The relative reduced Redlich–Kister equations for correlating excess properties of N,N-dimethylacetamide + 2-methoxyethanol binary mixtures at temperatures from 298.15 K to 318.15 K

Knowledge and prediction of physicochemical properties of binary mixtures is of great importance for understanding intermolecular interactions. The literature shows that most such systems exhibit non-linear behaviour. Excess molar volumes, viscosity deviations and isentropic compressibility changes in N,N-dimethylacetamide?+?2-methoxyethanol binary mixtures at 298.15, 308.15 and 318.15?K were calculated from experimental density, viscosity and sound velocity data presented in previous work. Here these experimental values were used to test the applicability of the correlative reduced Redlich–Kister equation and the recently proposed Herráez equation as well as their corresponding relative functions. Their correlation ability at different temperatures, and the use of different numbers of parameters, is discussed for the case of limited experimental data. These relative functions are important to reduce the effect of temperature and, consequently, to reveal the effects of different types of interactions. Limiting excess partial molar volume at infinite dilution were deduced from different methods, activation parameters and partial molar Gibbs energy of activation of viscous flow against compositions were investigated. The results of these observations have been interpreted in terms of structural effects of the solvents. In this frame, a correlating equation is recently proposed by Belda and in order to assess the validity of the proposed equation, it has also been applied to the present system for molar volume properties.     

Investigations of the reduced Redlich–Kister excess properties of 1,4-dioxane + isobutyric acid binary mixtures at temperatures from 295.15 to 313.15 K

Excess molar volumes and refractive index, molar refraction deviations and isentropic compressibility changes in 1,4-dioxane + isobutyric acid binary mixtures (from 295.15 to 313.15) K. were calculated from experimental density, refractive index and sound velocity data presented in previous work. Here, these experimental values were used to test the applicability of the correlative reduced Redlich–Kister equation as well as their corresponding relative functions which are important to reduce the effect of temperature and, consequently, to reveal the effects of different types of interactions. The results of these observations have been interpreted in terms of structural effects of the solvents. The correlating equation recently proposed by Belda, has also been applied to the present system in order to assess the validity of this equation and to give thermodynamic limiting partial molar quantities interesting to evaluate solute–solvent interaction.     

Reduced Redlich–Kister functions and interaction studies of Dehpa + Petrofin binary mixtures at 298.15 K

In order to understand the effect of different types of interactions in liquid mixtures by applying the correlative reduced Redlich–Kister equation, excess molar volume, excess dielectric constant, deviation in refractive index, deviation in molar refraction and molar polarisation were calculated at the temperature 298.15 K and atmospheric pressure P = 101.325 kPa for the binary mixture Petrofin (1) + Dehpa (2). The experimentally determined data of density and refractive index which were published earlier were used for these calculations. The results were interpreted in terms of structural effects of the solvents.     

Viscosity Arrhenius activation energy and derived partial molar properties in of N,N-dimethylacetamide + 2-ethoxyethanol binary mixtures at temperatures from 298.15 K to 318.15 K.

Calculation of excess properties in N,N-dimethylacetamide + 2-ethoxyethanol binary mixtures at (298.15, 308.15 and 318.15) K from experimental density, viscosity and sound velocity values were presented in previous work. Applications of these experimental values to test different correlation equations as well as their corresponding relative functions were also reported. Considering the quasi-equality between the Arrhenius activation energy Ea and the enthalpy of activation of viscous flow ?H*, here we can define partial molar activation energy Ea1 and Ea2 for N,N-dimethylacetamide and 2-ethoxyethanol, respectively, along with their individual contribution separately. Correlation between the two Arrhenius parameters of viscosity in all the domains of composition shows the existence of two main distinct behaviours separated by a stabilised structure in a short range of mole fraction in N,N-dimethylacetamide from 0.14 to 0.45. We add that correlation reveals interesting Arrhenius temperature, which is closely related to the vaporisation temperature in the liquid vapour equilibrium.     

The reduced Redlich–Kister excess molar Gibbs energy of activation of viscous flow and derived properties in 1,4-dioxane + water binary mixtures from 293.15 to 309.15 K

The excess molar volume, viscosity deviation and excess Gibbs free energy of activation of viscous flow have been investigated from the density and shear viscosity measurements of water–dioxane mixtures over the entire range of mole fractions from 293.15 to 309.15?K. The results were fitted by the Redlich–Kister equation. Partial molar volume and Gibbs energy at infinite dilution were deduced from four methods, activation parameters and partial molar Gibbs energy of activation of viscous flow against compositions were investigated. The water–dioxane interactions have principally an H-bound character and there are two principal types’ structures limited by 0.08?mole fraction in dioxane. The reduced Redlich–Kister excess properties provide an indication of the intermolecular interactions and for dioxane–water cluster formation as suggested in the literature.     

