Search Results (2,004)

This work develops a novel phosphate-functionalized extraction resin (HEHEHP + Cyanex272)/SiO₂-P via the vacuum impregnation method for efficient separation of light rare earth element impurities from lanthanum (La³⁺) in nitric medium through synergistic extraction. Batch experiments have demonstrated superior adsorption selectivity toward impurity ions over La³⁺ in a pH 4 nitric acid solution. Column studies confirmed exceptional performance under ambient conditions, achieving a lanthanum treatment capacity of 120.6 mg/g and over 98% impurity removal, which surpasses most reported values. Notably, this purification process enables direct production of purified La³⁺ solutions through a single-column system without desorption, significantly enhancing efficiency and reducing costs. Mechanistic insights revealed combined ion exchange and coordination interactions between metal ions and P-OH/P=O groups, corroborated by advanced characterization and density functional theory calculations. These findings indicate a higher binding affinity of light rare earth compared with La³⁺. This strategy provides a scalable approach for ultra-high-purity lanthanum compound production in advanced optical and electronic applications. Full article

To achieve efficient desilication and improve the grade of magnesite, an environmentally friendly surfactant, cocamidopropyl dimethylamine (PKO-H), was employed as a collector for the flotation separation of magnesite and quartz. The flotation performance and adsorption mechanism of PKO-H was systematically investigated through flotation experiments, Fourier-transform infrared spectroscopy (FTIR), contact angle measurements, zeta potential analysis, and molecular simulations. The flotation results demonstrated that PKO-H exhibited excellent selectivity, achieving a MgO recovery rate of 98.8% and a concentrate grade of 45.7% in artificially mixed mineral samples. Contact angle measurements, FTIR spectra, zeta potential analysis, and molecular simulations revealed that the adsorption of PKO-H on quartz is primarily driven by electrostatic attraction. In contrast, due to electrostatic repulsion, the interaction between PKO-H and magnesite is weak, preventing stable adsorption. This study establishes PKO-H as a sustainable and efficient collector for magnesite beneficiation and provides new insights into interfacial mechanisms for the design of eco-friendly flotation reagents. Full article

The sensitive detection of n-butanol is of high scientific and practical importance for ensuring safety in industrial production. In this study, hollow Cu₂O@CuS core–shell nanocubic heterostructures were fabricated via a multistep templating method. The Cu₂O@CuS heterostructures demonstrated exceptional performance, with an ultrahigh Brunauer–Emmett–Teller specific surface area that provided abundant active sites and a unique hollow architecture that enhanced mass transport and improved gas adsorption/desorption kinetics. High-density surface oxygen vacancies on the Cu₂O@CuS nanocubic heterostructures provide a key structural basis for the preferential adsorption of n-butanol molecules on its surface. The p–p heterojunction configuration further enhanced selective sensor response by optimizing the charge carrier separation and band structure modulation. The developed sensor achieved a detection limit of 3.18 ppm while exhibiting outstanding sensitivity, stability, and response time, meeting the stringent requirements for n-butanol detection in both industrial and agricultural settings. This work provides new insights on how to design materials for gas sensors. Full article

Photocatalysis is a promising strategy for the treatment of dangerous chemical pollutants in the ocean. In this work, a stable copper-based photocatalyst, i.e., {[Cu(BPA)₂]·2I₃}_n (1, BPA = 4,4′-bipyridinium-N-pentanoic acid), exhibited excellent degradation performance in dye pollutant in seawater. According to the structural analysis, this photocatalyst consists of 1-D cationic [Cu(BPA)₂]_n²ⁿ⁺ infinite chain and two I³⁻ polyiodide anions. In the [Cu(BPA)₂]_n²ⁿ⁺ chain, the distorted CuO₄N₂ octahedra are bridged by asymmetric viologen ligand (BPA), which result in a 1-D ladder-shaped chain. Strong C–H···O/I hydrogen bonds contribute to the formation of a 2-D layer along bc-plane, in which I³⁻ anions are stacked among the cationic chains. The strong adsorption from ultraviolet to visible regions together with its high charge separation efficiency implies its usage as excellent visible-light-driven catalysis. Interestingly, good photocatalytic performance for the degradation of Rhodamine B (RhB) in seawater can be observed by using this hybrid as photocatalyst. In detail, 90.6% degradation ratio of RhB can be achieved in 150 min under visible light, which was monitored on a UV–Vis spectrum. This work could pave the way for new ocean pollutant treatments for shipping accidents. Full article

