Effect of ZrB2 content on phase assemblage and mechanical properties of Si3N4–ZrB2 ceramics prepared at low temperature

Based on the previous work on Si₃N₄–ZrB₂ [Wu et al. J Eur Ceram Soc;2017,37:4217], the influence of ZrB₂ addition on the phase and microstructure evolution of Si₃N₄–ZrB₂ composites was emphatically investigated, and the mechanical properties were compared with pure Si₃N₄ ceramics. It was revealed that the ratio of β‐ to (α+β)‐Si₃N₄ significantly increased from 14.3% in pure Si₃N₄ ceramics to 39.8% in Si₃N₄ with 15 vol% ZrB₂ addition, indicating that the introduction of ZrB₂ promoted α‐ to β‐Si₃N₄ phase transformation. As a consequence, the microstructure of the composite showed the bimodal distribution, containing both elongated and equiaxed Si₃N₄ grains. For the pure Si₃N₄, Vickers hardness, fracture toughness and flexural strength was 22.8 GPa, 7.6 MPa m^1/2, and 334.5 MPa, respectively. In contrast, the composite of Si₃N₄–30 vol% ZrB₂ simultaneously possessed an excellent combination of mechanical properties: 19.5 GPa in hardness, 9.8 MPa m^1/2 in toughness and 702.0 MPa in strength. Present study suggested that Si₃N₄‐based ceramics with high hardness, high toughness, and high strength could be obtained by the combination of appropriate ZrB₂ content and low hot‐pressing temperature.     

Effect of ZrB2 on promoting the phase transformation mechanism of Si3N4-based ceramics at low temperature

In this study, the mechanism of the effect of ZrB₂ on phase transformation of Si₃N₄ at a low temperature and the influence of its content on Si₃N₄-based ceramics were investigated. Previous study has shown that oxide impurities, i.e., B₂O₃ and ZrO₂ on ZrB₂ particles, alone cannot contribute to phase transformation of Si₃N₄ at a low temperature. But, the introduction of 0.5 vol% ZrB₂ into Si₃N₄ ceramics can promote the α-β phase transformation of Si₃N₄, which is confirmed to be the role of boron by comparison of the experimental results obtained from the addition of 0.5 vol% Zr and 0.5 vol% B. Increasing the ZrB₂ content from 0 vol% to 2.5 vol% intensifies the α-β phase transformation while decreasing the α phase content of Si₃N₄-based ceramics, accompanied by a slight grain growth, leading to a decrease in hardness. At the same time, aspect ratio and the quantities of elongated grains per square micron increase, and thus the fracture toughness increases significantly. However, when the content of ZrB₂ increases to 5 vol%, the Si₃N₄-based ceramics not only have a substantial decrease in hardness, but also the fracture toughness fails to be effectively improved due to high porosity and the decrease in aspect ratio and the quantity of elongated grains per square micron. The current study demonstrates that the dense Si₃N₄-based ceramics with high hardness and toughness (hardness ∼19.9 ± 0.2 GPa, toughness ∼6.27 ± 0.19 MPa m^1/2) can be prepared successfully at 1600 °C by introducing 0.5 vol% ZrB₂.     

Thermal conductivity and mechanical properties of Si3N4 ceramics with binary fluoride sintering additives

Silicon nitride (Si₃N₄) ceramics were fabricated by gas pressure sintering (GPS) using four sintering additives: Y₂O₃–MgO, Y₂O₃–MgF₂, YF₃–MgO, and YF₃–MgF₂. The phase composition, grain growth kinetics, mechanical properties, and thermal conductivities of the Si₃N₄ ceramics were compared. The results indicated that the reduction of YF₃ on SiO₂, induced a high Y₂O₃/SiO₂ secondary phase ratio, which improved the thermal conductivity of the Si₃N₄ ceramics. The depolymerization of F atom reduces the diffusion energy barrier of solute atom and weakens the viscous resistance of anion group, which was beneficial to grain boundary migration. Besides exhibiting a lower grain growth exponent(n = 2.5)and growth activation energy (Q = 587.94 ± 15.35 kJ/mol), samples doped with binary fluorides showed excellent properties, including appreciable thermal conductivity (69 W m⁻¹ K⁻¹), hardness (14.63 ± 0.12 GPa), and fracture toughness (8.75 ± 0.18 MPa m^1/2), as well as desirable bending strength (751 ± 14 MPa).     

