QV is derived from laboratory measurements of the cation exchange capacity of the rock (CEC) CEC is expressed as milli-equivalents per gram of sample. To determine QV, CEC must be corrected for density and porosity by the relationship: QV = CEC RHOMA (1.0-PHIT) / PHIT EQ 18. This is the value of QV used by PETROLOG when an external QV is not supplied as an input curve.
QV is derived from laboratory measurements of the cation exchange capacity of the rock (CEC) CEC is expressed as milli-equivalents per gram of sample. To determine QV, CEC must be corrected for density and porosity by the relationship: QV = CEC RHOMA (1.0-PHIT) / PHIT EQ 18. This is the value of QV used by PETROLOG when an external QV is not supplied as an input curve.
QV is derived from laboratory measurements of the cation exchange capacity of the rock (CEC) CEC is expressed as milli-equivalents per gram of sample. To determine QV, CEC must be corrected for density and porosity by the relationship: QV = CEC RHOMA (1.0-PHIT) / PHIT EQ 18. This is the value of QV used by PETROLOG when an external QV is not supplied as an input curve.
The Waxman-Smits general equation for saturation can be expressed as:
SW^n1 = F1*RW / (RT * (1.0 + RW * B * QV / SW)) Eq 17a
or SW^n1 = F1*CT / (CW * (1.0 + B * QV /(CW * SW))) Eq 17b The term QV QV is expressed as cation concentration per unit volume of fluid in the pore space. (Equivalents per litre or meq/m) QV is derived from laboratory measurements of the cation exchange capacity of the rock (CEC) CEC is expressed as milli-equivalents per gram of sample. To determine QV, CEC must be corrected for density and porosity by the relationship: QV = CEC * RHOMA * (1.0-PHIT) / PHIT EQ 18 Where PHIT = Total Porosity which includes clay associated water RHOMA = Matrix density EQ 18 should be applied with caution as the matrix density used in the relationship must include the proportional clay and clean matrix densities. This is best achieved by obtaining matrix density values from pieces of the same core samples on which the CEC measurements are made. Where no CEC is available, Lavers has suggested the following relationship: QV = Aq * PHIT^Bq EQ 19 Where PHIT Total Porosity which includes clay associated water Aq Constant: Default = 0.0029 Bq Exponent: Default = -3.0590 This is the value of QV used by PETROLOG when an external QV is not supplied as an input curve. This relationship was used in the North Sea initially however can be modified for other locations. The term B B quantifies the conductance of the clay exchange cation as a specific temperature and a specific cation concentration. Juhasz (1981) published the expression linking B with Salinity and temperature as: B = (-1.28 + 0.225 * T - 0.0004059 * T^2) / (1.0+RW*0.045* T - 0.27) EQ 20 Where B Is expressed in mho.m-1/meq.cm-3 RW Formation water resistivity at formation temperature T Temperature in DegC B is automatically computed as a Zone Parameter in PETROLOG whenever BHT or RW is changed in a zone. B can also be modified manually by the user in the zone control file. Gravestock (1991) The term F1 = (Waxman-Smits Formation factor) According to Waxman and Thomas F1 is temperature independent. The reciprocal of the slope Co/CW line is F1 It is essential to determine the slope on the linear section of Co/CW (see Fig 5) because the term B accounts for the curved portion. The method to determine F1 is as follows 1. Saturate a core is a brine of a given salinity and measure Co 2. Flush the core and replace with a brine of different salinity and measure Co again 3. Repeat above as many time as necessary to trace the Co vs. CW plot and derive F1 This method is often referred to as The Waxman-Smits multiple salinity method. This is an expensive and time consuming exercise. The term F1 (Hoyer & Spann method) Hoyer and Spann (1975) in their paper Comments on Obtaining Accurate Electrical Properties of Cores established this simple relationship of F1 vs. F where F is determined from a single measurement of Co vs. CW. F1 = F * (1.0 -RW*B*QV) = F * (1.0 - B*QV/CW) EQ 21 Where F Formation resistivity factor from a single measurement of CW/Co F1 Waxman-Smits Formation resistivity factor The values of B and QV used in EQ 21 should be determined from the same core at the same temperature that was used to measure F in the laboratory. The terms a1, m1 (Waxman-Smits intercept and cementation exponent) Once a few F1 have been calculated using cores with different porosities, the values of a1 and m1 can be determined using the same conventional method to determine a and n. See figure 1. The porosity values used to determine a1 and m1 are total porosity PHIT which must be obtained by a dehumidified core analysis procedure. The terms n1 (Waxman-Smits saturation exponent) n1 should be measured with high conductivity water. The practice is to saturate a core with 100% brine (SW=1.0) and then remove gradually a percentage of the brine for partial saturations. See "Saturation Exponent" above. Modified Waxman Smits Equation This equation is based on the Juhasz model and makes do without the BQV and uses the apparent bound water resistivity. Rwb Rwa where VCLAY = 100% Rwb is the bound water resistivity using PHICP from the D-N Z-Plot. Two sets of equations are used: 1- When RW > Rwb Ro = F * Rwb * RW / (Rwb * (1 - VCLAY) + Vclay * RW) SWT = (Ro/RT)^(1/n) 2- When RW <= Rwb X = VCLAY * (Rwb - RW) / (2 8 Rwb) SWT = (X^2 + F * RW)/RT)^(1/n) + X Note that if RW = Rwb, the equation becomes a simple Archie formula since X = 0