Carbon nanotube/graphene oxide‐added CaO‐B2O3‐SiO2 glass/Al2O3 composite as substrate for chip‐type supercapacitor

A CaO‐B₂O₃‐SiO₂ (CBS) glass/40 wt% Al₂O₃ composite sintered at 900°C exhibited a dense microstructure with a low porosity of 0.21%. This composite contained Al₂O₃ and anorthite phases, but pure glass sintered at 900°C has small quantities of wollastonite and diopside phases. This composite was measured to have a high bending strength of 323 MPa and thermal conductivity of 3.75 W/(mK). The thermal conductivity increased when the composite was annealed at 850°C after sintering at 900°C, because of the increase in the amount of the anorthite phase. 0.25 wt% graphene oxide and 0.75 wt% multi‐wall carbon nanotubes were added to the CBS/40 wt% Al₂O₃ composite to further enhance the thermal conductivity and bending strength. The specimen sintered at 900°C and subsequently annealed at 850°C exhibited a large bending strength of 420 MPa and thermal conductivity of 5.51 W/(mK), indicating that it would be a highly effective substrate for a chip‐type supercapacitor.     

The influence of different SiC amounts on the microstructure,densification, and mechanical properties of hot-pressed Al2O3-SiC composites

The hot pressing process of monolithic Al₂O₃ and Al₂O₃-SiC composites with 0-25 wt% of submicrometer silicon carbide was done in this paper. The presence of SiC particles prohibited the grain growth of the Al₂O₃ matrix during sintering at the temperatures of 1450°C and 1550°C for 1 h and under the pressure of 30 MPa in vacuum. The effect of SiC reinforcement on the mechanical properties of composite specimens like fracture toughness, flexural strength, and hardness was discussed. The results showed that the maximum values of fracture toughness (5.9 ± 0.5 MPa.m^1/2) and hardness (20.8 ± 0.4 GPa) were obtained for the Al₂O₃-5 wt% SiC composite specimens. The significant improvement in fracture toughness of composite specimens in comparison with the monolithic alumina (3.1 ± 0.4 MPa.m^1/2) could be attributed to crack deflection as one of the toughening mechanisms with regard to the presence of SiC particles. In addition, the flexural strength was improved by increasing SiC value up to 25 wt% and reached 395 ± 1.4 MPa. The scanning electron microscopy (SEM) observations verified that the increasing of flexural strength was related to the fine-grained microstructure.     

Mechanical and dielectric properties of reduced graphene oxide nanosheets/alumina composite ceramics

Reduced graphene oxide (rGO) nanosheets/alumina (Al₂O₃) composite ceramics were fabricated by hot-pressing sintering. The density, porosity, microhardness, flexural strength and complex permittivity were investigated to study their mechanical and dielectric properties. The results revealed that the rGO nanosheets were uniformly distributed in the Al₂O₃ matrix and that the composite ceramics were highly dense at 3.67–3.99 g/cm³. Due to low rGO hardness and elevated porosity, the microhardness exhibits a decreasing trend as the rGO content increases. The flexural strength first increased and then decreased with the escalation of rGO content, and the highest strength of 313.75 MPa was obtained at 3 wt%, increasing by 37.61% relative to that of the hot-pressing sintered Al₂O₃ ceramic. Owing to the enhanced interfacial polarization, dipole polarization, polarization relaxation loss and conductance loss, the real part and imaginary part of complex permittivity increase from 10.40 to 52.73 and from 0.08 to 28.86 as the rGO content rose from 0 wt% to 4 wt%, respectively.     

Selective laser sintering of porous Al2O3-based ceramics using both Al2O3 and SiO2 poly-hollow microspheres as raw materials

Porous Al₂O₃-based ceramics with improved mechanical strength and different pore size were fabricated using Al₂O₃ and SiO₂ poly-hollow microspheres (PHMs) as raw materials by selective laser sintering (SLS). The effects of different contents of SiO₂ PHMs on phase compositions, microstructures, mechanical properties and pore size distribution of the prepared ceramics were investigated. It is found that moderate content of SiO₂ PHMs (≤30 wt%) could work as a sintering additive, which could enhance the bonding necks between Al₂O₃ PHMs. When the content of SiO₂ PHMs increased from 0 wt% to 30 wt%, the compressive strength of Al₂O₃-based ceramics increased from 0.3 MPa to 4.0 MPa, and the porosity decreased from 77.0% to 65.0% with open pore size decreased from 52.0 μm to 38.3 μm. However, SiO₂ PHMs could provide pores by keeping its integrity when the content of SiO₂ PHMs increased to 40 wt%, which could result in the porosity increasing to 66.8% and pore size decreasing to 30.1 μm. Selective laser sintering of different kinds of ceramic PHMs is a feasible method to fabricate porous ceramics with complex shape, controllable pore size and improved properties.     

