X-ray Diffraction Methods Research Articles

Plasma Spraying NiCoCrAlY-Cr2O3-AgMo Coatings: Fabrication and Tribological Mechanisms

The increasing demand for high-performance aircraft engines has led to a greater emphasis being placed on advanced sealing coating technologies. Developing long-life, self-lubricating, and wear-resistant coatings is of significant research value. This study focuses on the fabrication of a novel self-lubricating and wear-resistant NiCoCrAlY-Cr2O3-AgMo composite coating. This coating was deposited onto a GH4169 substrate utilizing plasma spraying. Scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS) and X-ray diffraction (XRD) methods were employed to characterize the elemental composition and microstructure of the fabricated NiCoCrAlY-Cr2O3-AgMo composite coating. Microhardness measurements across the coating cross-section indicated a gradual increase in hardness from the GH4169 substrate to the NiCoCrAlY-Cr2O3-AgMo coating. The average hardness of the GH4169 substrate was 413.92 HV0.2, while the CoNiCrAlY bonding layer region exhibited an average hardness of 467.60 HV0.2. The NiCoCrAlY-Cr2O3-AgMo coating itself demonstrated an average microhardness of 643.22 HV0.2. Room temperature friction tests indicated that the average coefficient of friction (COF) of the GH4169 substrate was 0.665. In contrast, the NiCoCrAlY-Cr2O3-AgMo coating exhibited a significantly lower average COF of 0.16, representing a 75.94% reduction compared to the uncoated GH4169 substrate. High-temperature friction tests were conducted at 400 °C, 500 °C, and 600 °C, indicating average COF values of 0.438, 0.410, and 0.268, respectively, for the NiCoCrAlY-Cr2O3-AgMo coating. Specifically, at 600 °C, the formation of a lubricious NiMoO4 tribofilm on the coating surface was observed. This tribofilm effectively reduced the wear rate of the GH605 pin to 2.78 × 10−6 mm3/N·m, highlighting the potential of the NiCoCrAlY-Cr2O3-AgMo coating to reduce wear in high-temperature sliding contact applications.

Preparation, characterization and thermal properties of the PS+Si based polymer nanocomposites

Polymer nanocomposites based on polystyrene and polycrystalline Si nanoparticles have been successfully synthesized using the solution-casting method. The scanning electron microscope and x-ray diffraction methods show that the Si nanoparticle size in the obtained nanocomposite was up to 50 nm. The thermostability of the obtained nanocomposite was studied depending on the concentration of Si nanoparticles in the PS matrix. It was found that Si nanoparticles that are distributed homogeneously in the polymer matrix act as a thermal barrier. By adding 3% Si nanoparticles into polystyrene polymer, the thermal degradation temperature of PS increases by 20°, and the decomposition rate reduces from −42,460 mg/min to −35,099 mg/min. In addition, it was shown that Si nanoparticles do not affect the PS glass transition temperature, which explains that the porous Si does not reduce the free volume for the polymer molecules to move. The polymer macromolecules just are adsorbed on the porous silicon surface, which partially limits their mobility.

Новый катодный материал La2/3Cu3Ti4−xFex O12−δ для твердооксидного топливного элемента: синтез и электропроводность

Copper lanthanum titanate La2/3Cu3Ti4−xFexO12−δ x = 0–1 was doped with Fe3+ cations. The diagram of the dependence of the tolerance factor on the relative electronegativity of cations for all studied compositions was represented. It was shown that all the compositions exist in the region of existence of distorted perovskite. X-ray diffraction and X-ray phase analysis methods established the region of existence of solid solutions of La2/3Cu3Ti4−xFexO12−δ obtained by ceramic technology, which was 0 ⩽ x ⩽ 0.4. The temperature dependences of electrical conductivity for the compositions from the region of existence of solid solutions La2/3Cu3Ti4−xFexO12−δ were obtained. The ionic-electronic nature of conductivity was suggested. It was shown that the decrease of electronic conductivity under the increase of iron content was due to the compensation of electronic carriers formed during acceptor doping.

