[0001] This invention relates generally to gamma ray well logging and, more particularly,
to a method of gamma ray well logging for use in determining the radial distance of
a radioisotope tracer from a gamma ray spectroscopy tool in a well bore.
[0002] Radioactive isotopes are widely used in the petroleum industry in a variety of field
operations. The most common applications include their use as radioactive tracer elements
in techniques for monitoring the effectiveness of downhole operations, such as well
completion operations wherein a well is cased and cemented before being placed in
production so that the geologic zones of interest can be isolated and so that a seal
can be maintained between adjacent geologic formations and the surface. In this respect,
techniques utilizing radioactive tracers have been devised for determining cement
thickness, in addition to the extent of cement covering throughout the well bore.
Radioactive tracers are also used in techniques for monitoring the effectiveness of
flow stimulating operations, such as hydraulic fracturing of geologic formations for
stimulating the flow of oil or gas from hydrocarbon-bearing formations. By such techniques
it has become possible to improve estimates of vertical fracture height or to determine
the mean depth of penetration of one or more radioactive tracers injected by a hydraulic
fracturing process into a fractured formation disposed about the well bore as an indication
of the extent of radial fractures.
[0003] In the construction of artificial structures such as gravel packs, it is helpful
to tag the sand in the pack itself as well as in the pre-packed sand placed in the
artificial formations outside the perforated casing.
[0004] In the various techniques noted above, it is customary procedure to add one or more
radioactive tracers to the materials or slurries which are pumped downhole. A gamma
ray energy-detecting tool for detecting the gamma rays emitted by each radioactive
tracer is then run in the well for obtaining a well log of spectroscopy measurements
which shows the locations of the tracers, presumably where the accompanying materials
or slurries which have been placed in the well are also located.
[0005] Many times the desired well completion or stimulation procedures can require that
several different materials be placed in a single operation. In the past, it has usually
been necessary to limit the complexity of such operations because only one tracer
could be monitored by means of gross gammas ray counting tools which are sensitive
only to the overall presence of gamma rays and not to the individual gamma ray energy
signatures characteristic of different tracers. However, gamma ray spectroscopy tools
have since been devised which make it possible to efficiently and accurately monitor
multiple radioactive tracers, and thus multiple materials, in downhole operations.
In particular, these tools measure the energies of gamma rays emitted by radioactive
tracers located in a well and the geologic formations in the immediate vicinity. Gamma
ray spectroscopy logs utilizing this technique have been found useful in a variety
of situations and an increasing number of applications.
[0006] We have now devised a way of utilizing gamma ray well logging to obtain a relative
distance indication of the placement of a radioisotope tracer with respect to the
well bore.
[0007] According to the present invention, there is provided a method of gamma ray well
logging of one or more radioactive tracer isotopes in an unknown cased or uncased
well borehole to obtain a relative distance indication of each radioisotope trace
with respect to the well bore, said method comprising: obtaining standard gamma ray
energy spectra for one or more individual tracer elements disposed in at least two
different geometrical regions spaced apart from a gamma ray detector in a known well
bore environment; moving a well logging instrument through the unknown well bore and
detecting gamma radiation emitted from one or more selected radioactive tracer isotopes
at different depth levels in the well borehole; separating said detected gamma radiation
into a measured unknown gamma ray energy spectrum at each of a plurality of depth
levels in the unknown borehole; separating said measured unknown gamma ray energy
spectrum into component parts attributable to each such selected radioactive tracer
isotope disposed in each of said geometrical regions by comparing said measured unknown
gamma ray energy spectrum with said one or more standard gamma ray energy spectra
of said selected tracer elements taken with said tracer elements disposed in said
geometrical regions; and obtaining a relative distance indicator with respect to said
well borehole for each tracer from the component parts of the unknown spectrum attributable
to each tracer disposed in each said geometrical region.
