Boron Oxide Research Articles

Investigation of the Effect of Boron Oxide and Beeswax on Workability and High-Temperature Performance of Bitumen

AbstractIn recent years, various studies have shown that boron-containing additives improve the rutting performance of the bituminous pavements. However, in these studies, it was stated that these additives would decrease the workability of the bitumen and increase energy required for the construction of the pavement. On the other hand, it has been shown in many studies that waxes increase the workability of the bitumen. In this study, it was aimed to obtain bitumen with high rutting resistance and workability by adding boron oxide (BO) and beeswax (BW) to bitumen. Therefore, modified bitumen was produced by adding BO and BW at different ratios to a 50/70 penetration grade base bitumen. Then, the chemical, physical, and rheological properties of modified bitumen samples were investigated by various experiments. As a result, it has been observed that BO increases the high-temperature performance and viscosity of bitumen; on the other hand, BW decreases rutting resistance and viscosity. When BO and BW were added together to the bitumen, the negative impact of BO on workability and the negative impact of BW on high temperature performance were significantly eliminated. Especially, in 1BO + 1BW and 3BO + 3BW bitumens, the high-temperature performance of the bitumen improved without decreasing the workability.

Effect of B2O3 and Basic Oxides on Network Structure and Chemical Stability of Borosilicate Glass

Glass properties play crucial roles in ensuring the safety and reliability of electronic packaging. However, challenges, such as thermal expansion and resistance to acid corrosion, pose long-term service difficulties. This study investigated the impact of the microstructure on acid resistance by adjusting the glass composition. A glass material with excellent acid resistance was obtained by achieving a similar coefficient of thermal expansion to tantalum; it exhibited a weight loss rate of less than 0.03% when submerged in 38% sulfuric acid at 85 °C for 200 h. Theoretically, this glass can be used to seal wet Ta electrolytic capacitors. Differential scanning calorimetry (DSC) was used to analyze the glass transition temperature and thermal stability of borosilicate glasses. X-ray diffractometry (XRD), scanning electron microscopy (SEM), and Raman spectroscopy were used to study the microstructure of the amorphous phase of the borosilicate glass, which revealed a close relationship between the degree of network phase separation in the borosilicate glass and the degree of polymerization (isomorphic polyhedron value, IP) of the glass matrix. The IP value decreased from 3.82 to 1.98 with an increasing degree of phase separation. Boron transitions from [BO4] to [BO3] within the glass network structure with increasing boron oxide content, which diminishes the availability of free oxygen provided by alkaline oxide, resulting in a lower acid resistance. Notably, the glass exhibited optimal acid resistance at boron trioxide and mixed alkaline oxide contents of 15% and 6%, respectively. Raman experiments revealed how the distributions of various bridging oxygen atoms (Qn) affect the structural phase separation of the glass network. Additionally, Raman spectroscopy revealed the depolymerization of Q4 into Q3, thereby promoting high-temperature phase separation and highlighting the unique advantages of Raman spectroscopy for phase recognition.

A dual-layer ceramic coating based on silicon carbide and boron oxide on the graphite surface to establish high temperature oxidation resistance

A dual-layer ceramic coating based on silicon carbide and boron oxide on the graphite surface to establish high temperature oxidation resistance

Unidentical Twins: Geometrically Similar but Chemically Distinct Metal-Free Sites in Boron Oxide for Methane Oxidation to HCHO, CO and CO2.

Metal-free boron-based catalysts such as boron oxide (B2O3) and boron nitride (h-BN) are promising catalysts for methane oxidation to HCHO and CO. The B2O3 catalyst contains various probable boron sites (B1 to B6), which may be responsible for methane oxidation. In this work, we utilized density functional theory to compare two relevant geometrically identical boron sites (B2 and B4) for their reactivities. The two sites are explored in-detail for the conversion of methane to formaldehyde (M2F), carbon monoxide and carbon dioxide. The B4 site activates the methane C-H bond easily as compared to the B2 site. In M2F conversion, the rate-determining step for the B2 site is the co-activation of dioxygen and methane, whereas over the B4 site, formaldehyde formation is the rate-determining step. The computationally-determined RDS for the B4 site coincides well with the reported experiments. It is further revealed that this site also prefers the formation of CO over CO2, which is in-line with the experiments in literature. It is also shown through orbital analysis that methanol formation does not occur during methane oxidation. We employed descriptors such as condensed Fukui functions and global electrophilicity index to chemically distinct these twin sites.

