Search Results (2,008)

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

The adsorptive removal of tetracycline (TC) in aqueous solution, a widely used antibiotic, was investigated using activated carbon derived from cotton textile waste. The valorization of textile waste provides a sustainable strategy that not only reduces the growing accumulation of discarded textiles but also supports a circular economy by transforming waste into efficient adsorbent materials for the removal pharmaceutical contaminants. This dual environmental and economic benefit underscores the novelty and significance of using cotton-based activated carbons in wastewater treatment. In this study, cotton textile waste was utilized as a raw material for the preparation of adsorbents via pyrolysis under nitrogen at 600 °C followed by chemical modification with H₂SO₄ solutions (1, 2, and 3 M). The sulfuric-acid modified-carbons (SMCs) were characterized by BET surface area analysis, FTIR spectroscopy and SEM imaging. Batch adsorption experiments were carried out to evaluate the effects of key operational parameters including contact time, initial TC concentration and solution pH. The results showed that the material treated with 2 M H₂SO₄ displayed the highest adsorption performance, with a specific surface area of 700 m²/g and a pore volume of 0.352 m³/g. The pH has a great influence on TC adsorption; the adsorbed amount increases with the initial TC concentration from 5 to 100 mg/L and the maximum adsorption capacity (74.02 mg/g) is obtained at pH = 3.8. The adsorption behavior was best described by Freundlich isotherm and pseudo-second-order kinetic models. This study demonstrates that low-cost and abundantly available material, such as cotton textile waste, can be effectively repurposed effective adsorbents for the removal of pharmaceutical pollutants from aqueous media. Full article

Fluoride contamination in groundwater is a pressing environmental and public health issue, with chronic exposure linked to skeletal and dental fluorosis. Here, we report the synthesis of magnesium oxide nanoparticles via a controlled co-precipitation method employing dimethylformamide (DMF) as solvent and either ammonium hydroxide (MgO-1) or ammonium carbonate (MgO-2) as precipitating agents. The resulting materials were comprehensively characterized using thermogravimetric analysis (TGA/DSC), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM/EDS). Additionally, BET surface area and porosity analyses revealed mesoporous structures, with MgO-1 showing a slightly higher surface area (14.12 m² g⁻¹) than MgO-2 (13.87 m² g⁻¹). Both MgO-1 and MgO-2 exhibited high crystallinity, nanoscale particle sizes (81.6 nm and 128.1 nm, respectively), and distinct morphological features. Batch adsorption studies revealed maximum fluoride uptake capacities of 117.6 mg/g (MgO-1) and 94.5 mg/g (MgO-2) at neutral pH, with MgO-1 exhibiting superior performance due to its smaller particle size and higher specific surface area. Fluoride removal remained above 98% between pH 3–9, confirming stability across a wide pH range, with a minor decline at pH 11 due to OH⁻ competition. Adsorption equilibrium data were best described by the Temkin isotherm model, suggesting heterogeneous surface interactions and an exothermic process, while kinetic analyses indicated pseudo-second-order behavior for MgO-1 and pseudo-first-order for MgO-2. Both materials maintained high fluoride selectivity in the presence of competing anions and successfully reduced fluoride in tap water from 2.11 mg/L to below the WHO limits without altering water hardness. These findings underscore the potential of engineered MgO nanomaterials as efficient, selective, and sustainable adsorbents for water defluoridation, offering a promising pathway toward scalable remediation technologies in fluoride-affected regions. Full article

