Page 173 - Materials Chemistry, Second Edition
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156       Practical Design Calculations for Groundwater and Soil Remediation



                   Thus, partial pressure of toluene = 0.0155 atm = 15,500 ppmV.

                                         x ) (10 mm-Hg)(0.464)=
                            P xylenes =  P (  vap  )( A
                                  =  4.64 mm-Hg = 0.0061 atm


                   Thus, partial pressure of xylenes = 0.0061 atm = 6,100 ppmV.
                   The volumetric (or molar) composition of the extracted vapor
                       = (15,500)/[15,500 + 6,100] = 71.8% (toluene)

               (d)  The mass concentration can be found by using Equation (2.1) as:

                        1 ppmV toluene = (92.1)/24.05 = 3.83 mg/m 3
                        So, 15,500 ppmV  = (15,500)(3.83) = 59,400 mg/m  = 59.4 mg/L
                                                                3
                         1 ppmV xylenes = (106.2)/24.05 = 4.42 mg/m 3
                        So, 15,500 ppmV  = (6,100)(4.42) = 27,000 mg/m  = 27.0 mg/L
                                                               3
                   The weight composition of the extracted vapor
                       = (59.4)/[59.4 +27.0] = 68.8% (toluene)

              Discussion:
                1.  The toluene concentration in the extracted vapor is 68.8% by
                   weight and 71.8% by volume. Both are higher than its concentra-
                   tion in the liquid solvent, 50% by weight. The higher percentage
                   of toluene in the vapor is mainly due to its higher vapor pressure.
                2.  This saturated vapor concentration would be higher than the
                   actual concentration of the extracted vapor due to the fact that
                   (1) not all the air flows through the impacted zone and (2) limita-
                   tions on mass transfer exist.

             As  mentioned,  the  presence  or  absence  of  a  free-product  phase  greatly
           affects the extracted vapor concentration. Equation (2.40) in Chapter 2 can be
           used as a starting point for discussion.

                                    [( w + ρ  K p + φ  H 
                                     φ
                                                 ( )]
                                       )( )
                               X =         b      a    × C
                                             t ρ      
                                      ( w )  +  ( b ) K p  + ()       (2.40)
                                          ρ
                                     φ
                                                 a φ
                                   
                                                     ×
                                 =    H  H          G
                                           t ρ     
                                                   
             Let soil saturation concentration (X ) correspond to the COC concentra-
                                             sat
           tion in soil at which the adsorptive limits of soil grains, the solubility of soil
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