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CRAIN'S PETROPHYSICAL HANDBOOK
c. 1978 - 2008 E. R. (Ross) Crain, P.Eng.
Rocky Mountain House, Alberta Canada T4T 2A2
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Updated 15 Jan 2008

CHAPTER EIGHT: CALCULATING HYDROCARBON CONTENT

Table Of Contents 8.00 Introduction To This Chapter
8.01 Definition Of Saturation
8.02 Visual Overlays Of Resisitivity And Porosity
8.03 Density Neutron Crossover
8.04 Other Indicators Of Hydrocarbons
8.05 Environmental Corrections For Resistivity
8.06 Calculating Diameter Of Invasion
8.07 Formation Water Resistivity
8.08 Water Saturation From The Porosity Water Saturation Product
8.09 Water Saturation From Archie Method
8.10 Water Saturation From Simandoux Method
8.11 Saturation From Waxman-Smits (CEC) Method
8.12 Water Saturation From Dual Water Method
8.13 Water Saturation From Ratio Method
8.14 Apparent Water Resistivity (Rwa) Method
8.15 Water Saturation From Pulsed Neutron Logs
8.16 Material Balance And Smoothing For Water Saturation
8.17 Selection of Water Resistivity
8.18 Selection Of Saturation Exponents
  
1. Selection of tortuosity exponent (A) from Log and DST Data
  
2. Selection of Cementation Exponent (M) from Special Core Data
  
3. Selection of Cementation Exponent (M) from Log Data
(Pickett, Shell, Nurmi, Rasmus)

  
4. Selection of Saturation xponent (N) from Special Core Data
8.19 Invaded Zone Water Saturation From Resistivity Logs
8.20 Invaded Zone Water Saturation From Electromagnetic Logs
8.21 Moveable Hydrocarbon Saturation
8.22 Fluid Volume Calculations
8.23 Hydrocarbon Density
8.24 Identifying Fluid Contacts
8.25 Iterative Saturation/Porosity Solutions
8.26 Selection Of Water Saturation Method
8.27 Water Saturation Routines
8.28 Summary Water Saturation Method
8.29 Calibrating Water Saturation to Core and Sample Data
8.30 Resistivity and Saturation in Laminated Shaly Sands
8.31 Water Saturation in Fractured Rocks
8.32 Sensitivity Analysis
8.33 Effect of Pyrite on Saturation
8.34 In Conclusion
8.35 Exercises For Chapter Eight
8.36 Bibliography For Chapter Eight

TABLE 8.01: Summary Water Saturation Method

Click here to go to NEXT CHAPTER


Publication History: Originally published as Chapter Seven of the Log Analysis Handbook, Pennwell 1986. Sections 8.18, 8.24, 8.28, 8.30, and 8.31 added for this electronic edition Feb 2001. Section 8.00 and 8.01 revised Sept 2001. Section 8.29 added Oct 2003. Section 8.33 added Jan 2008.

CHAPTER EIGHT: CALCULATING HYDROCARBON CONTENT

8.00 Introduction to This Chapter
This Chapter provides a few of the many equations available for determining water saturation. As for porosity, these methods correct for the effects of shale. In addition, the material covers hydrocarbon indicators, water resistivity determination, and selection of related parameters.

Water saturation is the ratio of water volume to pore volume. Water bound to the shale is not included, so shale corrections must be performed if shale is present. We calculate water saturation from the effective porosity and the resistivity log. Hydrocarbon saturation is 1 (one) minus the water saturation.

Most oil and gas reservoirs are water wet; water coats the surface of each rock grain. The water is held in place by surface tension. The surface water does not move while the oil or gas is being produced. This situation is shown in Figure 8.00 (left).

FIGURE 8.00: Water wet formation with hydrocarbon before invasion (left) and after invasion (right)

When a reservoir is drilled, some of the fluids near the wellbore are pushed away and the zone is invaded by the drilling fluid. If hydrocarbons were present, the water saturation after invasion will be higher than the original reservoir conditions (Figure 8.00 right). A shallow resistivity log will see the invaded zone water saturation. A deep resistivity log should see the original formation water saturation as long as invasion was not too deep.

