Currently there are no available methods for in-line measurement of gas-liquid interfacial tension during the flotation process. Microfluidic devices have the potential to be deployed in such settings to allow for a rapid in-line determination of the interfacial tension, and hence provide information on frother concentration. This paper presents the development of a simple method for interfacial tension determination based on a microfluidic device with a flow-focusing geometry. The bubble generation frequency in such a microfluidic device is correlated with the concentration of two flotation frothers (characterized by very different adsorption kinetic behavior). The results are compared with the equilibrium interfacial tension values determined using classical profile analysis tensiometry. Full article

In mixed solutions of anionic and cationic surfactants, called catanionics, ion pairs are formed which behave like non-ionic surfactants with a much higher surface activity than the single components. In equimolar mixtures of NaC_nSO₄ and C_mTAB, all surface-active ions are paired. For mixtures with n + m = const, the interfacial properties are rather similar. Catanionics containing one long-chain surfactant and one surfactant with medium chain length exhibit a strong increase in surface activity as compared with the single compounds. In contrast, catanionics of one medium- and one short chain surfactant have a surface activity similar to that of the medium-chain surfactant alone. Both the Frumkin model and the reorientation model describe the experimental equilibrium data equally well, while the adsorption kinetics of the mixed medium- and short-chain surfactants can be well described only with the reorientation model. Full article

Nowadays, the search for and development of new forms of materials with biocides is an actual problem of the modern science of nanosized materials due to the problem of microbiological contamination, which can be solved by using nanocontainers carrying biocides. Depending on the morphology of the nanocontainers and the filled active agents, it is possible to create coatings with specially designed self-healing functionality or multifunctional properties. The purpose of this work was to produce submicro-containers (SMCs) with a shell of SiO₂ nanoparticles and a core of polymerized 3-(trimethoxysilyl) propyl methacrylate filled with 5-dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT) in an oil in water (O/W) emulsion. The chemical nature of the individual components of the system and nano-capsules were investigated using NMR spectroscopy. The size and zeta potential of the SMCs were measured by a dynamic light scattering method (d = 170–180 nm, polydispersity index PDI = 0.125 and zeta-potential = 55 mV), the morphology of their outer surface was determined using SEM. The results of NMR analysis showed that during the addition of the biocide into the SMCs, its chemical structure is retained, as is its activity. Minor changes in the chemical shifts of the ¹H NMR spectra of the SMCs with DCOIT, as well as of the biocide itself, confirm the inclusion of DCOIT inside the SMCs. Full article

We investigate the equilibrium orientation and adsorption process of a single, ellipsoidal Janus particle at a fluid–fluid interface. The particle surface comprises equally sized parts that are hydrophobic or hydrophilic. We present free energy models to predict the equilibrium orientation and compare the theoretical predictions with lattice Boltzmann simulations. We find that the deformation of the fluid interface strongly influences the equilibrium orientation of the Janus ellipsoid. The adsorption process of the Janus ellipsoid can lead to different final orientations determined by the interplay of particle aspect ratio and particle wettablity contrast. Full article

Aqueous mixtures of cationic hexadecyltrimethylammonium chloride (CTAC) and nonionic pentaethyleneglycol monododecyl ether (C₁₂E₅) are investigated. Adsorption layer properties are systematically studied within a wide concentration range for a 1:1 molar ratio of the surfactants. Surface tension and dilatational rheology measurements are conducted by profile analysis tensiometry. The interfacial data are juxtaposed to drainage kinetics and stability results for microscopic foam films, investigated by microinterferometric thin liquid film instrumentation. The obtained results give experimental evidence of synergistic interactions in the studied solutions, as compared to the corresponding single surfactant systems. Specific runs of dynamic and equilibrium surface tension curves are registered against the total surfactant quantity; the surface dilatational elasticities for the mixtures are systematically higher. A clear correlation is established between adsorption layer performance and foam film characteristics. The maxima of the film lifetimes are well outlined, and the respective values are shifted towards lower overall concentrations. The reported results substantiate the key role of the adsorption layers, and the surface dilatational properties in particular, for foam film drainage kinetics and stability. The well-expressed synergy observed in adsorption layer and foam film properties suggests the substantial benefits of using mixed surfactant systems in the design and fine-tuning of foam systems for innovative applications. Full article

In this work, the wetting and evaporation behaviour of non-polar solvent droplets on thin soluble coatings is investigated experimentally. The wetting process on spin-coated polymer layers by toluene is captured using shadowgraphy. Initial spontaneous dynamic wetting as well as later stages of wetting are recorded and evaluated. Furthermore, structures obtained by wetting and subsequent evaporation of solvents on polymer coatings are studied by confocal microscopy. The solubility of the substrate has been varied by using polymers with different molecular masses. We observe that initial spreading dynamics does not depend on the molar mass in the studied range. However, we find a strong influence of the molar mass on the late stage wetting dynamics and on the surface structure after solvent evaporation. Full article