Hydrometallurgy is currently the mainstream industrial process for recovering valuable components (nickel, cobalt, manganese, lithium, etc.) from spent ternary lithium-ion battery cathode materials. During the crushing of lithium batteries, cathode materials, anode materials (graphite), and electrolytes become mixed. Consequently, fluoride ions inevitably enter the leaching solution during the hydrometallurgical recycling process, with concentrations as high as 100–300 mg/L. These fluoride ions not only adversely affect the quality of the recovered precursor products but also pose environmental risks. To address this issue, this study employs a synthesized lanthanum–zirconium (La@Zr) composite material, with a specific surface area of 67.41 m²/g and a pore size of 2–50 nm, which can reduce the fluoride ion concentration in the leaching solution to below 5 mg/L, significantly lower than the 20 mg/L or higher that is typically achieved with traditional calcium salt defluorination processes, without introducing new impurities. Under optimal adsorption conditions, the lanthanum–zirconium adsorbent exhibits a fluoride ion adsorption capacity of 193.4 mg/g in the leaching solution, surpassing that of many existing metal-based adsorbents. At the same time as the valuable metals, Li, Ni, and Co, are basically not adsorbed, the selective adsorption of fluoride ions can be achieved. Adsorption isotherm studies indicate that the adsorption process follows the Langmuir model, suggesting monolayer adsorption. The secondary adsorption process is primarily governed by chemical adsorption, and elevated temperatures facilitate the removal of fluoride ions. Kinetic studies demonstrate that the adsorption process is well described by the pseudo-second-order model. After desorption and regeneration with NaOH solution, the adsorbent still has a favorable fluoride removal performance, and the adsorption rate of fluoride ions can still reach 95% after four cycles of use. With its high capacity, rapid kinetics, and excellent selectivity, the adsorbent is highly promising for large-scale implementation. Full article

High denitration efficiency and strong adaptability to flue gas temperature fluctuations are the core properties of the NH₃-SCR catalyst. In this study, Fe₂O₃ modification is used as a means to explore the mechanism of adding Fe₂O₃ to broaden the temperature range of the 6CeO₂-40MnO₂/TiO₂ catalyst during the preparation process. The results show that the 6Fe₂O₃-6CeO₂-40MnO₂/TiO₂ catalyst exhibits excellent denitration performance, with a denitration efficiency higher than 90%. The temperature range is from 129 to 390 °C. N₂ selectivity and resistance to SO₂ and H₂O are good, and the denitration performance is significantly improved. When the Fe₂O₃ content is 6%, it promotes lattice shrinkage of TiO₂, improves its dispersion, refines the grain size, and increases the specific surface area of the catalyst. At the same time, Fe₂O₃ enhances the chemical adsorption of oxygen on the catalyst surface and increases the proportion of low-cost metal ions, thereby promoting electron transfer between active elements, generating more surface reactive oxygen species, increasing the oxygen vacancy content and adsorption sites for NO_x and NH₃, and significantly improving the redox performance of the catalyst. This effect is particularly conducive to the formation of strong acid sites on the catalyst surface. The NH₃-SCR reaction on the surface of the 6Fe₂O₃-6CeO₂-40MnO₂/TiO₂ catalyst follows both the L-H and E-R mechanisms, with the L-H mechanism being dominant. Full article

The quality and safety of agricultural products are important factors in safeguarding human health and promoting sustainable agricultural development. However, for the purpose of improving the yield and quality, the misuse of pesticides often occurs, causing pesticide residues to remain in vegetables, posing threats to both the environment and human health. In order to detect and adsorb pesticide residues in vegetables, a coral-like novel magnetic porous nanomaterial (Fe@MDZ) was developed in this study as an adsorbent to adsorb thiabendazole (TBZ). Fe@MDZ has a large specific surface area (229.254 m²/g) and high saturation magnetization intensity (57.38 emu/g) with good adsorption capacity for TBZ. When the initial concentration was 2 mg/L, the adsorption capacity for TBZ was 1.23 mg/g. The static adsorption process matched the Langmuir isotherm model and was consistent with the pseudo-second-order kinetic model. In addition, the recovery of TBZ in both tomato and Chinese cabbage samples at different concentrations was above 70%. This work provides a new idea for the detection of TBZ pesticide residues in vegetables. Full article

