Search Results (6,389)

This study aims to develop a high-performance, formaldehyde-free particleboard for sustainable housing using halloysite nanotube (HNT)-reinforced isocyanate adhesive. HNTs were incorporated into the isocyanate matrix via magnetic stirring followed by mechanical mixing, with loading levels systematically optimized from 0 to 3.0 wt%. Particleboard panels were fabricated and tested according to standard procedures. The optimal HNT loading was found to be 1.5 wt%. Compared with panels bonded with unmodified adhesive, those fabricated with the optimized HNT-reinforced adhesive exhibited significantly enhanced performance: surface bonding strength increased by 71.79% (to 2.01 MPa), internal bonding strength by 54.35% (to 0.71 MPa), modulus of rupture by 107.53% (to 19.3 MPa), modulus of elasticity by 59.95% (to 3191 MPa), and the 2 h water absorption thickness swelling rate decreased by 95.83% (to 0.1%). These results demonstrate that the optimized dispersion process and HNT loading are critical for achieving superior adhesive performance, providing a viable pathway toward high-performance, formaldehyde-free particleboard for sustainable housing. Full article

Soil nematodes are integral to soil micro-food webs and serve as sensitive bioindicators of soil ecological condition. However, how forest vegetation and soil properties interact to shape nematode community assembly, network structure, and functional stability remains inadequately understood. Using 18S rRNA gene amplicon sequencing coupled with phylogenetic null modeling, we examined soil nematode communities across four forest types along a succession gradient. Although taxonomic diversity (e.g., Shannon and Pielou indices) differed significantly among forest types, network topology and stochastic assembly processes were more closely associated with community restructuring and co-occurrence patterns. This suggests that, while diversity is not irrelevant, network- and assembly-based metrics provide complementary and often more sensitive indicators of nematode community responses to forest type. Co-occurrence network analysis revealed that mixed forests fostered more complex and potentially stable networks, whereas plantations formed dense but potentially vulnerable networks. Assembly processes were not dominated by strong deterministic selection (|βNTI| ≤ 2 for most comparisons), a pattern consistent with undominated processes (e.g., ecological drift, weak environmental filtering). Dispersal limitation played a negligible role in this system. Partial Least Square Path Modeling identified spatial factors and key soil properties (e.g., pH, electrical conductivity, soil water content, and organic carbon) as primary drivers of community structure. Our findings indicate that assessing soil food web health should integrate network analysis and stochasticity metrics rather than rely solely on taxonomic diversity. For sustainable forest management, mixed-species stands are preferable to monoculture plantations, and maintaining soil physicochemical heterogeneity is critical for community stability. Full article

The uncontrolled discharge of synthetic azo dyes such as methyl orange (MO) into water bodies has become a major environmental concern because of their strong chemical stability, limited biodegradability, and harmful effects on aquatic ecosystems. In this study, MgNiFe layered double hydroxides (LDHs) were synthesized through a co-precipitation route using a molar ratio of (Mg + Ni)/Fe equal to 3, and their adsorption ability toward MO in aqueous media was investigated. The prepared materials were characterized by X-ray diffraction (XRD), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDX), Fourier-transform infrared spectroscopy (FTIR), and inductively coupled plasma atomic emission spectroscopy (ICP-AES). The characterization results revealed the successful formation of a hydrotalcite-like layered structure with good crystallinity, a relatively uniform distribution of metallic species, and the incorporation of carbonate anions within the interlayer galleries. In addition, the adsorption performance was evaluated by studying the effects of several operational factors, namely adsorbent dosage, initial pH, and contact time. To better understand the interaction between these parameters and identify the optimum operating conditions, a Box–Behnken response surface design was applied. The results indicate solution pH is the most influential parameter in the adsorption process. Under optimized conditions, a maximum removal efficiency of 86.86% was obtained, corresponding to an adsorption capacity of approximately ~86.86 mg·g⁻¹ (based on 100 mL solution volume). The enhanced adsorption performance may be attributed to the combined effect of the multivalent metal cations (Mg²⁺, Ni²⁺, and Fe³⁺), likely increases the surface positive charge density of the LDH and promotes interactions with anionic dye molecules. These interactions are suggested to involve electrostatic attraction and possible surface adsorption processes. However, in the absence of post-adsorption characterization, the exact adsorption mechanism remains hypothetical. Overall, the results demonstrate the promising potential of MgNiFe LDHs as efficient adsorbent materials for the treatment of dye-contaminated wastewater. Full article

