Extraction Of Ions Research Articles

Metal-phenolic networks-engineered polyimide aerogels for high-efficiency gold extraction and separation from e-waste mixture

Engineering adsorption materials that offer easy handling, efficient, and selective recovery of precious metals, such as gold, from electronic waste (e-waste) are of significant interest, especially given the escalating volume of discarded electronic devices. However, the harsh digested solvents (e.g., aqua regia), ultralow gold concentrations (several ppm), and competitive interference from various metals present significant challenges. Herein, we engineer a porous polyimide (PI) aerogel with chemically reductive, mechanically resilient, and environmentally recyclable capabilities, using biomass-derived metal-phenolic networks (MPNs), for highly selective and efficient gold extraction and separation. The resulting aerogels show a high adsorption efficiency (∼97.4 %), selective extraction of gold ions from 12 metal ions in simulated leached solutions, and superior purity (∼100 %) in the reduced gold particles. The gold ions are reduced, nucleate, and grow into large agglomeration (∼12 μm) as observed in experiments and confirmed by density functional theory (DFT) calculations, facilitating their separation from the aerogels without the need for complex processes (e.g., membrane separation). On application to a central processing unit (CPU), our aerogels effectively extracted > 96 % of gold ions even at ultralow concentrations of 3.6 ppm in aqua regia, generating at least 66 times more profit compared to the cost (profit/cost = ∼52.9/∼0.8 $⋅g−1). These results demonstrated that MPNs-engineered aerogels are promising economical and practical adsorbents for gold recovery in e-waste.

Electric-field enhanced three-dimensional flexible carbon felt as a host for Pt4+ ions extraction

The extraction of the precious metal Pt4+ ions from aqueous solution are of great importance for both economic development and environmental protection. In this study, an electric field assisted adsorption process with high efficiency and recyclability was explored in a self-made device using three-dimensional (3D) flexible carbon felt (FCF) as the adsorbent without using conductive adhesive. Under the aid of an electric field (0.4 V), 3D pristine FCF (p-FCF) showed a considerable adsorption capacity for Pt4+ (82 mg/g). As high as 203 mg/g was obtained when o-NFCF adsorbents modified with N doping and surface oxygen-containing groups was used. Kinetic and thermodynamic studies show that the electric field would enhance the interactions between the adsorbent and Pt4+ ions, and improve the intraparticle diffusions. Mechanism study showed that the synergistic effect between N doping and oxygen-containing groups might efficiently tune the electrochemical properties of 3D FCF materials, which significantly contributed to the enhanced adsorption of Pt4+. The electroadsorption technology developed in this study provides a simple and efficient method for industrial recovery of precious metal ions.

Flotation Extraction of Copper and Zinc Ions with N-Nonanoyl-N'-Methanesulfonylhydrazine

Flotation Extraction of Copper and Zinc Ions with N-Nonanoyl-N'-Methanesulfonylhydrazine

The extraction of both positive and negative ions from a volume cusp H− ion source

The TRIUMF licensed H− ion source is known to produce 15 mA of H− ions, but some applications, such as cyclotrons, require the injection of both positive and negative ions. Furthermore, when using a tandem accelerator, there would be a benefit in using an ion source that can directly extract H− and He+. A charge exchange chamber would only have to be used with the He+ beam for the production of He−. In this paper, we present the conversion of the H− ion source to allow for the extraction of both positive (He+, H+, H2+ and H3+ ) and negative (H− and D−) ions. In the modified design, up to 3 mA of protons and 2 mA of He+ can be extracted when using positive extraction power supplies and up to 5 mA of H− can be extracted when the polarity of the power supplies switched to negative extraction. We study how the ion source parameters affect the proton fraction and we look at the influence of the magnetic filter field in the plasma chamber.

