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Performance of supported Co3O4 catalysts in the preferential oxidation of carbon monoxide: effect of support type and synthesis method

Performance of supported Co3O4 catalysts in the preferential oxidation of carbon monoxide: effect of support type and synthesis method
Performance of supported Co3O4 catalysts in the preferential oxidation of carbon monoxide: effect of support type and synthesis method

This study investigated the performance of supported Co3O4 catalysts during the preferential oxidation of carbon monoxide (CO-PrOx) in a H2-rich environment, focusing on the effects of different catalyst synthesis methods, namely, wetness impregnation (WI) and solution combustion synthesis (SCS), and different support materials, namely, Al2O3 and SiC. During CO-PrOx, the SiC-supported Co3O4 catalysts attained higher CO2 yields when compared with the Al2O3-supported Co3O4 catalysts possibly because of the existence of weaker interactions between Co3O4 and SiC. Moreover, the catalysts prepared via SCS achieved higher CO2 yields than the catalysts prepared via WI likely due to the presence of smaller and well-dispersed Co3O4 particles in the SCS-prepared catalysts. Significantly high amounts of unwanted CH4 were produced over the SiC-supported catalysts between 225 and 250 °C. The high CO methanation activity was also attributed to the weaker Co3O4-SiC interactions, which enabled the easier reduction of Co3O4 to methanation active metallic Co.

Catalyst reduction, Catalyst synthesis methods, CO-PrOx, CO and CH yields, CoO, Support type
0021-9517
Fadlalla, Mohamed I.
f1188dbb-fe38-480c-ba6c-5395f7721a07
Nyathi, Thulani M.
e5a3f8fb-63de-4b2c-a7d2-3b6be6f8107e
Farahani, Majid D.
3dc6dcdf-6a10-4776-97bb-a066b495b9a4
Zheng, Ying
24824a82-fcb3-4d81-9ae5-071ae86e174f
Wells, Peter P.
bc4fdc2d-a490-41bf-86cc-400edecf2266
Friedrich, Holger B.
78485da7-026e-4e66-87c3-584e27e5c0a9
Claeys, Michael
19cb6adb-b243-4dba-b0a8-94fd2c1f9658
Fadlalla, Mohamed I.
f1188dbb-fe38-480c-ba6c-5395f7721a07
Nyathi, Thulani M.
e5a3f8fb-63de-4b2c-a7d2-3b6be6f8107e
Farahani, Majid D.
3dc6dcdf-6a10-4776-97bb-a066b495b9a4
Zheng, Ying
24824a82-fcb3-4d81-9ae5-071ae86e174f
Wells, Peter P.
bc4fdc2d-a490-41bf-86cc-400edecf2266
Friedrich, Holger B.
78485da7-026e-4e66-87c3-584e27e5c0a9
Claeys, Michael
19cb6adb-b243-4dba-b0a8-94fd2c1f9658

Fadlalla, Mohamed I., Nyathi, Thulani M., Farahani, Majid D., Zheng, Ying, Wells, Peter P., Friedrich, Holger B. and Claeys, Michael (2024) Performance of supported Co3O4 catalysts in the preferential oxidation of carbon monoxide: effect of support type and synthesis method. Journal of Catalysis, [115777]. (doi:10.1016/j.jcat.2024.115777).

Record type: Article

Abstract

This study investigated the performance of supported Co3O4 catalysts during the preferential oxidation of carbon monoxide (CO-PrOx) in a H2-rich environment, focusing on the effects of different catalyst synthesis methods, namely, wetness impregnation (WI) and solution combustion synthesis (SCS), and different support materials, namely, Al2O3 and SiC. During CO-PrOx, the SiC-supported Co3O4 catalysts attained higher CO2 yields when compared with the Al2O3-supported Co3O4 catalysts possibly because of the existence of weaker interactions between Co3O4 and SiC. Moreover, the catalysts prepared via SCS achieved higher CO2 yields than the catalysts prepared via WI likely due to the presence of smaller and well-dispersed Co3O4 particles in the SCS-prepared catalysts. Significantly high amounts of unwanted CH4 were produced over the SiC-supported catalysts between 225 and 250 °C. The high CO methanation activity was also attributed to the weaker Co3O4-SiC interactions, which enabled the easier reduction of Co3O4 to methanation active metallic Co.

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Fadlalla et al_J Catal_manuscript - Accepted Manuscript
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Accepted/In Press date: 25 September 2024
e-pub ahead of print date: 26 September 2024
Keywords: Catalyst reduction, Catalyst synthesis methods, CO-PrOx, CO and CH yields, CoO, Support type

Identifiers

Local EPrints ID: 495918
URI: http://eprints.soton.ac.uk/id/eprint/495918
ISSN: 0021-9517
PURE UUID: bb895d90-c892-4af8-be3d-47cf161843a7
ORCID for Peter P. Wells: ORCID iD orcid.org/0000-0002-0859-9172

Catalogue record

Date deposited: 27 Nov 2024 17:48
Last modified: 28 Nov 2024 02:39

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Contributors

Author: Mohamed I. Fadlalla
Author: Thulani M. Nyathi
Author: Majid D. Farahani
Author: Ying Zheng
Author: Peter P. Wells ORCID iD
Author: Holger B. Friedrich
Author: Michael Claeys

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