Pressure Changes Across a Membrane Formed by Coacervation of Oppositely Charged Polymer-Surfactant Systems.

We investigate the mass transfer and membrane growth processes during capsule formation by the interaction of the biopolymer xanthan gum with CnTAB surfactants. When a drop of xanthan gum polymer solution is added to the surfactant solution, a membrane is formed by coacervation. It encapsulates the polymer drop in the surfactant solution. The underlying mechanisms and dynamic processes during capsule formation are not yet understood in detail. Therefore, we characterized the polymer-surfactant complex formation during coacervation by measuring the surface tension and surface elasticity at the solution-air interface for different surfactant chain lengths and concentrations. The adsorption behavior of the mixed polymer-surfactant system at the solution-air interface supports the understanding of observed trends during the capsule formation. We further measured the change in capsule pressure over time and simultaneously imaged the membrane growth via confocal microscopy. The cross-linking and shrinkage during the membrane formation by coacervation leads to an increasing tensile stress in the elastic membrane, resulting in a rapid pressure rise. Afterward, the pressure gradually decreases and the capsule shrinks as water diffuses out. This is not only due to the initial capsule overpressure but also due to osmosis caused by the higher ionic strength of the surfactant solution outside the capsule compared to the polymer solution inside the capsule. The influence of polymer concentration and surfactant type and concentration on the pressure changes and the membrane structure are studied in this work, providing detailed insights into the dynamic membrane formation process by coacervation. This knowledge can be used to produce capsules with tailored membrane properties and to develop a suitable encapsulation protocol in technological applications. The obtained insights into the mass transfer of water across the capsule membrane are important for future usage in separation techniques and the food industry and allow us to better predict the capsule time stability.

Evaluation of Interfacial Structure of Self-Assembled Nanoparticle Layers: Use of Standard Deviation between Calculated and Experimental Drop Profiles as a Novel Method.

The self-assembly of nanoparticles (NPs) at interfaces is currently a topic of increasing interest due to numerous applications in food technology, pharmaceuticals, cosmetology, and oil recovery. It is possible to create tunable interfacial structures with desired characteristics using tailored nanoparticles that can be precisely controlled with respect to shape, size, and surface chemistry. To address these functionalities, it is essential to develop techniques to study the properties of the underlying structure. In this work, we propose an experimental approach utilizing the standard deviation of drop profiles calculated by the Laplace equation from experimental drop profiles (STD), as an alternative to the Langmuir trough or precise microscopic methods, to detect the initiation of closely packed conditions and the collapse of the adsorbed layers of CTAB-nanosilica complexes. The experiments consist of dynamic surface/interfacial tension measurements using drop profile analysis tensiometry (PAT) and large-amplitude drop surface area compression/expansion cycles. The results demonstrate significant changes in STD values at the onset of the closely packed state of nanoparticle-surfactant complexes and the monolayer collapse. The STD trend was explained in detail and shown to be a powerful tool for analyzing the adsorption and interfacial structuring of nanoparticles. Different collapse mechanisms were reported for NP monolayers at the liquid/liquid and air/liquid interfaces. We show that the interfacial tension (IFT) is solely dependent on the extent of interfacial coverage by nanoparticles, while the surfactants regulate only the hydrophobicity of the self-assembled complexes. Also, the irreversible adsorption of nanoparticles and the increasing number of adsorbed complexes after the collapse were observed by performing consecutive drop surface compression/expansion cycles. In addition to a qualitative characterization of adsorption layers, the potential of a quantitative calculation of the parameter STD such as the number of adsorbed nanoparticles at the interface and the distance between them at different states of the interfacial layer was discussed.

Pickering foams and parameters influencing their characteristics.

