Page 120 - Hybrid Enhanced Oil Recovery Using Smart Waterflooding
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112     Hybrid Enhanced Oil Recovery using Smart Waterflooding


          Because the first-contact miscibility between the  DETERMINATION OF SOLVENT PHASE
          displacing and displaced fluids results in a completely  BEHAVIOR
          single phase, the displacing fluid is able to recover all  There are several experiments to characterize the solvent
          displaced fluid contacted. The miscible displacement  phase behavior such as single contact, multiple contact,
          achieving the first-contact miscibility indicates that the  and slim tube tests (Lake, 1989). The single contact
          injecting gas is miscible in all proportions with  experiment is useful to construct the P-z diagram, which
          the reservoir fluid under the prevailing reservoir temper-  only shows the number and types of phases and liquid
          ature and pressure conditions. It is termed as first-  volume, since the pressure can be changed. The multiple
          contact miscible process.                     contact experiment can formulate the ternary diagram
            Another immiscible displacement can be classified  and imparts the compositional information, which is
          with two processes (Slobod & Koch, 1953), and it  not described from P-z diagram. The experiment of
          corresponds to the CO 2 injection in the real field. In  slim tube displacement can bridge the static experiment
          the first immiscible process of type I, the equilibrium  and coreflood. Although it does not exactly mimic the
          phases at the gas-oil front area are essentially immiscible.  displacement process, it still offers the dynamic proper-
          In other words, the CO 2 -rich phase displaces oil-rich  ties of phase behavior. Although the slim tube test
          phase with the interface between the two phases. It intro-  measures an effluent concentration, its main objective
          duces the advantages of more viscous displacing gas, oil  is to identify the MMP. The pressure, in which certain
          swelling, and oil viscosity reduction. In the second  amount of oil recovery is produced, is the MMP or
          immiscible flood of type M, the injected gas is suffi-  minimum dynamic miscibility pressure. Although there
          ciently enriched at the front as to be completely miscible  are a number of definitions to indicate MMP, they
          with the reservoir fluid. It is the miscible process  show the similar trends in correlations. Corresponding
          achieving multiple-contact miscibility. In the CO 2  to MMP, the critical tie line passes through the crude
          injection, CO 2 - and oil-rich phases are miscible on not  composition. The MMP is conventionally less than the
          the first contact but multiple contacts. During the multi-  pressure of first-contact miscibility. The determination
          ple contacts between oil- and CO 2 -rich phases, the mass  of MMP using slim tube test requires a high cost. There-
          transfer between oil and CO 2 proceeds until the oil-rich  fore, alternative approaches to determine MMP are (1)
          phase cannot be distinguished from the CO 2 -rich phase.  mathematical models and (2) thermodynamic MMP
          The transfer process between oil- and CO 2 -rich phases is  correlations (Jarrell et al., 2002). The mathematical
          described with condensing/vaporizing mechanisms  model uses phase equilibrium data and EOS to estimate
          (Zick, 1986). Following the condensing mechanism,  the thermodynamic MMP. Once the appropriate data are
          the CO 2 firstly condenses into the hydrocarbon liquid,  given, an excellent determination of MMP is possible at
          i.e., oil-rich phase. The condensation makes the oil-rich  low cost. When the acquisition of phase equilibrium
          phase lighter and, often, drives some lightest methane  data is unavailable, MMP correlations can be applied
          out ahead of oil bank. Because of the succeeding vapor-  for the specific condition.
          izing mechanism, the lighter oil components vaporize
          into the CO 2 -rich phase. The vaporization makes the
          CO 2 -rich phase denser to be soluble in the oil phase.  SOLUBILITY OF CO 2 IN WATER
          When the multiple-contact miscibility between the  The solubility of most hydrocarbon components in water
          CO 2 - and oil-rich phases is achieved, the two phases  is negligible over the range of temperature and pressure
          cannot be distinguishable in terms of properties. During  conditions. However, the solubility of CO 2 in water is
          the multiple-contact miscible process of CO 2 injection,  much higher than that of hydrocarbon components in
          there are some advantages of viscosity ratio, oil swelling,  water. The solubility of CO 2 is a function of pressure,
          and condensing/vaporization to recover oil. The misci-  temperature, and salinity. Søreide and Whitson (1992)
          bility between CO 2 and oil is sensitive to the reservoir  developed the numerical model of PR EOS considering
          fluid composition, pressure, and temperature. Because  the temperature-, pressure-, and salinity-dependent
          the real production commonly undergoes little change  aqueous solubility of CO 2 based on the experimental
          in the temperature except for the thermal EOR process,  database. Chang, Coats, and Nolen (1998) also
          the main interesting factor on the miscibility is the  developed the EOS model using CO 2 solubility, as well
          pressure. The condensing CO 2 in oil-rich phase and  as the properties of CO 2 -saturated water including
          vaporizing oil in CO 2 -rich phase increase with an  formation volume factor, compressibility, and viscosity
          increase in pressure.                         based on the experimental database.
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