Effect of ZrB2 and its oxide impurities (ZrO2 and B2O3) on hot-pressed Si3N4 ceramics at low temperature

Based on the previous work on Si₃N₄-ZrB₂, the addition of 2.5 vol.% ZrB₂ promoted α- to β-Si₃N₄ phase transformation, bimodal microstructure, and toughness and strength improvement after hot-pressing at 1500 °C. However, the mechanism needed to be further explored. In the present work, the effect of ZrB₂ and its oxide impurities (ZrO₂ and B₂O₃) on phase composition, microstructure and mechanical properties of Si₃N₄ ceramics with MgO-Yb₂O₃ additives were studied. Results showed that the addition of B₂O₃ had no influence on Si₃N₄ ceramics, whereas the addition of ZrO₂ inhibited the α- to β-Si₃N₄ phase transformation, formed an uniform equiaxed microstructure, and deceased the toughness and strength. The positive effect of oxide impurities can be eliminated. Based on the STEM analysis, the possible reason was that the addition of ZrB₂ led to the formation of Si-Mg-O-N-Yb-Zr-B liquid phase, and then promoted α- to β-Si₃N₄ phase transformation.     

Stereolithographical fabrication of dense Si3N4 ceramics by slurry optimization and pressure sintering

Photocurable gray-colored Si₃N₄ ceramic slurry with high solid loading, suitable viscosity and high curing depth is critical to fabricate dense ceramic parts with complex shape and high surface precision by stereolithography technology. In the present study, Si₃N₄ ceramic slurry with suitable viscosity, high solid loading (45 vol %) and curing depth of 50 μm was prepared successfully when surface modifier KH560 (1 wt%) and dispersant Darvan (1 wt%) were used. The slurry exhibits the shear thinning behavior. Based on the Beer-Lambert formula, D_p (the attenuation length) and E_c (the critical energy dose) of Si₃N₄ ceramic slurry with solid loading of 45 vol % were derived as 0.032 mm and 0.177 mJ/mm², respectively. Si₃N₄ ceramic green parts with complex shape and high surface precision were successfully fabricated by stereolithography technology. After optimizing the debinding and sintering process for green parts, dense Si₃N₄ ceramics with 3.28 g/cm³ sintering density were fabricated. The microhardness and fracture toughness of as-sintered Si₃N₄ ceramics are ~14.63 GPa and ~5.82 MPa m^1/2, respectively, which are comparable to those of the samples by traditional dry-pressed and pressureless sintering technology. These results show that ceramic stereolithography technology could be promising to fabricate high performance ceramics, especially for gray-colored monolithic Si₃N₄ ceramics.     

Si3N4-ZrB2 ceramics prepared at low temperature with improved mechanical properties

Si₃N₄-ZrB₂ ceramics were hot-pressed at 1500 °C using self-synthesized fine ZrB₂ powders containing 2.0 wt% B₂O₃ together with MgO-Re₂O₃ (Re = Y, Yb) additives. Both Si₃N₄ and ZrB₂ grains in the hot-pressed ceramics were featured with elongated and equiaxed morphology. The presence of elongated Si₃N₄ and ZrB₂ grains led to the partial texture of the ceramics under the applied pressure. Vickers hardness and fracture toughness of Si₃N₄-ZrB₂ ceramics with MgO-Re₂O₃ additives prepared at low temperature were about 19–20 GPa and 9–11 MPa m^1/2, respectively, higher than the reported values of Si₃N₄-based ceramics prepared at high temperature (1800 °C or above) under the same test method.     

