A Hele-Shaw Newton's cradle: Circular bubbles in a Hele-Shaw channel. (Daniel Booth)

We present a model for the motion of approximately circular bubbles in a Hele-Shaw cell. The bubble velocity is determined by a balance between the hydrodynamic pressures from the external flow and the drag due to the thin films above and below the bubble. We find that the qualitative behaviour depends on a dimensionless parameter and is found to agree well with experimental observations.  Furthermore, we show how the effects of interaction with cell boundaries and/or other bubbles also depend on the value of this dimensionless parameter For example, in a train of three identical bubbles travelling along the centre line, the middle bubble either catches up with the one in front or is caught by the one behind, forming what we term a Hele-Shaw Newton's cradle.
 

Reciprocity in Fluids (Matthew Cotton)

Reciprocity is a useful, and often underused, way to calculate integrated quantities when a to solution to a related problem is known. In the remaining time, I will overview these ideas and give some example use cases

Elkem is developing a new method for categorising the reactivity between silicon carbide (SiC) powder and silicon monoxide gas (SiO(g)). Experiments have been designed which pass SiO gas through a powdered bed of SiC inside of a heated crucible, resulting in a reaction between the two. The SiO gas is produced via a secondary reaction outside of the SiC bed. Both reactions require specific temperature and pressure constraints to occur. Therefore, we would like to mathematically model the temperature distribution and gas flow within the experimental set-up to provide insight into how we can control the process.

Complexities arise from:

• Endothermic reactions causing heat sinks
• Competing reactions beyond the two we desire
• Dynamically changing properties of the bed, such as permeability

In this presentation, I will discuss the construction and results of numerical simulations quantifying flows around several species of soft corals. In the first project, the flows near the tentacles of xeniid soft corals are quantified for the first time. Their active pulsations are thought to enhance their symbionts' photosynthetic rates by up to an order of magnitude. These polyps are approximately 1 cm in diameter and pulse at frequencies between approximately 0.5 and 1 Hz. As a result, the frequency-based Reynolds number calculated using the tentacle length and pulse frequency is on the order of 10 and rapidly decays as with distance from the polyp. This introduces the question of how these corals minimize the reversibility of the flow and bring in new volumes of fluid during each pulse. We estimate the Péclet number of the bulk flow generated by the coral as being on the order of 100–1000 whereas the flow between the bristles of the tentacles is on the order of 10. This illustrates the importance of advective transport in removing oxygen waste. In the second project, the flows through the elaborate branching structures of gorgonian colonies are considered.  As water moves through the elaborate branches, it is slowed, and recirculation zones can form downstream of the colony. At the smaller scale, individual polyps that emerge from the branches expand their tentacles, further slowing the flow. At the smallest scale, the tentacles are covered in tiny pinnules where exchange occurs. We quantified the gap to diameter ratios for various gorgonians at the scale of the branches, the polyp tentacles and the pinnules. We then used computational fluid dynamics to determine the flow patterns at all three levels of branching. We quantified the leakiness between the branches, tentacles and pinnules over the biologically relevant range of Reynolds numbers and gap-to-diameter ratios, and found that the branches and tentacles can act as either leaky rakes or solid plates depending upon these dimensionless parameters. The pinnules, in contrast, mostly impede the flow. Using an agent-based modeling framework, we quantified plankton capture as a function of the gap-to diameter ratio of the branches and the Reynolds number. We found that the capture rate depends critically on both morphology and Reynolds number.