Liquid-liquid interfacial tension of equilibrated mixtures of ionic liquids and hydrocarbons

Ionic liquids are possible alternative solvents for the separation of aromatic and aliphatic hydrocarbons by liquid-liquid extrac- tion. Interfacial tension is an important property to consider in the design of liquid-liquid extraction processes. In this work, the liquid-liquid interfacial tension and the mutual solubility at 25 °C have been measured for a series of biphasic, equilibrated mixtures of an ionic liquid and a hydrocarbon. In particular, the ionic liquids 1-alkyl-3-methylimidazolium bis(trifluorome- thanesulfonyl)imide (with the alkyl substituent being ethyl, hexyl or decyl), 1-ethyl-3-methylimidazolium ethylsulfate, and 1-ethyl-3-methylimidazolium methanesulfonate have been selected, as well as the hydrocarbons benzene, hexane, ethylben- zene, and octane. The selected sets of ionic liquids and hydrocarbons allow the analysis of the influence of a series of effects on the interfacial tension. For example, the interfacial tension decreases with an increase in the length of the alkyl substituent chain of the cation or with an increase of the degree of charge delocalisation in the anion of the ionic liquid. Also, the interfa- cial tension with the aromatic hydrocarbons is markedly lower than that with the aliphatic hydrocarbons. A smaller effect is caused by variation of the size of the hydrocarbon. Some of the observed trends can be explained from the mutual solubility of the hydrocarbon and the ionic liquid.     

Anomalous temperature dependence of a dielectric relaxation rate

A polypropylene film containing 2,4,6-triiodophenol had, at 8 K, a dielectric absorption peak at 13.5 Hz. The peak moved to 22 Hz at 20 K, back to 15.5 Hz at 48 K, then rapidly to higher frequency with further increase in temperature. This probably results from a change in regime as the thermal phonon wavelengths become comparable to the size of the molecules.     

Liquid-vapor interfacial properties of water-ammonia mixtures: dependence on ammonia concentration

The equilibrium and dynamical properties of the liquid-vapor interfaces of water-ammonia mixtures are investigated by means of molecular-dynamics simulations. Altogether, we have simulated seven different systems of different concentration of ammonia. The inhomogeneous density, anisotropic orientational profiles, surface tension, and the pattern of hydrogen bonding are calculated for both water and ammonia molecules in order to characterize the location, width, thermodynamic aspects, and microscopic structure of the liquid-vapor interfaces of each of the water-ammonia systems. The dynamical aspects of the interfaces are investigated in terms of the anisotropic diffusion and dipole orientational relaxation of water and ammonia molecules. The properties of the interfaces are compared with those of the corresponding bulk phases. The present theoretical results are also compared with experimental findings wherever available.     

On the curvature dependence of the interfacial tension in a symmetric three-component interface

We consider a symmetric interface between two polymers A(N) and B(N) in a common monomeric solvent S using the mean-field Scheutjens-Fleer self-consistent field theory and focus on the curvature dependence of the interfacial tension. In multi-component systems there is not one unique scenario to curve such an interface. We elaborate on this by keeping either the chemical potential of the solvent or the bulk concentration of the solvent fixed, that is we focus on the semi-grand canonical ensemble case. Following Helfrich, we expand the surface tension as a Taylor series in the curvature parameters and find that there is a non-zero linear dependence of the interfacial tension on the mean curvature in both cases. This implies a finite Tolman length. In a thermodynamic analysis we prove that the non-zero Tolman length is related to the adsorption of solvent at the interface. Similar, but not the same, correlations between the solvent adsorption and the Tolman length are found in the two scenarios. This result indicates that one should be careful with symmetry arguments in a Helfrich analysis, in particular for systems that have a finite interfacial tension: one not only should consider the structural symmetry of the interface, but also consider the constraints that are enforced upon imposing the curvature. The volume fraction of solvent, the chain length N as well as the interaction parameter chi(AB) in the system can be used to take the system in the direction of the critical point. The usual critical behavior is found. Both the width of the interface and the Tolman length diverge, whereas the density difference between the two phases, adsorbed amount of solvent at the interface, interfacial tension, spontaneous curvature, mean bending modulus as well as the Gaussian bending modulus vanish upon approach of the critical point.     

