Self-propagating high temperature synthesis (SHS) of porous Si3N4-based ceramics with considerable dimensions and study on mechanical properties and oxidation behavior

The aim of present work is to fabricate porous Si₃N₄ ceramics with considerable dimensions and homogeneous microstructure by self-propagating high temperature synthesis (SHS) using Si, Si₃N₄ diluent and Y₂O₃ as raw materials. The results indicate that Si₃N₄ diluent with coarse particle sizes and appropriate β-phase content is beneficial to obtain porous Si₃N₄ ceramics with homogeneous microstructure and excellent mechanical property by controlling the shrinkage inside the sample. The produced Si₃N₄ ceramics possessed excellent flexural strength of 168 MPa～259 MPa, and high Weibull modulus of 11.0～17.2. Additionally, BN and SiC are added as second phase to modify the properties of Si₃N₄-based ceramics. Optimum flexural strength of 170 MPa and 137 MPa were obtained with 10 wt.% addition of BN and SiC respectively. After oxidation at 1100 °C～1300 °C, second phase-doped Si₃N₄ ceramics also presented higher residual strength than pure Si₃N₄ ceramics.     

Preparation of high-strength Si3N4 antenna window using selective laser sintering

In this study, a high-strength silicon nitride (Si₃N₄) antenna window was successfully developed via selective laser sintering (SLS) with cold isostatic pressing (CIP) after debinding before final sintering. The effects of CIP after debinding and sintering aids on the bulk density, total porosity, bending strength and microstructure of Si₃N₄ ceramics were examined. The results show that the bending strength of SLS Si₃N₄ ceramics can be greatly improved by adding sintering aids between Si₃N₄ granules and by CIP after debinding. Optimal performance of ceramics is obtained by CIP after debinding and the use of inter-granule sintering aids. The porosity, bulk density, and bending strength are 18.7%, 3.11 g/cm³, and 685 MPa, respectively. Eliminating the pores by the CIP after debinding and by inter-granule sintering aids promotes the growth of rod-like β-Si₃N₄, which lock with each other contribute to the strengthening of Si₃N₄ ceramics.     

Mechanical characterization of highly porous β-Si3N4 ceramics fabricated via partial sintering & starch addition

In this study, porous β-Si₃N₄ ceramics containing limited amount of Sm₂O₃ and CaO as sintering aids were produced by addition of potato starch (10 and 20 vol.%) and partial sintering. Two different Si₃N₄ powders, α- and β-, were used as starting materials. Scanning electron microscopy investigations revealed that development of elongated β-Si₃N₄ grains were much more pronounced when α-Si₃N₄ starting powder was used. Even though porosity values of the compositions prepared by using α-Si₃N₄ (～57.0–58.4%) is significantly higher than the samples produced by β-Si₃N₄ (42.6%), no significant change was observed for the bending strength, fracture toughness and Weibull modulus. This indicates that microstructural features have a significant contribution to the mechanical properties of the porous materials in terms of bending strength and fracture toughness.     

Prediction of bending strength of Si3N4 using machine learning

The bending strength of silicon nitride (Si₃N₄) plays a vital role in its application and is influenced by various process factors. Current experimental methods for investigating Si₃N₄ ceramics exhibiting low efficiency and high cost are incapable of systematically analysing the effect of process factors on the bending strength of Si₃N₄ ceramics and quantitatively predicting the optimum process parameters. In this study, machine learning (ML) approaches based on extreme gradient boosting (XGBoost) were applied to predict and analyse the bending strength of Si₃N₄ ceramics. Because the classification model of XGBoost is easily interpretable, the factors affecting the bending strength could be quantitatively evaluated. The current model can provide a suitable order of adding sintering additives to obtain excellent bending strength in Si₃N₄ ceramics. Although this study focuses on the bending strength of Si₃N₄ ceramics, the new approach reported herein is applicable for the in silico design and analysis of other ceramic materials.     

