Search Results (6)

This study investigates the impact of zirconium substitution on the structural, elastic and magnetic properties of CoCr₂O₄ nanoparticles. A series of CoCr_2−xZr_xO₄ nanoparticles, x = 0.00, 0.05, 0.10, 0.15 and 0.20, are synthesized via the co-precipitation method. X-ray diffraction (XRD) patterns affirm the formation of single-phase cubic structure with the space group Fd3m. Special attention is given to accurately calculating the average crystallite size (D) and lattice parameter (a) using Williamson–Hall (W–H) analysis and the Nelson–Riley (N–R) extrapolation function, respectively. The increase in Zr⁴⁺ content leads to a reduction in crystallite size and an increase in the lattice parameter. Elastic properties are estimated from force constants and the lattice constant, determined from FTIR and XRD, respectively. The observed changes in the elastic constants are attributed to the strength of interatomic bonding. The stiffness constants decrease, while Poisson’s ratio increases with increasing Zr⁴⁺ content, reflecting the increase in the ductility of the prepared samples. As the Zr⁴⁺ content increases, the stiffness constants decrease, and Poisson’s ratio increases, reflecting enhanced ductility of the samples. Furthermore, as Zr⁴⁺ content rises, Young’s modulus, the rigidity modulus and Debye temperature decrease. The magnetic hysteresis loop measurements are carried out at room temperature using a vibrating sample magnetometer (VSM) over a field range of 25 kg. Unsubstituted CoCr₂O₄ exhibits ferrimagnetic behavior. As Zr⁴⁺ content increases, saturation magnetization (M_s) and magnetic moment decrease, while remanent magnetization (M_r) and coercivity (H_c) initially decrease up to x = 0.10, then increase with further increases in x. The novel key of this study is how Zr⁴⁺ substitution in CoCr₂O₄ nanoparticles can effectively modify their elastic moduli and magnetic properties, making them suitable for various applications such as flexible electronics, protective coatings, energy storage components and biomedical implants. Full article

This work describes the characterization of pigments and ground layers in two paintings by the renowned Argentinian painter Antonio Berni (1905–1981). The studied paintings are “Toledo” and “Figure” from the collection of the Provincial Museum of Fine Arts in Santa Fe (Argentina). To approach this goal, an integrated investigation comprising in situ X-ray fluorescence measurements by means of a portable system (pXRF), micro-Raman spectroscopy, Attenuated Total Reflection–Fourier transform infrared spectroscopy (ATR-FTIR), and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDS) was carried out. The results revealed a chromatic palette with inorganic pigments, such as ultramarine blue, cobalt blue, lead white, zinc white, yellow cadmium, and hydrated chromium oxide (viridian), together with a preparation layer consisting of a mixture of earth, lead white, and calcite in “Toledo”. On the other hand, the preparation layer in “Figure” was characterized as lithopone, a mixture of barium sulfate and zinc sulfide. ATR-FTIR-analysis revealed the formation of metallic soaps in both paintings due to the reaction of fatty acids from a drying oil used as a binder with lead and zinc pigments, as confirmed by comparison with the infrared spectra of synthetic lead and zinc soaps. This study contributes to the understanding of Berni’s painting style and the future restoration of both artworks. Full article

A chromate of copper and cobalt (Φy) was synthesized and characterized. Φy activated peroxymonosulfate (PMS) to degrade ciprofloxacin (CIP) in water. The Φy/PMS combination showed a high degrading capability toward CIP (~100% elimination in 15 min). However, Φy leached cobalt (1.6 mg L⁻¹), limiting its use for water treatment. To avoid leaching, Φy was calcinated, forming a mixed metal oxide (MMO). In the combination of MMO/PMS, no metals leached, the CIP adsorption was low (<20%), and the action of SO₄•⁻ dominated, leading to a synergistic effect on pollutant elimination (>95% after 15 min of treatment). MMO/PMS promoted the opening and oxidation of the piperazyl ring, plus the hydroxylation of the quinolone moiety on CIP, which potentially decreased the biological activity. After three reuse cycles, the MMO still presented with a high activation of PMS toward CIP degradation (90% in 15 min of action). Additionally, the CIP degradation by the MMO/PMS system in simulated hospital wastewater was close to that obtained in distilled water. This work provides relevant information on the stability of Co-, Cu-, and Cr-based materials under interaction with PMS and the strategies to obtain a proper catalyst to degrade CIP. Full article

