Search Results (845)

Mycotoxin contamination is a crucial issue in food safety. However, the removal of trace amounts of mycotoxins from complex food and feed matrices without significant loss of nutritional and flavor quality remains a significant challenge. The integrated adsorption–catalysis strategy involves immobilizing catalytic modules onto adsorption materials, enabling in situ degradation while enriching the mycotoxins. This approach can significantly reduce the dosage of detoxification agents and achieve efficient removal of trace mycotoxins in food. This review provides an overview of adsorbents with enrichment capabilities and their applications in the targeted removal of mycotoxins from food. The adsorption–degradation coupled systems are categorized into the following two main types: adsorption–photocatalysis coupled systems and adsorption–biocatalysis coupled systems. The review introduces recent advances in the design of bifunctional catalysts, focusing on their synergistic mechanisms and practical applications for detoxifying various mycotoxins in food matrices. Finally, the review discusses current industrial challenges and offers insights into future directions for this field. Full article

Most risk assessment and source apportionment studies of the heavy metals in the surface soils in China have focused primarily on East China, whereas studies focused on Northwest China, particularly regarding heavy metals in surface soils in the central and western areas, remain limited. In this study, surface soils in the central–western Ali region were investigated, and the concentrations of nine heavy metals were determined. Moreover, the distribution patterns and ecological risks of these heavy metals were elucidated via a combination of the geoaccumulation index, pollution load index ($PLI$), comprehensive potential ecological risk index ($RI$), and integrated X-ray diffraction (XRD)–multivariate statistical techniques. Additionally, the pollution characteristics and sources were analyzed. The results indicated the following: (1) The spatial distribution of heavy metal pollution is closely linked to the geological background, and high–pollution zones (e.g., Cr, Ni, Co, Cu, As, and Cd) conform well with the distributions of ultramafic rocks and iron/chromite ore beds. The geoaccumulation index revealed that Cd caused slight and moderate contamination at 29.1% and 5.5% of the sites, respectively, whereas As affected 14.6% of the sites. The pollution load index indicated moderate pollution in 20% of the sites, and the potential ecological risk index indicated that 41.8% of the sites posed moderate risks, which was largely driven by Cd (mean $E_r^i$ = 43.1). The comprehensive ecological risk index ($RI$ = 115) confirmed a moderate risk level overall. Principal component analysis revealed three primary sources: natural weathering (Cr–Ni–Co–Cu, 39.1%); a mixed source influenced by nonagricultural anthropogenic activities such as transport and regional deposition, combined with natural processes such as arid climate and alkaline soil conditions that influence Cd mobility (Cd–Mo–Pb, 20.8%); and industrial/mining activities (As–Sb, 14.2%). Mineralogical analyses further indicated that heavy metals are present via lattice substitution, adsorption, and precipitation. This study systematically clarifies the composite pollution pattern and sources of heavy metals in the alpine Ali region, supporting targeted contamination control. Full article

Soil degradation, declining fertility, and rising greenhouse gas emissions highlight the urgent need for sustainable soil management strategies. Among them, biochar has gained recognition as a multifunctional material capable of enhancing soil fertility, sequestering carbon, and valorizing biomass residues within circular economy frameworks. This review synthesizes evidence from 186 peer-reviewed studies to evaluate how feedstock diversity, pyrolysis temperature, and elemental composition shape the agronomic and environmental performance of biochar. Crop residues dominated the literature (17.6%), while wood, manures, sewage sludge, and industrial by-products provided more targeted functionalities. Pyrolysis temperature emerged as the primary performance driver: 300–400 °C biochars improved pH, cation exchange capacity (CEC), water retention, and crop yield, whereas 450–550 °C biochars favored stability, nutrient concentration, and long-term carbon sequestration. Elemental composition averaged 60.7 wt.% C, 2.1 wt.% N, and 27.5 wt.% O, underscoring trade-offs between nutrient supply and structural persistence. Greenhouse gas (GHG) outcomes were context-dependent, with consistent Nitrous Oxide (N₂O) reductions in loam and clay soils but variable CH₄ responses in paddy systems. An emerging trend, present in 10.6% of studies, is the integration of artificial intelligence (AI) to improve predictive accuracy, adsorption modeling, and life-cycle assessment. Collectively, the evidence confirms that biochar cannot be universally optimized but must be tailored to specific objectives, ranging from soil fertility enhancement to climate mitigation. Full article