Effects of ultrasonic vibration on residual stress distribution and local mechanical properties of AA6061/Ti6Al4V dissimilar joints by resistance spot welding

The joining of dissimilar titanium and aluminum alloys has potential applications in railway and aerospace industries, owing to substantial weight reduction and better economic viability. In this study, the residual stress distribution and local mechanical performance of ultrasonic-assisted resistance spot welding (UaRSW) welds were investigated. The welding current, welding time, and electrode force of the RSW process were set as 9.0 kA, 350 ms, and 1.0 kN respectively, and the frequency and power of ultrasonic vibration were 20 kHz and 800 W. The residual stress was evaluated by X-ray diffraction (XRD) method and numerical simulation, and these methods showed a reasonable match. There was tensile residual stress distributed on RSW welds and UaRSW welds, but the value of residual stress was reduced by about 30% at welding nugget and 20% at heat affected zone (HAZ) with the ultrasonic vibration, the reduction of residual stress in UaRSW welds was attributed to the more uniform temperature distribution and lower plastic deformation resistant of AA6061. The welding peak temperature was decreased from 1673.4 °C to 1584.2 °C with the ultrasonic vibration, resulted from the modified Al/Ti contact surface and reduced contact resistance. The miniature tensile test results showed the improvement of mechanical performance by ultrasonic vibration. The maximum load of welding nugget region increased from 19.6 N to 22.3 N, and the elongation obtained 10% increase. This hybrid welding technique shows a potential to improve the quality of welds with ensured efficiency, which is also simple to realize automation in the manufacturing industry.

Structural Study on the Novel Plasmonic Optical Materials with Copper Selenide Nanoparticles

Background: Semiconductor-doped materials have been treated actively throughout the last decades and continue to be of great interest because of the challenges of the features due to various nanosize effects. Among other semiconductors, copper chalcogenides demonstrate the interesting plasmonic properties in line with quantum confinement effects provided by the size factor. Objective: This study aims to study the structural and optical features of the sol-gel-derived silica glasses with copper selenide nanoparticles, demonstrating the appearance of the plasmonic light absorption in the near IR range. Method: The samples under study were fabricated through an original sol-gel technique, which realized the simultaneous synthesis of copper selenide and sintering of mesoporous silica. The copper selenide glasses were characterized with X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM), and optical absorption spectroscopy. Results: Formation of nanocrystalline Cu2-xSe particles of the size range from 10 nm through 100-150 nm is established with XRD and TEM techniques. The principal optical properties are presented by the featured absorption in the visible and near-IR ranges. Eg was evaluated for the direct transitions in the range of 2.10-2.36 eV. The plasmonic resonance in the nanoparticles due to increased carrier concentration originated by intrinsic deficiency of Cu2-xSe nanoparticles with variable stoichiometry. Its energy can be controlled by the Cu/Se ratio in the synthesis procedure. Conclusion: The silica sol-gel glasses with copper selenide nanoparticles were fabricated and characterized by XRD and TEM methods, and their optical absorbance spectra were investigated. The principal optical properties are presented by the featured absorption in the visible and near-IR ranges: the steplike proper absorption of the semiconductor particles characterized by Eg and the intense near-IR band is associated with the localized plasmonic resonance in the nanoparticles due to increased carrier concentration.

Synthesis, crystal structure, spectroscopic, electronic and vibrational properties of N′-[(E)-3-pyridinylmethylene]nicotinohydrazide trihydrate: Experimental and computational study

