Synergistic Effects In Solvent Extraction Systems Based On Alkylsalicylic Acids Iv Extraction Of The Trivalent Rare Earth Metals In The Presence Of Bifunctional C PDF Download

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Synergistic Effects in Solvent-extraction Systems Based on Alkylsalicylic Acids. IV. Extraction of the Trivalent Rare-earth Metals in the Presence of Bifunctional C

Synergistic Effects in Solvent-extraction Systems Based on Alkylsalicylic Acids. IV. Extraction of the Trivalent Rare-earth Metals in the Presence of Bifunctional C
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Total Pages: 20
Release: 1998
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ISBN:

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Several bifunctional compounds of different types (diamides, diphosphonates and disulphoxides) were synthesized, and their effect on the extraction of the trivalent rare-earth metals from chloride media by solutions of some alkylsalicylic acids (HA) in xylene was investigated. Appreciable synergistic shifts in the individual pH50 values were observed in most cases, the shifts generally increasing in the order S=O


Synergistic Effects in Solvent-extraction Systems Based on Alkylsalicylic Acids. I. Extraction of Trivalent Rare-earth Metals in the Presence of Aliphatic Amides

Synergistic Effects in Solvent-extraction Systems Based on Alkylsalicylic Acids. I. Extraction of Trivalent Rare-earth Metals in the Presence of Aliphatic Amides
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Total Pages: 16
Release: 1995
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ISBN:

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Aliphatic carboxlic acid amides were found to cause synergistic shifts in the pH50 values for the extraction of trivalnet rare-earth metlas form chloride media by solutions of alkylsalicyclic acids in xylene. Fro the different types of amide examined, the synergistic shifts for the extraction of neodymium by 3,5-diisopropylsalicyclic acid (DIPSA) generally decrease in the order : R.CO.NR'2 > R.CO.NHR' > R.CO.NH2, where R and R' alkyl groups. With the N,N-dialkyl amides (R.CO.NR2') and the N-alkyl amides (R.CO.NHR'), the extent of the synergistic effect decreases with increasing chain-branching in either of the alkyl groups R and R'. Fro additions to 0.25 M alkylsalicyclic acid, the syngergistic effect increases with concentrations of up to 0.1 M amide, and decrease with higher concentrations. The extent of the synergistic shift produced by a given amide, as well as the separation in pH50 values form lanthanum to lutetium, increase with increasing steric bulk of the alkylsalicyclic acid used. The separations between adjacent lanthanides are too small to be any practical interest, however. Measurement of the solubility of salicyclic acids (LA) in xylene containing various amounts of N,N-dialkyl amide (L) indicate that essentially complete formation of the HA.L adduct takes place. Treatment of metal-distribution data by slope analysis, and measurement of the solubility of the neodymium-DIPSA complx in xylene in the presence of amide suggest that the mixed-ligand complex has the stiochiometry NdA3L2.


Synergistic Effects in Solvent Extraction Systems Based on Alkylsalicylic Acids. Part 2. Extraction of Nickel, Cobalt, Cadmium and Zinc in the Presence of Some Neutral N-, O- and S-donor Compounds

Synergistic Effects in Solvent Extraction Systems Based on Alkylsalicylic Acids. Part 2. Extraction of Nickel, Cobalt, Cadmium and Zinc in the Presence of Some Neutral N-, O- and S-donor Compounds
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Total Pages: 22
Release: 1996
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ISBN:

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Nine alkyl- and dialkyl-substituted salicyclic acids were prepared and their solvent extraction behaviour towards divalent nickel, cobalt, cadmium and zinc in nitrate media was examined, both in the absence and in the presence of some neutral N-, O- and S-donor compounds (n-octyl 3-pyridinecarboxylate and octanal oxime as N-donors, tri-n-butylphosphine oxide as O-donor, and tri-n-butylphosphine sulphide as S-donor.


Metals Abstracts

Metals Abstracts
Author:
Publisher:
Total Pages: 1042
Release: 1998
Genre: Metallurgy
ISBN:

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Chemical Abstracts

Chemical Abstracts
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Total Pages: 2762
Release:
Genre: Chemistry
ISBN:

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An Investigation of Aggregation in Synergistic Solvent Extraction Systems

An Investigation of Aggregation in Synergistic Solvent Extraction Systems
Author: Andy Steven Jackson
Publisher:
Total Pages: 122
Release: 2017
Genre:
ISBN: 9780355065541

