X-ray Phase Research Articles

Formation of nanosized copper silicides in a high-speed electric discharge plasma jet

Relevance. The search for suitable materials for creating a new generation of anodes in lithium-ion batteries that have not only high capacity, but also high electrical conductivity. For this purpose, the attempts have been made to use silicon Si, which has a high specific capacitance, instead of graphite C, but this material does not have high electrical conductivity. Copper silicides, in addition to high specific capacity, have high electrical conductivity values, since they do not react with lithium during operation, and therefore can be used to solve problems in the development of the above-mentioned lithium-ion anodes. Aim. To obtain dispersed materials in a high-speed jet of electric discharge plasma in the Cu-Si-C system. Objects. Dispersed materials obtained in the Cu-Si-C system. Methods. Plasma dynamic synthesis, X-ray diffractometry (X-ray phase analysis), scanning electron microscopy, transmission electron microscopy. Results. The authors have carried out the experimental studies to obtain dispersed materials of the Cu-Si-C system in a high-speed electric-discharge plasma jet and studied the microstructure and composition of the synthesized materials. It was revealed that the product consists of nanodispersed particles, which is confirmed by the results of scanning and electron microscopy. According to the results of X-ray diffractometry, crystalline phases of copper of the cubic system and copper silicides Cu3Si and Cu7Si of the hexagonal system are identified in the composition of the synthesized material.

THE MECHANICALLY ACTIVATED COMPOSITES BASED ON TUNGSTEN DISULFIDE: SYNTHESIS AND PROPERTIES

In this work, the physicochemical properties of mechano-activated composites (hereinafter referred to as the mechanocomposites) obtained by mechanical activation of commercial tungsten disulfide powder in a planetary mill were studied. Mechanical activation was carried out for 2, 4 and 8 h, but this work presents the results for the last two experiments. The acceleration of the grinding media was controlled through frequency adjustment; a frequency value of 15.5 Hz, according to calculations, corresponds to an acceleration of the grinding media of 50 m/s2 or 5G. The material of the balls from which the grinding balls are made is stainless steel. Due to the relatively low acceleration values, the problem of contamination of the sample with stainless steel components does not occur as a result of surface erosion that occurs when the balls collide with each other and with the walls of the grinding bowl. Mechanical activation was carried out in an inert argon environment, since these were preliminary studies and therefore there was a need to minimize the environmental parameters taken into account. However, the oxidation process will occur during the process of discharging the sample from the grinding bowl of the planetary mill. The resulting mechanocomposites are precursors for the synthesis of monocomponent catalysts for the processing of heavy oil residue. For this purpose, it is necessary to obtain mechanocomposites containing tungsten trioxide and tungsten disulfide. The results of an experimental study of the influence, mainly, of the duration of mechanical activation on the production of tungsten mechanocomposites are presented. The resulting compounds were characterized by X-ray phase analysis (XRD), IR spectroscopy, scanning electron microscopy (SEM), thermogravimetry (TGA) and simultaneous thermal analysis (STA). For citation: Akimov Al.S., Zhirov N.A., Sudarev E.A., Akimov A.S. The mechanically activated composites based on tungsten disulfide: synthesis and properties. ChemChemTech [Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol.]. 2024. V. 67. N 8. P. 36-43. DOI: 10.6060/ivkkt.20246708.2t.

Solid solutions in disulfide systems Re(IV)S<sub>2</sub>–Ti(IV)S<sub>2</sub>, Re(IV)S<sub>2</sub>–Mo(IV)S<sub>2</sub>, and Re(IV)S<sub>2</sub>–W(IV)S<sub>2</sub>