Pickering foams are available in many applications and have been continually gaining interest in the last two decades. Pickering foams are multifaceted, and their characteristics are highly dependent on many factors, such as particle size, charge, hydrophobicity and concentration as well as the charge and concentration of surfactants and salts available in the system. A literature review of these individual studies at first might seem confusing and somewhat contradictory, particularly in multi-component systems with particles and surfactants with different charges in the presence of salts. This paper provides a comprehensive overview of particle-stabilized foams, also known as Pickering foams and froths. Underlying mechanisms of foam stabilization by particles with different morphology, surface chemistry, size and type are reviewed and clarified. This paper also outlines the role of salts and different factors such as pH, temperature and gas type on Pickering foams. Further, we highlight recent developments in Pickering foams in different applications such as food, mining, oil and gas, and wastewater treatment industries, where Pickering foams are abundant. We conclude this overview by presenting important research avenues based on the gaps identified here. The focus of this review is limited to Pickering foams of surfactants with added salts and does not include studies on polymers, proteins, or other macromolecules.

Experimental techniques to study protein-surfactant interactions: New insights into competitive adsorptions via drop subphase and interface exchange.

Protein surfactant (PS) interactions is an essential topic for many fundamental and technological applications such as life science, nanobiotechnology processes, food industry, biodiesel production and drug delivery systems. Several experimental techniques and data analysis approaches have been developed to characterize PS interactions in bulk and at interfaces. However, to evaluate the mechanisms and the level of interactions quantitatively, e.g., PS ratio in complexes, their stability in bulk, and reversibility of their interfacial adsorption, new experimental techniques and protocols are still needed, especially with relevance for in-situ biological conditions. The available standard techniques can provide us with the basic understanding of interactions mainly under static conditions and far from physiological criteria. However, detailed measurements at complex interfaces can be formidable due to the sophisticated tools required to carefully probe nanometric phenomena at interfaces without disturbing the adsorbed layer. Tensiometry-based techniques such as drop profile analysis tensiometry (PAT) have been among the most powerful methods for characterizing protein's and surfactant's adsorption layers at interfaces via measuring equilibrium and dynamic interfacial tension and dilational rheology analysis. PAT provides us with insightful data such as kinetics and isotherms of adsorption and related surface activity parameters. However, the data analysis and interpretation can be challenging for mixed protein-surfactant solutions via standard PAT experimental protocols. The combination of a coaxial double capillary (micro flow exchange system) with drop profile analysis tensiometry (CDC-PAT) is a promising tool to provide valuable results under different competitive adsorption/desorption conditions via novel experimental protocols. CDC-PAT provides unique experimental protocols to exchange the droplet subphase in a continuous dynamic mode during the in-situ analysis of the corresponding interfacial adsorbed layer. The contribution of diffusion/convection mechanisms on the kinetics of the adsorption/desorption processes can also be investigated using CDC-PAT. Here, firstly, we review the commonly available techniques for characterizing protein-surfactant interactions in the bulk phase and at interfaces. Secondly, we give an overview for applications of the coaxial double capillary PAT setup for investigations of mixed protein-surfactant adsorbed layers and address recently developed protocols and analysis procedures. Exploring the competitive sequential adsorption of proteins and surfactants and the reversibility of pre-adsorbed layers via the subphase exchange are the particular experiments we can perform using CDC-PAT. Also the sequential and simultaneous competitive adsorption/desorption processes of some ionic and nonionic surfactants (SDS, CTAB, DTAB, and Triton) and proteins (bovine serum albumin (BSA), lysozyme, and lipase) using CDC-PAT are discussed. Last but not least, the fabrication of micro-nanocomposite layers and membranes are additional applications of CDC-PAT discussed in this work.

Interfacial Behavior of Particle-Laden Bubbles under Asymmetric Shear Flow.

