Co-processing of fossil feedstock with lignin-derived model compound isoeugenol over Fe-Ni/H-Y-5.1 catalysts

dc.contributor.authorVajglova Zuzana
dc.contributor.authorGauli Bibesh
dc.contributor.authorMäki-Arvela Päivi
dc.contributor.authorSimakova Irina L.
dc.contributor.authorKumar Narendra
dc.contributor.authorEränen Kari
dc.contributor.authorTirri Teija
dc.contributor.authorLassfolk Robert
dc.contributor.authorPeurla Markus
dc.contributor.authorDoronkin Dmitry E.
dc.contributor.authorMurzin Dmitry Yu
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id179298051
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/179298051
dc.date.accessioned2025-08-28T02:36:16Z
dc.date.available2025-08-28T02:36:16Z
dc.description.abstractCo-processing of n-hexadecane with lignin derived isoeugenol as a model compound was investigated in this work using low-cost mono-and bimetallic iron and nickel supported on H-Y-5.1 zeolite. Different Fe-Ni metal ratios in the catalyst led to different reaction rates of processes and product distribution. The presence of just 0.26 wt% isoeugenol in the mixture with n-hexadecane made hydroisomerization-hydro cracking of the latter two-fold less active. Catalysts with smaller metal particle sizes, lower than 6 nm were more efficient pointing out on structure sensitivity. Extremely high activity in co-processing was obtained over 2 wt% Fe - 8 wt% Ni/H-Y-5.1 catalysts with the median metal particle size of 4.6 nm and metals-to-acid site ratio of 8.6. Fe catalyst were much less active in isoeugenol hydrodeoxygenation, while high cracking activity of hexadecane was observed in the presence of Ni. Alkylation of n-hexadecane was a feature of 8 wt% Fe - 2 wt% Ni/H-Y-5.1, whereas, over the 5 wt% Fe - 5 wt% Ni/H-Y-5.1 bifunctional catalyst no undesired oxygen-containing cyclic products were detected. This catalyst exhibited the highest hydrogen consumption according to temperature programmed desorption, which can serve as a marker for efficient hydrodeoxygenation. The spent catalysts contained ca 40 wt% of coke with predominantly aliphatic species. (c) 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
dc.format.pagerange101
dc.format.pagerange116
dc.identifier.eissn1090-2694
dc.identifier.jour-issn0021-9517
dc.identifier.olddbid209380
dc.identifier.oldhandle10024/192407
dc.identifier.urihttps://www.utupub.fi/handle/11111/44937
dc.identifier.urlhttps://doi.org/10.1016/j.jcat.2023.03.016
dc.identifier.urnURN:NBN:fi-fe2023042538612
dc.language.isoen
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.publisherACADEMIC PRESS INC ELSEVIER SCIENCE
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1016/j.jcat.2023.03.016
dc.relation.ispartofjournalJournal of Catalysis
dc.relation.volume421
dc.source.identifierhttps://www.utupub.fi/handle/10024/192407
dc.titleCo-processing of fossil feedstock with lignin-derived model compound isoeugenol over Fe-Ni/H-Y-5.1 catalysts
dc.year.issued2023

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