RESUMEN

A first comprehensive survey was carried out in a university campus in Italy in order to investigate in terms of natural elements an area where medium-high values of natural radiation are expected because of its peculiar geological features. The content of terrestrial radionuclides in 20 topsoil samples from the campus was determined with the aim to provide an important database of the soil characteristics. 226Ra, 232Th, and 40K concentrations were analysed by High Purity Germanium (HPGe) gamma-ray spectrometer in order to determine the background levels of natural radionuclides characteristics of the original area. The mean concentrations of radionuclides in the investigated soil samples ranged from 58.95 ± 4.20 to 158.05 ± 19.95 Bq kg-1 for 226Ra, from 72.28 ± 7.61 to 146.00 ± 22.27 Bq kg-1 for 232Th and, for 40K, from 550.76 ± 33.24 to 1367.50 ± 18.73 Bq kg-1. The radiological hazard indices, including radium equivalent activity, external hazard index, annual effective dose, absorbed dose rate, lifetime excess cancer risk, were also evaluated and compared with global averages, revealing values above the worldwide ones. Finally, a spatial modelling methodology of the site-specific radionuclides levels as graphical tool for the monitoring of the potential land redevelopment of urban soils was proposed.

RESUMEN

Gallium-72 is an important Comprehensive Nuclear-Test-Ban Treaty relevant radionuclide that arouses significant interest. However, the reported half-lives of 72Ga are discrepant. In the current work, three solution samples of different concentrations were prepared and sequentially measured by a high-purity Germanium (HPGe) spectrometer. The count rates as a function of time of the 834.1 keV and 630.0 keV γ-lines were followed for the half-life determination. Through mass normalization, the datasets of three samples are combined and the statistical uncertainties are reduced. Half-life values were derived from datasets of each sample and mass normalization and corresponding complete uncertainty budgets are presented. The final half-life determined for 72Ga is 13.94 (2) h, showing a deviation of 1.12% from the last nuclear data sheets (NDS) recommended value. Comparing with the values of previous publications, the result from this work is smaller than most results and consistent with the latest value which has one large uncertainty. A recommended value of 14.07 (3) h is estimated using the power-moderated mean (PMM) method.

RESUMEN

For the first time, charge distribution studies have been carried out in the epi-cadmium neutron induced fission of 235U by measuring the fractional cumulative yields (FCY) and independent yields (IY) of various fission products. An off-line γ-ray spectrometric technique was used for the measurements. The average energy of the epi-cadmium neutron spectrum is 1.9 MeV. From the FCY values, the isobaric width parameter (σZ), most probable charge (ZP) and the charge polarization (ΔΖEXPT) as a function of fragment mass were obtained. Similarly, from the IY values, isotopic width parameter (σA), the most probable mass (AP) and the elemental yields (YZ) of Sn, Sb, Te, I, Xe, Cs, Ba, La, Ce and Pr were determined by using a non-linear fit. From the YZ values, the proton even-odd effect (δp) was obtained for the first time. The present data in the 235U(n, f) reaction were compared with the similar data in the 235U(nth, f) and 238U(n, f) reactions as well as of other actinides to examine the role of excitation energy and pairing effect.

RESUMEN

Measurement of independent isomeric yield ratios (IR) of 128,130,132Sb, 131,133Te, 132.134,136I, 135Xe and 138Cs have been carried out for the first time in the epi-cadmium neutron induced fission of 239Pu by using an off-line gamma-ray spectrometric technique. The average neutron energy () of the epi-cadmium reactor neutron spectrum is 1.9 MeV. From the IR values, root mean square fragment angular momenta (JRMS) were deduced by using spin dependent statistical model analysis. Effect of nuclear structure on JRMS values was examined. The present data in the epi-cadmium neutron induced fission of 239Pu were compared with the similar data in the thermal neutron induced fission of 239Pu to examine the role of excitation energy on JRMS values.

RESUMEN

Studies on charge distribution have been carried out in the epi-cadmium neutron induced fission of 238Pu for the first time. Experimentally fractional cumulative yields (FCY) and independent yields (IY) of various fission products have been measured by using an off-line γ-ray spectrometric technique. From the FCY values, the charge distribution parameters such as the isobaric width parameter (σZ), most probable charge (ZP) and the charge polarization (ΔΖEXPT) as a function of fragment mass were obtained. On the other hand, from the measured IY values, isotopic width parameter (σA), the most probable mass (AP) and the elemental yields (YZ) of Sn, Sb, Te, I, Xe, Cs, Ba, La, Ce and Pr were determined by using a non-linear fit. From the YZ values, the proton even-odd effect (δp) was obtained for the first time. The isobaric and isotopic charge distribution parameters in the 238Pu(nf, f) reaction were compared with the similar data in the thermal neutron induced fission of 238Pu and other actinides to examine the role of excitation energy.

