Search Results (160)

The efficient recovery of highly concentrated cadmium (44.55 g/L) from zinc smelting dust leachate is recognized as a significant metallurgical challenge. In this study, we focused on the selective separation of Cd from coexisting arsenic and zinc using trioctylamine (N235) as the extractant. Accordingly, key operational parameters including initial pH, extractant concentration, phase ratio, and temperature were optimized in a systematic manner. Under the optimized conditions of 30% N235, 15% TBP, and 55% sulfonated kerosene by volume, together with an initial pH of 0.5, an organic to aqueous phase ratio of 1 to 1, and a temperature of 20 °C, a three-stage countercurrent extraction process was found to dramatically enhance the Cd extraction efficiency to 99.80% while successfully rejecting As. Subsequently, stripping with 0.7 mol/L aqueous ammonia achieved an 81.4% stripping efficiency in a single stage, and washing with 1.0 mol/L HCl ensured complete regeneration of the organic solvent. Furthermore, Fourier transform infrared spectroscopy (FT-IR) and electrospray ionization mass spectrometry (ESI-MS) analyses corroborate that the extraction proceeds via an anion exchange mechanism. Specifically, within the chloride rich acidic environment, protonated N235 was shown to preferentially coordinate with the tetrachlorocadmate anion CdCl₄²⁻ to form the highly stable and lipophilic complex (R₃NH)₂CdCl₄. Overall, this work provides a scalable technological framework and a robust theoretical foundation for the extraction of highly concentrated heavy metals from complex secondary metallurgical resources. Full article

Metal–organic frameworks (MOFs) exhibit high specific surface area and porosity, which may facilitate electron transfer during electrochemical reactions. Therefore, it is clear that MOFs are promising materials for the development of electrochemical sensors. In particular, zinc (Zn) based MOFs offer several advantages such as high specific surface area, porosity, environmental friendliness and low cost. Thus, Zn-based MOF materials and their composites have been extensively utilized in the detection of various pollutants, biomolecules and food additives. The Zn-MOF-based materials have been extensively utilized in electrochemical and fluorescence sensing applications. Previously, various Zn-MOF-based sensing systems such as pristine Zn-MOF, carbon-supported Zn-MOF composites, MXene hybrids with Zn-MOF, and bimetallic/trimetallic Zn-based MOFs were explored to enhance sensing performance. Such materials exhibit remarkable analytical performance, such as a low limit of detection (LOD) (nM to pM range), wide linear response range (LR), fast response times, and high selectivity in the presence of interfering species. In electrochemical sensing, Zn-MOF-modified electrodes demonstrated improved charge-transfer kinetics and sensitivity, enabling accurate determination of the biomolecules, drugs and heavy metal ions in real samples. Similarly, Zn-MOF-based fluorescence sensors showed high luminescent properties and displayed sensitive detection of pollutants and biomolecules. Despite such promising sensing performances, some challenges, such as low stability, reproducibility and selectivity in real-time monitoring, etc., remain that need to be overcome. This review article summarizes the previously reported literature on the fabrication of Zn-MOFs, their composites and Zn-MOF-derived materials for the development of electrochemical and fluorescence sensors. We have also discussed the future directions for the rational design of the high-performance Zn-MOF-based sensing systems for environmental and biomedical applications. We believe that the present review article would be useful for the scientific community working on the fabrication of Zn-MOF-based sensors. Full article

Background/Objectives: Attention-deficit/hyperactivity disorder (ADHD) is increasingly recognized as a neurodevelopmental condition shaped by early-life biological and environmental factors. Emerging evidence highlights the role of nutrition in modulating key brain processes involved in ADHD, from gestational development through childhood. This review aims to examine how dietary interventions influence neuroimaging outcomes in individuals with ADHD, assessing whether nutritional approaches can modulate brain structure, function, or connectivity. Methods: A systematic search of PubMed, Scopus, and Web of Science was conducted to identify studies examining the effects of dietary interventions on neuroimaging outcomes in individuals with ADHD. Study quality was assessed using Cochrane RoB 2.0, ROBINS-I, the Newcastle–Ottawa Scale, and the JBI Critical Appraisal Checklist, according to study design. Results: A total of 1059 records were identified, and 4 studies met the final inclusion criteria. The included studies suggest that prenatal vitamin D exposure, omega-3 fatty acids, and micronutrients such as zinc may be associated with structural, functional, and neurometabolic brain characteristics relevant to ADHD. Reported findings included associations with brain volume, glutamatergic regulation, white matter organization, resting-state network integrity, and inattentive symptom. Conclusions: Current evidence supports the hypothesis that nutrition may influence neurodevelopmental processes involved in ADHD, including brain maturation and neural network organization. Although findings remain heterogeneous and limited in number, nutrition appears to represent a biologically plausible and potentially modifiable factor within the developmental framework of ADHD. Further longitudinal and multimodal neuroimaging studies are needed to clarify the mechanisms linking nutrition, brain development, and ADHD. Full article

