Search Results (3,236)

Innovations in nanomaterial science, engineering and printing technologies have increasingly driven advances in electrochemical sensing. Screen-printed electrodes (SPEs) have become a versatile, low-cost, and scalable solution for developing portable electrochemical detection platforms. However, their analytical performance remains intrinsically limited by surface area, electron transfer efficiency, and the immobilization of biomolecules. Recent developments in nanostructured materials, ranging from two-dimensional (2D) materials such as graphene, MXenes, and transition metal dichalcogenides, to one-dimensional nanostructures and hybrid nanocomposites, have transformed the signal transduction landscape of SPE-based electrochemical sensors. Integration of nanomaterials into SPEs has successfully transformed their analytical capabilities, but the diversity of materials and modification strategies has made it difficult to consolidate current knowledge in the field. Strategies that integrate nanomaterials via ink formulation, surface modification, or in situ growth have yielded sensors with unprecedented sensitivity, reproducibility, and selectivity across various chemical and biological targets. This review offers a cross-material synthesis of how nanomaterial engineering transforms the electrochemical performance of SPEs. By integrating insights across morphology, interfacial chemistry, and device-level behavior, it establishes a unified perspective that has been missing from the current literature and clarifies the design principles driving next-generation SPE-based sensing platforms. Full article

A heteroatom-rich pyridine-based adsorbent (Pyridine PC) was synthesized through a multicomponent strategy and structurally confirmed by ¹H/¹³C NMR spectroscopy and mass spectrometry. To further enhance adsorption activity and surface reactivity, waste-derived CuO nanoparticles were immobilized onto the porous heterocyclic framework, generating a sustainable CuO@Pyridine PC hybrid nanocomposite. Batch adsorption experiments demonstrate highly efficient removal of malachite green (MG) dye and Cd(II) ions from aqueous solutions. Kinetic analysis reveals that adsorption follows the pseudo-second-order model, while equilibrium data are best described by the Freundlich isotherm, indicating adsorption on heterogeneous surfaces. Thermodynamic parameters confirm that the adsorption processes are spontaneous and exothermic. Surface and structural characterization using SEM/EDX, elemental mapping analysis and FT-IR before and after adsorption verifies strong pollutant binding and highlights the role of nitrogen- and oxygen-containing functional groups as dominant interaction sites. BET measurements show that CuO incorporation increases surface area and pore volume, while zeta potential analysis indicates excellent colloidal stability of the composite in aqueous media. Consequently, the CuO-modified sorbent exhibits enhanced adsorption capacities, increasing from 169.8 to 176.13 mg g⁻¹ for MG and from 276.5 to 368 mg g⁻¹ for Cd(II). The adsorbent demonstrated effective pollutant removal from real wastewater. The adsorption mechanism involves synergistic interactions between functional groups in the Pyridine PC matrix and CuO nanoparticles, providing enhanced active binding sites. Full article

Antibiotic contamination of water, particularly tetracycline (TC), poses significant environmental risks and requires sustainable treatment solutions. This study reports a green and cost-effective synthesis of a ZnO/chitosan nanocomposite (ZnO/CS) for photocatalytic TC removal. ZnO nanoparticles were synthesized using lime juice as a natural stabilizing agent and subsequently incorporated into a chitosan matrix. The physicochemical properties of the composite were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET) surface area analysis. The results confirmed the successful formation of hexagonal wurtzite ZnO and strong interfacial interactions between ZnO nanoparticles and the –NH₂/–OH functional groups of chitosan. The incorporation of chitosan significantly increased the specific surface area from 10.7 to 21.7 m² g⁻¹ and reduced the band gap from 3.18 to 3.03 eV, thereby improving visible-light absorption. The photocatalytic performance was evaluated under varying pH, initial TC concentration, and catalyst dosage, with optimal conditions identified at pH 6, 20 mg/L TC, and 1 g/L catalyst. Under these conditions, the ZnO/CS nanocomposite achieved 94.1% TC degradation within 120 min under visible-light irradiation. Scavenger experiments revealed that •OH and •O₂⁻ radicals are the dominant reactive species, and a possible degradation mechanism was proposed. These findings demonstrate the potential of the green-synthesized ZnO/CS nanocomposite for antibiotic removal from aqueous environments. Full article