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With an increasing focus on anthropogenic climate change, nuclear reactors present an attractive option for base load power generation with regard to air pollution and carbon emissions, especially when compared with traditional fossil fuel based options. However, used nuclear fuel (UNF) is highly radiotoxic and contains minor actinides (americium and curium) which remain more radiotoxic than natural uranium ore for hundreds of thousands of years, presenting a challenge for long-term storage . Advanced nuclear fuel recycling can reduce this required storage time to thousands of years by removing the highly radiotoxic minor actinides. Many advanced separation schemes have been proposed to achieve this separation but none have been implemented to date. A key feature among many proposed schemes is the use of more than one extraction reagent in a single extraction phase, which can lead to the phenomenon known as "synergism" in which the extraction efficiency for a combination of the reagents is greater than that of the individual extractants alone. This feature is not well understood for many systems and a comprehensive picture of the mechanism behind synergism does not exist. There are several proposed mechanisms for synergism though none have been used to model multiple extraction systems.This work examines several proposed advanced extractant combinations which exhibit synergism: 2-bromodecanoic acid (BDA) with 2,2':6',2"-terpyridine (TERPY), tri-n-butylphosphine oxide (TPBO) with 2-thenoyltrifluoro acetone (HTTA), and dinonylnaphthalene sulfonic acid (HDNNS) with 5,8-diethyl-7-hydroxy-dodecan-6-oxime (LIX). We examine two proposed synergistic mechanisms involving and attempt to verify the ability of these mechanisms to predict the extraction behavior of the chosen systems. These are a reverse micellar catalyzed extraction model and a mixed complex formation model. Neither was able to effectively predict the synergistic behavior of the systems. We further examine these systems for the presence of large reverse micellar aggregates and thermodynamic signatures of aggregation. Behaviors differed widely from system to system, suggesting the possibility of more than one mechanism being responsible for similar observed extraction trends.


Solvent-extraction Processes for the Separation of the Rare-earth Metals

Solvent-extraction Processes for the Separation of the Rare-earth Metals
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Total Pages:
Release: 1990
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ISBN:

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In this paper the application of different classes of solvent-extraction reagents to the recovery and separation of the rare-earth metals is reviewed, and some aspects of the chemistry of these systems are discussed. Solvating extractants such as tri-n-butyl phosphate (TBP) are useful both in the recovery of mixed rare-earth products from nitrate liquors (complexes of the type Ln(NO3)3(TBP)3 being formed in the organic phase) and in the highly selective separation of cerium(IV) from the trivalent lanthanides (when complexes of stoichiometry Ce(NO3)4(TBP)2 or H2Ce(NO3)6(TBP)2 are extracted). Cation-exchange extractants, especially organophosphorus acids such as D2EHPA, are invaluable in the preliminary division of the rare earths into light, middle and heavy fractions, as well as for the subsequent separation of individual metals within these fractions. In some cases, as for the lanthanum-cerium pair, improved separations can be obtained with extractants of the phosphonic and phosphinic acid types. The characteristics of the extraction of the trivalent lanthanides and yttrium by different carboxylic acids can be related to the steric parameter of the substituent alkyl group. For sterically hindered acids such as Versatic 10, complexes of stoichiometry LnA3(HA)3 are extracted, and the pH(0,5) values decrease steadily from lanthanum to lutetium. For non-hindered acids such as 3-cyclohexylpropanoic acid, dimeric complexes such as (LnA3(HA)3)2 are formed, and the pH(0,5) values decrease to a minimum near the middle of the lanthanide series and thereafter increase again. Anion-exchange extractants, particularly quaternary ammonium salts, offer distinct advantages over other reagent types in certain instances, such as the separation of yttrium from the heavy rare-earth fraction in thiocyanate media, and the separation of neodymium from praseodymium in nitrate media. In these systems, complexes of the types (R4N)LnX4 and (R4N)2LnX5 are extracted, where X represents the thiocyanate or nitrate anion. The order of extraction of the individual rare earths is reversed in the nitrate system (La > Ce... > Lu) compared with the thiocyanate system (La


Solvent Extraction

Solvent Extraction
Author: G. M. Ritcey
Publisher:
Total Pages: 386
Release: 1984
Genre: Science
ISBN:

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Advances in Solvent Extraction

Advances in Solvent Extraction
Author: Kevin L. Lyon
Publisher:
Total Pages: 324
Release: 2020
Genre: Rare earth metals
ISBN:

