Professional Documents
Culture Documents
CONTENTS
1
POROSITY DETERMINATION IN
COMPLEX CONDITIONS
NEUTRON-DENSITY CROSSPLOTS
SONIC-DESITY CROSSPLOTS
SONIC-NEUTRON CROSSPLOTS
DENSITY-PHOTOELECTRIC CROSS
SECTION CROSSPLOTS
NGS CROSSPLOTS
10
EFFECT OF HYDROCARBONS ON
CROSSPLOTS
11
M-N PLOT
12
MID PLOT
13
1
LEARNING OBJECTIVES
Having worked through this chapter the Student will be able to:
1.
2.
3.
Describe the technique and the assumptions used for deriving porosity from
a neutron-density crossplot.
4.
Describe the technique and the assumptions used for deriving porosity from
a sonic-density crossplot.
5.
Describe the technique and the assumptions used for deriving porosity from
a sonic-neutron crossplot.
6.
Describe the technique and the assumptions used for deriving porosity
from a density-Pe crossplot.
7.
Describe the technique and the assumptions used for deriving minerals
from an NGS crossplot.
8.
9.
Describe the technique and the assumptions used for deriving minerals
from an M-N plot.
10. Describe the technique and the assumptions used for deriving minerals
from a MID plot.
1
in porosity units, or a single mineral point (e.g., salt point) may be defined. This
chart is entered with porosities computed as if the matrix had the same properties as
water-saturated limestone; as a result, the limestone line is the straight line of equal
density and neutron porosities.
When the matrix lithology is a binary mixture (e.g., sandstone-lime or lime-dolomite
or sandstone-dolomite) the point plotted from the log readings will fall between
the corresponding lithology lines.
2 NEUTRON-DENSITY CROSSPLOTS
Charts CP-1a and -1b are for SNP neutron versus density data. These charts were
constructed for clean, liquid-saturated formations and boreholes filled with water or
water-base mud. The charts should not be used for air-gas-filled boreholes; in these,
the SNP matrix effect is changed. Charts CP-1c and -1d are similar plots for CNL*
neutron versus density data.
The separations between the quartz, limestone, and dolomite lines indicate good
resolution for these lithologies. Also, the most common evaporites (rock salt,
anhydrite) are easily identified.
In the example shown on Figure 1, Dis = 15 and Nls = 21. This defines Point P,
lying between the limestone and dolomite curves and falling near a line connecting
the 18% porosity graduations on the two curves. Assuming a matrix of limestone
and dolomite and proportioning the distance between the two curves, the point
corresponds to a volumetric proportion of about 40% dolomite and 60% limestone;
porosity is 18%.
Figure 1
Porosity and lithology
determination from FDC
density and CNL neutron
logs in water-filled holes.
4
An error in choosing the matrix pair does not result in large error in the porosity value
found, as long as the choice is restricted to quartz (sandstone or chert), limestone,
dolomite, and anhydrite; shaliness and gypsum are excluded. For instance, in the
above example, if the lithology were sandstone and dolomite instead of limestone
and dolomite, the porosity found would be 18.3%; the mineral proportions would,
however, be about 40% sandstone and 60% dolomite.
In fact, the plotted Point P of Figure 1 could correspond to various mixtures of
sandstone, limestone, and dolomite. In all cases, the porosity would be in the
18% range. Thus, although the rock volumetric fractions estimated from the
neutron-density data could be considerably in error, the porosity value will always
be essentially correct if only sandstone, limestone, and/or dolomite are present. This
feature of the neutron-density combination, coupled with its use as a gas-finder, has
made it a very popular log combination.
