Search Results (26)

Rhodamine B dye is a hazardous pollutant that poses significant risks to human health and aquatic ecosystems due to its toxic, carcinogenic nature and high chemical stability. To address this issue, analcime@nickel orthosilicate nanocomposites were synthesized via the hydrothermal method for efficient rhodamine B dye removal. Two nanocomposites were synthesized: EW (without a template) and ET (with polyethylene glycol 400 as a template, followed by calcination at 600 °C for 5 h). X-ray diffraction (XRD) confirmed the formation of analcime (NaAlSi₂O₆) and nickel orthosilicate (Ni₂SiO₄), with crystallite sizes of 72.93 nm (EW) and 63.60 nm (ET). Energy-dispersive X-ray spectroscopy (EDX) showed distinct distributions of oxygen, sodium, aluminum, silicon, and nickel. Field-emission scanning electron microscopy (FE-SEM) revealed irregular morphology for EW and uniform spherical nanoparticles for ET. The maximum adsorption capacities (Q_max) were 174.83 mg/g for EW and 210.53 mg/g for ET. Adsorption followed the pseudo-second-order kinetic model and was best described by the Langmuir isotherm, indicating monolayer chemisorption. Thermodynamic studies showed that adsorption was exothermic (ΔH = −45.62 to −50.92 kJ/mol) and spontaneous (ΔG < 0) and involved an entropy increase (ΔS = +0.1441 to +0.1569 kJ/mol·K). These findings demonstrate the superior adsorption efficiency of the ET composite and its potential application in dye-contaminated wastewater treatment. Full article

Phospholipase D (PLD) plays a pivotal role in the biosynthesis of phosphatidylserine (PS), but its practical application is constrained by limitations in stability and reusability. In this study, we successfully fabricated the Fe₃O₄@SiO₂–graphene oxide (GO) nanocomposite by chemical binding of Fe₃O₄@SiO₂ and GO. Subsequently, PLD was immobilized onto the nanocomposite via physical adsorption, with the aim of enhancing catalytic stability, reducing mass transfer resistance, and improving reusability. Under optimal conditions, the immobilization efficiency reached 84.4%, with a PLD loading capacity of 111.4 mg/g_support. The optimal pH for PS production by immobilized PLD shifted from 6.0 to 6.5, while the optimal temperature increased from 45 °C to 50 °C. Notably, the immobilized PLD demonstrated a shorter reaction time and a higher PS yield, achieving a 95.4% yield within 90 min, compared to the free PLD (78.1% yield within 150 min), representing a 1.04-fold improvement in production efficiency. Furthermore, the immobilized PLD exhibited outstanding storage stability and thermal stability, along with remarkable reusability. Even after being reused for 10 cycles, the PS yield still stays as high as 78.3%. These findings strongly suggest that the Fe₃O₄@SiO₂–GO immobilized PLD has the potential for the efficient production of PS. Full article

This study for the first time reports that insights into microstructure and thermal and compressive responses can be best achieved following exposure to different cryogenic temperatures and that the lowest cryogenic temperature may not always produce the best results. In the present study, a Mg-SiO₂ biocompatible and environment-friendly nanocomposite was synthesized by using the Disintegrated Melt Deposition method followed by hot extrusion. Subsequently, it was subjected to four different sub-zero temperatures (−20 °C, −50 °C, −80 °C, and −196 °C). The results reveal the best densification at −80 °C, marginally improved ignition resistance at 50 °C, the best damping response at −80 °C, the best microhardness at −50 °C, and the best compressive response at −20 °C. The results clearly indicate that the cryogenic temperature should be carefully chosen depending on the property that needs to be particularly enhanced governed by the principal requirement of the end application. Full article

