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In this present investigation, novel hybrid magnesium composites were synthesized by the inclusion of self-lubricating (BN/MoS 2) and ceramic (ZrO 2) particulates with the help of the powder metallurgy technique. ZE41 magnesium (Mg–4Zn-1RE-0.7Zr) was applied for a broad range of components, including the gearbox casing, the framework of the door, and transmission in aircraft like the Sikorsky UH-60 and the Boeing 727. Apart from its structural application, its usage was limited because of its deficient wear and mechanical properties. This research focuses on enhancing the potential applications of the ZE41 magnesium alloy by improving its mechanical and tribological characteristics. The design of the experiment scheme was applied to explore the effect of individual reinforcements and their synergistic effects on various properties of prepared composites. Microstructural inspection was employed to inspect the morphological characteristics of prepared specimens through scanning electron microscope (SEM) and Energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction analysis (XRD). By analysing SEM, EDS, and X-ray diffraction patterns, the microstructural evaluation reveals uniform phase dispersion and the existence of reinforcements with some minor defects. As a result of the inclusion of reinforcements in composites, the hardness of the reinforced specimen improved to 39.65%, while the wear rate of the reinforced specimen decreased to 40.90% compared with monolithic alloy. A multi-objective grey relational analysis (GRA) optimization method was used to perform a detailed tribological analysis on Specimen G (ZE41 mg + 3% ZrO 2 + 3% MoS 2). According to the results of GRA, the optimized rate of wear and frictional coefficient were achieved on sliding velocity (4 ms−1), sliding distance (2000 m), and load (10 N). The worn surface micrograph reveals that the reinforced composite underwent abrasion and delamination wear, while the unreinforced alloy experienced plastic deformation. [ABSTRACT FROM AUTHOR]

Silicon carbide fiber reinforced silicon carbide ceramic matrix composite (CMC SiC f /SiC) has the advantages of high temperature resistance, corrosion resistance, high strength, low density, and oxidation resistance. It is a high-performance advanced material in aerospace, energy and other fields. However, due to its high hardness, brittleness and anisotropy of fiber structure, the research on application-oriented high-quality processing technology has become a hot issue. In this paper, a new process of rotational thirteen-beam coupling nanosecond laser processing of CMC-SiC f /SiC was studied. The rotational thirteen-beam coupling ablation experiments were carried out on CMC-SiC f /SiC workpiece. A laser beam is divided into thirteen beams and rotated around the beam center by using a beam splitter element. The morphology, structure and composition of ablation holes at different speeds were observed and analyzed by laser confocal microscope, scanning electron microscope, and X-ray energy dispersive spectrometer. It is found that the characteristics of rotational beam coupling have a significant effect on the laser ablation morphologies. The results show that the ablation region of CMC-SiC f /SiC is elliptical due to the fast heat transfer of fibers. The energy density distribution of the waist section of the Gaussian like beam after beam coupling is similar to the "W" shape, and the central energy is lower than the surrounding energy, and the ablation holes also show a similar "W" shape. With the increase of rotational speed, the hole depth first decreased and then increased, the hole diameter and roundness first increased and then decreased, and the hole section was "W" shaped. The ablation area can be divided into five parts: the white granular SiO 2 solid coverage area, the recast layer, the lower recast layer, the molten layer, and the heat affected zone. The rotational characteristics will make the reaction intensity of the whole ablation area more uniform in the circumferential direction. The formation mechanism and element distribution of each part were explored. The research work in this paper will provide a new technical way for the high-performance application of CMC-SiC f /SiC. [ABSTRACT FROM AUTHOR]

The effectiveness of silicon carbide (SiC) planarization mostly relies on the chemical and mechanical effects during chemical mechanical polishing (CMP). Nevertheless, the alumina (Al 2 O 3) abrasive only provides a mechanical effect and is incapable of achieving a high-efficiency polishing of SiC. To address this issue, a series of novel Al 2 O 3 @MnO 2 composite abrasives were prepared by encapsulating varying amounts of manganese dioxide (MnO 2) on Al 2 O 3 abrasive, and the polishing performance on SiC wafers was evaluated. The X-ray diffraction (XRD) and scanning electron microscope (SEM) images, along with the size and zeta potential data, show that MnO 2 is successfully coated on the surface of Al 2 O 3 , and the dispersion of Al 2 O 3 @MnO 2 composite abrasive is significantly improved when compared with the pure Al 2 O 3. Furthermore, the CMP experiment and surface profile analysis demonstrate that the material removal rate (MRR) can reach a maximum value of 640.47 nm/h when using a 0.05 wt% MnO 2 -coated Al 2 O 3 composite abrasive, which is 76 % higher than that of traditional Al 2 O 3 abrasive. Furthermore, the average surface roughness (Sa, arithmetic mean height) of SiC is reduced to 0.73 nm. X-ray photoelectron spectroscopy results reveal that the surface of SiC is oxidized and forms a chemical bond known as Mn–O–Si after CMP. The results of the friction coefficient test and contact angle test indicate that slurries containing composite abrasive have exceptional wettability and a higher friction coefficient. Under the synergistic chemical and mechanical effects, SiC is oxidized to soft oxide and then removed circularly to reach excellent flatness. [ABSTRACT FROM AUTHOR]

