Magnetic separation, sunlight-driven photocatalytic activity, and antibacterial studies of Sm-doped Co0.33Mg0.33Ni0.33Fe2O4 nanoparticles.

Magnetic nanoparticles have emerged as a promising tool for wastewater treatment due to their unique properties. In this regard, Co0.33Mg0.33Ni0.33SmxFe2-xO4 (0.00 ≤ x ≤ 0.08) nanoparticles were prepared to examine their magnetic separation efficiency (MSE), photocatalytic, antibacterial, and antibiofilm performances. Pure nanoparticles, having the highest saturation magnetization (Ms = 31.87 emu/g), exhibit the highest MSE, where 95.6% of nanoparticles were separated after 20 min of applying a magnetic field of 150 mT. The catalytic performance of the prepared samples is examined by the photodegradation of rhodamine B (RhB) dye exposed to direct sunlight radiation. Improved photocatalytic activity is exhibited by Co0.33Mg0.33Ni0.33Sm0.04Fe1.96O4 nanoparticles, labeled as Sm0.04, where the rate of the degradation reaction is enhanced by 4.1 times compared to pure nanoparticles. Rising the pH and reaction temperature improves the rate of the photodegradation reaction of RhB. The incorporation of 15 wt% reduced graphene oxide (rGO) with Sm0.04 enhanced the rate of the reaction by 1.7 and 2.4 times compared with pure Sm0.04 sample and rGO, respectively. The antibacterial and antibiofilm activities against Escherichia coli, Leclercia adecarboxylata, Staphylococcus aureus, and Enterococcus faecium are assessed by the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) broth microdilution, the agar well diffusion, the time-kill assays, the biofilm formation, and destruction assays. The bacteria used in these assessments are isolated from wastewater. The nanoparticles exhibit a bacteriostatic activity, with a better effect against the Gram-positive isolates. Co0.33Mg0.33Ni0.33SmxFe2O4 (x = 0.00) nanoparticles have the best effect. The effect is exerted after 2-3 h of incubation. Gram-positive biofilms are more sensitive to nanoparticles.

Aluminum oxide, cobalt aluminum oxide, and aluminum-doped zinc oxide nanoparticles as an effective antimicrobial agent against pathogens.

Since the clock of antimicrobial resistance was set, modern medicine has shed light on a new cornerstone in technology to overcome the worldwide dread of the post-antimicrobial era. Research organizations are exploring the use of nanotechnology to modify metallic crystals from macro to nanoscale size, demonstrating significant interest in the field of antimicrobials. Herein, the antimicrobial activities of aluminum oxide (Al2O3), cobalt aluminum oxide (CoAl2O4), and aluminum doped zinc oxide (Zn0.9Al0.1O) nanoparticles were examined against some nosocomial pathogens. The study confirmed the formation and characterization of Al2O3, CoAl2O4, and Zn0.9Al0.1O nanoparticles using various techniques, revealing the generation of pure nanoscale nanoparticles. With inhibition zones ranging from 9 to 14 mm and minimum inhibitory concentrations varying from 4 mg/mL to 16 mg/mL, the produced nanoparticles showed strong antibacterial activity against Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Staphylococcus aureus. Meanwhile, the bactericidal concentrations ranged from 8 mg/mL to 40 mg/mL. In culture, Zn0.9Al0.1O NPs demonstrated a unique ability to inhibit the development of nosocomial infections with high bactericidal activity (8 mg/mL). Transmission electron microscope images revealed changes in cell shape, bacterial cell wall morphology, cytoplasmic membrane, and protoplasm due to the introduction of tested nanoparticles. These results pave the way for the use of these easily bacterial wall-piercing nanoparticles in combination with potent antibiotics to overcome the majority of bacterial strains' resistance.

Influence of Ru doping on structural, optical, and photocatalytic properties of (Cd-Ni-Mn) nanoferrites.

