Spatially Resolved Measurements in a Stagnation-Flow Reactor: Kinetics of Catalytic NH3 Decomposition

被引:0
|
作者
Davari, Sadaf [1 ]
Cardenas, Camilo [1 ]
Hettel, Matthias [1 ]
Lott, Patrick [1 ]
Tischer, Steffen [2 ]
Angeli, Sofia [2 ]
Deutschmann, Olaf [1 ,2 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Chem Technol & Polymer Chem ITCP, Engesserstr 20, D-76131 Karlsruhe, Germany
[2] Karlsruhe Inst Technol KIT, Inst Catalysis Res & Technol IKFT, Hermann Von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
Ammonia decomposition; Heterogeneous kinetics; Nickel catalyst; Stagnation-flow reactor; CHEMICAL-VAPOR-DEPOSITION; SURFACE-REACTION KINETICS; ON-SITE GENERATION; AMMONIA DECOMPOSITION; PARTIAL OXIDATION; DOPED AL2O3; FLUID-FLOW; METHANE; COMBUSTION; PRESSURE;
D O I
10.1002/cite.202400100
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A stagnation-flow reactor was employed to investigate the decomposition of ammonia over a Ni/Al2O3 catalyst across a range of system pressures and ammonia mole fractions. The results indicate that the system pressure has a negligible impact on the light-off behavior and the concentration profiles of NH3. A comparison of 1D modelling with 3D computational fluid dynamics (CFD) computations justifies the use of the simpler flow model. Good agreement between experiments and the 1D simulation is achieved for two different kinetic models from literature in the mainly diffusion-controlled regime. For lower temperatures, at which the process is kinetically controlled, the two mechanisms exhibit significant differences. The stagnation-flow reactor concept is shown to be a promising tool for understanding, developing, and validating the reaction kinetics of heterogeneous catalytic processes.
引用
收藏
页码:1735 / 1750
页数:16
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