This disclosure relates generally to the field of pulsed neutron well logging for determining macroscopic thermal neutron capture cross section (sigma) and/or its converse thermal neutron decay time constant. More specifically, the invention relates to techniques for making such determinations which account for wellbore effect of neutron diffusion.
Formation sigma determination based on measurements of capture gamma rays resulting from a pulsed neutron source has been used in the petroleum industry for several decades. It is essentially a thermal neutron “die-away” measurement, which responds to the macroscopic thermal capture cross section of the formation. The decay of the thermal neutron population is close to exponential in an ideal situation (for example, a homogeneous uniform condition), while the actual shape of the decay curve with respect to time may not be representable by an analytic formula. An apparent decay constant (based on either a fitting or moments method) is not always equal or close to the actual formation decay constant. Wellbore decay contamination and thermal neutron diffusion affect the apparent decay constant. In some conditions (for example, high salinity water in the wellbore and a formation sigma that is much smaller than the corresponding borehole sigma), at least two decay constants can be observed, and the decay of the thermal neutron population is very close to a dual exponential decay. However, such dual exponential decay is not always evident. Obtaining accurate and precise formation sigma measurements under all formation and wellbore conditions is very challenging.
A method according to one aspect for determining thermal neutron decay constant for a formation includes counting radiation events corresponding to numbers of thermal neutrons with respect to time (decay spectrum) after irradiating the formation with neutrons. At least one moment of a first order of the decay spectrum or a single exponential curve to fit the decay spectrum is determined. A first apparent decay constant from the at least one moment or the single exponential curve. A second apparent decay constant is determined either by repeating the calculating a moment or exponential curve for different time segments of the decay spectrum or by using radiation events detected by at least a second radiation detector at a different spacing from a position of the irradiating than the at least a first radiation detector to determine a second apparent decay constant. A wellbore corrected thermal neutron decay constant is determined from the first and second apparent decay constants.
Other aspects and advantages will be apparent from the description and claims that follow.
The instrument housing 12 contains a pulsed neutron source 14, and two or more gamma ray detectors 18, 20 at different axial spacings from the pulsed neutron source. The pulsed neutron source 14 (hereinafter “source”), when activated, will emit controlled duration “bursts” of high energy neutrons (approximately 14 MeV, and which may be emitted isotropically). One example of a pulsed neutron source is described in U.S. Pat. No. 5,293,410 issued to Chen et al. and incorporated herein by reference.
Shielding 16 may be interposed between the source 14 and the axially closest detector (e.g., 16) to reduce the effects of direct neutron communication between the source 14 and the detectors 18, 20. The detectors 18, 20 may be scintillation counters each coupled to a respective counter or pulse height analyzer (not shown separately). Thus, numbers of and, with the use of a pulse height analyzer, energy of detected gamma rays may be characterized at each of a plurality of distances from the source 14.
The gamma ray detectors 18, 20 may detect gamma rays arriving at the detector as a function of time. There are two principal mechanisms, through which a neutron-induced gamma ray can be generated. One is neutron inelastic scattering, which can be triggered only by “fast” neutrons (with energy above approximately 1 MeV, the exact energy threshold depending on the type of nucleus). The other is through neutron capture, which can be triggered primarily by thermal neutrons (with energy around 0.025 eV at room temperature) or epithermal neutrons (with energy from about 0.4 to 100 eV) being absorbed into a susceptible nucleus, as non-limiting examples, chlorine, boron and cadmium. Gamma rays arriving at the detectors 18, 20 may be generated through both mechanisms because the source keeps emitting fast neutrons which can slow down to epithermal or thermal almost instantly (relative to the acquisition system timing. For purposes of the present disclosure, gamma rays corresponding to capture of thermal neutrons by susceptible nuclei are those of interest.
The detectors 18, 20 may also be any type of thermal neutron detector, e.g., 3He proportional counters. Gamma ray detectors may be preferable because of their higher sensitivity, and resulting higher count rates and associated statistical precision.
