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dc.contributor.authorJeantelot, Gabriel Antoine Alexandre
dc.contributor.authorFølkner, Simen Prang
dc.contributor.authorManegold, Johanna Ilse Sieglinde
dc.contributor.authorIngebrigtsen, Morten Grunnaleite
dc.contributor.authorJensen, Vidar Remi
dc.contributor.authorLe Roux, Erwan
dc.date.accessioned2022-09-07T09:35:35Z
dc.date.available2022-09-07T09:35:35Z
dc.date.created2022-08-16T11:10:58Z
dc.date.issued2022
dc.identifier.issn2470-1343
dc.identifier.urihttps://hdl.handle.net/11250/3016242
dc.description.abstractThe dominating catalytic approach to aromatic hydrocarbons from renewables, deoxygenation of phenol-rich depolymerized lignin bio-oils, is hard to achieve: Hydrodeoxygenation (HDO) of phenols typically leads to loss of aromaticity and to non-negligible fractions of cyclohexanones and cyclohexanols. Here, we report a catalyst, niobia-supported iridium nanoparticles (Ir@Nb2O5), which combines full conversion in HDO of lignin-derived phenols with appreciable and tunable selectivity for aromatics (25-95%) under mild conditions (200–300 °C, 2.5–10 bar of H2). A simple approach to removal of Brønsted-acidic sites via Hünig’s base prevents coking and allows reaction conditions (T > 225 °C, 2.5 bar of H2) promoting high yields of aromatic hydrocarbons.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectHetrogen katalyseen_US
dc.subjectHeterogeneous catalysisen_US
dc.subjectLigninen_US
dc.subjectLigninen_US
dc.titleSelective Hydrodeoxygenation of Lignin-Derived Phenols to Aromatics Catalyzed by Nb2O5-Supported Iridiumen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright the authorsen_US
cristin.ispublishedfalse
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1021/acsomega.2c04314
dc.identifier.cristin2043339
dc.source.journalACS Omegaen_US
dc.source.pagenumber31561–31566en_US
dc.relation.projectNorges forskningsråd: 255373en_US
dc.subject.nsiVDP::Uorganisk kjemi: 442en_US
dc.subject.nsiVDP::Inorganic chemistry: 442en_US
dc.identifier.citationACS Omega. 2022, 7 (35), 31561–31566.en_US
dc.source.volume7en_US
dc.source.issue35en_US


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