Chromium Research Articles

Rapid repair of thermal aging embrittlement in 17-4PH martensitic stainless steel using pulsed electric current

The 17-4PH stainless steel serves as the main steam isolation valve in a light water reactor due to excellent comprehensive mechanical properties and corrosion resistance. Nonetheless, the thermal aging resulting from prolonged service poses a threat to the safe operation of nuclear power plants. The mechanism of thermal-aging embrittlement of 17-4PH stainless steel and its repairing behavior under the action of the pulsed electric current were studied using transmission electron microscopy and 3D atom probe tomography. The ductile to brittle transition occurred following the spinodal decomposition and G phase formation during the thermal aging of 5000 h at 673 K, resulting in a 100 HV increase in hardness of the 17-4PH stainless steel, of which 94.4 HV was attributed to the spinodal decomposition. Under the action of a pulsed electric current at 733 K, the hardness and impact energy can be restored to its original state, whereas heat treatment at the same temperature is unable to restore these properties. This is because the pulsed electric current treatment decreased the thermodynamic barrier to dissolution for the spinodal decomposition and G phases. The Kolmogorov-Johnson-Mehl-Avrami model was used to calculate the kinetics of spinodal decomposition dissolution. The results suggest that the pulsed electric current could increase the diffusion pre-exponential factor of Cr element and accelerate the elimination of spinodal decomposition. This process ultimately facilitates the quick regeneration of the 17-4PH stainless steel's performance.

Impact of CeO2 modification on the quality and wear performance of Al2O3/SiC reinforced metal-based coatings

In the pursuit of enhancing the quality and performance of metal-based composite coatings, we utilized Al2O3 and SiC as reinforcement particles to create Ni62 composite coatings on 65Mn surfaces through laser cladding. This study systematically delves into the influence of various mass fractions of CeO2 on the coating's forming quality and wear resistance. An in-depth analysis of the friction and wear mechanisms of these composite coatings is presented, with particular emphasis on CeO2's inhibitory effect on coating cracks. Our research findings reveal that the addition of an appropriate quantity of CeO2 can notably enhance the surface quality of the coating. However, an excessive amount of CeO2 can introduce defects on the coating surface. Within the central part of the cladding layer, longitudinal cracks propagate horizontally, forming what we term “r-type” cracks. Simultaneously, cracks extend both horizontally and vertically at the bonding interface, creating “T-type” cracks. CeO2 enhances the melt pool's fluidity, reducing the occurrence of pores and inclusions within the cladding layer. It also improves the dispersion of hard ceramic particles within the cladding layer, leading to a more uniform distribution of Cr and Ni elements within the coating. This refinement of grain structure in the coating reduces stress concentration and sensitivity to crack formation. Furthermore, the addition of CeO2 results in the accumulation of Ce elements on the coating surface. This accumulation promotes the movement of ceramic particles within the cladding layer towards the coating surface, ultimately forming a dense protective film on the surface. This protective film includes a new phase known as AlNi3. The primary wear mode observed in the composite coating is abrasive wear, with a minor presence of adhesive wear. Importantly, the incorporation of CeO2 significantly enhances the wear resistance of the composite coating.

Influence of Cooling Rate and Alloying by “Cr, V, and Ni” on Microstructure and High-Temperature Wear Behavior of SiMo Ductile Iron

