Elemental Composition Analysis Research Articles

Green synthesis of g-C3N4 decorated with SnO2 nanocomposites using a novel Ananas comosus crown extract for boosted performance of asymmetric supercapacitors

The recent development of green chemistry, when preparing nanoparticles using plants and their various parts has received a lot of attention in today's world. Metal and metal oxide nanoparticles have gained recognition for their recent advances in green synthesis. In this work, the green synthesis of a 2D g-C3N4 nanosheet decorated with SnO2 nanocomposite was prepared by Ananas comosus crown extract for electrochemical storage applications. The novel Ananas comosus crown extract acts as a reducing or capping agent for a green approach. The prepared g-C3N4/SnO2 nanocomposites were studied with structural, functional group, morphological, elemental composition, chemical state, and surface area analysis of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman, Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), Energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and Brunauer-Emmett-Teller (BET). SnO2 and various concentrations of g-C3N4 (25, 50, 75 & 100 mg) nanocomposite were investigated for electrochemical performance. At a current density of 1 Ag−1, the green synthesized (SnO2/g-C3N4 (50 mg)) SCN-50 nanocomposite displays a high specific capacitance of 302.7 Fg−1, as well as the composite demonstrates excellent capacitance retention of 94 % after 10,000 loops. Moreover, the asymmetric supercapacitor device of SnO2/g-C3N4//Activated carbon performed good reversible and cyclic stability with high energy and power density. The green synthesis of SnO2/g-C3N4 nanocomposite has promising electrode materials for future energy storage devices.

Elemental profiling of agricultural soil in Hoshiarpur utilizing analytical techniques.

Our study aimed to assess the soil quality in Punjab's Hoshiarpur district through a meticulous analysis of nutrient and elemental composition. Using a variety of analytical techniques, including Neutron Activation Analysis (NAA), external Particle-induced Gamma-ray Emission (PIGE) an Ion beam analysis Technique, and energy-dispersive X-ray fluorescence (ED-XRF), we delved into soil characterization for 22 agricultural soil samples in the Punjab region. Within the NAA framework, utilizing the Pneumatic Carrier Facility and the self-serve facility at Dhruva reactor in Mumbai, a brief 1-min irradiation procedure identified pivotal elements-Na, Mg, V, Al, Mn, and K. Conversely, an extended neutron irradiation process of approximately 4h within the self-serve facility enabled the estimation of nearly 12 elements, including Rare Earth Elements (REEs), Transition elements, and other significant elements. The external PIGE technique quantified low Z elements (Na, Mg, Al, and Si), contributing to our analytical arsenal. Rigorously validating both NAA and PIGE methodologies, we compared results meticulously against established geological standard reference materials-specifically USGS RGM-1 and USGS AGV-1.Instrumental in elemental analysis, ED-XRF spectroscopy fortified our investigative endeavors by quick assessment of ten crucial elements. The elemental analysis revealed notable accumulations of Mn and Zn in the soil, surpassing the suggested permissible limits, whereas Co, Cr, and Pb were found to be within the recommended thresholds set by WHO/UNEP. Beyond elemental profiling, our study extended to estimate the accumulation levels of various elements utilizing ecological risk factors such as Contamination Factor, Potential Ecological Risk Index, Pollution Load Index, and Geoaccumulation Factor. Our findings highlighted significant accumulation of REEs including La, Sm and Yb.. This evaluation sheds new light on the interplay between soil composition and environmental health, emphasizing the need for advanced accessible agricultural technologies to prevent and forecast contaminant discharge in arable soil. This commitment aligns with our broader goal of advancing sustainable practices in soil management.