Preparation and thermal stability investigation of Al2O3–mullite–ZrO2–SiC composite ceramics for solar thermal transmission pipelines

To obtain composite ceramics with excellent thermal shock resistance and satisfactory high?temperature service performance for solar thermal transmission pipelines, SiC additive was incorporated into Al₂O₃?mullite?ZrO₂ composite ceramics through a pressureless sintering process. The effect of the SiC additive on thermal shock resistance was studied. Also, the variations in the microstructure and physical properties during thermal cycles at 1300 °C were discussed. The results showed that both thermal shock resistance and thermal cycling performance could be improved by adding 20 wt% SiC. In particular, the sample with 50 wt% Al₂O₃, 35 wt% Coal Series Kaolin (CSK), 15 wt% partially yttria?stabilized zirconia (PSZ), and 20 wt% SiC additional (denoted as sample A2) exhibited the best overall performance after firing at 1600 °C. Furthermore, the bending strength of sample A2 increased to 124.58 MPa, with an increasing rate of 13.63% after 30 thermal shock cycles. The increase in thermal conductivity and the formation of mullite were the factors behind the enhancement of thermal shock resistance. During the thermal cycles, the oxidation of SiC particles was favorable as it increased the microstructure densification and also facilitated the generation of mullite, which endowed the composite ceramics with a self?reinforcing performance.     

Vacuum impregnation treatment of microporous Al2O3-MgAl2O4 refractory raw materials with sub-micron pores and high strength

In the present work, we propose a novel method to decrease the pore size as well as to enhance the strength of microporous Al₂O₃-MgAl₂O₄ refractory raw materials, which were prepared by the vacuum impregnation treatment of porous Al₂O₃ powders with at MgCl₂ solution. The effect of the MgCl₂ content (0–32.5 wt%) on the phase distribution, microstructures, and physical properties of the refractory raw materials was thoroughly investigated. The results demonstrated that the sub-micron pore structure inside the pseudomorph particles was effectively preserved due to the volume expansion effect of spinel and the spinel sintering neck formation between Al₂O₃ microcrystallites. With the MgCl₂ content increasing from 0 to 11.9 wt%, the pseudomorph particles contained many sub-micron pores resulting from the introduction of the MgCl₂ solution, resulting in the decrease of the intra-particle pore size as well as the development of spinel sintering necks between pseudomorph particles. The strength of the aggregates was therefore enhanced. With a further increase of MgCl₂ content to 24.2 and 32.5 wt%, the inter-particle pore sizes increased due to the volume expansion and Kirkendall effect associated with the spinel formation between pseudomorph particles, which were responsible for the progressive decrease of the strength. Overall, the optimized samples were microporous Al₂O₃-MgAl₂O₄ refractory aggregates with the addition of 11.9 wt% MgCl₂, which exhibited an apparent porosity of 45.0%, a high compressive strength of 45.6 MPa, a median pore size of only 1.49 µm, and a high sub-micron pore volume content of 42.5 vol%. Meanwhile, it is possible to obtain the porous Al₂O₃-MgAl₂O₄ powders with a large number of sub-micron pores by crushing and sieving the optimized aggregates.     

Ternary hydroxyapatite/chitosan/graphene oxide composite coating on AZ91D magnesium alloy by electrophoretic deposition

In this work, ternary HA/chitosan/graphene oxide (GO) coating was applied via electrophoretic deposition on AZ91D magnesium alloy as bone implants, successfully. Subsequently, phase composition, surface morphology, hardness, corrosion behavior, bioactivity and antibacterial of the composite coatings were studied. Hardness and Young's modulus of the composite coatings increased from 40 ± 1.5 MPa and 3.1 ± 0.42 GPa to 60 ± 3.12 MPa and 8 ± 0.53 GPa for composite coatings with 0 and 2 wt% GO, respectively. The results of the SBF solution soaking of the composites after 24 days, indicated the improvement of HA growth due to the increasing of the GO addition in composite coating. New HA grains with leaf-like morphology grew uniformly at higher amounts of GO (1 and 2 %wt) in a perfectly balanced composition. Rate of the substrate corrosion significantly decreased from 4.3 to 0.2 (mpy), when the amount of GO increased from 0 to 2 wt% due to reduction of the surface cracks at the presence of the GO reinforcement. Also, there was no Escherichia coli and Staphylococcus aureus bacteria growth in broth medium after 24 h and OD₆₀₀ results at 24 h post inoculation for the 2%wt GO addition in coating.     