AbstractSiMo ductile irons, typical heat-resistant materials, are subjected to varied wear environments during operation in high-temperature applications. SiMo ductile iron castings of different thicknesses were cast in investment and greensand molds, achieving a wide range of cooling rates. The present work aims to investigate the effect of the cooling rate and alloying elements (Cr, V, and Ni) on the microstructure and the abrasive wear behavior of these grades of SiMo ductile iron at high-temperature 700 °C under different loads. Thermodynamic calculations were used to propose the phase diagrams, critical transformation temperatures, and phase volume fractions in all SiMo alloys by using the Thermo-Calc software then verified by and Differential Scanning Calorimetry (DSC). The microstructure of unalloyed SiMo ductile cast iron consists of graphite nodules and carbides embedded in the precipitates at the grain boundary regions in a ferrite matrix. The alloyed SiMo microstructure contains nodular graphite and the carbides promoted by the alloying elements (Cr and V). The alloyed SiMo alloys exhibit higher wear resistance than unalloyed ones. These wear results support that the microstructure plays a chief role in wear loss. The combination of M6C, VC, and M7C3 carbides embedded in a ferrite-pearlite matrix (alloyed SiMo) seems to be more resistant to wear than the ferritic matrix with lamellar pearlite and eutectic M6C carbides (unalloyed SiMo).

Environmental Radioactivity, Ecotoxicology (238U, 232Th and 40K) and Potentially Toxic Elements in Water and Sediments from North Africa Dams

The natural radioactivity of 238U, 232Th and 40K was measured in water and sediment samples collected from Sidi Salem dam (Tunisia) and Aïn Dalia dam (Algeria) in the Tuniso-Algerian transboundary basin. The samples were measured using a TERRA detector of gamma, beta, and alpha rays, and atomic absorption and gamma-ray spectrometry were used to analyze the levels of radionuclides and toxic elements, respectively. Potentially toxic elements (Fe, Pb, Zn, Ni, Cr, Cu and Cd) and associated health risks in surface water and sediment of dams were investigated in this present study. The concentrations of Fe, Pb, Zn, Ni, Cr, Cu and Cd in surface water ranged from 5.430 to 9.700 mg·L−1, 0.022 to 0.168, 0.018 to 0.142, 0.065 to 0.366, BDL to 0.0351, BDL to 0.071 and BDL to 0.048 mg·L−1, respectively. In the sediments, the concentrations of Fe, Pb, Zn, Cu, Ni, Cd and Cr were of the order of 136.7, 3.41, 3.22, 0.213, 0.182, 0.15 mg·L−1 and BDL, respectively. The mean radioactivity rates in the water samples were 1.72, 0.068 and 94.6 Bq·L−1 for 238U, 232Th and 40K, respectively (Tunisia dam), and were 1.9, 0.09 and 131.43 Bq·L−1 for 238U, 232Th and 40K, respectively (Algeria dam). The mean 238U, 232Th and 40K radioactivity concentrations measured in the sediment samples were 2.67, 0.18 and 197.87 Bq·kg−1, respectively (Tunisian dam), and were 4.34, 0.27 and 287.61 Bq·kg−1, respectively (Algeria dam). The activity concentration of 40K was higher than that of 238U and 232Th for the water and sediment samples. The activity concentrations follow the order 40K > 238U > 232Th. The cumulative impact of these radio-geochemical elements can cause immediate serious problems in the ecosystem due to their high potential toxicity to the environment and human health in this study area and can be transposable to any other similar region. A good knowledge of monitoring quality and quantity for transboundary water resources and international collaborations are essential to safeguard human health (women’s breast cancer, thyroid cancer, neurological impact) and avoid conflicts, especially during climatic upheavals of drought.

Mechanochemical synthesis, purification, and optimization studies of Cr boride@MgO particles

