Intrinsic kinetics of steam methane reforming on a thin, nanostructured and adherent Ni coating

被引:23
|
作者
Minette, Florent [1 ]
Lugo-Pimentel, Michael [2 ]
Modroukas, Dean [3 ]
Davis, Andrew W. [4 ]
Gill, Rajinder [4 ]
Castaldi, Marco J. [2 ]
De Wild, Juray [1 ]
机构
[1] Catholic Univ Louvain, Mat & Proc Engn IMAP, Pl St Barbe 2, B-1348 Louvain, Belgium
[2] CUNY City Coll, Dept Chem Engn, New York, NY 10031 USA
[3] Innoveering LLC, Ronkonkoma, NY USA
[4] Alloy Surfaces Co Inc ASC, Chester Township, PA USA
关键词
Catalyst coating; Structured catalyst; Natural gas steam reforming; Intrinsic reaction kinetics; Hydrogen; FISCHER-TROPSCH SYNTHESIS; PROMOTED IRON CATALYST; NATURAL-GAS; TRANSPORT LIMITATIONS; STRUCTURED CATALYST; MESOPOROUS ALUMINA; AXIAL-DISPERSION; NANOTUBE ARRAYS; BED DILUTION; REACTOR;
D O I
10.1016/j.apcatb.2018.07.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The intrinsic kinetics of Steam Methane Reforming (SMR) on a non-conventional nanostructured and strongly adherent Ni coating on a metal substrate was experimentally studied using an integral packed bed reactor. The coating was characterized by means of SEM, N-2 adsorption/desorption, EDX, XRD and TPR. The reactor was designed and the operating conditions selected to guarantee negligible interfacial and intra-particle transport limitations, plug flow, isothermal operation and a sufficiently small pressure drop. Experiments were carried out at temperatures between 450 and 600 degrees C, space times between 0.033 and 0.1 mol/(g(cat).s) and steam-to-carbon ratios of 2.87 to 5.53. Discrimination between potential reaction mechanisms and rate determining steps and estimation of the rate parameters and their confidence intervals followed from regression and statistical and physicochemical testing. Measurements confirmed that the water gas shift reaction reached equilibrium for each condition. A comparison with reported intrinsic kinetics for a conventional SMR catalyst was made and optimal catalyst coating thickness, accounting for intra-catalyst diffusion limitations was evaluated.
引用
收藏
页码:184 / 197
页数:14
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