Search Results (101)

Metal-organic frameworks (MOFs) offer high porosity for water remediation but face challenges in handling as powders. We address these limitations by physically immobilizing Fe–BTC MOF within calcium-crosslinked low-methoxyl pectin matrices (PE–Ca–MOF). Solvent-cast films and freeze-dried foams were fabricated using water-based and polyvinylpyrrolidone (PVP)-assisted Fe–BTC dispersions, preserving MOF and pectin structures confirmed by FT–IR. PVP improved Fe–BTC dispersion and reduced particle size, enhancing distribution and plasticizing the matrix proved by DSC. Incorporation of water-dispersed Fe–BTC increased the equilibrium adsorption capacity but reduced the initial adsorption rate, while the PVP-assisted foam further enhanced uptake in comparative batch tests through its more open porous structure. At pH 7, PE–Ca–5%MOF films showed high adsorption capacities and removal efficiencies for paraquat (35.5 mg/g, 70.6%) and tetracycline (14.5 mg/g, 46.8%), while maintaining Zn²⁺ uptake compared to calcium-pectin films without MOF. Adsorption followed pseudo-first-order kinetics and Langmuir isotherms. Green regeneration with acetic acid enabled >80% capacity retention over five adsorption–desorption cycles. Foam architectures increased porosity and active-site accessibility (SEM), improving performance even at lower MOF loadings. Overall, controlling MOF dispersion and composite morphology enables efficient, reusable, and environmentally friendly bio-based adsorbents for water purification. Full article

Metal–organic framework (MOF) materials were extensively studied in the removal of pollutants in wastewater. However, catalysts in the powder form usually suffered from the strong tendency to agglomerate and the intricate operation for recycling, which significantly limited their practical application. In comparison, monolithic catalysts with their high macroscopic operability and recoverability as well as impressive specific surface area have attracted tremendous attention in recent years. To address these issues, a monolithic Fe-based catalyst was prepared via in situ synthesis, using nickel–iron foam (NFF) as the substrate with cobalt (Co) incorporation. XPS analysis showed that Co doping enhanced the synergistic interaction among Fe, Ni, and Co, accelerating the redox cycle among species, thus improving electron transfer and laying a kinetic foundation for efficient peroxymonosulfate (PMS) activation. Quenching experiments and EPR indicated singlet oxygen (¹O₂) as the main reactive species; Co doping shifted the degradation pathway from radicals to non-radicals. Under optimized conditions (PMS: 0.08 mmol/L; catalyst: 1 cm²; initial Chlortetracycline (CTC): 50 mg/L), 95.7% CTC degradation was achieved within 60 min, and efficiency only dropped to 90.5% after 5 cycles. This catalyst provided theoretical and technical support for the application of monolithic MOF-derived catalysts and highly efficient PMS activators. Full article

It is well known that nitrite is widely used in industrial and agricultural sectors as a preservative, corrosion inhibitor, and intermediate in chemical synthesis; consequently, nitrite residues are often present in food, water, and the environment as a result of meat curing, fertilizer use, and wastewater discharge. Despite having several applications, nitrite exerts toxic effects on human beings and aquatic life. Therefore, the monitoring of nitrite is of particular significance to avoid negative impacts on human health, the environment, and aquatic life. Previously, the electrochemical method has been extensively used for the development of nitrite sensors using various advanced electrode materials. Additionally, zinc oxide (ZnO), cerium oxide (CeO₂), titanium dioxide (TiO₂), copper oxide (CuO), iron oxides, nickel oxide (NiO), polymers, MXenes, reduced graphene oxide (rGO), carbon nanotubes (CNTs), graphitic carbon nitride (gCN), metal–organic frameworks (MOFs), and other composites have been utilized as electrocatalysts for the fabrication of nitrite electrochemical sensors. This review article provides an overview of the construction of nitrite sensors using advanced electrode materials. The electrochemical activities of the reported nitrite sensors are discussed. Furthermore, limitations and future perspectives regarding the determination of nitrite are discussed. Full article

