Valenzstabilisierung von Neptunium in salpetersauren Medien bei der Wiederaufarbeitung abgebrannter Brennelemente
Valenzstabilisierung von Neptunium in salpetersauren Medien bei der Wiederaufarbeitung abgebrannter Brennelemente
A possibility of standarizing the extraction-behavior of Neptunium during the reprocessing of spent nuclear fuel corresponding to PUREX-Process was investigated. The aim of the work was a quantitative dirigation of the Transuraniumelement (TRUE) into the raffinat of the first extraction cycle by a c...
Saved in:
Personal Name(s): | Feldhaus, P. (Corresponding author) |
---|---|
Contributing Institute: |
Publikationen vor 2000; PRE-2000; Retrocat |
Imprint: |
Jülich
Forschungszentrum Jülich GmbH Zentralbibliothek, Verlag
1996
|
Physical Description: |
110 p. |
Document Type: |
Report Book |
Research Program: |
Addenda |
Series Title: |
Berichte des Forschungszentrums Jülich
3309 |
Link: |
OpenAccess OpenAccess |
Publikationsportal JuSER |
A possibility of standarizing the extraction-behavior of Neptunium during the reprocessing of spent nuclear fuel corresponding to PUREX-Process was investigated. The aim of the work was a quantitative dirigation of the Transuraniumelement (TRUE) into the raffinat of the first extraction cycle by a complete redoxconversion of the Neptunium valence states to unextractable Np(V). In the beginning the theoretical and experimental research focussed on the redoxchemistry of the actinide during the fuel dissolution and the feed preparation. Thereby the nitrous acid, which is produced by a radiological, photochemical and reductive degradation of the nitric acid, revealed an ambivalent influence on the Neptunium valences. By a short-term increase in HNO$_{2}$-concentration the Np(V)-fraction could be obviously risen. The use of some stabilizing reagents inhibited a later reoxidation to Np(VI) also catalyzed by nitrous acid. The urea used for this purpose also led to a further increase in the obtained conversion rates due to a Np(VI)-reduction. The analysis of the valence distribution was performed by an extraction method. This had been compared to chromatographic separation in some preliminary investigations and had tumed out to be comparably reliable and easily manageable. |