Chemical evaluation and bioactivity of humic substances isolated from the mangrove ecosystem

Mangroves are an ecosystem that features dark colored sediment, rich in organic matter, with humic substances as its main component, which were the target of this work that aimed to characterize those humic substances chemically and spectroscopically and compare the biological activity of different humic materials isolated from mangrove areas with different levels of anthropic interference (Maria Ortiz high and Canal dos Escravos low). The chemical and spectroscopic characterization of the humic materials was performed through the analysis of elemental composition, E4/E6 ratio, fluorescence intensity and infrared and their biological activity was tested by evaluating changes in the root growth of corn seedlings in hydroponics. The humic materials, from the Maria Ortiz area, presented higher values in the C/N ratio, higher values in the fluorescence index and lower values in the E4/E6 ratio, when compared with the humic materials from the area of Canal dos Escravos. The absorption bands of the infrared spectrum indicated similarities with respect to the chemical functionality of the humic materials, however, it was possible to notice clear differences between the study areas. All humic materials promoted, in general, changes in the root architecture of corn seedlings when compared to the control treatment. This work shows that there are differences in the chemical and spectroscopic characteristics and in the biological activity of the studied humic materials, demonstrating that the anthropic activity alters the quality of the organic matter of the mangrove sediments, which may interfere in the survival and development of the mangrove forests.

Development of a dissolution method for analyzing the elemental composition of fuel debris using sodium peroxide fusion technique

ABSTRACT A dissolution method for analyzing the elemental composition of fuel debris using the sodium peroxide (Na2O2) fusion technique has been developed. Herein, two different types of simulated fuel debris (such as solid solution of (Zr,RE)O2 and molten core – concrete interaction products (MCCI)) were taken. At various temperatures, these debris samples were subsequently fused with Na2O2 in crucibles, which are made of different materials (Ni, Al2O3, Fe, and Zr). Then, the fused samples are dissolved in nitric acid. Effects of the experimental conditions on the elemental composition analysis were evaluated using inductively coupled plasma-atomic emission spectroscopy (ICP – AES), which suggested the use of a Ni crucible at 923 K as an optimum testing condition. The optimum testing condition was then applied to the demonstration tests with Three Mile Island unit-2 (TMI-2) debris in a shielded concrete cell, thereby achieving complete dissolution of the debris. The elemental composition of TMI-2 debris revealed by the proposed dissolution method has good reproducibility and has an insignificant contradiction in the mass balance of the sample. Therefore, this newly developed dissolution method can be effectively utilized in practical applications by dissolving fuel debris and analyzing its elemental composition.

Structure of Silicon Wafers Planar Surface before and after Rapid Thermal Treatment

Presently it is important to remove mechanically disturbed layer on wafer surface during creation of up-to-date microelectronic products. Rapid thermal treatment with optical pulses of second duration is one of the applicable methods for removing disturbances in crystal lattice emerging after ion implantation. However the crystal structure of mechanically disturbed layer on wafer planar side is still unclear. Researches by transmission electronic method, analysis of diffraction reflection curve and electronic Auger spectroscopy has failed to provide reliable data about the state of crystal lattice in surface layer of at least 30 nm thickness. Hence it was impossible to suggest a model of solid phase recrystallization and to present its mathematical description. The goals of the work were as follows: – identify of silicon crystal lattice state in surface layer of 30 nm thickness before and after rapid thermal treatment by backward reflected electrons diffraction method using raw Si wafers surface; – analysis of contamination element composition on the surface of raw silicon before and after rapid thermal treatment; – model development for solid phase recrystallization of surface disturbed layer after rapid thermal treatment and its mathematical description. Images of back ward reflected electrons diffraction using surface layer of raw silicon wafers' of 30 nm thickness and also the results of the planar surface of raw silicon wafers' cleaning from impurities are provided. Processes reducing the activating energy of mechanically disturbed silicon layer recrystallization process were suggested and its mathematical description was provided. Parameters of rapid thermal treatment mitigating the thermal impact on silicon wafer for recrystallization of mechanically disturbed layer on its planar surface ware defined.

Synthesis and characterization of hierarchical Sr-doped ZnO hexagonal nanodisks as an efficient photocatalyst for the degradation of methylene blue dye under sunlight irradiation