The emerging demand for water pollution control has driven a significant interest in advanced porous materials for sustainable and effective wastewater treatment technologies. Metal–organic frameworks (MOFs) have been employed as promising substrates due to their versatile properties, especially their high surface area, tunable properties, and chemical functionality. However, their practical applications are often limited by poor aqueous stability, instability during recovery, and high production costs. Lignocellulosic biomass (LCB) is an abundant, low-cost, and renewable resource, primarily composed of cellulose, hemicellulose, and lignin, offering a sustainable solution for these challenges. This review critically examines the recent advances in design and applications of LCB-MOF materials for wastewater remediation. Several synthesis strategies, including in situ growth, ex situ impregnation, and post-synthetic modification, are systematically discussed in relation to their significance in enhancing stability, recyclability, and dispersibility of MOFs. The key, structural, morphological, and physicochemical properties of these LCB-MOFs were analyzed, along with their performance in removing organic dyes and heavy metal ions. Current drawbacks in long-term stability, scalability, and real-world wastewater performance are highlighted. Overall, LCB-MOFs demonstrate a promising class of sustainable materials that align with the principles of the circular economy and green chemistry, making them ideal for next-generation wastewater remediation technologies. Full article

This study investigates the separation performance of transformer oil–water mixtures using gravity separation and chemical demulsification. The synthetic emulsion had an initial oil concentration (C₀) of approximately 246,000 mg/L. For gravity separation, the effects of compartment volume ratio, influent flow rate, initial water level, and oil discharge strategy were systematically evaluated. Under optimal conditions (volume ratio 2:1:1, flow rate 0.0055 L/s, initial water level 5 cm), the effluent oil concentration was reduced to as low as 0.020 mg/L, corresponding to a removal efficiency higher than 99.99%. For chemical demulsification, polyaluminum chloride (PAC), polyferric sulfate (PFS), polyacrylamide (PAM), and an organosilicon polyether demulsifier (MCL-D) were tested. The effects of pH, dosage, and temperature on demulsification efficiency (DE) and dehydration rate (DR) were investigated. Under optimal conditions (pH 3–5, dosage 300 mg/L, temperature 50 °C), MCL-D achieved the best performance, with a DE of 95.09% and a DR of 99.50%. Overall, gravity separation is effective for removing free and dispersed oil with low operational cost, whereas chemical demulsification is more suitable for treating stable emulsified oil. The combination of these two methods provides an efficient strategy for the treatment of transformer oil-containing wastewater. Full article

Large-scale disasters can result in chronic pollution of coastal environments with unanticipated and poorly quantified impacts, such as the reshaping of marine connectivity. A recent example is the collapse of the Fundão tailings dam in 2015, which released about 50 million m³ of mine waste into the Doce River, affecting one of Brazil’s largest estuarine–mangrove systems. Here, we combine a high-resolution CROCO hydrodynamic simulation with an individual-based Lagrangian model (Ichthyop) to track the dispersal of mangrove crab (Ucides cordatus) larvae from four estuaries along the southeastern Brazilian margin between 2022 and 2024. Trajectories crossing seasonal msPAF fields derived from in situ water-quality measurements were used to quantify larval exposure to contaminants from mine waste. These fields were based on measured concentrations of As, Ba, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, V, Zn, and Al. Results show that surface shelf flow and mesoscale activity in the vicinity of the Doce River mouth contribute to offshore export of larvae, while the reef-dominated Abrolhos shelf promotes retention. Interannual variability alternates between long-distance export and local retention, associated with regional climate variability. Larval mortality rates caused by offshore advection and lethal temperature are high (65–75%). In addition to these modeled mortality sources, surviving cohorts frequently crossed areas with elevated msPAF values during transport, indicating potential exposure to metal(loid) mixtures. This suggests that the regional connectivity of U. cordatus is under chronic stress that likely compromises the integrity and resilience of coastal populations, since southern estuaries depend strongly on northern larval sources. The integration of Lagrangian simulations with in situ contaminant monitoring and spatially explicit exposure metrics demonstrates that transport pathways regulate not only connectivity among estuaries but also the duration and intensity of larval exposure to pollutants. Full article