A composite coating of Ni–W–Ti 2 AlC was fabricated through direct current electrodeposition. The characterization of the composite coatings included analysis using X-ray diffractometry, scanning electron microscope, energy spectrum analysis, Vickers microhardness testing, electrochemical testing, and tribological testing. The findings indicate that the inclusion of Ti 2 AlC alters both the grain size and microstructure of the coatings. The presence of Ti 2 AlC particles facilitates the nucleation process during Ni–W–Ti 2 AlC deposition. The Ti 2 AlC content influences the coating's performance in the bath. Specifically, the microhardness of the Ni–W-(5 g/L) Ti 2 AlC coating exhibits the highest value, experiencing a 41.89 % increase compared to that of the Ni–W coating. Ti 2 AlC contributes to the rectification of defects in the Ni–W–Ti 2 AlC coating. This composite coating exhibits the lowest corrosion current and superior corrosion resistance, particularly with a Ti 2 AlC concentration of 5 g/L. The wear mechanism of the coating encompasses abrasive wear, adhesive wear, and oxidation wear. Notably, the Ni–W–Ti 2 AlC composite coating demonstrates enhanced friction resistance compared to the Ni–W composite coating. Incorporating Ti 2 AlC introduces a novel approach and avenue for fabricating high-performance tungsten-based functional coatings. [ABSTRACT FROM AUTHOR]

The applications of Si 3 N 4 ceramics are hindered by their brittleness and susceptibility to fracture, despite their high strength and wear resistance. To address this challenge, layered ceramics were prepared using lamination and plasma sintering techniques, inspired by the structure of shell pearl layers. The bio-inspired layered ceramics were alternately arranged with Si 3 N 4 as the matrix layer (hard) and BN as the interfacial layer (soft). During the study, ceramic specimens with different microstructures were obtained by modulating the layer thickness ratio (ratio of Si 3 N 4 to BN) and sintering temperature. The microstructure of the specimens was characterized using SEM (Scanning Electron Microscope) and EDS (Energy Dispersive Spectrometer). The mechanical of various specimens were assessed by measuring the flexural strength and fracture toughness. The results of the investigation revealed that the mechanical characteristics of the samples reached their optimum state (with a toughness of 13.51 ± 1.56 MPa m1/2 and a strength of 429 ± 4.28 MPa) when the ratio of Si 3 N 4 to BN was 5:1, and the sintering temperature was maintained at 2000 °C. [ABSTRACT FROM AUTHOR]

A nanostructure of lithium-zinc copper ferrite (LiZnCu-Ferrite) prepared experimentally by the auto-combustion method depends on different parameters. The auto-combustion method operates at a temperature (160 °C) suitable for preparing the required nanostructure ferrite phase. The dependent composition was [Li 0.5-x Zn x Cu x Fe 2.5-x O 4 at (x = 0, 0.05, 0.15, 0.25, 0.35, and 0.45)]. A pre-firing at temperature (650 °C) was applied during the calcination process that was suitable to remove unwanted products. The sintering at temperature (800 °C) was suitable for a pelletized shape of ferrite samples. The X-ray diffraction (XRD) pattern showed a spinel structure of ferrite phase produced for all samples under study with the lattice constant in the range (8.345–8.368 Å) as a function of (x). The crystallite size was in the range (18.41–30.27 nm) calculated by the Scherrer method. The transmission electron microscope (TEM) showed a production of nanorods in the size range (10–45 nm) and nanoparticles in the size range (10–40 nm). There was a coincidence between the results of the XRD and TEM analyses. On the other hand, the scanning electron microscope (SEM) showed the surface morphology and the nature of grain size, which was a sign of the presence of nanostructure; it agreed with the XRD analysis. FTIR spectra showed evidence that the system Li0.5-xZnxCuxFe2.5-xO4 had spinal ferrite nanoparticles successfully prepared by sol-gel auto-combustion. A vibrating sample magnetometer (VSM) showed a change in magnetic parameters as compensation factor (x) increased for all composites of LiZnCu-ferrite such as saturation magnetization (Ms), initial magnetic permeability (μi), remanence (Mr), and coercive force (Hc) that measured from M − H loops. A saturation magnetization increased as a function of (x) and recorded a maximum value at (x = 0.15). While the coercivity, initial magnetic permeability (μi), and remanence magnetization enhanced as a function of (x) and recorded a maximum value at (x = 0.45). [ABSTRACT FROM AUTHOR]

