Search Results (3,060)

This research explores the dual role of biochar in addressing the escalating challenges of water salinity and pollution, focusing on its potential for both wastewater treatment and agricultural resilience. We investigated the adsorption capacity and efficiency of various biochar treatments to remove crystal violet dye from contaminated water. Biochar treated with H₂SO₄ demonstrated the highest adsorption capacity (450 mg/g). It consistently achieved 100% removal efficiency in all crystal violet concentrations tested, while silver-modified biochar showed a 99.95% removal rate at 50 ppm and an adsorption capacity of 5 mg/g. In agricultural applications, we evaluated the impact of biochar applications at concentrations of 1% and 3% on wheat crops irrigated with saline water of varying conductivity levels (0.63 and 10 dS/m). Wheat plants treated with 1% biochar exhibited the highest yield (26.6 cm) under 0.63 dS/m water conductivity, significantly outperforming the control group (17 cm). Biochar also resulted in elevated chlorophyll levels, with chlorophyll a ranging from 29.8 to 20.9 µg/mL and chlorophyll b ranging from 54 to 23 µg/mL, showing a marked improvement over the control. These findings demonstrate biochar’s potential to mitigate salinity-induced damage, with lower salinity conditions further enhancing chlorophyll a levels, while untreated plants showed reduced chlorophyll under high salinity. Full article

Constructed wetlands (CWs) are eco-technologies used for wastewater treatment, where vegetation is a key component. In recent decades, the adaptability and phytoremediation functions of ornamental plants (OPs)—which are not typically found in natural wetlands— have been tested. However, few comprehensive studies address the processes or mechanisms by which these OPs enhance pollutant removal in CWs and their artisanal applications. It is also vital to understand the most used OP species in CWs and their advantages in phytoremediation. Thus, this study enhances the understanding of the processes involved in pollutant degradation within CWs, specifically focusing on absorption, adsorption, translocation, radial oxygen loss, and root exudates. It reaffirms the essential role that plants play in these systems, as suggested in previous scientific reports, and discusses some potential applications for the ornamental plants produced in CWs, such as flower arrangements and crafts. This also includes the social aspect, emphasizing community engagement through social capital initiatives for the adoption and appropriation of the ecotechnology. Additionally, a bibliometric analysis revealed that Mexico is among the countries with the most significant research on OPs in CWs, particularly concerning commercially valuable species, followed by India and China. These findings can be instrumental in planning future community projects focused on wastewater treatment using CWs using OPs. Full article

This study systematically investigated the influence of catalyst formulation parameters (precious metal loading and Pt/Pd ratio) in diesel oxidation catalysts (DOCs)+catalyzed diesel particulate filter (CDPF)+selective catalytic reduction (SCR) on gaseous pollutant emissions from diesel engines. Results indicate that under varying conditions, the impact of catalyst formulation on DOC system performance—such as temperature rise characteristics, pressure drop, and brake specific fuel consumption (BSFC)—remains limited. Notably, exhaust temperature exerts a decisive influence on carbon monoxide (CO) and hydrocarbon (HC) conversion efficiency, significantly outweighing the impact of exhaust flow rate. Increasing precious metal loading and Pt proportion markedly optimizes CO and HC ignition characteristics by lowering ignition temperatures. However, under high-load conditions, conversion efficiencies across different catalyst formulations tend to converge. Specifically, under low-load conditions, a competitive adsorption mechanism between CO and HC causes HC conversion efficiency to exhibit an inverse trend relative to CO. Furthermore, higher precious metal loading and Pt content significantly enhance the catalyst’s NO₂ formation capacity at equilibrium temperatures, while higher Pd content contributes to improved thermal stability. Higher precious metal loading and Pt content increase nitrogen oxides (NO_x) conversion efficiency. CDPF possesses the ability to further oxidize NO. Full article