Enhanced bending strength and microwave dielectric properties of Li2MgTi3O8 ceramics by adding Si3N4 reinforcing phase

In the 5G era, the dielectric materials used in microwave electronic components must have not only have good microwave dielectric characteristics but also excellent structural characteristics. Li₂MgTi₃O₈ (LMT) ceramics have excellent microwave dielectric properties; however, their low bending strength limits their further applications in the 5G era. In this work, the dielectric properties and bending strength of LMT ceramics were optimized by the addition of Si₃N₄ reinforcing phase using a solid-phase method, and the effects of Si₃N₄ addition on the sintering properties, microscopic structure, crystalline phase, dielectric properties and bending strength of ceramics were investigated. The X-ray diffraction pattern indicates that all ceramics exhibit spinel structure. Combined with the phenomenon of grain reduction in the SEM graph, it indicates that the addition of Si₃N₄ can inhibit the grain growth and achieve the purpose of fine-grain strengthening. The dispersion enhancement of second phase particles is also one of the reasons for the increase of bending strength. LMT ceramics doped with 0.5 wt% Si₃N₄ exhibited the maximum bending strength after sintering at 1050 °C for 4 h, which was 76.97% higher than that of pure LMT ceramics. In addition, the ceramics exhibited outstanding dielectric properties: a dielectric constant of 23.20, quality factor of 49344 GHz, and temperature coefficient of ?5.90 ppm/°C. The high bending strength and good microwave dielectric properties indicate that Si₃N₄-added LMT ceramics can be effectively applied in the 5G era.     

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.     

Fused deposition modeling of Si3N4 ceramics: A cost-effective 3D-printing route for dense and high performance non-oxide ceramic materials

Dense Si₃N₄ ceramics were prepared by fused deposition molding method accompanied by gas pressure sintering. In this study, the surface steps, inter layer bonding and microstructure evolution were characterized and dense Si₃N₄ ceramics without obvious defects were obtained. It was verified that layer thickness and nozzle diameter have little impact on the density and flexural strength of both green and sintered parts. As to the filling strategy, contour offset path was more effective to obtain sintered part with higher flexural strength than parallel lines and grid path, which was due to the possible voids appeared at the intersection of print paths with different directions. The highest flexure strength 824.74 ± 85 MPa was obtained with layer thickness 0.15 mm, nozzle size 0.6 mm and contour offset path. The reliability of the obtained Si₃N₄ ceramics was also investigated and complex shaped Si₃N₄ ceramic parts with good shape keeping was prepared successfully.     

Microstructure and mechanical properties of tantalum carbide ceramics: Effects of Si3N4 as sintering aid

Stoichiometric Tantalum carbide (TaC) ceramics were prepared by reaction spark plasma sintering using 0.333–2.50 mol% Si₃N₄ as sintering aid. Effects of the Si₃N₄ addition on densification, microstructure and mechanical properties of the TaC ceramics were investigated. Si₃N₄ reacted with TaC and tantalum oxides such as Ta₂O₅ to form a small concentration of tantalum silicides, SiC and SiO₂, with significant decrease in oxygen content in the consolidated TaC ceramics. Dense TaC ceramics having relative densities >97% could be obtained at 0.667% Si₃N₄ addition and above. Average grain size in the consolidated TaC ceramics decreased from 11 µm at 0.333 mol% Si₃N₄ to 4 µm at 2.50 mol% Si₃N₄ addition. The Young's modulus, Vickers hardness and flexural strength at room temperature of the TaC ceramic with 2.50 mol% Si₃N₄ addition was 508 GPa, 15.5 GPa and 605 MPa, respectively. A slight decrease in bending strength was observed at 1200 °C due to oxidation of the samples.     

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.     

Effect of the molecular weight and concentration of PEG solution on microstructure and mechanical properties of Si3N4 ceramics fabricated by gel-casting

Gel-casting is a promising preparation technology of Si₃N₄ structural ceramics. The process involves drying of the “green” gel-cast parts before densification. And the drying of green gel-cast bodies is an important step in the gel-casting manufacturing process. In this work, the Si₃N₄ gel-cast green bodies were dried in polyethylene glycol (PEG) solution with the purpose of obtaining Si₃N₄ ceramics with good mechanical properties. The effect of the molecular weight and concentration of PEG solution on drying rate, microstructure and mechanical properties of Si₃N₄ ceramics was studied. The results indicated that with the increase of molecular weight of PEG, the drying rate increased obviously and the structure became more uniform and dense when the concentration of solution was 20?wt%. The Si₃N₄ ceramics after sintering have the excellent flexural strength (662.6?MPa) under PEG600 drying condition. Furthermore, the concentration of PEG600 solution had a positive effect on drying and sintering of the green body. Therefore, the bending strength reached 871.1?MPa under 65?wt% PEG 600 solution drying condition. Overall, the drying process (drying in 65?wt% PEG600 solution) promotes the efficiency and quality of drying of Si₃N₄ gel-cast green bodies, which is beneficial for the subsequent drying and sintering process.     

