Feasibility study on rare earth ion exchange resin saturation analysis based on PGNAA technique.

In this work, prompt gamma ray neutron activation analysis technique was used to monitor the REEs saturation in resin. A facility consisted of a D-T neutron generator, a BGO detector and a 3He detector was established and applied to analyze REEs (Gd and Sm) samples. Neutron self-shielding effect was also corrected. The enriched Gd and Sm in resin were close to saturation at about 400 min. The results showed a satisfactory agreement with the XRF tests, which demonstrated that PGNAA was sufficient for monitoring REEs saturation in resin.

Measurements of epithermal neutron properties of ITU Triga Mark II research reactor.

The k0 standardization method is one of the most commonly used neutron activation analyses to determine the concentrations of elements in the sample. To perform this method, it is required to know the neutron spectrum parameters such as epithermal neutron flux shape factor (α) and thermal to epithermal neutron flux ratio (f). In this study, the α and f parameters were determined using the Cd-ratio dual monitor method and bare triple monitor method. In both methods, irradiation studies were performed in the central thimble at the ITU Triga Mark II research reactor. A gamma-ray counting system (HpGe detector) was used for measuring foil activation values. The selected monitors were 197Au and 94Zr for the Cd-ratio dual monitor method and 197Au/94Zr/96Zr for the bare triple monitor method. The α and f parameters were -0.221 ± 0.018 and 41.826 ± 4.701 for 197Au/94Zr (724 keV) monitors, -0.231 ± 0.019 and 42.626 ± 4.791 for 197Au/94Zr (756 keV) monitors, 0.228 ± 0.025 and 43.917 ± 3.596 for 197Au/94Zr/96Zr monitors, respectively.

Discovery of neutron activation analysis.

It is well known that George Hevesy and Hilde Levi were the original discoverers of neutron activation analysis. However, there were many other researchers in Europe that firstly unknowingly and knowingly discovered the neutron, and others who experimented in neutron induced radioactivity. A historical timeline of the several parallel experiments in a very short period is given in this synopsis. It eventually was Hevesy and Hilde to first use the powerful technique of neutron activation analysis for analytical chemistry.

A pilot study on the use of neutron activation analysis and multivariate statistics for the provenance of Jamaican Cannabis sativa L (Marijuana).

The aim of this study was to use instrumental neutron activation analysis and multivariate analysis to determine the provenance of Jamaican Cannabis sativa L. Sixty-three samples were collected from various areas in Jamaica, with no other data but their known or self-reported growing regions. The samples were analysed for Al, As, Br, Ca, Cd, Co, Cs, Fe, K, La, Mg, Mn, Na, Rb, Sb, Sc, Sm, Sr, V, and Zn. The resulting elemental data were statistically evaluated using agglomerative hierarchical cluster analysis and principal component analysis. Cluster analysis was able to group the samples into their known or reported growing regions with a high degree of accuracy. Principal component analysis was also able to elucidate some of the underlying geochemical factors that could explain the clustering. These included the underlying bauxitic geochemistry and the influence of fertilizer inputs. Of the analysed elements, Al, As, Cd, Co, Fe, K, La, Mg, Mn, Sc, Sm, V, and Zn appear to be most significant in identifying the growing regions of the cannabis samples. Results indicate the promise of this methodology with an increased dataset and potentially further refinement of the identifying elements.

Performance of various mathematical functions for the in-situ relative detector efficiency towards its applicability for k0 IM-NAA.

The in-situ relative detection efficiency strongly influences the characteristics of the k0-based internal monostandard neutron activation analysis (IM-NAA). In the present work, various mathematical functions were explored for the establishment of in-situ relative detector efficiency calibration and compared their performance based on the reduced chi-square (χ2) values. Among the various mathematical functions, the polynomial logarithm with 6th order was found to be associated with the minimum mean standard deviation for the experimental data and the lowest value of reduced χ2 after carrying out multiple iterations using Nelder-Mead algorithm. Quality assurance of the function was tested by carrying out elemental quantification of the NIST SRM 1633b coal fly ash. Gamma energies of the activation products, 152mEu, 59Fe, 140La, 24Na and 46Sc of the irradiated NIST standard were used for the in-situ relative full energy peak efficiency calibration of 30% HPGe detector. The sample was counted for different time intervals for the complete profiling of the elements present in the NIST SRM. The deviations for most of the elements were found to be within ±5% with respect to the certified values and ξ-score values were within ±2, demonstrating its better accuracy. This method was also applied satisfactorily to profile the elemental concentrations of alloy materials used in a thermal sensor guide tube of the steam generator in a test reactor.

