Rare earth element mobility in and around carbonatites controlled by sodium, potassium, and silica
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Anenburg, Michael
Mavrogenes, John
Frigo, Corinne
Wall, Frances
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American Association for the Advancement of Science
Abstract
Carbonatites and associated rocks are the main source of rare earth elements (REEs), metals essential to modern
technologies. REE mineralization occurs in hydrothermal assemblages within or near carbonatites, suggesting
aqueous transport of REE. We conducted experiments from 1200°C and 1.5 GPa to 200°C and 0.2 GPa using light
(La) and heavy (Dy) REE, crystallizing fluorapatite intergrown with calcite through dolomite to ankerite. All experiments
contained solutions with anions previously thought to mobilize REE (chloride, fluoride, and carbonate),
but REEs were extensively soluble only when alkalis were present. Dysprosium was more soluble than lanthanum
when alkali complexed. Addition of silica either traps REE in early crystallizing apatite or negates solubility increases
by immobilizing alkalis in silicates. Anionic species such as halogens and carbonates are not sufficient for REE
mobility. Additional complexing with alkalis is required for substantial REE transport in and around carbonatites
as a precursor for economic grade-mineralization.
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Science Advances
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Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC)
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