708 research outputs found

    Structure of polydisperse inverse ferrofluids: Theory and computer simulation

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    By using theoretical analysis and molecular dynamics simulations, we investigate the structure of colloidal crystals formed by nonmagnetic microparticles (or magnetic holes) suspended in ferrofluids (called inverse ferrofluids), by taking into account the effect of polydispersity in size of the nonmagnetic microparticles. Such polydispersity often exists in real situations. We obtain an analytical expression for the interaction energy of monodisperse, bidisperse, and polydisperse inverse ferrofluids. Body-centered tetragonal (bct) lattices are shown to possess the lowest energy when compared with other sorts of lattices and thus serve as the ground state of the systems. Also, the effect of microparticle size distributions (namely, polydispersity in size) plays an important role in the formation of various kinds of structural configurations. Thus, it seems possible to fabricate colloidal crystals by choosing appropriate polydispersity in size.Comment: 22 pages, 8 figure

    Optimal packing of polydisperse hard-sphere fluids II

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    We consider the consequences of keeping the total surface fixed for a polydisperse system of NN hard spheres. In contrast with a similar model (J. Zhang {\it et al.}, J. Chem. Phys. {\bf 110}, 5318 (1999)), the Percus-Yevick and Mansoori equations of state work very well and do not show a breakdown. For high pressures Monte Carlo simulation we show three mechanically stable polydisperse crystals with either a unimodal or bimodal particle-size distributions.Comment: 17 pages, 8 figures, revtex (accepted by J. Chem. Phys.

    Jamming at Zero Temperature and Zero Applied Stress: the Epitome of Disorder

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    We have studied how 2- and 3- dimensional systems made up of particles interacting with finite range, repulsive potentials jam (i.e., develop a yield stress in a disordered state) at zero temperature and applied stress. For each configuration, there is a unique jamming threshold, ϕc\phi_c, at which particles can no longer avoid each other and the bulk and shear moduli simultaneously become non-zero. The distribution of ϕc\phi_c values becomes narrower as the system size increases, so that essentially all configurations jam at the same ϕ\phi in the thermodynamic limit. This packing fraction corresponds to the previously measured value for random close-packing. In fact, our results provide a well-defined meaning for "random close-packing" in terms of the fraction of all phase space with inherent structures that jam. The jamming threshold, Point J, occurring at zero temperature and applied stress and at the random close-packing density, has properties reminiscent of an ordinary critical point. As Point J is approached from higher packing fractions, power-law scaling is found for many quantities. Moreover, near Point J, certain quantities no longer self-average, suggesting the existence of a length scale that diverges at J. However, Point J also differs from an ordinary critical point: the scaling exponents do not depend on dimension but do depend on the interparticle potential. Finally, as Point J is approached from high packing fractions, the density of vibrational states develops a large excess of low-frequency modes. All of these results suggest that Point J may control behavior in its vicinity-perhaps even at the glass transition.Comment: 21 pages, 20 figure

    Geometrical properties of rigid frictionless granular packings as a function of particle size and shape

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    Three-dimensional discrete numerical simulation is used to investigate the properties of close-packed frictionless granular assemblies as a function of particle polydispersity and shape. Unlike some experimental results, simulations show that disordered packings of pinacoids (eight-face convex polyhedron) achieve higher solid fraction values than amorphous packings of spherical or rounded particles, thus fulfilling the analogue of Ulam's conjecture stated by Jiao and co-workers for random packings [Y. Jiao and S. Torquato, Phys. Rev. E 84\textbf{84}, 041309041309 (20112011)]. This seeming discrepancy between experimental and numerical results is believed to lie with difficulties in overcoming interparticle friction through experimental densification processes. Moreover, solid fraction is shown to increase further with bidispersity and peak when the volume proportion of small particles reaches 30%30\%. Contrarywise, substituting up to 50%50\% of flat pinacoids for isometric ones yields solid fraction decrease, especially when flat particles are also elongated. Nevertheless, particle shape seems to play a minor role on packing solid fraction compared to polydispersity. Additional investigations focused on the packing microstructure confirm that pinacoid packings fulfill the isostatic conjecture and that they are free of order except beyond 3030 to 50%50\% of flat or flat \& elongated polyhedra in the packing. This order increase progressively takes the form of a nematic phase caused by the reorientation of flat or flat \& elongated particles to minimize the packing potential energy. Simultaneously, this reorientation seems to increase the solid fraction value slightly above the maximum achieved by monodisperse isometric pinacoids, as well as the coordination number. Finally, partial substitution of elongated pinacoids for isometric ones has limited effect on packing solid fraction or order.Comment: 12 figures, 12 page

    Predicting phase equilibria in polydisperse systems

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    Many materials containing colloids or polymers are polydisperse: They comprise particles with properties (such as particle diameter, charge, or polymer chain length) that depend continuously on one or several parameters. This review focusses on the theoretical prediction of phase equilibria in polydisperse systems; the presence of an effectively infinite number of distinguishable particle species makes this a highly nontrivial task. I first describe qualitatively some of the novel features of polydisperse phase behaviour, and outline a theoretical framework within which they can be explored. Current techniques for predicting polydisperse phase equilibria are then reviewed. I also discuss applications to some simple model systems including homopolymers and random copolymers, spherical colloids and colloid-polymer mixtures, and liquid crystals formed from rod- and plate-like colloidal particles; the results surveyed give an idea of the rich phenomenology of polydisperse phase behaviour. Extensions to the study of polydispersity effects on interfacial behaviour and phase separation kinetics are outlined briefly.Comment: 48 pages, invited topical review for Journal of Physics: Condensed Matter; uses Institute of Physics style file iopart.cls (included

    Self-assembly of magnetic iron oxide nanoparticles into cuboidal superstructures

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    This chapter describes the synthesis and some characteristics of magnetic iron oxide nanoparticles, mainly nanocubes, and focus on their self-assembly into crystalline cuboids in dispersion. The influence of external magnetic fields, the concentration of particles, and the temperature on the assembly process is experimentally investigated
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