Utilization of accelerator and reactor based nuclear analytical techniques for chemical characterization of automobile windshield glass samples and potential of statistical analyses using trace elements towards glass forensics.

Glass forensics is an important area in forensic crime investigations, wherein glass origin or source finding is necessary mainly through chemical composition. In the present work, Nuclear Analytical Techniques namely external (in air) Particle Induced Gamma-ray Emission (PIGE) and Instrumental Neutron Activation Analysis (INAA) were utilized for complete chemical characterization of twenty-five "as received" windshield glass samples of six car manufactures. Concentrations of four major elements (Si, Na, Mg and Al) by PIGE using proton beam and nineteen elements including sixteen trace elements by INAA using research reactor neutrons were determined. Both the methods were validated by analysing matrix matched glass certified (standard) reference materials. Trace elemental concentrations including rare earth elements (REEs) and ternary plot using concentrations of major, transition elements and REEs were utilized to obtain preliminary grouping of the analyzed glass samples. Statistical tools namely K-mean, Cluster Analysis and Principal Component Analysis (PCA) using trace elemental concentrations were utilized for grouping studies, important for forensic applications. Among these statistical analysis techniques, PCA results confirmed that windshield glasses from six manufactures clearly belong to six different groups.

Measurement of talc in flour by the prompt-gamma ray neutron activation analysis method.

Prompt gamma-ray neutron activation analysis method (PGNAA) was used to measure the talc content in flour. Neutron activation prompt gamma spectrum measured by NaI(Tl) detector has complex components, poor energy resolution, and high Compton plateau, how to obtain accurate element content from the prompt γ spectrum is one of the core problems of PGNAA. To reduce the systematic uncertainty caused by the variation of the neutron energy spectrum and γ self-absorption in different samples, the spectral decomposition method based on library least-squares was improved. As a result, the average relative deviation between the calculated values from measured spectra and the theoretical values based on the known composition was reduced from 6.1% to 0.3%. The relative uncertainty of 30 measurements on the same sample was reduced from 4.8% to 3.0%. The detection time can be reduced to 1 min, which meets the requirement of on-line measurement for talc in flour.

Simulation of the cement measurement based on the pulse DT neutron generator: A Monte Carlo study.

The PGNAA system for the cement measurement was simulated based on Monte Carlo method. The sizes of the moderator and reflector for the 14 MeV DT neutron generator were optimized for fast and thermal neutron outputs. The DT neutron generator was simulated at the pulse mode, and the gamma-ray detector was set as LaBr3(Ce) scintillator. The characteristic peaks of the major elements (Ca, Si, Al, Fe) can be identified from the gamma-ray spectra which induced at the different time intervals of the neutron radiation. For the different thicknesses of the cement sample the ratios of the gamma-ray peaks were observed, and the result showed that when the thickness was between 20 to 30 cm, the ratios became stable. With the ratios, we can calculate the iron modulus, silica modulus and lime saturation factor.

In situ experimental measurement of mercury by combining PGNAA and characteristic X-ray fluorescence.

In our previous research, a new detection method was proposed to measure Hg and Pb simultaneously by combining Prompt Gamma-ray Neutron Activation Analysis (PGNAA) and X-ray Fluorescence (XRF) and proved by the Monte Carlo N-Particle (MCNP) simulation code. For further experimental verification, a combined measurement experimental facility, comprising an 241Am-Be neutron source, SAINT-GOBAIN Bismuth Germanate (BGO) as the γ-ray detector, and an NaI detector with 25 µm Be window as the X-ray detector, was presented. Specifically, the characteristic X-ray fluorescence of the Hg directly induced in this experimental facility was utilized to improve the limits of detection (LOD) of Hg instead of traditional excitation sources. The simulation and experiment results indicated that LOD for Hg by the combined measurement instrument was 19.4 mg kg-1. The empirical formula of the calibration curve in this method was given based on the aforementioned calculations.

