Search Results (1,198)

Due to their excellent physicochemical properties, the nanoparticles (NPs) have been utilized in various potential applications, including environmental remediation, energy storage, and nanomedicine. In this work, the ultrasonic and manual stirring approaches were used to integrate yttrium oxide (Y₂O₃) nanoparticles (NPs) into reduced graphene oxide (RGO) and carbon nanotubes (CNTs) to enhance their photocatalytic and anticancer properties. Pure Y₂O₃NPs, Y₂O₃/RGO NCs, and Y₂O₃/CNTs NCs were characterized using different analytical techniques, such as XRD, SEM, EDX with Elemental Mapping, FTIR, UV-Vis, PL, and DLS to investigate their improved structural, surface morphological, chemical bonding, optical, and surface charge properties. XRD data confirmed the successful integration of Y₂O₃into RGO and CNTs, with minor changes in crystallite sizes. SEM images with EDX analysis revealed that Y₂O₃NPs were uniformly distributed on RGO and CNTs, reducing aggregation. Chemical bonding and interactions between Y₂O₃and carbon materials were investigated using Fourier Transform Infrared (FTIR) analysis. UV and PL results suggest that the optical studies showed a shift in absorption peaks upon integration with RGO and CNTs. This indicates enhanced light absorption and modifications to the band gap between (3.79–4.40 eV) for the obtained samples. In the photocatalytic experiment, the degradation efficiency of bromophenol blue (BPB) dye for Y₂O₃RGO NCs was up to 87.3%, outperforming pure Y₂O₃NPs (45.83%) and Y₂O₃/CNTs NCs (66.78%) after 120 min of UV irradiation. Additionally, the MTT assay demonstrated that Y₂O₃/RGO NCs exhibited the highest anticancer activity against MG-63 bone cancer cells with an IC50 value of 45.7 µg/mL compared to Y₂O₃CNTs NCs and pure Y₂O₃NPs. This work highlights that Y₂O₃/RGO NCs could be used in significant applications, including environmental remediation and in vivo cancer therapy studies. Full article

Lead (Pb) in soil poses serious environmental and health risks, and its removal requires complex and costly treatment methods to meet strict regulatory standards. To effectively address this challenge, innovative and efficient techniques are essential. Sepiolite-supported MnFe₂O₄ (MnFe₂O₄/SEP) composites were synthesized via a chemical co-precipitation method. The effects of MnFe₂O₄/SEP on soil pH, cation exchange capacity (CEC), available Pb content, Pb²⁺ uptake, and the activities of antioxidant enzymes in Brassica chinensis (Pak Choi) were examined. MnFe₂O₄/SEP showed superior Pb²⁺ adsorption compared to SEP alone, fitting Langmuir models, Dubinin-Radushkevich (D-R) models, Temkin models and pseudo-second-order kinetics. The maximum adsorption capacities at 298, 308, and 318 K were 459, 500 and 549 mg·g⁻¹, respectively. XPS analysis indicated that chemisorption achieved through ion exchange between Pb²⁺ and H⁺ was the main mechanism. MnFe₂O₄/SEP increased the soil pH by 0.2–1.5 units and CEC by 18–47%, while reducing available Pb by 12–83%. After treatment with MnFe₂O₄/SEP, acid-extractable and reducible Pb in the soil decreased by 14% and 39%, while oxidizable and residual Pb increased by 26% and 21%, respectively. In Brassica chinensis, MnFe₂O₄/SEP reduced Pb²⁺ uptake by 76%, increased chlorophyll content by 36%, and decreased malondialdehyde (MDA) levels by 36%. The activities of antioxidant enzymes—superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT)—were decreased by 29%, 38% and 17%, respectively. These findings demonstrate that MnFe₂O₄/SEP is an efficient Pb²⁺ adsorbent that immobilizes Pb in soil mainly through ion exchange, thereby providing a highly effective strategy for remediating Pb-contaminated soils and improving plant health. Full article

