X-ray Diffraction Patterns Research Articles

Effects of Eucommia ulmoides leaf powder on the gelatinization, rheology, and gel properties of sweet potato starch

Effects of Eucommia ulmoides leaf powder on the gelatinization, rheology, and gel properties of sweet potato starch

Influence of Laser Energy on the Structural and Optical Properties of Sn Nanoparticles produced with Laser-Induced Plasma

This study aimed to investigate the structure and optical properties of Sn nanostructures. Thin tin (Sn) films were deposited on glass substrates using the pulsed laser deposition method. Nd:YAG laser with fundamental wavelengths of 532 nm and 1064 nm was used to create Sn nanostructures with varying energies of 400 mJ to 700 mJ and the same frequency of 6 Hz. The tin powder was compressed into a disc with a one-centimetre diameter to serve as a sample. The X-ray diffraction (XRD) pattern showed a crystalline structure with several Sn nanostructures peaks at various energies (400–700 mJ). The results revealed a crystalline size of 65.90 nm and 86.55 nm at 700 mJ, while the size was 40.19 nm and 17.19 at 400 mJ for the given wavelengths (532nm and 1064 nm), respectively. The appearance of Sn nanostructures and the aggregation of, particularly in the form of cauliflower, were revealed in Field emission scanning electron microscopy (FE-SEM) images. The results of the dispersive energy X-ray spectroscopy (EDS) analysis showed that various amounts of tin, carbon, and oxygen were present. Additionally, the optical characteristics were investigated of each film using absorbance spectra, which covered a range of wavelengths from 190 to 1100 nm. As the laser power increased, the band gap energy values in the optical properties decreased, falling into the ranges of 3.06 to 1.65 eV and 3.22 to 1.82 eV at 1064nm and 532nm, respectively.

Synthesis of Nano Sulfur/Chitosan-Copper Complex and Its Nematicidal Effect against Meloidogyne incognita In Vitro and on Coffee Pots.

Sulfur is one of the inorganic elements used by plants to develop and produce phytoalexin to resist certain diseases. This study reported a method for preparing a material for plant disease resistance. Sulfur nanoparticles (SNPs) stabilized in the chitosan-Cu2+ (CS-Cu2+) complex were synthesized by hydrolysis of Na2S2O3 in an acidic medium. The obtained SNPs/CS-Cu2+ complex consisting of 0.32% S, 4% CS, and 0.7% Cu (w/v), contained SNPs with an average size of ~28 nm as measured by transmission electron microscopy images. The X-ray diffraction pattern of the SNPs/CSCu2+ complex showed that SNPs had orthorhombic crystal structures. Interaction between SNPs and the CS-Cu2+ complex was also investigated by ultraviolet-visible. Results in vitro nematicidal effect of materials against Meloidogyne incognita showed that SNPs/CS-Cu2+ complex was more effective in killing second-stage juveniles (J2) nematodes and inhibiting egg hatching than that of CS and CS-Cu2+ complex. The values of LC50 in killing J2 nematodes and EC50 in inhibiting egg hatching of SNPs/CS-Cu2+ complex were 75 and 51 mg/l, respectively. These values were lower than those of CS and the CS-Cu2+ complex. The test results on the nematicidal effect against M. incognita on coffee pots showed that the SNPs/CS-Cu2+ complex was 100% effective at a concentration of 150 mg/l. Therefore, the SNPs/CS-Cu2+ complex could be considered as a biochemical material with potential for agricultural applications to control root-knot nematodes.

Green Synthesis of Silver Nanoparticles using Coriandrum sativum and Murraya koenigii Leaf Extract and its Thrombolytic Activity.

