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CHAPTER 2 Mechanisms of Low-Salinity and Smart Waterflood   35

                                        Total dissolved salts concentration, C TDS  (g/L)
                                       1         5  10       50 100
                                  90                                        0.00
                                           Calcite Surface (R)  Calcite Surface (R)
                                                    θ w       Crude Oil  θ w
                                             Crude Oil   High lonic Strength Water (W)  0.25
                                                               (CO)
                            Increasing water-wettability  Contact angle,     w  (°)  θ  60  0.50  COS    w  θ
                                              (CO)
                                        Low lonic Strength Water (W)






                                  30           Increasing oil recovery      0.75

                                   0                                        1.00
                                   0.01          0.1          1            10
                            [DI water]
                                   [SW]/100  [SW]/20 [SW]/10  [SW]/2  [SW]  [FW]
                                         NaCI equivalent concentration, C TDS  (mol/L)
                                               Decreasing ionic stregnth
                FIG. 2.7 The effect of salinity on the contact angle and wettability. (Credit: From Chen, S.-Y., Kaufman, Y.,
                Kristiansen, K., Dobbs Howard, A., Cadirov Nicholas, A., Seo, D., & et al. (2018). New Atomic to molecular
                scale insights into smart water flooding mechanisms in carbonates. In Paper presented at the SPE improved oil
                recovery Conference, Tulsa, Oklahoma, USA, 1418 April. https://doi.org/10.2118/190281-MS.)

          j 0 is the surface potential; d is the distance; A and Ddare  show complex surface, not flat, and become further
          the Hamaker constant and offset distance, respectively,  roughened because of mineral dissolution during
          for the van der Waals attraction; and d is the “hard-wall”  LSWF. The second mechanism on the roughening of
          hydration repulsion layer thickness.          the underlying calcite surface overcomes the limitations,
                                                        which are involved with the first mechanism. The initial
                              r ffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi
                               ε 0 ε r k B T
                         k  1  ¼                 (2.7)  surface roughness and more roughening due to mineral
                                2Ce 2                   dissolution on the adhesion energy are included in the
          where ε r is the dielectric constant and ε 0 is the permit-  modified Young-Dupré equation of Eq. (2.9),which
          tivity in free space.                         introduces the concept of an effective adhesion energy.
                                                        Notably, the mineral dissolution roughens the calcite
                        o


                      W o=w=r  ¼ g o=w 1   cos q o w  (2.8)  surface  and  decreases  contact  angle  improving
                         o
          where W o  and q are the intrinsic adhesion energy  wettability toward water-wetness.
                 o=w=r   w
          and intrinsic contact angle, respectively, on molecularly        o              o
                                                           W effective; o=w=r ¼ f o=r W o=w=r  ¼ g o=w 1   cos q w  (2.9)
          smooth, nonstructured, and flat surfaces and g o/w is the
          interfacial tension between oil and water.    where W effective, o/w/r is the effective adhesion energy and
            The proposed mechanisms of LSWF with the    f o/r is a surface roughness factor, defined as the ratio
          potential-determining ions, EDL expansion, and surface  between real contact area of oil and rock across the
          charge change can be explained with the first mechanism  aqueous brine film and the projected, flat contact area
          using extended DLVO theory and Young-Dupré    on the smooth surface.
          equation. However, they ignore the changes in (nano-  In addition to the physical-chemical considerations,
          scale to microscale) surface roughness and roughening,  the third mechanism takes account of the removal of
          which can significantly influence on the overall adhesion  preadsorbed organic-ionic ad-layer, i.e., flakes, from
          energy. The extended DLVO theory and Young-Dupré  the calcite surface. During LSWF, the flakes are released
          equation, conventionally, are strictly appropriate to  from calcite surface and suspended in the brine. The
          molecularly smooth and flat surface. Typical reservoirs  detachment of organic materials with the flakes
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