Dynamic surface elasticity of mixed poly(diallyldimethylammonium chloride)/sodium dodecyl sulfate/NaCl solutions

被引:19
|
作者
Lyadinskaya, V. V. [1 ]
Bykov, A. G. [1 ]
Campbell, R. A. [2 ]
Varga, I. [3 ]
Lin, S. Y. [4 ]
Loglio, G. [5 ]
Miller, R. [6 ]
Noskov, B. A. [1 ]
机构
[1] St Petersburg State Univ, Fac Chem, St Petersburg 198504, Russia
[2] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[3] Eotvos Lorand Univ, Inst Chem, H-1518 Budapest 112, Hungary
[4] Natl Taiwan Univ Sci & Technol, Dept Chem Engn, Taipei 106, Taiwan
[5] Univ Florence, Dipartimento Chim Organ, I-50019 Florence, Italy
[6] MPI Kolloid & Grenzflachenforsch, D-14424 Potsdam, Germany
关键词
Polyelectrolyte/surfactant complexes; Surface viscoelasticity; Dynamic surface tension; Relaxation processes in the surface layer; Colloidal dispersion; AIR-WATER-INTERFACE; OPPOSITELY CHARGED POLYELECTROLYTES; AIR/WATER INTERFACE; ADSORPTION LAYERS; DILATIONAL VISCOELASTICITY; POLY(DIMETHYLDIALLYLAMMONIUM CHLORIDE); ANIONIC SURFACTANTS; COMPLEXES; MIXTURES; STABILITY;
D O I
10.1016/j.colsurfa.2014.01.041
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
The non-monotonic concentration and kinetic dependencies of the dynamic dilational surface elasticity of mixed poly(diallyldimethylammonium chloride)/sodium dodecyl sulfate(SDS)/NaCl solutions indicate the formation of micro-aggregates in the surface layer. The increase of the solution's ionic strength results in strong changes of the surface dilational rheological properties and thereby of the interfacial layer structure at lower SDS concentrations due to the large increase of the adsorption rate. Close to the charge match point of the components, however, the rheological properties are influenced by the presence of micro-aggregates embedded in the adsorption layer. In this case, effects of changing the sample history on the rheological behavior and heterogeneity of the interface were further investigated. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:3 / 10
页数:8
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