Search arXivSearch

arXiv · 2110.15212

Kinetic theory of granular particles immersed in a molecular gas

Abstract

The transport coefficients of a dilute gas of inelastic hard spheres immersed in a molecular gas are determined. We assume that the number density of the granular gas is much smaller than that of the surrounding molecular gas, so that the latter is not affected by the presence of solid particles. In this situation, the molecular gas may be treated as a thermostat (or bath) of elastic hard spheres at a fixed temperature. This system (granular gas thermostated by a bath of elastic hard spheres) can be considered as a reliable model for describing the dynamic properties of particle-laden suspensions. The Boltzmann kinetic equation is the starting point of the present work. First step is to characterise the reference state in the perturbation scheme, namely the homogeneous state. Theoretical results for the granular temperature and kurtosis obtained in the homogeneous steady state are compared against Monte Carlo simulations showing a good agreement. Then, the Chapman-Enskog method is employed to solve the Boltzmann equation to first order in spatial gradients. As expected, the Navier-Stokes-Fourier transport coefficients of the granular gas are given in terms of the solutions of a coupled set of linear integral equations which are approximately solved by considering the leading terms in a Sonine polynomial expansion. Our results show that the dependence of the transport coefficients on the coefficient of restitution is quite different from that found when the influence of the interstitial molecular gas is neglected (dry granular gas). When the granular particles are much more heavier than the gas particles (Brownian limit) the expressions of the transport coefficients are consistent with those previously derived from the Fokker-Planck equation. Finally, a linear stability analysis of the homogeneous steady state is performed showing this state is always linearly stable.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Rubén Gómez González, Vicente Garzó. 2021-10-28. Kinetic theory of granular particles immersed in a molecular gas. https://doi.org/10.1017/jfm.2022.410

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft

Taylor dispersion in a soft tube

Diffusion of a solute along a tube is enhanced by hydrodynamic flow, a phenomenon known as Taylor dispersion. In microfluidic applications, the compliance of the tube boundaries modifies the hydrodynamic flow and thus solutal transport. Here, we develop the theory of solutal dispersion in a soft, axisymmetric tube where the tube walls respond to the hydrodynamic pressure through a Winkler response. By deriving the modified macro-transport equation for the solutal concentration dynamics based on multiple-time-scale analysis, we explore the influence of softness on solutal transport for steady and pulsatile configurations. Our main finding is that softness enhances the effective advection velocity and dispersion coefficient, which might have practical implication in biology and microfluidic technology.

cond-mat.soft