Stannous Research Articles

Metal Contamination and Human Health Risk Assessment of Soils from Parks of Industrialized Town (Galati, Romania)

The aim of the present study was to evaluate the contamination state of the surface soil from 10 parks from Galati, Romania, and the health hazards of the soil. The soil samples, collected in each site from the playing ground and from the edge of the park, were analyzed by using combined Wavelength- (WDXRF) and Energy-Dispersive (EDXRF) X-ray fluorescence techniques. A total number of 27 chemical elements (Ag, Al, As, Ba, Ca, Cd, Cr, Co, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Ti, V, Zn and Zr) were quantified in the urban soils, and the results were compared to the normal and alert values from Romanian legislation for toxic trace elements, as well as with European and world average values of element concentrations. The mineralogical analyses were performed by Scanning Electron Microscopy with Energy-Dispersive X-ray Analysis (SEM-EDX) and the Attenuated Total Reflectance–Fourier Transform Infrared technique (ATR-FTIR). To assess the soil contamination and the impact on human health of the presence of potential toxic elements and heavy metals in the soil, a series of pollution and health risk indices were used. All the results indicated an unpolluted to moderately polluted soil. The soil samples collected from the edge of the parks presented higher values for the specific pollutants, which originated from heavy traffic, such as Cu, Cr, Zn and Pb. The non-carcinogenic and carcinogenic risk to children was assessed using estimated daily intake (EDI) in relation to the pathways whereby pollutants can enter the human body, such as ingestion, dermal contact, inhalation and vaporization. Using the obtained values for EDI, the hazard quotient and hazard index were determined, which strengthen the formerly issued presumption that soil pollution is moderate and, by itself, does not present any threat to children’s health.

Distribution of Pb, Zn, Fe, As, Sn, Sb, Bi, and Ni Between Oxide Liquid and Metal in the ‘CuO0.5’-CaO-AlO1.5 System in Equilibrium with Cu Metal at 1400 °C

AbstractThe increasing complexity of ore resources and recycled materials in the feed of pyrometallurgical processes present a technical challenge to the metallurgical engineers working on maximizing the recovery of the valuable elements and minimizing the environmental impact of the processes. To address this challenge, the availability of computational tools that can predict the mass and energy balance in complex systems is required. Then, the accurate description of phase equilibria in the complex multicomponent systems describing the chemistry of the pyrometallurgical processes becomes critical for the correct implementation of the indicated tools and facing the outlined industrial challenges. In the present study, the distribution of selected elements (Pb, Zn, Fe, As, Sn, Sb, Bi, and Ni) between oxide liquid and metal in the ‘CuO0.5’–CaO–AlO1.5 system in equilibrium with Cu metal at 1400 °C (liquidus of CaAl2O4) was experimentally studied using the equilibration and quenching technique followed by the electron probe X-ray microanalysis of the resulted samples. The study covered a wide range of effective p(O2) over the system from 10−11 to 10−3.5 (corresponding to formation of immiscible CuO0.5-rich slag). To avoid loss of volatile elements (Pb, Zn, As, Sn, Sb, and Bi), a correlation between ‘CuO0.5’ in oxide liquid and p(O2) in open system was obtained first, followed by studying the volatile elements distribution in closed conditions (Al2O3 crucible sealed in SiO2 ampoule), where ‘CuO0.5’ concentration was used as a marker to evaluate the effective p(O2) over the system. The experimental results were then used for the optimization of the thermodynamic model parameters of the system as part of the integrated experimental and self-consisting thermodynamic modeling research program of phase equilibria in the Cu–Pb–Zn–Fe–Ca–Si–Al–Mg–O–S–(As, Sn, Sb, Bi, Ag, Au, Ni, Cr, Co, and Na) gas/oxide liquid/matte/speiss/metal/solids system. Graphical Abstract

Dopant effects on the environment-dependent chemical properties of NiO(100) surfaces

