Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Diffusion parameters

The derivation of the flux relations given here is a simplified treatment which yields the correct algebraic form but does not provide estimates of the various diffusion parameters. A more complete discussion is given by Mason et al. [21]. [Pg.19]

This solution describes a plume with a Gaussian distribution of poUutant concentrations, such as that in Figure 5, where (y (x) and (y (x) are the standard deviations of the mean concentration in thejy and directions. The standard deviations are the directional diffusion parameters, and are assumed to be related simply to the turbulent diffusivities, and K. In practice, Ct (A) and (y (x) are functions of x, U, and atmospheric stability (2,31—33). [Pg.380]

The parameters about which the least is known are the diffusion parameters and Og, which govern diffusion transport of pollutants within a plume. These parameters are not monitored by meteorological stations and must always be approximated through indirect methods. Figure 4 illustrates the role each of these parameters has on the transport of airborne pollutants. [Pg.290]

Make an accurate estimate of the effects produced by diffusion parameters and arrange the process to proceed in a kinetic or a diffusion region. The reactor efficiency is determined on the basis of the chosen model. [Pg.1035]

Fig. 8.3-1 iMteral diffusion parameter vs distance from the source. This does not consider meander and building effects... [Pg.322]

Lateral diffusion parameter vs distance from the source. ... [Pg.533]

In permeation measurements the first signs of hydrogen diffusing through 1 mm steel membranes can be observed in a few minutes. The practical measurement of diffusion parameters tends to be rather unreproducibie. [Pg.1233]

Sykova E, Vargova L (2008) Extrasynaptic transmission and the diffusion parameters of the extracellular space. Neurochem Int 52 5-13... [Pg.376]

Whether Knudsen or bulk diffusion dominates the mass transport process depends on the relative magnitudes of the two terms in the denominator of equation 12.2.6. The ratio of the two diffusivity parameters is obviously important in establishing these magnitudes. In this regard, it is worth noting that DK is proportional to the pore diameter and independent of pressure whereas DAB is independent of pore size and inversely proportional to the pressure. Consequently, the higher the pressure and the larger the pore, the more likely it is that ordinary bulk diffusion will dominate. [Pg.434]

Additives promote filling by diffusing to the metal surface, where they adsorb and influence the kinetics of ion-discharge and crystal-growth. The diffusion parameter can be written for an additive by replacing the current density with an interfacial flux Na-... [Pg.182]

In order to estimate the region of this approximation applicability, it is necessary to examine macrokinetics of a polymeranalogous reaction with explicit allowance for the diffusion of a reagent Z into a globule. In this case, the profile of its constituent monomeric units will be fuzzy rather than stepwise (see Fig. 1). This brings up two questions. The first one is how this profile depends on kinetic and diffusion parameters of a reaction system. The second question is concerned with the effect of the profile shape on the statistical characteristics of the chemical structure of the products of a polymeranalogous reaction. A rigorous theory has been developed [22,23] which enables us to answer these questions. The main concepts of this theory are outlined in the subsequent Sections. [Pg.151]

If R is known, it is possible to fit the parameters k, ktCC0, A, At, fcp and fct using kinetic data from a single experiment. Thus, if the reaction diffusion parameter is known from the unsteady state after-effect experiments, the kinetic constant evolution can be determined as a function of free volume, and thus conversion. More details about this method will be published elsewhere (18). [Pg.55]

Figure 12 Relationship between the diffusion parameter, to.3 and p-xylene selectivity in toluene disproportionation. Temperature 550°C. Pressure 41 bar. Conversion 20%. tQ 3 time to reach 30% of amount sorbed at infinite time. Figure 12 Relationship between the diffusion parameter, to.3 and p-xylene selectivity in toluene disproportionation. Temperature 550°C. Pressure 41 bar. Conversion 20%. tQ 3 time to reach 30% of amount sorbed at infinite time.
For the dependence of the translational diffusion parameter we assumed a model of an unfolded polymer in a good solvent (upper limit) where Rg MW3 5. It should be noted that the figure should only be read qualitatively, as the results for the NOE-based parameters will be influenced to a large degree by spin diffusion. [Pg.338]

When the pollutant concentration difference between the source and collection reservoir becomes smaller (i. e., when the concentration of pollutants in the collection reservoir approaches that of the source reservoir), the flux rate of pollutants decreases, and a near steady state flux (Js) is obtained (Fig. 3c). At this time, the diffusion parameter (D) can be calculated using Fick s model as follows ... [Pg.201]

