Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (206)

Search Parameters:
Keywords = anion resin

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
19 pages, 2033 KB  
Article
Galactooligosaccharide Production Using Immobilized Aspergillus oryzae β-Galactosidase, Part I: Characterization and Influence of Reaction Conditions
by Monika Antošová, Jana Krázel Adamíková and Milan Polakovič
Int. J. Mol. Sci. 2025, 26(23), 11266; https://doi.org/10.3390/ijms262311266 - 21 Nov 2025
Viewed by 210
Abstract
The enzymatic production of prebiotic galactooligosaccharides (GOS), functional food ingredients with established health benefits, remains an active research area driven by a rising global demand for GOS. These oligosaccharides are synthesized from lactose via transgalactosylation catalyzed by β-galactosidase, accompanied by hydrolysis of both [...] Read more.
The enzymatic production of prebiotic galactooligosaccharides (GOS), functional food ingredients with established health benefits, remains an active research area driven by a rising global demand for GOS. These oligosaccharides are synthesized from lactose via transgalactosylation catalyzed by β-galactosidase, accompanied by hydrolysis of both substrate and products, and the competition between these reactions critically determines the maximum achievable GOS yield. In this study, β-galactosidase from Aspergillus oryzae was immobilized on an anion-exchange resin (Dowex Marathon MSA) using three glutaraldehyde-based crosslinking strategies. The resulting immobilized biocatalysts were characterized and evaluated for GOS synthesis, with product yield as the principal performance indicator. The results demonstrated that the immobilized biocatalysts markedly modulated the balance between transgalactosylation and hydrolytic activities. The biocatalyst prepared by simultaneous resin activation and enzyme crosslinking provided the highest GOS yield and operational stability. This biocatalyst was subsequently used to study the effects of lactose concentration, pH, enzyme loading, and temperature. Among these, lactose concentration most strongly influenced GOS yield, whereas the other factors primarily affected the reaction rate. These findings offer practical insights into enzyme immobilization strategies for optimizing GOS production. Full article
(This article belongs to the Section Biochemistry)
Show Figures

Figure 1

21 pages, 2068 KB  
Article
Multi-Objective Optimization of Supercritical Water Oxidation for Radioactive Organic Anion Exchange Resin Wastewater Using GPR–NSGA-II
by Yabin Jin, Tiantian Xu, Le Zhang, Qian Zhang, Liang Zhou, Zhe Shen and Zhenjie Wan
Processes 2025, 13(12), 3759; https://doi.org/10.3390/pr13123759 - 21 Nov 2025
Viewed by 264
Abstract
Radioactive organic anion exchange resins present a significant challenge in nuclear power plant waste disposal due to their volatility, instability, and biotoxicity. Based on experimental degradation data from the supercritical water oxidation (SCWO) of organic anion exchange resin waste liquids from the nuclear [...] Read more.
Radioactive organic anion exchange resins present a significant challenge in nuclear power plant waste disposal due to their volatility, instability, and biotoxicity. Based on experimental degradation data from the supercritical water oxidation (SCWO) of organic anion exchange resin waste liquids from the nuclear industry, this study conducted correlation analysis, cluster analysis, and Sobol sensitivity analysis of key process parameters. The results indicate that temperature is the primary factor influencing chemical oxygen demand (COD) and total nitrogen (TN) removal, while oxidant dosage exhibits a notable synergistic effect on nitrogen transformation. A Gaussian Process Regression–Non-Dominated Sorting Genetic Algorithm II (GPR–NSGA-II) multi-objective optimization model was developed to balance COD/TN removal rate and treatment cost. The optimal operating conditions were identified as a temperature of 472.2 °C, an oxidant stoichiometric ratio (OR) of 136%, an initial COD concentration of 73,124 mg·L−1, and a residence time of 3.8 min. Under these conditions, COD and TN removal efficiencies reached 99.63% and 32.92%, respectively, with a treatment cost of 128.16 USD·t−1. The proposed GPR–NSGA-II optimization strategy provides a methodological foundation for process design and economic assessment of SCWO in treating radioactive organic resin waste liquids and can be extended to other studies involving high-concentration, refractory organic wastewater treatment. Full article
(This article belongs to the Section Environmental and Green Processes)
Show Figures