Chromium boride, an advanced ceramic material, is commonly produced by powder metallurgy methods using elemental boron and chromium powder, borothermic reactions, or boron carbide reduction of Cr2O3. In this study, a mechanochemical method for the production of chromium boride was developed, subsequent purification was performed, and the whole process was optimized. The amounts of Cr2O3, B2O3, and Mg in the initial powder blends were determined by computational thermodynamic methods based on their equilibrium compositions. Firstly, stoichiometric starting-powder blends were milled at different durations (1, 2, 3, 4, 5, and 8 h). The optimum purification route was determined using acid leaching experiments carried out with different acids, at different temperatures, and concentrations. Secondly, powders prepared in excess amounts were synthesized at the optimum duration (5 h) and leaching condition (0.1 M HCl, 25 °C). For the 100 wt % excess B2O3, 25 wt % excess Mg and 0.8 moles of Cr2O3 composition, annealing was conducted at 1100 °C. Characterization studies, X-ray diffractometry (XRD), scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS), transmission electron microscopy (TEM), and atomic absorption spectroscopy (AAS) were conducted on the milled and leached powders. After annealing, CrB, CrB2, Cr3B4 and MgO phases were obtained in the XRD patterns. The particle sizes of the resulting materials were also analyzed, and it was found to be nearly 3.11 μm after annealing. Finally, the TEM analysis revealed that the MgO peak evident in the XRD patterns was MgO shell covering the Cr boride particles having submicron sizes; hence, a pure Cr boride@MgO core-shell structure was obtained.

Synthesis of (WZrNbTaM)C (M = Cr, Ni, Ti) ceramic powders and the electromagnetic wave absorption in 2–18 GHz

AbstractWith the advent of the 5G era, while enjoying the convenience of information in our daily lives, we also face the challenge of dealing with increased and more complex electromagnetic (EM) radiation issues. Therefore, finding EM wave absorbing materials for the operating frequency range (2–18 GHz) of most electronic products has become an important aspect of ensuring human health and environmental safety. In this study, a variety of elements were incorporated into (WZrNbTaM)C powders by calculation and design, where M is Ni, Cr, or Ti. Phase and microstructural analysis demonstrated the successful preparation of a single‐phase solid solution with uniform elements distribution. The magnetic properties of the powders containing Ni and Cr elements exhibited significant improvement. Further analysis revealed that both the impedance matching and EM wave attenuation capabilities of (WZrNbTaCr)C and (WZrNbTaNi)C were enhanced, thereby improving their absorption performance. Compared to (WZrNbTaTi)C, (WZrNbTaCr)C and (WZrNbTaNi)C exhibit a significant improvement in minimum reflection loss (RL), with an increase of 27.1% and 37.2%, reaching −45.21 and −48.79 dB, respectively. The maximum effective absorption bandwidth (EAB) has also increased by 22.9% and 48.6%, reaching 3.44 and 4.16 GHz, respectively. It is noteworthy that (WZrNbTaCr)C and (WZrNbTaNi)C achieved these excellent absorption properties while maintaining a matching thickness of 1.07 and 1.17 mm. This lightweight and thin performance meets the requirements for use in special scenarios while ensuring the outstanding absorption performance.

Wintertime investigation of PM10 concentrations, sources, and relationship with different meteorological parameters

Meteorological factors play a crucial role in affecting air quality in the urban environment. Peshawar is the capital city of the Khyber Pakhtunkhwa province in Pakistan and is a pollution hotspot. Sources of PM10 and the influence of meteorological factors on PM10 in this megacity have yet to be studied. The current study aims to investigate PM10 mass concentration levels and composition, identify PM10 sources, and quantify links between PM10 and various meteorological parameters like temperature, relative humidity (RH), wind speed (WS), and rainfall (RF) during the winter months from December 2017 to February 2018. PM10 mass concentrations vary from 180 – 1071 µg m−3, with a mean value of 586 ± 217 µg m−3. The highest concentration is observed in December, followed by January and February. The average values of the mass concentration of carbonaceous species (i.e., total carbon, organic carbon, and elemental carbon) are 102.41, 91.56, and 6.72 μgm−3, respectively. Water-soluble ions adhere to the following concentration order: Ca2+ > Na+ > K+ > NH4+ > Mg2+. Twenty-four elements (Al, Si, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Co, Zn, Ga, Ge, As, Se, Kr, Ag, Pb, Cu, and Cd) are detected in the current study by PIXE analysis. Five sources based on Positive Matrix Factorization (PMF) modeling include industrial emissions, soil and re-suspended dust, household combustion, metallurgic industries, and vehicular emission. A positive relationship of PM10 with temperature and relative humidity is observed (r = 0.46 and r = 0.56, respectively). A negative correlation of PM10 is recorded with WS (r = − 0.27) and RF (r = − 0.46). This study’s results motivate routine air quality monitoring owing to the high levels of pollution in this region. For this purpose, the establishment of air monitoring stations is highly suggested for both PM and meteorology. Air quality standards and legislation need to be revised and implemented. Moreover, the development of effective control strategies for air pollution is highly suggested.

