Neutron Logging
Neutron Logging
15.2 Theory
In neutron logging there are three processes of interest: neutron emission, neutron scattering and
neutron absorption.
9
4 Be + 42 He ⇒ 126 C + 01n + γ (15.1)
1
Slowing Down Power
Hydrogen
0.1
Oxygen
0.01
Silicon
0.001
5 7
0.1 10 1000 10 10
Neutron Energy (eV)
Figure 15.2 The fast neutron slowing efficiency of hydrogen, silicon and oxygen atoms as a function
of neutron energy for a clean sandstone, φ = 0.15.
The initially fast neutrons (>0.5 MeV) quickly lose their energy and become slower (Fig. 15.3),
passing through stages called intermediate neutrons (102 to 105 eV), epithermal neutrons (0.1 to 100
eV), and finally thermal neutrons (<0.1 eV). In solid materials containing reasonable amounts of low
atomic mass elements, this process can happen very quickly for a given neutron (of the order of micro-
seconds). However, the time taken to slow down to a given energy will vary from neutron to neutron,
depending on the chance collisions with nuclei. Thermal neutrons are so called because they have
energies which are those that a particle has as a result of it existing a room temperatures. In other
words, they only have the small energies associated with the random kinetic motion associated with
room temperatures.
8
10
Fast Neutrons
7
10
Neutron Tool Release Energy
Neutron Energy (eV)
6
10
5
10
Intermediate Neutrons
4
10
1000
100
Epithermal Neutrons
10
0.1
Thermal Neutrons
0.01
0.001
Approx. 1 ms
Emission
Time Time
Figure 15.3 The slowing of fast neutrons with time by elastic collision with formation nuclei.
When the neutrons attain epithermal or thermal energies, collisions occur much less frequently
because the neutrons are moving from nucleus to nucleus much more slowly. Within a few
microseconds of being exposed to the fast neutron source, the formation has slowed the incoming
neutrons down to epithermal and thermal levels, and a cloud of these thermal neutrons exists in the
formation surrounding the source. Collisions continue resulting in little further loss of energy and the
slow diffusion of the thermal neutrons from the zone around the detector. During this process the
neutrons are absorbed by the formation nuclei.
1
1 H + 01 n ⇒ 21 H + γ (15.2)
and
(15.3)
35
17 Cl + 01n ⇒ 36
17 Cl + γ
In neutron logging, some tools measure the epithermal neutrons, some the thermal neutrons and some
the gamma rays emitted when a neutron is absorbed.
(15.4)
(C H )mass = n H AH
∑ ni Ai + n H AH
i
where: AH = the atomic mass of hydrogen atoms in the material
Ai = the atomic mass of non-hydrogen element i
nH = the number of hydrogen atoms in a molecule of the material
ni = the number of non-hydrogen atoms of element i in a molecule of the material
Note: i is summed over every non-hydrogen element in the material.
Thus, for pure water (H2O), where the atomic mass of hydrogen is 1.0 and the atomic mass of oxygen
is 16.0, the partial concentration of hydrogen (CH)mass = (2×1.0)/(1×16.0 + 2×1.0) = 1/9.
It is simple to obtain the partial concentration of hydrogens per unit volume (CH)vol, by multiplying the
partial concentration of hydrogens per unit mass by the density of the material, (CH)vol = ρb×(CH)mass.
Hence, the partial concentration of hydrogens per unit volume (CH)vol = ρbwater/9 = 1/9, because the
density of pure water is 1.000 g/cm3.
Now, the Hydrogen Index of a material is defined as the partial concentration of hydrogens per unit
volume relative to water. So, if the hydrogen index of water is constrained by the definition to be
unity, and water has a partial concentration of hydrogens per unit volume of 1/9, the hydrogen index of
a material is
9 n H AH (15.5)
HI = ρb
∑ ni Ai + n H AH
i
where: AH = the atomic mass of hydrogen atoms in the material
Ai = the atomic mass of non-hydrogen element i
Table 15.1 shows Eq. (15.5) in practice for a few minerals and fluids commonly found in reservoirs.
Table 15.1 Hydrogen index calculations for some reservoir minerals and fluids.
Compound Formula Ai ni nH ρb HI
• If the tool is in 100% water (a large tank of the stuff, say), the HI = 1.000. This is equivalent to a
rock of 100% porosity saturated with water. So we have a fixed point that HI = 1 represents φ = 1.
• If the tool is in a pure limestone rock with zero porosity, the HI = 0.000, because there are no
hydrogen atoms in the solid matrix of calcite. So we have a second fixed point where HI = 0
represents φ = 0.
• If the tool is in a pure limestone with a given porosity φ, the hydrogen index will be directly
proportional to the amount of water in the formation. Hence HI = φ for completely water saturated
limestones.
