Monte Carlo Simulation Study of Hot-Particle Detection in Voluminous Samples by Gamma Spectrometry

Abstract

In this work, we addressed the inhomogeneity problem in gamma spectrometry caused by hot particles, which are dispersed into environment from large nuclear reactor accidents such as at Chernobyl and Fukushima. Using Monte Carlo simulation, we have determined the response of a gamma spectrometer to individual and grouped hot particles randomly distributed in a soil matrix of 1-L and 0.6-L sample containers. By exploring the fact that the peak-to-total ratio of efficiencies in gamma spectrometry is an empirical parameter, we derived and verified a power-law relationship between the peak efficiency and peak-to-total ratio. This enabled creation of a novel calibration model which was demonstrated to reduce the bias range and bias standard deviation, caused by measuring hot particles, by several times, as compared with the homogeneous calibration. The new model is independent of the number, location, and distribution of hot particles in the samples. In this work, we demonstrated successful performance of the model for a single-peak 137Cs radionuclide. An extension to multi-peak radionuclide was also derived.

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Chu, L. , Burn, A. , Bradt, C. and Semkow, T. (2021) Monte Carlo Simulation Study of Hot-Particle Detection in Voluminous Samples by Gamma Spectrometry. Journal of Applied Mathematics and Physics, 9, 1522-1540. doi: 10.4236/jamp.2021.97104.

1. Introduction

In gamma spectrometry of environmental, food, and industrial matrices, voluminous samples are usually analyzed in quantities ranging from a fraction of to several L or kg. This is done in order to increase the sensitivity as well as to better assess the extent of any contamination present. Germanium gamma detector (Ge) calibration for voluminous samples is accomplished with either the physical traceable standards or computational methods. Both types of calibrations assume homogeneous distribution of radioactivity in large samples, using bulk peak efficiency pb of the Ge detector. In many types of samples, however, distribution of radioactivity may be heterogeneous. This can lead to substantial bias in activity determination.

One type of inhomogeneity may be referred to as geometrical, where different sections of the sample may have varied radionuclide activities. This has been investigated for spiked reference materials [1], where analysis of variance was used to determine homogeneity. Assumptions about geometrical inhomogeneity were studied in terms of cylinder and disc [2], fraction of volume not containing radiation [3], or two sections of Marinelli beaker [4] [5].

Another type of inhomogeneity can arise from sample granularity. It was shown, using Monte-Carlo (MC) simulation, that the Ge detector peak efficiency dropped with increased granularity [6]. However, this effect has not been seen experimentally for grains of soil or polystyrene much smaller than the container size, in which spiking solution occupied an interstitial space [7].

Yet another important type of inhomogeneity of interest to this investigation is due to suspension of “hot particles” in the sample matrix. The problem of hot particles was originated from nuclear detonation fallout [8] and was extensively observed and studied following the 1986 Chernobyl [9] [10] and 2011 Fukushima nuclear accidents [11] [12]. Hot particles from nuclear accidents are the results of several formation mechanisms: disintegration of nuclear fuel in the explosion and fires; condensation of liquid droplets; and deposition of volatile fission products such as Cs on fly ash and atmospheric aerosols [13]. The composition of hot particles depends on the formation mechanism. The Chernobyl particles can be mono-elemental, bi-elemental, or fuel fragments [13], whereas Fukushima particles contain predominately 137Cs, referred to as Cs microparticles [12]. Hot particles can have diameters from a fraction of a micrometer to over 100 μm [14] and their size distribution is often assumed as lognormal [15] or arbitrary [16].

Hot particles travel significant distances with the plume [17] [18]. Gas-phase and aerosol 131I from Fukushima were observed as far as New York State [19]. Hot particles deposit on the ground and cause contamination of soil, water, crops, food, etc. Additional mechanisms for hot particle dispersion from nuclear accidents involve weathering of radioactive lava (melted fuel elements) [20] and sorption of ionic 137Cs on soil particles [21].

An entirely different source of hot particles, also referred to as discrete radioactive particles, is corrosion of neutron irradiated steel in normal nuclear reactor operation [22] as well as fuel reprocessing [23]. The presence of hot particles in potential dirty bomb explosions has been described [24].

