Surface Tension Research Articles

Innovations and Insights in Superhydrophobicity: Learning from Nature to Surpass It

Abstract. Superhydrophobic surfaces, inspired by natural examples, have emerged as a promising area of research due to their unique properties. This paper reviews the characteristics and challenges of creating surfaces that can exceed the capabilities of natural counterparts. Key aspects include surface tension, contact angle, and morphology, with a focus on natural models such as lotus leaves and gecko feet. The paper highlights knowledge gaps in durability and manufacturing, and discusses design challenges in achieving roughness, hierarchy, and balance between hydrophobicity and durability. Methods for enhancing durability, such as chemical and roughness restoration, are explored, alongside the potential of AI in optimizing material and design choices. The paper concludes with recommendations for future research directions in the field.

Direct numerical simulation of bubble rising in turbulence

We describe the rising trajectory of bubbles in isotropic turbulence and quantify the slowdown of the mean rise velocity of bubbles with sizes within the inertial subrange. We perform direct numerical simulations of bubbles, for a wide range of turbulence intensity, bubble inertia and deformability, with systematic comparison with the corresponding quiescent case, with Reynolds number at the Taylor microscale from 38 to 77. Turbulent fluctuations randomise the rising trajectory and cause a reduction of the mean rise velocity $\tilde {w}_b$ compared with the rise velocity in quiescent flow $w_b$ . The decrease in mean rise velocity of bubbles $\tilde {w}_b/w_b$ is shown to be primarily a function of the ratio of the turbulence intensity and the buoyancy forces, described by the Froude number $Fr=u'/\sqrt {gd}$ , where $u'$ is the root-mean-square velocity fluctuations, $g$ is gravity and $d$ is the bubble diameter. The bubble inertia, characterised by the ratio of inertial to viscous forces (Galileo number), and the bubble deformability, characterised by the ratio of buoyancy forces to surface tension (Bond number), modulate the rise trajectory and velocity in quiescent fluid. The slowdown of these bubbles in the inertial subrange is not due to preferential sampling, as is the case with sub-Kolmogorov bubbles. Instead, it is caused by the nonlinear drag–velocity relationship, where velocity fluctuations lead to an increased average drag. For $Fr > 0.5$ , we confirm the scaling $\tilde {w}_b / w_b \propto 1 / Fr$ , as proposed previously by Ruth et al. (J. Fluid Mech., vol. 924, 2021, p. A2), over a wide range of bubble inertia and deformability.

Ion-Specific Surface Tension of Aqueous Electrolyte Solutions: Analytical Insights from a Restricted Primitive Model.

The ion-specific surface tension of aqueous electrolyte solutions is of fundamental importance in physical chemistry, solution chemistry, electrochemistry, and biochemistry, yet it remains a challenge to be qualitatively predicted. In this work, an analytical theory of ion-specific surface tension is developed. By modeling the solution to a restricted primitive model (RPM), the surface tension increment of the electrolyte solution reduces to the surface tension of the RPM, which is further determined analytically by using the integral equation theory and the morphological thermodynamics theory. According to our formula, the surface tension increment of the electrolyte solution consists of a dominant and positive hard sphere contribution, which depends on the salt concentration, and a secondary electrostatic contribution, which depends on the inverse Debye length and the salt concentration. Our theory is applied to 1:1, 2:2, 1:2, 2:1, 3:1, and 3:2 electrolyte solutions with typical salt concentrations up to several mol/L and compared with experimental data. Without introducing any adjustable parameters, our theory leads to a good prediction of the surface tension increment of more than 50 kinds of aqueous solutions. Such a good agreement demonstrates the great potential of our theory for a fundamental understanding of specific ion effects in a variety of electrolyte solutions.

Antifeedant Nanosuspension Formula of <i>Tithonia diversifolia</i> Leaf Extract by Emulsion Inverse Method to Control <i>Crocidolomia pavonana</i> Cabbage Pest Insect