3 SONIC-DENSITY CROSSPLOT
Crossplots of sonic t versus density b or D have poor porosity and reservoir rock
(sandstone, limestone, dolomite) resolution, but they are quite useful for determining
some evaporite minerals. As can be seen from Figure 2 (Chart CP-7), an error in
the choice of the lithology pair from the sandstone-limestone-dolomite group can
result in an appreciable error in porosity. Likewise, a small error in the measurement
of either transit time or bulk density can result in an appreciable error in porosity
and lithology analysis. The good resolution given by the chart for salt, gypsum, and
anhydrite is shown by the wide separation of the corresponding mineral points on
the figure. Several log-data points are shown that correspond to various mixtures of
anhydrite and salt and, perhaps, dolomite.
Figure 2
Porosity and lithology
determination from FDC
density and sonic logs.
4 SONIC-NEUTRON CROSSPLOTS
Chart CP-2a is a plot of sonic t versus porosity from an SNP log. As with
the density-neutron plots, resolution between sandstone, limestone, and dolomite
lithologies is good, and errors in choosing the lithology pair will have only a
small effect on the porosity value found. However, resolution is lost if evaporites
are present. Chart CP-2b is a similar plot of sonic t versus porosity from
the CNL log.
The sonic crossplots (Charts CP-2 and -7) are constructed for both the weightedaverage (Wyllie) and the observed (Raymer, Hunt, and Gardner) sonic transit time-toporosity transforms. Chart CP-2b is shown in Figure 3. For mineral identification
and porosity determination, use the transform previous experience has shown most
appropriate for the area.
Figure 3
Porosity and lithology
determination from sonic
log and CNL*
If one knows which pair of minerals is present in the matrix and the b-N porosity
is less than the b-Pe porosity, the presence of gas may be suspected. The location
of the log point on the porosity rib of the b-Pe plot permits the computation
of the matrix density (mixture of two minerals in known proportions). If maa
(from the b-N plot) is less than maa (from the b - Pe plot), the presence
of gas is confirmed.
6 NGS CROSSPLOTS
Because some minerals have characteristic concentrations of thorium, uranium, and
potassium, the NGS log can be used to identify minerals or mineral type. Chart
CP-19 compares potassium content with thorium content for several minerals; it can
be used for mineral identification by taking values directly from the recorded NGS
curves. Usually, the result is ambiguous and other data are needed. In particular, Pe
is used with the ratios of the radioactive families: Th/K, U/K, and Th/U. Use care
when working with these ratios because they are not the ratios of the elements within
the formation but rather the ratios of the values recorded on the NGS log, ignoring the
units of measurement. Charts have been constructed that allow Pe to be compared
with either the potassium content, Figure 5 (upper part of Chart CP-18), or the ratio
of potassium to thorium, Figure 6 (lower part of Chart CP-18).
Figure 4
Porosity and lithology
determination from LithoDensity* log; fresh water,
liquid-filled holes, f =
1.0.
Figure 5
Mineral identification from
Litho-Density log and natural gamma ray spectrometry log.
Figure 6
Mineral identification from
Litho-Density log and natural gamma ray spectrometry log.
High uranium concentrations in a shale suggest that the shale is a source rock. In
igneous rocks the relative proportions of the three radioactive families are a guide to
the type of rock, and the ratios Th/K and Th/U are particularly significant.
The radioactive minerals found in a formation are, to some extent, dependent on
the mode of sedimentation. The mode of transportation and degree of reworking and
Institute of Petroleum Engineering, Heriot-Watt University
1
alteration are also factors. As an example, because thorium has a very low solubility,
it has limited mobility and tends to accumulate with the heavy minerals. On the
other hand, uranium has a greater solubility and mobility, and so high uranium
concentrations are found in fault planes, fractures, and formations where water flow
has occurred. Similarly, high concentrations can build up in the permeable beds
and on the tubing and casing of producing oil wells. Chemical marine deposits
are characterised by their extremely low radioactive content, with none of the three
families making any significant contribution. Weathered zones are often indicated
by pronounced changes in the thorium and potassium content of the formation but
a more or less constant Th/K ratio.
10
Equation 1
Secondary porosity index
Figure 7
Effect of hydrocarbon.
