Magnetoelastic effects in rare‐earth iron‐aluminum compounds

1993 ◽  
Vol 73 (10) ◽  
pp. 6171-6173 ◽  
Author(s):  
K. Prajapati ◽  
A. G. Jenner ◽  
M. P. Schulze ◽  
R. D. Greenough
Keyword(s):  
Rare Earth ◽  
Iron Aluminum ◽  
Aluminum Compounds

Fluoride processing of oil hydrocarbon cracking catalyst with REE concentrate extraction

2021 ◽  
Vol 1 (1) ◽  
pp. 28-35
Author(s):  
A. O. Puzhel ◽  
V. A. Borisov ◽  
A. R. Osipov ◽  
I. V. Petlin ◽  
A. D. Kiselev ◽  
...  
Keyword(s):  
Rare Earth ◽  
Ir Spectroscopy ◽  
Phase Analysis ◽  
Second Order ◽  
Order Model ◽  
X Ray ◽  
Before And After ◽  
Aluminum Compounds ◽  
Oil Cracking ◽  
Second Order Model

It is proposed to use a spent cracking catalyst of petroleum hydrocarbons containing 1 wt.% of rare earth element (REE) oxides as an alternative REE feed source. The study covers the process of removing silicon in the form of ammonium hexafluorosilicate (NH4)2SiF6 by sintering an oil cracking catalyst sample with NH4F and subsequent (NH4)2SiF6 sublimation to produce an aluminum-containing concentrate of rare earth elements. The orthogonal central compositional planning of the experiment was used to study the effect of three factors: sublimation temperature (350 to 400 °С), duration (40 to 80 min), and weight of the catalyst fluorinated sintered mass (5 to 10 g) on the (NH4)2SiF6 sublimation completeness. Results obtained in the experiment were used to build a second-order model, which correlate with experimental data. The dynamics of (NH4)2SiF6 sublimation removal was determined for sublimation durations of τ = 10, 20, 40 and 80 min at processing temperatures of 350, 375 and 400 °C. The (NH4)2SiF6 removal degree values calculated based on the second-order model for τ = 44, 48, 52, 56, 60, 64, 68, 72, and 76 min fit well the experimental curves. Spectra of fluorinated catalyst samples before and after sublimation were studied using X-ray phase analysis and IR spectroscopy. The data of IR spectroscopy and X-ray phase analysis are in good agreement and show that (NH4)2SiF6, (NH4)3AlF6 and unreacted NH4F are present in the catalyst with NH4F sintered mass, and only aluminum compounds are detected – NH4AlF4 and AlF3 after sublimation. These data indicate the completeness of the sublimation removal of silicon from the catalyst and NH4F sintered mass with NH4AlF4 and AlF3 aluminum compounds only observed after sublimation. REE concentration is 15 % due to silicon removal.

Processes for the Treatment of NORM and TENORM

2003 ◽  
Author(s):  
Andreas Vesely
Keyword(s):  
Rare Earth ◽  
Sodium Hydroxide ◽  
Sodium Hydroxide Solution ◽  
Selective Dissolution ◽  
Electrochemical Process ◽  
Electrolysis Cell ◽  
Molybdenum Oxides ◽  
Radioactive Elements ◽  
Rare Earth Compound ◽  
Aluminum Compounds

