Search Results (5)

This study focused on the measurement of anthropogenic radionuclides such as americium (Am) and plutonium (Pu) in environmental samples. Plutonium isotopes, particularly ${}^{239}\mathrm{Pu}$, ${}^{240}\mathrm{Pu}$, and ${}^{241}\mathrm{Pu}$, originated from nuclear weapons testing, nuclear power plants, and accidents like Chernobyl and Fukushima Daiichi. Accurate measurement of these isotopes, considering their half-lives and trace concentrations, provides critical information about their persistence and environmental transport. Using the 1 MV Tandetron accelerator, we expanded the measurement capabilities to include ${}^{241}\mathrm{Pu}$, ${}^{241}\mathrm{Am}$. Chemical separation of these isotopes was achieved through ion chromatography, employing reference isotopes ${}^{242}\mathrm{Pu}$ and ${}^{243}\mathrm{Am}$ for method validation. Certified reference materials, including IAEA-410 (Bikini Atoll sediment) and Sample 05, were analyzed to ensure accuracy. We validated the ${}^{241}\mathrm{Am}$/${}^{243}\mathrm{Am}$ ratio in an Am standard (IFIN-STD-Am, our laboratory produced standard for Am), achieving a measured value of 0.158 at·at⁻¹ (3%), in good agreement with the nominal value of 0.154 at·at⁻¹. Additionally, we determined the ${(}^{241}\mathrm{Pu}$ + ${}^{241}\mathrm{Am}){/}^{242}\mathrm{Pu}$ ratio in the ColPuS standard to be equal to 0.029 at ·at⁻¹ (7%). These results demonstrate the potential of AMS for improved detection of actinides at low concentrations and contribute to understanding the behavior of Pu and Am isotopes. Full article

The Dual-beam ion irradiation facility for Fusion materials (DiFU) has been developed and installed at the Ruđer Bošković Institute with the purpose to perform irradiation of samples of fusion materials by one or two ion beams. Ion beams are delivered to the DiFU chamber by a 6 MV EN Tandem Van de Graaff and a 1 MV HVE Tandetron accelerator, enabling irradiation of areas up to 30 × 30 mm². The sample holder enables the three-dimensional positioning of samples that can be irradiated while being heated, cooled, or kept at room temperature. Ion fluxes are measured indirectly by the insertion of two large Faraday cups. Besides, the ion flux is monitored continuously by two sets of horizontal and vertical slits, which, in turn, define the limits of the irradiation area on the sample. Sample temperature and conditions during irradiation are additionally monitored by a set of thermocouples, an IR camera, and a video camera. Particular care is dedicated to the mitigation of carbon contamination during ion irradiation. Full article

Structural materials of the new generation of nuclear reactors, fission as well as fusion, must often cope with high production rates of transmutation helium. Their testing hence requires either a powerful source of fast neutrons or a high-fluence ion-irradiation facility providing sufficient amounts of high-energy helium to investigate its effect on the material. Most ion irradiation studies, however, concentrate on basic effects such as defect evolution or bubble swelling in narrow near-surface regions modified by ion bombardment. Studies on bulk samples with a relatively thick implanted region, which would enable, for instance, micromechanical testing, are underrepresented. This gap might be filled by high-fluence multi-energy ion irradiations modifying several tens of micrometres of the investigated substrate. High-energy ion accelerators providing reasonable currents with energies of tens of MeV are rarely employed in such studies due to their scarcity or considerable beamtime costs. To contribute to this field, this article reports a unique single-beam He implantation experiment aimed at obtaining quasi-uniform displacement damage across >60 μm with the He/dpa ratio roughly one order of magnitude above the typical spallation neutron target irradiation conditions. Some technical aspects of this irradiation experiment, along with recent developments and upgrades at the 6 MV Tandetron accelerator of the Slovak university of technology in Bratislava, are presented. Full article

Rutherford backscattering spectrometry (RBS) in channeling regimes (RBS/C), as an ion beam analysis method performed on a Tandetron 6MV accelerator, generally gives precise information about the structure of crystalline samples by combining RBS signals in the random and aligned configurations. This paper presents details about the design and implementation of tailored RBS/C measurements (coarse and fine) and data evaluation application developed in MATLAB for in situ accelerator control system ARGUS, delivered by High Voltage Engineering Europa BV (HVEE). Additionally, we examined two different ways of stepping during the measurement to reduce the possible inaccuracies related with goniometer’s backslash affecting the evaluation of spectra. Verification experiment was carried out using a 2-MeV ⁴He+-beam directed on a Si (100) substrate. The channeling effect is seen as channeling dips of a lower signal in an otherwise rather homogeneous plane. Implemented application significantly facilitates the RBS/C measurement and analysis of the experiments, and also extends the ion beam analysis portfolio of Advanced Technologies Research Institute. Finally, software is ready-to-use for any Tandetron based ion beam facility with the ARGUS software for accelerator control. Full article

In the framework of an extensive environmental investigation, promoted by the Italian Health Ministry, the ISPESL (Istituto Superiore per la Prevenzione e la Sicurezza del Lavoro) and the CNR (Consiglio Nazionale della Ricerca), aerosol samples were collected in Taranto (one of the most industrialized towns in southern Italy) with high time resolution and analyzed by PIXE. The samples were collected in two periods (February–March and June 2004) and in two different sites: an urban district close to the industrial area and a small town 7 km N-NW of Taranto. The use of ‘‘streaker’’ samplers (by PIXE International Corporation) allowed for the simultaneous collection of the fine (<2.5 μm) and coarse (2.5–10 μm) fractions of particulate matter. PIXE analyses were performed with a 3 MeV proton beam from the 3 MV Tandetron accelerator of the INFN-LABEC laboratory. Particulate emissions as well as their atmospheric transport and dilution processes change within a few hours, but most of the results in literature are limited to daily time resolution of the input samples that are not suitable for tracking these rapid changes. Furthermore, since source apportionment receptor models need a series of samples containing material from the same set of sources in different proportions, a higher variability between samples can be obtained by increasing the temporal resolution rather than with samples integrated over a longer time. In this study, the high time resolution of the adopted approach allowed us to follow in detail the changes in the aerosol elemental composition due to both the time evolution of the industrial emissions and the time changes in meteorological conditions, and thus, transport pathways. Moreover, the location of the sampling sites, along the prevalent wind direction and in opposite positions with respect to the industrial site, allowed us to follow the impact of the industrial plume as a function of wind direction. Positive matrix factorization (PMF) analysis on the elemental hourly concentrations identified eight sources in the fine fraction and six sources in the coarse one. Full article