Search

In this study, we report the synthesis of iron oxide nanoparticles (FeONPs) using micro-emulsion-hydrothermal method. By adjusting the synthesis temperature, we successfully produced FeO nanorods and nanospheres. In addition, the 2-octanol, and the surfactant cetyltrimethylammonium bromide served as a solvent in the synthesis process. Using iron nitrate hexahydrate as the salt precursor allowed for the formation of FeONPs with varied sizes, shapes and phases. The synthesized materials were extensively characterized using XRD, SEM, TEM, EDS, FTIR, and XPS techniques. However, the structural analysis revealed rhombohedral (hematite), and (magnetite) crystal structures in the materials synthesized at different temperature and durations, with particles ranged in size from 12 to 97 nm. More importantly, the magnetic characterization, performed with a vibrating sample magnetometer and SQUID magnetometer, indicated that the NPs showed not clear superparamagnetic behavior. In conclusion, this work demonstrates the synthesis of FeONPs with controlled size, shape and phase using microemulsion hydrothermal technique, with detailed characterization offering valuable insights into their magnetic and structural properties., Competing Interests: Declarations. Competing interests: The authors declare no competing interests., (© 2025. The Author(s).)

A novel nickel-molybdenum carbide-graphite nanofiber composite is introduced as an electrocatalyst for ethanol electrooxidation. The proposed nanofibers have been prepared by calcinating electrospun nanofibers composed of nickel acetate tetrahydrate, molybdenum chloride, and polyvinyl alcohol. The calcination process was conducted at different temperatures (700, 850, and 1000°C) under a nitrogen gas atmosphere with a heating rate of 2.5 deg/min and a holding time of 5 h. Physicochemical characterizations have indicated that nickel acetate is entirely reduced to nickel metal during the sintering process, and molybdenum has bonded with carbon to produce molybdenum carbide. At the same time, the used polymer has been pyrolyzed to produce a carbon nanofiber matrix embedding formed inorganic nanoparticles. Electrochemical measurements concluded that molybdenum content and calcination temperature should be controlled to maximize the electrocatalytic activity of the proposed catalyst. Typically, the oxidation peak current density was 28.5, 28.8, 51.5, 128.3, 25.6, and 3 mA/cm2 for nanofibers prepared from an electrospun solution containing 0, 5, 10, 15, 25, and 35 wt% molybdenum carbide, respectively. Moreover, it was observed that increasing the calcination temperature distinctly improves the electrocatalytic activity. Kinetic studies have indicated that the reaction order is close to zero with a reaction temperature-dependent value. Moreover, it was detected that the electrooxidation reaction of ethanol over the proposed nanofiber composite follows the Arrhenius equation. The determined activation energy is 33 kJ/mol, which indicates good catalytic activity for the introduced nanofibers. Through the application of a set of visualization-based tools and the general linear model (GLM), the optimal conditions that generate the highest current density were identified. The computations unveiled that the optimal parameter settings are as follows: Mo content at 15 wt.%, methanol concentration of 1.55 M, and reaction temperature of 59°C., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2024 Barakat et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)

This work addresses the problem of converting waste methane, a significant greenhouse gas, using customized nickel-zeolite catalysts to produce profitable syngas. The investigation employs 5 wt % of Ni on various zeolite supports with Si/Al ratios ranging from 13 to 25. Comprehensive characterization methods, including temperature-programmed reduction, N 2 adsorption-desorption, and X-ray diffraction, were used to identify critical structural characteristics that greatly impact the catalyst's performance. The study indicates that the reducibility and basicity of the catalyst, the type of zeolite support, and the kind of carbon deposits formed during the reaction at 800 °C all influence the efficiency of methane conversion to syngas. The best catalyst was found to be 5Ni-Z3, which at 800 °C produced high conversion rates of carbon dioxide (60%) and methane (50%). Lastly, the response surface methodology, in conjunction with numerical simulation, was used to determine the best operating settings for maximizing syngas production with the 5Ni-Z3 catalyst. Reaction temperature, space velocity, and the methane-to-carbon dioxide feed ratio were considered in this analysis. With a methane conversion rate exceeding 92%, a carbon dioxide conversion rate exceeding 90%, and a hydrogen-to-carbon monoxide ratio of 1.00, the catalyst produced experimental results very similar to the SRM predictions when the reaction was conducted at conditions close to the predicted values [temperature around 845 °C, space velocity around 22,000 mL/(h·gcat), and feed ratio close to 0.94]. The effectiveness of the identified operating conditions for the dry reforming process is validated by the near alignment of expected and experimental outcomes., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