Almost all saturation computation methods rely on work originally done by Gus Archie in 1940-41. He found from laboratory studies that, in a shale free, water filled rock, the Formation Factor (F) was a constant defined by:
1: F = R0 / RW

He also found that F varied with porosity:

2: F = A / (PHIt ^ M)

For a tank of water, R0 = RW. Therefore F = 1. Since PHIt = 1, then A must also be 1.0 and M can have any value. If porosity is zero, F is infinite and both A and M can have any value. However, for real rocks, both A and M vary with grain size, sorting, and rock texture. The normal range for A is 0.5 to 1.5 and for M is 1.7 to about 3.2. Archie used A = 1 and M = 2. In fine vuggy rock, M can be as high as 7.0 with a correspondingly low value for A. In fractures, M can be as low as 1.1. Note that R0 is also spelled Ro in the literature.

For shale free rocks with both hydrocarbon and water in the pores, he also defined the term Formation Resistivity Index (I) as:

3: I = Rt / R0
4: Sw = (1 / I) ^ (1 / N)

Archie used an N of 2 and the usual range is from 1.3 to 2.6, depending on rock texture. It is often taken to equal M, but this is not supported by core data in all cases.

Rearrangement of these four equations gives the more usual Archie water saturation:

5: Swa = (A * RW@FT / (PHIe ^ M) / RESD) ^ (1 / N)

True resistivity (Rt) is estimated from the deep resistivity log (RESD) or RESD corrected for borehole effects and invasion (RESDc). RESD can come from many different logging tools, such as the Electrical Survey (64 inch Normal), induction log, laterolog, and all their modern siblings. The actual curve name and abbreviation must be determined from the log heading

Porosity is determined as in Chapter Seven. A, M, and N are called the saturation exponents or the electrical properties of the rock. These are determined from log or core data as described later in Section 8.18. A more thorough explanation of Archie’s Laws is contained in Chapter Eighteen.

Shale corrections are applied by adding a shale conductivity term with an associated shale porosity and shale formation factor relationship. Numerous authors have explored this approach, leading to numerous potential solutions for water saturation, some of which are described in this Chapter.

8.01 Definition of Saturation
Saturation of any given fluid in a pore space is the ratio of the volume of that fluid to the pore space volume. For example, a water saturation of 10% means that 1/10 of the pore space is filled with water; the balance is filled with something else (oil, gas, air, etc. - a pore cannot be “empty”). As for porosity, saturation data is often reported in percentage units but is always a fraction in equations.

Porosity is the capacity of the rock to hold fluids. Saturation is the fraction of this capacity that actually holds any particular fluid. Porosity, hydrocarbon saturation, the thickness of the reservoir rock and the real extent of the reservoir determine the total hydrocarbon volume in place. Hydrocarbon volume, recovery factor, and production rate establish the economic potential of the reservoir.

Irreducible water saturation is the minimum water saturation obtainable in a rock. Water is usually the wetting fluid in oil or gas reservoirs, so a film of water covers each pore surface. The surface area thus defines the irreducible water saturation. Formations at irreducible water saturation cannot produce water until water encroaches into the reservoir after some oil or gas has been withdrawn. Small pores have larger surface area relative to their volume so the irreducible water saturation is higher. If pores are small enough, the irreducible water saturation may be 1.0, leaving no room for oil or gas to accumulate.

Of the total amount of oil or gas present in a reservoir, only a fraction of it can be produced, depending on the recovery efficiency. This recovery factor, normally determined by experience, is typically in the 20% to 50% range for oil, and may be as high as 95% for gas zones, or as low as 5% in heavy oil. Recovery factor can sometimes be estimated from log data by observing the moveable hydrocarbon volume.

Here are the standard definitions needed to understand this Chapter. Note that definitions 1 through 10 are in Chapter Seven.

