Influence of the content of polymethyl methacrylate on the properties of porous Si3N4 ceramics fabricated by digital light processing

Porous Si₃N₄ ceramics are highly regarded as ideal materials for radomes due to their unique characteristics. However, the slurry used for the preparation of porous Si₃N₄ ceramics suffers from a low cure depth, making it challenging to fabricate ceramic components using DLP technology. In this study, porous Si₃N₄ ceramics were prepared by combining DLP technology with pore-forming agent method. The addition of polymethyl methacrylate (PMMA) powders with lower refractive index than that of Si₃N₄ powders can improve the penetration depth of ultraviolet light in the Si₃N₄ slurry. A systematic study was conducted to investigate the influence of the addition of PMMA powders on the properties of Si₃N₄ slurries and porous Si₃N₄ ceramics. When PMMA powders were added at 10 wt%, the slurry with a lowest viscosity of 0.13 Pa s (the shear rate is 30 s⁻¹) and cure depth of 40.0 μm (the exposure energy is 600 mJ/cm²) was obtained. With the increase of PMMA content, porous Si₃N₄ ceramics experienced a gradual decrease in both the flexural strength and bulk density, while the porosity increased from 14.41% to 27.62%. Specifically, when 20 wt% PMMA was added, the resulting porous Si₃N₄ ceramics had a lowest bulk density (2.41 g/cm³), a maximum porosity (27.62%), and a flexural strength (435.87 MPa). The study is of great significance in establishing an experimental foundation for fabricating porous Si₃N₄ ceramics by using DLP technology.     

Influence of α-Si3N4 coarse powder on densification,microstructure, mechanical properties,and thermal behavior of silicon nitride ceramics

Silicon nitride (Si₃N₄) ceramics, with different ratios of fine and coarse α-Si₃N₄ powders, were prepared by spark plasma sintering (SPS) and heat treatment. Further, the influence of coarse α-Si₃N₄ powder on densification, microstructure, mechanical properties, and thermal behavior of Si₃N₄ ceramics was systematically investigated. Compared with fine particles, coarse particles exhibit a slower phase transition rate and remain intact until the end of SPS. The remaining large-sized grains of coarse α-Si₃N₄ induce extensive growth of neighboring β-Si₃N₄ grains and promote the development of large elongated grains. Noteworthy, an appropriate number of large elongated grains distributed among fine-grained matrix forms bimodal microstructural distribution, which is conducive to superior flexural strength. Herein, Si₃N₄ ceramics with flexural strength of 861.34 MPa and thermal conductivity of 65.76 W m⁻¹ K⁻¹ were obtained after the addition of 40 wt% coarse α-Si₃N₄ powder.     

Porous SiC–Si3N4 composite ceramics with excellent EMW absorption property prepared by gelcasting using DMAA

The porous SiC–Si₃N₄ composite ceramics with good EMW absorption properties were prepared by combination of gelcasting and carbothermal reduction. The pre-oxidation of Si₃N₄ powders significantly improved the rheological properties of slurries (0.06 Pa s at 103.92 s⁻¹) and also suppressed the generation of NH₃ and N₂ from Si₃N₄ hydrolysis and reaction between Si₃N₄ and initiator APS, thereby reducing the pore defects in green bodies and enhancing mechanical properties with a maximum value of 42.88 MPa. With the extension of oxidation time from 0 h to 10 h, the porosity and pore size of porous SiC–Si₃N₄ composite ceramics increased from approximately 41.86% and 1.0–1.5 μm to 46.33% and ~200 μm due to the production of CO, N₂ and gaseous SiO, while the sintering shrinkage decreased from 16.24% to 10.50%. With oxidation time of 2 h, the Si₂N₂O fibers formed in situ by the reaction of Si₃N₄ and amorphous SiO₂ effectively enhanced the mechanical properties, achieving the highest flexural strength of 129.37 MPa and fracture toughness of 4.25 MPa m^1/2. Compared with monolithic Si₃N₄ ceramics, the electrical conductivity, relative permittivity and dielectric loss were significantly improved by the in-situ introduced PyC from the pyrolysis of three-dimensional network DMAA-MBAM gel in green bodies and the SiC from the carbothermal reduction reaction between PyC and SiO₂ and Si₃N₄. The porous SiC–Si₃N₄ composite ceramics prepared by the unoxidized Si₃N₄ powders demonstrated the optimal EMW absorption properties with reflection loss of −22.35 dB at 8.37 GHz and 2 mm thickness, corresponding to the effective bandwidth of 8.20–9.29 GHz, displaying great application potential in EMW absorption fields.     