Perfluoroalkyl carboxylic acids (PFCAs) are sub-class of perfluoroalkyl substances commonly detected in water matrices. They are persistent in the environment, hence highly toxic to living organisms. Their occurrence at trace amount, complex nature and prone to matrix interference make their extraction and detection a challenge. This study consolidates current advancements in solid-phase extraction (SPE) techniques for the trace-level analysis of PFCAs from water matrices. The advantages of the methods in terms of ease of applications, low-cost, robustness, low solvents consumption, high pre-concentration factors, better extraction efficiency, good selectivity and recovery of the analytes have been emphasized. The article also demonstrated effectiveness of some porous materials for the adsorptive removal of the PFCAs from the water matrices. Mechanisms of the SPE/adsorption techniques have been discussed. The success and limitations of the processes have been elucidated., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Nanomaterials and nanoparticles are a burgeoning field of research and a rapidly expanding technology sector in a wide variety of application domains. Nanomaterials have made exponential progress due to their numerous uses in a variety of fields, particularly the advancement of engineering technology. Nanoparticles are divided into various groups based on the size, shape, and structural morphology of their bodies. The 21st century's defining feature of nanoparticles is their application in the design and production of semiconductor devices made of metals, metal oxides, carbon allotropes, and chalcogenides. For the researchers, these materials then opened a new door to a variety of applications, including energy storage, catalysis, and biosensors, as well as devices for conversion and medicinal uses. For chemical and thermal applications, ZnO is one of the most stable n-type semiconducting materials available. It is utilised in a wide range of products, from luminous materials to batteries, supercapacitors, solar cells to biomedical photocatalysis sensors, and it may be found in a number of forms, including pellets, nanoparticles, bulk crystals, and thin films. The distinctive physiochemical characteristics of semiconducting metal oxides are particularly responsible for this. ZnO nanostructures differ depending on the synthesis conditions, growth method, growth process, and substrate type. A number of distinct growth strategies for ZnO nanostructures, including chemical, physical, and biological methods, have been recorded. These nanostructures may be synthesized very simply at very low temperatures. This review focuses on and summarizes recent achievements in fabricating semiconductor devices based on nanostructured materials as 2D materials as well as rapidly developing hybrid structures. Apart from this, challenges and promising prospects in this research field are also discussed., Competing Interests: The authors declared no potential conflicts of interest., (This journal is © The Royal Society of Chemistry.)

The main objective of this work is to develop a variety of hybrid high-density polyethylene (HDPE) micro- and nanocomposites and to investigate their thermal, mechanical, and morphological characteristics as a function of number of fillers and their contents percentage. In this study, 21 formulations of the composites were prepared using fillers with different sizes including micro fillers such as talc, calcium carbonate (CaCO 3 ), as well as nano-filler (fumed silica (FS)) though the melt blending technique. The morphological, mechanical, and thermal properties of the composite samples were evaluated. The morphological study revealed negligible filler agglomerates, good matrix-filler interfacial bonding in case of combined both CaCO 3 and FS into the composites. Sequentially, improvements in tensile, flexural and Izod impact strengths as a function of fillers loading in the HDPE matrix have been reported. The maximum enhancement (%) of tensile, flexural and impact strengths were 127%, 86% and 16.6%, respectively, for composites containing 25% CaCO 3 and 1% FS without any inclusion of talc filler; this indicates that the types/nature, size, quantity and dispersion status of fillers are playing a major role in the mechanical properties of the prepared composites more than the number of the used fillers.