RESUMEN

Soil contamination in outdoor shooting ranges (OSRs) is a major threat for human health, particularly when, after the end of activities, the land is used for recreational areas or agricultural production. The status of land degradation of an OSR in southern Italy was assessed using a multisensor approach. It was based on: i) proximal sensors, including electromagnetic induction (EMI) for measuring soil electrical conductivity (ECa) and magnetic susceptibility (MSa), γ-ray spectrometry for K, eU and eTh analyses and ultrasonic penetrometry detecting cone index (CI) data representative of soil's strength, ii) field surveys on soil thickness (ST), and iii) laboratory analyses of potentially-toxic-elements (PTEs) by portable X-ray fluorescence spectrometry and polycyclic aromatic hydrocarbons (PAHs) by gas-chromatography. Spatial variability of measurements was modelled and mapped using geostatistical methods. The most densely measured covariate (i.e., the ECa of the topsoil) was used within kriging with external drift to improve the PTEs predictions. The PTEs maps were complemented by maps of spatial uncertainty. A robust multivariate principal component analysis (rPCA) was applied to proximal sensor and laboratory data and allowed to identify associations of PAHs, lead, CI with the topsoil ECa along the first component (PC1), highlighting the correlation between land anthropogenic effects and EMI measures; while the association between the ST (estimating the depth of underground travertine hard-layers) and the bottom soil ECa and MSa along the second component (PC2) evidenced the influence of soil stratigraphy on the EMI measures. This study demonstrates that the simultaneous use of different proximal sensors associated with laboratory analysis can allow to assess and model the spatial variability of the land degradation status of an OSR, including soil compaction, organic and inorganic contamination. The correlation between EMI data with the PTEs content highlights the potential of this technique in the field of soil contamination.

RESUMEN

The independent isomeric yield ratios (IR) of 128,130,132Sb, 131,133Te, 132,134,136I, 135Xe and 138Cs have been measured in the epi-cadmium neutron induced fission of 233U by using an off-line gamma-ray spectrometric technique. The average neutron energy of the epi-cadmium reactor neutron spectrum is 1.9 MeV. The root mean square fragment angular momenta (JRMS) were deduced from the IR values by using spin dependent statistical model analysis. The IR and JRMS values of considered fission products in the epi-cadmium neutron induced fission of 233U were compared with the literature data in the thermal neutron induced fission of 233U to examine the influence of excitation energy on nuclear structure effect.

RESUMEN

The cross sections for the 55Mn(n,2n)54Mn, 181Ta(n,2n)180gTa, and 181Ta(n,p)181Hf reactions were measured to be 705.1 ± 26.1 mb at 14.0 MeV, 1362.7 ± 87.2 mb at 13.6 MeV, and 2.31 ± 0.09 mb at 13.6 MeV, respectively, by using an off-line γ-ray spectroscopic technique. The neutrons were produced via the 3H(d,n)4He reaction. The monitor reactions 27Al(n,α)24Na and 93Nb(n,2n)92mNb were used for neutron flux determination. The results from the present work were compared with those of the literature and the evaluated data from ENDF/B-VIII.0, JEFF-3.3, JENDL-5, CENDL-3.2, and BROND-3.1 libraries. Besides, the cross sections were also estimated with the TALYS-1.96 nuclear model code using different level density models for a better description of the present work and literature data. The present experimental results were found to be in good agreement with most of the available literature data and with the evaluated data.

RESUMEN

Fractional cumulative yields (FCY) of various light mass fission products in the 233U(nth, f), 235U(nth, f) and 239Pu(nth, f) reactions were measured by using an off-line γ-ray spectrometric technique. The values of most probable charge (ZP) were obtained by using the width of isobaric charge distribution (σZ) of nearby fissioning systems with proper apportion. From the ZP values, the experimental charge polarization (ΔΖEXPT) as a function of fragment mass were also deduced. The ΔΖEXPT values for the light mass chains from the present work and for the heavy mass chains from earlier work show an oscillating nature in the interval of five mass units due to even-odd staggering. A local effect around the shell region and a systematic decreasing trend with the approach of symmetric split was also observed. The ΔΖMPE values based on minimum potential energy surface were theoretically calculated, which shows no oscillation but only a systematic decreasing trend with the approach of symmetric split due to the assumption of liquid drop behaviour of the fissioning nucleus.

