On the fabrication and mechanical properties of Si3N4 ceramics with low content sintering additives

Si₃N₄ ceramics were prepared by hot pressing (HP) and spark plasma sintering (SPS) methods using low content (5 mol%) Al₂O₃–RE₂O₃(RE = Y, Yb, and La)–SiO₂/TiN as sintering additives/secondary additives. The effects of sintering additives and sintering methods on the composition, microstructures, and mechanical properties (hardness and fracture toughness) were investigated. The results show that fully density Si₃N₄ ceramics could be fabricated by rational tailoring of sintering additives and sintering method, and TiN secondary additive could promote the density during HP and SPS. Besides, SN-AYS-SPS possesses the most competitive mechanical properties among all the as-prepared ceramics with the Vickers hardness as 17.31 ± .43 GPa and fracture toughness as 11.07 ± .48 MPa m^1/2.     

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.     

Low temperature sintering of Si3N4 ceramics by spark plasma sintering technique

Abstract

Abstract

Low temperature sintering of α‐Si₃N₄ matrix ceramics was developed in the present study using 4?wt‐%MgO together with Al₂O₃ or AlPO₄ as the sintering additives and spark plasma sintering technique. The results suggested that α‐Si₃N₄ ceramics could be densified at low sintering temperature by adjusting both the sintering temperature and sintering additive content. For low temperature sintered α‐Si₃N₄ ceramics, using MgO and Al₂O₃ as the sintering additives, the densification is not complete at a temperature lower than 1600°C, and the mechanical strength is <200?MPa. When MgO and AlPO₄ were used as the sintering additives, the increase in AlPO₄ content not only declines the sintering temperature but also promotes the mechanical property of the sintered Si₃N₄ ceramics. It was the AlPO₄ phosphate binder that played a significant role in low temperature sintering of Si₃N₄ ceramics.     

Influences of rare-earth oxide additives on the formation and properties of porous Si2N2O ceramic

Here we prepared porous silicon oxynitride (Si₂N₂O) ceramics by reaction sintering of SiO₂ and Si₃N₄ using five different rare-earth oxides (RE₂O₃, RE = Lu, Yb, Y, Sm, and La) as sintering aids. The influences of RE₂O₃ on the formation, densification, microstructure, and mechanical properties of Si₂N₂O ceramics have been investigated in detail. The results have indicated that with the increase in RE ionic radius, the formation temperature of Si₂N₂O decreases, and the densification process could be promoted by RE₂O₃ with larger RE³⁺ ionic radius. In addition, microstructures and mechanical properties are highly dependent on the RE₂O₃ additives. With the increase in RE³⁺ ionic radius, Si₂N₂O changes from platelike crystals to elongated crystals. The samples doped with La₂O₃ and Sm₂O₃ with elongated crystals exhibit higher flexural strength and higher Vickers hardness.     

Preparation and characterization of Si3N4-based composite ceramic tool materials by microwave sintering

Si₃N₄-based composite ceramic tool materials with (W,Ti)C as particle reinforced phase were fabricated by microwave sintering. The effects of the fraction of (W,Ti)C and sintering temperature on the mechanical properties, phase transformation and microstructure of Si₃N₄-based ceramics were investigated. The frictional characteristics of the microwave sintered Si₃N₄-based ceramics were also studied. The results showed that the (W,Ti)C would hinder the densification and phase transformation of Si₃N₄ ceramics, while it enhanced the aspect-ratio of β-Si₃N₄ which promoted the mechanical properties. The Si₃N₄-based composite ceramics reinforced by 15 wt% (W,Ti)C sintered at 1600 °C for 10 min by microwave sintering exhibited the optimum mechanical properties. Its relative density, Vickers hardness and fracture toughness were 95.73 ± 0.21%, 15.92 ± 0.09 GPa and 7.01 ± 0.14 MPa m^1/2, respectively. Compared to the monolithic Si₃N₄ ceramics by microwave sintering, the sintering temperature decreased 100 °C,the Vickers hardness and fracture toughness were enhanced by 6.7% and 8.9%, respectively. The friction coefficient and wear rate of the Si₃N₄/(W,Ti)C sliding against the bearing steel increased initially and then decreased with the increase of the mass fraction of (W,Ti)C., and the friction coefficient and wear rate reached the minimum value while the fraction of (W,Ti)C was 15 wt%.     

