Ethanol Dehydrogenation to Acetaldehyde over Co@N-Doped Carbon

乙醛 脱氢 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 [Multidisciplinary Digital Publishing Institute]
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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