Effects of ion solvation on phase equilibrium and interfacial tension of liquid mixtures

We study the bulk thermodynamics and interfacial properties of electrolyte solution mixtures by accounting for electrostatic interaction, ion solvation, and inhomogeneity in the dielectric medium in the mean-field framework. Difference in the solvation energy between the cations and anions is shown to give rise to local charge separation near the interface, and a finite Galvani potential between two coexisting solutions. The ion solvation affects the phase equilibrium of the solvent mixture, depending on the dielectric constants of the solvents, reflecting the competition between the solvation energy and translation entropy of the ions. Miscibility is decreased if both solvents have low dielectric constants and is enhanced if both solvents have high dielectric constant. At the mean-field level, the ion distribution near the interface is determined by two competing effects: accumulation in the electrostatic double layer and depletion in a diffuse interface. The interfacial tension shows a nonmonotonic dependence on the salt concentration: it increases linearly with the salt concentration at higher concentrations and decreases approximately as the square root of the salt concentration for dilute solutions, reaching a minimum near 1 mM. We also find that, for a fixed cation type, the interfacial tension decreases as the size of anion increases. These results offer qualitative explanations within one unified framework for the long-known concentration and ion size effects on the interfacial tension of electrolyte solutions.     

Critical behavior and interfacial tension of mixtures of propylene glycol and ethylene glycol oligomers

This investigation presents an analysis of the critical behavior of mixtures of oligomers of propylene glycol, PG₁₇, and ethylene glycol, EG_n, withn=3, 4, 5, 6.4, 8.7, 12.1 and 22.1. The critical coordinates, _c andT _c were determined from the phase diagrams. The critical compositions compare very well with the Huggins-Flory predictions. The interaction parameter _n is around one for EG₃, EG₄ and EG₅ and it increases up to two for the higher oligomers. The break in the interaction parameter also corresponds to a minimum in the critical temperature. The phase diagrams and the interfacial tension were used to get the critical exponents and , respectively. The data were analysed with two approaches. First, from the temperature dependence of the length of the tie-lines and of the interfacial tension up to the upper critical solution temperature, UCST. Second, with the data at 30°C using the critical temperature of the systems as the variable. The first method led to =0.39±0.05 in good agreement with the result of the second method, =0.37±0.04. The exponents for the interfacial tension, , determined with the first method for PG₁₇ with EG_6.4, EG_8.7 and EG_12.1 are =1.66±0.11, 1.46±0.25 and 1.73±0.18, respectively. The second method led to =1.17±0.14. The critical exponents are compared to mean field and ising-3D predictions.     

Investigation of the dependence of inferred interfacial tension on rotation rate in a spinning drop tensiometer

The spinning drop tensiometer is widely used to study the interfacial properties of many systems. However, there have also been several reported limitations with the spinning drop tensiometer. In this paper, it is shown that there is a relationship between the measured interfacial tension and the rotation rate of the drop. A detailed investigation of this relationship is presented.     

Anomalous temperature dependence of the dielectric and optical properties in ferroelectric liquid crystals

The anomalous temperature dependence of the sign of the spontaneous polarization in a biphenyl ester series of ferroelectric liquid crystals is reported. The reversal of the sign of the spontaneous polarization in the chiral smectic C phase of 2MBNCBC ((S)-2′-methylbutyl-4′-n- nonylcarbonyloxy-(l,l′-biphenyl)-l-carboxylate) is observed at T _m. This anomaly is studied in detail as functions of the length of the terminal alkyl chain, the applied electric field, the frequency and the applied hydrostatic pressure. T _m has been confirmed to depend on the length of the terminal chain and the applied pressure. However, it is independent of the applied field and the measuring frequency. In the mixture of these compounds, this anomaly is also observed.     

Anomalous temperature dependence of the dielectric and optical properties in ferroelectric liquid crystals

The anomalous temperature dependence of the sign of the spontaneous polarization in a biphenyl ester series of ferroelectric liquid crystals is reported. The reversal of the sign of the spontaneous polarization in the chiral smectic C phase of 2MBNCBC ((S)-2'-methylbutyl-4'-n- nonylcarbonyloxy-(l,l'-biphenyl)-l-carboxylate) is observed at T_m. This anomaly is studied in detail as functions of the length of the terminal alkyl chain, the applied electric field, the frequency and the applied hydrostatic pressure. T_m has been confirmed to depend on the length of the terminal chain and the applied pressure. However, it is independent of the applied field and the measuring frequency. In the mixture of these compounds, this anomaly is also observed.     

Concentration dependence of the interfacial tension for aqueous two-phase polymer solutions of dextran and polyethylene glycol

We studied the interfacial tension between coexisting phases of aqueous solutions of dextran and polyethylene glycol. First, we characterized the phase diagram of the system and located the binodal. Second, the tie lines between the coexisting phases were determined using a method that only requires measuring the density of the coexisting phases. The interfacial tension was then measured by a spinning drop tensiometer over a broad range of polymer concentrations close to and above the critical point. In this range, the interfacial tension increases by 4 orders of magnitude with increasing polymer concentration. The scaling exponents of the interfacial tension, the correlation length, and order parameters were evaluated and showed a crossover behavior depending on the distance to the critical concentration. The scaling exponent of the interfacial tension attains the value 1.50 ± 0.01 further away from the critical point, in good agreement with mean field theory, but the increased value 1.67 ± 0.10 closer to this point, which disagrees with the Ising value 1.26. We discuss possible reasons for this discrepancy. The composition and density differences between the two coexisting phases, which may be taken as two possible order parameters, showed the expected crossover from mean field behavior to Ising model behavior as the critical point is approached. The crossover behavior of aqueous two-phase polymer solutions with increasing concentration is similar to that of polymer solutions undergoing phase separation induced by lowering the temperature.     

