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Two Different Scenarios for the Equilibration of Polycation—Anionic Solutions at Water–Vapor Interfaces

dc.contributor.authorGuzmán Solís, Eduardo
dc.contributor.authorFernández Peña, Laura
dc.contributor.authorAkanno, Andrew
dc.contributor.authorLlamas, Sara
dc.contributor.authorOrtega Gómez, Francisco
dc.contributor.authorGonzález Rubio, Ramón
dc.date.accessioned2023-06-17T12:36:06Z
dc.date.available2023-06-17T12:36:06Z
dc.date.issued2019-07-13
dc.description.abstractThe assembly in solution of the cationic polymer poly(diallyldimethylammonium chloride) (PDADMAC) and two different anionic surfactants, sodium lauryl ether sulfate (SLES) and sodium N-lauroyl-N-methyltaurate (SLMT), has been studied. Additionally, the adsorption of the formed complexes at the water–vapor interface have been measured to try to shed light on the complex physico-chemical behavior of these systems under conditions close to that used in commercial products. The results show that, independently of the type of surfactant, polyelectrolyte-surfactant interactions lead to the formation of kinetically trapped aggregates in solution. Such aggregates drive the solution to phase separation, even though the complexes should remain undercharged along the whole range of explored compositions. Despite the similarities in the bulk behavior, the equilibration of the interfacial layers formed upon adsorption of kinetically trapped aggregates at the water–vapor interface follows different mechanisms. This was pointed out by surface tension and interfacial dilational rheology measurements, which showed different equilibration mechanisms of the interfacial layer depending on the nature of the surfactant: (i) formation layers with intact aggregates in the PDADMAC-SLMT system, and (ii) dissociation and spreading of kinetically trapped aggregates after their incorporation at the fluid interface for the PDADMAC-SLES one. This evidences the critical impact of the chemical nature of the surfactant in the interfacial properties of these systems. It is expected that this work may contribute to the understanding of the complex interactions involved in this type of system to exploit its behavior for technological purposes.
dc.description.departmentDepto. de Química Física
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/66155
dc.identifier.doi10.3390/coatings9070438
dc.identifier.issn2079-6412
dc.identifier.officialurlhttps://doi.org/10.3390/coatings9070438
dc.identifier.relatedurlhttps://www.mdpi.com/2079-6412/9/7/438
dc.identifier.urihttps://hdl.handle.net/20.500.14352/12594
dc.issue.number7
dc.journal.titleCoatings
dc.language.isoeng
dc.page.initial438
dc.publisherMDPI
dc.relation.projectIDCTQ-2016-78895-R
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.keywordpolyelectrolyte
dc.subject.keywordsurfactants
dc.subject.keywordkinetically trapped aggregates
dc.subject.keywordinterfaces
dc.subject.keywordsurface tension
dc.subject.keywordinterfacial dilational rheology
dc.subject.keywordadsorption
dc.subject.ucmFísica (Química)
dc.subject.ucmQuímica física (Química)
dc.titleTwo Different Scenarios for the Equilibration of Polycation—Anionic Solutions at Water–Vapor Interfaces
dc.typejournal article
dc.volume.number9
dspace.entity.typePublication
relation.isAuthorOfPublication8461433f-f4e7-40b0-9549-b14c34817028
relation.isAuthorOfPublication868be429-b538-45d8-a4c1-e1fac224c804
relation.isAuthorOfPublicationffe9a2c2-caca-446f-a49e-14cacb7984df
relation.isAuthorOfPublication.latestForDiscovery868be429-b538-45d8-a4c1-e1fac224c804

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