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dc.contributor.authorPrice, C.A.H.
dc.contributor.authorEarles, E.
dc.contributor.authorPastor-Pérez, L.
dc.contributor.authorLiu, J.
dc.contributor.authorReina, T.R.
dc.date.accessioned2023-03-14T08:04:41Z
dc.date.available2023-03-14T08:04:41Z
dc.date.issued2019
dc.identifier.citationPrice, C.A.H. and Earles, E. and Pastor-Pérez, L. and Liu, J. and Reina, T.R. 2019. Advantages of Yolk Shell Catalysts for the DRM: A Comparison of Ni/ZnO@SiO2 vs. Ni/CeO2 and Ni/Al2O3. Chemistry (Switzerland). 1 (1): pp. 3-16.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/90942
dc.identifier.doi10.3390/chemistry1010003
dc.description.abstract

Encapsulation of metal nanoparticles is a leading technique used to inhibit the main deactivation mechanisms in dry reforming of methane reaction (DRM): Carbon formation and Sintering. Ni catalysts (15%) supported on alumina (Al2O3) and ceria (CeO2) have shown they are no exception to this analysis. The alumina supported catalysts experienced graphitic carbonaceous deposits, whilst the ceria showed considerable sintering over 15 h of DRM reaction. The effect of encapsulation compared to that of the performance of uncoated catalysts for DRM reaction has been examined at different temperatures, before conducting longer stability tests. The encapsulation of Ni/ZnO cores in silica (SiO2) leads to advantageous conversion of both CO2 and CH4 at high temperatures compared to its uncoated alternatives. This work showcases the significance of the encapsulation process and its overall effects on the catalytic performance in chemical CO2 recycling via DRM.

dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/LP150101158
dc.titleAdvantages of Yolk Shell Catalysts for the DRM: A Comparison of Ni/ZnO@SiO2 vs. Ni/CeO2 and Ni/Al2O3
dc.typeJournal Article
dcterms.source.volume1
dcterms.source.number1
dcterms.source.startPage3
dcterms.source.endPage16
dcterms.source.titleChemistry (Switzerland)
dc.date.updated2023-03-14T08:04:41Z
curtin.accessStatusOpen access
dcterms.source.eissn2624-8549
curtin.repositoryagreementV3


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