Identification of core carcinogenic elements based on the age-standardized mortality rate of lung cancer in Xuanwei Formation coal in China.

In this study, the core carcinogenic elements in Xuanwei Formation coal were identified. Thirty-one samples were collected based on the age-standardized mortality rate (ASMR) of lung cancer; Si, V, Cr, Co, Ni, As, Mo, Cd, Sb, Pb, and rare earth elements and yttrium (REYs) were analyzed and compared; multivariate statistical analyses (CA, PCA, and FDA) were performed; and comprehensive identification was carried out by combining multivariate statistical analyses with toxicology and mineralogy. The final results indicated that (1) the high-concentration Si, Ni, V, Cr, Co, and Cd in coal may have some potential carcinogenic risk. (2) The concentrations of Cr, Ni, As, Mo, Cd, and Pb meet the zoning characteristics of the ASMR, while the Si concentration is not completely consistent. (3) The REY distribution pattern in Longtan Formation coal is lower than that in Xuanwei Formation coal, indicating that the materials of these elements in coal are different. (5) The heatmap divides the sampling sites into two clusters and subtypes in accordance with carcinogenic zoning based on the ASMR. (6) PC1, PC2, and PC3 explain 62.629% of the total variance, identifying Co, Ni, As, Cd, Mo, Cr, and V. (7) Fisher discriminant analysis identifies Ni, Si, Cd, As, and Co based on the discriminant function. (8) Comprehensive identification reveals that Ni is the primary carcinogenic element, followed by Co, Cd, and Si in combination with toxicology. (9) The paragenesis of Si (nanoquartz), Ni, Co, and Cd is an interesting finding. In other words, carcinogenic elements Ni, Co, Cd, and Si and their paragenetic properties should receive more attention.

High-temperature oxidation behaviors and mechanical properties of TiAlCrMnHEAs during heat treatment

A series of TiAlCrMn high entropy alloys (HEAs) with variable atomic ratios of Al, Cr, and Mn were prepared using vacuum melting. High-temperature oxidation behaviors and mechanical properties were investigated before and after heat treatment. The oxidation mass gain rate is declined dramatically with increasing Al, Cr, and Mn element contents. Enhanced oxidation resistance is attributed to a continuously dense (Al,Cr)-rich oxidation layer, which can hinder the inter-diffusion of O and alloying elements. Furthermore, microhardness increases monotonously with increasing Al, Cr, and Mn element contents of the alloys before and after heat treatment. Grain coarsening can result in lower microhardness, but precipitation strengthening contributes to higher hardness of the alloys with high alloying element contents. Meanwhile, deformation-induced strengthening also contributes to higher compressive strength. The value after heat treatment at 500 °C is lower than that of as-cast samples while an increased value occurs after heat treatment at 900 °C accompanied by sacrificing the malleability.