It is pivotal to precisely detect food preservatives to ascertain food quality and safety. In this work, we report the sensitive electrochemical detection of widely used cytotoxic food preservative tert-butylhydroquinone (TBHQ). A novel nanocomposite was sonochemically prepared by embedding ternary metal oxide (TMO) comprising ZnO, CuO, and MgO in β-cyclodextrin (β-CD) functionalized carbon black (CB). The properties of the prepared nanocomposite were evaluated by employing multiple characterization methods. The nanocomposite fabricated on a screen printed carbon electrode exhibited exceptional electrocatalytic activity towards TBHQ detection, evident from the resultant very low detection limit of 1 nM and high sensitivity of 22.67 μA μM -1 cm -2 . Moreover, the developed TBHQ sensor evinced all the important traits of a good electrochemical sensor including excellent selectivity, stability, reproducibility, and repeatability. Furthermore, for validating practical feasibility of TBHQ detection, we successfully determined this food additive in edible oils., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Nanomolar-level detection of priority toxic pollutant 4-nitrophenol (4-NP) in environment using a novel ternary nanocomposite based electrochemical sensor and its photocatalytic degradation is reported in this paper. A non-toxic and renewable natural biopolymer, chitosan wrapped carbon nanofibers was embedded with Ag doped spinel Co 3 O 4 to prepare the bi-functional ternary nanocomposite. Economical and ecofriendly sonochemical method was employed in preparation of this porous nanocomposite. We used one-pot aqueous solution approach to synthesize Ag-Co 3 O 4 nanoflowers and ultrasound-assisted method was utilized to prepare CS-CNFs. Morphological and structural properties of synthesized materials were analyzed using different characterization techniques. Electrochemical investigations using cyclic voltammetry and differential pulse voltammetry carried out with prepared ternary nanocomposite modified carbon electrode revealed its outstanding electrocatalytic activity in 4-NP quantification. The developed 4-NP sensor showcased excellent sensitivity of 55.98 μAμM -1 cm -2 and nanomolar detection limit of 0.4 nM. Moreover, reproducibility, repeatability, stability, and selectivity were evaluated to confirm reliability of developed sensor. Further, real sample analyses were conducted using domestic sewage, underground water, and tomato to affirm the practical feasibility of 4-NP detection using the proposed sensor., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Synthetic food colorants are extensively used across the globe regardless of the fact that they induce deleterious side effects when used in higher amounts. In this work, a novel electrochemical sensor based on nickel nanoparticles doped lettuce-like Co 3 O 4 anchored graphene oxide (GO) nanosheets was developed for effective detection of sulfonated azo dye sunset yellow widely used as a food colorant. Hydrothermal synthesis was adopted for the preparation of lettuce-like spinel Co 3 O 4 nanoparticles and Ni-Co 3 O 4 NPs/GO nanocomposite was prepared using ecofriendly and economical sonochemical method. The prepared ternary nanocomposite meticulously fabricated on a screen-printed carbon electrode exhibited remarkable electrocatalytic activity towards sunset yellow determination. This is apparent from the resultant well-defined and intense redox peak currents of Ni-Co 3 O 4 NPs/GO nanocomposite modified electrode at very low potentials. The developed sunset yellow sensor exhibited a high sensitivity of 4.16 μA μM -1  cm -2 and a nanomolar detection limit of 0.9 nM in the linear range 0.125-108.5 μM. Furthermore, experiments were conducted to affirm excellent stability, reproducibility, repeatability, and selectivity of proposed sensor. The practicality of sunset yellow determination using the developed sensor was analyzed in different varieties of food samples including jelly, soft drink, ice cream, and candy resulting in recovery in the range of 96.16%-102.56%., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Background and Objective: Arterial diseases would lead to several serious disorders in the cardiovascular system such as atherosclerosis. These disorders are mainly caused by the presence of fatty deposits, cholesterol and lipoproteins inside blood vessel. This paper deals with the analysis of non-Newtonian magnetic blood flow in an inclined stenosed artery., Methods: The Casson fluid was used to model the blood that flows under the influences of uniformly distributed magnetic field and oscillating pressure gradient. The governing fractional differential equations were expressed using the Caputo Fabrizio fractional derivative without singular kernel., Results: The analytical solutions of velocities for non-Newtonian model were then calculated by means of Laplace and finite Hankel transforms. These velocities were then presented graphically. The result shows that the velocity increases with respect to Reynolds number and Casson parameter, while decreases when Hartmann number increases., Conclusions: Casson blood was treated as the non-Newtonian fluid. The MHD blood flow was accelerated by pressure gradient. These findings are beneficial for studying atherosclerosis therapy, the diagnosis and therapeutic treatment of some medical problems., Competing Interests: Declaration of Competing Interest There is not any conflict of interest for all authors of this manuscript., (Copyright © 2021. Published by Elsevier B.V.)