Climate-based suitable habitats were projected for the endangered submerged macrophyte Ottelia acuminata under current and future climates (2050s–2090s) across three Shared Socioeconomic Pathways (SSPs: SSP126, SSP245, and SSP585, corresponding to SSP1-2.6, SSP2-4.5, and SSP5-8.5, respectively) using the Maximum Entropy (MaxEnt) model with 126 occurrence points and eight environmental variables. The four dominant climatic factors were Precipitation of the Driest Quarter (34.7%), Isothermality (24.2%), Temperature Annual Range (17.9%), and Mean Temperature of the Coldest Quarter (11.7%). Under the current climate, the total suitable area is 121.07 × 10⁴ km², mainly in northern and eastern Yunnan. Under future scenarios, the total suitable area expands, peaking at +17.1% under SSP245 in the 2070s, but undergoes substantial internal reconfiguration: moderately suitable areas increase by 95.2% under SSP585 in the 2090s while low-suitability areas decline sharply, and core-habitat loss is greatest under SSP126. The distribution centroid consistently shifts westward (maximum 83.3 km), driven by newly suitable areas in the west and north. We propose a zonal conservation strategy grounded in these climate-envelope projections, while emphasizing that additional data on hydrology, water quality, and dispersal are required to translate these results into operational conservation actions. These findings provide a macroecological basis for informing climate-adaptive conservation of O. acuminata. Full article

The wettability of dust is fundamental to its dispersion and control in mining operations. Current research, however, focuses largely on isolated properties, leaving the synergistic mechanisms of multi-scale factors-such as particle size, morphology, and surface chemistry-poorly understood. This study integrates field measurements, laboratory characterization, and theoretical analysis to investigate the spatial distribution and wetting behavior of dust in fully mechanized mining faces. The results show that respirable dust preferentially accumulated in mechanically disturbed and personnel-exposure zones. At the shearer operator’s station, respirable dust concentrations reached 328.6 mg/m³ in Mine A and 278.4 mg/m³ in Mine B, which were 1.8 and 1.6 times higher than those at the shearer cutting point, respectively. Mine A dust also showed poorer wettability, with a higher water contact angle of 148.9° ± 2.1° compared with 134.7° ± 1.8° for Mine B, mainly due to its larger agglomerates, rougher surface morphology, and more hydrophobic surface chemistry. Accordingly, targeted development pathways for spray and foam technologies are outlined, including compound wetting agents and micro-nano enhanced foaming systems. The integrated multi-scale framework linking concentration, particle size, morphology, surface chemistry, and wettability provide an application-oriented basis for understanding coal mine dust behavior and for supporting more precise and intelligent dust-control strategies. Full article

At present, human activity is the main source of water pollution. The tanning industry is a primary source of water contamination with Cr(III), which can cause various diseases if ingested. A circular economy approach proposes an effective, low-cost solution. The utilization of waste from the food industry is used for the removal of Cr(III) through biosorption. This study evaluated the adsorption capacity of orange peel (OP) and pineapple crown (PC) pretreated with H₂O₂ and NaOH was evaluated under different operating conditions. The physicochemical properties of the biosorbents were characterized using techniques such as Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). The results show that treatment with NaOH at 60 °C obtained an adsorption capacity of 61.63 mg/g and 64.19 mg/g for OP and PC, respectively. The combined biosorbents resulted in an approximately 50% increase in the adsorption capacity of Cr(III) compared to individual biosorbents. The isotherms that best fit the experimental data were Sips and Redlich–Peterson (RP) models, suggesting heterogeneous adsorption behavior in biosorbents. Thermodynamic parameters indicated that biosorption process was spontaneous and endothermic. Full article

