Page 43 - Geochemistry of Oil Field Waters
P. 43

32                                        ANALYSIS OF OILFIELD WATERS


            values  below  this  level  and  the  results  multiplied  by  the  correct  dilution
            factor.
              To  obtain  maximum  accuracy  and  precision  the  following  precautions
            should be observed:
              (a) Protect the Lucite standard from scratches, nicks, and fingerprints.
              (b) While  calibrating  the  instrument,  use  a  constant  orientation  of  the
            Lucite standard.
              (c) Use a homogeneous sample in the sample cuvette; do not take readings
            until finely dispersed bubbles have disappeared.
              (d)  Dilute  samples  containing. excess  tubidity  to some value  below  40
            JCU; take reading, and multiply results by correct dilution factor.

            Suspended solids analysis

              To  determine  the  composition  of  the  suspended  solids  they  can  be
            removed  by  filtration  using a 0.45-pm membrane or less porous filter. The
            filtered solids can then be subjected to chemical analysis. To determine the
            exact composition  of  the solids may require the filtration of  a large sample
            in  order  to procure  enough solid material.  The heavy-metal content can be
            determined  by  subjecting a  portion  of  the  sample to an emission spectro-
            metric  analysis;  X-ray diffraction  can  be  used  to determine which, if  any,
            clays are present; extraction  with organic solvents followed by infrared mass
           spectrometric,  chromatographic,  and gas chromatographic  analysis will give
           an indication  of  organic compounds present; thermogravimetric analysis will
           provide  clues; wet chemical analysis can be used to determine many of  the
           anions; and X-ray fluorescence can be used to determine some of the anions.

            Resistivity

              The resistivity of  petroleum-associated waters is used  in electric log inter-
           pretations  (Wyllie,  1963), and  for  such use the values must be adjusted to
           the formation temperature. This can be done by referring to curves such as
           those  shown  in  Fig.3.1,  which  gives resistivity  values for  sodium  chloride
           solutions. The resistivity of a formation water will not be exactly the same as
            that  of  a  pure  sodium  chloride  solution of  equal dissolved solid (DS) con-
           tent,  but  for  practical  purposes  the  assumption  that  the  resistivities  are
            approximately equal is satisfactory.
              It is possible  to  calculate  the resistivity  from  water-mineral analysis by
            using methods such as those developed by Dunlap and Hawthorne (1951) or
            Jones (1944). The calculated values are less accurate and usually lower than
            the directly  measured resistivities. The direct-measurement method is essen-
            tially  the  electrical  resistance  of  a  cube  of  oilfield  water.  In  well-logging
            practice, the edge of  the cube considered is 1 m in length. Therefore, resis-
            tivity of  an oilfield water is expressed in ohm-meters (am).
              Temperature has a profound effect on resistivity; therefore, all resistivities
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