Search Results (24)

The hydrothermal synthesis of CuO/NiO composites was conducted using banana fruit biomass waste. In this study, X-ray powder diffraction, scanning electron microscopy, and Fourier transform infrared spectroscopy were used to investigate the crystalline properties, shape structure, and functional group characterization of CuO/NiO composites. The typical morphology of the prepared materials consisted of irregular nanoparticles arranged into clusters of less than 200 nanometers in size. In spite of this, the CuO/NiO composites showed monoclinic CuO and cubic NiO phases and were therefore successfully synthesized. It was observed that rotten banana fruit juice had a significant impact on the particle size and crystal quality of CuO/NiO composites. This was due to the presence of capping, reducing, and stabilizing agents in banana fruit juice. Under alkaline conditions, the CuO/NiO composites were found to be highly electro catalytically active toward the oxidation of urea. Sample 2, which was prepared by adding 1.2 g of CuO decorated with NiO, showed a linear increase in urea detection ranging from 0.1 mM to 17 mM, with a limit of detection of 0.004 mM. Furthermore, sample 2 of the CuO/NiO composite demonstrated exceptional stability, selectivity, and reproducibility. Consequently, sample 2 of CuO/NiO could effectively detect urea in spinach, lotus root, milk, and curd. The improved performance of sample 2 of the CuO/NiO composite can be attributed to its favorable surface properties, which contain enriched active sites and a rapid charge transfer rate. Full article

Green approaches for nanoparticle synthesis have emerged as biocompatible, economical, and environment-friendly alternatives to counteract the menace of microbial drug resistance. Recently, the utilization of honey as a green source to synthesize Fe₂O₃-NPs has been introduced, but its antibacterial activity against one of the opportunistic MDR pathogens, Klebsiella pneumoniae, has not been explored. Therefore, this study employed Apis mellifera honey as a reducing and capping agent for the synthesis of iron oxide nanoparticles (Fe₂O₃-NPs). Subsequent to the characterization of nanoparticles, their antibacterial, antioxidant, and anti-inflammatory properties were appraised. In UV-Vis spectroscopic analysis, the absorption band ascribed to the SPR peak was observed at 350 nm. XRD analysis confirmed the crystalline nature of Fe₂O₃-NPs, and the crystal size was deduced to be 36.2 nm. Elemental analysis by EDX validated the presence of iron coupled with oxygen in the nanoparticle composition. In ICP-MS, the highest concentration was of iron (87.15 ppm), followed by sodium (1.49 ppm) and other trace elements (<1 ppm). VSM analysis revealed weak magnetic properties of Fe₂O₃-NPs. Morphological properties of Fe₂O₃-NPs revealed by SEM demonstrated that their average size range was 100–150 nm with a non-uniform spherical shape. The antibacterial activity of Fe₂O₃-NPs was ascertained against 30 clinical isolates of Klebsiella pneumoniae, with the largest inhibition zone recorded being 10 mm. The MIC value for Fe₂O₃-NPs was 30 µg/mL. However, when mingled with three selected antibiotics, Fe₂O₃-NPs did not affect any antibacterial activity. Momentous antioxidant (IC₅₀ = 22 µg/mL) and anti-inflammatory (IC₅₀ = 70 µg/mL) activities of Fe₂O₃-NPs were discerned in comparison with the standard at various concentrations. Consequently, honey-mediated Fe₂O₃-NP synthesis may serve as a substitute for orthodox antimicrobial drugs and may be explored for prospective biomedical applications. Full article

The electrochemical performance of NiCo₂O₄ with urea precursors was evaluated in order to develop a non-enzymatic urea sensor. In this study, NiCo₂O₄ nanostructures were synthesized hydrothermally at different concentrations of urea and characterized using scanning electron microscopy and X-ray diffraction. Nanostructures of NiCo₂O₄ exhibit a nanorod-like morphology and a cubic phase crystal structure. Urea can be detected with high sensitivity through NiCo₂O₄ nanostructures driven by urea precursors under alkaline conditions. A low limit of detection of 0.05 and an analytical range of 0.1 mM to 10 mM urea are provided. The concentration of 006 mM was determined by cyclic voltammetry. Chronoamperometry was used to determine the linear range in the range of 0.1 mM to 8 mM. Several analytical parameters were assessed, including selectivity, stability, and repeatability. NiCo₂O₄ nanostructures can also be used to detect urea in various biological samples in a practical manner. Full article