This study investigates the capacity of green and brown algae to sustainably remove oxyanions from contaminated waters, highlighting their cost-effectiveness. Often considered biomass waste and contributors to organic contamination, these algae can be used as effective biosorbents, aligning with circular economy principles and sustainable waste management. Various pre-treatments were tested to enhance adsorption capacity, with mixed results regarding their effectiveness. The focus then shifted to the use of Cladophora sericea algae for the uptake and removal of selenium species, specifically selenite (Se(IV)) and selenate (Se(VI)). The effects of different operational parameters on oxyanion uptake by algae were studied in batch mode. The assessments were conducted on a single-component and a multi-component synthetic matrix. The results indicate that pH significantly impacts biosorption, with equilibrium achieved in 90 min. Both pseudo-first-order and pseudo-second-order models provided a good fit to the experimental data. The algae’s retention capacity for selenium remained largely unaffected by the presence of other anions, a key advantage for application in complex real effluent matrices. Kinetic studies performed under different values of initial pollutant concentration and biosorbent mass indicate a biosorbed amount at an equilibrium of 570 µg g⁻¹. Full article

Microplastic pollution represents a significant environmental challenge, as microplastics accumulate in effluents and soils, causing serious risks to ecosystems and human health. Efficient removal of these contaminants is essential to mitigate their potential adverse effects. This review summarizes and critically analyses current methods for the removal of microplastics from effluents and soils, focusing on their effectiveness, advantages, and limitations. Conventional techniques—including filtration, flotation, chemical coagulation, flocculation, and adsorption—are discussed in the context of wastewater treatment and soil remediation. Emerging approaches, such as flocculation processes with special focus on the application of bio-based flocculants, are also highlighted as promising solutions. Key challenges in microplastic removal, including the diversity of microplastic types, their small size, and the complexity of environmental matrices, are addressed. This work intends to contribute to the urgent need for further research to develop more efficient and sustainable strategies for microplastic removal from environmental systems. Full article

Unsymmetrical dimethylhydrazine (1,1-Dimethylhydrazine, UDMH) is widely used as a high-performance liquid rocket propellant for the space industry globally. The release and leakage of UDMH into the environment, especially the soil environment, pose serious threats to ecosystems and human beings. In order to reveal the hazards of UDMH to soil and facilitate subsequent remediation, the adsorption behavior of UDMH in typical soil (yellow-brown soil, red soil, and black soil) matrices was explored, the environmental fate and toxicity of UDMH were presented by simulation calculation, and the phytotoxicity was evaluated by germination assay in the present study. The results showed that the adsorption performance of red soil, yellow-brown soil, and black soil for UDMH increased sequentially by integrating the findings from kinetic and thermodynamic studies. A highly significant correlation between the physicochemical and adsorption parameters for various soil matrices indicated a considerable impact of soil physicochemical properties on the adsorption behavior of UDMH in soils. The environmental fate simulation calculation indicated that UDMH and its transformation products were prone to being dissolved in soil water and migrating; however, once these compounds were present in the surface layer of dry soil, severe ecological and environmental pollution would occur. Based on a thorough evaluation of the toxicity parameters, formaldehyde dimethylhydrazone has been identified as demonstrating the most pronounced environmental toxicity profile, thus warranting prioritized attention. The results of a germination assay demonstrated that more than 100 mg·kg⁻¹ of UDMH in the soil would lead to strong phytotoxicity to plants, and more than 200 mg·kg⁻¹ of UDMH would significantly affect the early germination of seeds. Hence, this research provided helpful insights and theoretical support for the environmental fate and remediation of UDMH. Full article

