Electromigration method for destructive determination of spent nuclear fuel burnup

1980 ◽  
Vol 58 (1-2) ◽  
pp. 113-121 ◽  
Author(s):  
T. P. Makarova ◽  
A. V. Stepanov ◽  
A. M. Fridkin ◽  
B. A. Bibichev ◽  
A. V. Lovtsyus
Keyword(s):  
Nuclear Fuel ◽  
Spent Nuclear Fuel ◽  
Fuel Burnup

scholarly journals Thermal Ionization-Isotope Dilution Mass Spectrometry Determination of Ruthenium in Spent Nuclear Fuel

2013 ◽  
Vol 25 (12) ◽  
pp. 7044-7046 ◽  
Author(s):  
Young-Shin Jeon ◽  
Yang-Soon Park ◽  
Jung-Suk Kim ◽  
Sun-Ho Han ◽  
Yong Joon Park
Keyword(s):  
Mass Spectrometry ◽  
Nuclear Fuel ◽  
Isotope Dilution ◽  
Spent Nuclear Fuel ◽  
Isotope Dilution Mass Spectrometry ◽  
Thermal Ionization

The determination of mode shapes of a scaled model TN-32 spent nuclear fuel dry storage cask

2017 ◽  
Vol 142 (4) ◽  
pp. 2517-2518
Author(s):  
Kevin Y. Lin ◽  
Wayne E. Prather ◽  
Zhiqu Lu ◽  
Joel Mobley ◽  
Josh R. Gladden
Keyword(s):  
Nuclear Fuel ◽  
Spent Nuclear Fuel ◽  
Mode Shapes ◽  
Scaled Model ◽  
Dry Storage

scholarly journals An Automated SeaFAST ICP-DRC-MS Method for the Determination of 90Sr in Spent Nuclear Fuel Leachates

Molecules ◽  
2020 ◽  
Vol 25 (6) ◽  
pp. 1429 ◽  
Author(s):  
Víctor Vicente Vilas ◽  
Sylvain Millet ◽  
Miguel Sandow ◽  
Luis Iglesias Pérez ◽  
Daniel Serrano-Purroy ◽  
...  
Keyword(s):  
Nuclear Fuel ◽  
Safety Assessment ◽  
Analytical Approach ◽  
Source Term ◽  
Spent Nuclear Fuel ◽  
Spent Fuel ◽  
Chemical Purification ◽  
Radiochemical Method ◽  
Good Agreement

To reduce uncertainties in determining the source term and evolving condition of spent nuclear fuel is fundamental to the safety assessment. ß-emitting nuclides pose a challenging task for reliable, quantitative determination because both radiometric and mass spectrometric methodologies require prior chemical purification for the removal of interfering activity and isobars, respectively. A method for the determination of 90Sr at trace levels in nuclear spent fuel leachate samples without sophisticated and time-consuming procedures has been established. The analytical approach uses a commercially available automated pre-concentration device (SeaFAST) coupled to an ICP-DRC-MS. The method shows good performances with regard to reproducibility, precision, and LOD reducing the total time of analysis for each sample to 12.5 min. The comparison between the developed method and the classical radiochemical method shows a good agreement when taking into account the associated uncertainties.

Sign in / Sign up

Export Citation Format

Share Document