Search Results (40)

This study addresses the environmental challenge of end-of-life tire accumulation, a major source of toxic metals such as lead and cadmium in marine ecosystems. As a sustainable solution, multicomponent metal-oxide nanoparticles (Fe₃O₄, ZnO, CaO, MgO, and minor CaCO₃) were green-synthesized from sugarcane bagasse and stabilized with blackberry (Rubus glaucus) extract. Structural characterization (XRD, SEM, TEM, and EDS) confirmed their crystalline inorganic composition. Pb²⁺ was almost completely removed (95–99%) within 15–30 min using 50–100 mg of nanoparticles, with ~80–90% efficiency at 75 mg. Cd²⁺ removal showed dose-dependent kinetics: ~90% removal occurred within 10 min at 75 mg, while 50 and 100 mg reached ~60–70% after 60 min. Equilibrium, kinetic, and thermodynamic analyses revealed that Pb²⁺ adsorption followed the Langmuir model (R² = 0.982) with monolayer chemisorption, whereas Cd²⁺ obeyed the Freundlich model (R² = 0.945), indicating heterogeneous multilayer adsorption. Pb²⁺ removal fitted a pseudo-second-order model (R² = 0.991), while Cd²⁺ followed a pseudo-first-order behavior (R² = 0.958). Thermodynamic parameters (ΔG° < 0, ΔH° > 0, ΔS° > 0) confirmed a spontaneous and endothermic process. Sugarcane-bagasse-derived Fe₃O₄–ZnO–CaO–MgO nanomaterials act as sustainable and effective adsorbents for marine heavy metal removal. Full article

Difficult, extreme operating conditions of parabolic antennas under precipitation and sub-zero temperatures require the creation of effective heating systems. The purpose of the research is to develop a multilayer coating containing two metal-ceramic layers, epoxy composite layers, carbon fabric, and an outer layer of basalt fabric, which allows for effective heating of the antenna, and to study the properties of this coating. The multilayer coating was formed on an aluminum base that was subjected to abrasive jet processing. The first and second metal-ceramic layers, Al₂O₃ + 5% Al, which were applied by high-speed multi-chamber cumulative detonation spraying (CDS), respectively, provide maximum adhesion strength to the aluminum base and high adhesion strength to the third layer of the epoxy composite containing Al₂O₃. On this not-yet-polymerized layer of epoxy composite containing Al₂O₃, a layer of carbon fabric (impregnated with epoxy resin) was formed, which serves as a resistive heating element. On top of this carbon fabric, a layer of epoxy composite containing Cr₂O₃ and SiO₂ was applied. Next, basalt fabric was applied to this still-not-yet-polymerized layer. Then, the resulting layered coating was compacted and dried. To study this multilayer coating, X-ray analysis, light and raster scanning microscopy, and transmission electron microscopy were used. The thickness of the coating layers and microhardness were measured on transverse microsections. The adhesion strength of the metal-ceramic coating layers to the aluminum base was determined by both bending testing and peeling using the adhesive method. It was established that CDS provides the formation of metal-ceramic layers with a maximum fraction of lamellae and a microhardness of 7900–10,520 MPa. In these metal-ceramic layers, a dispersed subgrain structure, a uniform distribution of nanoparticles, and a gradient-free level of dislocation density are observed. Such a structure prevents the formation of local concentrators of internal stresses, thereby increasing the level of dispersion and substructural strengthening of the metal-ceramic layers’ material. The formation of materials with a nanostructure increases their strength and crack resistance. The effectiveness of using aluminum, chromium, and silicon oxides as nanofillers in epoxy composite layers was demonstrated. The presence of structures near the surface of these nanofillers, which differ from the properties of the epoxy matrix in the coating, was established. Such zones, specifically the outer surface layers (OSL), significantly affect the properties of the epoxy composite. The results of industrial tests showed the high performance of the multilayer coating during antenna heating. Full article

We developed a novel and portable magnetic nanochannel electrochemical sensor for the sensitive detection of cadmium ions (Cd²⁺), which pose serious risks to food safety and human health. The sensor was fabricated by co-modifying an anodic aluminum oxide (AAO) nanochannel membrane with a composite of glutathione (GSH) and ferric oxide nanoparticles (Fe₃O₄), denoted as GSH@Fe₃O₄. This modified membrane was then integrated with a screen-printed carbon electrode (SPCE) to construct the GSH@Fe₃O₄/GSH@AAO/SPCE sensing platform. The performance of the sensor was evaluated using differential pulse voltammetry (DPV), which demonstrated a strong linear correlation between the peak current response and the concentration of Cd²⁺ in the range of 5–120 μg/L. The calibration equation was I_DPV(μA) = −0.31 + 0.98·C_{Cd²⁺(μg/L)}, with an excellent correlation coefficient (R² = 0.999, n = 3). The calculated limit of detection (LOD) was as low as 0.1 μg/L, indicating the high sensitivity of the system. These results confirm the successful construction of the GSH@Fe₃O₄/GSH@AAO/SPCE portable nanochannel sensor. This innovative sensing platform provides a rapid, sensitive, and user-friendly approach for the on-site monitoring of heavy metal contamination in agricultural products, especially grains. Full article