Water pollution, caused by selenium contamination, is a significant global issue due to its toxic effects on humans and animals. Selenium occurs in several oxidation states, among which selenite and selenate are the most mobile and bioavailable forms. Traditional water treatment methods are often limited in efficiency, whereas adsorption offers a simple, cost-effective, and efficient solution. Various adsorbents, including metal and mineral oxides, carbon-based materials (activated carbon, graphene oxide), biosorbents, and nanocomposites, have shown high potential for Se removal. Adsorbent modifications—physical, chemical, or composite—significantly enhance adsorption capacity, selectivity, and material stability. Studies have demonstrated that nanomaterials and nanocomposites, such as MnFe₂O₄, PAA-MGO, magnetic MOFs, and magnetite-based biochars, enable rapid removal of Se(IV) and Se(VI) with high adsorption capacities. Se(IV) is primarily adsorbed through innersphere complexation, while Se(VI) forms weaker outer-sphere interactions, explaining differences in removal efficiency. Factors such as pH, the presence of surface hydroxyl and amino groups, surface charge, and competing ions strongly influence the adsorption process. Multivalent ions reduce Se adsorption efficiency, whereas monovalent ions (NO₃⁻ and Cl⁻) have minimal impact. Modified adsorbents, nanomaterials, and nanocomposites provide sustainable and practical solutions for selenium removal from water, combining high efficiency, selectivity, and reusability, making them suitable for real-world water treatment applications. Full article

This study investigated the comparative effects of various maleic anhydride-grafted polymeric compatibilizers such as polyethylene-graft-maleic anhydride, polypropylene-graft-maleic anhydride, polyethylene(alt)-graft-maleic anhydride and poly(styrene-ethylene/butylene-styrene)-graft-maleic anhydride on the final properties of polypropylene (PP) carbon nanotube (CNT) composites. Polypropylene nanocomposites (PP-CNT) were prepared by melt mixing using a laboratory scale twin-screw extruder. The mechanical test results showed that the incorporation of CNTs along with various compatibilizers increased the tensile strength (10.3%) and tensile modulus (24.2%). The tensile modulus and yield stress of the PP-CNT nanocomposites were significantly higher than those of the pristine PP. Differential Scanning Calorimetry (DSC) analysis revealed that the addition of CNTs slightly increased the melting temperature of the crystallization peaks. In the compatibilized PP-CNT composites, the CNTs were well dispersed to enhance the onset of degradation and maximum decomposition temperatures. The frequency-dependent rheological behaviors of PP-CNT nanocomposites indicated that the storage modulus (G’), loss modulus (G”), and complex viscosity (η*) PP increased for the compatibilized system. The XRD results indicated that the addition of CNTs and compatibilizers slightly affected the crystalline nature of PP. Scanning electron microscopic images of the fractured surfaces presented in the micrographs showed the brittle nature of the surface morphology of PP-CNT nanocomposites. Full article