Figure 1

21 pages, 3548 KB  
Article
Anti-Inflammatory and Antioxidant Mechanisms of Dendrobium moschatum Polysaccharide in Intestinal Epithelial Cells via TLR4-NF-κB and Nrf2 Signaling Pathways
by Ji Chen, Chunyan Ma, Xu Mo, Linhong Li, Lijuan Wu, Chaowen Zhang, Rui Li, Yuanfeng Zou, Fan Liu and Mengliang Tian
Antioxidants 2025, 14(11), 1384; https://doi.org/10.3390/antiox14111384 - 20 Nov 2025
Viewed by 550
Abstract
Dendrobium moschatum neutral polysaccharide (DMP-NP) was isolated using a water extraction–ethanol precipitation method, followed by purification with DEAE-cellulose anion-exchange resin and a dextran gel column. The resulting DMP-NP1 exhibited a weight-average molecular weight of 16.23 kDa. The molar ratio of monosaccharides was as [...] Read more.
Dendrobium moschatum neutral polysaccharide (DMP-NP) was isolated using a water extraction–ethanol precipitation method, followed by purification with DEAE-cellulose anion-exchange resin and a dextran gel column. The resulting DMP-NP1 exhibited a weight-average molecular weight of 16.23 kDa. The molar ratio of monosaccharides was as follows: glucose–mannose–galactose–fucose–rhamnose = 78.54:19.11:1.59:0.53:0.23, with a glucose-to-mannose ratio of 4.1:1. Infrared spectroscopic analysis revealed characteristic carbohydrate absorption peaks and confirmed the presence of pyranosidic linkages. NMR analysis revealed that DMP-NP1 possesses a backbone mainly formed by 1→4 glycosidic linkages, a small number of 1→6 branches, and O-acetyl substitutions at the C2 and C3 positions of mannose residues. In vitro experiments demonstrated that treatment with 0–20 μg/mL (0–1.23 μM) DMP-NP significantly enhanced the activities of catalase (CAT) and superoxide dismutase (SOD) in IPEC-J2 cells, along with upregulation of the corresponding antioxidant genes. Concurrently, DMP-NP reduced the secretion of key pro-inflammatory cytokines, including TNF-α, IL-1β, and IL-6, and downregulated the expression of genes associated with both antioxidant and inflammatory signaling pathways. Collectively, these findings indicate that DMP-NP not only prevents but also ameliorates LPS-induced inflammatory injury in intestinal epithelial cells, thereby providing a basis for the application of DMP-NP in intestinal inflammation mitigation. Full article
(This article belongs to the Section Health Outcomes of Antioxidants and Oxidative Stress)
Show Figures

Graphical abstract

10 pages, 1814 KB  
Article
Preparation and Characterization of a Dual-Layer Coating with Synergistic Ionic Selectivity and Photocathodic Protection Property
by Chuyuan Cui, Yongsheng An, Xiangpeng Wang and Ping Qiu
Corros. Mater. Degrad. 2025, 6(4), 60; https://doi.org/10.3390/cmd6040060 - 17 Nov 2025
Viewed by 340
Abstract
Inspired by the mechanism of ion exchange resins, this study is a first-report in constructing a dual-layer photocathodic protective coating with ionic selectivity to enhance corrosion resistance property. The microstructure, composition, and ion selectivity of the coating are characterized by scanning electron microscopy, [...] Read more.
Inspired by the mechanism of ion exchange resins, this study is a first-report in constructing a dual-layer photocathodic protective coating with ionic selectivity to enhance corrosion resistance property. The microstructure, composition, and ion selectivity of the coating are characterized by scanning electron microscopy, Raman spectroscopy, infrared spectroscopy, and membrane potential. It shows that the outer g-C3N4/TiO2 cation-selective layer plays a role in preventing corrosive Cl ions passing through the coating; the inner g-C3N4-TiO2-CTAB anion-selective layer could prevent Fe2+ ions from diffusing through the coating. Furthermore, the coated carbon steel sample demonstrates a minimum OCP (open circuit potential) value of −770 mV (vs. SCE) under illumination in 3.5% NaCl media. Interestingly, the OCP remains around −720 mV (vs. SCE) even after light deprivation. The synergistic effect between ion selectivity and photocathodic protection is described, in detail, in the following. Full article
Show Figures