The main objective of this study is to fabricate composite materials having excellent thermal, mechanical and electrical properties for thermal and electronic applications. In this work, strontium feldspar-containing composites (Sr-feldspar/cordierite and Sr-feldspar/Sr-osumilite) were prepared by solid-state sintering of SrO-containing cordierite (MgSrAl 4 Si 5 O 18)/borosilicate glass powder mixtures. The phase composition, physical properties and microstructure of sintered composites were investigated by X-ray diffraction technique, water displacement method and scanning electron microscope, respectively. Moreover, the thermal expansion coefficient, hardness, and electrical properties were also measured. The results of X-ray patterns revealed the crystallization of Sr-feldspar and cordierite in the composites that contain up to 20% borosilicate glass. On the other hand, the composites that include more than 20% glass, displayed the crystallization of Sr-feldspar and Sr-osumilite with little amount of cristobalite. The bulk density values of sintered composites were decreased from 2.41 to 1.84 g/cm3 with increasing the amount of added glass. The microhardness values were increased from 519 to 710 kg/mm2 with increasing the glass content. Low thermal expansion coefficient (2.65 × 10−6, 2.22 × 10−6, 3.45 × 10−6 and 4.26 × 10−6 K-1 for C0, CG91, CG73, CG55, respectively) and low dialectic constant (7–8.5) were obtained for the prepared composites. [ABSTRACT FROM AUTHOR]

This research delved into the structural, morphological, and magnetic characteristics of rare earth doped strontium ferrites (SrRE x Fe 12-x O 19 (x = 0.05–0.2, RE = La, Sm, Eu, Dy, Er, Lu)) synthesized via the sol-gel method. The dopant ion radius is correlated with the performance of the material to a certain extent. Barium and calcium doping and related iron deficiency state experiments were designed to substantiate the reciprocal dependence between ion radius and coercivity. X-ray diffraction results revealed that doping ions had the capacity to modify lattice dimensions. The lattice size does not exhibit a clear linear relationship with the radius of the doping ion, nor does it inherently correlate with the grain size. The scanning electron microscope demonstrated that ion doping had the capacity to influence the size of grains. A general consequence of rare earth doping is the reduction in the saturation magnetization of strontium ferrites. The lanthanide contraction effect significantly influences the changes in coercivity. It is noteworthy that the variations in lattice internal space induced by doping constitute a primary driving factor for the observed coercivity dependence on the radius of the doping ion. [ABSTRACT FROM AUTHOR]

Osteogenic differentiation and bone regeneration can be effectively aided by porous scaffolds with multiscale cellular structures, making it easier to repair defects in bone tissue. Due to the scarcity of pore-forming agents, it is extremely challenging to fabricate interconnected hierarchically porous zirconia at multi-scale. This work described a novel and straightforward method for directly imprinting a slurry containing two pore-forming agents (microspherical and filamentary) to produce strong and highly porous zirconia (ZrO 2) ceramics with four levels of porosity ranging from nanometers to millimeters. The concentration of hemp fibers significantly affected printability when the rheological behavior of a zirconia slurry was examined. Utilizing a scanning electron microscope (SEM) to monitor the development of powder interstices under various sintering techniques. The permeability performance was assessed when simulated plasma had fully filled the scaffolds. The structure had a high compressive strength of 24.18 MPa, a porosity of 80.9 %, an apparent porosity of 55.7 %, and took just 1.11 s to fill a scaffold that was 15 mm high. It is anticipated that the proposed route will be expanded to include various engineering materials for structural and practical applications. [ABSTRACT FROM AUTHOR]