N′-[(E)-3-pyridinylmethylene]nicotinohydrazide trihydrate (C12H10N4O·3(H2O)) was synthesized and its structure was determined by single crystal X-ray diffraction method. X-ray analysis showed that the compound crystalized in the triclinic system P-1 with a = 7.1134 (3) Å, b = 10.0208 (4) Å, c = 10.3601 (4) Å, α = 96.386 (3)°, β = 96.995 (3)°, γ = 101.219 (4)°, V = 712.05 (5) Å3 and Z = 2 and exhibits that the title compound (I) consists of N′-[(E)-3-pyridinylmethylene]nicotinohydrazide (II) (C12H10N4O), and three water molecules of crystallization. The two water molecules are attached to the third water molecule through intermolecular two OH…O hydrogen bonds. At the same time, this water molecule is linked to the NH amide group of the hydrazone by an intermolecular NH…O hydrogen bond. Hirshfeld surface (HS) analyses were carried out are to visualise the intermolecular interactions in the crystals of Compound I. The geometric optimization of the titled compound has been carried out by different computational methods such as by Hatree Fock (HF) and Density Functional Theory (DFT) methods with the 6–311++G (d,p) basis set. The vibrational frequency, dipole moment (μ), polarizability (α), hyperpolarizability (β), and electronic properties including the highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO–LUMO) of the compound have been calculated at the level of both theories. In the results of crystal analysis and geometry calculations of the compound I, it was observed that intermolecular hydrogen bonds, N2H2A…O3, O3H31…O2 and O3H32…O4, were formed. The energy band gap (Eg = ELUMO-EHOMO) values were also obtained by using ELUMO and EHOMO at the level of both theories. The value of equilibrium (ground state) dipole moment of the studied molecule was calculated to be 8.31 Debye in B3LYP and 7.55 Debye in HF. The calculated hyperpolarizability values at the B3LYP/6–311++G(d,p) of the compound are 2.53 × 10−30 esu and this value corresponds to 6.79 times the hyperpolarizability value of urea.

WO2–N co-doped 2D Carbon nanosheets as multifunctional additives for enhancing the electrochemical hydrogen storage performance of Co2B

Co2B, with its high theoretical hydrogen storage capacity, is a potential solid-state hydrogen storage material. However, its poor cycling life limits its practical application. In this work, in order to improve the cycling stability and reversibility of hydrogen absorption and desorption of Co2B, we propose to use WO2–N–C nanosheets as dopants to mix with Co2B, thereby enhancing its practical performance. Two-dimensional tungsten oxide-nitrogen-carbon (WO2–N–C) nanosheets was syntheized via a liquid-phase approach, using a tungstenate-polydopamine precursor followed by thermal treatment. Subsequently, these WO2–N–C nanosheets were compounded with cobalt boride (Co2B) particles through ball milling at various ratios of 1%, 3%, and 5%, which were confirmed by XRD (X-ray diffraction) and SEM (Scanning Electron Microscope) methods. Employing a comprehensive suite of electrochemical analyses, including corrosion potential measurements, polarization curves, step voltammetry, and electrochemical impedance spectroscopy (EIS), we found that the incorporation of WO2–N–C significantly enhances the corrosion resistance and electrochemical activity of Co2B. Furthermore, cyclic life tests revealed that the WO2–N–C-doped Co2B composites exhibit superior discharge capacities and capacity retention rates compared to pristine Co2B. Notably, the 3% WO2–N–C-doped Co2B composite demonstrated the optimal electrochemical performance, achieving a maximum discharge specific capacity of 555 mAh g−1 and maintaining 82% of its initial capacity after 50 cycles. Our findings underscore the dual role of WO2–N–C in not only augmenting the surface electrochemical activity of Co2B but also providing a protective surface layer, thereby enhancing its overall electrochemical performance.

