Search Results (184)

This investigation has yielded a remarkably efficient metallic catalyst. Copper (Cu), cobalt (Co), and nickel (Ni) nanoparticles were concurrently deposited onto micron-sized aluminum (µAl) through a displacement reaction, resulting in the formation of [nCu+nCo+nNi]/µAl composites. The interfacial layer of the nanocomposite facilitates the creation of efficient oxygen transport pathways, significantly augmenting thermal release. In the context of the ADN/AP oxidizer, the [nCu+nCo+nNi]/µAl configuration demonstrates a substantial synergistic catalytic effect, reducing its thermal decomposition temperature by an impressive 104.1 °C. Combustion experiments have corroborated that this composite markedly enhances flame intensity, combustion temperature, and the burning rate of the ADN/AP system. The underlying thermal-oxidative mechanism was elucidated through comprehensive thermal analysis of the composite both prior to and following a heat treatment at 1100 °C. Moreover, through an integration of thermal analysis and combustion experiments, the catalytic mechanism of [nCu+nCo+nNi]/µAl on the thermolysis of ADN/AP was elucidated, and a plausible reaction pathway under thermal stimulation was proposed (e.g., ${\mathrm{NH}}_4{\mathrm{ClO}}_4+{{\mathrm{NH}}_4\mathrm{N}({\mathrm{NO}}_2)}_2\stackrel{\mathrm{Cu},\mathrm{Co},\mathrm{Ni}}{\to }{\mathrm{N}}_2+{\mathrm{H}}_2\mathrm{O}+\mathrm{HCl}+{\mathrm{O}}_2+\left[\mathrm{O}\right]$). The developed nanocomposite significantly enhances the performance of oxidizers, presenting considerable potential for a wide array of applications in solid propellants. Full article

The paper studied the effect of high-voltage short-pulse electrohydraulic discharge (HVSPED) on the processes of catalytic cracking of oil sludge in order to increase the yield of light hydrocarbon fractions. A set of laboratory experiments was carried out varying the key parameters of HVSPED—discharge voltage, capacitance of capacitor banks and processing time. As a catalyst, the developed nanocomposite catalyst bentonite was used, with nickel packed. The optimal electrophysical parameters of oil sludge treatment by HVSPED were determined, providing the maximum yield of gasoline and kerosene fractions. The effectiveness of HVSPED treatment of oil sludge in the presence of a catalyst was confirmed by DTA–thermogravimetric analysis and chromatographic-mass spectral analysis of the light and middle fractions of the hydrogenate. The proposed approach made it possible to enhance the resource and energy efficiency of oil sludge processing using HVSPED, demonstrating high potential for further industrial application Full article

Binary metallic nickel–copper nanocatalysts were anchored onto a polyvinylidene fluoride-co-hexafluoropropylene membrane [NiCu/PVdF–HFP] using the electrospinning technique, followed by the chemical reduction of the relevant precursor salts by introducing sodium borohydride to the synthesis mixture. A series of varied Ni:Cu weight % proportions was developed in order to optimize the electroactivity of this binary nanocomposite towards the investigated oxidation process. A number of physicochemical tools were used to ascertain the morphology and chemical structure of the formed metallic species on polymeric films. Cyclic voltammetric studies revealed a satisfactory performance of altered NiCu/PVdF–HFP membranes in alkaline solution. Ethylene glycol molecules were successfully electro-oxidized at their surfaces, showing the highest current intensity [564.88 μA cm⁻²] at the one with Ni:Cu weight ratios of 5:5. The dependence of these metallic membranes’ behavior on the added alcohol concentration to the reaction electrolyte and the adjusted scan rate during the electrochemical measurement was carefully investigated. One hundred repeated scans did not significantly deteriorate the NiCu/PVdF–HFP nanostructures’ durability. Decay percentages of 76.90–87.95% were monitored at their surfaces, supporting the stabilized performance for prolonged periods. A much-decreased R_ct value was estimated at Ni₅Cu₅/PVdF–HFP [392.6 Ohm cm²] as a consequence of the feasibility of the electron transfer step for the electro-catalyzing oxidation process of alcohol molecules. These enhanced study results will hopefully motivate the interested workers to explore the behavior of many binary and ternary combinations of metallic nanomaterials after their deposition onto convenient polymeric films for vital electrochemical reactions. Full article

