SORPTION KINETICS CONSIDERED AS A RENORMALIZED DIFFUSION PROCESS

被引:97
作者
RAVERA, F
LIGGIERI, L
STEINCHEN, A
机构
[1] CNR,IST CHIM FIS APPLICATA MAT,VIA DE MARINI 6,I-16149 GENOA,ITALY
[2] FAC SCI & TECH ST JEROME,THERMODYNAM LAB,F-13397 MARSEILLE 13,FRANCE
关键词
D O I
10.1006/jcis.1993.1088
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
A theoretical study of the sorption kinetics is performed by using a new approach in which the adsorption-desorption process is considered as an extended diffusion process with a renormalized diffusion coefficient taking into account an interfacial potential barrier. This model allows us to describe the time dependence of the process by considering both the crossing of an interfacial potential barrier and the diffusion in the neighboring phase. This model leads us to write an expression for the surface concentration as a function of the time, in terms of the molecular activation energies of adsorption and desorption. The possibility of using this theoretical approach to interpret experimental data of dynamic interfacial tension during the absorption at liquid-liquid and liquid-gas interfaces is discussed. © 1993 Academic Press, Inc.
引用
收藏
页码:109 / 116
页数:8
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