Thus the hydrogen index is a proxy measure of porosity if the solid minerals of the formation contain
no hydrogen and if the pores are completely saturated with water. But, it is the hydrogen index that
controls the count rate observed by the neutron tool. Hence we have a tool that can measure porosity in
water saturated formations where the matrix minerals contain no hydrogen.
In practice, it is not only hydrogen that affects the passage of neutrons in a formation. As we can see
from Fig. 15.2, other rock forming elements have an effect on the slowing down of neutrons in the
formation, but their effect is small compared with hydrogen, and when it comes to neutron absorption,
both chlorine and hydrogen have a part to play. The small errors that are introduced by assuming that
it is just hydrogen that affects neutrons are overcome by calibrating the tool. The tool is calibrated in
pure limestone, and hence does not give true porosities. Instead it gives equivalent porosities that
would occur if the rock was measuring limestone. This will be discussed in further detail in Section 4.
The Hydrocarbon Effect. Note in Table 15.1 that the hydrogen indices of water and oil are
approximately the same because the effect of their different compositions on the partial concentration
of hydrogens per unit volume is approximately balanced by the difference in their density.
As with the formation density tool, the zone of investigation of the neutron tool is constrained to the
flushed zone. Hence, the tool will measure the hydrogen index associated mainly with the mud filtrate,
together with whatever remains of the hydrocarbons and formation water in the formation. Imagine,
for example that we are in an oil zone in a limestone, the mud filtrate almost completely replaces the
formation fluids such that there is a saturation of mud filtrate SXO, and a residual saturation of
hydrocarbons (1- SXO). The porosity read by the neutron tool is related to the actual porosity in the
formation by
[ ]
(15.5)
φ N = φ HI mf S XO + HI hc (1− S XO )
If the hydrocarbon is oil, this equation reduces to φN ≈ φ , because, as we have seen in Table 15.1 the
hydrogen index of water and oils is similar; HImf ≈HIhc. This is true whether the mud filtrate is oil-
based or water-based.
If the hydrocarbon is methane gas with a density of 0.1 g/cm3, the equation reduces to
If the saturation in the flushed zone SXO = 0.7, Eq. (15.7) reduces to φN = 0.77 φ. This is known as the
hydrocarbon effect in the neutron log.
The Chlorine Effect. Some types of neutron tool measure the thermal neutrons and gamma rays
produced during the capture of neutrons. There are only two elements that are found in reservoirs that
contribute significantly to neutron absorption; hydrogen and chlorine. The presence of hydrogen in the
fluids is what we want to measure, so this is not a problem.
However, if the drilling mud, mud filtrate or formation fluids contain a significant amount of dissolved
chloride ions, as is often the case, the tool will measure a lower flux of neutrons and hence
overestimate the porosity. This is called the chlorine effect, and is present in wells drilled or logged in
the presence of drilling muds containing dissolved chlorine, or in formations where the formation
waters are particularly salty.
The Shale Effect. Shale contain clays that have a significant amount of surface absorbed (bound)
water. Hence shales can contain a significant proportion of hydrogens despite being low porosity. The
apparent porosity read from the neutron tool in shale formations is therefore always significantly
higher than it really is. This is called the shale effect or the bound-water effect, and will be discussed
further later in this chapter.
Because the tool measures the thermal neutrons and the capture gamma rays, it is effected by the
process of neutron capture by chlorine. Since drilling mud, mud filtrate and formation waters may
contain significant amounts of dissolved chloride ions, the measurement can give erroneous values.
Erroneous values take the form of overestimated porosities in formations either drilled with muds
containing dissolved chloride ions, or salty formation fluids.
The detector is sensitive to epithermal neutrons. These neutrons are not yet slow enough to take part in
absorption reactions with hydrogen and chlorine. Hence, the SNP tool readings are unaffected by the
presence of chlorine in high salinity muds and formation fluids.
in the count rate despite the longer source-detector spacing for this tool compared to the GNT and SNP
tools. The stronger source permits a deeper depth of investigation as well as allowing the tool to
operate in cased holes. The CNL tool is run eccentred in the hole by an arm which presses the tool
against the side of the borehole. This means that the tool is insensitive to the type of mud in the hole,
but implies that the readings are only for one portion of the borehole wall. The CNL log is shown in
Fig. 15.4.
Formation Wire or
other tool
Far Detector
Near Detector
Source
End of tool
or other tool
Sprung-loaded
arm
The data from the GNT tool is given in API units as shown in Fig. 15.5.
The data from the SNP tool is given in equivalent limestone porosity units, with the scale running
from approximately –10% to 30%, as shown in Fig. 15.6.
Data from the CNL tool is given in equivalent limestone porosity units, with the scale running from
approximately –10% to 30%, as shown in Fig. 15.7.
