Please use this identifier to cite or link to this item: http://publications.jrc.ec.europa.eu/repository/handle/JRC120114
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dc.contributor.authorCOLLE JEAN-YVESen_GB
dc.contributor.authorSTOHR SARAHen_GB
dc.contributor.authorCREMER BERTen_GB
dc.contributor.authorVAN WINCKEL STEFAANen_GB
dc.contributor.authorRASMUSSEN GERTen_GB
dc.contributor.authorDIESTE BLANCO OLIVERen_GB
dc.contributor.authorWISS THIERRYen_GB
dc.contributor.authorKONINGS RUDYen_GB
dc.date.accessioned2020-06-11T00:05:38Z-
dc.date.available2020-06-10en_GB
dc.date.available2020-06-11T00:05:38Z-
dc.date.created2020-06-08en_GB
dc.date.issued2020en_GB
dc.date.submitted2020-02-21en_GB
dc.identifier.citationJOURNAL OF AEROSOL SCIENCE vol. 148 p. 105588en_GB
dc.identifier.issn0021-8502 (online)en_GB
dc.identifier.urihttps://publications.jrc.ec.europa.eu/repository/handle/JRC120114-
dc.description.abstractAerosols were produced from a MOX (Mixed Oxide of uranium and plutonium) sample by laser heating up to 4000 K under atmospheric conditions. They were collected with a cascade impactor as function of their aerodynamic size, and studied by SEM, EDS, TEM, EELS, SAED and ICPMS. The uranium and plutonium concentrations were related to the aerosol morphology, size and formation temperature. A clear decrease of the Plutonium concentration was observed as function of the Aerodynamic Equivalent Diameter (AED). Some bigger aerosols enriched in Plutonium were found which originated from solidification of ejected droplets of the liquid phase at the surface of the sample.en_GB
dc.description.sponsorshipJRC.G.I.3-Nuclear Fuel Safetyen_GB
dc.format.mediumOnlineen_GB
dc.languageENGen_GB
dc.publisherELSEVIER SCI LTDen_GB
dc.relation.ispartofseriesJRC120114en_GB
dc.titleUranium-Plutonium partitioning in aerosols produced from (U,Pu)O2 mixed oxide by laser heatingen_GB
dc.typeArticles in periodicals and booksen_GB
dc.identifier.doi10.1016/j.jaerosci.2020.105588 (online)en_GB
JRC Directorate:Nuclear Safety and Security

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