Page 244 - Geochemistry of Oil Field Waters
P. 244

228                                          ORIGIN OF OILFIELD WATERS


            TABLE 7 .XV
            Bioconcentrated bromide and iodide in seaweeds and corals

                                              Bromide (ppm)      Iodide (ppm)
            Seaweed
            Laminaria digitata (dry matter)    1,380               5 10-8,000
            Laminaria  saccharina (dry matter)   340              2,000
            Desmaresta (ash)                   6,800              5,200


            Corals*
            Gorgonia uerrucosa                16,200             69,200
            Gorgonellidae                     19,800             22,100
            Isididae                           7,400             20,300

            * After Vinogradov  (1953).

            However, with each crystallization, more  bromide is left in  solution than is
            entrained in the precipitate.
              Sylvite  (KC1)  begins  to  precipitate  when  the  chloride  concentration  is
            about 360,000 mg/l (Table 7.111), followed by carnallite (MgC12 *KCI *6H2  0)
            and bischoffite (MgC12 *6H, 0). During evaporation the concentration rate of
            bromide  in  solution  increases. The change in the slope of  the curve in Fig.
            7.4 illustrates this approximately.
              Other concentration  mechanisms operate to account for the high bromide
            concentrations  (6,000  mg/l  and  up)  found  in  some  brines.  One  of  the
            mechanisms is related  to bioconcentrators such as seaweeds and corals. The
            seaweeds and corals concentrate the bromide, they  die, and are buried with
            the sediments. Later the bromide is leached by the surrounding waters. Table
            7.XV  illustrates  some  of  the  concentrations  of  bromide  and  iodide  that
            Vinogradov (1953) found in various seaweeds and corals.
              Laboratory  experiments  have  demonstrated  that  bromide  is  accommo-
           dated  in  the  halite  crystal  lattice  and  replaces  chloride  in  solid  solution
            (Borchert and Muir,  L964). The weight percentage of  bromide in solid solu-
           tion in the halite lattice is related to its weight percentage in the parent brine
           as  :
                   wt.% Br  (in halite)
              C=
                  wt.% Br  (in solution)
           where C = the pa@ition coefficient.
              In  most  natural  environments  C = 0.14  (Braitsch  and  Herrmann,  1964).
           In a marine salt sequence the wt.% Br/NaCl rises from about 0.007 wt.% at
           the bottom  to 0.02 wt.% at the beginning of  potassium precipitation. How-
           ever,  the  bromide  concentration  with  a  given  natural  halite sequence may
           vary considerably, even though theoretically  it should increase continuously
   239   240   241   242   243   244   245   246   247   248   249