The removal of nickel from industrial wastewater necessitates efficient sorbent materials. This study investigates nanostructured potassium- and sodium-substituted aluminosilicate-based nanocomposites for this application. Materials were synthesized and characterized using SEM-EDS, XPS, XRD, FTIR, low temperature N₂ adsorption–desorption and Ni²⁺ adsorption experiments. SEM and XRD confirmed an X-ray amorphous structure attributable to fine crystallite size. The sodium-substituted material Na₂Al₂Si₂O₈ exhibited the lowest specific surface area (48.3 m²/g) among the tested composites. However, it demonstrated the highest Ni(II) sorption capacity (64.6 mg/g, 1.1 mmol/g) and the most favorable sorption kinetics, as indicated by a Morris-Weber coefficient of 0.067 ± 0.008 mmol/(g·min¹/²). Potassium-substituted analogs with higher Si/Al ratios showed increased surface area but reduced capacity. Analysis by XPS and SEM-EDS established that Ni(II) uptake occurs through a complex mechanism, involving ion exchange, surface complexation, and chemisorption resulting in the formation of new nickel-containing composite surface phases. The results indicate that optimal sorption performance for Ni(II) is achieved with sodium-based aluminosilicates at a low Si/Al ratio (Si/Al = 1). The functional characteristics of Na₂Al₂Si₂O₈ compare favorably with other silicate-based sorbents, suggesting its potential utility for wastewater treatment. Further investigation is needed to elucidate the precise local coordination environment of the adsorbed nickel. Full article

In this work, nickel ferrite/carbon nanotubes–polyaniline (NiFe₂O₄@CNTs-PANI) nanocomposites with positive magnetoresistance (MR) phenomenon was obtained by the hydrothermal method combined with the surface-initiated polymerization (SIP) method. The NiFe₂O₄@CNTs-PANI nanocomposites’ resistivity decreased as the temperature increased, exhibiting typical semiconductor behavior. This temperature-dependent resistivity revealed a quasi-three-dimensional (3D) variable range hopping (VRH) charge carrier transport mechanism. Based on the wave function shrinkage model, its positive MR was studied. It was found that the localization length (a₀) and average hopping distance (R_hop) were decreased with increasing magnetic field strength, indicating the reduction in the hopping probability of the charge carrier, which was beneficial for the positive MR. Meanwhile, the values of a₀ and R_hop were decreased with increasing NiFe₂O₄@CNTs loading, expressing a nanofiller loading-dependent behavior. Full article

Esophageal squamous cell carcinoma (ESCC) accounts for the majority of esophageal cancers worldwide, with a poor prognosis and increasing resistance to conventional treatments. Faced with these limitations, nanoparticles (NPs) are attracting growing interest as innovative therapeutic agents capable of improving specificity and efficacy and reducing systemic toxicity. This study critically examines the pharmacological effects, mechanisms of action, and toxicity profiles of different metallic or organic nanoparticles tested on ESCC cell lines. Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) 2020 guidelines were followed by a meticulous literature search of Google Scholar, Web of Science, PubMed/Medline, and Scopus databases to achieve this goal. The results show that the anti-tumor properties vary according to the type of nanoparticle (copper(II) oxide (CuO), silver (Ag), gold (Au), nickel(II) oxide (NiO), nano-curcumin, etc.), the synthesis method (chemical vs. green), and the biological activity assessment method (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), Bromodeoxyuridine (BrdU), Cell Counting Kit-8 (CCK8) assays, etc.). NPs derived from green synthesis, such as those based on Moringa oleifera, Photinia glabra, or pomegranate bark, exhibit moderate cytotoxic activity (50% inhibitory concentration (IC₅₀) between 92 and 500 µg/mL) but show good tolerance on normal cells. In contrast, chemically synthesized NPs, such as Cu(II) complexes with 1,3,5-benzenetricarboxylic acid (H₃btc) or 1,2,4-triazole (Htrz), show lower IC₅₀ (34–86 µM), indicating more marked cytotoxicity towards cancer cells, although data on their toxicity are sometimes lacking. In addition, multifunctional nanoparticles, such as gold-based nano-conjugates targeting Cluster of Differentiation 271 (CD271) or systems combined with doxorubicin, show remarkable activity with IC₅₀ below 3 µM and enhanced tumor selectivity, positioning them among the most promising candidates for future clinical application against ESCC. The most frequently observed mechanisms of action include induction of apoptosis (↑caspases, ↑p53, ↓Bcl-2), oxidative stress, and inhibition of proliferation. In conclusion, this work identifies several promising nanoparticles (silver nanoparticles derived from Photinia glabra (PG), gold-based nano-immunoconjugates targeting CD271, and silver–doxorubicin complexes) for future pharmaceutical exploitation against ESCC. However, major limitations remain, such as the lack of methodological standardization, insufficient in vivo and clinical studies, and poor industrial transposability. Future prospects include the development of multifunctional nanocomposites, the integration of biomarkers for personalized targeting, and long-term toxicological assessment. Full article

