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000048085 084__ $$2WoS$$aEngineering, Chemical
000048085 1001_ $$0P:(DE-HGF)0$$aSerrano-Purroy, D.$$b0
000048085 245__ $$aFirst demonstration of a centrifugal solvent extraction process for minor actinides from a concentrated spent fuel solution
000048085 260__ $$aAmsterdam [u.a.]$$bElsevier Science$$c2005
000048085 300__ $$a157 - 162
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000048085 440_0 $$014501$$aSeparation and Purification Technology$$v45$$x1383-5866$$y2
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000048085 520__ $$aThe efficiency of minor actinides (MA) recovery in the diamide extraction (DIAMEX) process has already been demonstrated using high active raffinate (HAR). In view of an industrial application, the next development step aims at the partitioning of MA from high active concentrate (HAC) as feed. The volume reduction reduces the size of the installation, and thereby the amount of waste and the costs of the process. In this work, MA recovery by DIAMEX partitioning using genuine HAC has for the first time been demonstrated. The experiment was successfully carried out in a 16-stage centrifugal extractor battery, installed in the hot cell facilities at ITU, using N,N'-dimethyl-N,N'-dioctyl-2-(2-(hexyloxy)ethyl)-malonamide (DMDOHEMA) as extractant. In order to produce a representative HAC, a concentration-denitration process was applied to a genuine HAR solution produced by small scale plutonium uranium redox extraction (PUREX) reprocessing of a mixed oxide (MOX) fuel solution. In the DIAMEX process, five extraction stages were sufficient to achieve feed decontamination factors above 10,000 for Am and Cm. Co-extraction of molybdenum, zirconium and palladium was prevented using oxalic acid and HEDTA scrubbing. The back-extraction proved to be very efficient, yielding in four stages recoveries for Am and Cm in the product fraction above 99.7 and 99.9%, respectively, which can be further improved by process flowsheet optimisation. This work is a major contribution in the field of partitioning and an important step towards the industrial implementation of MA partitioning. (C) 2005 Elsevier B.V. All rights reserved.
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000048085 65320 $$2Author$$aactinide partitioning
000048085 65320 $$2Author$$aDIAMEX
000048085 65320 $$2Author$$aminor actinides
000048085 65320 $$2Author$$ahigh active concentrate
000048085 65320 $$2Author$$acentrifugal extractors
000048085 7001_ $$0P:(DE-HGF)0$$aBaron, P.$$b1
000048085 7001_ $$0P:(DE-HGF)0$$aChristiansen, S. H.$$b2
000048085 7001_ $$0P:(DE-HGF)0$$aGlatz, J.-P.$$b3
000048085 7001_ $$0P:(DE-HGF)0$$aMadic, C.$$b4
000048085 7001_ $$0P:(DE-HGF)0$$aMalmbeck, R.$$b5
000048085 7001_ $$0P:(DE-Juel1)130383$$aModolo, G.$$b6$$uFZJ
000048085 773__ $$0PERI:(DE-600)2022535-0$$a10.1016/j.seppur.2005.03.001$$gVol. 45, p. 157 - 162$$p157 - 162$$q45<157 - 162$$tSeparation and purification technology$$v45$$x1383-5866$$y2005
000048085 8567_ $$uhttp://dx.doi.org/10.1016/j.seppur.2005.03.001
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000048085 915__ $$0StatID:(DE-HGF)0010$$aJCR/ISI refereed
000048085 9201_ $$0I:(DE-Juel1)VDB182$$d31.12.2006$$gISR$$kISR$$lInstitut für Sicherheitsforschung und Reaktortechnik$$x0
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