalytic activity towards the reduction of NO with propene was enhanced. However, almost no effect was observed when a voltage was applied. Additionally, when the cells were infiltrated with Pt, an electrochemical promotion was observed with respect to CO2 formation. http://pub.iapchem.org/ojs/index.php/JESE/article/view/419NOPropeneLSMCGO |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anja Zarah Friedberg Kent Kammer Hansen |
spellingShingle |
Anja Zarah Friedberg Kent Kammer Hansen NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells Journal of Electrochemical Science and Engineering NO Propene LSM CGO |
author_facet |
Anja Zarah Friedberg Kent Kammer Hansen |
author_sort |
Anja Zarah Friedberg |
title |
NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells |
title_short |
NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells |
title_full |
NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells |
title_fullStr |
NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells |
title_full_unstemmed |
NOx and propene conversion in La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells |
title_sort |
nox and propene conversion in la0.85sr0.15mno3+d/ce0.9gd0.1o1.95 symmetrical cells |
publisher |
International Association of Physical Chemists (IAPC) |
series |
Journal of Electrochemical Science and Engineering |
issn |
1847-9286 |
publishDate |
2017-12-01 |
description |
The catalytic electrochemical reduction of NO with propene was investigated on La0.85Sr0.15MnO3+d/Ce0.9Gd0.1O1.95 symmetrical cells. The electrodes were infiltrated with BaO and Pt. The cells were catalytically active towards the selective catalytic reduction of NOx with propene, but BaO infiltration lowered the NO conversion, probably because of active-site blocking on La0.85Sr0.15MnO3+d. Pt infiltration enhanced the reduction of NOx with propene. When a voltage was applied to the cell with BaO infiltrated electrodes, the NO conversion increased in absence and presence of propene in the feed gas and presence of 10 % O2. The addition of propene into the feed gas did not enhance the conversion of NO when the electrodes were infiltrated with BaO. When platinum was co-infiltrated with BaO, the catalytic activity towards the reduction of NO with propene was enhanced. However, almost no effect was observed when a voltage was applied. Additionally, when the cells were infiltrated with Pt, an electrochemical promotion was observed with respect to CO2 formation.
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topic |
NO Propene LSM CGO |
url |
http://pub.iapchem.org/ojs/index.php/JESE/article/view/419 |
work_keys_str_mv |
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