Search Results (3,528)

The development of biodegradable, biocompatible materials with inherent antibacterial properties, suitable for 3D printing, is a key challenge in modern materials science. Composites based on PLA and copper nanoparticles (NPs) are promising candidates for such a material. A protocol of the low-temperature incorporation of 0.1% Cu NPs or 0.1% CuO NPs into a PLA was developed. The dependence of the materials’ physicochemical properties on nanoparticle composition was evaluated. Cu and CuO NPs were synthesized via liquid-phase laser ablation and had sizes of 25 and 80 nm, with modal zeta potential values of +31 and +42 mV, respectively. The incorporation of Cu NPs enhances the tensile strength and Young’s modulus of PLA, and improves antibacterial properties. The PLA + 0.1% CuO or PLA + 0.1% Cu nanoparticles inhibited the growth of E. coli by ~60% and >80%, respectively. PLA + 0.1% Cu NPs destructed of bacterial cell walls. The antibacterial action mechanisms are an 8-oxoguanine and LRPS generations. The obtained materials did not exhibit cytotoxic effects against normal human fibroblasts, did not alter the pH or redox potential of water, and did not release of Cu²⁺ in concentrations toxic to humans. The material PLA + 0.1% Cu NPs is the most optimal. This material may find applications in food production and biomedical applications. Full article

Silver-coated copper (Cu@Ag) core–shell nanoparticles are promising interconnect materials for electronic packaging due to their high conductivity, oxidation resistance, and reduced use of precious metals. However, the key factors governing their sintering behavior and mechanical performance are not fully understood. In this study, molecular dynamics simulations were performed to examine the effects of sintering pressure (300–700 MPa), temperature (500–700 K), particle size, and silver shell thickness on atomic diffusion, microstructural evolution, and mechanical properties. Results show that higher pressure improves particle contact, accelerates densification, and strengthens interfacial bonding, with optimal performance achieved at 600–700 MPa. Elevated temperatures enhance atomic mobility, promoting neck growth and pore elimination, with the most active diffusion observed between 650 K and 700 K. Particle size and shell thickness also affect sintering: the Ag6Cu3 configuration exhibits the highest atomic mobility and a balanced combination of strength and ductility. Moderately thick silver shells facilitate surface diffusion and interfacial interdiffusion, while mechanisms such as the Kirkendall effect and local plastic relaxation reduce defect density, yielding stable sintered structures. These findings provide atomic-scale insights into the sintering mechanisms of Cu@Ag nanoparticle solder pastes and offer guidance for optimizing processing parameters in high-performance electronic packaging applications. Full article

In the present study, room temperature (RTR) and cryogenic (CR) rolling of electrolytic tough pitch copper (ETP-Cu) was performed to elucidate how deformation temperature and reduction ratio (40% and 80% thickness reductions) control dislocation storage, local stored energy (SE), and self-annealing. Correlated SEM/EDS and EBSD analyses were used to (i) locate Cu₂O particles, (ii) quantify local misorientation, and (iii) map the SE for self-annealing. Point EDS confirms that the intermetallic particles are copper oxides (Cu₂O), with apparent O content varying with particle size and EDS interaction volume. RTR80 (80% rolled) exhibits systematically higher KAM values and a larger area fraction of high SE than RTR40 (40% rolled), explaining the greater frequency and spatial density of self-annealed grains at higher reduction. Cryogenic rolling produces more severe fragmentation and a higher fraction of subgrains than RTR at equivalent reductions. CR80 shows the high KAM structures and locally highest SE regions among all conditions, and a higher fraction of self-annealed grains. Nevertheless, the mapped average SE for CR80 (2.93 × 10⁶ J/m³) was lower than for RTR80 (3.34 × 10⁶ J/m³) due to rapid post-deformation dislocation annihilation/self-annealing upon warming at RT. In all conditions, Cu₂O particles and bulged/irregular grain boundaries concentrate dislocations and SE and act as dominant particle-stimulated nucleation (PSN) sites and RT recrystallization, respectively. These results demonstrate that deformation temperature and reduction jointly determine the spatial distribution of SE and hence the propensity for self-annealing in ETP Cu. Full article

