Adsorption of surfactants and proteins at fluid interfaces

被引:200
作者
Fainerman, VB [1 ]
Lucassen-Reynders, E [1 ]
Miller, R [1 ]
机构
[1] Max Planck Inst Colloid & Surface Chem, D-12489 Berlin, Germany
关键词
adsorption isotherms; proteins; surface reorientation; surface aggregation; surfactants; thermodynamic theory;
D O I
10.1016/S0927-7757(98)00585-8
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
This review presents some new equations of state and adsorption isotherms which describe mixed monolayers of surfactants possessing different molar area values, monolayers which comprise surfactants and proteins capable of reorientation or reconformation. For systems allowing reorientation and aggregation, the effect of self-regulation of the surface layer composition caused by surface pressure is considered. This effect is especially pronounced in protein adsorption layers, where not only the composition, but also the thickness of the adsorption layer depends on surface pressure. This principle was first proposed by Paul Joos for describing surface layers. The results of the proposed models have a direct impact on dynamic surface phenomena. The rate of adsorption for a diffusion-controlled mechanism depends on molecular reorientation or aggregation processes within the surface layer. For protein surface layers mainly conformational changes at the surface determine the rate of adsorption/desorption and other dynamic and mechanical properties of surface layers. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:141 / 165
页数:25
相关论文
共 111 条
[61]   DYNAMIC INTERFACIAL-TENSION MEASUREMENTS BY A CAPILLARY-PRESSURE METHOD [J].
LIGGIERI, L ;
RAVERA, F ;
PASSERONE, A .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1995, 169 (01) :226-237
[62]   EFFECT OF COHESIVE ENERGIES BETWEEN ADSORBED MOLECULES ON SURFACTANT EXCHANGE PROCESSES - SHIFTING FROM DIFFUSION CONTROL FOR ADSORPTION TO KINETIC-DIFFUSIVE CONTROL FOR RE-EQUILIBRATION [J].
LIN, SY ;
MCKEIGUE, K ;
MALDARELLI, C .
LANGMUIR, 1994, 10 (10) :3442-3448
[63]   Adsorption kinetics of soluble surfactants and the phase transition model 2. Experimental demonstration of 1-decanol [J].
Lin, SY ;
Hwang, WB ;
Lu, TL .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 1996, 114 :143-153
[64]   DIFFUSION-LIMITED INTERPRETATION OF THE INDUCTION PERIOD IN THE RELAXATION IN SURFACE-TENSION DUE TO THE ADSORPTION OF STRAIGHT CHAIN, SMALL POLAR GROUP SURFACTANTS - THEORY AND EXPERIMENT [J].
LIN, SY ;
MCKEIGUE, K ;
MALDARELLI, C .
LANGMUIR, 1991, 7 (06) :1055-1066
[65]   SURFACE EQUATION OF STATE FOR IONIZED SURFACTANTS [J].
LUCASSEN, EH .
JOURNAL OF PHYSICAL CHEMISTRY, 1966, 70 (06) :1777-+
[66]   SURFACE EQUATION OF STATE FOR MIXED SURFACTANT MONOLAYERS [J].
LUCASSEN.EH .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1972, 41 (01) :156-&
[67]   INTERACTIONS IN MIXED MONOLAYERS .2. EFFECT ON EQUILIBRIUM SURFACE PROPERTIES, WITH APPLICATION TO FATTY-ACID SOAP SOLUTIONS [J].
LUCASSEN.EH .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1973, 42 (03) :563-572
[68]   SURFACE EXCESSES OF SURFACE-ACTIVE IONS + OF GEGENIONS AT AIR-SOLUTION INTERFACE [J].
LUCASSEN.EH .
JOURNAL OF COLLOID SCIENCE, 1964, 19 (06) :584-&
[69]  
Lucassen-Reynders E, 1976, PROG SURF MEMBRANE S, V10, P253
[70]  
LUCASSENREYNDER.EH, 1981, ANIONIC SURFACTANTS, P1