Arrow B-A represents correction of log Point B
for hydrocarbon effect for
a gas case. The arrows
at lower right represent
approximate hydrocarbon
shifts for various values of
for f Shr = 0.15, Pmf =
h
0, and mf = 1.
Arrow B-A on Figure 7 illustrates the correction for this hydrocarbon shift. Log
Point B is for a clean limestone containing gas of density 0.1 g/cm3. Corrected Point
A falls near the limestone line, and porosity can be read directly.
Equation 2
Hydrocarbon shift (b)h
Equation 3
Hydrocarbon shift (N)h
(b)h = - AShr
(N)h = - BShr - Nex,
Equation 4
B = 1
h + 0.30
mf (1 Pmf )
11
1
A = (1.19 - 0.16 Pmf) mf - 1.33h
and
B = 1
2.2 h
,
mf (1 Pmf )
Equation 5
where
Shr
h
mf
Pmf
=
=
=
=
The arrows at the lower right of Figure 7 show, for various hydrocarbon densities, the
approximate magnitudes and directions of the hydrocarbon shifts as computed from
the above relations for Shr = 15%. (Fresh mud filtrate was assumed and excavation effect was neglected.) This value of Shr could occur in a gas sand (e.g.,
= 20%, Shr = 75%).
Gas will also shift the points on a sonic-neutron plot as a result of the decrease in
N. Similarly, gas will shift points on a sonic-density plot as a result of the increase
in D because of the presence of gas. In uncompacted formations, the sonic t
reading may also be increased by the effect of the gas.
Hydrocarbon shifts in oil-bearing formations are usually negligible; for clean
formations, porosities can be read directly from the porosity graduations on
the chart.
11 M-N PLOT
In more complex mineral mixtures, lithology interpretation is facilitated by use of
the M-N plot. These plots combine the data of all three porosity logs to provide
the lithology-dependent quantities M and N. M and N are simply the slopes of the
individual lithology lines on the sonic-density and density neutron crossplot charts,
respectively. Thus, M and N are essentially independent of porosity, and a crossplot
provides lithology identification.
M and N are defined as:
M =
N =
tf t
x 0.01
b f
Nf N
.
b f
Equation 6
Equation 7
porosity units. The multiplier 0.01 is used to make the M values compatible for easy
scaling.
If the matrix parameters (tma, ma, Nma) for a given mineral are used in Equations 6
and 7 in place of the log values, the M and N values for that mineral are defined. For
water-bearing formations, these will plot at definitive points on the M-N plot. Based
on the matrix and fluid parameters listed in Table 1, M and N values are shown in
Table 2 for several minerals in both fresh mud- and salt mud-filled holes. (N is
computed for the CNL log.)
Points for a mixture of three minerals will plot within the triangle formed by connecting the three respective single-mineral points. For example, suppose a rock mixture
exhibits N = 0.59 and M = 0.81. In Figure 8 this point falls within a triangle defined
by the limestone-dolomite-quartz points. It would therefore be interpreted in most
cases as representing a mixture of limestone, dolomite, and quartz. However, it could
also be a limestone-quartz-gypsum mixture, since the point is also contained in those
triangles. The combination selected would depend on the geological probability of
its occurrence in the formation.
Secondary porosity, shaliness, and gas-filled porosity will shift the position of the
points with respect to their true lithology, and they can even cause the M-N points
to plot outside the triangular area defined by the primary mineral constituents. The
arrows on Figure 8 indicate the direction a point is shifted by the presence of each.
In the case of shale, the arrow is illustrative only since the position of the shale point
will vary with area and formation.
In combination with the crossplots using other pairs of porosity logs and
lithology-sensitive measurements, the M-N plot aids in the choice of the probable
lithology. This information is needed in the final solution for porosity and
lithology fractions.
