Showing papers on "Surface tension published in 2015"

Measurement of surface and interfacial tension using pendant drop tensiometry

Abstract: Pendant drop tensiometry offers a simple and elegant solution to determining surface and interfacial tension - a central parameter in many colloidal systems including emulsions, foams and wetting phenomena. The technique involves the acquisition of a silhouette of an axisymmetric fluid droplet, and iterative fitting of the Young-Laplace equation that balances gravitational deformation of the drop with the restorative interfacial tension. Since the advent of high-quality digital cameras and desktop computers, this process has been automated with high speed and precision. However, despite its beguiling simplicity, there are complications and limitations that accompany pendant drop tensiometry connected with both Bond number (the balance between interfacial tension and gravitational forces) and drop volume. Here, we discuss the process involved with going from a captured experimental image to a fitted interfacial tension value, highlighting pertinent features and limitations along the way. We introduce a new parameter, the Worthington number, Wo, to characterise the measurement precision. A fully functional, open-source acquisition and fitting software is provided to enable the reader to test and develop the technique further.

Liquid Phase Exfoliation of Two-Dimensional Materials by Directly Probing and Matching Surface Tension Components.

Abstract: Exfoliation of two-dimensional (2D) materials into mono- or few layers is of significance for both fundamental studies and potential applications. In this report, for the first time surface tension components were directly probed and matched to predict solvents with effective liquid phase exfoliation (LPE) capability for 2D materials such as graphene, h-BN, WS2, MoS2, MoSe2, Bi2Se3, TaS2, and SnS2. Exfoliation efficiency is enhanced when the ratios of the surface tension components of the applied solvent is close to that of the 2D material in question. We enlarged the library of low-toxic and common solvents for LPE. Our study provides distinctive insight into LPE and has pioneered a rational strategy for LPE of 2D materials with high yield.

Vapour-mediated sensing and motility in two-component droplets

Abstract: The ability to control the movement of fluid droplets is of practical use in many applications including microfluidic liquid handling. Existing techniques demand large energy gradients on the solid surfaces on which the droplets are placed or a carefully prepared surface to overcome contact line pinning (an effect which usually limits droplet motion). This paper reports a previously unrecognized phenomenon that could provide a convenient means of manipulating fluid droplets. Droplets consisting of two miscible components in which one component has both a higher vapour pressure and higher surface tension than the other such as water and propylene glycol exhibit a contact angle when deposited on a high-energy surface (clean glass), but rest on a fluid film so do not suffer from contact line pinning. The droplets are stabilized by evaporation-induced surface tension gradients and can move under the influence of tiny forces, including the vapour emitted by neighbouring droplets. A wide range of interesting interactions is recorded for example, one droplet bouncing off another, a droplet 'chasing' another in a circle and a rainbow of different droplets sorted according to their surface tensions.

Direct observation of drops on slippery lubricant-infused surfaces

Abstract: For a liquid droplet to slide down a solid planar surface, the surface usually has to be tilted above a critical angle of approximately 10°. By contrast, droplets of nearly any liquid “slip” on lubricant-infused textured surfaces – so termed slippery surfaces – when tilted by only a few degrees. The mechanism of how the lubricant alters the static and dynamic properties of the drop remains elusive because the drop–lubricant interface is hidden. Here, we image the shape of drops on lubricant-infused surfaces by laser scanning confocal microscopy. The contact angle of the drop–lubricant interface with the substrate exceeds 140°, although macroscopic contour images suggest angles as low as 60°. Confocal microscopy of moving drops reveals fundamentally different processes at the front and rear. Drops recede via discrete depinning events from surface protrusions at a defined receding contact angle, whereas the advancing contact angle is 180°. Drops slide easily, as the apparent contact angles with the substrate are high and the drop–lubricant interfacial tension is typically lower than the drop–air interfacial tension. Slippery surfaces resemble superhydrophobic surfaces with two main differences: drops on a slippery surface are surrounded by a wetting ridge of adjustable height and the air underneath the drop in the case of a superhydrophobic surface is replaced by lubricant in the case of a slippery surface.