Lithium has emerged as a critical element in contemporary society. It has been classified as an indispensable feedstock in the manufacture of lithium-ion batteries for electric mobility, portable electronics, and stationary energy storage systems, which are essential for the integration of intermittent renewable energy sources. This metal also has other industrial applications and is projected to support future developments in semiconductor and aerospace technology. However, the exponential growth in global Li demand driven by energy transition and technological innovation requires a resilient and sustainable supply chain where both technological and environmental challenges should be addressed. This review discusses and analyzes some of current challenges associated with the Li supply chain given a particular emphasis on its separation methods. First, statistics of the Li market and its applications are provided, including the main sources from which to recover Li and the environmental impact associated with conventional Li extraction techniques from mineral ores and salar brines. Different separation methods (e.g., solvent extraction, adsorption, ion exchange, membrane technology) to recover Li from different sources are reviewed. Recent advances and developments in these separation strategies are described, including a brief analysis of their main limitations and capabilities. The importance and potential of recycling strategies for end-of-life batteries and industrial residues are also highlighted. A perspective on the gaps to be resolved with the aim of consolidating the Li supply chain to support the energy transition agenda is provided in this review. Full article

Efficient and selective separation of gallium (Ga(III)) from alkaline industrial waste streams remains a significant challenge due to the coexistence of chemically similar ions such as Al(III) and V(V). In this study, a novel ion-imprinted chitosan-based adsorbent (CS/(H-CGCS)-Ga-IIP) was synthesized via a hybrid cross-linking strategy using glutaraldehyde and siloxane-modified chitosan. The optimized material exhibited a high adsorption capacity of 106.31 mg·g⁻¹ for Ga(III) at pH 9, with fast adsorption kinetics reaching equilibrium within 60 min. Adsorption behavior followed the pseudo-second-order kinetic and Langmuir isotherm models, and thermodynamic analysis indicated a spontaneous and endothermic process. In simulated Bayer mother liquor systems, the material demonstrated outstanding selectivity and a distribution coefficient ratio k_d-Ga/k_d-Al = 146.9, highlighting its strong discrimination ability toward Ga(III). Mechanistic insights from SEM-EDS, FTIR, and XPS analyses revealed that Ga(III) adsorption occurs via electrostatic interaction, ligand coordination, and structural stabilization by the siloxane network. The material maintained good adsorption performance over three regeneration cycles, indicating potential for reuse. These findings suggest that CS/(H-CGCS)-Ga-IIP is a promising candidate for the sustainable recovery of gallium from complex alkaline waste streams such as Bayer process residues. Full article

Although the exponential increase in photovoltaic installations does contribute to mitigating climate change, it has posed the problem of photovoltaic (PV) residue. As PV panels contain strategic metals, their recovery has become a priority. This paper therefore employs a mesoporous carbon impregnated with P507 extractant as adsorbent to selectively recover gallium and indium from solutions simulating the leachate of end-of-life CIGS (Copper Indium Gallium Selenide) cells in a fixed-bed. The previous batch results obtained in our lab show that both metals can be selectively separated by simply adjusting the initial pH, with large adsorption capacities (44.97 mg/g for gallium and 34.24 mg/g for indium). The obtained breakthrough curves were fitted to the Thomas, Yan, Yoon, and HSDM (Homogeneous Surface Diffusion Model) models using a simulation program developed in Python 3.12 obtaining good results in all cases (R² > 0.9). The estimated parameters were used to predict the experimental breakthrough curve for a different experiment that had not been used for parameter estimation, being the best predictive results the obtained with the HSDM. This is logical, given that unlike the other three models, it is mechanistic. Full article

The urgent need to address the climate crisis demands a swift transition from fossil fuels to renewable energy. Clean hydrogen, produced through ethanol steam reforming (ESR), offers a viable solution. Traditional ESR operates at atmospheric pressure, requiring costly separation and compression of hydrogen. High-pressure ESR, however, improves hydrogen purification, streamlines processes like pressure swing adsorption, and reduces operational costs while enhancing energy efficiency. High-pressure ESR also enables compact reactor designs, minimizing equipment size and land use by compressing reactants into smaller volumes. This study evaluates two nickel-based commercial catalysts, AR-401 and NGPR-2, under high-pressure ESR conditions. Key parameters, including reaction temperature, steam-to-ethanol ratio, and weight hourly space velocity, were optimized. At 30 bars, 700 °C, and a steam-to-ethanol ratio of 9, both catalysts demonstrated complete ethanol conversion, with hydrogen selectivity of 65–70% and yields of 4–4.5 moles of H₂ per mole of ethanol. Raising the temperature to 850 °C improved hydrogen selectivity to 74% and yielded 5.2 moles of H₂ per mole. High-pressure ESR using renewable ethanol provides a scalable, efficient pathway for hydrogen production, supporting sustainable energy solutions. Full article

