For an adequate choice or design of ionic liquids, the knowledge of their interaction with other solutes and solvents is an essential feature for predicting the reactivity and selectivity of systems involving these compounds. In this work, the activity coefficient of water in several imidazolium-based ionic liquids with the common cation 1-butyl-3-methylimidazolium was measured at 298.2 K. To contribute to a deeper insight into the interaction between ionic liquids and water, COSMO-RS was used to predict the activity coefficient of water in the studied ionic liquids along with the excess enthalpies. The results showed good agreement between experimental and predicted activity coefficient of water in ionic liquids and that the interaction of water and ionic liquids was strongly influenced by the hydrogen bonding of the anion with water. Accordingly, the intensity of interaction of the anions with water can be ranked as the following: [CF3SO3](-) < [SCN](-) < [TFA](-) < Br(-) < [TOS](-) < Cl(-) < [CH3SO3](-) [DMP](-) < [Ac](-). In addition, fluorination and aromatization of anions are shown to reduce their interaction with water. The effect of temperature on the activity coefficient of water at infinite dilution was measured by inverse gas chromatography and predicted by COSMO-RS. Further analysis based on COSMO-RS provided information on the nature of hydrogen bonding between water and anion as well as the possibility of anion-water complex formation.

Nanoparticles of CoFe2O4 and CoIn0.15Fe1.85O4 ferrites were prepared by citrate gel route and characterized to understand their structural, electrical, and magnetic properties. X-ray diffraction and Raman spectroscopy were used to confirm the formation of single phase cubic spinel structure. The average grain sizes from the Scherrer formula were below 50 nm. Microstructural features were obtained by scanning electron microscope and compositional analysis by energy dispersive spectroscopy. The hysteresis curve shows enhancement in coercivity while reduction in saturation magnetization with the substitution of In3+ ions. Enhancement of coercivity is attributed to the transition from multidomain to single domain nature. Electrical properties, such as dc resistivity as a function of temperature and ac conductivity as a function of frequency and temperature were studied for both the samples. The activation energy derived from the Arrhenius equation was found to increase in the doped sample. The dielectric constant (ε′) and dielectric loss (tan δ) are also studied as a function of frequency and temperature. The variation of dielectric properties ε′, tan δ, and ac conductivity (σac) with frequency reveals that the dispersion is due to Maxwell–Wagner type of interfacial polarization in general and the hopping of charge between Fe2+ and Fe3+ as well as between Co2+ and Co3+ ions at B-sites. Magnetization and electrical property study showed its dominant dependence on the grain size.

The industrial application of ionic liquids (ILs) requires the knowledge of their physical properties and phase behavior. This work addresses the experimental determination of the vapor−liquid equilibria (VLE) of binary systems composed of water + imidazolium-based ILs. The ILs under consideration are 1-butyl-3-methylimidazolium trifluoromethanesulfonate, 1butyl-3-methylimidazolium thiocyanate, 1-butyl-3-methylimidazolium tosylate, 1-butyl-3-methylimidazolium trifluoroacetate, 1butyl-3-methylimidazolium bromide, 1-butyl-3-methylimidazolium chloride, 1-butyl-3-methylimidazolium methanesulfonate, and 1-butyl-3-methylimidazolium acetate, which allows the evaluation of the influence of the IL anion through the phase behavior. Isobaric VLE data were measured at 0.05, 0.07, and 0.1 MPa for IL mole fractions ranging between 0 and 0.7. The observed increase in the boiling temperatures of the mixtures is related with the strength of the interaction between the IL anion and water. The Perturbed-Chain Statistical Associating Fluid Theory (PC-SAFT) was further used to describe the obtained experimental data. The ILs were treated as molecular associating species with two association sites per IL. The model parameters for the pure fluids and the binary interaction parameter k ij between water and ILs were determined by a simultaneous fitting to pure-IL densities, water activity coefficients at 298.15 K and VLE data at 0.1 MPa. Pure-IL densities, water activity coefficients, and VLE data were well described by PC-SAFT in broad temperature, pressure, and composition ranges. The PC-SAFT parameters were applied to predict the water activity coefficients at infinite dilution in ILs, and a satisfactory prediction of experimental data was observed.

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