The behavior of moving bubbles has mostly been studied in an axisymmetric flow field. To extend the knowledge to practical conditions, we investigate the interfacial and hydrodynamic properties of bubbles under asymmetric shear forces. Experiments are performed with a buoyant bubble at the tip of a capillary placed in a defined shear flow in the presence of surfactants, nanoparticles, and glass beads. The response of the interface to the surrounding asymmetric flow is measured under successive reduction of the surface area. Profile analysis tensiometry is utilized to investigate the dynamic surface tension and the surface rheology of the surfactant- and nanoparticle-laden interfaces. Microscopic particle image and tracking velocimetry are used to study the bulk flow and the interfacial mobility of the buoyant bubble. According to our results, the rotational component of the shear flow provokes an interfacial flow, which redistributes the adsorbed surfactants and particles at the interface. In the presence of NPSCs, a contiguous network of particles forms at the interface through densification of surface structures. We show that this interconnected nanoparticle network eventually stops the interfacial flow and decreases the mobility of the glass beads at the interface. The immobilization of the interface is characterized by a dimensionless number, defined as the ratio of the interfacial elasticity to bulk shear forces. This number provides an estimate of the interfacial forces required to impose interfacial immobility at a defined flow field. Our findings can serve as a basis to formulate boundary conditions for refined modeling and to predict the hydrodynamics of bubbles and droplets.

Enzymatic Hydrolysis of Triglycerides at the Water-Oil Interface Studied via Interfacial Rheology Analysis of Lipase Adsorption Layers.

The enzymatic hydrolysis of sunflower oil occurs at the water-oil interface. Therefore, the characterization of dynamic interfacial phenomena is essential for understanding the related mechanisms for process optimizations. Most of the available studies for this purpose deal with averaged interfacial properties determined via reaction kinetics and dynamic surface tension measurements. In addition to the classical approach for dynamic surface tension measurements, here, the evolution of the dilational viscoelasticity of the lipase adsorbed layer at the water-oil interface is characterized using profile analysis tensiometry. It is observed that lipase exhibits nonlinear dilational rheology depending on the concentration and age of the adsorbed layer. For reactive water-oil interfaces, the response of the interfacial tension to the sinusoidal area perturbations becomes more asymmetric with time. Surface-active products of the enzymatic hydrolysis of triglycerides render the interface less elastic during compression compared to the expansion path. The lipolysis products can facilitate desorption upon compression while inhibiting adsorption upon expansion of the interface. Lissajous plots provide an insight into how the hysteresis effect leads to different interfacial tensions along the expansion and compression routes. Also, the droplet shape increasingly deviates from a Laplacian shape, demonstrating an irreversible film formation during aging and ongoing hydrolysis reaction, which supports our findings via interfacial elasticity analysis.

Evolution of adsorbed layers of asphaltenes at oil-water interfaces: A novel experimental protocol.

HYPOTHESIS: Asphaltenes can form rigid interfacial films surrounding water droplets rendering water separation from crude oil sluggish. Therefore, the quantitative characterization of such complex film formation is of great importance. As the adsorbed layers of asphaltene illustrate crumpling under compression at certain conditions, the evolution process from soft to rigid states of the film can be evaluated considering standard deviations from Young-Laplace shape fitting. EXPERIMENTAL: In this study, novel experimental protocols are introduced to investigate the evolution of adsorbed asphaltene layer to a film of aggregates at model oil/water interface by means of dynamic interfacial tension (IFT) and dilational surface rheology measurements. In particular, the surface elasticity and standard deviation from the Young-Laplace shape fitting (YL-SD) are introduced as important indicators for the transformation of a regular asphaltene adsorbed layer to a film of aggregates. Different parameters affecting the film formation and stability, such as aging time, asphaltene concentration, and history of interfacial dynamics, are discussed and linked to emulsion stability. FINDINGS: It is shown for the first time that the standard deviation of drop profile fitting from the Young-Laplace equation can be used as a rigorous parameter to reveal the properties of the interfacial asphaltene film, which cannot be recognized by regular IFT measurements. Via this novel technique, it is revealed that the transformation of an asphaltene adsorbed layer to a rigid film depends not only on the asphaltene concentration but also on the aging time and the interfacial area perturbations. The results of this new method are supported by measurements of the dilational surface elasticity, which is known as an important parameter for the characterization of complex adsorbed layers, and further verified by an emulsion stability analysis.