Effects of Al2O3–Y2O3/Yb2O3 additives on microstructures and mechanical properties of silicon nitride ceramics prepared by hot-pressing sintering

Silicon nitride (Si₃N₄) ceramics doped with two different sintering additive systems (Al₂O₃–Y₂O₃ and Al₂O₃–Yb₂O₃) were prepared by hot-pressing sintering at 1800℃ for 2 h and 30 MPa. The microstructures, nano-indentation test, and mechanical properties of the as-prepared Si₃N₄ ceramics were systematically investigated. The X-ray diffraction analyses of the as-prepared Si₃N₄ ceramics doped with the two sintering additives showed a large number of phase transformations of α-Si₃N₄ to β-Si₃N₄. Grain size distributions and aspect ratios as well as their effects on mechanical properties are presented in this study. The specimen doped with the Al₂O₃–Yb₂O₃ sintering additive has a larger aspect ratio and higher fracture toughness, while the Vickers hardness is relatively lower. It can be seen from the nano-indentation tests that the stronger the elastic deformation ability of the specimens, the higher the fracture toughness. At the same time, the mechanical properties are greatly enhanced by specific interlocking microstructures formed by the high aspect ratio β-Si₃N₄ grains. In addition, the density, relative density, and flexural strength of the as-prepared Si₃N₄ ceramics doped with Al₂O₃–Y₂O₃ were 3.25 g/cm³, 99.9%, and 1053 ± 53 MPa, respectively. When Al₂O₃–Yb₂O₃ additives were introduced, the above properties reached 3.33 g/cm³, 99.9%, and 1150 ± 106 MPa, respectively. It reveals that microstructure control and mechanical property optimization for Si₃N₄ ceramics are feasible by tailoring sintering additives.     

Improved oxidation resistance properties of Si3N4/O′–SiAlON composite ceramics by a repeated sintering method

Si₃N₄/O′–SiAlON composite ceramics with superior oxidation resistance properties were fabricated by a repeated sintering method. The effects of sintering time on the phase evolution, microstructure, and oxidation resistance properties of the Si₃N₄/O′–SiAlON composite ceramics were investigated. The results indicated that the content of the O′–SiAlON phase and the densification of Si₃N₄/O′–SiAlON composite ceramics increased after two-time sintering. Furthermore, the thickness of the oxide layer of the Si₃N₄/O′–SiAlON composite ceramics after oxidation at 1100–1500°C for 30 h was not significant. Compared to the oxidation weight gain after the one-time sintering process, the oxidation weight gain of Si₃N₄/O′–SiAlON composite ceramics was 0.432 mg/cm² after two-time sintering when oxidized at 1500 C for 30 h, which was reduced by 43.3%. The mechanism of the improved oxidation resistance properties was ascribed to the formation of more O′–SiAlON and the enhancement of the densification.     

Effect of sintering activation energy on Si3N4 composite ceramics

This study investigated the activation energy and kinetic characteristics of silicon nitride (Si₃N₄) composite ceramics produced using different preparation methods. The effects of the linear shrinkage, expansion ratio, and heating rate on the sintering process were analysed in detail. The obtained results reveal that the finer particle size produced using the urea homogeneous precipitation method obviously enhanced the densification rate and reduced the atomic diffusion distance. Moreover, the densification sintering process was carried out efficiently, and the largest densification rate was achieved in advance. According to the Arrhenius curve, the activation energy of the Si₃N₄ composite ceramics calculated using the urea homogeneous precipitation method (310.94 kJ/mol) was lower than that achieved using the mechanical ball-milling method (365.11 kJ/mol). Additionally, the flexural strength and hardness of the Si₃N₄ composite ceramic prepared using the urea homogeneous precipitation method were 740 ± 42 MPa and 16.20 ± 30 GPa, respectively, which is attributed to this composite ceramic's higher diffusion rate and small grain size.     

High thermal conductivity silicon nitride ceramics prepared by pressureless sintering with ternary sintering additives

Silicon nitride ceramics were pressureless sintered at low temperature using ternary sintering additives (TiO₂, MgO and Y₂O₃), and the effects of sintering aids on thermal conductivity and mechanical properties were studied. TiO₂–Y₂O₃–MgO sintering additives will react with the surface silica present on the silicon nitride particles to form a low melting temperature liquid phase which allows liquid phase sintering to occur and densification of the Si₃N₄. The highest flexural strength was 791(±20) MPa with 12 wt% additives sintered at 1780°C for 2 hours, comparable to the samples prepared by gas pressure sintering. Fracture toughness of all the specimens was higher than 7.2 MPa·m^1/2 as the sintering temperature was increased to 1810°C. Thermal conductivity was improved by prolonging the dwelling time and adopting the annealing process. The highest thermal conductivity of 74 W/(m∙K) was achieved with 9 wt% sintering additives sintered at 1810°C with 4 hours holding followed by postannealing.     