Improving the ductile deformation behavior of Mg-SiC nanocomposites without compromising strength is critical to enhancing their mechanical properties. Mg-SiC nanocomposites are produced through mechanical milling, cold isostatic pressing, sintering, and hot extrusion processes. This study investigates the uniaxial stress–strain response and deformation behavior of the Mg-SiC nanocomposite compared to pure Mg samples with and without the milling process. The deformation behavior was investigated by two-dimensional (2D) digital image correlation (DIC) at two macroscopic and microscopic scales, employing light micrographs and in situ loading samples, respectively, in the scanning electron microscope. Compared to the pure Mg samples, the mechanical test results demonstrated a significant improvement in strength (80 MPa) and fracture strain (23.5%) of the Mg-SiC nanocomposite. The three-dimensional (3D) representative volume element (RVE) model revealed the particle dispersion effect on the mechanical properties of the nanocomposite. The RVE results demonstrate ductile deformation behavior in the sample with homogenous dispersion of SiC particles compared with the heterogeneous dispersion of SiC particles in Mg-SiC nanocomposite. The results demonstrated a good agreement between DIC and RVE predictions for Mg-SiC nanocomposites across macro- and microscales. Full article

In this study, novel V₂O₅-decorated garlic peel biochar (VO/GPB) nanocomposites are prepared via the facile hydrothermal technique. As-synthesized VO/GPB is characterized by various spectroscopic and analytical techniques. The surface morphology of the as-prepared samples was predicted by SEM analysis, which shows that the block-like V₂O₅ was uniformly decorated on the stone-like GPB surface. The elemental mapping analysis confirms the VO/GPB composite is composed of the following elements: C, O, Na, Mg, Si, P, K, and V, without any other impurities. The photocatalytic activity of the VO/GPB nanocomposite was examined by the degradation of methyl orange (MO) under the irradiation of visible light; 84% degradation efficiency was achieved within 30 min. The reactive oxidative species (ROS) study reveals that hydroxyl and superoxide radicals play an essential role in MO degradation. Moreover, the antioxidant action of the VO/GPB nanocomposite was also investigated. From the results, the VO/GPB composite has higher antioxidant activity compared to ascorbic acid; the scavenging effect increased with increasing concentrations of VO/GPB composite until it reached 40 mg/L, where the scavenging effect was the highest at 93.86%. This study will afford innovative insights into other photocatalytic nanomaterials with effective applications in the field of photocatalytic studies with environmental compensation. Full article

Achieving uniformly distributed reinforcement particles in a dense matrix is crucial for enhancing the mechanical properties of nanocomposites. This study focuses on fabricating Mg-SiC nanocomposites with a high-volume fraction of SiC particles (10 vol.%) using cold isostatic pressing (CIP). The objective is to obtain a fully dense material with a uniform dispersion of nanoparticles. The SiC particle size impact on the compressibility and density distribution of milled Mg-SiC nanocomposites is studied through the elastoplastic Modified Drucker-Prager Cap (MDPC) model and finite element method (FEM) simulations. The findings demonstrate significant variations in the size and dispersion of SiC particles within the Mg matrix. Specifically, the Mg-SiC nanocomposite with 10% submicron-scale SiC content (M10Sµ) exhibits superior compressibility, higher relative density, increased element volume (EVOL), and more consistent density distribution compared to the composite containing 10% nanoscale SiC (M10Sn) following CIP simulation. Under 700 MPa, M10Sµ shows improvements in both computational and experimental results for volume reduction percentage, 2.31% and 2.81%, respectively, and relative density, 4.14% and 3.73%, respectively, compared to M10Sn. The relative density and volume reduction outcomes are in qualitative alignment with experimental findings, emphasizing the significance of particle size in optimizing nanocomposite characteristics. Full article

Differences in the synthesis methods can affect the performance of nanocomposite materials. The synthesis methods of SiO₂-based nanocomposite pour point depressants synthesized by chemical hybrid are mostly in situ polymerization and chemical grafting. However, there are still some gaps in the synthesis of nanocomposites using chemical grafting. In this paper, the amino-modified Nano-SiO₂ and octamethyl methacrylate-maleic anhydride copolymer was used to prepare PM18-g-NSiO₂ by an amidation reaction, and the product was compared with PM18/SiO₂ prepared by the solution blending method. The characterization results of FT-IR and SEM showed that the chemical bond formed between PM18 and NSiO₂ and PM18-g-NSiO₂ showed a more regular morphology structure. The results of rheological tests showed that the optimal concentration of PM18-g-NSiO₂ and PM18/SiO₂ is 300 mg·kg⁻¹, but the decrease of PM18-g-NSiO₂ is 19 °C, while the decrease of PM18/SiO₂ is only 13 °C. The lowest viscosity of model oil added PM18-g-NSiO₂ was only 214 mPa·s while PM18/SiO₂ reached 453 mPa·s. The wax crystal structure after adding PM18-g-NSiO₂ is also more regular and smaller compared to PM18/SiO₂. We concluded that differences in the synthesis methods may lead to the different coverage of the polymer on the surface of the nanoparticle. Full article