Daqiuni clay is an aluminosilicate clay with unique properties that make it a promising ceramic precursor. Understanding its sintering behavior is crucial for quality control in manufacturing. This study aimed to investigate the phase evolution, densification process, and reaction kinetics during sintering of Daqiuni clay. A combination of X-ray diffraction (XRD), simultaneous thermogravimetric-differential scanning calorimetry (TG-DSC), scanning electron microscope (SEM) and Fourier transform infrared spectroscopy (FTIR) techniques were employed to comprehensively analyse the phase transformations. The densification behavior, apparent activation energies, and reaction mechanisms were elucidated through thermodilatometric analysis conducted at varying heating rates. Four stages were identified during sintering including dehydration, dehydroxylation, mullite formation, and partial melting. The maximum shrinkages at each stage were measured. Kissinger analysis yielded apparent activation energies of 122.90, 258.40, 361.98 and 348.69 kJ/mol for the dehydroxylation, mullite nucleation, mullite growth, and partial melting stages, respectively. The dehydroxylation and partial melting processes followed the mechanisms of 3rd order reaction and 3D diffusion. Mullite formation was a two-step nucleation and growth process following the JMA model. This study clarified the phase evolution of Daqiuni clay during sintering. [ABSTRACT FROM AUTHOR]

This study successfully synthesized novel phosphors Ca 2 GaTaO 6 : x Dy3+ (CGTO: x Dy3+) and Ca 2 GaTaO 6 :0.06Dy3+, y Sm3+ (CGTO:0.06Dy3+, y Sm3+) using the high temperature solid-phase reaction preparation. The microstructure, optical properties, and energy transfer mechanism of the phosphors were studied through X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence (PL) spectra and fluorescence lifetimes. XRD and corresponding refinement results indicate that Dy3+ and Sm3+ ions were effectively doped into the Ca 2 GaTaO 6 (CGTO) lattice. The SEM graphs show that the elements in CGTO:0.06Dy3+, 0.5Sm3+ phosphors are uniformly distributed. PL spectra analysis show the CGTO: x Dy3+ phosphors display two strong emission peaks located at 482 nm for blue emission and 575 nm for yellow emission when excited with 350 nm light. Under uniform conditions, when excited with 365 nm of light, the CGTO:0.06Dy3+, y Sm3+ phosphors emit light that can be tuned with adjustable color coordinates and correlated color temperature (CCT) by incorporating varying proportions of Sm3+ ions. This tunability is achieved through the effective energy migration from Dy3+ to Sm3+ ions within the phosphor material. Furthermore, the emission spectra and weaken lifetimes of the CGTO:0.06Dy3+, y Sm3+ confirm the energy transport between Dy3+ and Sm3+, and the energy transfer efficiency reached to 76 %. At 423 K, the luminescence intensity of CGTO:0.06Dy3+, 0.05Sm3+ phosphor retains 87 % of the intensity observed at 298 K, signifying its excellent thermal durability. Finally, the electroluminescent performance of the CGTO:0.06Dy3+ and CGTO:0.06Dy3+, 0.05Sm3+ phosphors packaged on 365 nm light-emitting diode (LED) chips respectively were studied to investigate the capability applications of the phosphors in white light-emitting diodes (WLEDs) field. The CCT of the packaged LEDs decline from 3396 to 2825 K, indicating CGTO:0.06Dy3+, 0.05Sm3+ phosphor shifts to warmer white light. At a voltage input of 3.4 V and a current of 600 mA, the thermal sensing shows that the WLEDs maintain aptitude for 90 min, showing that the packaged WLEDs can function consistently under elevated temperatures. These studies indicated the phosphors have potential applications in indoor lighting. [ABSTRACT FROM AUTHOR]

High-performance Sr 0.99 La 0.01 TiO 3 ceramics were synthesized using a conventional solid-phase method, and Sr 0.99 La 0.01 TiO 3 percolated (SLT10-P) samples with excellent resistivity were obtained by coating with an oxidant and heat treatment. In this work, simultaneous excellent dielectric properties (16667 of dielectric permittivity, 0.016 of loss tangent at 1 kHz) and high resistivity (1.44 × 1011 Ω·cm at DC100V) was achieved in SLT10-P ceramics at room temperature by modulating the duration of thermal treatment. X-ray Diffraction and scanning electron microscope analyses proved the diffusion of the oxidant in the grains and grain boundaries during the heat treatment. The increase in grain boundary resistance is mainly due to the fact that the insulating layer formed by the oxide ions entering the grain boundary hinders the long-range movement of electrons. In addition, the diffusion of oxygen from the air into the ceramic during the heat treatment process also contributes to the insulation of grain boundaries. [ABSTRACT FROM AUTHOR]

