Thermally integrated bio-syngas-production for biorefineries

被引:15
作者
Bludowsky, T. [1 ]
Agar, D. W. [1 ]
机构
[1] Tech Univ Dortmund, Dept Biochem & Chem Engn, Lab Tech Chem B, D-44227 Dortmund, Germany
关键词
Biorefinery; Thermal integration; Synthesis gas; Aqueous-phase reforming; Methanol synthesis; RENEWABLE HYDROGEN; OXYGENATED HYDROCARBONS; TRANSPORTATION FUELS; STEAM GASIFICATION; BIOMASS; ALKANES;
D O I
10.1016/j.cherd.2009.03.012
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Maximising the thermal efficiency of a biorefinery is a major challenge in the production of economically competitive biomass-based chemicals. This paper compares different bio-syngas to methanol routes with respect to their energy demands and proposes a novel heat integration concept. Previous studies on biorefineries have tended to focus on the chemical transformations involved. The defunctionalisation of biofeedstocks required to eliminate the excess oxygen they contain is also a very energy-consuming process, which exerts a considerable influence on the overall yields which can be achieved. In this article we deal with the less appreciated issue of thermal integration by analysing two principle routes for the generation of 'bio'-synthesis gas for methanol synthesis: a conventional high temperature biomass gasification process and a scheme based on aqueous-phase reforming (APR). Low temperature gasification processes below 250 degrees C, such as APR, permit one to use the heat liberated in the methanol synthesis for the endothermic synthesis gas production step. The composition of the resultant synthesis gas must be modified slightly to meet the demands of the methanol synthesis reaction using a low temperature retro-water-gas shift reaction in a special adsorptive reactor. The results indicate that the low temperature arrangement has an edge in terms of the net energy consumption for a given methanol production and the analysis reveals topics of interest for future research in this area. (C) 2009 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1328 / 1339
页数:12
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