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Ultrasonic Spectrometry of Aqueous Solutions of Alkyl Maltosides: Kinetics of Micelle Formation and Head‐Group Isomerization
Author(s) -
Haller  Julian,
Kaatze Udo
Publication year - 2009
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.200900457
Subject(s) - micelle , chemistry , relaxation (psychology) , alkyl , aqueous solution , isomerization , hydroxymethyl , ethylene glycol , critical micelle concentration , kinetics , thermodynamics of micellization , monomer , organic chemistry , polymer , catalysis , psychology , social psychology , physics , quantum mechanics
At frequencies between 100 kHz and 400 MHz, ultrasonic attenuation spectra are measured at 25 °C for aqueous solutions of hexyl‐, heptyl‐, octyl‐, nonyl‐, and decyl‐β‐ D ‐maltopyranoside as well as of decyl‐α‐ D ‐maltopyranoside. The spectra with surfactant concentration c above the relevant critical micelle concentration (cmc) display three relaxation terms with discrete relaxation times. That with a relaxation time between 0.1 and 1.2 μs is due to exchange of monomers between micelles and the suspending phase. It is discussed in the light of the Teubner–Kahlweit–Aniansson–Wall model of the formation/decay kinetics of systems with Gaussian size distribution of micelles. The relaxation parameters are compared to those for solutions of other non‐ionic surfactants, such as alkyl monoglycosides and poly(ethylene glycol) monoalkyl ethers. At c

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