Page 441 - Standard Handbook Petroleum Natural Gas Engineering VOLUME2
P. 441

Properties of  Hydrocarbon Mixtures   403


                                                        ( ) initial assumption of
                                                          dependent variable
                                 or T, (PI


                               Assume  IlquM
                             phase composition







                                 and  Ex,  I
                          I     Calculate XI














                                                                                 ,
                                                                               xI
                              Adjust dependent
                              Adjust dependent                           Exit wlth xI ,
                                                                         Exit
                                                                           wlth
                                                                               T
                                  varlable                               P.  and T
                                                                         P.
                                                                           and
                                  varlable
                                   f
                                Adjust llquld
                             phase composltbn
                           Figure 6-25.  Block diagram for  dew point calculations.

                 assume that the mole fraction of  the highest boiling component in the system
                 is equal to unity. The remaining component mole fractions are set to lo4.  Liquid
                 phase  compositions are  adjusted by  linear  combinations of the  assumed and
                 calculated value during each iteration. The convergence algorithms for (T) and
                 (P) dependent calculations are given in Figures 6-26 and 6-27.
                   The purpose of flash calculations is to predict the composition and amount
                 of  the coexisting vapor and liquid phases at a fixed temperature and pressure.
                   According to Equations 6-15 and 6-16


                                                                              (6-23a)
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