Searcharxiv⌕ Search

arXiv · cond-mat/0105395

Hydrodynamics for a granular binary mixture at low density

Abstract

Hydrodynamic equations for a binary mixture of inelastic hard spheres are derived from the Boltzmann kinetic theory. A normal solution is obtained via the Chapman-Enskog method for states near the local homogeneous cooling state. The mass, heat, and momentum fluxes are determined to first order in the spatial gradients of the hydrodynamic fields, and the associated transport coefficients are identified. In the same way as for binary mixtures with elastic collisions, these coefficients are determined from a set of coupled linear integral equations. Practical evaluation is possible using a Sonine polynomial approximation, and is illustrated here by explicit calculation of the relevant transport coefficients: the mutual diffusion, the pressure diffusion, the thermal diffusion, the shear viscosity, the Dufour coefficient, the thermal conductivity, and the pressure energy coefficient. All these coefficients are given in terms of the restitution coefficients and the ratios of mass, concentration, and particle sizes. Interesting and new effects arise from the fact that the reference states for the two components have different partial temperatures, leading to additional dependencies of the transport coefficients on the concentration. The results hold for arbitrary degree of inelasticity and are not limited to specific values of the parameters of the mixture. Applications of this theory will be discussed in subsequent papers.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Vicente Garzó, J. W. Dufty. 2001-12-05. Hydrodynamics for a granular binary mixture at low density. https://doi.org/10.1063/1.1458007

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

KEEP EXPLORING

Related papers

Dynamic clustering of active chemotactic Janus particles

Modeling self-propulsion as an emergent diffusiophoretic effect, we come back to the dynamic clustering experiment of active Janus colloids. Working in the original three-dimensional geometry, and using the chemical solute concentration as a control parameter, we find that the dynamic clustering region occupies a robust fraction of the phase diagram. This behavior is rationalized using a linear stability analysis that efficiently captures the instability of the gas phase to dynamic clusters. We also find that dynamic clustering results from the combined effects of a Keller-Segel collapse and of a motility-induced phase separation, either being arrested by the orientational coupling to the chemical field in agreement with previous work.

cond-mat.soft↗

Multi-Fidelity Machine Learning for Predicting Startup Stress Growth and Strain Hardening in Wormlike Micellar Solutions

Wormlike micellar solutions exhibit formulation-dependent nonlinear startup responses, including stress overshoot, undershoot, and strain hardening, making prediction across compositions and shear rates challenging. We developed a multi-fidelity machine-learning framework to predict stress-growth curves in cetylpyridinium chloride (CPyCl)-based wormlike micelles from sparse experimental measurements. The framework combines a low-fidelity analytical model describing the overall startup response with high-fidelity experimental data capturing formulation-specific nonlinear features. This approach addresses the limited and uneven coverage of salt chemistry, concentration, and shear rate without relying solely on data-intensive neural-network training. The trained model predicts complete stress-growth responses at untested shear rates and enables extraction of strain-hardening characteristics from interpolated curves. By augmenting sparse rheological measurements, the framework provides a basis for exploring relationships among formulation variables, linear viscoelastic properties, and nonlinear startup behavior, while supporting more efficient characterization of wormlike micellar solutions.

cond-mat.soft↗

Topology Does Not Determine Defect Mobility in Active Polar Matter

Topological defects are commonly characterized by their charge, although defects with the same charge can have different internal morphologies. We study the annihilation of isolated $\pm1$ defect pairs in a two-dimensional compressible Toner--Tu model, varying the morphology of the $+1$ defect while keeping the initial charges and separation fixed. Activity produces a morphology-dependent mobility asymmetry: reversing the radial orientation of an aster reverses which defect travels farther, and asters show the strongest response. An early-time analysis reveals that the initial morphology selects distinct density modes whose gradients subsequently feed back on the polarization. Consistently, removing the density-gradient coupling strongly suppresses the asymmetry. These results establish defect morphology, in addition to topological charge, as a dynamical variable governing defect-pair motion in active polar matter.

cond-mat.soft↗