Person:
Guzmán Solís, Eduardo

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First Name
Eduardo
Last Name
Guzmán Solís
Affiliation
Universidad Complutense de Madrid
Faculty / Institute
Ciencias Químicas
Department
Química Física
Area
Química Física
Identifiers
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Now showing 1 - 5 of 5
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    Surfactant-Like Behavior for the Adsorption of Mixtures of a Polycation and Two Different Zwitterionic Surfactants at the Water/Vapor Interface
    (Molecules, 2019) Akanno, Andrew; Guzmán Solís, Eduardo; Fernández Peña, Laura; Ortega Gómez, Francisco; González Rubio, Ramón
    The bulk and interfacial properties of solutions formed by a polycation (i.e., poly(diallyl-dimethylammonium chloride), PDADMAC) and two different zwitterionic surfactants (i.e., coco-betaine (CB) and cocoamidopropyl-betaine (CAPB)) have been studied. The bulk aggregation of the polyelectrolyte and the two surfactants was analyzed by turbidity and electrophoretic mobility measurements, and the adsorption of the solutions at the fluid interface was studied by surface tension and interfacial dilational rheology measurements. Evidence of polymer–surfactant complex formation in bulk was only found when the number of surfactant molecules was closer to the number of charged monomers in solutions, which suggests that the electrostatic repulsion associated with the presence of a positively charged group in the surfactant hinders the association between PDADMAC and the zwitterionic surfactant for concentrations in which there are no micelles in solution. This lack of interaction in bulk is reflected in the absence of an influence of the polyelectrolyte in the interfacial properties of the mixtures, with the behavior being controlled by the presence of surfactant. This work has evidenced the significant importance of the different interactions involved in the system for controlling the interaction and complexation mechanisms of in polyelectrolyte–surfactant mixtures.
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    Two Different Scenarios for the Equilibration of Polycation—Anionic Solutions at Water–Vapor Interfaces
    (Coatings, 2019) Guzmán Solís, Eduardo; Fernández Peña, Laura; Akanno, Andrew; Llamas, Sara; Ortega Gómez, Francisco; González Rubio, Ramón
    The 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.
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    Towards understanding the behavior of polyelectrolyte–surfactant mixtures at the water/vapor interface closer to technologically-relevant conditions
    (Physical Chemistry Chemical Physics, 2018) Llamas, Sara; Fernández Peña, Laura; Akanno, Andrew; Guzmán Solís, Eduardo; Ortega, Víctor; Ortega Gómez, Francisco; García Csaky, Aurelio; Campbell, Richard ; González Rubio, Ramón
    Polyelectrolyte–surfactant mixtures and their interactions with fluid interfaces are an important research field due to their use in technological applications. Most of the existing knowledge on these systems is based on models in which the polyelectrolyte concentration is around 50 times lower than that used in commercial formulations. The present work marks a step to close the gap on the understanding of their behavior under more practically-relevant conditions. The adsorption of concentrated mixtures of poly(diallyldimethyl-ammonium) chloride and sodium N-lauroyl-N-methyltaurate at the water/vapor interface with a crude mixing protocol has been studied by different surface tension techniques, Brewster angle microscopy, neutron reflectometry, and several bulk characterization techniques. Kinetically-trapped aggregates formed during mixing influence the interfacial morphology of mixtures produced in the equilibrium one-phase region, yet fluctuations in the surface tension isotherm result depending on the tensiometric technique applied. At low bulk surfactant concentrations, the free surfactant concentration is very low, and the interfacial composition matches the trend of the bulk complexes, which is a behavior that has not been observed in studies on more dilute mixtures. Nevertheless, a transition to synergistic co-adsorption of complexes and free surfactant is observed at the higher bulk surfactant concentrations studied. This transition appears to be a special feature of these more concentrated mixtures, which deserves attention in future studies of systems with additional components.
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    Study of the Liquid/Vapor Interfacial Properties of Concentrated Polyelectrolyte–Surfactant Mixtures Using Surface Tensiometry and Neutron Reflectometry: Equilibrium, Adsorption Kinetics, and Dilational Rheology
    (2018) Llamas, Sara; Guzmán Solís, Eduardo; Akanno, Andrew; Fernández Peña, Laura; Ortega Gómez, Francisco; Campbell, Richard; Miller, Reinhard; González Rubio, Ramón
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    Equilibration of a Polycation–Anionic Surfactant Mixture at the Water/Vapor Interface
    (Langmuir, 2018) Akanno, Andrew; Guzmán Solís, Eduardo; Fernández Peña, Laura; Llamas, Sara; Ortega Gómez, Francisco; González Rubio, Ramón
    The adsorption of concentrated poly(diallyldimethylammonium chloride) (PDADMAC)–sodium lauryl ether sulfate (SLES) mixtures at the water/vapor interface has been studied by different surface tension techniques and dilational viscoelasticity measurements. This work tries to shed light on the way in which the formation of polyelectrolyte–surfactant complexes in the bulk affects the interfacial properties of mixtures formed by a polycation and an oppositely charged surfactant. The results are discussed in terms of a two-step adsorption–equilibration of PDADMAC–SLES complexes at the interface, with the initial stages involving the diffusion of kinetically trapped aggregates formed in the bulk to the interface followed by the dissociation and spreading of such aggregates at the interface. This latter process becomes the main contribution to the surface tension decrease. This work aids our understanding of the most fundamental basis of the physicochemical behavior of concentrated polyelectrolyte–surfactant mixtures which present complex bulk and interfacial interactions with interest in both basic and applied sciences.