Page 341 - Enhanced Oil Recovery in Shale and Tight Reservoirs
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314                            Enhanced Oil Recovery in Shale and Tight Reservoirs


          which is for the matrix. The parameters for the capillary desaturation curves
          used in the base model for the fracture at (N C ) C are reported in Table 11.2,
          and the parameters for the fracture at (N C ) max are the same as those for the
          matrix in Table 11.3. The same values of T p in Table 11.3 are used for the
          matrix and the fracture.
             The model is symmetric along the Y direction. To cut the simulation
          running time, the model is cut into two halves along the Y direction.
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          Furthermore, 1 of matrix in the X direction (1/3 of model in the X
          direction) and one fracture (half model in the Y direction) are included in
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          the model. The final model sizes become 1   1.5   1 . The grids are
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          11   6   3. The injection rate is changed to one-sixth of that of the exper-
                                  3
          iment, that is, 0.00033 ft /day. Based on this smaller model, the
          permeability and porosity in the base model are replaced by shale properties
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          which are 300 nD (w3   10   19  m ) and 0.1 for the permeability and
          porosity, respectively.
             In general, a surfactant may change wettability and reduce IFT. Since the
          surfactant is injected with the alkali, the model assumes the surfactant
          reduces IFT and the alkali changes wettability. The degree of wettability
          alteration is controlled by interpolation scaling factor parameters u kr to
          represent the changes in relative permeability and u pc to represent the
          changes in capillary pressure:
                              k r ¼ u kr k ww  þð1  u kr Þk mw       (11.1)
                                      r             r
                              p C ¼ u pc p ww  þð1  u pc Þp mw       (11.2)
                                       C            C
          where the superscript ww and mw denote water-wet and initially mixed-wet
          conditions. The capillary pressure p C is a scaled with IFT, porosity, and
          permeability as follows:

                        r ffiffiffi  ww               ! E pc
                              jj
                ww        4 s 0         S j   S jr
               p Cjj 0 ¼ C pc  ow  1     P 3        j0; j ¼ 1; 2; 3  (11.3)
                              jj           j¼1 jr
                          k s 0      1        S
                   p ffiffiffiffiffiffiffiffi
          where C pc  f=k takes also into account the effect of permeability and
          porosity using the Leverett-J function (1941), f is the porosity and k is the
          permeability, s is the interfacial tension, S is the saturation at the water-wet
          condition, the subscripts j; j0 denote phases with j being the wetting phase,
          and S jr denotes the residual saturation of phase j. Phases 1, 2, and 3 represent
          water phase, oil phase, and microemulsion phase, respectively. The capillary
          pressure endpoints in Table 11.2 are C pc here. Assume the same C pc
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