4.4 Article

Nickel Supported on Multilayer Vanadium Carbide for Dry Reforming of Methane

期刊

CHEMISTRYSELECT
卷 7, 期 47, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202203873

关键词

dry reforming of methane; in situ infrared; m-V2C MXene; nickel; vanadium

资金

  1. National Natural Science Foundation of China [22078074, 21938001]
  2. Guangxi Natural Science Foundation [2020GXNSFDA297007]
  3. Opening Project of Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology [2020 K002]
  4. Special funding for Guangxi Bagui Scholars

向作者/读者索取更多资源

A multilayer vanadium carbide MXene was used as a support to prepare Ni/m-V2O3-V2C catalysts for dry reforming of methane. The addition of Ni increased the catalyst alkalinity and the interaction between Ni and the support. The catalyst showed excellent catalytic stability and anti-coking ability.
A multilayer vanadium carbide MXene (m-V2C) was used as a robust oxy-carbide support to prepare a series of Ni/m-V2O3-V2C catalysts with various Ni amounts by an impregnation method and used for dry reforming of methane (DRM). The results show that the Ni addition increases the catalyst alkalinity, and the interaction between the Ni metal and m-V2C increases with increasing Ni amount. Ni/m-V2O3-V2C with a Ni amount of 13 wt% showed optimal CH4 and CO2 conversions of 94 % and 89 %, respectively. In addition, 13Ni/m-V2O3-V2C exhibits excellent catalytic stability and anti-coking ability in a 90-hour stability test, which is attributed to the strong metal-support interaction. In situ DRIFTS analysis showed that methane activated on the Ni particles generates CHx and H, while CO2 interacts with m-V2O3-V2C to form carbonates on Ni/m-V2O3-V2C; carbonate species come into contact with methane pyrolysis products and quickly form formate species, which are further decomposed into CO.

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