Abstract
The low-frequency dielectric response of AOT micellar solutions in decane and hexadecane was studied and it was found that at low volume fractions of the spherical micelles, the dielectric relaxation was well explained by a single Debye relaxation process. At progressively higher volume fractions, the relaxation function first departed from the Debye equation, and at above 30%, a new and slow relaxation process was observed to coexist with the single particle relaxation process which eventually became the dominant process.
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