Understanding how redox-active ligands coordinate to metal centers of different oxidation states is essential for applications ranging from metal remediation and recycling to drug discovery. In this study, coordination complexes of nickel(II), copper(II), and zinc(II) chloride salts were synthesized by mixing the salts with either arylazoformamide (AAF) or arylazothioformamide (ATF) ligands in toluene or methanol. The AAF and ATF ligands coordinate through their 1,3-heterodienes, N=N–C=O and N=N–C=S, respectively, and, due to their known strong binding, the piperidine and pyrrolidine formamide units were selected, as was the electron-donating methoxy group on the aryl ring. A total of 12 complexes were obtained, representing potential chelation events from ligand-driven oxidation of zerovalent metals and/or coordination of oxidized metal salts. The X-ray crystallography revealed a range of coordination patterns. Notably, the Cu(II)Cl₂ complexes, in the presence of ATF, produce [ATF-CuCl]₂ dimers, supporting a potential reduction event at the copper, while other metals with ATF and all metals with AAF remain in the 2+ oxidation state. Hirshfeld analysis was performed on all complexes, and it was found that most interactions across the complexes were dominated by H…H, followed by Cl…H/H…Cl, with metals showing very little to no interaction with other atoms. Spectroscopic techniques such as UV–VIS absorption, NMR (when diamagnetic), and FTIR, in addition to electrochemical studies support the metal–ligand coordination. Full article

Accelerating urbanisation and industrial activity have led to the widespread release of polycyclic aromatic hydrocarbons (PAHs), a class of persistent organic pollutants with serious ecological and health consequences. While physical and chemical remediation techniques are widely used, they often require nonrenewable resources and generate secondary waste. Fungal-based bioremediation offers a promising alternative, leveraging the unique metabolic pathways and structural properties of fungi to break down or adsorb PAHs. This review focuses on three strategies of PAH remediation in aquatic environments: biofiltration, biosorption, and metabolic degradation. We conduct a comparison between conventional systems and fungal approaches with reference to the literature (2000–2025). Fungal matrices are identified as being able to capture and adsorb PAHs, facilitating localised remediation that capitalises on the biological capabilities of fungal organisms while requiring lower resource inputs than conventional methods. This review highlights fungal matrices as multifunctional water filtration membranes and provides insights for the application and development of engineered living materials (ELMs) for the water detoxification of PAHs. Full article

Rivers, vital for life and civilizations, face severe threats from human activities such as hydropower development, with heavy metal pollution emerging as a critical concern due to altered biogeochemical cycles. Understanding how river damming affects heavy metal transport processes and developing targeted remediation strategies are essential for safeguarding the health of river-reservoir ecosystems and enabling the sustainable utilization of hydropower resources. Therefore, this review first summarizes the global hydropower development, details how damming disrupts hydrology, environments, and ecosystems, and analyzes heavy metal distribution and transport in reservoir water, suspended sediments, and riverbed sediments. It reveals that river damming promotes heavy metal adsorption onto suspended particles, deposition in riverbed sediments, and re-release during reservoir regulation, and anthropogenic activities are a primary driver of significant pollution in key reservoirs worldwide. Additionally, we further evaluate in situ (e.g., stabilizing agents, sediment capping, and phytoremediation) and ex situ (e.g., dredging, chemical washing, electrochemical separation, and ultrasonic extraction) remediation techniques, highlighting the challenges of phytoremediation in deep, stratified reservoir environments. Moreover, solidification/stabilization emerges as a promising in situ strategy, emphasizing the need for specific approaches to balance pollution control with hydropower functionality in dammed river systems. Full article

Permafrost degradation, driven by the thawing of ground ice, results in the progressive thinning and eventual loss of the permafrost layer. This process alters hydrological and ecological systems by increasing surface and subsurface water flow, changing vegetation density, and destabilising the ground. The thermal and hydraulic conductivity of permafrost are strongly temperature-dependent, both increasing as the soil warms, thereby accelerating thaw. In addition, thawing permafrost releases large quantities of greenhouse gases, establishing a feedback loop in which global warming both drives and is intensified by permafrost loss. This paper reviews the mechanisms and consequences of permafrost degradation, including reductions in strength and enhanced deformability, which induce landslides and threaten the structural integrity of foundations and critical infrastructure. Permafrost has been investigated and modelled extensively, and various approaches have been devised to address the consequences of thawing permafrost on communities and the built environment. Some techniques focus on keeping the ground frozen via insulation, while others propose local replacement of permafrost with more stable materials. However, given the scale and pace of current changes, systematic remediation appears unfeasible. This calls for increased efforts towards adaptation, informed by interdisciplinary research. Full article