This study reports the synthesis of (Cd0.4Ni0.4Mn0.2)Fe2-xRuxO4 nanoparticles (NPs), where x = 0.00, 0.005, 0.01, 0.015, 0.02, and 0.04, via co-precipitation method. The synthesized samples were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM), and photoluminescence (PL) spectroscopy. The results confirmed the purity of the samples with the presence of a very small fraction of the hematite phase. Pseudo-spherical morphology was recognized from TEM images. Then, the prepared samples were further used as effective photocatalysts for the degradation of nitrobenzene under UV irradiation to examine the effect of doping on the photocatalytic activity. Among the synthesized samples, (Cd0.4Ni0.4Mn0.2)Fe1.985Ru0.015O4 NPs exhibited superior photocatalytic activity. This result is in good agreement with photoluminescence (PL) analysis in which (Cd0.4Ni0.4Mn0.2)Fe1.985Ru0.015O4 NPs revealed the slowest recombination rate of the electron-hole pair. To further improve the photocatalytic performance, different weight % of graphene was incorporated with (Cd0.4Ni0.4Mn0.2)Fe1.985Ru0.015O4 NPs. Finally, 81.41% of nitrobenzene was degraded after 180 min in the presence of 5 wt% graphene/(Cd0.4Ni0.4Mn0.2)Fe1.985Ru0.015O4 nanocomposites, and the degradation rate constant was estimated as 8.4 × 10-3 min-1.

Intraperitoneal hepato-renal toxicity of zinc oxide and nickel oxide nanoparticles in male rats: biochemical, hematological and histopathological studies.

In recent years, zinc oxide (ZnO) and nickel oxide (NiO) nanoparticles (NPs) have become more prevalent in commercial and industrial products. However, questions have been raised regarding their potential harm to human health. Limited studies have been conducted on their intraperitoneal toxicity in rats, and their co-exposure effects remain uncertain. Therefore, this study aimed to investigate some biological responses induced by a single intraperitoneal injection of ZnO-NPs (200 mg/kg) and/or NiO-NPs (50 mg/kg) in rats over time intervals. Blood and organ samples were collected from 36 male rats for hematological, biochemical, oxidative stress, and histological analysis. Results showed that the administration of NPs reduced the body and organ weights as well as red blood cell (RBC) indices and altered white blood cell (WBC) and platelet (PLT) counts. The experimental groups exhibited elevated levels of aspartate aminotransferase (AST), alanine transaminase (ALT), creatinine (CREA), urea, lipid profile, glucose (GLU), total protein (TP), albumin (ALB) and malondialdehyde (MDA), and decreased uric acid (UA), superoxide dismutase (SOD), and glutathione (GSH). Histological observations also revealed architectural damages in liver and kidneys. These alterations were time-dependent and varied in their degree of toxicity. Co-exposure of NPs initially lessened the damage but increased it afterwards compared to individual exposure. In conclusion, intraperitoneal injection of ZnO-NPs and/or NiO-NPs alters biological processes and induces oxidative stress in rats' liver and kidneys in a time-dependent manner, with NiO-NPs being more potent than ZnO-NPs. Furthermore, co-exposed NPs initially appeared to be antagonistic to one another while further aiming toward synergism.

Gamma-ray attenuation parameters of HDPE filled with different nano-size and Bulk WO3.

High-density polyethylene (HDPE) was obtained through a compression molding technique, and incorporated with different filler weight fractions (0, 10, 15, 25, and 35%) of bulk WO3, and two different WO3 nanoparticle sizes (45 nm and 24 nm). The radiation attenuation ability of the new category of polymer composite HDPE/WO3 was evaluated using gamma-ray energies ranging from 59.53 up to 1332.5keV of four radioactive sources 241Am, 133Ba, 137Cs, and 60Co. The mass attenuation coefficients µm, the total molecular cross-section σmol, the effective atomic cross-section σatom, the total electronic cross-section σel, the effective atomic number Zeff, electron density Neff, the half value layer (HVL), the tenth value layer (TVL), and the relaxation length were investigated. The obtained results of the gamma-ray attenuation parameters exhibited an outstanding influence of the size and weight fraction of WO3 filler on the gamma-ray shielding ability of the HDPE composite. A significant improvement was detected at low gamma-ray energies. The HVL of the synthesized HDPE composites is compared with that of pure lead as a conventional shielding material. HDPE composite filled with the smaller size of WO3 nanoparticle shows good improvement in the attenuation parameters, which suggests promising applications in radiation protection and gamma-ray shielding.

