Catalytic decomposition of methane over a wood char concurrently activated by a pyrolysis gas

被引:86
作者
Dufour, A. [4 ]
Celzard, A. [3 ]
Fierro, V. [2 ]
Martin, E. [1 ]
Broust, F. [1 ]
Zoulalian, A.
机构
[1] UPR Biomasse Energie, PERSYST, CIRAD, F-34398 Montpellier 5, France
[2] Nancy Univ, Fac Sci & Tech, UMR CNRS 7555, LCSM, F-54506 Vandoeuvre Les Nancy, France
[3] Nancy Univ, ENSTIB, UMR CNRS 7555, LCSM, F-88051 Epinal 9, France
[4] Gaz France, Res & Dev Div, F-93211 St Denis, France
关键词
hydrogen production; biomass gasification; methane decomposition; carbon-based catalyst; activation; surface properties;
D O I
10.1016/j.apcata.2008.05.023
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 catalytic activity of a wood char towards CH4 decomposition in a pyrolysis gas was investigated in a fixed bed reactor for maximising hydrogen production from biomass gasification. Wood char is suggested to be the cheapest and greenest catalyst for CH4 conversion as it is directly produced in the pyrolysis facility. The conversion of methane reaches 70% for a contact time of 120 ms at 1000 degrees C. Because steam and CO2 are simultaneously present in the pyrolysis gas, the carbon catalyst is continuously regenerated. Hence the conversion of methane quickly stabilises. Such a phenomenon is shown to be possible through the oxidation of the char by CO2 and H2O at high temperature, which prevents the blocking of the mouth of pores by the concurrent pyrolytic carbon deposition. In the experimental conditions, oxygenated functional Surface groups are continuously formed (by steam and CO2 oxidation) and thermally decomposed. The active sites for CH4 chemisorption and decomposition are suggested to be the unsaturated carbon atoms generated by the evolution of the oxygenated functions at high temperature. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 173
页数:10
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