A sustainable strategy was developed to valorize rabbit manure waste by synthesizing a porous quaternary Ni-Co-Zn-Fe layered double hydroxide/biochar nanocomposite (QL-RMB) for the efficient removal of Mn(VII) in the form of permanganate (MnO₄⁻) from aqueous solutions. The QL-RMB adsorbent exhibited a well-developed mesoporous structure with uniformly dispersed nanoparticles, achieving 73% MnO₄⁻ removal within 60 min under optimized conditions (pH 3.0; dosage 0.5 g L⁻¹). Adsorption followed pseudo-second-order kinetics and was best described by the Freundlich isotherm model (R² > 0.98), yielding a maximum Langmuir adsorption capacity (q_max) of 45.13 mg g⁻¹. Statistical physics modeling confirmed a multi-ionic, vertically oriented adsorption configuration, while thermodynamic analysis demonstrated that the process was spontaneous and exothermic, governed by electrostatic attraction, anion exchange, and surface complexation. The QL-RMB composite exhibited excellent MnO₄⁻ selectivity in the presence of competing ions (selectivity coefficients: 24.96 for Fe³⁺, 31.59 for Ni²⁺, 23.56 for Zn²⁺) and retained significant removal efficiency (73.96%) after five regeneration cycles. In a circular economy approach, the Mn (VII)-spent adsorbent (QL-RMB/Mn) was valorized as an electrocatalyst for urea electro-oxidation, achieving a current density of ~127.19 mA cm⁻² for pristine QL-RMB, which increased to ~217.07 mA cm⁻² after Mn(VII) adsorption (QL-RMB/Mn) in 1 M KOH/1 M urea. Batch scale-up studies revealed an efficiency of 42.55 g or 95% MnO₄⁻ removal from 50 L water, with a low estimated production cost of 0.0602 USD g⁻¹. Environmental sustainability was confirmed by the National Environmental Methods Index (NEMI), modified Green Analytical Procedure Index (Mo-GAPI), Eco-scale (score: 77), and Analytical GREEness (AGREE) assessment frameworks. Full article

Tetracycline antibiotics are increasingly detected in aquatic environments because of their ecological risks and persistence, while conventional wastewater treatment processes are often insufficient for their effective removal from water. Here, we introduce a novel 3D graphene oxide-based nanocomposite that stacks Cu-NPs and amino-functionalized MIL-101(Fe) (denoted by Cu/NH₂-MIL-101(Fe)@GO) to effectively remove tetracycline (TC) and oxytetracycline (OTC) from environmental water samples. XPS, XRD, TEM, SEM, and FTIR analyses were conducted to characterize the structure and surface morphology of the Cu/NH₂-MIL-101(Fe)@GO nanocomposite. Overall, it was confirmed that GO, NH₂-MIL-101(Fe), and Cu-NPs were successfully incorporated, resulting in a porous material with high access to Cu-related sites as well as oxygen- and nitrogen-based functionalities (such as amino-, hydroxy-, and carboxy-groups). This hybrid system facilitates the adsorption by complementary mechanisms like surface complexation/chelation at Cu and Fe centers with the pH-dependent tetracycline species in electrostatic interactions, hydrogen bonding, π–π stacking, and molecule confinement in the metal–organic framework (MOF) pores, and by the synergistic effects at the GO–MOF(Fe)–Cu junction interfaces. The batch adsorption studies showed that the quick and efficient uptake of the two antibiotics at pH 6.5, with removal rates of 99.65–99.83%, was achieved by 15.0 mg of Cu/NH₂-MIL-101(Fe)@GO at an initial concentration of 20 ppm in 40 min at 25 °C. Equilibrium data were found to be well-fitted by the Langmuir isotherm (R² = 0.908–0.909), suggesting monolayer-dominated adsorption with the maximum capacity of 769.8–775.2 mg g⁻¹. The adsorption kinetics was well-described by the pseudo-second order model (R² = 0.9641–0.9749), which agreed with the strong binding between the tetracyclines and active sites of the nanocomposite. The main novelty of this work consists of the design of a single recoverable platform integrating GO-based preconcentration, pore accessibility of NH₂-MIL-101(Fe), and Cu-driven complexation, which led to the strong removal of tetracyclines under a relevant range of water conditions. These findings demonstrate that Cu/NH₂-MIL-101(Fe)@GO could serve as a promising high-efficiency and potentially reusable adsorbent for removing tetracycline from aqueous solution, which provides a more sustainable approach for pharmaceutical wastewater treatment. Full article