Enhanced adsorption performance of magnetic Ni0.5Zn0.5Fe2O4/Zn0.95Co0.05O nanocomposites for the removal of malachite green dye.

This investigation reports the synthesis and characterization of (1-x)Ni0.5Zn0.5Fe2O4/(x)Zn0.95Co0.05O nanocomposites, with 0.0 ≤ × ≤ 0.5. Fourier transform infrared (FTIR) and Raman spectroscopies confirmed the purity of the samples and the presence of bands corresponding to octahedral and tetrahedral iron occupancies for Ni0.5Zn0.5Fe2O4 nanoparticles. A shift in peak positions of these bands was detected upon the addition of Zn0.95Co0.05O nanoparticles. The magnetic properties of the nanocomposites were examined using Mössbauer spectrometry at both room temperature and 77 K. Room temperature analysis showed the existence of both ferromagnetic and superparamagnetic behaviors, while at 77 K, all nanocomposites showed ferromagnetic behavior. The adsorption performance of the nanocomposite on the removal of malachite green (MG) dye solution was investigated by varying the contact time, adsorbent concentration, and reaction temperature. The adsorption reaction followed the second-order kinetics and the sample with x = 0.3 showed the highest adsorption rate. The adsorption rate showed an increase with the increase in the reaction temperature. The adsorption isotherm was determined by applying different adsorption isotherms (Langmuir, Freundlich, and Temkin isotherms), and the results are well-fitted with the Langmuir theoretical model.

Assessment of X-ray shielding properties of polystyrene incorporated with different nano-sizes of PbO.

PbO (lead oxide) particles with different sizes were incorporated into polystyrene (PS) with various weight fractions (0, 10, 15, 25, 35%). These novel PS/PbO nano-composites were produced by roll mill mixing and compressing molding techniques and then investigated for radiation attenuation of X-rays (N-series/ISO 4037) typically used in radiology. Properties of the PbO particles were studied by X-ray diffraction (XRD). Filler dispersion and elemental composition of the prepared nano-composites were characterized using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), revealing better filler distribution and fewer agglomerations with smaller PbO particle size. Linear and mass attenuation coefficients (µ and µm), total molecular and atomic cross-sections (σmol and σatm), as well as effective atomic number and electron density (Zeff and Neff), were calculated for the energy range N40 to N200. The influence of PbO weight percentage on the enhancement of the shielding parameters of the nano-composites was expected; however, the effect of PbO particle size was surprising. Linear and mass attenuation coefficients for PS/PbO composites increased gradually with increasing PbO concentrations, and composites with a small size of nanoparticles showed best performance. In addition, increasing PbO concentration raised the effective atomic number Zeff of the composite. Hence, the electron density Neff increased, which provided a higher total interaction cross-section of X-rays with the composites. Maximum radiation shielding was observed for PS/PbO(B). It is concluded that this material might be used in developping low-cost and lightweight X-ray shielding to be used in radiology.

The electrochemical corrosion behaviour of compacted (Bi, Pb)-2223 superconductors in aqueous solutions.

The corrosion behaviour of (Bi, Pb)-2223 samples compacted at 0.3-1.9 GPa in 0.5 M of HCl, NaCl, and NaOH solutions at 30 °C was investigated using potentiodynamic polarization curves measurements and electrochemical impedance spectroscopy (EIS) technique as well as scanning electron microscopy (SEM) and energy dispersive X-ray emission spectroscopy (EDX). Polarization results showed that the increase in compaction decreases both cathodic hydrogen evolution or oxygen reduction and anodic (BiPb)-2223 superconductor dissolution in 0.5 M HCl, and 0.5 M NaOH. On the other hand, compaction mainly affects the anodic part of the polarization curves of (Bi, Pb)-2223 in 0.5 M NaCl solution. EIS measurements revealed that the highest protection of the superconductors was achieved in 0.5 M NaCl, while the lowest degree of protection was observed in 0.5 M HCl. SEM images show a random plate-like morphology fitted with the marker of (Bi, Pb)-2223 material. The compacted sample at 1.9 GPa indicates deformation of the grains and the formation of a micro-crack. The corrosion mechanism of the superconductor at different pH values was also discussed.