Boron nanoparticles (BNPs) produced by ns-laser ablation in water: synthesis and characterization

Boron nanoparticles (BNPs) are attractive nanomaterials for their employment in many applications, such as neutron detection, boron neutron capture therapy, proton boron capture therapy and nuclear fusion. Depending on the specific application, 10B or 11B isotopes can be used.Nevertheless, there are significant challenges in developing suitable BNPs using both conventional chemical synthesis routes and dry fabrication techniques. In this study we report BNPs directly synthetised in water by pulsed Laser Ablation in Liquid (PLAL). Nanoparticles of elemental boron have been generated by laser ablation of a sintered 10B target in MilliQ water by employing ns laser pulse. The ablation resulted in BNPs and boron target micro-fragments with hydrogen gas and boric acid as by-products. Simple washing steps were used to obtain clean BNPs in water. The BNPs showed a narrow size distribution between 3 and 4 nm and their stability in water was induced by a thin layer of boron oxide surrounds BNPs. The BNPs were fully characterized by the chemical and structural point of view employing several techniques. A discussion on boron chemical reactions during laser ablation in water and after the NPs were released in solution was done.

Incorporating boron carbide into fused silica imparts multiple mechanisms to facilitate vat photopolymerization

Rapid manufacturing of complex-shaped ceramic components has long been a pressing issue in the aerospace industry. Recent progress in this direction takes advantage of additive manufacturing, by employing vat photopolymerization (VPP) followed by sintering. Here we demonstrate a new recipe/protocol that enables the VPP route to deliver silica products of high relative density as well as high strength. This is achieved by incorporating 2.5 wt% of boron carbide (B4C) into the fused silica slurry, which offers beneficial effects in multiple fronts. During the VPP process, the added black B4C, together with the refractive index difference between the two components in the mixture, effectively increased the light absorbance. Upon sintering, the boron oxide produced by the oxidation of B4C played the role of a sintering aid. The boron oxide also helped to suppress the crystallization of the amorphous silica and therefore the formation of cracks. As a result, the overall quality (forming precision, density, strength and dielectric constant) of the product surpasses by far those prepared previously via VPP-sintering. In particular, the flexural strength reached 60.7 MPa, a factor of 2.5 better than the previously reported highest value. Extending the success above further, we have manufactured a complex-structured silica radome, as a demonstration of the high-quality products achievable for practical applications.

Kinetic Insights into Boron-Based Materials Catalyzed Oxidative Dehydrogenation of Light Alkanes.

High selectivity toward alkenes in oxidative dehydrogenation (ODH) of light alkanes makes boron-based materials promising catalysts. However, many key mechanistic aspects are still debated due to the challenge of capturing fleeting reaction intermediates. Kinetic analysis, including determining reaction orders and activation energy, could be informative for reactions involving radical intermediates but has not been extensively exploited. This Review summarizes the current understanding of the apparent alkane reaction order and the apparent activation energy in the boron-catalyzed ODH. Despite varying compositions and structures, a majority of boron-based catalysts share many common features, including alkene selectivity, the evolution and the formation of active site, and the apparent kinetic properties. These common trends could be attributed to the shared gas-phase radical-mediated reaction pathways and the formation of active hydroxylated boron oxide species on boron-containing materials under ODH conditions. Values of apparent alkane reaction orders and apparent activation energies are sensitive and reliable experimental measures of the contributions of the gas-phase radical-mediated and surface-mediated pathways, suggesting the outline of a general mechanistic framework of the boron-catalyzed ODH.