[0008] The invention also provides a method of gamma ray well logging of one or more radioactive
tracer isotopes in an unknown cased well borehole to obtain a relative distance indication
of each radioisotope trace with respect to the well bore, said method comprising:
moving a well logging instrument through the unknown well bore and detecting gamma
radiation emitted from one or more selected radioactive tracer isotopes at different
depth levels in the well borehole and the formation adjacent said borehole; separating
said detected gamma radiation into a measured unknown gamma ray energy spectrum at
each of a plurality of depth levels in the unknown borehole; at such depth levels
in the unknown borehole, separating said measured unknown gamma ray energy spectrum
into component parts attributable to each such selected radioactive tracer isotope
disposed in specific geometrical regions relative to the borehole by comparing said
measured unknown gamma ray energy spectrum with said one or more standard gamma ray
energy spectra of said selected tracer elements; forming a composite spectrum for
each said radioactive tracer isotope by summing respective portions of the spectra
of the tracer attributable to such said geometrical regions; forming a Compton ratio
R
c of gamma ray counts in a first energy region of said composite gamma ray spectrum
which is sensitive to Compton scattering of gamma rays to gamma ray counts in a second
energy region of the composite gamma ray spectrum which is not sensitive to Compton
scattering of gamma rays to a degree sufficient to markedly affect said ratio R
c; and obtaining a relative distance indication for each said tracer with respect to
said well borehole from a predetermined functional relationship of the Compton ratio
R
c and the diameter of the annulus of the region of distribution of the tracer about
said well bore wherein said diameter represents the outer limit of tracer distribution
as measured from said well bore.
[0009] The standard spectra can, for example, be obtained from artificial geologic formations
simulating a standard cased hole environment, by placing a radioactive tracer in the
various annuli of the calibration formations and detecting the gamma radiation therefrom
using a detector positioned in the simulated well casing. Standard energy spectra
of the tracer can thus be obtained representing the presence of the tracer in specific
geometrical regions, such as tracer only in the formation, tracer only in the cement
annulus about the casing, and tracer only in the borehole.
[0010] These (or other) standard energy spectra, or signature spectra of the tracer, are
then used in the method of the invention in, for example, a weighted-least-squares
algorithm into which is input an arbitrary measured spectrum obtained from logging
a well borehole in a field operation. A solution is then obtained for the individual
tracer concentrations. In particular, using borehole and formation signature spectra
obtained from the calibration formations, it is possible to obtain, for example, the
borehole and formation concentrations for each radioisotope tracer present in the
field well and its immediate environment. This means that each tracer used in the
field well can be represented by a linear combination of the borehole and formation
components. Then, from these components, a composite spectrum for each individual
radioisotope tracer may be constructed by summing the component spectral from each
geometrical region. This composite spectrum contains peak structure due to unscattered
gamma rays reaching the detector, and also due to scattered, lower energy gamma rays.
The relative intensity of the lower energy scattered gamma rays to the higher energy
less scattered (or unscattered) gamma rays is indicative of the amount of scattering
material between the tracer and the detector, and therefore to the radial.
[0011] From each composite, a Compton ratio R
c, of gamma ray counts in a first energy region of the composite spectrum which is
sensitive to Compton scattering to gamma ray counts in a second energy region of the
composite spectrum which is not sensitive to Compton scattering, can be obtained and
transformed into a quantity proportional to the radial distribution of the associated
tracer.
[0012] In order that the invention may be more fully understood, reference is made to the
accompanying drawings, wherein:
Figure 1 is a view in perspective and part cut away, of a first tank structure containing
one embodiment of artificial geologic formation which can be used in calibrating the
tracer response of gamma ray spectroscopy tools;
Figure 2 is a view in perspective and part cutaway, of a second tank structure containing
a second embodiment of artificial geologic formation which can be used in calibrating
the tracer response of gamma ray spectroscopy tools;
Figure 3 is a schematic drawing of one form of well logging system which can be employed
in practising the present invention;
Figure 4 is a graphical representation of formation and borehole spectra for ¹⁹²Ir
obtained in gamma ray spectroscopy measurements of ¹⁹²Ir tracer distributed in the
casing fluid and artificial geologic structure contained in the tank of Figure 2;
Figure 5 is a graphical representation of formation and borehole spectra for ⁴⁶Sc
tracer obtained in gamma ray spectroscopy measurements of ⁴⁶Sc tracer distributed
in the casing fluid and formation annuli of the artificial geologic structure in the
tank of Figure 1;
Figure 6 is a graphical comparison of the cement annulus spectrum shown in Figure
5 with a composite annulus spectrum obtained by summing 61% of the formation spectrum
and 39% of the borehole spectrum of the spectra shown in Figure 5; and
Figure 7 is a graphical illustration of tracer concentration and radial distance curves
obtained by the method of the invention, from a sample well log where a fracturing
operation was performed using ⁴⁶Sc for tagging the fracturing fluid and ¹⁹²Ir for
tagging the proppant material.
