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dc.contributor.authorÁvila, Jocasta
dc.contributor.authorLozano-Martín, Daniel
dc.contributor.authorSimões Santos, Mirella
dc.contributor.authorZhang, Yunxiao
dc.contributor.authorLi, Hua
dc.contributor.authorPádua, Agilio
dc.contributor.authorAtkin, Rob
dc.contributor.authorCosta Gomes, Margarida
dc.date.accessioned2024-07-25T11:43:15Z
dc.date.available2024-07-25T11:43:15Z
dc.date.issued2023
dc.identifier.citationPhysical Chemistry Chemical Physics, 2023, vol. 25, p. 6808-6816.es
dc.identifier.issn1463-9076es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/69134
dc.description.abstractSurface active ionic liquids (SAILs) combine useful characteristics of both ionic liquids (ILs) and surfactants, hence are promising candidates for a wide range of applications. However, the effect of SAIL ionic structures on their physicochemical properties remains unclear, which limits their uptake. To address this knowledge gap, in this work we investigated the density, viscosity, surface tension, and corresponding critical micelle concentration in water, as well as gas absorption of SAILs with a variety of cation and anion structures. SAILs containing anions with linear alkyl chains have smaller molar volumes than those with branched alkyl chains, because linear alkyl chains are interdigitated to a greater extent, leading to more compact packing. This interdigitation also results in SAILs being about two orders of magnitude more viscous than comparable conventional ILs. SAILs at the liquid–air interface orient alkyl chains towards the air, leading to low surface tensions closer to n-alkanes than conventional ILs. Critical temperatures of about 900 K could be estimated for all SAILs from their surface tensions. When dissolved in water, SAILs adsorb at the liquid–air interface and lower the surface tension, like conventional surfactants in water, after which micelles form. Molecular simulations show that the micelles are spherical and that lower critical micelle concentrations correspond to the formation of aggregates with a larger number of ion pairs. CO2 and N2 absorption capacities are examined and we conclude that ionic liquids with larger non-polar domains absorb larger quantities of both gases.es
dc.format.mimetypeapplication/pdfes
dc.language.isospaes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleEffect of ion structure on the physicochemical properties and gas absorption of surface active ionic liquidses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1039/D2CP05145Aes
dc.identifier.publicationfirstpage6808es
dc.identifier.publicationissue9es
dc.identifier.publicationlastpage6816es
dc.identifier.publicationtitlePhysical Chemistry Chemical Physicses
dc.identifier.publicationvolume25es
dc.peerreviewedSIes
dc.identifier.essn1463-9084es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersiones


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