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Título
Dielectric and refractive index measurements for the systems 1-pentanol + 2,5,8,11,14-pentaoxapentadecane, or for 2,5,8,11,14-pentaoxapentadecane + octane at (293.15-303.15) K
Autor
Año del Documento
2013
Documento Fuente
Thermochimica Acta, 2013, 551, 70-77
Résumé
Relative permittivities, , and refractive indices, , have been measured at (293.15-303.15) K, for the mixtures 1-pentanol + 2,5,8,11,14-pentaoxapentadecane (TEGDME) or TEGDME + octane. These data have been used, together with density measurements available in the literature, to calculate the correlation factors, , according to the Kirkwood-Fröhlich equations. The curves of the deviations of from the ideal behaviour, , of the 1-pentanol + TEGDME system are shifted to high mole fractions of the alcohol, and show a rather large minimum. The shape of the curves of methanol + TEGDME or + polyethylene glycol dimethyl ether 250 (PEG-250) mixtures is similar. This reveals that polyethers can break the alcohol self-association even at high alkanol concentrations. The higher values of the methanol solutions are ascribed to large self-association of this alcohol. The curves of the 1-pentanol + dibutyl ether (DBE) system are nearly symmetrical, and the values are higher than those of the corresponding TEGDME mixture. This indicates that effects related to the alcohol self-association are much more relevant in the DBE system. These findings are supported by and molar polarization data. Values of molar refraction of 1-pentanol systems reveal that dispersion forces become more important in the sequence: octane < DBE < TEGDME. Such forces are also more relevant in the 1-pentanol + TEGDME system than in the methanol + TEGDME solution. The comparison of and data for TEGDME or DBE + octane mixtures shows than the polyether is a more structured liquid.
Revisión por pares
SI
Idioma
eng
Tipo de versión
info:eu-repo/semantics/submittedVersion
Derechos
restrictedAccess
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