Energy Dispersive X-ray Analysis Research Articles

Facile one step green synthesis of CdO-CdS hybrid nanocomposite: Its electrochemical and photoluminescence applications

This study reports the fabrication of a CdO-CdS hybrid nanocomposite (CDCS NC) and its application towards electrochemical sensing of dopamine (DA). The synthesis was conducted at various temperatures using Butea monosperma leaf powder as a green fuel and it was noticed in the XRD pattern that 400 °C was ideal for the formation of the CdO-CdS hybrid NC. Also, the samples were characterized by implementing Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Analysis (EDX), UV-Vis Diffused Reflectance Spectroscopy (UV-DRS) and Photoluminescence (PL) techniques. The electrochemical activity was investigated using Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV) techniques. A working electrode was fabricated by modifying a Glassy Carbon Electrode (GCE) using the CdO-CdS NC and it showed remarkable electrochemical activity towards dopamine (DA). Further, the electrochemical properties were investigated by varying the scan rate, pH and concentration. The fabricated electrode shows a low limit of detection of 23 µM. Hence by its unique composition and inherent properties, the NC stands as a potent tool for advancing the boundaries of electrochemical sensing, heralding a new era of innovation in sensor development.

Comprehensive characterization of modern industrial Argentinian paints for improved chronological painting attribution

Throughout the twentieth century, the paint industry developed a multitude of new binding media, pigments and additives that improved the appearance, ease of application, and performance of modern industrial paints. Depending on when and where they were first manufactured, and when they were introduced into paint formulations, some of these new paint components could conceivably be chronological markers useful in assigning attribution to specific artists or in the study of forgeries. The aim of this study was to develop a systematic methodology for characterizing organic and inorganic materials in modern paints, and search for potential chronological markers. Colored reference paints manufactured by local companies in Argentina from the 1940s and 1950s were studied with a multi-analytical approach that included Fourier-transform infrared spectroscopy, gas chromatography coupled with mass spectrometry, Raman spectroscopy, X-ray diffraction, X-ray fluorescence and scanning electron microscopy with energy dispersive X-ray analysis. A wide range of compounds was identified due to the complementarity use of the analytical techniques. Historical references, patents, books, and scientific publications about the materials used in that time period provided invaluable information in establishing tentative timelines for modern paint components. This investigation was part of a broader interdisciplinary investigation of Concrete Art, an international art movement of the beginning of the twentieth century, which took place in Argentina and other nearby countries during the 1940s and 1950s. To prove the concept, a micro-sample from “Obra N° 171” by Raúl Lozza was analyzed. Organic and inorganic fractions were studied and the information collected was correlated with developed timelines to support the authentication process. Ultimately, the information from this study may also have a direct impact on the key areas of material characterization, aging behavior, and conservation of works of art made from these products.

Defects assisted the enhancement of optical and ferromagnetism in Zn1-xCoxS Quantum Dots: Toward Efficient Optoelectronic and Spintronic Applications

Colloidal Co-doped ZnS Quantum dots (QDs) were successfully synthesized through a facile and effective chemical co-precipitation method using polyethylene glycol (PEG) as a capping agent. A comprehensive study on the structure, optoelectronic, and magnetic properties of ZnS: Co2+ QDs was thoroughly carried out using diverse characterization techniques. Transmission electron micrographs reveal spherical QDs with a mean particle size of 5 ± 0.5 nm, whereas the X-ray diffraction (XRD) analysis and Raman spectroscopy confirm the exclusive presence of cubic ZnS phase structure, without any signs of Co-related impurity phases. Energy-dispersive x-ray (EDX) analysis verifies the presence of only three elements: Zinc, Cobalt, and Sulphur, with nearly stoichiometric proportions. X-ray photoemission (XPS) analysis confirmed the presence of Co2+ ions in the divalent oxidation state as well as the fair existence of sulphur vacancies. Optical measurements demonstrate that Co-doping in ZnS leads to a decrease in the optical band gap owing to the presence of defects that create localized states within the band structure. In addition, the refractive index (n) is found to increase with Co-doping level due to the increase in the polarizability. The outcomes of optical properties reveal that the tunability of the optical band gap and dispersive oscillator parameters in Co-doped ZnS QDs results in an enhancement of the non-linear optical parameters, such as third-order non-linear optical susceptibility χ(3), and non-linear refractive index n2, rendering them well-suited for applications in optoelectronic devices. Furthermore, the room-temperature photoluminescence (PL) spectra revealed that the Co-doped ZnS QDs have two broad emission bands, including the blue emission, and the green emission. By varying the level of Co-doping, it becomes possible to effectively control the relative PL intensities of dual-color emissions, highlighting their potential for producing adjustable color outputs. The room temperature ferromagnetic behaviour of the QDs has been observed and analyzed in accordance with the bound magnetic polarons model. These findings suggest that Co-doped ZnS QDs can be utilized effectively in the design of spintronic devices.