This study presents the synthesis and comprehensive characterization of hierarchical hexagonal nanodisks of zinc oxide (ZnO) and strontium (Sr) doped ZnO, prepared via a hydrothermal method. The experimental synthesis procedure involved dissolving zinc nitrate in a water–ethanol mixture, followed by the addition of polyethylene glycol (PEG 200), sonication, and subsequent hydrothermal treatment. Different concentrations of Sr were introduced into the ZnO lattice to generate Sr-doped ZnO samples. Analysis of the obtained results revealed successful incorporation of Sr, evidenced by shifts in the X-ray diffraction (XRD) pattern and alterations in lattice parameters. Moreover, the Williamson-Hall plot indicated minimal strain and high structural stability in both pristine ZnO and Sr-doped ZnO. The morphology of the synthesized Sr-doped ZnO was confirmed through field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM), revealing a hexagonal nano disk-shaped morphology akin to pristine ZnO. Elemental composition analysis conducted via X-ray photoelectron spectroscopy (XPS) further confirmed the presence of Sr in the doped ZnO samples. Evaluation of photocatalytic activity against methylene blue dye demonstrated superior performance of the 5 % Sr-doped ZnO catalyst, attributed to its increased surface area compared to pristine ZnO. Notably, the highest degradation rate constant (k) of 0.0389 min−1 was observed for the 5 % Sr-doped ZnO catalyst, emphasizing its efficacy in environmental remediation applications. This research underscores the potential of Sr-doped ZnO as a promising photocatalyst, offering stability, reusability, and effective utilization of UV and visible light for catalytic processes.

Study of multi-elemental concentration and nano-micro structural morphology in medicinal plants by FE-SEM and EDX method.

Medicinal plants of the Moraceae family, such as Ficus racemosa linn, have been traditionally used in the North Karnataka region for treating various ailments. This study aims to analyze the elemental composition and nano-micro structural morphology of selected species of Moraceae family medicinal plants, focusing on their potential therapeutic applications. Samples were collected from the Dharwad and Gadag districts in North Karnataka. The surface morphology at nano and micro levels was examined using a field emission scanning electron microscope, while the elemental composition was analyzed through energy-dispersive X-ray spectroscopy. The study emphasizes the detailed examination of the specific weight percent of elemental concentration and the morphological features observed. The analysis revealed fine, irregularly shaped particles with an average diameter of 20 to 50 μm on the plant surface. Elemental composition analysis showed the presence of Mg, Al, Si, Cl, K, Ca, Mn, Fe, Cu, and Zn within WHO-recommended limits.

High-Efficiency Photo-Fenton-like Catalyst of FeOOH/g-C3N4 for the Degradation of PNP: Characterization, Catalytic Performance and Mechanism Exploration.

The composite photocatalyst FeOOH/g-C3N4 was prepared through thermal polycondensation and co-precipitation methods, followed by XRD, SEM and UV-vis characterization. The stability of FeOOH/g-C3N4 was explored by the recycling test. The active species in the reaction system were investigated by the capture experiment. The results indicated that the optimal preparation condition for g-C3N4 involved calcination at 600 °C for 4 h. XRD analysis revealed that g-C3N4 exhibits a high-purity phase, and Fe in FeOOH/g-C3N4 exists in a highly dispersed amorphous state. SEM analysis showed that FeOOH/g-C3N4 has a rough surface with an irregular layered structure. Element composition analysis confirmed that the content of elements in the prepared catalyst is consistent with the theoretical calculation. FeOOH/g-C3N4 possesses the largest specific surface area of 143.2 m2/g and a suitable pore distribution. UV-vis DRS analysis showed that the absorption intensity of FeOOH/g-C3N4 is stronger than that of g-C3N4. When the catalyst dosage was 1.0 g/L, the H2O2 dosage was 4 mmol/L, the PNP initial concentration was 10 mg/L and the initial pH value was 5, the PNP removal could reach 92% in 120 min. Even after 5 cycles, the efficiency of PNP removal by FeOOH/g-C3N4 remains nearly 80%. The capture experiment indicated that both •OH and •O2- play roles in the photocatalytic degradation of PNP, with •OH being more significant. These findings affirm that FeOOH has been successfully incorporated into g-C3N4, resulting in a conspicuous catalytic effect on the degradation of PNP in the visible light-assisted Fenton-like reaction.

