Adsorption Layer Characteristics of Mixed SDS/CnEOm Solutions. II. Dilational Viscoelasticity

被引:14
|
作者
Fainerman, V. B. [2 ]
Aksenenko, E. V. [3 ]
Zholob, S. A. [2 ]
Petkov, J. T. [4 ]
Yorke, J. [4 ]
Miller, R. [1 ]
机构
[1] Max Planck Inst Colloids & Interfaces, D-14424 Potsdam, Germany
[2] Donetsk Med Univ, UA-83003 Donetsk, Ukraine
[3] Inst Colloid Chem & Chem Water, UA-03680 Kiev, Ukraine
[4] Unilever R&D Port Sunlight, Bebington CH63 3JW, England
关键词
AIR/WATER INTERFACE; SURFACE-PROPERTIES; RHEOLOGY; MODELS;
D O I
10.1021/la9024926
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bubble profile a it it lysis tensiometry is used to Study the surface rheological behavior of mixed SDS/C12EO5 and SDS/C14EO8 Solutions. The experimental dependencies of the viscoclasticity modulus and phase angle are Studied in it wide range of surfactant concentrations of the individual Sodium dodecyl sulfate (SIDS) and CmEOn solutions and SDS/CnEOm mixtures at various mixing ratios. By generating harmonic oscillations of the bubble area at low oscillation amplitudes, the relaxation behavior at oscillation frequencies between 0.005 and 0.2 Hz Was Studied. The applied theoretical approach to describe the dilational rheology of surfactant mixtures requires the specification of the equations of state of the mixed surface layer and the adsorption isotherm of the mixture's components. For the systems, studies, the theoretical model considers different adsorption mechanisms For the different surfactants. In particular, the adsorption behavior of oxyethylated surfactants was described by the reorientation model (assumes two adsorption states of surfactant molecules with different molar areas), including all intrinsic compressibility of molecules in the state of minimal area. For the SDS component, the adsorption was assumed to be governed by the Frumkin model, which also accounts for the intrinsic compressibility. Satisfactory agreement between experimental data and theoretical calculations of the viscoelasticity modulus and the phase angle is obtained.
引用
收藏
页码:1796 / 1801
页数:6
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