کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
201421 460548 2013 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Excess volumes and excess heat capacities for alkanediol + water systems in the temperature interval (283.15–313.15) K
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Excess volumes and excess heat capacities for alkanediol + water systems in the temperature interval (283.15–313.15) K
چکیده انگلیسی


• Alkanediol + water density was obtained in the interval (283.15–313.15) K.
• Isobaric molar heat capacity was also measured in the same conditions.
• Excess isobaric heat capacities and excess volumes were determined from these data.
• Excess magnitudes show similar behavior than those of monoalcohol + water systems.

Density and isobaric heat capacity per unit volume were determined for aqueous mixtures of 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, and 1,2-hexanediol over the whole composition range in the temperature interval (283.15–313.15) K at atmospheric pressure. From these data, excess molar volumes and excess isobaric molar heat capacities were obtained. The comparison of experimental data with literature values shows quite good agreement, not only for absolute magnitudes, but also for excess quantities. Excess volumes are negative over the whole composition range and they become more ideal (less negative) as temperature increases. Excess isobaric molar heat capacity is mostly positive, although it is negative for some mixtures at several compositions and temperatures. Moreover, it was found that it presents a maximum at low mole fraction of the alcohol for most systems, as it was previously found for alkanol + water mixtures. As for temperature dependence, excess isobaric molar heat capacity increases with raising temperature in all cases. This increase is more pronounced for concentrated solutions of dialcohol, with the exception of the 1,2-hexanediol system. The obtained results are interpreted in terms of well-known arguments based on definition of excess magnitudes and chemical nature of the compounds.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Fluid Phase Equilibria - Volume 356, 25 October 2013, Pages 1–10
نویسندگان
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