Enhancing surface chemistry and wetting behavior of laser-modified Ti–6Al–4V surgical titanium alloy surfaces through wet deposition of biogenic hydroxyapatite

This study focuses on enhancing the surface properties of surgical titanium alloys (Ti–6Al–4V) to optimize their suitability for biomedical implant applications. Direct laser writing (DLW) was used to modify the titanium surface and facilitate the deposition of biohydroxyapatite (BHA) particles through wet deposition and the coalescence phenomenon. Four types of etching patterns were tested, resulting in biomimetic bone-like surfaces with microtextured features, exhibiting suitable hydrophilic characteristics for biomedical implants. The resulting surfaces were characterized structurally, morphologically, chemically, and in terms of wettability. X-ray diffraction was performed to validate the titanium alloy composition and determine the crystallite size of BHA particles, both before and after thermal treatment. Optical and electron microscopy results demonstrated that the etching pattern density directly impacts the distribution and anchoring of BHA particles, with denser patterns leading to better particle fixation. Dense etching patterns were found to reduce the wettability of Ti surfaces. However, after coating with BHA particles, the contact angle decreased, resulting in more wettable surfaces. Energy-dispersive X-ray spectroscopy (EDS) mapping revealed variations in elemental distribution across different samples, providing an elemental composition analysis that supports the findings from optical and electron microscopy. The effectiveness of BHA deposition is closely tied to the density and pattern of the surface texturization. Overall, this study presents a straightforward yet effective methodology to optimize the surface properties of titanium alloys, potentially enhancing their compatibility with biological tissues.

Experimental investigation of friction stir welding with special spherical ball shoulder different probe tools and parameters for enhanced material properties of AA2219 aluminium alloy

This research investigates the impact of unique spherical ball shoulder enhancement tool pin configurations on the friction stir welding (FSW) of AA2219 aluminum alloy under various parameters. FSW was performed using three different pin shapes: square, hexagonal, and octagonal. Testing samples were prepared using an L9 orthogonal array layout with varying welding parameters. The material behavior in the three distinct weld zones was evaluated for each pin configuration. Results indicated superior microhardness values in the heat-affected zone (HAZ) and thermo-mechanically affected zone (TMAZ) compared to the weld nugget zone. Elemental composition analysis of the TMAZ revealed significant differences, highlighting the influence of thermal stress and material behavior due to the tool pin and shoulder configuration. The square-headed tool demonstrated improved tensile strength and microhardness. Optimal welding performance was achieved with a spindle speed of 1000 RPM, a travel speed of 25 mm/min, and a tilt angle of 3°. Variations in Cu content in the TMAZ and HAZ underscored localized modifications within the material structure, driven by the spherical ball spinning effects on the shoulder. Tensile tests showed that welds made with the square pin consistently exhibited higher tensile strength compared to those made with hexagonal and octagonal pins.

Novel ordered dendritic InWO4-rGO p-n heterojunction for fast response to TEA

The ternary metal oxides that combine two different metal cations is an interesting candidate as sensing material based on their interesting properties. Hence, ordered dendrite InWO4 was successfully synthesized via a hydrothermal method, followed by the construction of an InWO4-rGO heterojunction to enhance detection capability for triethylamine (TEA) gas. The synthesized product underwent morphology and elemental composition analysis using various techniques. Gas sensing experiments revealed that the InWO4-rGO gas sensor, operating at the optimal temperature of 220 ℃, displayed a significantly improved response to 100 ppm TEA, with a high value of 59.5, in comparison to the pure InWO4 gas sensor (11.5 at 250 ℃). Additionally, the recovery time was reduced from 184s to 122s. Based on experimental data and gas sensing reaction theory, this study attributes the improved gas sensing performance to the formation of p-n heterojunction, a larger specific surface area and rGO's catalytic effect. This study not only introduces a novel addition to the gas sensing material family but also promotes the development of advanced gas sensors.

