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常见水模型的液-气相平衡性质的对应态分析。

A corresponding-states analysis of the liquid-vapor equilibrium properties of common water models.

机构信息

Bremen Center for Computational Materials Science, Universität Bremen, Am Fallturm 1, 28359 Bremen, Germany.

出版信息

J Chem Phys. 2017 Feb 14;146(6):064505. doi: 10.1063/1.4975778.

Abstract

Many atomistic potential models have been proposed to reproduce the properties of real water and to capture as many of its anomalies as possible. The large number of different models indicates that this task is by no means an easy one. Some models are reasonably successful for various properties, while others are designed to account for only a very few specific features of water accurately. Among the most popular models are SPC/E, TIP4P, TIP4P/2005, TIP4P/Ice, and TIP5P-E. Here, we report the equilibrium properties of the liquid-vapor coexistence, such as the densities of the liquid phase and the vapor phase, the interfacial tension between them, and the vapor pressure at saturation. From these data, the critical parameters are determined and subsequently used to cast the liquid-vapor coexistence properties into a corresponding-states form following Guggenheim's suggestions. Doing so reveals that the three TIP4P-based models display the same corresponding-states behavior and that the SPC/E model behaves quite similarly. Only the TIP5P-E model shows clear deviations from the corresponding-states properties of the other models. A comparison with data for real water shows that the reduced surface tension is well described, while the reduced coexistence curve is too wide. The models underestimate the critical compressibility factor and overestimate Guggenheim's ratio as well as the reduced boiling temperature (Guldberg's ratio). As demonstrated by the collapse of the data for the TIP4P-based models, these deviations are inherent to the specific model and cannot be corrected by a simple reparametrization. For comparison, the results for two recent polarizable models, HBP and BK3, are shown, and both models are seen to perform well in terms of absolute numbers and in a corresponding-states framework. The kind of analysis applied here can therefore be used as a guideline in the design of more accurate and yet simple multi-purpose models of water.

摘要

许多原子势模型被提出来以再现真实水的性质,并尽可能多地捕捉其异常。大量不同的模型表明,这项任务绝不是一件容易的事。有些模型在各种性质上相当成功,而另一些则旨在准确地解释水的极少数非常特定的特征。其中最受欢迎的模型包括 SPC/E、TIP4P、TIP4P/2005、TIP4P/Ice 和 TIP5P-E。在这里,我们报告了液体-蒸汽共存的平衡性质,如液相和气相的密度、它们之间的界面张力以及饱和时的蒸汽压力。从这些数据中,确定了临界参数,然后按照古根海姆的建议将液体-蒸汽共存性质转化为相应状态的形式。这样做表明,基于 TIP4P 的三个模型表现出相同的相应状态行为,而 SPC/E 模型的行为则非常相似。只有 TIP5P-E 模型表现出与其他模型的相应状态性质明显偏离。与真实水的数据比较表明,表面张力的降低得到了很好的描述,而共存曲线的降低则太宽。模型低估了临界压缩因子,并高估了古根海姆比以及降低的沸点(古尔伯格比)。正如基于 TIP4P 的模型数据的崩溃所表明的那样,这些偏差是特定模型固有的,不能通过简单的重新参数化来纠正。为了比较,还显示了两个最近的极化模型 HBP 和 BK3 的结果,并且可以看出这两个模型在绝对值和相应状态框架内都表现良好。因此,这里应用的分析可以用作设计更准确但仍然简单的多用途水模型的指南。

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