By contract with the Austrian government, the ARC is treating radioactive waste from research institutions and industries. In the last years, one focus was the development of processes for the treatment of NORM and TENORM. Our goal in developing such processes is to recycle valuable compounds for further industrial usage and to concentrate the radioactive elements as far as possible, to save space in the waste storage facilities. Austria is an important producer of tungsten-thoria- and tungsten-molybdenum-thoria-cermets. Scrap is generated during the production process in the form of turnings and grinding sludge and dust. Although big efforts have been undertaken to replace Thorium compounds, waste streams from past production processes are still waiting for treatment. The total amount of this waste stored in Austria may be estimated to be approx. 100 tons. In close co-operation with the tungsten industries, recycling processes were tested and further developed at ARC in laboratory, bench scale and pilot plants. Three different approaches to solve the problem were studied: Dissolution of tungsten in molten iron in an arc or induction furnace, thus producing an Fe-W or Fe-W-Mo alloy. Slag is produced upon the addition of lime and clay. This slag extracts nearly all of the Thorium contained in the metal melt. Selective dissolution of Tungsten in aqueous alkaline medium after oxidation of the metal to the hexavalent state by heating the scrap in air at temperatures of 500°C to 600°C. The resulting oxides are treated with sodium hydroxide solution. Tungsten and Molybdenum oxides are readily dissolved, while Thorium oxide together with silicon and aluminum compounds remain insoluble and are separated by filtration. Sodium tungstate solution is further processed by the usual hydrometallurgical tungsten mill process. Oxidation and dissolution of Tungsten can be achieved in one step by an electrochemical process. Thus, thoriated Tungsten scrap is used as an anode in an electrolysis cell, while sodium hydroxide or ammonia serve as electrolyte. After dissolution of Tungsten, the solids are separated from the liquid by filtration. With the electrochemical process, treatment of Tungsten-Thoria scrap can be achieved with high throughput in rather small reactors at moderate temperatures and ordinary pressure. The Tungsten solution exhibits high purity. Another process which we examined in detail is the separation of radium from rare earth compounds. Radium was separated by co-precipitation with barium sulfate from rare earth chloride solutions. The efficiency of the separation is strongly pH-dependent. Again, the valuable rare earth compound can be reused, and the radioactive elements are concentrated.

Complex Rare Earth Minerals Sulfate Decomposition Techniques Investigation

2019 ◽  
Vol 946 ◽  
pp. 580-584
Author(s):  
K.D. Naumov ◽  
K.A. Karimov ◽  
A.M. Klyushnikov
Keyword(s):  
Rare Earth ◽  
Sulfuric Acid ◽  
Atmospheric Pressure ◽  
Pressure Leaching ◽  
Decomposition Techniques ◽  
The Third ◽  
Iron Aluminum ◽  
Rare Earth Minerals ◽  
Concentrated Sulfuric Acid ◽  
Major Factors

This article presents a study of Tomtor rare earth ore decomposition. This material contains a lot of valuable components such as REE and niobium (mas., %: 12,8 ΣREO (rare earth oxides), 0.039 Sc, 18.4 P2O5, 9.9 Fe, 9.0 Al, 0.24 ThO2, 8.2 Nb2O5). The study aims to find efficient ways of processing this deposit. Technologies using the sulfuric acid as the main reagent to leach are described in this article. Investigation has three trends. The first trend is agitation leaching at low sulfuric acid concentrations, temperatures up to 95 °C and atmospheric pressure. The second trend is pressure leaching at low sulfuric acid concentrations, high temperatures (up to 180 °C) and high pressure. The third trend is high temperature sulfatization with concentrated sulfuric acid at elevated temperature (up to 180 °C) and atmospheric pressure followed by aqueous leaching. The dependence of target components (rare earth elements, scandium, phosphorus) and the impurity (iron, aluminum, thorium) extractions into solution from major factors was studied.

Recycling Red Mud of JSC Ural Aluminum Plant with the Recovery of Iron and Construction Materials

2017 ◽  
Vol 743 ◽  
pp. 331-337 ◽  
Author(s):  
Dmitry Zinoveev ◽  
Pavel Grudinsky ◽  
Vladimir Korneev ◽  
Valery Dyubanov ◽  
Mark Zheleznyi
Keyword(s):  
Rare Earth ◽  
Construction Industry ◽  
Red Mud ◽  
Rare Earth Metals ◽  
Construction Materials ◽  
Pig Iron ◽  
Iron Aluminum ◽  
Landfill Sites ◽  
Reduction Smelting ◽  
Alumina Industry

Red mud is a by-product of alumina industry which is currently almost completely stored in landfill sites without further use. It contains considerable amounts of valuable components such as iron, aluminum, titanium and rare-earth metals. The reduction smelting of red mud was carried out in laboratory scale to recover iron and obtain slag suitable for use in the construction industry. It has been shown that it is expedient to obtain pig iron and slag from the unprocessed red mud. Those two are suitable for the subsequent leaching of aluminum, titanium and rare-earth metals. It is practical to process dealkalized red mud, with composition adjustment by CaO and Al2O3 addition, in order to obtain pig iron and slag in the form of aluminous clinker.

