Hydrogen-enhanced catalytic hydrothermal gasification of biomass (vol 7, pg 521, 2017)

被引:2
|
作者
Reimer, J. [1 ]
Mueller, S. [1 ]
De Boni, E. [1 ]
Vogel, F. [1 ,2 ]
机构
[1] Paul Scherrer Inst, Lab Bioenergy & Catalysis, Res Div Energy & Environm, CH-5232 Villigen, Switzerland
[2] Fachhsch Nordwestschweiz, Hsch Tech, Inst Biomasse & Ressourceneffizienz, CH-5210 Windisch, Switzerland
关键词
Biomass; Carbon-supported ruthenium; Glycerol; Hydrogen co-feeding; Power to gas; Supercritical water gasification; Synthetic natural gas;
D O I
10.1007/s13399-017-0260-z
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 impact of hydrogen co-feeding on the catalytic hydrothermal gasification of wet biomass was explored in a continuous test rig using a feed of 10 wt% glycerol in water and a fixed bed of a carbon-supported ruthenium catalyst. The reactor was operated at a nominal temperature of 400 A degrees C and at pressures of 26-28 MPa. Variation of the hydrogen-to-glycerol ratio as well as of the total pressure showed clearly the methanation reaction to be promoted at the expense of carbon dioxide and hydrogen formation. This is explained by a higher hydrogen surface coverage and consecutively higher rates for hydrogenation of surface-bound carbon. An increase in peak temperature of ca. 75 K occurred in the catalytic fixed-bed when co-feeding hydrogen. The measured product gas composition was close to the thermodynamic equilibrium calculated at the outlet temperature of the reactor. A maximum methane concentration of 86 vol% in the raw gas was obtained at 28 MPa with a stoichiometric addition of hydrogen. Full catalytic activity was maintained during and after the hydrogen co-feeding experiments, verified by comparing the performance of a run with a 10 wt% glycerol in water feed after co-feeding hydrogen, for which the product distribution was very close to the experiments before hydrogen co-feeding.
引用
收藏
页码:521 / 521
页数:1
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