Determination of Chromium Mineral in Foodstuffs in Indonesia using INAA Method

The concentration of the element chromium (Cr) was determined in 76 types of food ingredients from four provinces in Indonesia. The element Cr is one of the essential elements needed by the human body for physiological processes. Although the amount needed for Cr is relatively small, this mineral is very important for the insulin hormone to function properly. Chromium deficiency can result in decreased insulin sensitivity, glucose intolerance and an increased risk of diabetes. The Cr element was determined using the Instrumental Neutron Activation Analysis (INAA) method in the GA. Siwabessy Multipurpose Research Reactor. The reactor which is located in the Puspiptek area has a thermal neutron flux of around 5.47 x 1013 n.cm-2s-1 . Bombardment Cr-50 in foodstuffs samples by thermal neutrons will produce Cr-51 through the n, nuclear reaction. The radiosotope Cr-51. The radiosotope Cr-51 which is the result of thermal neutron activation has a half-life of 27.7 days. The single energy peak of the Cr- 51 gamma-ray can be observed at 320.08 keV. The results showed that cassava leaves, melinjo leaves, watercress, sweet potato leaves, papaya leaves, ipomoea aquatica, kenikir, pumpkin leaves, spinach and mushrooms are foodstuffs rich in Cr compared to other foodstuffs. Foodstuffs from Pandeglang Regency-Banten Province have relatively higher Cr concentrations than other three locations.The concentration of Cr in foodstuffs ranges from 0.039 to 5.244 µg/g.

Corrosion behavior of aluminum reinforced austenitic steel in liquid lead bismuth at 550 ℃

The key material issue for the commercialization of advanced lead cooled fast reactors and accelerator driven subcritical systems is the compatibility between structural materials and lead based coolants. Structural steel materials require excellent corrosion resistance in high-temperature liquid lead bismuth eutectic (LBE) alloy. Aluminum forming austenitic steel (AFA steel) has excellent corrosion resistance in extreme environments due to its ability to form an Al<sub>2</sub>O<sub>3</sub> film on its surface. However, excessively high Ni elements are more easily dissolved or oxidized in LBE than Fe and Cr elements. Therefore, this work investigates the effect of reducing Ni element composition (25-Ni steel and 18-Ni steel) on the corrosion resistance of steel in LBE. Surface treatment can protect the substrate from corrosion to some extent, so herein we explore whether it has a protective effect on AFA steel in LBE by generating Al<sub>2</sub>O<sub>3</sub> through high-temperature pre oxidation. The morphology and structure of the oxide layer of AFA steel corroded for 600 h in LBE with saturated dissolved oxygen at 550 ℃ are characterized by scanning electron microscope (SEM), energy dispersive spectrometer (EDS), X-ray diffraction (XRD), and other technologies. The results indicate that the oxide film formed after corrosion of 18-Ni steel is thinner than that after corrosion of 25-Ni steel. Performing high-temperature pre oxidation is beneficial to forming a protective Al<sub>2</sub>O<sub>3</sub> oxide film on the surface of the sample, thereby reducing the thickness of the oxide layer and improving the material's LBE corrosion resistance. The reduction in thickness of the oxide layer generated after pre oxidation of 18-Ni steel is greater than that of 25-Ni steel, so the anti-corrosion effect of 18-Ni steel after pre oxidation is better than that of 25-Ni steel.

Atomic-scale Ru anchored on chromium-shavings as a precursor for a pH-universal hydrogen evolution reaction electrocatalyst.

In the leather manufacturing industry, the management of substantial quantities of solid waste containing chrome shavings remains a formidable challenge. Concurrently, there is a pressing need for the development of pH-universal and economically viable electrocatalysts for the hydrogen evolution reaction (HER). In response to these intertwined challenges, this study proposes an innovative approach wherein the amino groups present on the surface of chrome shavings are utilized to immobilize single ruthenium atoms during pyrolysis, thereby facilitating the synthesis of hydrogen evolution electrocatalysts. The optimized sample, denoted as CN/Cr2O3/Ru-1, demonstrates exceptional electrocatalytic performance, exhibiting an ultra-low overpotential of -28 mV in 1.0 M KOH at a current density of 10 mA cm-2, and it also exhibits good performance in acidic and neutral electrolytes. Importantly, these overpotentials surpass those reported for many previous ruthenium-based catalysts. Density functional theory (DFT) calculations elucidate that both oxygen (O) and chromium (Cr) moieties within Cr2O3 can engage in favorable interactions with the coordination patterns of the ruthenium (Ru) atoms, thereby elucidating the synergistic enhancement conferred by the chromium element in CN/Cr2O3/Ru, which ultimately facilitates and promotes the catalytic activity of the ruthenium atoms serving as the catalytic center. This facile synthesis route not only presents a green solution for addressing waste chromium pollutants but also offers a promising avenue for the development of high-performance, cost-efficient electrocatalysts.