Brilliant blue, as a pigment food additive, has all the characteristics of printing and dyeing wastewater and belongs to persistent and refractory organic compounds. The photocatalysis–Fenton reaction system consists of two parts: photocatalytic reaction and Fenton reaction. Electrons promote the decomposition of H₂O₂ to produce •OH. In addition, the effective separation of e- and h⁺ by light strengthens the direct oxidation of h⁺, and h⁺ reacts directly with OH⁻ to produce •OH, which can further promote the removal of organic pollutants. In this paper, g-C₃N₄ and Fe/g-C₃N₄ photocatalysts were prepared by the thermal polycondensation method. Fe/g-C₃N₄ of 15 wt% can reach 98.59% under the best degradation environment, and the degradation rate of g-C₃N₄ is only 7.6% under the same conditions. The photocatalytic activity of the catalysts was further studied. Through active species capture experiments, it is known that •OH and •O₂⁻ are the main active species in the system, and the action intensity of •OH is greater than that of •O₂⁻. The degradation reaction mechanism is that H₂O₂ combines with Fe²⁺ in Fe/g-C₃N₄ to generate a large amount of •OH and Fe³⁺, and the combination of Fe-N bonds accelerates the cycle of Fe³⁺/Fe²⁺ and promotes the formation of •OH, thereby accelerating the degradation of target pollutants. •O₂⁻ can reduce Fe³⁺ to Fe²⁺, Fe²⁺ reacts with H₂O₂ to produce •OH, which promotes degradation, and •O₂⁻ itself also plays a role in degradation. In addition, under the optimal experimental conditions obtained by response surface experiments, the fitting degree of first-order reaction kinetics is 0.96642, and the fitting degree of second-order reaction kinetics is 0.57884. Therefore, this reaction is more in line with first-order reaction kinetics. The adsorption rate is only proportional to the concentration of Fe/g-C₃N₄. Full article

Water resource management and agricultural practices in the Mediterranean region, characterised by the excessive use of pesticides, pose significant environmental and human health challenges. As they can be easily and inexpensively produced from various biomass sources, biochars are frequently recommended as a low-cost secondary decontamination strategy to address soil contamination problems. This study investigates the properties and sorption behaviours of biochars produced in a low-cost metallic kiln using local rosemary, giant reed, St. John’s wort, olive, cypress, and palm tree biomass residues to evaluate their potential for environmental remediation, with a special focus on the mobility and retention of contaminants. Analytical and experimental techniques were employed to characterise the biochars’ physicochemical attributes and sorptive capacities. The core analyses included measurement of basic physicochemical properties, including pH, electrical conductivity, functional group identification via Fourier transform infrared (FTIR) spectroscopy, and the molarity of ethanol droplet (MED) test to assess the surface hydrophobicity. Batch sorption experiments were conducted using methylene blue (MB) and two fluorescent tracers—uranine (UR) and sulforhodamine-B (SRB)—as proxies for organic contaminants to assess the adsorption efficiency and molecule–biochar interactions. Furthermore, the adsorption isotherms at 20 °C were fitted to different models to assess the biochars’ specific surface areas. Thermodynamic parameters were also evaluated to understand the nature and strength of the adsorption processes. The results highlight the influence of feedstock type on the resulting biochar’s properties, thus significantly affecting the mechanism of adsorption. Rosemary biochar was found to have the highest specific surface area (SSA) and cation exchange capacity (CEC), allowing it to adsorb a wide range of organic molecules. Giant reed and palm tree biochars showed similar properties. In contrast, wood-derived biochars generally showed very low SSA, moderate CEC, and low hydrophobicity. The contrasting properties of the three dyes—MB (cationic), UR (anionic), and SRB (zwitterionic)—enabled us to highlight the distinct interaction mechanisms between each dye and the surface functional groups of the different biochars. The reactivity and sorption efficiency of a biochar depend strongly on both the nature of the target molecule and the intrinsic properties of the biochar, particularly its pH. The findings of this study demonstrate the importance of matching biochar characteristics to specific contaminant types for optimised environmental applications, providing implications for the use of tailored biochars in pollutant mitigation strategies. Full article