Objectives. Chalcogenides of transition elements with low oxidation states, as well as their substituted derivatives, remain a poorly studied class of chemical compounds. Rhenium disulfide has many distinctive features and great application potential as a new twodimensional semiconductor. This is due to its unusual structure and unique anisotropic properties. The presence of weak interlayer bonding and a unique distorted octahedral (1T) structure suggests the possibility of creating new phases on its basis. The aim of this work is to obtain and study phases in systems Re(IV)S2–Ti(IV)S2, Re(IV)S2–Mo(IV)S2, and Re(IV)S2–W(IV)S2.Methods. The samples were obtained by high-temperature solid-phase ampoule synthesis in a vacuum. The study was carried out using X-ray phase analysis and X-ray photoelectron spectroscopy.Results. The regions of existence of solid solutions, intercalates and two-phase regions in the resulting systems were established.Diffraction patterns were obtained for the new phases and the crystal lattice parameters were calculated. Based on data relating to the binding energies of core electrons with the nucleus, the study showed the valence states of the elements after synthesis. The study also confirmed that all phases obtained as a result of synthesis contain transition elements in the oxidation state (IV).Conclusions. Intercalated solid solutions are formed in areas rich in rhenium, while in areas close to titanium and molybdenum disulfides, intercalated phases are attained. In the ReS2–WS2 system there is a region of solid solutions, including 30, 50, and 70 mol % rhenium disulfide. Their structure is a polymorphic modification of the structure of the original components. The presence of rhenium, molybdenum, and tungsten in these phases in the oxidation state (+IV) was confirmed. The data obtained on phase formation in dichalcogenide systems can be practically used in the creation of materials with unique electronic, magnetic, and optical properties with a wide range of applications.

In vivo imaging of nickel-rich laticifers: A breakthrough in metal hyperaccumulation

The discovery of the nickel-rich latex of the New Caledonian endemic tree Pycnandra acuminata introduced the term ‘hyperaccumulator’ and gave rise to a new field of research. This then instigated a global quest for these unusual hyperaccumulator plants, even while the underlying mechanisms of nickel acquisition, transport, and internal elemental distribution remained unknown for this original laticifer-bearing hyperaccumulator plant. Here we reveal for the first time the distribution of nickel-filled laticifers in the different plant organs of P. acuminata. The pressurised nickel laticifers were imaged multimodally with a combination of synchrotron X-ray fluorescence (XRF) microscopy, microtomography (XRF-μCT) and synchrotron X-ray phase contrast imaging microtomography (PCI-μCT). These advanced synchrotron methodologies allowed for complimentary non-invasive reconstructions of an in-situ model of the laticiferous system in this species. The data shows the distribution of the nickel-rich laticifers within whole plant tissues from roots to apical tip, thus suggesting nickel trafficking in the laticifer network. The extraordinary concentration of nickel within P. acuminata laticifers functions as an effective natural tracer for XRF-μCT and PCI-μCT to probe the structure and organization of these cells, thereby permitting insights into the development and physiological functioning of this unique duct system.

Magnetron carbon structures obtained by high-frequency magnetron sputtering in Argon and Nitrogen

Purpose of research. Creation and characterization of carbon nanostructures by high-frequency magnetron sputtering from a carbon target in argon on a silicon substrate and in a reactive nitrogen environment, obtained on a Ni catalyst buffer layer. Methods. High-frequency magnetron sputtering on a silicon substrate with changes in control parameters: sputtering time power and working gas pressure Ar and N. Research was carried out using X-ray phase analysis, atomic force microscopy and holographic microscopy, Raman scattering. Results. The formation of carbon nanotubes, including single-walled ones, was confirmed by the method of Raman scattering of light along the lines ID 1363 and IG 1564 cm-1, as well as ωRDМ 308 and 227 cm–1. Using atomic force microscopic images, the fractal dimension of the nanofilms was calculated, which indicated their 3D nature. Based on X-ray phase analysis of magnetron nanofilms, the dimensions of the coherence region, texture, microdeformations and interplanar deformation distortions were determined. Conclusion. In carbon magnetron nanofilms, deformations of both signs occur: both compressive (∆a < 0) and tensile (∆a > 0). Carbon magnetron nanofilms are represented, among other things, by single-walled carbon nanotubes, the chirality of which in an argon environment is (6, 6), and in a reactive mixture of nitrogen and argon on a Ni buffer layer (7, 7). It was discovered that in high-frequency magnetron mode, silicon carbide is formed in both inert and reactive environments.