DFN 11: Total water saturation (SWt) is the ratio of
  - total water volume (BVW + CBW) to
  - total porosity (PHIt)
  1: SWt = (BVW + CBW) / PHIt
DFN 12: Effective water saturation (SWe) is the ratio of:
  - free water volume (BVW) to
  - effective porosity (PHIe)
  2: SWe = BVW / PHIe

This is the standard definition of “water saturation”. Older books use this term to define total water saturation. Since all interpretation methods described here correct for the effects of shale, we are not normally interested in the total water saturation, except as a mathematical by-product. As effective porosity approaches zero, the water saturation approaches one (by edict, if not by calculus)

DFN 13: Useful water saturation (SWuse) is the ratio of:
  - useful water volume (BVW - BVI) to
  - useful porosity (PHIuse)
  3: SWuse = (BVW - BVI) / PHIuse
DFN 14: Irreducible water saturation (SWir) is the ratio of:
  - immobile or irreducible water volume (BVI) to
  - effective porosity (PHIe)
  4: SWir = BVI / PHIe
DFN 15: Residual oil saturation (Sor) is the ratio of:
  - immobile oil volume (BVHr) to
  - effective porosity (PHIe)
  5: Sor = BVHr / PHIe
DFN 16: The water saturation in the flushed zone (Sxo) is the ratio of :
  - free water in the flushed zone, to
  - effective porosity, which is assumed to be the same porosity as in the un-invaded zone.
  6: Sxo = BVWflushed / PHIe

The amount of free water in the invaded zone is usually higher than in the un-invaded zone, when oil or gas is present. Thus Sxo >= Swe. The water saturation in the invaded zone between the flushed and un-invaded zone is seldom used.

DFN 17: Further constraints that should be remembered are:
  7: PHIt >= PHIe >= PHIuse
  8: SWt >= SWe >= SWuse.
  9: PHIt = PHIe when Vsh = 0
  10: SWt = SWe when Vsh = 0

All volumes defined above are in fractional units. In tables or reports, log analysis results are often converted to percentages by multiplying fractional units by 100.

8.02 Visual Overlays of Resistivity and Porosity
The objective of many log analyses is to find the hydrocarbon bearing zones in an oil or gas well. The visual clues to hydrocarbons are often subtle. However, there are some general indicators that may be useful.

In a fairly porous, clean sand or carbonate sequence the hydrocarbon zone may stand out because of its increased resistivity relative to the same zone in another well or a deeper zone which is water bearing. High resistivity with moderate to high porosity is either hydrocarbon or fresh (or brackish) water.

Visual identification of such zones is based on the so called "Mae West" curve shape; that is, the porosity and shale indicators deflect to the left and resistivity deflects to the right. One of the easiest ways to see this effect is to overlay the porosity and resistivity logs on a light-table or a computer screen. In water zones, overlay the porosity and deep resistivity curves so as to track each other. They will have the same general shape and deflect in the same direction throughout all the beds. In a hydrocarbon zone, the resistivity log should deflect to the right when compared to the porosity log, This is shown in Figure 8.01.


FIGURE 8.01: Porosity Resistivity Overlay to locate possible hydrocarbon zones

The overlay approach is less effective in shaly sands, due to the conductivity of the clay minerals. When the zone is shaly, a resistivity log will often track the porosity log whether hydrocarbons are present or not. Figure 8.02 shows a set of logs from two offsetting wells, and it is evident that the curves track each other reasonably well. In addition, there is no obvious "Mae West" effect. It is thus difficult to observe by visual means alone that the well on the left will produce only water, and the well on the right will produce only gas.


FIGURE 8.02: Resistivity Porosity Overlay in shaly sand and fresher water may not be effective

These overlays can be produced on computerized logging trucks or at the computer center. Scales may be in porosity units (compatible scale overlays), or in units of formation factor, usually called Fr/Fs overlays. Another computed product which can be useful is the Rwa log, discussed later in this Chapter.

8.03 Density Neutron Crossover
In gas bearing zones, another indicator of hydrocarbon may be crossover, or at least close proximity of the density and neutron porosity curves. The example in Figure 8.03 is sandstone, and logs are recorded on a sandstone scale. The crossover is very large because the zone is quite porous (30% porosity), and the gas has not been flushed back from the borehole wall. The sonic log also reads too high (equivalent to cross-over) in this case.

FIGURE 8.03: Density Neutron Crossover may show gas

CAUTION: If the logs had been recorded on a limestone scale, there would always be some crossover in a clean sandstone, whether there was gas or not. Conversely, a gas filled limestone will infrequently show crossover if it is recorded on a sandstone scale, but it will (usually) if recorded on a limestone scale. Similarly, a dolomite logged on a limestone scale (a common occurrence) will show no crossover because of the lithology effect. The same well logged on a dolomite scale (not so common) will show crossover if the zone is dolomite and filled with gas, but also if the zone is limestone or sandstone without gas. Care should be taken to account for logging scales and lithology when using the crossover technique.