[0013] A series of calibration experiments was performed to establish the response of three
gamma ray spectroscopy tools to six common tracer isotopes with the principal purpose
of determining tool sensitivities to different isotopes so that a weighted-least-squares
algorithm could be implemented to process multi-tracer logs. Two artificial geologic
formations were constructed to simulate a typical cased hole environment. These artificial
test formations are illustrated in Figures 1 and 2. Each formation was constructed
utilizing a cylindrical steel tank 10, 30 inches (76cm) in diameter and 36 inches
(91cm) deep, mounted on four 30 inch (76cm) high steel legs 11. A 5½ inch (14cm) diameter,
17 lb/ft. (25.3 kg/m), 60 inch (1.52m) long casing 13 was welded to the center of
each tank 10 in coaxial relation thereto. A stainless steel cylinder 15 was also welded
to each tank 10 in concentric spaced relation to the casing 13 to provide a 1½ inch
(3.8cm) thick annulus adjacent to the casing 13 in order that a cement sheath 16 could
be simulated. The tank 10 in the test formation illustrated in Figure 1 was further
subdivided into inner, middle and outer annuli by means of additional stainless steel
cylinders 16 and 17. The diameters of the cylinders 16 and 17 were such as to provide
the inner annulus with a radial thickness of 2 inches (5.1cm), the middle annulus
with a radial thickness of 3 inches (7.6cm), and an outer annulus with a radial thickness
of 5-¾ inches (14.6cm).
[0014] On each tank the casing and each annulus were separately plumbed so that each individual
region could be isolated and filled or emptied as required. The formation and cement
"matrix" materials were simulated using loose-packed sandstone gravel such that each
test formation has a porosity of about 40%.
[0015] Each tracer used was in water-soluble form and added to fresh water in a supply barrel
in sufficient concentrations to give count rates in the range of 500-1000 gamma ray
API units. This corresponded to radioactivity levels of only a few tens of microcuries.
The tracer-tagged water was transferred between the formation and the supply barrel
through plastic tubing using a peristaltic pump driven by a reversible electric motor.
The experimental procedure was to make background measurements with fresh water in
the pore space and then to measure the tracer spectra in each annulus by successively
filling each annulus from the outermost to the innermost, as well as filling the casing
for the final measurement. The tracer spectra for each individual region were obtained
by subtracting the spectra from adjoining regions as appropriate.
[0016] Six of the most commonly used radioactive tracers, having half lives ranging from
2.7 to 250 days, were selected for the tracer calibration experiments with characteristics
as shown in TABLE 1 below.
TABLE 1.
ISOTOPES IN TRACER CALIBRATION EXPERIMENTS |
TRACER |
ISOTOPE |
HALF-LIFE |
GAMMA-RAY ENERGY* (keV) |
INTENSITY+ |
Gold-198 |
198Au |
2.70 days |
412 |
0.96 |
|
|
|
676 |
0.01 |
Iodine-131 |
131I |
8.04 days |
284 |
0.06 |
|
|
|
364 |
0.81 |
|
|
|
637 |
0.07 |
|
|
|
723 |
0.02 |
Antimony-124 |
124Sb |
60.2 days |
606* |
1.05 |
|
|
|
720* |
0.15 |
|
|
|
1353* |
0.05 |
|
|
|
1691 |
0.49 |
|
|
|
2091 |
0.06 |
Iridium-192 |
192Ir |
74.0 days |
311* |
1.42 |
|
|
|
468 |
0.48 |
|
|
|
603* |
0.18 |
Scandium-46 |
46Sc |
83.8 days |
889 |
1.00 |
|
|
|
1121 |
1.00 |
Silver-110m |
110mAg |
250 days |
666* |
1.32 |
|
|
|
773* |
0.34 |
|
|
|
885 |
0.73 |
|
|
|
937 |
0.34 |
|
|
|
1384 |
0.24 |
|
|
|
1502* |
0.18 |
+Intensity values give fraction of nuclear decays which result in gamma ray emission. |
*Energies of weak gamma ray transitions omitted. An asterisk indicates a weighted
composite of multiple gamma rays which cannot be resolved by Nal(Tl) detectors. |
[0017] Three gamma ray spectroscopy tools were used to collect the tracer spectra. Two were
large diameter (3-5/8 inch - 9.2cm) tools with 2 inch (5.1cm) diameter Na(T1) detectors.
