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EM 1110-1-4001 <br /> 3 Jun 02 <br /> V, _ (1—fm)$,(1—S,)V <br /> V. f m�.(1—S m)V <br /> H(1—S,) <br /> —b+ bz —4RmR,[r(O+Da)+Oct] <br /> 2Rn,R, <br /> —b— bz -4RmR,[F(O+(Da)+Oa] <br /> r2 = <br /> 2RmR, <br /> b = R,n((x+r)+R,(O+(D(x) <br /> Equations (F-20)and (F-21)are simple to use for matching contaminant extraction concentrations for a <br /> given extraction history Early data may not fit well because the initial distribution of contaminants at <br /> field sites is generally very different than the uniform,average concentration assumed by the theoretical <br /> formulation However, after the initial sweep of the mobile soils,the concentration history is generally <br /> . well-behaved and approaches an average concentration because of mechanical dispersion(i e , advective <br /> mixing) The equations provide an accurate engineering model for predicting site behavior in the later <br /> mass-transfer-limited phase if complicating factors do not exist(c g,NAPL) <br /> Because of the volume averaging over each soil region,very few parameters appear in the equations <br /> relative to the input required for detailed numerical modeling of an SVE system The input and/or fitting <br /> variables are, <br /> Soil Physical Properties 0,,,, 0„ Sm, S. <br /> Site-Specific Contaminant Properties H, Rm, R„y,,,,y, <br /> Initial Vapor Concentrations C,,,,o, CIO <br /> Representative Contaminated Volume V(or V,,,) <br /> Fraction of Soil Characterized as Mobile f,,, <br /> Field-Scale Mass Transfer Coefficient a <br /> This list of variables is very similar to the parameters used in two-region modeling of solute transport in <br /> saturated systems (Griffioen et al , 1998) Average soil physical properties in each region such as <br /> porosity and water saturation are usually available from independent measurements With these soil <br /> physical properties and Henry's constant for the contaminant, the retardation coefficient in each region <br /> can be estimated as described in Chapter 2 If degradation of the contaminant is considered significant, <br /> the degradation coefficient could be estimated from the appearance of daughter compounds in the <br /> extracted vapors, however, such an analysis is beyond the scope of this document By definition the <br /> concentration in extracted vapors is equal to the concentration in the mobile soils Therefore, the <br /> • measured extraction concentration at a specified start time to is the initial concentration in the mobile <br /> F-13 <br />