Fractionation of rare-earth elements during magmatic differentiation and weathering of calc-alkaline granites in southern Myanmar

2016 ◽  
Vol 80 (1) ◽  
pp. 77-102 ◽  
Author(s):  
Kenzo Sanematsu ◽  
Terumi Ejima ◽  
Yoshiaki Kon ◽  
Takayuki Manaka ◽  
Khin Zaw ◽  
...  
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Rare Earth Element ◽  
Earth Element ◽  
Geochemical Characteristics ◽  
Magmatic Differentiation ◽  
Calc Alkaline ◽  
Mineral Assemblages ◽  
Weathering Resistance

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.

scholarly journals Petrogenesis of Heavy Rare Earth Element Enriched Rhyolite: Source and Magmatic Evolution of the Round Top Laccolith, Trans-Pecos, Texas

Minerals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 423 ◽  
Author(s):  
Brent Elliott
Keyword(s):  
Rare Earth ◽  
Rare Earth Element ◽  
Earth Element ◽  
Geochemical Evolution ◽  
Magmatic Differentiation ◽  
Magmatic System ◽  
Heavy Rare Earth ◽  
Heavy Rare Earth Element ◽  
Element Concentrations ◽  
Stage Crystallization

The Round Top rhyolite located in Trans-Pecos Texas is enriched in Be, F, Li, Nb, Rb, Sn, Th, U, Y, Zr, and rare earth elements (REEs). REE-bearing minerals are mainly ubiquitous nano-scale accessory phases throughout the groundmass, incorporated in synchysite-group minerals, xenotime-(Y), Y- and Ce-rich fluorite, and zircon. The rhyolite is peraluminous, high-silica, alkaline (not peralkaline), with elevated heavy rare earth element concentrations and anonymously negative Eu values. Pervasive spongy groundmass and recrystallization textures are consistent with the elevated and remobilized Zr, Th, and Y + HREE (heavy rare earth element) concentrations and a high field strength element (HFSE) soluble, sub-alkalic, F-rich, magmatic system. REE-bearing minerals are present as late-magmatic, interstitial phases and attributed with closed-system, post-magmatic, hydrothermal alteration. Petrogenetic modeling provides scenarios that explain the geochemical evolution and REE complexing behavior in evolved rhyolite magmas, and determines possible source compositions and evolution. Trace element models suggest a system typical of having extensive magmatic differentiation. The resulting rhyolite magma is indicative of a silica-rich magmatic system enriched in H2O, Li, and/or F that could be considered transitional between pure silicate melt and hydrothermal fluid, where fluorine-ligand complexing was prevalent through late magmatic cooling and crystallization processes. Thorough differentiation and high fluorine activity contributed to the late stage crystallization of REE-bearing minerals in the Round Top rhyolite.

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
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Rare Earth Element ◽  
Earth Element ◽  
Element Mobility ◽  
Sodium Potassium ◽  
Ree Mineralization ◽  
Anionic Species ◽  
Ree Mobility ◽  
Modern Technologies

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.

scholarly journals The Occurrence States of Rare Earth Elements Bearing Phosphorite Ores and Rare Earth Enrichment Through the Selective Reverse Flotation

Minerals ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 698
Author(s):  
Wenxiang Chen ◽  
Feng Zhou ◽  
Hongquan Wang ◽  
Sen Zhou ◽  
Chunjie Yan
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Rare Earth Element ◽  
Earth Element ◽  
Ion Beam ◽  
Western China ◽  
Reverse Flotation ◽  
Flotation Process ◽  
Element Bearing ◽  
Element Contents

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.

Study on Mechanisms of Rare Earth Elements on Improving Thermoelectric Properties of RExCo4Sb12

2011 ◽  
Vol 71-78 ◽  
pp. 3737-3740
Author(s):  
Ke Gao Liu ◽  
Jing Li
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Mechanical Alloy ◽  
Spark Plasma Sintering ◽  
Thermoelectric Properties ◽  
Rare Earth Element ◽  
Figure Of Merit ◽  
Earth Element ◽  
Plasma Sintering ◽  
Spark Plasma

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.

Eocene Challis-Kamloops volcanism in central British Columbia: an example from the Buck Creek basin

1998 ◽  
Vol 35 (8) ◽  
pp. 951-963 ◽  
Author(s):  
J Dostal ◽  
D A Robichaud ◽  
B N Church ◽  
P H Reynolds
Keyword(s):  
British Columbia ◽  
Rare Earth ◽  
Rare Earth Element ◽  
Fractional Crystallization ◽  
Earth Element ◽  
Volcanic Rocks ◽  
Volcanic Belt ◽  
The United States ◽  
Calc Alkaline ◽  
Heavy Rare Earth Element

Eocene volcanic rocks of the Buck Creek basin in central British Columbia are part of the Challis-Kamloops volcanic belt extending from the United States across British Columbia to central Yukon. The volcanic rocks include two units, the Buck Creek Formation, composed of high-K calc-alkaline rocks with predominant andesitic composition, and the overlying Swans Lake unit made up of intraplate tholeiitic basalts. Whole rock 40Ar/39Ar data for both units show that they were emplaced at 50 Ma. They have similar mantle-normalized trace element patterns characterized by a large-ion lithophile element enrichment and Nb-Ta depletion, similar chondrite-normalized rare earth element patterns with (La/Yb)n ~4-14 and heavy rare earth element fractionation, and overlapping epsilonNd values (2.4-3.1) and initial Sr-isotope ratios ( ~ 0.704). These features suggest derivation of these two units from a similar mantle source, probably garnet-bearing subcontinental lithosphere. The differences between tholeiitic and calc-alkaline suites can be due, in part, to differences in the depth of fractional crystallization and the crystallizing mineral assemblage. Fractional crystallization of the calc-alkaline magmas began at a greater (mid-crustal) depth and included fractionation of Fe-Ti oxides. The volcanic rocks are probably related to subduction of the Farallon plate under the North American continent in a regime characterized by transcurrent movements and strike-slip faulting.

