Propane Ignition Characteristics in a Pt-Catalyzed Microreactor for SOFC Preheating: A Numerical Study of Catalyst Activity Effects

Leveraging catalytic microreactors as compact yet powerful thermal sources represents a promising approach to enable rapid and reliable startup of small-scale solid oxide fuel cell (SOFC) systems. In the present study, the homogeneous–heterogeneous (HH) combustion behavior of a propane/air mixture in a Pt-catalyzed microreactor is investigated using two-dimensional computational fluid dynamic (CFD) simulations. The catalytic reaction kinetics model is integrated into the general module of ANSYSY Fluent via a user-defined function (UDF) interface. By varying the surface area factor, the ignition characteristics of the propane/air mixture under different catalyst activities are systematically explored. Numerical results reveal that the relative catalyst activity range of 0–2 represents a sensitive region for propane/air ignition characteristics, characterized by a 541 K decrease in ignition temperature and a 50% reduction in ignition delay time. Nevertheless, further increases in relative catalyst activity from 2 to 10, yield a much smaller reduction—64 K in ignition temperature and 6.7 s in ignition delay time—indicating a weakly responsive regime. The relative contribution of the heterogeneous reaction (HTR) to the total heat release decreases with higher feed temperatures but increases with enhanced catalyst activity. Regarding the temporal evolution of HTR contribution, the initiation of homogeneous ignition undermines the dominance of HTR contribution. Irrespective of catalytic activity levels, the relative contributions of the two reaction pathways subsequently undergo dynamic redistribution and ultimately stabilize, reaching an equilibrium state within approximately 10 s. These findings provide critical insights into the role of catalyst activity in propane/air mixture ignition and the interplay between homogeneous and heterogeneous reactions in microscale combustion systems.

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Publication Details

Journal
Batteries
Published
2025-10-23
DOI
https://doi.org/10.3390/batteries11110390
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
0.00

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article

Propane Ignition Characteristics in a Pt-Catalyzed Microreactor for SOFC Preheating: A Numerical Study of Catalyst Activity Effects

Lili Ma, Guohe Jiang, Zhiwei Miao, Zunmin Li et al.
Batteries
Catalytic Processes in Materials Science
article

Propane Ignition Characteristics in a Pt-Catalyzed Microreactor for SOFC Preheating: A Numerical Study of Catalyst Activity Effects

Lili Ma, Guohe Jiang, Zhiwei Miao, Zunmin Li, Weiqiang Xu, Zhulong Wang, Zhen Wang, Zhiyuan Yang
article en

Abstract

Leveraging catalytic microreactors as compact yet powerful thermal sources represents a promising approach to enable rapid and reliable startup of small-scale solid oxide fuel cell (SOFC) systems. In the present study, the homogeneous–heterogeneous (HH) combustion behavior of a propane/air mixture in a Pt-catalyzed microreactor is investigated using two-dimensional computational fluid dynamic (CFD) simulations. The catalytic reaction kinetics model is integrated into the general module of ANSYSY Fluent via a user-defined function (UDF) interface. By varying the surface area factor, the ignition characteristics of the propane/air mixture under different catalyst activities are systematically explored. Numerical results reveal that the relative catalyst activity range of 0–2 represents a sensitive region for propane/air ignition characteristics, characterized by a 541 K decrease in ignition temperature and a 50% reduction in ignition delay time. Nevertheless, further increases in relative catalyst activity from 2 to 10, yield a much smaller reduction—64 K in ignition temperature and 6.7 s in ignition delay time—indicating a weakly responsive regime. The relative contribution of the heterogeneous reaction (HTR) to the total heat release decreases with higher feed temperatures but increases with enhanced catalyst activity. Regarding the temporal evolution of HTR contribution, the initiation of homogeneous ignition undermines the dominance of HTR contribution. Irrespective of catalytic activity levels, the relative contributions of the two reaction pathways subsequently undergo dynamic redistribution and ultimately stabilize, reaching an equilibrium state within approximately 10 s. These findings provide critical insights into the role of catalyst activity in propane/air mixture ignition and the interplay between homogeneous and heterogeneous reactions in microscale combustion systems.

BatteriesVol. 11(11)
Binzhou Technician College (CN), Shanghai Maritime University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 76%
Catalytic Processes in Materials Science
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