Brovchenko Ivan, Geiger Alfons, Oleinikova Alla
Physical Chemistry, Dortmund University, 44221 Dortmund, Germany.
J Chem Phys. 2005 Jul 22;123(4):044515. doi: 10.1063/1.1992481.
Liquid-liquid and liquid-vapor coexistence regions of various water models were determined by Monte Carlo (MC) simulations of isotherms of density fluctuation-restricted systems and by Gibbs ensemble MC simulations. All studied water models show multiple liquid-liquid phase transitions in the supercooled region: we observe two transitions of the TIP4P, TIP5P, and SPCE models and three transitions of the ST2 model. The location of these phase transitions with respect to the liquid-vapor coexistence curve and the glass temperature is highly sensitive to the water model and its implementation. We suggest that the apparent thermodynamic singularity of real liquid water in the supercooled region at about 228 K is caused by an approach to the spinodal of the first (lowest density) liquid-liquid phase transition. The well-known density maximum of liquid water at 277 K is related to the second liquid-liquid phase transition, which is located at positive pressures with a critical point close to the maximum. A possible order parameter and the universality class of liquid-liquid phase transitions in one-component fluids are discussed.
通过对密度涨落受限系统等温线的蒙特卡罗(MC)模拟以及吉布斯系综MC模拟,确定了各种水模型的液-液和液-气共存区域。所有研究的水模型在过冷区域均显示出多个液-液相变:我们观察到TIP4P、TIP5P和SPCE模型有两个相变,ST2模型有三个相变。这些相变相对于液-气共存曲线和玻璃化温度的位置对水模型及其实现高度敏感。我们认为,真实液态水在约228K的过冷区域中明显的热力学奇异性是由接近第一个(最低密度)液-液相变的旋节线引起的。液态水在277K时众所周知的密度最大值与第二个液-液相变有关,该相变位于正压下,临界点接近密度最大值。讨论了单组分流体中液-液相变可能的序参量和普适类。