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Dynamic Surface Tension and Adsorption Kinetics from Micellar Solutions on Planar Surfaces

โœ Scribed by Leonid K. Filippov; Nadezhda L. Filippova


Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
213 KB
Volume
187
Category
Article
ISSN
0021-9797

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โœฆ Synopsis


A qualitative theory of the dynamic surface tension and adsorption kinetics from micellar surfactant solutions on a planar surface is developed for the kinetic-diffusive-controlled adsorption process obeying any adsorption kinetics on a planar surface and any micellization-demicellization kinetics in the bulk. The time-dependent adsorption and dynamic surface tension is obtained in an analytical form for short and long times. It is shown that the adsorption process and dynamic surface tension over a wide range of surfactant (monomer) concentrations is governed by: (I) the adsorption kinetics of monomers and micelles for short times (0 /= tcr2). Formulas were derived to estimate the relaxation times tcr1, tcr2, and the parameters characterizing the adsorption process over a wide range of times. The existence of the (I), (II), and (III) regimes are justified by using the experimental data for the dynamic surface tension of a micellar Brij 58 solution.


๐Ÿ“œ SIMILAR VOLUMES


Dynamic Surface Tension and Adsorption/D
โœ Nadezhda L. Filippova ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 176 KB

The adsorption/desorption kinetics for individual polymers and polymer mixtures of the water-soluble associative polymers with molecular weights of 12, 62, and 100 kg/mol onto SiO 2 planar substrate have been studied by ellipsometry at room temperature under nonflow conditions. Equations were derive

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The adsorption/desorption kinetics for individual polymers and polymer mixtures of the water-soluble associative polymers with molecular weights of 12, 62, and 100 kg/mol onto a SiO2 planar substrate have been studied by ellipsometry at room temperature under flow conditions. Equations were derived

Dynamic Surface Tension and Adsorption K
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A quantitative theory is developed to describe the dynamic surface tension and the adsorption kinetics at a liquid-liquid interface, taking into account the molecular diffusion in both bulk phases and the adsorption isotherm for surfactant on the interface. Asymptotic analytical solutions are obtain

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โœ Nadezhda L. Filippova ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 251 KB

The adsorption and desorption kinetics of water-soluble associative polymers with different molecular weights on the silicon wafers were studied by ellipsometry. The parameters characterizing the adsorption and desorption processes such as (a) the maximum amount of adsorbate adsorbed, Gammainfinity,

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โœ Leonid K. Filippov ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 368 KB

equilibrium with the ion concentrations at the outer boundary A quantitative theory for dynamic surface tension has been deof the double layer. This model is discussed in Appendix A. veloped for the diffusion-controlled and diffusion-convective-con-Borwanker and Wasan (31) use the isotherm of Davies