Properties of alkali-promoted Cu-MgO catalysts and their activity for methanol decomposition and C2-oxygenate formation

被引:28
作者
Goodarznia, Shahin [1 ]
Smith, Kevin J. [1 ]
机构
[1] Univ British Columbia, Dept Biol & Chem Engn, Vancouver, BC V6T 1Z3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Catalyst; Promoter; Syngas; Cu-MgO; Basicity; Methyl formate; Ethanol; CO; Cu dispersion; HIGHER ALCOHOL SYNTHESIS; CARBON BOND FORMATION; CESIUM-DOPED CU/ZNO; MG/AL MIXED OXIDES; METHYL FORMATE; OXYGENATE SYNTHESIS; CO HYDROGENATION; KINETIC-MODEL; COPPER; DEHYDROGENATION;
D O I
10.1016/j.molcata.2010.01.002
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 decomposition of CH3OH in the presence of CO has been investigated over high surface area MgO, Cu-MgO, K-Cu-MgO and Cs-Cu-MgO catalysts. The catalysts were prepared by thermal decomposition of metal salts mixed with palmitic acid. The reduced catalysts had surface areas of 18-74 m(2) g(-1) and intrinsic basicities of 4-17 mu mol CO2 m(-2). Results revealed that methyl formate was a primary product of CH3OH decomposition, whereas CO was a secondary product. Although selectivity to C-2 species (ethanol and acetic acid) was low (<5 C-atom %) at the low pressure (101 kPa) conditions of the present study, there was an optimum intrinsic basicity (9.5 mu mol CO2 m(-2)) at which the selectivity to C-2 species and methyl formate reached a maximum. The role of catalyst basic properties in the formation of C-2 species from CH3OH is discussed. (c) 2010 Elsevier BM. All rights reserved.
引用
收藏
页码:1 / 13
页数:13
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