Browse
Submit Data
Databases
API
Help

Dataset Information

32 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Antagonistic Role of Aqueous Complexation in the Solvent Extraction and Separation of Rare Earth Ions.

ABSTRACT: Solvent extraction is used widely for chemical separations and environmental remediation. Although the kinetics and efficiency of this process rely upon the formation of ion-extractant complexes, it has proven challenging to identify the location of ion-extractant complexation within the solution and its impact on the separation. Here, we use tensiometry and X-ray scattering to characterize the surface of aqueous solutions of lanthanide chlorides and the water-soluble extractant bis(2-ethylhexyl) phosphoric acid (HDEHP), in the absence of a coexisting organic solvent. These studies restrict ion-extractant interactions to the aqueous phase and its liquid-vapor interface, allowing us to explore the consequences that one or the other is the location of ion-extractant complexation. Unexpectedly, we find that light lanthanides preferentially occupy the liquid-vapor interface. This contradicts our expectation that heavy lanthanides should have a higher interfacial density since they are preferentially extracted by HDEHP in solvent extraction processes. These results reveal the antagonistic role played by ion-extractant complexation within the aqueous phase and clarify the advantages of complexation at the interface. Extractants in common use are often soluble in water, in addition to their organic phase solubility, and similar effects to those described here are expected to be relevant to a variety of separations processes.

SUBMITTER: Sun P

PROVIDER: S-EPMC8614105 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

New Sustainable Solvent Extraction Pathways for Rare Earth Metals via Oximes Molecules

Project description: Not available

| S-EPMC10673299 | biostudies-literature

Advancing Rare-Earth Separation by Machine Learning.

Project description:Constituting the bulk of rare-earth elements, lanthanides need to be separated to fully realize their potential as critical materials in many important technologies. The discovery of new ligands for improving rare-earth separations by solvent extraction, the most practical rare-earth separation process, is still largely based on trial and error, a low-throughput and inefficient approach. A predictive model that allows high-throughput screening of ligands is needed to identify suitable ligands to achieve enhanced separation performance. Here, we show that deep neural networks, trained on the available experimental data, can be used to predict accurate distribution coefficients for solvent extraction of lanthanide ions, thereby opening the door to high-throughput screening of ligands for rare-earth separations. One innovative approach that we employed is a combined representation of ligands with both molecular physicochemical descriptors and atomic extended-connectivity fingerprints, which greatly boosts the accuracy of the trained model. More importantly, we synthesized four new ligands and found that the predicted distribution coefficients from our trained machine-learning model match well with the measured values. Therefore, our machine-learning approach paves the way for accelerating the discovery of new ligands for rare-earth separations.

| S-EPMC9241157 | biostudies-literature

Extraction of rare earth elements from aqueous solutions using the ionic liquid trihexyltetradecylphosphonium 3-hydroxy-2-naphthoate.

Project description:The task-specific ionic liquid trihexyltetradecylphosphonium 3-hydroxy-2-naphthoate has been described as a suitable extraction agent for numerous metals from aqueous phases, while additionally providing reduced leaching into the used matrices. Here, we investigate the extraction properties of this extractant towards rare earth elements. Of these, La, Ce, Nd, Ho und Lu were chosen as a representative mix of light and heavy elements. Single- as well as double-element extractions were carried out under varying conditions regarding pH, temperature and extraction time. The highest extraction efficacies and minimalized precipitation of the respective metals were recorded at a pH of 2.5. Satisfactory extraction efficacies (>80%) were achieved already after 6 hours for the elements Ce, Nd and Lu in single-element extraction experiments at room temperature. Increased temperatures improved the extraction efficacy for Nd from 36% at 20 °C to 80% at 30 °C after only 2 hours. Surprisingly, this effect was not observed for Ce in single-element experiments. In double-element feed solutions containing both Ce and Nd, however, the time-dependant extraction efficacy of Ce mirrored that of Nd. The pH in the aqueous extraction matrix changed during the extraction, showing a positive correlation with the extraction efficacy and revealing the extraction mechanism to be via anion exchange. The leaching was in good agreement with literature values, showed a positive correlation with extraction efficacies, and ranged for all extractions between 0.8 and 1.2%. Remarkably, increasing the temperature from 20 °C to 30 °C had no significant influence on leaching.

| S-EPMC10440728 | biostudies-literature

Rare earth elements show antagonistic interactions as revealed by transcriptome profiling in Chlamydomonas reinhardtii.

