Rare Earth Element Preconcentration from Various Primary and Secondary Sources by Polymeric Ion Exchange Resins

2021 ◽  
pp. 1-16
Author(s):  
Vladimir Rychkov ◽  
Evgeny Kirillov ◽  
Sergey Kirillov ◽  
Grigory Bunkov ◽  
Maxim Botalov ◽  
...  
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Rare Earth Element ◽  
Earth Element ◽  
Ion Exchange Resins ◽  
Secondary Sources ◽  
Exchange Resins

scholarly journals Terephthalaldehyde–Phenolic Resins as a Solid-Phase Extraction System for the Recovery of Rare-Earth Elements

Polymers ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 311
Author(s):  
Ruth Oye Auke ◽  
Guilhem Arrachart ◽  
Romain Tavernier ◽  
Ghislain David ◽  
Stéphane Pellet-Rostaing
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Solid Phase Extraction ◽  
Rare Earth Elements ◽  
Solid Phase ◽  
Extraction System ◽  
Ion Exchange Resins ◽  
Phase Extraction ◽  
Phenolic Resins ◽  
Exchange Resins

Rare-earth elements (REEs) are involved in most high technology devices and have become critical for many countries. The progress of processes for the extraction and recovery of REEs is therefore essential. Liquid–solid extraction methods are an attractive alternative to the conventional solvent extraction process used for the separation and/or purification of REEs. For this purpose, a solid-phase extraction system was investigated for the extraction and valorization of REEs. Ion-exchange resins were synthesized involving the condensation of terephthalaldehyde with resorcinol under alkaline conditions. The terephthalaldehyde, which is a non-hazardous aromatic dialdehyde, was used as an alternative to formaldehyde that is toxic and traditionally involved to prepare phenolic ion-exchange resins. The resulting formaldehyde-free resole-type phenolic resins were characterized and their ion-exchange capacity was investigated in regard to the extraction of rare-earth elements. We herein present a promising formaldehyde and phenol-free as a potential candidate for solid–liquid extraction REE with a capacity higher than 50 mg/g and the possibility to back-extract the REEs by a striping step using a 2 M HNO3 solution.

scholarly journals Selective Extraction of Rare Earth Elements from Phosphoric Acid by Ion Exchange Resins

Metals ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 682 ◽  
Author(s):  
Xavier Hérès ◽  
Vincent Blet ◽  
Patricia Di Natale ◽  
Abla Ouaattou ◽  
Hamid Mazouz ◽  
...  
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Phosphoric Acid ◽  
Rare Earth Elements ◽  
Moving Boundary ◽  
Cost Effective ◽  
Selective Extraction ◽  
Ion Exchange Resins ◽  
Maximum Sorption Capacity ◽  
Exchange Resins

Rare earth elements (REE) are present at low concentrations (hundreds of ppm) in phosphoric acid solutions produced by the leaching of phosphate ores by sulfuric acid. The strongly acidic and complexing nature of this medium, as well as the presence of metallic impurities (including iron and uranium), require the development of a particularly cost effective process for the selective recovery of REE. Compared to the classical but costly solvent extraction, liquid-solid extraction using commercial chelating ion exchange resins could be an interesting alternative. Among the different resins tested in this paper (Tulsion CH-93, Purolite S940, Amberlite IRC-747, Lewatit TP-260, Lewatit VP OC 1026, Monophos, Diphonix,) the aminophosphonic IRC-747, and aminomethylphosphonic TP-260 are the most promising. Both of them present similar performances in terms of maximum sorption capacity estimated to be 1.8 meq/g dry resin and in adsorption kinetics, which appears to be best explained by a moving boundary model controlled by particle diffusion.

scholarly journals Justification of the prospects of using phosphatotitanium ion exchangers for extracting rare earth metals from solutions of radionuclides

2019 ◽  
Vol 59 (9) ◽  
pp. 58-65
Author(s):  
Vladimir I. Ivanenko ◽  
◽  
Roman I. Korneykov ◽  
Nikita V. Zharov ◽  
◽  
...  
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Rare Earth Element ◽  
Rare Earth Metal ◽  
Earth Element ◽  
Earth Metal ◽  
Metal Cations ◽  
Sorption Properties ◽  
Ion Exchangers ◽  
Hydrated Titanium

