4.7 Article

Effect of pre-treatment and calcination temperature on Al2O3-ZrO supported Ni-Co catalysts for dry reforming of methane

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 44, Issue 39, Pages 21546-21558

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2019.06.085

Keywords

Bimetallic catalyst; Dry reforming; Methane; Stability; Deactivation; Regeneration

Funding

  1. Deanship of Scientific Research at King Saud University [RGP-1435-078]

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In this paper, the effect of pre-treatment and calcination temperature on a series of 5%Co/Al2O3-ZrO2, 5%Ni/Al2O3-ZrO2 and 2.5%Co-2.5%Ni/Al2O3-ZrO2 catalysts for dry reforming of methane was investigated. Main focus of our research was to improve the catalyst stability by proper pre-treatment and reaction conditions. The first approach aimed at the catalyst pre-treatment by using bimetallic systems and the second strategy at the in situ suppression of coke. The catalytic activity of bimetallic system was indeed higher compared to the monometallic in the temperature range of 500-800 degrees C (space velocity 18000 ml h(-1). at, CH4/CO2 = 1). The bimetallic catalyst calcined at 800 degrees C showed highest CH4 conversion without deactivation and gave a H-2/CO ratio of 91% and 0.96, respectively, and good stability with less coke deposition over 28 h at 800 degrees C reaction temperature. This improvement is assigned to the synergism between Co and Ni, their high dispersion according to interaction with support. It has been shown in our work that pretreatment temperatures and atmospheres have strong impact on stability of the catalyst. TEM, XRD and TPO investigations confirmed that the slight catalyst deactivation was related to the formation of multiwall carbon nanotubes with hollow inner tube structure. The addition of small amounts of steam or oxygen during DRM improved both the catalyst activity and stability as the bimetallic catalyst lost around 9.4% conversion in DRM, 5.4% in presence of water and only 3.2% in presence of O-2. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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