The present work aims to shed light on recent literature reports suggesting that ionic species are implicated in the electrical conductivity of 1-octanol and its mixtures with hydrocarbons. Other workers have questioned this interpretation, and herein, based on new experimentation and with reference to various literature studies, we consider that molecular interactions are more likely to be responsible. To investigate this, we have studied mixtures of 1-octanol and either silicone oil (SO) or n-dodecane as nonpolar components, using dielectric (in particular electrical conductivity) and viscometric measurements. With reference to the literature, the self-association of alcohols is known to create microheterogeneity in the neat liquids and in mixtures with nonpolar, low dielectric constant liquids, and it has previously been considered to be responsible for the particular solvent properties of alcohols. The present results suggest that the electrical conductivity of alkane/alcohol systems may have similar origins, with percolating pathways formed from octanol-rich nanodomains comprising polar regions containing hydrogen-bonded hydroxyl groups and nonpolar regions dominated by alkyl chains. The percolation threshold found for dodecane/octanol mixtures, in which interactions between the component molecules are found from viscosity measurements to be repulsive, agrees well with results from experimental and theoretical studies of disordered arrangements of packed spheres, and moreover, it is consistent with other published alkane/alcohol results. On the other hand, the situation is more complex for SO/octanol mixtures, in which interactions between the two components are attractive, based on viscosity data, and in which the phase separation of SO occurs at high octanol concentrations. Overall, we have concluded that electrical conductivity in octanol (and potentially all liquid alcohols) and its mixtures with nonpolar molecules, such as alkanes, is consistent with the presence of conducting networks comprising octanol-rich nanodomains formed by self-association, and not as a result of ionic conduction. Full article

It was reported in many papers that the magnetic field (MF) affects properties of water, and, among others, its surface tension. Thus, it should be reflected in changes of the wetting contact angle of a water droplet deposited on the solid surface. In this study, the water contact angles were measured on the glass and mica surface. The water was first exposed to the static magnetic field (MF) (15 mT or 0.27 T) for 1, 5, and 10 min under dynamic conditions. Then applying the van Oss et al. approach (LWAB), it was found that the MF effect is reflected in the changes of the calculated acid-base components of the solids, especially the electron donor parameter. However, the total surface free energy of the solids remained practically unchanged. Moreover, the apparent surface free energy of the solids calculated from the water contact angle hysteresis (CAH), i.e., the difference between the advancing and receding contact angles, changes in the same way as the electron donor parameter does. Since the solid surfaces were not magnetically treated, the acid-base components, which are mainly results from hydrogen bonding interactions, may be indirect evidence of the water structure changed by the MF action. All of the mentioned changes are greater for the glass than for a more hydrophilic mica surface and depend upon the time of MF exposure and its strength. The magnetic field effect on the changes of the surface-free energy parameters for the mica and glass is opposite what may be due to the difference in the surface hydrophilicity. A “magnetic memory” effect was also found. The effect of MF on the water surface tension depends on the circulation time. It increases with the field duration. Moreover, the changes in the work of water adhesion indicate the possibility of solid surface wettability changes by the external MF water treatment. However, these are preliminary results that need further confirmation by other techniques. Full article

The properties of binary colloidal systems have gained the interest of researchers because they have much richer structures than their one-component counterpart. Continuing efforts are being made on the theoretical side on binary colloidal systems, while many issues remained unsolved for the lack of solid experimental supports, especially for study in the field of two-dimensional (2D) binary colloids system. Oil–water interfaces can serve as a good stringent 2D confinement for colloidal particles and can avoid anomalous problems caused by the quasi-two-dimensional environment in previous experimental reports. In this work, we conduct experimental research of binary colloids system in an oil–water interface to revisit theoretical predication. We measure an ultra-long-range attraction and discuss the possible mechanism of this attraction by comparing the experimental result with existing model and theory. This study could contribute more understanding of the binary colloidal system in both experimental aspects and theoretical aspects. Full article

In view of emerging research on forced wetting under complex applied forces, a simple model for a droplet shape evolution is developed here. In particular, the model refers to droplet spreading under quasisteady conditions. The corresponding linearized two-dimensional Young–Laplace equation is solved analytically resulting in a system of two equations that relates the droplet shape features to each other. Despite its simplicity, the final model produces a wealth of droplet behaviors when combined with the physical requirement that the contact angle should be within a particular range of values. Indicative results of the droplet behavior under several forces scenarios are examined here exhibiting why the present model is useful for designing experimental campaigns on forced spreading. Full article