Effect of polystyrene addition on properties of porous Si3N4 ceramics fabricated by digital light processing

Porous Si₃N₄ ceramics with high strength and high transmittance have been widely used in the field of defense and military. Additive manufacturing (AM) technology is one of the effective means to fabricate porous Si₃N₄ ceramics. Nevertheless, it is difficult to prepare porous Si₃N₄ ceramics by using digital light processing (DLP) because of the large refractive index difference between Si₃N₄ powders and photosensitive resin. In this study, the effects of the amount of polystyrene (PS) powders on the properties of Si₃N₄ ceramic slurries and sintered ceramics were systematically discussed. The addition of PS reduced the overall refractive index of powders and increased the average particle size of powders, thus improving the cure depth of Si₃N₄ ceramic slurries from 11.0 ± 2.0 μm to 55.7 ± 1.8 μm. With the increase of PS content, the shrinkage and porosity of Si₃N₄ ceramics gradually increased, and the bulk density and flexural strength showed the opposite trend. The slurry with low viscosity (2.38 Pa٠s at a shear rate of 30 s⁻¹) and high cure depth (51.2 ± 4.6 μm) was obtained when the content of PS was 15 wt%, which met the thickness requirements for printing. The total porosity of Si₃N₄ ceramics reached the maximum values at 28.21 ± 2.58%. The addition of PS solved the problem of low cure depth of slurries, and PS as a pore-forming agent could help Si₃N₄ ceramics form porous structure. This research provides valuable insights into the fabrication of non-oxide ceramics with high refractive index using DLP technology.     

Effect of seeding on the thermal conductivity of self-reinforced silicon nitride

Thermal conductivity of Si₃N₄ containing large β-Si₃N₄ particles as seeds for grain growth was investigated. Seeds addition promotes growth of β-Si₃N₄ grains during sintering to develop the duplex microstructure. The thermal conductivity of the material sintered at 1900 °C improved up to 106 W m⁻¹ K⁻¹, although that of unseeded material was 77 Wm⁻¹ K⁻¹. Seeds addition leads to reduction of the sintering temperature with developing the duplex microstructure and with improving the thermal conductivity, which benefits in terms of production cost of Si₃N₄ ceramics with thermal conductivity. ©     

Preparation of Si3N4 ceramic based on digital light processing 3D printing and precursor infiltration and pyrolysis

The emergence of digital light processing (DLP) 3D printing technology creates favorable conditions for the preparation of complex structure silicon nitride (Si₃N₄) ceramics. However, the introduction of photosensitive resin also makes the Si₃N₄ ceramics prepared by 3D printing have low density and poor mechanical properties. In this study, high-density Si₃N₄ ceramics were prepared at low temperatures by combining DLP 3D printing with precursor infiltration and pyrolysis (PIP). The Si₃N₄ photocurable slurry with high solid content and high stability was prepared based on the optimal design of slurry components. Si₃N₄ green parts were successfully printed and formed by setting appropriate printing parameters. The debinding process of printed green parts was further studied, and the results showed that samples without defects and obvious deformation can be obtained by setting the heating rate at .1°C/min. The effect of the PIP cycle on the microstructure and mechanical properties of the Si₃N₄ ceramics was studied. The experimental results showed that the mass change and open porosity of the samples tended to be stable after eight PIP cycles, and the open porosity, density, and bending strength of the Si₃N₄ ceramics were 1.30% (reduced by 97%), 2.64 g/cm³ (increased by 43.5%), and 162.35 MPa.     

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.     

