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Thermodynamic properties of glycerol: Experimental and theoretical study
被引:32
|作者:
Verevkin, Sergey P.
[1
,2
,3
]
Zaitsau, Dzmitry H.
[3
]
Emel'yanenko, Vladimir N.
[3
]
Zhabina, Aleksandra A.
[1
,2
]
机构:
[1] Univ Rostock, Dept Phys Chem, D-18059 Rostock, Germany
[2] Univ Rostock, Dept Sci & Technol Life Light & Matter, D-18059 Rostock, Germany
[3] Kazan Fed Univ, Dept Phys Chem, Kazan 420008, Russia
关键词:
Glycerol;
Vapor pressure measurements;
Enthalpy of vaporization;
Enthalpy of formation;
Quantum-chemical calculations;
Thermodynamic properties;
Entropy;
VAPOR-PRESSURES;
VAPORIZATION ENTHALPIES;
EQUILIBRIUM;
SERIES;
WATER;
THERMOCHEMISTRY;
EVAPORATION;
PREDICTION;
SYSTEMS;
ENERGY;
D O I:
10.1016/j.fluid.2015.03.038
中图分类号:
O414.1 [热力学];
学科分类号:
摘要:
Vapor pressures of highly pure glycerol were measured by the static and the transpiration methods in a broad temperature range. The standard molar enthalpy of vaporization of glycerol was derived from the vapor pressure temperature dependencies. Thermodynamic data on glycerol available in the literature were collected, evaluated, and combined with own experimental results. We recommend the set of vaporization and formation enthalpies for glycerol at 298.15 K (in kJ mol(-1)): Delta H-f(m)degrees; (g) = -(578.8 +/- 0.6), Delta H-f(m)degrees (1) = -(669.3 +/- 0.5), and Delta H-g(I)m degrees = (90.5 +/- 0.3) as the reliable benchmark properties for further thermochemical calculations. Quantum-chemical calculations of the gas phase molar enthalpy of formation of glycerol have been performed using the G4 method and results were in agreement with the recommended experimental data. The standard molar entropy of formation and the standard molar Gibbs function of formation of glycerol were estimated. (C) 2015 Elsevier B.V. All rights reserved.
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页码:87 / 94
页数:8
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