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Mono‐ and Bimetallic Ni−Co Catalysts in Dry Reforming of Methane
Author(s) -
Zhang Xuliang,
Vajglova Zuzana,
MäkiArvela Päivi,
Peurla Markus,
Palonen Heikki,
Murzin Dmitry Yu.,
Tungatarova Svetlana A.,
Baizhumanova Tolkyn S.,
Aubakirov Yermek A.
Publication year - 2021
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.202100686
Subject(s) - bimetallic strip , catalysis , temperature programmed reduction , hydrogen , desorption , incipient wetness impregnation , materials science , oxide , inorganic chemistry , carbon dioxide reforming , fourier transform infrared spectroscopy , nuclear chemistry , adsorption , chemistry , syngas , metallurgy , chemical engineering , selectivity , organic chemistry , engineering
Several bimetallic Ni−Co catalysts supported on θ‐Al 2 O 3 together with 10 wt % Ni and 10 wt % Co on θ‐Al 2 O 3 were prepared via the incipient wetness method, characterized by X‐ray diffraction (XRD), nitrogen adsorption, transmission electron microscopy, temperature programmed reduction, temperature programmed CO 2 desorption, Fourier Transformed Infrared Spectroscopy (FTIR) with pyridine adsorption‐desorption and tested in dry methane reforming at 700 °C in a fixed bed reactor. According to XRD the metal oxide crystallite sizes decreased from 20 nm for 10 wt % Co/θ‐Al 2 O 3 to 13 nm for 5 wt % Ni‐5 wt % Co/θ‐Al 2 O 3 , which also showed formation of a mixed oxide alloy. The unit cell parameters for spinel in the fresh catalyst and fcc metal formed during the reaction followed the Vegard's rule. Although monometallic 10 wt % Co/θ‐Al 2 O 3 exhibited high hydrogen consumption, desorption temperature was also high resulting in a rather low activity of 10 wt % Co/θ‐Al 2 O 3 in comparison to bimetallic 5 wt % Ni‐5 wt % Co/θ‐Al 2 O 3 . The latter exhibited the highest initial activity for hydrogen formation due to its relatively small metal particle size. This catalyst suffered, however, from extensive coking. The most stable catalyst was 10 wt % Ni/θ‐Al 2 O 3 for which the hydrogen yield decreased form 56 % to 45 % during 100 h time‐on‐stream. For this catalyst no sintering occurred, opposite to 10 wt % Co/θ‐Al 2 O 3 .