| 
					
					
					 ELECTRICAL
					PROPERTIES BASICS Electrical properties are terms used in the Archie water
					saturation equation, and in its shale corrected cousins, to
					calibrate water saturation to the physical properties of the
					pore geometry of the rock. The parameters required are:
 1: tortuosity constant A
 2: cementation exponent M
 3: saturation exponent N
 These three terms are usually
			written in lower case font (a, m, n) but in keeping with the policy
			of this Handbook that input parameters be capitalized, they are
			referred to here and elsewhere in upper case 
			 M
			is defined as the slope of the best fit line drawn through a graph
			of formation factor (F = R0 / RW) versus porosity,  and A is
			the intercept of that line on the F axis. A sample of such a plot is
			show at the left and is discussed in more detail later in this
			Chapter. 
				 N is defined as the slope of the
			best fit line on a graph of resistivity index (RI = RT / R0) versus
			water saturation. A sample plot is shown at the right and discussed
			in more detail later.. Although there is not a lot of
			evidence to support the assertion, N is often taken as equal to M,
			probably because M can sometimes be found from available log data in
			the absence of core data, and N cannot. 
 Pore geometry in sandstones varies
			with lithology, grain size, sorting, shape, roughness, and shale
			volume. In carbonates, it varies with pore type and how well the
			pores are connected. Some examples are shown below, and combinations
			of these pore geometries are common. For example, fractured, moldic,
			intercrystalline porosity is relatively common.
 
			 Examples of different pore geometry models
 
					
					The cementation exponent has been studied the most and the
			following illustrations, keyed to the pore geometry shown above,
			give some idea of the complexity of the problem. The two images
			below are from "Cementation Exponents in Middle Eastern Carbonate
			Reservoirs" by J. W. Focke and D. Munn, SPE Paper 13175, June 1987. 
			 Formation factor plot and M versus porosity plot for intergranular
			and sucrosic pore geometry.
 A = 1.00, M = 2.00, and do not vary with porosity.
 
			 Similar plots for a moldic limestone. Formation factor data is
			scattered and M increases with
 increasing porosity. A variable M method is required for a
			satisfactory water saturation calculation.
 The equation for M is: M = 1.40 + 6.57 * PHIe where PHIe is a
			decimal fraction.(permeability
 regime 0.1 - 1.0 md)
 The
			slope and intercept of the variable M plots will of course vary from
			one reservoir to another, and vary with the permeability regime,
			which is an indicator of the connectedness of the moldic porosity.
 There are a number of methods for finding and adjusting the
					electrical properties of rocks. The common approaches are
					listed here.
 
  Tortuosity
			Constant (A) from Log and RW Data This
                is easy if there is a clean water zone on the log which also tested
                water. The formula is:    
                1: Rwa = (PHIt ^ M) * RESD / A
 1: Rwa = (PHIt ^ 2) * RESD
 2: RW@FTlog = Rwa
			from a relatively clean water bearing zone
 3: KT1 = 6.8 for English units 
  KT1 = 21.5 for Metric units
 4: RW@FTdst = RWlab * (TRW + KT1) / (FT +
			KT1)
 5: A = (RW@FTlog) / (RW@FTdst)
 Where:A = cementation exponent (unitless)
 RW@FTlog = RW@FT with A = 1.0 and M = 2.0 calculated from a
                water zone on logs (ohm-m)
 RW@FTdst = RW@FT from DST measured in the laboratory (ohm-m)
                and converted to formation temperature
 FT = formation temperature (degrees Fahrenheit or Celsius)
 RWlab = water resistivity at lab temperature (ohm-m)
 TRW = temperature at which water was measured (degrees Fahrenheit or Celsius)
 Data
                from several wells may be averaged to obtain a good value. The
                parameter A varies with grain size, so wells used should come
                from similar geologic settings (depth, distance from source of
                sediment, etc.).   
			
			 Cementation Exponent (M) from Special Core Data Plot
                porosity vs lab measured formation factor on log-log axes. Fit
                regression or eyeball line to data. Slope of line is M. Intercept
                at PHIe = 1 is A. The line force-fitted through F = PHIe = 1.0
                is called a pinned line. Some people prefer the pinned line but
                most data sets do not support this approach. Strictly speaking,
                the line must pass through F = 1 = PHIe, so the line must be non-linear
                approaching this point on the graph. An example is shown below.
 