Soil degradation and pollution pose significant threats to global agricultural sustainability and food security. Conventional remediation methods are often constrained by low efficiency, high cost, and potential secondary pollution. Nanobiotechnology, an emerging interdisciplinary field, offers innovative solutions by integrating functional nanomaterials with plant–microbe interactions to advance soil remediation and sustainable agriculture. This review systematically elaborates on the mechanisms and applications of nanomaterials in soil remediation and enhanced plant stress resilience. For contaminant removal, nanomaterials such as nano-zero-valent iron (nZVI) and carbon nanotubes effectively immobilize or degrade heavy metals and organic pollutants through adsorption, catalysis, and other reactive mechanisms. In agriculture, nanofertilizers facilitate the regulated release of nutrients, thereby markedly enhancing nutrient use efficiency. Concurrently, certain nanoparticles mitigate a range of abiotic stresses—such as drought, salinity, and heavy metal toxicity—through the regulation of phytohormone balance, augmentation of photosynthetic performance, and reinforcement of antioxidant defenses. However, concerns regarding the environmental behavior, ecotoxicity, and long-term safety of nanomaterials remain. Future research should prioritize the development of smart, responsive nanosystems, elucidate the complex interactions among nanomaterials, plants, and microbes, and establish comprehensive life-cycle assessment and standardized risk evaluation frameworks. These efforts are essential to ensuring the safe and scalable application of nanobiotechnology in environmental remediation and green agriculture. Full article

Basolite^® F300 and synthetic nano-{Fe-BTC} MOFs, two iron-trimesate MOFs, have been investigated, demonstrating broad pH range adsorption for monomethylarsenate (MMA), cacodylic acid (DMAA), 4-aminophenylarsonate (ASA), and arsenate, while arsenite adsorption was notable at pH > 9.5. A similar uptake trend was found for both MOFs, with Basolite^® F300 being the more effective given its higher porosity and greater surface area. Pseudo-second-order kinetic models were followed by MMA, DMAA, ASA, and As(V), suggesting a chemisorption mechanism with arsenic species diffusion into MOF pores as the controlling step. Equilibrium data for DMAA and ASA fit the Langmuir model whereas MMA adsorption fits the Redlich–Peterson model. The uptake of MMA, DMAA, and ASA by both Fe-MOFs is mainly attributed to their coordination with Fe(III). Aromatic units in ASA enhance adsorption through П-П stacking interactions. The competition between all arsenic species for the sorption sites of the Fe-MOFs led to an uptake decrease of 10% for MMA and ASA and higher than 30% for DMAA and As(V) with respect to the individual uptakes. The Fe-MOFs can be reused for four cycles by washing with acidic methanol. Basolite^® F300 and synthetic nano-{Fe-BTC} effectively removed organic and inorganic arsenic species, exhibiting rapid adsorption, selective uptake, stability, and easy regeneration. Full article

Coagulation–flocculation, historically reliant on simple inorganic salts, has evolved into a technically sophisticated process that is central to the removal of turbidity, suspended solids, organic matter, and an expanding array of micropollutants from complex wastewaters. This review synthesizes six decades of research, charting the transition from classical aluminum and iron salts to high-performance polymeric, biosourced, and hybrid coagulants, and examines their comparative efficiency across multiple performance indicators—turbidity removal (>95%), COD/BOD reduction (up to 90%), and heavy metal abatement (>90%). Emphasis is placed on recent innovations, including magnetic composites, bio–mineral hybrids, and functionalized nanostructures, which integrate multiple mechanisms—charge neutralization, sweep flocculation, polymer bridging, and targeted adsorption—within a single formulation. Beyond performance, the review highlights persistent scientific gaps: incomplete understanding of molecular-scale interactions between coagulants and emerging contaminants such as microplastics, per- and polyfluoroalkyl substances (PFAS), and engineered nanoparticles; limited real-time analysis of flocculation kinetics and floc structural evolution; and the absence of predictive, mechanistically grounded models linking influent chemistry, coagulant properties, and operational parameters. Addressing these knowledge gaps is essential for transitioning from empirical dosing strategies to fully optimized, data-driven control. The integration of advanced coagulation into modular treatment trains, coupled with IoT-enabled sensors, zeta potential monitoring, and AI-based control algorithms, offers the potential to create “Coagulation 4.0” systems—adaptive, efficient, and embedded within circular economy frameworks. In this paradigm, treatment objectives extend beyond regulatory compliance to include resource recovery from coagulation sludge (nutrients, rare metals, construction materials) and substantial reductions in chemical and energy footprints. By uniting advances in material science, process engineering, and real-time control, coagulation–flocculation can retain its central role in water treatment while redefining its contribution to sustainability. In the systems envisioned here, every floc becomes both a vehicle for contaminant removal and a functional carrier in the broader water–energy–resource nexus. Full article

