On the mechanisms and the selectivity determining steps in syngas conversion over supported metal catalysts: An IR study

被引:82
作者
Sanchez-Escribano, V.
Larrubia Vargas, M. A.
Finocchio, E.
Busca, G.
机构
[1] Univ Genoa, Dipartimento Ingn Chim & Proc, Lab Chim Superfici & Catalisi Ind, I-16129 Genoa, Italy
[2] Univ Salamanca, Dept Quim Inorgan, E-37008 Salamanca, Spain
[3] Univ Malaga, Dept Ingn Quim, E-29071 Malaga, Spain
[4] Consorzio INSTM, I-50121 Florence, Italy
关键词
methanol synthesis; methanation; Fischer Tropsch synthesis; IR spectroscopy; oxygenated intermediates; syngas conversions; selectivity; Cu-ZnO-Al2O3; catalyst; Ni-Al2O3; Co-Al2O3;
D O I
10.1016/j.apcata.2006.09.020
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
An IR study of syngas and methanol conversion has been performed over Cu-ZnO-Al2O3 methanol synthesis catalyst, Ni-Al2O3 methanation catalyst and Co-Al2O3 Fischer Tropsch catalyst. The data, obtained at low pressure, provide unequivocal evidence of the existence of a way via oxygenated intermediates (formates, possibly dioxymethylene, methoxy groups) in the three cases. In the selectivity determining step, methoxy groups desorb associatively as methanol on Cu-ZnO-Al2O3. Methoxy groups are selectively hydrogenolyzed to methane over Ni-Al2O3. Over Co-Al2O3 oxygenated surface species may be involved in the chain growth to give C2+ compounds. It is possible that this mechanism coexists with the via-carbide all-metallic catalysis reported for methanation and FT synthesis, on the basis of studies performed on pure metals. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 74
页数:7
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