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In this paper, a model that combines the lattice Boltzmann method with the singularity distribution method is proposed to simulate a self-propelled particle swimming (exhibiting translation and rotation) in a channel flow. The results show that the velocity distribution for a self-propelled particle swimming deviates from a Maxwellian distribution and exhibits high-velocity tails. The influence of an eccentric potential doublet on the translation velocity of the particle is significant. The velocity decay process can be described using a double exponential model form. No large differences in the velocity distribution were observed for different translation Reynolds numbers, rotation Reynolds numbers, or regular intervals.
Self-propelled particle swimming has gained wide attention due to its relevance to biological and technological applications. Micro-swimmers may use various driving mechanisms, such as flagellar propulsion, [1–3] beating cilia, [3] surface distortions, [4] chemical reactions, [5, 6] or actin-tail polymerisation. [7, 8] Although notable differences between these mechanisms exist, the universality in hydrodynamic behaviour is obvious. For many biologically relevant systems, it is typical that self-propulsive swimming contributes to non-equilibrium dynamics systems. [9, 10] The experimental observation that swimming particles enhance hydrodynamic diffusion has been confirmed by numerical simulations. [11, 12] The presence of swimming particles always affects the stability of suspensions. [13, 14] On the other hand, the rheological characteristics of suspensions that result from swimming particles may play a major role in channel flow. Bioconvection can occur when swimmers share a mean upward movement because of the effects of gravitational torque, chemotaxis, or phototaxis. [15] Therefore, investigation of the motion characteristics and effects of self-propelled swimmers on the properties of fluid media is important to understanding the transformation mechanism of biological system energy and improving the design of micro bionic robots.
Most of the research on the motion of self-propelled particles suspended in Newtonian fluids have employed analytical solutions or numerical methods to examine motion under the condition of low-Reynolds-number flow. From a microscopic perspective, Lighthill [16] first proposed the model of a squirmer, which has a spherical shape with surface tangential velocities, based on a solution of the Stokes equation in a spherical coordinate system. Blake [17] later extended this model to the dynamics of ciliary propulsion of a microscopic organism. Magar et al. [18] developed a model for nutrition uptake by a self-propelled steady squirmer. Recently, Ishikawa et al. [19] developed a database for an interacting pair of squirmers from which one can easily predict the motion of self-propulsion suspensions using a boundary element method. They used the interaction model to study the rheology of a semi-dilute suspension of bottom-heavy and non-bottom-heavy squirmers [20] and the diffusion of swimming micro-organisms in a semi-dilute suspension. [21] They also studied the orientation order in a concentrated suspension of spherical microswimmers. [22] This squirmer model is an accurate combination of an analytical solution and a boundary element method which is precise in dealing with a complex boundary and near-wall flow. However, this method requires a number of integrals and even a singular integral, which requires huge computing resources. Taking into consideration the interaction between particles, Hernández-Ortiz et al. proposed a model in which a force dipole is drawn into a fluid to describe the effects of self-propelled particles. [13, 23] Saintillan and Shelley [24] proposed a model based on the slender-body theory in which swimming particles are regarded as self-propelled rigid slender rods that impose a given shear stress on the surrounding fluid. These models seek to describe the movement mechanism of self-propelled particles and how they affect the characteristics of the surrounding fluid.
The lattice Boltzmann method (LBM), which is widely used in the simulation of various types of flow, [25–29] relies on the fact that the macroscopic dynamics of fluid flow does not depend on the microscopic details of the fluid field. The LBM was first proposed by Ladd et al. to simulate passive suspensions at finite Reynolds numbers. [30–32] Aidun et al. [33–35] developed this method and added ‘virtual nodes’ to the solid boundaries to simulate passive particles near contact. Recently, Ramachandran et al. [36] proposed an LBM model for active suspensions, in which two types of particles (movers and shakers) are defined by different distributions for point forces as a force dipole and a D2Q7 LBM model is used to simulate individual and multiple self-propelled colloidal particles. The researchers found that the velocity of the mover was directly proportional to the asymmetry of the position of the force distribution and that the statistical properties of the velocity field generated by the activity deviated from those of equilibrium fluids. Alarcón and Pagonabarraga [37] proposed a three-dimensional LBM for suspensions of self-propelled particles using a squirmer model in which the appropriate boundary conditions for the Stokes equation at the surfaces of spherical particles were imposed to induce a slip velocity between the fluid and the particles. They employed this method to characterise the hydrodynamic stresses induced by active swimmers, and they found that active stresses played a dominant role in decorrelating the collective motion of squirmers and that contractile squirmers formed significant aggregates.
