Role of CO in the Water-Induced Formation of Cobalt Oxide in a High Conversion Fischer-Tropsch Environment

被引:36
|
作者
Wolf, Moritz [1 ,2 ]
Mutuma, Bridget K. [3 ,4 ]
Coville, Neil J. [2 ,3 ,4 ]
Fischer, Nico [1 ,2 ]
Claeys, Michael [1 ,2 ]
机构
[1] Univ Cape Town, Dept Chem Engn, Inst Catalysis, ZA-7701 Rondebosch, South Africa
[2] DST NRF Ctr Excellence Catalysis C Change, ZA-7701 Rondebosch, South Africa
[3] Univ Witwatersrand, Sch Chem, DST NRF Ctr Excellence Strong Mat, ZA-2050 Johannesburg, South Africa
[4] Univ Witwatersrand, Sch Chem, Inst Mol Sci, ZA-2050 Johannesburg, South Africa
来源
ACS CATALYSIS | 2018年 / 8卷 / 05期
关键词
cobalt catalyst; Fischer-Tropsch synthesis; deactivation; oxidation; magnetometer; water; carbon monoxide; IN-SITU; CATALYSTS; DEACTIVATION; STABILITY; OXIDATION; NANOPARTICLES; BEHAVIOR; SILICA;
D O I
10.1021/acscatal.7b04177
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
A Co/C model catalyst was exposed to increasing partial pressures of water simulating high Fischer-Tropsch conversions at varying concentrations of synthesis gas. The stability of the metallic cobalt phase against oxidation and sintering under such conditions was monitored in an in situ magnetometer. Direct oxidation of cobalt to cobalt oxide with water-derived oxygen through a water splitting mechanism was shown to be kinetically hindered, even at high partial pressures of water. Combined threshold partial pressures of carbon monoxide and water were identified for rapid oxidation of cobalt, above which the removal of adsorbed oxygen species, originating from the dissociation of carbon monoxide on the metallic cobalt surface, by surface produced water was hindered resulting in water-induced oxidation.
引用
收藏
页码:3985 / 3989
页数:9
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