Search Results (62)

In this study, a simple and efficient hydrothermal strategy was developed to modify reduced graphene oxide (rGO) with copper (II) oxide (CuO) nanoparticles by varying the weight ratio of rGO relative to CuO (rGO@CuO_1:1, rGO@CuO_1:2, and rGO@CuO_2:1). The obtained materials were further characterized using analytical tools. Photocatalytic performance was assessed using adsorption–photocatalysis experiments under a household LED light source (10 W, λ > 400 nm), and the degree of degradation of doxycycline (DOX) was evaluated using UV-Vis spectrophotometer. The highest efficiency of 100% was achieved with a DOX concentration of 70 ppm, rGO@CuO_1:1 dosage of 1 mg/mL, and pH 7 within 30 min of irradiation. The degradation kinetics followed the pseudo-first-order model (R² ~0.99) and the Langmuir adsorption isotherm, indicating that DOX on the surface is governed by a dynamic equilibrium between adsorption and degradation rates. Furthermore, efficacy was tested using real water samples, and the recyclability of the catalyst was evaluated in up to five cycles. Full article

Copper (II) oxide nanoparticles (CuO NPs) attract much attention as a promising antimicrobial agent. We studied the antibacterial properties of three types of CuO NPs against Escherichia coli bacteria: flake-shaped particles with a diameter of 50–200 nm and a thickness of 10–20 nm (CuO-CD synthesized by chemical deposition), spherical particles with a size of 20–90 nm (CuO-EE obtained by electrical explosion), and rod-shaped particles with a length of 100–200 nm and a diameter of 30 × 70 nm (CuO-CS commercial sample). We tested how the shape, size, and concentration of the NPs, and composition of the dispersion medium affected the properties of the CuO NPs. We prepared dispersions based on distilled water, a 0.9% NaCl solution, and the LB broth by Lennox and used Triton X-100 and sodium dodecyl sulfate (SDS) as stabilizers. The concentration of NPs was 1–100 mg L⁻¹. We showed that the dispersion medium composition and stabilizer type had the greatest influence on the antibacterial effects of CuO NPs. We observed the maximum antibacterial effect for all CuO NP types dispersed in water without a stabilizer, as well as in LB broth with the SDS stabilizer. The maximum inhibition of culture growth was observed under the influence of CuO-EE (by 30%) and in the LB broth with the SDS stabilizer (by 1.3–1.8 times depending on the type of particles). In the saline solution, the antibacterial effects were minimal; in some cases, the CuO NPs even promoted bacterial culture growth. SDS increased the antibacterial effects of NPs in broth and saline but decreased them in water. Finally, among the particle types, CuO-CS turned out to be the most bactericidal, which is probably due to their rod-shaped morphology and small diameter. At the same time, the concentration and aggregation effects of CuO NPs in the colloidal systems we studied did not have a linear action on their antibacterial properties. These results can be used in the development of antibacterial coatings and preparations based on CuO NPs to achieve their maximum efficiency, taking into account the expected conditions of their use. Full article

In this paper, we present a one-step low-temperature solution combustion synthesis (SCS) of CuS nanoparticulated functional films processed via a simple blade-coating technique. This SCS route uses thiourea as a fuel and sulfur source, combined with copper(II) nitrate as an oxidant and a cupric ion source in an aprotic solvent such as non-toxic DMSO. It is hereby shown that the proposed SCS process formed a stable and completely dissolved molecular ink of thiourea and copper ion complexes, crucial for obtaining the pure crystalline phase of CuS nanoparticles (NPs). The CuS was formed by calcination at a low temperature of 200 °C during a brief annealing time of 20 min, to promote the synthesis of ~10 nm CuS NPs. The obtained CuS NPs were thoroughly analyzed in terms of structure and optoelectronic properties using various analytic and spectroscopic techniques, including TGA, XRD, FE-SEM, EDS, AFM, and four-point probe electrical resistivity measurements. The functionality of the prepared CuS nanoparticulated interlayers was evaluated by incorporating them as a hole injection layer (HIL) in Super Yellow (SY) organic light-emitting diodes (OLEDs). Full article

