A direct measurement of the influence of vapour, of liquid and of oriented monolayers on the interfacial energy of mica

A cleavage technique has been used to measure solid/fluid interfacial energies, and to study directly the effect of various media on these energies. Solid/vapour and solid/liquid interfacial energies were measured by cleaving mica specimens first in an atmosphere of vapour and then in the corresponding liquid. In this way we have a direct means of checking the validity of Young’s equation. Results obtained with water, as representative of a polar medium, and hexane, as representative of a non-polar medium show that Young’s equation holds for systems with zero contact angle. The effect of the humidity of the surrounding atmosphere on the cleavage of mica was also investigated. Water vapour was found to produce a marked reduction in the cleavage energy. In another set of experiments the cleavage technique was used to determine the work done in separating mica surfaces covered with an adsorbed monomolecular layer of fatty acid. The results yield a value of 37 erg/cm 2 for the surface energy of a lauric acid monolayer on mica.

2016 ◽  
Vol 6 (1) ◽  
pp. 96
Author(s):  
Ai-Jun Hu ◽  
Bao-Zhan Lv

<p class="1Body">Wetting of a spherical nanodroplet in smooth and homogeneous cylinder surface rotated by quadratic curve was studied by methods of thermodynamics. The solid-liquid-vapor system was separated into six parts using Gibbs method of dividing surface. The system free energy was calculated. A generalized Young equation for the equilibrium contact angle is proposed taking the line tension effects into consideration. On the basis of some assumptions, this generalized Young equation is the same as the classical Young’s equation.</p>


2009 ◽  
Vol 12 (05) ◽  
pp. 702-712 ◽  
Author(s):  
Dayanand Saini ◽  
Dandina N. Rao

Summary The two-century-old Young's equation has been widely used in petroleum engineering to depict the reservoir wettability in terms of contact angle, which is a function of surface free energies of the system. For solid/liquid/vapor (S/L/V) systems, Young's equation has been modified in the recent literature to include a line-tension term. This modification was sought to accommodate the imbalance of intermolecular forces experienced by the three-phase confluence zone. Also, Young's equation does not account for the vertical component of liquid/vapor surface tension. The present study aims to experimentally investigate the applicability of the line-tension-based modification of Young's equation to solid/liquid/liquid (rock/oil/brine) (S/L/L) systems of interest to the petroleum industry. Both the ambient- and reservoir-condition optical cells were used, with stock-tank and live oil, respectively, to determine the drop-size dependence of dynamic contact angle subtended by the oil/brine interface with the rock surface. The experimental data were correlated with the modified Young's equation to determine the magnitude of line tension for different rock/oil/brine systems. To the best of our knowledge, this is the first attempt to apply the modified Young's equation to rock/oil/brine systems and to measure line tension for a rock/live-crude-oil/brine system at reservoir conditions of pressure and temperature. The measured line tension for S/L/L systems, while being positive and of the same order of magnitude as in S/L/V systems, correlates well with the water-advancing contact angle and the adhesion number, a ratio of adhesion force to capillary force. This experimental study indicates that the extent of deviation from Young's equation exhibited by rock/oil/brine systems may be directly related to the rock/oil adhesion interaction. This study reinforces the need to include the rock/oil adhesion force in our consideration of rock/fluid interactions, wettability, and their impact on enhanced-oil-recovery (EOR)/improved-oil-recovery (IOR) processes.