To cope with environmental pollution caused by toxic emissions into water streams, high-performance photocatalysts based on ZnO semiconductor materials are urgently needed. In this study, ZnO nanostructures are synthesized using leafy spinach extract using a biogenic approach. By using phytochemicals contained in spinach, ZnO nanorods are transformed into large clusters assembled with nanosheets with visible porous structures. Through X-ray diffraction, it has been demonstrated that leafy spinach extract prepared with ZnO is hexagonal in structure. Surface properties of ZnO were altered by using 10 mL, 20 mL, 30 mL, and 40 mL quantities of leafy spinach extract. The size of ZnO crystallites is typically 14 nanometers. In the presence of sunlight, ZnO nanostructures mineralized methylene blue. Studies investigated photocatalyst doses, dye concentrations, pH effects on dye solutions, and scavengers. The ZnO nanostructures prepared with 40 mL of leafy spinach extract outperformed the degradation efficiency of 99.9% for the MB since hydroxyl radicals were primarily responsible for degradation. During degradation, first-order kinetics were observed. Leafy spinach extract could be used to develop novel photocatalysts for the production of solar hydrogen and environmental hydrogen. Full article

To determine urea accurately in clinical samples, food samples, dairy products, and agricultural samples, a new analytical method is required, and non-enzymatic methods are preferred due to their low cost and ease of use. In this study, bitter gourd peel biomass waste is utilized to modify and structurally transform nickel oxide (NiO) nanostructures during the low-temperature aqueous chemical growth method. As a result of the high concentration of phytochemicals, the surface was highly sensitive to urea oxidation under alkaline conditions of 0.1 M NaOH. We investigated the structure and shape of NiO nanostructures using powder X-ray diffraction (XRD) and scanning electron microscopy (SEM). In spite of their flake-like morphology and excellent crystal quality, NiO nanostructures exhibited cubic phases. An investigation of the effects of bitter gourd juice demonstrated that a large volume of juice produced thin flakes measuring 100 to 200 nanometers in diameter. We are able to detect urea concentrations between 1–9 mM with a detection limit of 0.02 mM using our urea sensor. Additionally, the stability, reproducibility, repeatability, and selectivity of the sensor were examined. A variety of real samples, including milk, blood, urine, wheat flour, and curd, were used to test the non-enzymatic urea sensors. These real samples demonstrated the potential of the electrode device for measuring urea in a routine manner. It is noteworthy that bitter gourd contains phytochemicals that are capable of altering surfaces and activating catalytic reactions. In this way, new materials can be developed for a wide range of applications, including biomedicine, energy production, and environmental protection. Full article

Wastewater treatment is indispensable as wastewater can lead to adverse health effects and deteriorate the quality of life on earth. Photocatalysis is a facile methodology to address this issue. In this study, nanocomposites (NCs) of manganese oxide (Mn₃O₄) and nickel oxide (NiO) were synthesized in different weight ratios via the solid-state reaction route. Structural properties, optical properties, surface morphology, and functional group analysis of the synthesized nanomaterials were conducted using X-ray diffraction (XRD), UV– Vis spectroscopy, scanning electron microscopy (SEM) along with energy-dispersive X-ray (EDX) analysis, and Fourier-transform infrared (FTIR) spectroscopy, respectively. The bandgap of the nanocomposite decreases significantly from 2.35 eV for the Mn₃O₄ NPs to 1.65 eV for the Mn₃O₄/NiO nanocomposite (NC). Moreover, adsorption studies followed by the photocatalytic performance of the Mn₃O₄/NiO NCs were evaluated to determine the removal of methylene blue (MB) dye from wastewater. The photocatalytic performance of the nanocomposite enhances as the ratio of Mn₃O₄ in the composite increases from one weight percentage to three weight percentage. The photocatalytic degradation efficiency was calculated to be 95%. The results show that the synthesized NCs could play an important role in photocatalytic wastewater purification and environmental remediation. Full article

