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dc.contributor.authorAronu, Ugochukwu Edwin
dc.contributor.authorCiftja, Arlinda Fejzo
dc.contributor.authorKim, Inna
dc.contributor.authorHartono, Ardi
dc.date.accessioned2020-12-16T12:02:57Z
dc.date.available2020-12-16T12:02:57Z
dc.date.created2014-11-27T09:56:44Z
dc.date.issued2013
dc.identifier.citationEnergy Procedia. 2013, 37 (0), 233-240.en_US
dc.identifier.issn1876-6102
dc.identifier.urihttps://hdl.handle.net/11250/2719809
dc.description.abstractRapid screening experiment has been used to acquire first-hand information on the precipitation characteristics of 14 aqueous amino acid salt systems. Absorption tests at 40°C have shown that at high concentrations, amino acid salt systems forms precipitate in the presence of CO2 resulting to 2 or 3 solid-liquid phase formation. Potassium salt of the amino acid salts generally showed better reaction kinetics than their sodium salt counterparts. 5m’ KSar and 4.3m’ KPro showed significantly higher reaction kinetics while 5m’ KSar, 5m’ KAla, 4.5m’ KSer, 5m’ KL-Ala were observed to have an upward shift in absorption rate at some point during absorption resulting to increased loading. Application of the conventional stripping process in the screening test, i.e. heating up the absorption solution to 80oC showed poor desorption characteristics for the precipitating amino acid salt solutions. Qualitative 13C NMR studies was used to identify the chemical species in the phases, 3-phase in 5m’ KSar and 2-phase in 4.5m’ KSer. The NMR results show that each phase contains HCO3 -/CO32- and carbamate fractions at varying degree.en_US
dc.language.isoengen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.subjectCO2 captureen_US
dc.subjectSpeciationen_US
dc.subjectNMRen_US
dc.subjectPhase formationen_US
dc.subjectPrecipitationen_US
dc.subjectScreening,en_US
dc.subjectAmino acid saltsen_US
dc.subjectDesorptionen_US
dc.subjectAbsorptionen_US
dc.titleUnderstanding precipitation in amino acid salt systems at process conditionsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2013 The Authors. Published by Elsevier Ltd.en_US
dc.source.pagenumber233-240en_US
dc.source.volume37en_US
dc.source.journalEnergy Procediaen_US
dc.identifier.doihttps://doi.org/10.1016/j.egypro.2013.05.107
dc.identifier.cristin1177625
dc.relation.projectNorges forskningsråd: 193816en_US
cristin.unitcode7401,80,3,4
cristin.unitnameCO2 innfangningsprosesser
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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