Preparation and mechanical properties of Si3N4 nanocomposites reinforced by Si3N4@rGO particles

A new type of reduced graphene oxide-encapsulated silicon nitride (Si₃N₄@rGO) particle was synthesized via an electrostatic interaction between amino-functionalized Si₃N₄ particles and graphene oxide (GO). Subsequently, the Si₃N₄@rGO particles were incorporated into a Si₃N₄ matrix as a reinforcing phase to prepare nanocomposites, and their influence on the microstructure and mechanical properties of the Si₃N₄ ceramics was investigated in detail. The microstructure analysis showed that the rGO sheets were uniformly distributed throughout the matrix and firmly bonded to the Si₃N₄ grains to form a three-dimensional carbon network structure. This unique structure effectively increased the contact area and load transfer efficiency between the rGO sheets and the matrix, which in turn had a significant impact on the mechanical properties of the nanocomposites. The results showed that the nanocomposites with 2.25 wt.% rGO sheets exhibited mechanical properties that were superior to monolithic Si₃N₄; the flexural strength increased by 83.5% and reached a maximum value of 1116.4 MPa, and the fracture toughness increased by 67.7% to 10.35 MPa·m^1/2.     

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.     

Novel porous Si3N4 ceramics prepared by aqueous gelcasting using Si3N4 poly-hollow microspheres as pore-forming agent

In this paper, novel porous Si₃N₄ ceramics were prepared by aqueous gelcasting using Si₃N₄ poly-hollow microspheres as pore-forming agent. The effect of Si₃N₄ poly-hollow microsphere content on the phase composition, microstructure, shrinkage, porosity and mechanical properties of the prepared porous Si₃N₄ ceramics were investigated. It is found that there is only β-Si₃N₄ phase in all the prepared porous Si₃N₄ ceramics. Meanwhile, the SEM results show that the pores in the porous Si₃N₄ ceramics distribute uniformly, the added Si₃N₄ poly-hollow microspheres and the basal body contact closely. With the increase of Si₃N₄ poly-hollow microsphere content, the shrinkage of the porous Si₃N₄ ceramics decreases gradually, and the porosity of the porous Si₃N₄ ceramics decreases firstly and then increases. Furthermore, the flexural strength and fracture toughness of the porous Si₃N₄ ceramics decrease with the increase of the Si₃N₄ poly-hollow microsphere content.     

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.     

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.     

Silicon nitridation mechanism in reaction‐bonded Si3N4–SiC and Si3N4‐bonded ferrosilicon nitride

Reaction‐bonded Si₃N₄–SiC and Si₃N₄‐bonded ferrosilicon nitride, with Si powder, SiC particles and Fe₃Si–Si₃N₄ particles as raw materials, respectively, are prepared in flame‐isolation nitridation shuttle kiln with flowing N₂ at 1723K. There is columnar β‐Si₃N₄ in both Si₃N₄–SiC and Si₃N₄‐bonded ferrosilicon nitride. However, fibrous α‐Si₃N₄ is only observed in Si₃N₄–SiC and Si₃N₄‐bonded ferrosilicon nitride contains much more Si₂N₂O than Si₃N₄–SiC. By analyzing the oxidation thermodynamics of Si and Si₃N₄, it is known that in the process of producing Si₃N₄–SiC, Si is oxidized first to gaseous SiO and fibrous α‐Si₃N₄ is generated with SiO and N₂. The existence of SiO is the reason of low silicon nitridation rate. But in the process of producing Si₃N₄‐bonded ferrosilicon nitride, Si₃N₄ is easier to be oxidized than Si and Si₂N₂O is generated on the surface of Si₃N₄ hexagonal prisms in ferrosilicon nitride particles. Meanwhile, Si in raw materials forms new ferrosilicon alloys with Fe₃Si, which decreases the temperature of liquid appearance and blocks some open pores in the samples, which stops the matter loss of nitridation. Liquid ferrosilicon alloys favors β‐Si₃N₄ generation from Si direct nitridation and fibrous α‐Si₃N₄ transformation, which used to exist in ferrosilicon nitride raw materials.     

