Page 326 - Characterization and Properties of Petroleum Fractions - M.R. Riazi
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         306 CHARACTERIZATION AND PROPERTIES OF PETROLEUM FRACTIONS
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                                                                                               TECHNICAL DATA BOOK
                                                                                                 February 1994
              0.1
               –50        –25       0      25     50    75   100       150     200   250   300      400    500


                                                                                       ◦    ◦
                          FIG. 7.4—Vapor pressure of some n-alkane hydrocarbons. Unit conversion: F = ( C) ×
                         1.8 + 32; psia = bar × 14.504. Taken with permission from Ref. [9].

          An expanded form of Antoine equation, which covers a  where P c is in bar. Equations (7.13) and (7.14) work better
         wider temperature range by including two additional terms  at superatmospheric pressures (T > T b ) rather than at sub-
         and a fourth parameter, is given in the following form as sug-  atmospheric pressures. The main advantage of this equation
         gested by Cox [12]:                                  is that it has only two constants. This was the reason that
                                                              it was used to develop Eq. (3.102) in Section (3.6.1.1) for
                                 B
        (7.12)        ln P vap  = A +  + CT + DT 2            calculation of Reid vapor pressure (RVP) of petroleum fuels.
                                 T
                                                              For RVP prediction, a vapor pressure correlation is applied at
         Another correlation is the Miller equation, which has the fol-  a single temperature (100 F or 311 K) and a two-parameter
                                                                                    ◦
         lowing form [12]:                                    correlation should be sufficient. Some other forms of equa-
                                                              tions used to correlate vapor pressure data are given in
                                 2
        (7.13)  ln P r vap  =−  A   1 − T + B (3 + T r)(1 − T r) 3    Ref. [12].
                                r
                          T r
         where A and B are two constants specific for each compound.
         These coefficients have been correlated to the reduced boiling  7.3.2 Predictive Methods—Generalized
         point T br (=T b /T c ) and P c of pure hydrocarbon vapor pressure  Correlations
         in the following form:
                                                              In Section 6.5, estimation of vapor pressure from an equa-
                             T br ln(P c /1.01325)            tion of state (EOS) through Eq. (6.105) was shown. When an
                        A 1 =
                                 1 − T br                     appropriate EOS with accurate input parameters is used, ac-
        (7.14)           A = 0.4835 + 0.4605A 1               curate vapor pressure can be estimated through Eq. (6.105)
                                                              or Eq. (7.65) [see Problem 7.13]. As an example, prediction of
                             A/A 1 − (1 + T br )              vapor pressure of p-xylene from a modified PR EOS is shown
                         B =
                             (3 + T br )(1 − T br ) 2         in Fig. 7.6 [14].












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