Cu-BTC (HKUST-1) metal–organic framework (MOF) is widely recognized for its carbon capture capability due to its unsaturated copper sites, high surface area, and well-defined porous structure. This study developed mixed matrix membranes (MMMs) using cellulose triacetate (CTA), incorporating bimetallic Ni-Cu-BTC MOFs for CO₂/CH₄ separation, and benchmarked them against membranes fabricated with monometallic Cu-BTC. CTA was selected for its biodegradability, membrane-forming properties, and cost-effectiveness. The optimized membrane with 10 wt.% Ni-Cu-BTC achieved a CO₂ permeability of 22.9 Barrer at 25 °C and 5 bar—more than twice that of pristine CTA—with a CO₂/CH₄ selectivity of 33.8. This improvement stems from a 51.66% increase in fractional free volume, a 49.30% rise in the solubility coefficient, and a 51.94% boost in the diffusivity coefficient. Dual-sorption model analysis further confirmed enhanced solubility and adsorption mechanisms. These findings establish CTA/Ni-Cu-BTC membranes as promising candidates for high-performance CO₂ separation in natural gas purification and related industrial processes. Full article

This study reports the separation of methyl ethyl ketone (MEK), a relevant compound in the biorefinery context, from aqueous solutions using activated carbons derived from avocado seed biomass. Two synthesis routes were explored via chemical and thermal activation with H₂SO₄ and KOH. A Taguchi experimental design was applied to tailor synthesis conditions, with MEK adsorption capacity as the target property. Adsorption kinetics and isotherms were evaluated to determine the thermodynamic behavior of MEK separation using the best-performing activated carbons. The carbon activated with H₂SO₄ achieved the highest adsorption capacity (142 mg g⁻¹) at 20 °C and pH 4, surpassing KOH-based materials. This enhanced performance correlated to increased surface area and acidic oxygenated functionalities. However, higher pH and temperature reduced the adsorption efficiency for all adsorbents. Comprehensive characterization was performed using XRD, XRF, FTIR, SEM, N₂ adsorption–desorption isotherms, pH at point of zero charge, and surface acidity/basicity analysis via Boehm titration. Thermodynamic data and surface characterization indicated that MEK adsorption occurs via a double-layer mechanism dominated by electrostatic interactions and hydrogen bonding. The findings highlight an optimized approach for tailoring avocado-based activated carbons to efficiently recover MEK from aqueous media, supporting its potential application in downstream purification of fermentation broths for biofuel production and energy transition processes. Full article

The TuguanZhai rare earth deposit in Tengchong, along with the Longan and Yingpanshan deposits in Longchuan, is a significant ion-adsorption type rare earth (iREE) deposit in Yunnan, China. Previous studies mainly focused on the geochemistry of residual regolith or the migration and enrichment mechanism of rare earth elements (REEs), but lacked systematic analysis of the protoliths. To constrain this deposit and its protolith rock, called Tuguanzhai granite, we systematically integrate petrology features, petrogeochemistry, zircon U-Pb date, and artificial heavy mineral separation (AHMS). Specifically, iREE-host granites include two main periods in this area: the Early Cretaceous (112.13 ± 0.75 Ma) and the Paleocene–Eocene (52.78 ± 0.28 Ma, 48.56 ± 0.19 Ma). The former includes three types of biotite monzogranite with different grain sizes, and the latter is mainly medium-grained biotite monzogranite with local mylonitization. Geochemical features show that these granites generally share high alkalinity compositions (w(K₂O + Na₂O): 7.15 to 12.75 wt%) and potassium contents (w(K₂O): 3.89 to 8.36 wt%). The mineralized granites exhibit significantly higher concentrations of the total REEs than non-mineralized granites, along with a strong enrichment of light REEs. Moreover, the results of AHMS reveal that the REE contents of apatite, allanite, and titanite in mineralized granites are 4.98, 1.29, and 1.90 times more abundant than in non-mineralized granites, respectively. Due to REEs being released from these REE-rich minerals in humid environments, there exists significant potential for iREE formation and exploration in the Early Cretaceous granites in western Yunnan. We innovatively propose the “abundance of easily leachable minerals” as a key indicator for iREE mineralization and exploration, having found it to be better than the traditional total REE contents. Full article

