Reforming of CH4 by partial oxidation: thermodynamic and kinetic analyses

Citation
J. Zhu et al., Reforming of CH4 by partial oxidation: thermodynamic and kinetic analyses, FUEL, 80(7), 2001, pp. 899-905
Citations number
19
Categorie Soggetti
Chemistry,"Chemical Engineering
Journal title
FUEL
ISSN journal
00162361 → ACNP
Volume
80
Issue
7
Year of publication
2001
Pages
899 - 905
Database
ISI
SICI code
0016-2361(200105)80:7<899:ROCBPO>2.0.ZU;2-F
Abstract
The traditional technology for synthetic-gas (H-2 and CO) production from n atural gas is steam reforming. A major drawback of this technology is the i ntensive energy requirement due to the high endothermicity of the reforming reactions. A possible alternative is methane partial oxidation, or in a co mbination with steam or CO2, which could offer an advantage of vastly reduc ed energy requirement of the reforming process. This paper reports on a fea sibility study of CH4 partial oxidation into H-2 and CO by means of thermod ynamic 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 CH 4 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 occu rring at an optimal initial O-2/CH4 ratio varying with temperature. The opt imal O-2/CH4 ratio decreases with increasing temperature and approaches 0.5 at temperatures greater than 1073 K. The synthetic-gas yields also increas e with increasing temperature but with decreasing pressure, yet high temper ature can suppress the pressure effect. The GRI mechanisms are found to be adequate for the CHEMKIN simulations of CH4 partial oxidation at temperatur es 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 oxida tion. 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 produc ts. Both thermodynamic and kinetic predictions of H-2 and CO yields compare well at high temperatures. The optimum operating conditions for CH4 partia l oxidation reforming are recommended at 0.5 O-2/CH4 ratio, 1473 K and 1 at m. (C) 2001 Elsevier Science Ltd. All rights reserved.