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Self-similar coalescence of clean foams
Published online by Cambridge University Press: 15 April 2013
Abstract
We consider the stability of a planar gas–liquid foam with low liquid fraction, in the absence of surfactants and stabilizing particles. We adopt a network modelling approach introduced by Stewart & Davis (J. Rheol., vol. 56, 2012, p. 543), treating the gas bubbles as polygons, the accumulation of liquid at the bubble vertices (Plateau borders) as dynamic nodes and the liquid bridges separating the bubbles as uniformly thinning free films; these films can rupture due to van der Waals intermolecular attractions. The system is initialized as a periodic array of equally pressurized bubbles, with the initial film thicknesses sampled from a normal distribution. After an initial transient, the first film rupture initiates a phase of dynamic rearrangement where the bubbles rapidly coalesce, evolving toward a new quasi-equilibrium. We present Monte Carlo simulations of this coalescence process, examining the time intervals over which large-scale rearrangement occurs as a function of the model parameters. In addition, we show that when this time interval is rescaled appropriately, the evolution of the normalized number of bubbles is approximately self-similar.
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- ©2013 Cambridge University Press
References
Stewart and Davis supplementary movie
Animation of bubble coalescence in a foam initially composed of 72 uniformly pressurized bubbles, corresponding to the snapshots shown in figure 4 and the time-traces shown in figures 5 and 6 in the paper. The movie illustrates how the breakage of the first film triggers a large-scale topological rearrangement of the foam, evolving toward a new quasi-equilibrium composed of only a few bubbles.
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