Study on Recovery of Rare Earth Elements from NdFeB Magnet Scrap by Using Selective Leaching

2020 ◽  
Vol 1009 ◽  
pp. 149-154
Author(s):  
Tanongsak Yingnakorn ◽  
Piamsak Laokhen ◽  
Loeslakkhana Sriklang ◽  
Tapany Patcharawit ◽  
Sakhob Khumkoa
Keyword(s):  
Rare Earth ◽  
Rare Earth Elements ◽  
Rare Earth Element ◽  
Earth Element ◽  
Rare Earth Metals ◽  
Hard Disk Drives ◽  
Selective Leaching ◽  
High Concentration ◽  
Neodymium Magnets ◽  
The Rare Earth

High power neodymium magnets have been used extensively, such as components of hard disk drives, electric vehicles, and maglev trains. This type of magnet contains of high concentration of rare earth elements. After the device is out of service, the magnet will be removed and the rare earth element contained in the magnet will be extracted in order to reuse for any purposes. Recently, the study on extraction of rare earth elements (REE) from neodymium magnets is increased. However, there was only few research regarding to the extraction of rare earth metals by using a water leaching method. In this study, rare-earth elements were extracted from neodymium magnet scrap by using selective leaching technique. Initially, magnets were leached with 2 M of sulfuric acid for 24 hrs. Then, the leached solution was heated at 110°C in order to remove water and the green powder was remained. The green powder was further roasted in a muffle furnace at various temperatures from 750°C to 900°C for 2 hrs. and subsequently leached by water. Finally, the iron oxide residue was separated from rare earth element solution by filtration. Based on this experiment, it was found that the purity of the rare earth metals can be achieved up to 99.4%.

Geochemical evolution in the Blake River Group, Abitibi Greenstone Belt, Superior Province

1980 ◽  
Vol 17 (9) ◽  
pp. 1292-1299 ◽  
Author(s):  
I. E. M. Smith
Keyword(s):  
Rare Earth ◽  
Volcanic Rock ◽  
Rare Earth Element ◽  
Greenstone Belt ◽  
Earth Element ◽  
Superior Province ◽  
Calc Alkaline ◽  
Abitibi Greenstone Belt ◽  
Rock Types ◽  
Element Fractionation

In well exposed, well developed greenstone belts of the Superior Province there is a clear progression from stratigraphically lower, geochemically primitive volcanic rock types (komatiites, tholeiites) to overlying geochemically evolved calc-alkaline volcanic rock types. In the western Blake River Group of the Abitibi Greenstone Belt the change from tholeiitic to calc-alkaline volcanics represents a geochemical discontinuity defined by an increase in incompatible elements and light/heavy rare-earth element fractionation in the overlying rocks. Quantitative modelling of the parameters of the discontinuity indicates that it can be explained by a change to very small amounts of melting of unmodified mantle lherzolite, although this is not a unique solution. In calc-alkaline suites showing high degrees of rare-earth element fractionation the calculated melt fraction required of unmodified mantle becomes unrealistically low and models involving a geochemically evolved source may have to be considered.

Quantitative trace-element modelling of the crystallization history of the Kinojévis and Blake River groups, Abitibi Greenstone Belt, Ontario

1989 ◽  
Vol 26 (7) ◽  
pp. 1356-1367 ◽  
Author(s):  
A. D. Fowler ◽  
L. S. Jensen
Keyword(s):  
Rare Earth ◽  
Rare Earth Element ◽  
Fractional Crystallization ◽  
Earth Element ◽  
Calc Alkaline ◽  
Quantitative Modelling ◽  
Ti Oxides ◽  
History Of ◽  
High Level ◽  
Ree Patterns

The Archean tholeiitic Kinojévis suite is characterized by an iron-enrichment trend and abundant Fe–Ti oxides in its evolved basalts, andesites, and rhyolites. The rare-earth-element (REE) patterns of the suite remain flat from the basalts through to the rhyolites, with the development of small, negative Eu anomalies. Quantitative modelling of the trace elements from little-altered samples is consistent with the mineralogy, suggesting that the suite was produced through fractional crystallization of olivine, pyroxene, plagioclase, and Fe–Ti oxides. The evolved rhyolites are interpreted as having developed by greater than 90% fractional crystallization in a high-level magma chamber.The calc-alkaline Blake River Group conformably overlies the Kinojévis rocks and is characterized by enrichment in alkalis and silica. The REE patterns are light rare-earth-element (LREE) enriched, and the felsic rocks have prominent negative Eu anomalies. Geochemical modelling shows that the suite could have developed either through fractional crystallization dominated by plagioclase and clinopyroxene or by assimilation of tonalite, coupled with fractional crystallization.

Sign in / Sign up

Export Citation Format

Share Document