4.7 Article

Ceria-modified nickel supported on porous silica as highly active and stable catalyst for dry reforming of methane

Journal

FUEL
Volume 301, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2021.121027

Keywords

CO2 reforming of methane; Ceria; Pore structure; Nickel; One-pot strategy

Funding

  1. National Natural Science Foundation of China [21673079, 21872056]
  2. Guangdong Provincial Natural Science Foundation [2021A1515010149]
  3. Guangzhou Municipal Science and Technology Project [20180410116]
  4. Guangdong Provincial Science and Technology Plan Project [2015A020216002]

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The addition of CeO2 enhances the carbon resistance of nickel-based catalysts for dry reforming of methane, improving catalytic activity and reducing the activation energy of CH4 and CO2, leading to decreased carbon deposition and graphitization. CeO2 hinders the formation of Ni-phyllosilicate species, weakens the interaction between Ni and silica, and prevents nickel sintering, resulting in catalysts with strong anti-sintering ability and carbon resistance.
Addition of CeO2 was regarded as a promising strategy to enhance the carbon resistance of nickel-based catalysts for dry reforming of methane (DRM) due to the high concentration of reactive oxygen species with excellent oxidation capacity. In this work, ceria-modified porous silica supported nickel catalysts (Ni-CeX-Y/SiO2) were prepared by one-pot method and employed to catalyze DRM reaction. Introduction of CeO2 hindered the formation of 1:1 Ni-phyllosilicate species and weakened the interaction between Ni and silica. The surrounding CeO2 on Ni nanoparticle efficiently prevented the nickel sintering. The number of active oxygen species gradually increased with increasing CeO2 loading, which was beneficial to improve the carbon resistance by means of participating in the oxidation of carbon. Therefore, Ni-CeX-Y/SiO2 catalysts exhibited lower carbon deposition and graphitization degree. Ni-Ce5-2/SiO2 and Ni-Ce5-3/SiO2 possessed strong anti-sintering ability and carbon resistance, showing relatively good stability that CH4 conversion decreased from 81.3 to 75.6% and 82.2 to 78.2% over 24 h time on stream. Kinetic study confirmed that introduction of CeO2 decreased the activation energy of CH4 decomposition and CO2 dissociation, hence enhancing the catalytic activity and carbon resistance.

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