In the search for new materials to open up creative pathways for industry and research, modification is one of the best methods to implement. Developing materials with high sensitivity and selectivity for specific applications, such as ion sensing, remains a significant challenge. This work aims to introduce a novel metal–organic framework (MOF) derived from the well-established 2-amino-[1,1′-biphenyl]-4,4′-dicarboxylic acid MOF by modifying its structure to enhance its properties and applications. A luminescent 2-naphthyl moiety was attached to the amino group of the linker to form the new luminescent Al-based MOF Al-BP-Naph with a surface area of 456 m² g⁻¹ and a pore volume of 0.55 cm³ g⁻¹. Al-BP-Naph showed high selectivity towards Fe³⁺ sensing due to the overlapping absorption and excitation spectra of both Fe³⁺ and MOF. The MOF demonstrated a detection limit of approximately 6 × 10⁻⁶ mol L⁻¹ with a limit of quantification of about 19 × 10⁻⁶ mol L⁻¹ and a very fast response time (less than 10 s). It also had a Stern–Volmer constant of approximately 0.09 × 10⁵ L mol⁻¹, distinguishing it from other ions. Our work contributes to the expanding repertoire of functional materials with promising applications in sensing technologies, offering a novel MOF with superior properties for iron(III) ion detection. Full article

This study presents a novel dual-temperature synthesis strategy for cobalt, zinc, and iron-based metal–organic frameworks (MOFs) integrated with tannic acid (TA) surface modification to enhance oxygen evolution reaction (OER) performance. MOFs were synthesized at room temperature and 80 °C, enabling controlled crystal growth and distinct morphologies. Subsequent TA treatment effectively tuned surface chemistry without altering core crystallinity, as confirmed by PXRD, FT-IR, and XPS analyses. Surface modification introduced oxygen-containing functional groups, improved charge transfer, and increased active-site accessibility. Among the catalysts, the tannic acid-modified Fe-based MOF synthesized at 80 °C (TAFeM-2) exhibited outstanding OER activity, achieving an overpotential of only 254 mV at 10 mA cm⁻², outperforming benchmark RuO₂ (276 mV) and unmodified counterparts. Tafel slope analysis revealed faster reaction kinetics for surface-tuned MOFs, while electrochemical impedance spectroscopy indicated reduced charge-transfer resistance (12 Ω for TAFeM-2). Chronoamperometry demonstrated exceptional long-term stability, maintaining constant current density over 20 h with minimal performance loss. Post-OER characterization suggested surface oxidation to iron oxyhydroxides without significant structural degradation. This work demonstrates that combining dual-temperature synthesis with TA surface engineering yields MOF-based catalysts with superior activity, conductivity, and durability, offering a promising pathway for developing high-performance electrocatalysts for sustainable energy applications. Full article

Arsenic (As) and cadmium (Cd) in rice grains are major global food safety concerns. Iron (Fe) can help reduce both, but current Fe treatments suffer from poor stability, low leaf absorption, and fast soil immobilization, with unclear underlying mechanisms. To address these issues, an Fe-based metal–organic framework (MIL-88) was modified with sodium alginate (SA) to form MIL-88@SA. Its stability as a foliar inhibitor and its leaf absorption were tested, and its effects on As and Cd accumulation in rice were compared with those of soluble Fe (FeCl₃) and chelating Fe (HA + FeCl₃) in a field study on As–Cd co-contaminated rice paddies. Compared with the control, MIL-88@SA outperformed or matched the other Fe treatments. A single foliar spray during the tillering stage increased the rice yield by 19% and reduced the inorganic As and Cd content in the grains by 22.8% and 67.8%, respectively, while the other Fe treatments required two sprays. Its superior performance was attributed to better leaf affinity and thermal stability. Laser ablation inductively coupled plasma–mass spectrometry (LA–ICP–MS) and confocal laser scanning microscopy (CLSM) analyses revealed that Fe improved photosynthesis and alleviated As–Cd stress in leaves, MIL-88@SA promoted As and Cd redistribution, and Fe–Cd co-accumulation in leaf veins enhanced Cd retention in leaves. Full article