The presence of hot particles in voluminous samples creates unusual challenges in gamma spectrometry regardless of their origin. There are several approaches to ameliorate these challenges, such as instrumental, radiochemical, and modeling. On the instrumental side, one can perform digital radiography to identify locations of hot particles [25]. Rotating waste drum scanning techniques can locate and determine heterogeneous distribution of radioactivity, utilizing emission/transmission measurements combined with modeling [26] [27] [28] [29] [30].

Among radiochemical methods, mechanical mixing only repositions hot particles in the sample without homogenization. Chemical homogenization of large samples is difficult. In addition, the particles formed as fuel elements, by condensation, or explosion are typically refractory and only high-temperature fusion [31] or HF digestion [32] can dissolve them. However, the ionic fraction, such as containing aerosol-deposited Cs and I, can be homogenized for some matrices as has been demonstrated for food using tetramethylammonium hydroxide and enzymes [33] [34].

A voluminous sample can contain both uniformly distributed radioactivity as well as inhomogeneous hot particles. It was estimated that at least 65% of total activity in the 30-km zone around Chernobyl was due to hot particles [14]. Statistical modeling methods have been developed based on either splitting of a large sample and measurement of several sub-samples on a gamma spectrometer [15] [35], or repetitive mixing and measuring of the same sample [36] [37] [38]. By analyzing the variance and modeling, some information about the fraction of activity in hot particles, their number, and size distribution could be inferred.

It follows from this introduction that a single gamma spectrometric measurement of a voluminous sample containing hot particles can be biased, i.e., the measured activity in the sample can significantly differ from true activity. By using techniques of sample splitting or mixing followed by repetitive measurements, that bias can be reduced, however, the resulting dispersion can be large.

In environmental health risk assessment, it is most important to obtain as accurate and precise determination of activity as possible. Therefore, the aim of this investigation was to reduce bias and improve precision, when measuring voluminous samples containing hot particles. We are seeking a novel gamma Ge detector calibration model in a functional form of p = f ( q ) , where detector peak efficiency p is a function of empirical parameter q. In this model, we are aiming at finding p which better represents sample inhomogeneity than the bulk efficiency pb, thereby reducing the bias and dispersion of measurement.

The methodology in this paper is by MC simulation, following [39] [40], and is described in detail in Section 2. This study focuses on a single radionuclide 137Cs, which is the most prominent gamma emitter remaining several years after the nuclear accident [36]. We use both the gamma radiation detected as a peak at 661.66 keV as well as Compton-scattered radiation. Scattered radiation has been used extensively in measuring void fraction using gamma radiation [41] [42] [43], medical image reconstruction [44], and geometrical inhomogeneity [5].

In gamma spectrometry, the most significant measures of Ge detector performance are peak efficiency p as well as the total efficiency t, the latter being a sum of peak and Compton radiations [45]. The ratio of peak efficiency to total efficiency p/t is larger for larger Ge crystals and for those with Compton-suppression systems. This ratio is used in analytical approaches to coincidence-summing corrections [46]. Some authors prefer using its inverse, t/p [47]. The p/t ratio is a directly measurable quantity, at least for a single radionuclide source, and it is a strong function of gamma energy. It has been demonstrated that p/t also depends on the radioactive source position with respect to the Ge detector [48], the feature we explore in the present work.

We design two calibration models: a 1-particle model and an n-particle model. For the 1-particle model, the relation of p = f ( p / t ) is derived using gamma attenuation [49], and its dependence on calibration is described in Section 3. The n-particle model is described in Section 4. The effect of p vs. p/t is more complicated for this model and has to be interpolated between those for single particles and bulk sample efficiency. We describe the interpolation process using Signal Detection Theory (SDT) [50] in Section 4. The performance of the n-particle model, when activities of the particles are not equal, and the extension of the model to multi-peak radionuclide are described in Section 5, followed by discussion in Section 6 and conclusions in Section 7. In this work, we are not considering radiation counting statistics and focus exclusively on the dispersion caused by inhomogeneity.

