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Dive into the research topics where Devin Conroy is active.

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Featured researches published by Devin Conroy.


Journal of Fluid Mechanics | 2008

Endothermic and exothermic chemically reacting plumes

Devin Conroy; Stefan G. Llewellyn Smith

We develop a model for a turbulent plume in an unbounded ambient that takes into account a general exothermic or endothermic chemical reaction. These reactions can have an important effect on the plume dynamics since the entrainment rate, which scales with the vertical velocity, will be a function of the heat release or absorption. Specifically, we examine a second-order non-reversible reaction, where one species is present in the plume from a pure source and the other is in the environment. For uniform ambient density and species fields the reaction has an important effect on the deviation from pure plume behaviour as defined by the source parameter Γ . In the case of an exothermic reaction the density difference between the plume and the reference density increases and the plume is ‘lazy’, whereas for an endothermic reaction this difference decreases and the plume is more jet-like. Furthermore, for chemical and density-stratified environments, the reaction will have an important effect on the buoyancy flux because the entrainment rate will not necessarily decrease with distance from the source, as in traditional models. As a result, the maximum rise height of the plume for exothermic reactions may actually decrease with reaction rate if this occurs in a region of high ambient density. In addition, we investigate non-Boussinesq effects, which are important when the heat of reaction is large enough.


Journal of Fluid Mechanics | 2005

Evolution of a chemically reacting plume in a ventilated room

Devin Conroy; Stefan G. Llewellyn Smith; C. P. Caulfield

The dynamics of a second-order chemical reaction in an enclosed space driven by the mixing produced by a turbulent buoyant plume are studied theoretically, numerically and experimentally. An isolated turbulent buoyant plume source is located in an enclosure with a single external opening. Both the source and the opening are located at the bottom of the enclosure. The enclosure is filled with a fluid of a given density with a fixed initial concentration of a chemical. The source supplies a constant volume flux of fluid of different density containing a different chemical of known and constant concentration. These two chemicals undergo a second-order non-reversible reaction, leading to the creation of a third product chemical. For simplicity, we restrict attention to the situation where the reaction process does not affect the density of the fluids involved. Because of the natural constraint of volume conservation, fluid from the enclosure is continually vented. We study the evolution of the various chemical species as they are advected by the developing ventilated filling box process within the room that is driven by the plume dynamics. In particular, we study both the mean and vertical distributions of the chemical species as a function of time within the room. We compare the results of analogue laboratory experiments with theoretical predictions derived from reduced numerical models, and find excellent agreement. Important parameters for the behaviour of the system are associated with the source volume flux and specific momentum flux relative to the source specific buoyancy flux, the ratio of the initial concentrations of the reacting chemical input in the plume and the reacting chemical in the enclosed space, the reaction rate of the chemicals and the aspect ratio of the room. Although the behaviour of the system depends on all these parameters in a non-trivial way, in general the concentration within the room of the chemical input at the isolated source passes through three distinct phases. Initially, as the source fluid flows into the room, the mean concentration of the input chemical increases due to the inflow, with some loss due to the reaction with the chemical initially within the room. After a finite time, the layer of fluid contaminated by the inflow reaches the opening to the exterior at the base of the room. During an ensuing intermediate phase, the rate of increase in the concentration of the input chemical then drops non-trivially, due to the extra sink for the input chemical of the outflow through the opening. During this intermediate stage, the concentration of the input chemical continues to rise, but at a rate that is reduced due to the reaction with the fluid in the room. Ultimately, all the fluid (and hence the chemical) that was originally within the room is lost, both through reaction and outflow through the opening, and the room approaches its final steady state, being filled completely with source fluid.


Bulletin of the American Physical Society | 2016

Three-dimensional simulations of thin ferro-fluid films and drops in magnetic fields

Devin Conroy; Alex Wray; Omar K. Matar


Bulletin of the American Physical Society | 2015

Dynamics and stability of thin films and drops subjected to magnetic fields

Devin Conroy; Alex Wray; Omar K. Matar


Bulletin of the American Physical Society | 2014

Viscous ferrofluid films under the effects of magnetic fields

Devin Conroy; Alex Wray; Omar K. Matar


Bulletin of the American Physical Society | 2013

Dynamics of a thin ferrofluid film subjected to a magnetic field

Devin Conroy; Alex Wray; Omar K. Matar


Bulletin of the American Physical Society | 2012

Electrosprays: cone-jet breakup in the presence of DC electric fields

Omar K. Matar; Devin Conroy; Richard V. Craster; Demetrios T. Papageorgiou; Hsueh-Chia Chang


Bulletin of the American Physical Society | 2011

Electric field-enhanced water dissociation in nanoporous membranes

Devin Conroy; Richard V. Craster; Omar K. Matar; Hsueh-Chia Chang


Bulletin of the American Physical Society | 2010

Breakup of an electrified jet in an AC field

Demetrios T. Papageorgiou; Devin Conroy; Richard V. Craster; Omar K. Matar


Bulletin of the American Physical Society | 2010

Breakup of an electrified viscous thread with charged surfactants

Devin Conroy; Richard V. Craster; Demetrios T. Papageorgiou; Omar K. Matar

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Alex Wray

Imperial College London

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