The leaf extract from Tithonia diversifolia is recognized for its ability to deter feeding in various Lepidoptera insect pests, including the larvae of Crocidolomia pavonana. Presently, transformation efforts from conventional formulations into nano-based formulations for biopesticides exhibit enhanced effectiveness and efficiency. Utilizing a low-energy process, an inversion emulsion facilitates the dispersion of the extract suspension in an organic solvent into a water-immiscible solvent using a suitable surfactant. The forming nano-size droplets in water (t1, t2, t3, t4) are influenced by the ratio of surfactant and organic suspension (Water: Tween 80: Organic suspension). The emulsification method successfully formulated T. diversifolia leaf extract, into dispersed nano-size and submicron suspensions in water. The t3 formula exhibits the smallest nano-size dispersed in water (D=23.6 ± 39.6 nm; polydispersity index IP=0.702) and enhanced wettability, evident in the lower contact angle of the droplet on the cabbage leaf surface (49.4°) compare with the control group. The Phytochemicals confirmed by IR-spectra analysis identified the phenols, alkaloids, and steroids constituents of leaf extract, which are known to have antifeedant properties. The enhanced antifeedant properties of T. diversifolia nanosuspension against C. pavonana third-instar larvae demonstrated by the antifeedant test results showing that t3 is the most successful deterrent larvae feeding activity compared to the control (P<0.05), due to the highest total antifeedant coefficient (74.27%) in a category medium antifeedant activity, while the non-emulsification displayed the lowest antifeedant coefficient (25.36%) in a category as low antifeedant activity. T. diversifolia leaf extract with a nano-based formula succeeded resulting in dispersed nano-size and submicron suspension in aqueous media, thereby reducing surface tension and enhancing wettability on the leaf surface during application. The improved dispersion of antifeedant nanosuspension on the leaf surface results in more effective delivery to target insects.

Soft Artificial Muscle of Poly(vinyl chloride) Gel with an Imperceptible Liquid Metal Electrode.

Electrodes with high electrical conductivity, yet good flexibility and mechanical compliance, are critical for electroactive artificial muscles. Herein, a promising liquid metal (LM) electrode is proposed by transforming eutectic gallium-indium (EGaIn) LM with high surface tension into paste-like LM with solid Ga2O3 shells. The developed compliant LM electrode not only shows high conductivity and negligible additional stiffness but also displays excellent electrical stability during cyclic actuation. Based on the LM electrode, the poly(vinyl chloride) gel (PVCG) artificial muscle developed exhibits the maximum actuation strain of 18.7% at a low electric field strength of 9 V μm-1 and maintains excellent durability without obvious performance attenuation after 10,000 s. A comparison shows that the as-developed PVCG artificial muscle is superior over that based on widely used carbon electrodes. Moreover, an artificial upper limb and crawling worm were manufactured to explore the great potential of PVCG artificial muscle in the robotic field. In addition, the practical application demonstration of the PVCG artificial muscle in the biomimetics field is also successfully fulfilled through the design of reasonable structures. Due to its easy fabrication, excellent electrical conductivity, and high mechanical compliance, the newly developed LM electrode is promising for high-performance PVCG artificial muscles in bionic robots.

Insights into surrogate respiratory droplet behaviour on inclined surfaces: Implications for disease transmission

Disease transmission via fluid ejections from infected individuals presents a significant public health challenge. The ejected droplet frequently lands on substrates with varying orientations, including horizontal, vertical, and inclined. However, the behaviour of disease-causing droplets on inclined substrates remains unexplored. Recent research has demonstrated that droplet evaporation, flow, and colloidal deposition are significantly altered when surfaces are inclined. Changes in contact angle impact evaporative flux and induce flow between the top and bottom edges of the droplet. This study examines the behaviour of simulated respiratory droplets containing NaCl, mucin, and micrometer-sized particles as pathogen surrogates, focusing on substrate inclinations of 0°, 45°, and 90° on glass surfaces. As respiratory droplets evaporate, their solute concentration rises, altering both surface tension and viscosity. The study explores the coupled effects of solute concentration variations and asymmetric evaporative flux at varying relative humidity conditions and droplet volumes. The presence of salt and mucin induces Marangoni flow, potentially altering evaporation, flow patterns, and deposition dynamics. Additionally, sedimentation flow influences crystal nucleation sites and precipitation patterns. Results reveal unprecedented crystallization dynamics on inclined substrates, with notable differences in nucleation and growth based on the angle of inclination. Optical profilometry and confocal microscopy further show that surrogate bacterial particles accumulate excessively at the bottom edge of inclined droplets, suggesting an elevated risk of pathogen survival on inclined fomites. These findings highlight the critical importance of considering substrate orientation in understanding the transmission of disease through surface-bound droplets, offering insights that could inform public health strategies.