Microstructure and mechanical properties of reaction-hot-pressed zirconium diboride based ceramics

ZrB₂ ceramics were prepared by in-situ reaction hot pressing of ZrH₂ and B. Additions of carbon and excess boron were used to react with and remove the residual oxygen present in the starting powders. Additions of tungsten were utilized to make a ZrB₂-4 mol%W ceramic, while a change in the B/C ratio was used to produce a ZrB₂-10 vol% ZrC ceramic. All three compositions reached near full density. The baseline ZrB₂ and ZrB₂–ZrC composition contained a residual oxide phase and ZrC inclusions, while the W-doped composition contained residual carbon and a phase that contained tungsten and boron. All three compositions exhibited similar values for flexure strength (~520 MPa), Vickers hardness (~15 GPa), and elastic modulus (~500 to 540 GPa). Fracture toughness was about 2.6 MPa m^1/2 for the W-doped ZrB₂ compared to about 3.8 MPa m^½ for the ZrB₂ and ZrB₂–ZrC ceramics. This decrease in fracture toughness was accompanied by an observed absence of crack deflection in the W-doped ZrB₂ compared with the other compositions. The study demonstrated that reaction-hot-pressing can be used to fabricate ZrB₂ based ceramics containing solid solution additives or second phases with comparable mechanical properties.     

Texture,microstructures, and mechanical properties of AlN‐based ceramics with Si3N4–Y2O3 additives

Textured AlN‐based ceramics with improved mechanical properties were prepared by hot pressing using Si₃N₄ and Y₂O₃ as additives. The introduction of Si₃N₄–Y₂O₃ into AlN matrix led to the formation of secondary Y₃AlSi₂O₇N₂ and fiber‐like 2H^δ AlN‐polytypoid phases, the partial texture of all crystalline phases, and the fracture mode change from intergranular to transgranular. Consequently, Vickers hardness, fracture toughness and flexural strength of AlN‐based ceramics by the replacement of Y₂O₃ by Si₃N₄–Y₂O₃ increased significantly from 10.4±0.3 GPa, 2.4±0.3 MPa m^½ and 333.3±10.3 MPa to 14.2±0.4 GPa, 3.4±0.1 MPa m^½ and 389.5±45.5 MPa, respectively.     

Fabrication and wear behaviors of graded Si3N4 ceramics by the combination of two-step sintering and β-Si3N4 seeds

Graded Si₃N₄ ceramics with sandwich-like microstructure were fabricated by the combination of hot-pressing, spark plasma sintering and β-Si₃N₄ seeds. Phase compositions, microstructures, mechanical properties, and wear behaviors were investigated. Main α-Si₃N₄ phase were detected in the outer layers, and only β-Si₃N₄ phase were observed in the inner layers. The outer layer with ultra-fine equiaxed grains were well bonded to the inner layer with a distinct bimodal grain size distribution. Vickers hardness of outer layer (～21.2?GPa) was much higher than that of inner layer (～16.1?GPa), whereas fracture toughness of outer layer (～3.5?MPa?m^1/2) was much lower than that of inner layer (～5.9?MPa?m^1/2), indicative of the hard surface and tough core. Due to the ultra-fine microstructure and high hardness of outer layer, the graded Si₃N₄ ceramics exhibited superior wear resistance with low wear rate.     