Characterization of Rare-Earth Fluoride Anti-Stokes Phosphors by Scanning arid Transmission Electron Microscopy

1971 ◽  
Vol 29 ◽  
pp. 142-143
Author(s):  
N. M. P. Low ◽  
L. E. Brosselard
Keyword(s):  
Electron Microscopy ◽  
Rare Earth ◽  
Elevated Temperatures ◽  
Stoichiometric Composition ◽  
Rare Earth Ions ◽  
Crystalline Solid ◽  
Precipitation Process ◽  
Rare Earth Fluoride ◽  
Earth Fluoride ◽  
Rare Earth Fluorides

There has been considerable interest over the past several years in materials capable of converting infrared radiation to visible light by means of sequential excitation in two or more steps. Several rare-earth trifluorides (LaF3, YF3, GdF3, and LuF3) containing a small amount of other trivalent rare-earth ions (Yb3+ and Er3+, or Ho3+, or Tm3+) have been found to exhibit such phenomenon. The methods of preparation of these rare-earth fluorides in the crystalline solid form generally involve a co-precipitation process and a subsequent solid state reaction at elevated temperatures. This investigation was undertaken to examine the morphological features of both the precipitated and the thermally treated fluoride powders by both transmission and scanning electron microscopy.Rare-earth oxides of stoichiometric composition were dissolved in nitric acid and the mixed rare-earth fluoride was then coprecipitated out as fine granules by the addition of excess hydrofluoric acid. The precipitated rare-earth fluorides were washed with water, separated from the aqueous solution, and oven-dried.

Study of segregation in La1.8Sr0.2CuO4 superconductor by STEM-EDS microanalysis

1987 ◽  
Vol 45 ◽  
pp. 54-55
Author(s):  
T. F. Kelly ◽  
P. J. Lee ◽  
E. E. Hellstrom ◽  
D. C. Larbalestier
Keyword(s):  
Rare Earth ◽  
High Field ◽  
Transport Current ◽  
Total Thickness ◽  
New Class ◽  
Ceramic Superconductors ◽  
Current Densities ◽  
Group Ii ◽  
Eds Microanalysis

Recently there has been much excitement over a new class of high Tc (>30 K) ceramic superconductors of the form A1-xBxCuO4-x, where A is a rare earth and B is from Group II. Unfortunately these materials have only been able to support small transport current densities 1-10 A/cm2. It is very desirable to increase these values by 2 to 3 orders of magnitude for useful high field applications. The reason for these small transport currents is as yet unknown. Evidence has, however, been presented for superconducting clusters on a 50-100 nm scale and on a 1-3 μm scale. We therefore planned a detailed TEM and STEM microanalysis study in order to see whether any evidence for the clusters could be seen.A La1.8Sr0.2Cu04 pellet was cut into 1 mm thick slices from which 3 mm discs were cut. The discs were subsequently mechanically ground to 100 μm total thickness and dimpled to 20 μm thickness at the center.

Microstructural characterization of a cast RENi5-based alloy

1993 ◽  
Vol 51 ◽  
pp. 1176-1177
Author(s):  
G. M. Micha ◽  
L. Zhang
Keyword(s):  
Electron Microscopy ◽  
Rare Earth ◽  
Microstructural Characterization ◽  
Binary Compound ◽  
Nickel Metal ◽  
Cast Material ◽  
Nickel Metal Hydride ◽  
Transmission Electron ◽  
Cast Condition

RENi5 (RE: rare earth) based alloys have been extensively evaluated for use as an electrode material for nickel-metal hydride batteries. A variety of alloys have been developed from the prototype intermetallic compound LaNi5. The use of mischmetal as a source of rare earth combined with transition metal and Al substitutions for Ni has caused the evolution of the alloy from a binary compound to one containing eight or more elements. This study evaluated the microstructural features of a complex commercial RENi5 based alloy using scanning and transmission electron microscopy.The alloy was evaluated in the as-cast condition. Its chemistry in at. pct. determined by bulk techniques was 12.1 La, 3.2 Ce, 1.5 Pr, 4.9 Nd, 50.2 Ni, 10.4 Co, 5.3 Mn and 2.0 Al. The as-cast material was of low strength, very brittle and contained a multitude of internal cracks. TEM foils could only be prepared by first embedding pieces of the alloy in epoxy.

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