scholarly journals Rare earth element mobility in and around carbonatites controlled by sodium, potassium, and silica

2020 ◽  
Vol 6 (41) ◽  
pp. eabb6570 ◽  
Author(s):  
Michael Anenburg ◽  
John A. Mavrogenes ◽  
Corinne Frigo ◽  
Frances Wall

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.

Minerals ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 698
Author(s):  
Wenxiang Chen ◽  
Feng Zhou ◽  
Hongquan Wang ◽  
Sen Zhou ◽  
Chunjie Yan

The reserve of rare-earth element-bearing phosphorite ores in Guizhou province in western China is huge. Increased demand for the different products manufactured from rare-earth elements has resulted in an extreme need for reasonable and comprehensive extraction of rare-earth elements. An improved understanding of rare-earth element occurrence states in single minerals of ores is important for their further processing. In this paper, rare-earth element contents were analyzed by inductively coupled plasma (ICP), and the occurrence states in single minerals were further investigated through SEM-EDS and focused ion beam-scanning electron microscope (FIB-SEM) methods. The results indicate that rare-earth element contents of apatite are far more than that of dolomite. No independent mineral of rare-earth elements exists for the studied sample. Rare-earth elements are present in the form of ions in the lattices of apatite. Based on the analysis of occurrence states and properties in single minerals, the distribution of rare-earth elements in the flotation process was investigated by reverse flotation technology. It shows that rare-earth elements are mainly concentrated in apatite concentrate. Under the optimized conditions, the P2O5 grade increases from 11.36% in the raw ore to 26.04% in the concentrate, and the recovery is 81.92%, while the total rare-earth oxide grade increases from 0.09% to 0.21% with the recovery of 80.01%, which is similar to P2O5 recovery. This study presents the feasibility of extracting rare-earth elements from rare-earth element-bearing phosphorite ores through the flotation of apatite.


2011 ◽  
Vol 71-78 ◽  
pp. 3737-3740
Author(s):  
Ke Gao Liu ◽  
Jing Li

It is the important way to improve thermoelectric properties of skutterudite materials by doping with rare earth elements. The mechanisms of improving properties of bulk RExCo4Sb12materials prepared by mechanical alloy and spark plasma sintering (MA-SPS) at 650°C were investigated by analyzing the composition, microstructure and atomic occupying locations. According the results it can be considered that the mechanism to improve the thermoelectric properties of rare earth elements is that rare earth element Ce in the samples mainly plays the doping role in reducing the resistivity of the sample and improving the conductivity, so that it makes the figure of merit ZT of samples increase significantly.


2016 ◽  
Vol 80 (1) ◽  
pp. 77-102 ◽  
Author(s):  
Kenzo Sanematsu ◽  
Terumi Ejima ◽  
Yoshiaki Kon ◽  
Takayuki Manaka ◽  
Khin Zaw ◽  
...  

AbstractGeochemical characteristics and rare-earth element (REE)-bearing minerals of calc-alkaline granites in southern Myanmar were investigated to identify the minerals controlling fractionation between light and heavyREE(LREE and HREE) during magmatic differentiation and weathering. The granites were classified on the basis of the mineral assemblages into two contrasting groups: allanite-(Ce)- and/or titanite-bearing granites; and more HREE-enriched granites characterized by hydrothermal minerals including synchysite(Y), parisite-(Ce), bastnäsite-(Ce), xenotime-(Y), monazite-(Ce), Y-Ca silicate, waimirite-(Y) and fluorite. This suggests that allanite-(Ce) and titanite are not stable in differentiated magma and HREE are eventually preferentially incorporated into the hydrothermal minerals. The occurrence of theREE-bearing minerals is constrained by the degree of magmatic differentiation and the boundary of two contrasting granite groups is indicated by SiO2contents of ∼74 wt.% or Rb/Sr ratios of ∼3–8. Fractionation between LREE and HREE during weathering of the granites is influenced by weathering resistance of theREE-bearing minerals, i.e. allanite-(Ce), titanite, theREEfluorocarbonates and waimirite-(Y) are probably more susceptible to weathering, whereas zircon, monazite-(Ce) and xenotime-(Y) are resistant to weathering. Ion-exchangeableREEin weathered granites tend to be depleted in HREE relative to the whole-rock compositions, suggesting that HREE are more strongly adsorbed on weathering products or that HREE remain in residual minerals.


Nature ◽  
1979 ◽  
Vol 282 (5736) ◽  
pp. 247-250 ◽  
Author(s):  
Scott M. McLennan ◽  
S. R. Taylor

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