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dc.contributor.authorConconi, Roberto
dc.contributor.authorGentile, Paolo
dc.contributor.authorFumagalli, Patrizia
dc.contributor.authorNieto García, Fernando 
dc.contributor.authorCapitani, Giancarlo
dc.date.accessioned2025-04-04T08:11:01Z
dc.date.available2025-04-04T08:11:01Z
dc.date.issued2025-07
dc.identifier.citationR. Conconi et al. LITHOS 504-505 (2025) 108033. https://doi.org/10.1016/j.lithos.2025.108033es_ES
dc.identifier.urihttps://hdl.handle.net/10481/103439
dc.descriptionThis study was supported by FAQC (University Competitive Funds) 2022 “Carbon REE-Cycle” and by the Italian Ministry of University and Research (MIUR) through the “Dipartimenti di Eccellenza–2019” grants.es_ES
dc.description.abstractA variety of CaREE-fluorcarbonates with differing morphologies and compositions have been studied: i) synchysite-(Ce) forming hexagonal prisms and rosette-like aggregates; ii) bastnäsite-(Ce) forming blocky aggregates; iii) bastnäsite-(Nd) forming desert rose-like intergrowths and iv) combinations of synchysite-(Ce) and bastnäsite-(Nd) forming more complex micro and nanostructures. These minerals are retained to form from a hydrothermal fluid in a temperature range between 350 and 100 °C. After an investigation spanning from the microscale to the atomic scale, which employed optical stereomicroscopy, scanning and transmission electron microscopy, microanalysis and Raman spectroscopy, a possible scenario for their formation has been depicted. It is assumed that the different CaREE-fluorcarbonates crystallized sequentially under decreasing temperature and fluid fractionation, with synchysite-(Ce) forming first, followed by bastnäsite-(Ce) and finally bastnäsite-(Nd). The different morphologies, in this case, besides being influenced by the dominant REE in the fluid, were also due to varying temperatures and cooling rates. Our study highlights that nature may efficiently fractionate REE from one another, like Y from La, Ce and Nd; Ce from Nd and La. Additionally, Th, a radioactive and toxic element, seems to enter the structure of CaREE-fluorcarbonates during the final stages of crystallization. The understanding of these natural processes may suggest routes for improving current metallurgical separation processes.es_ES
dc.description.sponsorshipFAQC (University Competitive Funds) 2022es_ES
dc.description.sponsorshipItalian Ministry of University and Research (MIUR)es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectBastnäsitees_ES
dc.subjectSynchysitees_ES
dc.subjectNanoparticleses_ES
dc.subjectTransmission electron microscopy es_ES
dc.subjectRaman spectroscopy es_ES
dc.titleCaREE-fluorcarbonates: A variety of morphologies, compositions and nanostructures with insights into REE partitioning and mobilityes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.lithos.2025.108033
dc.type.hasVersionVoRes_ES


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Atribución 4.0 Internacional
Except where otherwise noted, this item's license is described as Atribución 4.0 Internacional