Project description:Purpose; Here we compare the transcriptomic effects of three REEs; Ce, Tm and Y, and a mixture of all three on Chlamydomonas reinhardtii in order to determine the degree of overlap of their effects. Methods; Transcriptome profiling (RNA-Seq) analysis performed on Chlamydomonas reinhardtii (wild-type strain, CC-125 aka 137c, Chlamydomonas resource center) exposed for 2 h to one of three soluble REEs (Ce, Tm, Y) salts at 0.5 μM or to an equimolar ternary mixture of these REEs. Illumina HiSeq (v.4) was used for the paired-end sequencing (2 × 100 base pairs) of 25 samples (5 replicates for each treatment: Ce; Tm; Y; Mix; Controls). For each sample, ca. 55 million of reads with their sequences, identification and quality scores were stored in two FastQ files. Results; Known functions of the differentially expressed genes support effects of REEs on protein processing in the endoplasmic reticulum, phosphate transport and the homeostasis of Fe and Ca. The only stress response detected related to protein misfolding in the endoplasmic reticulum. When the REEs were applied as a mixture, antagonistic effects were overwhelmingly observed with transcriptomic results suggesting that the REEs were initially competing with each other for bio-uptake. Conclusions; Our study represents the first detailed analysis of REE transcriptomic effects in a green microalga that is ubiquitous to fresh waters. Results generated by RNA-seq technology suggest that the approach of government agencies to regulate the REEs using biological effects data from single metal exposures may be a largely conservative approach.

2021-06-14 | GSE176268 | GEO

Application of a functionalized ionic liquid extractant tributylmethylammonium dibutyldiglycolamate ([A336][BDGA]) in light rare earth extraction and separation.

Project description:A type of functionalized ionic liquid extractant, tributylmethylammonium dibutyldiglycolamate ([A336][BDGA]), was synthesized, and its extraction ability of light rare earth elements, namely, La(III), Ce(III), Pr(III) and Nd(III), wascompared with that of other functionalized ionic liquid extractants, including tributylmethylammonium dioctyldiglycolamate and diglycolic amide extractants N,N,N,N-tetrabutyl-3-oxapentane-diamide (TBDGA) and N,N,N,N-tetraoctyl-3-oxapentane-diamide (TODGA). The study of extraction behavior indicated that the ionic liquids exhibited better extraction properties than the amides under lower acidity conditions. The effects of the pH and concentration of the extractant on the extraction behavior of [A336][BDGA] on light rare earths were determined. A separation strategy of mixed light rare earths was investigated by means of extraction chromatography using [A336][BDGA] as the stationary phase. As a result, nearly pure La(III), Ce(III), Pr(III) and Nd(III) were obtained, respectively. A new strategy of separating mixed light rare earths was established by means of extraction chromatography. The stationary phase of [A336][BDGA] was used in this strategy. The four rare earths elements, La(III), Ce(III), Pr(III) and Nd(III), achieved baseline separation.

| S-EPMC6107113 | biostudies-literature

Carbonate complexation enhances hydrothermal transport of rare earth elements in alkaline fluids.

Project description:Rare earth elements (REE), essential metals for the transition to a zero-emission economy, are mostly extracted from REE-fluorcarbonate minerals in deposits associated with carbonatitic and/or peralkaline magmatism. While the role of high-temperature fluids (100 < T < 500 °C) in the development of economic concentrations of REE is well-established, the mechanisms of element transport, ore precipitation, and light (L)REE/heavy (H)REE fractionation remain a matter of debate. Here, we provide direct evidence from in-situ X-ray Absorption Spectroscopy (XAS) that the formation of hydroxyl-carbonate complexes in alkaline fluids enhances hydrothermal mobilization of LREE at T ≥ 400 °C and HREE at T ≤ 200 °C, even in the presence of fluorine. These results not only reveal that the modes of REE transport in alkaline fluids differ fundamentally from those in acidic fluids, but further underline that alkaline fluids may be key to the mineralization of hydrothermal REE-fluorcarbonates by promoting the simultaneous transport of (L)REE, fluoride and carbonate, especially in carbonatitic systems.

| S-EPMC8933457 | biostudies-literature

Split-anion solvent extraction of light rare earths from concentrated chloride aqueous solutions to nitrate organic ionic liquids.

