4.7 Article

Synthesis, characterization and catalytic performance of MgO-coated Ni/SBA-15 catalysts for methane dry reforming to syngas and hydrogen

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 38, Issue 23, Pages 9718-9731

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2013.05.097

Keywords

In-situ coating; Mesostructure; Magnesium; Hydrogen; Dry reforming

Funding

  1. Fundamental Research Funds for the Central Universities of China [2010SCU22010]
  2. Special Funds for Scientific Research on Public Causes of China [201010236]
  3. National Basic Research Program of China (973 Program) [2011CB201202]

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A series of MgO-coated SBA-15 mesoporous silica with MgO contents ranging from 2 wt% to 15 wt% have been successfully synthesized by a simple one-pot synthesis method and further impregnated with 10 wt% Ni. Ni/SBA-15 modified with 8 wt% MgO was also prepared by conventional impregnation method. The materials were characterized by means of XRD, N-2 physisorption, TEM by applying high-angle annular dark field (HAADF), XPS, CO2-TPD, TGA and temperature-programmed hydrogenation (TPH) techniques, and their catalytic performance was tested for methane reforming with CO2. The results showed that MgO was successfully coated on the walls of mesoporous silica and the mesoporous structure of SBA-15 was well maintained after MgO modification. Compared to MgO-impregnated material, MgO-coated counterpart showed a better order in the mesostructure and more medium basic sites. The addition of MgO enhanced initial catalytic activity of Ni/SBA-15, and the catalyst with 8 wt% MgO coating showed the most excellent catalytic activity. The MgO coating induced an improved dispersion of Ni species and larger medium basic sites than that of MgO impregnation, which led to an enhanced long-term stability and resistance to carbon formation. The deposition of graphitic carbon species during the reaction was the main reason for the deactivation of Ni/SBA-15 catalyst. Crown Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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