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Dependence of Surface Tension of a Droplet Formed on the Molecular Condensation Nucleus or Ion on the Droplet Radius

机译:在液滴半径上形成在分子凝结核或离子上的液滴表面张力的依赖性

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The dependence of the thermodynamic surface tension of a small droplet formed on a molecular-size condensation nucleus on the droplet size, nucleus size, molecular field parameters, and nuclear charge in the case of an ion is investigated. Calculations have been performed for molecules of supersaturated argon vapor at different values of the chemical potential of the molecules in the framework of the gradient density functional theory (DFT) and the Carnahan-Starling model to take into account the contribution of hard spheres. The interaction of argon molecules with an uncharged condensation nucleus has been described by the Lennard-Jones potential. In the case of an ion, the long-range Coulomb potential of electric forces is additionally taken into account. The dielectric constant is defined as a function of the local density of the number of argon molecules. As a variable describing the size of the droplet, the radius of the equimolecular surface of the droplet is chosen. The obtained dependences of the surface tension of the droplets have been compared with the dependence of the surface tension on the size of droplet without a condensation nucleus. When the effect of the solvation layer is discarded, the dependence of the surface tension on the radius of the equimolecular surface of a small droplet with a condensation nucleus exhibits similar behavior as in the absence of the nucleus with almost the same negative Tolman correction. The effect of the rigidity constant, however, is clearly influenced by the existence of a condensation nucleus. It is shown that when the first solvation layer is divided around the condensation nucleus, the dependence of surface tension on the radius of the equimolecular surface of a small droplet with a condensation nucleus exhibits similar behavior with almost the same negative Tolman correction as in the absence of a nucleus, but with a different correction, namely, with effective rigidity constant for the surface layer.
机译:研究了在分子尺寸缩合核上形成的小液滴的热力表面张力对离子的液滴尺寸,核尺寸,分子场参数和核电荷的依赖性。在梯度密度泛函理论(DFT)框架中的分子的不同值下的超饱和氩气的分子进行了计算,以考虑到硬球的贡献。通过Lennard-Jones潜力描述了氩分子与不充分的冷凝核的相互作用。在离子的情况下,另外考虑电力的远程库仑电位。介电常数被定义为氩分子数量的局部密度的函数。作为描述液滴尺寸的变量,选择液滴的成分表面的半径。将所获得的液滴表面张力的依赖性与表面张力对没有冷凝核的液滴尺寸的依赖性进行了比较。当丢弃溶剂层的效果时,表面张力对具有缩合核的小液滴的成分表面的半径的依赖性表现出类似的行为,与具有几乎相同的负甲块校正的核心不存在。然而,刚性常数的影响明显受到缩合核的存在性的影响。结果表明,当第一溶剂层围绕冷凝核划分时,表面​​张力对具有冷凝核的小液滴的平位表面的半径的依赖性呈现类似的行为,其具有几乎相同的负耐药性校正如在缺失中核,但具有不同的校正,即表面层的有效刚度常数。

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