High-strength and wave-transmitting Si3N4–Si2N2O-BN composites prepared using selective laser sintering

In this study, high-strength and wave-transmission silicon nitride (Si₃N₄) composites were successfully developed via selective laser sintering (SLS) with cold isostatic pressing (CIP) after debinding and before final sintering, and the optimal moulding process parameters for the SLS Si₃N₄ ceramics were determined. The effects of the sintering aids and secondary CIP on the bulk density, porosity, flexural strength, fracture toughness, and wave-transmitting properties of the Si₃N₄ composites were studied. The results showed that the increased CIP pressure was beneficial to the densification of SLS Si₃N₄ ceramics and improved their mechanical properties. However, the wave-transmitting performance decreased as the CIP pressure increased. The Si₃N₄ ceramics prepared by the moulding of sample S₁₁ were more in line with the performance requirements of the radomes. To obtain good comprehensive performance, an additional 3% of interparticle Y₂O₃ was added to the pre-printed mixed powder of granulated Si₃N₄ particles and resin and the secondary CIP pressure was adjusted to 280 MPa. After sintering, the bending strength, fracture toughness, and dielectric constant of the Si₃N₄ ceramics were 651 MPa, 6.0 MPa m^1/2, and 3.48 respectively. This study provides an important method for preparing of Si₃N₄ composite radomes using SLS process.     

Mechanism of improving the mechanical properties of Si3N4/TiC ceramic tool materials prepared by spark plasma sintering

Spark plasma sintering (SPS) is a new sintering method having shorter sintering time and higher densification speed than the traditional sintering methods. In this paper, the Si₃N₄/TiC ceramic tool material is sintered by SPS. The microstructure and mechanical properties of the material under different sintering parameters are compared. The sintering process of the material is then analyzed, and the best sintering parameters are obtained. Heat the material to 1600°C and keep the temperature for 15 min, then continue to heat to 1700°C and keep the temperature for 10 min, Si₃N₄/TiC ceramic tool material has high mechanical properties, its bending strength, fracture toughness, and Vickers hardness are 959 MPa, 8.61 MPa·m^1/2, and 15.21 GPa, respectively. The scanning electron microscope (SEM) analysis shows that under this condition, the sintering additives and Si₃N₄/TiC material form the liquid phase, which makes the Si₃N₄ particles rearrange, dissolve, precipitate, and transform into rod shape β-Si₃N₄. In addition, under the action of pulse current and external pressure, electric sparks are generated between TiC particles, which allows the material transfer and particle refinement. Therefore, the β-Si₃N₄ has uniform grain size, and it is vertically and horizontally arranged in the structure, which makes the material have excellent mechanical properties.     

ZrSi2–MgO as novel additives for high thermal conductivity of β-Si3N4 ceramics

A novel ZrSi₂–MgO system was used as sintering additive for fabricating high thermal conductivity silicon nitride ceramics by gas pressure sintering at 1900°C for 12 hours. By keeping the total amount of additives at 7 mol% and adjusting the amount of ZrSi₂ in the range of 0-7 mol%, the effect of ZrSi₂ addition on sintering behaviors and thermal conductivity of silicon nitride were investigated. It was found that binary additives ZrSi₂–MgO were effective for the densification of Si₃N₄ ceramics. XRD observations demonstrated that ZrSi₂ reacted with native silica on the Si₃N₄ surface to generate ZrO₂ and β-Si₃N₄ grains. TEM and in situ dilatometry confirmed that the as formed ZrO₂ collaborated with MgO and Si₃N₄ to form Si–Zr–Mg–O–N liquid phase promoting the densification of Si₃N₄. Abnormal grain growth was promoted by in situ generated β-Si₃N₄ grains. Consequently, compared to ZrO₂-doped materials, the addition of ZrSi₂ led to enlarged grains, extremely thin grain boundary film and high contiguity of Si₃N₄–Si₃N₄ grains. Ultimately, the thermal conductivity increased by 34.6% from 84.58 to 113.91 W·(m·K)⁻¹ when ZrO₂ was substituted by ZrSi₂.     