Anomalous temperature dependence of nuclear quadrupole interactions in strongly hydrogen-bonded systems from first principles

We present an analysis of the effect of finite temperatures on the deuteron nuclear quadrupole coupling constants in a strongly hydrogen-bonded molecular crystal by means of first-principles Car-Parrinello molecular-dynamics simulations. Our findings agree well with experiments and provide a microscopic explanation of the anomalous increase of the quadrupole coupling in this class of systems. We show that a simple model based on the anharmonicity of the hydrogen bond potential fails to describe the temperature dependence of the couplings even qualitatively. Instead, the inclusion of fluctuations and disorder in terms of atomic motion of the surrounding molecules turns out to be important to obtain the correct magnitude of the temperature effect.     

pH dependence of the kinetics of interfacial tension changes during protein adsorption from sessile droplets on FEP-Teflon

Interfacial tension changes during protein adsorption at both the solid-liquid and the liquid-vapor interface were measured simultaneously by ADSA-P from sessile droplets of protein solutions on fluoroethylenepropylene-Teflon. Four globular proteins of similar size, viz. lysozyme, ribonuclease, -lactalbumin and Ca²⁺-free -lactalbumin, and one larger protein, serum albumin, were adsorbed from phosphate solutions at varying pH values (pH 3-12). The kinetics of the interfacial tension changes were described using a model accounting for diffusion-controlled adsorption of protein molecules and conformational changes of already adsorbed molecules. The contribution of conformational changes to the equilibrium interfacial pressure was shown to be relatively small and constant with respect to pH when compared to the contribution of adsorption of the protein molecules. The model also yields the diffusion relaxation time and the rate constant for the conformational changes at the interface. Around the isoelectric point of a protein the calculated diffusion relaxation time was minimal, which is ascribed to the absence of an energy barrier to adsorption. Energy barriers to adsorption become larger at pH values away from the isoelectric point and can therefore become rate-limiting for the adsorption process. The rate constants for conformational changes at the liquid-vapor interface were maximal around the isoelectric point of a protein, suggesting a smaller structural stability of the adsorbed protein. At the solid-liquid interface the rate constants were smaller and independent of pH. indicating that conformational changes more readily occur at the liquid-vapor than at the solid-liquid interface.     

Interfacial tension in aqueous biopolymer-surfactant mixtures

The current study offers a first insight into the interfacial properties of pullulan-sodium dodecyl sulphate (SDS) aqueous two-phase systems (ATPS) in the presence of sodium chloride (NaCl). The effect of composition on the interfacial tension (sigma) in these ATPS was investigated over a wide range of pullulan, SDS and NaCl concentrations. An increase in the interfacial tension was observed with increasing pullulan and SDS concentrations and a small increase was also observed as the NaCl concentration was increased. In both cases the interfacial tension increases were closely related to the phase behaviour of these systems; as a consequence of increasing the pullulan, SDS and/or NaCl concentrations, the system moves further away from the critical point. In all systems interfacial tensions (of the order of muN/m) were comparable with those reported for polymer-polymer ATPS. Interfacial tensions sigma can be well correlated with the difference in pullulan and SDS concentrations between the phases (DeltaC pul and DeltaC SDS) and also the tie-line length (TLL); all yield straight lines on a log-log scale.     

The temperature dependence of surface tension and critical micelle concentration of egg lysolecithin

Summary The surface tension of egg lysolecithin-water solutions has been investigated using a modified Wilhelmy technique in a temperature scanning mode. Use of this method has allowed a thorough analysis of both the surface conformational properties of the monomer, and the temperature dependence of the critical micelle concentration of the lipid, from 20– to 80 °C. Assuming that the lysolecithin is a non-ionic (zwitterionic) surfactantH _mic. has been calculated from the CMC values. The variation of log₁₀ CMC with temperature was complex and a least squares analysis had to be done over three overlapping temperature ranges.H _mic calculated from log₁₀ CMC versus 1/T plots, also showed a complex dependence on temperature.In the CMC concentration region experimental results were complicated by an apparent temperature dependent increase in the solubility of the micellar phase. This resulted in desorption from the surface, with a resultant increase in surface tension.