Water pollution, a significant environmental issue, is growing more urgent. This study evaluated the effectiveness of adsorption and electrocoagulation methods in removing Ba-sic Blue 3 (BB3), a common dye used in the textile industry, from water. For the adsorption process, linden tree leaves—often used for health benefits in existing literature—were employed, while in the electrocoagulation (EC) method, an aluminum electrode was used. The results show that the optimal conditions for adsorption were an initial BB3 concentration of 5 mg/L, 50 mL of 0.9 g Tilia L. adsorbent, 60 min, 180 rpm, 30 °C, and pH 10, achieving a removal efficiency of 99.21%. The optimal conditions for electrocoagulation were 1 L of 15 mg/L initial BB3, a current density of 2.64 mA/cm², 15 mL of 0.2 M KCl, a reaction time of 90 min, a stirring speed of 100 rpm, and a pH of 10, resulting in a removal efficiency of 97.98%. The results indicate that linden leaves, a natural and sustainable material, showed a slightly higher removal percentage (99.21%) in the EC method over a shorter period (60 min). Conversely, the EC method also achieved a significant removal rate (97.98%, 90 min). In summary, both methods demonstrate strong BB3 removal capabilities and could help improve wastewater treatment processes. Full article

Microalgae are considered to be a dual solution for CO₂ fixation and biogas slurry purification due to their high photosynthetic efficiency and strong environmental adaptability. However, their application is constrained by the low solubility of CO₂ in the solution environment, which restricts microalgal growth, resulting in low biomass production and poor slurry purification efficiency. In this study, we developed MgFe layered double hydroxide (LDH) that spontaneously combined with Chlorella pyrenoidosa to help it concentrate CO₂, thereby increasing biomass yield and purification capacity for food waste biogas slurry. The prepared MgFe-LDH exhibited a typical layered structure with a CO₂ adsorption capacity of 4.44 mmol/g. MgFe-LDH and C. pyrenoidosa carried opposite charges, enabling successful self-assembly via electrostatic interaction. Compared with the control, the addition of 200 ppm MgFe-LDH increased C. pyrenoidosa biomass and pigment content by 36.82% and 63.05%, respectively. The removal efficiencies of total nitrogen, total phosphorus, and ammonia nitrogen in the slurry were enhanced by 20.04%, 31.54% and 14.57%, respectively. The addition of LDH effectively alleviated oxidative stress in C. pyrenoidosa and stimulated the secretion of extracellular polymeric substances, thereby enhancing the stress resistance and pollutant adsorption capabilities. These findings provided a new strategy for the industrial application of microalgal technology in CO₂ fixation and wastewater treatment. Full article

The development of efficient and sustainable advanced oxidation processes (AOPs) for organic pollutant removal is of great significance for water purification. In this study, a CoFeNi-layered double hydroxide (CoFeNi-LDH) catalyst was synthesized and applied for the simultaneous activation of peroxymonosulfate (PMS) and ozone to degrade rhodamine B (RhB) in aqueous solution. The CoFeNi-LDH/PMS/ozone system achieved a remarkable RhB removal efficiency of 95.2 ± 1.2% within 8 min under neutral pH conditions. Systematic parametric studies revealed that synergistic interactions among CoFeNi-LDH, PMS, and ozone contributed to the generation of reactive oxygen species (ROS), primarily sulfate radicals (SO₄^•−) and singlet oxygen (¹O₂), as confirmed by EPR and quenching experiments. Density functional theory (DFT) calculations demonstrated that ozone enhanced PMS adsorption and activation at CoFeNi catalytic sites. The catalyst exhibited robust magnetic recyclability and structural stability after repeated use. This work highlights a synergistic catalytic strategy for PMS/ozone activation, offering an effective and environmentally friendly platform for dye wastewater remediation. Full article

The escalating issue of water pollution driven by rapid industrialization necessitates the development of advanced remediation technologies. In this study, a novel method for producing chromium (Cr(VI)) ion-imprinted biochar (Cr(VI)-IIP-PEI@NBC) from wheat residue was proposed. After acid-oxidative modifications, polyethyleneimine (PEI) and glutaraldehyde (GA) were employed as the functional monomer and crosslinker, respectively, to enhance the biochar’s selectivity and adsorption capacity. Under optimized conditions (pH 2.0, 55 °C), the adsorbent achieved a maximum Cr(VI) uptake of 212.63 mg/g, which was 2.3 times higher than that of the non-imprinted biochar. The material exhibited exceptional specificity (99.64%) for Cr(VI) and maintained >80% adsorption efficiency after five regeneration cycles, demonstrating excellent reusability. Comprehensive structural characterization via Fourier transform infrared spectroscopy (FT-IR), thermal gravimetric analysis (TGA), Brunner–Emmet–Teller measurements (BET), and Scanning Electron Microscopy (SEM) confirmed successful Cr(VI) imprinting in the biochar and its high thermal stability and mesoporous architecture, elucidating the mechanisms behind its superior performance. This study presents a sustainable and high-performance adsorbent for the efficient treatment of chromium-contaminated wastewater, with significant potential for industrial applications. Full article