Plants have been used for ages in traditional medicine, and it is exciting to perceive how recent research has recognized the bioactive compounds liable for their beneficial effects. Green synthesis of metal nanoparticles is a hastily emergent research area in nanotechnology. This study describes the synthesis of silver nanoparticles (AgNPs) using Coriandrum sativum and Murraya koenigii leaf extract and its thrombolytic activity. The aim of the study was to determine the clot lysis activity of Coriandrum sativum and Murraya koenigii synthesized silver nanoparticles. Leaves of Coriandrum sativum and Murraya koenigii were collected. Methanolic extraction of the plant sample was done through a Soxhlet extractor. The methanolic extract obtained from both the leaves was subjected to GC-MS analysis. The synthesized NPs from leaf extracts were monitored for analysis, where the typical X-ray diffraction pattern and its diffraction peaks were identified. 3D image of the NPs was analysed by Atomic Force Microscopy. The surface charge of nanoparticles was identified by Zeta potential. The Clot lysis activity of Coriandrum sativum and Murraya koenigii synthesized silver nanoparticles were analysed by the modified Holmstorm method. The thrombolytic property of the methanolic extract of plants Coriandrum sativum showed clot lysis activity at 2.5 mg/mL with 45.99% activity, and Murraya koenigii extract with 66.56% activity. The nanoparticles (Nps) from Coriandrum sativum showed clot lysis activity at 2.5 mg/mL with 58.29% activity, and NPs from Murraya koenigii with 54.04% activity. Coriandrum sativum in GC-MS exhibited 3 peaks, whereas Murraya koenigii extract showed five peaks with notable bioactive compounds. These NPs were further used for biomedical applications after being fixed by an organic encapsulation agent. The present research reveals the usefulness of Coriandrum sativum and Murraya koenigii for the environmentally friendly manufacture of silver nanoparticles.

Preparation, Characterization, and Evaluation of the Anticancer Effect of Mesoporous Silica Nanoparticles Containing Rutin and Curcumin.

The aim of this study was the preparation of mesoporous silica nanoparticles co-loaded with rutin and curcumin (Rut-Cur-MSNs) and the assessment of its physicochemical properties as well as its cytotoxicity on the head and neck cancer cells (HN5). Besides, ROS generation of HN5 cells exposed to Rut-Cur-MSNs was evaluated. Several investigations showed that rutin and curcumin have potential effects as anticancer phytochemicals; however, their low aqueous solubility and poor bioavailability limited their applications. The assessment of physicochemical properties and anticancer effect of prepared nanoparticles was the objective of this study. The physicochemical properties of produced nanoparticles were evaluated. The toxicity of Rut-Cur-MSNs on HN5 cells was assessed. In addition, the ROS production in cells treated with Rut- Cur-MSNs was assessed compared to control untreated cells. The results showed that Rut-Cur-MSNs have mesoporous structure, nanometer size and negative surface charge. The X-ray diffraction pattern showed that the prepared nanoparticles belong to the family of silicates named MCM-41. The cytotoxicity of Rut-Cur-MSNs at 24 h was significantly higher than that of rutin-loaded MSNs (Rut-MSNs) and curcumin-loaded MSNs (Cur-MSNs) (p<0.05). The achieved results recommend that the prepared mesoporous silica nanoparticles containing rutin and curcumin can be a useful nanoformulation for the treatment of cancer. The produced nanomaterial in this study can be helpful for cancer therapy.

Constrution of Quinazoline-Linked Covalent Organic Frameworks via a Multicomponent Reaction for Photocatalysis.

Quinazoline (Qz)-linked covalent organic frameworks (COFs) have been constructed via a three-component reaction of ortho-acylanilines, benzaldehydes and NH4OAc. The structure of Qz-COFs has been confirmed by solid-state nuclear magnetic resonance spectroscopy, Fourier transform infrared and powder X-ray diffraction patterns. The Qz-COFs possess high chemical stability, showing good endurance to strong acid, strong base, oxidant, reductant and other conditions. Particularly, Qz-COF-3 can catalyze the aerobic photooxidation of toluene and other compounds containing C(sp3)-H bonds.