For complexation of mRNA into polyplexes, double-pH-responsive lipo-xenopeptides (XP), comprising tetraethylene pentamino succinic acid (Stp) and lipoamino fatty acids (LAFs), were combined with PEGylated lipids, either DMG-PEG 2 kDa (DMG-PEG) or azido-group-containing DSPE-PEG 2 kDa (DSPE-PEG-N3), to increase colloidal stability and to facilitate ligand-mediated targeted mRNA delivery. LAF-XPs mixed with DMG-PEG at low (1.5% and 3%) molar ratios improved colloidal stability and retained transfection efficiency. PEGylation also enabled the formulation of otherwise unstable carrier complexes and prevented aggregation induced by salt, proteins, and serum. PEGylation of more positively charged Stp-LAF₂ mRNA polyplexes decreased fibrinogen adsorption. More neutral, LAF-rich Stp-LAF₄ polyplexes exhibited low fibrinogen binding without PEGylation. Intravenous administration of these stabilized mRNA complexes demonstrated enhanced biosafety while preserving transfection efficiency. DSPE-PEG-N3 was selected for cell targeting after strain-promoted azide-alkyne cycloaddition (SPAAC)-mediated click-coupling of DBCO-modified ligands. Higher PEG ratios (10% and 20%) provided effective shielding but reduced transfection efficiency, a drawback known as the “PEG dilemma”. Functionalization with an EGFR-targeting ligand restored transfection in EGFR-positive cell lines in a ligand-specific manner. High transfection efficiency is consistent with a lipophilic-to-hydrophilic polarity switch of LAF-XP carriers upon endosomal protonation, triggering dissociation of the PEG lipids and deshielding of the polyplex. Full article

Depression is becoming more common in the face of modern life’s obstacles. Antidepressants are a fast-expanding pharmaceutical category. Antidepressant residues in water must be closely monitored and kept at levels that do not endanger human health, just like those of other psychotropic medications. Additionally, research has shown that these pollutants severely hinder aquatic life’s ability to migrate, reproduce, and interact with one another when they enter natural ecosystems. Antidepressants released into the natural environment can therefore be expected to have an impact on exposed fish and other aquatic species. There is a lot of information available about how exposure affects fish, but much of it is for exposure levels higher than those seen in their natural habitats. Antidepressants can bioaccumulate in fish tissues, and some behavioral effects have been documented for exposures that are relevant to the environment. As a result, antidepressant residue removal methods must be incorporated into contemporary wastewater treatment plant technology. In addition to covering a wide range of suggested treatment options and their ecotoxicological consequences on non-target organisms, this study discusses recent efforts to accomplish this goal. First, a thorough analysis of the harmful impacts on non-target people is provided. This work describes a variety of adsorptive methods that can make use of modern materials like molecularly imprinted polymers or ion-exchange resins or can rely on well-known and efficient adsorbents like silicates or activated carbon. Although extractive methods are also taken into consideration, they are now impractical due to the lack of reasonably priced and ecologically suitable solvents. Lastly, sophisticated oxidation methods are discussed, such as electrochemical alternatives, UV and gamma radiation, and ozone therapy. Notably, some of these techniques could totally mineralize antidepressant toxicants, either alone or in combination. Lastly, the topic of biological treatment with microorganisms is covered. This method can be very specific, but it usually prevents full mineralization. Full article

The renewable-energy-powered electrocatalytic CO₂ reduction reaction (CO₂RR) efficiently converts CO₂ into high-value chemicals and fuels, offering a promising approach to addressing environmental and energy sustainability challenges. This process is of immense significance for constructing a sustainable artificial carbon cycle. Cu-based catalysts exhibit remarkable catalytic activity and broad product selectivity in CO₂RR, which can be attributed to their excellent electrical conductivity, moderate adsorption energy, and unique electronic structure. This review comprehensively summarizes the advantages, practical applications, and mechanistic insights of Cu-based catalysts in CO₂RR, with a systematic based on recent advances in tuning strategies via electronic effects and structural design. Specifically, it emphasizes the influence of electronic structure tuning (electron-donating/-withdrawing effects and steric hindrance effects), active center tuning (single-atom catalysts, heterogeneous synergetic effects, and polymer modification), and surface structure (morphology effect, valence-state effect, and crystalline-facet effect) influences on catalytic performance. By rationally designing the catalyst structure, the adsorption behavior of reaction intermediates can be effectively regulated, thereby enabling the highly selective generation of target products. The objective of this paper is to provide a theoretical framework and actionable strategies for the structural design and catalytic performance optimization of Cu-based catalysts, with the ultimate goal of promoting the development and practical application of efficient CO₂RR catalytic systems. Full article