Comprehensive characterization and optoelectronic significance of Ho3+ and Cr3+ Co-doped ZnAl2O4 spinels.

The spinels ZnAl1.99-xHoxCr0.01O4 (with x = 0 and 0.001) were synthesized using a solid-state method, and various techniques were employed for their characterization. X-ray diffraction (XRD) analysis confirmed a cubic spinel structure with the Fd3̄m space group for both spinels. The morphology and homogeneity of the chemical composition were determined using scanning electron microscopy (SEM) and energy dispersive X-ray analysis. Raman and infrared vibrational spectroscopy techniques were also employed for analysis. The optical band gap (Eg) was determined from UV/vis absorption spectra, and the direct transition behavior was confirmed by Tauc's law. The observed large disorder and defect concentration are attributed to the presence of Cr3+ and Ho3+ ions, explaining this behavior. The electron paramagnetic resonance (EPR) measurement presented different types of traps. Room temperature absorption spectra exhibited multiple peaks corresponding to the 3d-3d and 4f-4f transitions of Cr3+ and Ho3+ ions. The results obtained validate the significance of our compounds in optoelectronic device applications.

Enhancing Corrosion Resistance of Mild Steel in 1M HCl: Investigation of New Benzoxazepine Derivatives Through Synthesis, Electrochemical Analysis, Surface Analysis, XPS, DFT, and Molecular Dynamics Simulation

AbstractThis research delineates the corrosion inhibitory efficiency of two newly synthesized benzoxazepine derivatives – [3,3‐dimethyl‐11‐phenyl‐3,4,5,11‐tetrahydrodibenzo[b,e] [1,4]oxazepine‐1(2 H)‐one (S1)] and [11‐(4‐chlorophenyl)‐3,3‐dimethyl‐3,4,5,11‐tetrahydrodibenzo[b,e][1,4]oxazepine‐1(2 H)‐one (S2)] – on mild steel in 1M HCl milieu. These derivatives were characterized by proton (1H NMR) and carbon (13C NMR) nuclear magnetic resonance spectroscopy. The experimental approach encompassed potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) techniques. The corrosion inhibition efficacy of S1 and S2 was concentration‐dependent, with their efficiencies peaking at 92.0 % and 92.1 %, respectively, at a 10−3 M concentration. Surface characterization, conducted using scanning electron microscopy (SEM), energy‐dispersive X‐ray analysis (EDS), X‐ray diffraction (XRD), contact angle measurements, and X‐ray photoelectron spectroscopy (XPS), corroborated the formation of a protective barrier layer on the mild steel surface. Additionally, using an inductive approach, UV‐visible spectrometry was employed to elucidate the adsorption behaviors of these inhibitors on the steel surface. Density functional theory (DFT) and molecular dynamics (MD) simulations were utilized to decipher the interaction mechanisms and adsorption modalities, unveiling critical insights into the interactions of S1 and S2 with the mild steel surface. This comprehensive analysis highlights the robust corrosion inhibition potential of the newly synthesized benzoxazepine derivatives and illuminates their prospective utility as effective inhibitors for mild steel in corrosive environments.

