Adsorption-enhanced steam-methane reforming

被引:259
作者
Ding, Y [1 ]
Alpay, E [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn & Chem Technol, London SW7 2BY, England
关键词
SMR; sorption enhancement; transient kinetics; Ni-catalyst; hydrotalcite; CO2; adsorbent; mathematical modelling;
D O I
10.1016/S0009-2509(99)00597-7
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Experimental and theoretical studies of steam-methane reforming in the presence of a hydrotalcite-based CO, adsorbent are presented. Attention is given to the analysis of the transient behaviour of a tubular (integral) reactor when an Ni-based catalyst is admired with the adsorbent. Considerable enhancement of the methane conversion is experimentally demonstrated. Enhancement arises from the favourable shifts in the reaction equilibria of the reforming and water-gas shift reactions towards further CO, production. As predicted, the potential for conversion enhancement is shown to increase under the conditions of a high reactor space time, high operating pressure, or a low steam-to-methane feed ratio, i.e. when reaction equilibrium limitations are important. A mathematical model, accounting for mass transfer limited adsorption kinetics, non-linear (Langmuirian) adsorption equilibria and a general reaction kinetic model, is shown to accurately predict the observed elution profiles from the reactor, and thus the degree of conversion enhancement. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3929 / 3940
页数:12
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