Measurement of the full shear-induced self-diffusion tensor of noncolloidal suspensions

2002 ◽  
Vol 116 (23) ◽  
pp. 10529-10535 ◽  
Author(s):  
V. Breedveld ◽  
D. van den Ende ◽  
M. Bosscher ◽  
R. J. J. Jongschaap ◽  
J. Mellema
2003 ◽  
Vol 15 (1) ◽  
pp. 1-4 ◽  
Author(s):  
Alexandre F. M. DaSilva ◽  
David S. Tuch ◽  
Mette R. Wiegell ◽  
Nouchine Hadjikhani

In this article, the authors review the application of diffusion tensor (DT) magnetic resonance (MR) imaging to demonstrate anatomical substructures that cannot be resolved by conventional structural imaging. They review the physical basis of DT imaging and provide illustrative anatomical examples. The DT imaging technique measures the self-diffusion, or random thermal motion, of the endogenous water in nerve tissue. Because of the preferred diffusion of water molecules along the nerve fiber direction, DT imaging can measure the orientation of the neural fiber structure within each voxel of the MR image. The fiber orientation information yielded by DT imaging provides a new contrast mechanism that can be used to resolve images of anatomical substructures that cannot otherwise be visualized using conventional structural imaging. The authors illustrate how DT imaging can resolve individual pathways in the brainstem as well as individual nuclei of the thalamus and conclude by describing potential applications in neurosurgery.


1972 ◽  
Vol 38 (5) ◽  
pp. 335-336 ◽  
Author(s):  
K. Otnes ◽  
R. Pynn ◽  
J.A. Janik ◽  
J.M. Janik

2001 ◽  
Vol 87 (20) ◽  
Author(s):  
Patrice Porion ◽  
Stéphane Rodts ◽  
Muzahim Al-Mukhtar ◽  
Anne-Marie Faugère ◽  
Alfred Delville

1994 ◽  
Vol 103 (3) ◽  
pp. 247-254 ◽  
Author(s):  
P.J. Basser ◽  
J. Mattiello ◽  
D. Lebihan

1997 ◽  
Vol 348 ◽  
pp. 85-101 ◽  
Author(s):  
CHARLES S. CAMPBELL

The collisionally induced random particle velocities in a rapid granular shear flow drive the diffusion of particles in manner directly analogous to the thermal diffusion of molecules or the eddy-induced diffusion in a turbulent flow. This paper reports measurements, via computer simulation, of the anisotropic diffusion tensor for a granular shear flow. The components are determined both by particle tracking and through velocity correlations, which are found to agree with reasonable accuracy. As might be expected from symmetry arguments, there are four non-zero components generated in a simple shear flow: the three diagonal components and one off-diagonal component.


1996 ◽  
Vol 312 ◽  
pp. 223-252 ◽  
Author(s):  
Jeffrey F. Morris ◽  
John F. Brady

Self-diffusion in a suspension of spherical particles in steady linear shear flow is investigated by following the time evolution of the correlation of number density fluctuations. Expressions are presented for the evaluation of the self-diffusivity in a suspension which is either raacroscopically quiescent or in linear flow at arbitrary Peclet number $Pe = \dot{\gamma}a^2/2D$, where $\dot{\gamma}$ is the shear rate, a is the particle radius, and D = kBT/6πa is the diffusion coefficient of an isolated particle. Here, kB is Boltzmann's constant, T is the absolute temperature, and η is the viscosity of the suspending fluid. The short-time self-diffusion tensor is given by kBT times the microstructural average of the hydrodynamic mobility of a particle, and depends on the volume fraction $\phi = \frac{4}{3}\pi a^3n$ and Pe only when hydrodynamic interactions are considered. As a tagged particle moves through the suspension, it perturbs the average microstructure, and the long-time self-diffusion tensor, D∞s, is given by the sum of D0s and the correlation of the flux of a tagged particle with this perturbation. In a flowing suspension both D0s and D∞ are anisotropic, in general, with the anisotropy of D0s due solely to that of the steady microstructure. The influence of flow upon D∞s is more involved, having three parts: the first is due to the non-equilibrium microstructure, the second is due to the perturbation to the microstructure caused by the motion of a tagged particle, and the third is by providing a mechanism for diffusion that is absent in a quiescent suspension through correlation of hydrodynamic velocity fluctuations.The self-diffusivity in a simply sheared suspension of identical hard spheres is determined to O(øPe3/2) for Pe ≤ 1 and ø ≤ 1, both with and without hydro-dynamic interactions between the particles. The leading dependence upon flow of D0s is 0.22DøPeÊ, where Ê is the rate-of-strain tensor made dimensionless with $\dot{\gamma}$. Regardless of whether or not the particles interact hydrodynamically, flow influences D∞s at O(øPe) and O(øPe3/2). In the absence of hydrodynamics, the leading correction is proportional to øPeDÊ. The correction of O(øPe3/2), which results from a singular advection-diffusion problem, is proportional, in the absence of hydrodynamic interactions, to øPe3/2DI; when hydrodynamics are included, the correction is given by two terms, one proportional to Ê, and the second a non-isotropic tensor.At high ø a scaling theory based on the approach of Brady (1994) is used to approximate D∞s. For weak flows the long-time self-diffusivity factors into the product of the long-time self-diffusivity in the absence of flow and a non-dimensional function of $\bar{P}e = \dot{\gamma}a^2/2D^s_0(\phi)$. At small $\bar{P}e$ the dependence on $\bar{P}e$ is the same as at low ø.