Influence of the composition and structure of sodium borosilicate glasses on the optical-color characteristics of chromium aventurine glass in the presence of cobalt (II) oxide

We investigated the influence of cobalt (II) oxide additive in the amount of 1–3 mol.% on the structure and optical-color characteristics of chromium-containing glass with the following composition (mol.%): 29.6 Na2O; 19.7 В2О3; 49.3 SiO2; and 1.5 Cr2O3. The dependence of the optical-color characteristics of the glasses under study on the thermal treatment of the glass melt at a temperature of 10500C for 20 minutes was established. The thermal treatment resulted in the volumetric crystallization with the subsequent development of the aventurine effect. According to X-ray phase analysis data, the decorative effect was caused by Cr2O3 crystals. By using IR spectroscopy and differential thermal analysis, the structure of the experimental glasses was studied, and the influence of thermal treatment of glass melts on the formation of the structure of glass-ceramic material was established. Aventurine glass of dark blue-green color was obtained with a color tone =490 nm, color purity P=11.35%, and lightness L=5.454 %. The nature of the influence of cobalt (II) oxide on the optical-color characteristics of chromium-containing aventurine glass based on the Na2O–В2О3–SiO2 system is of interest for further development of new compositions of decorative ceramic glazes and enamel coatings.

Synthesis of Eu-doped TiO<sub>2</sub> nanoparticles by hydrothermal method

Purpose of research. Synthesis, characterization and comparison of the photocatalytic properties of europium-doped titanium dioxide nanoparticles. Methods. Europium-doped titanium dioxide nanoparticles were synthesized via a hydrothermal method followed by post-treatment processes including washing and annealing. Characterization was conducted using transmission electron microscopy, X-ray phase analysis, and energy-dispersive analysis. The bandgap width of the nanoparticles was determined through diffuse reflectance spectroscopy. Photoluminescence properties were studied using scanning probe microscopy and Raman spectroscopy. The photocatalytic properties were studied by spectrophotometry to determine the degradation of methylene blue under ultraviolet radiation. Results. Transmission electron microscopy identified the average particle sizes of europium-doped titanium dioxide. Using X-ray phase analysis, it was established that the nanoparticles were in the anatase phase regardless of the europium content percentage. Energy-dispersive spectroscopy confirmed the presence of the dopant in the samples. The photoluminescence intensity peak increased proportionally with the increase in europium content percentage. The strongest photocatalytic properties were exhibited at the lowest europium content among the samples studied. Conclusion. Synthesized and processed europium-doped titanium dioxide nanoparticles with anatase polymorphic modification exhibit photoluminescent properties. The luminescence intensity depends on the concentration of europium in the particles, due to the formation of additional energy levels inside the band gap. The photocatalytic properties of europium-doped nanoparticles are significantly improved in comparison with samples synthesized without impurities. However, a europium concentration above 0,5% leads to the growth of structural defects that reduce the mobility of photogenerated charge carriers and creates a high energy barrier that prevents them from reaching the surface.

In Ukrainian

The paper describes the method of obtaining the SiC/porous-Si/Si heterostructure and the study of its structural and morphological properties. The method of obtaining heterostructures consisted of several stages: electrochemical etching of single-crystal silicon p-Si (111), annealing of porous Si in a CO atmosphere. The fabricated structures were characterized using scanning electron microscopy, X-ray spectral microanalysis, X-ray phase analysis, high-resolution diffractometry, X-ray reflectometry, and photoluminescence. The method of high-resolution diffractometry made it possible to assess the state of the SiC/Si(001) system. On the 2Theta-omega diffractograms, in addition to the (111) reflection of the Si substrate in the region of 2 Theta = 35.67, the (111) reflection of the cubic SiC film is observed. This means that the formed SiC film is textured in the (111) growth direction of the silicon substrate. The classical technique of X-ray phase analysis showed the presence of a hexagonal phase in the SiC film. The concentration ratio of cubic to hexagonal phase is 80 % cubic and 20 % hexagonal. The RMS deformation of the lattice (ε) in such a structure is ε = 1∙10–2. The photoluminescence spectra of the SiC films of the experimental samples in most cases consist of narrow and broad bands and extend from the near ultraviolet to the entire visible spectrum. At the same time, in the range of wavelengths corresponding to the energy forbidden zones of hexagonal polytypes and cubic polytypes, a noticeable glow was observed in most of the samples. In some samples, luminescence in the area of hexagonal phases was predominant. In the photoluminescence spectra both at T = 77 K and at T = 300 K, a narrow line at a wavelength of ~ 371 nm is observed.