The diffusion parameter calculated by the root time method is an average parameter, and is generally considered to be operative over the range of time from initial diffusion flux to near steady state flux conditions. The method is applicable for the situation where adsorption and desorption occur, and for various pH values of the influent. The closer (DE) is to (DB) in Fig. 5 d, the greater is the accuracy of the D coefficient. It is important to note that in the case of low pH values of the influent, desorption of cations from a clay soil could produce conditions where C2 > C1. Accordingly, the experimental values for relative change in concentration would then become negative. [Pg.205]

In leaching field-aged residues of Atrazine and Metolachlor from a soil column, a model with a single diffusion parameter underestimated desorption at early times and overestimated desorption at late times. [Pg.215]

However, we must keep in mind the limitations of this approach, especially the transfer of consistent sets of dispersion parameters to the propagation of air pollution in the vicinity of a source. The Gaussian plume formula should be used only for those downwind distances for which the empirical diffusion coefficients have been determined by standard diffusion experiments. Because we are interested in emissions near ground level and immissions nearby the source, we use those diffusion parameters which are based on the classification of Klug /12/ and Turner /13/. The parameters are expressible as power functions,... [Pg.117]

From equation (3.13) we can deduct a rough approximation of the location where maximum ground-level concentration occurs. It is argued that the turbulent diffusion acts more and more on the emitted substances, when the distance from the point source increases therefore the downwind distance dependency of the diffusion coefficients is done afterwards. If we drop this dependency, equation (3.13) leads to xmax=34,4 m for AK=I (curve a) and xmax=87,7 m for AK=V (curve b), what is demonstrated in fig n The interpolated ranges of measured values are lined in. Curve a overestimates the nondimensional concentration maximum, but its location seems to be correct. In the case of curve b the situation is inverted. Curve c is calculated with the data of AK=II. The decay of the nondimensional concentration is predicted well behind the maximum. Curve d is produced with F—12,1, f=0,069, G=0,04 and g=l,088. The ascent of concentration is acceptable, but that is all, because there is no explanation of plausibility how to alter the diffusivity parameters. Therefore it must be our aim to find a suitable correction in connection with the meteorological input data. [Pg.122]

Here, m = is the electrode kinetic parameter typical for surface electrode processes (see Sect. 2.5.1) and 7= rg is dimensionless diffusion parameter. The latter parameter represents the inflnence of the mass transfer of electroactive species. [Pg.101]


See other pages where Diffusion parameters is mentioned: [Pg.503]    [Pg.503]    [Pg.105]    [Pg.184]    [Pg.59]    [Pg.565]    [Pg.575]    [Pg.233]    [Pg.310]    [Pg.99]    [Pg.55]    [Pg.180]    [Pg.303]    [Pg.592]    [Pg.201]    [Pg.202]    [Pg.122]    [Pg.123]    [Pg.125]    [Pg.125]    [Pg.562]    [Pg.565]   
See also in sourсe #XX -- [ Pg.125 ]

See also in sourсe #XX -- [ Pg.88 ]

See also in sourсe #XX -- [ Pg.125 ]

See also in sourсe #XX -- [ Pg.240 ]




SEARCH



Apparent diffusion parameter

Atmospheric diffusion equation parameters

Correlations Between Oxygen Diffusion Parameters

Diffusant parameters

Diffusant solvent interaction parameters

Diffusion Jump parameters

Diffusion Parameters of the System

Diffusion fitting parameters

Diffusion parameters, intracrystalline

Diffusion pollutant physical parameters

Diffusion solubility parameter

Diffusion-parameter image

Diffusivity evaluation parameters

Diffusivity parameters

Effect of intraparticle diffusion on experimental parameters

Effects of intraparticle diffusion on the experimental parameters

Kinetic Parameters Diffusion Controlled Conditions

Kinetic parameters diffusion coefficient, double-layer

Optimising diffusion parameters

Parameters for diffusion

Parameters in the Atmospheric Diffusion Equation

Reaction parameters pore diffusion

Scaled 2-Propanol Parameters Diffusion Controlled

Scavenging Kinetics and Diffusion Parameters

Surface diffusion parameters, table

Turing Instabilities in Reaction-Diffusion Systems with Temporally or Spatially Varying Parameters

© 2024 chempedia.info