Disclosed embodiments relate generally to nuclear logging operations such as neutron and natural gamma ray logging and more specifically to a method of correcting natural gamma ray logs for measurement bias caused by drilling fluid (e.g., oxygen) activation gamma rays induced by fast neutrons.
Natural gamma ray logging is one of the most common logging techniques in the oil and gas industry. Such logging operations measure the naturally occurring gamma radiation emitted by a subterranean formation, primarily from potassium, uranium, and thorium containing minerals in the formation. Both total gamma ray and spectral gamma ray sensors are commonly employed. Total gamma ray sensors measure the total number of detected gamma rays (e.g., with energy above one or more predetermined thresholds). Radioactive elements tend to concentrate in shales and clays, while clean sands and limestone formations tend to have low levels of natural radioactivity. A gamma ray log indicates the shale content of a formation, with shale reading high radioactivity and sands and limestone reading low. Natural gamma ray logging is traditionally used for correlating zones from well to well, for preliminary identification of lithology, and for rough estimation of the volume of shale present in the formation. Spectral gamma ray sensors measure the energy spectrum of the emitted gamma rays and may be used to determine the weight concentrations of potassium, uranium, and thorium in the formation. This elemental analysis can provide a means to identify clay minerals, and help for the resolution of radioactive anomalies in clean formations that may be misinterpreted as shale zones using only a total gamma ray log.
In operations in which the tool string further includes a neutron source, such as a pulsed neutron generator, as found in common nuclear logging tools, drilling fluids (mud) in the borehole may be activated by the generated neutrons. Such activated mud is known to emit gamma rays that may be detected by a natural gamma ray sensor and thereby bias the natural gamma ray logging measurements. While methods are known for correcting natural gamma ray measurements for activated mud effects (e.g., activated oxygen gamma rays), there remains a need in the art for improved methods, for example, for reducing or minimizing error.
A method for making a natural gamma ray measurement is disclosed. The method includes circulating drilling fluid in a logging while drilling tool deployed in a subterranean wellbore. The LWD tool (or tool string) includes an electrical neutron source and a natural gamma ray sensor. The neutron output of the electrical neutron source is modulated and the natural gamma ray sensor is used to make a corresponding gamma ray measurement during at least a portion of the modulation. The gamma ray measurement is processed to obtain a corrected total natural gamma ray measurement of the subterranean formation.
The disclosed embodiments may provide various technical advantages. For example, the disclosed methods may advantageously reduce or substantially eliminate the influence of drilling fluid activation induced by fast neutrons. The disclosed embodiments may therefore provide corrected total natural gamma ray measurements that account for drilling fluid activation (e.g., oxygen activation) during a natural gamma ray logging operation and may therefore provide for an accurate determination of the total natural radioactivity in the subterranean formation. The correction methodology may improve both the accuracy and precision of total natural gamma ray measurements and therefore provide for improved formation evaluation.
This summary is provided to introduce a selection of concepts that are further described below in the detailed description. This summary is not intended to identify key or essential features of the claimed subject matter, nor is it intended to be used as an aid in limiting the scope of the claimed subject matter.
For a more complete understanding of the disclosed subject matter, and advantages thereof, reference is now made to the following descriptions taken in conjunction with the accompanying drawings, in which:
It will be understood that the deployment depicted on
In
With continued reference to
The gamma-ray detector 155, while intended to measure the natural gamma-ray activity of the formation, may also detect the above-described gamma-rays that originate in the mud. For example, oxygen activation induced gamma rays may be detected when downwardly flowing mud 112 in the tool string and/or upwardly flowing mud 113 in the annulus emits gamma rays in the vicinity of the detector 155. The resulting natural gamma ray measurements are thereby corrupted and commonly require correction to accurately reflect the properties of the formation.
One approach for correcting natural gamma ray measurements includes determining one or more standard spectra for gamma rays emitted by activated mud (e.g., by oxygen activation). The measured gamma-ray spectrum may then be analyzed as a combination of the standard spectra of the elements of the formation generating natural gamma-ray as well as the one or more standard spectra of the mud activation. From this analysis, it is possible to derive the part of the spectrum due to the mud activation and to correct the total count rate measured by the gamma ray detector by subtracting the count rate due to the detection of gamma rays from activated mud.