Clinical boundary conditions for propagation-based X-ray phase contrast imaging: from bio-sample models targeting to clinical applications.

Typical propagation-based X-ray phase contrast imaging (PB-PCI) experiments using polyenergetic sources are tested in very ideal conditions: low-energy spectrum (mainly characteristic X-rays), small thickness and homogeneous materials considered weakly absorbing objects, large object-to-detector distance, long exposure times and non-clinical detector. Explore PB-PCI features using boundary conditions imposed by a low power polychromatic X-ray source (X-ray spectrum without characteristic X-rays), thick and heterogenous materials and a small area imaging detector with high low-detection radiation threshold, elements commonly found in a clinical scenario. A PB-PCI setup implemented using a microfocus X-ray source and a dental imaging detector was characterized in terms of different spectra and geometric parameters on the acquired images. Test phantoms containing fibers and homogeneous materials with close attenuation characteristics and animal bone and mixed soft tissues (bio-sample models) were analyzed. Contrast to Noise Ratio (CNR), system spatial resolution and Kerma values were obtained for all images. Phase contrast images showed CNR up to 15% higher than conventional contact images. Moreover, it is better seen when large magnifications (>3) and object-to-detector distances (>13 cm) were used. The influence of the spectrum was not appreciable due to the low efficiency of the detector (thin scintillator screen) at high energies. Despite the clinical boundary condition used in this work, regarding the X-ray spectrum, thick samples, and detection system, it was possible to acquire phase contrast images of biological samples.

Features of the iron determination in dust emissions of gas purification of electrometallurgical production

Features of the iron determination in dust emissions of gas purification at electrometallurgical facilities are considered. The elemental and phase compositions of dust emissions were determined using energy dispersive x-ray fluorescence analysis (EDXRF) and inductively coupled plasma atomic emission spectrometry (ICP-AES). Sample preparation conditions were optimized with allowance for the analytical methods used. The phase composition of dust emissions represented mainly by zincite, zinc ferrite, halite and sylvite was preliminary determined by X-ray phase analysis. Model mixtures were prepared and used to construct calibration dependences taking into account the results of diffractometric studies. A technique for rapid x-ray fluorescence determination of iron in dust emissions of gas purification has been developed. The methods for iron determination tested on real samples of dust emissions of electrometallurgical production demonstrated a satisfactory convergence of the results obtained by EDXRF (Sr = 1.3%) and ICP-AES (Sr = 2.6%).

Production of ceramic bricks using nickel slags as contribution to decarbonization

PurposeThe study suggests that the high concentration of mining and metallurgical enterprises on the territory of the Russian Ural region determines the need to consider industrial waste, including nickel slag, as a possible raw material for the production of ceramic bricks. The article describes the properties of clays and nickel slag obtained at metallurgical enterprises in the Orenburg region and the features of their use as components in the composition of ceramic bricks.Design/methodology/approachTo achieve this purpose, such tasks as determining the technological parameters of production, conducting the X-ray phase and microstructural analysis of the obtained samples were solved.FindingsCompositions of ceramic mass using clay from the Khalilovsky deposit (Orenburg region) with the addition of nickel slag (20 and 40% by weight) have been developed, and their physical and mechanical properties (compressive strength, bending strength, water absorption and density) have been determined. With the help of modern research methods involving high-tech equipment, the microstructure is considered and the phase composition of the finished samples is determined. As a result of the conducted research, it was found that the composition of the selected clay and nickel slag in the obtained rational composition ensures the production of ceramic bricks of grades M175 and M200.Originality/valueThis is the first study on the use of nickel slag for the production of ceramic bricks. The results relate primarily to Russian feedstocks, but a methodology is presented that can be applied to other countries as well as to other silica-containing feedstocks.

