Page 201 - Characterization and Properties of Petroleum Fractions - M.R. Riazi
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                        AT029-Manual-v7.cls
                                                        21:30
                                           June 22, 2007
  AT029-04
            AT029-Manual
            4.5.4.6 Prediction of Property Distributions
                                                                  This equation can be used for narrow boiling range fractions
            Using Bulk Properties     T1: IML  4. CHARACTERIZATION OF RESERVOIR FLUIDS AND CRUDE OILS 181
                                                                  with M between 70 and 350. In this molecular weight range
            As discussed above, Eq. (4.56) can be used as a two-parameter  this equation is slightly more accurate than Eq. (2.117). Once
            relation with fixed values of B for each property (B M = 1,  distribution of I is determined from these equations, if the
                                                                                                          ∗
            B T = 1.5, and B SG = B I = 3). In this case Eq. (4.56) is referred  initial values of M o and SG o are correct then I av  calculated
            as a two-parameter distribution model. In such cases only  from the distribution coefficients and Eq. (4.72) should be
            parameters P o and A must be known for each property to ex-  close to the experimental value obtained from n 7+ . For cases
            press its distribution in a hydrocarbon plus fraction. The two-  that experimental data on n 7+ is not available it can be esti-
            parameter model is sufficient to express property distribu-  mated from M 7+ and SG 7+ using Eq. (4.95) or (2.117). Equa-
            tion of light oils and gas condensate systems. For very heavy  tion (2.117) estimates values of n 7+ for 48 systems [23] with
            oils two-parameter model can be used as the initial guess to  an average error of 0.4%. Steps to predict M, T b , SG, and I
            begin calculations for determination of the three parameters  (or n) distributions can be summarized as follows [24]:
            in Eq. (4.56). In some cases detailed composition of a C 7+
            fraction in a reservoir fluid is not available and the only infor-
            mation known are M 7+ and SG 7+ , while in some other cases
            in addition to these properties, a third parameter such as re-  1. Read values of M 7+ ,SG 7+ , and I 7+ for a given C 7+ sample.
            fractive index of the mixture or the true boiling point (TBP)  If I 7+ is not available Eq. (2.117) may be used to estimate
            curve are also known. For these two scenarios we show how  this parameter.
            parameters P o and A can be determined for M, T b , SG, and  2. Guess an initial value for M o (assume M o = 72) and cal-
                                                                            ∗
            I 20 .                                                   culate M from Eq. (4.93).
                                                                            av
              Method A: M 7+ , SG 7+ , and n 7+ are known—Three bulk  3. Calculate A M from Eq. (4.72) or Eq. (4.74) when B = 1.
            properties are the minimum data that are required to predict  4. Choose 20 (or more) arbitrary cuts for the mixture with
            complete distribution of various properties [24, 43]. In ad-  equal mole fractions (x mi ) of 0.05 (or less). Then calculate
                                                                                                                  --`,```,`,``````,`,````,```,,-`-`,,`,,`,`,,`---
            dition to M 7+ and SG 7+ , refractive index, n 7+ , can be easily  M i for each cut from Eq. (4.56).
            measured and they are known for some 48 C 7+ fractions [24].  5. Convert mole fractions (x mi ) to weight fractions (x wi )
            As shown by Eqs. (4.74)–(4.76), if P is known, parameter A  through Eq. (1.15) using M i from step 4.
                                         ∗
                                         av
            can be determined for each property. For example, if M o is  6. Guess an initial value for S o (assume S o = 0.59 as a starting
            known, M can be determined from definition of M as:       value).
                                                       ∗
                    ∗
                    av
                                                                   7. Calculate 1/J from Eq. (4.80) using SG o and SG 7+ . Then
                                                                     calculate A SG from Eq. (4.79) using Newton’s method.
            (4.93)            M =
                                    M av − M ◦
                                ∗
                                av                                 8. Using Eq. (4.56) with A SG and S o from steps 6 and 7 and
                                       M ◦
                                                                     B = 3, SG distribution in terms of x cw is determined and
            where M av is the mixture molecular weight of the C 7+ fraction,  for each cut SG i is calculated.
            which is known from experimental measurement. Similarly,  9. Convert x wi to x vi using Eq. (1.16) and SG i values from
            SG ∗ av  and I av  can be determined from S 7+ and n 7+ (or I 7+ ).  step 8.
                     ∗
            Parameters A M , A SG , and A I are then calculated from Eqs.  10. For each cut calculate T bi from M i and SG i through
            (4.72) and (4.81). For fixed values of B, Eqs. (4.74)–(4.76)  Eq. (2.56) or (2.57).
            and (4.79) and (4.80) may be used. One should realize that  11. For each cut calculate I i from M i and SG i through
            Eq. (4.74) was developed based on cumulative mole fraction,  Eq. (2.95).
            while Eqs. (4.79) and (4.80) are based on cumulative weight  12. From distribution of I versus x cv find parameters I o , A I
            fraction. Once distribution of M and SG are known, distribu-  and B I through Eqs. (4.56)–(4.57). Then calculate I av from
            tion of T b can be determined using equations given in Chapter  Eq. (4.72) and (4.81).
            2, such as Eqs. (2.56) or (2.57), for estimation of T b from M  13. Calculate ε 1 =|(I av,calc. − I 7+ )/I 7+ |.
            and SG. Based on data for 48 C 7+ samples, the following re-  14. If ε 1 < 0.005, continue from step 15, otherwise go back
            lation has been developed to estimate I o from M o and SG o  to step 6 with SG o,new = SG o,old + 0.005 and repeat steps
            [24]:                                                    7–13.
                                                                  15. Calculate I o from Eq. (4.94).
                                                                  16. Calculate ε 2 =|(I ◦,step15 − I ◦,step12 )/I ◦,step15 |.
                   I ◦ = 0.7454 exp (−0.01151M ◦ − 2.37842SG ◦
            (4.94)      + 0.01225M ◦ SG ◦ )M 0.2949 SG 1.53147    17. Go back to step 2 with a new guess for M o (higher than the
                                        ◦     ◦
                                                                     previous guess). Repeat steps 2–16 until either ε 2 < 0.005
            This equation can reproduce values of I o with an average  or ε 2 becomes minimum.
            deviation of 0.3%. Furthermore, methods of estimation of  18. For heavy oils large value of ε 2 may be obtained, because
            parameter I from either T b and SG or M and SG are given in  value of B M is greater than 1. For such cases values of
            Section 2.6.2 by Eqs. (2.115)–(2.117). Equation (2.117) may  B M = 1.5, 2.0, and 2.5 should be tried successively and
            be applied to the molecular weight range of 70–700. However,  calculations from step 2 to 17 should be repeated to min-
            a more accurate relation for prediction of parameter I from  imize ε 2 .
            M and SG is Eq. (2.40) with coefficients from Table 2.5 as  19. Using data for T b versus x cw , determine parameters T o , A T ,
            follows:                                                 and B T from Eqs. (4.56) and (4.57).
                                                                  20. Print M o , A M , B M ,SG o , A SG , T o , A T , B T , I o , A I , and B I .
                  I = 0.12399 exp(3.4622 × 10 −4 M + 0.90389SG    21. Generate distributions for M, T b , SG, and n 20 from
            (4.95)    −6.0955 × 10 −4 MSG)M 0.02264 SG 0.22423       Eq. (4.56).









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