Abstract

Exploiting Ni-based catalysts with excellent catalytic activity and anti-coking ability is significant for dry reforming of CH4 with CO2 (DRM) which is a promising route to CO2 utilization. In this work, the Ni/Al2O3 catalyst with hydrotalcite precursor (NiAl-LDH) was synthesized by a facile in-situ growth method. And the effect of the NiAl-LDH structure on the catalytic activity and anti-coking ability of Ni/Al2O3 catalyst was revealed. The H2-temperature programmed desorption (H2-TPD) revealed that better Ni dispersion and more Ni–Al2O3 interface could be obtained by the NiAl-LDH precursor, which were vital for the activation of CH4 and CO2. Moreover, the NiAl-LDH precursor with non-LDH phase or turbostratic structure was also created by insufficient or extra amount of urea, and the obtained catalysts exhibited a poor catalytic stability, further confirming the importance of the LDH structure. In comparison with the Ni-IMP catalyst prepared by the conventional impregnation method, the CH4 conversion increased by 16% and the carbon deposition decreased by 75% over Ni-6 catalyst with well-organized LDH precursor under the same reaction conditions. Hence, this work represents an important step toward developing Ni-based catalysts with excellent catalytic activity and anti-coking ability for DRM with the LDH precursor.

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