Synthesis and structure of polycrystals MnCo2O4-GdCrO4

The article discusses the synthesis and structure of polycrystalline nanocomposite MnCo2O4-GdCrO4 material. The sol-gel method was used as a synthesis of the study. Using X-ray phase analysis (XPA), the structure of the synthesized nanomaterial composition was determined: spinel – cobalt manganate and perovskite – gadolinium chromite. Based on the results of the analysis, it was established that the polycrystalline two-phase composite is a system of spinel-cubic and perovskite-tetragonal types. Morphological analysis of the nanocomposite was carried out using a scanning electron microscope (SEM). According to the data obtained as a result of SEM, the elemental composition was confirmed and the average nanosize of the nanomaterial was obtained, and the content of the compound increased to x2000 was determined, the particle size of MnCo2O4 is 383-281 nm, GdCrO4 – 1.63-1.34 µm; increased to x4000, particle size – MnCo2O4 277-219 nm, GdCrO4 – 1.48-1.27 µm; increased to x6000, particle size – MnCo2O4 239-209 nm, GdCrO4 –1.21-1.07 µm.

Physical and chemical processes during nitriding of chromium ferrosilicon by filtration combustion

In this paper, the nitriding of chromium ferrosilicon is carried out in the combustion mode under the condition of natural nitrogen filtration. The authors studied the effect of the key parameters (pressure of gaseous nitrogen, diameter and dispersity of starting samples) on the maximum temperature and combustion of the starting powder mixture based on chromium ferrosilicon. The combustion synthesis of chromium ferrosilicon proceeds steadily in the stationary mode with formation of a macrohomogeneous nitrided composition which, according to the results of X-ray phase analysis, contains two nitride phases - chromium nitride and silicon nitride. Interaction of the initial powder with gaseous nitrogen in the filtration combustion mode proceeds by the following probable chemical reaction: 3CrSi2 + 3Si + 3FeSi2 + 11.5N2 = 3CrN + 5Si3N4 + 3Fe. Increasing the diameter of the starting samples slightly affects the amount of absorbed nitrogen and slows the propagation of the combustion wave front. An increase in the pressure of gaseous nitrogen increases the amount of absorbed nitrogen and the combustion rate. Increasing the dispersity of the starting powder increases the amount of absorbed nitrogen and the combustion rate. It was found that the combustion reaction is not possible with a dense initial sample. The maximum combustion temperature, depending on the nitriding conditions, varies between 2400 and 2650 °C and increases with increasing gaseous nitrogen pressure, diameter of the initial samples and dispersion of chromium ferrosilicon powder. It is possible to realise nitriding of chrome ferrosilicon in the combustion mode at the pressure of gaseous nitrogen not less than 3 MPa, diameter of initial samples not less than 3.5 cm and size of initial particles not more than 100 μm. Optimal parameters of nitriding are gaseous nitrogen pressure of 5 MPa, diameter of samples 5 cm, size of initial particles less than 100 μm and bulk density of samples (2.23 g/cm3).

Cerium Dioxide-Dextran Nanocomposites in the Development of a Medical Product for Wound Healing: Physical, Chemical and Biomedical Characteristics.