Comparison of three analytical techniques for determination of Th and U in environmental samples.

Alpha-particle spectrometry, gamma spectrometry and neutron activation analysis techniques for determination of Th and U in environmental samples have been compared. The analytical parameters studied include detection limit, accuracy, repeatability, reproducibility and surrogate recovery. The results show that neutron activation analysis technique has the best accuracy among the studied techniques; the other two techniques were assessed relative to it. The percentage difference between the three techniques results is about [-20, 20]. In addition, U and Th concentrations are generally overestimated by gamma spectrometry and alpha-particle spectrometry in all cases except Th concentration in the former technique, which is underestimated.

Investigation of mammoth remains using the neutron activation analysis at the Training Reactor VR-1.

At the time when the importance of the interdisciplinary research increases, the nuclear analytical techniques supported by the small research reactors represent a useful tool for investigation of human society, culture, history etc. The historical, archaeological, and palaeontological samples and objects of cultural heritage can be easily studied using the radioanalytical methods such as the neutron activation analysis. This paper deals with the detailed investigation of fragments of mammoth remains from the Mid-Upper Palaeolithic site Pavlov VI by means of the instrumental neutron activation analysis at the Training Reactor VR-1 of the Czech Technical University in Prague. Six mammoth hard tissue samples (fragments of bones, tusk, and molar) from the Institute of Archaeology of the Czech Academy of Sciences were irradiated in the dry vertical irradiation channel with thermal neutron field (φ=2×109cm-2s-1) at maximum reactor power (80 W). The activated mammoth samples were analysed employing the nuclear γ-spectrometry and semiconductor HPGe detector, and the composition of the remains was determined (qualitative and quantitative analysis). The presence of Na, Cl, K, As, Fe, Sr, Mn, Br, I, Ba, and U was revealed in studied mammoth samples. Based on obtained production rates, the concentrations of Fe, Sr, Na, K, As, and U were determined. The results presented in this paper show clearly that the low-power Training Reactor VR-1 is excellent tool for the neutron activation analysis experiments within the interdisciplinary research and can provide experimental data important for archaeologists and palaeontologists.

Neutron Autoradiography Combined With UV-C Sensitization: Toward the Intracellular Localization of Boron.

Our group has reported the imprint formation of biological material on polycarbonate nuclear track detectors by UV-C exposure, which is used as an approach to simultaneously visualize cell imprints and nuclear tracks coming from the boron neutron capture reaction. Considering that the cell nucleus has a higher UV-C absorption than the cytoplasm and that hematoxylin preferentially stains the nucleus, we proposed to enhance the contrast between these two main cell structures by hematoxylin staining before UV-C sensitization. In this study, several experiments were performed in order to optimize UV-C exposure parameters and chemical etching conditions for cell imprint formation using the SK-BR-3 breast cancer cell line. The proposed method improves significantly the resolution of the cell imprints. It allows clear differentiation of the nucleus from the rest of the cell, together with nuclear tracks pits. Moreover, it reduces considerably the UV-C exposure time, an important experimental issue. The proposed methodology can be applied to study the boron distribution independently from the chosen cell line and/or boron compounds.

Estimation of daily selenium intake by 3- to 5-year-old Japanese children based on selenium excretion in 24-h urine samples.

