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dc.contributor.authorGavrilovic, Ljubisa
dc.contributor.authorBrandin, Jan
dc.contributor.authorHolmen, Anders
dc.contributor.authorVenvik, Hilde Johnsen
dc.contributor.authorMyrstad, Rune
dc.contributor.authorBlekkan, Edd Anders
dc.date.accessioned2020-06-17T12:24:20Z
dc.date.available2020-06-17T12:24:20Z
dc.date.created2019-06-18T14:13:07Z
dc.date.issued2019
dc.identifier.citationReaction Kinetics, Mechanisms and Catalysis. 2019, 127 (1), 231-240.en_US
dc.identifier.issn1878-5190
dc.identifier.urihttps://hdl.handle.net/11250/2658487
dc.descriptionPostprint version of published articleen_US
dc.description.abstractThe effect of ash salts on Co-based Fisher–Tropsch catalysts was studied using an aerosol deposition technique. The major elements in the ash were found to be K, S and Cl. The ash was deposited on a calcined catalyst as dry particles with an average diameter of approx. 350 nm. The loading of ash particles was varied by varying the time of exposure to the particles in a gas stream. Catalyst characterization did not reveal significant differences in cobalt dispersion, reducibility, surface area, pore size, or pore volume between the reference and the catalysts with ash particles deposited. Activity measurements showed that following a short exposure to the mixed ash salts (30 min), there were no significant loss of activity, but a minor change in selectivity of the catalyst . Extended exposure (60 min) led to some activity loss and changes in selectivity. However, extending the exposure time and thus the amount deposited as evidenced by elemental analysis did not lead to a further drop in activity. This behavior is different from that observed with pure potassium salts, and is suggested to be related to the larger size of the aerosol particles deposited. The large aerosol particles used here were probably not penetrating the catalyst bed, and to some extent formed an external layer on the catalyst bed. The ash salts are therefore not able to penetrate to the pore structure and reach the Co active centers, but are mixed with the catalyst and detected in the elemental analysis.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.subjectFischer-Tropschen_US
dc.subjectCobalten_US
dc.subjectAsh saltsen_US
dc.titleThe effect of aerosol-deposited ash components on a cobalt-based Fischer–Tropsch catalysten_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionacceptedVersionen_US
dc.source.pagenumber231-240en_US
dc.source.volume127en_US
dc.source.journalReaction Kinetics, Mechanisms and Catalysisen_US
dc.source.issue1en_US
dc.identifier.doi10.1007/s11144-019-01578-w
dc.identifier.cristin1705763
dc.relation.projectNorges forskningsråd: 280846en_US
dc.relation.projectNorges forskningsråd: 228741en_US
cristin.unitcode7401,80,40,0
cristin.unitnameProsessteknologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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