Response to "Comment on 'A simple molecular thermodynamic theory of hydrophobic hydration' " [J. Chem. Phys. 119, 10448 (2003)]

被引:0
|
作者
Ashbaugh, Henry S. [1 ]
Truskett, Thomas M. [2 ,3 ]
Debenedetti, Pablo G. [4 ]
机构
[1] Los Alamos Natl Lab, Theoret Div, Los Alamos, NM 87545 USA
[2] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
[3] Univ Texas Austin, Inst Theoret Chem, Austin, TX 78712 USA
[4] Princeton Univ, Dept Chem Engn, Princeton, NJ 08544 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2003年 / 119卷 / 19期
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中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this response, we present a generalized condition for the observation of entropy convergence behavior for hydrophobic hydration. Applied within the context of our previously developed partition function for aqueous mixtures with nonpolar solutes, it is shown that entropy convergence is observed at a unique temperature when the thermal expansion coefficient of liquid water satisfies specific criterion. Hydrogen-bonding is essential and van der Waals-type fluids never display this phenomenon. Comparing these results to the discussion of Graziano who contends transient hydrogen-bond fluctuations in water dominate entropy convergence, we find that both van der Waals and hydrogen-bonding contributions are significant within the context of our model. In addition, it is pointed out that molecular-level conclusions drawn from a mean-field model should be made with caution.
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页码:10450 / 10451
页数:2
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