Background/Objectives: Numerous diseases such as diabetes, Alzheimer’s disease, and cancer have spread in the whole world, especially in the Arab world. Also, various applications of Schiff-base functionalized nanoparticles and copper oxide nanoparticles (CuO-NPs) such as therapeutic applications have been discovered. Thus, the current research highlights (i) the synthesis of copper oxide nanoparticles (CuO-NPs) produced with a Schiff base (SB) serving as a capping agent during their synthesis and (ii) assessment of the in vitro biological activities of Schiff base-synthesized copper oxide nanoparticles (SB-CuO-NPs) and a Schiff base (SB). Methods: SB-CuO-NPs were characterized using ultraviolet-visible (UV-Vis) spectroscopy, zeta potential, DLS analysis, and transmission electron microscope (TEM). It also focuses on assessing the in vitro biological applications and activities, including antioxidant, scavenging, anti-diabetic, anti-Alzheimer, anti-arthritic, anti-inflammatory, cytotoxic activities, and enzymes inhibitory potential, of Schiff base-synthesized copper oxide nanoparticles (SB-CuO-NPs) and a Schiff base (SB) using methods described in the literature. Results: The results of the biological activities of the SB-CuO-NPs were compared with those of the SB. The SB-CuO-NPs demonstrated superior in vitro biological activities when compared to the SB from which they were produced. Conclusions: The results of this investigation concluded that the CuO-NPs, synthesized with the SB serving as an alternative capping agent, exhibited enhanced biological efficacy relative to the original SB. In the future, the biological efficiency of SB-CuO-NPs against diabetes, Alzheimer’s, and cancer diseases will be assessed in experimental animals (in vivo). Full article

Background/Objectives: With the increase of reactive oxygen species (ROS) production, cancer cells can avoid cell death and damage by up-regulating antioxidant programs. Therefore, it will be more effective to induce cell death by using targeted strategies to further improve ROS levels and drugs that inhibit antioxidant programs. Methods: Considering that dihydroartemisinin (DHA) can cause oxidative damage to protein, DNA, or lipids by producing excessive ROS, while, disulfiram (DSF) can inhibit glutathione (GSH) levels and achieve the therapeutic effect by inhibiting antioxidant system and amplifying oxidative stress, they were co-loaded onto the copper peroxide nanoparticles (CuO₂) coated with copper tannic acid (Cu-TA), to build a drug delivery system of CuO₂@Cu-TA@DSF/DHA nanoparticles (CCTDD NPs). In response to the tumor microenvironment, DHA interacts with copper ion (Cu²⁺) to produce ROS, and a double (diethylthiocarbamate)-copper (II) (CuET) is generated by the complexation of DSF and Cu²⁺, which consumes GSH and inhibits antioxidant system. Meanwhile, utilizing the Fenton-like effect induced by the multi-copper mode can achieve ROS storm, activate the MAPK pathway, and achieve chemotherapy (CT) and chemodynamic (CDT). Results: Taking pancreatic cancer cell lines PANC-1 and BxPC-3 as the research objects, cell line experiments in vitro proved that CCTDD NPs exhibit efficient cytotoxicity on cancer cells. Conclusions: The CCTDD NPs show great potential in resisting pancreatic cancer cells and provides a simple strategy for designing powerful metal matrix composites. Full article

This paper presents a comparative study on the temperature resistance of solid-contact ion-selective electrodes, depending on the type of solid-contact material. Five types of potassium electrodes, with a valinomycin-based model membrane, were developed using different types of mediation layers, namely a conductive polymer (poly(3-octylthiophene-2,5-diyl) and a perinone polymer), multi-walled carbon nanotubes, copper(II) oxide nanoparticles, and a nanocomposite consisting of multi-walled carbon nanotubes and copper(II) oxide. We examined how the measurement temperature (10 °C, 23 °C, and 36 °C) affects the sensitivity, measurement range, detection limit, selectivity, as well as the stability and reversibility of the electrode potential. Electrodes modified with a nanocomposite (GCE/NC/ISM) and a perinone polymer (GCE/PPer/ISM) showed the best resistance to temperature changes. An almost Nernst response and a stable measurement range and the lowest detection limit values for each temperature were obtained for them. The introduction of mediation layers significantly improved the stability and potential reversibility of all the modified electrodes relative to the unmodified electrode (GCE/ISM). Still, it was the GCE/PPer/ISM and GCE/NC/ISM that stood out from the others, with stability of 0.11 and 0.12 µV/s for 10 °C, 0.05 and 0.08 µV/s for 23 °C, and 0.06 and 0.09 µV/s for 36 °C, respectively. Full article