The SPES Laser Ion Source: Time Structure and Laser Enhancement Measurements with Sm+ beam

A two-step resonance photo-ionization scheme has been used to ionize samarium atoms in the SPES tantalum hot-cavity ion source. The effect of the ion load on the ion beam time structure and the laser enhancement of the ion yield has been studied at different ion source temperatures. Generally, the introduction of more positive ions (ion load) affects negatively the overall confinement of the laser ions inside the volume of the ion source. Possible enhancement of the laser ion confinement through the introduction of neutrals is observed as well. The ion load is also observed to affect the confinement in the transfer line much more than in the hot cavity. Measurement of the time structure with inverted polarity of the cavity DC heating supply confirmed the significance of the longitudinal potential for ion extraction. The laser enhancements of the ion yield are found to be sensitive to the ion load at low operating temperature of the ion source i.e. 1800°C, whereas at 2050°C and 2200°C, they are relatively stable till an ion load value of 1.2 µA.

Solvent Extraction of Silver(I) using N,N-Diethylacetamido Substituted p-t-Octylcalix[4]arene in Nitrate Media

Solvent extraction of silver ions using tetrakis(N,N-diethylaminocarbonylmethoxy)-p-t-octylcalix[4]arene (EATOC) in chloroform from nitrate medium is presented. The influences on the extraction conditions affecting the behaviour of extraction depending upon the factors such as concentrations of acids, extractants and silver ions as well as extraction time were investigated. Various stripping reagents for back extraction to recover the loaded silver ions by forward extraction process were applied. The extraction mechanism of silver ions using EATOC was established on the 1H NMR chemical shift of the extractant as well as the slope assessments of extraction conditions both before and after loading the silver ions.

NA-ALGINATE BEADS OF CALCIUM / IRON-LAYERED DOUBLE HYDROXIDE FOR TREATING WATER CONTAMINATED WITH AMOXICILLIN ANTIBIOTIC

The objective of this study was to prepare an adsorbent material from eggshells of chicken banished to the ambient as wastes to satisfy the ecological requirements of sustainable. The preparation process based on the extraction of calcium ions from eggshells and these ions must be reacted with iron to form nanoparticles of (Ca/Fe)-layered double hydroxides (LDHs) which immobilized as Na-alginate beads. Molar ration of calcium to iron, pH and dosage of LDH nanoparticles must be equal to 1, 12 and 5 g/100 mL to ensure that the prepared beads have highest ability to remove of Amoxicillin (AMOX) antibiotic with removal efficiency equal to 32% for operational conditions of Co=100 mg/L, beads dosage=0.5 g/50 mL, speed=200 rpm, pH=7 for 3 hrs. To increase this efficiency to ≥ 90%, best conditions must be time 90 min, pH 7, and beads mass 1.2 g/ 50 mL for Co 100 mg/L at 200 rpm in the batch mode. The Pseudo second order has high capability in the description of such tests with coefficient of determination (R2) ≥ 0.9924 and sum of squared error (SSE) ≤ 0.1287. Hence, the sorption of AMOX onto beads is governed by the chemisorption process. The reflections of XRD analysis proved the presence of (Ca/Fe)-LDH nanoparticles with size of 13.49 nm, calcium hydroxide (Ca(OH)2) and calcium carbonate (CaCO3)

Entropy optimization of lid-driven micropolar hybrid nanofluid flow in a partially porous hexagonal-shaped cavity with relevance to energy efficient storage processes