Mechanical properties of in situ synthesized mullite-based composite ceramics with three-dimensional network structure

Needle-like nanocrystalline mullite powders were prepared through the molten salt process at the temperature of 900°C using coal gangue as raw material. Then, mullite-based composite ceramics were prepared by a conventional solid-state reaction between in situ synthesized mullite and Al₂O₃ powders. Effects of Al₂O₃ content and sintering temperatures on phase compositions, microstructure, and mechanical properties of the mullite-based composite ceramics were also studied. The results show that mullite content productivity increase from 72% to 95%, as the sintering temperature increased from 1480°C to 1580°C, which led to the improvement in the bulk density and flexural strength of the samples. The three-dimensional interlocking structure for mullite-based composite ceramics was obtained by the in situ solid-state reaction process. The maximum bulk density, flexural strength, and fracture toughness for the sample with 15 wt% Al₂O₃ content are 2.48 g/cm³, 139.79 MPa, and 5.62 MPa··m^1/2, respectively, as it was sintered at the temperature of 1560°C for 3 h. The improved mechanical properties of mullite-based composite ceramics maybe ascribed to good densification and increased mullite phase content, as well as to the in situ three-dimensional network structure. Therefore, the results would provide new ideas for high-value utilization of coal gangue.     

Role of CeAl11O18 in reinforcing Al2O3/Ti composites by adding CeO2

This work discusses the reinforcement effect of elongated CeAl₁₁O₁₈ phase on multifunctional Al₂O₃/Ti composites by adding CeO₂ to inhibit interfacial reaction and strengthen interface for inducing optimized performances. For this purpose, Al₂O₃/Ti composite with different contents of CeO₂ was fabricated and the microstructure, mechanical and electrical properties were studied. Results indicated that after CeO₂ was added, elongated CeAl₁₁O₁₈ phase was formed within these composites. Owing to inhibited interfacial reaction between Al₂O₃ and Ti, Ti content was increased and compositions of composites were calculated using Rietveld method based on X-ray diffraction patterns. Attributed to the strengthening and toughening effects of CeAl₁₁O₁₈ phase, 2 mol% CeO₂ added composite showed the highest flexural strength and fracture toughness of 576 MPa and 5.15 MPa·m^1/2, which increased by 21% and 20% compared to Al₂O₃/Ti composite without CeO₂ addition. In this case, crack bridging by both Ti and CeAl₁₁O₁₈ particles was the major toughening mechanism and the additional fracture toughness caused by CeAl₁₁O₁₈ toughening effect reached a maximum. The role (crack bridging or particle pull-out mechanism) of CeAl₁₁O₁₈ in toughening Al₂O₃/Ti composites depended on the aspect ratio of these elongated particles, which was directly related to CeO₂ content. Because of the inhibition of interfacial reaction and the increase in Ti content, excellent electrical resistivity of composites after CeO₂ addition was maintained in spite of the formation of insulated CeAl₁₁O₁₈ phase. All samples showed relatively low electrical resistivity of ~10⁻³ Ωcm.     

Fabrication and microstructure of Al2O3–ZrO2(3Y)–SiC nanocomposites

Al₂O₃–ZrO₂(3Y)–SiC composite powder was prepared by the heterogeneous precipitation method. Calcinating temperature of the powder was important to obtain dense sintered body. The nanocomposites were got by hot-pressing, and addition of ZrO₂ did not raise the sintering temperature. Some Al₂O₃ grain shape was elongated, and Al₂O₃ grain size was about μm. Nano SiC particles were observed uniformly distributing throughout the composites, and most of them were located within the matrix grains. Because SiC particles located within ZrO₂ grains influenced the phase transformation of ZrO₂, the sintering of nanocomposites, which controlled grain size and transformable ZrO₂ amount, become important to get high performance. The strength of 80 wt% Al₂O₃–15 wt% ZrO₂–5 wt% SiC nanocomposites was 555 MPa, and toughness was 3·8 MPa m^1/2, which were higher than those of monolithic Al₂O₃ ceramics. ©     

