2005
DOI: 10.1016/j.cis.2004.11.001
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Interfacial rheology of adsorbed layers with surface reaction: On the origin of the dilatational surface viscosity

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Cited by 99 publications
(57 citation statements)
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“…In the static case, P dyn = 0. Unlike the case of mechanical equilibrium when the capillary pressure is exactly proportional to the surface tension, r, during surface deformations the capillary pressure fluctuations are proportional to the total surface stress, which contains also contributions from the surface viscosity [7,8,15,20]. Substituting Eqs.…”
Section: Theoreticalmentioning
confidence: 98%
“…In the static case, P dyn = 0. Unlike the case of mechanical equilibrium when the capillary pressure is exactly proportional to the surface tension, r, during surface deformations the capillary pressure fluctuations are proportional to the total surface stress, which contains also contributions from the surface viscosity [7,8,15,20]. Substituting Eqs.…”
Section: Theoreticalmentioning
confidence: 98%
“…They concluded that, in the case of their systems, surface rheology properties changed with macromolecule backbone rigidity [8] and that the adsorption kinetics depended on whether the system was below or above the equivalent point of charges [9]. On the other hand, Ivanov et al [10] stated that the correlation between the dynamic properties of the interface and the dispersion stability should be analyzed with caution.…”
Section: Introductionmentioning
confidence: 97%
“…to the adsorption layer such as reorientation, aggregation phase transitions, intrinsic two-dimensional compressibility and interfacial chemical reactions [27][28][29]. However, the experimental proofs for these processes are still unavailable.…”
Section: Introductionmentioning
confidence: 98%