NiO is a promising material for applications such as electronic devices and catalysts due to its low cost, environmental friendliness, and optimal chemical and electronic properties. Inclusion of a dopant element into the NiO near surface structure can further tune material properties. Despite extensive studies on doped NiO (M−NiO) materials, there remains a lack of knowledge regarding the connection between dopant, environment-dependent dominant near surface structures, and overall chemical properties. Here, the dopant effects on the near surface structure and electronic properties on M−NiO(100) are systematically examined using a combination of density functional theory (DFT) and ab initio phase diagrams. The simultaneous factors tested include dopant element (Al, Mo, Nb, Sn, Ti, V, W, or Zr), dopant placement (surface or subsurface), Ni/O vacancies (surface or subsurface), and oxygen species (O* or O2*) adsorption. The results reveal the dominant structures and compositions of M−NiO(100) under a wide range of environmental conditions (i.e. varying temperature and pressure). Subsequent electronic analyses of the dominant M−NiO(100) structures show non-uniform changes in charge redistribution, band gap, work function, and d-band center with dopant and near surface structure, emphasizing the role of dopants in tuning M−NiO(100) both geometric and electronic properties. Overall, these multiscale modeling results enable a rapid, effective, and a priori prediction of dominant M−NiO(100) structures with distinct chemical properties, crucial for guiding NiO-based materials design with enhanced performance for advanced electronics, energy storage, and catalytic systems.

Multiple generations of garnet and their genetic significance in the Niukutou cobalt-rich Pb-Zn-(Fe) skarn deposit, East Kunlun orogenic belt, western China

The Niukutou deposit, situated within the Qimantagh ore-concentrated area of the East Kunlun Orogenic Belt (EKOB), represents a typical skarn-type Pb-Zn-(Fe) deposit that is also associated with cobalt (Co) mineralization. The main ore minerals include galena, sphalerite, magnetite, hematite, Co-bearing arsenopyrite, cobaltite and glaucodot. This study conducted geochronological and chemical composition analyses of multi-generational garnets from the deposit, aiming to elucidate their genetic significance in the mineralization process. Field and mineralogical observations indicate the presence of three generations of garnets: Grt-I, Grt-II, and Grt-III. The earliest garnet generation (Grt-I) formed during the prograde stage, typically in garnet skarns, and is often replaced by epidote. The second generation (Grt-II), which coexists with pyroxene, also formed during the prograde stage, whereas the third generation (Grt-III) is associated with pyrrhotite stockworks, suggesting its formation during the sulfide stage. Using in-situ LA-ICP-MS U-Pb dating, garnets yield ages of approximately 230–234 Ma, which aligns with the age of 231.8 ± 7.5 Ma obtained from hydrothermal titanite in the deposit. These ages, combined with those of the previous studies, indicate major magmatic and metallogenic activity of 220–240 Ma in the Qimantagh area. Each generation of garnets displays oscillatory zoning characterized by alternating andradite and grossular compositions. The variations in Sn and high field-strength element (HFSE) contents across different garnet generations indicate an increasing trend in oxygen fugacity as mineralization progresses. The high Sn contents in the Niukutou garnets provide geochemical clues for the potential of Sn-W mineralization in this deposit, which should pay attention to in future exploration. Additionally, the high As concentrations in the Niukutou garnets suggest an As-rich hydrothermal fluid, which, owing to the stronger affinity of cobalt for sulfarsenides over sulfides, provides a geochemical indicator for the formation of abundant Co-bearing sulfarsenides rather than cobaltiferous sulfides in the deposit.

Room- and elevated-temperature strength of as-cast Mg-Sn-Y alloys mediated by Sn and Y solubility via intrinsic stability and deformation resistance

Microstructure evolution and first-principles calculations were adopted to explore alloying elements Sn and Y proportion influence on room- and elevated-temperature mechanical properties of as-cast Mg-Sn-Y alloy in the present study. The results show that the room- and elevated-temperature compression yield strength and ultimate compression strength of Mg-1Sn-yY alloy simultaneously improves with Y addition from 0.5 wt.% to 2 wt.%. Decreasing Sn to 0.5 wt.% in Mg-1Sn-2Y alloy, Mg-0.5Sn-2Y alloy yields comparable room-temperature strength to Mg-1Sn-1.5Y alloy with similar alloying element addition. Notably, the elevated-temperature strength of Mg-0.5Sn-2Y alloy is even greater than that of counterpart Mg-1Sn-1.5Y alloy and achieves increment by ∼42 MPa at 200 °C, 48 MPa at 250 °C, and 29 MPa at 300 °C, respectively. Combined with microstructure analysis and first-principles calculations, the mechanism behind this is mainly attributed to increased Y solubility in the matrix. Sn content reduction leads to the MgSnY ternary phase (4.97%) in Mg-1Sn-1.5Y alloy being replaced by the low-content Sn3Y5 phase (2.30%) so as to high Y solid solution in the Mg-0.5Sn-2Y alloy. Raised Y solubility is more favorable to decrease cohesive energy and increase bulk modulus, shear modulus and Young’s modulus, which avails enhancing intrinsic cohesive strength and deformation resistance of alloy other than Sn solubility. Thus, improvement of cohesive strength and deformation resistance by Y solubility promotes Mg-0.5Sn-2Y alloy to endure high loading at elevated temperatures.