Processing,microstructure, and mechanical properties of hot-pressed ZrB2 ceramics with a complex Zr/Si/O-based additive

Densification behavior, microstructure, and mechanical properties of zirconium diboride (ZrB₂) ceramics modified with a complex Zr/Si/O-based additive were studied. ZrB₂ ceramics with 5–20 vol.% additions of Zr/Si/O-based additive were densified to >95% relative density at temperatures as low as 1400°C by hot-pressing. Improved densification behavior of ZrB₂ was observed with increasing additive content. The most effective additive amount for densification was 20 vol.%, hot-pressed at 1400°C (∼98% relative density). Microstructural analysis revealed up to 7 vol.% of residual second phases in the final ceramics. Improved densification behavior was attributed to ductility of the silicide phase, liquid phase formation at the hot-pressing temperatures, silicon wetting of ZrB₂ particles, and reactions of surface oxides. Room temperature strength ranged from 390 to 750 MPa and elastic modulus ranged from 440 to 490 GPa. Vickers hardness ranged from 15 to 16 GPa, and indentation fracture toughness was between 4.0 and 4.3 MPa·m^1/2. The most effective additive amount was 7.5 vol.%, which resulted in high relative density after hot-pressing at 1600°C and the best combination of mechanical properties.     

Pressureless sintered in situ toughened ZrB2-SiC platelets ceramics

ZrB₂-SiC composite ceramics were densified by pressureless sintering with addition of Si₃N₄ or MoSi₂ at temperatures that induced SiC anisotropic growth from particles to platelets, within a ZrB₂ matrix with rounded grains. Si₃N₄ addition resulted in the formation of large amounts of liquid phase which enhanced mass transfer mechanisms in terms of matrix grain growth and homogeneous distribution of SiC platelets having an aspect ratio of 3. On the contrary, MoSi₂ helped the densification with local formation of liquid phases leading to a finer matrix with finer SiC platelets, though more agglomerated and with a lower aspect ratio (about 2). These different microstructures had very different fracture properties values, namely a toughness of 3.8 MPa m^1/2 and a strength of 300 MPa for the Si₃N₄-doped composite; toughness of 5 MPa m^1/2 and strength of 410 MPa for the MoSi₂-doped one.     

Effect of ZrB2 content on the densification,microstructure, and mechanical properties of ZrC-SiC ceramics

ZrC ceramics containing 30 vol% SiC-ZrB₂ were produced by high-energy ball milling and reactive hot pressing. The effects of ZrB₂ content on the densification, microstructure, and mechanical properties of ceramics were investigated. Fully dense ceramics were achieved as ZrB₂ content increased to 10 and 15 vol%. The addition of ZrB₂ suppressed grain growth and promoted dispersion of the SiC particles, resulting in fine and homogeneous microstructures. Vickers hardness increased from 23.0 ± 0.5 GPa to 23.9 ± 0.5 GPa and Young’s modulus increased from 430 ± 3 GPa to 455 ± 3 GPa as ZrB₂ content increased from 0 to 15 vol%. The increases were attributed to a combination of the higher relative density of ceramics with higher ZrB₂ content and the higher Young’s modulus and hardness of ZrB₂ compared to ZrC. Indentation fracture toughness increased from 2.6 ± 0.2 MPa⋅m^1/2 to 3.3 ± 0.1 MPa⋅m^1/2 as ZrB₂ content increased from 0 to 15 vol% due to the increase in crack deflection by the uniformly dispersed SiC particles. Compared to binary ZrC-SiC ceramics, ternary ZrC-SiC-ZrB₂ ceramics with finer microstructure and higher relative densities were achieved by the addition of ZrB₂ particles.     

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.     

Enhanced mechanical properties,thermal shock resistance and ablation resistance of Si2BC3N ceramics with nano ZrB2 addition

The mechanical properties, thermal shock resistance, and ablation resistance of nano ZrB₂ modified Si₂BC₃N ceramics were investigated. The results show that ZrB₂ stimulated microstructure evolution obviously. Therefore, the maximum strength and fracture toughness reach 559.6 MPa and 6.77 MPa·m^1/2, which are improved by 61.0% and 29.4%, respectively. Furthermore, the residual strengths of 10 wt% ZrB₂ containing composites tested at 1000 ℃ retain 363.6 MPa, which is much higher than 97.7 MPa of pristine Si₂BC₃N ceramics. Besides, the ablation resistance of ZrB₂ modified Si₂BC₃N ceramics at 3000 ℃ is enhanced remarkably and the linear and mass ablation rates of ZrB₂-10 are only 0.009 mm/s and 1.91 mg/s, respectively. The ablation in the ultra-high temperature zone is totally dominated by the ZrB₂ component, and the thermochemical erosion is determined by the oxidation resistance of ZrB₂ in the thermal affected zone.     

