scholarly journals High Level Waste Demonstration of the Caustic-Side Solvent Extraction Process with Optimized Solvent in the 2-CM Centrifugal Contactor Apparatus Using Tank 37H/44F Supernate

2003 ◽  
Author(s):  
M A Norato
2003 ◽  
Vol 38 (12-13) ◽  
pp. 2647-2666 ◽  
Author(s):  
M. A. Norato ◽  
M. H. Beasley ◽  
S. G. Campbell ◽  
A. D. Coleman ◽  
M. W. Geeting ◽  
...  

2019 ◽  
Vol 107 (9-11) ◽  
pp. 917-929 ◽  
Author(s):  
Rikard Malmbeck ◽  
Daniel Magnusson ◽  
Stéphane Bourg ◽  
Michael Carrott ◽  
Andreas Geist ◽  
...  

Abstract The EURO-GANEX process was developed for co-separating transuranium elements from irradiated nuclear fuels. A hot flow-sheet trial was performed in a counter-current centrifugal contactor setup, using a genuine high active feed solution. Irradiated mixed (carbide, nitride) U80Pu20 fast reactor fuel containing 20 % Pu was thermally treated to oxidise it to the oxide form which was then dissolved in HNO3. From this solution uranium was separated to >99.9 % in a primary solvent extraction cycle using 1.0 mol/L DEHiBA (N,N-di(2-ethylhexyl)isobutyramide in TPH (hydrogenated tetrapropene) as the organic phase. The raffinate solution from this process, containing 10 g/L Pu, was further processed in a second cycle of solvent extraction. In this EURO-GANEX flow-sheet, TRU and fission product lanthanides were firstly co-extracted into a solvent composed of 0.2 mol/L TODGA (N,N,N′,N′-tetra-n-octyl diglycolamide) and 0.5 mol/L DMDOHEMA (N,N′-dimethyl-N,N′-dioctyl-2-(2-hexyloxy-ethyl) malonamide) dissolved in Exxsol D80, separating them from most other fission and corrosion products. Subsequently, the TRU were selectively stripped from the collected loaded solvent using a solution containing 0.055 mol/L SO3-Ph-BTP (2,6-bis(5,6-di(3-sulphophenyl)-1,2,4-triazin-3-yl)pyridine tetrasodium salt) and 1 mol/L AHA (acetohydroxamic acid) in 0.5 mol/L HNO3; lanthanides were finally stripped using 0.01 mol/L HNO3. Approximately 99.9 % of the TRU and less than 0.1 % of the lanthanides were found in the product solution, which also contained the major fractions of Zr and Mo.


2000 ◽  
Author(s):  
J. Banaee ◽  
C. M. Barnes ◽  
T. Battisti ◽  
S. Herrmann ◽  
S. J. Losinski ◽  
...  

2019 ◽  
Vol 107 (5) ◽  
pp. 423-429 ◽  
Author(s):  
Parveen Kumar Verma ◽  
Rajesh Bhikaji Gujar ◽  
Prasanta Kumar Mohapatra

Abstract Ruthenium (106Ru), a notorious fission product in nuclear reprocessing cycle, which gets partitioned at each step needs to be recovered. The recovery of Ru from acidic high level waste (HLW) is of great importance to the nuclear fuel cycle. Quantitative recovery of Ru was achieved from acidic feeds using oxidative trapping mechanism strategy where NaIO4 was used as an oxidant to convert different species of Ru in acidic phase to RuO4 while n-dodecane was used as trapping agent for RuO4. Stripping was attempted using NaOH and NaClO mixture. Attempt was made to optimize various parameters for 103Ru extraction and stripping. 103Ru tracer spiked simulated high level waste was used to understand the 103Ru behaviour in actual waste. The composition of stripping solution (alkaline hypochlorite) was also optimized to have >95% Ru into the aqueous phase in ca. 180 min.


2009 ◽  
Vol 27 (2) ◽  
pp. 172-198 ◽  
Author(s):  
Lætitia H. Delmau ◽  
Tamara J. Haverlock ◽  
Eve Bazelaire ◽  
Peter V. Bonnesen ◽  
Mary E. Ditto ◽  
...  

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