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Rare earth elements have become essential materials in advanced clean energy technologies and national security applications due to their unique properties. Despite their importance, the United States remains almost completely dependent upon foreign supply chains, notably imports from China, for both raw and finished commodities containing rare earth elements. This dissertation explores the implementation of a neutral ligand, N, N, N', N' tetraoctyl diglycolamide (TODGA), for the separation of rare earth elements. TODGA offers distinct advantages over traditional phosphonic acid extractants, notably the elimination of saponification to achieve high recovery in a solvent extraction circuit and improved adjacent lanthanide separation factors, ultimately requiring fewer solvent extraction stages to achieve high degrees of purity and recovery. This work marks the first use of TODGA's unique chemistry to separate and purify the rare earths from each other in hydrochloric acid media using counter-current solvent extraction.Chapter 1 introduces the concept of rare earths as a critical material and highlights historic and future challenges associated with the rare earth supply chain. Separations remains as one of the greatest challenges due to high capital and operating costs to purify individual rare earth elements, thus emphasizing the need for advances in solvent extraction to enable a viable domestic supply chain in the United States. Chapters 2 and 3 provide background context that motivated the research by describing commercial rare earth separation processes and an overview of TODGA's known applications and uses for trivalent lanthanide extraction and separation. While TODGA's lanthanide extraction chemistry has been studied extensively for separations relevant to the nuclear fuel cycle, it has not been successfully applied in the field of rare earth mining and hydrometallurgy to separate individual lanthanides with high degrees of recovery and purity in a continuous counter-current solvent extraction cascade. TODGA exhibits a unique extraction trend among "light" low molecular weight lanthanides, with an observed 50% increase in adjacent light lanthanide separation factors as compared to the industry standard phosphonic acid PC88A. This suggests that a counter-current solvent extraction cascade with a reduced number of stages may be implemented for the purification of light rare earth elements.Chapter 4 outlines the various experimental methods that were utilized to conduct this research. A variety of techniques were utilized in the approach, including laboratory batch equilibrium solvent extraction experiments, counter-current mixer-settler testing, and process modeling and simulation using MATLAB/Simulink.Chapter 5 provides the rationale behind counter-current solvent extraction modeling and simulation for process design. Mass balances around a solvent extraction cascade may be written as a system of ordinary differential equations and coupled with empirical laboratory equilibrium data to model the approach to steady state. Alternative techniques for steady state cascade modeling using algebraic equations written in the form of a tridiagonal matrix and solved using the Thomas Algorithm are discussed. This approach may also be coupled with empirical expressions for calculating distribution ratios as a function of free TODGA and aqueous phase chloride concentration at equilibrium.Chapter 6 describes experimental results that were used to evaluate the feasibility of TODGA's extraction chemistry in a counter-current solvent extraction circuit. While TODGA demonstrates improved light rare earth separation factors, they are still relatively low, implying that neighboring lanthanides essentially co-extract. Commercially, high degrees of purity and recovery are achieved by implementing a selective scrubbing technique through which the purified REE product stream is refluxed into the scrub section. Batch solvent extraction experiments and simplified counter-current solvent extraction experiments in mixer-settlers revealed that TODGA is indeed capable of selective scrubbing to purify REEs under proper solvent loading conditions.Chapter 7 describes the applied culmination of TODGA's extraction chemistry through the design and experimental testing of a solvent extraction process to produce the permanent magnet precursor material didymium (75% neodymium and 25% praseodymium by mass), from a mixed light rare earth chloride feed representative of that produced from the processing of bastnasite ore. The chapter includes single metal extraction data with empirically determined expressions for calculating distribution ratios, followed by batch counter-current extraction experiments for light REE separations. Batch experimental results were used to design a 24-stage counter-current solvent extraction cascade to purify PrNd from a mixture of La, Ce, Pr, and Nd. While experimental results of the cascade design did not achieve optimum recovery or purity, they indicate that TODGA can successfully be used to for the continuous separation and purification of light rare earths. Single metal distribution ratio correlations did not accurately model cascade behavior; a "pseudo single-metal" approach is presented to calculate distribution ratios under saturated loading conditions in a solvent extraction cascade.Chapter 8 discusses the implications of utilizing TODGA in an industrial setting. While the use of a neutral ligand has distinct benefits over phosphonic acids, there are several limitations to the solvent system that require additional research efforts to address. Furthermore, implementing TODGA chemistry has economic impacts that may potentially limit its commercial viability. Notable limitations discussed include organic phase loading capacity, ligand synthesis and production costs, and high molarity salt-bearing raffinate streams that must be recycled or disposed of. A structure/property relationship was identified for DGA extractants with varying alkyl chain substituents, indicating that short alkyl chains make stronger, more selective extractants but are prone to gelling and third phase formation. Longer alkyl chains maintain selectivity and slightly reduce overall extraction strength. Branched alkyl chains prevent gelling and third phase formation but comes at the cost of poor selectivity due to steric hindrance caused by the branched alkyl chains in the outer coordination sphere.Chapter 9 summarizes the general conclusion of this work: TODGA is capable of performing industrially relevant rare earth separations in continuous counter-current solvent extraction equipment, achieving high degrees of REE recovery and purity. However, its practical application is limited at this time due to its low organic phase loading. Ongoing research in collaboration with Oak Ridge National Laboratory is currently underway to synthesize and test novel DGA extractants with tailored alkyl chain substituents that achieve high degrees of organic phase loading capacity, maintain enhanced adjacent lanthanide selectivity among light rare earths, and demonstrate acceptable hydrodynamic behavior suitable for use in solvent extraction equipment.