2. Monte Carlo Simulations

All calculations were performed for the 661.66-keV gamma ray from 137Cs, using sand as sample matrix with measured density of 1.55 g∙cm−3. Two counting geometries were considered as depicted in Figure 1: 0.6-L and 1-L cylindrical containers. Two coaxial p-type Ge detectors were used, with efficiencies of 134% and 48% relative to a 7.6-cm (3-inch) by 7.6-cm sodium iodide detector, which are also depicted in Figure 1. The dimensions in Figure 1 are to scale, whereas the actual values are given in Table 1. These configurations are existing in our laboratory. They can be compared in terms of detectability, which is defined as a ratio of the sample volume to the Ge crystal volume for the same activity in both samples. The configuration 0.6 L/134% Ge has such detectability 4.8 times better than the 1 L/48% Ge configuration. However, when the samples are assumed as having the same specific activity, the detectability is the product of sample volume and the Ge crystal volume. Then, such detectability is respectively 1.7 times better.

The calculations were performed using the MC code Gespecor, version 4.2 [39]. This program is especially designed for calculations in gamma spectrometry. It tracks every gamma ray randomly emitted at randomly selected location in the sample matrix. Gamma attenuation in terms of absorption and scattering is included in the sample matrix of a given geometrical shape, as well as attenuation in the Ge detector endcap and Ge crystal dead layer. Finally, gamma absorption in the Ge crystal leads to events recorded in the gamma peak, quantified as peak efficiency of the detector. Gamma scattering with partial escape from the Ge crystal leads to events outside of gamma peak in the gamma spectrum, contributing to the total efficiency of the detector. Also, gamma scattering from the lead shielding (not shown in Figure 1) is included. The Gespecor program accepts as input all materials elemental composition, dimensions, and densities. We performed simulations with 106 gamma-emission events in each studied case. Therefore, the calculations are realistic representations of the laboratory measurement systems. The density corrections are built into the calculations, whereas the coincidence-summing corrections [46] [48] can be included but are negligible for 137Cs.

In the initial step, we calculated peak and total efficiencies assuming homogeneous samples, referred to as bulk efficiencies, or Bulk efficiency model. They

Figure 1. Two counting geometries which are subjects of Monte Carlo simulations: 0.6-L and 1-L cylindrical containers, and 134% and 48% Ge detectors. The relative dimensions are to scale. The actual dimensions are given in Table 1.

Table 1. Dimensions of containers and Ge crystals. Peak and total efficiencies for bulk sample as well as max, min, and average positions of hot particle.

are given in Table 1. We also calculated efficiencies for hypothetical hot particles positioned at the closest and farthest locations, designated as max and min in Figure 1, respectively. It is seen that the bulk efficiency values are between those for the min and max positions. The ratio of peak efficiencies for the max and min positions is 73.6 for 1 L and 18.5 for 0.6 L. This can create significant bias in determination of hot-particle activity.

Let us abbreviate counting rate in the peak as R. The “true” activity determined using particle peak efficiency p is equal to A = R / p . The activity determined using bulk peak efficiency pb is equal to A b = R / p b . The Bias is defined as

Bias ( % ) = 100 ( A b / A 1 ) = 100 ( p / p b 1 ) . (1)

It is seen that the Bias does not depend on the activity, only on the efficiencies. Therefore, this investigation focuses on the efficiencies only. The discussion about hot particles having different activities is deferred to Section 5.

To study the effects associated with hot particles, we calculated the peak and total efficiencies of 2048 individual particles randomly distributed in either 0.6-L or 1-L containers, one particle at a time. The random positions of particles were calculated first using the algorithm for cylindrical coordinates [40]. In this algorithm, the height of particle position is proportional to a random number, while the radius of particle position is proportional to the square root of a random number. The azimuth angle is not important in this case because of a cylindrical symmetry. Then, the 2048 random particle positions were supplied to the Gespecor program, which calculated peak and total efficiencies at these positions. To verify the randomness of particle positions, we hypothesize that the average efficiency for all particles should approximate that of the bulk efficiency calculated above. The average peak and total efficiencies for all 2048 particles are also listed in Table 1. The deviations of average efficiencies from the bulk efficiencies are about −0.5% for 1-L container and about −1% for 0.6-L container, whereas the deviations for thep/t ratios are substantially smaller. The randomness of particle positions is judged satisfactory for the purpose of this study.