One of the large tools had a tool case of low atomic number (Low-Z) material so that
photoelectric gamma rays could be observed and the other was provided with a titanium
housing designed for high temperature, high pressure applications. The third tool
had a small diameter (1 11/16 inches - 4.29cm) and a steel tool housing.
[0018] A typical gamma ray logging system which may be used for practising the invention
is illustrated schematically in Fig. 3. The system, which can be used in field applications,
comprises a logging tool 30 suspended in a well borehole 31 from a logging cable 32
supported by a reel 34 on a logging truck or the like. The borehole 31 passes through
earth formations 33 and may be lined with a steel casing 35 set in place by an annulus
of cement. The tool 30 can however, be used in an uncased borehole as well. The casing
contains a well bore fluid 36. In conventional manner, rotation of the reel 34 provides
an indication of tool depth as the cable 32 is moved in or out of the borehole. The
tool 30 is provided with a steel housing 37 having a section 37a which surrounds the
radiation detector 38. The section 37a is constructed from a material having a low
atomic number (Z) and low density to facilitate observation and measurement of photoelectric
absorption of low energy gamma rays. Such a tool case is described in our U.S. patent
specification no. 4,405,354. For high temperature, high pressure applications, section
37a could be made of titanium. Incident gamma rays, whether from natural radiation
or from tracers, are detected in a large NaI(T1) scintillation detector crystal 38,
the scintillations of which are coupled to a photomultiplier 40 to produce electrical
pulses of magnitudes proportional to the energies of the impinging gamma rays.
[0019] The system gain can be maintained with ± 0.5% by a coincidence stabilization technique
for which purpose the apparatus includes in close proximity to detector 38, a smaller
crystal 42 containing an embedded ²⁴¹Am source. Such a technique is described in U.S.
patent specification no. 4,585,939. Other gain stabilization techniques, such as are
common in the art, could alternatively be used if desired.
[0020] After amplification by photomultiplier 40, coincidence and anti-coincidence data
pulses are digitized by an analog-to-digital converter 44, accumulated in a data accumulator
46, and sorted by a microprocessor controller 48 which synchronizes transmission of
data from the tool 30 to equipment at the surface. The coincidence (stabilizer) events
are converted into a 256 channel spectrum which spans the energy range from 0-350
keV so as to enable the automatic downhole gain stabilizer feedback circuit to maintain
system gain to approximately ± 0.5%. The anti-coincidence (external gamma radiation)
events are converted into two spectra, one of which spans the low energy range from
0-350 keV and the other of which spans the high energy range from 0-3000 keV. The
three spectra are accumulated in accumulator 46 and then transmitted along the cable
conductors, approximately each 0.25 ft. (7.6cm) while logging, to the logging system
located at the surface. At the earth surface, the data are demodulated by a demodulator
50 prior to recording in a magnetic tape recorder 52 and display in a spectral display
device 54. The external gamma ray spectra are also transferred to the computer 56
in which the high energy spectrum is separated into energy windows or regions dependent
on the particular tracers used. High energy windows are selected to encompass specific
gamma ray energy peaks between 150 keV and 0-3000 keV characteristic of the particular
tracer being used, whereas low energy windows are selected to include primarily downscattered
radiation, generally between 150 and 350 keV. For the low energy spectrum, windows
are selected for providing photoelectric sensitivity ratios under the constraint of
minimizing statistical uncertainty.
[0021] The primary purpose of the tracer calibration measurements was to determine the sensitivities
of the three spectroscopy tools to different tracer isotopes so that a weighted-least-squares
(WLS) algorithm could be implemented for processing gamma ray spectroscopy logs. The
WLS method has been described previously in a paper by Smith, H.D. Jr., Robins, C.A.,
Arnold, D.M., Gadeken, L.L. and Deaton, J.G., "A Multi-Function Compensated Spectral
Natural Gamma Ray Logging System", SPE Paper No. 12050, Fifty-Eighth Annual Technical
Conference, San Francisco, California, October 5-8, 1983. The WLS method thus described
was applied to the estimation of the potassium, uranium, and thorium concentrations
from natural gamma ray spectra. For that application, the elements of the sensitivity
matrix were defined to be the individual window count rates per unit concentration
for each natural constituent. Since for tracer applications, the parameters of interest
are generally the relative amounts of each tracer present, the elements of the tracer
sensitivity matrix were defined to be the individual window count rates per unit gamma
ray API for each isotope. The sensitivity matrices for each tracer isotope were constructed
by summing together the spectral count rates in each of the standard 13 energy windows
and dividing by the observed API value for the appropriate calibration spectra. Also
in this respect, reference is made to our European patent specification no. 198615A
and to our U.S. patent specification no. 4825071. These specifications disclose techniques
of weighted-least squares fitting of standard gamma ray spectra for tracer elements
utilized in well bore logging to measured gamma ray spectra taken in arbitrary boreholes.