The effect of alumina-based sintering aid on the microstructure,selected mechanical properties,and coefficient of friction of Cf/SiC composite prepared via spark plasma sintering (SPS) method

C_f-SiC air brake discs are being developed due to their high-temperature oxidation resistance compared to conventional C_f/C discs. The C_f-SiC air brake discs should have a coefficient of friction (COF) close to 0.4, a low wear rate, a density higher than 95% of the theoretical density, and flexural strength of more than 200 MPa. To reach the properties of C_f-SiC composite to the required characteristics of the air brake disc, different amounts of alumina-based sintering aid were used. For this purpose, first silicon carbide nanoparticles, sintering aids Al₂O₃–MgO, MgAl₂O₄, Al₂O₃–Y₂O₃, Al₂O₃–SiO₂–MgO, and carbon fiber (20 wt%) with a 5-mm length were prepared. Next, the final composite bulk was created via the SPS method at 1900 °C under a pressure of 50 MPa. The density of the sample sintered with the Al₂O₃–SiO₂–MgO sintering aid was higher than that of other sintering aids. The density value was obtained at 98% and 100% at 8 wt% and 4 wt% respectively. It was also found that the use of 4 wt% of Al₂O₃–SiO₂–MgO offered better mechanical properties compared to 8 wt%, due to the absence of Al₈Si₄O₂₀ phase at 4 wt%. The examination of mechanical properties showed that the hardness (3564 Vickers) and flexural strength (479 MPa) of the sample with the Al₂O₃–SiO₂–MgO sintering aid were higher than those of other sintering aids. The samples with the Al₂O₃–SiO₂–MgO sintering aid with 4 wt% revealed a COF of 0.41, showing the closest feature to the desired indices of aircraft brake discs.     

Microstructure and strengthening behavior in high content SiC nanowires reinforced SiC composites

In this study, the high-content SiC_nw reinforced SiC ceramic matrix composites (SiC_nw/SiC CMC) were successfully fabricated by hot pressing β-SiC and sintering additive (Al₂O₃-Y₂O₃) with boron nitride interphase modification SiC_nw. The effects of sintering additive content and mass fraction (5–25 wt%) of SiC_nw on the density, microstructure, and mechanical properties of the composites were investigated. The results showed that with the increase of sintering additives from 10 wt% to 12 wt%, the relative density of the SiC_nw/SiC CMC increased from 97.3% to 98.9%, attributed to the generated Y₃Al₅O₁₂ (YAG) liquid phase from the Al₂O₃-Y₂O₃ that promotes the rearrangement and migration of SiC grains. The comprehensive performance of the obtained composite with 15 wt% SiC_nw possessed the optimal flexural strength and fracture toughness of 524 ± 30.24 MPa and 12.39 ± 0.49 MPa·m^1/2, respectively. Besides, the fracture mode of the composites with 25 wt% SiC_nw content revealed a pseudo-plastic fracture behavior. It concludes that the 25 wt% SiC_nw/SiC CMC was toughened by the fiber pull-outs, debonding, bridging, and crack deflection that can consume plenty of fracture energy. The strategy of SiC nanowires worked as a main bearing phase for the fabrication of SiC/SiC CMC providing critical information for understanding the mechanical behavior of high toughness and high strength SiC nanoceramic matrix composites.     

Effects of residual stress and intragranular particles on mechanical properties of hot-pressed Al2O3/SiC ceramic composites

Al₂O₃/SiC ceramic composites with different SiC contents have been prepared by powder metallurgy at 1600 °C for 120 min at 30 MPa pressure. The effect of second phase particles on the microstructure and mechanical properties of composites have been studied. The results show that SiC particle has a significant impact on the matrix subjected to residual stress, and on the microstructure of the composites as well. The average grain size of alumina matrix decreases as the SiC particle content increases. Simultaneously, it has been found that the mechanical properties of the material are significantly enhanced in comparison with monolithic Al₂O₃. The highest strength and toughness are obtained when the SiC content is 15 vol%, and the values are 1237 MPa and 5.68 MPa m^1/2, respectively. The mechanisms of strengthening and toughening have been discussed.     

