Page 210 - Characterization and Properties of Petroleum Fractions - M.R. Riazi
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                                           June 22, 2007
            AT029-Manual
  AT029-04
                        AT029-Manual-v7.cls
         190 CHARACTERIZATION AND PROPERTIES OF PETROLEUM FRACTIONS
         properties of such mixtures. Application of this approach is
                                                                                 in Example 4.16.
         shown through estimation of sulfur content of crude oils. 21:30  TABLE 4.25—Pseudoization of the C 7+ for the Kuwaiti crude
                                                              Pseudocomponent  1       2      3       4      5
                                                              Weight fraction  0.097  0.162   0.281  0.197   0.264
                                                              Mole fraction    0.230  0.255   0.280  0.129   0.106
         4.8.1 General Approach                               Molecular weight  112.0  169.1  267.1  405.8  660.9
                                                              Specific gravity  0.753  0.810   0.864  0.904   0.943
         For a reservoir fluid accurate properties can be calculated
         through detailed compositional analysis of pure compounds
         from C 1 to C 5 and SCN groups from C 6 and heavier groups  by an adequate number of pseudocomponents with known
         up to at least C 50 . The remaining part can be grouped as C 50+ .  parameters.
         For very heavy oils, SCN group separation may be extended
         up to C 80 and the residue grouped as C 80+ . To estimate various  Example 4.16—Compositional data on a Kuwaiti crude oil is
         properties of these SCN groups at least two characterizing pa-  given as follows:
         rameters such as T b and SG or M and SG should be known.  Component
         This is shown in Table 4.24, where known data are indicated      C 2  C 3  iC 4  nC 4  iC 5  nC 5  C 6  C 7+
         by + sign. Methods outlined in Sections 4.5 and 4.6 can lead  Wt%  0.03  0.39  0.62  1.08  0.77  1.31  1.93  93.87
         to generate such information for a reservoir fluid. For SCN  The characteristics of the C 7+ fraction are M 7+ = 266.6 and
         groups of C 6 and heavier, methods in Chapter 2 can be used  SG 7+ = 0.891 [44]. Divide the C 7+ fraction into 5 pseudocom-
         to estimate various properties (T b , T c , P c ,...) using M and  ponents and present the crude in terms of mole and weight
         SG as available input parameters. For pure compounds up  fractions of representative constituents with known M, SG,
         to C 5 , all basic properties are given in Tables 2.1 and 2.2 and  and T b . Estimate M and SG for the whole crude.
         no estimation method is required. For more accurate pre-
         diction of properties of a reservoir fluid, each SCN groups
         from C 6 up to C 50+ may be divided into further three pseudo-  Solution—For the C 6 group from Table 4.6 we have M 6 = 82,
         components as paraffinic, naphthenic, and aromatic. Meth-
                                                              SG 6 = 0.69, and T b6 = 337 K. For pure components from C 2
         ods of Section 3.5 can be used to determine PNA composition  to C 5 , M and SG can be taken from Table 2.1. Using M and
         of each SCN group. In this way number of components in  x w , mole fraction x m can be estimated through Eq. (4.61).
         Table 4.24 increases to 152. For heavy oils the number of com-  Using Method A in Section 4.5.4.6 distribution coefficients
         ponents would be even higher. For each homologous group,  in Eq. (4.56) for the C 7+ fraction are found as M o = 90,
         different properties may be estimated from molecular weight  A M = 1.957, and B M = 1.0. From Method II outlined in Sec-
         of individual SCN group through the relations given in Sec-
         tion 2.3.3. Obviously calculation of mixture properties when  tion 4.6.1.2 and specifying 5 carbon number ranges the C 7+
                                                              can be split into 5 pseudocomponents with known mole frac-
         it is expressed in terms of large number of components is not  tion (normalized), M and SG as given in Table 4.25. In this
         an easy task. For this reason the number of components in  table the weight fractions are calculated through Eq. (1.15)
         Table 4.24 may be reduced by grouping to SCN components  using mole fraction and molecular weight. Values of weight
         or splitting the C 7 fraction into just 3 or 5 pseudocomponents.  fractions in Table 4.25 should be multiplied by wt% of C 7+ in
         Furthermore, iC 4 and nC 4 may be grouped as C 4 and iC 5 and  the whole crude to estimate wt% of each pseudocomponent
         nC 5 could be grouped as C 5 . In this way the mixture can be pre-  in the crude. Values of mol% in the original fluid are cal-  --`,```,`,``````,`,````,```,,-`-`,,`,,`,`,,`---
         sented by 10–15 components with known specifications. The  culated from wt% and molecular weight of all components
         following example shows how a crude oil can be presented
                                                              present in the mixture as shown in Table 4.26. For the 5 pseu-
                                                              docomponents generated by splitting the C 7+ , boiling points
                                                              are calculated from M and SG using Eq. (2.56). From T b and
             TABLE 4.24—Matrix table of components for estimation  SG of pseudocomponents given in Table 4.26, one may esti-
                       of properties of reservoir fluids.      mate basic characterization parameters to estimate various
            No.       Compound    Mole fraction  M   SG
             1         H 2 S          +
             2         CO 2           +                             TABLE 4.26—Characterization of the Kuwait crude oil
             3         N 2            +                                          in Example 4.16.
             4         H 2 O          +                       Component    Wt%      Mol%     M        SG     T b , C
                                                                                                               ◦
             5         C 1            +
                                                              C 2           0.03     0.22    30.1   0.356
             6         C 2            +
                                                              C 3           0.39     1.99    44.1   0.507
             7         C 3            +                       iC 4          0.62     2.40    58.1   0.563
             8         iC 4           +                       nC 4          1.08     4.18    58.1   0.584
             9         nC 4           +                       iC 5          0.77     2.40    72.2   0.625
            10         iC 5           +                       nC 5          1.31     4.08    72.2   0.631
            11         nC 5           +                       C 6           1.93     5.29    82     0.690     64
            12         C 6            +        +      +       C 7+ (1)      9.1     18.28   112.0   0.753     123
            13         C 7            +        +      +       C 7+ (2)     15.2     20.22   169.1   0.810     216
            14         C 8            +        +      +       C 7+ (3)     26.4     22.23   267.1   0.864     333
            15–55 a    C 9 –C 49      +        +      +       C 7+ (4)     18.5     10.26   405.8   0.904     438
            56         C 50+          +        +      +       C 7+ (5)     24.8      8.44   660.9   0.943     527
            a Compounds from 15 to 55 represent SCN groups from C 9 to C 49 .
            For compounds 1–11, properties are given in Tables 2.1 and 2.2.  Total  100  100  225.2  0.8469















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