Hydromagnetically associated heat convection can greatly enhance the performance of high-efficiency thermal appliances and renewable energy sources through an optimized design. This investigation examines the production of thermodynamic irreversibility and heat convection for a double lid-driven flow within a partially porous stratified hexagonal enclosure. The top and bottom-wall are moving in the opposite direction with an equal velocity U0. The top-wall and the bottom-wall are kept at temperature Tc and Th (Th >\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$>$$\\end{document} Tc) while the slanted walls are assumed to be thermally insulated. A constant magnetic field is employed in the horizontal x-direction. The hexagonal cavity was filled with a micropolar hybrid nanofluid Ag-MgO/water. The system of dimensionless equations was solved by the finite difference method (FDM) associated with successive over-relaxation (SOR), successive under-relaxation (SUR), and Gauss–Seidel iteration tactics and required results are computed with problem specific program in MATLAB code. The results indicate that the Ra and the thickness of the porous layer (Xp) significantly influences heat convection and thermal irreversibility processes. The Nuavg and STotal rises 6.299% and 3.373% as ‘ϕhnf\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\\upphi }_{{\ ext{hnf}}}$$\\end{document}’ enhances from 0 to 4%, respectively. Furthermore, as the values of Ra, Ha, K0, and ϕhnf\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\\upphi }_{{\ ext{hnf}}}$$\\end{document} increase, Beavg experiences a decline of 53.73%, 11.04%, 38.36%, and 0.09% respectively. Also, movement of wall has a significant impact on heat transfer rates and entropy production. The present study may be extended in numerous areas to mimic the problems like—(1) onset of thermo-mechanical process for solid–fluid interaction in a conduit. (2) Thermos-chemical process with extraction of ions in two-phase fluid for double layer plating on a continuously moving sheet, as region of porous stratum saturated with a class of fluid and region without porous medium occupied with other fluid.

Extraction of Metal Ions Using Novel Deep Eutectic Solvents with Chelating Amine

Extraction of Metal Ions Using Novel Deep Eutectic Solvents with Chelating Amine

Ionic Covalent Organic Frameworks in Adsorption and Catalysis

AbstractThe ion extraction and electro/photo catalysis are promising methods to address environmental and energy issues. Covalent organic frameworks (COFs) are a class of promising template to construct absorbents and catalysts because of their stable frameworks, high surface areas, controllable pore environments, and well‐defined catalytic sites. Among them, ionic COFs as unique class of crystalline porous materials, with charges in the frameworks or along the pore walls, have shown different properties and resulting performance in these applications with those from charge‐neutral COFs. In this review, current research progress based on the ionic COFs for ion extraction and energy conversion, including cationic/anionic materials and electro/photo catalysis is reviewed in terms of the synthesis strategy, modification methods, mechanisms of adsorption and catalysis, as well as applications. Finally, we demonstrated the current challenges and future development of ionic COFs in design strategies and applications.

Ionic Covalent Organic Frameworks in Adsorption and Catalysis.

The ion extraction and electro/photo catalysis are promising methods to address environmental and energy issues. Covalent organic frameworks (COFs) are a class of promising template to construct absorbents and catalysts because of their stable frameworks, high surface areas, controllable pore environments, and well-defined catalytic sites. Among them, ionic COFs as unique class of crystalline porous materials, with charges in the frameworks or along the pore walls, have shown different properties and resulting performance in these applications with those from charge-neutral COFs. In this review, current research progress based on the ionic COFs for ion extraction and energy conversion, including cationic/anionic materials and electro/photo catalysis is reviewed in terms of the synthesis strategy, modification methods, mechanisms of adsorption and catalysis, as well as applications. Finally, we demonstrated the current challenges and future development of ionic COFs in design strategies and applications.

Understanding the separation of trivalent lanthanides and actinides using multiple diglycolamide-containing ligands: a review

Abstract The complexation and separation behaviour of trivalent actinides and lanthanides with various multiple diglycolamide (DGA) group-containing ligands are compiled in the present review. The DGA arms are anchored on various scaffolds, viz., C- and N-pivot tripodal backbones, benzene-centred tripodal backbones, calix[4]arene, pillar[5]arene and azamacrocycle scaffolds. Dendrimers of different generations having DGA arms were also evaluated for the extraction and complexation studies of trivalent actinide and lanthanide ions. The extraction efficiency of the DGA units increases significantly when they are grouped together on a single backbone/scaffold. Furthermore, the selectivity was found to improve in many cases, particularly with respect to the UO2 2+ ion. This is very important for the development of suitable ligands for the extraction/separation of the actinide and lanthanide ions. Combined experimental, luminescence and DFT studies on the complexation of trivalent actinides and lanthanides with these DGA-based ligands are quite useful to understand their extraction and separation behaviour and this review article gives a critical analysis of the results available in the literature.