The biases were calculated using Eq. 1 for the 2048 particles and are plotted as histogram in Figure 2 for 1-L container. They range from about −100% to 700%, or by a factor of 8. This is less than 73.6 listed in Table 1, however, it is statistically unlikely to have a particle located at either a min or a max position. The frequency distribution of the biases is depicted in Figure 3 (distribution a, green points). This distribution resembles an exponential, reflecting exponential attenuation of gamma radiation in the sample.

3. One-Particle Model

The 1-particle model assumes presence of a single hot particle in the sample. This model provides a foundation for the n-particle model to be described in the next section. Let us consider a particle in the sample matrix located at a distance r from the Ge detector. In a simplified picture, we neglect all possible angles and

Figure 2. Histogram of Bias from single particle efficiency when using bulk efficiency for 1-L container.

Figure 3. Frequency plots for various Bias distributions for 1-L container. (a) Bias bulk from single particle, bin size 25%; (b) Bias for 1-particle model, bin size 5%; (c) Bias for n-particle model applied to 1 particle, bin size 10%.

finite sizes of both sample and the detector. For a gamma photon to be detected in the peak with efficiency pr, it must be attenuated in the sample and detected with an intrinsic peak efficiency of the detector pd. We thus have

p r = p d exp ( μ 0 r ) . (2)

Similar considerations apply to the total efficiency tr and intrinsic detector td. However, the total efficiency is enhanced by the scattered radiation in the sample originating from gamma photons emitted at the particle location r. Therefore,

t r = t d exp ( μ 0 r ) exp ( μ s r ) . (3)

Also,

μ 0 = μ a + μ s + minorterms , (4)

where μ 0 is a total gamma attenuation coefficient, μ a is a gamma absorption coefficient, and μ s is an incoherent (Compton) scattering coefficient [49].

By manipulation of Equations (2) and (3), we obtain

p r p d = ( t d p d p r t r ) μ 0 / μ s . (5)

It follows that p should be a power function of p/t,

p = g ( p / t ) h , (6)

where g and h are coefficients. In this way p/t carries some information about hot-particle peak efficiency and thus its position.

The p values are plotted as a function of p/t for the 1-L container in Figure 4. The densely located 2048 points lump into a gray area. The reason for such wide distribution is that it involves random particle locations and all directions of gamma emissions from a particle, as well as taking the ratio of two random variables p/t. Then an unconstrained power-law fit was made to the points according to Equation (6) resulting in pu, depicted by the green curve in Figure 4 representing the most probable p.

The sequence of analyzing the data is as follows. For each simulated particle at its location, one calculates p/t obtained from the MC simulation. Experimentally, for a single radionuclide, it would correspond to taking a ratio of the counts in the peak to the total counts in the gamma spectrum. Then, one reads the most probable value pu from the green curve in Figure 4. Subsequently, one calculates the Bias from Equation (1), by substituting pu for pb.

The histogram of Bias values for 1-particle model is depicted in Figure 5. It is seen that bias now spans the range between about −60% and 60%, and it is significantly reduced from that for the bulk efficiency in Figure 2. The frequency distribution for 1-particle model is depicted as curve b in Figure 3 (blue points).

Figure 4. Plots of p as a function of p/t for the MC data and various fits described in the text.

Figure 5. Histogram of Bias from single particle efficiency when using 1-particle model efficiency for 1-L container.

It is a narrow symmetric distribution reflecting significant reduction in the dispersion of the results.