Effects of solid loading and calcination temperature on microstructure and properties of porous Si3N4 ceramics by aqueous gelcasting using DMAA system

Herein, a low–toxic N, N–dimethylacrylamide (DMAA) system was used in preparation of porous Si₃N₄ ceramics by aqueous gelcasting, and variations in microstructure and properties with solid loading and calcination temperature were systematically investigated. In the considered solid loading range of 28–44 vol%, all the slurries exhibited superior rheological properties (≤145 mPa⋅s at 95.40 s⁻¹ for 44 vol% solid loading) perfectly suitable for casting. With increasing solid loading, a decreased bulk density (1.71–1.69 g/cm³), volume shrinkage (37.73–13.77%) and flexural strength (46.56–26.75 MPa) of green bodies were obtained, exhibiting better mechanical properties than those derived from the conventional acrylamide (AM) system. Regarding Si₃N₄ ceramics with various solid loadings, the increase in calcination temperature favored the phase transformation α→β–Si₃N₄ and β–Si₃N₄ growth, however, the increased solid loading exhibited an inhibiting effect on those since mass transport in gas phase was blocked due to the disruption of pore connectivity. The resulting microstructure changes imparted Si₃N₄ ceramics increasing flexural strength (110.36–367.88 MPa), fracture toughness (2.54–5.03 MPa⋅m^1/2), as well as decreasing porosity (54.21–41.05%) and pore size (0.38–0.33 μm). This work demonstrates the potential research value of DMAA system in preparing high–performance porous Si₃N₄ ceramics through gelcasting technique.     

A novel method of strong and tough Si3N4 ceramic from the particle-stabilized foam

The brittleness of Si₃N₄ ceramics has always limited its wide application. In this paper, Si₃N₄ ceramics were prepared based on foam. Combining the unique honeycomb structure of the ceramic foams and the self-toughening mechanism of Si₃N₄, the strengthening and toughening of Si₃N₄ ceramics can be further achieved by adjusting the microstructure of Si₃N₄ ceramic foams. The powder particles are self-assembled by particle-stabilized foaming to form a foam body with a honeycomb structure. It was pretreated at different temperatures (1450–1750°C). The microstructure evolution of foamed ceramics at different pretreatment temperatures and the conversion rate of α-Si₃N₄ to β-Si₃N₄ at different pretreatment temperatures were explored. Then the foamed ceramics with different microstructures are hot-press sintered to prepare Si₃N₄ dense ceramics. The effects of different microstructures of foamed ceramics on the strength and toughness of Si₃N₄ ceramics were analyzed. The experimental results show that the relative density of Si₃N₄ ceramics prepared at a particle pretreatment temperature of 1500°C is 97.8%, and its flexural strength and fracture toughness are relatively the highest, which are 1089 ± 60 MPa and 12.9 ± 1.3 MPa m^1/2, respectively. Compared with the traditional powder hot-pressing sintering, the improvement is 21% and 33%, respectively. It is shown that this method of preparing Si₃N₄ ceramics based on foam has the potential to strengthen and toughen Si₃N₄ ceramics.     

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.     

Tailoring the microstructure of high porosity Si3N4 foams by direct foaming with mixed surfactants

The mixed surfactants were successfully applied to fabricate the highly porous Si₃N₄ ceramic foams by the direct foaming method. The oppositely charged surfactants mixed in slurries could combined into catanionic surfactant by the electrostatic attraction and facilitate the formation of ultra-stable foams. The microstructure of the Si₃N₄ ceramic foams, including pore structure, mean pore size, pore size distribution and porosity were tailored by varying the mixing ratio of surfactant, mixed surfactants concentration and solid content of the initial slurries. Si₃N₄ ceramic foams with porosity of 92%-97%, mean pore size of 140-240 µm and compressive strength of 0.85-5.38 MPa were obtained by adjusting mixed surfactants between 0.1 and 0.4 wt% and solid content between 22 and 30 vol%. The compressive strength of Si₃N₄ ceramic foams in current work was much higher than most reported results.     

Effect of carboxymethyl cellulose addition on the properties of Si3N4 ceramic foams

The effect of carboxymethyl cellulose (CMC) addition on the preparation of Si₃N₄ ceramic foam by the direct foaming method was investigated. The addition of CMC in the foam slurry can reduce the surface tension, increase the viscoelasticity of foams, and improve their stability and fluidity. The foam ceramics show low shrinkage during drying owing to the CMC and the gelation of acrylamide monomers. The surface structure of dried foam is uniform, and there are no macropores and cracks on the surface. The sintered Si₃N₄ foam ceramics have very uniform pore distribution with average pore size of about 16 μm; the flexure strength is as high as 3.8–77.2 MPa, and the porosity is about 60.6–82.1%.     