Cd(II) and Cu(II) ions cause many diseases in humans. Therefore, they should be removed from water sources using simple and cost-effective adsorbents. Consequently, sodium magnesium silicate hydroxide/sodium magnesium silicate hydrate nanostructures were synthesized and functionalized using 2,3-dihydroxybenzaldehyde as a novel nanocomposite. Several instruments were used to characterize the synthetic products, such as an X-ray diffractometer (XRD), a Fourier-transform infrared spectrophotometer (FT-IR), an N₂ adsorption/desorption analyzer, a CHN elemental analyzer, an energy-dispersive X-ray spectrophotometer (EDS), and a field emission scanning electron microscope (FE-SEM). The functionalization of the nanostructures with 2,3-dihydroxybenzaldehyde led to the disappearance of the XRD peaks of the nanostructures and the presence of a broad XRD peak at 2θ = 32°. In addition, the FE-SEM images revealed that the nanostructures consisted of spheres, cubes, and irregular shapes with an average grain size of 115 nm, and the nanocomposite consisted of spherical conglomerates consisting of needle-like shapes. The anticipated morphology following the functionalization of the nanostructures with 2,3-dihydroxybenzaldehyde resulted from the presence of 2,3-dihydroxybenzaldehyde on the backbones of the nanostructures. The EDS results showed that the nanostructures were composed of O, Na, Mg, and Si with weight percentages equal to 38.59%, 5.95%, 16.60%, and 38.86%, respectively. Additionally, the nanocomposite was composed of C, N, O, Na, Mg, and Si with weight percentages equal to 55.31%, 2.23%, 30.09%, 6.56%, 2.98%, and 12.83%, respectively. The synthesized nanostructures and nanocomposite samples were utilized for the efficient removal of cadmium and copper ions from aqueous media using the ion exchange and chelation adsorption procedures, respectively. Optimum conditions for removing the cadmium and copper ions were achieved at a pH, time, and temperature equal to 7.5, 80 min, and 298 K, respectively. The maximum uptake capacities of the synthesized nanostructures and nanocomposite samples toward cadmium ions were 89.44 mg/g and 155.04 mg/g, respectively, and the maximum uptake capacities of the synthesized nanostructures and nanocomposite samples toward copper ions were 103.73 mg/g and 177.94 mg/g, respectively. Moreover, the adsorption processes were exothermic, chemical, and followed the pseudo-second-order model and Langmuir equilibrium isotherm model. Full article

Novel (Ca, Mg)CO₃&SiO₂ NPs-decorated multilayer graphene sheets could be successfully prepared from corn stalk pith using a simple alkaline hydrothermal treatment process followed by calcination in an inert atmosphere. The produced nanocomposite was characterized by SEM, EDX, TEM, FTIR, and XRD analytical techniques, which confirm the formation of multilayer graphene sheets decorated by inorganic nanoparticles. The nanocomposite shows efficient activity as a photocatalyst for water-splitting reactions under visible light. The influence of preparation parameter variations, including the alkaline solution concentration, hydrothermal temperature, reaction time, and calcination temperature, on the hydrogen evolution rate was investigated by preparing many samples at different conditions. The experimental work indicated that treatment of the corn stalk pith hydrothermally by 1.0 M KOH solution at 170 °C for 3 h and calcinating the obtained solid at 600 °C results in the maximum hydrogen production rate. A value of 43.35 mmol H₂/gcat.min has been obtained associated with the energy-to-hydrogen conversion efficiency of 9%. Overall, this study opens a new avenue for extracting valuable nanocatalysts from biomass wastes to be exploited in hot applications such as hydrogen generation from water photo-splitting under visible light radiation. Full article