Nitrogen dioxide (NO 2) exposure can have several adverse health impacts on people, especially the respiratory system. Low selectivity, a lack of long-term stability, and structural and morphological optimization are some challenges associated with using ZnO for NO 2 gas sensing. Therefore, we intended copper (Cu) doping in ZnO to alter its shape and gas-sensing characteristics. This study explores the synthesis, properties, and gas-sensing capabilities of bitter gourd-shaped Cu-doped zinc oxide (ZnO) nanostructures for the detection of nitrogen dioxide (NO 2). A facile hydrothermal synthesis method was employed to synthesize bitter gourd-shaped Cu-doped ZnO nanostructures and comprehensively characterized by several techniques. Comprehensive characterizations of our produced Cu-doped ZnO nanomaterial demonstrated by X-ray diffraction (XRD), Scanning electron microscope (SEM), Energy-dispersive X-ray spectroscopy (EDS), and different energy spectrum. The material was annealed at 400 °C in a controlled dry air environment to improve its suitability for gas sensor applications. A series of temperature-ranging experiments were conducted to get gas-sensing readings from 25 °C to 300 °C. The resulting sensor, founded upon the distinctive morphology of Cu-doped ZnO structures reminiscent of the intricate shape of bitter gourd, unveiled good selectivity with a pronounced affinity for detecting NO 2 gas. Notably, the zenith of its performance was attained at an operating temperature of 200 °C, where its selectivity and sensitivity were most pronounced. Even at a low concentration of 1 ppm, the sensors displayed a maximum response of 3.7, highlighting their high sensitivity. The sensors demonstrated excellent reproducibility, selectivity, and a low detection limit. These findings position bitter gourd-shaped Cu-doped ZnO nanostructures as promising candidates for NO 2 sensing applications across diverse environments. [ABSTRACT FROM AUTHOR]

This study aimed to investigate the impact of incorporating nanoparticles on the energy absorption properties of nanocomposites using low-velocity impact (LVI) testing and molecular modeling. Various types of thermoset polymer-based nanocomposites reinforced with carbon nanotubes (CNTs) and alumina were analyzed, and the effect of adding two types of nanofillers and microfiber as a filler material was investigated. The results show that the addition of nanoparticles significantly improved the elastic energy absorption properties of the nanocomposites at the atomic level. The LVI tests demonstrated that adding both types of nanoparticles, along with microfiber, significantly enhanced the energy absorption capacity of the four-phase composite under practical conditions. The scanning electron microscope (SEM) analyses revealed the morphology behavior of the nanoparticles. Incorporating both types of nanoparticles simultaneously with the polymer and fibers increased the elastic modulus by up to 163 %. These findings have significant implications for designing structures with energy-absorbing materials to reduce sports-related injuries. The use of nanocomposites with enhanced energy absorption properties can help to improve the performance of energy-absorbing structures and reduce the risk of sports-related injuries. [ABSTRACT FROM AUTHOR]

Magnetoelectric (ME) multiferroic composites are more promising candidates for low-power consumption devices, next-generation spintronic devices, and multistate memory devices since they exhibit significantly higher Magnetoelectric interaction over single-phase multiferroics. In this regard magnetic behaviour, dielectric, and magnetoelectric characteristics of a novel Pb-free (1-x) Na 0.5 Bi 0.5 TiO 3 -(x) Ni 0.5 Co 0.5 Fe 2 O 4 , (x = 0, 0.2, 0.4, 0.6, 0.8 & 1) particulate composites were explored. Solid-state synthesis was adopted to prepare the single-phase Na 0.5 Bi 0.5 TiO 3 (NBT), Ni 0.5 Co 0.5 Fe 2 O 4 (NCFO), and their composites. The presence of rhombohedral NBT and cubic inverse spinel NCFO in the composites were confirmed with X-ray diffraction (XRD) patterns. Microstrain (ε) induced in the prepared samples was estimated by using the Williamson-Hall (W-H) method. The piezoelectric NBT phase shows the tensile strain and the ferromagnetic NCFO shows the comprehensive strain. Among all the composites 0.8NBT-0.2NCFO shows a higher strain value of 0.012%, and the decrement in the strain values was observed upon increases in ferrite concentration. Backscattered scanning electron microscope (BS-SEM) images revealed the existence of highly dense uniformly distributed elements and Energy dispersive spectroscopy (EDS) confirmed the existing elements in the composites. UV–vis absorbance spectra disclosed a rise in energy gap values from 1.14 eV to 3.0 eV with increasing NBT percentage. Variations of dielectric permittivity and dielectric loss with respect to AC frequency were studied at room temperature (RT), and the 0.2NBT-0.8NCFO sample shows a high dielectric permittivity of 8500 at ∼100Hz. M − H (Magnetization-Magnetic field) hysteresis loops demonstrate the pure ferrite phase has a coercive field (H c) = 578 Oe, remnant magnetization (M r) = 21.43 emu/g and saturation magnetization (M s) = 71.29 emu/g. The M s and M r values in the composites are enhanced with increasing ferrite percentage. Studies on ME behaviour of (1-x) NBT-(x) NCFO, (x = 0.2,0.4,0.6 & 0.8) show the coupling effect between both the phases at room temperature and the highest coupling coefficient value 3.16mV/Cm. Oe was observed for the 0.8NBT-0.2NCFO further the reasons and mechanisms are discussed. [Display omitted] [ABSTRACT FROM AUTHOR]

