Transient bubble rising in the presence of a surfactant at very low concentrations

We study the formation of the dynamic adsorption layer when a bubble is released in a tank containing water with a tiny amount of surfactant. The influence of the sorption kinetic constants is examined by comparing the experiments with Sodium Dodecyl Sulfate (SDS) and Triton X-100. The experiments allowed us to determine the parameter conditions that lead to a stable bubble rising and to validate the simulation. A simple scaling analysis and the simulation show that the formation of the dynamic adsorption layer can be split into three phases characterized by disparate time scales. The mechanisms controlling those phases are surfactant convection, adsorption–desorption, and diffusion. The amount of surfactant adsorbed onto the interface increases monotonously throughout the three phases. The experiments and the simulation show that the rising velocity reaches a maximum at times of the order of k d − 1 ( k d is the desorption constant) when the dynamic adsorption layer is practically formed. This occurs even when only traces of surfactant are present in the liquid. The non-monotonous behavior of the maximum surfactant surface concentration is explained in terms of the reverse flow in the rear of the bubble right after the bubble release. This work contributes to the understanding of the complex interplay between hydrodynamics and surfactant transport and kinetics over bubble rising. • We study the formation of the dynamic adsorption layer for a rising bubble. • We solve the complete model for realistic Reynolds and Peclets numbers. • Three phases are observed dominated by: convection, adsorption, and diffusion. • The results explain why there is a maximum in the velocity profile (overshooting).

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Publication Details

Journal
International Journal of Multiphase Flow
Published
2025-03-08
DOI
https://doi.org/10.1016/j.ijmultiphaseflow.2025.105205
Citations
3
Primary Topic
Fluid Dynamics and Mixing
Type
article
Field-Weighted Citation Impact
2.02
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article

Transient bubble rising in the presence of a surfactant at very low concentrations

J. M. Montanero, Daniel Fernández‐Martínez, Miguel A. Herrada, José M. López-Herrera et al.
3 citations
International Journal of Multiphase Flow
Fluid Dynamics and Mixing
2.02
article

Transient bubble rising in the presence of a surfactant at very low concentrations

J. M. Montanero, Daniel Fernández‐Martínez, Miguel A. Herrada, José M. López-Herrera, M.G. Cabezas
article en
3 citations

Abstract

We study the formation of the dynamic adsorption layer when a bubble is released in a tank containing water with a tiny amount of surfactant. The influence of the sorption kinetic constants is examined by comparing the experiments with Sodium Dodecyl Sulfate (SDS) and Triton X-100. The experiments allowed us to determine the parameter conditions that lead to a stable bubble rising and to validate the simulation. A simple scaling analysis and the simulation show that the formation of the dynamic adsorption layer can be split into three phases characterized by disparate time scales. The mechanisms controlling those phases are surfactant convection, adsorption–desorption, and diffusion. The amount of surfactant adsorbed onto the interface increases monotonously throughout the three phases. The experiments and the simulation show that the rising velocity reaches a maximum at times of the order of k d − 1 ( k d is the desorption constant) when the dynamic adsorption layer is practically formed. This occurs even when only traces of surfactant are present in the liquid. The non-monotonous behavior of the maximum surfactant surface concentration is explained in terms of the reverse flow in the rear of the bubble right after the bubble release. This work contributes to the understanding of the complex interplay between hydrodynamics and surfactant transport and kinetics over bubble rising. • We study the formation of the dynamic adsorption layer for a rising bubble. • We solve the complete model for realistic Reynolds and Peclets numbers. • Three phases are observed dominated by: convection, adsorption, and diffusion. • The results explain why there is a maximum in the velocity profile (overshooting).

International Journal of Multiphase FlowVol. 188
Universidad de Sevilla (ES), Universidad de Extremadura (ES)
Openalex Percentile: Top 15%
Fluid Dynamics and Mixing
2.02
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