[0022] The original assumption for such data was that it was generally sufficient to consider
only two regions containing tracers. These two WLS solution components were (1) the
borehole region inside the casing and (2) the formation region outside the cement
annulus. It was assumed that the cement annulus was impervious to the tracer. If conditions
were such that the tracers were in the cement annulus, then this contribution would
be approximated by combining appropriate fractions of the borehole and formation components.
The spectral signatures for ⁴⁶Sc from these three regions are shown in Figure 4 for
the Low-Z tool. The differences due to increased Compton downscattering effects as
more and more material is interposed between the source region and the detector are
clearly evident. For the illustration of Fig. 4 the spectra were normalized so that
each 1121 keV (channel 99) peak had the same amplitude.
[0023] Figure 5 compares the cement annulus spectrum from Figure 4 with a composite spectrum
obtained by summing 61% of the formation tracer spectrum and 39% of the borehole tracer
spectrum from Figure 4. The Values of 61% and 39% were found by analyzing the cement
annulus tracer spectrum using the WLS algorithm and assuming that the input data were
made up of a formation component and a borehole component. Figure 5 illustrates a
fact that has been observed in the spectroscopy log field data and verified using
various combinations of calibration spectra from different annuli in the test formations.
It is generally possible to determine a linear combination of formation and borehole
standard spectra which matches any observed tracer spectrum, no matter where the isotope
is located. The quality of the fit is good enough in most cases that the composite
spectrum cannot be distinguished from the true spectrum for typical logging statistics.
[0024] A corollary of this observation is that a negative component is perfectly legitimate,
at least mathematically. For example, if a spectrum was measured for which a tracer
was present only in the outer annulus of test formation # l shown in Figure 1, the
WLS solution assuming only formation and borehole components would result in a positive
formation value and a negative borehole value. The reason for this can be seen easily.
The tracer spectrum from the outer annulus has a greater Compton downscattered component
than that for the whole formation annulus. Therefore, the borehole value determined
from the WLS algorithm must be negative since it represents a less Compton scattered
portion of the signal. A fraction of the borehole must be subtracted from the formation
signature to obtain the composite spectrum which most closely matches the spectrum
from the outer annulus. This mathematically sound, yet physically unreasonable, concept
of negative concentrations has led to a reformulation of the gamma ray spectroscopy
log presentation in terms of a relative distance indicator for each tracer. Although
mathematically consistent with the division into formation and borehole components,
it has the desirable feature of eliminating negative concentration values from the
output log as well as providing information on the radial distributions of the tracers
which is independent of the actual tracer concentrations.
[0025] For a particular downhole operation, where information is desired as to the distribution
of radioisotope tracers in the vicinity of the zone of interest in a well bore, the
unknown gamma ray spectrum is measured by moving a well logging instrument, such as
shown in Figure 3, through the well borehole. The resulting gamma ray spectrum as
measured in the depth region of interest in the well bore in the field is fitted to
the standard energy signature spectra for the individual tracers by a weighted-least-square
technique as referred to above. Accordingly, using borehole and formation signature
spectra obtained from the calibration formations, it is possible to obtain the borehole
and formation concentrations for each radioisotope tracer present in the field well
and its immediate environment. This means that each tracer can be represented by a
linear combination of the computed borehole and formation components (. Then, from
these components, a composite spectrum for each individual radioisotope tracer may
be constructed and from each composite spectrum a Compton ratio, R
c, of gamma ray counts in a first energy region of the composite spectrum which is
sensitive to Compton scattering to gamma ray counts in a second energy region of the
composite spectrum which is not sensitive to Compton scattering is obtained. As will
thereafter be shown, the Compton ratio can then be transformed into a quantity proportional
to the radial distribution of the associated tracer.