Влияние технологических параметров на микроструктуру и свойства сплава AlSiMg, полученного методом селективного лазерного плавления

Introduction. The development of additive technologies is aimed at the synthesis of new powder compositions for selective laser melting plants, the study of the effect of mode parameters on the stable quality of products. The purpose of this work is to study the effect of the scanning strategy on the microstructure, elemental composition, porosity and density of specimens obtained by selective laser melting from non-spherical powders (Al — 91 wt. %, Si — 8 wt. %, Mg — 1 wt. %), subjected to special preparation to determine the optimal conditions for selective laser melting. The research methods are methods of X-ray diffraction and X-ray phase analysis, transmission electron microscopy. The paper examines specimens formed using four different scanning strategies. Results and discussions. A promising aluminum alloy AlSi8Mg is developed for selective laser melting. The material has good manufacturability and low powder cost. The technological parameters of melting make it possible to form a thin structure with a low level of porosity. The mechanism of influence of the scanning strategy on porosity, surface morphology, relative density and microstructure is investigated. A specimen from the AlSi8Mg powder composition with a high relative density of 99.97 % is produced by selective laser melting with an energy density of 200 J/mm3, a specimen scanning circuit when the direction of laser movement changes by an angle of 90° each odd layer. It is proved that the density of the AlSiMg alloy depends on the scanning strategy used. The calculated density of the specimen was 2.5 g/cm3, which corresponds to the density of silumin. Analysis of SEM images and maps of the distribution of elements (Al, Mg, Si) of the specimens showed that different specimen formation strategies do not affect the nature of silicon distribution. A unique grain structure is observed in the resulting AlSi8Mg alloy. The melt pool consists of small grains along the border and large grains in the center. The formation of fine grains is explained by the addition of Si and the high cooling rate during selective laser melting.

Tetraaza macrocyclic complexes of Cu(II), Co(III) and Ni(II) derived from template condensation of 2,6-pyridinedicarbohydrazide and 2,6-diacetylpyridine: Stability investigation and coloring properties on plastics

Completely conjugated 14-membered ring hexaaza ligand complexes of Cu(II), Co(III) and Ni(II) were synthesized by the template cyclo-condensation reaction of 2,6-diacetylpyridine and 2,6-pyridinedicarbohydrazide: [Cu(HL)Cl]·1.35H2O (1), [Cu(HL)Br]·CH3OH (2), [Cu(L)(H2O)]·4H2O (3), [Co(HL)Cl2]·CH3OH (4), (H3O)[Co(H2L)Cl2][Co(HL)Cl2]Cl2·H2O (5), [Co(HL)(SCN)2]·CH3OH (6), [Ni(L)]·3H2O (7) and (H3O)[Ni(L)]Cl·H2O (8). The structure of all complexes derived from this novel diprotic macrocyclic ligand H2L (5,7-dimethyl-3,4,8,9-tetraaza-1,6(2,6)-dipyridinacyclodecaphane-4,7-diene-2,10-dione) were determined by single crystal X-ray diffraction method. The tetraaza 14-membered conjugated macrocycle is N4-tetracoordinated to metal, adopts an essentially planar configuration and forms four fused metallocycles rings, two five-membered and two six-membered chelates. The structures of the studied complexes reveal three isomers out of three possible: with a 5-6-5-6 order of alternation of metallocycles for 1–6, the 5-5-6-6 isomer in 8 and the coexistence of two different isomers with 5-5-6-6 and 6-6-5-5 alternation of metallocycles in 7. Based on the protonation state of the macrocyclic ligand, four forms of the ligand have been registered: bis-deprotonated L2− (compounds 3, 7 and 8), monodeprotonated HL− (1, 2 and 4), neutral H2L (5) and for compound 6 tautomeric (amide → imidic acid) HL− form. The organisation of crystal structures 1–8 depends on the nature of the metal and the composition of the solvents and outer-sphere ions, but shows clear common features for the same type of metal. The hydrolytic study demonstrated a high stability of the Co(III) and Ni(II) complexes in acidic solutions and the most thermally stable are the complexes 3 and 7 with the limit of 350 °C for Ni(II) complex. Testing of the coloring properties of the [Ni(L)] (8) complex on plastics indicates a high coloring efficiency, especially for polyamide polymers.