Dynamics of Competitive Adsorption of Lipase and Ionic Surfactants at the Water-Air Interface.

Lipase is one of the most important enzymes playing a key role in many biological and chemical processes, in particular for fat hydrolysis in living systems and technological applications such as food production, medicine, and biodiesel production. As lipase is soluble in water, the major hydrolysis process occurs at the water-oil interface, where lipase can get in contact with the oil. To provide optimum conditions, the emulsification of the oil is essential to provide a large interfacial area which is generally done by adding surfactants. However, the presence of surfactants can influence the lipase activity and also cause competitive adsorption, resulting in a removal of lipase from the interface or its conformational changes in the solution bulk. Here we have studied the dynamics of competitive adsorption and interfacial elasticity of mixed solutions containing lipase and the anionic surfactant sodium dodecyl sulfate (SDS) or the cationic surfactant cetyltrimethylammonium bromide (CTAB), respectively, at the water-air interface. The experiments were performed with a special coaxial double capillary setup for drop bulk-interface exchange developed for the drop profile analysis tensiometer PAT with two protocols: sequential and simultaneous adsorption of single components and mixed systems. The results in terms of dynamic surface tension and dilational viscoelasticity illustrate fast and complete desorption of a preadsorbed CTAB and SDS layers via subphase exchange with a buffer solution. In contrast, the preadsorbed lipase layer cannot be removed either by SDS or CTAB from the interface during drop bulk exchange with a buffer solution due to the unfolding process and conformation evolution of the protein molecules at the interface. In the opposite case, lipase can remove preadsorbed SDS and CTAB. The dynamic surface tension and viscoelasticity data measured before and after subphase exchange show joint adsorption of lipase and CTAB in the form of complexes, while SDS is adsorbed in competition with lipase. The results are in good correlation with the determined surface charges of the lipase gained by computational simulations which show a dominant negatively charged surface for lipase that can interact with the cationic CTAB while partial positively charged regions are observed for the interaction with the anionic SDS.

The influence of negatively charged silica nanoparticles on the surface properties of anionic surfactants: electrostatic repulsion or the effect of ionic strength?

The presence of negatively charged nanoparticles affects the surface activity of anionic surfactants in an aqueous phase. Recent studies suggest that electrostatic repulsive forces play an important role in increasing the surface activity of surfactants. However, the addition of nanoparticles also increases the ionic strength of the system, which has a significant impact on the surfactant's properties, e.g. its critical micelle concentration (CMC). To investigate how and to what extent electrostatic forces and ionic strength influence the behavior of ionic surfactants, the surface tension and elasticity of different solutions were measured using drop profile tensiometry as a function of the surfactant (SDBS), nanoparticle (silica) and salt (KNO3) concentration. It is observed that the surface activity of the surfactants is mainly influenced by the change in the system's ionic strength due to the presence of nanoparticles. Several characteristic parameters including the equivalent concentration of the surfactant, the CMC and the apparent partial molar area of the adsorbed surfactant are theoretically calculated and further employed to validate experimental observations. Both the nanoparticles and electrolyte decrease the CMC, while the equivalent concentration of the surfactant remains nearly constant. This paper presents a criterion to estimate the possible influence of such forces for nanoparticles of different sizes and mass fractions.

Particular Behavior of Surface Tension at the Interface between Aqueous Solution of Surfactant and Alkane.

A two-component interfacial layer model was employed to describe the experimental results obtained for various surfactants. In contrast to the previous works, here it is shown that the adsorption activity of alkane depends on its interaction with the adsorbed surfactant and is proportional to the surface coverage by this surfactant. Also, it is assumed that this increase of the adsorption activity parameter is limited by some maximum value. This model provides a good description of the influence of hexane and dodecane, which results in the decrease of surface tension by 2-5 mN/m at very low surfactant concentrations. The adsorbed amounts of the surfactant and alkane molecules in this low surfactant concentration range have been calculated. The reorientation model of surfactant adsorption predicts a smaller number of alkane molecules per one surfactant molecule than that which follows from the Frumkin model.

