Page 111 - Separation process principles 2
P. 111

76  Chapter 3  Mass Transfer and Diffusion


                 Table 3.5  Parachors for Representative Compounds
                                     Parachor,                          Parachor,                         Parachor,
                                  ~m~-~~/~/s'/~-mol                  ~m~-~'/~/s'/~-mol                 ~m~-~'/~/s'/~-mol
                 Acetic acid           131.2        Chlorobenzene         244.5        Methyl amine          95.9
                 Acetone               161.5        Diphenyl              380.0        Methyl formate       138.6
                 Acetonitrile          122          Ethane                110.8        Naphthalene          312.5
                 Acetylene             88.6         Ethylene              99.5         n-Octane             350.3
                 Aniline              234.4         Ethyl butyrate        295.1        1-Pentene            218.2
                 Benzene              205.3         Ethyl ether           211.7        1-Pentyne            207.0
                 Benzonitrile         25 8          Ethyl mercaptan       162.9        Phenol               221.3
                 n-Butyric acid       209.1         Formic acid           93.7         n-Propanol           165.4
                 Carbon disulfide      143.6        Isobutyl benzene      365.4        Toluene              245.5
                 Cyclohexane          239.3         Methanol              88.8         Triethyl mine        297.8
                 Source: Meissner, Chem. Eng. Prog., 45, 149-153  (1949).

                                  Table 3.6  Structural Contributions for Estimating the Parachor












                                  Alkyl groups
                                    1-Methylethyl                    0 (not noted above)
                                    1-Methylpropyl                   N (not noted above)
                                    1 -Methylbutyl                   s
                                    2-Methylpropyl                   P
                                    1-Ethylpropyl                    F
                                    1,l-Dimethylethyl                C1
                                    1,l-Dimethylpropyl               Br
                                    1,2-Dimethylpropyl               I
                                    1,1,2-Trimethylpropyl            Ethylenic bonds:
                                  C6H5                                 Terminal
                                                                       2,3-position
                                  Special groups:                      3,4-position
                                    -coo-
                                    -COOH                            Triple bond
                                    -OH
                                    -NH2                             Ring closure:
                                    -0-                                Three-membered
                                    -NO2                               Four-membered
                                    -NO3  (nitrate)                    Five-membered
                                    -CO(NH2)                           Six-membered
                                  Source: Quale [a].





                Estimate the diffusivity of formic acid (A) in benzene (B) at 25°C   However, because formic acid is an organic acid, ??A  is doubled
                and infinite dilution, using the appropriate correlation of  Hayduk   to 187.4.
                and Minhas [7]. The experimental value is 2.28 x   cm2/s.
                                                                    From (3-42),
                SOLUTION                                                                  [298'~29(205.30~5/ 187.4°.42)]
                                                                                                0.60.92960.23
                                                                        (DAB)co = 1.55 x
                Equation (3-42) applies, with T = 298 K
                                                                              = 2.15 x 10-'  crn21s
                YA = 93.7 ~m~-~~/~/s~/~-mol
                                          9g = 205.3 ~m~-~~/~/s'/~-mol
                   =
                 IJ.~ 0.6 cP at 25°C      vg = 96 cm3/mol at 80°C   which is within 6% of the the experimental value.
   106   107   108   109   110   111   112   113   114   115   116