Creation of Excitation-Driven Hypervalent Tin(IV) Compounds For Aggregation-Induced Emission and Application to Thermoresponsive Luminescent Films Below Freezing Point.

Although many researchers have devoted their much effort to establish the strategy for developing a stimuli-responsive molecule and tuning of their properties according to the preprogrammed design, it is still challenging to create desired molecules from the scratch. We recently demonstrated that the molecules with a large structural difference between the theoretically optimized structures in the ground and excited states have a potential to exhibit stimuli-responsive luminescent properties. We defined these molecules as an excitation-driven molecule and have shown that they are a versatile platform for designing stimuli-responsive luminescent molecules. Herein, based on the concept of excitation-driven molecules, we show that the hypervalent tin-fused azomethine (TAm) compounds possessing aggregation-induced emission (AIE) properties can be obtained by simple chemical modification with a methyl group although conventional TAm derivatives are well known to be highly luminescent compounds in solution. Furthermore, by combining the solid-state luminescence property of AIE and the coordination number shifts of the hypervalent tin atom, the thermoresponsive films operating below the freezing point are fabricated with the polymer. In this study, we apply the concept of excitation-driven molecules to the hypervalent compounds and demonstrate to obtain the novel functional materials.

Assessment of heavy metal pollution in soil-parent material relationship across ecosystems.

The works of assessing the pollution posed by metals in agricultural areas in developing countries are limited. This study aims to assess metal concentrations and pollution indices of parent materials and soils representing the mantle and oceanic crust units of the ophiolite in the Eastern Mediterranean region, specifically in Kahramanmaraş Province. A total of 88 samples, comprising 44 soil (0-30cm) and 44 parent material (90 + cm), were collected from the study area. Arsenic (As), mercury (Hg), selenium (Se), uranium (U), molybdenum (Mo), tin (Sn), and cesium (Cs) concentrations were analyzed in these samples, along with the reference metal, iron (Fe). Pollution levels were assessed using enrichment factor (EF) and contamination factor (CF) calculations. Results showed that elemental concentrations (Hg, Se, U, Mo, Sn, and Cs) in soils from the mantle and oceanic crust generally reflected those of the parent material. However, the average As concentration in soils from oceanic crust and mantle units was notably elevated, showing a 3 to fourfold increase compared to the parent material. Based on pollution index values, soils from these units demonstrated a moderate level of enrichment (2 < EF < 5) for As, while other elements (Hg, Se, U, Mo, Sn, and Cs) fell into the low enrichment class (EF < 2). Furthermore, the CF index indicated significant contamination (3 < CF < 6) for As. These findings suggest As contamination in soils from different units of the ophiolite (mantle and oceanic crust), potentially resulting from agricultural chemicals like pesticides and fertilizers.

Synthesis, characterization, and antioxidant activity of novel diorganotin(IV) complexes derived from Ibuprofen-5-aminosalicylic acid ligand

This study focuses on the preparations of a new ligand prepared by the condensation reaction between two substances ibuprofen and 5-aminosalicylic acid, and complexes of di organotin(IV) salts were prepared using this produced ligand to yield the appropriate complexes. The generated compounds were identified using FTIR and elemental analysis, in addition (tin, proton and carbon) magnetic resonance (119Sn, 1H, and 13C, NMR). Octahedral geometry was suggested for the synthesized complexes based on the observations of the spectra. Two techniques were used to examine the antioxidant activity of the compounds: DPPH and CUPRAC. Because the tin element was present, the resultant complexes exhibited a higher rate of inhibition than the ligand. Di-methyltin-di-IAS also showed a greater effect as antioxidants than the other compounds. KEY WORDS: Diorganotin(IV), Antioxidant activity, Ligand (IAS), DPPH method, CUPRAC method Bull. Chem. Soc. Ethiop. 2025, 39(1), 101-110. DOI: https://dx.doi.org/10.4314/bcse.v39i1.8