Commonly assigned U.S. Pat. No. 7,081,616, which is incorporated by reference in its entirety herein, discloses another approach in which the measured gamma ray spectrum is evaluated to determine a count rate corresponding to gamma rays having an energy in a correction interval above a predetermined threshold (the threshold corresponding generally to an energy threshold that natural gamma rays do not reach, for example, above about 3 MeV). A correction count rate, corresponding to the gamma rays derived from mud activation, is determined from the count rate above the threshold and is subtracted from the total count rate. Assuming that the spectral shape of gamma rays induced by activated drilling fluid remains unchanged during the measurement, the number of counts above the threshold (referred to in the art as T4) is directly proportional to the total number of gamma rays induced by the activated drilling fluid (referred to in the art as T1). A ratio R=T1/T4 may be computed based on laboratory measurements of oxygen activation spectra (e.g., based on gamma ray spectra measured from activated mud circulating inside a logging tool and/or outside a logging tool). During a logging operation, the count rate above the threshold (e.g., above about 3 MeV) may be multiplied by R to determine the correction count rate which may then be subtracted from the total count rate. This correction methodology is commonly referred to in the art as a T1/T4 correction.
While the above described correction methods are serviceable, they can be prone to error. For example, the relative contribution of mud based gamma rays and the shape of the mud activation gamma ray spectra can vary during a logging operation.
Gamma rays are detected at 206 using a natural gamma ray detector. In certain embodiments, the detected gamma rays are substantially free of activation gamma rays (i.e., are essentially entirely natural gamma rays emitted by the formation). In certain other embodiments, the detected gamma rays may include both natural gamma rays emitted by the formation and the activation gamma rays emitted by the activated drilling fluid (e.g., activated oxygen in the drilling fluid). In embodiments in which the detected gamma rays include activation gamma rays, the detected gamma rays may be processed at 208 to obtain a corrected natural gamma ray measurement (to thereby remove the activation gamma rays counts from the measurement). The corrected natural gamma ray measurement provides an indication of the total natural radioactivity of the subterranean formation. The corrected total natural gamma ray log may be evaluated, for example, to provide well to well correlation of formation layers within a field, to distinguish between shale and radioactively clean layers, to identify formation lithology, and/or to estimate a volume of shale present in the formation.
It will be understood that the neutron modulation in 204 may be applied to substantially any type of electrical neutron generator. For example, the neutron generator may be a pulsed neutron generator in which neutrons are emitted in high frequency bursts such as described in U.S. Pat. Nos. 4,926,044; 6,703,606 and 7,365,307. The neutron generator may also run in a “DC” mode without any high frequency pulses or bursts.
It will be further understood that the neutron modulation in 204 is a low frequency modulation in comparison to the high frequency bursts or pulses commonly utilized in pulsed neutron generators. The neutron modulation frequency in 204 may be one or more orders of magnitude (e.g., two or three orders of magnitude) less than the high frequency bursts or pulses. For example, the neutron modulation in 204 is generally less than 10 Hertz (e.g., in a range from about 0.01 to about 10 Hz, in a range from about 0.02 to about 5 Hz, or in a range from about 0.05 to about 2 Hz) while the high frequency bursts or pulses utilized in pulsed neutron generators are generally on the order of 10 kHz (10,000 Hz) to 100 kHz (100,000 Hz). In embodiments that employ pulsed (or burst) neutron generation, the modulation applied in 204 may be thought of as providing a low frequency modulation of (or envelope about) the high frequency pulse amplitude.
Gamma rays are detected at 226 using a natural gamma ray detector. A start time for the natural gamma ray measurement interval may be determined based on the count rate of high energy gamma rays (e.g., above 3 MeV). For example, the natural gamma ray measurement acquisition may be triggered when the count rate of high energy gamma rays falls below a predetermined threshold sufficient to ensure acceptable accuracy and precision of the natural gamma ray measurement. For example, high energy count rate may be essentially zero to ensure optimum precision and accuracy. In another embodiment, the initiation time of the natural gamma ray measurement interval may be computed based upon the drilling fluid flow rate and the bottom hole assembly configuration. For example, the natural gamma ray measurement acquisition may be initiated at some time interval after the neutron source is turned off. The time interval may be intended to provide sufficient time for the activated drilling mud to travel from the neutron source downhole to the drill bit and then uphole past the natural gamma ray sensor. The natural gamma ray measurement may be evaluated, for example, to provide well to well correlation of formation layers within a field, to distinguish between shale and radioactively clean layers, to identify formation lithology, and/or to estimate a volume of shale present in the formation.
It will be understood that method 220 may advantageously provide a highly accurate natural gamma ray measurement having minimal (essentially zero) activated drilling fluid gamma ray counts. One drawback of method 220 is that it requires the neutron source to be turned off for relatively long intervals so that the activated drilling fluid can flow through the tool string and then uphole through the annulus past the natural gamma ray sensor. These “off” intervals may reduce the statistical precision of other measurements that use the neutron source as a primary source of radiation (e.g., neutron logging measurements). The natural gamma ray measurements may also have reduced statistical precision since the gamma ray detector is active for only a portion of the drilling time as depicted on
In a related embodiment, the natural gamma ray measurements made while the neutron source is off may be used to correct natural gamma ray measurements made when the neutron source is active.