Four novel Pseudomonas strains with record resistance to copper (Cu²⁺) previously isolated from ecologically diverse samples (P. lactis UKR1, P. panacis UKR2, P. veronii UKR3, and P. veronii UKR4) were tested against sonochemically synthesised copper-oxide (I) (Cu₂O) and copper-oxide (II) (CuO) nanoparticles (NPs). Nanomaterials characterisation by X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), and High-Resolution Transmission Electron Microscopy (HRTEM) confirmed the synthesis of CuO and Cu₂O NPs. CuO NPs exhibited better performance in inhibiting bacterial growth due to their heightened capacity to induce oxidative stress. The greater stability and geometrical shape of CuO NPs were disclosed as important features associated with bacterial cell toxicity. SEM and TEM images confirmed that both NPs caused membrane disruption, altered cell morphology, and pronounced membrane vesiculation, a distinctive feature of bacteria dealing with stressor factors. Finally, Cu₂O and CuO NPs effectively decreased the biofilm-forming ability of the Cu²⁺-resistant UKR strains as well as degraded pre-established biofilm, matching NPs’ antimicrobial performance. Despite the similarities in the mechanisms of action revealed by both NPs, distinctive behaviours were also detected for the different species of wild-type Pseudomonas analysed. In summary, these findings underscore the efficacy of nanotechnology-driven strategies for combating metal tolerance in bacteria. Full article

Defining the copper-based catalysts that are responsible for the catalytic behaviour of oil-paper insulation systems and implementing effective regulation are of great significance. Accelerated ageing experiments were conducted to reveal variations in copper scales and deterioration in insulation properties. As ageing progressed, TEM images demonstrated that copper species were adsorbed and aggregated on the fibre surface in the form of nanoparticles (NPs). The scale of NPs exhibited a continuous increase, from 27.06 nm to 94.19 nm. Cu(I) and Cu(II) species were identified as the active sites for inducing intense free radical reactions, which significantly reduced the activation energy, making the insulating oil more susceptible to oxidation. The role of the antioxidant di-tert-butyl-p-cresol (DBPC) in extending the insulation life was regulated by determining the optimal addition time based on variations in the interfacial tension. After the second addition of DBPC, the ageing rates of the dissipation factor, acidity, micro-water and breakdown voltage in the Cu+DBPC group decreased by 28.8%, 43.2%, 52.9% and 46.7%, respectively, compared to the Cu group. This finding not only demonstrates the crucial role of DBPC in preventing the copper-based catalyst-induced oxidation of insulating oil, but also furnishes a vital foundation for enhancing the long-term stability of transformer insulation systems. Full article

In the present study, the feasibility to achieve localized induction heating and debonding of multi-material composite structures is assessed in testing coupons prepared by Automated Fiber Placement (AFP) and extrusion-based additive manufacturing (AM) technologies. Nano-compounds of Polyether-ketone-ketone (PEKK) with iron oxide nanoparticles acting as electromagnetic susceptors have been processed in a parallel co-rotating twin-screw extruder to produce filament feedstock for extrusion-based AM. The integration of nanocomposite interlayers as discrete debonding zones (DZ) by AFP-AM manufacturing has been investigated for two types of sandwich-structured laminate composites, i.e., laminate-DZ-laminate panels (Type I) and laminate-DZ-AM gyroid structures (Type II). Specimens were exposed to an alternating magnetic field generated by a radio frequency generator and a flat spiral copper induction coil, and induction heating parameters (frequency, power, heating time, sample standoff distance from coil) have been investigated in correlation with real-time thermal imaging to define the debonding process window without compromising laminate quality. For the optimized process parameters, i.e., 2–3 kW generator power and 20–25 mm standoff distance, corresponding to magnetic field intensities in the range of 3–5 kA m⁻¹, specimens were effectively heated above PEKK melting temperature, exhibiting high heating rates within the range of 5.3–9.4 °C/s (Type I) and 8.0–17.5 °C/s (Type II). The results demonstrated that localized induction heating successfully facilitated debonding, leading to full unzipping of the debonding zones in both laminate structures. Further insight on PEKK nanocomposites debonding performance was provided by thermal, morphological characterization and non-destructive inspection via X-ray micro-computed tomography at different processing stages. The developed framework aims to contribute to the development of rapid, on-demand joining, repair and disassembly technologies for thermoplastic composites, towards more efficient maintenance, repair and overhaul operations in the aviation sector and beyond. Full article

