Structure-performance relations of molybdenum- and tungsten carbide catalysts for deoxygenation

被引:122
|
作者
Stellwagen, Daniel R. [1 ]
Bitter, Johannes H. [1 ,2 ]
机构
[1] Univ Utrecht, Dept Inorgan Chem & Catalysis, NL-3584 CG Utrecht, Netherlands
[2] Wageningen Univ, NL-6708 WG Wageningen, Netherlands
关键词
SELECTIVE DEOXYGENATION; CARBON NANOTUBES; MICROALGAE OIL; HYDRODEOXYGENATION; ACID; REDUCTION; OXYGEN; ISOMERIZATION; PATHWAYS; OXIDES;
D O I
10.1039/c4gc01831a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work demonstrates for the first time that carbide particle size is a critical factor for the activity and stability of carbon supported tungsten-and molybdenum carbide catalysts in (hydro-) deoxygenation reactions. The stability of the catalyst was shown to increase for larger particles due to the improved resistance of the metal carbide phase against full oxidation to crystalline metal oxides under reaction conditions. In addition to the improved catalyst stability, supported molybdenum carbides were found to more than double their weight-based catalytic activity upon increasing carbide particle size from 2 to 10 nanometers. The strongly improved (de-) hydrogenation activity of these larger carbide particles also facilitated a new deoxygenation pathway for fatty acids, in which an initial hydrogenation to fatty-aldehyde is combined with a decarbonylation step. This is the first time in which this deoxygenation pathway is observed over supported tungsten-or molybdenum carbide catalysts.
引用
收藏
页码:582 / 593
页数:12
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