The results of a study of the sorption properties of ion-exchange materials based on hydrated titanium (IV) oxohydroxophosphates with respect to rare-earth metal cations are presented in this paper. A high affinity of the latters for the sorption matrix in nitrate media was established, which is determined by the ion radius of the sorbate and increases in the series Y3+  Gd3+  Eu3+ Sm3+ Nd3+ Ce3+ at pH=4 and La3+  Ce3+  Y3+  Yb3+ at pH=1.5 for all the studied sample compositions. It was experimentally shown that the doping of sorbents based on titanium (IV) oxyhydroxophosphates with zirconium (IV) cations, which differs from titanium (IV) in acid-base properties, leads to an increase in the sorption properties of ion exchangers, which allows the use of modified compositions for sorption of rare-earth metal cations from solutions with high acidity. It was established that partial dehydration of the sorption matrix and increase in temperature increase the sorption ability of ion-exchange materials. Sorption extraction of rare-earth element cations by sorbents of various compositions was carried out from solutions simulating real technological objects generated during the processing of nuclear fuel waste. It is shown that sorption materials based on hydrated titanium (IV) oxohydroxophosphates are promising ion exchangers for the extraction of rare-earth element cations from technological solutions with complex chemical composition. It was established that unmodified sorbent compositions are promising for the selective extraction of rare-earth element cations, while modified compositions are of interest for group sorption. The thermal treatment of a sorbent saturated with radioisotopes leads to the formation of crystalline insoluble mineral-like compounds, which ensures reliable immobilization of the sorbed components during long-term storage of the spent product.

scholarly journals EASILY LEACHABLE RARE EARTH ELEMENT PHASES IN THE PARNASSUS-GIONA BAUXITE DEPOSITS, GREECE

2017 ◽  
Vol 50 (4) ◽  
pp. 1952 ◽  
Author(s):  
E. Mouchos ◽  
F. Wall ◽  
B.J. Williamson ◽  
B. Palumbo-Roe
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Rare Earth Elements ◽  
Ammonium Sulphate ◽  
Rare Earth Element ◽  
Earth Element ◽  
Preliminary Results

The Parnassus-Giona karst bauxite deposits contain significant concentrations of rare earth elements (400-500 ppm). Preliminary results from a pilot leaching study show that between 19 and 47% of rare earth elements in the bauxite are easily leachable using ion exchange agents such as ammonium sulphate.

scholarly journals Rare Earth Metals Leaching from Coal Ash and Theirs Concentration

2016 ◽  
Vol 5 (1) ◽  
pp. 48-55
Author(s):  
Сеник ◽  
E. Senik ◽  
Виноградов ◽  
M. Vinogradov ◽  
Таранов ◽  
...  
Keyword(s):  
Rare Earth ◽  
Ion Exchange ◽  
Rare Earth Metals ◽  
Experimental Studies ◽  
Cation Exchange Resin ◽  
Acid Leaching ◽  
Coal Ash ◽  
Flow Diagram ◽  
Ion Exchange Resins ◽  
Exchange Resins

Problems related to rare earth metals leaching from coal ash and theirs ion-exchange concentration from sulfuric solutions, in particular the characteristics of scandium, yttrium and lanthanum sorption by different ion exchange resins have been considered in this work. It has been shown that the best way to leach rare earth metals from coal ash is a complex acid and biological treatment of ash waste. Kinetics related to the process of scandium, yttrium and lanthanum acid leaching from ash and slag waste of CHPP in Kumertau has been investigated. Subsequent metal solutions concentration was achieved using ion exchange resins. The results of experimental studies related to the processes of rare-earth metals (in particularly scandium) ion exchange concentration by cation exchange resin in the Naform PC-100 have been presented, as well as the results of experimental studies related to rare earth metals (scandium including) sedimentation process, using special sedimentators. Dependences of rare earth metals (in particular scandium) sedimentation efficiency against pH value have been constructed, and recommendations for pH values, that are optimal for rare earth metals sedimentation, have been given. Based on obtained experimental results it was created and tested an experimental laboratory prototype of plant for rare earth metals (scandium, yttrium and lanthanum including) extraction from located near Moscow brown coal basin’s slag heaps, and from ash dumps of Russian Federation’s energy enterprises. This plant’s process flow diagram as well as its operation description has been presented. The created plant was tested in modes previously fulfilled in laboratory conditions. At the same time, carried out integrated exploration have showed the prospects for implementation of developed technical solutions for processing of ash dumps of Russian Federation’s various energy enterprises.

Embedding Procedure for Water Swollen Samples

1970 ◽  
Vol 28 ◽  
pp. 504-505
Author(s):  
Ann M. Thomas ◽  
Virginia Shemeley
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Ion Exchange ◽  
Structural Changes ◽  
Cross Linking ◽  
Ion Exchange Resins ◽  
Transmission Electron ◽  
First Pass ◽  
Exchange Resins

Those samples which swell rapidly when exposed to water are, at best, difficult to section for transmission electron microscopy. Some materials literally burst out of the embedding block with the first pass by the knife, and even the most rapid cutting cycle produces sections of limited value. Many ion exchange resins swell in water; some undergo irreversible structural changes when dried. We developed our embedding procedure to handle this type of sample, but it should be applicable to many materials that present similar sectioning difficulties.The purpose of our embedding procedure is to build up a cross-linking network throughout the sample, while it is in a water swollen state. Our procedure was suggested to us by the work of Rosenberg, where he mentioned the formation of a tridimensional structure by the polymerization of the GMA biproduct, triglycol dimethacrylate.

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