Eco-synthesis route: Developing bis-hydrazono[1,2,4]-thiadiazoles via a green synthetic approach with calcium oxide-chitosan nanocomposite

Modern environmental organic chemistry is focused on developing cost-efficient, versatile, environmentally acceptable catalytic chemicals that are also highly effective. Herein, hybrid calcium-chitosan nanocomposite films was prepared by doping calcium oxide molecules into a chitosan matrix at weight percentage (15, 20, and 25 % wt. chitosan‑calcium) using an easy and affordable simple co-precipitation process. The CS–CaO nanocomposite's structure was elucidated using analytical techniques such as Fourier transform infrared (FTIR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). Based on the X ray diffraction (XRD) measurements, the crystallinity was reduced by the incorporation of the CaO molecules. Also, from the calculation of the Debye-Scherrer equation on this X-ray diffraction (XRD) pattern, the crystallite size was found to be 17.2 nm for the nanocomposite film with 20 % wt. The energy dispersive spectroscopy graph demonstrated the presence of the distinctive Ca element signals within the chitosan, with the amount in a sample of 20 % wt. being discovered to be 21.32 % wt. For the synthesis of bis-hydrazono[1,2,4]thiadiazoles, the obtained CS–CaO nanocomposite could be employed as a potent heterogeneous recyclable catalyst. Better reaction yields, quicker reactions, softer reaction conditions, and green reusable efficient biocatalysts for several uses are just a few advantages of this approach.

Dy3+ doped KCa(PO3)3 phosphor for white light generation: structural and luminescent studies

Using the traditional solid-state reaction approach, Dy3+ ions doped KCa(PO3)3 phosphors have been synthesized to investigate their luminescent properties to produce high-quality white light for solid-state lighting applications, particularly in white LEDs. x-ray diffraction (XRD) patterns were used to examine the structure and phase of the phosphors. Using scanning electron microscopy (SEM), the morphology of the as-synthesized phosphor has been investigated. Fourier transform infrared spectroscopy (FT-IR) has been used to investigate several vibrational bands seen in the phosphor. Using diffuse reflectance spectra (DRS), the as-synthesized phosphors’ optical band gap values have been estimated. When Dy3+ ions are excited at 350 nm, the photoluminescence (PL) spectra characteristics observed for the activated KCa(PO3)3 phosphor show strong white area emission due to both 575 nm, which is related to the 4F9/2 → 6H13/2 and 482 nm that is ascribed to 4F9/2 → 6H15/2 transition of Dy3+ ions. Additionally, the concentration quenching of Dy3+ ions doped at 4 mol% is seen in the PL spectra. Based on the observed PL spectra, the computed CIE chromaticity coordinates for the optimised KCa(PO3)3 phosphors are located in the deep white area. The lifespan of the as-titled phosphors decreases as the amount of Dy3+ ions increases in the host lattice. Additionally, the PL decay profiles shows a dual exponential behaviour when excited at 350 nm, with an emission wavelength at 575 nm. The lifetime values were used to calculate the quantum efficiency of the as prepared phosphors. On the basis of the results of the aforementioned studies, we wish to project Dy3+ ion doped KCa(PO3)3 phosphors as white light generating materials in w-LEDs and for other photonic applications.

Eco-Friendly Synthesis of CuO@ZnO Nanocomposites Using Artemisia vulgaris Leaf Extract and Study of Its Photocatalytic Activity for Methylene Blue