Novel chromium (III)-based compound for inhibition of oxaliplatin-resistant colorectal cancer progression.

Colorectal cancer (CRC) ranks as the third leading cause of cancer-related mortality worldwide. The current standard of care includes systemic chemotherapy with cytotoxic agents, offering palliative relief for severe CRC cases and serving as the primary therapy for metastatic recurrence. However, the development of chemoresistance poses a substantial obstacle in the realm of chemotherapy. This study delved into the potential of a novel chromium (III)-based compound, hexaacetotetraaquadihydroxochromium (III) diiron (III) nitrate, for CRC treatment. The therapeutic promise of this innovative chromium (III)-based compound was explored by utilizing LoVo colon cancer cells and an in-vivo mouse model of CRC. Various dosages of the compound were administered to LoVo parental cells and LoVo oxaliplatin-resistant cells. Findings unveiled that a concentration of 2000 μg/mL of the chromium (III) compound significantly inhibited mesenchymal transition and the migratory and invasive properties of LoVo oxaliplatin-resistant cells. This novel chromium (III)-based compound also demonstrated similar efficacy in other different CRC cell lines. The tumor growth was in the in-vivo mouse model was reduced by this compound. Moreover, the chromium (III)-based compound induced apoptosis by triggering the endoplasmic reticulum (ER) stress pathway in LoVo oxaliplatin-resistant cells. This study illuminates the capacity of the novel chromium (III)-based compound to impede the progression and growth of chemotherapy-resistant CRC. This discovery instills confidence in the potential of this compound as a therapeutic agent for CRC, even in the face of drug resistance. It holds the promise of serving as a valuable asset in the future treatment of chemotherapy-resistant CRC.

Anthropogenic impact on soil and vegetation in Turkistan region: Chemical composition and heavy metal contamination

The main purpose of this study is to analyze the anthropogenic impact on the soil and vegetation cover of the landscapes of the Turkistan region (southern part of Kazakhstan), and to investigate the chemical composition of elements and pollutants. The current state of landscapes with patterns of distribution of chemical elements and the influence of anthropogenic activity have been revealed. Quantitative indicators of the content of chemical elements (carbon, oxygen, sodium, magnesium, aluminum, silicon, potassium, calcium, titanium, iron, lead, arsenic, copper, zinc, nickel, cobalt, vanadium, thallium, manganese, and strontium) were studied based on soil samples. The levels of concentration of chemical elements of vegetation cover, aboveground and underground parts (carbon, oxygen, sodium, magnesium, aluminum, silicon, phosphorus, sulphur, chlorine, potassium, calcium, iron and copper) were assessed. The results of the chemical analysis of the soil cover revealed an excess of the maximum permissible concentration of chemical elements (lead, copper, zinc, arsenic, and chromium), while elevated levels of insoluble ash were observed in plants.

Accurate prediction analysis of steel alloy elements by femtosecond laser-ablation spark-induced breakdown spectroscopy and out-of-bag random forest regression

Femtosecond laser-ablation spark-induced breakdown spectroscopy (fs-LA-SIBS) and out-of-bag random forest regression (OOB-RFR) were developed for accurate quantitative analysis of the elements manganese (Mn), chromium (Cr), and nickel (Ni) in steel alloys.