To evaluate the daily Se intake of 3- to 5-year-old Japanese children, we used seventy-two urine samples collected from fifty-three children (twenty-seven male and twenty-six female) from two cities in Miyagi prefecture, Japan. For measuring low Se concentrations with high precision, accuracy and rapidity in the 24-h urine samples, we developed an instrumental neutron activation analysis (INAA) method, that is without any chemical separation, using the short-lived 77mSe (t1/2 = 17·4 s) nuclide. The estimated Se intake of the fifty-three children was 51·5 (sd 30·2) µg/d (geometric mean: 42·7 µg/d). Ten subjects (three male and seven female), successfully provided 24-h urine samples over two or three consecutive days; their Se intake was 37·4 (sd 5·9) µg/d. Based on the logarithmically transformed data of these ten subjects, the ratio of intra-/inter-individual variances of usual Se intake was 16·7 (28·0/1·7) and geometric mean was 27·7 µg/d. The 5th to 95th percentile of usual Se intake of these ten subjects was 17·5 to 40·4 µg/d, which ranged between the recommended dietary allowance and tolerable upper intake level of Se by the Dietary Reference Intakes for Japanese (2015).

Elemental Characterization of Medicinal Plants and Soils from Hazarganji Chiltan National Park and Nearby Unprotected Areas of Balochistan, Pakistan.

The aim of this work was to evaluate the variability in elemental composition of seven medicinal plants and their respective soils belonging to protected and nearby unprotected sites of the Hazarganji Chiltan National Park. The medical plants under study were Achillea wilhelmsii C. Koch, Peganum harmala Linn, Sophora mollis (Royle) Baker, Perovskia atriplicifolia Benth, Seriphidium quettense (Podlech.) Ling, Hertia intermedia (Bioss) O. Ktze, and Nepeta praetervisa Rech. F. Macro (C, H, N, S, K, Ca), micro (Cl, Cu, Fe, Mn, and Zn), beneficial (Al, Co, Na), others (As, Br, Cr, Cs, Hf, Pb, Rb, Sb, Sr, Sn, V and Th) and rare earth elements (Ce, Eu, La, Lu, Nd Sc, Sm, Tb and Yb) were characterized by means of standard organic elemental and instrumental neutron activation methodologies and by flame atomic absorption spectroscopy. Results showed that, among macro nutrients, carbon concentration was the highest element in both plant and soil samples followed by H and K. Elements such as Cl, Na and Fe were detected in considerably good amounts; all the other elements were found in trace quantities. Principal component analysis (PCA) was applied to identify spatial variation in elemental composition of medicinal plants, in which 80-90% of the total variance in whole set of data was found. In particular, the findings highlighted the presence of essential and beneficial elements such as C, H, N, K, Ca, Fe, Mn and Na, in samples from protected sites, while potentially dangerous elements such as Al, As, Br and Cr were detected in samples from unprotected sites. These results emphasized on the need for rational exploitation of valuable medicinal plants and supporting protected areas as an excellent source of biodiversity conservation.

The use of HPLC-NAA and HPLC-ICP-MS for the speciation of As in infant food.

Arsenic and its inorganic species: As (III), As (V), dimethylarsenic acid (DMA) and monomethylarsenic acid (MMA) were determined in hypoallergenic formulas and grain porridges commercially available on Polish market, dedicated for infant 0-8 months. After quantitative extraction with 0.5% HNO3, separation of individual species was performed by high performance liquid chromatography (HPLC), and their determination by neutron activation analysis (NAA) and inductively coupled plasma mass spectrometry (ICP-MS). Due to relatively low content of As in the analysed samples, it was only possible to determine DMA using the HPLC-ICP-MS mode. HPLC separation coupled with off-line determination by NAA enabled the determination of more extracted As species (especially inorganic) with good accuracy. Certified reference material (CRM) Rice Flour SRM 1568b (NIST) was used for the validation of both procedures.

Evaluation of ions and metals in the blood of GRMD dogs submitted to hASCs therapy by NAA and XRF techniques.

The elements Br, Ca, Cl, Cr, Fe, K, Mg, Na, P, Rb, S, and Zn were investigated in the whole blood samples of Golden Retriever dogs submitted to cell therapy (hASCs). These analyses were performed over 2 years using Neutron Activation Analysis and X-Ray Fluorescence techniques. The results were compared with control and untreated dog's. A significant increase was observed in K blood levels. There was also variation in blood levels of Br, Cr, Fe, Rb, S, and Zn.