RESUMEN

44Sc is a promising radionuclide for positron emission tomography (PET) in nuclear medicine. As a part of the implementation of a production site for 44Sc, precise knowledge of the activity of the product is necessary. At the Paul Scherrer Institute (PSI) and the University of Bern (UniBE), 44Sc is produced by enriched 44CaO-target irradiation with a cyclotron. The two sites use different techniques for activity measurement, namely a dose calibrator at the PSI and a gamma-ray spectrometry system at UniBE and PSI. In this work, the 44Sc was produced at the PSI, and samples of the product were prepared in dedicated containers for onsite measurements at PSI, UniBE, and the Institute of Radiation Physics (IRA) in Lausanne for precise activity measurement using primary techniques and for the calibration of the reference ionization chambers. An accuracy of 1% was obtained for the activity measurement, allowing for a precise calibration of the dose calibrator and gamma-ray spectrometry of the two production sites. Each production site now has the capability of measuring 44Sc activity with an accuracy of 2%.

RESUMEN

Greek honey was examined for 238U, 234U, 210Pb, 210Po, 40K, and 137Cs levels. 238U was calculated from 0.013 ± 0.007 Bq kg-1 to 0.10 ± 0.02 Bq kg-1 while 234U ranged from 0.017 ± 0.009 Bq kg-1 to 0.11 ± 0.03 Bq kg-1. 210Pb measured from 0.04 ± 0.02 Bq kg-1 to 1.70 ± 0.26 Bq kg-1 whereas 210Po activity determined between 0.02 ± 0.01 Bq kg-1 and 2.31 ± 0.34 Bq kg-1. 40 K found at the range of 7.9 ± 1.6 Bq kg-1 to 102.2 ± 19.7 Bq kg-1 and 137Cs 0.3 ± 0.1 Bq kg-1 up to 0.8 ± 0.1 Bq kg-1. Uranium isotopes and 210Po were determined via alpha spectrometry. 210Pb was also indirectly determined by alpha spectrometry. 40 K and 137Cs were measured through γ-ray spectrometry. An annual dose calculation was performed for different age groups.

Asunto(s)

RESUMEN

Isobaric charge distribution has been carried out in the thermal neutron induced fission of 233U, 235U and 239Pu by measuring the fractional cumulative yields (FCY) of various heavy mass fission products within the range of 127-149. An off-line γ-ray spectrometric technique was used for the measurement of fission product activities. The width of the isobaric charge distribution (σZ), most probable charge (ZP) and thus the experimental charge polarization (ΔΖEXPT) as a function of fragment mass were obtained. It was found that the σZ values around the mass number 127-129 and 132-136 are lower due to the presence of spherical 50p and 82n shells. The ΔΖEXPT values show an oscillating nature in the interval of five mass units due to even-odd effect. The ΔΖEXPT values also show a decreasing trend with the approach of symmetric split besides an oscillating nature. The most probable charge (ZMPE) and thus the ΔΖMPE values based on the minimum potential energy surface were theoretically calculated, which show a systematic decreasing trend with the approach of symmetric split due to the liquid drop behaviour of the fissioning nucleus.

RESUMEN

The activation cross-sections of 93Nb(n,2n)92Nbm and 88Sr(n,2n)87Srm reactions were measured using the activation and off-line γ-ray spectrometry technique in the neutron energy range 13.97-20.02 MeV. The present measurements have been done at the neutron energies where there are deficiencies and scarcity in the reaction cross-section data. The neutron flux was determined using the 27Al(n,α)24Na monitor reaction. The γ-ray self-attenuation effect and the low energy background neutron corrections were done in this experiment. The results of the present work were compared with the previously published data and evaluated nuclear data libraries. Theoretically, the cross-section for 93Nb(n,2n)92Nbm and 88Sr(n,2n)87Srm reactions was predicted by TALYS-1.9 nuclear code and compared with the present results.

RESUMEN

Considering the probable health risks due to radioactivity input via drinking tea, the concentrations of 226Ra, 232Th,40K and 137Cs radionuclides in the soil and the corresponding tea leaves of a large tea plantation were measured using high purity germanium (HPGe) γ-ray spectrometry. Different layers of soil and fresh tea leaf samples were collected from the Udalia Tea Estate (UTE) in the Fatickchari area of Chittagong, Bangladesh. The mean concentrations (in Bq/kg) of radionuclides in the studied soil samples were found to be 34 ± 9 to 45 ± 3 for 226Ra, 50 ± 13 to 63 ± 5 for 232Th, 245 ± 30 to 635 ± 35 for 40K and 3 ± 1 to 10 ± 1 for 137Cs, while the respective values in the corresponding tea leaf samples were 3.6 ± 0.7 to 5.7 ± 1.0, 2.4 ± 0.5 to 5.8 ± 0.9, 132 ± 25 to 258 ± 29 and <0.4. The mean transfer factors for 226Ra, 232Th and 40K from soil to tea leaves were calculated to be 0.12, 0.08 and 0.46, respectively, the complete range being 1.1 × 10-2 to 1.0, in accordance with IAEA values. Additionally, the most popularly consumed tea brands available in the Bangladeshi market were also analyzed and, with the exception of 40K, were found to have similar concentrations to the fresh tea leaves collected from the UTE. The committed effective dose via the consumption of tea was estimated to be low in comparison with the United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) reference ingestion dose limit of 290 µSv/y. Current indicative tea consumption of 4 g/day/person shows an insignificant radiological risk to public health, while cumulative dietary exposures may not be entirely negligible, because the UNSCEAR reference dose limit is derived from total dietary exposures. This study suggests a periodic monitoring of radiation levels in tea leaves in seeking to ensure the safety of human health.