Құрамында бор бар силикохромды қолдану арқылы төмен көміртекті феррохромды балқыту процесін термодинамикалық модельдеу

The TERRA program for calculating multicomponent heterogeneous systems, based on the principle of maximum entropy, was used to study systems with a complex chemical composition, in which the task of numerical modeling is chemical and phase transformations play an important role. The effect of charge composition and temperature on the chemical and phase composition of melting products was studied, the degree of transition of charge elements into metal was determined, and optimal conditions for obtaining the alloy were found. The thermodynamic analysis of the ferrochromium production process showed that in order to approach the real process of low-carbon ferrochromium smelting, it is necessary to take into account the degree of silicon use by introducing oxygen into the working fluid to oxidize excess silicon according to the calculation. On the basis of the performed thermodynamic analysis, it is also shown that the choice of the process temperature (1750-1800°C and more) is associated with the kinetic conditions of melting, the melting temperature of the formed metal and slag. Therefore, it is expected that the presence of boron oxide, in addition to stabilizing slag from decomposition, will reduce its melting point, and the early appearance of the liquid phase due to low-temperature boron phases will ensure a shift in the reduction reactions of chromium with silicon to the low-temperature region. All these provisions will be implemented during high-temperature experimental work on the development of technological parameters.

Tribological impact on borosilicate glass powder reinforced Al-MMC by variation of sliding velocity and the study of its machinability

Now-a-days, metal matrix composites based on pure aluminium are widely used as a replacement for a wide range of applications thanks to their high strength-to-weight ratio, ductility, and thermal conductivity. Micron-sized (10−3 mm) borosilicate (mixer of Silica (SiO2) and Boron Oxide (B2O3)) glass particles were used to create a dispersion in an aluminium matrix composite (Al7075- borosilicate glass MMC) utilizing a stir casting technique while in a liquid condition. The present study examines the effect of borosilicate glass particle content (0, 3, 6, and 9 wt%) and changes in sliding velocity (0.5, 1, 1.5, and 2 m s−1) on the wear behaviour of a composite rubbing against an EN31 steel disc at a constant load of 20N and a sliding distance of 1000 m. Analysis of wear showed that the presence of borosilicate glass increased the wear rate and countered the trend shown in the coefficient of friction. In a similar vein, the sliding velocity of the counter plate rotated faster resulted in a higher coefficient of friction and a higher wear rate. A reliable mathematical model is developed to find the best combination of machining parameters for Al7075-borosilicate glass metal matrix composite (MMC). This model will consider important performance measures like surface smoothness and material removal rate. The authors will also use a sophisticated statistical method called the Taguchi L9 orthogonal array design of experiments (DOE) to understand how different machining settings affect how easily the composite can be machined. By analyzing the results from the DOE, it can optimize the machining parameters for efficient and cost-effective processing. This work can lead to manufacturing innovation in the future.

Effects of nano-metal oxide additives on ignition and combustion properties of MICs-boron rich fuels

Boron has been considered a promising powdered metal fuel for enhancing composite propellants' energy output due to its high energy density. However, the high ignition temperature and low combustion efficiency limit the application of boron powder due to the high boiling point of the boron oxide layer. Much research is ongoing to overcome these shortcomings, and one potential approach is to introduce a small quantity of metal oxide additives to promote the reaction of boron. This study prepared boron-rich fuels with 10 wt% of eight nano-metal oxide additives by mechanical ball milling. The effect of metal oxides on the thermo-oxidation, ignition, and combustion properties of boron powder was comprehensively studied by the thermogravimetric analysis (TG), the electrically heated filament setup (T-jump), and the laser-induced combustion experiments. TG experiments at 5 K/min found that Bi2O3, MoO3, TiO2, Fe2O3, and CuO can promote thermo-oxidation of boron. Compared to pure boron, Tonset can be reduced from 569 °C to a minimum of 449 °C (B/Bi2O3). Infrared temperature measurement in T-jump tests showed that when heated by an electric heating wire at rates from 1000 K/s to 25000 K/s, the ignition temperatures of B/Bi2O3 are the lowest, even lower than the melting point of boron oxide. Ignition images and SEM for the products further showed that the high heating rate is beneficial to the rapid reaction of boron powder in the single-particle combustion state. Fuels (B/Bi2O3, B/MoO3, and B/CuO) were mixed with the oxidant AP and ignited by laser to study the combustion performance. The results showed that B/CuO/AP has the largest flame area, the highest BO2 characteristic spectral intensity, and the largest burn rate for powder lines. To combine the advantages of CuO and Bi2O3, binary metal oxide (CBO, mass ratio of 3:1) was prepared and the test results showed that CBO can very well improve both ignition and combustion properties of boron. Especially B/CBO/AP has the highest burn rate compared with all fuels containing other additives. It was found that multi-component metal-oxide additive can more synergistically improve the reaction characteristics of boron powder than unary additive. These findings contribute to the development of boron-rich fuels and their application in propellants.