The preparation of silicon nitride ceramics by gelcasting and pressureless sintering

A new gelling system based on the polymerization of hydantion epoxy resin and 3,3′-Diaminodipropylamine (DPTA) was successfully developed for fabricating silicon nitride (Si₃N₄) ceramics. The effects of pH value, the dispersant content, solid volume fraction and hydantion epoxy resin amount on the rheological properties of the Si₃N₄ slurries were investigated. The relative density of green body obtained from the solid loading of 52 vol% Si₃N₄ slurry reached up to 62.7%. As the concentration of hydantion epoxy resin increased from 5 wt% to 20 wt%, the flexural strength of Si₃N₄ green body enhanced from 5.3 MPa to 31.6 MPa. After pressureless sintering at 1780 °C for 80 min, the sintered samples exhibited the unique interlocking microstructure of elongated β-Si₃N₄ grains, which was beneficial to improve the mechanical properties of Si₃N₄ ceramics. The relative density, flexural strength and fracture toughness of Si₃N₄ ceramics reached 97.8%, 687 MPa and 6.5 MPa m^1/2, respectively.     

Effects of surfactant and particle size on the microstructure and strength of Si3N4 foams with high porosity

The highly porous Si₃N₄ ceramic foams were prepared by direct foaming with mixed surfactants. The surface tension and viscosity of slurries were tailored by different carbon chain length of surfactants and different mean Si₃N₄ particle size to achieve the pore size controlling. The nearly linear relationship between the pore size and the ratio of surface tension to viscosity was observed, which indicates that the pore size could be precisely tailored by the slurry properties. Si₃N₄ ceramic foams with porosity of nearly 94%, mean pore size of 110–230 µm, and compressive strength of 1.24–3.51 MPa were obtained.     

Porous Si3N4 ceramics prepared by aqueous gelcasting using low–toxicity DMAA system: Regulatable microstructure and properties by monomer content

In this study, the low–toxicity monomer N, N–dimethylacrylamide (DMAA), serving as both gelling agent and pore–forming agent, was adopted to fabricate porous Si₃N₄ ceramics with a regulatable microstructure and property by aqueous gelcasting. Results indicate that monomer content played an important role in regulating and optimizing the properties of sintered bodies. With increasing monomer content (5.94–30.69?wt%), both slurry viscosity (maximum 0.14?Pa?s at 95.40 s^?1) and green body strength (11.35–49.23?MPa) exhibited monotonic increasing trends, demonstrating superior mechanical properties to those obtained using the neurovirulent acrylamide (AM) gelling system. The increased monomer content not only improved porosity, but also promoted α→β–Si₃N₄ transformation as well as β–Si₃N₄ grain growth through enhancing the connectivity of interlocking pores and accelerating the vapor phase transport during liquid–phase sintering. These variations in phase composition and microstructure derived from the varied monomer content further resulted in monotonic changes in porosity (40.32–51.50%), mean pore size (0.27–0.38?μm), flexural strength (202.77–132.15?MPa), fracture toughness (2.93–2.32?MPa?m^1/2), dielectric constant (3.48–2.78) and loss (3.52–3.09?×?10^?3) at 10?GHz for sintered bodies, displaying an excellent comprehensive properties. This study suggests a promising prospect for DMAA in preparation of high–performance porous Si₃N₄ ceramics by aqueous gelcasting.     