The Relative Reduced Redlich–Kister Equations for Correlating Excess Properties of N,N-Dimethylacetamide + Water Binary Mixtures at Temperatures from 298.15 K to 318.15 K

Excess molar volumes, viscosity deviations, and isentropic compressibility changes in N,N-dimethylacetamide + water binary mixtures at (298.15, 308.15 and 318.15)?K were calculated from experimental density, viscosity and sound velocity results presented in previous work. Here these experimental values were used to test the applicability of the correlative reduced Redlich?CKister equation and the recently proposed Herráez equation, as well as their corresponding relative functions. Their correlation ability at different temperatures, and the use of different numbers of parameters, are discussed for the case of limited experimental data. The relative functions are important to reduce the effect of temperature and, consequently, to reveal the effects of different types of interactions. Values of the limiting excess partial molar volume at infinite dilution were deduced using different methods. Also, the activation parameters and partial molar Gibbs energy of activation of viscous flow were analyzed as functions of composition. Correlation between the two Arrhenius parameters of viscosity in all composition domains show the existence of two distinct behaviors, separated by a stabilized structure over a short range of mole fractions from (0.2?to?0.3) in N,N-dimethylacetamide. In this regard, a correlation equation recently proposed by Belda has also been applied to the present system for deriving molar volume properties, in order to assess the validity of the proposed equation,     

The Relative Reduced Redlich–Kister and Herráez Equations for Correlating Excess Properties of N,N-Dimethylacetamide + Formamide Binary Mixtures at Temperatures from 298.15 K to 318.15 K

Excess molar volumes and viscosity deviations in binary mixtures of N,N-dimethylacetamide with formamide at (298.15, 308.15 and 318.15) K were calculated from experimental density and viscosity data presented in previous work. The density and viscosity data as well as their corresponding derived functions were used to test the applicability of two correlative equations: the reduced Redlich?CKister equation and the recently proposed Herráez equation. Their correlation abilities at different temperatures, and the use of different numbers of parameters, are discussed for the case of limiting experimental data. These relative functions are important to reduce the effect of temperature and, consequently, to reveal the effects of different types of interactions. Correlation between the two Arrhenius parameters of viscosity over the composition domains shows the existence of two distinct behaviors.     

Ultrasonic and viscometric studies of molecular interactions in binary mixtures of tetrahydrofuran with some aromatic hydrocarbons at temperatures from 288.15 to 318.15 K

Densities of the binary systems of 2,2′-oxybis[propane] with ethyl acrylate, butyl acrylate, methyl methacrylate, and styrene have been measured as a function of the composition, at 298.15 K and atmospheric pressure, using an Anton Paar DMA 5000 oscillating U-tube densimeter and used to calculate the partial and excess volumes. The latter were correlated with the Redlich-Kister equation and with a series of Legendre polynomials. The excess volumes are negative for all the systems reported here.     

Isothermal vapour–liquid equilibrium data for the binary propan-2-one+chloroalkanes mixtures at temperatures from 298.15 K to 313.15 K

Isothermal vapour–liquid equilibrium data are reported for binary mixtures of propan-2-one with 1,1,2,2-tetrachloroethane (I) and 1,4-dichlorobutane (II) within the 298.15–313.15 K temperature range. Total vapour pressures were measured by a static method, the mixtures beeing prepared by weight and degased directly into the working cell. The experimental data were correlated by Barker's method and different expressions for excess Gibbs energy were tested. The results indicate negative deviation from ideality for mixture (I), while mixture (II) behaves almost ideally, with slightly positive deviations.     

Viscometric and volumetric properties of benzene + methyl acetate,or + methyl propanoate,or + methyl butanoate binary systems at 283.15, 298.15 and 313.15 K

Viscosities and densities of three binary liquid mixtures, benzene?+?methyl acetate, benzene?+?methyl propanoate and benzene?+?methyl butanoate, have been measured at 283.15, 298.15 and 313.15?K, and atmospheric pressure. From experimental data, viscosity deviation, excess energy of activation for viscous flow, and excess molar volume were calculated and satisfactorily correlated with Redlich and Kister equation. Empirical and semiempirical equations and the predicted group-contribution method, universal automatic computer, were applied.     

Isobaric vapour–liquid phase diagram and excess properties for the binary system 1,4-dioxane + water at 298.15 K, 318.15 K and 338.15 K

Isobaric vapour–liquid equilibrium (VLE) data have been measured for the binary system (1,4-dioxane + water) at atmospheric pressure. The compositions of the two phases in equilibrium were taken from the refractive indices curve of the system. The equilibrium data show a positive deviation from ideality and reveal an azeotrope. VLE data have been used to calculate the activity coefficients of the two components at 298.15 K, 318.15 K and 338.15 K. The excess properties have been deduced at these temperatures. Molar Gibbs free energy at liquid state was expressed as a function of composition and temperature. At the liquid state, excess entropies of the present system are negative over the entire composition range. Molecular-scale segregation in this system was proved.     