Much progress has been made in the determination of As (III), while numerous electrochemical sensors based on metal nanomaterials with significant sensitivity and precision have been developed. However, further research is still required to achieve rapid detection and avoid interference from other metal ions (especially copper ions). In this study, bimetallic AuPt nanoparticles are electrochemically modified with screen printing electrodes. What’s more, L-cysteine also self-assembles with AuNPs through Au-S bond to enhance the electrochemical performance. To overcome the interference of Cu (II) in the sensing process, the reduced iron powder was chosen to remove Cu (II) and other oxidizing organics in aqueous solutions. The lowest detectable amount is 0.139 ppb, a linear range of 1~50 ppb with superlative stability by differential pulse anodic stripping voltammetry. Fortunately, the reduced iron powder could eliminate the Cu (II) with no effect on the As (III) signal. Full article

The widespread application of nanoparticles (NPs) in agriculture has not only enhanced the efficiency of agrochemical use but also introduced environmental pollution, potentially impacting human health through absorption and accumulation in edible plants. The purpose of this study was to evaluate the toxic effects and ecological risks of Cu₂O nanoparticles (nCu₂O) in the life cycle of soybean, and to provide a theoretical basis for the safe application of NPs in agriculture. Soybeans were grown in natural soil modified with nCu₂O, bulk cuprous oxide (bCu₂O) and copper sulfate (CuSO₄) at concentrations of 0, 50, 200, and 800 mg/kg. Samples and grains from treated soybeans were collected at the flowering, podding, and seed-filling stages for analysis. The results indicated that treatments with nCu₂O, bCu₂O, and Cu²⁺ reduced the chlorophyll content in soybean leaves, thereby affecting photosynthesis. Significant reductions were observed in the net photosynthetic rate (Pn), the transpiration rate (Tr), stomatal conductance (Gs), the quantum yield of photosystem II (Y(II)), photochemical quenching (qP), and the electron transport rate (ETR) at high concentrations. However, the toxicity of nCu₂O to photosynthesis recovers as the plant grows. Almost all treatments increased the levels of antioxidant enzymes (SOD, POD, CAT) and reduced oxidative stress. In the nCu₂O and bCu₂O treatments, grain protein content was significantly reduced, while fat and water content increased. Phosphorus (P) content decreased, whereas sulfur (S), potassium (K), magnesium (Mg) and calcium (Ca) contents increased. The accumulation of copper in plants followed the order nCu₂O > bCu₂O > Cu²⁺, with the bCu₂O treatment being slightly more toxic than the nCu₂O treatment, and both being more toxic than the Cu²⁺ treatment. The above data indicated that nCu₂O had a dose-dependent effect, which significantly inhibited soybean growth and changed grain quality at high concentrations. Full article

In this study, we investigated the influence of pH on the hydrothermal synthesis of copper (II) oxide CuO nanostructures with the aim of tuning their morphology. By varying the pH of the reaction medium, we successfully produced CuO nanostructures with three distinct morphologies including nanoparticles, nanorods, and nanosheets according to the pH levels of 4, 7, and 12, respectively. The observed variations in surface morphology are attributed to fluctuations in growth rates across different crystal facets, which are influenced by the presence of intermediate species within the reaction. This report also compared the structural and optical properties of the synthesized CuO nanostructures and explored their potential for photoelectrochemical glucose sensing. Notably, CuO nanoparticles and nanorods displayed exceptional performance with calculated limits of detection of 0.69 nM and 0.61 nM, respectively. Both of these morphologies exhibited a linear response to glucose within their corresponding concentration ranges (3–20 nM and 20–150 nM). As a result, CuO nanorods appear to be a more favorable photoelectrochemical sensing method because of the large surface area as well as the lowest solution resistance in electroimpedance analysis compared to CuO nanoparticles and nanosheets forms. These findings strongly suggest the promising application of hydrothermal-synthesized CuO nanostructures for ultrasensitive photoelectrochemical glucose biosensors. Full article

