焦炭
催化作用
甲烷
二氧化碳重整
碱金属
化学
化学工程
合成气
碳纤维
无机化学
材料科学
冶金
有机化学
复合材料
复合数
工程类
作者
Robert Franz,Tobias Kuehlewind,Genrikh Shterk,Edy Abou‐Hamad,Alexander Parastaev,Evgeny A. Uslamin,Emiel J. M. Hensen,Freek Kapteijn,Jorge Gascón,Evgeny A. Pidko
标识
DOI:10.26434/chemrxiv.12174879
摘要
Coke deposition is one of the main challenges in the commercialisation of dry reforming of methane over supported Ni catalysts. Besides the coke quantity, the structure of the deposits is also essential for the catalyst lifetime. Accordingly, in this study, we analysed the effect of Na, K, and Cs promoters on both these variables over Ni/ ZrO<sub>2</sub> catalysts. Besides blocking the most active coke-forming sites already at low loading, the promoting effect of the alkali metals is also contributed by their coke gasification activity. To evaluate the additional impact of the latter, the behaviour of alkali-doped catalysts was compared to that for Mn-doped catalysts, exclusively featuring the site-blocking promotion mechanism. While the conversion is barely affected by the type of promoter, it has a profound effect on the amount and the composition of carbon deposits formed during the reaction. Promoting with K or Mn reduces the coke content to a similar degree but with less carbon fibres observed in the case of K. The promotion by Cs and Na results in the lowest coke content. The superior performance of Cs and Na-doped Ni/ZrO<sub>2</sub> catalysts is attributed to the enhanced coke gasification via carbonate species on top of the site blocking effects.
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