Sorption of divalent metal ions from aqueous solutions on activated carbon with its further separation through electroflotation

Currently, there are multiple methods for wastewater treatment from metal ions. One of the leading methods is the sorption process. The advantage of sorption purification is its ability to extract substances from multi-component mixtures and its high efficiency with low concentrations of wastewater contamination. The purpose of this work was to study the sorption capacity of the “OU-B” activated carbon in relation to metal ions (Cu2+, Zn2+, Mn2+). The following tasks were set: establishing optimal parameters for sorption in a static mode, approximating the obtained data by linear forms of kinetic and adsorption equations, as well as obtaining the ability to separate coal particles from aqueous solutions by electroflotation. To study the patterns, we used the following research methods: low-temperature nitrogen adsorption, atomic absorption spectrometry, and nephelometry. The optimal parameters for sorption in a static mode (sample size of coal, process time, initial concentration of metal ions) were established experimentally. The maximum degree of extraction of metal ions in the course of sorption was achieved with a 1:133 ratio of coal to aqueous solution during 60 minutes and was 82% for Cu2+, 73% for Zn2+, and 63% for Mn2+. The obtained sorption results were analysed using the kinetic models of Zeldovich-Chen-Clayton of pseudo-first and pseudo-second order and adsorption models of Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, and Flory-Higgins. The analysis showed that the sorption of Cu2+, Zn2+, and Mn2+ on OU-B carbon occurred according to the mechanism of physical adsorption, which was described by the sorption models of Langmuir and Freundlich and the Zeldovich-Chen-Clayton kinetic model. The separation of used sorbents and the aqueous phase was a difficult task from a technological point of view due to the small size of carbon particles. The article showed the prospects of using electroflotation for extracting OU-B carbon from aqueous solutions: the degree of extraction of coal particles reached 97-99% when cationic or non-ionic SAS were added to the solution.

Dynamic Interfacial Tension Measurement for the Kinetic Study of Eu(III) Extraction in the NaNO3/Tributyl Phosphate System Based on an Increase in Interfacial Tension.

We demonstrated for the first time that interfacial tension measurements can be used to evaluate the kinetics of the solvent extraction of metal ions. The Eu(III) extraction mechanism in the nitrate ion/tributyl phosphate (TBP) system was investigated on the basis of dynamic interfacial tension. Interestingly, the interfacial tension of the TBP droplet (γ) increased with Eu(III) extraction. This behavior can be explained by the electrocapillary effect. The time dependence of γ was kinetically analyzed, and we demonstrated that the rate-determining process was the interfacial reaction of Eu(III). Furthermore, the dependence of the mass transfer rate constant upon the concentration of the nitrate ions revealed that two nitrate ions were involved in the interfacial reaction during Eu(III) extraction. However, no change in the rate constant upon TBP concentration was observed, because the change in the TBP concentration did not affect the electrocapillary effect. We determined the forward and backward reaction rates to be k1 = (1.5 ± 0.7) × 10-6 m M-2 s-1 and k-MT = (6.9 ± 3.9) × 10-7 m s-1. Therefore, for the first time, we demonstrated that dynamic interfacial tension, which is involved in the electrocapillary effect, can be used to elucidate the kinetics of Eu(III) extraction. We expect that this study will attract the attention of researchers in several fields, including physical and analytical chemistry.