Alumina/zirconia composites toughened by the addition of graphene flakes

The effect of added graphene flakes on the mechanical properties of a composite containing 20 wt% Al₂O₃ and 80 wt% ZrO₂ (stab. 3 mol% Y₂O₃) was studied. To obtain samples, a commercial ceramic powder produced by Tosoh (Japan), and graphene oxide (GO) made at the Institute of Electronic Materials Technology (Poland) were used. The obtained composites were based on aqueous mixtures of both components. After drying, they were sintered in an uniaxial pressure (HP) furnace. The composites contained from 0% to 3% of GO by weight. Results showed the influence of GO content i.e. fracture toughness has a maximum for 0.02% GO (increase by 42% in comparison to GO-free matrix) and afterwards decreased, strength decreased in the whole GO content range. Young's modulus and Vickers hardness remained constant up to 0.2% GO, and then decreased.     

Effects of oxide addition on structure and properties of WC–10Co cemented carbide obtained by in situ synthesized powder

Combining spray drying and in situ synthesized technology, WC–10Co cemented carbide with uniform composition was prepared by vacuum sintering. The effects of Al₂O₃ and additions of different rare-earth oxides (La₂O₃, Y₂O₃ and CeO₂) on the microstructure and mechanical properties of WC–10Co were investigated. As the Al₂O₃ content increased from .5 to 2 wt%, the hardness of the sintered sample increased, whereas the relative density and fracture toughness decreased. Compared with the addition of .5 wt% Al₂O₃, the WC–10Co alloy with .5 wt% rare-earth oxides had higher hardness. In addition, compared with the alloy without an inhibitor (.80 μm), after adding .5 wt% Al₂O₃, La₂O₃, Y₂O₃ and CeO₂, the WC grain sizes were reduced to .73, .65, .71 and .62 μm, respectively, which indicated that the addition of Al₂O₃ and rare-earth oxides could refine WC grain during sintering. Among these additives, CeO₂ had the best effect. With the addition of .5 wt% CeO₂, the hardness and the fracture toughness increased from 1299 to 1710 HV₃₀ and from 16.18 to 18.90 MPa m^1/2, respectively.     

Effect of high energy milling on microstructure and mechanical properties of Al2O3-10 wt% Co composites consolidated by spark plasma sintering (SPS)

Al₂O₃-10 wt% Co composites were prepared by high energy milling in the presence of ethyl alcohol and with subsequent spark plasma sintering (SPS). The powders milled for 5 and 30 h were sintered by SPS at 1350 °C for 5 min. The effect of milling time on the sinterability and mechanical properties was studied. The morphology and structure of milled powders were investigated by scanning electron microscopy, dynamic light scattering and X-ray diffraction. The Co phase forms plate-like particles of different sizes, while finely fragmented Al₂O₃ particles are incorporated in the Co phase, forming composite particles. The average size of the composite particles decreases with increasing milling time, achieving 1.33 μm after 30 h. Crystallite size and micro-strain are inversely proportional. Overall, all the samples display homogeneous microstructures, high density (85.29–91.60%) and microhardness in the range 11.41–14.37 GPa.     

Enhanced mechanical strength and bactericidal activity of macro-porous Al2O3 ceramics through the introduction of Cu for membrane support application

Enhancing the mechanical strength of macro-porous ceramics and simultaneously endowing them with bactericidal activity are considered to be beneficial for their application as membrane support materials for water and wastewater treatment. In this study, Cu-containing Al₂O₃ porous ceramics were prepared by powder mixing, cold pressing and subsequent sintering. The microstructures of as-fabricated ceramics consisted of large α-Al₂O₃ particles as matrix, as well as inter-particle NaAlSiO₄, CuAl₂O₄ and CuO phase. With increased sintering temperature from 1430 to 1560 °C, the proportion of band-shaped CuO phase, which exhibited stronger binding tendency with Al₂O₃ than NaAlSiO₄, gradually increased, while that of particle-shaped CuAl₂O₄ phase decreased. Increasing the Cu content from 2 to 8 wt% at a fixed sintering temperature of 1500 °C resulted in the presence of more band-shaped CuO phase in Al₂O₃ matrix which tightly bonded Al₂O₃ particles together. The increase of sintering temperature and Cu content could both lead to enhanced bending strength and reduced porosity, while the later factor showed stronger modulatory effects than the former one. Moreover, the bactericidal rates of Cu-containing Al₂O₃ porous ceramics towards Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) were found to increase with increased Cu content in a Cu content-dependent manner. Together, the Cu-containing Al₂O₃ porous ceramic added with 8 wt% Cu and sintered at 1500 °C exhibited the highest bending strength and strongest bactericidal activity, which could be a promising candidate material for membrane support application.     