The effectiveness of periodate-assisted photocatalysis in removing the cationic dye Safranin O (SO) was evaluated using a UV/TiO₂/IO₄⁻ process operated at room temperature under near-neutral pH conditions. Under base conditions ([IO₄⁻] = 0.15 mM, [TiO₂] = 0.4 g/L, [SO] = 10 mg/L), the ternary system achieved a pseudo-first-order rate constant of 0.6212 min⁻¹, outperforming the UV/TiO₂ and UV/IO₄⁻ processes by approximately 21- and 29-fold, respectively. This yielded a synergy ratio of about 12 compared to the sum of the binary processes. Targeted quenching experiments revealed the operative pathways. Strong inhibition by ascorbic acid and phenol indicates that interfacial holes and ^•OH are key oxidants. Methanol caused a moderate slowdown, consistent with ^•OH and hole scavenging. Benzoquinone and oxalate suppressed removal by intercepting the electron and O₂^•− pathways, respectively. Dichromate markedly inhibited the process via optical screening and competition for electrons. Azide had little effect, suggesting a minor role for singlet oxygen. Matrix studies showed progressively slower kinetics from deionized water to mineral water to seawater. This was due to halides, sulfate, alkalinity, and TiO₂ aggregation driven by ionic strength. Additional tests confirmed that the dominant modulators of performance were humic acid (site fouling and light screening), chloride and sulfate (radical speciation and surface effects), nitrite (near-diffusion radical quenching), and bicarbonate at pH 8.3 (conversion of ^•OH to CO₃^•−). Nonionic surfactants (Tween 80, Triton X-100) also depressed SO removal through micellar sequestration and competitive adsorption on TiO₂. The study confirms the potential of UV/TiO₂/IO₄⁻ as a tunable AOP capable of delivering rapid and reliable dye degradation under a wide range of water quality conditions. The mechanistic mapping unifies two roles for IO₄⁻, an electron acceptor that inhibits recombination and a photochemical precursor of iodine centered and ^•OH radicals and connect these roles to the observed synergy and to the trend across deionized water, mineral water, and seawater. The scavenger outcomes assign the main oxidant flux to holes and ^•OH radicals with a contributory electron or O₂^•− branch from IO₄⁻ reduction. Full article

Metal–organic frameworks (MOFs) have been increasingly recognized as promising platforms for enzyme modulation, owing to their tunable porosity, high surface area, and versatile chemical functionality. In this review, the potential of MOFs for the inhibition and modulation of protein kinases and phosphatases—key regulators of cellular signaling and disease progression—is examined. The structural fundamentals of MOFs are outlined, followed by a discussion of common synthesis strategies, including solvothermal, microwave-assisted, sonochemical, and mechanochemical methods. Emphasis is placed on how synthesis conditions influence critical features such as particle size, crystallinity, surface chemistry, and functional group accessibility, all of which impact biological performance. Four primary mechanisms of MOF–enzyme interaction are discussed: surface adsorption, active site coordination, catalytic mimicry, and allosteric modulation. Each mechanism is linked to distinct physicochemical parameters, including pore size, surface charge, and metal node identity. Special focus is given to biologically relevant metal centers such as Zr⁴⁺, Ce⁴⁺, Cu²⁺, Fe³⁺, and Ti⁴⁺, which have been shown to contribute to both MOF stability and enzymatic inhibition through Lewis acid or redox-mediated mechanisms. Recent in vitro studies are reviewed, in which MOFs demonstrated selective inhibition of disease-relevant enzymes with minimal cytotoxicity. Despite these advancements, several limitations have been identified, including scalability challenges, limited physiological stability, and potential off-target effects. Strategies such as post-synthetic modification, green synthesis, and biomimetic surface functionalization are being explored to overcome these barriers. Through an integration of materials science, coordination chemistry, and molecular biology, this review aims to provide a comprehensive perspective on the rational design of MOFs for targeted enzyme inhibition in therapeutic contexts. Full article