CAL (in)
Depth (m)
GNT (NAPI)
6 16
Bit Size (in) 160 3360
6 SGR (GAPI) 16
0 100
1050
1055
CAL (in)
Depth (m)
SNP (%)
6 16 45 -15
Bit Size (in)
6 GR (GAPI) 16
0 150
1050
1055
CAL (in)
Depth (m)
CNL(%)
6 16
Bit Size (in) 45 -15
6 SGR (GAPI) 16
0 100
1050
1055
15.5 Calibration
IMPORTANT The common use of limestone porosity units as the calibrating unit for these logs
means that the reading of porosity in a limestone formation will be exact, but the reading of porosity in
these units in any other formation lithology will need correction (Fig. 15.8).
Figure 15.8 Correction chart for obtaining porosity values for lithologies other than limestone.
The SNP tool is calibrated at the wellsite uses a U-shaped polyethylene baffle (artificial formation)
with a two position baffle, where the geometry of the block and baffle arrangements are known to
result in readings equivalent to 11% porosity and 22% porosity.
The calibration of the CNL tool is checked at the wellsite before and after each logging run by the use
of a neutron source of accurately known activity placed a standard distance from each detector.
The presence of gas in a formation increases the depth of investigation because, although the gas may
contain hydrocarbons, the gas has a vary low density compared to liquid water and oil, and hence a
very low hydrogen index.
The presence of shales decreases the depth of investigation because even low porosity shales contain
many waters (i.e., hydrogen) that are bound to the surface of the clay crystals.
The depth of investigation of the CNL tool in a water saturated formation of 35% porosity is about 12
inches, and that of the SNP tool in the same formation is about 8 inches.
As usual, the true bed resolution (the thinnest bed for which the true neutron porosity reading in that
bed is measured) is approximately three times the vertical resolution (i.e., 36 to 48 inches). Thinner
beds will be noticed by the tool, but the apparent porosity will not be the same as the true porosity of
the bed.
The measuring point for these tools is half way between the source and the detector for single detector
tools, and half way between the two detectors for the dual detector tool.
The SNP and CNL tools are run pressed up against the borehole wall. In this case, the roughness of the
borehole wall due to caving or wash-out can result in the detectors or source not being pressed directly
up against the borehole wall. This will cause erroneous porosity readings.
The GNT tool is sensitive to chloride-rich muds, and its results must then be corrected for the drilling
mud, mudcake and mud filtrate.
The SNP tool is not sensitive to the chloride effect and is run pressed against the borehole wall. The
mudcake tends to increase the apparent porosity because the mudcake has a high hydrogen index. This
effect can be corrected for.
The detectors of the CNL tool are sensitive to the chloride effect. However, the tool is run pressed
against the borehole wall so the effect of the drilling mud is not included in the measurement.
Furthermore, the use of two detectors automatically compensates for the effect of chloride-rich
mudcake and mud filtrate.
The density of the mud also affects the readings, because high density muds attenuate the radiation to
a greater extent. This is usually only a problem for the GNT tool, where the effect can be compensated
for using correction charts.
The tool is sensitive to the amount of hydrogens in the formation and to a less extent upon other
elements. It is assumed that the contribution to the measurement by elements other than hydrogen is
negligible, and that the contribution to the measurement from hydrogen comes entirely from the fluids
fully occupying the pore space.
However, in real rocks elements other than hydrogen that exist in the rock matrix do contribute to the
measurement (e.g., chlorine in formation water, mud filtrates and in some evaporite formations), and
hydrogen is present in the matrix (e.g., bound water in shales).
The problem is partially overcome by calibrating the tool to give the porosity in limestone units. Pure
limestone saturated with fresh water is chosen because it contains no elements which contribute
significantly to the measured signal other than hydrogen.
The porosities that are read by the tool are accurate in limestone formations that contain fresh water.
The porosities that are read by the tool in other lithologies or with other fluids need to be corrected by
a chart such as that shown in Fig. 15.8.
There are three effects that are not corrected for in the log data, that need to be briefly mentioned.
The Hydrocarbon Effect. The presence of hydrocarbon liquid (oil) does not effect the tool response
as it has approximately the same hydrogen index as fresh water. Hydrocarbon gas, however, has a
much lower hydrocarbon index resulting from its low density, and its presence will give rise to
underestimations in porosity (Fig. 15.9).
The Shale Effect. Shale contain clays that have a significant amount of bound water molecules on
their surfaces. This increases the hydrogen index of the formation. Even very low porosity shales can
give erroneously high porosity readings due to the presence of these bound waters.
The Chloride Effect. Chlorine is a good absorber of neutrons, and can lead to overestimations of
porosity if present either as formation fluid or mud filtrate.
Table 15.2 Lithological and fluid indicators for the neutron tool.