Improving strength-conductivity synergy of Al-Cu-(Sn/Er) alloy with nanoscale substructure

As a conductive material for power transmission, Al-Cu alloy is widely used in power engineering, microelectronics and other fields. In view of the contradiction between the conductivity and strength of aluminum alloy, Sn and Er elements were selected to micro-alloy Al-Cu alloy. Al-Cu, Al-Cu-Sn and Al-Cu-Sn-Er alloys were prepared by near-liquidus casting. After solution treatment, it was subjected to three-stage alternating process of rolling and aging. The effects of micro-alloying and alternating process on the microstructure and properties of Al-Cu alloy were studied. The results show that the precipitated phase Al2Cu of Al-1.12 Cu alloy is rod-shaped after the first-stage process, and the average size is about 278±87 nm. The precipitated phases in the Al-Cu-Sn alloy are Al2Cu (average size of about 206±79 nm) and nano-sized β-Sn particles. The fine β-Sn nanoparticles in the Al-Cu-Sn-Er alloy heterogeneously nucleated on Al8Cu4Er (average size of about 167±45 nm), making Al8Cu4Er grow into particles. After secondary processing, stacking faults (SFs) appeared in the substructures of the three alloys, and the precipitated phases were further refined. The size of most precipitated phases in Al-1.13Cu-0.12Sn and Al-1.01Cu-0.15Sn-0.22Er alloys is reduced to nanometer level. After the three-stage process, some of the Al2Cu precipitates in the Al-Cu alloy are also refined to the nanometer level, and the precipitates in the other two alloys are all refined to the nanometer level. Nanotwins also appear in Al-1.01Cu-0.15Sn-0.22Er alloy. The tensile strength of Al-1.13Cu-0.12Sn and Al-1.01Cu-0.15Sn-0.22Er alloys after three-stage alternating process is 303 MPa and 327 MPa, respectively. The elongations are 21.6 % and 23.3 %, respectively. The relative conductivity was 61.7 %IACS and 59.8 %IACS, respectively. The synergistic effect of microalloying of Sn and Er elements and three-stage alternating processing technology not only reduces the size of precipitates and twins in the alloy to the nanometer level, but also adjusts the distribution of dislocation tangles and stacking faults (SFs), improves the substructure configuration, and improves the mechanical and electrical properties of conductive aluminum alloys.

The elemental variance between the "rice" and "non-rice" portions of Maifanitum and its health risk assessment

BackgroundMaifanitum, a mineral used in Chinese medicine, was first documented during the Song Dynasty (960–1279). Historical records suggest its multifaceted therapeutic properties, including detoxification and stasis resolution, necrosis removal and tissue regeneration, diuretic and calculi dissolution and prolonging life. The concentration of elements in Maifanitum may vary depending on its origin, different parts, which can affect its effectiveness in different fields of applications. Therefore, the analysis of elements in Maifanitum and the subsequent health risk assessment have been conducted. This provides an important basis for the quality control and application safety of Maifanitum. MethodThe analytical techniques employed in this study are inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma optical emission spectrometry (ICP-OES), utilized for the quantitative assessment of 60 elements (Refer to Appendix 1) within Maifanitum samples. Based on the test results, chemometric methods are employed to evaluate the characteristics and differences in elemental concentration from different sources and locations. Additionally, a preliminary health risk assessment is conducted for Maifanitum from different origins and various parts. ResultsWe have established a fingerprint of the elements within Maifanitum, demonstrating a commendable level of similarity. The findings from hierarchical cluster analysis（HCA） corroborated with those from principal component analysis (PCA), collectively unveiling a systematic profile of elemental disparities between Maifanitum samples of diverse origins and applications. It also revealed that there are differences in the concentration of Al, Ga, Be, Hf, Na, Sn, Ti, Zr, Gd, Tb, Sr, Pb, Ce, Ba and other elements in different parts of Maifanitum. While Cd, As, and Cu levels in all samples were within the permissible limits as defined by the Chinese Pharmacopeia, Pb concentrations in the majority of samples were found to surpass these standards, albeit slightly in the ''non-rice'' fraction. The assessment of both beneficial and deleterious elements indicates that the ''non-rice'' fraction of Maifanitum possesses superior quality attributes. Moreover, the overall concentration of rare earth elements in Maifanitum is substantially below the established lower threshold for daily human consumption, with no immediate evidence suggesting any adverse health risks. ConclusionThis study provides a basis for the quality control and safety evaluation of Maifanitum in clinical use.

