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Effect and Motility-Induced Phase Separation

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Introduction

Active Matter Systems

Self-motion, which is the defining feature of active matter, is ubiquitous in living systems, and this is one of the reasons why research interest in active matter systems has increased significantly over the past decade. One of the main questions in the field of active matter research is about the consequences of self-motion.

Active Brownian Particles

The behavior of an active suspension is governed by the Péclet number𝑃𝑒=𝑈0ℓ0/𝐷𝑇 = (ℓ0/𝛿)2, which serves as a measure of the activity of ABPs. The evolution of the probability density in the phase space (𝒙,𝒒) is governed by Smoluchowski.

Mechanics of Active Suspensions

The usefulness of swimming pressure can be clearly revealed by considering the concept of equivalent pressure. When calculating the pressure exerted by the fluid on a wall, the "true" fluid pressure 𝑝 must be used, not the equivalent pressure.

Thesis Outline

As the activity 𝑃𝑒 decreases, the difference between the number densities in the two regions disappears. In both cases, the direction of the phoretic movement aligns with the total osmotic force 𝑭𝑜 𝑠𝑚 𝑜.

Active Matter with Spatially Varying Transport Properties

Introduction

We also present an interesting transient behavior of the Green's function of the Smoluchowski equation for active particles with a sudden change in activity. Since isothermal suspensions are considered, the variation of 𝐷𝑇 is equivalent to the spatially varying Stokes drag coefficient 𝜁, which depends on the suspended fluid viscosity and hydrodynamics.

Infinite Active Suspensions

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Figure 2.10: A schematic of a suspension of ABPs with an abrupt change in activity bounded by a circular wall of radius 𝑅
Figure 2.10: A schematic of a suspension of ABPs with an abrupt change in activity bounded by a circular wall of radius 𝑅

Transient Behavior of Microswimmers with Abrupt Variation in Ac-

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Figure 2.12: (Left) Snapshots from BD simulations of purely active particles re- re-leased at 𝑡 = 0 from the center (white dashed line) where the reorientation time or swim speed abruptly changes
Figure 2.12: (Left) Snapshots from BD simulations of purely active particles re- re-leased at 𝑡 = 0 from the center (white dashed line) where the reorientation time or swim speed abruptly changes

Conclusions

When 𝜏𝑅,1=𝜏𝑅,2regardless of the swimming speed in the two regions, the landmarks of the rescaled probability density 𝐴= 𝑃𝑈 are symmetric and also fall on a single curve on the rescaled domain 𝒙 =𝒙/ℓ. When the reorientation time during a suspension is uniform, the Smoluchowski equation can be rescaled so that it has no swimming speed and the transient distributions fall on a single symmetrical master curve regardless of the swimming speeds in the two regions.

Appendix: Brownian Dynamics Simulations of Active Brownian

The total pressure 𝑃 is the sum of the local osmotic pressure Π𝑜 𝑠𝑚 𝑜 = 𝑛 𝑘𝐵𝑇 exerted by particles and the fluid pressure 𝑝𝑓. The equilibrium condition for the system is given by the minimization of the large potential𝑊.

Reverse Osmotic Effects in Active Matter

Particle Phase Pressure on Walls

Since 𝑛𝑏𝑢𝑙 𝑘𝑈 is nearly constant for highly active particles, as shown in the previous chapter (see Figure 2.3), the pressure exerted by particles on the walls Π𝑤 ≈ Π𝑠𝑤𝑖 𝑚 ∼ 𝑛𝑏𝑢𝑙 𝑘𝜁 𝐷 𝑠𝑤𝑖 𝑚 ∼ 𝜁(𝑛𝑏𝑢𝑙 𝑘𝑈)ℓ will otherwise are in the two regions if the run lengths are differentℓ1 ≠ℓ2. In both cases, the ratio of the pressure exerted by particles on the walls is ℓ1/ℓ2 when the activity is high (𝑃𝑒≫ 1).

Mechanical Description of Active Matter with Spatially Varying Ac-

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Figure 3.2: A schematic of a suspension of ABPs with an abrupt change in activity confined between two parallel planar walls (see Fig
Figure 3.2: A schematic of a suspension of ABPs with an abrupt change in activity confined between two parallel planar walls (see Fig

Reverse Osmotic Effect in Active Matter

For spherical active particles with radii 𝑎 and Stokes drag coefficient𝜁 =6𝜋𝜂𝑎, |Δ𝑝𝑓| = (3/4)𝜂 𝜙𝑈ℎ|Δℓ|/𝑎2, where 𝜙 is the average volume fraction of suspended particles and 𝜂 is the viscosity of the liquid. Assuming a cylindrical connecting pipe and laminar flow, the pressure drop across the pipe is |Δ𝑝𝑡| = 𝜂𝑄 𝑅𝑡, where 𝑅𝑡 = 8𝐿𝑡/(𝜋𝑟4 . 𝑡) is the resistance of the pipe and 𝐿𝑡and𝑟𝑡 are the length and radius of the pipe.

Reverse Diffusiophoresis in Active Bath

The results obtained from the BD simulations confirm Brady's prediction [7] of reverse diffusiophoresis that the total osmotic force and thus the phoretic velocity is linearly proportional to the swimming velocity gradient. We also confirm that the magnitude of the total osmotic force is linearly proportional to the swimming velocity gradient.