The study of wide-bandgap nanomaterials has gained considerable attention in recent years, especially in the case of semiconductor oxides that exhibit full or partial optical transparency in fundamental research and technological applications. These include optoelectronic devices, gas sensors and photovoltaic cells, among others. The activation or adjustment of optical and structural properties, especially the bandgap and the parameters of unit cell lattice, can be achieved by varying the dopant concentration during the synthesis of semiconductor thin films in these applications. In this context, copper oxide has emerged as a valuable material, owing to its thoroughly analyzed structural behavior and its broad potential across multiple technological fields. The present work focuses on the synthesis of zinc-doped copper oxide (Zn_xCu_1−xO) thin films on silicon and quartz substrates through ultrasonic spray pyrolysis. The effects of varying the zinc doping concentration (0.0, 5.0, 10.0 and 20.0 at. %) on the morphological, structural, and optical characteristics of the Zn_xCu_1−xO films were analyzed. Scanning electron microscopy (SEM) analysis indicated a gradual increase in nanoparticle size, rising from 221 nm for CuO to approximately 322 nm for the Zn_0.2Cu_0.8O samples as the zinc content increased. Structural characterization via X-ray diffraction (XRD) confirmed a monoclinic crystal arrangement belonging to the $C_{2h}^6$ (c2/c) space group. As the percentage of zinc increased, the XRD peaks shifted to lower angles, consequently increasing the volume and crystal lattice parameters of the Zn_xCu_1−xO structure; this finding was additionally supported by a redshift observed in the Raman analysis. The transmittance spectra of the films showed low transmittance between 40 and 44%. The optical bandgap of the Zn_xCu_1−xO thin films was estimated from the transmittance data by applying the Tauc plot method. A decrease in the band gap was observed at higher doping concentrations. It can be confirmed that no secondary phases are observed at a doping level of 20.0 at. % of zinc, indicating good solubility of zinc in CuO. The analysis and discussion of these findings are included throughout this work to elucidate the controversies noted in the literature. Full article

This study utilized polysiloxane as the raw material to successfully prepare black spherical silica fillers with varying internal carbon content. Through different thermal treatment processes, a dense silica layer was formed on the particle surface, while the internal hydrocarbon groups were thermally decomposed into carbon. Four types of spherical silica with different carbon contents were systematically characterized in terms of particle size distribution (D50 ≈ 2.0 μm, D100 < 5 μm), scanning electron microscopy morphology, moisture content (<0.1%), specific surface area (~1.0–1.1 m²/g), true density (~1.90–1.97 g/cm³), carbon content, blackness (L* values), and volume resistivity. The results indicate that the prepared black spherical silica exhibits a narrow particle size distribution, low moisture content, and high electrical insulation properties. Furthermore, the prepared black spherical silica was used as a filler in a polyphenylene oxide-based binder system to fabricate copper-clad laminates (CCLs), and their dielectric properties were systematically investigated. The study found that at electric field frequencies of 1 GHz and 10 GHz, the dielectric constant (D_k) and dielectric loss (D_f) of CCLs prepared with fillers containing less than 5% carbon remained largely consistent with those of carbon-free control samples. However, the D_f of CCLs prepared with fillers containing 9.00% carbon increased nearly tenfold, indicating that when the internal carbon content of the filler exceeds a certain threshold, it adversely affects the high-frequency dielectric properties of the copper-clad laminate. Full article

Surface modification can regulate surface properties through the design of surface structures and chemical compositions. Heparin has good anticoagulant properties and is widely used in the surface modification of blood-contact materials. However, the molecular structure of heparin has often been overlooked in terms of its application and further utilization in the design process. In this study, heparin was grafted onto substrate materials through polydopamine/polyethyleneimine co-deposition coating and connected with cysteine to obtain PP-Hep-Cys. The sulfhydryl content of PP-Hep-Cys reached about 2.06 nmol/cm², and the NO generation was about 0.2415 nmol/cm². In the absence of NO donors, the introduction of heparin contributed to the inhibition of platelets, but when NO donors were added, the inhibition of platelets was caused by the synergistic effect of heparinization and NO generation. In addition, the clotting time of PP-Hep-Cys was significantly prolonged compared with PP, and the hemolysis rate declined to 0.33 ± 0.01%. Regarding the adsorption performance of Cu²⁺, the adsorption capacity of PP-Hep-Cys was higher than that of PP-Hep and PP-Cys, and monolayer adsorption was dominant. Overall, these results indicated that heparin, as a spacer, and cysteine, as a ligand, exerted a synergistic effect on blood compatibility and adsorption. Full article

