Tri-cobalt Carboxylate as a Catalyst and Catalyst Precursor in the Fischer-Tropsch Synthesis

被引:2
作者
Fischer, N. [1 ,2 ]
van Steen, E. [1 ,2 ]
Claeys, M. [1 ,2 ]
机构
[1] Univ Cape Town, Dept Chem Engn, Ctr Catalysis Res, ZA-7701 Cape Town, South Africa
[2] Univ Cape Town, Dept Chem Engn, Change DST NRF Ctr Excellence Catalysis C, ZA-7701 Cape Town, South Africa
关键词
cobalt; hydrogenation; hydrocarbons; nanostructures; supported catalysts; CO HYDROGENATION ACTIVITY; PARTICLE-SIZE; HYDROCARBON SYNTHESIS; STRUCTURE SENSITIVITY; PARTIAL OXIDATION; CARBON-DIOXIDE; SELECTIVITY; METHANOL; FORMALDEHYDE; DISPERSION;
D O I
10.1002/cctc.201300932
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
In recent years, several groups have invested significant research capacity to investigate the effect of the metal crystallite size on the various primary and secondary reactions taking place during the Fischer-Tropsch synthesis. Most publications agree that with decreasing crystallite size (d(cryst) < 10 nm) the surface-specific CO hydrogenation activity (turnover frequency) decreases. In parallel, an increased selectivity to the undesired methane was observed. In the present study we combined and extended previously published data on alumina-supported cobalt nanocrystallites with observations on an alumina-supported cobalt carbonyl complex ((CO)(9)Co3CCOOH) and its decomposition products under Fischer-Tropsch reaction conditions. We could show that with an increased degree of sintering of the complex, that is, a larger cobalt crystallite size, the turnover frequency increased and the tendency to form methane decreased. The results connect seamlessly with those obtained for the nanocrystallites suggesting that the catalyst performance features extend into the sub-2 nm range.
引用
收藏
页码:1707 / 1713
页数:7
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