Page 128 - Characterization and Properties of Petroleum Fractions - M.R. Riazi
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         108 CHARACTERIZATION AND PROPERTIES OF PETROLEUM FRACTIONS
         3.2.2.3.2 Conversion of a Distillation Curve from Sub- or
                                                                                                          ◦
                                                              kelvin.
         Super- Atmospheric Pressures to a Distillation Curve at  in the above relations all temperatures are either in Corin
         Atmospheric Pressure—The method of conversion of boil-
         ing points through Eqs. (3.29)–(3.32) can be used to every  3.2.2.4 Summary Chart for Interconverion of Various
         point on a distillation curve under either sub- or superatmo-  Distillation Curves
         spheric pressure conditions. In these equations T b or T (760  A summary of all conversion methods is shown in Fig. 3.20.
         mm Hg) represent a point along the distillation curve at at-  It should be noted that any distillation curve at low pressure
         mospheric pressure. It can be applied to any of TBP, EFV,  (i.e., ASTM D 1160 or EFV at 1, 10, 50, mm Hg or TBP at
         or ASTM D 1160 distillation curves. However, it should be  1 mm Hg) should be first converted to TBP distillation curve
         noted that these equations convert distillation curves from  at 10 mm Hg before they are converted to TBP at atmospheric
         one pressure to another within the same type. For example, it  pressure.
         is not possible to use these equations to directly convert ASTM
         D 1160 at 10 mm Hg to TBP at 760 mm Hg. Such conversions  Example 3.6—For a petroleum fraction the ASTM D 1160
         require two steps that are discussed in the following section.  distillation data at 10 mm Hg are given in Table 3.13. Predict
         The only distillation curve type that might be reported un-  the TBP curve at atmospheric pressure.
         der superatmospheric pressure (P > 1.01325 bar) condition
         is the EFV distillation curve. TBP curve may be at 1, 10, 100,  Solution—ASTM D 1160 data have been converted to TBP
         or 760 mm Hg pressure. Experimental data on ASTM D 1160  at 10 mm Hg by Eq. (3.34). Then Eq. (3.29) with P = 10
         are usually reported at 1, 10, or 50 mm Hg. ASTM D 86 distil-  mm Hg and Q = 0.001956 is used to convert TBP from 10
         lation is always reported at atmospheric pressure. It should  to 760 mm Hg. A summary of results is given in Table 3.13.
         be noted that when ASTM D 1160 distillation curve is con-  The second and less accurate method to convert TBP from 10
         verted to or reported at atmospheric pressure (760 mm Hg)  to 760 mm Hg is through Eq. (3.32), which in its reverse form
         it is not equivalent to or the same as ASTM D 86 distillation  becomes T (760 mm Hg) = 1.17T (10 mm Hg) + 67.51. Esti-
         data. They are different types of distillation curves and there  mated TBP at 760 mm Hg through this relation is presented
         is no direct conversion between these two curves.
                                                              in the last column of Table 3.13.
         3.2.2.3.3 Conversion of ASTM D 1160 at 10 mm Hg to
         TBP Distillation Curve at 10 mm Hg—The only method   3.2.3 Prediction of Complete Distillation Curves
         widely used under subatmospheric pressure condition for  In many cases distillation data for the entire range of percent
         conversion of distillation curves is the one developed by  distilled are not available. This is particularly the case when a
         Edmister–Okamoto [17], which is used to convert ASTM  fraction contains heavy compounds toward the end of distilla-
         D 1160 to TBP, both at 10 mm Hg. This method is graphi-  tion curve. For such fractions distillation can be performed to
         cal and it is also recommended by the API-DTB [2]. In this  a certain temperature. For example, in a TBP or ASTM curve,
         method it is assumed the at 50% points ASTM D 1160 and  distillation data may be available at 10, 30, 50, and 70% points
         TBP temperatures are equal. The Edmister–Okamoto chart  but not at 90 or 95% points, which are important for process
         is converted into equation form through regression of values  engineers and are characteristics of a petroleum product. For
         read from the figure in the following form [2]:       heavier fractions the distillation curves may even end at 50%
                                                              point. For such fractions it is important that values of temper-
                 TBP(100%) = ASTM D 1160(100%)                atures at these high percentage points to be estimated from
                  TBP(90%) = ASTM D 1160(90%)                 available data. In this section a distribution function for both
                  TBP(70%) = ASTM D 1160(70%)                 boiling point and density of petroleum fractions is presented
                                                              so that its parameters can be determined from as few as three
        (3.34)    TBP(50%) = ASTM D 1160(50%)
                                                              data points on the curve. The function can predict the boiling
                  TBP(30%) = ASTM D 1160(50%) − F 1           point for the entire range from initial point to 95% point. This
                                                              function was proposed by Riazi [31] based on a probability
                  TBP(10%) = ASTM D 1160(30%) − F 2
                                                              distribution model for the properties of heptane plus fractions
                   TBP(0%) = ASTM D 1160(10%) − F 3
                                                              in crude oils and reservoir fluids and its detailed characteris-
                                                              tics are discussed in Section 4.5.4. The distribution model is
         where functions F 1 , F 2 , and F 3 are given in terms of temper-
         ature difference in the ASTM D 1160:                 presented by the following equation (see Eq. 4.56):
                                                                                                
 1/B

            F 1 = 0.3 + 1.2775( T 1 ) − 5.539 × 10 ( T 1 ) + 2.7486  (3.35)  T − T ◦  =  A  ln  1
                                         −3
                                               2
               ×10 ( T 1 ) 3                                                  T ◦    B    1 − x
                   −5
            F 2 = 0.3 + 1.2775( T 2 ) − 5.539 × 10 ( T 2 ) + 2.7486  in which T is the temperature on the distillation curve in
                                               2
                                         −3
                   −5
               ×10 ( T 2 ) 3                                  kelvin and x is the volume or weight fraction of the mixture
                                           2
                                     −4
            F 3 = 2.2566( T 3 ) − 266.2 × 10 ( T 3 ) + 1.4093  distilled. A, B, and T ◦ are the three parameters to be deter-
                   −4
               ×10 ( T 3 ) 3                                  mined from available data on the distillation curve through a
            T 1 = ASTM D 1160(50%) − ASTM D 1160(30%)         linear regression. T ◦ is in fact the initial boiling point (T at x =
                                                              0) but has to be determined from actual data with x > 0. The
            T 2 = ASTM D 1160(30%) − ASTM D 1160(10%)         experimental value of T ◦ should not be included in the regres-
            T 3 = ASTM D 1160(10%) − ASTM D 1160(0%)          sion process since it is not a reliable point. Equation (3.35)






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