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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Main Authors: Anja Zarah Friedberg, Kent Kammer Hansen
Format: Article
Language:English
Published: International Association of Physical Chemists (IAPC) 2017-12-01
Series:Journal of Electrochemical Science and Engineering
Subjects:
NO
LSM
CGO
Online Access:http://pub.iapchem.org/ojs/index.php/JESE/article/view/419
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spelling 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.
topic NO
Propene
LSM
CGO
url http://pub.iapchem.org/ojs/index.php/JESE/article/view/419
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