We investigated the application of an adsorbent fabricated from satsuma mandarin peel biomass using coating with poly(glycidyl methacrylate) followed by sequential treatment with hydroxylamine and hydrochloric acid for the remediation of hexavalent chromium-polluted water. The adsorbent was characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). Batch adsorption experiments were conducted wherein initial solution pH, initial chromium concentration, contact time, and temperature were varied. The adsorption equilibrium experimental data were well simulated by the Langmuir and Jovanovic models, pointing toward the formation of a monolayer of adsorbed chromium ions. The total chromium adsorption capacity of the functionalized satsuma mandarin peel adsorbent reached 219.28 mg g⁻¹ at initial pH 1.4 and 60 °C, markedly higher than 110.23 mg g⁻¹ at 30 °C. Where Cr(VI) was the sole chromium oxidation state in the initial solutions synthesized from potassium dichromate, the presence of Cr(III) ions in the final solutions confirmed Cr(VI) reduction. The results of this study show that the functionalized satsuma mandarin peel biomass is a potential candidate for use in the removal of hexavalent chromium from aqueous solution through reduction-coupled adsorption. Full article

Today, hydrogen is already widely regarded as up-and-coming source of energy. It is essential to meet energy needs while reducing environmental pollution, since it has a high energy capacity and does not emit carbon oxide when burned. However, for the widespread application of hydrogen energy, it is necessary to search new technical solutions for both its production and storage. A promising effective and cost-efficient method of hydrogen generation and storage can be the use of solid materials, including nanomaterials in which chemical or physical adsorption of hydrogen occurs. Focusing on the recommendations of the DOE, the search is underway for materials with high gravimetric capacity more than 6.5% wt% and in which sorption and release of hydrogen occurs at temperatures from −20 to +100 °C and normal pressure. This review aims to summarize research on hydrogen generation and storage using silicon nanostructures and silicon composites. Hydrogen generation has been observed in Si nanoparticles, porous Si, and Si nanowires. Regardless of their size and surface chemistry, the silicon nanocrystals interact with water/alcohol solutions, resulting in their complete oxidation, the hydrolysis of water, and the generation of hydrogen. In addition, porous Si nanostructures exhibit a large internal specific surface area covered by SiH_x bonds. A key advantage of porous Si nanostructures is their ability to release molecular hydrogen through the thermal decomposition of SiHx groups or in interaction with water/alkali. The review also covers simulations and theoretical modeling of H₂ generation and storage in silicon nanostructures. Using hydrogen with fuel cells could replace Li-ion batteries in drones and mobile gadgets as more efficient. Finally, some recent applications, including the potential use of Si-based agents as hydrogen sources to address issues associated with new approaches for antioxidative therapy. Hydrogen acts as a powerful antioxidant, specifically targeting harmful ROS such as hydroxyl radicals. Antioxidant therapy using hydrogen (often termed hydrogen medicine) has shown promise in alleviating the pathology of various diseases, including brain ischemia–reperfusion injury, Parkinson’s disease, and hepatitis. Full article