Because of the large matrix effect due to dolomite, crossover can seldom be seen in dolomitic limestone, dolomitic sandstone, or pure dolomite unless an appropriate scale shift is made to the density and neutron logs. In the absence of a computer, this may be accomplished by overlaying the density and neutron curves in known oil or water zones, and looking for crossover that might indicate gas or limestone above or below the water or oil zones.

8.04 Other Indicators of Hydrocarbons
Even with such aids, it is obvious that hydrocarbon zones can be missed by a visual interpretation of the logs. Only the most obvious hydrocarbon zones will stand out and it is often necessary to compute log analyses for all the zones in a well, and possibly from other adjacent wells, in order to sort out those zones which are likely to be hydrocarbon bearing and those that are not.

Other indicators of hydrocarbons such as gas or oil in the mud, a gas or mud log at the well site with shows of oil and gas, drill stem test results, production from offset wells, and sample or core staining or fluorescence, are often relied upon to narrow down the possible zones which may contain hydrocarbons. All the data in the well history is therefore very important to the log analyst.

Sonic log skipping may be an indicator of gas in the formation or in the mud, or a fractured formation, but may be due only to poor logging instruments or poor quality control. It is hoped that logs are run to minimize skipping and the log analyst should not rely on the presence of skips to indicate gas.

8.05 Calculating Environmental Corrections for Resistivity Logs
Water saturation calculations require a good value for formation resistivity, commonly called true resistivity or Rt, as well as shale corrected porosity and the shale content. Therefore, the resistivity log may need some environmental corrections before use in the saturation equations.

Borehole corrections for mud salinity and hole diameter should be applied first, if needed. Most computer aided log analysis software has this capability. Fortunately, borehole corrections can often be safely ignored when the log is run in a good borehole with a good mud system. The newest array induction logs attempt to produce Rt with all corrections applied. Do not over correct your data.

1. Borehole Environment Corrections to Resistivity

For those who insist on superfluous detail, formulae are provided here for the deep induction log (Figure 8.04) for no standoff and in Figure 8.05 for 1.5 inches standoff (the usual case).


FIGURE 8.04: Borehole correction for deep induction - standoff = 0.0 inches


FIGURE 8.05: Borehole correction for deep induction - standoff = 1.5 inches

Note that the abbreviations shown above are those used in this FORTRAN program and do not conform to abbreviations used in this book. Hole size is in inches and correction to the code for metric dimensions is required. Charts for these formulae are given in Figures 8.06 to 8.10 for various tool types.


FIGURE 8.06: Borehole correction for medium induction log


FIGURE 8.07: Borehole correction for deep induction log


FIGURE 8.08: Borehole correction for deep laterolog (dual)


FIGURE 8.09: Borehole correction for shallow laterolog (dual)


FIGURE 8.10: Borehole correction for laterolog (single)

It is instructive to determine the borehole corrections for some typical cases and run a sensitivity study with one of the saturation equations to see if the corrections have a measurable impact.

NAME: RESDc1 - Induction Log Borehole Corrections

The borehole signal for induction logs is subtracted from the induction conductivity measurement and reciprocated to obtain corrected resistivity.
1: RESDc = 1000 / (1000 / RESD - BHGD)
2: RESMc = 1000 / (1000 / RESM - BHGM)

WHERE:
BHGD = deep resistivity correction (mS/m)
BHGM = medium resistivity correction (mS/m)
RESD = deep resistivity reading (ohm-m)
RESDc = deep resistivity corrected for borehole effect (ohm-m)
RESM = medium resistivity reading (ohm-m)
RESMc = medium resistivity corrected for borehole (ohm-m)

COMMENTS:
The values for BHGD and BHGM are to be taken from Figure 8.06 and 8.07, or from curve fits to these charts. Some computer programs use a look-up table. These charts are for Schlumberger’s 6FF40 tool. Different charts and look-up tables are needed for other induction logging tool designs.