Synthesis, Characterization, and Antibacterial Activity of Mg-Doped CuO Nanoparticles.

This study aims to investigate the effect of magnesium (Mg) doping on the characteristics and antibacterial properties of copper oxide (CuO) nanoparticles (NPs). The Mg-doped CuO NPs were fabricated by the co-precipitation method. NPs were characterized by X-ray Powder Diffraction (XRD), Transmission Electron Microscope (TEM), Energy Dispersive X-ray (EDX) analysis, Fourier Transform Infrared Spectroscopy (FTIR), and Photoluminescence (PL). Broth microdilution, agar-well diffusion, and time-kill assays were employed to assess the antibacterial activity of the NPs. XRD revealed the monoclinic structure of CuO NPs and the successful incorporation of Mg dopant to the Cu1-xMgxO NPs. TEM revealed the spherical shape of the CuO NPs. Mg doping affected the morphology of NPs and decreased their agglomeration. EDX patterns confirmed the high purity of the undoped and Mg-doped CuO NPs. FTIR analysis revealed the shifts in the Cu-O bond induced by the Mg dopant. The position, width, and intensity of the PL bands were affected as a result of Mg doping, which is an indication of vacancies. Both undoped and doped CuO NPs exhibited significant antibacterial capacities. NPs inhibited the growth of Gram-positive and Gram-negative bacteria. These results highlight the potential use of Mg-doped CuO NPs as an antibacterial agent.

Structural and magnetic properties of hard-soft BaFe12O19/(Zn0.5Co0.5)Fe2O4ferrites.

Hard-soft nanocomposites of (1 -x) BaFe12O19/x(Zn0.5Co0.5)Fe2O4, forx= 0.00, 0.25, 0.50, 0.75 and 1.00, were prepared via co-precipitation and high-speed ball milling techniques, respectively. The synthesized samples were characterized via x-ray diffraction, transmission electron microscope, Fourier transform infrared (FTIR), and vibrating sample magnetometer. XRD revealed the formation of hard-soft nanocomposites. TEM indicated that the two phases are well distributed and the particle size distribution is narrower for low content of soft phase, leading to better exchange coupling between the grains. Magnetic measurements were performed at 300 K and 77 K. The results showed a good single-phase magnetic behavior, verifying the good exchange coupling between hard and soft phases. For low (Zn0.5Co0.5)Fe2O4content, the dipolar interactions were dominated by the exchange-coupling interactions. Additionally, the optimum values of saturation and remanent magnetizations, coercivity, and squareness ratio were obtained forx= 0.5. This was attributed to the dominance of exchange-coupling interaction. The enhancement of magnetic properties and energy product (BH)maxfor nanocomposites at low temperature is skilled in the reduction of the thermal fluxes of magnetic moments at the surface. The maximum energy product (BH)maxwas observed in C2 at both temperatures with a smaller value than that of pure BaFe12O19.

Ab initio calculations of the electronic structure of the low-lying states for the ultracold LiYb molecule.

Ab initio techniques have been applied to investigate the electronic structure of the LiYb molecule. The potential energy curves have been computed in the Born-Oppenheimer approximation for the ground and 29 low-lying doublet and quartet excited electronic states. Complete active space self-consistent field, multi-reference configuration interaction, and Rayleigh Schrödinger perturbation theory to second order calculations have been utilized to investigate these states. The spectroscopic constants, ωe, Re, Be, …, and the static dipole moment, µ, have been investigated by using the two different techniques of calculation with five different types of basis. The eigenvalues, Ev, the rotational constant, Bv, the centrifugal distortion constant, Dv, and the abscissas of the turning points, Rmin and Rmax, have been calculated by using the canonical functions approach. The comparison between the values of the present work, calculated by different techniques, and those available in the literature for several electronic states shows a very good agreement. Twenty-one new electronic states have been studied here for the first time.