In this study, a magnetic/polyetherimide-acrylonitrile composite nanofiber membrane with effective adsorption of nickel ions in an aqueous solution was created using a simple electrospinning method. Iron oxide nanoparticles (NPs) were stirred and ultrasonically dispersed into a polyetherimide-acrylonitrile solution to create a homogenous NPs suspension, which was placed in an electrospinning machine to produce a uniform and smooth nanofiber composite membrane. Nanoparticle incorporation into this membrane was confirmed using scanning electron microscope, energy dispersive X-ray spectroscopy (EDX), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and NPs aqueous stability from a leaching test. The high adsorption capability of the membrane on nickel ions was attributed to the combination of magnetic NPs, polyetherimide-acrylonitrile matrix, and the nanostructure of the membrane. A membrane containing magnetic NPs demonstrated the maximum adsorption capabilities (102 mg/g) of nickel ions in an aqueous solution. Various kinetic and isotherm models were applied to understand the adsorption behavior, such as pseudo-second-order kinetic and Langmuir isotherm models. A polyetherimide-acrylonitrile composite nanofiber membrane containing magnetic NPs could be used as an environmentally friendly and nontoxic adsorbent for the removal of nickel ions in an aqueous medium due to its ease of preparation and use and stability in aqueous mediums.

In this study, N-doped and TiO 2 -decorated graphene oxides were developed as efficient nonprecious electrodes for capacitive deionization. The activity of this new material was evaluated in situ and in vivo. The performance of the synthesized material was measured in different saline solutions (0.1, 0.5 and 1.0 M NaCl) as an electrolyte. The results showed that the new material exhibits very good performance (157 F/g at 5 mV/s and 1.0 M NaCl compared to 19.5 F/g for pure graphene oxide). In the desalination test, which was performed in batch mode, the salt adsorption capacity and the efficiency of salt removal were 9.2 mg/g and 98%, respectively. To check the stability, the desalination test was repeated several times, and no change in the performance was observed. The results provide evidence that the newly synthesized material is a potential electrode material for CDI water desalination with satisfactory salt removal ability.