Role of Surfactants in Promoting Gas Hydrate Formation

Abstract: Gas hydrates have been proposed as a potential technology for a number of applications, such as separation of gas mixtures, CO2 capture, transportation, and sequestration, methane storage and transport, and seawater desalination. Most of these applications will benefit from reduced induction time of hydrate nucleation, enhanced hydrate growth rate, and maximum water-to-hydrate conversion. The addition of surfactants to the gas–water system serves this purpose in a very effective manner. This review focuses on different surfactants that were utilized for gas hydrate formation studies; insights have been provided on the possible mechanisms of action through which these surfactants affect hydrate formation kinetics. A thorough analysis of the existing literature on surfactants suggests that enhanced rate of hydrate nucleation and growth kinetics may not be directly linked to micelle formation. Conversely, reduced surface tension in the presence of surfactants not only enhances the mass transfer but also chan...

Stiffening solids with liquid inclusions

Abstract: Solids embedded with fluid inclusions are intuitively softer than their pure counterparts. But experiments show that when the droplets are small enough, material can become stiffer—highlighting a role for surface tension.

Microemulsions: a novel approach to enhanced oil recovery: a review

Abstract: The trend of growing interest in alternative source of energy focuses on renewable products worldwide However, the situation of petroleum industries in many countries needs much concern in improving the oil recovery technique Chemical method, especially microemulsion flooding, plays an important role in enhanced oil recovery technique due to its ability to reduce interfacial tension between oil and water to a large extent as well as alter wettability of reservoir rocks Surfactant-based chemical systems have been reported in many academic studies and their technological implementations are potential candidates in enhanced oil recovery activities This paper reviews the role of different types of surfactants in enhanced oil recovery, structure of microemulsion, phase behavior of oil–brine–surfactant/cosurfactant systems with variation of different parameters such as salinity, temperature, pressure and physicochemical properties of microemulsions including solubilization capacity, interfacial tension, viscosity and density under reservoir conditions The enhanced oil productivity by microemulsion flooding with different surfactant/cosurfactant systems has also been discussed in this paper This review introduces a new opening in enhanced oil recovery by microemulsion flooding with some new aspects

Tailoring surface quality through mass and momentum transfer modeling using a volume of fluid method in selective laser melting of TiC/AlSi10Mg powder

Abstract: A selective laser melting (SLM) physical model of coupled radiation transfer and thermal diffusion is proposed, which provides a local temperature field. A strong difference in thermal conductivity between the powder bed and dense material is taken into account. Both thermo-capillary force and recoil pressure induced by the material evaporation, which are the major driving forces for the melt flow, are incorporated in the formulation. The effect of the laser energy input per unit length (LEPUL) on the temperature distribution, melt pool dynamics, surface tension and resultant surface morphology has been investigated. It shows that the surface tension plays a crucial role in the formation of the terminally solidified surface morphology of the SLM-processed part. The higher surface tension of the lower temperature metal near the edge of the melt pool and the thermal-capillary force induced by the surface temperature gradient tend to pull the molten metal away from the center of the melt pool. For a relatively high LEPUL of 750 J/m, the molten material in the center of the melt pool has a tendency to flow towards the rear part, resulting in the stack of molten material and the attendant formation of a poor surface quality. For an optimized processing condition, LEPUL=500 J/m, a complete spreading of the molten material driven by the surface tension is obtained, leading to the formation of a fine and flat melt pool surface. The surface quality and morphology are experimentally acquired, which are in a good agreement with the results predicted by simulation.

Quantification of surface tension and internal pressure generated by single mitotic cells

Abstract: During mitosis, adherent cells round up, by increasing the tension of the contractile actomyosin cortex while increasing the internal hydrostatic pressure. In the simple scenario of a liquid cell interior, the surface tension is related to the local curvature and the hydrostatic pressure difference by Laplace's law. However, verification of this scenario for cells requires accurate measurements of cell shape. Here, we use wedged micro-cantilevers to uniaxially confine single cells and determine confinement forces while concurrently determining cell shape using confocal microscopy. We fit experimentally measured confined cell shapes to shapes obeying Laplace's law with uniform surface tension and find quantitative agreement. Geometrical parameters derived from fitting the cell shape and the measured force were used to calculate hydrostatic pressure excess and surface tension of cells. We find that HeLa cells increase their internal hydrostatic pressure excess and surface tension from ≈ 40 Pa and 0.2 mNm−1 during interphase to ≈ 400 Pa and 1.6 mNm−1 during metaphase. The method introduced provides a means to determine internal pressure excess and surface tension of rounded cells accurately and with minimal cellular perturbation and should be applicable to characterize the mechanical properties of various cellular systems.

