ORIGINAL RESEARCH article

Front. Energy Res., 23 March 2022

Sec. Nuclear Energy

Volume 10 - 2022 | https://doi.org/10.3389/fenrg.2022.835495

Study on the Fast Neutron Multiplicity Measurement of Uranium Material

  • Xi’an Research Institute of Hi-Tech, Xi’an, China

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Abstract

As a non-destructive testing and analysis technology, the neutron multiplicity measurement method plays an important role in the field of arms control verification. Great progress has been achieved in the fast neutron multiplicity measurement of plutonium, while there are few studies that have been conducted in the fast neutron multiplicity measurement of uranium. In this study, a set of fast neutron multiplicity measurement devices based on the BC501A liquid scintillation detector was built, and two small mass uranium samples with low density were studied. It is found that the change of the total neutron counting rate is irregular, and the coincidence counting rate will increase linearly with the mass. It is due to the energy loss caused by the scatter of the Am-Li source neutron with the sample, resulting in part of the neutron energy below the threshold. A simulation detection system is built by Geant4 to verify the reliability. On this basis, four kinds of packaging materials such as steel, copper, aluminum, and graphite were studied. The measurement results of different materials were compared and analyzed. The thickness of the material was studied, and the functional relationship curve was fitted. In this study, the fast neutron multiplicity measurement of small-mass and low-density uranium samples was carried out and verified. The influence of different packaging materials on the multiplicity measurement was analyzed, which is of great significance for the development of the fast neutron multiplicity measurement technology.

Introduction

With the continuous development of the nuclear technology, nuclear energy has been applied in various fields. As the important fissile materials, uranium and plutonium play an important role in the nuclear energy utilization technology. Due to the particularity of nuclear materials, especially with the advancement of nuclear arms control and nuclear disarmament, the attribute certification analysis of nuclear materials has attracted more and more attention. The neutron multiplicity measurement method is an important non-destructive analysis technique. The effective mass of nuclear materials can be calculated by establishing the functional relationship between fission neutron and nuclear material properties. According to the spontaneous fission rate and induced fission rate of nuclear materials, different measurement methods can be adopted. 240Pu has a higher spontaneous fission rate, often using the passive measurement method (Sarwar, 2016). The passive measurement method does not need the external neutron source and mainly relies on the spontaneous fission reaction, while 235U and 237Np have higher induced fission rates, often adopting the active measurement method (Hua et al., 2020; Krick et al., 1996; Dolan et al., 2014). The active measurement method irradiates the nuclear material through the external neutron source to induce fission. At present, the neutron multiplicity measurement method is relatively mature, using 3He tube as the neutron detector, and the measurement model is AWCC (Stewart et al., 2000). The fast neutron multiplicity measurement is carried out by using a scintillation detector (BC501A, EJ-309, Stilbene) (Di et al., 2018; Li et al., 2018). The influence of the neutron scattering crosstalk is considered in the measurement, and the equation is corrected (Shin et al., 2017). Compared with the neutron multiplicity measurement equation, the fast neutron multiplicity measurement equation of plutonium deduces the high-order equation (Zhang et al., 2019). At present, the fast neutron multiplicity measurement mostly focuses on nuclides with a high spontaneous fission rate, such as 240Pu. There are few studies on nuclides with a high induced fission rate, such as 235U and 237Np, and most of them are concentrated on large mass and high-density samples (Kerr et al., 2007). Based on the six-probe liquid scintillation detection system, this work studies the fast neutron multiplicity measurement of two small-mass and low-density uranium samples, which is of great significance to broaden the application range of fast neutron multiplicity measurement technology.

Principle

Different from the coincidence counting method, the fast neutron multiplicity measurement method establishes an analysis model through neutron counting rate and sample parameters. The model is established on the basis of the “point model” and a series of assumptions, and the equations are deduced by introducing mathematical knowledge such as the probability-generating function and factorial moment (Favalli et al., 2015; Westcott, 1972), as shown in the following equations.In Eqs 13, are the first-, second-, and third-order factorial moments of neutron distribution induced by an external neutron source, and are the first-, second-, and third-order factorial moments of neutron distribution induced by the secondary fission, respectively. ε is the detection efficiency of the system. is the double and triple coincidence factor of the system, respectively. Since the active measurement method uses external neutrons to induce fission, the induced fission rate is related to the uranium material mass, the intensity of the Am-Li source, and the coupling coefficient, as shown as follows.