Textile wastewater is among the most challenging industrial effluents due to its complex composition, high pollutant load, and low biodegradability. Conventional treatment methods often fall short in achieving complete removal of dyes and emerging contaminants. Photocatalytic composite membranes have emerged as a promising solution by integrating membrane separation and advanced oxidation processes. This review provides a comprehensive overview of the design, fabrication, and performance of photocatalytic composite membranes for textile wastewater treatment. Key aspects include the types of photocatalysts employed, methods of incorporation into membranes, and their synergistic role in pollutant removal and membrane fouling mitigation. Recent advancements in materials science, such as visible-light-responsive catalysts, carbon-based nanocomposites, and self-cleaning surfaces, are discussed, along with current limitations related to catalyst stability, operational scalability, and cost. This review underscores the potential of photocatalytic composite membranes as a next-generation platform for sustainable and effective textile wastewater treatment. Full article

This work reports on the synthesis and electrochemical investigation of sustainable carbon–TiO₂ nanocomposites derived from marine biowaste, designed to elucidate light-assisted charge storage mechanisms in non-aqueous electrolytes. Porous carbons obtained from prawn chitin and blue shark gelatin were decorated in situ with TiO₂ nanoparticles using a deep eutectic solvent (DES) as a green synthesis medium. Structural and morphological characterisation revealed that TiO₂ incorporation induces significant nanoscale reorganisation of the carbon framework, resulting in hierarchical porosity, increased surface area, and intimate semiconductor–carbon interfaces. Electrochemical evaluation in a three-electrode configuration using an ethaline-based DES electrolyte demonstrated that TiO₂ decoration substantially enhances capacitive performance and cycling stability, with the prawn chitin-derived composite achieving a specific capacitance of 54 ± 3 F g⁻¹ and 91% retention after 10,000 cycles. Under illumination, all TiO₂-containing composites exhibited a pronounced increase in anodic current response and discharge time, indicating photo-assisted surface charge accumulation. Although the absolute capacitance values are modest compared to those of aqueous supercapacitor systems, the results provide mechanistic insight into the interplay among nanostructure, semiconductor photoactivity, and ion transport in viscous, hydrogen-bonded DES electrolytes. By combining waste-derived carbons, green synthesis routes, and photo-responsive nanostructures, this study highlights a sustainable strategy for developing multifunctional carbon-based nanomaterials with light-modulated electrochemical behaviour. Full article

The quantitative analysis of cardio selective beta-blockers, such as the antihypertensive and antiarrhythmic medication acebutolol (ABT), is critical for biomedical and environmental monitoring. This study describes the development of a high-performance electrochemical sensing platform for ABT based on a screen-printed carbon electrode (SPCE) modified with a silver nanoparticle/hexagonal boron nitride (Ag NPs/h-BN) nanocomposite. The morphological and structural properties of the synthesized materials were examined by using a microscopic and spectroscopic techniques. The Ag NPs/h-BN/SPCE demonstrated exceptional electrocatalytic activity toward ABT oxidation, characterized by a significant reduction in overpotential and a substantial enhancement in peak current relative to unmodified and mono-component electrodes. This superior performance is attributed to the synergistic integration of Ag NPs and h-BN, which provides a high density of active sites, an expanded electroactive surface area, and accelerated charge transfer kinetics. Under optimized experimental conditions, the sensor exhibited a broad linear dynamic range of 0.01–284 μM, a remarkably low limit of detection (LOD) of 0.0049 μM, and a high sensitivity of 0.873 µA µM⁻¹ cm⁻² for ABT detection. Furthermore, the platform displayed excellent selectivity in the presence of common interfering species and robust reproducibility (RSD of 4.8%). The practical utility of the Ag NPs/h-BN/SPCE was successfully validated through the precise quantification of ABT in complex biological and environmental matrices. This work provides a versatile strategy for the rational design of metal nanocatalysts confined within h-BN frameworks for the development of advanced electrochemical diagnostic tools. Full article