This study presents a combined process of sulfide precipitation followed by hydrogen peroxide leaching for rhenium recovery from copper smelting waste acid under ambient temperature and pressure. The process first removed copper through selective sulfide precipitation, then achieved co-precipitation of rhenium and arsenic to obtain a rhenium-rich precipitate. Subsequently, exploration of rhenium-containing precipitate leaching using H₂O₂ solution was conducted under isothermal conditions at 20 °C. The effects of H₂O₂ concentration, liquid-to-solid ratio, acidity, and leaching time rhenium extraction efficiency were examined systematically. The optimal leaching conditions were determined as: H₂O₂ concentration of 150 g/L, liquid-to-solid ratio of 5:1 mL/g, stirring speed of 350 r/min, and leaching time of 30 min. Under these conditions, the leaching conversions of rhenium and arsenic reached 96.0% and 93.8%, respectively. Through characterization of precipitate and leaching residue using ICP, SEM-EDS, XRD, and XPS analyses, the process and related reactions were elucidated. Results demonstrated that low-valence rhenium oxides and sulfides serve as the main reactive species during H₂O₂ leaching, whereas organic sulfur, high-valence oxides, and copper sulfide remained stable and resistant to leaching. Selective precipitation of copper effectively eliminated insoluble metal sulfides from rhenium-containing precipitates, thereby enabling efficient separation of rhenium under mild conditions. Full article

The enzymatic saccharification of cellulose remains a key step in biomass conversion processes, often influenced by enzyme stability, distribution, and accessibility at solid–liquid interfaces. Immobilization of cellulolytic enzymes on nanostructured supports has been proposed as a strategy to modulate catalytic behavior; however, the relationship between enzyme loading and catalytic response remains insufficiently understood. In this study, CuO-based nanobiocatalysts were prepared through controlled cellulase immobilization and systematically evaluated under defined experimental conditions. Structural and physicochemical characterization was performed using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and integrated thermal analysis (TGA–DTG–DSC), enabling a comparative assessment of the analyzed systems. SEM analysis showed that the average particle diameter increased from 39.5 ± 14.8 nm (CuO nanoparticles) to 95.6 ± 21.8 nm (NPI10), 106.6 ± 27.7 nm (NPI15), and 113.5 ± 23.1 nm (NPI20), indicating progressive variations in particle organization with increasing enzyme loading. Catalytic performance was evaluated through enzymatic hydrolysis of cellulose filter paper as a model substrate, with products quantified by HPLC at a representative reaction time. The system prepared at lower enzyme loading (NPI10) exhibited product formation comparable to that of the free enzyme, with apparent average glucose formation values of 1.054 and 1.047 mg·mL⁻¹·h⁻¹, respectively. In contrast, higher immobilization levels were associated with reduced catalytic output. Across all systems, glucose was the predominant product, with negligible accumulation of intermediate oligomers under the evaluated conditions. These results indicate that increasing enzyme loading does not correspond to proportional increases in product formation and highlight the influence of enzyme distribution and accessibility within the system. The combined structural and catalytic observations provide a controlled framework for evaluating how immobilization conditions influence system behavior in nanobiocatalytic systems. Full article

Continental remobilization is a crucial driver of metallogenesis and the formation of ore deposits. Some of the world’s largest mineral deposits of the economically valuable elements tin (Sn), tungsten (W), gold (Au), copper (Cu), lead (Pb), and zinc (Zn) formed during the Mesozoic Era. Additionally, the chemistry and distribution of the elements Sn and W have been investigated in previous studies to understand planetary formation and differentiation processes. These two elements are largely co-located during certain South China Mesozoic metallogenic events but are not co-located during other time periods in the same regions. Here, we investigated the mineral chemistry network similarities and dissimilarities of Sn and W to understand their mineral formation and distribution during the Mesozoic Era and throughout Earth history. Mineral chemistry network community detection analysis and electronegativity associations among mineral constituent elements of Sn minerals and W minerals indicate that the elements have similar chemistry among their oxide minerals. However, Sn forms a much wider range of minerals that also contain S compared to W, which occurs in a limited number of S-containing minerals. The divergent constituent element interactions among S-containing Sn minerals and W minerals reflect the redox sensitivity and importance of oxygen (O) fugacity in Sn mineral formation. Conversely, extensive W mineral deposits are known to form at both high and low O fugacities. The similarities and differences between the mineral chemistry networks of Sn and W reflect the mineral distribution of the two elements in the Sn-W mineralization event from 160 to 139 Ma vs. the Sn–uranium (U) mineralization event from 125 to 98 million years ago (Ma). The mineral chemistry and distribution of Mesozoic Sn and W deposits illustrate the contrasting importance of redox and O fugacity on the mineral formation of different elements, and the dynamic crustal evolution that took place during this period of Earth history. Full article