Gamma rays are detected at 246 using a natural gamma ray detector. A start time for the natural gamma ray measurement interval may be determined based upon the drilling fluid flow rate and the distance between the neutron source and the natural gamma ray detector with the time interval being computed to provide sufficient time for the activated drilling mud to travel from the neutron source past the gamma ray sensor. The gamma rays detected at 246 may include natural gamma emitted by the formation and activation gamma rays emitted by the activated drilling fluid flowing uphole through the annulus. The acquired gamma ray counts may be processed at 248, for example, using a conventional T4/T1 correction in combination with a standard spectrum for activated drilling fluid flowing outside the logging tool to remove the activation gamma ray counts and obtain a corrected gamma ray measurement. The standard spectra may be obtained, for example, via laboratory measurements and/or modeling. As noted above, the corrected measurement may be evaluated, for example, to provide well to well correlation of formation layers within a field, to distinguish between shale and radioactively clean layers, to identify formation lithology, and/or to estimate a volume of shale present in the formation.
Method 240 may advantageously provide a highly accurate natural gamma ray measurement having significantly lower oxygen activation gamma ray counts than a conventional measurement. These measurements may therefore further have improved accuracy after an activation correction is applied (e.g., a T4/T1 correction). Moreover, the neutron source “off” intervals are relatively short thereby enabling neutron logging measurements to be made with good statistical precision.
Gamma rays are detected at 266 using a natural gamma ray detector. The detected gamma rays may be evaluated, for example, using frequency spectrum analysis techniques and/or filtering techniques at 268 to remove at least a portion of the gamma rays resulting from drilling fluid activation and to obtain a corrected gamma ray measurement. The corrected measurement may then be evaluated, for example, as described above to provide well to well correlation of formation layers within a field, to distinguish between shale and radioactively clean layers, to identify formation lithology, and/or to estimate a volume of shale present in the formation.
A true (corrected) total natural gamma ray measurement may be computed, for example, from first and second natural gamma ray measurements corresponding to the maximum 273 and minimum 274 values of neutron emission in the neutron modulation scheme. It will be understood that neutron source modulation only modulates the drilling fluid (e.g., oxygen) activation gamma rays (e.g., as depicted at 275) but does not modulate (or in any way influence) the true (real) total natural gamma ray emission of the formation. The first and second natural gamma ray measurements may expressed mathematically, for example, as follows:
GRM1=NGR+AGR
GRM2=NGR+X·AGR
where GRM1 and GRM2 represent the first and second gamma ray measurements corresponding to the maximum and minimum neutron outputs in the modulation scheme (GRM1 and GRM2 are depicted, for example, at 281 and 282), NGR represents the true natural gamma ray count rate, AGR represents the activation gamma ray count rate at the maximum neutron output, and X represents a ratio of the minimum to maximum neutron output in the modulation scheme such that 0≤X<1. These equations may be solved simultaneously to obtain a mathematical expression for the true natural gamma ray count rate, for example, as follows:
It will be understood that the above equation assumes that the activation gamma ray count is substantially proportional to the neutron source output. The disclosed embodiments are of course not limited in this regard. In the above equation X may be substituted with X′ indicating that the activation gamma ray count is a non-proportional (or non-linear) function of the neutron output.
Method 260 may advantageously provide a highly accurate corrected natural gamma ray measurement in which gamma rays emitted by activated drilling fluid are removed based on a characteristic frequency rather than other assumptions such as the spectral shape of the activation gamma rays. Method 260 further provides for accurate neutron logging measurements having good statistical precision since the neutron source remains on (modulating between relatively high and low values).
As noted above, the neutron modulation in the disclosed embodiments is a very low frequency modulation (e.g., in a range from about 0.01 to about 10 Hz) in comparison to the high frequency bursts or pulses commonly utilized in pulsed neutron generators (which is on the order of 10 kHz to 100 kHz). For example, the neutron modulation frequency may be on the order of two, three, or more orders of magnitude less than the high frequency bursts or pulses. As further noted above, in embodiments employing pulsed (or burst) neutron generation, the disclosed modulation may be thought of as providing a low frequency modulation of (or envelope about) the high frequency pulse amplitude such that the amplitude of (or number of neutrons generated in) the high frequency pulses is modulated. This is depicted schematically in
With continued reference to
With reference again to
While not depicted in the FIGS., it will be understood that a portion of the disclosed method embodiments may be implemented downhole (e.g., by a downhole controller deployed in the logging string). Moreover, it will be further understood that the aspects and features of the disclosed embodiments may be embodied as logic that may be processed by, for example, a computer, a microprocessor, hardware, firmware, programmable circuitry, or any other processing device known in the art. Similarly the logic may be embodied on software suitable to be executed by a processor, as is also well known in the art. The disclosed embodiments are not limited in any of these regards.