A well logging instrument including a scintillation detector type radiation counter is shown at 210 in
The present example of the well logging instrument may be an instrument that makes measurements corresponding to selected properties of the Earth formations 215 based on analysis of detected capture gamma rays, or detected thermal neutrons, with respect to time after each operation of the pulsed neutron source (14 in
One or more radiation detectors (e.g., 18 and 20 as explained with reference to
While the example conveyance of a well logging instrument as shown in
The present disclosure explains use of the moment method to compute the apparent decay constant. There are some varieties of the moment methods, which are described in more detail below. “Moment” as used herein may be broadly defined as the shape of a set of data points. All the described methods are based on the assumption that the thermal neutron decay curve is a single exponential decay, and the decay constant thus determined corresponds to the thermal neutron capture cross section of the formation adjacent to the logging instrument. In reality, this assumption is generally incorrect because there are borehole contamination and diffusion effects in addition to formation decay in the counting rate of the detected thermal neutrons or capture gamma rays. Thus correction may be performed after computing the apparent sigma from
In addition to moment methods, one can also compute the apparent decay constant by using a single exponential fit. The results of the single exponential fit are very similar to the ones of the first order moment method.
Instruments such as shown in
Equation 1 shows how to compute an apparent thermal neutron decay constant using the first order moment from a measured thermal neutron decay time spectrum, where fi is the count rate in the i-th time bin and ti is the time of the i-th time bin with respect to the end of the neutron bust generated by the pulsed neutron source (14 in
Assuming the decay time spectrum is a single exponential decay, Equation 2 shows the theoretical first order moment method, which is the first order moment divided by the zero order moment.
If it were possible to integrate Equation 2 from t=0 to infinite time, the result of Equation 2 provides the decay constant x of the single exponential decay. Since in reality one cannot measure the decay time spectrum to infinity, the integration can only be performed from time=0 to a certain time T. This is shown in Equation 3.
Equation 4 shows the result of the finite integration of Equation 3 is x′.
Equation 5 shows an approximation for the decay constant expressed in terms of x′ and the finite correction.
When T goes to infinity, x′ converges to x. In order to obtain x from x′, a correction is needed for the finite integral effect. The correction term is defined in Equation 6, which is a function of T/x. t1 represents the ending time of the measurement gate, which as will be further explained below, may be selected or optimized for particular purposes.
Since x is unknown, one may estimate the correction term using x′. This cannot be performed analytically, but may be performed empirically. One can generate a good approximation of the exact correction term for a wide, realistic range of T/x, and try to reproduce the correction term using T/x′ based on an empirical equation, lookup table or similar means when processing data from the logging instrument. The formula in Equation 6 shows an example of such an empirical equation. One may different equations or may estimate the correction term iteratively. Then, one may estimate the decay constant x using the approximated correction term and x′ from the moments as shown in Equation 6. Similarly, for a measured discrete neutron decay time spectrum, one can apply the same correction term to τ′ in Equation 1 to obtain the apparent decay constant, as shown in Equation 6. At the end, one may compute the apparent sigma from the apparent decay constant T using Equation 7.
The apparent sigma thus computed is related to the starting time (t0) and end time (T) of the measurement time gate (wherein the gate ending time is represented by t1 as explained above). Varying the starting time will not only change the borehole and diffusion effect in the apparent decay constant, but will also change the statistical precision. An apparent sigma based on an early gate starting time will have more borehole and diffusion effect than one with a later starting time, because borehole decay and diffusion typically occur early after the end of the neutron burst, and formation decay often happens later. Varying the end time of the measurement gate will only change the statistical precision due to the presence of activation background radiation, which needs to be subtracted from the measurements before determining the decay constant.
The second order moment method is similar to the first order moment method. Instead of computing a first order moment divided by a zero order moment, this method computes a second order moment divided by a first order moment, as shown in Equation 8.
Equation 9 shows if the decay time spectrum is a single exponential, the second order moment method will compute the decay constant x by integrate from 0 to infinity.
Equation 10 shows if the integration is not infinite, the computed x′ can be written as the decay constant x multiplied by a correction term.
Equation 11 shows the correction term can be approximated by T/x′.
Equation 12 shows one can obtain the decay constant x by applying the approximated correction term to x′.
Equation 13 shows the apparent decay constant T can be computed by applying the same approximated correction term to a measured discrete neutron decay time spectrum. At the end, the apparent sigma can be computed from the apparent decay constant T using Equation 7.
By comparing the first and second order moment methods, one can easily extend the above methods to higher order moments by computing, e.g., (n+1)th order moment divided by the nth order moment, or nth order moment divided by an mth order moment and then raise the result of the division to the power of m/n.
