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dc.contributor.authorJoseph, Prajin
dc.contributor.authorTanase-Opedal, Mihaela
dc.contributor.authorMoe, Størker T.
dc.date.accessioned2023-12-11T10:19:20Z
dc.date.available2023-12-11T10:19:20Z
dc.date.created2023-09-18T09:33:05Z
dc.date.issued2023
dc.identifier.issn0006-3525
dc.identifier.urihttps://hdl.handle.net/11250/3106815
dc.description.abstractLignin, the second most abundant biopolymer on earth and with a predominantly aromatic structure, has the potential to be a raw material for valuable chemicals and other bio-based chemicals. In industry, lignin is underutilized by being used mostly as a fuel for producing thermal energy. Valorization of lignin requires knowledge of the structure and different linkages in the isolated lignin, making the study of structure of lignin important. In this article, lignin samples isolated from two types of reactors (autoclave reactor and displacement reactor) were analyzed by FT-IR, size exclusion chromatography, thermogravimetric analysis (TGA), and Py-GC-MS. The average molecular mass of the organosolv lignins isolated from the autoclave reactor decreased at higher severities, and FT-IR showed an increase in free phenolic content with increasing severity. Except for molecular mass and molecular mass dispersity, there were only minor differences between lignins isolated from the autoclave reactor and lignins isolated from the displacement reactor. Carbohydrate analysis, Py-GC–MS and TGA showed that the lignin isolated using either of the reactor systems is of high purity, suggesting that organosolv lignin is a good candidate for valorization.en_US
dc.language.isoengen_US
dc.publisherWiley Periodicals LLC.en_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titlePolymer properties of softwood organosolv lignins produced in two different reactor systemsen_US
dc.title.alternativePolymer properties of softwood organosolv lignins produced in two different reactor systemsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume114en_US
dc.source.journalBiopolymersen_US
dc.source.issue12en_US
dc.identifier.doi10.1002/bip.23566
dc.identifier.cristin2175895
dc.relation.projectNorges forskningsråd: 226247en_US
dc.relation.projectNorges forskningsråd: 257622en_US
dc.relation.projectNorges teknisk-naturvitenskapelige universitet: 70441799en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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