Assessment of drinking water quality based on trace elements concentrations in the semi-arid region, Morocco

Human health and sustainable socio-economic growth are closely linked to water quality. Due to increasingly intense human activity, pollutants, and in particular trace elements, are entering the aquatic system and harming humans. The main objective of this study is to analyse and compare the impact of the trace elements on the water quality of natural springs. The concentrations of ten trace elements in 12 spring water samples collected in 2022 were analyzed using ICP-MS to determine the spatial variability of natural water quality in the Ouislane watershed. Nine major trace elements (boron, cobalt, chromium, copper, manganese, nickel, lead, zinc, and vanadium) were measured using the inductively coupled plasma mass spectrometry (ICP-MS) technique. The average values of these elements followed the descending trend: B > Ni > Cr > Co > Zn > Mn > V > Cu > Pb in spring water samples. Some trace elements measured in certain water samples exceed the upper limits set by Moroccan drinking water quality standards (NM) and the World Health Organization (WHO). From the principal components analysis (PCA), 83% of the variation is explained by the first three main components. B, Co, Cr and Ni have a strongly impact on water quality explain by their strong correlation with CP1 (R2 > 0.70). The calculated water quality index (WQI) values ranged from 61.18 to 95.11, with an average of 78.47. Approximately 17% of the water samples were categorized as excellent quality water (WQI < 50), with the remaining 83% classified as good quality water (50 < WQI < 100). According to the WQI index, all the natural spring waters investigated are deemed suitable for human consumption.

A Combined Microscopy Study of the Microstructural Evolution of Ferritic Stainless Steel upon Deep Drawing: The Role of Alloy Composition

Ferritic stainless steel (FSS) is widely used to manufacture deep-drawn products for corrosion resistance applications, being the alloy drawability strongly affected by its microstructural anisotropy. This study combines a variety of microscopy techniques enabling in-depth analyses of the microstructural evolution of two different FSSs correlated to their deep drawing performance. One of the steels has a good correspondence with the standard EN-1.4016 (AISI 430). The other is a modified version of the previous one with higher contents of the ferrite-stabilising elements Si and Cr, and lower contents of the austenite-stabilising elements C, N, and Mn. Electron Backscatter Diffraction results confirm that the microstructural properties and drawability of FSS in the deep drawing process are improved in the modified steel version. Scanning transmission electron microscopy under low-angle annular dark field conditions evidences that the deformation mechanism of FSS during deep drawing follows a microstructural distortion model based on the grain size gradient and shows a variation of the deformation texture depending on the alloy composition. This work demonstrates the potential of advanced microscopy techniques for optimising the processing and design of ferritic stainless steels, with slight variations in the alloy composition, for deep drawing applications.

First-principles study of magnetic properties and electronic structure of 3d transition-metal atom-adsorbed SnSSe monolayers.

We investigated the electronic structure and magnetic characteristics of 3d transition metal elements (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) adsorbed onto monolayer SnSSe by employing first-principles calculations. After the calculation, we found that Sc, Ti, V, Cu, and Zn atoms adsorbed onto monolayer SnSSe do not have magnetic moments, while the rest of the atoms adsorbed onto SnSSe are able to produce magnetic moments, and their magnetic moments in the adsorption systems are in the range of 1.0-3.0 μB, in which the magnetic distance of Mn is the largest. The results of MAE calculations indicate that there is a big difference in the MAE of the systems with TM atoms adsorbed to the S-side and the Se-side; for V adsorbed to the S-side on the Sn atoms, the MAE is the largest, which reaches 8.277 meV f.u.-1, showing an in-plane magnetic anisotropy, and for Co adsorbed to the Se-side on the Sn atoms, the MAE is the smallest, which is -0.673 meV f.u.-1, showing a perpendicular magnetic anisotropy. Calculations of binding energies show that all atoms are able to adsorb stably. Our results indicate the potential application of TM-adsorbed SnSSe monolayers in spintronics and magnetic memory devices.