In this study, novel chitosan/silica composites with different mass ratios were prepared by in-situ hydrolysis using chitosan (from shrimp shell) as a carrier, triblock copolymer (P123) as the structure-directing agent, and ethyl orthosilicate as a silicon source. These nanocomposites were characterized by different techniques, including the FT-IR, XRD, TGA, SEM, TEM and N₂ adsorption–desorption. The results indicated that the morphology and properties of composites changed with the introduction of silica. When the CS/TEOS mass ratio was 0.0775, the CS−2/SiO₂ composite displayed a coral-like three-dimensional porous structure with specific surface area of 640.37 m²/g and average pore size of 1.869 nm. The adsorption properties for methylene blue (MB) were investigated as well and the CS−2/SiO₂ showed better adsorption performance. The removal rate for MB reached 94.01% with absorbents dosage of 6 g/L, initial concentration of 40 mg/L, initial pH value of 7, temperature of 35 °C, and adsorption time of 40 min. The adsorption process well fitted the Langmuir isothermal model and quasi-second-order adsorption kinetics model. The maximum adsorption capacity for MB was 13.966 mg/g based on Langmuir fitting. The surface functional groups of the composites can play an important role in the adsorption. The adsorption mechanism of CS−2/SiO₂ on MB involved electrostatic interaction, hydrogen bonding and functional group complexation. In addition, the prepared chitosan/silica composites showed good reusability at six cycles, making them a promising material in the application of removing dyeing wastewater. Full article

A series of novel Mn_xFe_y@SiO₂ (x,y = 1–20%) nanocomposites were synthesized for the first time via the sol-gel/combustion method with different content of precursors (Mn and Fe acetate salts). The effect of precursor content and ratio on physicochemical properties were observed by various characterization methods. Moreover, Rhodamine B (RhB) was chosen as the target pollutant to test the performance of these nanocomposites under a photocatalytic Fenton-like reaction. The results showed that the nanocomposite morphology improved by increasing Fe and Mn content. In this study, interesting behavior was observed in BET results which were different from the fact that increasing metal content can decrease the surface area. This study revealed that one metal could be more critical in controlling the properties than another. Moreover, the precursor ratio appears to have a more tangible effect on the surface area than the effect of precursor content. Among all synthesized nanocomposites, Mn₁Fe₅@SiO₂ showed the highest surface area of 654.95 m²/g. At optimum batch conditions (temp = 25 °C, catalyst dosage = 1 g L⁻¹, H₂O₂ = 75 mmolL⁻¹, and initial RhB concentration = 50 mg L⁻¹), complete removal (simultaneous adsorption/degradation) occurred using Mn₁Fe₅@SiO₂ at neutral pH. This study showed that the designed nanomaterial could be used as a dual functional adsorbent/photocatalyst in different environmental applications. Full article

Magnesium silicate nanosheets (MgSiNS) and graphitic carbon nitride (g-C₃N₄) nanocomposites were produced by varying different weight percentages of g-C₃N₄. The obtained nanocomposites were characterized by various techniques such as X-Ray diffraction (XRD), Fourier transformed infrared spectroscopy (FT-IR), diffuse reflectance UV–vis spectroscopy (DR UV–vis), N₂-physisorption, transmission electron microscopy (TEM), and X-ray photon spectroscopy (XPS). The photocatalytic activities of the nanocomposites were measured using visible light irradiation to degrade methylene blue (MB) and Pb²⁺ adsorption in aqueous solution. The ideal physicochemical properties such as porosity, band gap energy, and functional groups in the MgSiNS-GN20 composite (80% MgSiNS and 20 wt % of g-C₃N₄) offered high Pb²⁺ adsorption (0.005 mol/g) and excellent MB degradation efficiency (approximately 93%) at pH 7 within 200 min compared to other composites. In addition, the influences of different reaction parameters such as the effect of pH, the load catalyst, and the concentration of MB and Pb⁺² ions were examined. The obtained results indicate that inexpensive and eco-friendly MgSiNS and g-C₃N₄ composites could be recycled several times, hence representing a promising material to purify water from both organic and inorganic contaminants. Full article

