scholarly journals New Insights in the Hydrothermal Synthesis of Rare-Earth Carbonates

Materials ◽  
2019 ◽  
Vol 12 (13) ◽  
pp. 2062 ◽  
Author(s):  
Luca Spiridigliozzi ◽  
Claudio Ferone ◽  
Raffaele Cioffi ◽  
Mauro Bortolotti ◽  
Gianfranco Dell’Agli

The rare-earth carbonates represent a class of materials with great research interest owing to their intrinsic properties and because they can be used as template materials for the formation of other rare earth phases, particularly of rare-earth oxides. However, most of the literature is focused on the synthesis and characterization of hydroxycarbonates. Conversely, in the present study we have synthesized both rare-earth carbonates—with the chemical formula RE2(CO3)3·2-3H2O, in which RE represents a generic rare-earth element, and a tengerite-type structure with a peculiar morphology—and rare-earth hydroxycarbonates with the chemical formula RECO3OH, by hydrothermal treatment at low temperature (120 °C), using metal nitrates and ammonium carbonates as raw materials, and without using any additive or template. We found that the nature of the rare-earth used plays a crucial role in relation to the formed phases, as predicted by the contraction law of lanthanides. In particular, the hydrothermal synthesis of rare-earth carbonates with a tengerite-type structure was obtained for the lanthanides from neodymium to erbium. A possible explanation of the different behaviors of lighter and heavier rare-earths is given.

Author(s):  
Luca Spiridigliozzi ◽  
Mauro Bortolotti ◽  
Grazia Accardo ◽  
Alessandro Vergara ◽  
Domenico Frattini ◽  
...  

2017 ◽  
Vol 81 (6) ◽  
pp. 1367-1395 ◽  
Author(s):  
Emma Dowman ◽  
Frances Wall ◽  
Peter J. Treloar ◽  
Andrew H. Rankin

AbstractCarbonatites are enriched in critical raw materials such as the rare-earth elements (REE), niobium, fluorspar and phosphate. A better understanding of their fluid regimes will improve our knowledge of how to target and exploit economic deposits. This study shows that multiple fluid phases penetrated the surrounding fenite aureole during carbonatite emplacement at Chilwa Island, Malawi. The first alkaline fluids formed the main fenite assemblage and later microscopic vein networks contain the minerals of potential economic interest such as pyrochlore in high-grade fenite and rare-earth minerals throughout the aureole. Seventeen samples of fenite rock from the metasomatic aureole around the Chilwa Island carbonatite complex were chosen for study. In addition to the main fenite assemblage of feldspar and aegirine ± arfvedsonite, riebeckite and richterite, the fenite contains micro-mineral assemblages including apatite, ilmenite, rutile, magnetite, zircon, rare-earth minerals and pyrochlore in vein networks. Petrography using a scanning electron microscope in energy-dispersive spectroscopy mode showed that the rare-earth minerals (monazite, bastnäsite and parisite) formed later than the fenite feldspar, aegirine and apatite and provide evidence ofREEmobility into all grades of fenite. Fenite apatite has a distinct negative Eu anomaly (determined by laser ablation inductively coupled plasma mass spectrometry) that is rare in carbonatite-associated rocks and interpreted as related to pre-crystallization of plagioclase and co-crystallization with K-feldspar in the fenite. The fenite minerals have consistently higher midREE/lightREEratios (La/Sm ≈ 1.3 monazite, ≈ 1.9 bastnäsite, ≈ 1.2 parisite) than their counterparts in the carbonatites (La/Sm ≈ 2.5 monazite, ≈ 4.2 bastnäsite, ≈ 3.4 parisite). Quartz in the low- and medium-grade fenite hosts fluid inclusions, typically a few micrometres in diameter, secondary and extremely heterogeneous. Single phase, 2- and 3-phase, single solid and multi solid-bearing examples are present, with 2-phase the most abundant. Calcite, nahcolite, burbankite and baryte were found in the inclusions. Decrepitation of inclusions occurred at ∼200°C before homogenization but melting-temperature data indicate that the inclusions contain relatively pure CO2. A minimum salinity of ∼24 wt.% NaCl equivalent was determined. Among the trace elements in whole-rock analyses, enrichment in Ba, Mo, Nb, Pb, Sr, Th and Y and depletion in Co, Hf and V are common to carbonatite and fenite but enrichment in carbonatitic type elements (Ba, Nb, Sr, Th, YandREE) generally increases towards the inner parts of the aureole. A schematic model contains multiple fluid events, related to first and second boiling of the magma, accompanying intrusion of the carbonatites at Chilwa Island, each contributing to the mineralogy and chemistry of the fenite. The presence of distinct rare-earth mineral microassemblages in fenite at some distance from carbonatite could be developed as an exploration indicator ofREEenrichment.


