Rapid aging as a key to understand deactivation of Ni/Al2O3 catalysts applied for the CO2 methanation

dc.contributor.authorBeierlein, Dennis
dc.contributor.authorHäussermann, Dorothea
dc.contributor.authorTraa, Yvonne
dc.contributor.authorKlemm, Elias
dc.date.accessioned2023-04-11T09:41:55Z
dc.date.available2023-04-11T09:41:55Z
dc.date.issued2021de
dc.date.updated2023-03-25T15:41:09Z
dc.description.abstractWe developed a rapid aging method for Ni/Al2O3 methanation catalysts mimicking the real aging in the actual application. The method is based on hydrothermal deactivation of the catalyst at 600 or 700 °C, which leads to a catalyst with nearly constant conversion after a much shorter time period compared to normal aging. The hydrothermally aged catalysts are characterized by N2 adsorption, X-ray powder diffraction, temperature-programmed reduction and H2 chemisorption. The catalytic performance of the aged catalysts is comparable to the one of a catalyst deactivated in a long-term measurement with up to 720 h on stream. The time needed for reaching a stable conversion can be diminished by rapid aging by a factor of 10. The investigations also showed that the long-term deactivation is caused by Ni particle sintering and that the support pores limit the Ni particle size.en
dc.description.sponsorshipProjekt DEALde
dc.identifier.issn1011-372X
dc.identifier.issn1572-879X
dc.identifier.other1843323915
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-129488de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/12948
dc.identifier.urihttp://dx.doi.org/10.18419/opus-12929
dc.language.isoende
dc.relation.uridoi:10.1007/s10562-021-03884-2de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/de
dc.subject.ddc540de
dc.titleRapid aging as a key to understand deactivation of Ni/Al2O3 catalysts applied for the CO2 methanationen
dc.typearticlede
ubs.fakultaetChemiede
ubs.institutInstitut für Technische Chemiede
ubs.publikation.seiten2908-2919de
ubs.publikation.sourceCatalysis letters 152 (2022), S. 2908-2919de
ubs.publikation.typZeitschriftenartikelde

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