Investigating the Role of Microclimate and Microorganisms in the Deterioration of Stone Heritage: The Case of Rupestrian Church from Jac, Romania

Natural stone can undergo disaggregation from various causes, including physical actions such as freeze–thaw cycles, temperature and humidity variations, chemical actions such as the solubilization of minerals by organic and inorganic acids, as well as biological actions due to the colonization of organisms that can produce biocorrosion and biomineralization. This research investigates the impact of microclimatic conditions and microbial activity on the physical and chemical integrity of stone heritage, particularly the biodeterioration caused by fungi in the case of a Romanian rock church. Various analytical techniques were employed, including macroscopic and optical microscopy, Raman spectroscopy, X-ray diffraction, and culture-based identification methods, to characterize the mineral composition and microbial contamination of the rock samples. The analyses revealed that the sandstone consists primarily of quartz (over 90%), muscovite (5–10%), and feldspars. The identified fungi included Cladosporium herbarium, Aspergillus niger, and Mortierella hyalina. The SEM images showed fungal hyphae and spores within the kaolinite–illite matrix, indicating significant microbial colonization and its role in rock deterioration. Additionally, microclimatic data collected over a 12-week period highlighted the substantial fluctuations in temperature and relative humidity within the church, which contribute to the physical and chemical weathering of the stone. This study also noted high levels of particulate matter (PM2.5 and PM10) and volatile organic compounds, which can exacerbate microbial growth and stone decay. The comprehensive analysis underscores the need for targeted preservation strategies that consider both microclimatic factors and microbial colonization to effectively conserve stone heritage sites, ensuring their longevity and structural integrity.

Corrosion of Chromium Coating Fabricated on Zircaloy-4 Substrate.

In the nuclear industry, coated cladding is a topical problem and it is chosen as the near-term and most promising ATF (Accident-Tolerant Fuel) cladding concept. The main objective of this concept is to enhance the accident tolerance of nuclear power plants and accordingly, the performance of cladding is expected to be improved. This work assesses the corrosion performance of a Zircalloy-4 alloy coated with a thin chromium coating by MS (magnetron sputtering), tested under a CANDU (CANada Deuterium Uranium) reactor primary circuit simulated condition (LiOH solution, 10 MPa, 310 °C, pH = 10.5). The anticorrosive performance is evaluated by a gravimetric analysis, a metallographic analysis, X-ray diffraction, electronic microscopy, and electrochemical methods. A four times less gain mass was noticed compared to uncoated Zircaloy-4, indicating a smaller corrosion rate. The SEM micrographs illustrate that the coatings are still adherent, and they are keeping the initial morphological characteristics during the autoclaving process. A SEM cross-section analysis shows values of the thickness of the coatings between 0.8 and 1.46 µm. By XRD, the presence of Cr2O3 oxide is identified. Electrochemical testing confirms good stability and good corrosion performance of Cr coating over time under autoclave conditions.

Electrocatalytic efficiency of carbon nitride supported gold nanoparticle based sensor for iodide and cysteine detection

Extensive investigations are being conducted on gold nanoparticles focusing on their applications in biosensors, laser phototherapy, targeted drug delivery and bioimaging utilizing advanced detection techniques. In this work, an electrochemical sensor was developed based on graphite carbon nitride supported gold nanoparticles. Carbon nitride supported gold nanoparticles (Au–CN) was synthesized by applying a deposition-precipitation route followed by a chemical reduction technique. The composite system was characterized by X-ray diffraction and X-ray photo electron spectroscopy methods. Electron microscopy analysis confirmed the formation of gold nanoparticles within the size range of 5–15 nm on the carbon nitride support. Carbon nitride supported gold based sensor was employed for the electrochemical detection of iodide ion and l-cysteine. The limit of detection and sensitivity of the sensor was attained 8.9 μM and 0.96 μAμM⁻1cm⁻2, respectively, for iodide ion, while 0.48 μM and 5.8 μAμM⁻1cm⁻2, respectively, was achieved for the recognition of cysteine. Furthermore, a paper-based electrochemical device was developed using the Au–CN hybrid system that exhibited promising results in detecting iodide ions, highlighting its potential for economic and portable device applications.

