Intrinsic kinetics of steam methane reforming over a monolithic nickel catalyst in a fixed bed reactor system

被引:3
|
作者
Shen, Ziqi [1 ]
Nabavi, Seyed Ali [1 ]
Clough, Peter T. [1 ]
机构
[1] Cranfield Univ, Energy & Sustainabil Theme, Cranfield MK43 0AL, Beds, England
关键词
Steam methane reforming; Structured catalyst; Intrinsic kinetic; Hydrogen production; Reaction mechanism; PROCESS INTENSIFICATION; CHEMICAL CONVERSION; HYDROGEN-PRODUCTION; FLUIDIZED-BED; ACTIVATION; CO2; REQUIREMENTS; MECHANISM; ENERGY; H2O;
D O I
10.1016/j.ces.2024.120482
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The intrinsic kinetics of steam methane reforming were experimentally investigated using a monolithic nickelbased catalyst in a specially designed fixed bed system. All kinetic tests were performed under various operating conditions: steam to carbon ratio of 2 to 5, methane volumetric concentration in feed gas of 3 % to 9 %, temperature of 500 to 650 degrees C, and typical biogas compositions with N 2 dilution (carbon dioxide 35.7 - 55.6 %, methane 44.4 - 64.3 %, with 86 - 91 % nitrogen dilution). A deconvolution process was applied during the rate calculation and the reaction orders with respect to different gases were determined, coupled with thermodynamic system analysis. The reaction mechanism was then proposed and a Langmuir-Hinshelwood-HougenWatson (LHHW) kinetic model was established, followed by kinetic parameter estimations for the model and a further model validation with experimental data. Based on the model, the intrinsic kinetic of SMR reaction using monolithic catalysts was described. The validity and feasibility of applying the faster approach for kinetic parameter estimation were demonstrated, and this work is the first demonstration of a complex reaction system. Also, the reaction mechanism appeared to show a suitably high correlation with alternative and more sustainable methane sources (i.e. biogas).
引用
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页数:13
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