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dc.contributor.authorGhoreishi, Solmaz
dc.contributor.authorBarth, Tanja
dc.contributor.authorHermundsgård, Dag Helge
dc.date.accessioned2020-03-19T12:25:40Z
dc.date.available2020-03-19T12:25:40Z
dc.date.issued2019
dc.PublishedGhoreishi S, Barth T, Hermundsgård. Effect of Reaction Conditions on Catalytic and Noncatalytic Lignin Solvolysis in Water Media Investigated for a 5 L Reactor. ACS Omega. 2019;4:19265-19278eng
dc.identifier.issn2470-1343en_US
dc.identifier.urihttps://hdl.handle.net/1956/21536
dc.description.abstractThe high content of oxygen in the lignin polymer and the prevalence of phenolic functional groups make the conversion of lignin to fuels and value-added products with well-defined chemical properties challenging. The lignin-to-liquid process using a water/formic acid reaction medium has been shown to convert the lignin polymer to monomers with a molecular weight range of 300–600 Da. The bio-oil comprises a complex mixture of monomeric phenols, aromatics, and aliphatic hydrocarbons with a high H/C and low O/C ratio. This study investigates the effect of the stirring rate, level of loading, and catalyst at 305 and 350 °C in a 5 L pilot scale reactor. The oil yields are found to be highest for experiments conducted using the maximum stirring rate, maximum level of loading, and Ru/Al2O3 catalyst with yields of more than 69 wt % on lignin intake. Goethite as a catalyst does not show good conversion efficiency at either reaction temperatures. The carbon recovery is highest for products produced at 305 °C. Furthermore, results from solid phase extraction on a DSC-CN solid phase show that 65–92 wt % the bio-oils can be recovered as fractions separated based on polarity.en_US
dc.language.isoengeng
dc.publisherACSen_US
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/4.0eng
dc.titleEffect of Reaction Conditions on Catalytic and Noncatalytic Lignin Solvolysis in Water Media Investigated for a 5 L Reactoren_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2020-02-10T07:22:55Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2019 American Chemical Societyen_US
dc.identifier.doihttps://doi.org/10.1021/acsomega.9b02629
dc.identifier.cristin1755234
dc.source.journalACS Omega


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