Mechanical properties of CoCrFeNi-X (X = Ti,Sn) high entropy alloy and tribological properties in simulated seawater environment

Five multimajor element CoCrFeNi-X(X = Ti,Sn) high entropy alloys (HEA) were prepared by vacuum hot press sintering. The phase composition, mechanical properties and tribological properties of CoCrFeNi-X(X = Ti,Sn) alloys in simulated seawater were investigated. The phase structure of CoCrFeNiTi high-entropy alloy is solid solution FCC phase, R phase, σ phase, and Laves phase. But after addition Sn elements, the phase structure become the FCC phase and Ni-Sn solid solution phase. CoCrFeNiTi alloy has lower density (7.17 g/cm3) and higher hardness (750 HV) than that of CoCrFeNiSn. The compressive yield strength of CoCrFeNiTi HEA is better than CoCrFeNiSn HEA. The CoCrFeNiSn high-entropy alloys showed lower wear rates. The main reason is that SnO2 is generated on the wear scar surface, which has good wetting and corrosion inhibition effects, so CoCrFeNiSn HEA shows better wear resistance in simulated seawater. The main wear mechanism of the CoCrFeNiSn HEA is abrasive wear, oxidative wear, exfoliation wear and corrosive wear.

Oxidative stability of chelated Sn(II)(aq) at neutral pH: The critical role of NO3- ions.

Tin(II) compounds are versatile materials with applications across fields such as catalysis, diagnostic imaging, and therapeutic drugs. However, oxidative stabilization of Sn(II) has remained an unresolved challenge as its reactivity with water and dioxygen results in loss of functionality, limiting technological advancement. Approaches to slow Sn(II) oxidation with chelating ligands or sacrificial electron donors have yielded only moderate improvements. We demonstrate here that the addition of nitrate to pyrophosphate-chelated Sn(II)(aq) suppresses Sn(II) oxidation in water across a broad pH range. Evidence of hydroxyl radical concentration reduction and detection of a radical nitrogen species that only forms in the presence of chelated Sn(II) point to a radical-based reaction mechanism. While this chemistry can be broadly applied, we present that this approach maintains Sn(II)'s antibacterial and anti-inflammatory efficacies as an example of sustained oral chemotherapeutic functionality.

Effect of alloying elements (Ni, Co, Cr, and Sn) on the mechanical properties of W–Cu alloy system predicted from first principles

Effect of alloying elements (Ni, Co, Cr, and Sn) on the mechanical properties of W–Cu alloy system predicted from first principles

Efficient bis(indoyl)methanes synthesis enabled by SnO2/SiO2 nanocomposite

This study focuses on the synthesis of SnO2/SiO2 nanocomposite materials using sol-gel method and investigates their role in the synthesis of bis(indoyl)methanes via the Friedel–Craft alkylation route. The results, based on TON and TOF, show that 15 wt % SnO2/SiO2 exhibits high production efficiency and greater stability, with yields reaching 91–93% within 80–93 min. The prepared catalysts were characterized using various analytical techniques. The XRD revealed a crystalline size of 25.05 nm. The TEM analysis indicated a reduced particle size of about 25–30 nm. The SEM reflected the porous nature of the material and EDS showed the constituent elements Sn, O and Si with 3.65, 54.93, and 41.44 atomic %, respectively. FT-IR identified the composite framework with bands at 3408, 1620, 1093, 806 and 631 cm−1. The NH3-TPD indicated the presence of both Lewis acidic and Bronsted acidic sites in the composite materials. The BET method revealed a specific surface area and average pore diameter of 331.5814 m2/g. The developed method offers several advantages, such as a simple workup procedure, high yield, nontoxicity, cleanliness, and the ability to recycle and reuse the catalytic materials three times without loss in catalytic activity. These findings demonstrate the potential of SnO2/SiO2 nanocomposites as efficient and environmentally friendly catalysts for the synthesizing bis(indoyl)methane derivatives.

