No Arabic abstract
Ferrofluids belong to an important class of highly functional soft matter, benefiting from their magnetically controllable physical properties. Therefore, it is of central importance to quantitatively predict the dynamic magnetic response of ferrofluids. Traditional dynamic theories, however, are often restricted to the near-equilibrium regime and/or only apply to nearly ideal ferrofluids that are monodisperse, dilute enough, and weakly interacting. In this paper I develop a self-consistent and nonperturbative dynamical mean field theory for typical ferrofluids which are often polydisperse, concentrated, and strongly interacting, possibly driven far from equilibrium. I obtain a general nonperturbative expression for the dynamic magnetic susceptibility, quantitatively agreeing with the spectra obtained from Brownian Dynamics simulations on both mono- and bidisperse samples. Furthermore, I derive a generic magnetization relaxation equation (MRE) for both mono- and polydisperse ferrofluids by employing the projection operator technique in nonequlibrium statistical mechanics. This MRE is in simple closed form and independent of which model is employed to approximate the equilibrium magnetization curve. Existing models can be recovered as low-order approximations of my generic and nonperturbative MRE. My theory can play a key role in studying the dynamics of ferrofluids and other polar fluids. It may also have substantial and immediate consequences to various ferrofluid applications.
Taking into account the structural transition and long-range interaction (lattice effect), we resort to the Ewald-Kornfeld formulation and developed Maxwell-Garnett theory for uniaxially anisotropic suspensions to calculate the effective permeability of inverse ferrofluids. And we also consider the effect of volume fraction to the magnetophoretic force on the nonmagnetic spherical particles submerged in ferrofluids in the presence of nonuniform magnetic field. We find that the coupling of ac and dc field case can lead to fundamental and third harmonic response in the effective magnetophoresis and changing the aspect ratio in both prolate and oblate particles can alter the harmonic and nonharmonic response and cause the magnetophoretic force vanish.
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.
A new theoretical model for self dynamic response is developed using Vibration-Transit (V-T) theory, and is applied to liquid sodium at all wavevectors q from the hydrodynamic regime to the free particle limit. In this theory the zeroth-order Hamiltonian describes the vibrational motion in a single random valley harmonically extended to infinity. This Hamiltonian is tractable, is evaluated a priori for monatomic liquids, and the same Hamiltonian (the same set of eigenvalues and eigenvectors) is used for equilibrium and nonequlibrium theory. Here, for the self intermediate scattering function Fself(q,t) we find the vibrational contribution is in near perfect agreement with molecular dynamics (MD) through short and intermediate times, at all q. This is direct confirmation that normal mode vibrational correlations are present in the motion of the liquid state. The primary transit effect is diffusive motion of the vibrational equilibrium positions, as the liquid transits rapidly among random valleys. This motion is modeled as a standard random walk, and the resulting theoretical Fself(q,t) is in excellent agreement with MD results at all q and t. In the limit for q to infinity, the theory automatically exhibits the correct approach to the free-particle limit. Also in the limit for q to zero, the hydrodynamic limit emerges as well. In contrast to the benchmark theories of generalized hydrodynamics and mode coupling, the present theory is near a priori, while achieving modestly better accuracy. Therefore, in our view, it constitutes an improvement over the traditional theories.
We discuss the motion of colloidal particles relative to a two component fluid consisting of solvent and solute. Particle motion can result from (i) net body forces on the particle due to external fields such as gravity; (ii) slip velocities on the particle surface due to surface dissipative phenomena. The perturbations of the hydrodynamic flow field exhibits characteristic differences in cases (i) and (ii) which reflect different patterns of momentum flux corresponding to the existence of net forces, force dipoles or force quadrupoles. In the absence of external fields, gradients of concentration or pressure do not generate net forces on a colloidal particle. Such gradients can nevertheless induce relative motion between particle and fluid. We present a generic description of surface dissipative phenomena based on the linear response of surface fluxes driven by conjugate surface forces. In this framework we discuss different transport scenarios including self-propulsion via surface slip that is induced by active processes on the particle surface. We clarify the nature of force balances in such situations.
The recently proposed dynamical effective field model (DEFM) is quantitatively accurate for describing dynamical magnetic response of ferrofluids. In paper I it is derived under the framework of dynamical density functional theory, via which the original ensemble of bare Brownian particles is mapped to an ensemble of dressed particles. However, it remains to clarify how the characteristic rotational relaxation time of a dressed particle, denoted by $tau_r$, is quantitatively related to that of a bare particle, denoted by $tau^0_r$. By building macro-micro connections via two different routes, I reveal that under some gentle assumptions $tau_r$ can be identified with the long-time rotational self-diffusion time. I further introduce two simple but useful integrated correlation factors, describing the effects of quasi-static (adiabatic) and dynamic (nonadiabatic) inter-particle correlations, respectively. In terms of both correlation factors I reformulate the dynamic magnetic susceptibility in an illuminating and elegant form. Remarkably, it shows that the macro-micro connection is established via two successive steps: a dynamical coarse-graining with nonadiabatic effects accounted for by the dynamic factor, followed by equilibrium statistical mechanical averaging captured by the static factor. Surprisingly, $tau_r/tau^0_r$ is found insensitive to changes of particle volume fraction. I provide a physical picture to explain it. Furthermore, an empirical formula is proposed to characterize the dependence of $tau_r/tau^0_r$ on dipole-dipole interaction strength. The DEFM supplemented with this formula leads to parameter-free predictions in good agreement with results from Brownian dynamics simulations. The theoretical developments presented in this paper may have important consequences to studies of ferrofluid dynamics in particular and other systems modelled by DDFTs in general.