In this study, copper oxide nanoparticles (CuO NPs), zinc oxide nanoparticles (ZnO NPs), and copper oxide/zinc oxide nanocomposites (CuO@ZnO NPs) were synthesized by green synthetic route where bioactive compounds inherently present in the leaf extract of Artemisia vulgaris act as stabilizing and reducing agents. Phytochemicals present in leaf extract were assessed by qualitative chemical tests and spectroscopic measurements. UV-visible spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, Energy Dispersive X-ray (EDX) spectroscopy, X-ray Diffraction (XRD), and Field Emission Scanning Electron Microscopy (FESEM) were used to characterize the as-synthesized nanomaterials, i.e., CuO, ZnO, and CuO@ZnO NPs. XRD pattern revealed the crystalline nature of nanoparticles. Based on the Debye–Scherrer formula, the sizes of CuO NPs, ZnO NPs, and CuO@ZnO NCs were found to be 17.24, 20.74, and 22.50 nm, respectively. The band gap of the as-prepared nanomaterials was measured using the Tauc plot. Using the nanomaterials, MB degradation was studied at room temperature under exposure to UV light. The degradation efficiency of CuO, ZnO, and 2% CuO@ZnO was found to be 52%, 68%, and 98%, respectively. Kinetic degradation process reveals that the CuO@ZnO NCs showed a better photocatalytic activity on MB dye with the degradation constant of 0.04124 min−1 compared to those of either constituent. Based on the findings, it was found that CuO@ZnO nanocomposites have the potential to degrade MB as an organic dye and can be used for wastewater treatment.

Effect of stabilization and carbonization treatment on the chemical and physical transformation of polyacrylonitrile (PAN) based electrospun carbon nanofibers

The present study delves into the production of carbon nanofibers (CNFs) utilising electrospun polyacrylonitrile (PAN) nanofiber mats, with a specific focus on the influence of oxidative stabilisation and carbonisation treatments. This research aims to thoroughly understand how variations in stabilisation time and temperature, as well as carbonisation temperature, impact the CNFs properties. These properties include fiber size, morphology, chemical and crystal structure transformation, thermal behaviour, and surface characteristics. Our methodology involved a detailed examination of the thermal treatment processes, where we observed a significant decrease in fiber size, though the surface morphology of the fibers remained largely unaffected. We employed Fourier-transform infrared (FTIR) spectroscopy to track the transformation of nitrile groups in PAN to imine groups, which indicated the progression of cyclisation reactions. Complementary analyses through differential scanning calorimetry (DSC) confirmed a high degree of these reactions, particularly at stabilisation temperatures extending to 250 °C and beyond. The cyclisation process was found to be complete during the carbonisation phase, at temperatures reaching 450 °C and above. Further, x-ray diffraction (XRD) patterns offered insight into the changes in the crystal structure, particularly in the packing of the d(002) spacing because of the stabilisation and carbonisation processes. This findings from this study not only elucidate the intricate process of CNFs production from electrospun PAN nanofiber mats but also highlight the critical factors that influence their final properties. These insights are invaluable for the development of advanced CNFs with tailored properties suitable for a range of applications, including but not limited to energy storage, electronics, and as supporting materials in various technological domains.

Effect of annealing temperature on physical properties and photoelectrochemical behavior of electrodeposited nanostructured NiO thin films for optoelectronic applications

Our paper used a low-cost electrodeposition technique to grow Nickel Oxide (NiO) thin films on fluorine-doped tin oxide (FTO) substrate. As-deposited films were annealed at different temperatures (350, 400, 450, and 500 °C). X-ray diffraction (XRD), Raman spectroscopy (RAM), scanning electron microscopy (SEM), UV–vis spectrophotometer, photoluminescence (PL), Cyclic voltammetry (CV), photocurrent (PC), electrochemical impedance spectroscopy (EIS), and Mott-Schottky analysis (MS) were used to study and investigate the effect of annealing temperatures on the structural, morphological, electrical, and optical properties of prepared thin films. XRD patterns proved the cubic phase of all NiO samples with the preferential orientation in (111) direction. SEM results showed that the grain size increased with increasing annealing temperature. The optical transmission was studied by a UV–vis spectrophotometer, where high transmittance for NiO thin films was found to vary in the range of 73–84 % in the visible wavelength region, depending on the annealing temperatures. At the same time, UV–visible measurements indicate an absorption band edge at 311 nm, mainly recognized as a characteristic direct band gap for prepared NiO. The optical gap calculated from the Tauc relation showed a decreasing trend from 3.97 to 3.86 eV with increasing annealing temperature from 300 °C to 500 °C. PL spectra of synthesized samples revealed two distinct emission peaks at around 400 nm and 490 nm. RAM analysis confirmed the presence of three characteristic peaks related to the vibration of Ni–O bonds. The NiO film annealed at 500 °C displays the highest specific capacitance value by CV analysis. The P-type conductivity of manufactured arrays and enhanced electrical properties were confirmed by PC, EIS, and MS analysis. The highest carrier concentration values (9.19 × 1018 cm−3) and flat band potential (0.82 V) were obtained for samples annealed at 500 °C. Our outcomes proved that NiO-500 °C thin films are ideal candidates for optoelectronic applications.

