Page 80 - Well Logging and Formation Evaluation
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70                Well Logging and Formation Evaluation

            This plot was made assuming an m* value of 2.0. From the plot it was
          possible to determine: R w = 0.05ohmm; f c = 0.13; and C = 0.01. Using
          an assumed value of n*, it is then possible to calculate Waxman-Smits
          saturations in the hydrocarbon leg.
            If SCAL (special core analysis) data are available, it is possible to
          derive  m* and  n* from the experiments as follows. In a conventional
          cementation-exponent (m) measurement, the formation factor F is plotted
          against f on a log-log scale. In Archie’s model, the following would be
          true:

            F = ( R R w ) = f - m                                    (5.1.6)
                  o

          where  R o is the resistivity of the 100% water-saturated rock. Hence
          log(F)  =-m*log(f) and the gradient of the line yields  m. Since for
          the Waxman-Smits equation it is clearly not the case that F =f -m * , a cor-
          rection must be made. Let:

            F* = (1 +  R BQ v * )  F = f - m*                        (5.1.7)
                      w
          Now, if F* is plotted against f on a log-log scale, it is indeed the case that
          the gradient yields m*.
            Having derived m*, it should then be used to rederive C wa from R t and
          f. This will then lead to revised values of R w, f c , and C. This may in turn
          lead to a revised value of m*. Usually a couple of iterations are sufficient
          to get m* to converge to a value that fits both the C wa vs. 1/f plot and the
          F* vs. f plot. Since F* will exceed F by a larger amount at low porosi-
          ties than at high porosities, m* will always be greater than m. Typically,
          if an m value of 2.0 is measured, the value of m* will be around 2.2. A
          similar procedure is followed for n*. Archie’s model assumes that:

            I = ( R R o ) =  S w - n                                 (5.1.8)
                  t
          Hence, if log(I) is plotted against log(S w ), the gradient should yield n.
            For Waxman-Smits, it is necessary to derive I*, which is given by

                                                n
                                               -
                                           )
            I* = (1 +  R BQ S w * )  I (1 +  R BQ v =  S w *.        (5.1.9)
                                      w
                         v
                     w
          Plotting log(I*) versus log(S w ) yields the corrected saturation exponent
          n*. As  with  m*,  n* will be found to be lower than  n, typically by
          about 0.2.
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