Measuring Forces and Spatiotemporal Evolution of Thin Water Films between an Air Bubble and Solid Surfaces of Different Hydrophobicity

Abstract: A combination of atomic force microscopy (AFM) and reflection interference contrast microscopy (RICM) was used to measure simultaneously the interaction force and the spatiotemporal evolution of the thin water film between a bubble in water and mica surfaces with varying degrees of hydrophobicity. Stable films, supported by the repulsive van der Waals-Casimir-Lifshitz force were always observed between air bubble and hydrophilic mica surfaces (water contact angle, θ(w) < 5°) whereas bubble attachment occurred on hydrophobized mica surfaces. A theoretical model, based on the Reynolds lubrication theory and the augmented Young-Laplace equation including the effects of disjoining pressure, provided excellent agreement with experiment results, indicating the essential physics involved in the interaction between air bubble and solid surfaces can be elucidated. A hydrophobic interaction free energy per unit area of the form: WH(h) = -γ(1 - cos θ(w))exp(-h/D(H)) can be used to quantify the attraction between bubble and hydrophobized solid substrate at separation, h, with γ being the surface tension of water. For surfaces with water contact angle in the range 45° < θ(w) < 90°, the decay length DH varied between 0.8 and 1.0 nm. This study quantified the hydrophobic interaction in asymmetric system between air bubble and hydrophobic surfaces, and provided a feasible method for synchronous measurements of the interaction forces with sub-nN resolution and the drainage dynamics of thin films down to nm thickness.

Classical nucleation theory of homogeneous freezing of water: thermodynamic and kinetic parameters

Abstract: The probability of homogeneous ice nucleation under a set of ambient conditions can be described by nucleation rates using the theoretical framework of Classical Nucleation Theory (CNT). This framework consists of kinetic and thermodynamic parameters, of which three are not well-defined (namely the interfacial tension between ice and water, the activation energy and the prefactor), so that any CNT-based parameterization of homogeneous ice formation is less well-constrained than desired for modeling applications. Different approaches to estimate the thermodynamic and kinetic parameters of CNT are reviewed in this paper and the sensitivity of the calculated nucleation rate to the choice of parameters is investigated. We show that nucleation rates are very sensitive to this choice. The sensitivity is governed by one parameter – the interfacial tension between ice and water, which determines the energetic barrier of the nucleation process. The calculated nucleation rate can differ by more than 25 orders of magnitude depending on the choice of parameterization for this parameter. The second most important parameter is the activation energy of the nucleation process. It can lead to a variation of 16 orders of magnitude. By estimating the nucleation rate from a collection of droplet freezing experiments from the literature, the dependence of these two parameters on temperature is narrowed down. It can be seen that the temperature behavior of these two parameters assumed in the literature does not match with the predicted nucleation rates from the fit in most cases. Moreover a comparison of all possible combinations of theoretical parameterizations of the dominant two free parameters shows that one combination fits the fitted nucleation rates best, which is a description of the interfacial tension coming from a molecular model [Reinhardt and Doye, J. Chem. Phys., 2013, 139, 096102] in combination with the activation energy derived from self-diffusion measurements [Zobrist et al., J. Phys. Chem. C, 2007, 111, 2149]. However, some fundamental understanding of the processes is still missing. Further research in future might help to tackle this problem. The most important questions, which need to be answered to constrain CNT, are raised in this study.