The coupling coefficient is the key parameter in the active multiplicity measurement, which is related to the geometry structure, density, material composition, and the neutron spectrum of the Am-Li source (Weinmann-Smith et al., 2017), and it is difficult to calculate theoretically. The empirical relationship between the coupling coefficient and multiplication coefficient was revealed by (Ensslin et al., 1991), as shown in Eq. 5.

The parameters are substituted into Eq. 4 to obtain the coupling coefficient , and the scale coefficient is obtained by fitting the coupling coefficient with the multiplication coefficient . According to the determined curve, the value of the coupling coefficient is calculated, and then, the effective mass of 235U is obtained from Eq. 4.

Experimental Measurement

System Composition

The detection system consists of six liquid scintillation detectors, iron support, high-voltage power supply, NIM chassis, two four-channel pulse shape discriminators MPD-4, multi-channel scaler MCS6A, and computer. The structure is shown in Figure 1.

FIGURE 1

FIGURE 1

Model of the detection system: (A) Theoretical model diagram (B) Actual model diagram.

The liquid scintillator detector is BC501A with a density of 0.874 g/cm3 and a size of Φ 12.7 cm × 5.08 cm. The sample chamber is a closed square with a length of 15.24 cm. Six detectors are located at the center of each surface of the sample chamber. The threshold of the detector is set to 0.15 MeV.

System Calibration

The 252Cf standard source (1.9 × 105cps) was placed at the center of the sample chamber, and the measurement time of the MCS6A scaler was set to 200 s. The measurement result is shown in Table 1. Taking the average neutron counting rate as , the detection efficiency is obtained by Eq. 6.

TABLE 1

Measurement timesNeutron counting rate
115632.3
215594.01
315585.02
415571.45
515581.41
Average15592.84

Measurement result of the 252Cf standard source.

In the absence of radioactive sources, the background counting rate is almost close to 0. The average neutron counting rate and the intensity of the standard source are substituted into Eq. 6 to obtain the detection efficiency of 8.21%. The 252Cf source is measured under two gate width settings, and the gate width was determined as G1, G2 = 2G1. The 252Cf standard source is placed at the center of the sample chamber. The measurement time under each gate width is 200 s, and the coincidence counting rates D1 and D2 are obtained, respectively. The neutron decay time of the device is calculated by the following formula , which is = 58.27. After measuring the neutron decay time, the gate width G can be determined by the formula . The double coincidence gate factor and triple coincidence gate factor are determined by experimental calibration. The calculation formula is as following: are the factorial moments of 252Cf source distribution, = 3.757, = 11.948, and = 31.636. The 252Cf standard source is placed in the center of the sample chamber. The measurement time is set as 200 s, and the result is shown in Table 2.

TABLE 2

Measurement timesSDT
115632.31546.8872.03
215594.011543.5269.5
315585.021539.368.9
415571.451539.9169.13
515581.411537.1568.68
Average value15592.841541.35269.648

Multiplicity measurement of the 252Cf standard source.

Substituting the average value to Eqs 7, 8, the coincidence factors , are obtained as 0.757 and 0.472, respectively.

Sample Measurement

Two samples are measured, and they are all uranium trioxide (U3O8). Sample 1 is composed of 10 screw samples. The size of a single sample is about 1.2 cm × 3.2 cm. The abundance of 235U is 90%, and the uranium mass of each sample is about 2 g. The size of sample 2 is about 8 cm × 9 cm, the abundance of 235U is 19%, and the mass is 200 g, as shown in Figure 2.

FIGURE 2

FIGURE 2

Uranium sample: (A) sample 1 (B) sample 2.

The Am-Li source with an intensity of 5 × 104cps is placed on the two opposite corners of the device, respectively, as shown in Figure 3.

FIGURE 3

FIGURE 3

Plane distribution of Am-Li sources.

Points 1 and 3 are Am-Li sources, and point 2 is the sample. The background measurement of the Am-Li sources is performed, and the measurement time is set to 1,800 s. The result is shown in Tables 35.

TABLE 3

Measurement timesSDT
14557.513.580.01
24555.923.450.01
34472.823.510.01
Average4528.753.510.01

Background measurement.

TABLE 4

Mass/gSDT
204696.59511.130.245
144746.8759.490.22
84566.217.140.12
44518.225.8350.095
24504.0754.620.06

Sample 1 measurement.

TABLE 5

SDT
13939.6716.560.4
23888.7516.370.41
33876.7616.510.41
43884.7616.420.44
Average3897.48516.4650.415

Sample 2 measurement.