Environmental radioactivity of soils and sediments: Egyptian sector of the Nile valley.

The activity concentrations of natural 40K, 232Th, and 238U in 89 soil and 84 sediment samples collected over the entire Egyptian Nile River basin including the Nile delta are reported based on the results of epithermal neutron activation analysis. The average activity concentrations of 40K, 232Th, and 238U equal to 15.3 ± 6.6, 15.6 ± 11.1 and 220 ± 31 Bq/kg, respectively, are significantly lower than those reported for the Upper Continental Crust, World Average Sediments as well as World Average Soils, suggesting the presence of a considerable portion of mafic material, most probably originating from the Ethiopian High Plateau. Their average activity concentrations are statistically the same in soil and sediments, indicating that the Nile sediments and soil material are of the same origin. The main goal of this study was not only to estimate the radiological hazards but also to show the influence of sedimentary material transportable by the Blue Nile from the Ethiopian High Plateau. The different hazard indices like the radium equivalent, gamma index, external hazard as well as the internal hazard show a low radiological exposure either on direct contact or if local mud bricks are used in the construction of dwellings.

In vivo measurement of bone manganese and association with manual dexterity: A pilot study.

We used neutron activation analysis (NAA) to measure hand bone manganese (BnMn) in 19 adult males. Median BnMn was 0.89µg/g dry bone (interquartile range = 1.07). After adjustment for age and occupation, higher ln(BnMn) was significantly associated with lower manual dexterity based on the Purdue Pegboard assembly task: ß = -1.77, standard error = 0.79, p = 0.04. Due to the small sample size, these results should be interpreted cautiously. BnMn appears to be a promising biomarker, and should be further studied.

Customized compact neutron activation analysis system to quantify manganese (Mn) in bone in vivo.

OBJECTIVE: In the US alone, millions of workers, including over 300 000 welders, are at high risk of occupational manganese (Mn) exposure. Those who have been chronically exposed to excessive amount of Mn can develop severe neurological disorders similar, but not identical, to the idiopathic Parkinson's disease. One challenge of identifing the health effects of Mn exposure is to find a reliable biomarker for exposure assessment, especially for long-term cumulative exposure. APPROACH: Mn's long biological half-life as well as its relatively high concentration in bone makes bone Mn (BnMn) a potentially valuable biomarker for Mn exposure. Our group has been working on the development of a deuterium-deuterium (D-D)-based neutron generator to quantify Mn in bone in vivo. Main results and significance: In this paper, we report the latest advancements in our system. With a customized hand irradiation assembly, a fully characterized high purity germanium (HPGe) detector system, and an acceptable hand dose of 36 mSv, a detection limit of 0.64 µg Mn/g bone (ppm) has been achieved.

New generation non-stationary portable neutron generators for biophysical applications of Neutron Activation Analysis.

BACKGROUND: Neutron sources are increasingly employed in a wide range of research fields. For some specific purposes an alternative to existing large-scale neutron scattering facilities, can be offered by the new generation of portable neutron devices. SCOPE OF REVIEW: This review reports an overview for such recently available neutron generators mainly addressed to biophysics applications with specific reference to portable non-stationary neutron generators applied in Neutron Activation Analysis (NAA). MAJOR CONCLUSIONS: The review reports a description of a typical portable neutron generator set-up addressed to biophysics applications. GENERAL SIGNIFICANCE: New generation portable neutron devices, for some specific applications, can constitute an alternative to existing large-scale neutron scattering facilities. Deuterium-Deuterium pulsed neutron sources able to generate 2.5MeV neutrons, with a neutron yield of 1.0×106n/s, a pulse rate of 250Hz to 20kHz and a duty factor varying from 5% to 100%, when combined with solid-state photon detectors, show that this kind of compact devices allow rapid and user-friendly elemental analysis. "This article is part of a Special Issue entitled "Science for Life" Guest Editor: Dr. Austen Angell, Dr. Salvatore Magazù and Dr. Federica Migliardo".