Trace element bioaccumulation in the plumage of common blackbirds (Turdus merula Linnaeus, 1758) from Agigea, Romania

The purpose of this research was to establish the baseline concentrations of thirteen trace elements (Cd, Co, Cr, Cu, Ni, Pb, Fe, Mg, Na, K, Sr, Ca, and Zn) in feathers of the common blackbird Turdus merula (n=9) at the Natura 2000 site “Marine Dunes from Agigea” (ROSCI0073). Both remiges and rectrices were pooled, and the quantification of trace elements was accomplished using two spectrometry analysis methods: high-resolution continuum source atomic absorption spectrometer with a graphite furnace (HR-CS GF-AAS) and flame atomic absorption spectrometer (FL-AAS). The concentration of Ca was the highest of the thirteen trace elements, registering at 209.9146±192.4098 µg·g-1 w.w., while Cd had the lowest concentration levels in feathers, 0.0243±0.0158 µg·g-1 w.w., respectively. However, the results obtained were significantly lower than those in the relevant literature. These findings suggest that the bioavailability of the analysed trace elements is minimal in our study area. Thus, it is imperative to conduct further research on the impact of these trace elements' accumulation and effects on avifauna in the Natura 2000 site “Marine Dunes from Agigea”.

Rare Earth Element Characteristics of Shales from Wufeng-Longmaxi Formations in Deep-Buried Areas of the Northern Sichuan Basin, Southern China: Implications for Provenance, Depositional Conditions, and Paleoclimate.

To explore the sedimentary environment and the background of the source area of organic-rich shales in the Wufeng-Longmaxi Formations in the northern Sichuan Basin, samples from Well XX1 in the area were subjected to geochemical testing and analysis of organic carbon content, trace elements, and rare earth elements (REEs). The results show that the total content of REE (ΣREE) of the shale in the Wufeng-Longmaxi Formations varied from 183.08 to 234.66 μg/g with an average of 212.59 μg/g, which is significantly higher than the content of the North American shale composite. The fluctuations in the total amount of REEs in the shale of the Wufeng-Longmaxi Formations reflect certain differences in the geochemical conditions of the Upper Ordovician-Lower Silurian shale. The ratios of LREE/HREE, LaN/YbN, LaN/SmN, and GdN/YbN and the distribution of normalized REE patterns indicate that the source supply or sedimentary structural background may have changed during the shale deposition period of the Wufeng Formation, while the shale deposition period of the Longmaxi Formation may be in a relatively stable source supply and sedimentary structural background. There is no significant correlation between δCe and ΣREE, and the obviously negative Eu abnormity and the weak Ce abnormity indicated that the diagenesis had a limited impact on REEs. Geochemical parameters such as values of ∑REE, δEu, δCe, Ceanom, and LaN/YbN indicate that the climate during the Wufeng-Longmaxi Formation shale deposition period was warm and humid, and the shale was deposited mainly in the suboxic-anoxic water environment. The deposition rate was stable and slow, providing good conditions for the production and preservation of organic matter. At the same time, this shows that the water environment of Wufeng Formation is more anoxic and reductive than that of Longmaxi Formation, which is more conducive to the preservation of organic matter. The correlation between ΣREE and the content of Sc, Ti, Cr, Co, Zr, Nb, Th, Hf, Ta, and other elements indicates that the sources of REEs in the shale of Wufeng and Longmaxi Formations in the study area are similar, mainly terrestrial clasts, and some may come from the sea. The REE distribution pattern shows that the shale provenance of the Wufeng-Longmaxi Formations mainly comes from the upper crust. The La/Yb-∑REE diagram shows that the sediment-parent rocks are mainly early sedimentary rocks and these sediment-parent rocks have granite provenance characteristics. Compared to La/Yb, LREE/HREE, LaN/YbN, and other REE characteristic parameters, it is inferred that the tectonic background of the study area is dominated by passive continental margin.