Smoluchowski/Stokes-Einstein expression

Perrin model and the Johansson and Elvingston model fall above the experimental data. Also shown in this figure is the prediction from the Stokes-Einstein-Smoluchowski expression, whereby the Stokes-Einstein expression is modified with the inclusion of the Ein-stein-Smoluchowski expression for the effect of solute on viscosity. Penke et al. [290] found that the Mackie-Meares equation fit the water diffusion data however, upon consideration of water interactions with the polymer gel, through measurements of longitudinal relaxation, adsorption interactions incorporated within the volume averaging theory also well described the experimental results. The volume averaging theory had the advantage that it could describe the effect of Bis on the relaxation within the same framework as the description of the diffusion coefficient. 

The rate of diffusion controlled reaction is typically given by the Smoluchowski/Stokes-Einstein (S/SE) expression (see Brownian Dynamics), in which the effect of the solvent on the rate constant k appears as an inverse dependence on the bulk viscosity r), i.e., k oc (1// ). A number of experimental studies of radical recombination reactions in SCFs have found that these reactions exhibit no unusual behavior in SCFs. That is, if the variation in the bulk viscosity of the SCF solvent with temperature and pressure is taken into accounL the observed reaction rates are well described by S/SE theory. However, these studies were conducted at densities greater than the critical density, and, in fact, the data is inconclusive very near to the critical density. Additionally, Randolph and Carlier have examined a case in which the observed diffusion controlled, free radical spin exchange rates are up to three times faster than predicted by S/SE theory, with the deviations becoming most pronounced near the critical point. This deviation was attributed to some sort of solvent-solute clustering effect. It is presently unclear why this system is observed to behave differently from those which were observed to follow S/SE behavior. Possible candidates are differences in thermodynamic conditions or molecular interactions, or even misinterpretation of the data arising from other possible processes not considered. 

In the Smoluchowski limit, one usually assumes that the Stokes-Einstein relation (Dq//r7)a = C holds, which fonns the basis of taking the solvent viscosity as a measure for the zero-frequency friction coefficient appearing in Kramers expressions. Here C is a constant whose exact value depends on the type of boundary conditions used in deriving Stokes law. It follows that the diffiision coefficient ratio is given by ... 

In electrochemistry several equations are used that bear Einsteins name [viii-ix]. The relationship between electric mobility and diffusion coefficient is called Einstein relation. The relation between conductivity and diffusion coefficient is called - Nernst-Einstein equation. The expression concerns the relation between the diffusion coefficient and the viscosity and is known as the - Stokes-Einstein equation. The expression that shows the proportionality of the mean square distance of the random movements of a species to the diffusion coefficient and the duration of time is called - Einstein-Smoluchowski equation. A relationship between the relative viscosity of suspension and the volume fraction occupied by the suspended particles - which was derived by Einstein - is also called Einstein equation [ix]. 

Application of the Smoluchowski equation (1.3) requires a knowledge of the sizes and diffusion coefficients of molecules. An estimate of the effective values of r can usually be made from molecular volumes. Diffusion coefficients present more of a problem, since not very many have been experimentally determined over a range of temperature. They may, however, be eliminated from Equation (1.3) by using the Stokes-Einstein relation, which is theoretically derived from the same molecular model and is often in fairly good accord with experimental data it expresses D in terms of the viscosity of the solvent (t)) and the... 

The fundamental rate expression to be considered is the Smoluchowski relation k = 4n iVDAB AB (Equation (2.1)). The derived expression ART/r] (Equation (2.3a)), is a useful approximation, but deviations from it are observed, because the Stokes-Einstein equation which is involved is derived by hydrodynamic theory for spherical particles moving in a continuous fluid, and does not accurately represent the measured values of translational diffusion coefficients in real systems. Although the proportionality Da 1 /rj is indeed a reasonable approximation for many solutes in common solvents, the numeral coefficient 1 /4 is subject to uncertainty. In the first place, this theoretical value derives from the assumption that in translational motion there is no friction between a solute molecule and the first layer of solvent molecules surrounding it, i.e., that slip conditions hold. If, however, one assumes instead that there is no slipping ( stick conditions), so that momentum is... 

---