Interfacial Properties of Colloidal Silica Dispersions in Contact with Solutions of Fatty Amines in Hexane

Many natural phenomena and technologies are concerned with the interactions between micro- or nano-metre sized particles and surfactant molecules at liquid interfaces. Highly stable emulsions are produced by using surfactants to modify the surfaces of nanoparticles. Particle attachment to bubbles is controlled by surfactant adsorption in flotation technologies. So far, however, few experimental studies have explored the properties of these complex interfacial layers

Effect of Silica Nanoparticles on Rheological and Structural Properties of DPPC Langmuir Monolayers

The study of the interaction between nanoparticles and model of lung surfactant is of great relevance to understand possible adverse effects of inhalable nanoparticles on the respiratory function [1,2]. We report therefore a study on the interfacial properties, structure and dilational rheology of monolayers of the major lipidic component of the lung surfactant, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), in the presence of silica nanoparticles. Investigations are performed by a Langmuir trough equipped with Brewster Angle Microscopy

Evaluating the Impact of Hydrophobic Silicon Dioxide in the Interfacial Properties of Lung Surfactant Films

CRUE-CSIC (Acuerdos Transformativos 2022)The interaction of hydrophobic silicon dioxide particles (fumed silicon dioxide), as model air pollutants, and Langmuir monolayers of a porcine lung surfactant extract has been studied in order to try to shed light on the physicochemical bases underlying the potential adverse effects associated with pollutant inhalation. The surface pressure−area isotherms of lung surfactant (LS) films including increasing amounts of particles revealed that particle incorporation into LS monolayers modifies the organization of the molecules at the water/vapor interface, which alters the mechanical resistance of the interfacial films, hindering the ability of LS layers for reducing the surface tension, and reestablishing the interface upon compression. This influences the normal physiological function of LS as is inferred from the analysis of the response of the Langmuir films upon the incorporation of particles against harmonic changes of the interfacial area (successive compression−expansion cycles). These experiments evidenced that particles alter the relaxation mechanisms of LS films, which may be correlated to a modification of the transport of material within the interface and between the interface and the adjacent fluid during the respiratory cycle.Depto. de Química FísicaFac. de Ciencias QuímicasTRUEUnión Europea. Horizonte 2020Ministerio de Ciencia e Innovación (MICINN)pu

Interaction of Particles with Langmuir Monolayers of 1,2-Dipalmitoyl-Sn-Glycero-3-Phosphocholine: A Matter of Chemistry?

Lipid layers are considered among the first protective barriers of the human body against pollutants, e.g., skin, lung surfactant, or tear film. This makes it necessary to explore the physico-chemical bases underlying the interaction of pollutants and lipid layers. This work evaluates using a pool of surface-sensitive techniques, the impact of carbon black and fumed silica particles on the behavior of Langmuir monolayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC). The results show that the incorporation of particles into the lipid monolayers affects the surface pressure–area isotherm of the DPPC, modifying both the phase behavior and the collapse conditions. This is explained considering that particles occupy a part of the area available for lipid organization, which affects the lateral organization of the lipid molecules, and consequently the cohesion interactions within the monolayer. Furthermore, particles incorporation worsens the mechanical performance of lipid layers, which may impact negatively in different processes presenting biological relevance. The modification induced by the particles has been found to be dependent on their specific chemical nature. This work tries to shed light on some of the most fundamental physico-chemical bases governing the interaction of pollutants with lipid layers, which plays an essential role on the design of strategies for preventing the potential health hazards associated with pollution

Short Time Dynamic Interfacial Tension as Measured with Capillary Pressure Technique

Dynamic interfacial tension measurements in the short time range are a major request for controlling interfacial processes in modern, highly dynamic technologies. Capillary pressure measurements for growing and oscillating drops represent a good way to fulfil these requirements. The corresponding quantitative data analysis, however, requires the solution of rather complex theories on the hydrodynamics of growing drops and the adsorption dynamics at the drop surface and possible mass transfer across interfaces for liquid/liquid systems

Particle and Particle-Surfactant Mixtures at Fluid Interfaces: Assembly, Morphology, and Rheological Description

We report here a review of particle-laden interfaces. We discuss the importance of the particle’s wettability, accounted for by the definition of a contact angle, on the attachment of particles to the fluid interface and how the contact angle is strongly affected by several physicochemical parameters. The different mechanisms of interfacial assembly are also addressed, being the adsorption and spreading the most widely used processes leading to the well-known adsorbed and spread layers, respectively. The different steps involved in the adsorption of the particles and the particle-surfactant mixtures from bulk to the interface are also discussed. We also include here the different equations of state provided so far to explain the interfacial behavior of the nanoparticles. Finally, we discuss the mechanical properties of the interfacial particle layers via dilatational and shear rheology. We emphasize along that section the importance of the shear rheology to know the intrinsic morphology of such particulate system and to understand how the flow-field-dependent evolution of the interfacial morphology might eventually affect some properties of materials such as foams and emulsions. We dedicated the last section to explaining the importance of the particulate interfacial systems in the stabilization of foams and emulsions.Peer Reviewe

Interfacial Properties of Tridecyl Dimethyl Phosphine Oxide Adsorbed at the Surface of a Solution Drop in Hexane Saturated Air

The surface tension of C₁₃DMPO aqueous solution drops in hexane vapor is studied using the drop profile method. The hexane was injected into the measuring cell at three different conditions: before the formation of the solution drop, at a certain moment during the adsorption process, and after reaching the equilibrium of surfactant adsorption. The surface tension values for all experiments at the same concentration and different injection situations ultimately coincide with each other after attaining the final equilibration stage. The equilibrium surface tension isotherms of C₁₃DMPO solutions, and the adsorption of both components—surfactant and hexane—were calculated. It was shown that the presence of surfactant leads to an increased hexane adsorption

Thermodynamics, Kinetics and Dilational Visco-Elasticity of Adsorbed CnEOm Layers at the Aqueous Solution/Air Interface

The adsorption behaviour of linear poly(oxyethylene) alkyl ether (CnEOm) is best described by a reorientation model. Based on a complete set of experimental data, including the adsorption kinetics, the equilibrium surface tension isotherm and the surface dilational visco-elasticity, the thermodynamic and kinetic adsorption parameters for some CnEOm at the water/air interface were determined. For the study, six CnEOm surfactants were selected (n = 10, 12 and 14 and m = 4, 5 and 8) and were studied by bubble profile analysis and maximum bubble pressure tensiometry. A refined theoretical model based on a reorientation-adsorption model combined with a diffusion-controlled adsorption kinetics and exchange of matter allowed us to calculate the surface layer composition by adsorbing molecules in different orientations. It turns out that at larger surface coverage, the adsorption rate decreases, i.e., the apparent diffusion coefficients are smaller. This deceleration can be explained by the transition of molecules adsorbed in a state of larger molar surface area into a state with smaller molar surface area

Sistema automatico di acquisizione dati e calcolo della tensione superficiale

No abstract availabl

Dilational properties of fluid interfaces and adsorption kinetics. Application to FAST experiments

No abstract availabl