A novel single-walled carbon nanotube (SWNT), silver (Ag) nanoparticle, and zinc benzene carboxylate (ZnBDC) metal–organic framework (MOF) composite was synthesised and systematically characterised to develop an efficient platform for mercury ion (Hg²⁺) detection. X-ray diffraction confirmed the successful incorporation of Ag nanoparticles and SWNTs without disrupting the crystalline structure of ZnBDC. Meanwhile, field-emission scanning electron microscopy and energy-dispersive spectroscopy mapping revealed a uniform elemental distribution. Thermogravimetric analysis indicated enhanced thermal stability. Electrochemical measurements (cyclic voltammetry and electrochemical impedance spectroscopy) demonstrated improved charge transfer properties. Electrochemical sensing investigations using differential pulse voltammetry revealed that the SWNTs/Ag@ZnBDC-modified glassy carbon electrode exhibited high selectivity toward Hg²⁺ ions over other metal ions (Cd²⁺, Co²⁺, Cr³⁺, Fe³⁺, and Zn²⁺), with optimal performance at pH 4. The sensor displayed a linear response in the concentration range of 0.1–1.0 nM (R² = 0.9908), with a calculated limit of detection of 0.102 nM, slightly close to the lowest tested point, confirming its high sensitivity for ultra-trace Hg²⁺ detection. The outstanding sensitivity, selectivity, and reproducibility underscore the potential of SWNTs/Ag@ZnBDC as a promising electrochemical platform for detecting trace levels of Hg2+ in environmental monitoring. Full article

In this study, we report the synthesis and characterization of a novel NH₂-MIL-101(Fe) magnetic composite, developed via in situ formation of NH₂-MIL-101(Fe) in the presence of Fe₃O₄ nanoparticles embedded within a chloropropyl-modified mesoporous silica layer. This hybrid composite retains the high adsorption capacity of NH₂-MIL-101(Fe) while benefiting from the easy magnetic separation enabled by Fe₃O₄ nanoparticles. The mesoporous silica forms a protective porous coating around the magnetic nanoparticles, significantly enhancing its chemical stability and preventing clumping. Beyond protection, the mesoporous silica layer provides a high-surface-area scaffold that promotes the uniform in situ growth of NH₂-MIL-101(Fe). Functionalization of the silica surface with chloride groups enables strong electrostatic interactions between the magnetic component and metal organic framework (MOF), ensuring a homogeneous and stable hybrid structure. The new composite’s capacity to remove Pb(II) and Cd(II) ions from aqueous solutions was systematically investigated. The adsorption data showed a good fit with the Langmuir isotherm model for both ions, the maximum adsorption capacities calculated being 214.6 mg g⁻¹ for Pb(II) and 181.6 mg g⁻¹ Cd(II). Furthermore, the kinetic behavior of the adsorption process was accurately described by the pseudo-second-order model. These findings confirm the effectiveness of this composite for the removal of Pb(II) and Cd(II) ions from aqueous solutions, demonstrating its potential as an efficient material for environmental remediation. The combination of magnetic recovery, high adsorption capacity, and stability makes this novel composite a promising candidate for heavy metal removal applications in water treatment processes. Full article

The development of metal–organic framework (MOF)-based composites for photocatalytic hydrogen evolution has garnered significant attention due to their tunable structures, high surface area, and abundant active sites. Recent advancements focus on enhancing light absorption, charge separation, and catalytic efficiency through strategies such as ligand functionalization, metal doping, heterojunction formation, and plasmonic coupling effects. For instance, modifications with Ir (III) complexes and Pt nanoparticles have significantly improved hydrogen evolution rates, while sandwich-structured MOF composites demonstrate optimized charge separation through tailored micro-environments and proton reduction efficiency. Additionally, integrating MOFs with semiconductors (e.g., CdS, g-C₃N₄) or plasmonic metals (e.g., Au) enhances visible-light responsiveness and stability. This review highlights key design principles, performance metrics, and mechanistic insights, providing a roadmap for future research in MOF-based photocatalysts for sustainable hydrogen production. Challenges such as long-term stability and scalable synthesis are also discussed to guide further innovations in this field. Full article