13
14
Mineral
Mineral
tma
tma
mama
maSNP
maSNP
maCNL
maCNL
Sandstone
Sandstone
1 1
(Vma
= 18,000)
(Vma
= 18,000)
> 10%
f > f10%
55.5
55.5
2.65
2.65
-0.035*
-0.035*
-0.05*
-0.05*
Sandstone
Sandstone
2 2
(Vma
= 19,500)
(Vma
= 19,500)
> 10%
f > f10%
51.2
51.2
2.65
2.65
-0.035*
-0.035*
-0.05*
-0.05*
Limestone
Limestone
47.5
47.5
2.71
2.71
0.00
0.00
0.00
0.00
Dolomite
43.5
Dolomite
1 1
43.5
= 5.5%
to 30%)
(f =(f5.5%
to 30%)
2.87
2.87
0.02*
0.02*
0.065*
0.065*
Dolomite
43.5
Dolomite
2 2
43.5
= 1.5%
to 5.5%
(f =(f1.5%
to 5.5%
> 30%)
& >&30%)
2.87
2.87
0.02*
0.02*
0.065*
0.065*
Dolomite
43.5
Dolomite
3 3
43.5
= 0.0%
to 1.5%)
(f =(f0.0%
to 1.5%)
2.87
2.87
0.005*
0.005*
0.04*
0.04*
Anhydrite
Anhydrite
50.0
50.0
2.98
2.98
-0.005*
-0.005*
-0.0020
-0.0020
Gypsum
Gypsum
52.0
52.0
2.35
2.35
0.49**
0.49**
Salt
Salt
67.0
67.0
2.03
2.03
0.04
0.04
-0.01
-0.01
Fluids
Fluids
tf tf
f f
fNfN
Primary
Porosity
Primary
Porosity
(Liquid
- Filled):
Fresh
mud
(Liquid
- Filled):
Fresh
mud
Salt
mud
Salt mud
189.0
189.0
185.0
185.0
1.00
1.00
1.10
1.10
1 1
Secondary
Porosity
Secondary
Porosity
(In
Dolomite):
Fresh
mud
(In Dolomite): Fresh
mud
Salt
mud
Salt
mud
43.5
43.5
1.00
1.00
1.10
1.10
1 1
Limestone):
Fresh
mud
(In (In
Limestone):
Fresh
mud
Salt
mud
Salt mud
47.5
47.5
1.00
1.00
1.10
1.10
1 1
Sandstone):
Fresh
mud
(In (In
Sandstone):
Fresh
mud
Salt
mud
Salt mud
55.5
55.5
1.00
1.00
1.10
1.10
1 1
Table 1a
Matrix and fluid coefficients of several minerals
and types of porosity (liquid-filled boreholes).
Table 1b
Matrix and fluid coefficients of several minerals
and types of porosity (liquid-filled boreholes).
Figure 8
M-Nplot showing the
points for several singlemineral formations. This
plot is a simplified version
of Chart CP-8.
12 MID PLOT
Indications of lithology, gas, and secondary porosity can also be obtained using the
matrix identification (MID) plot (Chart CP-15).
To use the MID plot, three data are required. First, apparent total porosity, ta, must be
determined using the appropriate neutron-density (Chart CP-1a or CP-1b depending
upon whether it is fresh or salt water) and empirical (red curves) neutron-sonic crossplots (Charts CP-2a). For data plotting above the sandstone curve on these charts,
the apparent total porosity is defined by a vertical projection to the sandstone curve.
Equation 8
Apparent grain density
Next, an apparent matrix transit time, tmaa and an apparent grain density, maa,
are calculated:
maa =
b ta f
1 - ta
Equation 9
Apparent matrix transit
time
tmaa =
Equation 10
Apparent matrix transit
time (field observed)
tmaa = t -
t - ta t f
time- average relationship
1 - ta
tat
field- observed relationship
c
15
1
where,
b is bulk density from density log,
t is interval transit time from sonic log,
f is pore fluid density,
tf is pore fluid transit time,
ta is apparent total porosity,
and
c is a constant (c approx. = 0.68)
The apparent total porosity is not necessarily the same in the equations. For use in the
tmaa equations (Equations 9 and 10), it is the value obtained from the neutron-density
crossplot (Chart CP-1a or CP-1b).