9-Mesitylacridinium salts are widely recognized as efficient organic photoredox catalysts owing to their strong excited-state oxidizing power and stability under visible-light irradiation. In this study, a new mesityl acridinium derivative bearing a di-tert-butylphenyl substituent on the nitrogen atom was synthesized. The introduction of tert-butyl groups on the N-aryl moiety was primarily aimed at improving solubility and chemical stability of the acridinium salt. Starting from a 9(10H)-acridinone precursor, the target compound was obtained in high overall yield through a concise synthetic sequence. The synthesis consists of a copper-catalyzed C–N coupling reaction to install the aryl substituent on the nitrogen atom, followed by a Grignard reaction and subsequent acid treatment to afford the corresponding acridinium salt. All transformations proceeded smoothly, providing efficient access to the desired novel acridinium derivative. This work presents a practical example of the structural modification of mesitylacridinium derivatives directed toward enhanced solubility and stability, and provides a useful synthetic platform for the preparation of structurally diverse acridinium salts. Full article

The current work aims to enhance the structural, optical, photocatalytic, and cytotoxic properties of CuO NPs at varied rGO concentrations of 5% and 10%. In the present work, a one-step hydrothermal method was successfully applied to prepare rGO/CuO NCs at different concentrations of RGO. The novelty of this work was to enhance the structural, optical, photocatalytic, and cytotoxic properties of CuO using the addition of rGO sheets. XRD, TEM, SEM-EDX, XPS, FTIR, UV-vis, PL, and DLS techniques were used to characterize the prepared samples. XRD data confirmed the formation of the monoclinic phase of CuO with a decrease in crystallite size, from 21.14 nm for CuO to 16.94 nm for the 10% rGO/CuO NCs nanocomposite. SEM and TEM images verified the uniform anchoring and excellent dispersion of CuO nanoparticles on the rGO sheets, and the EDX spectra showed the presence of Cu, O, and C elements in the obtained rGO/CuO NCs. DLS measurements showed that the hydrodynamic radius dropped from 69.98 ± 17.81 nm for CuO to 51.72 ± 10.48 nm for 10% rGO/CuO NCs. The zeta potential values remained negative for all samples, ranging from −20.50 ± 8.69 mV for CuO to −25.60 ± 9.08 mV for 10% rGO/CuO NCs, suggesting enhanced colloidal stability with rGO incorporation. Furthermore, FTIR and XPS analyses confirmed that Cu–O–C bonding formed between CuO and rGO. UV-Vis analysis revealed a redshift in the absorption edges as rGO content increased, reducing the band gap from 3.65 eV to 3.60 eV. Additionally, PL spectra showed a marked reduction in emission intensity due to a decrease in the recombination rate between electron (e⁻)–holes (h⁺) pairs. The CuO/(10%)rGO NCs showed the best photocatalytic performance with a 93.56% degradation of methylene blue (MB) after 120 min under UV irradiation, and followed pseudo-first-order kinetics with k = 0.0203 min⁻¹. Cytotoxicity studies on HT1080 cells showed a dose-dependent decrease in viability. 10% rGO/CuO NCs exhibited the highest cytotoxicity effect, resulting in 58% and 50% viability at 1.4 mg/mL, respectively. The presented results showed that the presence of rGO in CuO NPs played a role in enhancing the structural stability, charge mobility, and biological reactivity of Cu NPs. This study highlighted that the rGO/CuO NCs are a promising multi-functional material for environmental and biomedical applications. Full article

Successive ionic layer adsorption reaction (SILAR) was used to deposit Cu₂O nanosheets on anodized TiO₂ nanotubes at different deposition cycles (4, 8, 15, and 20). Compared to the bare TiO₂ nanotubes, these coatings were investigated for their tribological behavior (friction, wear and energy loss), scanning and transmission electron microscopy (SEM, TEM), X-ray Diffraction (XRD) was used to characterize Cu₂O/TiO₂ coatings to study the effect of number of cycles on the morphological and structural properties of the samples; these characteristics engage in determining the wear mechanisms. The assessment of the coating’s adhesion was determined by the obtained critical loads from the scratch test; the 15 cycles Cu₂O/TiO₂ exhibited higher critical loads, which corresponds to improved adhesion. This sample also showed a low wear volume of 7.5 × 10⁶ µm³ compared to other samples but higher energy loss due to the low shear strength of copper oxide. The friction coefficient, however, decreased from 0.7 for bare TiO₂ nanotubes to 0.48 for 20 cycles Cu₂O/TiO₂ coatings at higher loads, which proves the wear resistance enhancement. Since these coatings will be manufactured for orthopedic and dental implant applications, the corrosion resistance was tested, and the 15 cycles Cu₂O-NPs/TiO₂-NTs where these coatings exhibited the most favorable combination of a low corrosion current density (1.9 × 10⁻⁴ A/cm²) and a noble corrosion potential (−0.3 V/SCE); furthermore, there was a polarization resistance of 2.4 × 10⁴ Ω·cm² and a protection efficiency of 96.7%, indicating significantly enhanced corrosion resistance as opposed to the other samples. Full article