Currently, few studies have revealed the comprehensive effects of environmental organic matter, freeze–thaw and oxidative aging on the adsorption performance of cadmium (Cd(II)), which is essential for the sustainable stability evaluation of the adsorbent. Herein, we observed that humic acids (HAs) extracted from different soils inhibited the adsorption performance of Cd(II) onto the cuttlebone-derived samples by occupying the different major adsorption active sites of the adsorbent, and the lower cadmium-complexation ability of HAs would increase the occupation of adsorption sites. The freeze–thaw process increased the pore size and volume of the cuttlebone-derived samples, while oxidative aging enhanced the specific surface area and introduced additional C–O/C=O groups. These changes promoted the adsorption performance of Cd(II) in the cuttlebone-derived samples after freeze–thaw or oxidative aging. Additionally, the resistances of cuttlebone-based adsorbents to HAs, freeze–thaw, and oxidative aging were elucidated and optimized by simple alkali boiling or carbonization treatment. Furthermore, the adsorption capacities of Cd(II) by samples in the natural cadmium-contaminated river ranged from 548.99 mg g⁻¹ to 571.55 mg g⁻¹, which are higher values than those of most reported adsorbents. Therefore, this work provides an important experimental basis for the practical application and sustainable design of adsorbents under real environmental conditions. Full article

Industrial air pollution, particularly acidic gases such as hydrogen chloride (HCl), poses serious environmental and health hazards. Here, hopcalite catalysts were introduced into activated carbon fibers via the impregnation process to enhance HCl capture. The Cu/Mn molar ratio was fixed at 1:1 while the Cu precursor loading was varied with the weight of Cu (Cu 0.04–0.1). Structural and surface modifications were examined using scanning electron microscope, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, inductively coupled plasma mass spectrometer, and Brunauer–Emmett–Teller analyses. Progressive CuMnOx deposition increased Cu and Mn contents up to 4 at.% and 3.7 at.%, respectively, but decreased the specific surface area from 1565.1 to 1342.7 m²/g owing to pore blocking. Fixed-bed breakthrough tests (50 ppm HCl, 1000 mL/min) showed that moderate catalyst addition (Cu 0.04) yielded the highest total removal (83.6%) and adsorption capacity (12,354.6 mg/g), benefiting from combined physical and catalytic chemisorption. Higher loadings (Cu 0.06–0.1) further reduced microporosity and led to lower removal efficiencies. These results demonstrate that an optimal CuMnOx level effectively promotes chemical adsorption without compromising the intrinsic microporous network of ACFs. Full article

This study aimed to develop a high-performance Modified Activated Carbon Fiber (ACF) filter for the effective removal of Volatile Organic Compounds (VOCs) generated in workplaces and for application in indoor VOCmitigation devices. ACF was modified with CuMnOx catalysts and evaluated for the removal of formaldehyde, acetaldehyde, and benzene. The modified ACF filter was prepared by introducing CuMnOx via an impregnation method using Cu(NO₃)₂⋅3H₂O and Mn(NO₃)₂⋅6H₂O precursors, followed by a crucial high-concentration oxygen plasma surface treatment (50 sccm gas flow) to effectively incorporate oxygen functional groups, thereby enhancing catalyst dispersion and activity. Characterization of the fabricated ACF/CuMnOx composite revealed that the optimized sample, now designated ACF-P-0.1 (representing both CuMnOx catalyst impregnation and O₂ plasma treatment), exhibited uniformly dispersed CuMnOx particles (<500 nm) on the ACF surface. This stability retained a high specific surface area (1342.7 m²/g) and micropore ratio (92.23%). H₂-TPR analysis demonstrated low-temperature reduction peaks at 140 °C and 205.8 °C, indicating excellent redox properties that enable high catalytic VOC oxidation near room temperature. The oxygen plasma treatment was found to increase the interfacial reactivity between the catalyst and ACF, contributing to further enhancement of activity. Performance tests confirmed that the ACF-P-0.1 sample provided superior adsorption–oxidation synergy. Benzene removal achieved a peak efficiency of 97.5%, demonstrating optimal interaction with the microporous ACF structure. For formaldehyde, a removal efficiency of 96.6% was achieved within 30 min, significantly faster than that of Raw ACF, highlighting the material’s ability to adsorb VOCs and subsequently oxidize them with high efficiency. These findings suggest that the developed ACF/CuMnOx composite filters can serve as promising materials for VOCs removal in indoor environments such as printing, coating, and conductive film manufacturing processes. Full article