the creation of a dextran coating on cerium oxide crystals using different ratios of cerium and dextran to synthesize nanocomposites, and the selection of the best nanocomposite to develop a nanodrug that accelerates quality wound healing with a new type of antimicrobial effect. Nanocomposites were synthesized using cerium nitrate and dextran polysaccharide (6000 Da) at four different initial ratios of Ce(NO3)3x6H2O to dextran (by weight)-1:0.5 (Ce0.5D); 1:1 (Ce1D); 1:2 (Ce2D); and 1:3 (Ce3D). A series of physicochemical experiments were performed to characterize the created nanocomposites: UV-spectroscopy; X-ray phase analysis; transmission electron microscopy; dynamic light scattering and IR-spectroscopy. The biomedical effects of nanocomposites were studied on human fibroblast cell culture with an evaluation of their effect on the metabolic and proliferative activity of cells using an MTT test and direct cell counting. Antimicrobial activity was studied by mass spectrometry using gas chromatography-mass spectrometry against E. coli after 24 h and 48 h of co-incubation. According to the physicochemical studies, nanocrystals less than 5 nm in size with diffraction peaks characteristic of cerium dioxide were identified in all synthesized nanocomposites. With increasing polysaccharide concentration, the particle size of cerium dioxide decreased, and the smallest nanoparticles (<2 nm) were in Ce2D and Ce3D composites. The results of cell experiments showed a high level of safety of dextran nanoceria, while the absence of cytotoxicity (100% cell survival rate) was established for Ce2D and C3D sols. At a nanoceria concentration of 10-2 M, the proliferative activity of fibroblasts was statistically significantly enhanced only when co-cultured with Ce2D, but decreased with Ce3D. The metabolic activity of fibroblasts after 72 h of co-cultivation with nano composites increased with increasing dextran concentration, and the highest level was registered in Ce3D; from the dextran group, differences were registered in Ce2D and Ce3D sols. As a result of the microbiological study, the best antimicrobial activity (bacteriostatic effect) was found for Ce0.5D and Ce2D, which significantly inhibited the multiplication of E. coli after 24 h by an average of 22-27%, and after 48 h, all nanocomposites suppressed the multiplication of E. coli by 58-77%, which was the most pronounced for Ce0.5D, Ce1D, and Ce2D. The necessary physical characteristics of nanoceria-dextran nanocomposites that provide the best wound healing biological effects were determined. Ce2D at a concentration of 10-3 M, which stimulates cell proliferation and metabolism up to 2.5 times and allows a reduction in the rate of microorganism multiplication by three to four times, was selected for subsequent nanodrug creation.

Autofinding egg parasitoids in moth eggs by using machine learning methods in synchrotron-coherent X-ray imaging

The use of a non-destructive technique, such as the propagation-based X-ray phase contrast radiography (PBR) can be an innovative method for automatic parasitism analysis, especially if it presents standard structures. Herein, an artificial intelligence (AI) model is applied in order to establish a computer vision of egg parasitoids in PBRs of parasitized moth eggs acquired at the Synchrotron Radiation for Medical Physics (SYRMEP) beamline at ELETTRA. PBRs of eggs parasitized in four different stages of parasitism (0 days, 3 days, 5 days and 7 days) have been tested. The AI model performance was evaluated by using different metrics. Average Precision (AP), which measures the accuracy of object detection, was found to be 0.866 and 0.741 for the moth eggs and for the parasites, respectively. Additionally, we found that as stage of parasitism becomes longer, the accuracy of parasitism detection also increases (76 % at 7 days).

Влияние технологических параметров процесса прямого лазерного выращивания на качество формируемого объекта из титанового сплава ВТ23

Introduction. Laser engineered net shaping (LENS) or Direct metal deposition (DMD) is considered as a promising method for manufacturing products of complex configurations from titanium-based alloys, as it allows minimizing the use of machining and loss of material to waste. Currently, neither the LENS technological process of titanium alloy VT23 has not been developed, nor the structural features of the alloy after LENS have not been studied, which will make it possible to determine the scope of application of the material after LENS. The purpose of this study is to determine optimal modes of the LENS process for manufacturing of quality parts from titanium alloy VT23. Methodology. The alloy specimens obtained with laser power 700÷1300 W in increments of 100 W and scanning speed 600÷1,000 mm/min in increments of 200 mm/min and distance between adjacent laser tracks 0.5–0.9L (L — track width) in increments of 0.2L were analyzed in the study. The elemental composition of the powder material was studied by X-ray fluorescence analysis and reducing combustion in a gas analyzer, the structure of the objects obtained by LENS was analyzed by metallographic and X-ray phase analysis methods as well as microhardness was determined. Results and discussion. It is established that high-quality objects without cracks, with low porosity can be synthesized from VT23 alloy by LENS method using the following modes: laser power 700÷1100 W, scanning speed 800–1,000 mm/min, track spacing 0.5–0.7 of the individual track width L. It is shown that after all investigated LENS modes, the VT23 alloy had a dispersed (α+β) structure of the “basket weave” type. It is revealed that regardless of LENS mode the amount of β-phase in the alloy structure is about 30 %. It is shown that the microhardness of the deposited material does not depend on LENS modes and is 460 HV.