SrFe 12 O 19 is widely used due to its low cost, stability and corrosion resistance. In this study, Sm-doped porous SrFe 12 O 19 powder with high coercivity was synthesized using KCl- assisted spray pyrolysis. The Sm doping, microstructure and magnetic properties were studied by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM) and vibrating sample magnetometer (VSM). The results showed that when Sm-doping amount was 0.2, the ferrite powder prepared by KCl-assisted spray pyrolysis had high coercivity of 7.286 kOe and saturation magnetization of 56.422 emu/g. The coercivity of the Sm-doped samples increased by 39.23 % compared with that of the undoped samples. The significant increase in coercivity was associated with the improvement of super-exchange interaction between Fe3+ particles caused by Sm doping, and the size decrease of the hexagonal plate Sr-ferrite particle caused by KCl action. The influencing mechanism of coercivity was discussed in detail based on the analysis of crystal structure and microstructure observation. [ABSTRACT FROM AUTHOR]

With the increasing consumption of non-renewable energy sources such as fossil fuels, human beings are facing the crisis of energy shortage. Therefore, researchers in most regions and countries in the world are actively committed to designing and developing new dielectric energy storage components with high energy storage density and high energy storage efficiency. In this work, 2-dimensional flaky Na 0.5 Bi 0.5 TiO 3 (NBT) inorganic powders were prepared by the two-step molten salt method and compounded with polymer polyvinylidene fluoride (PVDF). NBT/PVDF monolayer and 'sandwich' structure composites were prepared by the tape casting method, and the flaky NBT powders were arranged in parallel in the PVDF matrix. The phase and microstructure of the prepared NBT powders were analyzed by X-ray diffractometer and scanning electron microscope. The dielectric, conductivity, ferroelectric, and energy storage properties of the prepared composites were tested. The results show that the critical breakdown field strength of the prepared single-layer NBT/PVDF and 'sandwich' structure composites with a volume fraction of 0.75 vol.% NBT inorganic powder is 380 kV/mm and 540 kV/mm, respectively. The energy storage density reaches 13.78 J/cm3 and 21.57 J/cm3, which is about 1.87 and 3.01 times the volume fraction of 0 vol.%. [ABSTRACT FROM AUTHOR]

La3+ substituted Mn 0.5 Co 0.5 Fe 2 O 4 ferrites were synthesized through sol-gel auto-combustion route. The impacts of varying doping concentrations (0.03, 0.06 and 0.09) were studied on synthesized samples' structural, optical, morphological, vibrational, and dielectric properties. The spinel cubic phase of synthesized samples was confirmed by X-ray diffraction (XRD) analysis; increased La3+ concentration has altered the structural parameters of prepared ferrites. Diffuse Reflectance Spectroscopy (DRS) shows a decrease in band gap with increasing concentration of La3+. Morphology has been reviewed by Field Effect Scanning Electron Microscope (FE-SEM), and elemental composition was confirmed by Energy Dispersive X-ray (EDAX) spectra. In addition, M − O stretching bonds were verified employing Fourier Transform Infrared (FTIR) spectroscopy. Raman Spectroscopy shows five modes, further confirming the spinel structure. The XPS spectra verified the +2 oxidation state of Manganese. Finally, the dielectric constant, tangent loss, and AC (Alternating Current) conductivity were analyzed with temperature at several frequencies. The experimental results have unveiled intriguing findings: the dielectric constant exhibited its maximum value at the lowest frequency within the investigated range, and it demonstrated an increasing trend with the rising temperature at a specific frequency. Notably, introducing La3+ through substitution has led to a noteworthy enhancement in the dielectric constant, underscoring the novel impact of this dopant on the material's electrical properties. A positive correlation existed between AC conductivity and temperature; as the temperature increases, so does the AC conductivity. Also, it was found to be maximum at maximum frequency value for all samples. Additionally, it can be deduced that raising the La3+ concentration in crystal improves the dielectric characteristics of Manganese Cobalt ferrites. [Display omitted] [ABSTRACT FROM AUTHOR]