As key intermediate products in petroleum and chemical units, C4 hydrocarbons can be converted to ethene and propylene. While C4 olefins can be cracked into ethene and propylene on acid catalysts, such reactions with C4 paraffins are difficult under these conditions. In this study, a bifunctional metal–acid catalyst, BDHC, was prepared for catalytic dehydrogenation and catalytic cracking, using ZSM-5 zeolite for cracking active groups and Fe₂O₃ and Cr₂O₃ for dehydrogenation active groups. In the catalyzed reaction, C4 paraffins are converted to C4 olefins, which are subsequently cracked into ethene and propylene. The BDHC catalyst’s high relative crystallinity and large specific surface area and pore volume promote adsorption of reactant molecules. Moreover, the appropriate acid content suppresses side pathways and produces more ethene and propylene. Under optimized conditions, the ethene yield was 11.20%, the propylene yield was 27.51%, and the sum of the ethene and propylene yields was 38.71%. Full article

N-doped carbon aerogels have garnered increasing research interest in the field of energy and environment due to their unique structural features. Organic dyes, which contain redox-active sites and act as pollutants, are attractive candidates for cathode materials in Li-ion batteries but still suffer from poor cycle stability and rate performance. Therefore, there is still a lack of an easy and effective approach to rationally design the pore structure of N-doped carbon aerogels for efficiently and stably trapping dye molecules and converting them into high-performance cathode materials. Herein, we propose an innovative strategy for preparing nitrogen-doped carbon aerogels with a well-defined micropore structure (MNCAs) for efficient adsorption of dye molecules, subsequently converting them into high-performance lithium-ion battery cathode materials. MNCAs were synthesized via Schiff-based polymerization using polyhedral oligomeric silsesquioxane (POSS) as a template, resulting in a carbon framework with well-defined micropores. Benefiting from their high specific surface area and well-defined micropore structure, MNCAs exhibited a maximum adsorption capacity at equilibrium of 2273 mg g⁻¹ for indigo. Notably, the indigo@nitrogen-doped carbon aerogel composite (IDG@MNCAs) exhibits high specific capacity, outstanding cycling stability, and remarkable rate capability. The discharge specific capacity of IDG@MNCAs retains 89% of its capacity (120 mAh g⁻¹) after 200 cycles at 100 mA g⁻¹ and maintains 70% capacity retention after 1200 cycles at the higher current density of 1000 mA g⁻¹, surpassing many recently reported organic cathode materials. 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

The valorization of volcanic ash as a raw material for advanced functional materials offers dual benefits for both the environment and technology. Firstly, it diverts waste from landfills, thereby reducing the environmental footprint of volcanic deposits. Secondly, it contributes to the circular economy by transforming an abundant natural residue into a high-value product. In this study, zeolites were synthesized from the ash of the Ubinas volcano via the hydrothermal method in an alkaline medium. A systematic investigation was conducted to ascertain the influence of NaOH concentration and reaction temperature on synthesis efficiency and final material properties. The crystalline phases and morphology of the products were characterized using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), and Scanning Electron Microscopy (SEM), while textural and thermal properties were evaluated through the Brunauer–Emmett–Teller (BET) method and Thermogravimetric Analysis (TGA). The results revealed that both temperature and NaOH concentration significantly affected the physicochemical properties of the zeolites. Four zeolite types were obtained; among them, Zeolite Z4 (synthesized with 3 M NaOH at 150 °C) exhibited the highest adsorption capacity, with a specific surface area of 35.60 m²/g, while Zeolite Z1 (synthesized at 120 °C with 1.5 M NaOH and 27.85 m²/g) displayed superior thermal stability and crystallinity. These variations in thermal and textural properties were reflected in the catalytic pyrolysis performance of polypropylene (PP). Zeolite Z3 (synthesized at 150 °C with 1.5 M NaOH) achieved the highest gaseous product yield (80.2%), despite lacking the expected zeolitic crystalline phases. In contrast, Zeolite Z2 (synthesized at 120 °C with 3 M NaOH) yielded 57.7% gaseous products and stood out for its predominant analcime phase, characteristic of zeolitic materials. In summary, this study demonstrates that volcanic ash-derived zeolites not only enhance synthesis efficiency and functional performance but also represent a sustainable strategy for waste valorization, closing material loops and enabling the recovery of high-calorific gaseous products from plastic waste. Full article

