Page 375 - Characterization and Properties of Petroleum Fractions - M.R. Riazi
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                                                  8. APPLICATIONS: ESTIMATION OF TRANSPORT PROPERTIES 355















                                FIG. 8.12—Schematic and dimensions of a constant volume cell. Taken with per-
                              mission from Ref. [56].

              This method can be extended to multicomponent systems  model and the assumptions made in its formulation. Methods
            and it has been successfully used to measure gas diffusiv-  that use unrealistic assumptions, i.e., neglecting natural con-
            ity in heavy oils [57, 58]. In this method, pressure mea-  vection terms when it exists, or oversimplified boundary con-
            surement is more accurate than measuring the interphase  ditions (i.e., semiinfinite assumption) lead to predictions that
            location. Furthermore, the initial measurements are more  do not match the entire curve. In these cases, reported diffu-
            critical than measurements near the final equilibrium condi-  sion coefficients are based on a portion of experimental data
            tion. The amount of initial liquid or gas determines diffusivity  and this is the reason that in such cases differences as large
            of which phase can be measured more accurately [56]. As it  as ±100% are reported for diffusion coefficients in liquids at
            can be seen from Fig. 8.13 once a correct value of diffusion co-  high pressures for the same systems under the same condi-
            efficient is used, the model prediction matches experimental  tions. The technique can also be used to measure diffusivity
            data throughout the curve. This confirms the validity of the  in porous media by placing a reservoir core in the bottom of a
                                                                  PVT cell saturated initially with liquid oil. With such experi-
                                                                  ments and availability of more data, Eq. (8.67) can be further
                                                                  studied, modified, and improved.







             Pressure, bar
                                                                    Diffusion Coefficient × 10 5 , m 2 /s















                                     Time, hr

             FIG. 8.13—Variation of pressure for the C 1 –C 5 constant vol-               Time, hr
            ume diffusion experiment at 311 K. — Diffusion coefficient from
            Eq. (8.67); ------ diffusion coefficient from Eq. (8.67) multiplied  FIG. 8.14—Diffusion coefficient of the methane–n-pentane
            by 1.1; ······ diffusion coefficient from Eq. (8.65). Taken with  system at 311 K for the liquid and gas phases. Taken with
            permission from Ref. [56].                           permission from Ref. [56].














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