In this work, a bright white oxide coating was successfully prepared on 6061 Al alloy by PEO process from an environmentally friendly and low-cost concentrated silicate electrolyte as an alternative for commonly used fluozirconate electrolyte. The characteristics of PEO processes and resulting coatings both in diluted and concentrated silicate electrolytes were investigated by using Optical Emission Spectrometer (OES), Scanning Electron Microscope (SEM), X-ray Energy Dispersive Spectrometer (EDS) and X-ray Diffraction Spectrometer (XRD). The thermal control properties of the coatings were evaluated by UV-VIS-NIR spectrophotometer and infrared emissivity spectrometer, respectively. The corrosion protection performances of the coatings were investigated by potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) tests. Results show that the discharges in diluted silicate electrolyte are more pronounced than those in concentrated silicate electrolyte. The more intensive discharges in diluted silicate electrolyte are related to plasma electrochemical reactions at the material surface or at the metal-oxide interface, facilitating to a relatively dense structure and complex oxides including α -Al 2 O 3 , γ -Al 2 O 3 and mullite. The weaker discharges in concentrated silicate are associated with the fast silicate anions deposition process, resulting in the formation of amorphous SiO 2 with a porous microstructure and high thickness. The coating prepared in concentrated silicate electrolyte is characterized by a bright white color in appearance and has much lower solar absorptance (α s) of 0.159 and higher emissivity (ε) of 0.90 than the coating prepared in diluted silicate electrolyte with α s of 0.429 and ε of 0.79. However, the coating prepared in concentrated silicate electrolyte has a little inferior corrosion protection performance compared with that prepared in diluted silicate electrolyte due to the more porous microstructure. [ABSTRACT FROM AUTHOR]

Photocatalyst technology is the most feasible method for the degradation of industrial pollutants as it requires lesser energy and is also highly efficient. In this study, we report for the first time the synthesis of strontium nitrate nanocubes (ST NCs) by two-step decoration strategy using silver nanoparticles (Ag NPs) and graphene oxide nanosheets (GO NSs) to form Ag/ST and Ag/ST/GO nanocomposites via facile ultrasonication route. The crystallinity, chemical composition, morphology, optical, photocatalytic and electrochemical measurements of the samples were characterized using x-ray diffractometer (XRD), x-ray photoelectron spectrometer (XPS), high-resolution scanning electron microscope (HRSEM), high-resolution transmission electron microscope (HRTEM), ultraviolet–visible (UV–Vis) spectrophotometer and electrochemical workstation. The synthesized 3%Ag/ST and 3%Ag/ST/3%GO nanocomposites demonstrated highest degradation efficiency for the degradation of methylene blue (MB) dye, resulting in 97 % and 99 % degradation in 60 min and 45 min. The samples demonstrated good stability and reproducibility throughout the degradation process. [Display omitted] [ABSTRACT FROM AUTHOR]

The present study presents an analysis of the structural, morphological and magnetic properties of multiferroic YbMnO 3 (YBO) due to Lu doping. YbMnO 3 (YBO) and Yb 0.85 Lu 0.15 MnO 3 (YBLu) were prepared using a conventional solid state reaction method. The investigation employed techniques such as X-ray diffraction (XRD), Field Effect Scanning Electron Microscope (FE-SEM), Raman spectroscopy and magnetic measurements. The X-ray diffraction (XRD) patterns of both samples confirmed the growth of these samples in a polycrystalline single hexagonal phase having space group P6 3 cm with no detectable impurities. The evaluation of crystalline parameters, such as lattice parameters, cell volume, specific bond lengths etc. has been carried out. The Lu-doped sample shows a minor reduction in cell parameters and cell volume which can be attributed to the smaller ionic radius of Lu3+. Lu doping in YBO results in slight shift in Raman Lines towards slightly frequencies which is the result of a small change in the average bond length. The effective magnetic moment of YBLu is found to decrease ∼6 % and the antiferromagnetic ordering temperature T N nearly remains the same because Lu3+ has zero magnetic moment. Both samples show ferri/ferromagnetic behaviour below 5 K due to the ordering of the Yb3+ lattice. [ABSTRACT FROM AUTHOR]