Varying the starting time (t0) and end time (T) of the measurement time gate will change the borehole and diffusion effect in the apparent sigma computed using the second order moment method, similar to the first order moment method. An apparent sigma with an early measurement gate starting time will have more wellbore and diffusion effect than the one with a late starting time, because borehole decay and diffusion typically happen early and formation decay often happens late. The apparent sigma computed by the first and second order moment methods based on the same timing gate will have different borehole and diffusion effects. The moment is essentially a weighted sum with the current time as the weight. A higher order moment will have higher weight for the later time compared to a lower order moment. Since borehole effects and diffusion typically happen earlier than the formation decay, an apparent sigma computed using a higher order moment will have less borehole and diffusion effects than the one computed using a lower order moment method.
The zero order moment method is somewhat different from the higher order moment methods. As shown in Equation 14, the apparent decay constant may be computed by a zero order moment (simply a sum of the decay spectrum) within one timing gate (t0 to tN) divided by another zero order moment within different timing gate (t0 to tM).
Ideally, tN would be infinity and tM equal to t0 as shown in Equation 15.
Essentially, this method computes the decay constant by using the sum of the decay curve divided by the value of the decay curve (i.e., the counting rate) at time 0. As explained above, the decay curve is not measured to infinite time. In addition, one cannot measure the decay curve instantaneously but only as a summation of the number of detected radiation events in a discrete time bin. Equation 16 shows the result of the zero order moment method x′ for a single exponential decay.
If TN goes to infinity and TM goes to 0, x′ will converge to x/TM. Based on Equation 16, one can study the relationship between x′ and x giving a TN and TM, then use x′ to approximate x empirically.
Equation 17 shows one example of approximating x using x′ based on a fifth order polynomial equation obtained by data fit. The coefficients of the polynomial are a function of TM and TN.
x≈a
1
·x′
5
+a
2
·x′
4
+a
3
·x′
3
+a
4
·x′
2
+a
5
·x′+a
6 (17)
Applying the same polynomial equation, one can obtain τ T from τ′ as shown in Equation 18. At the end the apparent sigma can be computed using Equation 7.
τ≈a1·τ′5+a2·τ′4+a3·τ′3+a4·τ′2+a5·τ′+a6 (18)
Similarly to the two previous methods, varying the timing gate from early to late, the borehole and diffusion effects in the apparent sigma computed using the zero order moment method will become less. The apparent sigma from the zero order moment method has more borehole and diffusion effects than the higher order moment methods due to the relatively smaller weight applied to later in the time gate.
One can also compute the apparent decay constant by applying a single exponential fit within a certain timing gate of the decay time spectrum. This may be a non-linear fit, due to the present of activation gamma rays and nature gamma rays from formation. One can periodically turn off the PNG and measure the background, then remove them from the decay spectrum. The fitting can become a linear fit after taking a log of the background corrected decay spectrum.
Because the measured thermal neutron decay time spectrum is usually not a single decay constant exponential decay, the apparent sigma computed using the methods described earlier will need additional correction to compensate for wellbore and diffusion effects. The finite integral correction terms as shown in Equation 6, Equation 13, and Equation 18 do not correct the computed apparent decay constant to the true formation decay constant, but they are necessary to determine in the present example methods. Without them, compensation techniques described below will not behave linearly so that the correction may be more difficult to perform
Different wellbore and diffusion compensation methods will be described below. All of them may use the difference between the borehole and diffusion effects in two or more apparent values of sigma, which are computed using either different calculation methods or different timing gates, or based on measurements from different detectors, to compensate those effects and obtain an accurate formation sigma without needing a wellbore sigma value as an input. The examples shown are not exhaustive and do not limit the scope of the present disclosure. One can combine two or more different compensation methods or extend them readily. Different example methods which can be applied to single detectors will be described first, and then example methods for multiple detectors will be described.
The examples shown are based on modeling data, which were computed using a Monte Carlo method (MCNP) in an 8 inch wellbore with a 5.5-in. OD casing with 4.95 in. ID. The wellbore can be filled with either fresh water or saline water (250 ppk). 33 different formation conditions were modeled: sandstone, limestone, dolomite with 0-pu, (pu represents “porosity units” or fractional volume of pore space times 100 in a particular formation) 2.5-pu, 5-pu, 10-pu, 20-pu, and 40-pu filled with fresh water in the pore spaces; sandstone 10-pu, 20-pu, and 40-pu with saline water (100 ppk, 200 ppk and 260 ppk) in the pore spaces; and sandstone, limestone, dolomite with 5-pu or 10-pu filled with methane gas (0.15 g/cc).