Figure 1

17 pages, 515 KB  
Article
A Complete Mobile Treatment Chain to Produce Drinking Water from Sources Heavily Contaminated by Inorganic and Organic Compounds
by Jean-François Blais, Vincent Taillard, Geneviève Rioux, Justine Dionne, Richard Lévesque, Pejman Abolhosseini, Lan Huong Tran and Richard Martel
Water 2025, 17(22), 3246; https://doi.org/10.3390/w17223246 - 14 Nov 2025
Viewed by 571
Abstract
The provision of potable water for armed forces at their operational sites necessitates a robust treatment chain to ensure the production of safe drinking water from potentially contaminated local water sources. Relying on single-use water bottles is not considered an eco-friendly option and [...] Read more.
The provision of potable water for armed forces at their operational sites necessitates a robust treatment chain to ensure the production of safe drinking water from potentially contaminated local water sources. Relying on single-use water bottles is not considered an eco-friendly option and on-site production may exhibit limited efficiency depending on the water contamination. This study therefore aimed to define a mobile processing chain that could efficiently produce drinking water on-site while offering a multi-barrier level of protection. To evaluate the system, contaminated water was prepared from different water sources and then spiked with various inorganic contaminants (metals, anions: Cl, F, I, NO2, NO3, SO42−, CN), organic contaminants (e.g., pesticides, petroleum hydrocarbons, polycyclic aromatic hydrocarbons, chlorinated solvents), and energetic compound (perchlorate) at levels ranging from 5 to 50 times the standard water quality criteria. A specific treatment process was defined optimized and evaluated at flow rates reaching 500 L/h. This treatment chain includes the following: a sediment filter, a greensand filter, a cation exchange resin, an anion exchange resin, an activated carbon adsorption filter, ultrafiltration, a UV lamp, and a reverse osmosis (RO) unit. This treatment system successfully met all water quality criteria, providing a reliable and effective alternative to an RO-only treatment regime. Full article
(This article belongs to the Section Wastewater Treatment and Reuse)
Show Figures

Graphical abstract

17 pages, 3863 KB  
Article
Adsorption of Cr(III) by IRA-900 Resin in Sodium Phosphite and Sulfuric Acid System
by Tingjie Xu, Dahuan Gan, Guowang Wei, Yingjie Yang, Qiankun Wei and Chunlin He
Separations 2025, 12(10), 270; https://doi.org/10.3390/separations12100270 - 5 Oct 2025
Viewed by 493
Abstract
Chromium (Cr), a toxic heavy metal, poses significant environmental and health risks when industrial effluents containing Cr are discharged untreated. Addressing this challenge, this study developed a selective chromium removal strategy using IRA-900 resin in a sulfuric acid system with sodium phosphite (NaH [...] Read more.
Chromium (Cr), a toxic heavy metal, poses significant environmental and health risks when industrial effluents containing Cr are discharged untreated. Addressing this challenge, this study developed a selective chromium removal strategy using IRA-900 resin in a sulfuric acid system with sodium phosphite (NaH2PO3) as a complexing agent. In the NaH2PO3-H2SO4 system, IRA-900 resin exhibited exceptional selectivity for Cr3+ with minimal co-adsorption of competing ions. The adsorption process followed the Langmuir isotherm model (R2 > 0.99), indicating monolayer chemisorption dominated by homogeneous active sites, and achieved a maximum capacity of 103.56 mg·g−1. Characterization via XPS, FT-IR, and SEM-EDS revealed a two-step mechanism: Cr3+ reacts with H2PO3 to form an anionic complex, and then the complex undergoes electrostatic interaction and ion exchange with chloride ions (Cl) on the quaternary ammonium groups of the resin. The chromium-loaded resin demonstrated remarkable structural stability, resisting Cr3+ desorption under conventional elution conditions. This property provides a novel pathway for chromium solidification in industrial wastewater, effectively minimizing secondary pollution risks. This work advances the design of ligand-assisted ion-exchange systems for targeted heavy metal removal, offering both high selectivity and environmental compatibility in wastewater treatment. Full article
(This article belongs to the Topic Advances in Separation Engineering)
Show Figures