The sludge produced by the Fenton process contains mixed-valence iron particulates (hereafter called Fenton wastes). Using a solvothermal method, we fabricated a new heterogeneous photo-Fenton catalyst using Fenton wastes and metal–organic frameworks (MOFs). Nanoporous metal carboxylate (MIL-88) MOF impregnated with Fenton waste was functionalized using 2,5-dihydroxyterephthalic acid (x-HO-MIL-88-C, x, concentration of the 2,5-dihydroxyterephthalic acid). The efficiency of x-HO-MIL-88-C was examined under visible light radiation using methylene blue (MB) as an index pollutant. We observed the best catalytic performance for MB degradation by 4-HO-MIL-88-C. In the photo-Fenton process, the simultaneous presence of singlet oxygen, superoxide, and hydroxyl radicals is confirmed by free radical quenching and electron spin resonance spectral data. These free radicals associate with holes in the non-selective degradation of MB. The 4-HO-MIL-88-C catalyst shows good stability and reusability, maintaining over 80% efficiency at the end of five consecutive cycles. This work opens up a new path for recycling Fenton wastes into usable products. Full article

The phototherapeutic applications of porphyrin-based nanoscale metal–organic frameworks (nMOFs) are limited by the poor penetration of conventional excitation light sources into biological tissues. Radiodynamic therapy (RDT), which directly excites photosensitizers using X-rays, can overcome the issue of tissue penetration. However, RDT faces the problems of low energy conversion efficiency, requiring a relatively high radiation dose, and the potential to cause damage to normal tissues. Researchers have found that by using some metals with high atomic numbers (high Z) as X-ray scintillators and coordinating them with porphyrin photosensitizers to form MOF materials, the excellent antitumor effect of radiotherapy (RT) and RDT can be achieved under low-dose X-ray irradiation, which can not only effectively avoid the penetration limitations of light excitation methods but also eliminate the defect issues associated with directly using X-rays to excite photosensitizers. This review summarizes the relevant research work in recent years, in which researchers have used metal ions with high Z, such as Hf⁴⁺, Th⁴⁺, Ta⁵⁺, and Bi³⁺, in coordination with carboxyl porphyrins to form MOF materials for combined RT and RDT toward various cancer cells. This review compares the therapeutic effects and advantages of using different high-Z metals and introduces the application of the heavy atom effect. Furthermore, it explores the introduction of a chemodynamic therapy (CDT) mechanism through iron coordination at the porphyrin center, along with optimization strategies such as oxygen delivery using hemoglobin to enhance the efficacy of these MOFs as radiosensitizers. This review also summarizes the potential of these materials in preclinical applications and highlights the current challenges they face. It is expected that the summary and prospects outlined in this review can further promote preclinical biomedical research into and the development of porphyrin-based nMOFs. Full article

The bioavailability of heavy metals is profoundly influenced by their interactions with active soil components (microorganisms, organic matter, and iron minerals). However, the effects of urease-producing bacteria combined with organo-Fe hydroxide coprecipitates (OFCs) on Cd accumulation in wheat, as well as the mechanisms underlying these effects, remain unclear. In this study, pot experiments integrated with high-throughput sequencing were employed to investigate the impacts of the urease-producing bacterial strain TJ6, ferrihydrite (Fh), and OFCs on Cd enrichment in wheat grains, alongside the underlying soil–microbial mechanisms. The results demonstrate that the strain TJ6-Fh/OFC consortium significantly (p < 0.05) reduced (50.1–66.7%) the bioavailable Cd content in rhizosphere soil while increasing residual Cd fractions, thereby decreasing (77.4%) Cd accumulation in grains. The combined amendments elevated rhizosphere pH (7.35), iron oxide content, and electrical conductivity while reducing (14.5–21.1%) dissolved organic carbon levels. These changes enhanced soil-colloid-mediated Cd immobilization and reduced Cd mobility. Notably, the NH₄⁺ content and NH₄⁺/NO₃⁻ ratio were significantly (p < 0.05) increased, attributed to the ureolytic activity of TJ6, which concurrently alkalinized the soil and inhibited Cd uptake via competitive ion channel interactions. Furthermore, the relative abundance of functional bacterial taxa (Proteobacteria, Gemmatimonadota, Enterobacter, Rhodanobacter, Massilia, Nocardioides, and Arthrobacter) was markedly increased in the rhizosphere soil. These microbes exhibited enhanced abilities to produce extracellular polymeric substances, induce phosphate precipitation, facilitate biosorption, and promote nutrient (C/N) cycling, synergizing with the amendments to immobilize Cd. This study for the first time analyzed the effect and soil science mechanism of urease-producing bacteria combined with OFCs in blocking wheat’s absorption of Cd. Moreover, this study provides foundational insights and a practical framework for the remediation of Cd-contaminated wheat fields through microbial–organic–mineral collaborative strategies. Full article