Poly(ethylene terephthalate)/graphite (PET/G) micro-composites were fabricated by the melt compounding method using a minilab extruder. The carbon fillers were found to act as nucleating agents for the PET matrix and hence accelerated crystallization and increased the degree of crystallinity. TGA showed that carbon fillers improved the resistance to thermal and thermo-oxidative degradation under both air and nitrogen atmospheres. However, a poor agreement was observed at higher loadings of the filler where the composites displayed reduced reinforcement efficiency. The results demonstrate that the addition of graphite at loading >14.5 wt.% made electrically conductive composites. It was calculated that the electric conductivities of PET/graphite micro-composites were enhanced, above the percolation threshold values by two orders of magnitudes compared to the PET matrix. The minimum value of conductivity required to avoid electrostatic charge application of an insulating polymer was achieved, just above the threshold values. The addition of graphite also improved thermal stability of PET, accelerated its crystallization process and increased the degree of crystallinity. Microscopic results exhibit no indication of aggregations at 2 wt.% graphite, whereas more agglomeration and rolling up could be seen as the graphite content was increased in the PET matrix (in particular, above the percolation threshold value). Furthermore, based on the mechanical experimental characterization of the PET/graphite micro-composites, a large deformation-based mathematical model is proposed for material behavior predictions. The model fits well the experimental data and predicts other mechanical data that are not included in the parameter identification.

The nanofibers membranes were fabricated by poly(vinyl alcohol)/chitosan (PVA/Chi) using an electro-spun technique for selective and high adsorption of lead (Pb(II)) and cadmium (Cd(II)) ions based on the solution acidity. The PVA/Chi NFs membranes were characterized systematically using several instrumentations. In addition, several experimental parameters such as initial metal ions concentration, interaction time, adsorbent dosage, solution pH and the effects of competing ions on Pb(II) and Cd(II) adsorption were evaluated. The adsorption data were also clarified that the PVA/Chi NFs membranes were exhibited high kinetic performances towards the both toxic ions at the optimum conditions. The adsorption data were manipulated using different kinetics models, and it was confirmed that only pseudo-second-order model obeyed the adsorption kinetics for Pb(II) and Cd(II) ions. Similarly, the equilibrium data were well fitted with the Langmuir adsorption isotherms model, and the maximum adsorption capacity was 266.12 and 148.79 mg/g for Pb(II) and Cd(II) ions, respectively. The Pb(II) and Cd(II) ions adsorptions were also measured to know the selectivity with simulated environmental solution, and the data were confirmed the high selectivity to Pb(II) and Cd(II) ions at the optimum condition and the nanofibers membrane shown the potentiality for possible use in efficient removal of the selected toxic ions from waste samples. Thus, the PVA/Chi NFs are considered to be effective and promising materials for Pb(II) and Cd(II) ions from wastewaters with high efficiency., (Copyright © 2018 Elsevier Inc. All rights reserved.)

Synthesis of NiSn alloy nanoparticle-incorporated carbon nanofibers was performed by calcining electrospun mats composed of nickel acetate, tin chloride and poly(vinyl alcohol) under vacuum. The electrochemical measurements indicated that utilization of tin as a co-catalyst could strongly enhance the electrocatalytic activity if its content and calcination temperature were optimized. Typically, the nanofibers prepared from calcination of an electrospun solution containing 15 wt% SnCl 2 at 700 °C have a current density almost 9-fold higher than that of pristine nickel-incorporated carbon nanofibers (77 and 9 mA/cm 2 , respectively) at 30 °C in a 1.0 M urea solution. Furthermore, the current density increases to 175 mA/cm 2 at 55 °C for the urea oxidation reaction. Interestingly, the nanofibers prepared from a solution with 10 wt% of co-catalyst precursor show an onset potential of 175 mV ( vs. Ag/AgCl) at 55 °C, making this proposed composite an adequate anode material for direct urea fuel cells. Optimization of the co-catalyst content to maximize the generated current density resulted in a Gaussian function peak at 15 wt%. However, studying the influence of the calcination temperature indicated that 850 °C was the optimum temperature because synthesizing the proposed nanofibers at 1000 °C led to a decrease in the graphite content, which dramatically decreased the catalyst activity. Overall, the study opens a new venue for the researchers to exploit tin as effective co-catalyst to enhance the electrocatalytic performance of the nickel-based nanostructures. Moreover, the proposed co-catalyst can be utilized with other functional electrocatalysts to improve their activity toward oxidation of different fuels.