[0026] In a previous publication by Gadeken, L.L.; Smith, H.D. Jr.; and Seifert, D.J.: "Calibration
and Analysis of Borehole and Formation Sensitivities for Gamma Ray Spectroscopy Measurements
with Multiple Radioactive Tracers", The Log Analyst (May-June, 1988) 159-177, a Compton
ratio, R
c, was defined to be a high energy count rate (350 keV-3000 keV) divided by a low energy
count rate (150 keV-350 keV). This makes it convenient to quantify the effects of
Compton downscattering on the observed gamma ray spectra. An additional result illustrated
in Figure 6 is that the Compton ratio obtained from the formation-plus-borehole composite
spectrum is nearly the same (usually within measurement statistics) as the Compton
ratio found from the actual spectrum. This observation makes it possible to determine
an R
c value for each tracer, even when more than one tracer is present, since borehole
and formation components are obtained for each isotope using the WLS algorithm.
[0027] It was also shown in the Log Analyst publication noted above that the Compton ratio
is directly related to the inverse square of the annulus diameter. By data analysis,
it has been found that the Compton ratio data can be linearized by parameterizing
it with the inverse square of the annulus diameter, D, as follows:
R
c = A +

where A and B are constants which are dependent on the tracer type and the casing
diameter. This relation was used in this invention as the basis for the development
of a relative distance indicator. Detailed data analysis has shown that this indicator
is best used only qualitatively, which is mainly a result of the uncertainty in the
diameter estimate induced by the statistics of the Compton ratio measurement. The
effects of borehole size, casing size and tool position also contribute to the problem.
Nevertheless, such analysis has established that this relative distance measurement
can be qualitatively used to indicate the average depth of tracer penetration. Further
development may permit quantitative results to be obtained.
[0028] One of the unique features of the gamma ray spectroscopy logging system described
herein is that measurements in the low energy photoelectric region can be made when
using the Low-Z toolcase. As with Compton scattering effects, it is convenient to
parameterize the photoelectric information using the ratio of a higher energy count
rate window (80-150 keV) to a lower energy count rate window (20-80 keV). The measurement
principle is that gamma rays from tracers inside the well casing undergo much less
low energy photoelectric absorption than those from outside the casing. It was shown
that the photoelectric ratio, R
p, usually makes it possible to distinguish the location of tracers inside versus outside
the casing. Operationally, however, the R
p log value must also be used qualitatively due to a number of factors including counting
statistics, borehole and casing diameter effects and increased sensitivity to tool
response variations as well as whether or not the natural gamma ray background was
removed.
[0029] It is to be noted therefore, that the Compton relative distance indicator is related
to the average placement distance for individual tracers and that the photoelectric
ratio is primarily an indicator of the relative tracer count rate inside versus outside
the casing. These relative distance indicators which are derived from gamma ray spectroscopy
logs of radiation from tracer tagged materials placed downhole are quite helpful in
the interpretation of the effectiveness of the particular downhole operations.
Log Example
[0030] The gamma ray spectroscopy log presented in Fig. 7 is a typical field example which
shows the utility of the WLS processing algorithm for tracer concentrations coupled
with both Compton and photoelectric relative distance indicators. It is to be noted,
however that since the depth of investigation of any gamma ray tool is about one foot
from the borehole wall, the tracer concentrations and average distances shown on the
log reflect information from a limited radial region surrounding the borehole. Nonetheless
in many situations the near well bore environment reflects approximately the state
of affairs in the formations far removed from the well bore.
[0031] There are four steps recommended to obtain a complete set of gamma ray spectra: (1)
a "before" log is run to determine the natural gamma ray background, (2) the materials
tagged with radioactive tracers are placed downhole, (3) an "after" log is run to
measure the gamma ray spectra from the tracers and from the natural background, and
(4) the "before" data is subtracted from the "after" data and a resulting log is generated
which shows the tracer concentrations and the relative distance of the tracers as
a function of depth. It should be recognized that it is possible to skip Step 1 and
estimate the natural background contribution together with the tracer response, or
to ignore the natural background if the tracer concentrations used are high enough
such that the natural gamma ray background is not a significant contribution to the
total observed spectra. However, not subtracting the natural background does degrade
the quality of the tracer estimates since in general one should solve the three natural
gamma concentrations (K,U,Th), as well as each of the tracer concentrations in the
WLS algorithm. This leads to greater uncertainty in the calculated tracer results.
An approximate composite natural gamma ray sensitivity treated in the WLS algorithm
just like another tracer sensitivity can give an adequate result for the value of
the natural gamma ray background in many cases.