Figure 1

15 pages, 1246 KB  
Article
Removal of Aggregates During Bispecific Antibody Purification Using Hydrophobic Interaction Chromatography
by Puya Zhao, Yue Qi and Kai Gao
Membranes 2025, 15(10), 299; https://doi.org/10.3390/membranes15100299 - 1 Oct 2025
Viewed by 1217
Abstract
In the production of recombinant antibody/Fc-fusion proteins using mammalian cells, many aggregates often form alongside the target proteins, particularly with bispecific antibodies. To ensure the safety of biological products, it is essential to control the amount of aggregates within a specific range. A [...] Read more.
In the production of recombinant antibody/Fc-fusion proteins using mammalian cells, many aggregates often form alongside the target proteins, particularly with bispecific antibodies. To ensure the safety of biological products, it is essential to control the amount of aggregates within a specific range. A traditional downstream process typically involves using Protein A (ProA) resin to capture the target antibody, followed by two polishing steps to ensure purity; for instance, using an anion exchange chromatography (AEX) in flow-through mode and a cation exchange chromatography (CEX) in binding–elution mode. In this study, we choose a Dual Action Fab (DAF), which can bind two antigens and is prone to aggregation when expression in CHO (Chinese Hamster Ovary) cells. We introduce hydrophobic interaction membrane chromatography (HIMC) operating in flow-through mode, which enhances production efficiency while reducing costs and the risks associated with column packing. We evaluated the impact of the operating buffer system, as well as the pH and conductivity of the loading samples, on aggregate removal using HIMC. Additionally, we investigated the mechanism of aggregate binding and found that loading conditions had a limited impact on this process. Overall, our findings indicate that employing HIMC can achieve a 20% reduction in aggregate levels. These results demonstrate that HIMC in flow-through mode is an effective and robust approach for reducing aggregates during antibody purification. Full article
Show Figures

Figure 1

20 pages, 5226 KB  
Article
Design and Performance of 3D-Printed Hybrid Polymers Exhibiting Shape Memory and Self-Healing via Acrylate–Epoxy–Thiol–Ene Chemistry
by Ricardo Acosta Ortiz, Alan Isaac Hernández Jiménez, José de Jesús Ku Herrera, Roberto Yañez Macías and Aida Esmeralda García Valdez
Polymers 2025, 17(19), 2594; https://doi.org/10.3390/polym17192594 - 25 Sep 2025
Cited by 1 | Viewed by 942
Abstract
This study presents a novel strategy for designing photocurable resins tailored for the additive manufacturing of smart thermoset materials. A quaternary formulation was developed by integrating bis(2-methacryloyl)oxyethyl disulfide (DADS) with an epoxy/thiol-ene system (ETES) composed of diglycidyl ether of bisphenol A (EP), pentaerythritol [...] Read more.
This study presents a novel strategy for designing photocurable resins tailored for the additive manufacturing of smart thermoset materials. A quaternary formulation was developed by integrating bis(2-methacryloyl)oxyethyl disulfide (DADS) with an epoxy/thiol-ene system (ETES) composed of diglycidyl ether of bisphenol A (EP), pentaerythritol tetrakis(3-mercaptopropionate) (PTMP), and 4,4′-methylenebis(N,N-diallylaniline) (ACA4). This unique combination enables the simultaneous activation of four polymerization mechanisms: radical photopolymerization, thiol-ene coupling, thiol-Michael addition, and anionic ring-opening, within a single resin matrix. A key innovation lies in the exothermic nature of DADS photopolymerization, which initiates and sustains ETES curing at room temperature, enabling 3D printing without thermal assistance. This represents a significant advancement over conventional systems that require elevated temperatures or post-curing steps. The resulting hybrid poly(acrylate–co-ether–co-thioether) network exhibits enhanced mechanical integrity, shape memory behavior, and intrinsic self-healing capabilities. Dynamic Mechanical Analysis revealed a shape fixity and recovery of 93%, while self-healing tests demonstrated a 94% recovery of viscoelastic properties, as evidenced by near-overlapping storage modulus curves compared to a reference sample. This integrated approach broadens the design space for multifunctional photopolymers and establishes a versatile platform for advanced applications in soft robotics, biomedical devices, and sustainable manufacturing. Full article
(This article belongs to the Section Smart and Functional Polymers)
Show Figures