Fundamental understanding of the biomass pyrolysis process on a molecular level provides important guidelines for designing advanced porous carbon materials. In this study, the effects of KOH and K₂CO₃ activators on the thermal decomposition of agarose were elucidated using TG-FTIR-GCMS coupling techniques. The results demonstrate that the presence of KOH/K₂CO₃ shifts the pyrolysis gaseous products from organic fragments to CO₂ and H₂O, thereby preserving more C-C bonds in the solid phase and facilitating the subsequent aromatization process. Furthermore, compared to using KOH as the sole activator, the K₂CO₃/KOH co-activation strategy suppresses the violent evolution of CO₂ within the 300–400 °C range, thereby alleviating the structural shock to the material skeleton and ensuring its integrity. Therefore, the HPC-KCO prepared via a synergistic KOH/K₂CO₃ co-activation and one-step carbonization process exhibits a high specific surface area of 1670 m² g⁻¹ and successfully retains its interconnected hierarchical porous framework. Benefiting from its well-developed porous structure, HPC-KCO exhibits an impressive specific capacitance of 370 F g⁻¹ when employed in zinc-ion capacitors. Furthermore, the assembled symmetric supercapacitor demonstrates robust stability over a wide temperature range from −60 to 100 °C, delivering a remarkable capacitance of 121 F g⁻¹ even at −60 °C. This work offers a new insight for synthesizing porous structures of biomass-derived carbon. Full article

The growing concern over greenhouse gas emissions has prompted the need for efficient carbon dioxide (CO₂) capture technologies. This study focuses on simulating CO₂ adsorption using a zinc-based metal–organic framework (Zn-MOF-5). The primary aim is to develop and refine a robust MATLAB-based approach for equilibrium and kinetic modelling using the Linear Driving Force (LDF) model and Langmuir isotherm, capable of accurately predicting CO₂ adsorption performance under varying operational conditions. By employing advanced computational methods, this research seeks to streamline the process design and enhance the feasibility of sustainable CO₂ capture solutions. Excel was used for statistical analysis and validation, while MATLAB R2025a was utilised for equilibrium and kinetic modelling using the LDF model and the Langmuir isotherm. The independent effects of temperature, pressure, and flow rate were evaluated using the variable effect method. The study found a significant negative association between temperature and CO₂ uptake, consistent with the exothermic nature of the adsorption process. Pressure had a significant impact on adsorption, whereas flow rate had little effect within the investigated range. The simulated CO₂ uptake (21.196 mmol/g) closely matched the experimental data (21.07 mmol/g) with a 0.59% variance, validating the model’s trustworthiness. The research shows that Zn-MOF-5 has a strong adsorption potential and that simulation tools can significantly minimise experimental costs and time. Furthermore, it underscores the potential of simulation tools to significantly reduce experimental costs and time, paving the way for more efficient and effective carbon capture solutions. This initiative not only contributes to optimising process design but also promotes sustainable practices in addressing global CO₂ emissions. By contributing to process optimisation, this study aligns with the United Nations Sustainable Development Goal (SDG) 13: Climate Action, which emphasises the urgent need for innovative solutions to combat climate change and its impacts. Furthermore, it promotes sustainable practices to address global CO₂ emissions, thereby supporting broader efforts for environmental sustainability. Full article

Effective regulation of the adsorption strength of oxygen reduction reaction (ORR) intermediates on active sites is the key to enhancing their catalytic performance. This study proposes an axial coordination modulation strategy by successfully anchoring the dioxin-linked FePcF₁₆-based covalent organic frameworks (COFs) onto amino-functionalized multi-walled carbon nanotubes (NH₂-MWCNTs), constructing a FePcF₁₆-COF/NH₂-MWCNT hybrid catalyst. Experimental results demonstrate that the catalyst exhibits outstanding ORR activity (E_1/2 = 0.901 V; J_L = 5.133 mA cm⁻²), outperforming commercial 20% Pt/C and most reported Fe-based non-precious metal catalysts. Furthermore, the robust dioxin-linked COF skeleton endows the catalyst with excellent electrochemical stability. A zinc–air battery using this catalyst as the cathode also demonstrates superior power density and cycling performance. This work provides a new strategy for designing highly efficient ORR catalysts through axial coordination environment engineering. Full article