Synthesis of Quaternary-Ammonium-Lignin-Based Ionic Liquids and Comparison of Extraction Behavior of Co(II) and Ni(II) with 2-Ethylhexyl Phosphoric Acid Mono-2-Ethylhexyl Ester

The escalating demand for cobalt in modern industry necessitates the recycling or extraction of this resource for sustainable development. Despite the abundance of lignin in nature, its utilization remains low, highlighting the need to enhance its value-added potential. This study focuses on the synthesis of quaternary ammonium lignin (QAL) and 2-ethylhexyl phosphoric acid mono-2-ethylhexyl ester (P507) as ionic liquid (QP–IL) compounds for the extraction of metal ions. A comparison of the extraction behavior of Co(II) and Ni(II) from chloride solution between QP–IL and P507 revealed varying extraction ratios under different conditions, with QP–IL demonstrating a higher cobalt extractability than P507. Furthermore, under identical conditions, QP–IL exhibited superior Co/Ni separation performance (βCo/Ni) compared to P507. Ultimately, QP–IL proved to be more effective than P507 in separating cobalt from mixed solutions.

Research on the Synthesis of Zinc-Ammonium Phosphate Using Galvanic Waste Sludge as a Source of Zinc.

This paper presents the extraction of zinc ions from waste resulting from the galvanic industry, such as sludge from acid zinc electroplating baths, and their revaluation in mineral fertilizer as zinc-ammonium phosphate. The purpose of this work is to extract zinc ions from the sludge that forms directly in the zinc bath, which can only contain zinc and small amounts of iron, to revalorize zinc into the form of zinc-ammonium phosphate. The process of obtaining zinc-ammonium phosphate is presented using waste sludge from the galvanic industry. In order to obtain zinc-ammonium phosphate, the solution resulting from the dissolution of the sludge with a 20% hydrochloric acid solution was used in reaction with diammonium phosphate and a 25% ammonia solution. After the chemical analysis of the obtained products, zinc-ammonium phosphate was characterized using X-ray powder diffraction, infrared FT-IR spectroscopy and electronic microscopy (SEM) analysis. The results obtained indicate a promising approach to sustainable resource utilization in the production of zinc-ammonium phosphate.

Update of high voltage isolation control and monitoring system for HVE-400 ion implanter

HVE-400 ion implanter is special ion implantation equipment for semiconductor materials boron and phosphorus doping. The ion source and extraction deflection system are at high voltage platform, while the corresponding control system is at ground voltage position. The control signals and measurement signals of various parameters at the high-voltage end need to be transmitted between ground voltage and high voltage through optical fibers to isolate high voltage. Upgrading is carried out due to the aging of the optical fiber transmission control and monitoring system, which cannot work stably. The transformation replaces the original distributed single-point control method with an advanced distributed centralized control method, and integrates all control and monitoring functions into an industrial control computer for digital operation and display. In the computer software, two kinds of automatic calculation of ion mass number are designed. After upgrading, the implanter high-voltage platform control and monitoring system features digitalization, centralized control, high reliability, strong anti-interference, fast communication speed, and easy operation.

Ordered Vacancies as Sodium Ion Micropumps in Cu-Deficient Copper Indium Diselenide to Enhance Sodium Storage.

Unordered vacancies engineered in host anode materials cannot well maintain the uniform Na+ adsorbed and possibly render the local structural stress intense, resulting in electrode peeling and battery failure. Here, the indium is first introduced into Cu2Se to achieve the formation of CuInSe2. Next, an ion extraction strategy is employed to fabricate Cu0.54In1.15Se2 enriched with ordered vacancies by spontaneous formation of defect pairs. Such ordered defects, compared with unordered ones, can serve as myriad sodium ion micropumps evenly distributing in crystalline host to homogenize the adsorbed Na+ and the generated volumetric stress during the electrochemistry. Furthermore, Cu0.54In1.15Se2 is indeed proved by the calculations to exhibit smaller volumetric variation than the counterpart with unordered vacancies. Thanks to the distinct ordered vacancy structure, the material exhibits a highly reversible capacity of 428mAhg-1 at 1C and a high-rate stability of 311.7mAhg-1 at 10C after 5000 cycles when employed as an anode material for Sodium-ion batteries (SIBs). This work presents the promotive effect of ordered vacancies on the electrochemistry of SIBs and demonstrates the superiority to unordered vacancies, which is expected to extend it to other metal-ion batteries, not limited to SIBs to achieve high capacity and cycling stability.