The catalytic properties of three copper complexes, [Cu(en)₂](ClO₄)₂ (1), [Cu(amp)₂](ClO₄)₂, (2) and [Cu(bpy)₂](ClO₄)₂ (3) (where en = ethylenediamine, amp = 2-aminomethylpyridine and bpy = 2,2′-bipyridine), were explored upon the oxidation of benzyl alcohol (BnOH). Maximized conversions of the substrates to their respective products were obtained using a multivariate analysis approach, a powerful tool that allowed multiple variables to be optimized simultaneously, thus creating a more economical, fast and effective technique. Considering the studies in a fluid solution (homogeneous), all complexes strongly depended on the amount of the oxidizing agent (H₂O₂), followed by the catalyst load. In contrast, time seemed to be statistically less relevant for complexes 1 and 3 and not relevant for 2. All complexes showed high selectivity in their optimized conditions, and only benzaldehyde (BA) was obtained as a viable product. Quantitatively, the catalytic activity observed was 3 > 2 > 1, which is related to the π-acceptor character of the ligands employed in the study. Density functional theory (DFT) studies could corroborate this feature by correlating the geometric index for square pyramid Cu(II)-OOH species, which should be generated in the solution during the catalytic process. Complex 3 was successfully immobilized in silica-coated magnetic nanoparticles (Fe₃O₄@SiO₂), and its oxidative activity was evaluated through heterogenous catalysis assays. Substrate conversion promoted by 3-Fe₃O₄@SiO₂ generated only BA as a viable product, and the supported catalyst’s recyclability was proven. Reduced catalytic conversions in the presence of the radical scavenger (2,2,6,6-tetrametil-piperidi-1-nil)oxil (TEMPO) indicate that radical and non-radical mechanisms are involved. Full article

Graphene oxide and its magnetic nanoparticle-based composites are a well-known tool to remove heavy metals from wastewater. Unfortunately, one of the major issues in handling such small particles consists of their difficult removal from treated wastewater (even when their magnetic properties are exploited), due to their very small diameter. One possible way to overcome this problem is to embed them in a macroscopic biopolymer matrix, such as alginate or chitosan beads. In this way, the adsorbent becomes easier to handle and can be used to build, for example, a packed column, as in a traditional industrial adsorber. In this work, the removal performances of two different embedded magnetic nanocomposite adsorbents (MNAs) are discussed. The first type of MNA is based on ferrite magnetic nanoparticles (MNPs) generated by coprecipitation using iron(II/III) salts and ammonium hydroxide, while the second is based on a 2D material composed of MNP-decorated graphene oxide. Both MNAs were embedded in cross-linked alginate beads and used to treat artificial water contaminated with chromium(III), nickel(II), and copper(II) in different concentrations. The yield of removal and differences between MNAs and non-embedded magnetic nanomaterials are also discussed. From the results, it was found that the time to reach the adsorption equilibrium is higher when compared to that of the nanomaterials only, due to the lower surface/volume ratio of the beads, but the adsorption capacity is higher, due to the additional interaction with alginate. Full article

The biogenic synthesis of copper oxide nanoparticles was explored using the Myriophyllum spicatum plant through a process involving co-precipitation and was utilized as an effective photocatalyst for the reduction of Cr(VI) and Pb(II) ions in an aqueous solution. The plant-mediated CuO nanoparticles were characterized using microscopic techniques (TEM and SEM), FT-IR, and XRD analyses. The amount of the reduced metal ions was determined by UV–visible and Atomic Absorption (AA) spectrophotometers. The analyses of the functional group present in the leaf extract revealed the type of bioactive molecules that were involved in the formation of copper oxide nanoparticles. The nanoparticles were used in the photo-enhanced reduction of hexavalent Cr and divalent Pb ions, and the impact of solution pH, initial metal concentrations, and photocatalyst dosage was investigated to establish the optimal performance of the CuO nanoparticles. Results revealed a direct association between the reduction of metal ions and catalyst dosage in both cases. A maximum percentage reduction of 89.2% and 79.1% was achieved for Cr(VI) and Pb(II), respectively, using 3 g of the CuO nanoparticles. This confirms that the CuO nanoparticles exhibited higher efficiency for Cr(VI) reduction as compared to Pb(II) reduction and indicates that CuO nanoparticles are a promising photocatalyst that is capable of reducing these metal ions into less toxic products. Full article