The spontaneous reduction of one Cu(II) center to Cu(I) in a series of three dinuclear copper complexes in acetonitrile is described. These complexes feature ligands that include nitrogen donors from a diazecine ring and imidazole, designated as promeim, thiopromeim, and thioenmeim; the latter two incorporate a thioether as a third donor component. The mechanism of metal reduction was elucidated through spectroscopic and spectrometric techniques (UV-vis, EPR, XANES, ESI-MS) and electrochemical tools, in combination with DFT electronic structure calculations. Based on these and on spectroelectrochemical results, a mechanism is proposed in which the one-electron reduction of one of the copper ions is achieved by a one-electron oxidation in the adjacent imidazole group, while the other copper ion remains as Cu(II). The persistent detection of superoxide and peroxide over long periods suggests a mechanism in which a catalytic cycle involving electron transfer occurs between copper, ligand, and dioxygen. Full article

Copper functions as an exceptionally efficient conductor, garnering considerable interest in electrical and thermal applications; however, its relatively malleable nature and insufficient durability may hinder its structural effectiveness. This study focused on the development of copper-based nanocomposites by reinforcing a copper matrix with co-precipitated CuO/Al₂O₃ nanoparticles (varying from 0 to 10 wt% in increments of 2%). A thorough examination was conducted regarding the microstructural characteristics, mechanical properties, and the electrical and thermal conductivities of the composites. X-ray diffraction (XRD) and energy-dispersive spectroscopy (EDS) analysis validated the successful synthesis of nano-sized CuO and Al₂O₃ phases, with an estimated crystallite size of 33.2 ± 2.4 nm. Scanning electron microscopy revealed a relatively uniform distribution of nano-oxides within the copper matrix, albeit with signs of particle agglomeration at higher loading levels. The durability of the copper exhibited a significant enhancement attributed to the nano-oxide reinforcement, achieving an 180% increase relative to pure copper with a 10% reinforcement addition. Consequently, the tensile strength increased by approximately 68% (from around 154 MPa to nearly 260 MPa), while maintaining an exceptional level of ductility. The electrical conductivity of copper remained largely unchanged with the addition of nanoparticles; rather, a slight improvement in conductivity and a ~30% rise in thermal conductivity were observed at the maximum reinforcement level. This research work presents a copper-based nanocomposite that offers remarkable potential for applications requiring enhanced strength, wear resistance, and exceptional electrical and thermal conductivity. Full article

Modern genetic selection for high productivity has created a physiological conflict in ruminants, where the metabolic demands of lactation compete directly with the energy requirements of reproduction. This review provides a mechanistic synthesis of how key nutritional factors modulate the endocrine and cellular pathways governing reproductive success in cattle and sheep. Negative energy balance (NEB), characteristic of the early postpartum period, suppresses the hypothalamic–pituitary–gonadal (HPG) axis by impairing the pulsatile secretion of gonadotropin-releasing hormone (GnRH) and luteinizing hormone (LH), mediated through reduced kisspeptin signaling, growth hormone (GH) resistance, and decreased circulating insulin, insulin-like growth factor-1 (IGF-1), and leptin. At the macronutrient level, excess rumen-degradable protein elevates blood urea nitrogen and impairs the uterine environment, while omega-3 polyunsaturated fatty acids inhibit prostaglandin F2α synthesis to support corpus luteum maintenance. At the micronutrient level, selenium, copper, and zinc are essential antioxidant cofactors protecting gametes and embryos from oxidative stress, while vitamins A, D, and E regulate gene expression in reproductive tissues. Furthermore, maternal nutrition during critical gestational windows programs the reproductive capacity of offspring through epigenetic modifications, with profound implications for long-term herd fertility. Understanding these nutritional–reproductive interactions is crucial for developing precision feeding strategies that optimize herd fertility, improve animal welfare, and ensure the economic sustainability of livestock management. A thorough understanding of these nutritional–reproductive interactions is essential for developing precision feeding strategies that optimize fertility in high-producing ruminants. Full article