A comparative study of thin-film transistors based on mist-CVD deposited InAlZnO with different Al contents

In this study, amorphous InAlZnO thin films with varying In:Al:Zn mole ratios of 2:1:2, 4:1:4, and 8:1:8 are deposited using mist chemical vapor deposition (mist-CVD). The X-ray diffraction patterns suggest that these InAlZnO thin films are amorphous. Besides, the O 1s binding energy spectra observed by X-ray photoelectron spectroscopy, photoluminescence, and Tauc plots indicate that oxygen vacancy within the InAlZnO films decreases and bandgap energy of the InAlZnO films increases when the InAlZnO films have higher Al content. The 2:1:2 ratio yields insufficient electrical performance, while the 4:1:4 ratio obtains higher field-effect mobility of 11.42 ± 2.09 cm2V−1s−1, the steepest subthreshold swing of 168.57 ± 27.66 mV/dec, the largest on/off current ratio of (1.76 ± 0.3) × 106, and more stable behavior under negative/positive bias illumination stress. The 8:1:8 ratio reaches the highest field-effect mobility of 27.31 ± 5.13 cm2V−1s−1 while scarifying the stability. This study highlights the impact of Al content on InAlZnO for thin-film transistor applications.

Synergistic effects of La-doping on ZnO nanostructured photocatalysts for enhanced MB dye degradation

In this work, we present the design and characterization of pristine and La-doped ZnO photocatalysts, prepared via a facile co-precipitation technique. A comprehensive range of characterization techniques was employed to analyze the physicochemical properties of these synthesized nanostructured photocatalysts. The slight shift in the position of peaks in the X-ray diffraction (XRD) pattern confirms successful doping (La3+) of ZnO. Additionally, the identified wurtzite phase further validates the presence of ZnO nanostructures. Subsequent photocatalytic investigations were conducted using model solutions of water and methylene blue (MB) dyes under solar irradiation, meticulously comparing the performance of pure ZnO with La3+ doped ZnO. Over the time span of 90 min, the 5 % La-doped ZnO photocatalysts exhibited an impressive 98 % degradation efficiency for MB dye, surpassing the performance of the pristine ZnO counterpart (0 % La), which achieved only 51 % degradation. This emphasizes the pronounced enhancement resulting from the incorporation of La ions. The photoluminescence (PL) spectra insights with 5 % La3+doping exhibit significant quenching, caused by the suppression of charge carrier recombination, which enhances the photocatalyst's charge transport. X-ray photoelectron spectroscopy (XPS) spectra provided crucial insights into the elemental composition and chemical states of the 5 % La3+ doped ZnO nanostructures. Through systematic reusability assessments, it was established that the 5 % La-doped ZnO photocatalysts maintain their efficiency for up to four cycles, without displaying a significant reduction in removal efficacy. This emphasizes the inherent reliability and robustness of the developed photocatalysts.

