drodynamic coupling between the vertical motion of the sur-The behavior of solubilized alkanes at the surface of DoTAB face and the surface area changes is preserved. ## solutions for various surfactant bulk concentrations below and In the case of alkanes, the preparation of thin oil phases above
Viscoelasticity of Surfactant Monolayers
โ Scribed by Y. Jayalakshmi; L. Ozanne; D. Langevin
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 434 KB
- Volume
- 170
- Category
- Article
- ISSN
- 0021-9797
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โฆ Synopsis
Dilatational viscoelasticities of a nonionic surfactant monolayer are measured at the air/water interface using the excitedcapillary-wave technique. The data are compared with the diffusion-exchange model for surfactant adsorption. This model requires the knowledge of the equation of state for the monolayer. We have used the Frumkin equation of state. Although the measured elasticities show the same qualitative trends predicted by the model, their absolute values fall well below the calculated ones in the diffusion-dominated regime. In order to quantitatively fit the model to our data, rather high values of the diffusion coefficient must be used. However, we independently determine the diffusion coefficient for this system, via dynamic surface tension measurements using the relaxing pendent-drop technique, and our results agree with the expected bulk value within the experimental uncertainty. When the diffusion-model parameters are calculated numerically without assuming any form of equation of state to relate (\gamma, \Gamma), and (c), the model fits the data with the bulk diffusion coeflicient value within experimental uncertainties. This suggests that the current monolayer equations of state are not able to accurately describe the response of a monolayer to small periodic dilatations around equilibrium. (O) 1995 Academic Press, Inc.
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