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dc.contributor.authorDadgar, Farbod
dc.contributor.authorMyrstad, Rune
dc.contributor.authorPfeifer, Peter
dc.contributor.authorHolmen, Anders
dc.contributor.authorVenvik, Hilde Johnsen
dc.date.accessioned2020-12-15T12:51:16Z
dc.date.available2020-12-15T12:51:16Z
dc.date.created2017-05-23T11:56:54Z
dc.date.issued2017
dc.identifier.citationCatalysis Letters. 2017, 147 (4), 865-879.en_US
dc.identifier.issn1011-372X
dc.identifier.urihttps://hdl.handle.net/11250/2719575
dc.description.abstractCatalysts for direct synthesis of dimethyl ether (DME) from synthesis gas should essentially contain two functions, i.e., methanol synthesis and methanol dehydration. In the present work, the deactivation of both functions of hybrid catalysts during direct DME synthesis under industrially relevant conditions has been investigated with special focus on the influence of each reaction step on the deactivation of the catalyst function corresponding to the other step. A physical mixture of a Cu–Zn-based methanol synthesis catalyst and a ZSM-5 methanol dehydration catalyst was used. The metallic catalyst appears to deactivate due to Cu sintering, with no apparent effect from the methanol dehydration step under the conditions applied. The acid catalyst deactivates due to accumulation of hydrocarbon species formed in its pores. Synthesis gas composition, i.e., {H}2/CO ratio and {CO}2-content (which directly affects partial pressure of water), seems to influence the zeolite deactivation.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.subjectCu/ZnO/Al2O3en_US
dc.subjecthybrid catalysten_US
dc.subjectdeactivationen_US
dc.subjectmethanol dehydrationen_US
dc.subjectmethanol synthesisen_US
dc.subjectDMEen_US
dc.subjectH-ZSM-5en_US
dc.titleCatalyst Deactivation During One-Step Dimethyl Ether Synthesis from Synthesis Gasen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionacceptedVersionen_US
dc.rights.holderThis is the authors' manuscript to the article. The final publication is available at Springer via https://link.springer.com/article/10.1007%2Fs10562-017-1971-2 .en_US
dc.source.pagenumber865-879en_US
dc.source.volume147en_US
dc.source.journalCatalysis Lettersen_US
dc.source.issue4en_US
dc.identifier.doi10.1007/s10562-017-1971-2
dc.identifier.cristin1471558
dc.relation.projectNorges forskningsråd: 208351en_US
cristin.unitcode7401,80,5,5
cristin.unitnameKinetikk og katalyse
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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