Thermoviscosimetric characteristics of borosilicate glasses with regard to the promising area of low-melting compositions currently being developed for the removable small-scale melter designed by Mayak Production Association

Relevance. The need to obtain experimental data on dependence of thermoviscosimetric properties of the examined borosilicate glasses on temperature, in order to solve the problem of developing a low-melting composition of borosilicate glass for a small-scale melter designed by Mayak Production Association. Aim. To get the most complete characterization of the glasses under study using thermoviscometric measurements. Methods. Mathematical modelling, simplex-lattice design. Results and conclusions. One of the most effective methods of experiment planning, which allows, with a relatively small number of experiments, obtaining a mathematical model reflecting the dependence of the studied property of the mixture on the content of components in it, is the simplex experiment planning method. To simplify the solution of such a task, a group or groups of components are usually distinguished, in which the ratio of the mass fraction of the components does not change. In this article, three groups of components are taken – simulators of high-level radioactive waste, sodium and boron oxides, and glass frit. The authors have identified the most promising area, where the mass fraction of glass frit is from 67.5 to 75%, the mass fraction of sodium and boron is from 25 to 32.5% and the mass fraction of high-level waste components is from 0 to 20%. The paper presents the results of thermoviscometric measurements of 15 melts of low-melting borosilicate glasses of different compositions at temperatures ranging from 700 to 1,200°C. Using simplex-based mathematical models of experiment planning, domains of dependence of thermoviscosimetric characteristics of glass melts on their compositions were created. The authors identified the compositions of glass melts that are found within the viscosity limits determined as allowable for glass melt discharge during operation of the removable small-scale melter of Mayak Production Association design.

Formation of bubbles and microexplosions in burning boron agglomerates

Combining laser ignition tests with quenched particle cross-sectional analyses, this study explores the formation of bubbles and microexplosions in burning boron agglomerates, and discusses the plausible mechanisms behind the microexplosion (expansion–rupture) phenomenon. High-resolution images reveal that these phenomena are caused by bubble nucleation and growth within the molten droplet. Based on the timescale, it is categorized into weak expansion and strong expansion phenomena. The expansion rate of droplets during the weak expansion process mostly ranges between 0.006 m/s and 0.4 m/s, while during the strong expansion process, it predominantly falls between 0.4 m/s and 1 m/s. An increase in ambient pressure results in the delayed occurrence and reduced frequency of the expansion–rupture phenomenon. When the ambient pressure exceeds 3 atm, the expansion phenomenon no longer occurs. In addition, a decrease in the initial diameter of the agglomerates lowers the overall occurrences of expansion–rupture. Analysis of the quenched particle cross-sections reveals that the size and density distributions of the pores within the boron agglomerates reduce gradually during the combustion process. In addition, the surface oxide layers of certain pores are removed during combustion. Estimates of the vaporization rates of (BO)n and B2O3 support the speculation that the expansion of molten boron droplets is attributed to the evaporation of boron oxide layer. In this process, the molten boron acts as a heating surface to evaporate the boron oxide trapped inside the droplet, thus producing B2O3, B2O2, and BO, and leading to droplet growth and tearing of the liquid film. Analysis of bubble growth indicates that the merging of adjacent bubbles to reach the critical nucleation size is probable the starting point of the expansion process. These results can be helpful in promoting the combustion efficiency of boron within the combustion chamber.

