Anomalous corresponding-states surface tension of hydrogen fluoride and of the Onsager model -: art. no. 084705

被引:20
|
作者
Weiss, VC
Schröer, W
机构
[1] Int Univ Bremen, Sch Sci & Engn, D-28725 Bremen, Germany
[2] Univ Bremen, Inst Anorgan & Phys Chem, D-28359 Bremen, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 2005年 / 122卷 / 08期
关键词
D O I
10.1063/1.1849152
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 a corresponding-states analysis of the liquid-vapor surface tension originally suggested by Guggenheim, we study the behavior of different simple (i.e., nonpolar), polar and ionic fluids. The results are compared to the corresponding ones for model fluids of each of the three types. For simple and weakly polar fluids (both real and model), the data map onto a master curve, as demonstrated by Guggenheim. For strongly dipolar, associating fluids, which also exhibit hydrogen bonding, one finds deviations from the master curve at low temperatures and, thus, observes the characteristic sigmoid behavior of the reduced surface tension as a function of temperature. The same is obtained for the model ionic fluid, the restricted primitive model. Truly exceptionally low values of the reduced surface tension are found for hydrogen fluoride and for the Onsager model of dipolar fluids, the surface tension of which we evaluate using an approximate hypernetted chain relation to obtain the square-gradient term in a modified van der Waals theory. Remarkably, in the corresponding-states plot, the surface tensions of HF and of the Onsager model agree very closely, while being well separated from the values for the other fluids. We also study the gradual transition of a model fluid from a simple fluid to a strongly dipolar one by varying the relative strength of dipolar and dispersion forces. (C) 2005 American Institute of Physics.
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页数:11
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