Fabrication and properties of Si3N4 bioscaffolds with orderly–interconnected big pore channels and well–distributed small pores

This paper focuses on investigating the technical potential for fabricating porous ceramic bioscaffolds for the repair of osseous defects from trauma or disease by inverse replication of three–dimensional (3–D) printed polymer template. Si₃N₄ ceramics with pore structure comprising orderly–interconnected big pore channels and well–distributed small pores are successfully fabricated by a technique combining 3–D printing, vacuum suction filtration and oxidation sintering. The Si₃N₄ ceramics fabricated from the Si₃N₄ powder with addition of 10?wt% talcum by sintering at 1250?°C for 2?h have little deformation, uniform microstructure, low linear shrinkage of 4.1%, high open porosity of 58.2%, relatively high compression strength of 6.4?MPa, orderly–interconnected big pore channels and well–distributed small pores, which are promising bioscaffold in the field of bone tissue engineering.     

Porous Si3N4/SiC Ceramics Prepared via Nitridation of Si Powder with SiC Addition

Porous Si₃N₄/SiC ceramics with high porosity were prepared via nitridation of Si powder, using SiC as the second phase and Y₂O₃ as sintering additive. With increasing SiC addition, porous Si₃N₄/SiC ceramics showed high porosity, low flexural strength, and decreased grain size. However, the sample with 20wt% SiC addition showed highest flexural strength and lowest porosity. Porous Si₃N₄/SiC ceramics with a porosity of 36–45% and a flexural strength of 107‐46MPa were obtained. The linear shrinkage of all porous Si₃N₄/SiC ceramics is below 0.42%. This study reveals that the nitridation route is a promising way to prepare porous Si₃N₄/SiC ceramics with favorable flexural strength, high porosity, and low linear shrinkage.     

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.     

Effects of pore diameters on phase,oxidation resistance,and thermal shock resistance of the porous Si2N2O ceramics

Porous silicon oxynitride (Si₂N₂O) ceramics were prepared by gas pressure sintering at 1650°C for 2 hour under 1.5 MPa N₂ in two different powder beds, that is, h‐BN/Si₃N₄ or h‐BN/(Si₃N₄ + SiO₂). Effects of the gaseous atmosphere in the powder bed and the pore diameter in the ceramics on formation of the Si₂N₂O phase and the oxidation resistance of the sintered porous ceramics were investigated. Results showed that presence of the gaseous SiO in the powder bed played a crucial role in suppressing decomposition of the Si₂N₂O phase at the outer surface of the material. Permeability of the gaseous substances was decreased when the pore diameter was small, to affect the phase composition and the oxidation behavior of the porous Si₂N₂O ceramics. The oxidation weight gain curves of the porous Si₂N₂O ceramics fitted the asymptotic law. No significant changes in the dielectric constant of the Si₂N₂O ceramics were observed after oxidation at 1000°C‐1200°C for up to 30 minutes, whereas the dielectric loss tangent was reduced by oxidation due to formation of SiO₂. The as‐obtained porous Si₂N₂O ceramics could withstand a highest thermal shock of 1200°C when the outer surface could be sealed by the oxidation‐derived SiO₂ layer.     

Design,thermal shock resistance of dense BaO-Al2O3-SiO2 glass/Si3N4-barium feldspar coating for porous Si3N4 ceramic

Silicon nitride-monoclinic barium feldspar (Si₃N₄-m-BAS) composite possesses great dielectric properties, low density, and low thermal expansion coefficient (CTE). Preparing dense Si₃N₄-m-BAS coating on porous Si₃N₄ ceramic is an effective strategy to improve its water resistance and ensure its dielectric performances. However, this promising coating has not been reported yet, because the synthesis of m-BAS is difficult, and the densification of Si₃N₄-BAS composite requires very high temperature. Here, the BaO-Al₂O₃-SiO₂ glass/Si₃N₄-BAS coating was first fabricated by a manual spray method and pressureless sintering at 1450°C. Combining the influence of Si⁴⁺ on the crystal phase composition of BAS and the volume expansion effect of silicon in N₂, an effective coating structure design scheme was proposed. By changing the content of silicon powder, the CTE and horizontal shrinkage of the coating during sintering were controlled. Besides, the prepared coatings exhibited low water absorption and high bonding strength. During the thermal shock tests, SiO₂ produced by the oxidation of Si₃N₄ healed the cracks in the coating, thus delaying the degradation of the properties. The coating prepared in this work is expected to be applied to radome in extreme service environments.     