Structural Changes in High-Entropy Alloys CoCrFeNi and CoCrFeMnNi, Irradiated by He Ions at a Temperature of 700 °C.

High-entropy alloys (HEA) are promising structural materials that will successfully resist high-temperature irradiation with helium ions and radiation-induced swelling in new generations of nuclear reactors. In this paper, changes in the elemental and phase composition, surface morphology, and structure of CoCrFeNi and CoCrFeMnNi HEAs irradiated with He2+ ions at a temperature of 700 °C were studied. Structural studies were mainly conducted using the X-ray diffraction method. The formation of a porous surface structure with many microchannels (open blisters) was observed. The average diameter of the blisters in CoCrFeMnNi is around 1.3 times smaller than in CoCrFeNi. It was shown that HEAs' elemental and phase compositions are stable under high-temperature irradiation. It was revealed that, in the region of the peak of implanted helium, high-temperature irradiation leads to the growth of tensile macrostresses in CoCrFeNi by 3.6 times and the formation of compressive macrostresses (-143 MPa) in CoCrFeMnNi; microstresses in the HEAs increase by 2.4 times; and the dislocation density value increases by 4.3 and 7.5 times for CoCrFeNi and CoCrFeMnNi, respectively. The formation of compressive macrostresses and a higher value of dislocation density indicate that the CoCrFeMnNi HEA tends to have greater radiation resistance compared to CoCrFeNi.

Influence of stabilized zirconium dioxide and high hydrostatic pressure on the kinetics of sintering nanopowders of metastable aluminum oxide

The paper presents an analysis of the effect of processing powders with high hydrostatic pressure (HHP) (300, 500, 700 MPa) and stabilized zirconium dioxide (ZrO2 + 3 mol.% Y2O3, (YSZ)) doping on the compaction of metastable nanopowders mixture with γ+θ-Al2O3 + n% YSZ (n = 0, 1, 5, 10, 15 wt%) composition during sintering. The behavior of nanopowders at the initial stage of sintering was studied by dilatometry at a constant heating rate of 5 °C/min, in temperature range from 20 °C to 1500 °C. It has been determined that sintering of compacts occurs in two stages: compaction of γ + θ-Al2O3 (Ⅰ-st stage metastable phases), compaction of the stable α-Al2O3 (ⅠⅠ-nd stage), accompanied by inhibition between them. An “effect of mutual protection against crystallization” of powder mixtures was determined using the X-ray diffraction method. This is characteristic of systems obtained by co-precipitation. A connection between the above mentioned inhibition and an increase in the YSZ additive was found. That, also, correlates to the effect of “mutual protection against crystallization” of Al2O3 – YSZ powder mixtures. A study of the mechanisms and activation energies of γ+θ-Al2O3 + n% YSZ systems’ (n = 0, 1, 5, 10, 15 wt%) sintering depending on the YSZ additive amount and the HHP value showed that a dopant and pressure increase leads to activation energy decrease of the initial sintering stage, and the prevailing sintering mechanism is volumetric diffusion in corundum grains. Also, the work shows that for γ+θ-Al2O3 + ≥5 wt% YSZ systems, the optimal compaction pressure is HHP ≥500 MPa, which corresponds to the transition of the sintering mechanism from grain-boundary diffusion to volumetric diffusion.

Crystal structure and magnetic properties of Fe doped BaTiO3 at morphotropic phase boundary