The wide variety of uses for nanoparticles (NPs) is due to their unique combination of features in a single assembly. The arc melted copper-cobalt ingot sample were qualitatively studied using laser induced breakdown spectroscopy (LIBS). Later, using the fabricated alloy as a target material for Nd:YAG laser ablation, CuCo₂O₄ NPs were synthesized. The magnetic properties of the synthesized NPs were studied using a vibrating sample magnetometer (VSM). To determine the composition and morphology of the synthesized NPs, X-ray diffraction (XRD), energy dispersive X-ray (EDX) analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and dynamic light scattering (DLS) techniques were used. The TEM and DLS showed that particles were spherical in shape with an average size of 32 nm and 28 nm, respectively. The antibacterial activity of the synthesized NPs was studied against S. aureus and E. coli strains as positive and negative controls using a standard approach. CuCo₂O₄ nanoparticles exhibited non-mutagenic potential against S. typhimurium TA-98 and TA-100 strains. Furthermore, the magnetic hyperthermia study of CuCo₂O₄ nanofluid was examined using a lab-made apparatus. The specific absorption rates (SAR) of 4.57 and 5.17 W/g were determined for the magnetic field strength of 230 μT and 247 μT, respectively. The study shows antibacterial activity and magnetic hyperthermia potential of the synthesized nanoparticles. Full article

Magneto-plasmonic Ag/Ni and Ag/Fe nanoparticles (NPs) were synthesized in this work using the environmentally safe and contaminant-free dual-pulsed Q-switched Nd:YAG 1064 nm laser ablation method. The optical and magnetic characteristics of synthesized nanomaterials were investigated using a vibrating sample magnetometer and an ultraviolet-visible absorption spectrometer. According to transmission electron microscopy (TEM), the shape of Ag/Ni and Ag/Fe NPs seems to be spherical, with mean diameters of 7.3 nm and 11.5 nm, respectively. X-ray diffraction (XRD) was used in order to investigate and describe the phase structures of the synthesized nanomaterials. The synthesized NPs reached maximum temperatures such as 48.9, 60, 63.4, 70, 75, and 79 °C for Ag/Ni nanofluid and 52, 56, 60, 68, 71, and 72 °C for Ag/Fe nanofluid when these nanofluids were subjected to an NIR 808 nm laser with operating powers of 1.24, 1.76, 2.36, 2.91, 3.5, and 4 W, respectively. Because of the plasmonic hyperthermia properties of nanoparticles, nanofluids display higher temperature profiles than pure water. According to these findings, plasmonic nanoparticles based on silver might be used to treat hyperthermia. Full article

This research is aimed at the up-gradation of indigenous Pakistani iron ore, i.e., Dilband iron ore (hematite), by utilizing common metallurgical processes. First, the magnetic properties of the ore were determined. Initially, the iron ore samples contained 34 wt. % Fe in addition to other gangue materials. Therefore, the ore was subjected to a high-temperature reduction roasting process between 800 °C and 1000 °C. Additionally, the magnetic separation process was also employed. The influence of different roasting parameters, such as the reduction time, coal-to-ore ratio, and temperature, was examined. This was followed by characterization techniques using XRD (X-ray diffraction analysis), the Rietveld method, wet chemistry analysis, and a VSM (Vibrating Sample Magnetometer). The results suggest an excellent reduction at 900 °C for a coal/ore ratio of 20 wt. %, which was achieved within 2 h of the process. The Fe concentration increased tremendously from 34 to 56 wt. %, and in conjunction, magnetic properties were also induced (1.5 emu). The recovery was found to be substantial for the ore when the Fe content was 75 wt. %. Additionally, the economic feasibility of the processed ore was also studied, followed by an extensive analysis of the roasting and magnetic separation processes. Full article

