Page 66 - Formation Damage during Improved Oil Recovery Fundamentals and Applications
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48                                            David A. Wood and Bin Yuan


          divalent cations by the monovalent cations (Lager et al., 2008). This
          makes the system more water-wet and thereby increases the oil recov-
          ery factor. If the MIE mechanism is dominant, there should be an
          inverse correlation between oil recovery factors and divalent cation
          adsorption. The higher the divalent adsorption, the lower the oil
          recovery should be.
             By injecting cores with solutions of different concentrations of both
          NaCl and CaCl 2 , Pouryousefy et al. (2016) showed that the results did
          not match with those predicted by MIE. The expectations for MIE are
          that high concentration of NaCl should lead to higher oil recoveries than
          lower concentrations, and that all concentrations of CaCl 2 should lead to
          lower recoveries than NaCl with little variation in oil recovery due to dif-
          ferent CaCl 2 concentrations. Experimental results showed that lower con-
          centration of Ca 21   achieved higher oil recoveries than higher
          concentrations of Ca 21 . Also, although the oil recoveries with CaCl 2
          were lower than for NaCl (consistent with MIE), the highest overall oil
          recovery was achieved with the lowest NaCl concentrations.
             Based on these results, Pouryousefy et al. (2016) conclude that MIE
          can only be one of the mechanisms at play with LSWF and suggest that
          DLE, induced by LSWF (and perhaps in part by MIE) is also playing a
          role. The exact mechanism(s) by which this might occur remain unclear.
          Several possible chemical bonding mechanisms are likely involved, where
          polar components of crude oil are directly attached to the surface of the
          rock, or at least the thin water film covering its pore linings and its associ-
          ated electrical double layers (Fig. 2.1). These include cation bridging,
          cation exchange, ligand bonding, anion bridging, which are all impacted
          by the electrolyte concentrations in the formation fluids. Myint and
          Firoozabadi (2015) have shown how some of the chemical mechanisms
          proposed by Austad et al. (2010) (e.g., organometallic bridges, hydrogen
          bonding, acid/base interactions) impact the expansion of the electrical
          double layer in sandstones and carbonates during LSFW.






               2.8 RELATIONSHIPS BETWEEN OIL RECOVERY,
               SALINITY, AND WETTABILITY VARIABLES

               The wettability of a porous rock refers to the ability of one fluid to
          spread across or adhere to the solid surface in presence of another
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