Biofabrication of Silver Nanoparticles by Azadirachta indica Rhizosphere Bacteria with Enhanced Antibacterial Properties

Microorganisms (MOs) are prominent in ecological functioning and balance. The rhizosphere is considered one of the most diverse ecosystems on Earth and serves as a breeding spot for many MOs. Rhizosphere microbial diversity changes according to plant species, genotype, and the nature of the soil. The current study reports the possible use of bacteria isolated from the rhizosphere of Azadirachta indica for synthesizing silver nanoparticles (AgNPs). The physicochemical characterization and antibacterial activity of these green synthesized AgNPs are also reported. The gene (16S rRNA) sequence of bacteria isolated from the rhizosphere showed a maximum similarity of 99.25% with Bacillus subtilis. After incubation, the colorless reaction mixture transformed to brown, which indicates the formation of AgNPs, and UV-vis spectral analysis also confirmed the biosynthesis of AgNPs. Compared to lower temperatures, the efficiency of AgNP synthesis was high at the higher temperature. The scanning electron microscope image demonstrated spherical-shaped AgNPs with sizes ranging from 18 to 21 nm. Energy-dispersive X-ray analysis established the elemental analysis of synthesized AgNPs. The synthesized AgNPs showed strong bactericidal properties against pathogenic bacteria Klebsiella pneumonia, Pseudomonas aeruginosa, Escherichia coli, and methicillin-resistant Staphylococcus aureus.

Characterization of polymetallic ore of zinc, copper and lead

The study aimed to characterize a sample of approximately 150 kg of polymetallic zinc, copper and lead ore from the Aripuanã region, Mato Grosso. Due to the strategic importance of these minerals in the Brazilian economy and the complexity of processing. To achieve the objective, techniques such as scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDS), X-ray diffraction (XRD) and inductively coupled plasma mass spectrometry (ICP) were used to identify the minerals and determine its chemical composition. Furthermore, the Bond Work Index (WI) test was performed to evaluate resistance to fragmentation, and helium gas pycnometry was used to analyze the specific mass. The results showed a specific mass of 2.89 g/cm³, a WI of 9.22 kWh/st and contents of 5.15% zinc, 0.15% copper and 1.30% lead. The presence of minerals carrying the study elements, such as galena, sphalerite and chalcopyrite, highlights the relevance of these findings for the mining and metallurgy industry, boosting sustainable development and consolidating Brazil's position as a producer of valuable mineral resources.

Structural, spectroscopi c and laser properties of transparent Tm:YScO3 ceramic based on gas-phase synthesized nanoparticles

Owing to the combination of good thermo-optical properties and inhomogeneously broadened fluorescence spectra suitable for ultrashort laser pulse generation, rare-earth doped solid solutions of sesquioxides (Y,Lu,Sc)2O3 have attracted considerable interest in recent years. In this study, compositionally disordered Tm3+-doped YScO3 transparent ceramic was fabricated using solid-state vacuum sintering of nanopowder produced using laser ablation of solid target in air flow. The as-synthesized powder consisted of weakly aggregated spherical particles having 20 nm diameter and a mostly monoclinic (space group C2/m) crystal structure, whose symmetry was transformed into cubic (space group Ia-3) by calcination at 1050 °C. From high resolution transmission electron microscopy (HRTEM) and energy dispersive X-ray analysis (EDX), we observed a homogeneous distribution of components both throughout individual nanoparticles and 100-nm-thick ceramic foil resulting in high structural and optical quality of the obtained samples. The sintered ceramic featured an optical transmission of 77% at 600 nm and above 81% near 2 μm, an average grain size of 24.2 μm and a content of scattering centers of 26.1 ppm. The absorption spectra at several temperatures, from 93 K to 293 K, were measured and the corresponding absorption coefficients were obtained by Lambert-Beer formula in the range from 600 nm to 900 nm and from 1400 nm to 2100 nm. In particular, the room temperature absorption cross section at 794 nm and 1634 nm were determined to be σabs = 4.25 × 10−21 cm2 and σabs = 5.01 × 10−21 cm2 respectively. Concerning the emission cross section it was calculated by Fuchtbauer-Ladenburg equation starting from the fluorescence spectrum acquired at the laser work temperature: at 1951 nm and 2106 nm corresponding to the main two emission peaks belonging the curve, it was found σem = 9.2 × 10−21 cm2 and σem = 4.9 × 10−21 cm2, respectively. Finally, it was tested the laser behavior of the ceramic: pumped at 793 nm in quasi-CW mode it delivered 1.27 W of output power with a slope efficiency of 10.33% at 2081 nm. The tunability curve spans from 1942 nm to 2110 nm (i.e. 168 nm).