A suitable downhole controller may include, for example, a programmable processor, such as a microprocessor or a microcontroller and processor-readable or computer-readable program code embodying logic. A suitable processor may be utilized, for example, to execute a portion of the method embodiments described above with respect to
A suitable controller may be further configured to control operation of the natural gamma ray detector(s) and the neutron generator(s) (e.g., to modulate the neutron source and/or to initiate a natural gamma ray measurement cycle). A suitable controller may also optionally include other controllable components, such as data storage devices, power supplies, timers, and the like and may optionally communicate with other instruments in the drill string, for example, including telemetry systems that communicate with the surface. A suitable controller may further optionally include volatile or non-volatile memory or a data storage device for storing measured gamma ray spectra for further post-processing.
Although a method for making natural gamma ray logging measurements and certain advantages thereof have been described in detail, it should be understood that various changes, substitutions and alternations can be made herein without departing from the spirit and scope of the disclosure as defined by the appended claims.
This application claims the benefit of U.S. Provisional Application Ser. No. 62/694,354 entitled Pulsed Neutron Generator (PNG) Output Modulation for Error Reduction in the Oxygen Activation Correction, filed Jul. 5, 2018.
Filing Document | Filing Date | Country | Kind |
---|---|---|---|
PCT/US2019/040669 | 7/5/2019 | WO |
Publishing Document | Publishing Date | Country | Kind |
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WO2020/010294 | 1/9/2020 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
2856537 | Clark | Oct 1958 | A |
3281599 | Baker | Oct 1966 | A |
3825753 | Givens | Jul 1974 | A |
3914603 | Paap | Oct 1975 | A |
3928762 | Peelman | Dec 1975 | A |
3930152 | Pitts, Jr. | Dec 1975 | A |
3940611 | Arnold | Feb 1976 | A |
3940613 | Paap | Feb 1976 | A |
3979300 | Paap | Sep 1976 | A |
4180728 | Goldstein | Dec 1979 | A |
4857729 | Gadeken | Aug 1989 | A |
4926004 | Pelrine | May 1990 | A |
4926044 | Wraight | May 1990 | A |
5408097 | Wraight | Apr 1995 | A |
5459314 | Plasek | Oct 1995 | A |
6051830 | Moake | Apr 2000 | A |
6703606 | Adolph | Mar 2004 | B2 |
7081616 | Grau | Jul 2006 | B2 |
7361886 | Stoller | Apr 2008 | B2 |
7365307 | Stoller | Apr 2008 | B2 |
7800052 | Gadot | Sep 2010 | B2 |
8049164 | Kirkwood | Nov 2011 | B2 |
9329302 | Stoller | May 2016 | B2 |
9500753 | Moake | Nov 2016 | B2 |
10317568 | Mauborgne | Jun 2019 | B2 |
10564311 | Stoller | Feb 2020 | B2 |
10866336 | Stoller | Dec 2020 | B2 |
20050127282 | Grau | Jun 2005 | A1 |
20070241275 | Guo | Oct 2007 | A1 |
20090123071 | Iwasaki | May 2009 | A1 |
20090321622 | Stoller | Dec 2009 | A1 |
20140343856 | Zhou | Nov 2014 | A1 |
20150090870 | Stoller | Apr 2015 | A1 |
20170363770 | Mauborgne | Dec 2017 | A1 |
20180059283 | Xu | Mar 2018 | A1 |
20180364184 | Reiderman | Dec 2018 | A1 |
20210169417 | Burton | Jun 2021 | A1 |
Number | Date | Country |
---|---|---|
2016179516 | Nov 2016 | WO |
Entry |
---|
International Search Report and Written Opinion issued in International Patent application PCT/US2019/040669 dated Oct. 2019, 11 pages. |
Exam Report Under Section 18(3) issued in United Kingdom Patent Application GB2100088.0 dated Jan. 26, 2022, 5 pages. |
Number | Date | Country | |
---|---|---|---|
20210270994 A1 | Sep 2021 | US |
Number | Date | Country | |
---|---|---|---|
62694354 | Jul 2018 | US |