Impedance spectroscopy investigation on the electrical response and optical characteristics of novel Sr2TiZrO6 double perovskite

This study centers on the synthesis and characterization of a novel double perovskite, termed Sr2TiZrO6 (STZO), which was synthesized using the conventional solid-state reaction method and subsequently calcined at 1000 °C for 12 h. X-ray diffraction (XRD) pattern refinement confirmed the formation of the tetragonal phase Sr2TiZrO6 (space group P4mm), while both XRD and scanning electron microscope (SEM) analyses revealed that the resulting STZO displaying spherical-like grains with nanometric diameters. Thermogravimetric analysis revealed a minor weight loss attributed to the emergence of the ZrO2 phase and the formation of the STZO double perovskite. The diffuse reflectance spectroscopy (DRS) results demonstrated strong UV-light absorption, with an optical absorption onset below 400 nm. The obtained band gap for direct transitions of the STZO sample is equal to 3.26 eV. The conductance and impedance study of the STZO sample are investigated. The present properties provide crucial insights to enhance comprehension of the STZO double perovskite material, which holds promise as a viable candidate for a range of applications, such as solar cells and photodiodes.

Investigations of structural, photoluminescence, colorimetric, lifetime, and luminous efficiency of Tb3+ and Sm3+ co-doped calcium tungstate for WLEDs

Structure, photoluminescence, colorimetric, and thermoluminescence analysis of Ca1-x-yTb2x/3Sm2y/3WO4; x = 0.01; y = 0.01–0.05 ceramics are reported in this manuscript. The materials are made by the use of the solid-state method. Reitveld refinements of the obtained X-ray diffraction patterns are done by using the Fullprof Suite software. The obtained results denoted that the synthesized materials have a tetragonal structure and I41/a space group. Energy bandgaps are found in the UV–visible absorbance spectra. Photoluminescence investigations of the phosphors are done. The critical quenching concentrations of the phosphor are found to be x = 0.01; and y = 0.04. Moreover, the critical distance of energy shift with the adjacently presented ions is computed. Dexter’s theory is employed to elucidate that the dipole-dipole electronic interactions are the imperative reasons for the transfer of energy in the phosphor. The white color of emission is achieved for x = 0.01, y = 0.04 Tb, and Sm doped CaWO4 material. Moreover, great values in color purity, correlated color temperature, color rendering index as well as luminous efficiency of radiation are obtained from the CIE Chromaticity coordinates. Quantum yield efficiency of x = 0.01, y = 0.04 Tb & Sm codoped CaWO4 is measured. Photoluminescence decay analysis of all the samples is done to study the long-after glow properties and also the average lifetime values are evaluated. This is an indication of the suitable usage of the prepared materials in the white light-emitting diodes. Concentration as well as dose-dependent Thermoluminescence spectroscopy is investigated thoroughly. Kinetic parameters are calculated by deconvoluting the spectra of x = 0.01; y = 0.01 Tb & Sm codoped CaWO4 irradiated with 15 min of UV excitation dose. These results are denoted by high trap depth, second-order kinetics, and low UV dosimetry of the phosphor.

Exploring 2D X-ray diffraction phase fraction analysis with convolutional neural networks: Insights from kinematic-diffraction simulations

AbstractDeep-learning models are effective for analyzing the complex information in 2D X-ray diffraction (XRD) patterns. Accurately collecting parameters of the material sample is crucial during model training, significantly impacting model performance. In this study, we employ a kinematic-diffraction simulator to generate simulated 2D XRD patterns for Ti–6Al–4V alloy, allowing precise control of sample parameters. These simulated patterns are used to train convolutional neural networks, predicting $$\upbeta$$ β -phase volume fractions. The training data set consists exclusively of 2D XRD patterns with pure $$\upalpha$$ α - or pure $$\upbeta$$ β -phase, while the testing set incorporates patterns with intermediate phase volume fraction. In particular, we investigate how the architectures of the model influence prediction reliability and computational performance. Experimental results reveal that, with appropriate training, the convolutional neural network accurately detects intermediate phase volume fractions even trained with only pure-phase patterns, achieving a mean square error accuracy of $$9.4 \times 10^{-4}$$ 9.4 × 10 - 4 . Graphical abstract

Effect of manganese (Mn) doping on the structural, dielectric, ferroelectric, and ferromagnetic properties of ceria (CeO2)