This study investigates the development and sensing profile of synthetic melanin nanoparticle-coated electrodes for the electrochemical detection of heavy metals, including lead (Pb), cadmium (Cd), cobalt (Co), zinc (Zn), nickel (Ni), and iron (Fe). Synthetic melanin films were prepared in situ by the deacetylation of diacetoxy indole (DAI) to dihydroxy indole (DHI), followed by the deposition of DHI monomers onto indium tin oxide (ITO) and glassy carbon electrodes (GCE) using cyclic voltammetry (CV), forming a thin layer of synthetic melanin film. The deposition process was characterized by electrochemical quartz crystal microbalance (EQCM) in combination with linear sweep voltammetry (LSV) and amperometry to determine the mass and thickness of the deposited film. Surface morphology and elemental composition were examined using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). In contrast, Fourier-transform infrared (FTIR) and UV–Vis spectroscopy confirmed the melanin’s chemical structure and its polyphenolic functional groups. Differential pulse voltammetry (DPV) and amperometry were employed to evaluate the melanin films’ electrochemical activity and sensitivity for detecting heavy metal ions. Reproducibility and repeatability were rigorously assessed, showing consistent electrochemical performance across multiple electrodes and trials. A comparative analysis of ITO, GCE, and graphite electrodes was conducted to identify the most suitable substrate for melanin film preparation, focusing on stability, electrochemical response, and metal ion sensing efficiency. Finally, the applicability of melanin-coated electrodes was tested on in-house heavy metal water samples, exploring their potential for practical environmental monitoring of toxic heavy metals. The findings highlight synthetic melanin-coated electrodes as a promising platform for sensitive and reliable detection of iron with a sensitivity of 106 nA/ppm and a limit of quantification as low as 1 ppm. Full article

Introducing small-sized metal nanoparticles directly into biopolymers susceptible to thermal and chemical stimulations remains a significant challenge. Recently, we showed a novel approach to fabricating gold nanoparticles through pulsed laser ablation in liquid (PLAL) using a microchip laser (MCL). Despite its lower pulse energy compared to conventional lasers, this technique demonstrates high ablation efficiency, offering the potential to produce composites without compromising the distinctive structure of biopolymers. As a proof of concept, we successfully generated gelatin-stabilized gold nanoparticles with a smaller size (average diameter of approximately 4 nm), while preserving the unchanged circular dichroism (CD) spectra, indicating the retention of gelatin’s unique structure. Extending this technique to the preparation of type I collagen-stabilized gold nanoparticles yielded non-aggregated nanoparticles, although challenges in yield still persist. These results highlight the potential of the microchip laser ablation technique for producing metal nanoparticles within a vulnerable matrix. Full article

Pollution by heavy metal ions has a serious impact on human health and the environment, which is why the monitoring of heavy metal ions is of great practical importance. In this work, we describe the development of an electrochemical sensor for the detection of cadmium (Cd²⁺) involving the doping of porous SiO₂ spheres with ZnO nanoparticles. Zinc oxide is chosen as the central dopant in the composite material to increase the conductivity and thus improve the electrochemical detection of Cd²⁺ ions with the SiO₂ spheres. The resulting composite is characterized by electrochemical spectroscopic XRD and microscopic methods. As a result, the developed sensor shows good selectivity towards the targeted Cd²⁺ ions compared to other divalent ions. After optimization of the experimental conditions, the electrochemical sensor shows two different linear ranges between 2.5 × 10⁻¹¹ molL⁻¹ to 1.75 × 10⁻¹⁰ molL⁻¹ and 2 × 10⁻⁹ molL⁻¹ to 1.75 × 10⁻⁹ molL⁻¹, indicating a change from diffusion-controlled to surface-controlled oxidation of Cd²⁺. A detection limit was reached at 4.4 × 10⁻¹¹ molL⁻¹. In addition, it offers good repeatability and recovery, and can detect accurate trace amounts of Cd²⁺ ions in real samples such as tap water or seawater by spiking these samples with known Cd²⁺ concentrations. This setup also provides satisfactory recovery rates in the range of 89–102%. Full article