Chart CP-14 (Figure 9) can be used to solve graphically for maa (Equation 8)
and for tmaa using the empirical field-observed transit time-to-porosity relationship
(Equation 10). The north-east half (upper right) of the chart solves for the apparent
matrix interval transit time, tmaa. The south-west half (lower left of the same chart)
solves for the apparent matrix grain density, maa.
Figure 9
Determination of apparent
matrix parameters from
bulk density or interval
transit time and apparent
total porosity;
fluid density = 1.
The crossplot of the apparent matrix interval transit time and apparent grain density on
the MID plot will identify the rock mineralogy by its proximity to the labelled points
on the plot. On Chart CP-15 the most common matrix minerals (quartz, calcite,
dolomite, anhydrite) plot at the positions shown (Figure 10). Mineral mixtures would
plot at locations between the corresponding pure mineral points. Lithology trends
may be seen by plotting many levels over a zone and observing how they are grouped
on the chart with respect to the mineral points.
The presence of gas shifts the plotted points to the north-east on the MID plot. Secondary
porosity shifts points in the direction of decreased tmaa; i.e., to the left. For the SNP
log, shales tend to plot in the region to the right of anhydrite on the MID plot. For
the CNL log, shales tend to plot in the region above the anhydrite point.
16
Sulfur plots off the chart to the north-east at tmaa approx. = 122 and maa approx.
= 2.02. Thus, the direction to the sulfur point from the quartz, calcite, dolomite,
anhydrite group is approximately the same as the direction of the gas-effect shift.
Gypsum plots to the south-west.
The concept of the MID plot is similar to that of the M-N plot. However, instead of
having to compute values of M and N, values of maa and tmaa are obtained from charts
(Chart CP-14). For most accurate results, lot readings should, of course, be depth
matched and corrected for hole effect, etc. The need for such corrections can often
be seen from the trend of the plotted points on the MID plot (Figure 10).
Figure 10
Matrix identification (MID)
Plot
17
1
Umaa =
Pe e - ta U f
1 - ta
Equation 11
Apparent matrix volumetric cross section
where
Pe is photoelectric absorption cross section index,
e is electron density ,
a is apparent total porosity.
The apparent total porosity can be estimated from the density-neutron crossplot
if the formation is liquid filled.
Chart CP-20 solves Equation 11 graphically. A simplified version is shown in Figure 11.
Table 3 lists the photoelectric absorption cross section index, the bulk density, and
the volumetric cross section for common minerals and fluids. For the minerals, the
listed value is the matrix value (ma, Uma); for the fluids, it is the fluid value (ma, Uf).
Chart CP-21 (Figure 12) shows the location of these minerals on a maa crossplot.
The triangle encompassing the three common matrix minerals of quartz, calcite, and
dolomite has been scaled in the percentages of each mineral. For example, a point
exhibiting an apparent matrix grain density of 2.76 g/cm3 and volumetric cross section
of 10.2 barns/cm3 would be defined by 40% calcite, 40% dolomite, and 20% quartz
provided no other minerals exist and the pores are liquid saturated.
On this crossplot, gas saturation displaces points upwards on the chart and
heavy minerals displace points to the right. Clays and shales plot below the
dolomite point.
Figure 11
Matrix identification Plot
maa vs. Umaa
18
Figure 12
Matrix identification Plot
19
1
LIST OF INTERPRETATION CHARTS FOR CHAPTER 6
Chart
Chart
Chart
Chart
Chart
Chart
Chart
Chart
Chart
Chart
Chart
Chart
Chart
Chart
20
CP-1a
CP-1b
CP-1c
CP-2a
CP-2b
CP-7
CP-14
CP-15
CP-16
CP-17
CP-18
CP-19
CP-20
CP-21