The aim of the present study is to investigate the influence of Nickel–Hexagonal Boron Nitride (Ni-hBN) nanocomposite coatings, deposited using the pulse reverse current electrodeposition technique. This experimental study focuses on assessing the tribological and corrosion properties of the produced coatings on the SS304 substrate. The microhardness of the as-deposited (AD) sample and heat-treated (HT) sample were 49% and 83.8% higher compared to the control sample. The HT sample exhibited a grain size which was approximately 9.7% larger than the AD sample owing to the expansion–contraction mechanism of grains during heat treatment and sudden quenching. Surface roughness reduced after coating, where the Ni-hBN-coated sample measured a roughness of 0.43 µm compared to 0.48 µm for the bare surface. The average coefficient of friction for the AD sample was 42.4% lower than the bare surface owing to the self-lubricating properties of nano hBN. In particular, the corrosion rate of the AD sample was found to be 0.062 mm/year, which was lower than values reported in other studies. As such, findings from the present study can be particularly beneficial for applications in the automotive and aerospace industries, where enhanced wear resistance, reduced friction, and superior corrosion protection are critical for components such as engine parts, gears, bearings and shafts. Full article

The rapid growth in population and industrialization have significantly increased global energy demand, placing immense pressure on finite and environmentally harmful conventional fossil fuel-based energy sources. In this context, the development of hybrid electrocatalysts presents a crucial solution for energy conversion and storage, addressing environmental challenges while meeting rising energy needs. In this study, the fabrication of a novel bifunctional catalyst, copper nickel aluminum spinel (Cu_0.5Ni_0.5Al₂O₄) supported on graphitic carbon nitride (GCN), using a solid-state synthesis process is reported. Because of its effective interface design and spinel cubic structure, the Cu_0.5Ni_0.5Al₂O₄/GCN nanocomposite, as synthesized, performs exceptionally well in electrochemical energy conversion, such as the oxygen evolution reaction (OER), the hydrogen evolution reaction (HER), and energy storage. In particular, compared to noble metals, Pt/C- and IrO₂-based water-splitting cells require higher voltages (1.70 V), while for the Cu_0.5Ni_0.5Al₂O₄/GCN nanocomposite, a voltage of 1.49 V is sufficient to generate a current density of 10 mA cm⁻² in an alkaline solution. When used as supercapacitor electrode materials, Cu_0.5Ni_0.5Al₂O₄/GCN nanocomposites show a specific capacitance of 1290 F g⁻¹ at a current density of 1 A g⁻¹ and maintain a specific capacitance of 609 F g⁻¹ even at a higher current density of 5 A g⁻¹, suggesting exceptional rate performance and charge storage capacity. The electrode’s exceptional capacitive properties were further confirmed through the determination of the roughness factor (Rf), which represents surface heterogeneity and active area enhancement, with a value of 345.5. These distinctive characteristics render the Cu_0.5Ni_0.5Al₂O₄/GCN composite a compelling alternative to fossil fuels in the ongoing quest for a viable replacement. Undoubtedly, the creation of the Cu_0.5Ni_0.5Al₂O₄/GCN composite represents a significant breakthrough in addressing the energy crisis and environmental concerns. Owing to its unique composition and electrocatalytic characteristics, it is considered a feasible choice in the pursuit of ecologically sustainable alternatives to fossil fuels. Full article