Graphical abstract

20 pages, 3129 KB  
Article
Selective Removal of Mo and W from Acidic Leachates Using Thiourea Modified Macroporous Anion Exchanger
by Akmaral Ismailova, Dilyara Rashit, Tomiris Kossova and Yerbol Tileuberdi
Molecules 2025, 30(18), 3803; https://doi.org/10.3390/molecules30183803 - 18 Sep 2025
Viewed by 542
Abstract
In this study, a commercial anion-exchange resin (D301), known for high regenerability but limited selectivity, was chemically modified to enhance its sorption performance. The modification included graft polymerization of glycidyl methacrylate followed by thiourea functionalization, yielding a new sorbent, TD301, with chelating functional [...] Read more.
In this study, a commercial anion-exchange resin (D301), known for high regenerability but limited selectivity, was chemically modified to enhance its sorption performance. The modification included graft polymerization of glycidyl methacrylate followed by thiourea functionalization, yielding a new sorbent, TD301, with chelating functional groups. Characterization using SEM/EDS, IR spectroscopy, XPS, and zeta potential measurements confirmed the successful introduction of sulfur- and nitrogen-containing groups, increased surface roughness, and decreased surface charge in the pH range 2–6. These changes shifted the sorption mechanism from nonspecific ion exchange to selective coordination. Sorption properties of TD301 were evaluated in mono- and bimetallic Mo–W systems, as well as in solutions obtained from real ore decomposition. The modified sorbent showed fast sorption kinetics and high selectivity for Mo(VI) at pH 1.5, while retaining high W(VI) uptake at pH 0.5. In binary systems, separation factors (α) reached 128.4, greatly exceeding those of unmodified D301. In real leachates (Mo ≈ W ≈ 0.04 g/L), TD301 selectively extracted W at pH 0.66 and Mo at pH 1.5. These findings demonstrate that TD301 is an effective sorbent for pH-dependent Mo/W separation in complex matrices, with potential for resource recovery, wastewater treatment, monitoring, and suitability for repeated use. Full article
(This article belongs to the Section Analytical Chemistry)
Show Figures

Graphical abstract

19 pages, 2165 KB  
Article
Structural Analysis of Acidic Glycosphingolipids in the Adductor Muscle of the Japanese Giant Scallop (Patinopecten yessoensis)
by Shunsuke Sonoda, Saki Itonori, Mutsumi Sugita, Ayako Higashino, Koki Sugimoto, Ryota Hosomi and Kenji Fukunaga
Fishes 2025, 10(9), 460; https://doi.org/10.3390/fishes10090460 - 12 Sep 2025
Viewed by 698
Abstract
Structural analysis of glycosphingolipids provides novel insights into organismal classification and reveals conserved functional roles that transcend taxonomic boundaries. To elucidate the structural characteristics of acidic glycosphingolipids (AGLs) in the adductor muscle of the Japanese giant scallop (Patinopecten yessoensis), AGLs were [...] Read more.
Structural analysis of glycosphingolipids provides novel insights into organismal classification and reveals conserved functional roles that transcend taxonomic boundaries. To elucidate the structural characteristics of acidic glycosphingolipids (AGLs) in the adductor muscle of the Japanese giant scallop (Patinopecten yessoensis), AGLs were isolated and purified by column chromatography using anion exchange resin and silica gel. Structural characterization was performed using mass spectrometry, proton nuclear magnetic resonance spectroscopy, and immunological techniques. The sugar chain structure was identified as GlcA4Meβ1-4(GalNAc3Meα1-3)Fucα1-4GlcNAcβ1-2Manα1-3Manβ1-4Glcβ1-Cer, consistent with the mollu-series core reported for mollusks. In addition to uronic acid, the structure was distinguished by internal fucose and methylated sugars, features commonly found in bivalves. The presence of xylose in the sugar chains of AGLs was also suggested. In contrast, the ceramide moiety was composed primarily of fatty acids C16:0 and C18:0 and the long-chain base d16:1. This chemical structure provides valuable insights into the biological classification of P. yessoensis and the mollu-series glycolipids containing fucose and methylated sugars, which may serve as bioactive components shared across species in the phylum Mollusca and class Bivalvia. Full article
Show Figures