As shown in Figure 4, the double counting rate of sample 1 is fitted, and the fitting equation is obtained. The goodness is 99.1%, which indicates that the double counting rate is approximately proportional to the 235U mass.

FIGURE 4

FIGURE 4

Fitting result of the coincidence counting rate.

From the sample 1 measurement, the change of the total counting rate is not obvious, while the change of the coincidence counting rate is obvious, which basically shows a linear relationship with the sample mass. The coincidence counting rate of sample 2 is relatively stable, but there is an experimental phenomenon that the total counting rate is lower than the background counting rate. Combined with the experimental results of sample 1 and sample 2, it is inferred that the background neutron emitted from the Am-Li source will scatter with the sample. Some low-energy neutrons are below the threshold of the detector after losing part of the energy, which makes it impossible to count. The coincidence neutron is mainly from the sample, which will not be affected and will increase with the sample mass.

Simulation Analysis

From the aforementioned experimental results, the variation of the total counting rate is irregular and even lower than the background counting rate, while the coincidence counting rate and the triple counting rate have a good law of growth with the mass. The preliminary analysis is that the energy loss of partial background neutron results in a lower total counting rate. To verify the accuracy of the experimental result and further demonstrate the reasons for the irregular change of the total neutron counting rate, a simulation detection system is built by Geant4. The model is shown in Figure 5.

FIGURE 5

FIGURE 5

Simulation model.

The spatial layout and geometric size of the simulation detection system are consistent with the experimental device. The Am-Li source is set at points 1 and 3, and the source intensity is 5 × 104. The sample with a density of 0.7 g/cm3 is set at point 2. Since the specific spectrum of the Am-Li source is unknown, the average energy of 0.3 MeV is adopted in the simulation, and the energy threshold of the detector is set to 0.15 MeV. The measurement result is shown in Table 6.

TABLE 6

Mass/gSDT
22.550595741−4.73796E-078.93108E-14
43.6029850520.132310888−1.32309E-08
87.0818099840.652288917−6.04186E-07
1413.391817910.76748276−1.41031E-06
2016.415565081.17560280.083655763

Measurement result of sample 1.

As shown in Figure 6, the fitting equation is , and the goodness reaches 94.1%.

FIGURE 6

FIGURE 6

Fitting result of the coincidence counting rate.

It can be seen from Table 6 that when the average energy is 0.3 MeV, the total counting rate and double counting rate will increase with the mass. Under the condition of the 0.15 MeV threshold, the background counting is 0, and the detector only records the neutron generated by the induced fission of the sample. So there is no decrease in the total counting rate. As the energy spectrum of the Am-Li source used in the experimental measurement is continuous, the background count cannot be 0. After placing the sample, the energy of some background neutrons is lower than the threshold due to scattering with the sample, resulting in the irregular change of the total counting rate. Referring to the neutron energy spectrum in reference (Weinmann-Smith et al., 2017), an approximate sectional energy spectrum is compiled to replace the real Am-Li source for measurement. The specific energy information is shown in Table 7, and the result is shown in Table 8.

TABLE 7

Interval0–1 keV1 keV–0.5 MeV0.5–1 MeV1–2 MeV
Probability0.40.150.30.15

Sectional energy spectrum.

TABLE 8

Mass/gSDT
21923.2833330.944758842−0.000207349
41921.850.8945563960.049787649
81927.051.5934280050.049652752
141927.9166672.1101183420.066173938
201948.4333332.7718656160.099350973

Sample 1 measurement.

As shown in Figure 7, the fitting equation is , and the goodness is 98.1%.

FIGURE 7

FIGURE 7

Fitting result of the coincidence counting rate.

Similar to the experimental measurement, the total counting rate changes irregularly with the mass, while the double counting rate and triple counting rate will increase regularly. However, the increase amplitude is obviously smaller than the experimental result, particularly due to the difference of the energy spectrum of the Am-Li source. Sample 2 is also measured, and the result is shown in Table 9.

TABLE 9

Measurement timesSDT
110481.360.105
210451.32−2.899e-04
Background counting rate10750.09−2.197e-05

Sample 2 measurement.

It can be seen from Table 9 that the total counting rate is lower than the background counting rate. Different from sample 1, sample 2 has lower density, larger volume, and smaller abundance, and the scattering effect is more obvious, which leads to more background neutrons unable to count. The experimental result is further verified by the simulation result.

Impact of Packaging Materials

To protect the sample from corrosion, pollution, and leakage, a layer of packaging material is usually installed on the outer layer of the sample. The U3O8 sample used in this study is wrapped with a layer of alloy material. To study the effect of packaging material, the measurement results of various packaging materials are analyzed.

