Blas Felipe J, MacDowell Luis G, de Miguel Enrique, Jackson George
Departamento de Fisica Aplicada, Facultad de Ciencias Experimentales, Universidad de Huelva, 21071 Huelva, Spain.
J Chem Phys. 2008 Oct 14;129(14):144703. doi: 10.1063/1.2989115.
We consider the computation of the interfacial properties of molecular chains from direct simulation of the vapor-liquid interface. The molecules are modeled as fully flexible chains formed from tangentially bonded monomers with truncated Lennard-Jones interactions. Four different model systems comprising of 4, 8, 12, and 16 monomers per molecule are considered. The simulations are performed in the canonical ensemble, and the vapor-liquid interfacial tension is evaluated using the test area and the wandering interface methods. In addition to the surface tension, we also obtain density profiles, coexistence densities, critical temperature and density, and interfacial thickness as functions of temperature, paying particular attention to the effect of the chain length on these properties. According to our results, the main effect of increasing the chain length (at fixed temperature) is to sharpen the vapor-liquid interface and to increase the width of the biphasic coexistence region. As a result, the interfacial thickness decreases and the surface tension increases as the molecular chains get longer. The interfacial thickness and surface tension appear to exhibit an asymptotic limiting behavior for long chains. A similar behavior is also observed for the coexistence densities and critical properties. Our simulation results indicate that the asymptotic regime is reached for Lennard-Jones chains formed from eight monomer segments. We also include a preliminary study on the effect of the cutoff distance on the interfacial properties. Our results indicate that all of the properties exhibit a dependence with the distance at which the interactions are truncated, though the relative effect varies from one property to the other. The interfacial thickness and, more particularly, the interfacial tension are found to be strongly dependent on the particular choice of cutoff, whereas the density profiles and coexistence densities are, in general, less sensitive to the truncation.
我们考虑通过汽液界面的直接模拟来计算分子链的界面性质。分子被建模为由具有截断的 Lennard-Jones 相互作用的切向键合单体形成的完全柔性链。考虑了四个不同的模型系统,每个分子分别包含 4、8、12 和 16 个单体。模拟在正则系综中进行,使用测试面积法和移动界面法评估汽液界面张力。除了表面张力外,我们还获得了密度分布、共存密度、临界温度和密度以及作为温度函数的界面厚度,特别关注链长对这些性质的影响。根据我们的结果,增加链长(在固定温度下)的主要作用是使汽液界面变锐,并增加双相共存区域的宽度。结果,随着分子链变长,界面厚度减小,表面张力增加。对于长链,界面厚度和表面张力似乎表现出渐近极限行为。对于共存密度和临界性质也观察到类似的行为。我们的模拟结果表明,由八个单体段形成的 Lennard-Jones 链达到了渐近区域。我们还包括了关于截止距离对界面性质影响的初步研究。我们的结果表明,所有性质都表现出对相互作用截断距离的依赖性,尽管相对影响因性质而异。发现界面厚度,特别是界面张力强烈依赖于截止的特定选择,而密度分布和共存密度通常对截断不太敏感。