Graphical abstract

22 pages, 6464 KB  
Article
Evaluation and Experiment of High-Strength Temperature- and Salt-Resistant Gel System
by Changhua Yang, Di Xiao, Jun Wang and Tuo Liang
Gels 2025, 11(8), 669; https://doi.org/10.3390/gels11080669 - 21 Aug 2025
Viewed by 689
Abstract
To address the issues of poor thermal stability, inadequate salt tolerance, and environmental risks in conventional gel systems for the development of high-temperature, high-salinity heterogeneous reservoirs, a triple-synergy gel system comprising anionic polyacrylamide (APAM), polyethyleneimine (PEI), and phenolic resin (SMP) was developed in [...] Read more.
To address the issues of poor thermal stability, inadequate salt tolerance, and environmental risks in conventional gel systems for the development of high-temperature, high-salinity heterogeneous reservoirs, a triple-synergy gel system comprising anionic polyacrylamide (APAM), polyethyleneimine (PEI), and phenolic resin (SMP) was developed in this study. The optimal synthesis parameters—APAM of 180 mg/L, PEI:SMP = 3:1, salinity of 150,000 ppm, and temperature of 110 °C—were determined via response surface methodology, and a time–viscosity model was established. Compared with existing binary systems, the proposed gel exhibited a mass retention rate of 93.48% at 110 °C, a uniform porous structure (pore size of 2–8 μm), and structural stability under high salinity (150,000 ppm). Nuclear magnetic resonance displacement tests showed that the utilization efficiency of crude oil in 0.1–1 μm micropores increased to 21.32%. Parallel dual-core flooding experiments further confirmed the selective plugging capability in heterogeneous systems with a permeability contrast of 10:1: The high-permeability layer (500 mD) achieved a plugging rate of 98.7%, while the recovery factor of the low-permeability layer increased by 13.6%. This gel system provides a green and efficient profile control solution for deep, high-temperature, high-salinity reservoirs. Full article
(This article belongs to the Special Issue Applications of Gels for Enhanced Oil Recovery)
Show Figures

Figure 1

14 pages, 1689 KB  
Article
Effect of Sulfoaluminate Clinker Addition on Boron Removal During Water Softening
by Marco Tagliabue, Alessandra de Folly d’Auris, Andrea Pacini, Michela Bellettato, Gianluigi Marra, Sara Perucchini, Cinzia Mazzara, Emanuele Lagrotta and Marco Vocciante
Appl. Sci. 2025, 15(16), 8890; https://doi.org/10.3390/app15168890 - 12 Aug 2025
Viewed by 559
Abstract
Boron is frequently present in saline water (e.g., seawater, geothermal water, and hydrocarbon production water) due to the natural release of boric acid from minerals. While essential to life, excess boron is toxic, particularly to citrus plants, necessitating its regulation for safe water [...] Read more.
Boron is frequently present in saline water (e.g., seawater, geothermal water, and hydrocarbon production water) due to the natural release of boric acid from minerals. While essential to life, excess boron is toxic, particularly to citrus plants, necessitating its regulation for safe water use. Current boron removal methods, such as reverse osmosis, chelating resin adsorption, and magnesium-based precipitation softening, increase water treatment complexity and cost. Ettringite, (Ca6Al2(SO4)3(OH)12·26H2O), is a clay and an effective anion adsorbent. It is also a key hydration product of Portland cement. This study explores boron removal via precipitation softening using sulfoaluminate clinker as an ettringite precursor. Raw water, a first-stage reverse-osmosis permeate from an Italian oil-and-gas site, contained approximately 15.0 mg/L of boron. Optimal removal required sulfoaluminate clinker in excess with respect to the stoichiometric dose and 150 min of contact time. The preliminary results demonstrate the feasibility of this approach, offering a viable alternative to existing methods. Full article
(This article belongs to the Special Issue New Approaches to Water Treatment: Challenges and Trends, 2nd Edition)
Show Figures

Graphical abstract

26 pages, 4818 KB  
Article
Novel Anion-Exchange Resins for the Effective Recovery of Re(VII) from Simulated By-Products of Cu-Mo Ore Processing
by Piotr Cyganowski, Pawel Pohl, Szymon Pawlik and Dorota Jermakowicz-Bartkowiak
Int. J. Mol. Sci. 2025, 26(15), 7563; https://doi.org/10.3390/ijms26157563 - 5 Aug 2025
Viewed by 1126
Abstract
The efficient recovery of rhenium (Re), a critical metal in high-tech industries, is essential to address its growing demand and reduce reliance on primary mining. In this study, we developed novel anion-exchange resins for the selective adsorption and recovery of Re(VII) ions from [...] Read more.
The efficient recovery of rhenium (Re), a critical metal in high-tech industries, is essential to address its growing demand and reduce reliance on primary mining. In this study, we developed novel anion-exchange resins for the selective adsorption and recovery of Re(VII) ions from acidic solutions, simulating industrial by-products. The resins were synthesized from a vinylbenzyl chloride-co-divinylbenzene copolymer modified with aliphatic, heterocyclic, and aromatic weakly basic amines, selected from among bis(3-aminopropyl)amine (BAPA), 1-(2-pyrimidinyl)piperazine (PIP), thiosemicarbazide (TSC), 2-amino-3-hydroxypyridine (AHP), 1-(2-hydroxyethyl)piperazine (HEP), 4-amino-2,6-dihydroxypyrimidine (AHPI), and 2-thiazolamine (TA). The adsorption of Re on BAPA, PIP, and HEP resins obeyed the Langmuir model, and the resins exhibited high adsorption capacities, with maximum values reaching 435.4 mg Re g−1 at pH 6. Furthermore, strong selectivity for ReO4 ions over competing species, including Mo, Cu, and V, was noted in solutions simulating the leachates of the by-products of Cu-Mo ores. Additionally, complete elution of Re was possible. The developed resins turned out to be highly suitable for the continuous-flow-mode adsorption of ReO4, revealing outstanding adsorption capacities before reaching column breakthrough. In this context, the novel anion-exchange resins developed offer a reference for further Re recovery strategies. Full article
Show Figures