2020 ◽  
Vol 12 ◽  
Author(s):  
Nihar Ranjan Biswal

Background: Surfactant adsorption at the interfaces (solid–liquid, liquid–air, or liquid–liquid) is receiving considerable attention from a long time due to its wide range of practical applications. Objective: Specifically wettability of solid surface by liquids is mainly measured by contact angle and has many practical importances where solid–liquid systems are used. Adsorption of surfactants plays an important role in the wetting process. The wetting behaviours of three plant-based natural surfactants (Reetha, Shikakai, and Acacia) on the glass surface are compared with one widely used nonionic synthetic surfactant (Triton X-100) and reported in this study. Methods: The dynamic contact angle study of three different types of plant surfactants (Reetha, Shikakai and Acacia) and one synthetic surfactant (Triton X 100) on the glass surface has been carried out. The effect of two different types of alcohols such as Methanol and amyl alcohol on wettability of shikakai, as it shows little higher value of contact angle on glass surface has been measured. Results: The contact angle measurements show that there is an increase in contact angle from 47° (pure water) to 67.72°, 65.57°, 68.84°, and 68.79° for Reetha, Acacia, Shikakai, and Triton X-100 respectively with the increase in surfactant concentration and remain constant at CMC. The change in contact angle of Shikakai-Amyl alcohol mixtures are slightly different than that of methanol-Shikakai mixture, mostly there is a gradual increase in contact angle with the increasing in alcohol concentration. Conclusion: There is no linear relationship between cos θ and inverse of surface tension. There was a linear increase in surface free energy results with increase in concentration as more surfactant molecules were adsorbing at the interface enhancing an increase in contact angle.


2021 ◽  
Author(s):  
Xu-Guang Song ◽  
Ming-Wei Zhao ◽  
Cai-Li Dai ◽  
Xin-Ke Wang ◽  
Wen-Jiao Lv

AbstractThe ultra-low permeability reservoir is regarded as an important energy source for oil and gas resource development and is attracting more and more attention. In this work, the active silica nanofluids were prepared by modified active silica nanoparticles and surfactant BSSB-12. The dispersion stability tests showed that the hydraulic radius of nanofluids was 58.59 nm and the zeta potential was − 48.39 mV. The active nanofluids can simultaneously regulate liquid–liquid interface and solid–liquid interface. The nanofluids can reduce the oil/water interfacial tension (IFT) from 23.5 to 6.7 mN/m, and the oil/water/solid contact angle was altered from 42° to 145°. The spontaneous imbibition tests showed that the oil recovery of 0.1 wt% active nanofluids was 20.5% and 8.5% higher than that of 3 wt% NaCl solution and 0.1 wt% BSSB-12 solution. Finally, the effects of nanofluids on dynamic contact angle, dynamic interfacial tension and moduli were studied from the adsorption behavior of nanofluids at solid–liquid and liquid–liquid interface. The oil detaching and transporting are completed by synergistic effect of wettability alteration and interfacial tension reduction. The findings of this study can help in better understanding of active nanofluids for EOR in ultra-low permeability reservoirs.


Author(s):  
Yeeli Kelvii Kwok

Wettability has been explored for 100 years since it is described by Young’s equation in 1805. It is all known that hydrophilicity means contact angle (θ), θ < 90°; hydrophobicity means contact angle (θ), θ > 90°. The utilization of both hydrophilic surfaces and hydrophobic surfaces has also been achieved in both academic and practical perspectives. In order to understand the wettability of a droplet distributed on the textured surfaces, the relevant models are reviewed along with understanding the formation of contact angle and how it is affected by the roughness of the textured surface aiming to obtain the required surface without considering whether the original material is hydrophilic or hydrophobic.


Author(s):  
Mercy Dicuangco ◽  
Susmita Dash ◽  
Justin A. Weibel ◽  
Suresh V. Garimella

The ability to control the size, shape, and location of particulate deposits is important in patterning, nanowire growth, sorting biological samples, and many other industrial and scientific applications. It is therefore of interest to understand the fundamentals of particle deposition via droplet evaporation. In the present study, we experimentally probe the assembly of particles on superhydrophobic surfaces by the evaporation of sessile water droplets containing suspended latex particles. Superhydrophobic surfaces are known to result in a significant decrease in the solid-liquid contact area of a droplet placed on such a substrate, thereby increasing the droplet contact angle and reducing the contact angle hysteresis. We conduct experiments on superhydrophobic surfaces of different geometric parameters that are maintained at different surface temperatures. The transient droplet shape and wetting behavior during evaporation are analyzed as a function of substrate temperature as well as surface morphology. During the evaporation process, the droplet exhibits a constant contact radius mode, a constant contact angle mode, or a mixed mode in which the contact angle and contact radius change simultaneously. The evaporation time of a droplet can be significantly reduced with substrate heating as compared to room-temperature evaporation. To describe the spatial distribution of the particle residues left on the surfaces, qualitative and quantitative evaluations of the deposits are presented. The results show that droplet evaporation on superhydrophobic surfaces, driven by mass diffusion under isothermal conditions or by substrate heating, suppresses particle deposition at the contact line. This preempts the so-called coffee-ring and allows active control of the location of particle deposition.


