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dc.contributor.authorBuvik, Vanja
dc.contributor.authorVevelstad, Solrun Johanne
dc.contributor.authorMoser, Peter
dc.contributor.authorWiechers, Georg
dc.contributor.authorWanderley, Ricardo R.
dc.contributor.authorMonteiro, Juliana
dc.contributor.authorKnuutila, Hanna K
dc.date.accessioned2023-10-30T08:52:32Z
dc.date.available2023-10-30T08:52:32Z
dc.date.created2023-05-16T13:42:25Z
dc.date.issued2023
dc.identifier.citationCarbon Capture Science & Technology (CCST). 2023, 7 100110-?.en_US
dc.identifier.urihttps://hdl.handle.net/11250/3099321
dc.description.abstractThe oxidative degradation of previously used ethanolamine from three different CO2 capture pilot plants was studied in a laboratory-scale degradation setup. Different solvents behave differently under the same experimental conditions, indicating that different solvent contaminants, resulting from different operational conditions, can act either stabilising or destabilising under oxidising conditions. Some ionic compounds in the solvent seem beneficial to amine stability under oxidising conditions, while the presence of some inorganic compounds appears to have a negative effect on the stability of the solvent. The most stable pre-used ethanolamine solutions were those that contained the highest total concentrations of heat-stable salts, calcium, sodium, sulphur, potassium, and silicon. These solutions were previously used for CO2 capture from a lignite-fired power plant and a waste-to-energy plant. The least stable amine solution had a higher concentration of metal ions like chromium, magnesium, and zinc, making these suspects of deteriorating solvent stability.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleDegradation behaviour of fresh and pre-used ethanolamineen_US
dc.title.alternativeDegradation behaviour of fresh and pre-used ethanolamineen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber100110-?en_US
dc.source.volume7en_US
dc.source.journalCarbon Capture Science & Technology (CCST)en_US
dc.identifier.doi10.1016/j.ccst.2023.100110
dc.identifier.cristin2147842
dc.relation.projectEC/H2020/271501en_US
dc.relation.projectNorges forskningsråd: 257579en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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