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6.8. LIQUID-GAS  FLOW  IN  PIPELINES
            particular flow pattern  is subjective and  all the pertinent  variables   64, 193-200  (1942)] is popular:
             apparently  have  not  yet  been  correlated,  boundaries  between
                                                                                 +
             regions are fuzzy, as in (d).                          l/kwo-phase = x/k - x)/@L.              (6.97)
                I is  to  be: expected  that  the  kind  of  phase  distribution will
             affect such phenomena as heat transfer and friction in pipelines. For   The specific volumes are weight fraction additive,
             the most part,  however, these operations have not been correlated
             yet with flow patterns, and the majority of  calculations of two-phase   Vtwo-phase = XVG + (1 - X)VL   (6.98)
            flow  are  made  without  reference  to  them.  A  partial  exception is
             annular flow which tends to exist at high gas flow rates and has been   so that
             studied in some detail from the point of  view of  friction and heat
            transfer.                                              l/Ptwo-phase = x/P~ +
                The usual procedure for  evaluating two-phase pressure drop is      - x)/pL,                (6.99)
            to combine pressure drops of individual phases in some way. To this
             end, multiplieris $i are defined by                where x  is  the  weight fraction of  the  gas.  Pressure  drops by  this
                                                                method tend to be underestimated, but are more nearly accurate at
                                                                higher pressures and higher flow rates.
                                                         (6.94)    With  the  Blasius equation  (6.96), the  friction factor  and  the
                                                                pressure gradient become, with this model,
             In the following table, subscript L refers to the liquid phase,  G to
             the gas phase,  and LO  to the total flow but with properties of  the   .  f =  0 32   x  1 -x  0.25

             liquid phase; x  is the weight fraction of  the vapor phase.   (DG)0.25 (E +   ’              (6.100)
             Subscript     e          AP/L           +2                                                    (6,101)
                G     DGx~PG      fGG2x2/2gcDpG   (APIL)I(APIL),
                L     DG(1 - X)i’p,   CG2(1 - X)~/~S,DPL (AP/L)/(Af/L),
                LO    DGIy,       iFLo~2/2&DP,L   (APIL)I(APIL),,   A  particularly simple expression is  obtained  for  the  multiplier in
                                                                terms of  the Blasius equation:
             In  view  of  the  many  other  uncertainties  of  two  phase  flow
             correlations, the friction factors are adequately represented by
                                                                                                           46.102)
                           e < 2000, Poiseuille equation,   (6.95)
                   .0.32/Re0-”,   We > 2000, Blasius equation.   (6.96)
                                                                Some values of +io from this equation for steam are
                OGENEOUS MODEL                                             x    P = 0.689 bar   P = 10.3 bar
            The simplest ?way to compute line friction in two-phase flow is  to   0.01   3.40   1.10
            adopt some kiinds of  mean properties of the mixtures and to employ   0.10   12.18   1.95
            the  single  phlase  friction  equation.  The  main  problem  is  the   0.50   80.2   4.36
            assignment of  a two-phase viscosity. Of  the  number of  definitions
            that  have been  proposed, thzt  of  McAdams et  al.  [Trans. ASME   High values of multipliers are not uncommon.






               EXAMPLE 5.13                                        ’          -0.0369   +  5.52W4)  + 0.0272
               Isothermad Flow of  a Nonideal Gas                    =     [(V - 0.00169)2   V3
            The  case  of  Example  6.12 will  be  solved  with  a  van  der  Waals
            equation  of  steam.  From  the  CRC  Handbook  of  Chemistry  and   The  integration  is  performed  with  Simpson’s  rule  with  20
            Physics  (CRC Press, Boca Raton, FL, 1979),         intervals. Values of  V2 are assumed until  one is found that  makes
                                                                + = 0.  Then the pressure is found from the v dW equation:
               Q  = 5.464 atm(m3/kg mol)’  = 1703.7 Pa(m3/kg)’,
                b = 0.03049 m3/kg mol = 0.001692 m3/kg,            P-   2.276(105)  -- 1703.7
               RT = 831,4(493.2)/18.02 = 2.276(105) N m/kg.         ’ - (V, - 0.00169)   V;

            Equation  (6.93) becornies                             Two  trials  and,  a  linear  interpolation  are  shown. The  value
                                                                P2 = 18.44 bar compares with the ideal gas 17.13.
                                                                             4         +
                                                                            0.120    -0.0540
                  +  0.0187(410.07)2(305) -                                 0.117    +0.0054
                                  - 0,
                       2(0.0777)                                            0.1 173     0      18.44 bar
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