In this work, we investigate advanced photocatalyst Bi₃TiNbO₉ as promising piezophotocatalyst in terms of the effect of synthesis methods on the surface chemistry, structure, and catalytic performance in process of contaminant removal. Samples were prepared via solid-state reaction (BTNO-900) and molten salt synthesis (BTNO-800), leading to distinct morphologies and defect distributions. SEM imaging revealed that BTNO-900 consists of agglomerated, irregular particles, while BTNO-800 exhibits well-faceted, plate-like grains. Nitrogen adsorption analysis showed that the molten-synthesized sample possesses a significantly higher specific surface area (5.9 m²/g vs. 1.4 m²/g) and slightly larger average pore diameter (2.8 nm vs. 2.6 nm). High-resolution XPS revealed systematic shifts in binding energies for Bi 4f, Ti 2p, Nb 3d, and O 1s peaks in BTNO-900, accompanied by a higher content of adsorbed oxygen species (57% vs. 7.2%), indicating an increased concentration of oxygen vacancies and surface hydroxylation due to the solid-state synthesis route. Catalytic testing demonstrated that BTNO exhibits enhanced piezocatalytic efficiency of Methylene Blue degradation (~78% for both samples), whereas BTNO-800 shows significantly reduced photocatalytic activity (45.6%) compared to BTNO-900 (84.1%), suggesting recombination effects dominate in the more defective material. Synergism of light and mechanical stress results in piezophotocatalytic degradation for both samples (92.4% and 93.4%, relatively). These findings confirm that synthesis-controlled defect engineering is a key parameter for optimizing the photocatalytic behavior of Bi₃TiNbO₉-based layered oxides and crucial role of its piezocatalytic activity. Full article

Lead (Pb(II)) contamination in water poses severe environmental and health risks due to its toxicity and persistence. This study compares almond shell-derived biochars produced by slow pyrolysis (SP) and microwave pyrolysis (MW), with and without KOH activation, focusing on structural properties and Pb(II) adsorption performance. Biochars were characterized by proximate and elemental analysis, BET surface area, FTIR spectroscopy, and adsorption experiments including pH dependence, kinetics, and equilibrium isotherms. Non-activated SP exhibited the highest surface area (S_BET = 693 m²·g⁻¹), pronounced mesoporosity (≈73% of total pore volume), and the largest observed equilibrium capacities. KOH activation increased surface hydroxyl content but degraded textural properties; in MW samples, it induced severe pore collapse. Given the very fast uptake, kinetic modeling was treated cautiously: for non-activated biochars, Elovich adequately captured the time-course trend, whereas activated samples returned non-physical kinetic constants (e.g., negative k₂) likely due to high post-adsorption pH (>11) and probable Pb(OH)₂ precipitation. Equilibrium data (fitted over 50–500 mg·L⁻¹) were better captured by the Freundlich and Redlich–Peterson models, indicating a mixed adsorption behaviour with contributions from heterogeneous site distribution and site-specific interactions. Optimal Pb(II) removal occurred at pH 4, with no measurable leaching from the biochar matrix. Overall, non-activated SP biochar is the most effective, sustainable and low-cost option among the tested materials for Pb(II) removal from water, avoiding aggressive chemical activation while maximizing adsorption performance. Full article