Background/Objectives: Carbonic anhydrase I (CAI) is a zinc-dependent metalloenzyme whose inhibitor discovery requires both effective navigation of chemical space and explicit evaluation of coordination-credible binding hypotheses. We aimed to develop an interpretable and reproducible QSAR-to-structure workflow for CAI inhibitor discovery. The workflow links potency prediction with zinc-site plausibility and early developability to support decision-oriented prioritization of new CAI inhibitor candidates. Methods: CAI inhibitors were retrieved from ChEMBL (CHEMBL261) and modeled as $p{K}_i=9-{\mathrm{l}\mathrm{o}\mathrm{g}}_{10}(K_i [\mathrm{n}\mathrm{M}\left]\right)$. AlvaDesc v3.0.8 generated 4224 2D descriptors, which were reduced using train-only preprocessing, variance filtering, correlation pruning, and bagged-tree ranking to a top-100 panel. Five regressors (elastic net, CART, bagging, GB, and XGB) were benchmarked on a held-out test set. Potent ChEMBL seeds (K_i ≤ 10 nM) were used for a 90% 2D similarity PubChem expansion. Predicted hits were then externally validated using independently available PubChem CAI $K_i$ records. Ten novel candidates lacking CAI $K_i$ data were docked to CAI (PDB: 1AZM) via SwissDock AutoDock Vina in neutral and relevant anionic states, with pose selection constrained by a Zn-donor filter (Zn-N/O $\le 2.6$ Å). SwissADME was used to profile physicochemical space, alerts, and absorption/distribution proxies. Results: The bagging model showed the best test generalization ($R^2=0.646$; RMSE = 0.61; MAE = 0.45). PFI and SHAP converged on sulfur/heteroatom connectivity and polar–lipophilic organization as dominant potency drivers. PubChem expansion yielded 25,315 analogs and 233 candidates at predicted $p{K}_i\ge 8.0$; external validation on 145 CAI-measured hits gave $R^2=0.358$ (RMSE = 0.456; MAE = 0.320). Across 20 ligand/protomer docking runs, 12 produced canonical Zn-anchored poses (10 Zn-N; 2 Zn-O). SwissADME indicated consensus logP values from −0.65 to 3.21, 0/10 PAINS alerts, and predominantly favorable drug-likeness (8/10 with zero Lipinski violations), supporting tiered advancement. Conclusions: Integrating interpretable QSAR, external PubChem validation, coordination-aware docking, and SwissADME yields a practical triage framework for CAI inhibitor discovery. The resulting tiered shortlist identifies two Zn-N-anchored N-alkyl sulfamides (CIDs 103935964 and 112684680) and one Zn-O-anchored carboxylate control (CID 122367674) as highest-priority computational hypotheses for staged biochemical evaluation. Full article

The increasing presence of microplastics in the aquatic and terrestrial food chains calls for the need to come up with innovative and effective remediation approaches. Such innovations as zinc oxide (ZnO) structures and metal–organic frameworks (MOFs) are examined as the second generation of photocatalysts for degrading microplastics under sunlight. We will focus on the latest advances and discuss the structure of photocatalytic processes, their functioning under various light conditions, and their environmental impacts, especially environmental safety and ecotoxicity. ZnO structures are even better photocatalysts because they form reactive oxygen species (ROS) as good as other metal oxides. However, their possible cytotoxicity and the ability to generate oxidative stress require serious evaluation. MOFs, on the contrary, offer physicochemical properties, environmental safety, ecotoxicity, and environmentally friendly synthesis pathways, making them a worthy substitute. The review underscores the urgency of incorporating environmental safety and ecotoxicity into the design of photocatalysts, thereby unlocking their full potential while avoiding environmental or human health risks. Moving forward in the field of sustainable nanotechnology to remove microplastics will provide the way to come up with green innovations and hence guarantee the effectiveness of combating plastic pollution in long-term stability. Full article