NAME: RESDc2 - Laterolog Borehole Corrections

The borehole correction for laterologs is a correction factor which is divided into the original log reading to obtain the corrected value.
1: RESDc = RESD / CFD
2: RESMc = RESM / CFM
3: RESEDITFLAG$ = "BH"

WHERE:
CFD = borehole effect correction factor for deep laterolog
CFM = borehole effect correction factor for shallow laterolog
RESD = deep resistivity reading (ohm-m)
RESDc = deep resistivity corrected for borehole effect (ohm-m)
RESM = medium resistivity reading (ohm-m)
RESMc = medium resistivity corrected for borehole (ohm-m)

COMMENTS:
The values for CFD and CFM are to be taken from Figure 8.08 and 8.09, or from curve fits to these charts. Some computer programs use a look-up table. These charts are for Schlumberger’s DLL tool. Different charts and look-up tables are needed for other laterolog tool designs.

2. Invasion Corrections

The second correction is for the effects of invasion of mud filtrate into the formation. Knowledge of the invasion profile can be used to correct the deep resistivity log for this effect. The profile knowledge comes from the medium and shallow resistivity data when compared to the deep resistivity.

NAME: RESDc3 - Invasion Correction for Induction Logs

The invasion corrections for dual induction logs are computed as follows:
1: IF RESD < RESM
2: AND IF RESM < RESS
3: THEN H = RESS / RESD - 1
4: B = RESM / RESD - 1
5: C = H / B
6: D = 0.59 * H - 2.21 * C + 1.35
7: E = -1.44 * H + 2.47 * C - 2.76
8: G = - 0.5 * (D ^ 2 - 4 * E) ^ 0.5 + D)
9: IF RESD >= RESM
10: OR IF RESM >= RESS
11: THEN G = 1.0
12: RESDc = G * RESD

WHERE:
B = intermediate term
C = intermediate term
D = intermediate term
E = intermediate term
G = intermediate term
H = intermediate term
RESD = deep resistivity log reading (ohm-m)
RESDc = deep resistivity log reading corrected for invasion (ohm-m)
RESM = medium resistivity log reading (ohm-m)
RESS = shallow resistivity log reading (ohm-m)

COMMENTS:
If the medium and deep resistivity logs read the same value, then either no correction is needed because invasion is very shallow, or no correction is possible because invasion is extremely deep. These formulae are shown graphically in Figure 8.11. Newer tools need different charts.

RESDc is often called Rt, the "true" resistivity - see warning below Figure 8.11.


FIGURE 8.11: Invasion correction for dual induction

CRAIN'S OPINIONATED OPINION
CAUTION: The invasion correction for induction logs as defined by service company charts always reduces Rt. This is fine in a water zone but is dead wrong in oil or gas zones, where Rt is usualy too low due to invasion of water. Lowering it even more is just too dumb for words. Therefore, DO NOT apply invasion corrections from these charts in hydrocarbon zones. Most software allows you to turn off these offensive corrections.

Below is a sample sensitivity analysis that shows the correction factor Rt/RESD is greater than 1.0 for many real situations. The same factor (Rt/Rild) on Figure 8.11 is never greater than 1.0.

SENSITIVITY ANALYSIS

WATER SATURATION AND RESISTIVITY WITH INVASION

Archie's Equation

 

Sw = (A * RW@FT / (PHIe ^ M) / Rt) ^ (1 / N)

   

Assume A=1.0, M = N = 2.0

  Sw = (RW@FT / (PHIe ^ 2) / Rt) ^ 0.5
   

Rearrange terms

 

Sw^2 = (RW@FT / (PHIe ^ 2) / Rt)

   

Solve for Rt in uninvaded oil zone

  Rt= (RW@FT / (PHIe ^ 2) / Sw^2)
   

Solve for Rxo in invaded oil zone

  Rxo= (RMF@FT / (PHIe ^ 2) / Sxo^2)
   
Solve for R0 in uninvaded water zone
  R0= (RW@FT / (PHIe ^ 2)
   

Assume RESD gets 50% of signal from invaded zone and 50% from uninvaded zone

 

RESD = 1 / ((1 / Rt + 1 / Rxo) / 2)

   
Solve for SWa in invaded oil or water zone
  Swa = (RW@FT / (PHIe ^ 2) / RESD) ^ 0.5
   

