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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.accessioned2017-05-29T08:07:23Z
dc.date.available2017-05-29T08:07:23Z
dc.date.created2017-05-23T11:56:54Z
dc.date.issued2017
dc.identifier.citationCatalysis Letters. 2017, 1-15.nb_NO
dc.identifier.issn1011-372X
dc.identifier.urihttp://hdl.handle.net/11250/2443640
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{H}2 /CO ratio and {CO}2{CO}2 -content (which directly affects partial pressure of water), seems to influence the zeolite deactivation.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Verlagnb_NO
dc.titleCatalyst Deactivation During One-Step Dimethyl Ether Synthesis from Synthesis Gasnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionsubmittedVersionnb_NO
dc.source.pagenumber1-15nb_NO
dc.source.journalCatalysis Lettersnb_NO
dc.identifier.doi10.1007/s10562-017-1971-2
dc.identifier.cristin1471558
dc.description.localcodeThis 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 . Locked until 20 February 2018 due to copyright restrictionsnb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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