Mechanical and dielectric properties of Si3N4-SiO2 ceramics prepared by digital light processing based 3D printing and oxidation sintering

Si₃N₄-SiO₂ ceramics are considered as the preferred high-performance wave-transmitting material in the aerospace field. However, traditional fabrication methods for Si₃N₄-SiO₂ ceramics have the disadvantages of high cost and complicated fabrication process. In this paper, Si₃N₄-SiO₂ ceramics with excellent mechanical and dielectric properties were fabricated by digital light processing-based 3D printing combined with oxidation sintering. Firstly, the curing thickness and viscosity of slurries with different solid loadings for vat photopolymerization-based 3D printing were studied. Then, the effects of the sintering temperature on the linear shrinkage, phase composition, microstructure, flexural strength, and dielectric properties of Si₃N₄-SiO₂ ceramics, and the influences of solid loading on them were explored. The curing thickness and viscosity of the slurry with a solid loading of 55 vol% were 30 μm and ∼1.5 Pa‧s, respectively. The open porosity and the flexural strength of Si₃N₄-SiO₂ ceramic with a solid loading of 55 vol% were 4.3 ± 0.61% and 76 ± 5.6 MPa, respectively. In the electromagnetic wave band of 8–18 GHz, the dielectric constant of Si₃N₄-SiO₂ ceramics was within the range of less than 4, and the dielectric loss remained below 0.09. The method of digital light processing-based 3D printing combined with oxidation sintering can be further extended in the preparation of Si₃N₄-based structure-function integrated ceramics.     

Graded Si3N4 ceramics with hard surface and tough core by two-step hot pressing

Graded Si₃N₄ ceramics with hard surface and tough core were prepared by two-step hot pressing with the homogenous starting composition. The inner Si₃N₄ layer was firstly hot-pressed at 1800 °C, subsequently covered with Si₃N₄ powders on both sides, and finally hot-pressed at 1600 °C. After two-step hot pressing, the resulting ceramics exhibited a zoned microstructure, differentiated by the phase assemblage of Si₃N₄ and grain size. The outer layers were well bonded to the inner layer. The outer layer exhibited bimodal and fine-grained microstructure, whereas the inner layer exhibited bimodal and coarse-grained microstructure. Vickers hardness of outer and inner layers were 18.1±0.2 GPa and 16.0±0.2 GPa, respectively, and fracture toughness were 4.2±0.1 MPa m^1/2 and 5.5±0.2 MPa m^1/2, respectively.     

Photosensitive Si3N4 slurry with combined benefits of low viscosity and large cured depth for digital light processing 3D printing

Digital light processing 3D printing can be applied to fabricate complex silicon nitride (Si₃N₄) components. However, because of the surface hydroxyl groups and large refractive index, it is still a foremost challenge to realize a stable photosensitive Si₃N₄ slurry with combined benefits of low viscosity and large curing depth. In this study, we propose a new formulation strategy to prepare Si₃N₄ slurry. Starting from the optimization of monomer ratio, we have systematically optimized powder particle size, dispersant and photoinitiator on the rheological properties and curing properties of Si₃N₄ slurry. Specifically, we have fabricated a stable photosensitive Si₃N₄ slurry (48 vol%) with a viscosity of 2.09 Pa s (30 s^?1), a critical curing energy of 126.09 mJ/cm² and a maximum curing depth of 80 µm. Finally, based on this optimized slurry, we have successfully obtained complex Si₃N₄ green body with no defect, which demonstrates great potential to fabricate arbitrary complex ceramic components for various applications.     

Effect of post-sintering heat-treatment on thermal and mechanical properties of Si3N4 ceramics sintered with different additives

To improve the thermal conductivity of Si₃N₄ ceramics, elimination of grain-boundary glassy phase by post-sintering heat-treatment was examined. Si₃N₄ ceramics containing SiO₂–MgO–Y₂O₃-additives were sintered at 2123 K for 2 h under a nitrogen gas pressure of 1.0 MPa. After sintering, the SiO₂ and MgO could be eliminated from the ceramics by vaporization during post-sintering heat-treatment at 2223 K for 8 h under a nitrogen gas pressure of 1.0 MPa. Thermal conductivity of 3 mass% SiO₂, 3 mass% MgO and 1 mass% Y₂O₃-added Si₃N₄ ceramics increases from 44 to 89 Wm⁻¹ K⁻¹ by the decrease in glassy phase and lattice oxygen after the heat-treatment. Relatively higher fracture toughness (3.8 MPa m^1/2) and bending strength (675 MPa) with high hardness (19.2 GPa) after the heat-treatment were achieved in this specimen. Effects of heat-treatment on microstructure and chemical composition were also observed, and compared with those of Y₂O₃–SiO₂-added and Y₂O₃–Al₂O₃-added Si₃N₄ ceramics.     

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.