The Ce1-xMnxO2 ceramics were prepared using a solid-state route, with Mn doping concentrations of (x = 0.00, 0.03, 0.08, 0.13, and 0.18). Examination of X-ray diffraction patterns confirms the effective insertion of Mn into the CeO2 lattice, resulting in discernible changes in oxygen vacancy concentration and lattice expansion. X-ray photoelectron spectroscopy (XPS) analysis confirmed the presence of Ce3+, Ce4+, Mn3+, and Mn2+ oxidation states. The Photoluminescence (PL) spectra reveal the existence of oxygen vacancies, as manifested by the appearance of peaks within the energy range spanning from 3.1 eV to 2.71 eV. Raman spectra reveal a symmetric vibration around 466.81 cm-1 in all samples. The surface morphology of the samples exhibited subtle changes in grain size upon the introduction of Mn into CeO2. The dielectric behavior, investigated across a range of frequencies with varying Mn doping concentrations, exhibits an increased dielectric constant in Mn-doped CeO2, particularly with a smaller dielectric loss at lower frequencies. The ferroelectric response revealed a maximum recoverable energy density of 0.56 mJ/cm2 with an efficiency of 47.86% for CeO2. The room temperature magnetic response of the samples improved as Mn concentration increased, which is well explained by the Bound Magnetic Polarons (BMPs) and exchange interactions model. Overall, the studies show the effect of structural, electrical, and magnetic properties after doping with Mn, opening avenues for diverse applications of these ceramics.

Optimizing luminescent properties of ZnO: Er3+ through temperature and dopant variation: XRD and emission spectroscopy studies

This study focuses on optimizing the synthesis conditions for the luminescent properties of ZnO:Er3[Formula: see text], a key step toward improving its applicability in optoelectronics. X-ray diffraction (XRD) patterns at [Formula: see text]C with Er3[Formula: see text] dopant concentrations (1, 3 and 5[Formula: see text]wt.%) show the preservation of the crystalline phase of ZnO, indicating that the dopants did not affect the structural integrity. Luminescence properties were observed in ZnO with 1[Formula: see text]wt.% erbium doping at 900–[Formula: see text]C, with the sample at [Formula: see text]C exhibiting the highest emission peak at 533[Formula: see text]nm. The optimal conditions for significant luminescence were identified at [Formula: see text]C, with 5[Formula: see text]wt.% Er3[Formula: see text] showing the most pronounced effect. The practical implications of the achievement of optimal luminescence in ZnO:Er3[Formula: see text] are profound for optoelectronics. These conditions are critical for efficient light-emitting devices, particularly in applications such as light-emitting diodes (LEDs) and lasers, where emission characteristics have a direct impact on performance. In addition, the enhanced luminescence holds great promise for sensors, especially in biomedical and environmental monitoring, as well as in quantum technologies. It contributes to the advancement of quantum sensors and quantum computing applications. This research provides a basis for tailoring the properties of ZnO:Er3[Formula: see text] for specific applications by identifying optimal luminescence conditions at different dopant concentrations. While the identification of optimal conditions has been successful, further research is essential to unravel the underlying mechanisms at the atomic and molecular levels. Overcoming these challenges and exploring additional applications will be critical to realizing the practical impact of these findings in various technological fields, as the study paves the way for advances in optoelectronics, sensing, and quantum information processing.

Photoremoval of Ibuprophenin and Oxytetracycline and some microorganisms from a pharmaceutical wastewater via Ag-Fe3O4 nanocomposites