				 Find A and M from special core data (electrical properties
                data) - M is slope of best fit line
 (pinned or free regression - your choice), A is intercept at
				PHIe = 1.0.
 
  Saturation Exponent (N) from Special Core Data Plot
                brine saturation from core analysis versus formation resistivity
                index (RESD / R0) on log-log axes. Draw line through the data
                to intercept at SW = 1.0. The slope of this line
                is N. Data from several wells may have to be combined to get a
                reasonable fit.
 
				 Find N from special core data (electrical properties
                data). Slope is N and line must pass
 through Sw = 1.0 at RI = 1.0..
 
				
					
			 Sample Special Core 
				REPORTS The graphs 
				described above are provided by the core analysis contractor 
				based on the measurements they have made. These data are also 
				provided as a table or spreadsheet. The layout may vary from the 
				examples shown here. You are free to edit or combine data sets 
				and make your own graphs and determine new A, M, and N values
				specific to a particular zone, facies, or rock type.
 
                
			 The final product from the lab includes formation factor and
			resistivity graphs and  a table of F, M, RI, and N values for 
			use in the appropriate water saturation equations. This example is
			from a clean, moderately tight, dolomitic sandstone.
 
 
			
			 A shaly sand special core analysis gives a table of BQv, F, F*,
			M, M*, RI, RI*, N, and N* for use in the appropriate water 
			saturation equations.This example is from a Cretaceous shaly sand in 
			southern Alberta.
 
  Cementation Exponent (M) from Log Data A variety of
				approaches are available to assess the electrical property M
				from log data. There
                is no direct method for finding N from log data, but there is an
				indirect approach. If you are satisfied that A, M, and RW are
				correct, you can compare the log analysis SW with the capillary
				pressure SW. Any difference can be repaired by adjusting
				N. Changing N will make no difference in a water zone, so it
				helps to be able to calibrate A, M, and RW in the water zones
				first.
 
 
  Pickett Plot Method Pickett
                proposed that the Archie formation factor and saturation equations
                be rearranged as follows:
 2: log(RESD) = - M * log(PHIe) +
				log(A*RW@FT)
 3: log(RESS) = - M * log(PHIe) + log(A*RMF@FT)
 
			In
                water zones:4: M = (log(A*RW@FT) - log(RESD)) / log(PHIe)
 In
                invaded water or hydrocarbon zones:5: M = (log(A*RMF@FT) - log(RESS)) / log(PHIe)
 Where:A = tortuosity exponent (unitless)
 M = cementation exponent (unitless)
 PHIe = porosity from any source (fractional
 RESD = deep resistivity of rock with water and oil (or mercury)
                (ohm-m)
 RESS = shallow resistivity of rock with water and oil (or mercury)
                (ohm-m)
 RW@FT = water resistivity at formation temperature (ohm-m)
 RMF@FT = mud filtrate resistivity at formation temperature (ohm-m)
 
			
			 COMMENTS Equation 1 represents a plot of deep resistivity vs effective
                porosity FROM KNOWN WATER ZONES on log-log paper. Draw a line
                through southwest data points. Slope of this line is M and intercept
                at PHIe = 1 is A*RW@FT.
 Equation
                2 may work in hydrocarbon zones if invasion is well developed
                and residual hydrocarbon is small. M will be too high if ROS is
                high. 
				 Find M and A*RW from Pickett plot
 Make
                a separate graph FOR EACH ROCK TYPE. Typical rock types in carbonates
                are intergranular (clastic texture), intercrystalline (fine, medium,
                or coarse), vuggy (fine, medium, or large), microporosity (unconnected
                pores), oomoldic, and fractured zones (with any other rock type).
                Rock typing is usually done from sample or core description. M
                can be made to vary by solving equation 1 or 2 for each data point
                instead of fitting a line through the average of the data set. 
					/ "VARIABLE M" METHODS 
 
  Shell Method Analysts
                at Shell Oil proposed a formula to vary M in carbonates with porosity.
                Other relationships could be found by fitting non-linear curves
                to the data used for the Pickett plot or by plotting individual
				M values versus porosity:
 6:
                M = 1.87 + 1.9 * PHIe
 