Study on the shielding performance of bismuth oxide as a spent fuel dry storage container based on Monte Carlo simulation

For traditional spent fuel shielding materials, due to physical and chemical defects and cost constraints, they have been unable to meet the needs. Therefore, this paper carries out the first discussion on the application and performance of bismuth in neutron shielding by establishing Monte Carlo simulation on the neutron flux model of shielded spent fuel. Firstly, functional fillers such as bismuth oxide, lead oxide, boron oxide, gadolinium oxide and tungsten oxide are added to the matrices to compare the shielding rates of aluminum alloy matrix and silicone rubber matrix. The shielding rate of silicone rubber mixture is higher than aluminum alloy mixture, reaching more than 56%. The optimal addition proportion of bismuth oxide and lead oxide is 30%, and the neutron radiation protection efficiency reaches 60%. Then, the mass attenuation coefficients of bismuth oxide, lead oxide, boron oxide, gadolinium oxide and tungsten oxide in silicone rubber matrix are simulated with the change of functional fillers proportion and neutron energy. This simulation result shows that the mixture with functional fillers has good shielding performance for low energy neutrons, but poor shielding effect for high energy neutrons. Finally, in order to further evaluate the possibility of replacing lead oxide with bismuth oxide as shielding material, the half-value layers and various properties of bismuth oxide and lead oxide are compared. The results show that the shielding properties of bismuth oxide and lead oxide are basically the same, and the mechanical properties, heat resistance, radiation resistance and environmental protection of bismuth oxide are better than that of lead oxide. Therefore, in the case of neutron source strengths in the range of 0.01–6 MeV and secondary gamma rays produced below 2.5 MeV, bismuth can replace lead in neutron shielding applications.

Preparation of super-hydrophobic BN nanotube mesh and theoretical research of wetting state

In this study, we have fabricated stainless steel mesh with columnar super-hydrophobic boron nitride nanotubes (BNNTs) through the ‘gas-liquid-solid’ mechanism annealing method. We employed iron (Fe) powder as the catalyst and utilized boron (B) and boron oxide (B2O3) as the raw materials. The synthesis took place within a tubular furnace, operating under an NH3 atmosphere at a temperature of 1250C∘. The contact angle of water droplets on the experimental surface measures approximately 150∘, while the sliding angle is approximately 3∘. In the next place, the laboratory carried out a series of experiments on the tensile properties, corrosion resistance, and erosion resistance of the prepared samples. The experimental results showed that the sample material had good mechanical properties and corrosion resistance. In addition, the erosion resistance test results showed that the sample material even at high speed (2800 rpm/min). After washing the sample for 5 min, the surface of the material still has good wettability (contact angle is 136.49∘). Finally, droplet bouncing experiments have demonstrated that the adhesion force on the surface of the boron nitride nanotube stainless steel mesh is notably minimal, indicating its substantial hydrophobic properties. Additionally, we conducted an investigation into the wetting interaction between droplets and the surface of the boron nitride nanotube stainless steel mesh. By applying the Wenzel and Cassie formulas and considering the pertinent geometric parameters of the material surface, we theoretically elucidated that, upon contact, the droplets assume a ‘Cassie’ state on the surface of the super-hydrophobic boron nitride nanotube stainless steel mesh. The research results show that the superhydrophobic boron nitride nanotube stainless steel mesh has broad application prospects in the fields of hydrogen storage, sewage treatment and oil-water separation.

Afterglow of Dual‐Confined Carbon Dots Ranging from Blue to Near‐Infrared

AbstractComprehensive research into afterglow emission in the near‐infrared (NIR) region of carbon dots (CDs) is currently lacking. In this study, highly efficient multicolor CDs are synthesized with fluorescence from blue to NIR using Rhodamine 6G. Boron oxide (B2O3) is employed as a matrix for encapsulating and confining the CDs, inhibiting triplet exciton quenching. Furthermore, structural rigidity is enhanced due to the formation of carbon‐boron (C─B) covalent bonds between CDs and B2O3, achieving tunable afterglow emission ranging from 463 to 722 nm with lifetimes up to 801 ms. The green–yellow afterglow composite exhibits an impressive quantum yield up to 37.67% while demonstrating thermally activated delayed fluorescence (TADF). Thus, this composite is coated onto a blue alternating‐current light‐emitting diode (BAC‐LED) to fabricate a white AC‐LED, which is successfully prepared with Commission Internationale de L'Eclairage (CIE) at coordinates of (0.32, 0.34), accompanied by the color rendering index (CRI) reaching 81.1. The bright afterglow compensates for zero‐point flickering in the BAC‐LED, resulting in stable and gentle emission. The potential applications of these luminescent materials in optoelectronic devices are undoubtedly widened by this remarkable advancement.

