Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/23792
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dc.contributor.authorWu, Gaowei-
dc.contributor.authorConstantinou, Achilleas-
dc.contributor.authorCao, Enhong-
dc.contributor.authorKuhn, Simon-
dc.contributor.authorMorad, Moataz-
dc.contributor.authorSankar, Meenakshisundaram-
dc.contributor.authorBethell, Donald-
dc.contributor.authorHutchings, Graham J.-
dc.contributor.authorGavriilidis, Asterios-
dc.date.accessioned2022-01-25T08:05:49Z-
dc.date.available2022-01-25T08:05:49Z-
dc.date.issued2015-04-29-
dc.identifier.citationIndustrial & Engineering Chemistry, 2015, vol. 54, no. 16, pp. 4183–4189en_US
dc.identifier.issn15205045-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/23792-
dc.description.abstractA Teflon AF-2400 tube-in-tube microreactor is investigated for the continuous, solvent-free, catalytic oxidation of benzyl alcohol with oxygen. The semipermeable Teflon AF-2400 tube acts as the interface between the gaseous oxidant and the liquid substrate. Because of the inherent safety of this contacting method, the use of pure oxygen is possible. The semipermeable tube was packed with 1 wt % Au–Pd/TiO2 catalyst particles and placed inside a PTFE tube to provide an annular region which was pressurized with pure oxygen. This design allowed continuous penetration of oxygen through the inner tube during the reaction, resulting in higher oxygen concentration in the catalyst bed and significantly improved conversion compared to a reactor operating with an oxygen presaturated feed. The amount of oxygen available for reaction in the tube-in-tube microreactor was 2 orders of magnitude higher than that in a nonpermeable reactor with oxygen presaturated feed. The semipermeable tube reactor performance in terms of both conversion and selectivity was enhanced by increasing the gas pressure, the catalyst contact time and by dilution of the catalyst. The highest conversion of benzyl alcohol obtained for the range of conditions investigated was 44.1%, with 73.0% selectivity to benzaldehyde, at 120 °C; catalyst contact time, 115 gcat·s/galcohol; and catalyst dilution factor, 4.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofIndustrial & Engineering Chemistryen_US
dc.rights© American Chemical Societyen_US
dc.subjectAlcoholsen_US
dc.subjectCatalystsen_US
dc.subjectOxygenen_US
dc.subjectMicroreactorsen_US
dc.subjectPharmaceuticalsen_US
dc.titleContinuous heterogeneously catalyzed oxidation of benzyl alcohol using a tube-in-tube membrane microreactoren_US
dc.typeArticleen_US
dc.collaborationUniversity College Londonen_US
dc.collaborationKU Leuvenen_US
dc.collaborationCardiff Universityen_US
dc.collaborationUniversity of Liverpoolen_US
dc.subject.categoryChemical Sciencesen_US
dc.journalsSubscriptionen_US
dc.countryUnited Kingdomen_US
dc.countryBelgiumen_US
dc.subject.fieldNatural Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1021/ie5041176en_US
dc.identifier.scopus2-s2.0-84929470601en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84929470601en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.contributor.orcid#NODATA#en
dc.relation.issue16en_US
dc.relation.volume54en_US
cut.common.academicyear2014-2015en_US
dc.identifier.spage4183en_US
dc.identifier.epage4189en_US
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.openairetypearticle-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.orcid0000-0002-7763-9481-
crisitem.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
crisitem.journal.journalissn1520-5045-
crisitem.journal.publisherACS Publications-
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