Bifunctional catalyst GaO-mZrO/SAPO-34 for CO hydrogenation: GaO-mZrO improving light olefins
CO 2 hydrogenation to light olefins is key for reducing environmental emissions and creating sustainable energy. Bifunctional oxide-zeolite (OX-ZEO) catalysts are widely used in this area. Metal oxides, crucial for CO 2 adsorption and H 2 dissociation, need careful selection and optimization. This p...
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Published in | Catalysis science & technology Vol. 14; no. 13; pp. 3652 - 3659 |
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Main Authors | , , , , |
Format | Journal Article |
Published |
01.07.2024
|
Online Access | Get full text |
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Summary: | CO
2
hydrogenation to light olefins is key for reducing environmental emissions and creating sustainable energy. Bifunctional oxide-zeolite (OX-ZEO) catalysts are widely used in this area. Metal oxides, crucial for CO
2
adsorption and H
2
dissociation, need careful selection and optimization. This paper presents a bifunctional catalyst where Ga
2
O
3
is loaded onto mZrO
2
(monoclinic zirconia) (Ga
2
O
3
-mZrO
2
) using citric acid complex method and combined with SAPO-34. Our study demonstrates that the loading method can significantly improve the adsorption capacity of the catalyst for CO
2
and had demonstrated impressive catalytic performance compared to common preparation methods. Further, Ga
2
O
3
-mZrO
2
, in comparison to Ga
2
O
3
loaded onto tZrO
2
(tetragonal zirconia) (Ga
2
O
3
-tZrO
2
), has a stronger ability to produce light olefins. The catalyst achieves 84.1% selectivity for C
2
=
-C
4
=
, 20.2% CO
2
conversion, and 45.3% CO selectivity, remaining stable over 100 hours. This offers a novel method for designing highly active Zr-based oxides for effective CO
2
conversion.
This study synthesized Ga
2
O
3
-mZrO
2
/SAPO-34 for CO
2
hydrogenation to light olefins, demonstrating the efficacy of citric acid complexation and mZrO
2
support. Achieving 84.1% C
2
=
-C
4
=
selectivity, it offers a novel strategy for active oxide preparation. |
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Bibliography: | https://doi.org/10.1039/d4cy00445k Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/d4cy00445k |