scholarly journals Drop Size Dependence of the Apparent Surface Tension of Aqueous Solutions in Hexane Vapor as Studied by Drop Profile Analysis Tensiometry

2020 ◽  
Vol 4 (3) ◽  
pp. 29
Author(s):  
Valentin B. Fainerman ◽  
Volodymyr I. Kovalchuk ◽  
Eugene V. Aksenenko ◽  
Altynay A. Sharipova ◽  
Libero Liggieri ◽  
...  
Keyword(s):  
Surface Tension ◽  
Drop Size ◽  
Profile Analysis ◽  
Pure Water ◽  
Dynamic Surface Tension ◽  
Dynamic Surface ◽  
Hexane Vapor ◽  
Wide Range ◽  
Drop Profile Analysis Tensiometry ◽  
Hexane Phase

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.

Experimental Investigation of Low Weber Number Post-Impact Drop Spreading on Solid Substrates

2010 ◽  
Author(s):  
Milind A. Jog ◽  
Raj M. Manglik
Keyword(s):  
Surface Tension ◽  
High Speed ◽  
Pure Water ◽  
Surfactant Solution ◽  
Video Camera ◽  
Dynamic Surface Tension ◽  
Temporal Variations ◽  
Dynamic Surface ◽  
Post Impact ◽  
Triton X

The post-impact spreading and recoil behaviors of droplets of pure liquids (water and ethanol) and aqueous solution of Triton X-100 (a surfactant) on a dry horizontal hydrophilic (glass) substrate are investigated for low Weber numbers. The evolution of drop shape during spreading and recoil are captured using a high-speed (4,000 frames per second) digital video camera. Digital image-processing was used to determine the spread and height of the liquid film on the surface from each frame. Unlike pure liquids, the liquid-gas interfacial tension for surfactant solution is a function of surface age, where surface tension is that of the solvent at zero time and then reaches an equilibrium value with increasing surface age. Furthermore, the equilibrium surface tension is a function of the surfactant concentration, which decreases from that of the solvent at zero concentration to that at the critical micelle concentration (CMC), and remains essentially constant thereafter. The surface tension of aqueous Triton X-100 solution varies from that of pure water to nearly that of ethanol. As such the comparison of transient droplet-impact-spreading-recoil behavior of the three liquids, or their temporal variations of the spread and the flattening factor, provides a basis for understanding the role of dynamic surface tension and surface wettability.

Visualization of Multiscale Processes - Bubble Dynamics in Surface Active Colloids

2015 ◽  
Vol 137 (8) ◽  
Author(s):  
S. Manoharan ◽  
D. Kalaikadal ◽  
R. M. Manglik ◽  
E. Iskrenova-Ekiert ◽  
S. S. Patnaik
Keyword(s):  
Molecular Dynamics ◽  
Surface Tension ◽  
Pure Water ◽  
Dynamic Surface Tension ◽  
Air Flow Rate ◽  
Dynamic Surface ◽  
Multi Scale ◽  
Macro Scale ◽  
Dynamics Simulations ◽  
Adsorption Desorption

The growth dynamics of isolated gas bubbles from a submerged capillary-tube orifice in a pool of aqueous solution of Cetyl Trimethyl Ammonium Bromide (CTAB) was studied by multi-scale modeling. The macro-scale bubble ebullience is controlled by the molecular scale surfactant adsorption/desorption on the liquid-gas interface. Molecular dynamics simulations were carried out to predict the interfacial adsorption/desorption kinetics. The results of the molecular dynamics simulations were input to the volume-of-fluid based macro-scale computations. The size and shape of bubbles from incipience to departure were measured using high speed videography for model validation. Predictions of the multi-scale model agree with the experimental measurements of bubble size evolution and bubble diameter at departure. The surfactant mass transfer and adsorption on the liquid gas interface gives rise to dynamic surface tension. As a result of the surfactant presence, the bubble departure diameters were smaller in CTAB solution compared to pure water. Furthermore, dynamic surface tension behavior of CTAB makes the bubble departure diameter a function of bubble Reynolds number (Re based on the orifice diameter and air flow rate). At low flow rates or low Re, the bubble departure diameters are smaller than those in water. As the air flow rate increases, the bubble departure diameters tend towards those in pure water. The authors gratefully acknowledge funding from AFOSR Thermal Science Program and AFRL DoD Supercomputing Resource Center for computing time and resources.

Adsorption of C14EO8 at the interface between its aqueous solution drop and air saturated by different alkanes vapor

2017 ◽  
Vol 19 (3) ◽  
pp. 2193-2200 ◽  
Author(s):  
R. Miller ◽  
E. V. Aksenenko ◽  
V. I. Kovalchuk ◽  
V. B. Fainerman
Keyword(s):  
Aqueous Solution ◽  
Surface Tension ◽  
Pure Water ◽  
Dynamic Surface Tension ◽  
Dynamic Surface ◽  
Equilibrium Surface ◽  
Equilibrium Surface Tension

The dynamic and equilibrium surface tension for drops of aqueous C14EO8 solutions at the interface to pure air or pentane, hexane, heptane and toluene saturated air, and the dynamic surface tension of pure water at these interfaces are presented.