Figure 3.4: A schematic of reverse diffusiophoresis in a bath of active hard-spheres.
Figure 3.4: A schematic of reverse diffusiophoresis in a bath of active hard-spheres.

Conclusions

Assume that two phases 𝛼 and 𝛽 coexist in equilibrium in the absence of external potential. From the particle force balance (4.49), the difference in collision pressures between the two phases is balanced by the integral of the buoyancy force: ΔΠ𝑐.

Mechanical Theory of Phase Coexistence

Phase Equilibrium Conditions

According to the second law, the entropy of a system has its maximum value at equilibrium. When the total molar volume of the system is 𝑣 ∈ (𝑣𝛼, 𝑣𝛽), the total Helmholtz free energy is minimized by two separate phases with (𝑣𝛼, 𝑇) and (𝑣𝛽, 𝑇): Helmholtz free energy minimization principle for fixed 𝑁 , 𝑉 and 𝑇.

Figure 4.1: (a) A schematic description of the double-tangent construction on an isotherm in the diagram of the molar Helmholtz free energy 𝐹 versus the molar volume 𝑣 at a fixed temperature 𝑇
Figure 4.1: (a) A schematic description of the double-tangent construction on an isotherm in the diagram of the molar Helmholtz free energy 𝐹 versus the molar volume 𝑣 at a fixed temperature 𝑇

Microscopic Structure of Phase Interfaces

Thus, the simple model of free energy density functional 𝑓 = 𝑓0(𝜌) only captures the macroscopic equilibrium condition (4.1) of classical thermodynamics - the microscopic structure of interfaces cannot be described. Equation (4.25) clearly shows that the interfacial tension is the result of the square gradient term which penalizes non-homogeneity in the density due to interparticle interactions.

Mechanical Description of Phase Interfaces

The stress deviates from −𝑝0𝑰 — the stress when the fluid is homogeneous — due to inhomogeneities in density. By integrating the balance of mechanical forces (4.29), we have 4.30) the pressure is the same deep within the coexisting phases due to the lack of density gradients in the bulk: a condition of mechanical equilibrium.

Motility-Induced Phase Separation

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Figure 4.2: (a) Generalized equal-area construction from the mechanical theory (eqs. (4.53) and (4.56)) in the (Π 𝑎 𝑐𝑡 = [Π 𝑐 + Π 𝑠𝑤𝑖 𝑚 ] , Π 𝑐 ) plane and (b) Maxwell construction for ℓ 0 / 𝐷 = 35 × 2 −1/6 in 2D
Figure 4.2: (a) Generalized equal-area construction from the mechanical theory (eqs. (4.53) and (4.56)) in the (Π 𝑎 𝑐𝑡 = [Π 𝑐 + Π 𝑠𝑤𝑖 𝑚 ] , Π 𝑐 ) plane and (b) Maxwell construction for ℓ 0 / 𝐷 = 35 × 2 −1/6 in 2D

Conclusions

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Appendix: Classical Density Functional Theory

For example, the functional derivative of the mean density with respect to the internal chemical potential gives the variance or fluctuation of the microscopic density: 4.65). Equations (4.64) and (4.65) clearly show that the mean density is a functional of the internal chemical potential in the grand canonical formulation.

Appendix: Orientational Moment Equations of Interacting Active

We first derive the evolution equation of the number density field to account for mass transport. The first term corresponding to the self-drive refers to the definition of the microscopic density of polar order.

Appendix: Effects of Correlation between Collisional Stress and

Bertin, "Lack of an equation of state for the non-equilibrium chemical potential of gases of active particles in contact," The Journal of Chemical Physics, vol. Waals, "The thermodynamic theory of capillarity under the hypothesis of a continuous variation of density," Journal of Statistical Physics, vol.

Figure 4.7: A schematic of Π 𝑎 𝑐𝑡 -Π 𝑐 plot with a van-der Waals-like loop. The corre- corre-lation between the collisional stress and orientation leads to ∫
Figure 4.7: A schematic of Π 𝑎 𝑐𝑡 -Π 𝑐 plot with a van-der Waals-like loop. The corre- corre-lation between the collisional stress and orientation leads to ∫

Gambar

Figure 2.1: A schematic of an infinite suspension of ABPs with an abrupt change in activity
Figure 2.2: Color map of 𝑛 +∞ / 𝑛 −∞ for 𝑈 2 / 𝑈 1 = 5. The modified Péclet numbers 𝐶 𝑖 = 0 when 𝑃𝑒 𝑖 = 0 and 𝐶 𝑖 → 1 when 𝑃𝑒 𝑖 → ∞
Figure 2.3: (a) Number densities scaled with the overall number density ⟨ 𝑛 ⟩, (b) the product of the number density and swim speed scaled with the overall number density and the harmonic mean of the swim speeds ( 𝑈 ℎ = 2 ( 𝑈 − 1
Figure 2.4: Relative magnitude of the nematic order 𝑄 𝑥 𝑥 compared to the number density 𝑛 as a function of the position 𝑥 scaled with the run length in the region 2 ℓ 2 = 𝑈 2 / 𝐷 𝑅 2 obtained by BD simulations
+7

Referensi

Dokumen terkait

MATERIALS AND METHODS The effects of temperature on the duration and survival of egg, larval and pupal stages, adult female weight and fecundity, and reproductive potential were