Multiply deep resistivity (RESD) by Rt/RESD ratio to obtain Rt from RESD


INVADED OIL ZONE Sw=0.25 RMF@FT=1.000  

Sxo=0.6

Sxo=0.8 Sxo=1.0 Sw=1.0
                     
RW@FT PHIe Rt Rxo R0 RESD SWa Rt/RESD Rt/RESD Rt/RESD Rt/RESD
0.25 0.25 64.0 44.4 4.0 52.5 0.28 1.22 1.78 2.50 0.63
0.25 0.15 177.8 123.5 11.1 145.7 0.28 1.22 1.78 2.50 0.63
0.10 0.25 25.6 44.4 1.6 32.5 0.22 0.79 1.01 1.30 0.55
0.10 0.15 71.1 123.5 4.4 90.2 0.22 0.79 1.01 1.30 0.55
0.03 0.25 7.7 44.4 0.5 13.1 0.19 0.59 0.65 0.74 0.52
0.03 0.15 21.3 123.5 1.3 36.4 0.19 0.59 0.65 0.74 0.52

INVADED OIL ZONE Sw=0.25 RMF@FT=0.50   Sxo=0.6 Sxo=0.8 Sxo=1.0 Sw=1.0
                     
RW@FT PHIe Rt Rxo R0 RESD SWa Rt/RESD Rt/RESD Rt/RESD Rt/RESD
0.25 0.25 64.0 22.2 4.0 33.0 0.35 1.94 3.06 4.50 0.75
0.25 0.15 177.8 61.7 11.1 91.6 0.35 1.94 3.06 4.50 0.75
0.10 0.25 25.6 22.2 1.6 23.8 0.26 1.08 1.52 2.10 0.60
0.10 0.15 71.1 61.7 4.4 66.1 0.26 1.08 1.52 2.10 0.60
0.03 0.25 7.7 22.2 0.5 11.4 0.21 0.67 0.81 0.98 0.53
0.03 0.15 21.3 61.7 1.3 31.7 0.21 0.67 0.81 0.98 0.56

INVADED OIL ZONE Sw=0.25 RMF@FT=0.25 RMF@FT   Sxo=0.6 Sxo=0.8 Sxo=1.0 Sw=1.0
                     
RW@FT PHIe Rt Rxo R0 RESD SWa Rt/RESD Rt/RESD Rt/RESD Rt/RESD
0.25 0.25 64.0 11.1 4.0 18.9 0.46 3.38 5.62 8.50 1.00
0.25 0.15 177.8 30.9 11.1 52.6 0.46 3.38 5.62 8.50 1.00
0.10 0.25 25.6 11.1 1.6 15.5 0.32 1.65 2.55 3.70 0.70
0.10 0.15 71.1 30.9 4.4 43.0 0.32 1.65 2.55 3.70 0.70
0.03 0.25 7.7 11.1 0.5 9.1 0.23 0.85 1.11 1.46 0.56
0.03 0.15 21.3 30.9 1.3 25.2 0.23 0.85 1.11 1.46 0.56

INVADED OIL ZONE Sw=0.25 RMF@FT=0.10 RMF@FT   Sxo=0.6 Sxo=0.8 Sxo=1.0 Sw=1.0
                     
RW@FT PHIe Rt Rxo R0 RESD SWa Rt/RESD Rt/RESD Rt/RESD Rt/RESD
0.25 0.25 64.0 4.4 4.0 8.3 0.69 7.70 13.30 20.5 1.75
0.25 0.15 177.8 12.3 11.1 23.1 0.69 7.70 13.30 20.5 1.75
0.10 0.25 25.6 4.4 1.6 7.6 0.46 3.38 5.62 8.50 1.00
0.10 0.15 71.1 12.3 4.4 21.0 0.46 3.38 5.62 8.50 1.00
0.03 0.25 7.7 4.4 0.5 5.6 0.29 1.36 2.04 2.90 0.65
0.03 0.15 21.3 12.3 1.3 15.6 0.29 1.36 2.04 2.90 0.65
 

NUMERICAL EXAMPLE:
1. For example, the data for Sand D gives:
RESS = 2.0
RESM = 1.5
RESD = 1.0
H = 2.0 / 1.0 - 1 = 1.0
B = 1.5 / 1.0 - 1 = 0.5
C = 1.0 / 0.5 = 2.0
D = 0.59 * 1.0 - 2.21 * 2.0 + 1.35 = -2.48
G = - 0.5 * (2.48 ^ 2 - 4 * 0.74) ^ 0.5) - 2.48) = 0.35
RESDc = 0.35 * 1.0 = 0.35

Thus, invasion is so deep that the dual induction reads nearly three times too high. If this is a water zone, the correction is reasonable. If it is hydrocarbon bearing, the correction makes no sense.