The deposition of layers of different polycations (synthetic or derived from natural, renewable resources) onto oppositely charged surfaces has been studied using ellipsometry and quartz crystal microbalance with dissipation monitoring (QCM-D). Information about the thickness of the deposited layers and their water content was ascertained. The adsorption of the different polycations onto negatively charged surfaces was found to be a complex process, which is influenced by the chemical nature of the polymer chains, ionic strength, polymer concentration and the addition of additives such as surfactants. The experimental picture shows a good agreement with theoretical calculations performed using the Self-Consistent Mean Field (SCF) approach. The results show that the electrostatically-driven deposition can be tuned by modifying the physico-chemical properties of the solutions and the chemical nature of the adsorbed polymer. This versatile approach is a big step forward in aiding the design of new polymers for many industrial applications and, in particular, the design of sustainable washing formulations for cosmetic applications. Full article

During the past 20 years, polymer flooding has become a successful enhanced oil recovery (EOR) technique for mature reservoirs with high water cut and recovery percent around the world. However, the high bulk viscosity of polymer solutions could slow down the separation rate of the crude oil emulsion and make it difficult to treat the produced fluid. Consequently, the efficient removal of oil from the polymer flooding produced sewerage has still drawn significant concern. In this research, a high flux super-hydrophobic copper mesh was prepared using two-stage processes to treat the sewerage from polymer flooding. The surface of the super-hydrophobic mesh was characterized using various techniques including scanning electron microscope (SEM), OCA 20-contact angle goniometer, etc. Accordingly, the static contact angle of the super-hydrophobic copper mesh reached up to 165°. Moreover, the performances of the mesh were systematically evaluated under different internal and external factors such as oil to water volume ratio, polymer concentration, shear rate, and pH. The corresponding configuration and separation mechanisms are further explained in detail. The prepared superhydrophobic mesh can be a potential candidate for sewerage with both a polymer solution and crude oil. Full article

A theory of the amount of foam produced by compression/decompression cycles of a soft porous media is developed. The amount of foam produced was found to be dependent on both the amount of surfactant within the media and the minimum separation between the plates of the compression device. The latter is determined by the mechanical properties of the soft media. The theory also shows the importance of the decompression of the media as this is the mechanism of where the air penetrates into the soft porous material. The accumulated air is used during the compression stage for foam formation. The theoretically predicted values of foam mass are found to have good agreement with experimental observations, which validates the theory predictions. The theory also predicts independence of the foam produced in terms of the frequency of compression/decompression cycles, which agrees with our experimental observations. Full article

Surface tension experiments were performed using the drop profile analysis tensiometry method. The hexane was injected into the measuring cell at certain times before the formation of the solution drop. The influence of the capillary diameter and solution drop size on the measured apparent dynamic surface tension was studied. The amount of hexane transferred from the vapor phase to the drop was estimated. For large pure water drops, it was shown that the ageing of the drop in the hexane vapor during a long time resulted in the formation of a liquid hexane phase covering the drop, but the volume of this phase did not exceed 0.5 mm³. On the contrary, for surfactant solution drops the volume of the hexane phase covering the drop was essentially larger. Experiments with solution drops were performed to measure the surface tension within a wide range of surfactant concentration. It was found that the dependencies of dynamic surface tension on the C₁₃DMPO and C₁₄EO₈ solutions concentration exhibit maxima at concentrations of about 1–2 μmol/L for C₁₄EO₈ and 2–5 μmol/L for C₁₃DMPO at ageing times of 100 to 1000 s; these maxima were shown to exist also at equilibrium. This phenomenon is presumably ascribed to the competitive character of simultaneous adsorption of hexane and surfactant. Full article

In this study, water-in-extra virgin olive oil emulsions were enriched with vitamins. Water-in oil emulsions are heterogeneous systems able to solubilize both hydrophilic and hydrophobic compounds. Thus, hydrophilic vitamin C and lipophilic vitamin E were loaded separately or together in emulsion. A suitable emulsion composition was selected after considering different surfactant (mono and diglycerides of fatty acids, E471; sorbitan monooleate, Span 80; polyoxyethylene sorbitan monooleate, Tween 80) and water concentrations. The most appropriate emulsion, for the high stability, resulted the one containing concentrations of Span 80 1% w/w and water 1% w/w. The antioxidant effect of vitamins in emulsions was studied considering the variation of the peroxide values during storage. The oxidation reaction was slowed down in emulsions containing vitamin C, but it was quickened by the loading of vitamin E for its high concentration. In emulsions containing vitamin E, indeed, the peroxide values were higher than in emulsions prepared in the absence of vitamins or in oil. The antioxidant activity generated by the co-loading of vitamin C and E was very effective to the point that in presence of high amounts of vitamins the peroxide values did not change in about 40 days of storage, due to the vitamin E regeneration by vitamin C. Full article

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. Full article