Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Dilational visco-elasticity of polyelectrolyte/surfactant adsorption layers at the air/water interface: Poly(vinyl pyridinium chloride) and sodium dodecylsulfate. / Носков, Борис Анатольевич; Быков, Алексей Геннадьевич; Grigoriev, D.O.; Lin, S. Y.; Loglio, Giuseppe; Miller, Reinhard.
в: Colloids and Surfaces A: Physicochemical and Engineering Aspects, Том 322, 2008, стр. 71-78.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Dilational visco-elasticity of polyelectrolyte/surfactant adsorption layers at the air/water interface: Poly(vinyl pyridinium chloride) and sodium dodecylsulfate
AU - Носков, Борис Анатольевич
AU - Быков, Алексей Геннадьевич
AU - Grigoriev, D.O.
AU - Lin, S. Y.
AU - Loglio, Giuseppe
AU - Miller, Reinhard
N1 - DOI: 10.1016/j.colsurfa.2008.02.036
PY - 2008
Y1 - 2008
N2 - The dilational dynamic surface elasticity of mixed aqueous polyvinylpyridinium chloride/sodium dodecyl sulfate solutions (PVPmCl/SDS) was measured as a function of time and surfactant concentration. This system represents a typical example of polyelectrolyte/surfactant complex formation and subsequentaggregation on the nano-scale. The concentration dependence of the real part of the dynamic surface elasticity for the mixed PVPmCl/SDS solutions in 0.1MNaCl and without added NaCl qualitatively agreed with the corresponding results for some previously studied polyelectrolyte/surfactant solutions. This similarityindicates that strong changes of the surface visco-elasticity in a narrow сoncentration range can be explained by the formation of microparticles in the surface layer. The addition of 0.1MNaCl to PVPmCl/SDS solutions led to an almost two times decrease of the surface elasticity at low concentrations and to the acceleration of the adsorption layer formation. At the same time the imaginary part of surface elasticity of PVPmCl/SDS solutions was significantly higher than the corresponding results for the earlier studied systems and the adsorption layers proved to be visco-elastic in a broad concentration range. The application of the Maxwell rheological model in this case allowed the calculation of the main relaxation time. The main relaxation process is the surfactant exchange between the surface layer and the bulk phase or in the surface layer between free surfactant molecules and those bound in aggregates. The distinction of the surface visco-elasticity of PVPmCl/SDS solutions from the previously studied systems can be explained by the lower stability of polyelectrolyte/surfactant complexes in the adsorption layer.
AB - The dilational dynamic surface elasticity of mixed aqueous polyvinylpyridinium chloride/sodium dodecyl sulfate solutions (PVPmCl/SDS) was measured as a function of time and surfactant concentration. This system represents a typical example of polyelectrolyte/surfactant complex formation and subsequentaggregation on the nano-scale. The concentration dependence of the real part of the dynamic surface elasticity for the mixed PVPmCl/SDS solutions in 0.1MNaCl and without added NaCl qualitatively agreed with the corresponding results for some previously studied polyelectrolyte/surfactant solutions. This similarityindicates that strong changes of the surface visco-elasticity in a narrow сoncentration range can be explained by the formation of microparticles in the surface layer. The addition of 0.1MNaCl to PVPmCl/SDS solutions led to an almost two times decrease of the surface elasticity at low concentrations and to the acceleration of the adsorption layer formation. At the same time the imaginary part of surface elasticity of PVPmCl/SDS solutions was significantly higher than the corresponding results for the earlier studied systems and the adsorption layers proved to be visco-elastic in a broad concentration range. The application of the Maxwell rheological model in this case allowed the calculation of the main relaxation time. The main relaxation process is the surfactant exchange between the surface layer and the bulk phase or in the surface layer between free surfactant molecules and those bound in aggregates. The distinction of the surface visco-elasticity of PVPmCl/SDS solutions from the previously studied systems can be explained by the lower stability of polyelectrolyte/surfactant complexes in the adsorption layer.
M3 - Article
VL - 322
SP - 71
EP - 78
JO - Colloids and Surfaces A: Physicochemical and Engineering Aspects
JF - Colloids and Surfaces A: Physicochemical and Engineering Aspects
SN - 0927-7757
ER -
ID: 35207527