Structural and spectroscopic correlation in barium-boro-tellurite glass hosts: effects of Dy2O3 doping

In this study, a series of barium-boro-tellurite glass hosts with varying concentration of Dy2O3 doping (0 to 1.25 mol%) were made by melt-quenching method. A study was conducted to investigate how Dy2O3 dopants affect the physical and spectroscopic traits of glasses. Raw materials including barium oxide (BaO), tellurium dioxide (TeO2), boron oxide (B2O3), and dysprosium oxide (Dy2O3) were used to produce these glasses. XRD patterns of the samples showed a broad hump and absence of long-range periodic lattice arrangements, indicating their amorphous nature. The Raman spectral analyses displayed the various vibration modes where the most intense band caused by BaO vibrations at 300 cm-1 and 450 cm-1 corresponding to the symmetric stretching vibration mode of Te–O–Te intra-chain bridges. The peak at 750 cm-1 was due to TeO4 and Te-O-Te vibration modes. The value of optical band gap energy was decreased from 3.155 to 2.1894 eV and then increase at higher Dy2O3 level (0.75 to 1.25 mol%). At Dy3+ contents between 0.25 to 1.25 mol% seven absorption bands were observed at 390, 424, 452, 750, 797, 895 and 1092 nm due to the electronic transitions in Dy3+. The glass refractive indices were raised from 2.3563 to 2.6584 and then decreased at higher Dy2O3 contents which was mainly because of the generation of more bridging oxygen (BO) in the glass matrix. The value of glass electronic polarizability and oxide ions polarizability calculated using LorentzLorenz equation showed a decrease with the rise of Dy2O3 contents, which was ascribed to the presence of fewer non-bridging oxygen (NBO). The optical basicity of the proposed glass hosts was calculated using Duffy and Ingram equation which was decreased with the increase of doping contents. In addition, the optical transmission was increased and reflection loss was reduced with increasing Dy+3 levels. The value of metallization parameter below 1 proved the true amorphous nature of the prepared samples. All the glasses revealed blue and yellow photoluminescence emission peaks due to 4F9/2→ 6H15/2, and 4F9/2 →6H13/2 transitions in Dy3+, respectively. The proposed glass compositions may be beneficial for the advancement of solid-state lasers.

The Synthesis of Three-Dimensional Hexagonal Boron Nitride as the Reinforcing Phase of Polymer-Based Electrolyte for All-Solid-State Li Metal Batteries.

Powdery hexagonal boron nitride (h-BN), as an important material for electrochemical energy storage, has been typically synthesized in bulk and one/two-dimensional (1/2D) nanostructured morphologies. However, until now, no method has been developed to synthesize powdery three-dimensional (3D) h-BN. This work introduces a novel NaCl-glucose-assisted strategy to synthesize micron-sized 3D h-BN with a honeycomb-like structure and its proposed formation mechanism. We propose that NaCl acts as the template of 3D structure and promotes the nitridation reaction by adsorbing NH3 . Glucose facilitates the homogeneous coating of boric acid onto the NaCl surface via functionalizing the NaCl surface. During the nitridation reaction, boron oxides (BO4 and BO3 ) form from a dehydration reaction of boric acid, which is then reduced to O2 -B-N and O-B-N2 intermediates before finally being reduced to BN3 by NH3 . When incorporated into polyethylene oxide-based electrolytes for Li metal batteries, 5 wt % of 3D h-BN significantly enhances ionic conductivity and mechanical strength. Consequently, this composite electrolyte demonstrates superior electrochemical stability. It delivers 300 h of stable cycles in the Li//Li cell at 0.1 mA cm-2 and retains 89 % of discharge capacity (138.9 mAh g-1 ) after 100 cycles at 1 C in the LFP//Li full cell.