The Impact of Four Kinds of Packaging Materials

To analyze the influence of material types, the thickness of the packaging layer is set to 2.5 cm uniformly. The radioactive source has a spherical shape with a density of 19.8 g/cm3. The intensity is 5 × 104cps, and the energy is 0.3 MeV. Under four kinds of packaging materials of steel, aluminum, copper, and graphite, the results are obtained, as shown in Figures 810. The density of steel is 7.85 g/cm3. The density of aluminum is 2.7 g/cm3. The density of metallic copper is 8.96 g/cm3, and the density of graphite is 2.2 g/cm3.

FIGURE 8

FIGURE 8

Detection efficiency of different packaging materials.

FIGURE 9

FIGURE 9

Total counting rate of different packaging materials.

FIGURE 10

FIGURE 10

Double counting rate of different packaging materials.

It is found that the detection efficiency is reduced after the packaging material is added to the outer layer of the sample. Among them, the detection efficiency of Cu and Fe is lower, while the detection efficiency of C and Al is higher. Compared with other materials, the total neutron counting rate and double counting rate of Cu and Fe are lower, which is the reason for the lower detection efficiency. The scattering cross section of neutrons with hydrogen atoms is relatively high, while the scattering cross section of nuclides with a high atomic number such as metals are relatively low, especially aluminum and zirconium. Therefore, Al has a smaller effect on the measurement result. However, due to the high scattering cross section of C with neutrons, the energy is reduced, which leads to the increase of the induced fission rate of the sample. So the total counting rate is higher than that without the packaging material. Taking 1 kg sample as an example, under the same condition of energy, intensity, and time, the number of induced fission rate under different packaging materials is recorded, as shown in Table 10.

TABLE 10

MaterialNo layerSteelCopperAluminumGraphite
Fission rate69095473681766047518

Fission rate under different packaging materials.

The Impact of Shell Thickness

To study the influence of thickness of the packaging layer on the measurement result, the thicknesses of 1.5, 2.0, and 2.5 cm are calculated by using the steel material, as shown in Figure 11.

FIGURE 11

FIGURE 11

Detection efficiency of different thicknesses.

As we can see, with the increase of the thickness, the detection efficiency will gradually decrease. For 3,000 g sample, the detection efficiency of the thickness from 0.5 to 3.5 cm is calculated. The result is shown in Figure 12.

FIGURE 12

FIGURE 12

Fitting result of the thickness.

The fitting equation is , = 0.063, and = −0.004, and the goodness is 96.3%. The curve well reflects the functional relationship between the detection efficiency and the thickness. It can be speculated that other materials will also show the same trend, and the difference lies in the change of coefficient. Only the coefficient needs to be changed when changing the type of packaging materials.

Summary

In this study, two kinds of small-mass and low-density U3O8 samples are measured by a six-probe detection system. It is found that the total neutron counting rate changes irregularly, and the coincidence counting rate increases with the mass. It is due to the energy loss of some neutrons emitted by the Am-Li source after scattering with the sample, which cannot be counted below the energy threshold, resulting in a decrease of the total counting rate. The coincidence neutron is almost from the sample, so it will increase with the mass. To verify this conclusion, a simulation detection system is built by Geant4. The monoenergetic neutron and sectional spectrum are used. It is found that the total counting rate and double counting rate will increase with the mass when using the monoenergetic neutron, while the total counting rate changed irregularly and the double counting rate increased linearly with the mass when using the sectional spectrum. The conclusion is verified through the simulation measurement. Meanwhile, different packaging materials such as steel, copper, aluminum, and graphite are studied, and the measurement results of different materials are analyzed and compared. In addition, the steel material with different thicknesses is studied. It is found that the detection efficiency is approximately linear with the thickness, and the fitting equation is obtained. In this study, a set of detection system is built to study the influence of neutron scattering and packaging material, which is of great significance for the development of the fast neutron multiplicity measurement technology.

