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BINARY NUCLEATION KINETICS .1. SELF-CONSISTENT SIZE DISTRIBUTION

机译:二元核动力学1。自洽大小分布

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Using the principle of detailed balance, we derive a new self-consistency requirement, termed the kinetic product rule, relating the evaporation coefficients and equilibrium cluster distribution for a binary system. We use this result to demonstrate and resolve an inconsistency for an idealized Kelvin model of nucleation in a simple binary mixture. We next examine several common forms for the equilibrium distribution of binary clusters based on the capillarity approximation and ideal vapor behavior. We point out fundamental deficiencies for each expression. We also show that each distribution yields evaporation coefficients that formally satisfy the new kinetic product rule but are physically unsatisfactory because they depend on the monomer vapor concentrations. We then propose a new form of the binary distribution function that is free of the deficiencies of the previous functions except for its reliance on the capillarity approximation. This new self-consistent classical (SCC) size distribution for binary clusters has the following properties: It satisfies the law of mass action; it reduces to an SCC unary distribution for clusters of a single component; and it produces physically acceptable evaporation rate coefficients that also satisfy the new kinetic product rule. Since it is possible to construct other examples of similarly well-behaved distributions, our result is not unique in this respect, but it does give reasonable predictions. As an illustrative example, we calculate binary nucleation rates and vapor activities for the ethanol-hexanol system at 260 K using the new SCC distribution and compare them to experimental results. The theoretical rates are uniformly higher than the experimental values over the entire vapor composition range. Although the predicted activities are lower, we find good agreement between the measured and theoretical slope of the critical vapor activity curve at a constant nucleation rate of 10(7) cm(-3) s(-2). (C) 1995 American Institute of Physics. [References: 34]
机译:使用详细平衡的原理,我们得出了一个新的自洽要求,称为动力学乘积规则,它涉及二元系统的蒸发系数和平衡簇分布。我们使用此结果来证明和解决理想的开尔文模型在简单的二元混合物中的成核问题。接下来,我们将基于毛细作用近似和理想蒸气行为,研究二元簇平衡分布的几种常见形式。我们指出了每种表达方式的基本缺陷。我们还表明,每种分布所产生的蒸发系数都正式满足新的动力学乘积法则,但在物理上并不令人满意,因为它们取决于单体蒸气浓度。然后,我们提出了一种新形式的二进制分布函数,该函数没有依赖于以前的函数的缺陷,除了它依赖于毛细管近似。这种针对二元簇的新的自洽经典(SCC)大小分布具有以下特性:满足质量作用定律;对于单个组件的集群,它简化为SCC一元分布;它产生的物理上可接受的蒸发速率系数也满足新的动力学乘积规则。由于可以构造行为类似的分布的其他示例,因此我们的结果在这方面不是唯一的,但确实给出了合理的预测。作为一个说明性的例子,我们使用新的SCC分布计算了260 K下乙醇-己醇系统的二元成核速率和蒸气活度,并将其与实验结果进行了比较。在整个蒸气组成范围内,理论速率均始终高于实验值。尽管预测的活性较低,但我们发现在恒定成核速率为10(7)cm(-3)s(-2)的情况下,临界蒸气活度曲线的实测斜率与理论斜率之间具有良好的一致性。 (C)1995年美国物理研究所。 [参考:34]

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