Organosilane Modification of Lignin and Lignosulfonate: Structure and Compatibility in PVDF Membrane

The high difference in surface tension between the filler and the polymer often constrains membrane compatibility. To reduce the surface tension, organosilane such as GPTMS is usually used to improve miscibility. In this study, GPTMS was introduced to produce lignin-GPTMS (LG) and lignosulfonate-GPTMS (LsG). The modification was done by reacting lignin and lignosulfonate with GPTMS using ethanol as the media. The product was characterized using Fourier Transform InfraRed (FTIR), X-ray Diffraction (XRD), Particle Size Analyzer (PSA), Scanning Electron Microscope-Energy Dispersive X-ray (SEM-EDX) and microscope. The success of functionalization was shown in FTIR spectra with the vibration of Si-O at 1034 cm-1 and 528 cm-1. The XRD analysis presents that the filler material has an amorph and crystalline structure. The functionalization using a 2:1 ratio increases zeta potential absolute and particle size due to the silane being a bridge and making a larger macromolecule. For a ratio of 1:1, a higher organosilane compound results in breaking siloxane linkages and making smaller molecules. Mixed LG and LsG into PVDF membrane conducted to analyze filler compatibility. The sulfonation and functionalization of GPTMS increase the compatibility of lignin in PVDF membrane with the best homogeneity achieved by a membrane with the addition of LsG 1:1.

Orientational Disorder of Alcohol Molecules at Their Solution Surfaces in Low Concentration Range: A Molecular Dynamics Simulation Study.

Molecular dynamics (MD) simulations of short-chain alcohols (methanol, ethanol, and 1-propanol) in solution were carried out to examine the orientational disordering (randomizing) of alcohol molecules at the surface under diluted conditions. Recent vibrational sum frequency generation (VSFG) spectroscopy, combined with photoelectron spectroscopy, has successfully measured the disordering structure at low concentrations. The present MD simulations accurately reproduce this observation for the first time. To ensure reliable results through MD simulations, several widely used force field models for water and alcohol, including polarizable models, were examined. This examination involved a comparison of structural and thermodynamic quantities, such as surface density times orientation and surface excess concentration, which were obtained through surface-specific measurements like VSFG spectroscopy and surface tension measurements. It is found that the width of the density profile for alcohol molecules at the surface, along the surface normal, increases as the concentration decreases in the diluted condition, which is consistent with the results obtained from the previous neutron and X-ray grazing incidence reflection experiments. A molecular mechanism explaining the disordering of alcohol molecules with decreasing concentration is also discussed.

Investigation of Surface Tension of Isobutane (R600a) and Isobutane–Hydrogen Solutions

Investigation of Surface Tension of Isobutane (R600a) and Isobutane–Hydrogen Solutions

Modeling for formation of microdroplets prepared by pulsated orifice ejection method

Abstract This study investigated the preparation of metallic microdroplets by pulsed orifice ejection method. Computational fluid dynamics simulations, combined with volume-of-fluid model, were employed to analyze the jet break-up and droplet formation behaviors of various metallic materials within a certain Weber number (We) range. An energy-based physical model under inlet boundary conditions was established to precisely control the generation of droplets. The results indicate that the break-up state of metal jets is significantly influenced by material properties within the range that We = 12 ∼ 24, which makes the materials exhibiting higher surface tension and density relatively favorable to the production of mono-sized microdroplets. Moreover, the break-up behavior of the jet is closely related to the ratio of volume force to surface tension (Bond number). And the proposed model effectively predicts the properties of droplets. This research provides theoretical guidance and technical support for the precise preparation of metallic microdroplets.

Laser-induced thermo-compression bonding for Cu–Au heterogeneous nanojoining

Abstract Surface tension-induced shrinkage of heterogeneously bonded interfaces is a key factor in limiting the performance of nanostructures. Herein, we demonstrate a laser-induced thermo-compression bonding technology to suppress surface tension-induced shrinkage of Cu–Au bonded interface. A focused laser beam is used to apply localized heating and scattering force to the exposed Cu nanowire. The laser-induced scattering force and the heating can be adjusted by regulating the exposure intensity. When the ratio of scattering forces to the gravity of the exposed nanowire reaches 3.6 × 103, the molten Cu nanowire is compressed into flattened shape rather than shrinking into nanosphere by the surface tension. As a result, the Cu–Au bonding interface is broadened fourfold by the scattering force, leading to a reduction in contact resistance of approximately 56%. This noncontact thermo-compression bonding technology provides significant possibilities for the interconnect packaging and integration of nanodevices.