Two zinc(II)-trimesate metal–organic frameworks were synthesized under hydrothermal conditions and structurally characterized by single-crystal X-ray diffraction. Although both compounds originate from the same Zn(II)-benzene-1,3,5-tricarboxylate (BTC) chemical system, they crystallize in different space groups and exhibit distinct coordination environments and secondary building units (SBUs). One framework adopts a cubic structure and is built from a binuclear Zn paddlewheel type SBU, characterized by a short Zn–Zn internuclear distance and four μ₂-bridging carboxylate groups. In contrast, the second framework crystallizes in a tetragonal lattice and features mixed Zn(II) coordination environments, with the coexistence of tetrahedral and octahedral metal centers assembled into a fundamentally different SBU. The comparison between these two structures highlights the coordination flexibility of Zn(II) and the sensitivity of Zn–BTC frameworks to crystallization conditions, such as solvent composition. These results underline the importance of detailed crystallographic analysis in revealing SBU diversity and provide insight into how variations in local coordination chemistry can lead to distinct framework architectures from identical chemical building blocks. Full article

Manganese-based cathodes offer high capacity, low cost, and safety for aqueous zinc-ion batteries (AZIBs), yet suffer from Mn dissolution, Jahn–Teller distortion, and sluggish Zn²⁺ kinetics. Herein, a Zn/Co co-doped MnO nanoporous carbon composite (denoted as ZnCo-MnO@NPC) derived from a bimetallic ZnCoMn metal–organic framework (ZnCoMn-MOF-74) is successfully synthesized and proposed as a high-performance cathode to address these challenges. The introduction of Zn²⁺ increases the initial specific capacity of MnO, while Co doping effectively suppresses the Jahn–Teller distortion and improves the integrity of the structure. Furthermore, the nanoporous carbon matrix facilitates electrolyte infiltration and accelerates ionic transport. To further suppress dendrite growth and enhance cycling stability, a zeolitic imidazolate framework (ZIF-8) protective layer is engineered on the zinc anode (denoted as ZIF-8@Zn), effectively mitigating dendrite formation. The ZnCo-MnO@NPC//ZIF-8@Zn full cell demonstrates superior electrochemical performance, delivering 281.3 mAh g⁻¹ at 0.1 A g⁻¹ and retaining 98.7% of this value after 3500 long-term cycles at 2.0 A g⁻¹, a remarkable finding that underscores its potential for high-performance energy storage. Collectively, this work highlights that transition metal ion doping represents an effective way to design efficient high-performance MOF-derived cathodes of AZIBs. Full article

High-sensitivity rapid detection of ammonia (NH₃) in environmental monitoring, industrial safety, early diagnosis, and other fields is of great significance. Covalent organic frameworks (COFs) have shown great potential in the field of gas sensing due to their designable porous structure and active sites. However, the traditional solvothermal synthesis method of COFs has problems such as cumbersome steps, high energy consumption and serious environmental pollution. Therefore, it is of great significance to invent a new method for COF synthesis that is green and efficient and makes it easy to conduct flexible ammonia gas sensing. This study first reported a solvent-free synthesis of imine connection 1,3,5-Triformylbenzene (TFB) and p-Phenylenediamine (PDA)—a new strategy for COF. This method innovatively employs zinc trifluoromethyl sulfonate (Zn(OTf)₂) as a bifunctional catalyst. This catalyst not only efficiently catalyzes para-phenylenediamine, but its zinc ions also play a unique structural guiding role, guiding the reactants to be arranged in a directional manner, thereby constructing a highly ordered porous crystal structure. A series of characterizations confirmed that the obtained TFB-PDA-COF had good crystallinity and a high proportion of imine bonds (C=N). The powder material was coated onto a flexible polyimide (PI) substrate, successfully constructing a resistive ammonia gas sensor that operates at room temperature. The test results show that this sensor has a high response value, rapid response/recovery capability, and good selectivity for ammonia gas. More importantly, based on a flexible PI substrate, the device can maintain stable sensing performance even under repeated bending conditions, demonstrating its great potential in practical flexible electronic applications. This work not only provides a brand-new “zinc ion-guided” paradigm for the green and controllable synthesis of COF but also lays a material foundation for their application in the next-generation flexible sensing field. Full article