In the last decade, magnetic nanoparticles (MNPs) have attracted much attention for the implementation of non-invasive approaches suitable for the diagnosis and treatment of vascular diseases. In this work, the optimization of novel vascular grafts loaded with Nickel-based nanoparticles via electrospinning is proposed. Two different polycarbonate urethanes—i.e., Corethane A80 (COT) and Chronoflex AL80 (CHF)—were used to fabricate 3D electrospun nanocomposite grafts. SEM analysis showed a homogeneous distribution of fibers, with slight differences in terms of average diameters as a function of the polymer used—(1.14 ± 0.18) µm for COT, and (1.33 ± 0.23) µm for CHF—that tend to disappear in the presence of MNPs—(1.26 ± 0.19) µm and (1.26 ± 0.213) µm for COT/NPs and CHF/NPs, respectively. TGA analyses confirmed the higher ability of CHF to entrap MNPs in the fibers—18.25% with respect to 14.63% for COT—while DSC analyses suggested an effect of MNPs on short-range rearrangements of hard/soft micro-domains of CHF. Accordingly, mechanical tests confirmed a decay of mechanical strength in the presence of MNPs with some differences depending on the matrix—from (6.16 ± 0.33) MPa to (4.55 ± 0.2) MPa (COT), and from (3.67 ± 0.18) MPa to (2.97 ± 0.22) MPa (CNF). The in vitro response revealed that the presence of MNPs did not negatively affect cell viability after 7 days in in vitro culture, suggesting a promising use of these materials as smart vascular grafts able to support the actuation function of vessel wall muscles. Full article

In Gen-IV nuclear reactors, structural materials must endure unprecedented levels of neutron irradiation and hydrogen exposure, posing significant challenges for traditional Ni-based alloys. This study evaluates Ni–graphene nanocomposites (NGNCs) as a promising solution, leveraging their inherent radiation tolerance and hydrogen diffusion suppression. Using molecular dynamics simulations, we investigate how Ni/graphene interfaces influence mechanical properties under combined hydrogen permeation and displacement damage. Key parameters, such as hydrogen concentration, displacement damage level, strain rate, and temperature, are systematically varied to assess their impact on stress–strain behavior (including Young’s modulus and tensile strength), with comparisons to single-crystal nickel. Our findings reveal that NGNCs exhibit distinct mechanical responses characterized by serrated stress–strain curves due to interfacial slip. Hydrogen and irradiation effects are complex: low hydrogen levels can increase Young’s modulus, while higher concentrations and irradiation generally degrade strength, with NGNCs being more affected than single-crystal nickel. Additionally, NGNCs show enhanced thermal stability but increased strain rate sensitivity. These results provide critical insights for designing materials that balance reinforcement with environmental resilience in nuclear applications. Full article

In this study, borophene and nickel phthalocyanine (NiPc): borophene nanocomposites were prepared using the sonication method. The NiPc: borophene nanocomposite was uniformly obtained as a 10–80 nm-sized spherically shaped particle. Electrical conductivities (s) were measured as 3 × 10⁻¹³ Scm⁻¹ and 9.5 × 10⁻⁹ Scm⁻¹ for NiPc and the NiPc: borophene nanocomposite, respectively. The SEM image showed that borophene was homogeneously distributed in the NiPc matrix and increased the charge transport pathways. This is the main reason for a 10⁶-fold increase in electrical conductivity. An indium tin oxide (ITO)/NiPc: borophene nanocomposite-based thermoelectric generator (TEG) was prepared and characterized. The Seebeck coefficients (S) were calculated to be 5 μVK⁻¹ and 30 μVK⁻¹ for NiPc and the NiPc: borophene nanocomposite, respectively. A positive Seebeck coefficient value for the NiPc: borophene showed the p-type nature of the nanocomposite. The power factors (PF = sS2) were calculated as 7.5 × 10⁻¹⁶ μW m⁻¹ K⁻² and 8.6 × 10⁻¹⁰ μW m⁻¹ K⁻² for NiPc and the NiPc: borophene nanocomposite, respectively. Compositing NiPc with borophene increased the power factor by ~10⁶-fold. It has been concluded that the electrical conductivity and Seebeck coefficient of the NiPc: borophene material increases due to energy band convergence because of combining p-type NiPc with p-type borophene. Therefore, the NiPc: borophene nanocomposite is a promising material for TEG. Full article

