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Handbook of Solvents - George Wypych - ChemTech - Ventech!

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1574 Hanadi S. Rifai, Charles J. Newell, Todd H. Wiedemeier<br />

dispersion, the solute front travels at a rate that is faster than would be predicted based solely<br />

on the average linear velocity <strong>of</strong> the ground water. Figure 23.1.1 illustrates the effects <strong>of</strong> hydrodynamic<br />

dispersion on an advancing solute front. Mechanical dispersion is commonly<br />

represented by the relationship:<br />

Mechanical Dispersion = α xv x<br />

[23.1.3]<br />

where:<br />

vx average linear ground-water velocity [L/T]<br />

αx dispersivity [L]<br />

Dispersivity represents the spreading<br />

<strong>of</strong> a contaminant over a given length <strong>of</strong><br />

flow and is characteristic <strong>of</strong> the porous medium<br />

through which the contaminant migrates.<br />

It is commonly accepted that<br />

dispersivity is scale-dependent, and that at a<br />

given scale, dispersivity may vary over<br />

three orders <strong>of</strong> magnitude 3,4 as shown in<br />

Figure 23.1.3.<br />

Several approaches can be used to estimate<br />

longitudinal dispersivity, α x ,atthe<br />

field scale. One technique involves conducting<br />

a tracer test but this method is time<br />

consuming and costly. Another method<br />

commonly used in solute transport modeling<br />

is to start with a longitudinal<br />

dispersivity <strong>of</strong> 0.1 times the plume<br />

lengths. 5-7 This assumes that dispersivity<br />

varies linearly with scale. Xu and Eckstein 8<br />

proposed an alternative approach. They<br />

evaluated the same data presented by<br />

Gelhar et al. 4 Figure 23.1.3. Relationship between dispersivity and<br />

scale. [From T.H. Wiedemeier, H. S. Rifai, C. J. Newell<br />

and J.T. Wilson, Natural Attenuation <strong>of</strong> Fuels and<br />

Chlorinated <strong>Solvents</strong> in the Subsurface. Copyright ©<br />

1999 John Wiley & Sons, Inc. Reprinted by permission <strong>of</strong><br />

John Wiley & Sons, Inc.]<br />

and, by using a weighted<br />

least-squares method, developed the following relationship for estimating dispersivity:<br />

( L )<br />

αx =083 . log10<br />

p<br />

2. 414<br />

[23.1.4]<br />

where:<br />

αx longitudinal dispersivity [L]<br />

Lp plume length [L]<br />

Both relationships are shown on Figure 23.1.3.<br />

In addition to estimating longitudinal dispersivity, it may be necessary to estimate the<br />

transverse and vertical dispersivities (αT and αZ, respectively) for a given site. Commonly,<br />

αT is estimated as 0.1αx (based on data 4 ), or as 0.33αx. 9,10 Vertical dispersivity (αZ) may be<br />

estimated as 0.05αx, 9 or as 0.025 to 0.1αx. 10<br />

23.1.2.3 Sorption<br />

Many organic contaminants, including chlorinated solvents, are removed from solution by<br />

sorption onto the aquifer matrix. Sorption <strong>of</strong> dissolved contamination onto the aquifer ma-

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