Page 217 - Geochemistry of Oil Field Waters
P. 217

204                                         ORIGIN OF OILFIELD WATERS


              Deffeyes  et al.  (1964) proposed that dolomitization of  limestone results
            from  the evaporation of  sea water and  precipitation  of  gypsum causing the
            ratio  of  magnesium  to calcium  in  the  water to increase. The concentrated
            water  flows  downward,  because  it  is more dense,  into the underlying  sedi-
            ments where it reacts with limestone to form dolomite.
              Modern evaporite deposits are thin and cover relatively small areas of  the
            earth;  however,  the  ancient  environments  indicate  that  these  depositions
            were  widespread  in  the  United  States  (Krumbein,  1951) and in the world
            (Lotze,  1938). The  majority  of  the  major  evaporite  bodies  are  of  marine
            origin, and range in age from Cambrian to Tertiary. They form in arid marine
            climates where water  lost by  evaporation equals or exceeds that supplied by
            rainfall,  rivers,  or  the open sea. They also form in deep-water environment
            (Brongersma-Sanders, 1971  ).
              The  data  in Table 7.111  illustrate how  the concentrations of  some of  the
            dissolved constituents change as sea water is evaporated to dryness (Collins,
            1969a). As sea water is evaporated to dryness and the chloride concentration
            approaches  178,000  mg/l,  calcium  sulfate  precipitates.  Halite  precipitates
            when  the  chloride  concentration  approaches  27  5,000  mg/l,  magnesium
            sulfate  precipitates  during  the  next  stage  as  the  chloride  concentration
            approaches 277,000 mg/l. The concentrations of the ions in solution at these
            various stages approximate  those  shown  in  Table  7.111.  The  data  in Table
            7.111  indicate  that,  as sea  water  evaporates, the  concentrations of  lithium,
            magnesium,  boron,  chloride,  bromide  and  iodide  in  the  residual liquor in-
            crease, and that the concentrations of  sodium, potassium, rubidium, calcium,
            and strontium decrease. In most depositional areas, the brines never reached
            the concentration necessary for the deposition of potassium and magnesium




            TABLE 7.111
            Concentration changes during evaporation of sea water and brine

            Element            Sea water  CaS04.l   NaCl 4   MgS04.l   KCI 4   MgClz.1
            Lithium                 0.2       2        11        12       27        34
            Sodium             11,000     98,000  140,000    70,000    13,000   12,000
            Potassium             350      3,600   23,000    37,000    26,000    1,200
            Rubidium                0.1       1         6         8       14        10
            Magnesium           1,300     13,000   74,000    80,000  130,000  153,000
            Calcium               400      1,700      100        10        0         0
            Strontium               7        60        10         1        0         0
            Boron                   5        40       300       310      750       850
            Chloride           19,000    178,000  275,000  27 7,000  360,000  425,000
            Bromide                65       600     4,000     4,300     8,600   10,000
            Iodide                  0.05      2         5         7        8         8
            Total                        295,000  517,000  469,000  538,000  602,000
   212   213   214   215   216   217   218   219   220   221   222