Microstructure and mechanical properties of α/β-Si3N4 composite ceramics with novel ternary additives prepared via spark plasma sintering

In this study, α/β-Si₃N₄ composite ceramics with high hardness and toughness were fabricated by adopting two different novel ternary additives, ZrN–AlN–Al₂O₃/Y₂O₃, and spark plasma sintering at 1550 °C under 40 MPa. The phase composition, microstructure, grain distribution, crack propagation process and mechanical properties of sintered bulk were investigated. Results demonstrated that the sintered α/β-Si₃N₄ composite ceramics with ZrN–AlN–Al₂O₃ contained the most α phase, which resulted in a maximum Vickers hardness of 18.41 ± 0.31 GPa. In the α/β-Si₃N₄ composite ceramics with ZrN–AlN–Y₂O₃ additives, Zr₃AlN MAX-phase and ZrO phase were found and their formation mechanisms were explained. The fracture appearance presented coarser elongated β-Si₃N₄ grains and denser microstructure when 20 wt% TiC particles were mixed into Si₃N₄ matrix, meanwhile, exhibited maximum mean grain diameter of 0.98 ± 0.24 μm. As a result, the compact α/β-Si₃N₄ composite ceramics containing ZrN–AlN–Y₂O₃ additives and TiC particles displayed the optimal bending strength and fracture toughness of 822.63 ± 28.75 MPa and 8.53 ± 0.21 MPa?m^1/2, respectively. Moreover, the synergistic toughening of rod-like β-Si₃N₄ grains and TiC reinforced particles revealed the beneficial effect on the enhanced fracture toughness of Si₃N₄ ceramic matrix.     

Microstructure and mechanical properties of Al2O3 ceramic and TiAl alloy joints brazed with Ag–Cu–Ti filler metal

Al₂O₃ ceramic was reliably joined to TiAl alloy by active brazing using Ag–Cu–Ti filler metal, and the effects of brazing temperature, holding time, and Ti content on the microstructure and mechanical properties of Al₂O₃/TiAl joints were investigated. The typical interfacial microstructure of joints brazed at 880 °C for 10 min was Al₂O₃/Ti₃(Cu,Al)₃O/Ag(s.s)+AlCu₂Ti+Ti(Cu,Al)+Cu(s.s)/AlCu₂Ti+AlCuTi/TiAl alloy. With increasing brazing temperature and time, the thickness of the Ti₃(Cu,Al)₃O reaction layer increased, and the blocky AlCu₂Ti compounds aggregated and grew gradually. The Ti dissolved from the TiAl substrate was sufficient to react with Al₂O₃ ceramic to form a thin Ti₃(Cu,Al)₃O layer when Ag–Cu eutectic alloy was used, but the dissolution of TiAl alloy was inhibited with an increase in Ti content in the brazing filler. Ti and Al dissolved from the TiAl alloy had a strong influence on the microstructural evolution of the Al₂O₃/TiAl joints, and the mechanism is discussed. The maximum shear strength was 94 MPa when the joints were brazed with commercial Ag–Cu–Ti filler metal, while it reached 102 MPa for the joint brazed with Ag–Cu+2 wt% TiH₂ at 880 °C for 10 min. Fractures propagated primarily in the Al₂O₃ substrate and partially along the reaction layer.     

In situ synthesis mechanism of 15R–SiAlON reinforced Al2O3 refractories by Fe–Si liquid phase sintering

15R–SiAlON bonded Al₂O₃ refractories were successfully synthesized using ferrosilicon nitride and alumina by liquid phase sintering. The phase composition and morphology were analyzed by means of X‐ray diffraction, scanning electron microscopy, and transmission electron microscopy. The results show that 15R–SiAlON reinforcement can be in situ obtained in the specimens with 5 wt% ferrosilicon nitride at 1500°C to 1700°C in flowing N₂ of 0.1 MPa. The morphology of 15R–SiAlON is strongly dependent on the morphology of intermediate AlON phases formed at different temperatures. Fe–Si alloys from ferrosilicon nitride form liquid phase and accelerate the formation of 15R‐SiAlON, in which process the wettability of Fe–Si alloys is improved by the increase in Si content, carbon coating on particle, solution process and reactions. The 15R–SiAlON reinforced Al₂O₃ refractory materials possess high cold crushing strength of 138‐171 MPa.