This work focuses on preparing TiO₂, CdS, and composite TiO₂:CdS thin films for photovoltaic applications by thermal evaporation. The suggested materials exhibit very good optical and electrical properties and can play a significant role in enhancing the efficiency of the device. Various microscopy and spectroscopy techniques were considered to investigate the optical, morphological, photoluminescence, and electrical properties. FTIR confirms the material identification by displaying some peaks in the fingerprint region. UV Vis spectroscopy yields high transmission (80–90%) and low absorbance (5–10%) within the spectral region from 500 nm to 800 nm for the composite thin films. The optical band gap values for CdS, TiO_2, and TiO₂:CdS thin films are 2.42 eV, 3.72 eV, and 3.6 eV. XRD was utilized to analyze the amorphous nature of the thin films, while optical and SEM microscopy were employed to examine the morphological changes caused by the addition of CdS to TiO₂. The decrease in the bandgap of the composite thin films was determined by the Tauc plot, which is endorsed due to the band tailing effects. Photoluminescence spectroscopy depicts several emission peaks in the visible region when they are excited at different wavelengths, and the electrical measurement enhances the material conductivity. Furthermore, the proposed electron transport materials (TiO₂, CdS, TiO₂:CdS) were simulated with different perovskite materials to validate their design by employing the SCAPS-1D program and assess their performance in commercial implementation. The observed results suggest that TiO₂:CdS is a promising candidate to be used as an ETM in PSC with enhanced productivity. Full article

Herein, polymeric cryogels containing poly(N-isopropylacrylamide) were synthesized by cryo-polymerization at subzero temperature. The synthesized cryogels were loaded with silver and palladium nanoparticles by the chemical reduction method at room temperature using the reducing agent NaBH₄. Moreover, for comparison with cryogels, pure poly(N-isopropylacrylamide) hydrogel and its silver hybrid were also prepared by the conventional method at room temperature. The chemical structure and functional group analysis of the pure cryogels was confirmed by Fourier transform infrared spectroscopy. The synthesis of hybrid cryogels was confirmed by the X-ray diffraction technique and energy dispersive X-ray. The pore size and surface morphology of the pure cryogels, their respective hybrid cryogels and of conventional hydrogels were studied by using the scanning electron microscopy technique. The hybrid cryogels were successfully used as a catalyst for the degradation of methyl orange dye. The degradation performance of the hybrid cryogels was much better than its counterpart hybrid hydrogel for methyl orange dye. The effect of temperature and amount of catalyst on catalytic performance was studied by UV-visible spectroscopy. The reduction follows pseudo-first-order reaction kinetics. In addition, the antibacterial activities of these cryogels were evaluated against Gram-positive bacteria (Staphylococcus aureus, ATCC: 2593) and Gram-negative bacteria (Escherichia coli, ATCC: 25922). Both hybrid cryogels have shown much better antibacterial activity for these two strains of bacteria compared to pure cryogels. The results indicate that these cryogels are potential candidates for water purification systems as well as biomedical applications. Full article

Nickel-supported hierarchical zeolite catalysts were prepared through a desilication reassembly process under optimized conditions and applied in one-pot menthol synthesis. In this work, the hierarchical zeolite-supported metal bifunctional catalysts were prepared with the help of desilication re-assembly and wetness impregnation techniques and applied in menthol synthesis via citral hydrogenation. The prepared catalysts were characterized using PXRD, BET, FE-TEM, NH₃-TPD, H₂-TPR, pyridine adsorption, and ICP-OES techniques. As a result, the physicochemical and acidic properties, such as mesopore surface area, metal dispersion, acidity, catalytic activity, and strong Lewis acid sites of pure microporous ZSM-5/USY zeolites, were significantly improved. Consequently, with the occurrence of superior physicochemical and acidic properties, the Ni/HZ-0.5 M catalyst exhibited outstanding catalytic activity (100% conversion, TOF 7.12 h⁻¹) and menthol selectivity (83%, 4 h) with uniform stability at 100 °C, 1.0 MPa hydrogen. Similarly, the cracking rate decreased with the decrease in Bronsted acid sites. Full article