RESUMEN

There are few long-lived radionuclides yielding high intensity gamma-rays emission with energies ranging from 100 keV to 500 keV that can be applied as radioactive gamma standard to calibrate HPGe detectors. Furthermore, this energy range represents the main emitted energies of the majority of radionuclides used in nuclear medicine. The Brazilian National Laboratory for Ionizing Radiation Metrology (LNMRI/IRD/CNEN) has attempted to identify radionuclides that have the potential to be used as a calibration source due to their long half-life as well as their emission spectrum. Hence, LNMRI promotes standardization studies of gamma-emitting radionuclides that meet these criteria on order to disseminate them. Thorium-229, with its well-defined energies and relatively high intensities, is one such candidate radionuclide for the energy and full-energy peak efficiency calibration of high-purity gamma spectrometers. Thorium-229 was standardized by the method of 4παß(LS)-γ(NaI(Tl)) live timed anticoincidence counting. The emission intensities of gamma-rays associated with the decay of 229Th have been determined by HPGe gamma ray spectrometry with accuracy and precision. The results are in agreement with current literature data.

RESUMEN

In 2017, JRC-Geel organised a proficiency test for 120 participants on the massic activity determination of 131I, 134Cs and 137Cs in maize powder. The proficiency test reference material was produced by spiking blank maize powder. The material was characterised for its radioactive content using γ-ray spectrometry. The z scores of the reported massic activity were acceptable in 92% of the results for 131I, and in 94% for both 134Cs and 137Cs. The ζ scores were consistent with the reference value for 66% of the results for 131I, 56% for 134Cs and 68% for 137Cs.

Asunto(s)

RESUMEN

This paper presents a sparse spectral unmixing algorithm for activity estimation of radionuclides in γ-ray spectrometry. The spectral unmixing method aims to decompose a measured spectrum into spectral signatures of radionuclides, which is sensitive to the choice of the spectral signatures. The sparsity of the solution is imposed to identify the active radionuclides. Experimental results on simulated and real spectra show that the proposed method yields significant improvement for estimating radioactivity at low statistics.

RESUMEN

The radium isotopes 226Ra and 228Ra can provide important data on the dynamics of deep-sea hydrothermal plumes that travel the oceans for decades and have great impact on the ocean chemistry. This study focuses on parameters important for obtaining low detection limits for 228Ra using gamma-ray spectrometry. It is present at mBq-levels in samples collected during the US GEOTRACES 2013 cruise to the Southeast Pacific Ocean.

RESUMEN

A new medium resolution gamma-ray spectrometer consisting of a cerium bromide (CeBr3) crystal (2˝ x 2˝), is developed and optimized for radioactivity measurements in aquatic environments. This apparatus named GeoMAREA (Gamma-ray spectrometer for in-situ Marine Environmental Applications) is designed to control and prevent radio-contaminants in aquatic environments as well as to estimate the variation of natural radionuclides in marine systems for studying oceanographic processes. The system offers activity concentrations in Bq/m3 for detected gamma-ray emitters in the energy range from 150 to 2600 keV, and can provide sequential continuous monitoring data in a stand-alone mode or it can be integrated in stationary/mobile platforms for (near) real-time applications. The photopeak efficiency values were estimated via the MCNPΧ code. Two experimental points were used to validate the theoretical estimations by deploying the system in a water tank with diluted reference sources such us Caesium-137 (137Cs) and Potassium-40 (40K). The system was subsequently deployed in the field along with a conductivity-temperature (CT) sensor, to measure 40K and radon daughters in a region where submarine groundwater discharges (Anavalos, Kiveri, Greece) are present. The experimental calibration data was utilized to provide a first estimation for the background contribution around the photopeak of 40K, attributed to the Cerium Bromide (CeBr3) intrinsic activity.

Asunto(s)

RESUMEN

A collimated source of 241Am was scanned over the endcap of a 21 year old coaxial HPGe-detector that had spent about 75% of its life at room temperature (and the remaining time at 77 K). The detector response was recorded and used as a measure of the relative thickness of the top deadlayer. This thickness was not homogeneous and was thicker near to the outer surface of the crystal compared to the centre, which could be a result of increased diffusion of Li atoms during times the detector was kept at room temperature. The results were compared with two newer HPGe-detectors that proved to have homogeneous top deadlayers.