Selective depression of serpentine remains a major challenge in the flotation of low-grade nickel sulphide ores because serpentine slimes impair concentrate grade and recovery. In this study, four structurally related micromolecular depressants bearing amino and phosphonic functionalities were designed, synthesized and systematically evaluated. Micro-flotation screening (depressant range: 0–20 mg·L⁻¹) and bench-scale tests identified an operational optimum near pH 9 and a reagent dosage of ≈18 mg·L⁻¹; potassium butyl xanthate (PBX) was used as a collector and methyl isobutyl carbinol (MIBC) as a frother. Phosphonate-containing molecules (PMIDA and GLY) delivered the largest gains in pentlandite recovery and concentrate selectivity compared with carboxylate analogues and a benchmark depressant. Mechanistic studies (zeta potential, adsorption isotherms, FT-IR, and XPS) indicated that selective adsorption of amino and phosphonate groups on serpentine occurs via coordination with surface Mg sites and by altering the electrical double layer. The DLVO modelling showed that these reagents generate an increased repulsive barrier, mitigating slime coating and entrainment. Contact-angle measurements confirmed selective hydrophilization of serpentine while pentlandite remained hydrophobic. These findings demonstrate that incorporating targeted phosphonate chelation into small-molecule depressants is an effective strategy to control serpentine interference and to enhance flotation performance. Full article

Eutrophication of freshwater bodies is primarily caused by excessive nitrogen and phosphorus, resulting in significant environmental challenges, including harmful algal blooms and hypoxia. This review examines the potential for natural and modified zeolites to act as adsorbents and regulate nutrient concentrations in eutrophic freshwater ecosystems, excluding applications for wastewater or industrial water effluents. Natural zeolites are effective adsorbents of ammonium, whereas modified zeolites (with aluminum, iron, calcium, and many others) have been noted to have enhanced phosphate adsorption and a higher overall nutrient removal efficiency. The application of modified zeolites for controlling eutrophication in freshwater bodies has proven to have high efficiency in adsorbing nitrogen and phosphorus, resulting in reduced nutrient release from sediments and improved water quality in shallow lakes and reservoirs. This review describes the adsorption mechanisms and modification methods, with an appreciation for the multifunctional role of zeolites in nutrient immobilization and capping sediments. Finally, it presents the potential to use zeolite-based materials in eutrophic freshwater restoration through sustainable circular economy approaches. Zeolite materials present ample environmental applications for cost-effective and targeted mitigation approaches to freshwater eutrophication. 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

The persistent contamination of water bodies by organic compounds, heavy metals, and pathogenic microorganisms represents a critical environmental and public health concern worldwide. In this context, polymer composite materials have emerged as promising multifunctional platforms for advanced water purification. These materials combine the structural versatility of natural and synthetic polymers with the enhanced physicochemical functionalities of inorganic fillers, such as metal oxides and clay minerals. This review comprehensively analyzes recent developments in polymer composites designed to remove organic, inorganic, and biological pollutants from water systems. Emphasis is placed on key removal mechanisms, adsorption, ion exchange, photocatalysis, and antimicrobial action, alongside relevant synthesis strategies and material properties that influence performance, such as surface area, porosity, functional group availability, and mechanical stability. Representative studies are examined to illustrate contaminant-specific composite designs and removal efficiencies. Despite significant advancements, challenges remain regarding scalability, material regeneration, and the environmental safety of nanostructured components. Future perspectives highlight the potential of bio-based and stimuli-responsive polymers, hybrid systems, and AI-assisted material design in promoting sustainable, efficient, and targeted water purification technologies. Full article

Heavy metal ions in wastewater endanger ecology and human health, requiring cost-effective treatments. This study innovatively converts abandoned basalt fibers (BFs) into high-performance adsorbents (BFSN) via NaOH etching and chelation with nitrilotriacetic acid (NTA)/carboxymethyl starch (CMS), introducing target functional groups. Characterizations (XPS, FTIR, zeta potential) reveal Cu²⁺/Pb²⁺ adsorption mechanisms: -COO⁻ chelation, N-containing group ion exchange, and electrostatic adsorption. Kinetics fit a pseudo-first-order model (R² > 0.98) and isotherms fit the Langmuir model, confirming monolayer chemisorption. BFSN has excellent thermal stability (≤2% mass loss at 800 °C) and post-adsorption integrity (≈0.11% mass loss post-loading). Waste-derived BFSN, cheaper than commercial adsorbents, has strong economic viability. This “waste-to-value” approach offers efficient, sustainable large-scale heavy metal wastewater remediation, advancing waste utilization and ecological restoration in water treatment. Full article