Thermodynamic Evaluation of Novel 1,2,4-Triazolium Alanine Ionic Liquids as Sustainable Heat-Transfer Media

Ionic liquids, which are widely recognized as environmentally friendly solvents, stand out as promising alternatives to traditional heat-transfer fluids due to their outstanding heat-storage and heat-transfer capabilities. In the course of our ongoing research, we successfully synthesized ionic liquids 1-ethyl-4-alkyl-1,2,4-triazolium alanine [Taz(2,n)][Ala], where (n = 4, 5); in this study, we present comprehensive data on their density, surface tension, isobaric molar heat capacity, and thermal conductivity for the first time. The key thermophysical parameters influencing the heat-transfer process, such as thermal expansibility, compressibility, isochoric heat capacity, and heat-storage density, were meticulously calculated from experimental data. Upon comparison with previously reported ionic liquids and commercially utilized heat-transfer fluids, [Taz(2,n)][Ala] demonstrated superior heat-storage and heat-transfer performance, particularly in terms of heat-storage density (~2.63 MJ·m−3·K−1), thermal conductivity (~0.190 W·m−1·K−1), and melting temperature (~226 K). Additionally, the presence of the alanine anion in [Taz(2,n)][Ala] provides more possibilities for its functional application.

Bubble Drainage Assisted Fabrication of Polyamide Membranes with Crater-like Structures for Efficient Desalination.

Bubble drainage (BD) occurs in various natural phenomena and industrial activities, in which bubbles rise toward the water surface and create a progressively thinned two-sided liquid film, called a lamella. Surfactant, as an important regulator in the BD process, not only assembles on both sides of the lamellae, generating a configuration of lamellae sandwiched by monolayers of surfactants (lamellae/MS), but also induces interfacial deformation by lowering interfacial tension. Herein, we developed a strategy of BD assisted interfacial polymerization for the fabrication of polyamide (PA) membranes. The regulated interfacial deformation at the water-oil interface produced a membrane with crater-like structures, which greatly increased the surface area of the PA membrane. Moreover, the lamellae/MS configuration served as a reservoir to spontaneously enrich amine monomers and thus modulate the diffusion-reaction kinetics. The resulting PA membranes exhibited superior separation performance with a water permeance of 44.7 L m-2 h-1 bar-1 and a Na2SO4 rejection of 99.2%.

Production and characterization of biosurfactants from lactic acid bacteria in Dadiah for strawberries edible coating

Biosurfactants are amphiphilic components applied in various fields, one of which is preserving agricultural products. Biosurfactants can be used as additives in edible coatings to prevent microbial adhesion by reducing surface tension on the fruit surface. They also play a role in increasing the moisture barrier and slowing down the physiological changes of fruit. Nonetheless, biosurfactants were often produced by non-GRAS bacteria. GRAS biosurfactant-producing bacteria are urgently needed for application in food products. This study aims to isolate and characterize biosurfactant-producing strains of lactic acid bacteria from Dadiah and evaluate their efficacy in reducing microbial adhesion on strawberries. From four selected isolates found in Dadiah, Lactiplantibacillus plantarum was the best candidate, producing biosurfactant with index emulsification (EI24) of 64.48 ± 0.37% with a CMC of 1 g/l. LC-MS and FT-IR characterized the biosurfactants as glycolipids. The rate of antibacterial and anti-adhesive tests on Escherichia coli ATCC 8739 were 18.79 ± 5.23% and 55.26 ± 0.02%, while on Staphylococcus aureus ATCC 6738 were 31.60 ± 2.63% and 74.63 ± 0.00% at a concentration of 3000 mg/l. However, no anti-fungal activity against Rhizopus stolonifer and Aspergillus niger was observed at the same concentration. Compared to SDS, biosurfactants demonstrated non-toxicity with an LC50 value of 2.94 x 108 mg/l. A combination of 1% chitosan reduced the number of fungal cells by 29.76 ± 3.25% on 125 mg/l biosurfactant and bacterial cells by 31.91 ± 5.06% on 1000 mg/l biosurfactant after 10 days, indicating their potential to reduce fruit spoilage and enhance microbial anti-adhesive properties of edible coatings.

Nonylphenol and Cetyl Alcohol Polyethoxylates Disrupt Thyroid Hormone Receptor Signaling to Disrupt Metabolic Health.