NAME: RESDc4 - Invasion Correction for Laterologs

The invasion corrections for dual laterologs are computed as follows:
1: IF RESD / RESS <= 1
2: THEN RESDc = 1.7 * RESD - 0.7 * RESM
3: IF RESD / RESM >= 1.1
4: THEN RESDc = 1.1 * RESD
5: C = RESM / RESS * (RESD - RESS) / (RESD - RESM)
6: IF C = 1 / 1.7
7: THEN RESDc = RESD
8: IF C # 1 / 1.78
9: THEN RESDc = 2.18 * C * RESD / (1.78 * C - 1)
10: OTHERWISE RESDc = RESD

WHERE:
C = intermediate term
RESD = deep resistivity log reading (ohm-m)
RESDc = deep resistivity log reading corrected for invasion (ohm-m)
RESM = medium resistivity log reading (ohm-m)
RESS = shallow resistivity log reading (ohm-m)

COMMENTS:
If the medium and deep resistivity logs read the same value, then either no correction is needed because invasion is very shallow, or no correction is possible because invasion is extremely deep. These formulae are shown graphically in Figure 8.12. Newer tools need different charts.


FIGURE 8.12: Invasion correction for dual laterolog

This chart can raise or lower the Rt. Use the correction only if the correction raises Rt. The reader is encouraged to run a sensitivity analysis, similar to the one shown earlier for induction logs, for the laterolog in a salt mud case and a fresh mud case.

NUMERICAL EXAMPLE:
1. Assume a dual laterolog had been run, the log might have read:
RESD = 2.0
RESM = 1.5
RESS = 1.0
C = 1.5 / 1.0 * (2.0 - 1.0) / (2.0 - 1.5) = 3.00
RESDc = 2.18 * 3.00 * 2.0 / (1.78 * 3.00 - 1) = 3.00

8.06 Calculating Diameter of Invasion
The invasion correction described above can also be used to calculate an apparent invasion diameter (Di). The formulae are:

NAME: Di - Diameter of Invasion

1: IF RESTYPE$ = "DIL"
2: THEN C = (RESM / RESDc) * (RESD - RESDc) / (RESM - RESD)
3: AND Di = 33 * (C + 1) - min (100, 10 ^ (0.5 * C - 0.04))
* (1 + 24.4 * (IF DEPTHUNIT$ = "METRIC"))
4: IF RESTYPE$ = "DLL"
5: AND IF RESDc / RESD > 1
6: THEN Di = 10 ^ (RESDc / RESD - 1) * (1 + 24.4 * (IF DEPTHUNIT$ = "METRIC"))
7: IF RESTYPE$ = "DLL"
8: AND IF RESDc / RESD < 1
9: THEN Di = 160 * (1 - RESD / RESDc) * (1 + 24.4 * (IF DEPTHUNIT$ = "METRIC"))
10: OTHERWISE Di = 0.0

WHERE:
Di = diameter of invasion (inches or mm)
RESD = deep resistivity log reading (ohm-m)
RESDc = corrected deep resistivity reading (ohm-m)
RESM = medium resistivity log reading (ohm-m)

COMMENTS:
If RESDc / RESD = 1; Di cannot be determined.

Solutions to these formulae are also shown in Figure 8.11 and 8.12. While diameter of invasion is not used to correct other data, it is a useful quality control indicator.

NUMERICAL EXAMPLE:
1. Data for Sand D gives:
RESS = 2.0
RESM = 1.5
RESD = 1.0
RESDc = 0.35 from previous example

C = (1.5 / 0.35) * (1.0 - 0.35) / (1.5 - 1.0) = 5.57
Di = 33 * (5.57 + 1) - min (100, 10 ^ (0.5 * 5.57 - 0.04)) = 116 inches

8.07 Formation Water Resistivity
Most methods for computing water saturation require knowledge of formation water resistivity at the formation temperature (RW@FT). There are four major sources of this data.

l. Drill stem test recoveries of water in your well or nearby wells, analyzed for chemical content and water resistivity in the laboratory.

