Production of Cycloalkanes in Hydrodeoxygenation of Isoeugenol Over Pt- and Ir-Modified Bifunctional Catalysts

dc.contributor.authorLouis Bomont
dc.contributor.authorMoldir Alda‐Onggar
dc.contributor.authorVyacheslav Fedorov
dc.contributor.authorAtte Aho
dc.contributor.authorJanne Peltonen
dc.contributor.authorKari Eränen
dc.contributor.authorMarkus Peurla
dc.contributor.authorNarendra Kumar
dc.contributor.authorJohan Wärnå
dc.contributor.authorVincenzo Russo
dc.contributor.authorPäivi Mäki‐Arvela
dc.contributor.authorHenrik Grénman
dc.contributor.authorMarina Lindblad
dc.contributor.authorDmitry Yu. Murzin
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=teollisuusfysiikan laboratorio|en=Laboratory of Industrial Physics|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.contributor.organization-code2606704
dc.converis.publication-id31494106
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/31494106
dc.date.accessioned2022-10-27T12:12:21Z
dc.date.available2022-10-27T12:12:21Z
dc.description.abstract<p>Hydrodeoxygenation of isoeugenol was investigated at 200 °C under 3 MPa total pressure in dodecane as a solvent, in hydrogen, over bifunctional Pt‐ and Ir‐modified Beta zeolites and mesoporous materials. As a comparison, Pt and Ir supported on Al<sub>2</sub>O<sub>3</sub>, SiO<sub>2</sub> and mesoporous MCM‐41 were also tested. The catalysts were characterized by XRD, CO pulse chemisorption, transmission electron microscopy, scanning electron microscopy, nitrogen adsorption and FTIR pyridine adsorption desorption. The results revealed that the most active and selective catalyst was Pt‐H‐Beta‐300, which exhibits the lowest acidity and largest crystal size of Beta zeolite among the studied Pt‐ and Ir‐modified Beta zeolites. Complete conversion of isoeugenol and 89 % selectivity to propylcyclohexane was obtained with this catalyst in 240 min. The overall deoxygenation selectivity was 100 %, giving dialkylated cyclohexanes as the second major product. The catalyst was regenerated, reduced and reused in the hydrodeoxygenation of isoeugenol with almost the same performance as the fresh catalyst. Thermodynamic analyses and kinetic modelling of the data were also performed.</p>
dc.format.pagerange2841
dc.format.pagerange2854
dc.identifier.jour-issn1434-1948
dc.identifier.olddbid173904
dc.identifier.oldhandle10024/156998
dc.identifier.urihttps://www.utupub.fi/handle/11111/31609
dc.identifier.urnURN:NBN:fi-fe2021042719194
dc.language.isoen
dc.okm.affiliatedauthorPeltonen, Janne
dc.okm.affiliatedauthorPeurla, Markus
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline116 Kemiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.relation.doi10.1002/ejic.201800391
dc.relation.ispartofjournalEuropean Journal of Inorganic Chemistry
dc.relation.issue24
dc.relation.volume2018
dc.source.identifierhttps://www.utupub.fi/handle/10024/156998
dc.titleProduction of Cycloalkanes in Hydrodeoxygenation of Isoeugenol Over Pt- and Ir-Modified Bifunctional Catalysts
dc.year.issued2018

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