In this study, chloride (Cl⁻) ions were successfully doped into ZnO nanostructures by the solvothermal method. The effect of various Cl⁻ concentrations on the photocatalytic activity of ZnO towards the photodegradation of methylene blue (MB) under the illumination of ultraviolet light was studied. The as-prepared Cl⁻-doped ZnO nanostructures were analyzed in terms of morphology, structure, composition and optical properties. XRD data revealed an average crystallite size of 23 nm, and the XRD patterns were assigned to the wurtzite structure of ZnO even after doping with Cl⁻. Importantly, the optical band gap of various Cl ion-doped ZnO nanostructures was successively reduced from 3.42 to 3.16 eV. The photodegradation efficiency of various Cl⁻ ion-doped ZnO nanostructures was studied for MB in aqueous solution, and the relative performance of each Cl ion-doped ZnO sample was as follows: 20% Cl⁻-doped ZnO > 15% Cl⁻-doped ZnO > 10% Cl⁻-doped ZnO > 5% Cl⁻-doped ZnO > pristine ZnO. Furthermore, the correlation of the pH of the MB solution and each Cl ion dopant concentration was also investigated. The combined results of varying dopant levels and the effect of the pH of the MB solution on the photodegradation process verified the crucial role of Cl⁻ ions in activating the degradation kinetics of MB. Therefore, these newly developed photocatalysts could be considered as alternative materials for practical applications such as wastewater treatment. Full article

Aluminum nitride (AlN) is a semiconductor material possessing a hexagonal wurtzite crystal structure with a large band gap of 6.2 eV. AlN thin films have several potential applications and areas for study, particularly in optoelectronics. This research study focused on the preparation of Ni-doped AlN thin films by using DC and RF magnetron sputtering for optoelectronic applications. Additionally, a comparative analysis was also carried out on the as-deposited and annealed thin films. Several spectroscopy and microscopy techniques were considered for the characterization of structural (X-ray diffraction), morphological (SEM), chemical bonding (FTIR), and emission (PL spectroscopy) properties. The XRD results show that the thin films have an oriented c-axis hexagonal structure. SEM analysis validated the granular-like morphology of the deposited sample, and FTIR results confirm the presence of chemical bonding in deposited thin films. The photoluminescence (PL) emission spectra exhibit different peaks in the visible region when excited at different wavelengths. A sharp and intense photoluminescence peak was observed at 426 nm in the violet-blue region, which can be attributed to inter-band transitions due to the incorporation of Ni in AlN. Most of the peaks in the PL spectra occurred due to direct-band recombination and indirect impurity-band recombination. After annealing, the intensity of all observed peaks increases drastically due to the development of new phases, resulting in a decrease in defects and a corresponding increase in the crystallinity of the thin film. The observed structural, morphological, and photoluminescence results suggest that Ni: AlN is a promising candidate to be used in optoelectronics applications, specifically in photovoltaic devices and lasers. Full article

The development of innovative technology for effective pollutant degradation is becoming more important as a result of major environmental issues. Here, ZnO nanoparticles were synthesized using facile and aqueous chemical growth routes. Analytical techniques such as scanning electron micrographs (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Zeta Seizer (ZS), and Zeta Potential were used to analyze the resultant nanoparticles (ZP). The ZnO reveals a nanocluster texture that has a medium scale of 27 nm and a surface charge (17 ± 3 mV) with a wurtzite phase and crystalline nature. Photo catalysts have a higher potential for the thermal disposal of chlorophenols pollutants due to their low cost and simple synthesis procedure. The as-prepared sample underwent photocatalysis for the simultaneous photo-degradation of PCP and TCP as a model dye under sunlight. The ZnO nanostructure exhibited an exceptional degradation of around 85–90% for PCP and TCP in the aqua liquid, with the lowest amount of catalyst dosage of 240–250 μg individually and simultaneously, over 3 min beneath the sun ray. The greater productivity of the ZnO nanostructure for natural deterioration during solar irradiation indicates that the aqueous chemical growth enables the creation of effective and affordable photocatalysts for the photodegradation of a variety of environmental contaminants. Full article