Type Examples
Fresh and salt water Formation water
Drilling mud
Mudcake
Mud filtrate
Hydrocarbons Gasses
Oils
Oil-based drilling mud
Oil-based mud filtrate
Oil-based mudcake
Coal
Organic-rich deposits
Bound water Shales
Water of Crystallization Evaporites
Hydrated minerals Igneous and metamorphic rocks
The values of apparent porosity in shales varies considerably, but is usually higher than the apparent
porosity in carbonate or sandstone rocks (i.e., 45 to 75%). This clearly high and unrealistic porosity is
a partial indicator of shale, and can become diagnostic when combined with the gamma ray log. One
may see a slight decrease in the apparent porosity in shales due to compaction, but only over large
depth intervals.
The apparent neutron limestone porosity is affected by the amount of shale and sand, or shale and
limestone in a mixture of the two. Hence we can recognize coarsening-up and fining-up sequences in
the neutron log (Fig. 15.11). While one can calculate a shale volume from the neutron log directly, it is
not recommended because of the effect of hydrocarbon gasses which may be present to disturb the log.
Shale
Sand
Figure 15.11 The neutron log response to mixtures of shales and sandstones.
Organic mater, often present in shales may cause an even higher apparent neutron limestone porosity
than the bound water in the shales alone (Fig. 15.11).
The neutron log can detect evaporites by either their waters of crystallization. The most common
example is gypsum (CaSO4.2H2O), but also include kainite, carnalite and polyhalite. The first three of
these give apparent limestone porosities of about 60%, while polyhalite give about 25%. The apparent
limestone porosities for halite, anhydrite, and sylvite are very low (-3, -2, and –3 respectively) as they
contain no water. Note that there is no effect of the chlorine atom in halite or sylvite (Fig. 15.12).
Both the formation density log and the neutron log give a direct measurement of TOTAL porosity.
Hence, if they are plotted on compatible scales, they should overlie each other (Fig. 15.13).
Note that the compatible scale here is Density (1.95 to 2.95 g/cm3) and Neutron (-15 to 45% limestone
porosity units). This is the most commonly used scale range, although other wider or more restricted
ones are possible.
Note also that good superimposition will ONLY occur for clean limestone formations 100% saturated
with fresh water.
• For limestone with 0% porosity, the density log reads 2.71 g/cm3 and the neutron log reads zero.
• For limestone with 100% porosity, the density log reads 1.00 g/cm3 and the neutron log reads 100.
These two points can be plotted on a graph of density (from the density log) on the y-axis against
neutron porosity (from the neutron log) on the x-axis. We can join up the two points with a straight
line, and calibrate the line for porosity (Fig. 15.14). The graph is called the density-neutron crossplot
and the line is called the clean limestone line.
The clean limestone line only works for clean limestones because of the effect of non-hydrogen
elements in the matrix on the neutron porosity values, and the different grain densities. However, we
can take account of the different densities and correct the neutron porosity units using Fig. 15.8, to
obtain lines of the cross-plot for clean sandstones and clean dolomite, the clean sandstone and clean
dolomite lines.
Figure 15.13 The density and neutron log responses for clean formations on a compatible scale (after
Rider, 1997).
One can see from the cross-plot that for density and neutron logs plotted on compatible scales, there
will be a separation of the density and the neutron logs for sandstone and dolomite, but no separation
for limestone (Fig. 15.15). The sandstone separation is called negative and the dolomite separation is
in the other direction and slightly larger, and is called positive.
If the shale volume decreases due to the intermixture of sandstone, the large positive separation
decreases, crosses-over and becomes eventually the small negative separation associated with pure
sandstone.
Thus, a sequence of clearly defined sand and shale formations shows switching between positive and
negative separations in the logs.
Often the beds will not be well defined, but coarsen-up or fine-up gradually. This can be seen by a
gradual switch from one separation to another. Hence the characteristic patterns (reviewed in the
chapter on the gamma ray log) can be recognized in the separations, and conclusions may be drawn
concerning the depositional environment.
The size of the separation is actually THE BEST quantitative estimator or shale volume. It is better
than the shale volume derived from the gamma ray log. We can write an equation for shale volume
based on separations
where Ω stands for the separation measured in 100% sandstone, 100% shale, and at the point of
interest in the log. Note that the separations may ALL be measured on the limestone porosity scale,
ALL on the density scale, or ALL using a simple ruler on the log! Each is valid, but you must keep it
consistent for the whole equation.
15.11.5 Evaporites
Remember from the section about the
formation density tool that evaporites can
often be recognized because their often pure
nature leads to well constrained density
values. Evaporites have apparent neutron
porosity values which are either very high or
very low. The combination of well
constrained density values and very high or
very low apparent neutron porosity values is
a characteristic and diagnostic combination
for evaporites (Fig. 15.17).