Composites of ferromagnetic and ferroelectric phases are of interest for studies on mechanical strain-mediated coupling between the two phases and for a variety of applications in sensors, energy harvesting, and high-frequency devices. Nanocomposites are of particular importance since their surface area-to-volume ratio, a key factor that determines the strength of magneto-electric (ME) coupling, is much higher than for bulk or thin-film composites. Core–shell nano- and microcomposites of the ferroic phases are the preferred structures, since they are free of any clamping due to substrates that are present in nanobilayers or nanopillars on a substrate. This review concerns recent efforts on ME coupling in coaxial fibers of spinel or hexagonal ferrites for the magnetic phase and PZT or barium titanate for the ferroelectric phase. Several recent studies on the synthesis and ME measurements of fibers with nickel ferrite, nickel zinc ferrite, or cobalt ferrite for the spinel ferrite and M-, Y-, and W-types for the hexagonal ferrites were considered. Fibers synthesized by electrospinning were found to be free of impurity phases and had uniform core and shell structures. Piezo force microscopy (PFM) and scanning microwave microscopy (SMM) measurements of strengths of direct and converse ME effects on individual fibers showed evidence for strong coupling. Results of low-frequency ME voltage coefficient and magneto-dielectric effects on 2D and 3D films of the fibers assembled in a magnetic field, however, were indicative of ME couplings that were weaker than in bulk or thick-film composites. A strong ME interaction was only evident from data on magnetic field-induced variations in the remnant ferroelectric polarization in the discs of the fibers. Follow-up efforts aimed at further enhancement in the strengths of ME coupling in core–shell composites are also discussed in this review. Full article

Nanocomposite laminates containing carbon fibers, epoxy, and multiwalled carbon nanotubes were fabricated using a vacuum bag process. Ecofriendly ionic liquid (5 wt%)-treated multiwalled carbon nanotubes (pristine and nickel-coated) were added to the epoxy independently, in amounts ranging from 1 wt% to 3 wt%, in order to tailor the mechanical, electrical, and thermal performance of manufactured carbon fiber epoxy composite laminates. These nanocomposite laminates were later characterized through flexural testing, dynamic mechanical analysis, impedance spectroscopy, thermal conductivity tests, and FTIR spectroscopy to evaluate their suitability for battery pack applications. The findings showed that both types of multiwalled carbon nanotubes exhibited multifaceted effects on the properties of bulk hybrid carbon fiber epoxy nanocomposite laminates. For instance, the flexural strength of the composites containing 3.0 wt% of ionic liquid-treated pristine multiwalled carbon nanotubes reached 802.8 MPa, the flexural modulus was 88.21 GPa, and the storage modulus was 18.2 GPa, while the loss modulus peaked at 1.76 GPa. The thermal conductivity of the composites ranged from 0.38869 W/(m · K) to 0.69772 W/(m · K), and the electrical resistance decreased significantly with the addition of MWCNTs, reaching a minimum of 29.89 Ω for CFRPIP-1.5 wt%. The structural performance of hybrid nanocomposites containing ionic liquid-treated pristine multiwalled carbon nanotubes was higher than that of the hybrid nanocomposite of ionic liquid-treated Ni-coated multiwalled carbon nanotubes, although the latter was found to possess better functional performance. Full article

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

A highly redox-active ternary nickel sulfide and cobalt-anchored carbon nanocomposite (NiS-Co@C) electrochemical electrode is synthesized by a two-step pyrolysis-hydrothermal method using biomass-derived carbon. The high-crystalline hierarchical porous nanostructure provides abundant voids and cavities, along with a large specific surface area, to improve the interfacial properties. The as-synthesized electrode achieved a specific capacity of 640 C g⁻¹ at 1 A g⁻¹, with a capacity retention of 93% over 5000 cycles, revealing outstanding electrochemical properties. Nickel sulfide nanoparticles embedded in the cobalt-anchored carbon framework improved redox activity, ion transport, and conductivity, resulting in a dominant diffusion-controlled battery-type behavior. Moreover, a hybrid supercapattery, based on battery-type NiS-Co@C as the positrode and capacitive-type activated carbon as the negatrode, achieved a maximum specific energy/power of 33 Wh kg⁻¹/7.1 kW kg⁻¹ with a 91% capacity retention after 5000 cycles. The synergistic effect of the combinatorial battery–capacitor behavior of the hybrid supercapattery has improved the specific energy–power considerably, leading the development of next-generation energy storage technologies. Full article