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Effect of Particle Size of Sintering Additives on Microstructure and Properties of Porous Silicon Nitride Ceramics
Journal of Ceramics 2025, 46(3): 562-569
Published: 01 June 2025
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Background and purpose

With the development of hypersonic aircraft, radomes must be used in harsher environments and have stronger electromagnetic wave transmission characteristics. As a strong covalent compound, silicon nitride ceramics have the advantages of high specific strength, high thermal shock resistance, low dielectric constant, etc., making them promising candidates as missile radome materials. Dense silicon nitride ceramics have extremely high hardness and bending strength. The bending strength could be as high as 1090 MPa, but it decreases sharply with increasing porosity. With the development of light weight and miniaturization of radomes, the performance of the base materials (silicon nitride ceramics) has higher requirements, so the preparation of low-density and high-strength porous silicon nitride ceramics is a challenge.

Methods

In this work, fiber α-Si3N4 was used as the main raw material and 5 wt.% nano-sized Y2O3 was used as the sintering aid. The Si3N4 powder was mixed with Y2O3 of different particle sizes through ball milling for 12 h. The mixtures were finally magnetically stirred for 2 h. The resulting slurries were evaporated in a rotary evaporator at 70–80 ℃ for 2 h and then dried in an oven at 80 ℃ for 12 h. The dried powder was sieved through a 150-mesh sieve (aperture 100 μm) and die pressed into samples with dimension of 5 mm×5 mm×50 mm. The green bodies were sintered in a furnace (Highmulti-5000, Fujidempa Co., Ltd., Osaka, Japan) at 1700 ℃ for 2 h, at N2 pressure of 0.5 MPa, at heating rate of 5 ℃·min-1. X-ray powder diffractometer (XRD) was used to determine phase composition of the samples. Microstructure was characterized by using scanning electron microscopy (SEM, Phenom pro X, accelerated voltage 10 k V, backscattered electron imaging mode). The samples were machined to bending test bars with a size of 3 mm×4 mm×50 mm. The tensile surface was ground by using an 800-grit diamond wheel and the edges were beveled to reduce the effect of edge cracks. Three-point bending testing was conducted to determine flexural strength on a testing machine (Instron1195, Instron Co., London, UK) with a span of 16 mm at a crosshead speed of 0.5 mm·min−1. Image J software was used to randomly select at least 500 grains for particle size distribution and at least 100 pores for pore size distribution statistics in SEM images of sample fractures.

Results

The addition of Y2O3 with different particle sizes as sintering additives had weak effect on the green density, linear shrinkage and bulk density of porous silicon nitride, with porosity of 54%–56%. The silicon nitride had completed the phase transformation from α to β after sintering at 1700 ℃ for 2 h. The average grain size decreased and the glass phase distribution became more uniform as the particle size of the sintering aid decreased. The decrease in pore size of the porous silicon nitride ceramics was observed with increasing grain size, which was attributed to the effective improvement in the bending strength from 82.3 MPa to 135.4 MPa. Dielectric constant of the porous silicon nitride ceramics changed slightly, ranging from 2.85 to 3.08, while the dielectric loss was less than 2×10-3. The dielectric properties of the materials met the needs of low dielectric wave-transmitting materials.

Conclusions

Porous silicon nitride ceramics with high strength and porosity were successfully prepared by using pressureless sintering. The Y2O3 with smaller particle size was more uniformly distributed in the matrix, resulted in uniform distribution of the liquid phase after sintering. With the decrease of Y2O3 particle size, the grain size decreased significantly and grain distribution was more uniform, which was attributed to the high nucleation rate of β-Si3N4 in the phase transformation. The pore size decreased with the decrease of grain size, while grain refinement and pore size reduction were the main factors for improving mechanical properties. As the particle size of Y2O3 decreased, the bending strength increased from 82.3 MPa to 135.4 MPa. Dielectric properties depend mainly on the porosity of the materials.

Issue
Preparation and Properties of Silicon Nitride Porous Ceramics through Molding with High Aspect Ratio β-Si3N4 Whiskers
Journal of Ceramics 2022, 43(4): 644-651
Published: 01 August 2022
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In order to improve the flexural strength and high temperature resistance of porous silicon nitride, porous ceramics composed of β-Si3N4 whisker bonded with α-Si3N4 were prepared by using press molding, phenolic resin impregnation and carbonization and carbothermic reduction reaction between SiO vapor and residual carbon, through pressureless sintering. The effects of whisker size, forming pressure and impregnation time of the β-Si3N4 whisker on properties of the porous ceramics were studied. It was found that the addition of sintering aid Y2O3 and the use of loose sintering are effective to increase the aspect ratio of the β-Si3N4 whiskers. Average aspect ratio of the β-Si3N4 whiskers reached 13.8, while the maximum is 25.7. Increasing the pressure during molding improved the densification of the materials and hence the orientation degree of the whiskers, increased overlap point number of the whiskers and reduced the porosity, thus leading to improvement in strength of the materials. Increasing the number of impregnations raised the content of α-Si3N4 after carbothermic reduction. Resin impregnation for 1–3 times improved the connecting of the whiskers, so that the strength could be greatly increased. Only a slight increase in strength was observed above three impregnations, whereas the porosity was reduced, due to the enhanced effective bonding among the whiskers. The porosity and flexural strength of the sample molded at 120 MPa after five times of dipping are 41.0% and 213.4 MPa.

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