Ceramic compounds BaTi1-xFexO with x = 0 – 0.2 prepared by solid state reaction technique were studied using X-ray diffraction, Raman spectroscopy, and magnetometry methods focusing on the correlation between the structure and magnetic properties. Chemical doping with Fe ions leads to a concentration driven structural transformation from the single phase tetragonal (T-) structure to the hexagonal (H-) structure with a mixed structural state stable in the concentration range 0.06 <x ≤ 0.2. Increase in the Fe ions content causes a stabilization of weak ferromagnetic state driven by the exchange interactions Fe3+ – O – Fe3+ ions strongly dependent on the structural positions of the Fe ions. Increase of the dopant content above x = 0.08 leads to a decrease of the remnant magnetization which is mainly caused by a stabilization of Fe4+ ions as well as by the lattice defects associated with oxygen vacancies formed to keep electroneutrality of the compounds. The results of the structural and magnetization measurements allowed to itemize the type of exchange interactions between Fe ions residing different structural positions of the hexagonal lattice as well as to reveal structural instability of the T- and H- phases under ambient conditions and applied electric field which shows a possibility to control the structure and magnetic properties of the mixed compounds via external stimuli.

Physical & mechanical properties of pervious concrete incorporating municipal solid waste incineration bottom ash

Municipal solid waste incineration bottom ash (BA) as a cementitious substitute in pervious concrete constitutes a viable strategy for waste recycling and carbon emission mitigation. Nonetheless, the resultant alterations in the cementitious matrix composition and the inter-aggregate macro-porous structure induced by BA incorporation still need to be explored, limiting a thorough understanding of the mechanical behavior and permeability. Macroscopic tests were employed to investigate the impact of BA and compaction densities on the physical and mechanical properties. The effects of BA on the hydration products were analyzed using X-ray diffraction (XRD) and thermogravimetric analysis (TG) methods. The results reveal that at a density of 2190 kg/m³, BA has minimal effect on the interconnected porosity and permeability. However, as the density increases, a higher BA substitution ratio leads to a narrowed pore distribution and a significant reduction in permeability. Furthermore, a power-function relationship exists between the compressive strength and dynamic modulus of elasticity. At a 15 % substitution ratio, a slight decrease in hydration products was observed, resulting in a minor reduction in compressive strength. Concurrently, a linear relationship was established between the proportion of tiny pores (less than two mm2) and the relative compressive strength. Considering both permeability and mechanical performance, pervious concrete with a density of 2310 kg/m3 and containing no more than 10 % BA meets the requirements of the CJJ/T135-2009 standard. These findings provide a scientific basis for the mix design of pervious concrete incorporating BA.

Impact of composition of AlGaInAs confining barriers on emission of InAs quantum dots embedded in AlGaAs/GaAs dot-in-a-well heterostructures

The emission of InAs quantum dots (QDs) grown on Al0.30 Ga0.70As/GaAs heterostructures and integrated into additional capping/buffer quantum wells (QW), known as dot-in-a-well (DWELL) structures, has been investigated. Two different AlGaInAs confining barriers (CBs) and buffer layers (BLs) are compared. The first QD structure includes the Al0.30 Ga0.70As CB (#1) and the In0.15Ga0.85As BL. The second QD structure consists of the Al0.40Ga0.45In0.15As CB (#2) and the In0.25Ga0.75As BL. Comparison of photoluminescence (PL) spectra has revealed that the ground state (GS) emission band in the structure #2 with Al0.40Ga0.45In0.15As CB is characterized by the lower peak energy, smaller PL linewidth (more homogeneous QD sizes) and higher GS emission intensity compared to that parameters in the structure #1 with Al0.30 Ga0.70As CB. The smaller potential barriers at the Al0.40Ga0.45In0.15As CB/QD interfaces in #2 lead to faster thermal decrease in the GS PL intensity at high temperatures compared with that in #1. High-resolution X-ray diffraction (HR-XRD) method was used for the study of the QD structures with the aim of monitoring the sizes and compositions of QDs and QWs. Numerical simulation of HR-XRD scans has shown that the material compositions of QDs and QW in #2 with Al0.40Ga0.45In0.15As CB has not changed in the process of QD structure growth at high temperatures compared to those in #1. The obtained results are interesting for further improvement of InAs/GaAs QD structures for telecommunication technology and optoelectronic applications.