Enhanced H2S gas sensing utilizing UV-assisted In2O3@ZnO nanosheets

In the realm of environmental protection, there is a growing demand for efficient and environmentally friendly gas sensors. In this study, we employed a simple hydrothermal method to synthesize nanosheets composed of zinc oxide (ZnO)-doped indium oxide (In2O3), utilizing zeolitic imidazolate framework-8 (ZIF-8) as a precursor. These nanosheets demonstrated exceptional sensitivity and selectivity in detecting hydrogen sulfide (H2S) gas. A comprehensive analysis of crystal structure, chemical states, elemental composition, surface area, and morphology was conducted. Brunauer–Emmett–Teller (BET) surface area measurements to assess the materials' textural properties revealed that the nanosheets labeled In2O3/0.1ZnO possessed a high specific surface area of 49.02 m2/g, greater than the 45.65 m2/g of pure In2O3 nanosheets, a crucial factor contributing to the observed exceptional sensitivity and selectivity in detecting H2S gas. Particularly noteworthy is the substantial improvement in gas detection response from 109.9 to 146.2 (approximately 24.7 %) observed in the In2O3/0.1ZnO material under UV irradiation at the optimal temperature of 250 °C. This enhancement emphasizes the material's potential for superior gas detection. The incorporation of ZIF-8-derived ZnO nanostructures played a crucial role in creating additional active sites, further enhancing the gas-sensing capabilities. Importantly, this innovative synthesis technique ensures the production of clean, non-toxic materials, aligning with environmental conservation objectives, and holds promise for achieving heightened sensitivity and selectivity in the detection of environmentally harmful gases.

Analysis of Morphological and Elemental Composition in Rice, Beans, and Groundnut Husk

The morphological characteristics and elemental composition of these agricultural products provides insights into their nutritional value, chemical properties, and potential industrial applications, contributing to advancements in food science, agriculture, and environmental sustainability. The comprehensive analysis of the morphological and elemental composition of three widely consumed agricultural products: rice, beans, and groundnut husk as a partial substitute for sand due to its high content of calcium, silicon, aluminum, iron, and other elements when properly controlled. Transforming them into practical materials in order to reduce their detrimental impact on the environment. An equal weight of 50 g of Rice husk, 25 g of bean husk, and 25 g of groundnut shell were measured out of 100 g of untreated samples and oven dried at 1000C for 4 hours. The samples were the crushed to fine particle and sieve, which was burned at a temperature of 5500C in an electric furnace for 4 hours. The result obtained microscopic techniques such as Scanning Electron Microscope (SEM) with Energy Disperse X-ray fluorescence (EDXRF) and X-ray diffraction (XRD), were used to observe the surface and element presence in RBGH. The result among other things shows that untreated RBGH atomic concentration of Si is 65.79%, K is 16.01.53%, P is 5.14% Ca is 3.36% and Mg is 3.35% respectively, and the SEM shows that it has a porous cellular structure and consists of irregular-shape particles. The findings shed light on the potential industrial applications of these agricultural byproducts

Photocatalytic, Antimicrobial, and Cytotoxic Efficacy of Biogenic Silver Nanoparticles Fabricated by Bacillus amyloliquefaciens

The biomass filtrate of the endophytic bacterial strain Bacillus amyloliquefaciens Fa.2 was utilized for the eco-friendly production of silver nanoparticles (Ag-NPs). The yellowish-brown color’s optical properties showed a maximum surface plasmon resonance at 415 nm. The morphological and elemental composition analysis reveals the formation of spherical shapes with sizes of 5–40 nm, and the Ag ion comprises the major component of the produced Ag-NPs. X-ray diffraction confirmed the crystalline structure, whereas dynamic light scattering reveals the high stability of synthesized Ag-NPs with a polydispersity index of 0.413 and a negative zeta potential value. The photocatalytic experiment showed the efficacy of Ag-NPs to degrade methylene blue with maximum percentages of 73.9 ± 0.5 and 87.4 ± 0.9% under sunshine and UV irradiation, respectively, compared with 39.8% under dark conditions after 210 min. Additionally, the reusability of Ag-NPs was still more active for the fifth run, with a percentage decrease of 11.6% compared with the first run. Interestingly, the biogenic Ag-NPs showed superior antimicrobial activity against different pathogenic Gram-negative bacteria (MIC = 6.25 µg mL−1), Gram-positive bacteria (MIC = 12.5 µg mL−1), and uni- and multicellular fungi (MIC = 12.5 µg mL−1). Moreover, the biosynthesized Ag-NPs could target cancer cells (Pc3 and Mcf7) at low concentrations compared with normal cell (Vero) lines. The IC50 of normal cells is 383.7 ± 4.1 µg mL−1 compared with IC50 Pc3 (2.5 ± 3.5 µg mL−1) and McF7 (156.1 ± 6.8 µg mL−1). Overall, the bacterially synthesized Ag-NPs showed multifunctional features to be used in environmental catalysis and biomedical applications.