4. n-Particle Model

The n-particle model assumes that there are 1 or more hot particles in the sample, all having the same activity. It can be realized by simple grouping of the 2048 MC points. For instance, one can group 2 particles (1024 cases), 4 particles (512 cases), etc., until finally arriving at 1 case of 2048 particles. The average variables for n independent particles are given by

p n = 1 n i = 1 n p i , (7)

t n = 1 n i = 1 n t i , (8)

p / t n = p n / t n , (9)

The reason for such definitions of averages is that Equation (9) is the one that would be realized experimentally. The averages are “true” values as calculated by the MC program, and the Bias when using Bulk efficiency model is generalized from Equation (1):

Bias ( % ) = 100 ( p n / p b 1 ) . (10)

The values of p 2048 , t 2048 , and p / t 2048 are listed in Table 1 under source position in the average row (both geometries). As discussed in Section 2, the averages for 2048 particles approximate bulk efficiency calculations pb, tb, and ( p / t ) b very well. This average for 1 L container is depicted as an open circle in Figure 4, which does not lay on the green pu curve. The reason is that p / t n (Equation (9)) is not equal to 1 / n i = 1 n p i / t i .

We performed another power-law fit to the data in Figure 4, this time we constrained the fit by passing through the p / t 2048 point, resulting in an orange pc curve. It follows that, regardless of the number of hot particles present, the most probable measured p/t will fall between these two curves. Therefore, we need to interpolate between them in such a way that if p/t is close to p / t 2048 , it will be weighted towards pc; if it is far from p / t 2048 , then it will be weighted towards pu. We tried linear and quadratic interpolations without success because the interpolation has to be steep in the vicinity of p / t 2048 .

A satisfactory interpolation can be obtained however, by application of the SDT [50]. SDT is concerned with distinguishing between the signal and noise. We assume Gaussian distributions for both signal and noise, with the mean and sigma given as { μ signal , σ signal } and { μ noise , σ noise } , respectively. We designate a Gaussian (normal) distribution function (an integral of the Gaussian probability density function from minus infinity to the Deviate) with mean and sigma, and its inverse as

Probability = Φ ( Deviate , { mean , sigma } ) , (11)

Deviate = Φ 1 ( Probability , { mean , sigma } ) . (12)

For the set of 2048 points, we find the minimum and maximum values of p/t, ( p / t ) min and ( p / t ) max , respectively. For any average of n particles, the SDT probability of signal rejection, Pr can be written as

P r = { p / t n ( p / t ) min p / t 2048 ( p / t ) min , p / t n p / t 2048 , ( 13 a ) ( p / t ) max p / t n ( p / t ) max p / t 2048 , p / t n > p / t 2048 . ( 13 b )

Then, by combining Equations (11)-(13), we obtain the SDT probability of misses Pm and hits Ph as

P m = Φ [ Φ 1 ( P r , { μ n o i s e , σ n o i s e } ) , { μ s i g n a l , σ s i g n a l } ] , (14a)

P h = 1 P m . (14b)

We determined that a mean and sigma of {0, 1} for the noise, and {0.6, 0.5} for the signal, provided sufficient convergence.

Finally, the interpolated value of pinterp between the unconstrained fit pu and the constrained fit pc from Figure 4 (green and orange curves, respectively) is given by

p i n t e r p = P h p u + P m p c . (15)

The Bias for the n-particle model is given by

Bias ( % ) = 100 ( p n / p i n t e r p 1 ) . (16)

The performance of various models is listed in Table 2 for 1-L container. The quantity of interest is the Bias(%) from “true” efficiencies known from the MC calculation, its minimum (Min) and maximum (Max) values, as well as standard deviation (Std Dev). Table 2 shows that for 1 particle, the Bulk efficiency model

resulted in a significant minimum and maximum bias and bias standard deviation. This was already seen in Figure 1 and Figure 2. As the number of particles increases, the bias and all its measures decrease since the inhomogeneity drops. Application of 1-particle model to 1 particle present significantly reduces the bias and its standard deviation. Application of n-particle model reduces all measures of bias as compared with the Bulk model, for all particles studied. The n-particle model applied to 1 particle performs slightly worse than the 1-particle model. This is seen in the bias measures in Table 2, as well as in the frequency distribution with right tail (curve c in Figure 3).

The results of the Bias for the 0.6-L container are listed in Table 3. They exhibit the same trends as for the 1-L container, however, of smaller magnitude

Table 2. Performance of the Bulk, n-particle, and 1-particle models expressed as bias from known efficiency for several number of particles and 1-L container.