Cutting performance improvement of Si3N4 ceramic cutting tools by adding boride

Cutting performances of silicon nitride (Si₃N₄) ceramic cutting tools with and without boride additive (2.5 vol% ZrB₂ or TiB₂) prepared by hot-pressing at 1500°C were investigated. Due to the α- to β-Si₃N₄ phase transformation and low densification temperature, boride-containing Si₃N₄ ceramics with high hardness and high toughness were obtained. The turning tests showed that the effective cutting lengths of the Si₃N₄–2.5 vol% TiB₂ ceramic (∼2480 m) and Si₃N₄–2.5 vol% ZrB₂ ceramic (∼2200 m) were higher than the monolithic Si₃N₄ ceramic (∼1780 m). As the toughness was improved while maintaining relative high hardness, the cutting performances of the boride-containing Si₃N₄-based inserts were improved by adding 2.5 vol% ZrB₂ or TiB₂. The improved cutting performance indicated that the boride-containing Si₃N₄ ceramics are expected to be used in the field of ceramic cutting tools.     

Effect of in situ synthesized and additives on the thermal performance of mullite thermal storage ceramics

High-performance thermal storage ceramics can enable utilization of solar thermal power generation plants. In this work, in situ synthesis was used to prepare mullite thermal storage ceramics. Calcined bauxite, talc, and kaolin were used as raw materials. The effects of additives (e.g., SiC, Si₃N₄, TiC, and ZrB₂) on the density, mechanical durability, phase components, microstructure, and thermal performance of the mullite ceramics were studied. The results showed that the thermal expansion coefficient, thermal conductivity, and heat storage density of the mullite ceramics were affected by their phase components. SiC and Si₃N₄ did not decompose during the in situ syntheses, but TiC and ZrB₂ decomposed. With the addition of 10 wt% SiC, the thermal conductivity improved to 2.72 W (m K)^?1 (298 K). The heat storage density of this material was 688 kJ kg^?1 (273–1073 K). Consequently, the in situ synthesized mullite thermal storage ceramic with added SiC could be a promising candidate material for a compound latent-sensible heat storage system.     

Effects of Gd2O3 and MgSiN2 sintering additives on the thermal conductivity and mechanical properties of Si3N4 ceramics

Si₃N₄ ceramics were prepared by gas pressure sintering at 1900°C for 12 h under a nitrogen pressure of 1 MPa using Gd₂O₃ and MgSiN₂ as sintering additives. The effects of the Gd₂O₃/MgSiN₂ ratio on the densification, microstructure, mechanical properties, and thermal conductivity of Si₃N₄ ceramics were systematically investigated. It was found that a low Gd₂O₃/MgSiN₂ ratio facilitated the thermal diffusivity of Si₃N₄ ceramics while a high Gd₂O₃/MgSiN₂ ratio benefited the densification and mechanical properties. When the Gd₂O₃/MgSiN₂ ratio was 1:1, Si₃N₄ ceramics obtained an obvious exaggerated bimodal microstructure and the optimal properties. The thermal conductivity, flexural strength, and fracture toughness were 124 W·m⁻¹·k⁻¹, 648 MPa, and 9.12 MPa·m^1/2, respectively. Comparing with the results in the literature, it was shown that Gd₂O₃-MgSiN₂ was an effective additives system for obtaining Si₃N₄ ceramics with high thermal conductivity and superior mechanical properties.     