Corrosion resistance of powder metallurgy fabricated Cu–10Sn/SiC/mica hybrid composite

Abstract For the first time, bronze/SiC/mica hybrid composite has been manufactured using powder metallurgy method. Mixture – process variable design has been applied to design of experiments and optimization of the composite composition, as well as the production process variables (compaction pressure and sintering temperature) to attain superior corrosion resistance. This involved mixing different compositions of bronze, SiC, and mica powders, which were subsequently subjected to varied pressures and temperatures during the pressing and sintering stages, all in accordance with the experimental design plan. The microstructure, chemical composition, and elemental distribution of the samples were examined using scanning electron microscope equipped by energy dispersive X-ray analyzer, and an optical microscope. In order to study the corrosion resistance, potentiodynamic polarization test and electrochemical impedance spectroscopy were performed in 3.5 wt.% NaCl solution. The results revealed that co-incorporation of SiC and mica particles in Cu–10Sn bronze matrix increases the corrosion resistance, with a synergistic effect between these particles. The result of optimization process showed that the highest corrosion resistance could be achieved for the composite with the composition of Cu–10Sn/9.85SiC/0.67mica. This outcome was subsequently validated through experimental procedures.

Investigation of electrical ageing effects on the structural and electrical properties of polystyrene by charging and discharging current method

Abstract This study focuses on isothermal charging and discharging currents in polystyrene (PS). It is a well known fact that the discharging current is almost the mirror symmetry of the charging current at low electric fields. However, the experimental results presented and discussed in this study have revealed the possibility of an abnormal discharging current (ADC) flowing in the same direction as the charging current. Furthermore, electrical measurements implied that the electrical ageing of PS resulted in a significant increase in the charging current, even for extended ageing periods. Moreover, the intensity and duration of the reverse discharging current have evolved with electrical ageing. This characteristic can be attributed to the presence of ionic impurities both trapped at the polymer surface and in the bulk structure. To highlight the structural changes induced by electrical ageing, detailed structural analyses were conducted using Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) analysis. 

ZnS@ fluorenone derived multifunctional quantum dots for simultaneous recognition of bovine serum albumin (BSA) and copper ions (Cu2+) in aqueous blood and urine samples

An efficient synthesis of water-stable and fluorescent ZnS quantum dots has been executed beginning with its organic predecessor possessing fluorenone for sensing bovine serum albumin (BSA) among other proteins. Moreover, the organic predecessor of quantum dots has also been utilized for sensing of F- ions with binding constant of 1.8 × 104 M−1. Various spectroscopic techniques such as high-resolution transmission electron microscopy (HRTEM), powder X-ray diffraction (PXRD), UV-visible (UV-vis), Fourier transform infrared (FTIR), thermogravimetric (TGA), Energy dispersive X-ray analysis (EDX), circular dichroism (CD) and Fluorescence (FL) spectroscopy have been utilized for the characterization of the developed quantum dots. The emission properties of quantum dots made them useful for the sensing of BSA and Cu2+ accompanied with secondary sensing of urea. The LODs value for BSA and Cu2+ were calculated as 213 and 211 nM, respectively. Demonstrating remarkable efficacy, these quantum dots have been successfully employed for the discernment of BSA in human blood and urine samples, achieving an outstanding recovery rate of up to 99.8%.

Characterizing boron-enhanced one-part alkaline-activated mortars: Mechanical properties, microstructure and environmental impacts