In order to solve the problem of high accumulation of silicon-manganese slag, this paper proposes a method to prepare foam ceramics with high porosity using silicon-manganese slag as raw material. Two types of silicon-manganese slag were obtained from different regions of Ningxia, China, and used to prepare foam ceramics. This was done with the help of one-step sintering method by adding SiC as a foaming agent and borax as a flux. The effects of chemical composition and crystal phase difference of silicomanganese slag on the physical properties, phase and micromorphology of foam ceramics were investigated. By adjusting the firing temperature and foaming agent content, the optimal process for the preparation of foam ceramics by two kinds of silicomanganese slag was determined. The phase and microstructure of the samples were characterized by X-ray diffractometer (XRD) and scanning electron microscope (SEM), and physical analysis was carried out. The results show that when the sintering temperature of the Huiyi silica manganese slag (HYSM) sample is 1100 °C, the bulk density reaches the minimum value of 0.41 g/cm3, while the porosity and compressive strength are 86.26 % and 0.95 MPa, respectively. On the other hand, when the sintering temperature of the Tianyuan silica manganese slag (TYSM) sample is 1110 °C, the packing density reaches a value of at least 0.51 g/cm3, while the porosity and compressive strength are 80.07 % and 2.09 MPa, respectively. The XRD and SEM results show that the crystalline phase of the HYSM sample is mainly magnesium feldspar, while that of the TYSM sample is mainly diopside. In this study, two kinds of silicon manganese slag with different physical and chemical properties were used to prepare foam ceramics with high porosity, and a theoretical basis for the large-scale use of silicon manganese slag in foam ceramics was presented. [ABSTRACT FROM AUTHOR]

The phase composition, microstructure, and hydration process of C 3 A with different MgO content were compared to elucidate the mechanism of hydration resistance of CaO improved by MgO–C 3 A solid solution. The process of hydration heat release was detected by isothermal calorimetry and the hydration products were analyzed by X-ray diffraction and scanning electron microscope. The results showed that the addition of MgO resulted in lattice distortion of C 3 A. In the middle and late stages of the hydration process, Mg(OH) 2 and amorphous gel-like substances covered the surface of the unreacted C 3 A and reduced the hydration reaction rate. The addition of MgO effectively reduced the hydration activity of the MgO–C 3 A solid solution that indicated the addition of MgO can improve the hydration resistance of CaO materials. [ABSTRACT FROM AUTHOR]

In order to solve the problem of high accumulation of silicon-manganese slag, this paper proposes a method to prepare foam ceramics with high porosity using silicon-manganese slag as raw material. Two types of silicon-manganese slag were obtained from different regions of Ningxia, China, and used to prepare foam ceramics. This was done with the help of one-step sintering method by adding SiC as a foaming agent and borax as a flux. The effects of chemical composition and crystal phase difference of silicomanganese slag on the physical properties, phase and micromorphology of foam ceramics were investigated. By adjusting the firing temperature and foaming agent content, the optimal process for the preparation of foam ceramics by two kinds of silicomanganese slag was determined. The phase and microstructure of the samples were characterized by X-ray diffractometer (XRD) and scanning electron microscope (SEM), and physical analysis was carried out. The results show that when the sintering temperature of the Huiyi silica manganese slag (HYSM) sample is 1100 °C, the bulk density reaches the minimum value of 0.41 g/cm3, while the porosity and compressive strength are 86.26 % and 0.95 MPa, respectively. On the other hand, when the sintering temperature of the Tianyuan silica manganese slag (TYSM) sample is 1110 °C, the packing density reaches a value of at least 0.51 g/cm3, while the porosity and compressive strength are 80.07 % and 2.09 MPa, respectively. The XRD and SEM results show that the crystalline phase of the HYSM sample is mainly magnesium feldspar, while that of the TYSM sample is mainly diopside. In this study, two kinds of silicon manganese slag with different physical and chemical properties were used to prepare foam ceramics with high porosity, and a theoretical basis for the large-scale use of silicon manganese slag in foam ceramics was presented. [ABSTRACT FROM AUTHOR]

The phase composition, microstructure, and hydration process of C 3 A with different MgO content were compared to elucidate the mechanism of hydration resistance of CaO improved by MgO–C 3 A solid solution. The process of hydration heat release was detected by isothermal calorimetry and the hydration products were analyzed by X-ray diffraction and scanning electron microscope. The results showed that the addition of MgO resulted in lattice distortion of C 3 A. In the middle and late stages of the hydration process, Mg(OH) 2 and amorphous gel-like substances covered the surface of the unreacted C 3 A and reduced the hydration reaction rate. The addition of MgO effectively reduced the hydration activity of the MgO–C 3 A solid solution that indicated the addition of MgO can improve the hydration resistance of CaO materials. [ABSTRACT FROM AUTHOR]