[0032] It appears that three isotopes are a practical limit for obtaining relative distance
indicators using a large (3-5/8 inch - 9.2cm) spectroscopy tool. The small (1-11/16
inch - 4.29cm) spectroscopy tool is limited to two isotopes due to its smaller gamma
ray detector and the corresponding reduced sensitivity to the different tracer signatures.
[0033] The log example shown in Fig. 7 is from a well (completed with a 7 inch (17.8cm)
diameter cemented casing in a 10 inch (25.4cm) diameter borehole) in California where
a single stage foam fracturing operation was performed. The fluid pumped downhole
was tagged with ⁴⁶Sc while the proppant was tagged with ¹⁹²Ir. The perforated interval
extended from X258 ft to X358 ft (X78.6m to 109.1m). The spectra data were obtained
with a large tool with a Low-Z housing around the detector, permitting the photoelectric,
as well as the Compton distance indicators to be measured. Figure 7 shows the resulting
log. The base log natural gamma ray curve and the Fit-Error curve are shown in Track
1. The total tracer concentrations (individual contributions shaded) are displayed
in Track 2 together with the Rp (photoelectric ratio) curve. The Compton relative
distance curves for ⁴⁶Sc and ¹⁹²Ir tracers are given in Track 3. The relative distance
curves were obtained by using the borehole and formation components to construct a
composite spectrum for each isotope. The Compton ratio values were obtained and converted
to relative distance values as described above.
[0034] The concentration curves indicate that the fracturing fluid and the proppant are
both present throughout the logged interval. The predominance of ⁴⁶Sc in the upper
and lower sections leads to the suspicion that this signal is due to residual fluid
in the borehole. This is supported by the consistently low value of the R
p curve which shows the presence of tracer material in the borehole above X230 and
below X358. The R
p curve gives a qualitative outside casing indication in the zone between X230 and
X300 since its values are greatest in this interval. The Compton relative distance
curves show that the most effectively fractured and propped interval in the well occurred
between X220 and X264. The ⁴⁶Sc relative distance curve shows the fractured zone extends
downwards to X356 while the ¹⁹²IR relative distance curve shows somewhat less effective
propping of the formation in this interval. The "peaky" fine structure of the relative
distance curves may be statistical artifacts and should not be interpreted unless
verified by repeat passes over the zone of interest. However, the similar trends for
both the Compton and photoelectric relative distance curves over extended intervals
in the well stand out clearly. It is apparent that these curves can be used to assist
in interpreting gamma ray spectroscopy logs.
[0035] Information from the operating company states that the quality of the cement job
across the logged interval was rather poor and that higher than desired pumping rates
were used in an attempt to avoid a premature screen-out. This could have resulted
in significant amounts of sand being deposited in or around the borehole and not out
into the formation as desired. The overall results of this log indicate that the
fractured interval extended beyond the perforations and that the proppant was not
placed as effectively as desired, which was confirmed by subsequent production rates
which were lower than anticipated.
[0036] It is therefore to be noted that calibration experiments and analysis results with
the use of both large and small gamma ray spectroscopy tools for six different isotopes
have been described from which it is possible to determine both formation and borehole
gamma ray spectral sensitivities for each tracer in a multi-tracer operation so that
a weighted-least-squares algorithm can be implemented. The use of borehole as well
as formation components in the solution results not only in more accurate total concentration
measurements for each tracer, but also in the qualitative determination of the radial
location of the tracers. This is possible by use of the two-component solution for
each isotope to find a Compton ratio for each. A relative distance estimate can then
be extracted from the composite Compton ratio for each material tagged with a distinct
radioactive isotope.
1. A method of gamma ray well logging of one or more radioactive tracer isotopes in
an unknown cased or uncased well borehole to obtain a relative distance indication
of each radioisotope trace with respect to the well bore, said method comprising:
obtaining standard gamma ray energy spectra for one or more individual tracer elements
disposed in at least two different geometrical regions spaced apart from a gamma ray
detector in a known well bore environment; moving a well logging instrument through
the unknown well bore and detecting gamma radiation emitted from one or more selected
radioactive tracer isotopes at different depth levels in the well borehole; separating
said detected gamma radiation into a measured unknown gamma ray energy spectrum at
each of a plurality of depth levels in the unknown borehole; separating said measured
unknown gamma ray energy spectrum into component parts attributable to each such selected
radioactive tracer isotope disposed in each of said geometrical regions by comparing
said measured unknown gamma ray energy spectrum with said one or more standard gamma
ray energy spectra of said selected tracer elements taken with said tracer elements
disposed in said geometrical regions; and obtaining a relative distance indicator
with respect to said well borehole for each tracer from the component parts of the
unknown spectrum attributable to each tracer disposed in each said geometrical region.