Mechanistic Insight into the Synthesis and Morphological Evolution of Superhydrophobic Silica Nanotubes.

Silica nanotubes have significant applications in various fields, including thermal insulation, self-cleaning, and catalysis. Currently, the synthesis methods of silica nanotubes are mostly limited to the template method. In this work, a template-free strategy and vapor-phase approach were used to prepare silica nanotubes. Poly(methylhydrosiloxane) (PMHS) was hydrolyzed and condensed in a high-temperature closed reactor by using ammonia as a catalyst. The resulting product was then subjected to template-free self-assembly to synthesize silica nanotubes incorporating methyl groups. The silica nanotubes were synthesized under varying conditions, resulting in lengths ranging from 50 nm to several micrometers, exterior diameters between 40 and 120 nm, and wall thicknesses varying from 7 to 30 nm. The synthesized products underwent morphology analysis using TEM and FESEM for morphology analysis, elemental composition analysis using XPS, and chemical structure identification using FTIR, and the possible formation mechanism of silica nanotubes formation was also speculated. Furthermore, the coatings formed by silica nanotubes exhibited remarkable superhydrophobic self-cleaning properties with a water contact angle of 162° and a rolling angle of less than 1°.

Formation of Ca, P, and Zn-doped ZrO2/TiO2 coating layer via plasma electrolytic oxidation and magnetic sputtering: Improving surface characteristics and biocompatibility of Ti–6Al–4V alloy

The study demonstrated the Ca, P, and Zn-doped ZrO2/TiO2 coating layer via plasma electrolytic oxidation (PEO) and radiofrequency magnetron sputtering (RF-MS) for improving surface characteristics and biocompatibility of Ti–6Al–4V alloy. The process involved sandblasting (SB) to create micro-scale irregularities on the alloy surface, followed by RF-MS and PEO. The coating's morphology, elemental composition, phase composition, and chemical analysis were examined by FE-SEM with energy-dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Raman analysis. The dual surface treatment resulted in the formation of composite coatings with TiO2, ZnO, ZrO2, and HA presence and displayed anisotropic multi-scale porous morphology while the surface texturing created by the SB process facilitated mechanical interlocking during the oxide layer growth. In the SB-Zr + PEO-Zn sample, the phase analysis indicated the strain-induced stabilization of t-ZrO2 in the PEO coating layer due to the incorporation of Ca2+ ions, and the formation of zinc-substituted hydroxyapatite was observed that showed enhanced roughness and wettability. Also, reduced hardness and elastic modulus (comparable to that of cortical bone) were observed due to transformation toughening under stress from t-ZrO2 to m-ZrO2. The presence of TiO2, ZrO2, ZnO, and HA within the coating, all act as protective barriers in effectively reducing corrosion rates. The biological analysis demonstrated better biocompatibility, including promoting cell proliferation, cell adhesion, osteoblast differentiation, ALP activity, and mRNA expression of several osteogenic markers of the cells cultured on the SB-Zr + PEO-Zn sample. These results demonstrated the higher potential of the PEO coating system with higher biocompatibility and osseointegration ability for dental implants.

Elemental Composition, Antioxidant, Anti-inflammatory and Anti-genotoxic Properties of Nitophyllum punctatum

ObjectivesMarine algae are important sources of nutritionally and pharmacologically important products. Here in the study, nutritional composition and biological activities of a marine red algae Nitophyllum punctatum were assessed. The present study aimed to analyze the nutritional composition and biological effects of the N. punctatum. MethodsThe marine algae N. punctatum was collected, shade dried and extracted using Soxhelet apparatus. The elemental composition was estimated using Atomic Absorption Spectroscopy; the anti-inflammatory effect was determined using Raw 264.7 macrophages. Genotoxicity was assessed by standard methods using Allium cepa root model. ResultsThe elemental composition analysis revealed the presence of essential minerals such as calcium, magnesium, potassium, and iron, indicating the potential nutritional value of the algae. The extract demonstrated significant inhibition of Nitric oxide (NO) production and downregulated the expression of pro-inflammatory cytokines such as TNF-α and IL-6, suggesting its potential as an anti-inflammatory agent. Furthermore, the anti-genotoxic potential of the methanol extract was evaluated using the Allium cepa model, a well-established system for assessing genotoxicity. Onion root tips were treated with various concentrations of the extract, and the chromosomal changes were performed as indicators of genotoxicity. Results indicated a protective effect against Ethyl methyl sulfonate (EMS) induced genotoxicity in onion roots. ConclusionsThe findings suggest that the methanol extract of N. punctatum possesses potent anti-inflammatory and anti-genotoxic properties, which may be attributed to the presence of bioactive compounds. The study highlights the potential pharmacological importance of N. punctatum as a source of natural compounds with anti-inflammatory and anti-genotoxic activities.