Membrane tension controls the assembly of curvature-generating proteins

Abstract: Proteins containing a Bin/Amphiphysin/Rvs (BAR) domain regulate membrane curvature in the cell. Recent simulations have revealed that BAR proteins assemble into linear aggregates, strongly affecting membrane curvature and its in-plane stress profile. Here, we explore the opposite question: do mechanical properties of the membrane impact protein association? By using coarse-grained molecular dynamics simulations, we show that increased surface tension significantly impacts the dynamics of protein assembly. While tensionless membranes promote a rapid formation of long-living linear aggregates of N-BAR proteins, increase in tension alters the geometry of protein association. At high tension, protein interactions are strongly inhibited. Increasing surface density of proteins leads to a wider range of protein association geometries, promoting the formation of meshes, which can be broken apart with membrane tension. Our work indicates that surface tension may play a key role in recruiting proteins to membrane-remodelling sites in the cell.

Plateau–Rayleigh crystal growth of periodic shells on one-dimensional substrates

Abstract: The Plateau-Rayleigh instability was first proposed in the mid-1800s to describe how a column of water breaks apart into droplets to lower its surface tension. This instability was later generalized to account for the constant volume rearrangement of various one-dimensional liquid and solid materials. Here, we report a growth phenomenon that is unique to one-dimensional materials and exploits the underlying physics of the Plateau-Rayleigh instability. We term the phenomenon Plateau-Rayleigh crystal growth and demonstrate that it can be used to grow periodic shells on one-dimensional substrates. Specifically, we show that for certain conditions, depositing Si onto uniform-diameter Si cores, Ge onto Ge cores and Ge onto Si cores can generate diameter-modulated core-shell nanowires. Rational control of deposition conditions enables tuning of distinct morphological features, including diameter-modulation periodicity and amplitude and cross-sectional anisotropy. Our results suggest that surface energy reductions drive the formation of periodic shells, and that variation in kinetic terms and crystal facet energetics provide the means for tunability.

Surfactants at the Design Limit

Abstract: This article analyzes how the individual structural elements of surfactant molecules affect surface properties, in particular, the point of reference defined by the limiting surface tension at the aqueous cmc, γcmc. Particular emphasis is given to how the chemical nature and structure of the hydrophobic tails influence γcmc. By comparing the three different classes of surfactants, fluorocarbon, silicone, and hydrocarbon, a generalized surface packing index is introduced which is independent of the chemical nature of the surfactants. This parameter ϕcmc represents the volume fraction of surfactant chain fragments in a surface film at the aqueous cmc. It is shown that ϕcmc is a useful index for understanding the limiting surface tension of surfactants and can be useful for designing new superefficient surfactants.

Stability of Constrained Capillary Surfaces

Abstract: A capillary surface is an interface between two fluids whose shape is determined primarily by surface tension. Sessile drops, liquid bridges, rivulets, and liquid drops on fibers are all examples of capillary shapes influenced by contact with a solid. Capillary shapes can reconfigure spontaneously or exhibit natural oscillations, reflecting static or dynamic instabilities, respectively. Both instabilities are related, and a review of static stability precedes the dynamic case. The focus of the dynamic case here is the hydrodynamic stability of capillary surfaces subject to constraints of (a) volume conservation, (b) contact-line boundary conditions, and (c) the geometry of the supporting surface.

Adsorption of soft particles at fluid interfaces

Abstract: Soft particles can be better emulsifiers than hard particles because they stretch at fluid interfaces. This deformation can increase adsorption energies by orders of magnitude relative to rigid particles. The deformation of a particle at an interface is governed by a competition of bulk elasticity and surface tension. When particles are partially wet by the two liquids, deformation is localized within a material-dependent distance L from the contact line. At the contact line, the particle morphology is given by a balance of surface tensions. When the particle radius R≪L, the particle adopts a lenticular shape identical to that of an adsorbed fluid droplet. Particle deformations can be elastic or plastic, depending on the relative values of the Young modulus, E, and yield stress, σp. When surface tensions favour complete spreading of the particles at the interface, plastic deformation can lead to unusual fried-egg morphologies. When deformable particles have surface properties that are very similar to one liquid phase, adsorption can be extremely sensitive to small changes of their affinity for the other liquid phase. These findings have implications for the adsorption of microgel particles at fluid interfaces and the performance of stimuli-responsive Pickering emulsions.