Rapid industrial growth is associated with an increase in the production of environmentally harmful waste. A potential solution to significantly reduce pollution is to replace current synthetic materials with readily biodegradable plastics. Moreover, to meet the demands of technological advancements, it is essential to develop materials with unprecedented properties to enhance their functionality. Polysaccharide composites demonstrate significant potential in this regard. Polysaccharides possess exceptional film-forming abilities and are safe for human use, biodegradable, widely available, and easily modifiable. Unfortunately, polysaccharide-based films fall short of meeting all expectations. To address this issue, the current study focused on incorporating carbon quantum dots (CQDs), which are approximately 10 nm in size, into the structure of a starch/chitosan biocomposite at varying concentrations. This modification has improved the mechanical properties of the resulting nanocomposites. The inclusion of nanoparticles led to a slight reduction in solubility and an increase in the swelling degree. The optical characteristics of the obtained films were influenced by the presence of CQDs, and the fluorescence intensity of the nanocomposites changed due to the specific heavy metal ions and amino acids used. Consequently, these nanocomposites show great potential for detecting these compounds. Cellular viability assessments and comet assays confirm that the resulting nanocomposites do not exhibit any cytotoxic properties based on this specific analytic method. The tested nanocomposites with the addition of carbon quantum dots (NC/CD II and NC/CD III) were characterised by greater genotoxicity compared to the negative control. The positive control, the starch/chitosan composite alone, was also characterised by a greater induction of chromatin damage in mouse cells compared to a pure mouse blood sample. Full article

This work reports the development of a functional photocatalytic coating based on a combination of polymeric electrospun fibres and nanoparticles that is intended to be activated in the visible light range. In this sense, the resulting fibres can act as an effective matrix for the incorporation of titanium dioxide (TiO₂) particles, which are covered by gold nanoparticles (AuNPs), in the outer surface of the metal oxide precursor. In the first step of the process, the optical properties of the nanoparticles were determined by UV-Vis spectroscopy. The extension of the visible absorption can be associated to the localized surface plasmon resonance (LSPR) of the metallic AuNPs. In addition, the resultant particle size distribution and average particle diameter was evaluated by dynamic light scattering (DLS) measurements. Furthermore, the phase composition and porosity of the functional particle powder were analysed by an XRD and N₂ adsorption test. In the second step, these synthesized particles have been successfully immobilized into a PAA + β-CD electrospun fibre matrix by using the two different deposition methods of dip-coating and solution-casting, respectively. The morphological characterization of the samples was implemented by means of scanning electron microscopy (SEM), showing uniform and homogeneous, free-beaded fibres with a random distribution of the synthesized particles deposited onto the electrospun fibres. Then, the functional coatings were removed from the substrate, and a thermogravimetric (TGA) analysis was carried out for each sample in order to obtain the precursor mass immobilized in the coating. Once the overall mass of precursor was obtained, the percentage of TiO₂ particles and AuNPs in the precursor was calculated by using inductively coupled plasma atomic emission spectrometry (ICP-AES). Finally, the photocatalytic activity of both functional solution and electrospun coatings were evaluated in terms of a gradual degradation of rhodamine B (RhB) dye after continuous exposition to a visible-light lamp. Full article

Soil heavy metal pollution has become an important environmental problem in the world. Therefore, it is particularly important to find effective remediation methods for heavy metal contaminated soil. Biochar (BC) is a kind of soil heavy metal passivator with a wide range of applications. It also has a good effect on the control of soil heavy metal pollution. However, BC does not have sufficient fixation capacity for para-anionic contaminants. Nano-zero-valent iron (nZVI) has a strong reducing ability, which can make up for this defect of BC. Therefore, to improve the passivation effect of heavy metals, nanomaterial modification is proposed to optimize biochar performance. Nanoparticles are used as carriers to impregnate biochar (BC). Biochar-supported nano-ferric zero-valent materials are prepared to repair soil contaminated by heavy metals. Results show that the physicochemical properties of modified biochar are significantly optimized. At 5%, the modified biochar (1:3) treatment group had the best remediation effect on Cd-contaminated soil, which significantly promoted soil catalase activity. The modified biochar (3:1) treatment group had the best remediation effect on As-contaminated soil, and significantly increased soil pH, Cation Exchange Capacity (CEC), and available Fe content. Modified biochar (1:3) with 3% added content was used to repair actual composite heavy metal contaminated soil, and the relative percentage content of Cu, Zn, As, Cd, and Pb residue state increased by 10.28%, 7.81%, 7.44%, 9.26%, and 12.75%, respectively. The effects of nZVI@BC on the remediation effect and soil enzymes of Cd- and As-contaminated soil under different factors such as mass ratio of carbon and iron and dosage were studied. The remediation mechanism of Cd- and As-contaminated soil was clarified, and a good solidification and stabilization effect was obtained. This provides a theoretical basis for nZVI@BC remediation of soil contaminated by Cd and As. It has good application value in the treatment and remediation of complex heavy metal contaminated soil. Full article

