Design of a core-shell catalyst : an effective strategy for suppressing side reactions in syngas for direct selective conversion to light olefins

dc.bibliographicCitation.firstPage4097eng
dc.bibliographicCitation.issue16eng
dc.bibliographicCitation.journalTitleChemical scienceeng
dc.bibliographicCitation.lastPage4105eng
dc.bibliographicCitation.volume11eng
dc.contributor.authorTan, Li
dc.contributor.authorWang, Fan
dc.contributor.authorZhang, Peipe
dc.contributor.authorSuzuki, Yuichi
dc.contributor.authorWu, Yingquan
dc.contributor.authorChen, Jiangang
dc.contributor.authorYang, Guohui
dc.contributor.authorTsubaki, Noritatsu
dc.date.accessioned2021-09-07T07:33:39Z
dc.date.available2021-09-07T07:33:39Z
dc.date.issued2020
dc.description.abstractAn elegant catalyst is designedviathe encapsulation of metallic oxide Zn-Cr inside of zeolite SAPO34 as a core-shell structure (Zn-Cr@SAPO) to realize the coupling of methanol-synthesis and methanol-to-olefin reactions. It can not only break through the limitation of the Anderson-Schulz-Flory distribution but can also overcome the disadvantages of physical mixture catalysts, such as excessive CO2formation. The confinement effect, hierarchical structure and extremely short distance between the two active components result in the Zn-Cr@SAPO capsule catalyst having better mass transfer and diffusion with a boosted synergistic effect. Due to the difference between the adsorption energies of the Zn-Cr metallic oxide/SAPO zeolite physical mixture and capsule catalysts, the produced water and light olefins are easily removed from the Zn-Cr@SAPO capsule catalyst after formation, suppressing the side reactions. The light olefin space time yield (STY) of the capsule catalyst is more than twice that of the typical physical mixture catalyst. The designed capsule catalyst has superior potential for scale-up in industrial applications while simultaneously extending the capabilities of hybrid catalysts for other tandem catalysis reactions through this strategy. © The Royal Society of Chemistry 2020.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/6723
dc.identifier.urihttps://doi.org/10.34657/5770
dc.language.isoengeng
dc.publisherCambridge : RSCeng
dc.relation.doihttps://doi.org/10.1039/c9sc05544d
dc.relation.essn2041-6539
dc.relation.issn2041-6520
dc.rights.licenseCC BY-NC 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/eng
dc.subject.ddc540eng
dc.subject.otherCatalystseng
dc.subject.otherChromium alloyseng
dc.subject.otherChromium compoundseng
dc.subject.otherMass transfereng
dc.subject.otherMetalseng
dc.subject.otherMethanoleng
dc.subject.otherMixtureseng
dc.subject.otherOxideseng
dc.subject.otherShells (structures)eng
dc.subject.otherZeoliteseng
dc.subject.otherZinc alloyseng
dc.subject.otherAdsorption energieseng
dc.subject.otherAnderson-Schulz-Flory distributionseng
dc.subject.otherConfinement effectseng
dc.subject.otherCore shell catalystseng
dc.subject.otherCore shell structureeng
dc.subject.otherHierarchical structureseng
dc.subject.otherMethanol to olefineng
dc.subject.otherSynergistic effecteng
dc.subject.otherLight olefinseng
dc.titleDesign of a core-shell catalyst : an effective strategy for suppressing side reactions in syngas for direct selective conversion to light olefinseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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