费托法
钴
催化作用
粒径
化学
粒子(生态学)
碳纳米纤维
多相催化
选择性
化学工程
无机化学
物理化学
有机化学
海洋学
工程类
地质学
作者
G. Leendert Bezemer,Johannes H. Bitter,H.P.C.E. Kuipers,Heiko Oosterbeek,Johannes E. Holewijn,Xiaoding Xu,Freek Kapteijn,A.J. van Dillen,Krijn P. de Jong
摘要
The influence of cobalt particle size in the range of 2.6−27 nm on the performance in Fischer−Tropsch synthesis has been investigated for the first time using well-defined catalysts based on an inert carbon nanofibers support material. X-ray absorption spectroscopy revealed that cobalt was metallic, even for small particle sizes, after the in situ reduction treatment, which is a prerequisite for catalytic operation and is difficult to achieve using traditional oxidic supports. The turnover frequency (TOF) for CO hydrogenation was independent of cobalt particle size for catalysts with sizes larger than 6 nm (1 bar) or 8 nm (35 bar), while both the selectivity and the activity changed for catalysts with smaller particles. At 35 bar, the TOF decreased from 23 × 10-3 to 1.4 × 10-3 s-1, while the C5+ selectivity decreased from 85 to 51 wt % when the cobalt particle size was reduced from 16 to 2.6 nm. This demonstrates that the minimal required cobalt particle size for Fischer−Tropsch catalysis is larger (6−8 nm) than can be explained by classical structure sensitivity. Other explanations raised in the literature, such as formation of CoO or Co carbide species on small particles during catalytic testing, were not substantiated by experimental evidence from X-ray absorption spectroscopy. Interestingly, we found with EXAFS a decrease of the cobalt coordination number under reaction conditions, which points to reconstruction of the cobalt particles. It is argued that the cobalt particle size effects can be attributed to nonclassical structure sensitivity in combination with CO-induced surface reconstruction. The profound influences of particle size may be important for the design of new Fischer−Tropsch catalysts.
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