The static dielectric constant (epsilon) of ethane-1,2-diol + 1,2-dimethoxyethane + water ternary mixtures was measured as a function of temperature (263.15 less than or equal to T (K) less than or equal to 353.15) and composition, over the complete mole fraction range 0 less than or equal to x(1), x(2), x(3) less than or equal to 1. The experimental values were analyzed by empirical relationships that accounted for the dependence epsilon = epsilon(T) and Y = Y(x(i)). A comparison between calculated and experimental data shows that these fitting relationships can be reliably used to predict epsilon values, along with other related properties, in areas of experimental data gaps. Starting from the experimental measurements, some derived quantities such as molar orientational polarization (P), dipolar interaction free energy (Fmu) and the relevant thermodynamic excess mixing properties (F-mu(E), (F) over bar (E)(mu,i)), were obtained. The values of the excess quantities are indicative of the presence of specific interactions between different components in the mixtures. A discussion of data in terms of the Kirkwood theory also provides information on the short-range intermolecular interactions, suggesting the formation of stable two-component adducts rather than of more complex moieties involving all three molecular species.
Dielectric properties in ternary mixtures of ethane-1,2-diol+1,2-dimethoxyethane + water / Foca, Giorgia; Manfredini, Matteo; Manzini, Daniela; Marchetti, Andrea; Pigani, Laura; Sighinolfi, Simona; Tassi, Lorenzo; Ulrici, Alessandro. - In: INTERNATIONAL JOURNAL OF THERMOPHYSICS. - ISSN 0195-928X. - STAMPA. - 25:3(2004), pp. 839-855. [10.1023/B:IJOT.0000034239.58332.be]
Dielectric properties in ternary mixtures of ethane-1,2-diol+1,2-dimethoxyethane + water
FOCA, Giorgia;MANFREDINI, Matteo;MANZINI, Daniela;MARCHETTI, Andrea;PIGANI, Laura;SIGHINOLFI, Simona;TASSI, Lorenzo;ULRICI, Alessandro
2004
Abstract
The static dielectric constant (epsilon) of ethane-1,2-diol + 1,2-dimethoxyethane + water ternary mixtures was measured as a function of temperature (263.15 less than or equal to T (K) less than or equal to 353.15) and composition, over the complete mole fraction range 0 less than or equal to x(1), x(2), x(3) less than or equal to 1. The experimental values were analyzed by empirical relationships that accounted for the dependence epsilon = epsilon(T) and Y = Y(x(i)). A comparison between calculated and experimental data shows that these fitting relationships can be reliably used to predict epsilon values, along with other related properties, in areas of experimental data gaps. Starting from the experimental measurements, some derived quantities such as molar orientational polarization (P), dipolar interaction free energy (Fmu) and the relevant thermodynamic excess mixing properties (F-mu(E), (F) over bar (E)(mu,i)), were obtained. The values of the excess quantities are indicative of the presence of specific interactions between different components in the mixtures. A discussion of data in terms of the Kirkwood theory also provides information on the short-range intermolecular interactions, suggesting the formation of stable two-component adducts rather than of more complex moieties involving all three molecular species.Pubblicazioni consigliate
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