Surfactants are molecules with both hydrophobic and hydrophilic structural groups that adsorb at the air-water or oil-water interface and serve to decrease the surface tension. Surfactants combine to form micelles that surround and break down or remove oils, making them ideal for detergents and cleaners. Two of the most important classes of nonionic surfactants are alkylphenol ethoxylates (APEOs) and alcohol ethoxylates (AEOs). APEOs and AEOs are high production-volume chemicals that are used for many industrial and residential purposes, including laundry detergents, hard-surface cleaners, paints, and pesticide adjuvants. Commensurate with better appreciation of the toxicity of APEOs and the base alkylphenols, use of AEOs has increased, and both sets of compounds are now ubiquitous environmental contaminants. We recently demonstrated that diverse APEOs and AEOs induce triglyceride accumulation and/or pre-adipocyte proliferation in vitro. Both sets of contaminants have also been demonstrated as obesogenic and metabolism disrupting in a developmental exposure zebrafish model. While these metabolic health effects are consistent across models and species, the mechanisms underlying these effects are less clear. This study sought to evaluate causal mechanisms through reporter gene assay assessments, relative binding affinity assays, co-exposure experiments, and use of both human cell and zebrafish models. We report that antagonism of thyroid hormone receptor signaling appears to mediate at least a portion of the polyethoxylate-induced metabolic health effects. These results suggest further evaluation is needed, given the ubiquitous environmental presence of these thyroid disrupting contaminants and reproducible effects in human cell models and vertebrate animals.

Synthesis of short-chain fluorocarbon surfactant: Enhancing surface and foam performance through hydrocarbon surfactants compounding

The research of short-chain fluorocarbon surfactants is crucial in effectively and environmentally extinguishing petrochemical fires. In this study, a short-chain fluorocarbon surfactant named 2H,2H-perfluorooctanoic acid sodium salt (PFH-CA) was synthesized, and then characterized its chemical structure, thermal stability, surface activity, and foam property. Subsequently, PFH-CA was compounded with hydrocarbon surfactants including sodium dodecyl sulfate (SDS), dodecyl trimethyl ammonium chloride (DTAC), and N,N-dimethyldodecylamine-N-oxid (OB-2) at different molar ratios. The surface tension, interaction parameters, and foam property of the PFH-CA/hydrocarbon surfactant compounding systems were investigated. The analysis indicates that PFH-CA exhibits excellent surface activity and thermal stability concomitant with poor foam property. Introducing SDS, DTAC, and OB-2 enhances the foam performance and reduces the consumption of PFH-CA through synergistic interactions. Especially, PFH-CA/DTAC (1:4) system possesses the strongest interactions and the best performance, with critical micelle concentration (CMC) and surface tension at CMC (γCMC) of 0.11 mmol/L and 20.90 mN/m, respectively. When concentration of PFH-CA exceeds 0.5 mmol/L, the foaming ability and foam stability stabilize at 30 cm and 90 %, respectively. The enhanced performance of PFH-CA/DTAC system is attributed to the electrostatic attraction between anionic and cationic surfactants, which facilitates the formation of micelles, subsequently leading to better surface activity and foam properties.

Validation of a phase-field approach for contact line hysteresis against a sloshing droplet case

AbstractUnderstanding liquid propellants behavior in microgravity conditions is critical for efficient spacecraft design. For a number of operations, ranging from engine restart to orbital propellant storage and transfer, insight is needed to characterize capillary-dominated flows. In such conditions, surface tension and wetting properties, including contact angle hysteresis, can greatly impact the fluid’s behavior and therefore spacecraft performance. Using experimental data from ESA Propulsion Laboratory, a contact line model for the Cahn–Hilliard phase-field method is validated. The case studied is that of a droplet confined between two oscillating plates, which aims to isolate and observe contact angle-driven physics, limiting the effect of gravity on the flow in a simple and reproducible way on ground. The contact line model allows for the prediction of contact line motion without requiring the computation of dynamic contact angles or contact line velocities, thus simplifying implementation and reducing computational overhead. For the validation, contact line pinning and motion under varying oscillation frequencies is investigated. Specifically, the length between the rear and front contact line edges, as well as the shape of the sloshing droplet are compared. The results show good agreement between simulations and experimental data, confirming the model’s accuracy in predicting contact line behavior and pinning.

