M. Carrott, C. Maher, C. Mason, M. Sarsfield, D. Whittaker, R. J. Taylor
{"title":"Experimental Test of a Process Upset in the EURO-GANEX Process and Spectroscopic Study of the Product","authors":"M. Carrott, C. Maher, C. Mason, M. Sarsfield, D. Whittaker, R. J. Taylor","doi":"10.1080/07366299.2022.2136488","DOIUrl":null,"url":null,"abstract":"ABSTRACT EURO-GANEX is an innovative hydrometallurgical process for the group separation of transuranic actinides from future spent nuclear fuels. A flowsheet test of a process upset (or ‘maloperation’) has been carried out involving the reduction in the concentration of the scrub acid feed to the extract-scrub contactors. The experimental test was completed in two stages. First, the extract-scrub contactors were run under normal flowsheet conditions before initiating the process upset by reducing the scrub acidity from 0.5 to 0.05 mol/L HNO3. At low acidity, a change in the online UV-Vis spectra of the solvent phase indicated the formation of hydrolyzed plutonium species or plutonium colloid formation. Surprisingly, however, this did not lead to the recycle and accumulation of plutonium in the extract-scrub contactors as expected indicating that the EURO-GANEX process is quite robust towards this process upset. Further spectroscopic investigations of the organic-phase species were also performed to characterize the conditions under which the hydrolyzed plutonium species form in the EURO-GANEX solvent as well as separate TODGA and DMDOHEMA phases. The spectroscopic studies supported the view that Pu(IV) hydrolyses at low acidity but the hydrolysis is limited by the organic ligands and is consequently reversible on raising the acidity again. The hydrolysis was also observed in separate TODGA and DMDOHEMA phases.","PeriodicalId":22002,"journal":{"name":"Solvent Extraction and Ion Exchange","volume":"41 1","pages":"88 - 117"},"PeriodicalIF":1.8000,"publicationDate":"2022-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solvent Extraction and Ion Exchange","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/07366299.2022.2136488","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 6
Abstract
ABSTRACT EURO-GANEX is an innovative hydrometallurgical process for the group separation of transuranic actinides from future spent nuclear fuels. A flowsheet test of a process upset (or ‘maloperation’) has been carried out involving the reduction in the concentration of the scrub acid feed to the extract-scrub contactors. The experimental test was completed in two stages. First, the extract-scrub contactors were run under normal flowsheet conditions before initiating the process upset by reducing the scrub acidity from 0.5 to 0.05 mol/L HNO3. At low acidity, a change in the online UV-Vis spectra of the solvent phase indicated the formation of hydrolyzed plutonium species or plutonium colloid formation. Surprisingly, however, this did not lead to the recycle and accumulation of plutonium in the extract-scrub contactors as expected indicating that the EURO-GANEX process is quite robust towards this process upset. Further spectroscopic investigations of the organic-phase species were also performed to characterize the conditions under which the hydrolyzed plutonium species form in the EURO-GANEX solvent as well as separate TODGA and DMDOHEMA phases. The spectroscopic studies supported the view that Pu(IV) hydrolyses at low acidity but the hydrolysis is limited by the organic ligands and is consequently reversible on raising the acidity again. The hydrolysis was also observed in separate TODGA and DMDOHEMA phases.
期刊介绍:
Solvent Extraction and Ion Exchange is an international journal that publishes original research papers, reviews, and notes that address all aspects of solvent extraction, ion exchange, and closely related methods involving, for example, liquid membranes, extraction chromatography, supercritical fluids, ionic liquids, microfluidics, and adsorption. We welcome submissions that look at: The underlying principles in solvent extraction and ion exchange; Solvent extraction and ion exchange process development; New materials or reagents, their syntheses and properties; Computational methods of molecular design and simulation; Advances in equipment, fluid dynamics, and engineering; Interfacial phenomena, kinetics, and coalescence; Spectroscopic and diffraction analysis of structure and dynamics; Host-guest chemistry, ion receptors, and molecular recognition.