Rare earth elements (REYs) are crucial components of billions of products worldwide. Transitioning from foreign to domestic REY sources requires utilizing both primary (i.e., carbonatites, alkaline igneous rocks, pegmatites, skarn deposits) and secondary (unconventional) sources (i.e., ion-adsorption clays, placer deposits, weathered rock, black and/or oil shales). Coal and coal-bearing strata, promising secondary REY resources, are the focus of this study. Understanding REY mineral associations in unconventional resources is essential to quantifying resource volume and identifying viable mineral separation and processing techniques. Highly REY-enriched (>750 ppm) coal or mudstone samples from the Uinta Region, Utah, USA, were selected for scanning electron microscopy (SEM) analysis. Energy dispersive X-ray spectroscopy (EDS)-determined REY enrichment occurs in: (1) a silt-size fraction (5–30 μm) of monazite and xenotime REY-enriched grains, (2) a clay-size fraction (2–5 μm) of monazite REY-enriched grains dispersed in the clay-rich matrix, and (3) organically confined REY domains < 2 μm. Findings suggest possible REY enrichment from multiple sources, including: (1) detrital silt-size grains, (2) volcanic ash fall, largely in clay-size grains, and (3) organic REY uptake in the peat swamp depositional environment. Full article

Formo-phenolic-like resins were synthesized by replacing phenol with phloroglucinol, a biobased and biocompatible compound, and using different aldehydes, such as biomass-derived furaldehyde and glyoxal. Studies on the adsorption of rare earth elements from an aqueous organic acid solution indicate that these resins follow the Langmuir isotherm model, with maximum adsorption capacities ranging from 0.38 to 0.75 mmol/g. Adsorption was temperature-independent but strongly influenced by pH, with an up to fourfold increase between pH 2 and 5. Extraction kinetics were rapid, reaching equilibrium within two hours. Complete metal recovery was achieved within ten minutes using a 1 mol/L HCl desorption solution. Selectivity also varied with pH; glyoxal- and furfural-based resins showed superior separation performance at pH 2–3 and 3–4, respectively. The application of this method to real-world samples, including permanent magnet and red mud organic acid leachates, demonstrated effective extraction of rare earth elements and promising selectivity over iron (Fe), cobalt (Co), and nickel (Ni). Full article

Against the backdrop of increasing global warming, exploring sustainable pathways to mitigate the greenhouse effect has become a central issue for the ecological and energy future. Photocatalytic reduction of CO₂ technology shows a broad application prospect due to its ability to directly convert CO₂ into high-value-added hydrocarbon fuels and to use solar energy, a clean energy source, to drive the reaction. However, traditional semiconductor catalysts generally suffer from insufficient activity and poor product selectivity in the actual reaction, which cannot meet the requirements of practical applications. In recent years, sulfur vacancy, as an effective material modulation strategy, has demonstrated a remarkable role in enhancing photocatalytic performance. This paper reviews a series of research reports on sulfur vacancies in recent years, introduces the methods of preparing sulfur vacancies, and summarizes the commonly used characterization methods of sulfur vacancies. Finally, the mechanism of introducing sulfur vacancies to promote CO₂ reduction is discussed, which improves the photocatalytic activity and selectivity by enhancing light absorption, facilitating carrier separation, improving CO₂ adsorption and activation, and promoting the stability of reaction intermediates. This review aims to provide theoretical support for an in-depth understanding of the role of sulfur vacancies in photocatalytic systems and to provide a view on the future direction and potential challenges of sulfur vacancies. Full article

Due to the nearly identical chemical properties of Lu and Yb, the production of no-carrier-added (NCA) ¹⁷⁷Lu faces significant challenges in their separation. Achieving efficient and streamlined separation of Lu and Yb is crucial for the production of NCA ¹⁷⁷Lu. This study systematically investigated the separation performance of the commercial Rext-P350 extraction resin for Lu and Yb. Static adsorption experiments revealed that, at a solid–liquid ratio of 8 g/L, both Lu³⁺ and Yb³⁺ were nearly completely adsorbed, with saturation adsorption capacities of 25.8 mg/g and 21.5 mg/g, respectively. An increase in the nitric acid concentration in the aqueous phase significantly inhibited adsorption, but the separation factor for Lu³⁺/Yb³⁺ remained above 1.88. The adsorption kinetics followed a pseudo-second-order model (R² > 0.99), with equilibrium reached within 15 min, demonstrating fast adsorption kinetics. Characterization by SEM, FT-IR, and XPS confirmed the chemical coordination between the resin and Lu³⁺/Yb³⁺. Dynamic chromatographic separation experiments showed that the Rext-P350 resin exhibited significantly better separation performance for Lu³⁺/Yb³⁺ compared to 2-ethylhexylphosphoric acid mono-2-ethylhexyl ester (P507) extraction resin. Leveraging the excellent performance of Rext-P350 resin, a two-stage continuous extraction chromatography process was designed, achieving efficient separation of 0.045 mg of Lu³⁺ from 200 mg of Yb³⁺ with a Lu³⁺ purity of 90.9% and a yield of 98.4%. This study provides a feasible separation technique for the purification of NCA ¹⁷⁷Lu. Full article