Pártay Lívia, Jedlovszky Pál
Department of Colloid Chemistry, Eötvös Loránd University, Pázmány Péter Setany 1/a, H-1117 Budapest, Hungary.
J Chem Phys. 2005 Jul 8;123(2):24502. doi: 10.1063/1.1953547.
The percolation transition of the hydrogen-bonded clusters of molecules is investigated in supercritical water by Monte Carlo computer simulations. Simulations have been performed at four thermodynamic state points located above the supercritical extension of the vapor-liquid coexistence curve on the p-T phase diagram and at four state points located below this curve. It is found in a temperature range of a few hundred Kelvin that the extension of the vapor-liquid coexistence curve separates the supercritical thermodynamic states in which the water molecules form infinite hydrogen-bonded clusters from those in which the hydrogen-bonded clusters are isolated oligomers. However, the difference between the size of the hydrogen-bonded clusters at thermodynamic states located at the two sides of the extension of the coexistence curve is found to decrease with increasing temperature, and the present results suggest that this difference is likely to vanish at high enough temperatures.
通过蒙特卡罗计算机模拟研究了超临界水中分子氢键簇的渗流转变。在p-T相图上位于气液共存曲线超临界延伸之上的四个热力学状态点以及位于该曲线之下的四个状态点进行了模拟。发现在几百开尔文的温度范围内,气液共存曲线的延伸将水分子形成无限氢键簇的超临界热力学状态与氢键簇为孤立低聚物的状态区分开来。然而,发现共存曲线延伸两侧的热力学状态下氢键簇大小的差异随温度升高而减小,目前的结果表明,在足够高的温度下这种差异可能会消失。