A continuum thermodynamic model of the influence of non-ionic surfactant on mass transfer from gas bubbles

A continuum thermodynamic model of the influence of non-ionic surfactant on mass transfer from gas bubbles
Notice: This research summary and analysis were automatically generated using AI technology. For absolute accuracy, please refer to the [Original Paper Viewer] below or the Original ArXiv Source.

Mass transfer of gaseous components from rising bubbles to the ambient liquid depends not only on the chemical potential difference of the transfer component but also on the interfacial free energy and composition. The latter is strongly affected by surface active agents that are present in many applications. Surfactants lead to local changes in the interfacial tension, which influence the mass transfer rates in two different ways. On the one hand, inhomogeneous interfacial tension leads to Marangoni stress, which can strongly change the local hydrodynamics. One the other hand, the coverage by surfactant molecules results in a mass transfer resistance. This hindrance effect is not included in current continuum physical models. The present work provides the experimental validation of a recently introduced extended sharp-interface model for two-phase flows with mass transfer that also accounts for the mass transfer hindrance due to adsorbed surfactant. The crucial feature is to account for area-specific concentrations not only of adsorbed constituents but also of transfer species, and to model mass transfer as a series of two bi-directional sorption-type bulk-interface exchange processes. The resulting model is shown to quantitatively describe experimental measurements on mass transfer reduction for the dissolution of CO$_2$ bubbles in different surfactant solutions.


💡 Research Summary

The paper addresses a long‑standing gap in the modeling of mass transfer across gas‑liquid interfaces when non‑ionic surfactants are present. Conventional sharp‑interface models treat the interface as a zero‑thickness surface and describe mass transfer solely by bulk concentration gradients and Henry’s law equilibrium, ignoring both the Marangoni stresses caused by surface‑tension gradients and the additional resistance introduced by surfactant adsorption layers. While numerous experimental studies have documented that surfactants can both slow bubble rise (through Marangoni‑induced flow retardation) and hinder the passage of dissolved gases (through a steric or energetic barrier), a thermodynamically consistent continuum framework that incorporates both effects has been lacking.

The authors build on a recently proposed extended sharp‑interface formulation (reference


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