TY - JOUR
T1 - Uranium beam characterization at CIRCE for background and contamination determinations
AU - De Cesare, M.
AU - De Cesare, N.
AU - D'Onofrio, A.
AU - Fifield, L. K.
AU - Gialanella, L.
AU - Terrasi, F.
N1 - Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - The Accelerator Mass Spectrometry (AMS) is the most sensitive technique, compared either to the Inductively Coupled Plasma (ICP-MS) or Thermal Ionization (TI-MS) mass spectrometer, for the actinide (e.g. 236U, xPu isotopes) measurements. They are present in environmental samples at the ultra trace level since atmospheric tests of Nuclear Weapons (NWs) performed in the past, deliberate dumping of nuclear waste, nuclear fuel reprocessing, on a large scale, and operation of Nuclear Power Plants (NPPs), on a small scale, have led to the release of a wide range of radioactive nuclides in the environment. At the Center for Isotopic Research on Cultural and Environmental heritage (CIRCE) in Caserta, Italy, an upgraded actinide AMS system, based on a 3-MV pelletron tandem accelerator, has been developed and routinely operated. At CIRCE a charge state distribution as a function of terminal voltage, the beam emittance, measured in the 20° actinides dedicated beam line, as well as the energy and position validation of the U ions were performed in order to determine the best measurement conditions. A 236U/238U isotopic ratio background level of about 5×10-12 or 3×10-13, depending on the Time of Flight-Energy (TOF-E) configurations, as well as the spatial distribution of the 235U, 238U interferences ions and a 236U contamination mass of about 0.5fg have been determined.
AB - The Accelerator Mass Spectrometry (AMS) is the most sensitive technique, compared either to the Inductively Coupled Plasma (ICP-MS) or Thermal Ionization (TI-MS) mass spectrometer, for the actinide (e.g. 236U, xPu isotopes) measurements. They are present in environmental samples at the ultra trace level since atmospheric tests of Nuclear Weapons (NWs) performed in the past, deliberate dumping of nuclear waste, nuclear fuel reprocessing, on a large scale, and operation of Nuclear Power Plants (NPPs), on a small scale, have led to the release of a wide range of radioactive nuclides in the environment. At the Center for Isotopic Research on Cultural and Environmental heritage (CIRCE) in Caserta, Italy, an upgraded actinide AMS system, based on a 3-MV pelletron tandem accelerator, has been developed and routinely operated. At CIRCE a charge state distribution as a function of terminal voltage, the beam emittance, measured in the 20° actinides dedicated beam line, as well as the energy and position validation of the U ions were performed in order to determine the best measurement conditions. A 236U/238U isotopic ratio background level of about 5×10-12 or 3×10-13, depending on the Time of Flight-Energy (TOF-E) configurations, as well as the spatial distribution of the 235U, 238U interferences ions and a 236U contamination mass of about 0.5fg have been determined.
KW - AMS
KW - Interferences ions
KW - TOF-E systems
KW - Uranium
UR - http://www.scopus.com/inward/record.url?scp=84934937410&partnerID=8YFLogxK
U2 - 10.1016/j.apradiso.2015.06.011
DO - 10.1016/j.apradiso.2015.06.011
M3 - Article
SN - 0969-8043
VL - 103
SP - 166
EP - 172
JO - Applied Radiation and Isotopes
JF - Applied Radiation and Isotopes
ER -