Thermodynamics and Modeling of Sorption Isotherms

被引:8
|
作者
Adolphs, Juergen [1 ]
机构
[1] POROTEC GmbH, Niederhofheimer Str 55, D-65719 Hofheim Ts, Germany
基金
美国国家科学基金会;
关键词
Capillary condensation; Disjoining pressure; Excess surface work; Sorption hysteresis; Sorption isotherm; Thermodynamics of sorption; EXCESS SURFACE WORK; PORE-SIZE ANALYSIS; CAPILLARY CONDENSATION; ADSORPTION-ISOTHERMS; NITROGEN; SYSTEMS; FILMS;
D O I
10.1002/cite.201500137
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
An extended version of the thermodynamic computation model for sorption isotherms and capillary condensation is introduced. With the combination of the excess surface work (ESW) and disjoining pressure approach sorption isotherms for various pore size distributions of cylindrical and slit-like mesopores are successfully modeled. The main idea is that during adsorption on pore walls the approaching films will collapse and capillary condensation proceeds, while evaporation is described with a modified Kelvin equation. In both cases adsorption and desorption, the surface tension dependency on the pore size is considered.
引用
收藏
页码:274 / 281
页数:8
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