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ABNORMALLY-HIGH FORMATION PRESSURE                                    63
             most pronounced AHFP zones in the Baku Archipelago and Lower Kura
             Depression.
                According to Chilingar (1957), the relationship between the chemical composition
             of the Absheron Peninsula waters and the stratigraphic depth is subject to the
             following rules:
             (1) The total salinity of formation waters decreases with stratigraphic depth (also see
                 Samedov and Buryakovsky, 1966; Rieke and Chilingarian, 1974, pp. 265–269).

             (2) The Cl , Ca 2+  and Mg 2+  contents decrease with depth.
                          +
                                                 +
                    +

                                            2
                                                      +
             (3) (Na +K ) and (HCO 3 +CO 3 +H +K ) contents gradually increase with
                 depth.
             (4) The transition from hard-to-alkaline waters occurs at maximum concentration,
                 not exceeding 0.1 g-eq. per 100 g of water (5–6.51Be). As a rule, the waters are
                 hard at concentration above 0.1 g-eq.


             (5) The HCO 3 content (in g-eq.) does not exceed the Cl content.
                                                      2
             (6) Usually, the waters do not contain SO 4  anion. If present, however, its
                 concentration does not exceed 0.0004 g-eq. per 100 g of water.
               Mekhtiev (1956) (in: Rieke and Chilingarian, 1974, pp. 265) also showed that in the
             Azerbaijan oilfields water salinity is decreasing with stratigraphic depth and calcium

                                    +
             chloride waters (rCl  rNa )/rMg 2+ 41, where r is percent-equivalent, are gradually

                                              +
                                                          2
             replaced by bicarbonate waters: (rNa  rCl )/rSO 4 41. For magnesium chloride

                             +
             water, (rCl  rNa )/rMg 2+ o1. For details on classification of waters, see Chilingar
             (1956, 1957, 1958), Samedov and Buryakovsky (1966), and Buryakovsky (1974).
                According to Chilingarian et al. (1994), the chemistry of pore water is determined
             mainly by the compaction of argillaceous rocks and squeezing-out of pore water.
             The formation water chemistry, in turn, influences the diagenetic and catagenetic
             transformation (of clay minerals) processes.
                Fig. 3.17 shows the dependence of montmorillonite content on the total salinity of
             formation water for the calcium chloride and sodium bicarbonate types of pore
             waters in sands of the South Caspian Basin. As shown, a direct relationship exists for
             the sodium bicarbonate type of water, i.e., with increasing water salinity, the
             conditions for preservation of montmorillonite are improved and its content in
             the clays increases. Increase in the total salinity of water is caused by an increase in
             the content of carbonate and bicarbonate salts of alkali-earth metals. Sodium
             bicarbonate-type waters are present in the Baku Archipelago and the Lower Kura
             Depression, as well as in the rocks from the Lower Productive Series of Absheron
             Peninsula and adjacent offshore area, i.e., sections in which the argillaceous rocks
             are characterized by higher montmorillonite content. There is an inverse relationship
             between the montmorillonite content and the presence of calcium chloride type of
             waters. The chloride content [in particular sylvite (KCl)] increases with increasing
             water salinity. Thus, alkaline medium is apparently favorable for the formation and
             preservation of montmorillonite.
                Thus, the geochemical environment at great depths in the South Caspian Basin
             deposits not only conducive to the preservation of allothigenic montmorillonite, but
             possibly allows the transformation of illite into secondary montmorillonite.
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