Aqueous redox flow batteries (ARFBs) are a promising solution for large-scale energy storage; however, the development of organic posolytes that combine high redox potential with long-term stability remains a significant hurdle. This study introduces sodium 3-(10H-phenoxazin-10-yl)propane-1-sulfonate (POZS), a novel sulfonate-functionalized phenoxazine derivative designed to overcome these limitations. By incorporating hydrophilic anionic sulfonic groups, this molecular engineering strategy enhances the structural stability of redox-active phenoxazine materials. Although POZS shows limited solubility in pure water, its solubility increases to 0.98 M (equivalent to a charge capacity of 26.3 Ah L⁻¹) upon the addition of 1.5 M tetraethylammonium chloride (TEAC). This enhancement suggests that the supporting electrolyte optimizes the ionic environment and mitigates intermolecular aggregation, thereby facilitating higher active species concentration. Electrochemical characterization of POZS reveals a highly positive redox potential of 1.51 V (vs. Zn/Zn²⁺) and rapid electron transfer kinetics (2.02 × 10⁻² cm s⁻¹). When tested in a zinc-based hybrid flow cell, the POZS posolyte demonstrates excellent rate capability (up to 50 mA cm⁻²) and a temporal capacity fade rate of 0.335% per hour over 500 cycles—a nearly five-fold improvement over previously reported quaternized phenoxazines. Post-cycling analyses indicate that while the phenoxazine core remains susceptible to nucleophilic ring substitution, the pendant sulfonate groups ensure that any resulting byproducts remain soluble, preventing the catastrophic depletion typically caused by the precipitation of degraded active species. These findings establish a robust molecular framework for the design of high-potential, durable organic posolytes for sustainable energy storage systems. Full article

Biomineralization has recently emerged as a highly effective strategy for enzyme immobilization. Zeolitic imidazolate frameworks (ZIFs), a subclass of metal–organic frameworks (MOFs), are particularly attractive carriers due to their structural tunability and chemical stability. While ZIF-8 has been extensively studied, its denser and thermodynamically more stable analog ZIF-zni has received far less attention. In this work, we report the biomineralization of glucose oxidase (GOx) from Aspergillus niger within the ZIF-zni framework and systematically investigate the influence of zinc and imidazole (Im) concentration on immobilization performance. The optimized biocomposite, obtained at 10 mM Zn²⁺ and a Zn:Im ratio of 1:10, exhibited a specific activity of 2051 IU g⁻¹, which is more than twice the activity obtained for GOx@ZIF-8 in our previous study (874 IU g⁻¹). Furthermore, the GOx@ZIF-zni biocomposite demonstrated remarkable resistance to sodium dodecyl sulfate (SDS) and retained up to 50% of its activity after incubation at 65 °C for one hour. These results demonstrate that ZIF-zni is a highly promising carrier for enzyme immobilization and suggest that framework topology and synthesis conditions play a crucial role in determining the catalytic performance and stability of enzyme@MOF biocomposites. Full article

p-Nitrophenol (PNP) and bis(4-nitrophenyl) phosphate (BNPP), as typical persistent and toxic organic contaminants, present significant risks to both ecological systems and human health. Accurately quantifying these compounds using luminescent sensors remains a formidable task. In this study, we successfully synthesized a zinc-based metal–organic framework (Zn-MOF) that functions as a luminescent sensing material. The synthesized Zn-MOF demonstrates exceptional dual-response luminescent detection toward PNP and BNPP, with detection limits as low as 3.49 × 10⁻⁶ and 8.43 × 10⁻⁶ mol/L, respectively. The sensor maintains high selectivity and functionality even in the presence of various potentially interfering substances commonly found in complex environmental samples. Moreover, the material can be fabricated into a visual sensing film, greatly facilitating its application in on-site rapid detection scenarios. Overall, this work introduces a novel luminescent sensor platform that enables fast and reliable monitoring of PNP and BNPP in environmental contexts, demonstrating strong potential for integration into real-time surveillance and early warning systems. Full article

The urgent need to mitigate carbon dioxide (CO₂) emissions from fossil-fuel-based electricity generation has driven research into advanced materials for post-combustion carbon capture. This paper presents a modified solvothermal technique to synthesize zinc (Zn) and magnesium (Mg) based MOF-74 suitable for CO₂ capture from coal-fired power plants. The materials were synthesized through a solvothermal method using N,N-dimethylformamide (DMF) as the primary solvent, and subsequently characterized using Brunauer–Emmett–Teller (BET) surface area analysis, Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), and thermogravimetric analysis (TGA). Both MOFs contained oxygen-containing functional groups and were thermally stable up to 430 °C and 600 °C respectively, making them ideal for carbon capture. The low-pressure N₂-BET surface areas were 55 m²/g and 24.73 m²/g. In conclusion, the Zn material had a mesoporous structure, making it more favorable for carbon capture. It was found that prolonged synthesis time weakened the MOF structure. Future work should experimentally evaluate CO₂ capture from coal-derived flue gas using Zn/Mg-MOF-74 materials, investigating adsorption behavior and kinetics through isotherm and kinetic models, while also assessing the effect of varying Zn: Mg ratios under optimized synthesis conditions. Full article