Since alkali activators negatively effect the environmental impact assessment, it is necessary to develop the alternative activators from natural sources with low environmental impact. Therefore, in this study, the usage of boron refined products colemanite, ulexite and boron pentahydrate as activators in slag-based alkali-activated mortar systems was investigated in detail. Flexural and compressive strength tests, isothermal calorimetry measurement, thermogravimetric and differential thermal analysis, inductively coupled plasma mass spectrometry analysis, field emission scanning electron microscopy, and energy dispersive analysis and elemental mapping and X-ray diffraction analysis were carried out on the samples. In addition, sample production was subjected to life cycle analysis (LCA) with a cradle-to-gate approach using two different transportation scenarios. According to the results obtained, it was determined that colemanite, ulexite and boron penta hydrate, when used in optimum proportions, had a positive effect on strength (up to increase 40% compressive strength by 20% ulexite replacement) and could be used as an activator in slag-based alkali-activated systems. The positive results obtained in strength as a result of using boron-refined products are also supported by other test results conducted within the scope of the study. Furthermore, according to the LCA results, it was observed that there was a significant decrease in global warming potential with the substitution of 20% colemanite, ulexite or boron pentahydrate as activators, not only compared to the reference sample but also traditional cementitious systems.

Hal-Py-SO3H as a novel and recyclable catalyst for highly efficient synthesis of xanthene and spiropyran derivatives

The aim of this research is to synthesize a new sulfonic acid catalyst based on halloysite nanotubes (Hal-Py-SO3H) and characterize it as a solid acid nanocatalyst by various analytical techniques such as Fourier-Transformed Infrared spectroscopy (FTIR), Thermal gravimetric Analysis (TGA), X-ray Diffraction (XRD) analysis, Scanning Electron Microscopy (SEM), Vibrating Energy-Dispersive X-ray analysis (EDX), Transmission electron microscopy (TEM) and X-ray atomic mapping. Furthermore, this new catalyst was evaluated in synthesizing spiropyran derivatives via multicomponent reactions (MCRs) and Xanthen derivatives under environmentally sustainable conditions. The main advantages of this approach include green conditions, excellent yields, quick reaction rates, and ease of preparation. Additionally it was observed that the catalyst exhibited robust stability even after multiple recycling processes, indicating its potential for practical applications in sustainable chemical transformations.

Facile Preparation of Gold Nanoparticles Silica Composite Film Embedded in Anodized Aluminium Oxide-Glass Substrate

Thin film based on gold nanoparticles or AuNPs is typically used as catalyst in the industrial processes due to their high stability and good reusability. In this work, a thin AuNPs-silica composite film was fabricated firstly from sol-gel method by mixing gold pyrazolate complex to a medium comprised of ethanol, deionized water, and hydrochloric acid followed by addition of tetrabutyl orthosilicate as silica source. Next, 70 microliters of the sol-gel solution were spin-coated on several type of substrates such as glass, anodized aluminium oxide or AAO, and combination of both to yield gold complex-silica composite film. It was found that gold complex-silica composite film fabricated on combination of both AAO-glass substrate gave the best quality based on its surface thickness, layer uniformity and film brittleness. Later, the film was selected and subjected to thermal hydrogen reduction at 210 degrees Celsius for 2 hours to facilitate the formation of gold nanoparticles to give AuNPs-silica in AAO-glass film. Before the heat treatment, the light-brownish colour of the original gold complex-silica in AAO-glass film in daylight will appear as a pinkish red film under UV light, suggesting the interaction between gold atoms and supported by its luminescence spectrum at 692 nm. Upon heat treatment, the resulting AuNPs-silica in AAO-glass film gave a deep-red colour indicating the successful formation of AuNPs. The presence of AuNPs in the film was further confirmed based on the absorption peak at 545 nm, X-ray diffraction pattern at 38.20 degrees for d111 plane in wide-angle region, transmission electron microscopy images showing a small and sphere shape particles as well as its elemental composition in energy dispersive X-ray analysis. Moreover, scanning electron microscope images also suggested that the AAO pores is fully filled with the composite and is in accordance with its surface roughness study via atomic force microscopy analysis.

