Diffusion coefficient Einstein equation

The proportionality factor D is called the diffusion coefficient. This equation was first developed by Einstein and is therefore called the Einstein equation. 

This too is a fundamental relation and will be used later (Section 3.4.1) to derive an expression for the rotational diffusion coefficient. The equation was originally due to Einstein in 1906 [3,d], and was found by Perrin in 1909 to fit the results of microscopic measurements on the random motion of spherical particles of resin about 10 cm in diameter suspended in water [3,a,c,d]. It was applied to molecules in solution by Debye [5], The evidence for its applicability to solutions rests on the results of experimental work on rotational diffusion coefficients (Section 3.4.3.2 below). 

There is also a traffic between the surface region and the adjacent layers of liquid. For most liquids, diffusion coefficients at room temperature are on the order of 10 cm /sec, and the diffusion coefficient is related to the time r for a net displacement jc by an equation due to Einstein ... 

The dififiision time gives the same general picture. The bulk self-diffusion coefficient of copper is 10"" cm /sec at 725°C [12] the Einstein equation... 

Reference 115 gives the diffusion coefficient of DTAB (dodecyltrimethylammo-nium bromide) as 1.07 x 10" cm /sec. Estimate the micelle radius (use the Einstein equation relating diffusion coefficient and friction factor and the Stokes equation for the friction factor of a sphere) and compare with the value given in the reference. Estimate also the number of monomer units in the micelle. Assume 25°C. 

The Stokes-Einstein equation has already been presented. It was noted that its vahdity was restricted to large solutes, such as spherical macromolecules and particles in a continuum solvent. The equation has also been found to predict accurately the diffusion coefficient of spherical latex particles and globular proteins. Corrections to Stokes-Einstein for molecules approximating spheroids is given by Tanford. Since solute-solute interactions are ignored in this theory, it applies in the dilute range only. 

A number of metals, such as copper, cobalt and h on, form a number of oxide layers during oxidation in air. Providing that interfacial thermodynamic equilibrium exists at the boundaries between the various oxide layers, the relative thicknesses of the oxides will depend on die relative diffusion coefficients of the mobile species as well as the oxygen potential gradients across each oxide layer. The flux of ions and electrons is given by Einstein s mobility equation for each diffusing species in each layer... 

In connection with the earlier consideration of diffusion in liquids using tire Stokes-Einstein equation, it can be concluded that the temperature dependence of the diffusion coefficient on the temperature should be T(exp(—Qvis/RT)) according to this equation, if the activation energy for viscous flow is included. 

Very commonly Eq. (4-5) is combined with Eq. (4-6), the Stokes-Einstein equation relating the diffusion coefficient to the viscosity -q. 

Equations (4-5) and (4-7) are alternative expressions for the estimation of the diffusion-limited rate constant, but these equations are not equivalent, because Eq. (4-7) includes the assumption that the Stokes-Einstein equation is applicable. Olea and Thomas" measured the kinetics of quenching of pyrene fluorescence in several solvents and also measured diffusion coefficients. The diffusion coefficients did not vary as t) [as predicted by Eq. (4-6)], but roughly as Tf. Thus Eq. (4-7) is not valid, in this system, whereas Eq. (4-5), used with the experimentally measured diffusion coefficients, gave reasonable agreement with measured rate constants. 

Following the general trend of looldng for a molecular description of the properties of matter, self-diffusion in liquids has become a key quantity for interpretation and modeling of transport in liquids [5]. Self-diffusion coefficients can be combined with other data, such as viscosities, electrical conductivities, densities, etc., in order to evaluate and improve solvodynamic models such as the Stokes-Einstein type [6-9]. From temperature-dependent measurements, activation energies can be calculated by the Arrhenius or the Vogel-Tamman-Fulcher equation (VTF), in order to evaluate models that treat the diffusion process similarly to diffusion in the solid state with jump or hole models [1, 2, 7]. 

T0 is a reference temperature which can be identified with T, and although the constant B is not related to any simple activation process, it has dimensions of energy. This form of the equation is derived by assuming an electrolyte to be fully dissociated in the solvent, so it can be related to the diffusion coefficient through the Stokes-Einstein equation. It suggests that thermal motion above T0 contributes to relaxation and transport processes and that... 

The same equation applies to other solvents. It is often easier to incorporate an expression for the diffusion coefficient than a numerical value, which may not be available. According to the Stokes-Einstein equation,6 diffusion coefficients can be estimated from the solvent viscosity by... 

Using the Stokes-Einstein equation of diffusion coefficient ... 

According to Stokes-Einstein equation, the diffusion coefficient is inversely proportional to the solution viscosity which increases with temperature. Hence, a lower diffusion coefficient corresponds to a lower size molecule. 

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. 

Self-diffusion coefficients are dynamic properties that can be easily obtained by molecular dynamics simulation. The properties are obtained from mean-square displacement by the Einstein equation ... 

This equation, called the Kubo equation, is equivalent to the Einstein equation. However, it is easier to estimate self-diffusion coefficients from the slope of the mean-square displacements. 

The ratio of the diffusion coefficient and the electrolytic mobility is given by the Nernst-Einstein equation (valid for dilute solutions)... 

The fundamental theory of electron escape, owing to Onsager (1938), follows Smoluchowski s (1906) equation of Brownian motion in the presence of a field F. Using the Nemst-Einstein relation p = eD/kRT between the mobility and the diffusion coefficient, Onsager writes the diffusion equation as... 

Substituting the diffusion coefficient D into its expression in the Stokes-Einstein equation, we... 

The Smoluchowski theory for diffusion-controlled reactions, when combined with the Stokes-Einstein equation for the diffusion coefficient, predicts that the rate constant for a diffusion-controlled reaction will be inversely proportional to the solution viscosity.16 Therefore, the literature values for the bimolecular electron transfer reactions (measured for a solution viscosity of r ) were adjusted by multiplying by the factor r 1/r 2 to obtain the adjusted value of the kinetic constant... 

Einstein to describe Brownian motion.5 The model can be used to derive the diffusion equations and to relate the diffusion coefficient to atomic movements. 

The gas A must transfer from the gas phase to the liquid phase. Equation (1) describes the specific (per m2) molar flow (JA) of A through the gas-liquid interface. Considering only limitations in the liquid phase, this molar flow notably depends on the liquid molecular diffusion coefficient DAL (m2 s ). Based on the liquid state theories, DA L can be calculated using the Stokes-Einstein expression, and many correlations have been developed in order to estimate the liquid diffusion coefficients. The best-known example is the Wilke and Chang (W-C) relationship, but many others have been established and compared (Table 45.4) [28-33]. 

Solutes diffuse in proportion to their diffusion coefficient, which is inversely proportional to their hydrodynamic radii, ah, (Stokes-Einstein equation) ... 

Photon correlation spectroscopy (PCS) has been used extensively for the sizing of submicrometer particles and is now the accepted technique in most sizing determinations. PCS is based on the Brownian motion that colloidal particles undergo, where they are in constant, random motion due to the bombardment of solvent (or gas) molecules surrounding them. The time dependence of the fluctuations in intensity of scattered light from particles undergoing Brownian motion is a function of the size of the particles. Smaller particles move more rapidly than larger ones and the amount of movement is defined by the diffusion coefficient or translational diffusion coefficient, which can be related to size by the Stokes-Einstein equation, as described by... 

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