Cationic and catanionic surfactant vesicle systems have been perturbed by addition of a single-chain surfactant to take the system from a vesicle-stable region to a micelle-stable region. The first vesicle system is based on a double-chain cationic surfactant cetyldecyldimethylammonium bromide (C16C10DMABr) and the second vesicle system is based on a mixture of anionic and cationic single-chain surfactants, namely, sodium octyl sulfate (SOS) and cetyltrimethylammonium bromide (CTAB). In both systems, vesicle breakdown will involve the initial incorporation of the single-chain surfactant into the vesicle, followed by subsequent disintegration of the vesicle. The progress of reaction has been observed by monitoring turbidity changes using a stopped-flow or conventional spectrophotometer. The rate of breakdown of vesicles was found to be linearly dependent on the concentration of added single-chain surfactant, which provides the driving force for the breakdown reaction. The breakdown reaction rates could be changed by factors up to 100 by adjusting the concentration of the solutions.

Kinetics of Induced Vesicle Breakdown for Cationic and Catanionic Systems

FONTANA, Antonella
2002-01-01

Abstract

Cationic and catanionic surfactant vesicle systems have been perturbed by addition of a single-chain surfactant to take the system from a vesicle-stable region to a micelle-stable region. The first vesicle system is based on a double-chain cationic surfactant cetyldecyldimethylammonium bromide (C16C10DMABr) and the second vesicle system is based on a mixture of anionic and cationic single-chain surfactants, namely, sodium octyl sulfate (SOS) and cetyltrimethylammonium bromide (CTAB). In both systems, vesicle breakdown will involve the initial incorporation of the single-chain surfactant into the vesicle, followed by subsequent disintegration of the vesicle. The progress of reaction has been observed by monitoring turbidity changes using a stopped-flow or conventional spectrophotometer. The rate of breakdown of vesicles was found to be linearly dependent on the concentration of added single-chain surfactant, which provides the driving force for the breakdown reaction. The breakdown reaction rates could be changed by factors up to 100 by adjusting the concentration of the solutions.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/122004
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