Progress on the chemical separation of fission fragments from 236Np produced by proton irradiation of natural uranium target
The aim of the current work is to develop and validate a radiochemical separation scheme capable of separating both 236gNp and 236Pu from a uranium target of natural isotopic composition (~1g uranium) and ~200 MBq of fission decay products. A target containing 1.2g of UO2 was irradiated with a beam...
Gespeichert in:
Veröffentlicht in: | Radiation physics and chemistry (Oxford, England : 1993) England : 1993), 2017-11, Vol.140, p.480-486 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The aim of the current work is to develop and validate a radiochemical separation scheme capable of separating both 236gNp and 236Pu from a uranium target of natural isotopic composition (~1g uranium) and ~200 MBq of fission decay products. A target containing 1.2g of UO2 was irradiated with a beam of 25MeV protons with a typical beam current of 30 μA for 19h in December 2013 at the University of Birmingham Cyclotron facility. Using literature values for the production cross-section for fusion of protons with uranium targets, we estimate that an upper limit of approximately 250Bq of activity from the 236Np ground state was produced in this experiment. Using a radiochemical separation scheme, Np and Pu fractions were separated from the produced fission decay products, with analyses of the target-based final reaction products made using Inductively Couple Plasma Mass Spectrometry (ICP-MS) and high-resolution α particle and γ-ray spectrometry.
•Development of a radiochemical separation scheme for separating 236gNp.•Measurements using α and high-resolution γ-ray spectrometry.•γ-ray spectroscopy used indicates presence of 236Np ground state.•Clear signature of 236Pu characteristic lines. |
---|---|
ISSN: | 0969-806X 1879-0895 |
DOI: | 10.1016/j.radphyschem.2017.02.004 |