1979 ◽  
Vol 34 (8) ◽  
pp. 1057-1058 ◽  
Author(s):  
Axel Czybulka ◽  
Günter Steinberg ◽  
Hans-Uwe Schuster

In the systems Li-M-X = (M = Y, Gd; X = Si, Ge) the compounds LiYSi, LiYGe and LiGdGe were prepared. Their crystal structures were determined by X-ray investigations. They crystallize hexagonally (space group P 6̄2m), and a C22-(Fe2P-type) lattice was found


Metals ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 131 ◽  
Author(s):  
Lisa Brückner ◽  
Tobias Elwert ◽  
Thomas Schirmer

Rare earth-bearing gypsum tailings from the fertilizer industry are a potential source for an economically viable and sustainable production of rare earth elements. Large quantities are generated inter alia in Catalão, Brazil, as a by-product in a fertilizer production plant. Hitherto, the gypsum has been used as soil conditioner in agriculture or was dumped. The cooperative project, “Catalão Monazite: Economical exploitation of rare earth elements from monazite-bearing secondary raw materials,” intends to extract rare earth elements from these gypsum tailings. In this paper, a chemical process route to obtain a mixed rare earth carbonate from a monazite concentrate, was investigated. The results of the digestion, leaching, and precipitation experiments are presented and discussed herein. This includes reagent choice, process parameter optimization through experimental design, mineralogical characterization of the feed material and residues, purification of the leach solution, and precipitation of the rare earth as carbonates. The results showed that a rare earth extraction of about 90% without the mobilization of key impurities is possible during a sulfuric acid digestion with two heating stages and subsequent leaching with water. In the following purification step, the remaining impurities were precipitated with ammonium solution and the rare earth elements were successfully recovered as carbonates with a mixture of ammonium solution and ammonium bicarbonate.


2013 ◽  
Vol 68b ◽  
pp. 29-38 ◽  
Author(s):  
Ernst Hinteregger ◽  
Gerhard Böhler ◽  
Thomas S. Hofer ◽  
Hubert Huppertz ◽  

2015 ◽  
Vol 48 ◽  
pp. 256-262 ◽  
Author(s):  
Liurukara D. Sanjeewa ◽  
Kyle Fulle ◽  
Colin D. McMillen ◽  
Fenglin Wang ◽  
Yufei Liu ◽  
...  

2015 ◽  
Vol 4 (4) ◽  
Author(s):  
Guo Lin ◽  
Libo Zhang ◽  
Shaohua Yin ◽  
Jinhui Peng ◽  
Shiwei Li ◽  
...  

AbstractThe heating behavior and effect of experimental parameters like holding time, calcination temperature and microwave power on the weight loss of the mixed rare earth carbonate using microwave heating have been studied, also characterized by X-ray diffraction, thermogravimetry-differential scanning calorimetry, scanning electron microscopy (SEM), particle analysis and Fourier transform infrared (FT-IR). The results show the following: rare earth oxides are obtained at 850°C for holding 1 h; FT-IR analysis indicates that the vibration absorption peak of carbonate disappears after calcination using microwave, confirming the feasibility of microwave calcination for the rare earth carbonates; SEM shows that the rare earth oxides have the characteristics of better and finer particles, have better dispersion and have surface that is more loose and porous than that of products using conventional calcination; particle analysis indicates that average size (D


2011 ◽  
Vol 110-116 ◽  
pp. 1928-1933 ◽  
Author(s):  
Yan Xiang Wang ◽  
Xiao Yan Li ◽  
Jian Sun ◽  
Yao Hui Hu

In the paper, ZnO nanopowders were synthesized by one-step hydrothermal synthesis using zinc acetate and sodium hydroxide as raw materials. The influences of molar concentration of NaOH and synthesis temperature on the properties of ZnO nanopowders were investigated. XRD and FSEM were used to characterize ZnO nanopowders. The results showed that; when the molar concentration of NaOH was 0.05 mol/L, 1mol/L and 2mol/L, ZnO micrometer powders were obtained. When the molar concentration of NaOH was 4mol/L, ZnO nanorods or nanosheets were obtained with different reaction temperature. When the temperature was 220°C, ZnO nanorods with the length of 500nm and diameter of 100nm, were synthesised. Pure ZnO nanopowders can be obtained at lower temperature of 100°C by using one-step hydrothermal synthesis. When the synthesis temperature was 100°C and the molar concentration of NaOH was 4mol/L, ZnO nanosheets were produced. The length, width and thickness of ZnO nanosheets were about 800 nm, 500nm and 80nm, respectively.


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