The main target of the current research work is effectively eliminating fossil fuel dependency and improving the exhaust air quality of conventional Compression Ignition (CI) engines. This research paper demonstrates for the first time that a nanofluid (water without surfactant) stored in separate tanks can be quantified, collected, and immediately emulsified by a high shear mixer before transfer into the combustion chamber of a diesel engine. The experiment was carried out under different load states (25%, 50%, 75% and 100%) with a constant speed of 1500 rpm. Biofuel was extracted from citronella leaves using an energy-intensive process. The 5% water share was used for preparing the biofuel emulsion and nano-biofuel emulsion. A cobalt chromate nanoadditive was used to make the nanofluid. An experimental investigation was performed with prepared test fuels, namely, ultra-low sulphur diesel (ULSD), 100% Citronella (B100), surfactant-free Diesel emulsion (SDE), surfactant-free bioemulsion (SBE), and Surfactant free nano-bioemulsion (SNBE), in a test engine. The properties of the sample test fuels was ensured according to EN and ASTM standards. The observation performance results show that the SNBE blend exhibited lower BTE (by 0.5%) and higher SFC (by 3.4%) than ULSD at peak load. The emission results show that the SNBE blend exhibited lower HC, CO, NO_x, and smoke emissions by 23.86%, 31.81%, 2.94%, and 24.63%, respectively, compared to USD at peak load. The CP and HRR results for SNBE were closer to ULSD fuel. Overall, the novel concept of an RTEFI (Real-time emulsion fuel injection) system was proved to be workable and to maintain its benefits of better fuel economy and greener emissions. Full article

In the present work, cobalt-chromite-based pigment Co_1-xNi_xCr₂O₄ chromate powder and nanoparticles with various transition metal concentrations (x = 0.2, 0.4, 0.6, and 0.8) were manufactured by applying aqueous synthesis approaches and sol–gel synthesis routes. XRD analysis of the powder shows that all samples formulated by the sol–gel method were crystalline with a spinel structure. Chromites show green color with a higher nickel concentration, while Co-substituent shows blackish pigments. Samples were annealed at distinct temperatures ranging from 600 °C to 750 °C. The nanoparticles obtained were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectroscopy (RS), photoluminescence (PL), and energy-dispersive X-ray spectroscopy (EDS). The particle size of the parent compound (CoCr₂O₄) ranges from 100 nm to 500 nm, as measured by SEM. The tendency of particles to form aggregates with increasing annealing temperature was observed. These compounds may be successfully used as an effective doped nickel-cobalt ceramic pigment. Full article

A simple titrimetric method is described for the determination of dothiepin hydrochloride. The method is based on titrating the cited drug with potassium salts of trioxalato-ferrate (III) (TOXFe), trioxalato-chromate (III) (TOXCr), trioxalatoaluminate (III) (TOXAI) and trioxalato-cobaltate (III) (TOXCo). The end point was located conductimetrically. The effect of solvent, molar ratio, reagent concentration and temperature were studied. Based on conductimetric measurements at 25 °C, the solubility, solubility product, free energy (ΔG) and entropy changes (ΔS) of the ion associates were calculated. Calculations of the enthalpy change (ΔH) are based on atomic absorption measurements of the solubility of the ion associates at different temperatures. The method allowed the determination of 6.63-29.87, 3.31-49.78, 9.95-49.78 and 3.31-33.19 mg of the studied drug using TOXFe, TOXCr, TOXAl and TOXCo, respectively. The method was further applied successfully to some dosage forms containing the cited drug, and the obtained results were compared favorably with those previously given by the official method. Full article