Studies on the Solid Oxide Cell Perovskite Electrode Materials for Soot Oxidation Activity

Solid Oxide Cells (SOCs) can work efficiently in reversible operation, allowing the energy storage as hydrogen in power to gas application and providing requested electricity in gas to power application. They can easily switch from fuel cell to electrolyzer mode in order to guarantee the production of electricity, heat or directly hydrogen as fuel depending on energy demand and utilization. The proposed modeling is able to calculate effectively SOC performance in both operating modes, basing on the same electrochemical equations and system parameters, just setting the current density direction. The identified kinetic core is implemented in different simulation tools as a function of the scale under study. When the analysis mainly focuses on the kinetics affecting the global performance of small-sized single cells, a 0D code written in Fortran and then executed in Aspen Plus is used. When larger-scale single or stacked cells are considered and local maps of the main physicochemical properties on the cell plane are of interest, a detailed in-home 2D Fortran code is carried out. The presented modeling is validated on experimental data collected on laboratory SOCs of different scales and electrode materials, showing a good agreement between calculated and measured values and so confirming its applicability for multiscale approach studies.

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Influence of the Preparation Method of Ag-K/CeO2-ZrO2-Al2O3 Catalysts on Their Structure and Activity for the Simultaneous Removal of Soot and NOx

Catalysts ◽

10.3390/catal10030294 ◽

2020 ◽

Vol 10 (3) ◽

pp. 294 ◽

Cited By ~ 2

Author(s):

Anna Cooper ◽

Thomas E. Davies ◽

David J. Morgan ◽

Stan Golunski ◽

Stuart H. Taylor

Keyword(s):

Preparation Method ◽

Catalyst Activity ◽

Chemical Vapor ◽

Soot Oxidation ◽

Simultaneous Removal ◽

Oxidation Activity ◽

Wet Impregnation ◽

Incipient Wetness ◽

The Difference ◽

Soot Oxidation Activity

Ag/CeO2-ZrO2-Al2O3, a known catalyst for the simultaneous removal of NOx and soot, was modified by the addition of K, and was prepared using various techniques: wet impregnation, incipient wetness, and chemical vapor impregnation at different temperatures. The effect of the preparation method on catalyst activity was studied. It was found that catalysts prepared via wet impregnation, incipient wetness, and chemical vapor impregnation at 80 °C were able to utilize in situ formed N2O at low temperatures, to simultaneously remove NOx and soot. The difference in preparation method affected the catalyst’s ability to produce and use N2O as an oxidant for soot. The temperature at which chemical vapor impregnation was performed greatly influenced the catalyst’s ability to oxidize soot. The introduction of K to the Ag/CeO2-ZrO2-Al2O3 vastly improved the soot oxidation activity, particularly for the catalyst prepared via wet impregnation. However, the incorporation of K had an adverse effect on the reduction of NOx.

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