Green Silver Nanoparticles Synthesized Using Lignin Extracted from Phoenix Dactylifera Seed: Application as Electrochemical Sensor for the Monitoring of Ornidazole

Abstract Lignin is the second most common biopolymer after cellulose and the most-available renewable source of aromatic groups in nature. The alkaline method was used to extract lignin from Phoenix dactylifera seeds powder. The current research aims to use extracted lignin as a reducing and stabilizing agent for ecofriendly manufacturing of silver nanoparticles (Lig-AgNPs). The prepared Lig-AgNPs were characterized by UV-Vis, scanning electron microscopy, and energy-dispersive X-ray analysis techniques. Moreover, they were further used to modify the surface of a carbon paste electrode (CPE), and the resulting modified electrode (Lig-AgNPs/CPE) was applied for electrochemical detection of ornidazole (ODZ) according to optimum square wave voltammetry conditions. The prepared sensor Lig-AgNPs/CPE was able to identify ODZ (at BR buffer pH 2.3) in a linear range between 8.0×10-6 and 1.0×10-3 M, with DL of 0.362 µM and QL equal 1.21 μM, the acquired RSD was 3%. Additionally, the developed electrode Lig-AgNPs/CPE was successfully applied to detect ODZ in commercial milk, river water, and tap water with agreeable results.

Temperature sensing materials based on the fluorescence intensity ratio in Li2Ba5W3O15:Dy3+ phosphors

One of the interesting uses of phosphors is the development of non-contact thermometers apart from their usage as visible photonic devices. A series of Dy3+-doped Li2Ba5W3O15 (LBW) phosphors were successfully synthesized using high temperature solid-state reaction process. The crystal structure and morphology of LBW:xDy3+ phosphors were studied using X-ray diffraction (XRD), Rietveld refinements and field effect scanning electron microscopy (FE-SEM) with energy dispersive x-ray (EDX) analysis. The XRD and photoluminescence (PL) analyses validated the effective substitution of Ba2+ ions with Dy3+ ions. Two prominent emission peaks were found at 493 and 583 nm corresponding to 4F9/2→6H15/2 and 4F9/2→6H13/2 transitions respectively under 368 nm excitation wavelength. A comprehensive analysis has been carried out on the usage of the Dy3+ doped LBW phosphors in fluorescence intensity ratio (FIR) thermometry. The optical temperature measurement performance of the LBW:xDy3+ phosphor was achieved by utilizing distinct thermal quenching transitions, specifically on 4F9/2→6H15/2,13/2, at temperatures ranging from 293 to 443 K. The as-prepared phosphors demonstrate excellent performance as optical thermometers, with a maximum relative sensitivity (Sr) of 0.7% K−1 at 293 K, an absolute sensitivity (Sa) of 4.68 K−1 at 443 K and a temperature resolution of ∼0.51 at 443 K. These values indicate that the phosphors are highly responsive to changes in temperature, making them suitable for non-contact thermometry applications.

Greener approach for the synthesis of Ag decorated ZnO–CeO2 nanostructure using Moringa oleifera LE and its investigation photocatalyst for degradation of ciprofloxacin and methylene orange

Green synthesis of silver decorated ZnO–CeO2 nanostructure (Ag@ZnO–CeO2 NS) mediated Moringa oleifera LE and its photocatalytic potential against ciprofloxacin antibiotic and Methylene orange dye under sunlight. The synthesized ZnO–CeO2 and Ag@ZnO–CeO2 NS were characterized using X-ray diffraction (XRD) analysis. The crystallite size and crystallinity were calculated to 74 nm and 89% respectively using XRD analysis. X-ray photoelectron spectroscopy (XPS) analysis confirmed the presence of Ag, Zn, Ce and oxygen vacancies in green synthesized Ag@ZnO–CeO2 NS. Also, PL spectroscopy analysis showed the oxygen vacancies due to defects in nanostructure. The bandgap of prepared nanostructure was calculated to 2.0 eV by UV–visible spectroscopy analysis. Ag@ZnO–CeO2 NS average particles size was evaluated to 40 nm by scanning electron microscopy (SEM) analysis and energy-dispersive X-ray (EDX) analysis confirmed the presence of Ag, Zn and Ce in nanostructure. The Ag@ZnO–CeO2 NS showed an excellent Brunauer-Emmett-Teller (BET) surface area of 165 m2g-1 and 15 nm of pore diameter. Moreover, Fourier transform infrared (FTIR) spectroscopy was used to analyze chemical bonding and interaction and RAMAN spectroscopy confirmed the presence of oxygen vacancies. The thermal decomposition and heat flow was accessed by thermogravimetric analysis (TGA) and Differential scanning calorimetry (DSC) The Ag@ZnO–CeO2 NS demonstrated great potential for environmental remediation which offered effective approach for the removal of Ciprofloxacin antibiotic and Methylene orange dye from wastewater with 74% and 85% photocatalytic activity respectively. The stability of catalyst after 5 cycles of reusability was evaluated by XRD analysis which showed the crystalline structure. This research contributes to the development of advanced nanomaterials with improved photocatalytic properties and the removal of emerging contaminants.