2. The water catalogue published by your local well logging society or similar catalogues created by searching in-house data bases.

3. Back calculation of RW@FT from log data in a clean (non shaly) zone - usually called the Rwa method, or the water zone (Ro) method.

4. Calculation from knowledge of the SP value in a clean zone.

A sample of the type of data found in a water catalogue is shown in Figure 8.13. Note that data is tabulated and also posted on a map, and is based on a standard temperature of 25 degrees Celcius (77 degrees Fahrenheit). Thus, catalogue or DST values must be converted to an equivalent value at the formation temperature.


FIGURE 8.13: Water resistivity catalog

The following relationships are needed to manipulate water resistivity data prior to calculations of water saturation.

NAME - RW@FT1 - Water Resistivity at Formation Temperature

1: FT = SUFT + (BHT - SUFT) / BHTDEP * DEPTH
2: C = 6.8 + 14.7 * (IF DEPTHUNIT$ = "METRIC")
3: RW@FT = RW@SUFT * (SUFT + C) / (FT + C)
4: RMF@FT = RMF@SUFT * (SUFT + C) / (FT + C)
5: RMC@FT = RMC@SUFT + (SUFT * C) / (FT + C)

WHERE:
BHT = bottom hole temperature (degrees Fahrenheit or Celcius)
BHTDEP = depth at which BHT was measured (feet or meters)
C = temperature offset (degrees Fahrenheit or Celcius)
FT = formation temperature (degrees Fahrenheit or Celcius)
RMC@FT = mud cake resistivity at formation temperature (ohm-m)
RMC@SUFT = mud cake resistivity at surface temperature (ohm-m)
RMF@FT = mud filtrate resistivity at formation temperature (ohm-m)
RMF@SUFT = mud filtrate resistivity at surface temperature (ohm-m)
RW@FT = water resistivity at formation temperatures (ohm-m)
RW@SUFT = water resistivity at surface temperature (ohm-m)
SUFT = surface temperature (degrees Fahrenheit or Celcius)

COMMENTS:
Use this relation when RW@SUFT is known from measured data. This transformation can be made on the chart in Figure 8.14. Typical Temperature gradients are shown in Figure 8.15.


FIGURE 8.14: Water resistivity - Temperature - Salinity relationships


FIGURE 8.15: Typical Depth - Temperature profiles

 

NUMERICAL EXAMPLE:
1. Water resistivity at formation temperature.
English units example:
RW@FT = (0.32 ohm-m @ 77'F) * (77 + 6.8) / (102 + 6.8) = 0.25 ohm @ 102'F

Metric units example:
RW@FT = (0.32 ohm-m @ 25'C) * (25 + 21.5) / (39 + 21.5) = 0.25 ohm-m @ 39'C

NAME: RW@FT2 - Water Resistivity from Salinity

1: FT1 = SUFT + (BHT - SUFT) / BHTDEP * DEPTH)
2: IF LOGUNITS$ = "METRIC"
3: THEN FT1 = 9 / 5 * FT1 + 32
4: RW@FT = (400000 / FT1 / WS) ^ 0.88

WHERE:
BHT = bottom hole temperature (degrees Fahrenheit or Celcius)
BHTDEP = depth at which BHT was measured (feet or meters)
FT1 = formation temperature (degrees Fahrenheit or Celcius)
RW@FT = water resistivity at formation temperatures (ohm-m)
SUFT = surface temperature (degrees Fahrenheit or Celcius)
WS = water salinity (ppm NcCl)

COMMENTS:
Use this relation if salinity is known from laboratory measurements. Figure 8.14 also solves this equation.

NUMERICAL EXAMPLE:
1. Salinity to water resistivity.
RW@FT = (400000 / 102'F / 200,000 ppm) ^ 0.88 = 0.031 ohm-m @ 102'F
(rounded to three significant digits)

2. Water resistivity to salinity.
WS = 400,000 / 102'F / ((0.250 ohm-m) ^ 1.14) = 19,000 ppm NaCl
(rounded to three significant digits)

NAME: WSa - Water salinity from chloride content:

1: WSa = Cc1 * 1.645

WHERE:
Ccl = water salinity (ppm Cl)
WSa = water salinity (ppm NaCl)

COMMENTS:
Use this relationship when chloride content of the water sample is known.