In-Situ Atomic-Scale Observation of Brownmillerite to Ruddlesden–Popper Phase Transition Tuned by Epitaxial Strain in Cobaltites

Phase transitions involving oxygen ion extraction within the framework of the crystallographic relevance have been widely exploited for sake of superconductivity, ferromagnetism, and ion conductivity in perovskite-related oxides. However, atomic-scale pathways of phase transitions and ion extraction threshold are inadequately understood. Here we investigate the atomic structure evolution of LaCoO3 films upon oxygen extraction and subsequent Co migration, focusing on the key role of epitaxial strain. The brownmillerite to Ruddlesden–Popper phase transitions are discovered to stabilize at distinct crystal orientations in compressive- and tensile-strained cobaltites, which could be attributed to in-plane and out-of-plane Ruddlesden–Popper stacking faults, respectively. A two-stage process from exterior to interior phase transition is evidenced in compressive-strained LaCoO2.5, while a single-step nucleation process leaving bottom layer unchanged in tensile-strained situation. Strain analyses reveal that the former process is initiated by an expansion in Co layer at boundary, whereas the latter one is associated with an edge dislocation combined with antiphase boundary. These findings provide a chemo-mechanical perspective on the structure regulation of perovskite oxides and enrich insights into strain-dependent phase diagram in epitaxial oxides films.

Charging behavior of ZnMn2O4 and LiMn2O4 in a zinc- and lithium-ion battery: an ab initio study

In the field of sustainable energy storage systems, zinc-ion batteries (ZIB) employing aqueous electrolytes have emerged as viable successors to the widely used lithium-ion batteries, attributed to their cost-effectiveness, environmental friendliness, and intrinsic safety features. Despite these advantages, the performance of ZIBs is significantly hindered by the scarcity of suitable cathode materials, positioning manganese zinc oxide (ZnMn2O4) as a potential solution. In this study, we describe the ZnMn2O4 (ZMO) compound focusing on its properties variations during Zn extraction and potential battery applications. For the sake of comparison, we also analyze the same properties of the LiMn2O4 in its tetragonal phase (TLMO), for the first time, motivated by a recent discovery that the substitution of Zn ions by Li in ZMO forms isostructural TLMO compound at room temperature. The study was conducted within the density functional theory (DFT) framework, where the structural, electronic, magnetic, electrochemical, and spectroscopic properties of ZMO and TLMO are investigated under various conditions. Although both systems crystallize in tetragonal structures, they demonstrate distinct electronic and magnetic properties due to different oxidation states of the Mn. Computationally optimized lattice parameters align closely with experimental values. The TLMO exhibits a narrower band gap compared to ZMO, indicating enhanced electrical conductivity. In addition, TLMO presented a lower diffusion energy barrier than ZMO, indicating better ionic conductivity. To evaluate the potential application of these materials in battery technologies, we further explored their volume changes during charging/discharging cycles, simulating Zn or Li ions extraction. TLMO underwent a significant volume contraction of 5.8% upon complete Li removal, while ZMO experienced a more pronounced contraction of 12.5% with full Zn removal. By adjusting ion extraction levels, it is possible to reduce these contractions, thereby approaching more viable battery applications. Voltage profiles, constructed from DFT-based simulation results, unveiled an average voltage of 4.05 V for TLMO, closely matching experimental values. Furthermore, spectroscopy results provide insights into the electronic transitions and validate the computational findings, consolidating our understanding of the intrinsic properties of ZMO and TLMO.