Room temperature ferromagnetism in undoped and Fe doped Zn3P2 nanoparticles: Structural, optical and magnetic properties

In the current study, the structural, optical, and magnetic characteristics of Fe-doped Zn3P2 nanoparticles prepared by the solid-state reaction technique with various concentrations of Fe (x = 0.00, 0.02, 0.04, 0.06, and 0.08) were investigated. Studies using X-ray diffraction (XRD) verified that all of the produced samples had a tetragonal structure without any other phase, and that the lattice parameters increased (a = 8.090 Å, c = 11.421 Å to a = 8.120 Å, c = 11.499 Å) as the amount of dopant increased. The scanning electron microscopy (SEM) performed on the sample demonstrates that the grain size is almost spherical. The size of agglomerations slightly increases with increasing dopant concentration. The results of an energy dispersive X-ray analysis (EDAX) are almost exactly what was anticipated for the atomic weight ratios. The optical bandgap of the samples went from being 1.406 eV to being 1.453 eV when the dopant concentration was raised. When excited at wavelengths of 210 nm and 240 nm, rather than 307 nm, very intensity Photoluminescence (PL) emission spectra were detected in all of the samples. Vibrating sample magnetometer (VSM) verified that magnetic moment is found to increase (0.08829 emu/g to 0.23125 emu/g) with increase of dopant concentration from 0.02 to 0.08.

Exploring tool geometry influence on EDD of Waspaloy

ABSTRACT Electric discharge drilling (EDD) is a competent method for drilling hard-to-cut materials despite its drawbacks, including minimum material removal rate (MRR), excess tool wear rate (TWR), high surface roughness (R a ), and power consumption (PC). To address these issues, EDD’s performance was explored by varying factors like tool electrode geometry (TEG), current (I), pulse-on-time (TON ), and tool electrode speed (TES) to investigate the effect on MRR, TWR, R a , and PC. Cu-6 produced the highest MRR of 36.26 mm³/min, surpassing Cu-7, Cu-8, and Cu-solid by 28.309%, 44.866%, and 51.843% respectively. Cu-solid revealed the lowest TWR of 4.397%, significantly lower than Cu-6, Cu-7, and Cu-8. R a followed the trend: Cu-solid < Cu-8 < Cu-7 < Cu-6. Cu-solid consumed more power than hollow electrodes. Microscopic analysis attributed rough surfaces to high currents. Energy dispersive X-ray (EDX) analysis exhibits material migration from a workpiece and tool electrode on the machined surface. .

Examining the effects of sintering temperature on double perovskite La2NiTiO6: Analysis of structural, optical, electrical properties, and leakage current characteristics

This study explores the influence of varying sintering temperatures on the structural, optical, electrical, and leakage current features of La2NiTiO6 (LNTO), a double perovskite material synthesized through the citrate auto-ignition method. The X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and energy dispersive X-ray (EDX) analysis were employed to investigate the structure, microstructure, and compositional distribution of the samples. The samples sintered at various temperatures showed the monoclinic structure with space group P21/n and were confirmed by Rietveld's refinement of the XRD patterns. The average grain size increased with higher sintering temperatures, which is consistent with the particle size estimated from the histogram plot of the FE-SEM data. The UV–visible (UV–Vis) spectroscopy showed that the energy band gap decreased as sintering temperatures increased. Impedance spectroscopy analysis revealed non-Debye type relaxation of charge carriers and confirmed the negative temperature coefficient of resistance (NTCR) behavior. Electrical analysis affirmed that the direct current (DC) conductivity is thermally activated, following the Arrhenius equation with an inverse temperature dependency. As the sintering temperature increases, the leakage current density decreases, and the leakage current conforms to the ohmic conduction mechanism.