Drill Hole Spacing Analysis for Evaluation of Quartz Sand Resources as Residual Material from On-Land Alluvial Tin Processing based on Global Estimation Variance and Kriging Variance, with Case Study in the Bangka and Belitung Islands, Indonesia

On-land alluvial tin mining activities produce residual materials from mineral processing or mineral washing; the major one of these is quartz sand, which can be utilized in the manufacturing industry. As time goes by, the reserves of alluvial tin are decreasing, which is in line with the increasing residual material from abundant mineral processing. Mining procedures are carried out following the Indonesian government regulations, covering mining as well as reprocessing. This motivated us to evaluate the potential of quartz sand at two mining sites in Bangka and Belitung Islands. This study evaluated alluvial tin processing residual quartz sand through drill hole spacing analysis (DHSA) by comparing two geostatistics parameters, namely global estimation variance (GEV) and kriging variance (KV). Drill hole samples were taken with varying spacing, ranging from 50 to 200 m, after which geostatistical analysis was carried out. With several simulations, the incorporation of GEV and KV was able to produce the optimal drill hole spacing with measured resource categories in the range of 40 to 55 m, indicated resources in the range of 55 to 85 m, and inferred resources &gt;85 m. Accordingly, the total estimated quartz sand resources of both sites were obtained.

Seasonal changes in the physicochemical characteristics of atmospheric aerosol at the research station “Ice Base Baranova Cape” (Severnaya Zemlya archipelago)

Since 2017 we have carried out aerosol sampling at the research station “Ice Base Baranova Cape” (Novaya Zemlya Archipelago) with the purpose of studying the variations in aerosol physicochemical characteristics: the concentrations of ions, microelements, organic and elemental carbon (ОС and ЕС), as well as the isotopic composition of carbon δ13C in the aerosol. The average summed concentrations of ions throughout the period of measurements were 1,99 μg/m3, the concentrations of elements were 51,1 ng/m3; and those of ОС and ЕС were 398 and 25 ng/m3, respectively; the isotopic composition of carbon δ13C was–27.6 ‰. The main contribution (73 %) to the ion composition of atmospheric aerosol is due to “marine” ions Na+ and Cl-, and the contribution to the elemental composition is due to terrogenic Fe and Al (71 %). The large enrichment coefficients (with respect to Na+ in sea water) were manifested for ions SO 2-, K+, and Ca2+. Aerosol enrichment by these ions is the largest in the warm period. In the aerosol elemental composition, we identified large enrichment coefficients (with respect to Al in the Earth’s crust) in elements Se, Sn, Sb, Mo, As, Zn, Cu, Cr, Pb, and Cd, indicating their technogenic origin. The nearest sources of aerosol enrichment by technogenic elements are plants for mining and processing mineral resources in the Taymyr Autonomous Okrug. The statistical generalization of the multiyear data allowed us to calculate for the first time the annual average behavior of the chemical composition of aerosol in the study region. With respect to the seasonal variations, the ions and elements can be divided into three groups: 1) with winter maximum (Na+, Cl-, Mg2+, Br-; Se, Cd, V, Co, As); 2) with summer (PO 3-, NH +, CH SO3-, F-) or autumn (Al, Ti, Li, Sr, Fe, Zn, Ba, Ni) maximum; 3) with poorly defined or indefinite variations in other ions (NO -, K+, SO 2-, Ca2+) and elements (Cu, Pb, Mo, W, Sn, Cr, Sb, Mn). As most of the other characteristics, the annual behaviors of the ОС and ЕС concentrations are characterized by the general maximum in the winter-spring period. In addition, a second maximum is manifested in the ОС content in the summer-autumn period. The average monthly carbon isotopic composition in the aerosol varies in the range from –28.3 ‰ (February) to –27.3 ‰ (May).

Multiple Tin Compounds Modified Carbon Fibers to Construct Heterogeneous Interfaces for Corrosion Prevention and Electromagnetic Wave Absorption

HighlightsExcellent impedance matching through component modulation engineering.Rich heterogeneous interfaces are constructed to realize excellent electromagnetic wave (EMW) absorption performance.Long-term corrosion protection and excellent EMW absorption properties.