Formation of Structured Membranes by Coacervation of Xanthan Gum with CnTAB Surfactants.

We present a novel approach for studying membrane formation by the interaction of polymers and surfactants with opposite charge using a Hele-Shaw experimental setup. A solution of the anionic biopolymer xanthan gum is placed in direct contact with a CnTAB surfactant solution (n = 10, 12, 14, and 16). Thereby, a polymer-surfactant membrane spontaneously forms between the two solutions due to the precipitation of polymer-surfactant complexes, which grows afterwards in the direction of the polymer solution. The dynamics of the growth of the membrane thickness and the mass transfer of polymer are evaluated for different surfactant types and concentrations. The experiments and supporting numerical calculations indicate that polymer mass transfer is driven by diffusion of the charged macromolecules along the concentration gradient, which is coupled to the electric field induced by the faster diffusion of the more mobile counterions. The properties and structure of the formed membrane significantly depend on the surfactant hydrophobicity and concentration. In addition, in a wide range of experiments, the formation of a porous structure in the membrane is observed whose characteristics can be tuned by the process parameters. A mechanism is proposed for the pore formation explaining it as an instability of the growing membrane surface in interaction with the supply of polymer across the depleted zone in the vicinity of the membrane front.

Synthesis and physicochemical properties of dual-responsive acrylic acid/butyl acrylate cross-linked nanogel systems.

HYPOTHESIS: A cross-linked amphiphilic nanogel containing a high mole% of hydrophilic pH-responsive moiety can provide enhanced functionality regarding stimuli-responsiveness, water-dispersibility, hydrophobic substance loading, and structural stability under harsh environmental conditions. These nanogels could be synthesized using a one-pot procedure for large-scale applications. Moreover, the interplay of various interaction forces in these colloidal systems is being investigated. EXPERIMENTS: Model nanogels consisting of acrylic acid-butyl acrylate-ethylene glycoldimethacrylate were synthesized using an emulsion copolymerization via a seeded semi-batch process under an acidic condition. The structures were assessed by Fourier transform infrared spectroscopy and potentiometric-conductometric titrations. Zeta potential, field-emission scanning electron microscopy, and transmission electron microscopy were used to evaluate the dispersion stability, size distribution, and structural distribution, respectively. Their stimuli-responsive behavior was studied by combining static and dynamic light scattering and titration analyses. FINDINGS: Monodisperse nanospheres of approximately 150 nm were successfully prepared by implementing a one-pot practical pathway. These nanogels displayed a dual thermo- and pH-responsive behavior, reflecting the high efficiency of physical cross-linking make it ideal for drug delivery and oil industry applications. Moreover, a novel symmetric pH-activated morphology transformation behavior was revealed. Accordingly, a compositional distribution was proposed and assessed by exploring the polymerization process.

Influence of hydrophilic silica nanoparticles on the adsorption layer properties of non-ionic surfactants at water/heptane interface.

There is a notable paucity of studies investigating the impact of charged nanoparticles on the interfacial behavior of nonionic surfactants, assuming that the interactions are negligible in the absence of electrostatic forces. Here, we argue about our observations and the existence of a complex interfacial behavior in such systems depending on the type and chemical structure of surfactant. This study set out to investigate the effects of interactions between hydrophilic silica nanoparticles (NP) and non-ionic surfactants on water/heptane dynamic interfacial properties using drop profile analysis tensiometry (PAT). Three surfactants were studied, namely Triton X-100 (significantly soluble in water phase), C12DMPO (well soluble in both phases) and SPAN 80 (oil-soluble). The different chemical structures and partition coefficients of the surfactants enabled us to cover possible interactions and differentiate between bulk and interfacial interactions. We observed that hydrophilic silica NPs had a negligible effect on the interfacial behavior of Triton X-100, that they increased the surface activity of C12DMPO when both compounds are initially in the aqueous phase. Most interestingly is that the added NPs generated unstable interfacial NP-surfactant complexes and reduced the pseudo-equilibrium interfacial tension of oil-soluble surfactant, Span 80, even though NPs and surfactants were in different bulk phases.