Table 3. Performance of the Bulk, n-particle, and 1-particle models expressed as bias from known efficiency for several number of particles and 0.6-L container.

reflecting relatively less inhomogeneity in this smaller container.

In order to compare model performances for the two containers, we define Bias Range (%) as the difference between the Max and Min bias. Then, the improvement factors for the Bias Range and Bias Std Dev (%) are calculated as the ratios of the corresponding values from the Bulk model to the ones for the 1-particle and n-particle models. The improvement factors are depicted in Figure 6 for 1 and more particles present in the sample. It is seen that there are significant improvements in Bias Range and Bias Std Dev when using the calibration models developed here. The highest improvements by a factor ranging from about 3 to 6.5 are when using 1-particle model. The same case of 1 particle present, when applying the n-particle model to it, resulted in improvement factors from about 3 to 4. As the number of particles increases, the improvement factors drop to between 1.5 and 2 for 64 particles. For small number of particles (1 to 4), the improvement factors are higher for 1-L container than for the 0.6-L container; this trend is reversed for larger number of particles in most cases.

5. Non-Equal Particles and Multi-Peak Radionuclide

The n-particle model assumes that all particles have the same activities. It was observed that hot particles from nuclear accidents exhibit distribution of sizes [14], often assumed lognormal [15]. Then, constant specific activity implies lognormal distribution of activities as well. This situation results in even more inhomogeneity than for equal particles, because a few of very hot particles dominate activity of the sample.

Non-equal particles can be easily simulated within the present data set by positioning several equal particles in the same location. Since the derived n-particle

Figure 6. Improvement factors for Bias Range and Bias Std Dev when using 1-particle and n-particle models compared with the Bulk model, for 1-L and 0.6-L containers.

model interpolates the efficiencies between 1 particle and the bulk sample, it should be independent of a specific assumption about the number or location of the particles. Therefore, it should apply to non-equal particles as well.

To test this hypothesis, we created two cases of non-equal particles, for 1-L container. In the first case we have 2 particles, one is assumed twice as radioactive as the other. Therefore, the average peak efficiency from Equation (7) is p 2 = 1 / 3 ( 2 p 1 + p 2 ) . We have used 2 equal particles from the MC set of 2048 and created a group of 2 non-equal particles. We have 1024 such groups to perform statistics on. For the second case, we repeated 1st particle 4 times, 2nd particle 2 times, and took the 3rd and 4th particles as is. The average peak efficiency is p 4 = 1 / 8 ( 4 p 1 + 2 p 2 + p 3 + p 4 ) . We thus have 512 such groups. Similarly, we calculated t n and p / t n , n = 2 , 4 . Then, we apply the n-particle model by calculating p i n t e r p from Equation (15) and study the Bias from Equation (16).

The results are given in Table 4 in terms of Bias Range and Bias Std Dev. Also, the results for equal 1, 2, and 4 particles are reproduced from Table 2. It is seen that the values for 2 non-equal particles are laying between those for 1 and 2 equal particles. The reason is that one particle dominates by assumption. For the case of 4 non-equal particles, the values are between those for 2 and 4 equal particles because of assumed distribution of activity among particles and domination by the hotter ones. Nevertheless, the n-particle model performed well and the calculated values of Bias Range and Bias Std Dev are significantly improved from those of the Bulk model.

In this work we have considered a single gamma peak of 661.11 keV from 137Cs. The n-particle model based on p/t can be extended to multi-peak radionuclide as follows. Let A represent the radionuclide activity of a hot particle. The counting rate in gamma peak j is given by

R p , j = A p e f f , j , (17)

where p e f f , j is an effective peak efficiency, which includes gamma intensity, density correction in the sample matrix and any coincidence-summing correction. For k peaks of the radionuclide in the gamma spectrum, the total counting rate in all peaks is equal to

R p = j = 1 k R p , j = A j = 1 k p e f f , j = A p e f f . (18)

Table 4. Performance of the n-particle model for non-equal particles in 1-L container.