This research focuses on the synthesis, characterization, and photocatalytic performance of Cu-based polyoxometalate (Cu-POM) as an effective catalyst for the degradation of organic dyes, specifically Congo Red (CR) and Phenol Red (PR). The main goals are to synthesize Cu-POM using a controlled self-assembly technique, characterize its optical and structural characteristics using FTIR, XRD, SEM, TGA, and UV-Vis spectroscopy, and estimate its photocatalytic activity when exposed to UV light. The outcomes confirm the successful formation of Cu-POM with well-defined nanostructures and a crystalline polyoxometalate framework. The determined optical bandgap of 3.65 eV indicates its strong UV-light responsiveness. The photocatalytic degradation experiments demonstrated high removal efficiencies of 58.1% for CR and 64.6% for PR under UV irradiation, corresponding kinetic rate constants of 0.00484 min⁻¹ and 0.00579 min⁻¹, respectively. The superior photocatalytic activity is attributed to the efficient charge carrier separation and high surface area of Cu-POM. These findings highlight the potential of Cu-POM as a promising heterogeneous photocatalyst for sustainable wastewater treatment and environmental remediation. Full article

The continuous increase in urbanization and global population has led to the generation of a substantial amount of kitchen waste, posing severe environmental and disposal challenges. The utilization of kitchen waste as organic biomass for biochar production offers a promising, sustainable, and cost-effective solution. This review comprehensively analyzes the recent developments in the transformation of kitchen waste into biochar. Moreover, the current study involves various synthesis techniques, the physicochemical characteristics of biochar, and its applications in soil and water remediation. Afterwards, the experimental parameters and feedstock types are critically evaluated in terms of their key characteristics for biochar. Moreover, the current study highlights the effectiveness of kitchen waste-derived biochar (KWBC) in decomposing organic pollutants, heavy metals, and pharmaceutical pollutants from contaminated environments. Additionally, the mechanisms of adsorption, ion exchange, complexation, and redox interactions are thoroughly illustrated to evaluate the pollutant removal pathways. At the end of the study, experimental parameters such as pH, dosage, contact time, and initial pollutant concentration are discussed, which play the main role in enhancing the adsorption capacity of biochar. Finally, this review outlines current limitations and proposes future directions for optimizing biochar performance and promoting its large-scale application in sustainable environmental management. Full article

Different treatments of fish scales from carps (Cyprinus carpio) (FS)—mechanical milling, modified with cerium dioxide (CeO₂) nanoparticles and controlled carbonization of FS and modification with CeO₂—were applied to obtain FS, FS-CeO₂ and CFS-CeO₂ bio-adsorbents. The synthesized adsorbents were used for As(V) and Cr(VI) oxyanion separation from water. Porosity and the amount of CeO₂ nanoparticles deposition were controlled using different experimental conditions. Response surface methodology (RSM) was used to select optimal parameters for adsorbent synthesis to obtain the highest adsorption capacity. The structural and surface characteristics of the synthesized adsorbents were examined using FTIR, XRD and SEM techniques. The efficiency of pollutant removal was analyzed in terms of varying experimental conditions: the mass of adsorbent, pH, temperature and contact time. RSM was also used to optimize adsorption and desorption processes. The adsorption data, obtained at 25, 35 and 45 °C, were processed using Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm and Van’t Hoff thermodynamic models. The FS-CeO₂ bio-adsorbent showed good adsorption capacities of 92.61 and 65.50 mg g⁻¹ for As(V) and Cr(VI) ion removal, respectively, obtained by using the Langmuir model. Thermodynamic parameters proved that adsorption was a viable, spontaneous and endothermic process. The results from kinetic modeling indicated that both adsorbate and surface functional group concentration determine overall kinetic law with the highest participation of intra-particle diffusion resistance to pollutant transport. Exceptional adsorption and desorption performances of FS-CeO₂ in conjunction with the bio-based origin of synthesized adsorbents offer valuable alternatives for the remediation of polluted water. Full article