This work aims to design versatile hybrids fabricated by poly(hydroxypropyl methacrylate-co-glycidyl methacrylate) gels loaded with pristine montmorillonite, P(HPMA-co-GMA)/Mmt, by varying the clay content. Insights into design of epoxy-functional hybrids were provided by combining in situ copolymerization reactions with solution mixing to evaluate the effect of aluminosilicate addition on structure–property changes in (alkyl)methacrylate-based gels. Comprehensive analyses were conducted regarding the composition and structural properties of hybrids in the presence of Mmt. The hybrids exhibited excellent swelling, salt surfactant tolerance, and pH sensitivity depending on the composition. The higher the Mmt concentration, the lower the swelling ratio; however, the compressive moduli did not change monotonically with increasing Mmt from 0.80 to 2.20% (w/v). Dye adsorption revealed the effects of variables (dye type, pH, contact time, concentration) on adsorptive properties of hybrids towards cationic methylene blue (MB) and anionic sunset yellow, allura red, blue brilliant, carmoisine, and tartrazine dyes. Adsorption kinetics of MB obeyed pseudo-second-order model, and the maximum dye adsorption capacity for hybrids increased from 5.01 mg g⁻¹ to 16.42 mg g⁻¹, while adsorption isotherms were defined by the Freundlich model. The proposed hybrids have emerged as alternative materials that enable multiple uses of same adsorbent for the removal of different types of pollutants. Full article

Chromium (Cr), a toxic heavy metal, poses significant environmental and health risks when industrial effluents containing Cr are discharged untreated. Addressing this challenge, this study developed a selective chromium removal strategy using IRA-900 resin in a sulfuric acid system with sodium phosphite (NaH₂PO₃) as a complexing agent. In the NaH₂PO₃-H₂SO₄ system, IRA-900 resin exhibited exceptional selectivity for Cr³⁺ with minimal co-adsorption of competing ions. The adsorption process followed the Langmuir isotherm model (R² > 0.99), indicating monolayer chemisorption dominated by homogeneous active sites, and achieved a maximum capacity of 103.56 mg·g⁻¹. Characterization via XPS, FT-IR, and SEM-EDS revealed a two-step mechanism: Cr³⁺ reacts with H₂PO₃⁻ to form an anionic complex, and then the complex undergoes electrostatic interaction and ion exchange with chloride ions (Cl⁻) on the quaternary ammonium groups of the resin. The chromium-loaded resin demonstrated remarkable structural stability, resisting Cr³⁺ desorption under conventional elution conditions. This property provides a novel pathway for chromium solidification in industrial wastewater, effectively minimizing secondary pollution risks. This work advances the design of ligand-assisted ion-exchange systems for targeted heavy metal removal, offering both high selectivity and environmental compatibility in wastewater treatment. Full article

Microplastics (MPs), as an emerging persistent contaminant, pose a potential threat to ecosystems and human health. The adsorptive removal of MPs from aqueous environments using magnetic nanoparticles has become a particularly promising remediation technology. Nevertheless, there remain significant knowledge gaps regarding its adsorption mechanism, especially how the key physical properties of magnetic nanoparticles regulate their adsorption behavior towards MPs. This study first investigated the relationship between the particle size of Fe₃O₄ nanoparticles and their adsorption efficacy for MPs. The results demonstrated a non-monotonic, size-dependent adsorption of MPs by Fe₃O₄ nanoparticles, with the adsorption efficiency and capacity following the order: 300 nm > 15 nm > 100 nm. This non-linear relationship suggested that factors other than specific surface area (which would favor smaller particles) are significantly influencing the adsorption process. Isotherm analysis indicated that the adsorption is not an ideal monolayer coverage process. Kinetic studies showed that the adsorption process could be better described by the pseudo-second-order model, while intra-particle diffusion played a critical role throughout the adsorption process. Furthermore, the effect of pH on adsorption efficiency was examined, revealing that the optimal performance occurs under neutral to weak acidic conditions, which is consistent with measurements of surface charges of nanoparticles. These findings suggest that the adsorption is not determined by specific surface area but is dominated by electrostatic interactions. The size-dependent adsorption of MPs by Fe₃O₄ nanoparticles provides new insights for the modification of magnetic adsorbents and offers a novel perspective for the sustainable and efficient remediation of environmental MPs pollution. Full article