Similarly, for the total counting rate,

R t = j = 1 k R t , j = A j = 1 k t e f f , j = A t e f f . (19)

Therefore, the observed peak-to-total ratio for a multi-peak radionuclide is given by

( p / t ) e f f = R p / R t = p e f f / t e f f . (20)

The left-hand side of Equation (20) can be measured, while the right-hand side calculated by the MC simulation. The n-particle model can be used as earlier in Sections 4, 5, with p and t replaced by peff and teff.

6. Discussion

A overview of the origins and behavior of hot particles was provided in Section 1. Such particles are normally encountered in environmental samples following nuclear accidents. Digital radiography is typically used for samples spread on a surface, while digital tomography is not always practical for measuring many environmental samples. Surveillance samples for gamma spectrometry are typically large to increase sensitivity and to provide better sampling of radioactive contamination. However, voluminous samples may be inhomogeneous due to the presence of hot particles. Applying the Bulk efficiency model leads to significant bias of measured activity. One approach to this problem is repetitive mixing and measuring of a sample (from 25 to 100 times [36] [38] ). While this method can provide relatively accurate average of the measured activity, is not very practical for many samples, and the dispersion evaluated by means of a standard deviation can be large and increasing as the number of hot particle decreases.

In this investigation we provided a method to reduce this dispersion. Our goal was to study the behavior of hot particles randomly distributed in the soil matrix, for two counting geometries: 1-L and 0.6-L cylindrical containers. Using MC simulation, we calculated the peak and total efficiencies of 2048 individual hot particles at random locations in each container. We focused on a single radionuclide of 137Cs and its 661.66-keV gamma ray. The presence of counts in the gamma peak in the spectrum represents gamma transmission, whereas anywhere in the gamma spectrum, both transmission and scattering. On this basis, we derived a power-law relationship between peak efficiency and peak-to-total ratio. This relationship was confirmed by the MC simulation. Since peak-to-total ratio is a measurable parameter, the power-law relationship can provide a more accurate value of the efficiency than the bulk efficiency. We called this approach 1-particle model. It was shown that the 1-particle model reduced the Bias Range 6.5 times and Bias Std Dev 4 times compared to the Bulk efficiency model for 1-L container, and 4 and 3 times for 0.6-L container, respectively.

Subsequently, identical individual particles were combined into n-particle groups, which resulted in the n-particle model. The averages for peak and total efficiencies were calculated as well as their peak-to-total ratio. From the power-law relationship, the most probable value of peak efficiency could be obtained from the empirically available peak-to-total ratio. The complication arose from the fact that the most probable peak efficiency lays between the single-particle power-law and the power-law constrained by the bulk efficiency point. Fortunately, an innovative interpolation was developed, based on a formulation from the Signal Detection Theory, between the two power-law curves. The n-particle model works well for any number of particles. When applied to a single-particle case, the reduction in Bias Range and Bias Std Dev was between 3 and 4. These are improvement factors when using this model compared with the Bulk model. As the number of hot particles increases, the inhomogeneity decreases, and improvement factors decrease to between 1.5 and 2 for 64 hot particles. We also simulated groups of non-equal hot particles and found that the n-particle model is independent of the number, location, and size distribution of hot particles.

If this approach is applied to repetitive mixing and measurement method for inhomogeneous sample, the accuracy of the average is expected to have low bias as before, however, the standard deviation will decrease several times. If only one measurement is made on an unknown sample, this method guarantees reduction of the bias several times for inhomogeneous samples without the need of knowing the details of inhomogeneity.

7. Conclusion

We developed a novel calibration of a gamma-ray spectrometer using the relationship p = g ( p / t ) h , where g and h are coefficients and p/t is a ratio of peak-to-total efficiencies. This method can be used to reduce the variance of measured activity in bulk environmental or food samples containing hot particles as compared with the homogenous calibration. So far, we were able to apply it to a single-peak single-radionuclide, such as 137Cs, which is known as the most important gamma emitter for aged fallout from nuclear-power accidents. We also derived equations to accommodate multiple-peak radionuclide. At this time, the method has not been shown suitable for characterizing samples containing mixtures of radionuclides.

Acknowledgements

This work was partially supported by the US FDA FERN Cooperative Agreement 1U18FD005514.

Conflicts of Interest

The authors declare no conflicts of interest regarding the publication of this paper.

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