					
			 Focke and Munn l Method The
			Focke and  Munn paper referred to earlier shows a variety of
			data sets, in which M increases with porosity, as shown
			below:
 7: M = 1.20 + 12.76 * PHIe (perm < 0.10)
 8: M = 1.40 + 6.57 * PHIe (perm = 0.1 - 1.0)
 9: M = 1.20 + 6.29 * PHIe (perm = 1.0 - 100)
 10: M = 1.22 + 3.49 * PHIe (perm > 100)
 
			Where:M = cementation exponent (unitless)
 PHIe = porosity from any source (fractional
 
					
			 Nugentl Method An
                equation proposed by Nugent uses the secondary porosity concept:
 11: M >= 2 * log(PHIsc) / log(PHIxnd)
 PHIsc
                represents the matrix porosity and PHIxnd represents the effective
                porosity in the carbonate rock. Both should be shale corrected
                as described in Chapter Seven. Use
				Nugent's method 
                in intergranular, intercrystalline, vuggy, and fossilmoldic rock
                types. Results
                are too low in oomoldic rock type. PHIsc
                must be calculated with a matrix value (DELTMA) that varies with
                the rock lithology. This can be derived from the results of a
                two or three mineral model or sample description with DELTMA =
                V1 * DELTMA1 + V2 * DELTMA2 + V3 * DELTMA3. 
					
			 Nurmi Method In
                oomoldic porosity, Nurmi proposed the following:
 12: PHIvug = 2 * (PHIxnd - PHIsc)
 13: PHIma = PHIxnd - PHIvug
 14: M >= 2 * log(PHIma) / log(PHIxnd)
 Use
				Nurmi method in oomoldic rock type. PHIsc
                must be calculated with a matrix value (DELTMA) that varies with
                the rock lithology. This can be derived from the results of a
                two or three mineral model or sample description. 
					
			 Rasmus Method The
                same techniques used to derive M for various carbonate rock types
                can also be used to find M in fractured carbonates. A standard
                Pickett plot in water zones, or a Pickett plot using a shallow
                resistivity log in the invaded zone, will usually suffice. The
                M value so derived will be the result of BOTH fractures and the
                rock type in the zone covered by the crossplot. Normally, M is
                chosen once for each fractured interval from Pickett plots over
                well-defined rock type zones or layers.
 However,
                there is no reason to believe M is a constant in a zone because
                fracture intensity probably varies dramatically from foot to foot
                within the layer.A
                method proposed by Rasmus, based on secondary porosity concepts,
                solves this problem:
 11: Md = log((1 - (PHIxnd - PHIsc)) * (PHIsc^Mb) + (PHIxnd - PHIsc))
                / log(PHIe)
 Mb
                is the formation factor exponent for the bulk matrix (un-fractured)
                rock and Md is the value for the combined matrix plus fracture,
                or double porosity, porosity. Mb should be determined separately
                in un-fractured zones if possible.
 
 
					
				
				
			 Typical A, M, N Parameters: for sandstone A = 0.62 
                M = 2.15 
                N = 2.00
 for
                carbonates A = 1.0 
                M = 2.00 
                N = 2.00
 NOTE:
                N is often lower than 2.0 For
                quick analysis use carbonate values. Values for local situations
                should be developed from special core data. Results will always
                be better if good local data is used instead of traditional values,
                such as those given above.
 Asquith (1980 page 67) quoted other authors, giving values for A
				and M, with N = 2.0, showing the wide range of possible values:
 
 Average sands sands    A = 1.45  M = 1.54
 Shaly sands                 
				A = 1.65  M = 1.33
 Calcareous sands        
				A = 1.45  M = 1.70
 Carbonates                  
				A = 0.85  M = 2.14
 Pliocene sands S.Cal.  A = 2.45  M = 1.08
 Miocene LA/TX            
				A = 1.97  M = 1.29
 Clean granular            
				A = 1.00  M = 2.05 - PHIe
 
 
 
  META/LOG 
				"FRF" --
										Electrical Properties Spreadsheet This spreadsheet
										provides a tool for summarizing Electrical Properties
										dara and
				includes crossplots to find
 A, M, and N.
 
 Download this spreadsheet:
 SPR-09 META/LOG PYRITE CORRECTION CALCULATOR
 Calculate effect of pyrite on resistivity logs.
 Metric Units
 
 
										 
 
  Sample output from "META/FRF"
										spreadsheet for summarizing electrical
										properties.
 
 |