2. A method according to claim 1, wherein the step of comparing said measured unknown
gamma ray energy spectrum and said standard gamma spectra is performed by fitting
said measured unknown spectrum to said standard spectra using a weighted-least-squares
fitting technique of all selected tracer isotope standard spectra components to the
measured unknown spectrum.
3. A method according to claim 1 or 2, wherein said relative distance indication for
each said tracer with respect to the well borehole is obtained by solving for the
quantity D in the linear relationship R
c = A +

where A and B are constants which are dependent on the particular tracer and the
casing diameter, and D is the outer diameter of an annulus cylindrical region of distribution
of the tracer with respect to the well borehole.
4. A method according to claim 1,2 or 3, which further includes modifying the measured
unknown gamma ray spectrum by removing therefrom the background gamma radiation due
to naturally occurring gamma rays in the formations adjacent the well borehole which
are emitted from uranium, thorium, and potassium isotopes and their daughter products,
to obtain a modified measured gamma ray spectrum representing solely the energy spectrum
of gamma radiation attributable to radioactive tracer elements.
5. A method according to any of claims 1 to 3, which further comprises the step of
including one or more standard spectra for natural gamma radiation as background standard
spectra in the step of separating the measured unknown spectrum into component parts,
wherein the natural gamma ray background is assumed to be a part of the measured unknown
spectrum.
6. A method of gamma ray well logging of one or more radioactive tracer isotopes in
an unknown cased well borehole to obtain a relative distance indication of each radioisotope
trace with respect to the well bore, said method comprising: moving a well logging
instrument through the unknown well bore and detecting gamma radiation emitted from
one or more selected radioactive tracer isotopes at different depth levels in the
well borehole and the formation adjacent said borehole; separating said detected gamma
radiation into a measured unknown gamma ray energy spectrum at each of a plurality
of depth levels in the unknown borehole; at such depth levels in the unknown borehole,
separating said measured unknown gamma ray energy spectrum into component parts attributable
to each such selected radioactive tracer isotope disposed in specific geometrical
regions relative to the borehole by comparing said measured unknown gamma ray energy
spectrum with said one or more standard gamma ray energy spectra of said selected
tracer elements; forming a composite spectrum for each said radioactive tracer isotope
by summing respective portions of the spectra of the tracer attributable to such said
geometrical regions; forming a Compton ratio Rc of gamma ray counts in a first energy region of said composite gamma ray spectrum
which is sensitive to Compton scattering of gamma rays to gamma ray counts in a second
energy region of the composite gamma ray spectrum which is not sensitive to Compton
scattering of gamma rays to a degree sufficient to markedly affect said ratio Rc; and obtaining a relative distance indication for each said tracer with respect to
said well borehole from a predetermined functional relationship of the Compton ratio
Rc and the diameter of the annulus of the region of distribution of the tracer about
said well bore wherein said diameter represents the outer limit of tracer distribution
as measured from said well bore.
7. A method according to claim 6, which further includes modifying the measured unknown
gamma ray spectrum by removing therefrom the background gamma radiation due to naturally
occurring gamma rays in the formations adjacent the well borehole which are emitted
from uranium, thorium, and potassium isotopes and their daughter products, to obtain
a modified measured gamma ray spectrum representing solely the energy spectrum of
gamma radiation attributable to radioactive tracer elements.
8. A method according to claim 6 or 7, wherein the step of comparing said modified
measured unknown gamma ray energy spectrum and said standard gamma ray spectra is
performed by fitting said measured unknown spectrum to said standard spectra using
a weighted-least-squares fitting technique of all selected tracer isotope standard
spectra components to the measured unknown spectrum.
9. A method according to claim 6,7 or 8, wherein said relative distance indication
for each said tracer with respect to the well borehole is obtained by solving for
the quantity D in the linear relationship R
c = A +

where A and B are constants which are dependent on the particular tracer and the
casing diameter, and D is the outer diameter of an annular cylindrical region of distribution
of the tracer with respect to the well borehole.