Marangoni propulsion is a form of locomotion wherein an asymmetric release of surfactant by a body located at the surface of a liquid leads to its directed motion. We present in this paper a mathematical model for Marangoni propulsion in the viscous
regime. We consider the case of a thin rigid circular disk placed at the surface of a viscous fluid and whose perimeter has a prescribed concentration of an insoluble surfactant, to which the rest of its surface is impenetrable. Assuming a linearized equation of state between surface tension and surfactant concentration, we derive analytically the surfactant, velocity and pressure fields in the asymptotic limit of low Capillary, Peclet and Reynolds numbers. We then exploit these results to calculate the Marangoni propulsion speed of the disk. Neglecting the stress contribution from Marangoni flows is seen to over-predict the propulsion speed by 50%.
Confinement and wall effects are known to affect the kinematics and propulsive characteristics of swimming microorganisms. When a solid body is dragged through a viscous fluid at constant velocity, the presence of a wall increases fluid drag, and thu
s the net force required to maintain speed has to increase. In contrast, recent optical trapping experiments have revealed that the propulsive force generated by human spermatozoa is decreased by the presence of boundaries. Here, we use a series of simple models to analytically elucidate the propulsive effects of a solid boundary on passively actuated filaments and model flagella. For passive flexible filaments actuated periodically at one end, the presence of the wall is shown to increase the propulsive forces generated by the filaments in the case of displacement-driven actuation, while it decreases the force in the case of force-driven actuation. In the case of active filaments as models for eukaryotic flagella, we demonstrate that the manner in which a solid wall affects propulsion cannot be known a priori, but is instead a nontrivial function of the flagellum frequency, wavelength, its material characteristics, the manner in which the molecular motors self-organize to produce oscillations (prescribed activity model or self-organized axonemal beating model), and the boundary conditions applied experimentally to the tethered flagellum. In particular, we show that in some cases, the increase in fluid friction induced by the wall can lead to a change in the waveform expressed by the flagella which results in a decrease in their propulsive force.
A fluid droplet located on a super-hydrophobic surface makes contact with the surface only at small isolated regions, and is mostly in contact with the surrounding air. As a result, a fluid in motion near such a surface experiences very low friction,
and super-hydrophobic surfaces display strong drag-reduction in the laminar regime. Here we consider theoretically a super-hydrophobic surface composed of circular posts (so called fakir geometry) located on a planar rectangular lattice. Using a superposition of point forces with suitably spatially-dependent strength, we derive the effective surface slip length for a planar shear flow on such a fakir surface as the solution to an infinite series of linear equations. In the asymptotic limit of small surface coverage by the posts, the series can be interpreted as Riemann sums, and the slip length can be obtained analytically. For posts on a square lattice, our analytical results are in excellent quantitative agreement with previous numerical computations.
Cell motility in viscous fluids is ubiquitous and affects many biological processes, including reproduction, infection, and the marine life ecosystem. Here we review the biophysical and mechanical principles of locomotion at the small scales relevant
to cell swimming (tens of microns and below). The focus is on the fundamental flow physics phenomena occurring in this inertia-less realm, and the emphasis is on the simple physical picture. We review the basic properties of flows at low Reynolds number, paying special attention to aspects most relevant for swimming, such as resistance matrices for solid bodies, flow singularities, and kinematic requirements for net translation. Then we review classical theoretical work on cell motility: early calculations of the speed of a swimmer with prescribed stroke, and the application of resistive-force theory and slender-body theory to flagellar locomotion. After reviewing the physical means by which flagella are actuated, we outline areas of active research, including hydrodynamic interactions, biological locomotion in complex fluids, the design of small-scale artificial swimmers, and the optimization of locomotion strategies.
Laminar flow over a bubble mattress is expected to experience a significant reduction in friction since the individual surfaces of the bubbles are shear-free. However, if the bubbles are sufficiently curved, their protrusion into the fluid and along
the flow direction can lead to an increase in friction as was recently demonstrated experimentally and computationally. We provide in this paper a simple model for this result. We consider a shear flow at low Reynolds number past a two-dimensional array of bubbles, and calculate analytically the effective slip length of the surface as function of the bubble geometry in the dilute limit. Our model is able to reproduce quantitatively the relationship between effective friction and bubble geometry obtained in numerical computations, and in particular: (a) The asymmetry in friction between convex and concave bubbles, and (b) the existence of a geometric transition from reduced to enhanced friction at a critical bubble protrusion angle.