Heavy metals (HMs) including cadmium (Cd), lead (Pb), arsenic (As), zinc (Zn), copper (Cu), chromium (Cr), and nickel (Ni) pose significant challenges to bioenergy crop production due to their persistence, toxicity, and bioaccumulation in soils and plants. This study not only summarizes the mechanisms of HM absorption, translocation, and accumulation in bioenergy crops, but also critically assesses their impact on crop development, biomass quality, and biorefinery processes. Heavy metals disrupt key physiological processes and modify lignocellulosic composition, which is important for biofuel and biogas production. Global soil contamination from sources like industrial emissions, mining, and agricultural activities exacerbates these problems, posing a threat to both energy security and environmental sustainability. Sustainable management strategies, including phytoremediation, microbial bioremediation, soil amendments, and genetic engineering, are explored to mitigate HM effects while enhancing crop resilience. This review emphasizes the importance of integrating techniques to balance bioenergy production with environmental and human health and safety, including the use of HM-tolerant crop varieties, enhanced biorefinery processes, and robust policy frameworks. Future research should focus on developing scalable remediation technologies and interdisciplinary solutions that align with the United Nations’ Sustainable Development Goals and meet global bioenergy needs. Full article

Functional hydrogels are a growing class of soft materials. Functional hydrogels are characterized by their three-dimensional (3D) polymeric network and high water-retention capacity. Functional hydrogels are deliberately engineered with specific chemical groups, stimuli-responsive motifs, or crosslinking strategies that impart targeted biomedical or environmental roles (e.g., drug delivery, pollutant removal). Their capacity to imitate the extracellular matrix, and their biocompatibility and customizable physicochemical properties make them highly suitable for biomedical and environmental applications. In contrast, non-functional hydrogels are defined as passive polymer networks that primarily serve as water-swollen matrices without such application-oriented modifications. Recent progress includes stimuli-responsive hydrogel designs. Stimuli such as pH, temperature, enzymes, light, etc., enable controlled drug delivery and targeted therapy. Moreover, hydrogels have shown great potential in tissue engineering and regenerative medicine. The flexibility and biofunctionality of hydrogels improve cell adhesion and tissue integration. Functional hydrogels are being explored for water purification by heavy metal ion removal and pollutant detection. The surface functionalities of hydrogels have shown selective binding and adsorption, along with porous structures that make them effective for environmental remediation. However, hydrogels have long been postulated as potential candidates to be used in clinical advancements. The first reported clinical trial was in the 1980s; however, their exploration in the last two decades has still struggled to achieve positive results. In this review, we discuss the rational hydrogel designs, synthesis techniques, application-specific performance, and the hydrogel-based materials being used in ongoing clinical trials (FDA–approved) and their mechanism of action. We also elaborate on the key challenges remaining, such as biocompatibility, mechanical stability, scalability, and future directions, to unlocking their multifunctionality and responsiveness. Full article

In this study, we report, for the first time, the tribo-catalytic degradation of methyl orange (MO) using Cu/Al₂O₃ nanoparticles under mechanical stirring conditions. The hybrid catalyst was synthesized via a wet impregnation method and characterized through different techniques, confirming structural integrity and compositional uniformity. When subjected to friction generated by a PTFE-coated magnetic stir bar, Cu/Al₂O₃ nanoparticles exhibited high tribo-catalytic activity, achieving up to 95% MO degradation within 10 h under dark conditions. The observed activity surpasses that of alumina alone and is attributed to the synergistic effects between copper and alumina, facilitating charge separation and enhancing reactive oxygen species (ROS) formation. Tribo-catalytic efficiency was further influenced by stirring speed and contact area, confirming the key role of mechanical friction. Reusability tests demonstrated stable performance over five cycles, highlighting the material’s durability and potential for practical environmental remediation applications. Full article

