Abstract

Mesoporous Ni-based catalysts with Ni confined in nanochannels are widely used in CO2 methanation. However, when Ni loadings are high, the nanochannels are easily blocked by nickel particles, which reduces the catalytic performance. In this work, three-dimensional mesoporous Ni-CeO2-CSC catalysts with high Ni loadings (20−80 wt %) were prepared using a colloidal solution combustion method, and characterized by nitrogen adsorption–desorption, X-ray diffraction (XRD), transmission electron microscopy (TEM) and H2 temperature programmed reduction (H2-TPR). Among the catalysts with different Ni loadings, the 50% Ni-CeO2-CSC with 50 wt % Ni loading exhibited the best catalytic performance in CO2 methanation. Furthermore, the 50% Ni-CeO2-CSC catalyst was stable for 50 h at 300° and 350 °C in CO2 methanation. The characterization results illustrate that the 50% Ni-CeO2-CSC catalyst has Ni particles smaller than 5 nm embedded in the pore walls, and the Ni particles interact with CeO2. On the contrary, the 50% Ni-CeO2-CP catalyst, prepared using the traditional coprecipitation method, is less active and selective for CO2 methanation due to the larger size of the Ni and CeO2 particles. The special three-dimensional mesoporous embedded structure in the 50% Ni-CeO2-CSC can provide more metal–oxide interface and stabilize small Ni particles in pore walls, which makes the catalyst more active and stable in CO2 methanation.

Highlights

  • In recent years, CO2 conversion has attracted much attention [1,2]

  • In order to increase the Ni–CeO2 interface and improve the thermal stability of a highly dispersed Ni-CeO2 catalyst, threethe Ni–CeO2 interface and improve the thermal stability of a highly dispersed Ni-CeO2 catalyst, dimensional mesoporous Ni-CeO2-CSC catalysts with Ni embedded in the pore walls were prepared three-dimensional mesoporous Ni-CeO2 -CSC catalysts with Ni embedded in the pore walls were using a colloidal solution combustion method

  • The results indicate that the 50% Ni-CeO2 -CSC catalyst is more stable than the 50% Ni-CeO2 -CSC

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Summary

Introduction

CO2 conversion has attracted much attention [1,2]. CO2 methanation can convert. The metal particles embedded in the pore wall can improve the thermal stability of the catalyst, and avoid embedded in the pore wall can improve the thermal stability of the catalyst, and avoid the the blockage of the channel, which is conducive to mass transfer. In order to increase the Ni–CeO2 interface and improve the thermal stability of a highly dispersed Ni-CeO2 catalyst, threethe Ni–CeO2 interface and improve the thermal stability of a highly dispersed Ni-CeO2 catalyst, dimensional mesoporous Ni-CeO2-CSC catalysts with Ni embedded in the pore walls were prepared three-dimensional mesoporous Ni-CeO2 -CSC catalysts with Ni embedded in the pore walls were using a colloidal solution combustion method.

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Physicochemical of theNi-CeO fresh Ni-CeO
CO an conversion
Characterization of the Used Catalyst
The results show that the mesoporous and visible inless
Synthesis of
Synthesis route of with the Ni-CeO
Characterization of Catalysts
Catalytic Performance
Conclusions
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