Search Results (50)

Magnetic polymer nanocomposites (MPNCs) have attracted considerable attention as advanced multifunctional materials for water purification due to their high adsorption capacity, magnetic recoverability, and excellent reusability. This review presents a comprehensive overview of recent developments in the synthesis, characterization, and environmental applications of MPNCs for wastewater treatment. Particular emphasis is placed on the principal synthesis strategies, including in situ and ex situ approaches, and their influence on nanoparticle dispersion, interfacial interactions, and the physicochemical properties of the resulting nanocomposites. The review covers the most widely investigated magnetic nanomaterials, such as Fe₃O₄, γ-Fe₂O₃, CoFe₂O₄, ZnFe₂O₄, and other ferrites, incorporated into natural and synthetic polymer matrices including chitosan, cellulose, alginate, polyaniline, polypyrrole, poly(vinyl alcohol), and polystyrene. Advanced characterization techniques, including X-ray diffraction (XRD), scanning and transmission electron microscopy (SEM/TEM), Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), and superconducting quantum interference device (SQUID) measurements, are discussed to evaluate the structural, chemical, thermal, and magnetic properties of these hybrid materials. The adsorption performance and underlying mechanisms of MPNCs for the removal of heavy metals, dyes, pharmaceutical compounds, organic pollutants, and oil contaminants are critically analyzed, highlighting the roles of polymer functionalization, nanocomposite architecture, and magnetic separation in enhancing treatment efficiency and reusability. In addition, the contribution of density functional theory (DFT) to understanding adsorption mechanisms and guiding the rational design of high-performance adsorbents is reviewed. Finally, current challenges and future perspectives, including green synthesis, multifunctional and stimuli-responsive materials, scalable manufacturing, and industrial implementation, are discussed. This review provides a comprehensive framework for the design and development of next-generation magnetic polymer nanocomposites for sustainable water remediation applications. Full article

With the pervasive deployment of 5G communication systems and electronic devices, electromagnetic (EM) pollution has emerged as a critical environmental concern. Due to their wide availability, low cost, and ease of acquisition, biomass materials have been widely used in the preparation of electromagnetic wave absorption materials. Compared with traditional in situ impregnation methods, this study first employs chemical reagents to reduce the lignin content within balsa wood, thereby opening more pores and enhancing the loading capacity of iron salts. Subsequently, magnetic Fe₃O₄ particles are synthesized in situ, enabling the fabrication of magnetic wood-based composites. Compared with the non-impregnated pure carbonized samples, the reflection loss value of the samples with magnetic particles increased to −42.37 dB, corresponding to a matching thickness of 1.5 mm. This is much better than the −8.79 dB of the pure carbonized samples, and is attributed to multiple loss mechanisms. In addition, modern physical and chemical analysis instruments such as SEM, TEM, XRD, XPS, and Raman were used to characterize the physical and chemical changes of the materials. Finally, its applications in aerospace and thermal response were identified. Full article

The Lantana genus, especially L. camara, has emerged as a potential yet underutilized lignocellulosic feedstock for various catalytic thermochemical conversion products and advanced carbon materials. This study reviews recent developments in the valorization of Lantana biomass to generate biofuels, bio-oil, syngas, and engineered biochar materials through pyrolysis, gasification, hydrothermal processing, and integrated biorefinery processes, in a critical manner. Particular focus will be on nanocomposite-modified, metal-doped biochar with catalytic elements such as ZSM-5, Fe₃O₄, TiO₂, and Ni-, Co-, and Zn-based oxides to enhance deoxygenation, catalytic cracking, tar reforming, pollutant remediation, and energy storage. Recent developments in catalyst synthesis techniques, such as impregnation, hydrothermal deposition, and in situ functionalization, are reviewed, along with characterization methods including BET, XRD, SEM/TEM, Raman spectroscopy, and XPS. The review further examines the impact of pore structure, surface chemistry, the presence of redox-active centers, and catalyst stability on product selectivity, syngas quality, and upgrading bio-oil performance. The effects of biochar on microbial immobilization, anaerobic digestion, and integrated biochemical conversion are discussed in detail, excluding thermochemical effects. The challenges of catalyst deactivation, biomass heterogeneities, scalability, techno-economic viability, and decentralized biomass logistics are also discussed. In summary, the development and implementation of catalytic reaction engineering, the design of nanocomposite biochar, and circular bioeconomy strategies have great potential to facilitate the conversion of invasive Lantana biomass into renewable fuels, multifunctional carbon materials, and environmentally friendly bioeconomy products. Full article

This work investigates the reciprocal adhesion of Polybenzoxazole (PBO) and silicon nitride (SiN) with a focus on the combined effects of surface chemistry and environmental conditions, i.e., temperature (T) and relative humidity (RH). A set of six samples, including standard and silicon-rich SiN substrates treated with oxygen (O₂) or carbon tetrafluoride (CF₄) plasma, was fabricated and characterized by AFM, XPS, and TEM/EDX to quantify surface roughness and interfacial chemical modifications. Adhesion with PBO was then assessed through nanoindentation both in situ, during ambient control, and ex situ, after aging in a climatic chamber. Compared to PBO adhesion with as-deposited standard and silicon-rich SiN, O₂ plasma treatment was shown to improve adhesion by 13% and 24%, respectively, whereas CF₄ plasma treatment was still beneficial but more limited, improving adhesion by 8% for both substrates. The different effects were ascribed to the formation of a surface oxide layer after O₂ plasma, enhancing chemical affinity and substantially equalizing the adhesion on the two SiN substrates, while CF₄ plasma was impacting adhesion by reducing the substrates’ activity and, thus, increasing the efficiency of the PBO curing procedure. Notably, the adhesion loss with increasing dew point of the ambient (dependent on temperature and relative humidity) was observed across all samples regardless of surface treatment, reinforcing the critical role of absorbed moisture on polymeric film adhesion. However, this trend was observed for all samples only for in situ testing, with a loss of 25% in the critical load of delamination for the most critical environment, while ex situ tests showed a marked recovery of adhesion properties, leading to measurements no longer reflecting the actual state of the samples inside the altered environment. The results presented in this paper highlight the effect of substrate preparation on the adhesion of an organic compound and a substantial difference in environmental control methods for adhesion testing, providing an alternative approach to classical aging treatments and subsequent characterization for qualifying polymer/inorganic interfaces exposed to stressful operational conditions. Full article

Owing to the substantial polarity difference and weak interfacial interaction, the large-scale application of fly ash (FA) in rubber materials still faces substantial challenges. To solve this issue, this study prepared a modified hybrid SSBR@FA filler through a solution mechanochemical reaction between solution-polymerized styrene-butadiene rubber (SSBR) and FA in a lab planetary ball mill. Fourier transform infrared spectroscopy (FTIR) and energy-dispersive spectroscopy (EDS) analyses demonstrated the in situ grafting-neutralization between the carboxyl in the SSBR chains and metal oxides in FA. Transmission electron microscopy (TEM) showed that surface-grafted SSBR formed a rubber-constrained layer on FA particle surfaces, which can reduce their surface energy and improve the wettability between FA and SBR matrix. Compared with the SBR vulcanizate, the mechanical properties, thermal conductivity, and flame-retardant properties of the SBR/SSBR@FA vulcanizates were obviously improved. This was because of the uniform distribution of FA and the improved interfacial interaction between FA and the rubber matrix. For example, the tensile strength, tear strength, and elongation at break increased by 66.3%, 52.9%, and 17.7%, respectively. This easy, efficient, and environmentally modified method for FA was expected offer a practical and creative solution for its application in rubber manufacturing. Full article

Designing and constructing heterojunctions has emerged as a pivotal strategy for improving the photocatalytic efficiency of semiconductors. In this study, we report the controlled synthesis of an Au/Zn₃In₂S₆ Schottky junction through a combination of hydrothermal and in situ photodeposition methods. The structural, morphological, and photoelectrochemical properties of the catalyst were meticulously characterized using a suite of techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), photoelectrochemical (PEC) measurements, and electron spin resonance (ESR) spectroscopy. The optimized 3% Au/Zn₃In₂S₆ composite exhibited a remarkable enhancement in both photocatalytic activity and stability, achieving a 90.4% removal of bisphenol A (BPA) under UV–visible light irradiation within 100 min. The corresponding first-order reaction rate constant was approximately 1.366 h⁻¹, nearly 4.37 times greater than that of the pristine Zn₃In₂S₆. This substantial improvement can be attributed to several key factors, including increased BPA adsorption, enhanced light absorption, and the efficient charge separation facilitated by the Au/Zn₃In₂S₆ heterojunction. Photogenerated holes, superoxide radicals, and hydroxyl radicals were identified as the primary reactive species responsible for the BPA degradation. This work highlights the potential of metal-modified semiconductors for advanced photocatalytic applications, offering insights into the design of highly efficient materials for environmental remediation. Full article

High-entropy alloys (HEAs) are a class of multi-principal element materials composed of five or more elements in near-equimolar ratios. This unique compositional design generates high configurational entropy, which stabilizes simple solid solution phases and reduces the tendency for intermetallic compound formation. Unlike conventional alloys, HEAs exhibit a combination of properties that are often mutually exclusive, such as high strength and ductility, excellent thermal stability, superior corrosion and oxidation resistance. The exceptional mechanical performance of HEAs is attributed to mechanisms including lattice distortion strengthening, sluggish diffusion, and multiple active deformation pathways such as dislocation slip, twinning, and phase transformation. Advanced characterization techniques such as transmission electron microscopy (TEM), atom probe tomography (APT), and in situ mechanical testing have revealed the complex interplay between microstructure and properties. Computational approaches, including CALPHAD modeling, density functional theory (DFT), and machine learning, have significantly accelerated HEA design, allowing prediction of phase stability, mechanical behavior, and environmental resistance. Representative examples include the FCC-structured CoCrFeMnNi alloy, known for its exceptional cryogenic toughness, Al-containing dual-phase HEAs, such as AlCoCrFeNi, which exhibit high hardness and moderate ductility and refractory HEAs, such as NbMoTaW, which maintain ultra-high strength at temperatures above 1200 °C. Despite these advances, challenges remain in controlling microstructural homogeneity, understanding long-term environmental stability, and developing cost-effective manufacturing routes. This review provides a comprehensive and analytical study of recent progress in HEA research (focusing on literature from 2022–2025), covering thermodynamic fundamentals, design strategies, processing techniques, mechanical and chemical properties, and emerging applications, through highlighting opportunities and directions for future research. In summary, the review’s unique contribution lies in offering an up-to-date, mechanistically grounded, and computationally informed study on the HEAs research-linking composition, processing, structure, and properties to guide the next phase of alloy design and application. Full article

The pervasive discharge of synthetic dyes into aquatic ecosystems poses a significant threat due to their chemical stability, low biodegradability, and carcinogenicity. Conventional dye remediation methods—such as biological treatments, coagulation, and adsorption—have demonstrated limited efficiency and poor reusability, particularly against resilient azo dyes. Cerium oxide (CeO₂) nanoparticles have gained traction as photocatalysts owing to their redox-active surfaces and oxygen storage capabilities; however, issues like particle agglomeration and rapid charge recombination restrict their catalytic performance. To address these challenges, this study presents the novel synthesis of a graphene oxide–cerium oxide (GO-CeO₂) nanocomposite via a facile in situ hydrothermal approach, using graphite from lead pencils as a sustainable precursor. The composite was structurally characterized using UV–visible spectroscopy, XRD, FTIR, and TEM. The GO matrix not only facilitates uniform dispersion of CeO₂ nanoparticles but also enhances interfacial electron mobility and active site availability. The nanocomposite demonstrated exceptional photocatalytic degradation efficiencies for methyl orange (94%), methyl red (98%), congo red (96%), and 4-nitrophenol (85.6%) under sunlight irradiation, with first-order rate constants significantly exceeding those of pure CeO₂. Notably, GO–CeO₂ retained strong catalytic activity over four degradation cycles, confirming its recyclability and structural stability. Total organic carbon (TOC) analysis revealed 79% mineralization of methyl orange, outperforming CeO₂ (45%), indicating near-complete conversion into benign byproducts. This work contributes a scalable, low-cost, and highly active heterogeneous photocatalyst for wastewater treatment, combining green synthesis principles with improved photodegradation kinetics. Its modular architecture and reusability make it a promising candidate for future environmental remediation technologies and integrated photocatalytic systems. Full article

In this study, the use of spent coffee waste as a green precursor of polyphenolic compounds, which are subsequently employed as reducing agents for the synthesis of zero-valent iron nanoparticles (nZVI) aimed at the efficient removal of dyes from aqueous systems, has been investigated. The nanoparticles, generated in situ in the presence of controlled amounts of hydrogen peroxide, were applied in the removal of organic dyes—including methylene blue, methyl orange, and orange G—through a heterogeneous Fenton-like catalytic process. The synthesized nZVI were thoroughly characterized by nitrogen adsorption at 77 K, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FT-IR), and powder X-ray diffraction (XRD). A statistical design of experiments and response surface methodology were employed to evaluate the effect of polyphenol, Fe(III), and H₂O₂ concentrations on dye removal efficiency. Results showed that under optimized conditions, a 100% removal efficiency could be achieved. This work highlights the potential of nZVI synthesized from agro-industrial waste through sustainable routes as an effective solution for water remediation, contributing to circular economy strategies and environmental protection. Full article

Organic dye pollution in industrial wastewater is severe and difficult to degrade, posing a significant challenge to environmental management and water resource security. To meet the demand for the efficient elimination of Congo Red (CR) dye from industrial wastewater, this work prepared two zirconium-based metal–organic framework (MOF)–biochar composites, UIO-66@BY and UIO-67@BY, by in situ loading zirconium-based MOFs (UIO-66 and UIO-67) onto biochar (BY) via a solvothermal method. The composite material was comprehensively characterized using transmission electron microscopy (TEM), BET surface area analysis, and X-ray photoelectron spectroscopy (XPS). The adsorption results indicate that UIO-67@BY exhibits a significantly higher maximum adsorption capacity for CR dye compared to pristine biochar (BY), while UIO-66@BY also shows enhanced adsorption performance, but one that is slightly lower than that of UIO-67@BY. Further investigations reveal that the adsorption behavior conformed to a pseudo-second-order kinetic model and was well described by the Langmuir isotherm, suggesting that the adsorbent exhibited a homogeneous adsorption surface, and that chemical adsorption played a dominant role in the process. The primary mechanisms responsible for CR dye uptake by the composite include pore structure characteristics, coordination with functional groups, π–π stacking interactions, and electrostatic forces. The composite material developed herein provides an environmentally sustainable and economically efficient strategy for mitigating wastewater contamination. Full article

With the continuous consumption of fossil energy and the related environmental problems, clean energy, especially the hydrogen energy-derived water electrolysis, has attracted wide attention. However, as a result of the high energy consumption of water electrolysis and the limitations of single-function catalysts, there is an urgent need for cheap and simple-to-make bifunctional catalysts. In this work, based on the NiFe-LDH that is usually used for OER (Oxygen Evolution Reaction), doping of heteroatoms was carried out and a bifunctional catalyst could be then prepared using biomass as the carbon source. The preparation of catalyst precursors and in situ reduction were performed through the coupling process of hydrothermal and pyrolysis to enhance the electrolytic activity of the catalyst. Results showed that the overpotentials required to reach a current density of 10 mA·cm⁻² for the HER and OER processes were 305.2 mV and 310.4 mV, respectively, which are superior to the commercial catalysts. In the subsequent characterization, the structural characteristics of the catalyst support and their structure–activity correlation with active metals were systematically investigated by TEM, XRD, and XPS analysis, providing mechanistic insights into the catalytic behavior. The basic catalytic mechanisms of HER and OER were also obtained: the HER process was due to the formation of a Ni₃Fe alloy structure during catalyst preparation, which changed the electronic structure of the catalyst, while the OER process was induced by the formation of a NiOOH intermediate. The research results are expected to provide new ideas and data support for the preparation of bifunctional catalysts. Full article

Understanding the formation, structural evolution, and response of water ice at the nanoscale is essential for advancing research in fields such as cryo-electron microscopy and atmospheric science. In this work, we used environmental transmission electron microscopy (ETEM) to investigate the formation of water ice nanostructures and the etching and charging behaviors of ice under fast electron irradiation. These nanostructures were observed to be suspended along the edges of copper grids and supported on few-layer graphene. We varied growth parameters (temperature and time) to produce water ice nanostructures characterized by uniform thickness and enhanced crystallinity. Moreover, we examined the lithographic patterning of water ice at the copper grid edges and its localized etching effects on graphene substrates. Off-axis electron holography experiments further revealed charging phenomena induced by electron beam irradiation, enabling a quantitative assessment of charge accumulation on the ice nanostructures. Our findings demonstrate the controlled growth of ice thin films under high vacuum conditions at cryogenic temperatures, elucidate the etching behavior and charging phenomena of water ice under rapid electron beam irradiation. Full article

Diesel particulate matter (DPM) represents a deleterious environmental contaminant that necessitates the development of effective catalytic oxidation methodologies. This research delineates a comparative analysis of silver-supported metal oxide catalysts (Ag/Al₂O₃, Ag/TiO₂, Ag/ZnO, and Ag/CeO₂), with an emphasis on the effects of silver distribution and the metal-support interaction on the oxidation of DPM. An array of characterization techniques including XRD, HRTEM, XPS, H₂-TPR, TEM, GC-MS, TGA, and in situ DRIFTS was employed. The novelty of this study resides in elucidating the oxidation mechanism through a tripartite pathway and recognizing Ag⁰ as the predominant active species involved in soot oxidation. The Ag/Al₂O₃ catalyst demonstrated superior catalytic performance, achieving a reduction in the ignition temperature by more than 50 °C, attributable to the optimal dispersion of Ag nanoparticles and a balanced metal-support interaction. Conversely, an excessive interaction observed in Ag/ZnO resulted in diminished catalytic activity. The oxidation of DPM transpires through the volatilization of VOCs (<300 °C), the oxidation by reactive oxygen species, and the combustion of soot (>300 °C). This investigation offers significant contributions to the formulation of highly efficient silver-based catalysts for emissions control, with a particular focus on optimizing Ag dispersion and support interactions to enhance catalytic efficacy. Full article

Background: Poultry litter is the main waste of poultry farming and is widely used as an agricultural fertilizer. However, owing to the use of antimicrobials in animal production, it can accumulate antimicrobial residues, antimicrobial-resistant bacteria (ARB), and antimicrobial resistance genes (ARGs). This study aimed to evaluate the impact of poultry litter use on the microbiome and resistome of agricultural soils. Methods: Soil samples from fertilized and unfertilized plots were collected from two horticultural farms that intensively use poultry litter. Microbiome composition was assessed using 16S rRNA sequencing. A culture-dependent method was used to isolate resistant strains on CHROMagar plates supplemented with sulfamethoxazole or ciprofloxacin. ARGs and integrase-encoding genes were identified by PCR. Results: Microbiome analysis revealed significant differences in structure and composition between poultry litter-fertilized and unfertilized soils. Fertilized soils exhibited greater alpha diversity and richness. Bacillota, commonly found in the avian gastrointestinal tract, were more abundant in fertilized soils. A total of 62 resistant strains were isolated, and 23 clinically relevant strains harbored ARGs, including fluoroquinolone (qnrA and qnrB) and β-lactam (bla_GES, bla_TEM, and bla_SHV) resistance genes. Class 1 and 2 integron-associated genes (intI1 and intI2) were also detected. Notably, the rare bla_GES gene was detected in Bacillus sp. from unfertilized soil. Similarly, qnrA co-occurred with bla_SHV in a Bosea sp. strain from unfertilized soil. Conclusions: These findings highlight the potential for ARB dissemination in agricultural environments, where ARB and ARGs, once introduced into soils, may spread by weathering and other environmental factors, complicating negative control selection in in situ studies. Full article

A stabilized biochar (BC)–nano-scale zero-valent iron (nZVI) composite (BC-nZVI@Cell-g-PAA) was prepared using cellulose-grafted polyacrylic acid (Cell-g-PAA) as the raw material through in situ polymerization and liquid-phase reduction methods for the remediation of hexavalent chromium (Cr(VI))-contaminated water. BC-nZVI@Cell-g-PAA was characterized by XRD, FT-IR, SEM, BET, TEM, and XPS. According to the batch experiments, under optimized conditions (Cr(VI) concentration of 50 mg/L, pH = 3, and dosage of 2 g/L), the BC-nZVI@Cell-g-PAA composite achieved maximum Cr(VI) removal efficiency (99.69%) within 120 min. Notably, BC, as a carrier, achieved a high dispersion of nZVI through its porous structure, effectively preventing particle agglomeration and improving reaction activity. Simultaneously, the functional groups on the surface of Cell-g-PAA provided excellent protection for nZVI, significantly suppressing its oxidative deactivation. Furthermore, the composite effectively reduced Cr(VI) to insoluble trivalent chromium(Cr(III)) species and stabilized them on its surface through immobilization. The synergistic effects of physical adsorption and chemical reduction greatly contributed to the removal efficiency of Cr(VI). Remarkably, the composite exhibited excellent reusability with a removal efficiency of 62.4% after five cycles, demonstrating its potential as a promising material for remediating Cr(VI)-contaminated water. In conclusion, the BC-nZVI@Cell-g-PAA composite not only demonstrated remarkable efficiency in Cr(VI) removal but also showcased its potential for practical applications in environmental remediation, as evidenced by its sustained performance over multiple reuse cycles. Moreover, Cr(VI), a toxic and carcinogenic substance, poses significant risks to aquatic ecosystems and human health, underscoring the importance of developing effective methods for its removal from contaminated water. Full article