Microbial spores are increasingly recognized as multifunctional platforms for enzyme immobilization, combining natural resilience with biotechnological versatility. Their inherent structural complexity enables high enzyme load, thermal and chemical stability, and robustness to be repeatedly used under industrially relevant conditions, largely widening their application scope. This review explores the growing role of spore-based systems in biocatalysis, from naturally active spores to engineered microbial hosts capable of producing immobilized enzymes in situ. Compared to conventional immobilization techniques, spore-based strategies offer simplified workflows, reduced environmental impact, and greater sustainability. Recent innovations also extend beyond traditional applications, introducing artificial spores and incorporating spores into biocomposite materials and biosensors. These developments reflect a shift from basic enzyme stabilization research toward scalable solutions in waste remediation, polymer degradation, green chemistry, and synthetic biology. Overall, spore-enabled biocatalysis represents a modular and robust toolset for advancing industrial biotechnology and sustainable manufacturing, instrumental in achieving a circular and bioeconomy. Full article

Enzymes are highly selective and efficient biological catalysts that play a critical role in modern industrial biocatalysis. Their ability to operate under mild conditions and reduce environmental impact makes them ideal alternatives to conventional chemical catalysts. This review provides a comprehensive overview of advances in enzyme-based catalysis, focusing on enzyme classification, engineering strategies, and industrial applications. The six major enzyme classes—hydrolases, oxidoreductases, transferases, lyases, isomerases, and ligases—are discussed in the context of their catalytic roles across sectors such as pharmaceuticals, food processing, textiles, biofuels, and environmental remediation. Recent developments in protein engineering, including directed evolution, rational design, and computational modeling, have significantly enhanced enzyme performance, stability, and substrate specificity. Emerging tools such as machine learning and synthetic biology are accelerating the discovery and optimization of novel enzymes. Progress in enzyme immobilization techniques and reactor design has further improved process scalability, reusability, and operational robustness. Enzyme sourcing has expanded from traditional microbial and plant origins to extremophiles, metagenomic libraries, and recombinant systems. These advances support the integration of enzymes into green chemistry and circular economy frameworks. Despite challenges such as enzyme deactivation and cost barriers, innovative solutions continue to emerge. Enzymes are increasingly enabling cleaner, safer, and more efficient production pathways across industries, supporting the global shift toward sustainable and circular manufacturing. Full article

Perovskite-type CaBiO₂Cl with a unique layered Sillen X1 structure exhibits great potential as an efficient visible-light photocatalyst. In this study, CaBiO₂Cl was synthesized through calcination at 800 °C and subsequently composited with varying amounts of g-C₃N₄ to optimize photocatalytic performance. The prepared catalysts were characterized by multiple techniques to confirm their structural and compositional features. Under visible-light irradiation, the photocatalytic activities toward Rh6G degradation were systematically evaluated using UV–vis PDA and EPR analyses. To further elucidate the degradation mechanism, radical scavenger experiments were conducted to identify the reactive species generated during the photodegradation process. Kinetic analysis revealed that the reaction rate constant (k) of pure CaBiO₂Cl was 0.0525 h⁻¹, while that of pure g-C₃N₄ was 0.0423 h⁻¹. Notably, the CaBiO₂Cl/10 wt% g-C₃N₄ composite exhibited an enhanced k value of 0.0568 h⁻¹, which is 1.1 and 1.3 times higher than those of CaBiO₂Cl and g-C₃N₄, respectively. Furthermore, under ambient conditions (25 °C, 1 atm), the CO₂-to-CH₄ photocatalytic conversion efficiency of the CaBiO₂Cl/10 wt% g-C₃N₄ composite reached 0.5652 μmol g⁻¹ h⁻¹. These findings demonstrate that CaBiO₂Cl-based composite photocatalysts not only achieve superior visible-light photocatalytic activity but also exhibit excellent stability, highlighting their potential for environmental remediation and alignment with the principles of green chemistry. Full article