Show simple item record

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


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal