Velocity distributions in trapped and mobilized non-wetting phase ganglia in porous media.

Understanding the mobilisation of trapped globules of non-wetting phase during two-phase flow has been the aim of numerous studies. However, the driving forces for the mobilisation of the trapped phases are still not well understood. Also, there is little information about what happens within a globule before, at the onset and during mobilization. In this work, we used micro-particle tracking velocimetry in a micro-fluidic model in order to visualise the velocity distributions inside the trapped phase globules prior and during mobilisation. Therefore, time-averaged and instantaneous velocity vectors have been determined using fluorescent microscopy. As a porous medium, we used a polydimethylsiloxane (PDMS) micro-model with a well-defined pore structure, where drainage and imbibition experiments were conducted. Three different geometries of trapped non-wetting globules, namely droplets, blobs and ganglia were investigated. We observed internal circulations inside the trapped phase globules, leading to the formation of vortices. The direction of circulating flow within a globule is dictated by the drag force exerted on it by the flowing wetting phase. This is illustrated by calculating and analyzing the drag force (per unit area) along fluid-fluid interfaces. In the case of droplets and blobs, only one vortex is formed. The flow field within a ganglion is much more complex and more vortices can be formed. The circulation velocities are largest at the fluid-fluid interfaces, along which the wetting phase flows and decreases towards the middle of the globule. The circulation velocities increased proportionally with the increase of wetting phase average velocity (or capillary number). The vortices remain stable as long as the globules are trapped, start to change at the onset of mobilization and disappear during the movement of globules. They reappear when the globules get stranded. Droplets are less prone to mobilization; blobs get mobilised in whole; while ganglia may get ruptured and get mobilised only partially.