Several numerical studies have been performed in the past few years to explore the mechanism of self-propulsive particle movement using the lattice Boltzmann method, in which a force dipole or a slip velocity is exerted on the boundaries of the particles as the driving mode. However, it is difficult to apply this approach to particles with irregular geometric shapes. Chwang and Wu [38–40] proposed a singularity distribution method, based on the theory for low-Reynolds-number flows, with which the real movement characteristics of self-propelled particles with complicated boundaries can be simulated. The Stokes flow around an object with arbitrary shapes can be simulated by properly adjusting the type, position, and intensity of fundamental Stokes flow singularities in the interior of an object using the singularity distribution method. In this paper, we present a model that combines the lattice Boltzmann method with the singularity distribution method to simulate a self-propulsive particle swimming in a channel flow. The behaviours of self-propelled particles’ translation, rotation, period of transition between translation and rotation, and decay of the particle velocity were analysed.
The LBM is different from schemes based on the continuum assumption of fluids. In the LBM, the discrete microscopic velocity space is given as follows: [41]
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In the nine-bit LBGK model, the two-dimensional velocity in the phase space is discretised in nine directions:
Within the limit of long wavelengths, the lattice Boltzmann equation recovers the following quasi-incompressible Navier–Stokes equation by the Chapman–Enskog multi-scaling expansion: [44]
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Ladd [31, 32] and Aidun et al. [34] used the momentum exchange method to propose a modified bounce-back rule for a moving wall. If we place the boundary nodes on the links connecting the interior and exterior nodes,
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For the case in which the inertial effects are negligible in comparison to the viscous forces, under the condition of low-Reynolds-number flow, the Navier–Stokes equations are usually simplified to the Stokes equations
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In the simulations, we modelled an active self-propelled particle in a typical two-dimensional static flow field, as shown in Fig.
Figure
Compared with the boundary element method that Ishikawa et al. [19–22] proposed for use in simulating active suspensions, the method we propose here can reduce the huge amount of computational effort required as a result of the large number of singular numerical integrations involved. The advantage of LBM is that it avoids the need to solve Poisson’s equation and is easy to employ using parallel computation, which greatly reduces the computational resources required. On the other hand, unlike previously proposed computational schemes that lacked the ability to address complicated boundaries, the proposed method can construct the exact velocity distributions of particles with complex geometric shapes by arranging the basic singularities of different types of Stokes flow within a certain law. That is to say, the method we propose here possesses the advantages of both the LBM and the method of singularity distribution.
A self-propelled particle can swim continuously or at regular intervals. We call the interval between two adjacent times the switching time. We define the Reynolds number
The velocity distributions for the translation of a single particle at different
The potential doublet at different positions along the orientation vector
The decrease in the velocity of a self-propelled particle when its activity is switched off was also studied at three Reynolds numbers. The results show that the shapes of the decay curves are consistent with a double exponential function. Figure
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The timescales t 1 and t 2 stem from different dissipative mechanisms. The short timescale t 2 stems from the friction generated by relative motion between the particle boundary and the fluid, and the long timescale t 1 stems from the fluid drag force that exists before the particle becomes stationary.
Different eccentric distances can also lead to a various self-propulsion velocities, even though we assigned an equal-intensity potential doublet to the particle. A fitted parabolic curve of the following form is shown in Fig.
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As the figure shows, the eccentric distance can determine the self-propulsion efficiency. The farther the eccentric point is from the centre, the higher the particle velocity is.
To explore the characteristics of the rotation of a single self-propelled particle in a channel, we defined a rotation Reynolds number
The decay process of the rotation of a single particle is different from that of its translation, in that rotation requires less time than translation. Figure
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The short timescale t 1 and the long timescale t 2 are determined by the friction and drag force, respectively.
A self-propelled micro-organism often switches its mode of motion between translation and rotation. For example, a bacterium cell usually exhibits a run-and-tumble motion in which it changes the direction of swimming by the rotation of any motor, i.e., unravelling of flagellar bundles. [15] Thus, it makes sense to study fluid velocity distributions after the sudden movement pattern changes of a single particle. Figure
A single particle rotating through a specific angle
A model that combines the lattice Boltzmann method with the singularity distribution method is proposed to simulate a self-propelled particle swimming (exhibiting translation and rotation) in a channel. Periodic boundary conditions were used in the simulations conducted, and the interaction between a single particle and the channel was not taken into account. The results show that the velocity distributions for translation and rotation of a single self-propelled particle deviate from a Maxwellian distribution, with high-velocity tails being observed because of the pumping of energy into the system. The effects of different potential doublet eccentricities on the translation velocity of a single self-propelled particle are significant. The double-exponential distributions decay when the swimming particle is switched off, which confirms that friction and drag force are the two major sources of resistance. The velocity distribution of a self-propelled particle is different from the Maxwellian distribution of a passive particle. No large differences in the velocity distribution were observed for different translation Reynolds numbers, rotation Reynolds numbers, or regular intervals.
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