This study describes the development of an electrochemical sensor for quantitatively measuring acetaminophen (ACOP) in drug tablets. The sensor design is based on the modification of glassy carbon electrode (GCE) using zinc oxide nanoparticles (ZnONPs) embedded in a naturally occurring clay matrix (Sa) functionalized with phenylalanine (Phe). To ensure that the ZnONPs are homogeneously dispersed on the clay surface, the nanocomposite was synthesized using an impregnation approach and low-temperature heat treatment. The amino acid promotes specific interactions with ACOP through hydrogen bonding and π-π stacking, acting as both a stabilizing agent and a molecular recognition moiety. FTIR, UV-Vis, XRD, and FESEM/EDX mapping were employed to fully characterize the developed material (ZnONPs-Sa/Phe). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used for the electrochemical determination of ACOP using the modified electrode GCE/ZnONPs-Sa/Phe. Parameters susceptible to affecting the sensitivity of the developed sensor were optimized, revealing that 5 µL of the suspension ZnONPs-Sa/Phe immobilized on GCE was ideal for the sensing of ACOP in a phosphate buffer solution at pH 2.0. The calibration curve obtained by plotting peak current intensity against ACOP concentration exhibited linear behavior within the concentration range between 0.02 µM and 0.28 µM, enabling determination of the limits of detection (LOD) and quantitation (LOQ) at 8.54 × 10⁻⁹ M and 2.84 × 10⁻⁸ M, respectively. The reproducibility, stability, and selectivity of the sensor were evaluated, followed by its application to the nano-sensing of ACOP in Africure and Doliprane tablets, yielding satisfactory results. The simplicity, affordability, and high analytical sensitivity of the developed sensor make this sensing platform a promising tool for pharmaceutical quality control applications. Full article

With the rapid development of electronic devices and wireless communication systems, electromagnetic interference pollution has become a critical concern, driving the urgent demand for high-performance, lightweight, and flexible electromagnetic interference (EMI) shielding materials. To endow fabrics with excellent electromagnetic shielding, a Fe₃O₄/Ag/RGO ternary nanocomposite-coated cotton fabric for electrical conductivity and EMI shielding application was developed. The cotton fabric pretreated with dopamine was coated with graphene oxide (GO), followed by silver nanoparticles (Ag) via a microwave-assisted chemical reduction method, and Ag/reduced graphene oxide (RGO)-coated cotton. Subsequently, nano-ferroferric oxide was deposited on Ag/RGO-coated cotton fabric using a coprecipitation method. The results show that the surface resistance of Fe₃O₄/Ag/RGO-coated cotton fabric arrives at 1.68 Ω/sq, demonstrating excellent electrically conductive performance. Fe₃O₄/Ag/RGO-coated cotton fabric demonstrates outstanding electromagnetic shielding performance, with SE values exceeding 45 dB across the entire 1–18 GHz range. The flexibility and superior electromagnetic shielding performance of Fe₃O₄/Ag/RGO-coated cotton fabric render it a promising candidate for applications in wearable electronics, aerospace, advanced protective systems, and military protective clothing. Full article

Developing an ultrasensitive electrochemiluminescence (ECL) detection platform remains challenging due to the limited enrichment efficiency of ECL emitters and co-reactants at the electrode interface, as well as the insufficient catalytic enhancement of co-reactant conversion. Moreover, simultaneous in situ analyte enrichment and efficient anti-interference capability are often difficult to achieve in a single sensing interface. Herein, a new ECL platform was developed based on nanocatalyst-supported nanochannel-confined surfactant micelle (SM) system, which integrates an enhanced luminol-dissolved oxygen (DO) ECL response for the ultrasensitive detection of antibiotic rifampicin (RIF). A nanocomposite comprising nitrogen-doped graphene quantum dots and a molybdenum disulfide nanosheet (NGQDs@MoS₂) was modified on an indium tin oxide (ITO) electrode. This nanocomposite layer catalyzed the oxygen reduction reaction (ORR), boosting the co-reactant efficiency of DO. Vertically ordered mesoporous silica film filled with surfactant micelles (SM@VMSF) was subsequently grown in situ on the NGQDs@MoS₂ surface. The hydrophobic micelles enable the simultaneous enrichment of luminol, DO, and RIF. Integrating the triple-enrichment effect of surfactant micelles with the high electrocatalytic effect of NGQDs@MoS₂ nanocomposite results in significant ECL enhancement of the luminol–DO. SM@VMSF also provides an excellent molecular sieving effect, endowing the sensor with high anti-interference capability and stability. RIF quenches the ECL signal by consuming superoxide anion radicals, enabling sensitive detection. Detection of RIF was established with a high sensitivity (2927 a.u. per nM) wide linear range (10 pM to 10 μM) and a low limit of detection (LOD, 2.5 pM). The fabricated sensor exhibits good selectivity and high fabrication reproducibility (relative standard deviation, RSD, of 1.9%). Additionally, the determination of RIF in eye drops and seawater samples was realized. This work offers new insights for the design of high-performance ECL sensing interfaces and sensitive detection of RIF. Full article