Excess volume and surface tension of some flavoured binary alcohols at temperatures 298.15, 308.15 and 318.15 K

ABSTRACT

From the measured work of Ching-Ta and Chein-Hsiun Tu, we have presented the theoretical results of Surface tension and excess volume for three binary systems: namely 2-Propanol+Benzyl alcohol(1), 2-Propanol+2-Phenylethnol(2) and Benzyl alcohol+2-Phenylethanol(3) at temperatures 298.15, 308.15 and 318.15 K and atmospheric pressure over the concentration range 0.05–0.95. Theoretical results were computed from Flory model, Ramaswamy and Anbananthan (RA) model and model devised by Glinski, and studied the mixing properties and interactions of these liquids. Deviations in the surface tension (?σ) were evaluated and fitted to the Redlich–Kister polynomial equation to derive the binary coefficients and standard errors. Moreover, McAllister multi-body interaction model based on Eyring’s theory of absolute reaction rates has also been applied. For liquid mixtures, the free energy of activation is additive, based on the proportions of the different components of the mixture and interactions of like and unlike molecules. The behaviour of the liquids was studied and correlated with the molecular interactions from these liquid state models. Conclusively, these non-associated and associated models were compared and tested for different systems showing that the McAllister multi-body interaction model yields good results as compared to associated models, while Flory model shows more deviations.     

Thermodynamic and transport properties for binary and ternary mixtures of 2-methyltetrahydrofuran?+?chlorobenzene?+?cyclopentanone at T?=?298.15?K

Abstract  

Experimental densities ρ, viscosities η, and refractive indices n _D of the ternary mixtures consisting of 2-methyltetrahydrofuran + chlorobenzene + cyclopentanone and constituted binary mixtures were measured at T = 298.15 K for the liquid region and at ambient pressure for the whole composition range. Excess molar volumes V_\textm^\textEV_{\text{m}}^{\text{E}}, deviations in the viscosity Δη, and deviations in the refractive index Δn _D from the mole fraction average for the mixtures were derived from the experimental data. The excess partial molar volumes V_\textm,i^\textEV_{{\text{m}},i}^{\text{E}} were also calculated. The binary and ternary data of V_\textm^\textEV_{\text{m}}^{\text{E}}, Δη, and Δn _D were correlated as a function of the mole fraction by using the Redlich–Kister and the Cibulka equations, respectively. McAllister’s three-body interaction model is used for correlating the kinematic viscosity of binary mixtures with the mole fraction.     

Correspondence between Grunberg-Nissan,Arrhenius and Jouyban-Acree parameters for viscosity of 1,4-dioxane + water binary mixtures from 293.15 K to 320.15 K

The study of physical properties of binary liquid mixtures is of great importance for understanding and characterisation of molecular interactions. In the same way, some models attempt to correlate viscosity in liquid mixtures to release eventual interactions, structures’ change and peculiar behaviours. Grunberg–Nissan (GN) parameters for viscosity (η) in 1,4-dioxane?+?water mixtures over the entire range of mole fractions under atmospheric pressure and from 293.15?K to 320.15?K were calculated from experimental dynamic viscosities presented in previous works. Many experimenters investigate physicochemical properties using numerous models to derive some interpretations and conclusions. The present work comes within the framework of correlating different used equations to restrict investigations with an optimal of number of these models. Relationship between the GN, Arrhenius and Jouyban–Acree parameters for viscosity is shown in one binary mixture which dielectric constants of their pure components are very distinct.     

Excess properties and spectroscopic studies of binary system of 1-methoxy-2-propanol + dimethyl sulfoxide at T = (298.15–318.15) K

Thermophysical property data for the binary system of 1-methoxy-2-propanol (PGME) + dimethyl sulfoxide (DMSO), a potential candidate for use as the scrubbing liquid for the absorption of SO₂, are lacking in the literature. This paper presents experimental data at 0.1 MPa on the density and viscosity for this binary system measured over the whole composition range at T = (298.15, 303.15, 308.15, 313.15 and 318.15) K. The extended combined uncertainty U_c with a 0.95 level of confidence for the pycnometer method and Ubbelohde viscometer used in this study is 0.002 g·cm^?3 and 0.028 cm²·s^?1, respectively. The PGME + DMSO system shows negative values of the excess molar volume at all temperatures and compositions. Based on UV-Vis and FTIR, the intermolecular interaction of PGME with DMSO was confirmed as hydrogen bonding between the hydroxyl hydrogen atom in PGME and the oxygen atom in DMSO.     

Volumetric properties and volumetric interaction parameters for the CsCl–monosaccharide (d-galactose,d-xylose and d-arabinose)–water systems at T=298.15 K

Density measurements have been carried out at T=298.15 K for the CsCl–monosaccharide (d-galactose, d-xylose and d-arabinose)–water systems. The apparent molar volume of saccharides V_φ,S in the ternary solutions, the corresponding infinite dilution apparent molar volume V_φ,S^∘, and the standard transfer volume Δ_tV_φ,S^∘ of saccharides from water to aqueous CsCl solutions have been determined. The McMillan–Mayer theory was employed to relate the excess thermodynamic functions to a series of interaction parameters to obtain the volumetric interaction parameters of CsCl with monosaccharide in water. These parameters are interpreted by the group additivity principle and the stereochemistry of these monosaccharide molecules.