Iron-based metal–organic frameworks (Fe-MOFs) are promising for biomedical and environmental applications due to their porosity, tunable chemistry, and biocompatibility. This study examines how particle size, morphology, and ligand composition affect the properties and cytotoxicity of MIL-101(Fe) and MIL-88A. MIL-101(Fe) (octahedral) and MIL-88A (rod-like) were synthesized with a controlled size (~200 nm to ~5 μm). Both showed a high crystallinity and stability. Cytotoxicity assays in A549 cells revealed size- and structure-dependent effects: smaller particles of MIL-88A caused greater toxicity (32.5% viability) than MIL-101(Fe) (66.1% viability at 100 μg/mL), while larger particles were less toxic. MIL-88A also induced higher reactive oxidative species (ROS) levels and degraded more rapidly, releasing more Fe ions. Toxicity predication analysis indicated the higher inherent toxicity of MIL-88A’s ligand (fumaric acid) compared to MIL-101(Fe)’s terephthalic acid. These results demonstrate that structural and chemical factors collectively influence Fe-MOFs’ biocompatibility and highlight the importance of rational design for safer MOF applications. Full article

The aim of this study is to investigate a green and efficient hydrothermal synthesis method for obtaining a high-purity MIL-100(Fe) metal–organic framework (MOF) without using hazardous HF acid or other toxic reagents. The influence of various synthesis conditions (reactant ratios and reaction times) and washing protocols on the MOF’s properties and crystallinity was investigated. Additionally, the adsorption capacities of the synthesized MIL-100(Fe) for hydrogen (H₂), carbon dioxide (CO₂), and water vapor were evaluated at different temperatures and pressures. By analyzing the adsorption behavior, this research study aims to assess the potential of this material for thermal or specific gas storage applications. MF-S1 synthesis, using less iron and water, produces the purest MIL-100(Fe), as confirmed by XRD and FTIR. MF-S1-W2, with additional washing, is ideal for gas adsorption due to its crystallinity, purity, and high surface area. It effectively stores hydrogen (0.25 wt.% at 5 °C), CO₂ (32.6 wt.% at 5 °C), and water vapor (47.5 wt.% at 30 °C). Full article

Understanding the reaction pathway of aldehyde deformylation catalyzed by natural enzymes has shown significance in developing synthetic methodologies and new catalysts in organic, biochemical, and medicinal chemistry. However, unlike other well-rationalized chemical processes catalyzed by cytochrome P450 (Cyt P450) superfamilies, the detailed mechanism of the P450-catalyzed aldehyde deformylation is still controversial. Challenges lie in establishing synthetic models to decipher the reaction pathways, which normally are homogeneous systems for precisely mimicking the structure of the active sites in P450s. Herein, we report a heterogeneous Cyt P450 aromatase mimic based on a porphyrinic metal–organic framework (MOF) PCN-224. Through post-metalation of iron(II) triflate with the porphyrin unit, a five-coordinated Fe^II(Porp) compound could be afforded and isolated inside the resulting PCN-224(Fe) to mimic the heme active site in P450. This MOF-based P450 mimic could efficiently catalyze the oxidative deformylation of aldehydes to the corresponding ketones under room temperature using O₂ as the sole oxidant and triethylamine as the electron source, analogous to the NADPH reductase. The catalyst could be completely recovered after the catalytic reaction without undergoing structural decomposition or compromising its reactivity, representing it as one of the most valid mimics of P450 aromatase from both the structural and functional aspects. A mechanistic study reveals a strong correlation between the catalytic activity and the C^α-H bond dissociation energy of the aldehyde substrates, which, in conjunction with various trapping experiments, confirms an unconventional mechanism initiated by hydrogen atom abstraction. Full article