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dc.contributor.authorCiftja, Arlinda
dc.contributor.authorHartono, Ardi
dc.contributor.authorSvendsen, Hallvard Fjøsne
dc.date.accessioned2014-09-29T07:20:38Z
dc.date.accessioned2016-01-25T14:14:52Z
dc.date.available2014-09-29T07:20:38Z
dc.date.available2016-01-25T14:14:52Z
dc.date.issued2013
dc.identifier.citationChemical Engineering Science 2013, 102:378-386nb_NO
dc.identifier.issn0009-2509
dc.identifier.urihttp://hdl.handle.net/11250/2374781
dc.description.abstract2-(Diethylamino)ethanol (DEEA) and 3-(Methylamino) propylamine (MAPA) in combination may represent a promising absorbent system for CO2 capture due to high CO2 loading capacity, high equilibrium temperature sensitivity, low energy requirement for regeneration and relatively high reaction rate. Three different systems: DEEA–CO2–H2O; MAPA–CO2–H2O and DEEA–MAPA–CO2–H2O were studied quantitatively by NMR spectroscopy and the data are reported in the present work. The main products quantified for these systems are: carbonate-bicarbonate for the DEEA–CO2–H2O system; primary, secondary carbamate, dicarbamate for the MAPA–CO2–H2O system, and primary/secondary carbamate, dicarbamate, carbonate/bicarbonate in blended DEEA–MAPA–CO2–H2O. The speciation data of the three systems were measured and reported in the present work. The blended system of 5 M DEEA–2 M MAPA can form two liquid phases after being loaded with CO2 and both phases were analyzed quantitatively by NMR spectroscopy. The experimental data shows that the lower phase is rich in CO2 and MAPA while the upper phase was lean in CO2 and rich in DEEA. The ratio DEEA–MAPA in the lower phase increases with increasing partial pressure whereas for the upper phase the opposite is true.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.titleExperimental study on phase change solvents in CO2 capture by NMR spectroscopynb_NO
dc.typeJournal articlenb_NO
dc.typePeer revieweden_GB
dc.date.updated2014-09-29T07:20:39Z
dc.source.volume102nb_NO
dc.source.journalChemical Engineering Sciencenb_NO
dc.identifier.doi10.1016/j.ces.2013.08.036
dc.identifier.cristin1049449
dc.description.localcode(c) 2013 Elsevier Ltd. All rights reserved. This is the authors' accepted and refereed manuscript to the article.nb_NO


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