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dc.contributor.authorPrado García, Raquel
dc.contributor.authorBrandt, Agnieszka
dc.contributor.authorErdocia Iriarte, Xabier
dc.contributor.authorHallett, Jason
dc.contributor.authorWelton, Tom
dc.contributor.authorLabidi, Jalel
dc.date.accessioned2024-02-08T11:01:13Z
dc.date.available2024-02-08T11:01:13Z
dc.date.issued2015-09
dc.identifier.citationGreen Chemistry 18(3) : 834-841 (2016)
dc.identifier.issn1463-9262
dc.identifier.urihttp://hdl.handle.net/10810/65382
dc.description.abstractThe depolymerisation of lignin directly in the black liquor was studied, comparing two ionic liquids as extracting solvents (butylimidazolium hydrogen sulphate and triethylammonium hydrogen sulphate), under oxidising conditions. H2O2 was chosen as the oxidant agent. It was observed that lignins derived from butylimidazolium hydrogen sulphate were more susceptible to degradation. The main degradation products found in the extracted oils were aromatic acids, such as vanillic acid, benzoic acid and 1,2-benzenedicarboxylic acid.es_ES
dc.description.sponsorshipDepartment of Education, Universities and Investigation of the Basque Government (project IT672-13)es_ES
dc.language.isoenges_ES
dc.publisherRSC
dc.rightsinfo:eu-repo/semantics/restrictedAccesses_ES
dc.subjectionic liquidses_ES
dc.subjectlignines_ES
dc.subjectoxidationes_ES
dc.titleLignin oxidation and depolymerisation in ionic liquidses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© The Royal Society of Chemistry 2016es_ES
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2016/gc/c5gc01950h
dc.identifier.doi10.1039/C5GC01950H
dc.departamentoesIngeniería química y del medio ambientees_ES
dc.departamentoeuIngeniaritza kimikoa eta ingurumenaren ingeniaritzaes_ES


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