Page 165 - Geochemistry of Oil Field Waters
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152                 INORGANIC CONSTITUENTS AND PHYSICAL PROPERTIES


            the  temperature  and  the redox  potential control its occurrence.  It is trans-
            ported in hot springs (White et al., 1963).
              Shales, sandstones, and carbonates contain about 0.4, 0.03, and 0.04 ppm,
            respectively,  of  mercury.  Sea water  contains 3 x  lo-’  mg/l, and subsurface
            oilfield  brines  contain  0-0.15  mg/l.  The  samples  containing  0.15 mg/l  of
            mercury  were  found  in  relatively  dilute brines taken  from the Cymric and
            the  Rio  Bravo  oilfields  in  California.  Free  mercury  is  found  in  the oils
            produced  from these fields, and the ages of  the producing formations range
            from Eocene to Pleistocene.
              The  mercury  content of  natural waters has been  used to locate cinnabar
            deposits  (Dall’Aglio,  1968). The amounts  of  mercury  in  waters  appear  to
            increase  with  increasing  bicarbonate  concentration.  Karasik  et  al.  (1965)
            found  that  saline  waters  containing  200,000 mg/l of  chloride contain very
            small amounts  of  mercury,  which  suggests that  anionic complexes such as
            HgC14-*  may not be important transporters of  mercury. Brackish waters con-
            taining up to 3,000 mg/l dissolved solids, up to 400 mg/l of  bicarbonate, and
            the iodide  ion sometimes contain up to 10 ppb of  mercury,  while stronger
            brines  contain  <0.1 ppb  of  mercury,  which suggests that mercury  may be
            transported as Hg14-*  in brackish waters.

            Lead

              Lead  is a member of the IV  A  group of  elements; it is ubiquitous in the
            earth,  but  its abundance  in  the crust  is only about 0.002  wt.% (Fleischer,
            1962). It is extracted from its minerals during weathering and migrates in the
            form  of  soluble-stable compounds.  It is  particularly  soluble in  acetic  and
            other acids. Because the bicarbonate  form is more soluble than the carbon-
            ate,  lead  can  be  transported  as  the  bicarbonate.  Most  of  the  lead  is
            precipitated  from waters before they reach the sea. Hemley (1953) studied
            lead  sulfide solubility related  to ore deposition from saline waters.  He con-
            cluded  that  lead-complex  concentrations  increase  with  increasing  concen-
           trations of  bivalent  sulfur and decrease at pH values above 7. The solubility
           of  lead  is  limited  primarily  by  the solubility  restrictions  of  its sulfide and
           sulfate in reducing and oxidizing systems. How its solubility is influenced by
           many  other  ions,  such  as those found in a brine, has not been sufficiently
           studied.
              Shales,  sandstones,  and  carbonates contain  about  20,  7, and  9 ppm  of
           lead,  respectively.  Sea  water  contains  about  0.003  mg/l,  and  subsurface
           brines contain trace amounts to more than 100 mg/l of  lead.

           Cadmium
              Cadmium is a member of  the I1 B group of  elements and may be consid-
           ered one of  the rarer elements; its abundance is about 3 x  lo-’  wt.% of the
           earth’s  crust  (Fleischer,  1962).  It  is strongly  thiophile,  but  its chemistry
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