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Hydrodynamic model structure-dependent

All the above formulas are one-parameter equations, i.e. they relate the dispersion viscosity only to the volume fraction of particles contained in it. This limits the range of applicability of the equations to not very high dispersion concentrations. To take account of the influence of the structure of concentrated dispersions on their rheological behavior, Robinson [12] suggested that the viscosity of dispersions is not only propertional to the volume fraction of solid phase, but is also inversely proportional to the fraction of voids in it. (At about the same time Mooney [40], who proceeded from a hydrodynamic model, arrived, using theoretical methods, at the same conclusion). Robinson s equation contains the relative sedimentation volume value — S, which depends on the particle size distribution of the dispersion... [Pg.108]

R), i.e. there is no effect due to caging of the encounter complex in the common solvation shell. There exist numerous modifications and extensions of this basic theory that not only involve different initial and boundary conditions, but also the inclusion of microscopic structural aspects [31]. Among these are hydrodynamic repulsion at short distances that may be modelled, for example, by a distance-dependent diffiision coefficient... [Pg.844]

The dynamical properties of polymer molecules in solution have been investigated using MPC dynamics [75-77]. Polymer transport properties are strongly influenced by hydrodynamic interactions. These effects manifest themselves in both the center-of-mass diffusion coefficients and the dynamic structure factors of polymer molecules in solution. For example, if hydrodynamic interactions are neglected, the diffusion coefficient scales with the number of monomers as D Dq /Nb, where Do is the diffusion coefficient of a polymer bead and N), is the number of beads in the polymer. If hydrodynamic interactions are included, the diffusion coefficient adopts a Stokes-Einstein formD kltT/cnr NlJ2, where c is a factor that depends on the polymer chain model. This scaling has been confirmed in MPC simulations of the polymer dynamics [75]. [Pg.123]

While it is evident that the Q dependence of the short-time star relaxation can be exclusively explained on the basis of the star structure, the time scale of these relaxations does not fit into this simple picture. In the model of hydrodynamic interaction this time scale is solely determined by the temperature... [Pg.106]

Computational fluid dynamics enables us to investigate the time-dependent behavior of what happens inside a reactor with spatial resolution from the micro to the reactor scale. That is to say, CFD in itself allows a multi-scale description of chemical reactors. To this end, for single-phase flow, the space resolution of the CFD model should go down to the scales of the smallest dissipative eddies (Kolmogorov scales) (Pope, 2000), which is inversely proportional to Re-3/4 and of the orders of magnitude of microns to millimeters for typical reactors. On such scales, the Navier-Stokes (NS) equations can be expected to apply directly to predict the hydrodynamics of well-defined system, resolving all the meso-scale structures. That is the merit of the so-called DNS. [Pg.10]

Although the diffusion layer model is the most commonly used, various alterations have been proposed. The current views of the diffusion layer model are based on the so-called effective diffusion boundary layer, the structure of which is heavily dependent on the hydrodynamic conditions, fn this context, Levich [102] developed the convection-diffusion theory and showed that the transfer of the solid to the solution is controlled by a combination of liquid flow and diffusion. In other words, both diffusion and convection contribute to the transfer of drug from the solid surface into the bulk solution, ft should be emphasized that this observation applies even under moderate conditions of stirring. [Pg.90]


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