Bubbles in water are stabilised against coalescence by the addition of salt. The white froth in seawater but not in freshwater is an example of salt-stabilised bubbles. A range of experiments have been carried out to investigate this simple phenomenon, which is not yet understood.¶
The process of thin film drainage between two colliding bubbles relates to surface science fields including hydrodynamic flow, surface forces, and interfacial rheology. Bubble coalescence inhibition also stands alongside the better known Hofmeister series as an intriguing example of ion specificity: While some electrolytes inhibit coalescence at around 0.1M, others show no effect. The coalescence inhibition of any single electrolyte depends on the combination of cation and anion present, rather than on any single ion.¶
The surfactant-free inhibition of bubble coalescence has been studied in several systems for the first time, including aqueous mixed electrolyte solutions; solutions of biologically relevant non-electrolytes urea and sugars; and electrolyte solutions in nonaqueous solvents methanol, formamide, propylene carbonate and dimethylsulfoxide. Complementary experimental approaches include studies of terminal rise velocities of single bubbles showing that the gas-solution interface is mobile; and measurement of thin film drainage in inhibiting and non-inhibiting electrolyte solution, using the microinterferometric thin film balance technique.¶
The consolidation of these experimental approaches shows that inhibiting electrolytes act on the non-equilibrium dynamic processes of thin film drainage and rupture between bubble surfaces and not via a change in surface forces, or by ion effects on solvent structure. In addition, inhibition is driven by osmotic effects related to solute concentration gradients, and ion charge is not important.¶
A new model is presented for electrolyte inhibition of bubble coalescence via changes to surface rheology. It is suggested that thin film stabilisation over a lifetime of seconds,
is caused by damping of transient deformations of film surfaces on a sub-millisecond timescale. This reduction in surface deformability retards film drainage and delays film rupture. It is proposed that inhibiting electrolyte solutions show a dilational surface viscosity, which in turn is driven by interfacial concentration gradients. Inhibiting electrolytes have two ions that accumulate at the surface or two ions that are surface excluded, while non-inhibiting electrolytes have more evenly distributed interfacial solute. Bubble coalescence is for the first time linked through this ion surface partitioning, to the ion specificity observed at biological interfaces and the wider realm of Hofmeister effects.¶
| Identifer | oai:union.ndltd.org:ADTP/256923 |
| Date | January 2009 |
| Creators | Henry, Christine L., christine.henry@alumni.anu.edu.au |
| Publisher | The Australian National University. Department of Applied Mathematics, Research School of Physical Sciences and Engineering, |
| Source Sets | Australiasian Digital Theses Program |
| Language | English |
| Detected Language | English |
| Rights | http://www.anu.edu.au/legal/copyrit.html), Copyright Christine L. Henry |
Page generated in 0.0094 seconds