Direct synthesis of dimethyl ether from carbon-monoxide-rich synthesis gas: Influence of dehydration catalysts and operating conditions

被引:82
|
作者
Stiefel, Miriam [1 ]
Ahmad, Ruaa [1 ]
Arnold, Ulrich [1 ]
Doering, Manfred [1 ]
机构
[1] IKFT, Karlsruhe Inst Technol, D-76344 Eggenstein Leopoldshafen, Germany
关键词
Dimethyl ether; Synthesis gas; Zeolite catalysts; ZSM-5; Mordenite; Biofuels; SOLID-ACID; HYBRID CATALYSTS; DME SYNTHESIS; METHANOL DEHYDRATION; SURFACE-ACIDITY; H-MORDENITE; SYNGAS; ZEOLITES; DEACTIVATION; CU/ZNO/AL2O3;
D O I
10.1016/j.fuproc.2011.03.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Various dehydration catalysts were studied in the synthesis of dimethyl ether (DME) directly from carbon-monoxide-rich synthesis gas under a series of different reaction conditions. The investigated catalyst systems consisted of combinations of a methanol catalyst (CuO/ZnO system) with catalysts for methanol dehydration based on gamma-Al2O3 or zeolites and gamma-Al2O3 was identified as the most favorable dehydration catalyst Various reaction parameters such as temperature, H-2/CO ratio and space velocity were studied. The impact of water on Cu/ZnO/Al2O3-gamma-Al2O3 catalysts was investigated and no deactivation could be observed at water contents below 10% during running times of several hours. A running time of several days and a water content of 10% led to a significant increase of CO conversion but the water gas shift reaction became dominating and CO2 was the main product. After termination of water feeding significant deactivation of the catalyst system was observed but the system returned to high DME selectivity. Catalyst stability and the influence of CO2 in the gas feed were studied in experiments lasting for about three weeks. The presence of 8% of CO2 caused an approximately 10% lower CO conversion and an about 5% lower DME selectivity compared to the reaction system without CO2. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1466 / 1474
页数:9
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