Search arXiv⌕ Search

arXiv · cond-mat/9805077

Bulk and Surface Properties of Dipolar Fluids

Abstract

Based on density-functional theory we analyze the full phase diagram, the occurrence of long-ranged orientational order, and the structural properties of dipolar fluids. As a model system we consider the Stockmayer fluid that consists of spherical particles interacting via a Lennard-Jones potential plus dipolar forces. For sufficiently strong dipole moments one finds a region where a fluid phase with long-ranged orientational order is stable. For all sample shapes with the exception of a long thin needle this phase exhibits a spatially inhomogeneous magnetization which depends on the actual shape. We determine the details of the magnetization structure in a cubic sample in the absence and in the presence of an external magnetic field. One obtains a vortexlike structure with an escape of the magnetization into the axis direction near the vortex axis and two point defects where the absolute value of the magnetization is strongly reduced. If the spherical cores of the particles are replaced by elongated or oblate shapes a nematic phase without spontaneous magnetization is also possible due to the anisotropic steric interactions. We study the interplay of this nematic ordering with ferromagnetism in fluids of dipolar hard ellipsoids. Orientational order arises locally in the isotropic fluid phases near the liquid-gas interface of the Stockmayer fluid. Density-functional theory allows us to determine density and orientational order profiles as well as the surface tension of this interface.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

B. Groh, S. Dietrich. 1998-05-07. Bulk and Surface Properties of Dipolar Fluids. https://arxiv.org/abs/cond-mat/9805077

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

KEEP EXPLORING

Related papers

Control of filament network rigidity by the condensation of crowding molecules

Understanding how liquid-liquid phase separation impacts the mechanics of filament networks is a fundamental physical problem at the heart of biological cellular processes and soft material design. While a few theoretical mechanisms have been proposed, a clear demonstration of the direct coupling of phase separation to the overall network stiffness is missing. We report experiments that reveal a universal mechanism by which the condensation of macromolecular crowders induces a rigidity transition in a model filament network. We reconstituted stiff sterically interacting helical filaments and polymeric crowders. Initially, the macromolecules were uniformly dissolved and the filaments formed bundles that assembled a rigid entangled network. Once the crowders condensed into droplets, the network structure lost its rigidity and its mechanical response weakened by an order-of-magnitude. The subsequent dissolution of the condensates was accompanied by the re-establishment of rigidity. Our results show that crowder phase separation modulates the mechanics of filament networks by tuning the osmotic pressure holding the network together. This principle may serve as a paradigm for devising dynamically tunable filamentous materials.

cond-mat.soft↗

Speed up of passive tracers in mixtures with active chemical reactions

Diffusivity of passive tracers in complex mixtures is widely relevant for industrial applications and for probing biological systems. Interactions with the surrounding medium typically generate a drag force that suppresses tracer diffusion, although self-propulsion can accelerate tracers via active fluctuations. Similar effects are not understood in mixtures with particle conversion and exchange, although these are particularly relevant in biological contexts, where actively driven reactions prevail. By studying a thermodynamically consistent model of chemical reactions in mixtures, we show that reactions provide an additional relaxation pathway that suppresses interaction-induced memory, reducing the drag on tracers and restoring their diffusivity toward the value expected in the absence of solutes. Moreover, active reactions generate nonequilibrium fluctuations that can push tracer diffusivity beyond this limit, an effect we confirm with particle-based simulations. Our results identify chemical activity as a distinct route to controlling mass transport and offer a framework for interpreting microrheology experiments in chemically active mixtures.

cond-mat.soft↗

Diffusion of charged rods across 3D varying section channels

We analyze the transport of rod-like particles by diffusion and drift in a three-dimensional channel with varying circular or elliptic cross section. Applying the Fick-Jacobs approximation to the transport equation of the particles' probability distribution, we derive an effective one-dimensional substitute model and the associated free energy profile. Our results show that the data for the mean first passage time of rods, once expressed as a function of the effective free energy barrier, collapse onto the same master curve as obtained for point or spherical particles. The observed universality provides a simple framework for predicting transport times of anisotropic particles in confined geometries without resolving the full multidimensional dynamics.

cond-mat.soft↗