Alpha-Photon Coincidence Spectroscopy Along Element 115 Decay Chains

Produced in the reaction 48Ca+243Am, thirty correlated α-decay chains were observed in an experiment conducted at the GSI Helmholzzentrum für Schwerionenforschung, Darmstadt, Germany. The decay chains are basically consistent with previous findings and are considered to originate from isotopes of element 115 with mass numbers 287, 288, and 289. A set-up aiming specifically for high-resolution charged particle and photon coincidence spectroscopy was placed behind the gas-filled separator TASCA. For the first time, γ rays as well as X-ray candidates were observed in prompt coincidence with the α-decay chains of element 115

Recoil-α-fission and recoil-α-α-fission events observed in the reaction 48Ca + 243Am

Products of the fusion-evaporation reaction 48Ca + 243Am were studied with the TASISpec set-up at the gas-filled separator TASCA at the GSI Helmholtzzentrum für Schwerionenforschung, Darmstadt, Germany. Amongst the detected thirty correlated α-decay chains associated with the production of element Z=115, two recoil-α-fission and five recoil-α-α-fission events were observed. The latter five chains are similar to four such events reported from experiments performed at the Dubna gas-filled separator, and three such events reported from an experiment at the Berkeley gas-filled separator. The four chains observed at the Dubna gas-filled separator were assigned to start from the 2n-evaporation channel 289115 due to the fact that these recoil-α-α-fission events were observed only at low excitation energies. Contrary to this interpretation, we suggest that some of these recoil-α-α-fission decay chains, as well as some of the recoil-α-α-fission and recoil-α-fission decay chains reported from Berkeley and in this article, start from the 3n-evaporation channel 288115

Tellurium determination by three modes of instrumental neutron activation analysis in aerosol filters and trap solutions for the simulation of a severe nuclear accident

Tellurium belongs to the elements not frequently determined by neutron activation analysis (NAA) or other analytical methods. We present results of a new methodological study using three independent modes of instrumental NAA (INAA) using the\ua0123mTe,\ua0131Te and\ua0131I radionuclides. We compare the results obtained in terms of accuracy, precision and limits of detection (LOD). We utilized the INAA procedures tested for the tellurium determination in aerosol filters and trap solutions in a model experiment aimed at reducing the knowledge gap concerning the behaviour of\ua0132Te, a radiologically significant fission product, which constitutes a considerable health risk towards the public in case of its release in a severe nuclear power plant accident. We found that the nuclear reaction\ua0130Te(n,γ)131Te and gamma-ray spectrometric measurement of\ua0131I, a descendant of\ua0131Te, is the most sensitive way of Te determination by INAA providing as low LOD values as 0.15\ua0\ub5g of Te in the Teflon aerosol filters and 0.22\ua0\ub5g mL-1\ua0in the 0.1\ua0M NaOH trap solutions. The three independent INAA modes allowed employing the self-verification principle of INAA for increasing the trustworthiness of our results. Finally, we also point to the indispensable role of the non-destructive feature of INAA for assay of samples, such as Teflon aerosol filters, that are difficult to be analysed by other analytical methods requiring complete sample destruction without analyte losses