Получение покрытий с высокой инфракрасной излучательной способностью

Introduction. One of the promising modern methods of coating formation is detonation gas dynamic sputtering. Coatings obtained by this method have high adhesion to the substrate, dense structure and specified functional properties. Development of technology for obtaining functional coatings with high emission coefficient in the infrared range is an urgent need for the development of high-temperature industrial processes and technologies. High-temperature industrial processes consume a large amount of energy, so improving the energy efficiency of industrial equipment is considered as one of the ways to overcome the ever-growing energy crisis. To this end, coatings with high infrared emissivity have been developed for industrial furnaces. These coatings are usually applied to the furnace walls, which significantly improves energy efficiency by increasing heat transfer from the heat-emitting surfaces of the furnace. The purpose of the work is to obtain coatings with high emission indices in the infrared range for further recommendation of its use in baking ovens of Shebekinsky machine-building plant. Methods for studying coating specimens obtained by detonation gas-thermal method: scanning electron microscopy, X-ray phase analysis, energy dispersive analysis, infrared spectroscopy. Results and discussion. The microstructure, phase composition, emissivity and thermal cycling resistance of Fe2O3; Al2O3 + 10 % Fe2O3; Ti + 10% Fe2O3 coatings obtained by detonation gas-dynamic powder spraying are investigated in this work. The results of the study showed that the obtained coatings have a dense structure, increased emissivity and resistance to thermal treatment cycles, as a result of which the structure of the crystal lattice of the coatings does not change.

Inline edge illumination X-ray phase contrast imaging through mask misalignment

Inline edge illumination X-ray phase contrast imaging through mask misalignment

Еffect of synthetic calcium hydrosilicate on the hydration of portland cement

The regularities of the synthesis of calcium hydrosilicates of tobermorite composition in the system “amorphous silica – calcium hydroxide – water” were investigated. The effect of calcium hydrosilicates additive on the hydration processes of Portland cement and the nature of changes in the strength of cement stone at different stages of its hardening was studied. The methods of determining the heat of hydration of cement dough during hardening and X-ray phase analysis showed that the addition of calcium hydrosilicates at the initial stages of hardening accelerates the physicochemical processes of hydration of clinker minerals.

A promising eco-sustainable wound dressing based on cellulose extracted from Spartium junceum L. and impregnated with Glycyrrhiza glabra L extract: Design, production and biological properties

Glycyrrhiza glabra extract is widely known for its antioxidant and anti-inflammatory properties and can improve the wound healing process. The aim of this work was to shorten the time of the healing process by using an eco-sustainable wound dressing based on Spanish broom flexible cellulosic fabric by impregnation with G. glabra extract-loaded ethosomes. Chemical analysis of G. glabra extract was performed by LC-DAD-MS/MS and its encapsulation into ethosomes was obtained using the ethanol injection method. Lipid vesicles were characterized in terms of size, polydispersity index, entrapment efficiency, zeta potential, and stability. In vitro release studies, biocompatibility, and scratch test on 3T3 fibroblasts were performed. Moreover, the structure of Spanish broom dressing and its ability to absorb wound exudate was characterized by Synchrotron X-ray phase contrast microtomography (SR-PCmicroCT). Ethosomes showed a good entrapment efficiency, nanometric size, good stability over time and a slow release of polyphenols compared to the free extract, and were not cytotoxic. Lastly, the results revealed that Spanish broom wound dressing loaded with G. glabra ethosomes is able to accelerate wound closure by reducing wound healing time. To sum up, Spanish broom wound dressing could be a potential new green tool for biomedical applications.