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Performance of Ni/Si‐MCM‐41 catalysts in CO 2 methanation
The production of methane from the methanation reaction between H 2 and CO 2 , also known as the Sabatier reaction, is one way to diversify the global energy matrix, providing a use for CO 2 . This work evaluates the performance in this reaction of Ni catalysts supported on type MCM‐41 silica, synth...
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Published in: | Canadian journal of chemical engineering 2024-08, Vol.102 (8), p.2724-2738 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | The production of methane from the methanation reaction between H
2
and CO
2
, also known as the Sabatier reaction, is one way to diversify the global energy matrix, providing a use for CO
2
. This work evaluates the performance in this reaction of Ni catalysts supported on type MCM‐41 silica, synthesized y a wet impregnation method. Catalytic tests were performed for 2.5 h under atmospheric pressure. The reaction variables considered were the catalyst nickel mass content (5% and 10%), temperature (
T
= 400 and 550°C), reactant ratio (H
2
/CO
2
= 4 and 2.5), and space velocity (VHSV = 5 and 10 L g
−1
h
−1
). The catalysts were characterized by Brunauer–Emmett–Teller (BET), X‐ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive x‐ray spectroscopy (EDS) analyses before the reactions, and by thermogravimetric analysis (TGA), SEM, and EDS analyses after the reactions. The reaction variables were evaluated using an experimental design with 2 factors and 4 variables, in order to determine the effects of the reaction conditions on catalyst selectivity, reactant conversion, and reaction yields in terms of CH
4
and CO. The best result was obtained using a reactant ratio of 2.5, space velocity of 5 L g
−1
h
−1
, and reaction temperature of 550°C, resulting in 93.7% selectivity for methane, 69.4% CO
2
conversion, 74% H
2
conversion, and methane yield of 20.69%. Findings show Ni/Si‐MCM‐41 catalyst's applicability in methanation, advancing CH
4
production technology, and addressing local demand while reducing CO
2
emissions. |
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ISSN: | 0008-4034 1939-019X |
DOI: | 10.1002/cjce.25224 |