Effect of CO2-assisted surfactant/polymer flooding on enhanced oil recovery and its mechanism

D oilfield is a typical heavy oil reservoir affected by bottom water and has the characteristics of high porosity, high permeability, and strong heterogeneity. However, water flooding leaves oil behind due to unfavorable mobility ratios and capillary forces. The layer (well section) with poor or no liquid entry ability originally has been improved in the process of surfactant/polymer flood. However, fluid entry distribution interlayers were not improved obviously in the middle and late stages. To further improve the recovery efficiency of surfactant/polymer flooding on bottom water reservoirs, the CO2-assisted surfactant/polymer flooding development method had been proposed. The optimal composition of the surfactant/polymer system was selected by evaluating the oil-water interfacial tension and viscosity. Three-dimensional cores with bottom water were used in CO2-assisted surfactant/polymer flooding experiments to improve oil recovery. On this foundation, the screening of oil displacement agents, optimization of oil production well location, and injection pressure were carried out. Based on the comprehensive analysis of the produced liquid, the CO2 assisted surfactant/polymer flooding to enhanced oil recovery mechanism was analyzed. The results showed that the surfactant named BS had a low oil-water interfacial tension of 3.79 × 10-3 mN/m. In addition, salinity decreases the viscosity of the surfactant/polymer solution. It was found that conducting CO2 huff and puff after chemical flooding can improve oil recovery. Among the four chemical agents, CO2-assisted the anionic nonionic surfactant and the salt-resistant polymer system flooding had the highest recovery. Moreover, the location of the oil production well, that is, the distance between it and the bottom water layer, has an impact on the recovery. During the experiment, 2.5 cm was the farthest distance between the oil production well and the bottom water layer, at which point the recovery was highest at 70.9%, and the bottom water breakthrough rate was 2.4%. These results provide theoretical and technical support for the development of CO2-assisted surfactant/polymer flooding and its application in wells.

The Effect of Wettability on Confinement-Induced Phase Behavior and Storage of Alkane in Nanoporous Media.

The impact of wettability on the confined phase behavior of fluids is paramount for various applications, such as gas storage, carbon dioxide sequestration, and water purification. However, the understanding of the fluid-solid intermolecular interactions in confined systems is still limited and requires further investigation. This work investigates the effect of hydrophilic and hydrophobic nanoporous materials on the adsorption and desorption isotherms of n-butane. The hydrophilic samples in this research are MCM-41 silica powder with two different pore sizes (80 and 100 Å). MCM-41 samples were successfully treated with hexamethyldisilazane (HMDS) to create hydrophobic adsorbents. Isotherms of n-butane in materials with different wetting states were generated at various temperatures using an upgraded gravimetric apparatus. The results demonstrated that n-butane was adsorbed more onto the hydrophilic MCM-41 materials during the initial adsorption process. The lower affinity between n-butane and the modified MCM-41 samples slightly increased the capillary condensation and evaporation pressures in these materials compared to those in the original ones. However, it is noted that wettability's influence on the confined phase transitions of n-butane was not significant in this study. Interestingly, the hysteresis behavior of the vapor-liquid and liquid-vapor phase transitions due to confinement was independent of the surface's wetting properties. Kelvin's equation for a hemispherical meniscus was adopted to evaluate the capillary evaporation pressures of n-butane in nanopores. The calculated pressures showed agreement with experimental data when appropriate pore size and surface tension values were applied. These findings provide valuable insights into the impacts of surface chemistry and wettability on the phase behavior of hydrocarbon gas in nanoporous media. Furthermore, this study enriches the experimental database on confined fluids, which is essential for developing accurate theoretical and modeling tools for numerous industrial and scientific applications.

Coalescence Frequency in O/W Emulsions: Comparisons of Experiments with Models.

We have studied the coalescence of oil in water emulsions under the influence of gravity. The emulsions were made with alkane oils and surfactants with varying physical chemistry. We chose cationic alkyl trimethylammonium bromides of different chain lengths and nonionic surfactants of ethylene oxide and sugar head groups, including polymeric surfactants. We observed phase separation in two steps. Creaming of the oil drops is followed by their rapid coalescence, increasing the average drop size and resulting in complete surfactant surface coverage of the interfaces. Full phase separation occurs after much longer times Tc when the emulsion drops coalesce dramatically. We have used a model by Dinh et al. to relate Tc to the coalescence frequency and hence to the activation energy for the rupture of the films between two neighboring drops. Our results support the view that the coalescence of stable emulsions (stable at least for a few hours) is a thermally activated process and is controlled by the surface compression elastic modulus. This modulus was determined using surface tension measurements and calculations using the Gibbs adsorption equation. The observed differences between ionic and nonionic systems are attributed to a two-step film rupture process in the case of ionic surfactants, which is not found in nonionic systems.