Fabrication of Si3N4 ceramics with high thermal conductivity and flexural strength via novel two-step gas-pressure sintering

Si₃N₄ ceramic substrates serving as heat dissipater and supporting component are required to have excellent thermal and mechanical properties. To prepare Si₃N₄ with desirable properties, a novel two-step gas-pressure sintering route including a pre-sintering step followed by a high-temperature sintering step was devised. The effects of pre-sintering temperature (1500 – 1600 °C) on the phase transformation, microstructure, thermal and mechanical properties of the samples were studied. The pre-sintering temperature played an important role in adjusting the Si₃N₄ particles’ rearrangement and α→β transformation rate. Furthermore, the densification process for the Si₃N₄ ceramics prepared via the two-step gas-pressure sintering was revealed. After sintered at 1525 °C for 3 h followed by a high-temperature sintering at 1850 °C for another 3 h, the prepared Si₃N₄ compact with a bimodal microstructure presented the highest thermal conductivity and flexural strength of 79.42 W·m^?1·K^?1 and 801 MPa, respectively, which holds great application prospects as ceramic substrates.     

Mechanical properties of hybrid multilayer graphene/whisker-reinforced ceramic composites: Simulation and experimental investigation

The trial-and-error method used in ceramics research has certain limitations such as the high blindness of material component design. Moreover, calculations of the toughness of ceramics using the extended finite element method, which is the most broadly applied technique, are complicated. To overcome these issues, in this study, multilayer graphene (MLG)/Si₃N₄ whisker (Si₃N_4w)-reinforced Si₃N₄ ceramics (MWSCs) were used as the model material, and the modeling of MWSCs was conducted using Voronoi tessellation. Additionally, a more concise novel approach was applied for the prediction of the fracture toughness of MWSCs. Furthermore, the optimal MLG and Si₃N_4w contents were predicted, and then they were verified by fabricating MWSCs using spark plasma sintering (SPS). Simulation results indicated that the optimum MLG and Si₃N_4w contents to enable the toughness and hardness to reach the maximum values (9.87 MPa·m^1/2 and 23.19 GPa) were 1 wt% and 3 wt%, which were consistent with the experimental results. Consequently, the effectiveness of the proposed method was verified. Moreover, the experimental values of the maximum fracture toughness and hardness were 11.04 MPa·m^1/2 and 20.29 GPa, which were 47.20% and 12.10% higher than those of Si₃N₄ ceramics reinforced with 1 wt% MLG, respectively. The synergistic toughening effects of MLG and Si₃N_4w were significantly reflected. The load-bearing effect, bridging, and crack deflection induced by MLG and Si₃N_4w were the key reasons for the improvement in the mechanical properties of MWSCs.     

The effect of BaTiO3 addition on the dielectric constant of Si3N4 ceramics

Si₃N₄ ceramics with different BaTiO₃ contents have been fabricated by pressureless sintering in a N₂ atmosphere at 1680°C for 2 h. Al₂O₃ and Nd₂O₃ were used as sintering additives to promote the densification of Si₃N₄ ceramics. The effect of BaTiO₃ addition on the densification, mechanical properties, phase compositions, microstructure, and dielectric properties of Si₃N₄ ceramics was investigated. The relative density and flexural strength of Si₃N₄ ceramics increased with the addition of BaTiO₃ up to 15 wt% and then decreased, while the dielectric constant increased continuously as the BaTiO₃ contents increased. The dielectric constant of Si₃N₄ ceramics can be tailored in the range from 8.42 to 12.96 by the addition of 5 wt%‐20 wt% BaTiO₃. Meanwhile, these Si₃N₄ ceramics all had flexural strength higher than 500 MPa.     

Effects of Y2O3/MgO ratio on mechanical properties and thermal conductivity of silicon nitride ceramics

In this work, the effects of Y₂O₃/MgO ratio on the densification behavior, phase transformation, microstructure evolution, mechanical properties, and thermal conductivity of Si₃N₄ ceramics were investigated. Densified samples with bimodal microstructure could be obtained by adjusting the ratio of Y₂O₃/MgO. It was found that a low Y₂O₃/MgO ratio facilitated the densification of Si₃N₄ ceramics while a high Y₂O₃/MgO ratio benefited the phase transformation of Si₃N₄ ceramics. Best mechanical properties (flexural strength of 875 MPa, and fracture toughness of 8.25 MPa·m^1/2, respectively) and optimal thermal conductivity of 98.04W/(m·K) were achieved in the sample fabricated with Y₂O₃/MgO ratio of 3:4 by sintering at 1900°C for 4 h.     