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Zusammenfassung Die Oberflächenspannung von wäßrigen Lösungen von Eilysolecithin wurde mittels einer modifizierten Wilhelmymethode bei kontinuierlicher Temperaturänderung untersucht. Die Benutzung dieser Methode gestattet eine sorgfältige Analyse sowohl der Konformationsänderungen an der Oberfläche als auch der Temperaturabhängigkeit der kritischen Mizellkonzentration des Lipids von 20°–80 °C. Die EnthalpieänderungH _mic der Mizellbildung wurde aus den Werten der kritischen Mizellkonzentration (CMC) berechnet. Der Verlauf von log₁₀ CMC mit der Temperatur erwics sich als komplex, so daß eine Analyse kleinster Fehlerquadrate über drei sich teilweise überschneidende Temperaturintervalle durchgeführt werden mußte.H _mic zeigte infolgedessen ebenfalls einen komplizierten Verlauf der Temperaturabhängigkeit.Im Bereich der kritischen Mizellkonzentration verursachte eine temperaturabhängige Zunahme der Löslichkeit der Mizellarphase eine Desorption von der Oberfläche und infolgedessen eine Erhöhung der Oberflächenspannung.

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With 5 figures and 2 tables     

Anomalous temperature dependence of gas chromatographic retention indices of polar compounds on nonpolar phases

The character of the temperature dependences of the retention indices RI(Т) of polar sorbates on nonpolar stationary phases was found to depend on the dosed amounts of sorbates, but not on column overloading. A physicochemical model was suggested to explain the observed anomalies in RI(Т).     

Nucleation-fluctuation approach to determining the temperature dependence of the surface tension of metals

An analysis of nucleation processes that occur during a vapor-liquid phase transition and temperature fluctuations that take place in clusters of stable phases is employed to derive a semiempirical relation between the capillary and thermophysical characteristics of substances. The relation enables one to calculate the surface tension of elementary substances based on their thermophysical characteristics in a wide temperature range from melting to boiling points. The surface tension of metals is calculated within this temperature range. In most cases, the calculated results agree with available experimental data.     

Transient interfacial tension of partially miscible polymers

The interfacial tension of three different binary polymer blends has been measured as function of time by means of a pendent drop apparatus, at temperatures ranging from 24 degrees C to 80 degrees C. Three grades of polybutene (PB), differing in average molecular weight and polydispersity, are used as dispersed phase, the continuous phase is kept polydimethylsiloxane (PDMS), ensuring different asymmetry in molecular weight across the interface. The interfacial tension changes with time and, therefore, this polymer blends can not be considered fully immiscible. Changes in interfacial tension are attributed to the migration of low-molecular weight components from the source phase into the interphase and, from there, into the receiving phase. In the early stages of the experiments, just after the contact between the two phases has been established, the formation of an interphase occurs and the interfacial tension decreases with time. As time proceeds, the migration process slows down given the decrease in driving force which is the concentration gradient and, at the same time, molecules accumulated in the interphase start to migrate into the "infinite" matrix phase. A quasi-stationary state is found before depletion of the low-molecular weight fraction in the drop occurs and causes the interfacial tension sigma(t) to increase. The time required to reach the final stationary value, sigma(stat), increases with molecular weight and is a function of temperature. Higher polydispersity leads to lower sigma(stat) and a weaker dependence of sigma(stat) on temperature is found. A model coupling the diffusion equation in the different regimes is applied in order to interpret the experimental results. Numerical solutions of the diffusion equation are proposed in the cases of a constant and a changing interphase thickness. In the latter case, the interphase is defined by tracking with time a fixed limiting concentration in the transient concentration profiles and the variations found in sigma(t) are attributed to the changes in the interphase thickness. A discrete version of this continuous model is proposed and scaling arguments are reported in order to compare the results obtained with the predictions of the continuous model. The kinetic model as proposed by Shi et al. [T. Shi, V.E. Ziegler, I.C. Welge, L. An, B.A. Wolf, Macromolecules 37 (2007) 1591-1599] appears as a special case of the discrete model, when depletion is not taken into account. Using the models, time scales for the diffusion process can be derived, which fit the experimental results quite well.     

Pressure and temperature dependence of the excess enthalpy of alkylchloride/alkane mixtures

There exist only few experimental data of the excess enthalpy of liquid mixtures at high pressure in literature. In this work some recent experimental results of the excess enthalpy H^E for alkylchloride/alkane mixtures are reported measured at different pressures and temperatures by using a high pressure flow calorimeter. H^E shows a relatively weak dependence on pressure compared with other polar/unpolar systems such as alcohol/alkane mixtures (ref.1).     

Anomalous temperature dependence of the intensity of the ΝP-H IR bands of dialkylphosphorous acids

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1709–1710, July, 1989.