乙醛
脱氢
钴
催化作用
化学
碳纤维
乙醇
氧合物
乙烯
无机化学
有机化学
材料科学
复合数
复合材料
作者
Aleksey N. Chernov,Tatiana V. Astrakova,Konstantin Yu. Koltunov,Vladimir Sobolev
出处
期刊:Catalysts
[MDPI AG]
日期:2021-11-21
卷期号:11 (11): 1411-1411
被引量:4
标识
DOI:10.3390/catal11111411
摘要
Cobalt and nitrogen co-doped carbon materials (Co@CN) have recently attracted significant attention as highly efficient noble-metal-free catalysts exhibiting a large application range. In a similar research interest, and taking into account the ever-increasing importance of bioethanol as a renewable raw material, here, we report the results on ethanol dehydrogenation to acetaldehyde over Co@NC catalysts. The catalyst samples were synthesized by a variety of affordable techniques, ensuring generation of various types of Co species incorporated in carbon, such as subnanosized cobalt sites and nano-sized particles of metallic cobalt and cobalt oxides. The catalytic activity was tested under both oxidative and non-oxidative gas-phase conditions at 200–450 °C using a fixed-bed flow reactor. The non-oxidative conditions proved to be much more preferable for the target reaction, competing, however, with ethanol dehydration to ethylene. Under specified reaction conditions, ethanol conversion achieved a level of 66% with 84% selectivity to acetaldehyde at 400 °C. The presence of molecular oxygen in the feed led mainly to deep oxidation of ethanol to COx, giving acetaldehyde in a comparatively low yield. The potential contribution of carbon itself and supported cobalt forms to the observed reaction pathways is discussed.
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