Effect of a new nonoxide additive,Y3Si2C2, on the thermal conductivity and mechanical properties of Si3N4 ceramics

Enhancement of the thermal conductivity of silicon nitride is usually achieved by sacrificing its mechanical properties (bending strength). In this study, β-Si₃N₄ ceramics were prepared using self-synthesized Y₃Si₂C₂ and MgO as sintering additives. It was found that the thermal conductivity of the Si₃N₄ ceramics was remarkably improved without sacrificing their mechanical properties. The microstructure and properties of the Si₃N₄ ceramics were analyzed and compared with those of the Y₂O₃-MgO additives. The addition of Y₃Si₂C₂ eliminated the inherent SiO₂ and introduced nitrogen to increase the N/O ratio of the grain-boundary phase, inducing Si₃N₄ grain growth, increasing Si₃N₄ grain contiguity, and reducing lattice oxygen content in Si₃N₄. Therefore, by replacing Y₂O₃ with Y₃Si₂C₂, the thermal conductivity of the Si₃N₄ ceramics was significantly increased by 31.5% from 85 to 111.8Wm⁻¹K⁻¹, but the bending strength only slightly decreased from 704 ± 63MPa to 669 ± 33MPa.     

Fabrication of Si3N4 ceramics substrates with high thermal conductivity by tape casting and gas pressure sintering

In this paper, high thermal conductivity Si₃N₄ ceramics were successfully fabricated through exploring and optimizing the tape casting process. The impact of various organic additives on the rheological characteristics of Si₃N₄ slurry was explored, and the pore size distribution and microstructure of the green tapes at different solid loadings were investigated, as well as the microstructure of Si₃N₄ ceramics. Green tapes with a narrow pore size distribution, a small average pore size, and a high density of 1.88 g cm⁻³ were prepared by the investigation and optimization of the Si₃N₄ slurry formulation. After gas pressure sintering, Si₃N₄ ceramics with a density of 3.23 g cm⁻³, dimensions of 78 mm × 78 mm, and a thickness of 0.55 mm were obtained. The microstructure of the Si₃N₄ ceramics showed a bimodal distribution and a low content of glassy phases. The thermal conductivity of the Si₃N₄ ceramics was 100.5 W m⁻¹ K⁻¹, the flexural strength was 735 ± 24 MPa, and the fracture toughness was 7.17 MPa m^1/2.     

Preparation,mechanical and thermal properties of Si3N4 ceramics by gelcasting using low–toxic DMAA gelling system and gas pressure sintering

In this work, Si₃N₄ ceramics were fabricated through an aqueous gelcasting method using a low–toxic monomer called N, N–dimethylacrylamide (DMAA) followed by gas pressure sintering at 1850 °C for 2 h under 6 MPa N₂ atmosphere. The effect of solid loading on performance of slurries, green and sintered bodies was investigated systematically. The results show that the slurries with a solid loading as high as 50 vol% (viscosity 0.17 Pa.s at 100 s^–1) were achieved. With the increase of solid loading (30–50 vol%), the green bodies exhibited a monotonically decreased, however high enough in general, flexural strength of 16.50–11.52 MPa, which was comparable to that of widely–used neurovirulent acrylamide (AM) gelling system. In regard to the sintered bodies, increasing solid loading significantly promoted sintering and improved mechanical properties and thermal conductivity as a result of the increased density, bimodal distribution structure, as well as suitable interfacial bonding strength. The best performance parameters of Si₃N₄ ceramics, bulk density of 3.25 g/cm³, apparent porosity of 0.67%, flexural strength of 898.92 MPa, fracture toughness of 6.42 MPa m^1/2, Vickers hardness of 2.81 GPa, and thermal conductivity of 34.69 W m^–1 K^–1, were obtained at 50 vol% solid loading. This work renders low–toxic DMAA gelling system promising prospect in preparation of high–performance Si₃N₄ ceramics by gelcasting.