RESUMEN
A method for absolute measurements of the 225Ac activity in equilibrium with its progeny was developed. Measurements were performed using the triple-to-double coincidence ratio (TDCR) method in two different TDCR counters. The activity concentration of an 225Ac solution was determined and the solution was sent to the SIR system for a comparison. The half-life of 225Ac was determined by one of the TDCR counters and found to be 9.9150(63) days.
RESUMEN
The activity of the 177Lu solution has been measured by means of the CIEMAT/NIST efficiency tracing method. This result has been compared to the previous obtained results received from 4πß(LS)-γ coincidence and anticoincidence counting. The activities determined with various methods have been found to be consistent. The decay curve of the 177Lu solution has been followed in the TDCR counter to determine the half-life of this isotope. The half-life has been separately determined for double and triple coincidence events. The arithmetic mean value of these two results has been found to be T1/2 = 6.6489(52) d.
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Activity measurements of 3H, 241Am and 60Co solutions were performed to compare digital coincidence modules used at PTB and POLATOM for TDCR and 4πß(LS)-γ coincidence counting. The activities determined with various coincidence modules connected in parallel to the same counter at PTB were found to be consistent. Observed discrepancies caused by differences in the coincidence resolving time did not exceed 0.14%. Accidental coincidences simulated by a frequency generator were registered, and the coincidence resolving time was determined.
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Application of a new coincidence module using the pulse-mixing method in the 4π(LS)-γ coincidence system with TDCR detector in the beta channel (TDCRG) is presented. The pulse-mixing method extended for the TDCR system with gamma channel was compared with the classical coincidence method where the coincidence resolving time is introduced. The characteristics of the resolving and dead time of the above two methods were investigated. The level of accidental coincidences in the system was determined. The new developed coincidence module was validated by activity measurement of a set of 51Cr, 54Mn, 60Co, 65Zn, 85Sr and 134Cs standards.
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An internal consistency test of the calculation of coincidence-summing correction factors FC for volume sources is presented. The test is based on exact equations relating the values of FC calculated for three ideal measurement configurations. The test is applied to a number of 33 sets of FC values sent by 21 teams. Most sets passed the test, but not the results obtained using the quasi-point source approximation; in the latter case the test qualitatively indicated the magnitude of the bias of FC.
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An international key comparison, identifier CCRI(II)-K2.Ge-68, has been performed. The National Institute of Standards and Technology (NIST) served as the pilot laboratory, distributing aliquots of a 68Ge/68Ga solution. Results for the activity concentration, CA, of 68Ge at a reference date of 12h00 UTC 14 November 2014 were submitted by 17 laboratories, encompassing many variants of coincidence methods and liquid-scintillation counting methods. The first use of 4π(Cherenkov)ß-γ coincidence and anticoincidence methods in an international comparison is reported. One participant reported results by secondary methods only. Two results, both utilizing pure liquid-scintillation methods, were identified as outliers. Evaluation using the Power-Moderated Mean method results in a proposed Comparison Reference Value (CRV) of 621.7(11)kBqg-1, based on 14 results. The degrees of equivalence and their associated uncertainties are evaluated for each participant. Several participants submitted 3.6mL ampoules to the BIPM to link the comparison to the International Reference System (SIR) which may lead to the evaluation of a Key Comparison Reference Value and associated degrees of equivalence.
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The aim of the work was to develop new radioactive standard sources based on epoxy resins. The optimal proportions of the components and the homogeneity of the matrices were determined. The activity of multigamma sources prepared in Marinelli beakers was determined with reference to the National Standard of Radionuclides Activity in Poland. The difference of radionuclides activity values determined using calibrated gamma spectrometer and the activity of standard solutions used are in most cases significantly lower than measurement uncertainty limits. Sources production method and quality control procedure have been developed.
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A new large-volume metal reference standard has been developed. The intended use is for calibration of free-release radioactivity measurement systems and is made up of cast iron tubes placed inside a box of the size of a Euro-pallet (80 × 120 cm). The tubes contain certified activity concentrations of (60)Co (0.290 ± 0.006 Bq g(-1)) and (110m)Ag (3.05 ± 0.09 Bq g(-1)) (reference date: 30 September 2013). They were produced using centrifugal casting from a smelt into which (60)Co was first added and then one piece of neutron irradiated silver wire was progressively diluted. The iron castings were machined to the desirable dimensions. The final material consists of 12 iron tubes of 20 cm outer diameter, 17.6 cm inner diameter, 40 cm length/height and 245.9 kg total mass. This paper describes the reference standard and the process of determining the reference activity values.
Asunto(s)
Radioisótopos de Cobalto/análisis , Monitoreo de Radiación/métodos , Residuos Radiactivos/análisis , Plata/análisis , Administración de Residuos/normas , Humanos , Estándares de ReferenciaRESUMEN
In 2011 the joint research project Metrology for Radioactive Waste Management (MetroRWM)(1) of the European Metrology Research Programme (EMRP) started with a total duration of three years. Within this project, new metrological resources for the assessment of radioactive waste, including their calibration with new reference materials traceable to national standards will be developed. This paper gives a review on national, European and international strategies as basis for science-based metrological requirements in clearance and acceptance of radioactive waste.
Asunto(s)
Guías como Asunto , Protección Radiológica/legislación & jurisprudencia , Protección Radiológica/normas , Residuos Radiactivos/legislación & jurisprudencia , Residuos Radiactivos/prevención & control , Administración de Residuos/legislación & jurisprudencia , Administración de Residuos/normas , Descontaminación/legislación & jurisprudencia , Descontaminación/normas , InternacionalidadRESUMEN
We present a complete systematics (excitation functions and system-size dependences) of global stopping and side flow for heavy ion reactions in the energy range between 0.09A and 1.93A GeV. For the heaviest system, Au+Au, we observe a plateau of maximal stopping extending from about 0.2A to 0.8A GeV with a fast drop on both sides. The degree of stopping, which is shown to remain significantly below the expectations of a full stopping scenario, is found to be highly correlated to the amount of side flow.