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dc.contributor.authorKupila, Riikka
dc.contributor.authorLappalainen, Katja
dc.contributor.authorHu, Tao
dc.contributor.authorHeponiemi, Anne
dc.contributor.authorBergna, Davide
dc.contributor.authorLassi, Ulla
dc.date.accessioned2021-08-26T06:01:30Z
dc.date.available2021-08-26T06:01:30Z
dc.date.issued2021
dc.identifier.citationKupila, R., Lappalainen, K., Hu, T., Heponiemi, A., Bergna, D., & Lassi, U. (2021). Production of ethyl lactate by activated carbon-supported Sn and Zn oxide catalysts utilizing lignocellulosic side streams. <i>Applied Catalysis A: General</i>, <i>624</i>, Article 118327. <a href="https://doi.org/10.1016/j.apcata.2021.118327" target="_blank">https://doi.org/10.1016/j.apcata.2021.118327</a>
dc.identifier.otherCONVID_100270718
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/77491
dc.description.abstractIn this study, activated carbon-supported Sn and Zn oxide catalysts were prepared from hydrolysis lignin and used for the conversion of model solutions of trioses, hexoses, and lignocellulosic biomass hydrolysates to ethyl lactate. Both catalysts, SnO2@AC and ZnO@AC, were able to produce ethyl lactate in high yields. SnO2@AC was a more active and selective catalyst in triose (dihydroxyacetone) conversion, providing 99% yield to ethyl lactate. ZnO@AC, by contrast, was more selective in glucose and hydrolysate conversion, with a yield of 60% and 85%, respectively. The ethyl lactate yields were significantly higher than those from the optimized model solution experiments when using ZnO@AC catalyst. These findings indicate that milder acidity of the ZnO@AC catalyst together with Na+ and SO42- in hydrolysate favored ethyl lactate production, preventing byproduct, furan derivatives and acetal, formation. Moreover, the catalysts were able to maintain their catalytic activity in recycling experiments.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesApplied Catalysis A: General
dc.rightsCC BY 4.0
dc.subject.otheractivated carbon
dc.subject.otherheterogeneous catalyst
dc.subject.othermetal oxide
dc.subject.otherethyl lactate
dc.subject.otherlignocellulosic biomass
dc.titleProduction of ethyl lactate by activated carbon-supported Sn and Zn oxide catalysts utilizing lignocellulosic side streams
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202108264654
dc.contributor.laitosKokkolan yliopistokeskus Chydeniusfi
dc.contributor.laitosKokkola University Consortium Chydeniusen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineSoveltavan kemian yksikköfi
dc.contributor.oppiaineOrganic Chemistryen
dc.contributor.oppiaineThe Unit of Applied Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn0926-860X
dc.relation.volume624
dc.type.versionpublishedVersion
dc.rights.copyright© 2021 The Author(s). Published by Elsevier B.V.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber20201508
dc.subject.ysokatalyysi
dc.subject.ysoaktiivihiili
dc.subject.ysooksidit
dc.subject.ysobiomassa (teollisuus)
dc.subject.ysokatalyytit
dc.subject.ysolaktaatit
dc.subject.ysokemian tekniikka
dc.subject.ysosinkkioksidi
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p8704
jyx.subject.urihttp://www.yso.fi/onto/yso/p25569
jyx.subject.urihttp://www.yso.fi/onto/yso/p2803
jyx.subject.urihttp://www.yso.fi/onto/yso/p6170
jyx.subject.urihttp://www.yso.fi/onto/yso/p15480
jyx.subject.urihttp://www.yso.fi/onto/yso/p9014
jyx.subject.urihttp://www.yso.fi/onto/yso/p2463
jyx.subject.urihttp://www.yso.fi/onto/yso/p27694
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1016/j.apcata.2021.118327
dc.relation.funderEuropean Commissionen
dc.relation.funderEuroopan komissiofi
jyx.fundingprogramInterreg, othersen
jyx.fundingprogramInterreg, muutfi
jyx.fundinginformationAuthors R.K. and K.L. would like to thank the Green Bioraff Solutions Project (EU/Interreg/Botnia-Atlantica, 20201508) for funding this research.
dc.type.okmA1


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