Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19337
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dc.contributor.authorAlmeida, Hugo F. D.pt
dc.contributor.authorFreire, Mara G.pt
dc.contributor.authorFernandes, Ana M.pt
dc.contributor.authorLopes-da-Silva, Jose A.pt
dc.contributor.authorMorgado, Pedropt
dc.contributor.authorShimizu, Karinapt
dc.contributor.authorFilipe, Eduardo J. M.pt
dc.contributor.authorCanongia Lopes, Jose N.pt
dc.contributor.authorSantos, Luis M. N. B. F.pt
dc.contributor.authorCoutinho, Joao A. P.pt
dc.date.accessioned2017-12-07T19:09:16Z-
dc.date.issued2014pt
dc.identifier.issn0743-7463pt
dc.identifier.urihttp://hdl.handle.net/10773/19337-
dc.description.abstractAiming at providing a comprehensive study of the influence of the cation symmetry and alkyl side chain length on the surface tension and surface organization of ionic liquids (ILs), this work addresses the experimental measurements of the surface tension of two extended series of ILs, namely R,R'-dialkylimidazolium bis-Rtrifluoromethyl)sulfonyllimide ([C(n)C(n)im][NTf2]) and R-alkyl-3-methylimidazolium bis[ (trifluoromethyl)sulfonyl] imide ([C-n C(1)im]-[NTf2D, and their dependence with temperature (from 298 to 343 K). For both series of ILs the surface tension decreases with an increase in the cation side alkyl chain length up to aliphatic chains no longer than hexyl, here labeled as critical alkyl chain length (CACL). For ILs with aliphatic moieties longer than CACL the surface tension displays an almost constant value up to [C(12)C(1)im][NTf2] or [C(16)C(1)im][NTf2]. These constant values further converge to the surface tension of long chain n-alkanes, indicating that, for sufficiently long alkyl side chains, the surface ordering is strongly dominated by the aliphatic tails present in the IL. The enthalpies and entropies of surface were also derived and the critical temperatures were estimated from the experimental data. The trend of the derived thermodynamic Properties highlights the effect of the structural organization of the IL at the surface with visible trend shifts occurring at a well-defined CACL in both symmetric and asymmetric series of ILs. Finally, the structure of a long-alkyl side chain IL at the vacuum-liquid interface was also explored using Molecular Dynamics simulations. In general, it was found that for the symmetric series of ILs, at the outermost polar layers, more cations point one of their aliphatic tails outward and the other inward, relative to the surface, than cations pointing both tails outward. The number of the former, while being the preferred conformation, exceeds the latter by around 75%.pt
dc.language.isoengpt
dc.publisherAMER CHEMICAL SOCpt
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132936/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/132962/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/124806/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/121274/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/121520/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F81748%2F2011/PTpt
dc.rightsrestrictedAccesspor
dc.subjectEXTENDED PRESSURE RANGEpt
dc.subjectMOLECULAR-FORCE FIELDpt
dc.subjectPHYSICAL-PROPERTIESpt
dc.subjectTHERMODYNAMIC PROPERTIESpt
dc.subjectREFRACTIVE-INDEXpt
dc.subjectTEMPERATUREpt
dc.subjectDENSITYpt
dc.subjectANIONpt
dc.subjectWATERpt
dc.subjectSIMULATIONSpt
dc.titleCation Alkyl Side Chain Length and Symmetry Effects on the Surface Tension of Ionic Liquidspt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage6408pt
degois.publication.issue22pt
degois.publication.lastPage6418pt
degois.publication.titleLANGMUIRpt
degois.publication.volume30pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1021/la501308qpt
dc.identifier.doi10.1021/la501308qpt
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