A new equation of state for H2O ice Ih

被引:299
作者
Feistel, R [1 ]
Wagner, W
机构
[1] Univ Rostock, Leibniz Inst Ostseeforsch, D-18119 Warnemunde, Germany
[2] Ruhr Univ Bochum, Lehrstuhl Thermodynam, D-44780 Bochum, Germany
关键词
compressibility; density; entropy; enthalpy; Gibbs energy; heat capacity; ice; melting point; sublimation pressure; thermal expansion; thermodynamic properties; water;
D O I
10.1063/1.2183324
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Various thermodynamic equilibrium properties of naturally abundant, hexagonal ice (ice Ih) of water (H2O) have been used to develop a Gibbs energy function g(T,p) of temperature and pressure, covering the ranges 0-273.16 K and 0 Pa-210 MPa, expressed in the temperature scale ITS-90. It serves as a fundamental equation from which additional properties are obtained as partial derivatives by thermodynamic rules. Extending previously developed Gibbs functions, it covers the entire existence region of ice Ih in the T-p diagram. Close to zero temperature, it obeys the theoretical cubic limiting law of Debye for heat capacity and Pauling's residual entropy. It is based on a significantly enlarged experimental data set compared to its predecessors. Due to the inherent thermodynamic cross relations, the formulas for particular quantities like density, thermal expansion, or compressibility are thus fully consistent with each other, are more reliable now, and extended in their ranges of validity. In conjunction with the IAPWS-95 formulation for the fluid phases of water, the new chemical potential of ice allows an alternative computation of the melting and sublimation curves, being improved especially near the triple point, and valid down to 130 K sublimation temperature. It provides an absolute entropy reference value for liquid water at the triple point. (c) 2006 American Institute of Physics.
引用
收藏
页码:1021 / 1047
页数:27
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