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.     

Pressureless sinterability of slip cast silicon nitride bodies prepared from coprecipitation-coated powders

The sinterability of compositions from different powder preparation methods (coprecipitation-coating of Si₃N₄ powder or mechanical mixing of Si₃N₄ with Y₂O₃ and Al₂O₃) and compaction routes (dry pressing or slip casting) was compared. Both the coating method and the slip casting process improved silicon nitride sinterability over the mechanical mixing method and dry pressing route. However, the minimisation of powder agglomeration in the green bodies achieved by slip casting is more determinant to the sintering behaviour than the homogeneous distribution of the sintering additives around the Si₃N₄ offered by the coated powder. The coating powder method in combination with the slip casting process is the most favourable processing route, leading to a homogeneous and fully dense microstructure by pressureless sintering at a relatively low temperature of 1750°C. This technique produced materials with hardness of 15·2 GPa, fracture toughness of 7 MPa  m^1/2 and flexural bending strength of 910 MPa.     

Preparation of Porous Si3N4 Ceramics with Controlled Porosity and Microstructure by Fibrous α‐Si3N4 Addition

Porous silicon nitride ceramics with various porosities were fabricated by liquid phase sintering of mixtures containing fibrous and equiaxed α‐Si₃N₄ powder with a various content ratios. The effects of the contents of the fibrous α‐Si₃N₄ powder (0%–100%) on the microstructure and mechanical properties of porous Si₃N₄ ceramics were studied. As the increase of the fibrous α‐Si₃N₄ powder content, both the density of green bodies and the linear shrinkage decreased, resulting in increased porosity due to the inhibited densification by the fibrous Si₃N₄ particle. XRD analysis proved the complete formation of single β‐Si₃N₄ phase. SEM analysis revealed that the microstructure of the low content of fibrous α‐Si₃N₄ porous ceramics was almost composed of fine elongated β‐Si₃N₄ grains with high aspect ratio while numerous coarse elongated β‐Si₃N₄ grains with low aspect ratio surrounding fine grains were formed as the content of the fibrous α‐Si₃N₄ powder increased. With the increase in content of the fibrous α‐Si₃N₄ powder from 0% to 100%, the porosity changed from 47.8% to 56.6%, and the flexural strength decreased from 146 to 62 MPa correspondingly, indicating a flexural adjustment of the porosity and mechanical properties.     

Effect of magnesium titanate content on microstructures,mechanical performances and dielectric properties of Si3N4-based composite ceramics

Silicon nitride-based composite ceramics with different contents of magnesium titanate have been fabricated via gas pressure sintering method. The phase compositions, microstructure, mechanical performances and dielectric properties of the composite ceramics were investigated. The density of the Si₃N₄-based composite ceramics firstly increased with additive of magnesium titanate powder up to 5 wt% and then gently decreased, and the mechanical properties firstly increased and then declined. Besides, the dielectric constant and dielectric loss increased with the increase of magnesium titanate contents. For the Si₃N₄-based composite ceramics with 5 wt% magnesium titanate powders, the flexural strength, elastic modulus, dielectric constant and dielectric loss reached 451 MPa, 274 GPa, 7.65, 0.0056, respectively. These results suggested that the magnesium titanate was beneficial for the improvement of mechanical performances and dielectric constant of Si₃N₄-based composite ceramics.     

A non-sintering fabrication method for porous Si3N4 ceramics via sol hydrothermal process

A non-sintering fabrication method for porous Si₃N₄ ceramics with high porosity and high mechanical strength was proposed. Strength of the porous ceramics can be obtained by silica sol mass transfer process in hydrothermal conditions rather than a traditionally controlled high temperature sintering process. Under hydrothermal circumstances, silica sol is continuously transferred to the necks of Si₄N₃ powder compact, depositing there and thus consolidating the ceramic skeleton. The key of the method to obtain homogeneous microstructure and mechanical strength is how to keep the silica sol from gelatin during hydrothermal procedure. The stabilization of silica sol and its affecting factors were studied. The results indicated that ultrasonic treatment makes alkali-catalyzed silica sol remain stable even in 200?℃ hydrothermal condition, which insures consecutive silica transportation. The effect of hydrothermal time on open porosity/mechanical strength of the porous Si₄N₃ ceramics were also thoroughly investigated. The porous Si₄N₃ ceramics with open porosity above 42% and flexural strength of 45?MPa were obtained without any high temperature sintering process. This method can be widely employed for the preparation of other porous ceramics as well.