To overcome graphene aggregation in aqueous nanofluids, polycarboxylate-modified structural graphene (PSG) was synthesized via surface functionalization. Characterizations indicate that the modification preserves the 3D hierarchical porous framework while ensuring exceptional dispersion stability through steric hindrance and enhanced hydrophilicity. Convective heat transfer evaluations demonstrated remarkable enhancement; notably, the 0.1 wt% PSG nanofluid achieved a 46% increase in the heat transfer coefficient over pure water at Re = 4000. Molecular dynamics simulations further revealed the underlying interfacial mechanisms. The surface-anchored oxygen-containing groups induce a dense, hydrogen-bonded hydration layer that restricts local water diffusion. This highly ordered interfacial structure may facilitate vibrational energy exchange across the solid–liquid boundary. Together with the intrinsic high-conductivity 3D skeleton, these microscopic interactions are likely to contribute to the enhanced macroscopic thermal performance, providing a promising framework for designing advanced graphene-based thermal management fluids. Full article

The low water solubility of numerous drug candidates and phytochemicals continues to pose a significant challenge in pharmaceutical development, greatly limiting their bioavailability and therapeutic performance. This review presents a detailed overview of formulation strategies aimed at improving the solubility and dissolution of poorly aqueous-soluble compounds. The biopharmaceutics classification system and the relevance of in vitro–in vivo correlation, as well as key challenges in formulation development, are briefed. Solid-state and particle engineering approaches, including micronization, supercritical fluid technology, electrospinning, and cryogenic techniques, are discussed. Extensive critical examination of amorphous solid dispersions and their preparation methods, as well as crystallization inhibition strategies, is covered. Cocrystallization is highlighted as a promising approach, with emphasis on design principles and preparation methods. Various solubilization techniques, such as pH modification, cosolvency, hydrotropy, micellar solubilization, and cyclodextrin-based complexation, including advanced hybrid systems, are also explored. Emerging solvent platforms, such as deep eutectic systems and lipid-based and nanotechnology-driven approaches, are reviewed for their role in improving solubility and drug delivery. Additionally, enabling technologies such as liquisolid systems and hydrophilic polymers are addressed. Despite notable progress, limitations such as scalability, reproducibility, regulatory constraints, and long-term safety persist. Overall, this review provides integrated insights into formulation design approaches to enhance the solubility and therapeutic efficacy of poorly soluble drugs. Full article

Facing the increasingly severe energy challenges and environmental problems, the development of thermally stable, lightweight, and thermal insulating materials is critical. Herein, we report an organic-inorganic composite strategy combined with a high-temperature carbonization step to fabricate aerogel-containing composites synergistically reinforced with chopped glass fibers and hollow glass microspheres. By systematically varying the ratio of acrylic emulsion to potassium silicate solution, we investigated the effects on the forming behavior, microstructure, hydrophobicity, thermal stability, and thermal insulation performance. Increasing the acrylic emulsion fraction substantially enhanced hydrophobicity, yielding a maximum water contact angle of 129.3°. Concurrently, the apparent density decreased from 0.18 g/cm³ to 0.09 g/cm³ and the thermal conductivity dropped from 57.9 mW/(m·K) to 29.0 mW/(m·K). Mechanical testing revealed that the compressive Young’s modulus decreased with increasing acrylic content, from 3.6 MPa for the purely inorganic sample to 0.55 MPa at 70% acrylic content, reflecting a trade-off between stiffness and organic-derived porosity. Microstructural characterization revealed a hierarchical porous network in which uniformly dispersed hollow glass microspheres and the aerogel-derived silica network form an efficient thermal barrier system. Thermogravimetric analysis demonstrated excellent thermal stability, with total weight loss below 5% up to 800 °C. Infrared thermography analysis showed that, after unilateral heating at 300 °C and 400 °C for 10 min, the backside surface temperature of the composites decreased as the acrylic emulsion content increased. At 300 °C, the temperature decreased from 176.1 °C for AP-1 to 151.0 °C for AP-4, while at 400 °C, it decreased from 228.5 °C to 199.3 °C. These results indicate that the composites exhibit effective thermal insulation and maintain structural stability under high-temperature exposure. Taken together, this facile and scalable approach yields these aerogel-containing composites that combine low density, low thermal conductivity, robust structural integrity, and good environmental resistance, as evidenced by a water contact angle of 129.3°, making them promising candidates for aerospace, building, and industrial high-temperature insulation applications. Full article

