Thermodynamic analysis of dry reforming of CH4 with CO2 at high pressures

被引:116
|
作者
Chein, R. Y. [1 ]
Chen, Y. C. [2 ]
Yu, C. T. [3 ]
Chung, J. N. [4 ]
机构
[1] Natl Chung Hsing Univ, Dept Mech Engn, Taichung 40227, Taiwan
[2] Natl United Univ, Dept Energy Engn, Miaoli 36003, Taiwan
[3] Inst Nucl Energy Res, Div Chem, Taoyuan 32546, Taiwan
[4] Univ Florida, Dept Mech & Aerosp Engn, Gainesville, FL 32611 USA
关键词
Dry reforming of methane (DRM); Gibbs free energy minimization; High pressures; CH4; conversion; CO2; Carbon formation; FIXED-BED REACTORS; CARBON-DIOXIDE; SYNTHESIS GAS; EQUILIBRIUM ANALYSIS; PARTIAL OXIDATION; SYNGAS PRODUCTION; OXYGEN ADDITION; METHANE; CATALYSTS; STEAM;
D O I
10.1016/j.jngse.2015.07.001
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
Thermodynamic equilibrium of dry reforming of methane (DRM) was studied by Gibbs free energy minimization at elevated pressures. CH4 and CO2 conversions, carbon formation, H-2 yield, H-2/CO ratio and H2O formation were used to characterize the DRM performance using the reaction temperature as the primary parameter. The result shows that DRM is unfavorable at high pressure. CO2 and CH4 conversions decrease while the carbon formation increases as the pressure increases. With increasing CO2/CH4 ratio in the reaction, CH4 conversion is enhanced, carbon formation is suppressed, but CO2 conversion is lower due to the excess CO2 supply. The simulation results indicated that the introduction of inert gas in the system did not produce a significant effect on DRM performance. The performances of combined DRM and partial oxidation of methane (POM) and combined DRM and methane-steam reforming (MSR) were also studied to suppress the carbon formation. It was found that carbon formation can be reduced by introducing oxygen. However, the resulted H-2/CO ratio is less than 1. Introducing H2O into the reaction system can eliminate carbon formation when amount of H2O is large. However, the system must be operated at high temperature to produce high CH4 and CO2 conversions. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:617 / 629
页数:13
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