Impact of copper and manganese on phase transformation, microstructural development and material strength in CoCrFeNi high-entropy alloys through mechanical alloying

CoCrFeNiX (X = Cu, Mn) equiatomic high-entropy alloys (HEAs) were prepared through mechanical alloying (MA) followed by sintering at moderate temperature. The prepared HEAs were subjected to X-ray diffraction and microscope techniques to evaluate their phase evolution, microstructure, and elemental composition. Alloyed CoCrFeNiCu powder consists of two face centered cubic (FCC) phases (FCC1 and FCC2), whereas, CoCrFeNiMn powder showed a major FCC phase with a minor body centered cubic (BCC) phase. After sintering, bulk CoCrFeNiMn alloy showed only a single solid solution FCC phase, and the bulk CoCrFeNiCu still contained dual FCC phases. The elemental composition analysis revealed that both HEAs are equiatomic in composition. The average microhardness of CoCrFeNiCu and CoCrFeNiMn HEAs was 85 ± 15 HV and 147 ± 20 HV, respectively. It was observed that the presence of Cu in CoCrFeNiCu reduces the hardness of the HEA due to segregation. This study demonstrates the influence of the fifth metal on the phase evolution, microstructure, and mechanical properties of the HEAs.

Failure Analysis of CRDINiCr Butterfly Valves for Nuclear Power Plant Applications

Corrosion-resistant iron with nickel and chromium (CRDINiCr) is often used in butterfly valves for flow control at nuclear power plants, where resistance to corrosion, oxidation, and wear is significant. In this study, a failure analysis of a CRDINiCr alloy butterfly valve was performed by combining morphology characterization and in situ elemental composition analysis of failure of various regions of the valve. Based on the testing and analysis conducted in this study, it was determined that the inspected valve body material exhibited several defects, including poor graphitization, porosity, and the presence of eutectic carbides. These imperfections compromised the required plasticity criteria, resulting in significant embrittlement of the material. Therefore, under the impact stresses applied during the pressure testing, these vulnerabilities facilitated rapid crack initiation and propagation. The presence of such defects significantly compromised the material’s resistance to fracture under dynamic loading conditions, underscoring the critical importance of stringent quality control in the production of such materials to ensure their reliability and performance in operational settings at nuclear power plants.

Valorisation of Spent Yeast Fermentation Media through Compositional-Analysis-Directed Supplementation

Spent fermentation media from bioprocessing represent a significant waste stream, and interest in recycling them as part of the developing circular bioeconomy is growing. The potential to reuse yeast spent culture media (YSM) to feed secondary bacterial fermentations producing recombinant protein was investigated in this study. Elemental and amino acid compositional analysis using inductively coupled plasma mass spectrometry (ICP-MS) and LC-MS/MS identified significant differences in the concentrations of 6 elements and 18/20 amino acids in YSM compared with rich microbiological media (LB). Restoration of levels of magnesium and sodium through addition of their salts and amino acids from tryptone supplementation led to the expression of equivalent titres of recombinant proteins by E. coli (0.275 g/L), compared to that in LB media (0.296 g/L) and BMMY media (0.294 g/L) in shake flask culture. When this supplementation strategy was employed in a bioreactor system, we observed a significant increase in recombinant protein titre using the supplemented YSM (2.29 (±0.02) g/L) over that produced using LB media (1.29 (±0.09) g/L). This study demonstrates through highly sensitive compositional analysis and identification of supplementation strategies the potential to valorise spent media from yeast fermentations that underpin industrial processes of significant scale, creating a circular approach to waste stream management.