Enhancing mechanical and microstructural properties of Pb composite anode by the addition of W-Co3O4 ceramic particles fabricated by Accumulative Roll Bonding

In this research, the accumulative roll bonding (ARB) technique was employed as a severe plastic deformation method to manufacture a unique bi-metal Pb/W composite reinforced by Co3O4 ceramic oxide. For this purpose, composites with different amounts of reinforcement particles (0.25, 0.5, 1, 1.5, and 2 wt%) were successfully produced using the ARB process (up to 10 cycles). Also, the mechanical properties were evaluated using microhardness, tensile, and shear punch tests. For microstructural investigations, the X-ray diffraction method (XRD), transmission electron microscopy (TEM), and fractography analysis by scanning electron microscopy (SEM) were employed. The Pb-0.5%W/Co3O4 following 10 ARB cycles exhibited optimal mechanical and microstructural properties. For this composite, the tensile strength showed a markable increase of 2.17 times, yield strength by 4.7 times, shear strength by 3.6 times, and hardness by 4.2 times compared to the pure Pb sample subjected to the same ARB cycles. However, the strain was reduced by 3.85 times. These enhanced properties are also followed by increased stiffness and improved anode dimensional stability, creep resistance, and operational lifespan.

Activated Iron-Porous Carbon Nanomaterials as Adsorbents for Methylene Blue and Congo Red.

The adsorption properties of microporous carbon materials modified with iron citrate were investigated. The carbon materials were produced based on resorcinol-formaldehyde resin, treated in a microwave assisted solvothermal reactor, and next carbonized in the tube furnace at a temperature of 700 °C under argon atmosphere. Iron citrate was applied as a modifier, added to the material precursor before the synthesis in the reactor, in the quantity enabling to obtain the nanocomposites with C:Fe mass ratio equal to 10:1. Some samples were additionally activated using potassium oxalate or potassium hydroxide. The phase composition of the produced nanocomposites was determined using the X-ray diffraction method. Scanning and transmission electron microscopy was applied to characterize the changes in samples' morphology resulting from the activation process and/or the introduction of iron into the carbon matrix. The adsorption of nitrogen from gas phase and dyes (methylene blue and congo red) from water solution on the obtained materials was investigated. In the case of methylene blue, the adsorption equilibrium isotherms followed the Langmuir isotherm model. However, in the case of congo red, a linear dependency of adsorption and concentration in a broad equilibrium concentration range was found and well-described using the Henry equation. The most efficient adsorption of methylene blue was noticed for the sample activated with potassium hydroxide and modified with iron citrate, and a maximum adsorption capacity of 696 mg/g was achieved. The highest congo red adsorption was noticed for the non-activated sample modified with iron citrate, and the partition coefficient for this material equaled 171 dm3/g.

Characterization of radon gas transmission rate in pore structures of different rock layers by radon daughters inversion calculation

Determining the transmission rate of radon gas in overburden strata is crucial for conducting a comprehensive study of radon gas's longitudinal and long-distance migration mechanisms. This study investigates the mineral components of rocks in the underground strata of the mining area using the X-ray diffraction method. Additionally, it examines the pore structure parameters of the rocks at different depths using the low-temperature nitrogen adsorption method. This research introduces an approach to inversion calculate the radon gas transmission rate through the activity ratio of radon's characteristic daughters based on the decay law and activity balance of 210Po and 210Pb daughters. In addition, it determines the transmission rates of radon gas in overlying strata at various depths through this method. The relationship between the rock's mineral composition and pore structure is investigated, and the effects of pore structure and mineral composition on the radon gas transmission rate are analyzed. The findings indicated that the pore structure exerts a dual impact on radon gas transport: macropores serve as channels for upward radon gas transport, while micropores offer most of the adsorption area. In contrast, the radon gas transmission rate is indirectly influenced by the mineral composition content associated with the medium's adsorption capacity and pore structure. In the studied lithologies, an increase in quartz content promotes radon gas transmission, while an increase in clay mineral content impedes it. Finally, the mechanisms of radon gas transport, daughter adsorption, and the impacts of rock pore structure and mineral composition on the radon transmission rate are discussed.