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Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Author contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Acknowledgments

The authors extend their sincere thanks to the staff of CIAE and the National Nature Science Fund of China Grants (Agreement Number 51309228) for the financial support for this work. The authors also thank the Shanxi Technology Committee Natural Science Basic Research Project for financially supporting this work (No. 2016JM6026).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • 1

    DiF. A.ShinT. H.BasleyA. (2018). Fast-neutron Multiplicity Counter for Active Measurements of Uranium Oxide Certified Material[J]. Nucl. Instr. Methods Phys. Res. Section A: Acc. Spectrometers, Detectors Associated Equipment907, 248257. 10.1016/j.nima.2018.05.049

  • 2

    DolanJ. L.MarcathM. J.FlaskaM. (2014). Active-interrogation Measurements of Fast Neutrons from Induced Fission in Low-Enriched Uranium[J]. Nucl. Instr. Methods Phys. Res.738 (feb), 99105. 10.1016/j.nima.2013.11.052

  • 3

    EnsslinN.KrickM. S.LangnerD. G. (1991). Active Neutron Multiplicity Counting of Bulk Uranium[C]. Institute of Nuclear Materials Management 32nd Annnul Meeting.

  • 4

    FavalliA.CroftS.PeterS. (2015). Point Model Equations for Neutron Correlation Counting: Extension of Böhnel׳ S Equations to Any Order. Nucl. Instr. Meth ods Phys. Res. Section A: Acc. Spectrometers, Detectors Associated Equipment795, 370375. 10.1016/j.nima.2015.06.009

  • 5

    HuaM. Y.PlummerT. A.HutchinsonJ. D. (2020). Measured Nondestructive Assay of $^{237$Np Using Organic Scintillators and Active Neutron Multiplicity Counting. INMM 61th Annual Meeting

  • 6

    KerrP.RowlandM.DanD. (2007). Active Detection of Small Quantities of Shielded Highly-Enriched Uranium Using Low-Dose 60-kev Neutron Interrogation[J]. Nucl. Inst. Methods Phys. Res. B261 (1-2), 347350. 10.1016/j.nimb.2007.04.190

  • 7

    KrickM. S.EnsslinN.CeoR. N. (1996). Analysis of Active Neutron Multiplicity Data for Y-12 Skull Oxide Samples[J].

  • 8

    LiX.YaoJ.MaJ. (2018). Analysis of Measurement Model of Uranium Multiplicity Based on the Liquid Scintillators[J]. J. Phys. Conf. Ser.1053 (1), 012067. 10.1088/1742-6596/1053/1/012067

  • 9

    SarwarR. (2016). Fast-neutron Multiplicity Analysis Based on Liquid Scintillation - ScienceDirect[J]. Appl. Radiat. Isot.110, 5358. 10.1016/j.apradiso.2015.12.064

  • 10

    ShinT. H.HuaM. Y.FulvioA. D. (2017). Validation of the Fast-Neutron Multiplicity Expressions for Fissile Mass Estimation[C]. Indian Wells, CA: Institute of Nuclear Materials Management 58th Annual Meeting.

  • 11

    StewartJ. E.MenloveH. O.MayoD. R. (2000). The Ephithermal Neutron Multiplicity Counter Design and Performance Manual: More Rapid Plutonium and Uranium Inventory Verifications by Factors of 5-20. office of scientific & technical information technical reports.

  • 12

    Weinmann-SmithR.BeddingfieldD. H.EnqvistA. (2017). Variations in AmLi Source Spectra and Their Estimation Utilizing the 5 Ring Multiplicity Counter[J]. Nucl. Instr. Methods Phys. Res. Section A Acc. Spectrometers Detectors Associated Equipment856, 1725. 10.1016/j.nima.2017.02.083

  • 13

    WestcottM. (1972). The Probability Generating Functional[J]. J. Aust. Math. Soc.14 (04), 448. 10.1017/s1446788700011095

  • 14

    ZhangQ.YangJ.LiX. (2019). High Order Fast Neutron Multiplicity Measurement Equations Based on Liquid Scintillation Detector[J]. Appl. Radiat. Isot.152, 4551. 10.1016/j.apradiso.2019.06.022

Summary

Keywords

fast neutron multiplicity, neutron scattering, packaging material, neutron counting rate, detection efficiency

Citation

Li S, Li K, Zhang Q and Cai X (2022) Study on the Fast Neutron Multiplicity Measurement of Uranium Material. Front. Energy Res. 10:835495. doi: 10.3389/fenrg.2022.835495

Received

14 December 2021

Accepted

28 February 2022

Published

23 March 2022

Volume

10 - 2022

Edited by

Guang Hu, Xi’an Jiaotong University, China

Reviewed by

Jianfu Zhang, Northwest Institute of Nuclear Technology, China

Mingjun Wang, Xi’an Jiaotong University, China

Updates

Copyright

*Correspondence: Sufen Li,

This article was submitted to Nuclear Energy, a section of the journal Frontiers in Energy Research

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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