Figure 1

12 pages, 6808 KB  
Communication
Research on Preventing High-Density Materials from Settling in Liquid Resin
by Lixin Xuan, Zhiqiang Wang, Xuan Yang, Xiao Wu, Junjiao Yang and Shijun Zheng
Materials 2025, 18(15), 3469; https://doi.org/10.3390/ma18153469 - 24 Jul 2025
Viewed by 443
Abstract
The applications of magnetic particles in anti-counterfeiting and anti-absorbing coatings and other functional materials are becoming increasingly widespread. However, due to their high density, the magnetic particles rapidly settle in organic resin media, significantly affecting the quality of the related products. Thereby, reducing [...] Read more.
The applications of magnetic particles in anti-counterfeiting and anti-absorbing coatings and other functional materials are becoming increasingly widespread. However, due to their high density, the magnetic particles rapidly settle in organic resin media, significantly affecting the quality of the related products. Thereby, reducing the density of the particles is essential. To achieve this goal, high-density magnetic particles were coated onto the surface of hollow silica using anion–cation composite technology. Further, the silane coupling agent N-[3-(trimethoxysilyl)propyl]ethylenediamine was bonded to the surface of magnetic particles to form an amino-covered interfacial layer with a pH value of 9.28, while acrylic acid was polymerized and coated onto the surface of hollow silica to form a carboxyl-covered interfacial layer with a pH value of 4.65. Subsequently, the two materials were compounded to obtain a low-density composite magnetic material. The morphologies and structural compositions of the magnetic composite materials were studied by FTIR, SEM, SEM-EDS, XRD, and other methods. The packing densities of the magnetic composite materials were compared using the particle packing method, thereby solving the problem of magnetic particles settling in the resin solution. Full article
Show Figures

Figure 1

15 pages, 2047 KB  
Article
Aluminum-Loaded Bifunctional Resins for Efficient Fluoride Removal from Aqueous Solutions
by Mengfei Ma, Yingpeng Gu, Ruijie Wang and Yue Sun
Appl. Sci. 2025, 15(14), 7829; https://doi.org/10.3390/app15147829 - 12 Jul 2025
Viewed by 863
Abstract
The deep defluorination of water remains a significant environmental challenge. In this work, aluminum was loaded onto the bifunctional resin S957 containing a phosphoric-sulfonic acid difunctional group for efficient fluoride removal. Al-S957 demonstrated excellent fluoride removal performance across a broad pH range. When [...] Read more.
The deep defluorination of water remains a significant environmental challenge. In this work, aluminum was loaded onto the bifunctional resin S957 containing a phosphoric-sulfonic acid difunctional group for efficient fluoride removal. Al-S957 demonstrated excellent fluoride removal performance across a broad pH range. When anions and organics coexisted, Al-S957 exhibited significantly better fluoride adsorption performance compared to aluminum-loaded monofunctional resins. The adsorption followed an endothermic chemisorption process on a monolayer surface. FTIR and XPS analyses further revealed that fluoride removal relied on a ligand exchange mechanism. Column adsorption conducted over five cycles highlighted the strong practical potential of Al-S957. The results suggested that Al-S957 exhibits significant potential for practical applications. Full article
(This article belongs to the Special Issue Advances in Pollutant Removal from Water Environments)
Show Figures

Figure 1

Back to TopTop