Author(s):  
C. A. Ward

A method for determining the surface tension of solid-fluid interfaces has been proposed. For a given temperature and fluid-solid combination, these surface tensions are expressed in terms of material properties that can be determined by measuring the amount of vapor adsorbed on the solid surface as a function of xV, the ratio of the vapor-phase pressure to the saturation-vapor pressure. The thermodynamic concept of pressure is shown to be in conflict with that of continuum mechanics, but is supported experimentally. This approach leads to the prediction that the contact angle, θ, can only exist in a narrow pressure range and that in this pressure range, the solid-vapor surface tension is constant and equal to the surface tension of the liquid-vapor interface, γLV. The surface tension of the solid-liquid interface, γSL, may be expressed in terms of measurable properties, γLV and θ: γSL = γLV(1 − cosθ). The value of θ is predicted to depend on both the pressure in the liquid at the three-phase, line x3L, and the three-phase line curvature, Ccl. We examine these predictions using sessile water droplets on a polished Cu surface, maintained in a closed, constant volume, isothermal container. The value of θ is found to depend on the adsorption at the solid-liquid interface, nSL = nSL(x3L,Ccl). The predicted value of θ is compared with that measured, and found to be in close agreement, but no effect of line tension is found.


Author(s):  
Dong-Lei Zeng ◽  
Biao Feng ◽  
Jia-Wen Song ◽  
Li-Wu Fan

Abstract Temperature-dependent wettability of water droplets on a metal surface in a pressurized environment is of great theoretical and practical significance. In this paper, molecular dynamic simulation is used to study this problem by relating the temperature-dependent apparent contact angles to the changes in solid-liquid and solid-vapor interfacial free energies and hydrogen bonds in the nano-sized water droplets with increasing the temperature. The temperature range of interest is set from 298 K to 538 K in a 20 K interval under a constant pressure of 7 MPa. The results show that the contact angle in general decreases with raising the temperature and decreasing trend can be divided into two sections with different slopes. The contact angle drops slowly when the temperature is below 458 K as a critical point. Beyond this point, the contact angle shows a much steeper decrease. The difference between solid-vapor and solid-liquid interfacial free energies is found to decrease slightly with temperature. Combining with that the surface tension drops with increasing the temperature, a decreasing trend of the contact angle is expected according to the Young’s equation. As the temperature increases, the number and average energy of the hydrogen bonds both decrease, and the hydrogen bonds tend to aggregate at the bottom of the nano-droplets.


Author(s):  
Kavic Rason ◽  
Brad Kinsey

Geometrically complex, high aspect ratio microstructures and limited aspect ratio nanostructures have been successfully fabricated in supercooled Bulk Metallic Glass (BMG) substrates by molding against patterned Silicon and Silicon dioxide substrates. However, demand exists for similar metallic substrates with high aspect ratio, nanoscale features. Van Der Waals based interfacial energies between the supercooled liquid BMG and the Silicon cavity represent a substantial obstacle to the direct scaling of the molding process to the nanoscale. In an effort to investigate these effects, experiments were conducted using molds of various compositions: Silicon, SiO2 and SiO2 coated with Gold. The Gold coating failed to impact molding performance due to the thin layer deposited. However, drastically superior results were obtained by using a Silicon mold because of the variation in interfacial interaction between the BMG and the mold material. In addition, a theoretical model to predict achievable aspect ratio is presented and was found to be in qualitative agreement with experimental results. Finally, a value for the surface tension of Viterloy-1b within it’s supercooled liquid state was deduced from experimental data.


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