Dynamic surface tension of xylem sap at the air-water interface

2021 ◽  
Author(s):  
Reddy Prasanna Duggireddy ◽  
Eran Raveh ◽  
Gilboa Arye
Keyword(s):  
Surface Tension ◽  
Surface Activity ◽  
Pure Water ◽  
Xylem Sap ◽  
Dynamic Surface Tension ◽  
Bulk Solution ◽  
Diffusion Control ◽  
Dynamic Surface ◽  
Equilibrium Surface Tension ◽  
Air Interface

<p>The surface tension (ST) of xylem sap at the water-air interface is a crucial phenomenon, influencing many physiological events such as air seeding and embolism, by which xylem vessels become air-filled and cease to function. Refilling of embolized, may relies on sap’s surface activity at the interface. It is commonly assumed that the ST of xylem sap is equal to the ST of pure water (72 mN/m). However, xylem sap is a complex solution and consists of surface-active molecules that may adsorb and accumulate at the water-air interface and thereby reduce the ST of water as a function of their aqueous concentration. However, when a new water-air interface is formed, equilibrium ST is not reached instantaneously. Specifically, amphiphilic molecules are kinetically adsorbed and undergo orientation at the interface following diffusion from the bulk solution. Dynamic ST of xylem sap and liquid-solid interactions, describing the surface phenomena of the xylem of vascular plants is currently not fully understood. This is mainly due to a lack of quantitative knowledge on the rate and extent of dynamic and equilibrium ST of sap. In this regard, the main objective of this study is to quantify the dynamic and equilibrium ST of xylem sap as a function of their aqueous concentration. We extracted xylem sap from lemon trees and measured ST as a function of time using the pendant drop technique. The dynamic ST data were analyzed using empirical and diffusion-control mathematical models which adequately described the exponential-like decay of the ST as a function of time. The results showed reduced ST of water in the xylem sap, indicating significant surface activity, reaching equilibrium ST values as low as 42 mN/m. The rate of ST decay was higher in high sap concentration and reduced in diluted one. The results of dynamic and equilibrium ST and the corresponding model will be presented and their implications for xylem hydraulic functioning will be discussed.</p><p> </p><p>Keywords: Dynamic surface tension, Equilibrium surface tension, Diffusion, Xylem sap.</p><p> </p>

scholarly journals A pH-Responsive Foam Formulated with PAA/Gemini 12-2-12 Complexes

2021 ◽  
Vol 5 (3) ◽  
pp. 37
Author(s):  
Hernán Martinelli ◽  
Claudia Domínguez ◽  
Marcos Fernández Leyes ◽  
Sergio Moya ◽  
Hernán Ritacco
Keyword(s):  
Surface Tension ◽  
Dynamic Surface Tension ◽  
Foam Formation ◽  
Ph Responsive ◽  
Dynamic Surface ◽  
X Ray ◽  
Equilibrium Surface Tension ◽  
Potential Applications ◽  
The Stability ◽  
Air Interfaces

In the search for responsive complexes with potential applications in the formulation of smart dispersed systems such as foams, we hypothesized that a pH-responsive system could be formulated with polyacrylic acid (PAA) mixed with a cationic surfactant, Gemini 12-2-12 (G12). We studied PAA-G12 complexes at liquid–air interfaces by equilibrium and dynamic surface tension, surface rheology, and X-ray reflectometry (XRR). We found that complexes adsorb at the interfaces synergistically, lowering the equilibrium surface tension at surfactant concentrations well below the critical micelle concentration (cmc) of the surfactant. We studied the stability of foams formulated with the complexes as a function of pH. The foams respond reversibly to pH changes: at pH 3.5, they are very stable; at pH > 6, the complexes do not form foams at all. The data presented here demonstrate that foam formation and its pH responsiveness are due to interfacial dynamics.

Pool Boiling Heat Transfer in Aqueous Solutions of an Anionic Surfactant

2000 ◽  
Vol 122 (4) ◽  
pp. 708-715 ◽  
Author(s):  
V. M. Wasekar ◽  
R. M. Manglik
Keyword(s):  
Anionic Surfactant ◽  
Pure Water ◽  
Pool Boiling ◽  
Sodium Dodecyl ◽  
Dynamic Surface Tension ◽  
Nucleate Boiling ◽  
Optimum Level ◽  
Lauryl Sulfate ◽  
Dynamic Surface ◽  
Influence Of Temperature On

Saturated nucleate pool boiling of aqueous surfactant solutions on a horizontal cylindrical heater has been experimentally investigated. Sodium dodecyl or lauryl sulfate (SDS or SLS), an anionic surfactant, is employed. Boiling performance, relative to that for pure water, is found to be enhanced significantly by the presence of SDS, with an early onset of nucleate boiling. An optimum level of enhancement is observed in solutions at or near critical micelle concentration of the surfactant; the enhancement, however, decreases considerably in higher concentration solutions. The dynamic surface tension measurements indicate a substantial influence of temperature on the overall adsorption isotherm. The diffusion kinetics of surfactant molecules and micelles is, therefore, expected to be quite different at boiling temperature than at room temperature. This greatly modifies the boiling mechanism that is generally characterized by the formation of smaller-size bubbles with increased departure frequencies, and a decreased tendency to coalesce which causes considerable foaming. [S0022-1481(00)00704-0]

An axisymmetric model for the analysis of dynamic surface tension

RSC Advances ◽  
2015 ◽  
Vol 5 (11) ◽  
pp. 7921-7931 ◽  
Author(s):  
S. I. Arias ◽  
J. R. Fernández ◽  
L. García-Rio ◽  
J. C. Mejuto ◽  
M. C. Muñiz ◽  
...  
Keyword(s):  
Surface Tension ◽  
Diffusion Length ◽  
Dynamic Surface Tension ◽  
Ionic Surfactants ◽  
Adsorption Behaviour ◽  
Dynamic Surface ◽  
Axisymmetric Model

An axisymmetric model accounts for dynamic surface tension of non-ionic surfactants under consideration of diffusive adsorption behaviour with a finite diffusion length.

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