In İzmir Turkey, a pharmaceutical industry wastewater produces drugs and antibiotics. The removals of these parameters were not sufficient with the conventional activated sludge process. In order to remove these organics some photocatalysts like Fe3O4 and FeO were solely used with enhanced magnetic properties. However low photodegradation yields (75% - 77%) were detected for the Ibuprophenin drug and Oxytetracycline antibiotic. Although Ag effectively destroys the pharmaceutical chemicals and the pathogenic microorganisms the low photogenerated carrier-separation efficiency limits its application in water treatment. Therefore, it is practically significant to develop a magnetic material to a couple of Ag with Fe3O4 through heterojunctions to separate the nanocomposite magnetically from wastewaters. In order to improve the photocatalytic degradation of Fe3O4, Ag was loaded onto a magnetic nanoparticle to develop Ag-Fe3O4 nanocomposite under laboratory conditions. On the other hand, the toilet wastewater was mixed with the process wastewater due to the dilution purpose of pollutants in the pharmaceutical wastewater. Due to the high working personnel capacity of the industry (10,000 people) the concentrations of Salmonella, Pseudomonas, yeast, fungi, total coliforms, fecal coliforms, and heterotrophic bacteria were found to be high in the raw pharmaceutical industry wastewaters. Therefore, in this study to maximize the removal yields of these pollutants and organisms with Ag-Fe3O4 photodegradation the operational conditions were optimized. The effect of increasing Ag-Fe3O4 nanocomposite concentrations (0.05 - 6.0 mg/l), pollutant concentrations (10 - 500 mg/l), contacting times (5 - 90 mins), pH levels (4.00 - 10.00), power (10 - 100 W/m2), on the photodegradation yields of organisms (Salmonella, Pseudomonas, yeast, fungi, total coliforms, fecal coliforms, heterotrophic bacteria) and ibuprophene, oxytetracycline removal yields were studied. The particle shapes and properties were investigated with field emission scanning electron microscope (FESEM) and fourier transform infrared spectrophotometer (FTIR), X-ray diffraction (XRD). The XRD pattern of Ag-Fe3O4 nanocomposites showed the same diffraction peaks at 26.9°, 33.0°, 38.3°, 55.1°, 65.7°, and 68.7° for Ag and at 28.26°, 34.53°, 44.01°, and 61.88° for Fe3O4, indicating a good coupling of Ag and Fe3O4 with no change in their crystal structure. The maximum organism and pollutant yields were detected at 1 mg/l Ag-Fe3O4 nanocomposite concentration, after 45 mins at a pH 7.00 and 5.00 for Ibuprophenin drug and Oxytetracycline antibiotic, respectively. 99% treatment yields were recorded for ibuprophene, oxytetracycline, and organisms during photocatalysis. The recovery studies with Ag-Fe3O4 NPs showed that all organisms and both pollutants can be used 120 times with the same yields. The photodegradation kinetics was found to be pseudo-first-order and the rate constants (k) for oxytetracycline and ibuprophene were calculated as 5 × 10−2 min−1, and 5.02 × 10−2 min−1, respectively. From 1.5 mg/l Ag- Fe3O4 nanocomposite 0,95 mg/l Fe3+ and 0,39 mg/l Ag +1 was leached during ibuprophene photodegradation. For oxytetracycline from 1.5 mg/l Ag- Fe3O4 nanocomposite 0,89 mg/l Fe3+ and 0,34 mg/l Ag +1 was leached.

Chemical characterization of cement samples by radio-analytical methods namely external (in air) PIGE, INAA and ED-XRF for assessing their quality and method validation of radioanalytical techniques

This paper demonstrates novel application of neutron and proton based nuclear analytical techniques for the rapid evaluation of cement quality in terms of compressive strength using Ca to Si ratios. Preliminary phase characterization was performed using X-ray diffraction patterns. External PIGE method was optimized and applied for direct analysis of “as received” samples in thin mylar foils with reduced turn-around time of analysis. Moreover, Pneumatic Carrier Facility at Dhruva reactor of BARC was utilized for NAA for rapid and short irradiation of samples followed by analysis. Quality control of both NAA and PIGE methods were done using several geological Certified / Standard Reference Materials (CRMs and SRMs). EDXRF was employed as alternative analytical technique for comparative evaluation. Statistical evaluation was performed in terms of t-test and F-tests to understand the reliability of measurement and acceptable variance of the results. Eight cementitious samples were analyzed and their compressive strengths were evaluated using NAA and PIGE.