Isotherms of capillary condensation influenced by formation of adsorption films - 1. Calculation for model cylindrical and slit pores

被引:40
作者
Churaev, NV
Starke, G
Adolphs, J
机构
[1] Russian Acad Sci, Inst Phys Chem, Lab Thin Liquid Layers, Moscow 117915, Russia
[2] Univ Essen Gesamthsch, Dept Math, D-45117 Essen, Germany
[3] Northwestern Univ, NSF, Ctr Adv Cement Based Mat ACBM, Evanston, IL 60208 USA
关键词
adsorption; capillary condensation; nanoporous systems; sorption isotherms; disjoining pressure; excess surface work; wetting films;
D O I
10.1006/jcis.1999.6592
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
Isotherms of capillary condensation are often used to determine the vapor sorption capacity of porous adsorbents as well as the pore size distribution by radii. In this paper, for calculating the volume of capillary condensate and of adsorption films in a porous body, an approach based on the theory of surface forces is used. Adsorption isotherms and disjoining pressure isotherms of wetting films are presented here in an exponential form discussed earlier. The calculations were made for straight cylindrical capillaries of different radii and slit pores of different width. The mechanisms of capillary condensation differ in cylindrical and slit pores. In cylindrical pores capillary condensation occurs due to capillary instability of curved wetting films on a capillary surface, when film thickness grows. In the case of slit pores, coalescence of wetting films formed on opposite slit surfaces proceeds under the action of attractive dispersion forces, Partial volumes of liquid in the state of both capillary condensate and adsorbed films are calculated dependent on the relative vapor pressure in a surrounding media. (C) 2000 Academic Press.
引用
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页码:246 / 253
页数:8
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