New Piezoceramic SrBi2Nb2-2xWxSnxO9: Crystal Structure, Microstructure and Dielectric Properties.

By using the method of high-temperature solid-phase reaction, the new piezoceramic SrBi2Nb2-2xWxSnxO9 was obtained, where partial substitution of niobium (Nb) atoms with Sn4+ and W6+ atoms in the compound SrBi2Nb2O9 occurred in the octahedra of the perovskite layer (B-position). X-ray diffraction investigations showed that these compounds are single-phase SrBi2Nb2-2xWxSnxO9 (x = 0.1, 0.2) and two-phase SrBi2Nb2-2xWxSnxO9 (x = 0.3, 0.4), but all of them had the structure of Aurivillius-Smolensky phases (ASPs) with close parameters of orthorhombic unit cells. It corresponded to the space group A21am. The temperature dependences of the relative permittivity ε/ε0 and the tangent of the dielectric loss angle tan d were defined at various frequencies. It was found that doping SrBi2Nb2-2xWxSnxO9 (x = 0.1) improved the electrophysical properties of the compound: losses decreased, and the relative permittivity increased. This result was obtained for the first time. Moreover, a new result was obtained that indicated an improvement in the electrophysical properties of SrBi2Nb2O9 using the chemical element Sn (tin). This refutes the previously existing opinion about the impossibility to use Sn as a doping element.

A Review of Nanocarbon-Based Anode Materials for Lithium-Ion Batteries

Renewable and non-renewable energy harvesting and its storage are important components of our everyday economic processes. Lithium-ion batteries (LIBs), with their rechargeable features, high open-circuit voltage, and potential large energy capacities, are one of the ideal alternatives for addressing that endeavor. Despite their widespread use, improving LIBs’ performance, such as increasing energy density demand, stability, and safety, remains a significant problem. The anode is an important component in LIBs and determines battery performance. To achieve high-performance batteries, anode subsystems must have a high capacity for ion intercalation/adsorption, high efficiency during charging and discharging operations, minimal reactivity to the electrolyte, excellent cyclability, and non-toxic operation. Group IV elements (Si, Ge, and Sn), transition-metal oxides, nitrides, sulfides, and transition-metal carbonates have all been tested as LIB anode materials. However, these materials have low rate capability due to weak conductivity, dismal cyclability, and fast capacity fading owing to large volume expansion and severe electrode collapse during the cycle operations. Contrarily, carbon nanostructures (1D, 2D, and 3D) have the potential to be employed as anode materials for LIBs due to their large buffer space and Li-ion conductivity. However, their capacity is limited. Blending these two material types to create a conductive and flexible carbon supporting nanocomposite framework as an anode material for LIBs is regarded as one of the most beneficial techniques for improving stability, conductivity, and capacity. This review begins with a quick overview of LIB operations and performance measurement indexes. It then examines the recently reported synthesis methods of carbon-based nanostructured materials and the effects of their properties on high-performance anode materials for LIBs. These include composites made of 1D, 2D, and 3D nanocarbon structures and much higher Li storage-capacity nanostructured compounds (metals, transitional metal oxides, transition-metal sulfides, and other inorganic materials). The strategies employed to improve anode performance by leveraging the intrinsic features of individual constituents and their structural designs are examined. The review concludes with a summary and an outlook for future advancements in this research field.

Enhancement of Wear and Corrosion Resistance of Ti6Al4V Alloy through Hollow Cathode Discharge-Assisted Plasma Nitriding.

In order to improve the wear and corrosion resistance of Ti6Al4V alloy, a Ti-N compound layer was formed on the alloy by plasma nitriding at a relatively low temperature (750 °C) and within an economical processing duration (4 h), in a mixture of NH3 and N2 gases with varying ratios. The influence of the gas mixture on the microstructure, phase composition, and properties of the Ti-N layer was investigated. The results indicated that the thickness of the nitrided layer achieved in a mixed atmosphere with optimal proportions of NH3 and N2 (with a ratio of 1:2) was substantially greater than that obtained in an atmosphere of pure NH3. This suggests that appropriately increasing the proportion of N2 in the nitriding atmosphere is beneficial for the growth of the nitrided layer. The experiments demonstrated that the formation of the surface nitrided layer significantly enhances the corrosion and wear resistance of the titanium alloys.