Project description:Despite its benefits, the extraction of rare earths (REEs) from chloride solutions with neutral or basic extractants is not efficient, so that separation is currently carried out by using acidic extractants. This work aims to improve this process by replacing the conventional molecular diluents in the organic phase by ionic liquids (ILs) which contain coordinating anions. The extraction of La(iii), Ce(iii) and Pr(iii) from concentrated chloride solutions was tested with a quaternary ammonium and a phosphonium nitrate IL extractant. Dissolution of a trialkylphosphine oxide neutral extractant (Cyanex 923) in the nitrate ILs changed the preference of the organic phase from lighter to heavier REE and increased the overall extraction efficiency and the loading capacity of the organic phase. An increase of the CaCl2 concentration in the feed solution resulted in higher extraction efficiencies, due to a lower activity of water and hence to a poorer hydration of the REE ions. In that respect, chloride ions were not coordinating to the REE ion after extraction from concentrated chloride solutions. To achieve selectivity, one should fine-tune the loading by varying the CaCl2 and/or Cyanex 923 concentrations. Adjustment of the CaCl2 concentration in the feed and stripping solutions is essential for the separation of mixtures of REE. However, and unlike in the case of acidic extractants, no control of equilibrium pH is required. The split-anion extraction offers the possibility to separate mixtures of REEs in different groups without having to change the chloride feed solution. It leads to safer and environmentally friendlier extraction processes by (1) using solvents that are not volatile, not flammable and do no accumulate static electricity, (2) consuming no acids or alkali, (3) easy stripping with water and (4) avoidance to create nitrate-containing effluents.

| S-EPMC9087025 | biostudies-literature

Rare-earth ions as antibacterial agents for woven wool fabric.

Project description:Woven fabrics were bestowed with antibacterial property by the simple adsorption of rare-earth metal ions, and the underlying mechanism was investigated using electron spin resonance (ESR) spectroscopy. The adsorption of Ce3+ ions on wool, silk, and cotton fabrics resulted in significant inhibition of Staphylococcus aureus (a gram-positive bacterium), with maximum antibacterial activities (viable bacterial count compared to the reference) of 4.7, 5.8, and 5.2, respectively. Even after 50 wash cycles, the values remained at 3.9, 2.9, and 4.8, respectively. The adsorption of La3+ and Gd3+ ions on wool fabrics also resulted in antibacterial activities of 5.8 and 5.9, respectively. In addition, wool adsorbed with Ce3+ exhibits a satisfactory antibacterial activity of 6.2 against Escherichia coli (a gram-negative bacterium). Such bacterial inhibition is attributed to Fenton reactions between the adsorbed rare-earth ions and hydrogen peroxide (H2O2) produced during bacterial metabolism, as determined from the ESR spectra collected using the spin trap method in the presence of H2O2. The safety of cerium nitrate was also investigated, and no significant issues arose, indicating that it was a safe antibacterial agent. This facile method of imparting antibacterial properties to natural fabrics may be useful for preventing infections in humans.Supplementary informationThe online version contains supplementary material available at 10.1007/s11696-021-01999-9.

| S-EPMC8853069 | biostudies-literature

Hydration counteracts the separation of lanthanides by solvent extraction.

Project description:The extraction of lanthanides from aqueous nitrate solutions by quaternary ammonium nitrate ionic liquids (e.g., [A336][NO3]) shows a negative sequence (i.e., light lanthanides are more efficiently extracted than heavy lanthanides), which conflicts with the lanthanide contraction. In this study, we explored the origin of the negative sequence by investigating the extraction of lanthanides from ethylammonium nitrate by [A336][NO3]. The extraction shows a positive sequence, which is converted to a negative sequence with the addition of water. The transformation from positive to negative sequences reveals that the negative sequence is caused by the hydration of lanthanide ions: hydration of lanthanide ions counteracts the extraction. Therefore, the use of solvents that have weak solvation with lanthanide ions might enhance the separation of the elements by solvent extraction.

| S-EPMC9285791 | biostudies-literature

Statistical determinants of selective ionic complexation: ions in solvent, transport proteins, and other "hosts".

Project description:To provide utility in understanding the molecular evolution of ion-selective biomembrane channels/transporters, globular proteins, and ionophoric compounds, as well as in guiding their modification and design, we present a statistical mechanical basis for deconstructing the impact of the coordination structure and chemistry of selective multidentate ionic complexes. The deconstruction augments familiar ideas in liquid structure theory to realize the ionic complex as an open ion-ligated system acting under the influence of an "external field" provided by the host (or surrounding medium). Using considerations derived from this basis, we show that selective complexation arises from exploitation of a particular ion's coordination preferences. These preferences derive from a balance of interactions much like that which dictates the Hofmeister effect. By analyzing the coordination-state space of small family IA and VIIA ions in simulated fluid media, we derive domains of coordinated states that confer selectivity for a given ion upon isolating and constraining particular attributes (order parameters) of a complex comprised of a given type of ligand. We demonstrate that such domains may be used to rationalize the ion-coordinated environments provided by selective ionophores and biological ion channels/transporters of known structure, and that they can serve as a means toward deriving rational design principles for ion-selective hosts.

| S-EPMC2894556 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data