Reforming of CH4 by partial oxidation:: thermodynamic and kinetic analyses

被引:162
作者
Zhu, J
Zhang, D
King, KD
机构
[1] Curtin Univ Technol, Sch Chem Engn, Perth, WA 6845, Australia
[2] Univ Adelaide, Dept Chem Engn, Adelaide, SA 5005, Australia
关键词
methane; partial oxidation; thermodynamic and kinetic analyses;
D O I
10.1016/S0016-2361(00)00165-4
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The traditional technology for synthetic-gas (H-2 and CO) production from natural gas is steam reforming. A major drawback of this technology is the intensive energy requirement due to the high endothermicity of the reforming reactions. A possible alternative is methane partial oxidation, or in a combination with steam or CO2, which could offer an advantage of vastly reduced energy requirement of the reforming process. This paper reports on a feasibility study of CH4 partial oxidation into H-2 and CO by means of thermodynamic and kinetic analyses. The thermodynamic analysis has been performed using the Gibbs free energy minimisation method, and the kinetic modelling has employed the CHEMKIN package incorporating the GRI 1.2 mechanisms of CH4 oxidation. The effects of initial O-2/CH4 ratio, temperature and pressure are examined. The thermodynamic analysis indicates that the synthetic-gas yields are strongly dependent on the initial O-2/CH4 ratio with maxima occurring at an optimal initial O-2/CH4 ratio varying with temperature. The optimal O-2/CH4 ratio decreases with increasing temperature and approaches 0.5 at temperatures greater than 1073 K. The synthetic-gas yields also increase with increasing temperature but with decreasing pressure, yet high temperature can suppress the pressure effect. The GRI mechanisms are found to be adequate for the CHEMKIN simulations of CH4 partial oxidation at temperatures greater than ca. 1273 K and O-2/CH4 ratio greater than 0.5. The CHEMKIN simulations suggest that two distinct stages exist during the partial oxidation. The first stage is a rapid 'oxidation' zone where H2O and CO2 are the main reaction products. The second stage is a slow 'conversion' zone where steam and CO2 reforming, water gas shift reaction as well as C2H2 coupling and C2H2 Steam reforming takes place with H-2 and CO being the main products. Both thermodynamic and kinetic predictions of H-2 and CO yields compare well at high temperatures. The optimum operating conditions for CH4 partial oxidation reforming are recommended at 0.5 O-2/CH4 ratio, 1473 K and 1 atm. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:899 / 905
页数:7
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