No Arabic abstract
We study the steady-state behavior of active, dipolar, Brownian spheroids in a planar channel subjected to an imposed Couette flow and an external transverse field, applied in the downward normal-to-flow direction. The field-induced torque on active spheroids (swimmers) is taken to be of magnetic form by assuming that they have a permanent magnetic dipole moment, pointing along their self-propulsion (swim) direction. Using a continuum approach, we show that a host of behaviors emerge over the parameter space spanned by the particle aspect ratio, self-propulsion and shear/field strengths, and the channel width. The cross-stream migration of the model swimmers is shown to involve a regime of linear response (quantified by a linear-response factor) in weak fields. For prolate swimmers, the weak-field behavior crosses over to a regime of full swimmer migration to the bottom half of the channel in strong fields. For oblate swimmers, a counterintuitive regime of reverse migration arises in intermediate fields, where a macroscopic fraction of swimmers reorient and swim to the top channel half at an acute `upward angle relative to the field axis. The diverse behaviors reported here are analyzed based on the shear-induced population splitting (bimodality) of the swim orientation, giving two distinct, oppositely polarized, swimmer subpopulations (albeit very differently for prolate/oblate swimmers) in each channel half. In strong fields, swimmers of both types exhibit net upstream currents relative to the laboratory frame. The onsets of full migration and net upstream current depend on the aspect ratio, enabling efficient particle separation strategies in microfluidic setups.
We present a quantitative analysis on the response of a dilute active suspension of self-propelled rods (swimmers) in a planar channel subjected to an imposed shear flow. To best capture the salient features of shear-induced effects, we consider the case of an imposed Couette flow, providing a constant shear rate across the channel. We argue that the steady-state behavior of swimmers can be understood in the light of a population splitting phenomenon, occurring as the shear rate exceeds a certain threshold, initiating the reversal of swimming direction for a finite fraction of swimmers from down- to upstream or vice versa, depending on swimmer position within the channel. Swimmers thus split into two distinct, statistically significant and oppositely swimming majority and minority populations. The onset of population splitting translates into a transition from a self-propulsion-dominated regime to a shear-dominated regime, corresponding to a unimodal-to-bimodal change in the probability distribution function of the swimmer orientation. We present a phase diagram in terms of the swim and flow Peclet numbers showing the separation of these two regimes by a discontinuous transition line. Our results shed further light on the behavior of swimmers in a shear flow and provide an explanation for the previously reported non-monotonic behavior of the mean, near-wall, parallel-to-flow orientation of swimmers with increasing shear strength.
Dense assemblies of self propelled particles, also known as active or living glasses are abundantaround us, covering different length and time scales: from the cytoplasm to tissues, from bacterialbio-films to vehicular traffic jams, from Janus colloids to animal herds. Being structurally disorderedas well as strongly out of equilibrium, these systems show fascinating dynamical and mechanicalproperties. Using extensive molecular dynamics simulation and a number of different dynamicaland mechanical order parameters we differentiate three dynamical steady states in a sheared modelactive glassy system: (a) a disordered phase, (b) a propulsion-induced ordered phase, and (c) ashear-induced ordered phase. We supplement these observations with an analytical theory based onan effective single particle Fokker-Planck description to rationalise the existence of the novel shear-induced orientational ordering behaviour in our model active glassy system that has no explicitaligning interactions,e.g.of Vicsek-type. This ordering phenomenon occurs in the large persistencetime limit and is made possible only by the applied steady shear. Using a Fokker-Planck descriptionwe make testable predictions without any fit parameters for the joint distribution of single particleposition and orientation. These predictions match well with the joint distribution measured fromdirect numerical simulation. Our results are of relevance for experiments exploring the rheologicalresponse of dense active colloids and jammed active granular matter systems.
We use a continuum model to report on the behavior of a dilute suspension of chiral swimmers subject to externally imposed shear in a planar channel. Swimmer orientation in response to the imposed shear can be characterized by two distinct phases of behavior, corresponding to unimodal or bimodal distribution functions for swimmer orientation along the channel. These phases indicate the occurrence (or not) of a population splitting phenomenon changing the swimming direction of a macroscopic fraction of active particles to the exact opposite of that dictated by the imposed flow. We present a detailed quantitative analysis elucidating the complexities added to the population splitting behavior of swimmers when they are chiral. In particular, the transition from unimodal to bimodal and vice versa are shown to display a re-entrant behavior across the parameter space spanned by varying the chiral angular speed. We also present the notable effects of particle aspect ratio and self-propulsion speed on system phase behavior and discuss potential implications of our results in applications such as swimmer separation/sorting.
Motivated by the structure of networks of cross-linked cytoskeletal biopolymers, we study the orientationally ordered phases in two-dimensional networks of randomly cross-linked semiflexible polymers. We consider permanent cross-links which prescribe a finite angle and treat them as quenched disorder in a semi-microscopic replica field theory. Starting from a fluid of un-cross-linked polymers and small polymer clusters (sol) and increasing the cross-link density, a continuous gelation transition occurs. In the resulting gel, the semiflexible chains either display long range orientational order or are frozen in random directions depending on the value of the crossing angle, the crosslink concentration and the stiffness of the polymers. A crossing angle $thetasim 2pi/M$ leads to long range $M$-fold orientational order, e.g., hexatic or tetratic for $theta=60^{circ}$ or $90^{circ}$, respectively. The transition is discontinuous and the critical cross-link density depends on the bending stiffness of the polymers and the cross-link geometry: the higher the stiffness and the lower $M$, the lower the critical number of cross-links. In between the sol and the long range ordered state, we always observe a gel which is a statistically isotropic amorphous solid (SIAS) with random positional and random orientational localization of the participating polymers.
Transport properties of dense fluids are fundamentally challenging, because the powerful approaches of equilibrium statistical physics cannot be applied. Polar fluids compound this problem, because the long-range interactions preclude the use of a simple effect-diameter approach based solely on hard spheres. Here, we develop a kinetic theory for dipolar hard-sphere fluids that is valid up to high density. We derive a mathematical approximation for the radial distribution function at contact directly from the equation of state, and use it to obtain the shear viscosity. We also perform molecular-dynamics simulations of this system and extract the shear viscosity numerically. The theoretical results compare favorably to the simulations.