Page 154 - Characterization and Properties of Petroleum Fractions - M.R. Riazi
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            AT029-Manual
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  AT029-03
         134 CHARACTERIZATION AND PROPERTIES OF PETROLEUM FRACTIONS



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                          FIG. 3.28—Equipment for measurement of flash point of petroleum fractions by ASTM
                         D 93 test method (courtesy of Chemical Engineering Department at KU).

         nearly independent of specific gravity. Based on data from  (3.114) is adopted by the API as the standard method to esti-
         pure hydrocarbons and some petroleum fractions, the con-  mate flash point of petroleum fractions [2]. It was shown that
         stants in Eq. (3.113) were determined as             Eq. (3.114) can be simplified into the following linear form
                                                              [73]:
                1               2.84947
        (3.114)    =−0.024209 +        + 3.4254 × 10 −3  ln T 10
                T F               T 10                        (3.115)        T F = 15.48 + 0.70704 T 10
         where for pure hydrocarbons T 10 is normal boiling point,
         while for petroleum fractions it is distillation temperature at  where both T 10 and T F are in kelvin. This equation is applica-
         10 vol% vaporized (ASTM D 86 at 10%) and it is in kelvin. T F is  ble to fractions with normal boiling points (i.e., ASTM D 86
         the flash point in kelvin determined from the ASTM D 93 test  temperature at 50%) less than 260 C (500 F). For such light
                                                                                                 ◦
                                                                                           ◦
         method (Pensky–Martens closed cup tester). This equation is  fractions, Eq. (3.115) is slightly more accurate than Eq.
         presented in Fig. 3.29 for a quick and convenient estimate  (3.114). For heavier fractions Eq. (3.114) should be used.
         of flash point. For 18 pure hydrocarbons and 39 fractions,  There are some relations in the literature that correlate flash
         Eq. (3.114) predicts flash points with an average absolute de-  points to either the initial boiling point (T 0 ) or the distillation
         viation (AD) of 6.8 C (12 F) while Eq. (3.111) predicts the  temperature at 50% point (T 50 ). Such correlations are not ac-
                         ◦
                              ◦
         flash points with AD of 18.3 C.                       curate over a wide range of fractions, especially when they are
                                ◦
          Equation (3.114) should be applied to fractions with nor-  applied to fractions not used in obtaining their coefficients.
         mal boiling points from 65 to 590 C (150–1100 F). Equation  Generally reported initial boiling points for petroleum frac-
                                                ◦
                                     ◦
                                                              tions are not reliable and if mid boiling point temperature is
                                                              used as the characteristics boiling point it does not truly rep-
                      150
                                                              resent the boiling point of light components that are initially
                                                              being vaporized. For this reason the correlations in terms of
                                                              distillation temperature at 10% point (T 10 ) are more accurate
                      100
                    Flash Temperature, °C  50 0               petroleum fractions. Flash points of petroleum fractions may
                                                              than the other correlations for estimation of flash points of
                                                              also be estimated from the pseudocomponent method using
                                                              the PNA composition and values of flash points of pure hy-
                                                              drocarbons from Table 2.2. However, volumetric averaging
                                                              predicts the flash point of the blend and the blending index
                      -50                                     of component flash point through Eq. (3.40) generally over-
                                                              approach described below should be used to estimate flash
                         0   100   200   300  400
                                                              point of defined mixtures.
                          ASTM  10% Temperature, °C
                                                                If the flash point of a petroleum fraction or a petroleum
                    FIG.  3.29—Prediction  of  flash           product does not meet the required specification, it can be
                   point of petroleum fractions from          adjusted by blending the fraction with other compounds hav-
                   Eq. (3.114).                               ing different flash points. For example in hot regions where













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