Lightweight magnesium-based materials have received attention in the automobile sector as a solution to minimize fuel consumption and greenhouse gas emissions. Magnesium has great weight-reduction potential in the aerospace sector, but its low ignition temperature limits its utilization. Improving magnesium’s ignition resistance is critical for aerospace applications. The present study developed Mg/Si₃N₄ nanocomposites to improve the ignition resistance to address this limitation. The nanocomposites were prepared by ultrasonically-assisted stir casting with 0.5, 1, and 1.5 vol% Si₃N₄ nanoparticles. The effect of Si₃N₄ nanoparticles on the ignition and compression characteristics was examined. SEM micrographs showed the homogeneous dispersion of Si₃N₄ nanoparticles with negligible clustering. Notably, the nanocomposites’ ignition resistance was increased by increasing the vol% of the Si₃N₄ nanoparticles. Adding 1.5 vol% Si₃N₄ nanoparticles resulted in the highest ignition temperature of 614 °C, 34 °C higher than pure magnesium. Similarly, the compressive properties were enhanced with the progressive addition of Si₃N₄ nanoparticles. The inclusion of 1.5 vol% Si₃N₄ nanoparticles resulted in a maximum compressive yield strength of 118 MPa and ultimate compressive strength of 323 MPa. Full article

Nanocomposites formed by clay and lipid carriers (NLCs) show a high potential for providing controlled release and specific delivery of bioactive molecules and have recently gained attention in the pharmaceutical sector due to their ability to transport hydrophilic and hydrophobic drugs. Recent studies have recognized the biological activity of the oil of Bixa orellana L. (AO) with regards to its healing, antioxidant, antibacterial, and anti-leishmanial properties. Therefore, the purpose of this study is the preparation and characterization of hybrid systems based on lipid nanocarriers and laponite for the delivery of AO. NLCs were prepared by the fusion-emulsification method, using cetyl palmitate (CP) or myristyl myristate (MM), AO, and Poloxamer 188. The morphology, hydrodynamic diameters, zeta potential (ZP), polydispersity index (PDI), thermal analysis, X-ray diffraction analysis (XRD), viscosity behavior, and cytotoxicity testing of the hybrid systems were performed. The thermal study and X-ray diffraction analyses (XRD) revealed polymorphic structural changes compatible with the amorphization of the material. Rheological assays highlighted a typical pseudoplastic behavior in all systems (MM and CP with LAP). The hybrid systems’ morphology, size diameters, and PDIs were similar, preset spherical and monodisperse structures (≈200 nm; <0.3), without significant change up to sixty days. The ZP values differed from each other, becoming higher with increasing AO concentration. XEDS spectra and elemental X-ray maps show peaks of lipids (organic components, C and O) and inorganic components O, Mg, and Si. All samples showed cell viability above 60%. The results indicated a stable, biocompatible hybrid system that can be an alternative for topical application. Full article

Sports are becoming an important part of everyday life. In this study, an excellent Ni-SiC nanocomposite was prepared on the dumbbell surface using the pulse electrodeposition (PE) method to improve the durability of sports equipment and prevent sports injuries. Transmission electron microscopy (TEM), scanning electron microscopy (SEM), abrasion testing, triboindentry, and X-ray diffraction (XRD) were used to evaluate the impact of plating conditions upon the microhardness, microstructure, morphology, and wear behavior of the fabricated coatings. The obtained results showed that several SiC and TiN nanoparticles were incorporated into Ni/TiN-SiC nanocomposites obtained at 4 A/dm². SiC and TiN nanoparticles had mean diameters of 37.5 and 45.6 nm, respectively. The Ni/TiN-SiC nanocomposite produced at 4 A/dm² showed an excellent mean microhardness value of 848.5 HV, compared to the nanocomposites produced at 2 and 6 A/dm². The rate of wear for Ni/TiN-SiC nanocomposite produced at 4 A/dm² was 13.8 mg/min, demonstrating outstanding wearing resistance. Hence, it has been suggested that the Ni/TiN-SiC nanocomposite can effectively reduce sports injuries. Full article