Stone heritage deteriorates through physical, chemical, and biological processes driven by water, climate, and microbial colonization. Multifunctional polymeric coatings combining hydrophobic and antimicrobial moieties have emerged as a promising conservation strategy, yet a substantial gap remains between laboratory innovation and real-world performance. This review critically examines advances from 2021 to 2026, covering wetting theory, antimicrobial mechanisms, and material architectures, including molecularly integrated systems, Sol–Gel hybrids, nanocomposites, and layered systems. Long-term studies on the Aurelian Walls in Rome and stone in Reims show that biocidal efficacy typically declines within one to two years despite the chemical persistence of the coatings. In parallel, hydrophobic performance often deteriorates over time due to UV exposure, particulate deposition, and surface chemical changes, leading to increased wettability and reduced protective efficiency. Substrate porosity governs durability and visual compatibility (ΔE* < 5 threshold), while treatments can reshape microbial communities, favoring stress-tolerant meristematic fungi. Regulatory pressure on fluorinated compounds drives the development of more sustainable alternatives. Emerging directions include stimuli-responsive systems, self-healing materials, slippery interfaces, and precision polymer architectures. However, future progress will depend on tailoring formulations to major lithotypes, improving compatibility with porous substrates, and validating performance through standardized accelerated aging and multi-year field trials. Bridging laboratory design with environmental exposure data and conservation practice will be essential for achieving durable and culturally acceptable protection strategies. Full article

The world’s growing need for energy, fueled by industrial expansion and a rising population, continues to be a challenge for the scientific community. The heavy reliance on fossil fuels that contribute to environmental degradation and public health concerns, is shifting toward sustainable alternatives, with hydrogen production via advanced catalysts as an energy source emerging as a promising solution. This transition addresses the challenges posed by harmful combustion emissions. In this study, we developed an innovative PANI@Cu-NA-MOF nanocomposite catalyst through a sol–gel synthesis approach that strategically integrates conducting polymers with metal–organic frameworks. The catalyst was characterized using different sets of techniques. Surface morphology and elemental composition were investigated using SEM-EDX, while structural analysis was carried out with FTIR that helped to identify the chemical bonds and functional groups, and UV-Vis spectroscopy provided information on its light absorption properties. In addition, TGA was used to evaluate thermal behavior, and XPS offered detailed surface chemical analysis. It was observed by morphology that PANI@Cu-NA-MOF is a noncapsular-like structure. It is thermally highly stable; a TGA study showed that up to 550 °C, almost 2.5% of weight was lost. The single peak in UV-Vis is the preparation of a successful composite. XPS and FTIR reveal the required peaks of functional groups and elements. The PANI@Cu-NA-MOF composite turned out to be quite effective for water electrolysis, requiring an overpotential of just 0.47 V to drive the reaction. When tested against the reversible hydrogen electrode, we observed onset potentials of 1.6 V/RHE for the oxygen evolution reaction and 0.2 V/RHE for the hydrogen evolution reaction. What makes this particularly interesting is that such performance significantly cuts down on the energy needed for electrolysis, which could make hydrogen production much more practical. Since hydrogen burns cleanly and offers a real alternative to fossil fuels, having an efficient catalyst like this brings us one step closer to sustainable energy. Full article