Seeking borophene on Ni3Al(111): an experimental characterization of boron segregation and oxidation

Synthesis of a stable, well ordered honeycomb borophene (hB) phase has been achieved to date by exploiting Al(111) as a growth substrate, which provides the necessary charge doping to compensate the high hexagonal-holes density. However, B/Al(111) is governed by a strong B–Al interaction so to yield the actual formation of an AlB2 hB phase. Dilution of aluminum by alloying could then in principle weaken the boron-support bonding. By means of a combined spectroscopy and microscopy experimental approach, we find instead that the growth of boron layers on the Ni3Al(111) alloy termination is driven by B dissolution into the bulk and surface segregation mechanisms. While no long-range ordered boron-induced phase is observed, locally ordered superstructural units with triangular appearance are stabilized by substrate pinning, following the chemical p(2 × 2) surface order. Oxidation involves both boron and aluminum, inducing surface segregation of B, while nickel remains in its metallic form.

Enhanced ignition and combustion performance of boron-based energetic materials through surface modification and titanium dioxides coating

The present study focuses on the removal of ineffective hydroxyl surface (B–OH) of the shell of pristine boron (B) particles, followed by its modification using a low-cost, eco-friendly, and non-hazardous ethylene glycol (EG). Subsequently, very small-sized titanium dioxide (TiO2) particles are coated onto the boron surface by adding titanium tetraisopropoxide (TTIP) precursors at room temperature. Characterization techniques were employed to investigate the structure and morphology of these materials. FTIR, XPS, and TEM analysis reveal that EG effectively removes ineffective boron hydroxyl surfaces and modifies the surface through passivation by its surface functionalities. Furthermore, EG assists in the coating very small-sized TiO2 particles on the boron surface. Thermal stability tests show that the modified boron surface and TiO2-coated boron surface exhibit earlier oxidation of the core boron compared to pristine boron. This enhanced capability for earlier oxidation of core boron was further investigated in the shock tube and bomb calorimeter for measurement of ignition delay time and heat of combustion. The findings demonstrate that room temperature synthesized TiO2-coated B particles (ignition delay time of ∼181 μs and heat of combustion of ∼17.3 kJ/g) outperform pristine B particles (ignition delay time of ∼284 μs and heat of combustion of ∼13.2 kJ/g). This improvement is attributed to the removal of ineffective boron hydroxyl surfaces, surface modification, uniform coating with very small TiO2 particles, the catalytic effect of TiO2 on oxygen diffusion, and effective oxidation of core boron. This study suggests that efficient energetic material can be achieved at room temperature with no potential harm to the environment.

Mechanical properties and microstructure evolution of KD‐SA SiCf/BN/SiC CMCs oxidized at different temperatures

AbstractSilicon carbide fiber‐reinforced SiC ceramic matrix composites (SiCf/SiC CMCs) based on a domestic KD‐SA SiC fiber were exposed to a wet oxygen atmosphere for 135 h at 800, 1100, and 1300°C. The evolution of the microstructure and mechanical properties of SiCf/SiC CMCs have been systematically investigated following oxidation. For weight change, CMC‐1300 showed the greatest gain (0.394%), followed by CMC‐1100 (0.356%) and CMC‐800 (0.149%). The volatilization of boron oxide (B2O3) combined with the slight oxidation of the SiC matrix at 800°C caused crack deflection and fiber pull‐out. The complete dissipation of the interphase could be found when the oxidation temperature increases to 1100°C, generated a fracture surface with brittle fracture characteristics. At 1300°C, crystalline SiO2 hindered oxygen diffusion, with evidence of fiber pull‐out. Based on thermodynamic calculations and microscopic observations, we propose a mechanism to explain the thermal degradation of SiCf/SiC CMCs. This work offers valuable guidance for the fabrication of SiCf/SiC CMCs that are suitable for high‐temperature applications.