1974 ◽  
Vol 15 (2) ◽  
pp. 227-229 ◽  
Author(s):  
I. Zupančič ◽  
J. Pirš ◽  
M. Luzar ◽  
R. Blinc ◽  
J.W. Doane

2016 ◽  
Vol 795 ◽  
pp. 739-783 ◽  
Author(s):  
N. J. Hoh ◽  
R. N. Zia

We study the influence of hydrodynamic, thermodynamic and interparticle forces on the diffusive motion of a Brownian probe driven by a constant external force through a dilute colloidal dispersion. The influence of these microscopic forces on equilibrium self-diffusivity (passive microrheology) is well known: all three act to hinder the short- and long-time self-diffusion. Here, via pair-Smoluchowski theory, we explore their influence on self-diffusion in a flowing suspension, where particles and fluid have been set into motion by an externally forced probe (active microrheology), giving rise to non-equilibrium flow-induced diffusion. The probe’s motion entrains background particles as it travels through the bath, deforming the equilibrium suspension microstructure. The shape and extent of microstructural distortion is set by the relative strength of the external force $F^{\mathit{ext}}$ to the entropic restoring force $kT/a_{\mathit{th}}$ of the bath particles, defining a Péclet number $\mathit{Pe}\equiv F^{\mathit{ext}}/(2kT/a_{\mathit{th}})$; and also by the strength of hydrodynamic interactions, set by the range of interparticle repulsion ${\it\kappa}=(a_{\mathit{th}}-a)/a$, where $kT$ is the thermal energy and $a_{\mathit{th}}$ and $a$ are the thermodynamic and hydrodynamic sizes of the particles, respectively. We find that in the presence of flow, the same forces that hinder equilibrium diffusion now enhance it, with diffusive anisotropy set by the range of interparticle repulsion ${\it\kappa}$. A transition from hindered to enhanced diffusion occurs when diffusive and advective forces balance, $\mathit{Pe}\sim 1$, where the exact value is a sensitive function of the strength of hydrodynamics, ${\it\kappa}$. We find that the hindered to enhanced transition straddles two transport regimes: in hindered diffusion, stochastic forces in the presence of other bath particles produce deterministic displacements (Brownian drift) at the expense of a maximal random walk. In enhanced diffusion, driving the probe with a deterministic force through an initially random suspension leads to fluctuations in the duration of probe–bath particle entrainment, giving rise to enhanced, flow-induced diffusion. The force-induced diffusion is anisotropic for all $\mathit{Pe}$, scaling as $D\sim \mathit{Pe}^{2}$ in all directions for weak forcing, regardless of the strength of hydrodynamic interactions. When probe forcing is strong, $D\sim \mathit{Pe}$ in all directions in the absence of hydrodynamic interactions, but the picture changes qualitatively as hydrodynamic interactions grow strong. In this nonlinear regime, microstructural asymmetry weakens while the anisotropy of the force-induced diffusion tensor increases dramatically. This behaviour owes its origins to the approach toward Stokes flow reversibility, where diffusion along the direction of probe force scales advectively while transverse diffusion must vanish.


2003 ◽  
Vol 16 (3) ◽  
pp. 121-128 ◽  
Author(s):  
Nan Li ◽  
Zhao Gong ◽  
Deborah Saucier ◽  
Edward J. Kendall ◽  
Gordon E. Sarty

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