Heavy metal contamination in water resources is a major issue worldwide. Metals released into the environment endanger human health, owing to their persistence and absorption into the food chain. Cadmium is a highly toxic heavy metal, which causes severe health hazards in human beings as well as in animals. To overcome the issue, current research focused on cadmium ion removal from the polluted water by using porous magnetic chitosan composite produced from Kaphal (Myrica esculenta) leaves. The synthesized composite was characterized by BET, XRD, FT-IR, FE-SEM with EDX, and VSM to understand the structural, textural, surface functional, morphological-compositional, and magnetic properties, respectively, that contributed to the adsorption of Cd. The maximum Cd adsorption capacities observed for the Fe₃O₄ nanoparticles (MNPs) and porous magnetic chitosan (MCS) composite were 290 mg/g and 426 mg/g, respectively. Both the adsorption processes followed second-order kinetics. Batch adsorption studies were carried out to understand the optimum conditions for the fast adsorption process. Both the adsorbents could be regenerated for up to seven cycles without appreciable loss in adsorption capacity. The porous magnetic chitosan composite showed improved adsorption compared to MNPs. The mechanism for cadmium ion adsorption by MNPs and MCS has been postulated. Magnetic-modified chitosan-based composites that exhibit high adsorption efficiency, regeneration, and easy separation from a solution have broad development prospects in various industrial sewage and wastewater treatment fields. Full article

The design and synthesis of efficient photocatalysts that promote the degradation of organic pollutants in water have attracted extensive attention in recent years. In this work, CdS nanoparticles are grown in situ on Co@C derived from metal–organic frameworks. The resulting hierarchical CdS/Co@C nanostructures are evaluated in terms of their adsorption and photocatalytic ciprofloxacin degradation efficiency under visible-light irradiation. The results show that, apart from offering a large surface area (55.69 m²·g⁻¹), the prepared material can effectively suppress the self-agglomeration of CdS and enhance the absorption of visible light. The CdS/Co@C-7 composite containing 7% wt Co@C has the highest photodegradation rate, and its activity is approximately 4.4 times greater than that of CdS alone. Moreover, this composite exhibits remarkable stability after three successive cycles of photocatalysis. The enhanced photocatalytic performance is largely ascribed to the rapid separation of electron–hole pairs and the effective electron transfer between CdS and Co@C, which is confirmed via electrochemical experiments and photoluminescence spectra. The active substance capture experiment and the electron spin resonance technique show that h⁺ is the main active entity implicated in the degradation of CIP, and accordingly, a possible mechanism of CIP photocatalytic degradation over CdS/Co@C is proposed. In general, this work presents a new perspective on designing novel photocatalysts that promote the degradation of organic pollutants in water. Full article

Heavy metal toxicity in water is a serious problem that may have harmful effects on human health and the ecosystem. Lead [Pb(II)] and cadmium [Cd(II)] are two such heavy metal ions, present in water, whose severity is well-known and well-studied. In the current research, magnetic biochar composite (MBC) is studied as an adsorbent material for the effective removal of lead and cadmium ions from water solutions. Magnetite (Fe₃O₄) nanoparticles and pine-needle-derived ultrasonicated magnetic biochar were used in different weight ratios to prepare APTES (3-aminopropyl triethoxysilane)-functionalized MBC (FMBC). An average crystalline size of ~10 nm for magnetite NPs was obtained via XRD analysis. The adsorption characteristics of both Pb(II) and Cd(II) ions were investigated in a batch experiment. The FTIR spectra of raw biochar, MBC, FMBC, and metal-loaded FMBC were obtained at different stages. The decrease in the intensity of the –NH₂ functional group in the FTIR spectra of the residue confirmed the successful adsorption of heavy metal ions. The SEM-EDX spectra of the residue showed the uniform adsorption of Pb(II) and Cd(II) heavy metal ions onto the surface of the adsorbent. Magnetic biochar composite (MBC) was found to be a very effective adsorbent at basic pH, as a maximum of 97% instantaneous heavy metal removal was observed for both ions in synthetic water solutions. The Langmuir isotherm model predicted the monolayer adsorption and good affinity between the metal ions and adsorbent. The prepared MBC is low-cost, environmentally friendly, and it has shown good adsorption performance. Therefore, our study suggests that the magnetic biochar composite under study is an effective adsorbent for lead and cadmium metal ion removal from aqueous solutions at normal room temperature. Only a few hundred milligrams of the adsorbent dose is sufficient to remove higher concentrations (~100 ppm) of lead and cadmium at basic pH conditions of aqueous solutions. Full article