Ophicarbonates provide an important natural record of mineral carbonation during serpentinization of ultramafic rocks and therefore offer insight into the mechanisms and limits of CO₂ fixation in low-temperature geological environments. This paper presents a synthesis and process-oriented reinterpretation of stable-isotope published and previously unpublished data, petrographic, and mineralogical evidence for carbonate formation under fluid-limited serpentinization conditions. Using mineralogical constraints together with a compiled δ¹³C–δ¹⁸O dataset that includes legacy measurements from the 1980s–1990s, we evaluate how multi-stage carbonate precipitation reflects evolving water–rock ratio, redox state, transport limitation, and deformation-controlled permeability. Particular attention is given to systematic differences between vein-hosted carbonates and dispersed intergranular or scattered-grain ophicarbonates, as these textural–isotopic relationships help identify fluid flux, carbon source, and reaction progress in ultramafic systems. The analysis shows that carbonation does not proceed uniformly but is restricted to overlapping reactive windows controlled by fluid availability, nucleation kinetics, and permeability evolution. These constraints help explain why carbonation may either intensify or stall during progressive serpentinization. The Author further discuss why kinetic barriers and Mg–Ca partitioning may redirect carbonate mineralogy toward calcite or metastable Mg-rich phases even where dolomite or magnesite may be thermodynamically favored. The results highlight the importance of coupling isotopic signatures with petrographic context in reconstructing carbonation pathways and provide a broader framework for understanding natural mineral sequestration of carbon in heterogeneous serpentinite systems. Full article

The use of flotation reagents in the form of microemulsions significantly enhances the recovery of noble metals during the processing of gold-bearing ore and technogenic materials by improving the flotation of finely dispersed sulfides. This study investigates the effect of dibutyldithiophosphate (DBDTP) applied as emulsion microbubbles in the form of emulsion microbubbles on the flotation of gold-bearing ores and technogenic materials. The research objects were gold-bearing ore and aged flotation tailings from a Kazakhstani deposit containing 3.20 g/t and 0.62 g/t of gold, respectively. Flotation beneficiation was carried out using dispersed DBDTP generated in a water–air microemulsion generator (WAMG). The flotation kinetics results demonstrated that the application of dispersed DBDTP accelerates the flotation process, increasing gold recovery by 4.65% and reducing the gold content in flotation tailings by 0.17 g/t. Under baseline conditions, 37.51% of gold was distributed in the −25 + 0 μm size fraction of tailings with a gold content of 0.98 g/t. When the dispersed reagent produced by the WAMG was applied, the gold distribution in the −25 + 0 μm size fraction decreased to 28.29% (9.22% lower than the baseline), with a gold content of 0.62 g/t. In the flotation of aged tailings, the use of dispersed DBDTP increased gold recovery in the concentrate by 5.88% while maintaining concentrate quality. Full article

Electrochemical water splitting for hydrogen production is a key technological route toward the large-scale generation of green hydrogen. However, the anodic oxygen evolution reaction (OER) suffers from sluggish kinetics and high overpotential, necessitating the development of non-noble metal catalysts that simultaneously possess low cost, high activity, and excellent stability. In this work, a nitrogen-doped graphene quantum dots@nickel–iron layered double hydroxide (N-GQDs@NiFe-LDH) composite catalyst was in situ constructed via a facile hydrothermal strategy. Benefiting from the electronic modulation and structural confinement effects of N-GQDs, the intrinsic catalytic activity and structural stability of the catalyst were simultaneously enhanced. The as-prepared catalyst requires an overpotential of only 320 mV to deliver a current density of 500 mA cm⁻² and maintains 98% of its initial activity after 100 h of chronoamperometric stability testing, demonstrating promising potential for practical applications. Multiscale characterizations revealed that N-GQDs formed strong electronic interactions with Ni/Fe active sites at the interface, significantly enhanced interfacial electron transport, and accelerated the OER kinetics. This study demonstrates that the N-GQDs@NiFe-LDH catalytic system constructed via an interfacial heterostructure engineering strategy provides a new insight for the rational design and development of efficient non-noble-metal OER electrocatalysts. Full article