The Role of Electrostatic Repulsion on Increasing Surface Activity of Anionic Surfactants in the Presence of Hydrophilic Silica Nanoparticles.

Hydrophilic silica nanoparticles alone are not surface active. They, however, develop a strong electrostatic interaction with ionic surfactants and consequently affect their surface behavior. We report the interfacial behavior of n-heptane/anionic-surfactant-solutions in the presence of hydrophilic silica nanoparticles. The surfactants are sodium dodecyl sulfate (SDS) and dodecyl benzene sulfonic acid (DBSA), and the diameters of the used particles are 9 and 30 nm. Using experimental tensiometry, we show that nanoparticles retain their non-surface-active nature in the presence of surfactants and the surface activity of surfactant directly increases with the concentration of nanoparticles. This fact was attributed to the electrostatic repulsive interaction between the negatively charged nanoparticles and the anionic surfactant molecules. The role of electrostatic repulsion on increasing surface activity of the surfactant has been discussed. Further investigations have been performed for screening the double layer charge of the nanoparticles in the presence of salt. Moreover, the hydrolysis of SDS molecules in the presence of silica nanoparticles and the interaction of nanoparticles with SDS inherent impurities have been studied. According to our experimental observations, silica nanoparticles alleviate the effects of dodecanol, formed by SDS hydrolysis, on the interfacial properties of SDS solution.

Adsorption of ß-casein-surfactant mixed layers at the air-water interface evaluated by interfacial rheology.

This work presents a detailed study of the dilational viscoelastic moduli of the adsorption layers of the milk protein ß-casein (BCS) and a surfactant at the liquid/air interface, over a broad frequency range. Two complementary techniques have been used: a drop profile tensiometry technique and an excited capillary wave method, ECW. Two different surfactants were studied: the nonionic dodecyldimethylphosphine oxide (C12DMPO) and the cationic dodecyltrimethylammonium bromide (DoTAB). The interfacial dilational elasticity and viscosity are very sensitive to the composition of protein-surfactant mixed adsorption layers at the air/water interface. Two different dynamic processes have been observed for the two systems studied, whose characteristic frequencies are close to 0.01 and 100 Hz. In both systems, the surface elasticity was found to show a maximum when plotted versus the surfactant concentration. However, at frequencies above 50 Hz the surface elasticity of BCS + C12DMPO is higher than the one of the aqueous BCS solution over most of the surfactant concentration range, whereas for the BCS + DoTAB it is smaller for high surfactant concentrations and higher at low concentrations. The BCS-surfactant interaction modifies the BCS random coil structure via electrostatic and/or hydrophobic interactions, leading to a competitive adsorption of the BCS-surfactant complexes with the free, unbound surfactant molecules. Increasing the surfactant concentration decreases the adsorbed proteins. However, the BCS molecules are rather strongly bound to the interface due to their large adsorption energy. The results have been fitted to the model proposed by C. Kotsmar et al. ( J. Phys. Chem. B 2009 , 113 , 103 ). Even though the model describes well the concentration dependence of the limiting elasticity, it does not properly describe its frequency dependence.

Characterisation of alkyl amines at the water/air surface with the drop and bubble profile analysis tensiometry.

Pendant drop and buoyant bubble methods have been used to study the surface characteristics of alkyl amines at the water/air surface. The investigated alkyl amines, triethylamine and octylamine, showed unusual changes in the surface tension as a function of time: an initially steep drop and a subsequent steady increase in the surface tension until a value close to the one of the pure water/air system was observed. This phenomenon is explained by the evaporation of the alkyl amines, for which several sets of experiments have been conducted with the pendant drop and buoyant bubble methods. Using an appropriate experimental protocol, the equilibrium adsorption behaviour of the two amines can be quantitatively measured.