Page 33 - Applied Process Design For Chemical And Petrochemical Plants Volume II
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22                        Applied Process Design for Chemical and Petrochemical Plants

          energy in the form of reboiler heat and condenser coolant   Because the feed tray is essentially non-effective it is sug-
          to maintain a total reflux condition with no feed, no over-   gested  that  an  additional theoretical  tray  be  added  to
          head and no bottoms products or withdrawals.          allow for  this.  This  can  be  conveniently solved by  the
            The conditions of  total liquid reflux in a column also   nornographs [21] of Figures 8-16 and 17. If the minimum
          represent the minimum number of  plates required for a   number of trays in the rectifying section are needed, they
          given separation. Under such conditions the column has   can be calculated by the Fenske equation substituting the
          zero  production  of  product,  and  infinite  heat  require-   limits of xF1 for XBh and XBl, and the stripping section can
          ments, and L,/V,  = 1.0 as shown in Figure 8-15. This is the   be calculated by difference.
          limiting condition for the number of trays and is a conve   From Fenske’s equation, the minimum number of equi-
          nient measure of the complexity or difficulty of separation.   librium stages at total reflux is related to their bottoms (B)
                                                                 and  distillate or  overhead  (D)  compositions using  the
          Fenske Equation: Overall Minimum Total Trays with      average relative volatility, see Equation 8-29.
          Total Condenser                                          To  solve for the component split [loo] in distillate or
                                                                 bottoms:
                                                                 (”)      = (“)          Sm

                                                        (8 - 29)                  (aLK-m                     (8-32)
               \--min  , -I                                        x~   D    X~~   D
                             log Q avg.
          This includes the bottoms reboiler as a tray in the system.   where   S,   = total number of calculated theoretical trays
          See tabulation below.                                                  at total reflux, from Equation &30
            Nmin includes  only  the  required  trays in  the  column   Xlk = XLK = liquid mol fraction of light key
          itself, and not the reboiler.                                xa  = xm = liquid mol fraction of heavy key
                                                                 lk - hk = LK - HK= average relative volatility of column (top to
                                                                                 bottom)
           aavg = (alk/hk)
          D refers to overhead distillate
           B refers to bottoms                                     Because a  column cannot operate at total reflux and
                                                                 produce net product from the column, a reflux ratio of
                                                                 about 1.1 to 1.5 times the minimum reflux will usually give
                                                        (8 - 30)   practical results. Be  aware that as the reflux ratio comes
                                                                 down approaching the minimum, the number of theoret-
             This applies to any pair of components. My experience   ical and then corresponding actua2 trays must increase.
           suggests adding +1 theoretical tray for the reboiler, thus
           making the total theoretical trays perhaps a bit conservative.   Relative Volatility
           But, they must be included when converting to actual trays
           using the selected or calculated tray efficiency:       Relative volatility is the volatility separation factor in a
                                                                 vapor-liquid system, i.e., the volatility of  one component
           S,+  1 =N,h                                  (8 - 31)   divided by the volatility of the other. It is the tendency for
                                                                 one component in a liquid mixture to separate upon dis-
             For a condition of  overall total trays allowance is to be   tillation from the other. The term is expressed as the ratio
           made for feed tray effect, then add one more theoretical tray to   of vapor pressure of the more volatile to the less volatile in
           the  total.  As  demonstrated  in  the  tabulation  to  follow,
           allowance should be made for the reboiler and condenser.   the liquid mixture, and therefore a1,2 is always equal to 1.0
                                                                 or greater. a1,2 means the relationship of the more volatile
                        Total                Partial             or low boiler to the less volatile or high boiler at a constant
                     Condenser  Reboiler  Condenser  Total       specific temperature. The greater the value of a, the easier
                                                                 will be the desired separation. Relative volatility can be cal-
               Nmin      +I          0         +O      Nm+l      culated between any two components in a mixture, binary
                                    +1         +O      Nm+2      or multicomponent. One of the substances is chosen as the
               Nmin      +O         +1         +1      N,+2      reference to which the other component is compared.
                                                                   Definition  of  Relative Volatility:  Relative Volatility  of
             Note  that the  approach recommended here is  not in
           agreement with Van Winkle [74], because he assumes the   Component 1 with respect to component 2.
           reboiler and partial condenser are included in the overall   Q1,2 = (p1 XZ)/(PZ  Xl) = (y1 X2)/(Y2  x1)   (8 - 33)
           calculation for NmiW
             Various average values of  a for use in these calculations   where   1,2, etc. are component identification
           are suggested in the following section on “Relative Volatility.”   p = partial pressure of a component
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