Bubble Coalescence during Acoustic Cavitation in Aqueous Electrolyte Solutions

• Published in: Langmuir 2011-10, Vol.27 (19), p.12025-12032
• Main Authors: Browne, Christine, Tabor, Rico F, Chan, Derek Y. C, Dagastine, Raymond R, Ashokkumar, Muthupandian, Grieser, Franz
• Format: Article
• Language: English
• Subjects: Chemistry; Exact sciences and technology; General and physical chemistry; Interfaces: Adsorption, Reactions, Films, Forces; Surface physical chemistry
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la202804c

Bubble coalescence behavior in aqueous electrolyte (MgSO4, NaCl, KCl, HCl, H2SO4) solutions exposed to an ultrasound field (213 kHz) has been examined. The extent of coalescence was found to be dependent on electrolyte type and concentration, and could be directly linked to the amount of solubilized gas (He, Ar, air) in solution for the conditions used. No evidence of specific ion effects in acoustic bubble coalescence was found. The results have been compared with several previous coalescence studies on bubbles in aqueous electrolyte and aliphatic alcohol solutions in the absence of an ultrasound field. It is concluded that the impedance of bubble coalescence by electrolytes observed in a number of studies is the result of dynamic processes involving several key steps. First, ions (or more likely, ion-pairs) are required to adsorb at the gas/solution interface, a process that takes longer than 0.5 ms and probably fractions of a second. At a sufficient interfacial loading (estimated to be less than 1–2% monolayer coverage) of the adsorbed species, the hydrodynamic boundary condition at the bubble/solution interface switches from tangentially mobile (with zero shear stress) to tangentially immobile, commensurate with that of a solid–liquid interface. This condition is the result of spatially nonuniform coverage of the surface by solute molecules and the ensuing generation of surface tension gradients. This change reduces the film drainage rate between interacting bubbles, thereby reducing the relative rate of bubble coalescence. We have identified this point of immobilization of tangential interfacial fluid flow with the “critical transition concentration” that has been widely observed for electrolytes and nonelectrolytes. We also present arguments to support the speculation that in aqueous electrolyte solutions the adsorbed surface species responsible for the immobilization of the interface is an ion-pair complex.