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Effect of polymer on the elasticity of surfactant membranes: a light scattering study.

作者信息

Iñiguez-Palomares Ramón, Acuña-Campa Heriberto, Maldonado Amir

机构信息

Departamento de Física, Universidad de Sonora, 83000 Hermosillo, Sonora, Mexico.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2011 Jul;84(1 Pt 1):011604. doi: 10.1103/PhysRevE.84.011604. Epub 2011 Jul 8.

DOI:10.1103/PhysRevE.84.011604
PMID:21867181
Abstract

We have performed a dynamic light-scattering (DLS) investigation of the effect of a water-soluble polymer, polyethylene glycol (PEG), on the bending elastic modulus κ of surfactant membranes. The polymer, in concentrations ranging from 0 to 8 g/L (0 to 0.4 mM), was incorporated into the solvent of sponge phases of the sodium dodecyl sulfate (SDS)-hexanol-brine system. PEG adsorbs into the SDS membranes. The correlation functions of the polymer-doped sponge phases displayed a stretched-exponential decay, appropriately described by the Zilman-Granek (Z-G) theory for fluctuating membranes. The dynamics of the surfactant bilayers was slowed down by the addition of the polymer: Increasing PEG concentrations increase the DLS relaxation times. From the Z-G model we extracted the membrane-bending elastic modulus, as a function of polymer concentration, C(PEG) = κ increases with C(PEG), a behavior opposite to that expected from available models for the interaction between fluid membranes and adsorbing polymers. Our results suggest that the polymer penetrates to some extent the surfactant bilayers.

摘要

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