The structure effect on the surface and interfacial properties of zwitterionic sulfobetaine surfactants for enhanced oil recovery

Abstract: The surface and interfacial properties of five zwitterionic surfactants, including three propyl sulfobetaines CSB (where the carbon atom number of the alkyl chain is 12, 14 and 16, respectively) and two hydroxypropyl sulfobetaine surfactants CHSB (where the carbon atom number of the alkyl chain is 12 and 14, respectively), were studied at both air–water and oil–water interfaces. The surface activity of these surfactants at the air–water interface in aqueous solutions was investigated by the Wilhelmy plate method at 30 °C and ambient pressure. The values of the critical micelle concentration (CMC) and surface tension at CMC (γCMC) were determined from the surface tension measurements. The obtained results indicate that CMC and surface tension strongly depend on the surfactant molecular structure. An increase in the alkyl chain length results in a decrease in the CMC and γCMC values. The presence of a hydroxyl group causes an increase in CMC values and a decrease in γCMC values. The hydroxypropyl sulfobetaine surfactants have better surfacial properties. In addition, the interfacial activity at the oil–water interface among the crude oil–reservoir water–surfactant systems was investigated by use of the spinning drop method under harsh reservoir conditions of high temperature (90 °C) and high salinity (11.52 × 104 ppm, including 7040 ppm Ca2+ and 614 ppm Mg2+). It is interesting that the transient minimum dynamic interfacial tension (DITmin) could be observed in a specific concentration range. The time to reach DITmin is different with different surfactant molecular structures and surfactant concentrations. The hydroxypropyl sulfobetaine surfactant C14HSB shows excellent interfacial properties: it can reduce interfacial tension (IFT) between oil and water to an ultralow level at a very low concentration, and the ultralow IFT phenomenon only occurs in a specific concentration range from 0.03 to 0.10 wt%. In this work, hydroxypropyl sulfobetaine surfactants exhibit remarkable ability and are good candidates for chemical agents to enhance oil recovery in harsh reservoirs.

Adsorption of soft particles at fluid interfaces

Abstract: Soft particles can be better emulsifiers than hard particles because they stretch at fluid interfaces. This deformation can increase adsorption energies by orders of magnitude relative to rigid particles. The deformation of a particle at an interface is governed by a competition of bulk elasticity and surface tension. When particles are partially wet by the two liquids, deformation is localized within a material-dependent distance $L$ from the contact line. At the contact line, the particle morphology is given by a balance of surface tensions. When the particle radius $R \ll L$, the particle adopts a lenticular shape identical to that of an adsorbed fluid droplet. Particle deformations can be elastic or plastic, depending on the relative values of the Young modulus, $E$, and yield stress, $\sigma_p$. When surface tensions favour complete spreading of the particles at the interface, plastic deformation can lead to unusual fried-egg morphologies. When deformable particles have surface properties that are very similar to one liquid phase, adsorption can be extremely sensitive to small changes of their affinity for the other liquid phase. These findings have implications for the adsorption of microgel particles at fluid interfaces and the performance of stimuli-responsive Pickering emulsions.

Nanofluids alter the surface wettability of solids.

Abstract: We report the results of our studies on the changes in the contact angle and interfacial tension using a nanofluid composed of silica nanoparticles dispersed in water on three different solid substrates: gold (partially hydrophobic), glass (hydrophilic), and a silicon wafer (hydrophilic). We used both the goniometric method and drop-shape analysis to make the measurements. On the basis of the results of the drop-shape analysis using the Laplace equation, we evaluated the contributions of the interfacial tension change to the equilibrium contact angle and the presence of nanoparticles near the solid substrate, thereby elucidating the change in the wettability of the solid substrate. We found that the nanoparticles decrease the contact angle of the substrate with the increase in the nanoparticle concentration. To rationalize our experimental observations on the decrease in the contact angle of the solid substrate in the presence of nanoparticles, we calculated the surface volume fraction of the nanoparticle...