The first example uses the first order moment method to compute two (or more) apparent sigma values based on different timing gates.
comp_term≡Σtrue−Σlate≈−a1·(Σearly−Σlate)+a2 (19)
The estimated sigma can then be computed as shown in Equation 20.
Σestimated=Σlate+comp_term=(1+a1)·Σlate−a1·Σearly+a2 (20)
Essentially, the estimated sigma is a linear function of the two apparent sigma values plus a constant offset. The sum of the two coefficients for the two apparent sigma is equal to 1 in Equation 20. One can relieve this constraint and fit the three coefficients in Equation 21 based on modeling data (or lab measured data in actual formations using an actual instrument).
Σestimated=b1·Σlate+b2·Σearly+b3 (21)
Another compensation method may be obtained by generating the contribution of the late exponential spectrum to the total measured spectrum. The first step in defining this contribution is to determine the apparent decay constant of the late spectrum using the moment method as shown in Equation 22.
In Equation 22, the sum is over the late bins of the measured spectrum (I is the last bin of the measured spectrum). The apparent decay constant may helpfully be corrected for the finite window used in its computation as shown in Equation 23 (Δ is the bin width [time duration] of the measured spectrum).
The starting bin, N, can be optimized. The late spectrum, Li, my be defined for each bin of the measured spectrum as shown in Equation 24.
The fraction of counts in the early portion of the measured spectrum that comes from this late contribution may then be defined in Equation 25.
The difference between early sigma and late sigma is close to a linear function of the late fraction, as may be observed in
Σestimated=b1·Σlate+b2·late_fraction+b3 (26)
Comparing the above described correction method to the previous one (early and late first-order moment sigma compensation), one minor difference is that the finite integral correction term is a little different (Equation 23 vs. Equation 6). An important difference is that the above described correction approach uses the late fraction term, which is a complex function of late apparent sigma and a zero order moment (the ratio of the two sum) without finite integral correction. In principle, this approach is the same as the previous one, because
The different methods to compensate the borehole and diffusion effects described above are based on different apparent sigma. All the foregoing methods can be applied to measurements from only a single detector. If more than one detector is available, depending on the detector spacings from the source, the apparent sigma computed using the same method and same timing gate but different detectors will have different borehole and diffusion effects. Thus, one may take advantage of the apparent sigma from different detectors.
Note that the accuracy in crossover conditions of the above described multi-detector method is higher than all the methods discussed for single detector. The crossover condition is defined as when the wellbore decay is slower than the formation decay; thus the formation component goes away at the later time and only the wellbore component may remain later in the time spectrum. This is the opposite of the non-crossover condition, in which the wellbore component dominates early in the time spectrum and decays away more quickly than the formation and leaves more formation component later in the time gate. The methods for a single detector are based on different borehole and diffusion effects in different timing. In crossover conditions, the compensation fails. The multi-detector method is not based on different timing so that it does not have this problem.
Methods according to the present disclosure may provide accurate formation sigma values under a wide range of wellbore and formation conditions, in particular without the need to have a known value of wellbore sigma as an input.
A processor can include a microprocessor, microcontroller, processor module or subsystem, programmable integrated circuit, programmable gate array, or another control or computing device.
The storage media 106 can be implemented as one or more computer-readable or machine-readable storage media. Note that while in the exemplary embodiment of
It should be appreciated that computing system 100 is only one example of a computing system, and that computing system 100 may have more or fewer components than shown, may combine additional components not depicted in the example embodiment of
Further, the steps in the processing methods described above may be implemented by running one or more functional modules in information processing apparatus such as general purpose processors or application specific chips, such as ASICs, FPGAs, PLDs, or other appropriate devices. These modules, combinations of these modules, and/or their combination with general hardware are all included within the scope of the present disclosure.
While the invention has been described with respect to a limited number of embodiments, those skilled in the art, having benefit of this disclosure, will appreciate that other embodiments can be devised which do not depart from the scope of the invention as disclosed herein. Accordingly, the scope of the invention should be limited only by the attached claims.
This application claims priority to and the benefit of U.S. Provisional Application Ser. No. 61/817,714 entitled “Compensated Sigma Calculation Based On Pulsed Neutron Capture Tool Measurements”, filed Apr. 30, 2013, the disclosure of which is hereby incorporated by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/US2014/036095 | 4/30/2014 | WO | 00 |
Number | Date | Country | |
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61817714 | Apr 2013 | US |