Non-additive sintering of Si2N2O ceramic with enhanced high-temperature strength,oxidation resistance,and dielectric properties

The high-temperature mechanical and dielectric properties of Si₂N₂O ceramics are often limited by the introduction of a sintering aid. Herein, dense Si₂N₂O was prepared at 1700 °C by hot-pressing oxidized amorphous Si₃N₄ powder without sintering additives. A homogeneous network with short-range order and a SiN₃O structure was formed in the oxidized amorphous Si₃N₄ powder during the hot-pressing process. Si₂N₂O crystals preferentially nucleated at positions within the SiN₃O structure and grew into rod-like and plate-like grains. Fully dense ceramics with mainly crystalline Si₂N₂O and some residual amorphous phases were obtained. The as-prepared Si₂N₂O possessed a good flexural strength of 311 ± 14.9 MPa at 1400 °C, oxidation resistance at 1500 °C, and a low dielectric loss tangent of less than 5 × 10⁻³ at 1000 °C.     

Densification of silicon nitride powder by spark plasma extrusion

The simultaneous extrusion and sintering of ceramic materials using the spark plasma extrusion (SPE) technique is an alternative densification route for the powders examined in this study. SPE with Y₂O₃ and Al₂O₃ as the additives was employed for the concurrent densification and extrusion of pure α-Si₃N₄ commercial powder. Three compositions of α-Si₃N₄ powders, namely SN-4, SN-12, and SN-20, were studied to understand the effect of additives on the sinter-extrusion process. The number in the mixture name corresponded to the weight percentage of additives in the samples. A mechanical shaker was used to thoroughly mix the selected powder compositions in isopropanol for 24 h at 720 rpm. It was then dried in a furnace at 100 °C for 3 h. The sinter-extrusion treatment was conducted for a holding time of 5 min at a heating rate of 300 °C/min and a sintering temperature of 1500 °C with a pressure in the range of 12–63 MPa. The maximum degree of extrusion was attained when the total amount of additives was at 20 wt% (SN-20 series). As the total amount of additives increased, the capillary pressure gradients led to an inhomogeneous liquid distribution throughout the specimen, which in turn promoted further densification of the Si₃N₄ ceramics. Owing to the conical geometry of the graphite die used for the extrusion process in this study, the largest densification values observed in the extruded ceramics corresponded to the base and the middle sections of the SN-20 series (relative density ~92%). The latter could only take place once the α-to β-Si₃N₄ phase transformation occurred, leading to significant shrinkage of the material.     

Rapid fabrication of Si3N4 ceramics with gradient appearance and microstructure

Si₃N₄ ceramics with tailored gradient in color and microstructure were prepared by a rapid cost-effective one-step approach. The gradient microstructure was obtained by the manipulation of the dissolution-reprecipitation process, by controlling the sintering temperature and sintering additive content. In the Si₃N₄ ceramics, the β-phase content gradually changed from 84% to 11%. The Si₃N₄ ceramics exhibited white color on one side and showed a hardness of 19 GPa and fracture toughness of 7 MPa·m^1/2 and may be suitable for bio-implantation applications.     

Effect of nano-size oxy-nitride starting precursors on spark plasma sintering of calcium sialons along the alpha/(alpha + beta) phase boundary

Several compositions of calcium stabilized sialon ceramics were synthesized by using nano-size starting powder precursors and spark plasma sintering technique at a relatively low temperature of 1500?°C. The formation of calcium alpha/beta-sialons was investigated for the compositions represented by Ca_m/2Si_12-(m+n)Al_m+nO_nN_16-n where m and n values were varied from 0.6 to 1.6 and 0.4–1.6, respectively. Phase analysis of the selected compositions helped in developing the phase boundary between alpha and alpha/beta phase regimes. Effect of m and n values on the evolution of the final phase(s), densification and mechanical properties were evaluated. All samples yielded densified ceramics with density values (3.13–3.19?g/cm³) comparable with those reported in the literature for similar compositions and synthesized at temperatures greater than 1700?°C via conventional sintering techniques. Vickers hardness value HV₁₀ of 20?GPa was measured for the Ca_0.5Si_10.6Al_1.4O_0.4N_15.6 composition (with m?=?1.0 and n?=?0.4) synthesized at 1500?°C. An increase in n value (higher oxide content) was observed to facilitate the formation of beta-sialon and AlN polytype phases leading to an increase in fracture toughness but a decrease in Vickers hardness.