Thermal,electrical, and mechanical properties of Si3N4 filled LLDPE composite

Silicon nitride (Si₃N₄) filled linear low-density polyethylene (LLDPE) composite was prepared. The effects of Si₃N₄ filler content, dispersion, and LLDPE particle size on the thermal conductivity, and Si₃N₄ filled content on the mechanical and electrical properties of Si₃N₄ reinforced LLDPE composites prepared using powder mixing were investigated. The results indicate that there existed a unique dispersion state of Si₃N₄ particles in LLDPE, shell-kernel structure, in which Si₃N₄ particles surrounded LLDPE matrix particles. With increasing filler content and LLDPE particles size, thermal conductivity increased, and reached 1.42 W/m K at 30 vol% of filler, seven times as that of unfilled LLDPE. Furthermore, the examinations of Agari model demonstrate that larger size LLDPE particles form thermal conductive networks easily compared with smaller ones. The values predicted by theoretical model underestimate the thermal conductivity of Si₃N₄/LLDPE composites. In addition, the composites still possessed rather higher electrical resistivity and dielectric properties, but the mechanical properties decreased. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Si3N4-BN-SiCN ceramics with unique hetero-interfaces for enhancing microwave absorption properties

SiCN-based ceramics with broadband and strong microwave absorption properties are desired for the structural and functional integration of ceramic matrix composites. The elemental composition and thermal expansion coefficients of the ceramics matrix crucially affect its microstructure and electromagnetic wave (EMW) absorption properties. BN layer with lower electrical conductivity and higher specific area, exhibits both the impedance matching characteristic and EMW attenuation in the process of multiple reflections, electrical conductivity loss, dipole polarization and interfacial polarization. Therefore, Si₃N₄-BN-SiCN ceramics, which were synthesized using chemical vapor infiltration (CVI) method, construct unique hetero-interface of Si₃N₄-BN, Si₃N₄–SiCN and BN-SiCN. Therefore, the Si₃N₄-BN-SiCN ceramics have outstanding EMW absorption performance and realize an effective absorption bandwidth (EAB) that covers the whole X band and the minimum reflection coefficient (RC) reaches -18.43 dB at a thickness of 3.37 mm.     

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.     

Low-temperature densification by plasma activated sintering of Mg2Si-added Si3N4

In this study, highly dense Si₃N₄ ceramics with excellent mechanical properties were fabricated using Mg₂Si as a sintering additive by plasma-activated sintering at 1400–1500 °C. The effects of the sintering temperature and content of Mg₂Si on the densification, microstructures, and mechanical properties of the Si₃N₄ ceramics were investigated. The mechanism responsible for the effect of Mg₂Si in the promotion of the sinterability of Si₃N₄ is discussed. The results showed that the addition of Mg₂Si could effectively remove the oxide layers on the Si₃N₄ particles and form a liquid phase during the sintering, promoting the densification and phase transition of the Si₃N₄ ceramics. The Si₃N₄ ceramic sintered at 1450 °C with 6.0 wt% of Mg₂Si exhibited the maximum strength of 1050 MPa.     

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.     

Thermal and mechanical properties of Si3N4 ceramics obtained via two-step sintering

Si₃N₄ ceramics were prepared using novel two-step sintering method by mixing α-Si₃N₄ as raw material with nanoscale Y₂O₃–MgO via Y(NO₃)₃ and Mg(NO₃)₂ solutions. Si₃N₄ composite powders with in situ uniformly distributed Y₂O₃–MgO were obtained through solid–liquid (SL) mixing route. Two-step sintering method consisted of pre-deoxidization at low temperature via volatilization of in situ-formed MgSiO₃ and densification at high temperature. Variations in O, Y, and Mg contents in Si₃N₄–Y₂O₃–MgO during first sintering step are discussed. O and Mg contents decreased with increasing temperature because SiO₂ on Si₃N₄ surface reacted with MgO to form low-melting-point MgSiO₃ compound, which is prone to volatilize at high temperature. By contrast, Y content hardly changed due to high-temperature stability of Y–Si–O–N quaternary compound. In the second sintering step, skeleton body was densified, and the formation of Y₂Si₃O₃N₄ secondary phase occurred simultaneously. Two-step sintered Si₃N₄ ceramics had lower total oxygen content (1.85 wt%) than one-step sintered Si₃N₄ ceramics (2.51 wt%). Therefore, flexural strength (812 MPa), thermal conductivity (92.1 W/m·K), and fracture toughness (7.6 MPa?m^1/2) of Si₃N₄ ceramics prepared via two-step sintering increased by 28.7%, 16.9%, and 31.6%, respectively, compared with those of one-step sintered Si₃N₄ ceramics.     

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.     

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).     

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.     

Thermal shock behavior of porous Si3N4 ceramics with Nd2O3 as sintering additive

The thermal shock behavior of porous Si₃N₄ ceramics with Nd₂O₃ as sintering additive was investigated by the water quenching method in the temperature difference range from 200 to 1500°C. The porosity and residual flexural strength of the specimens after single water quenching were measured to reveal the influence of thermal shock on porous Si₃N₄ ceramics. It was found that the critical temperature was 780°C, which was almost 230°C higher than its dense counterpart reported by other researchers. Scanning electron microscope was used to examine the microstructure evolution of the external surface and interior after water quenching. Surface oxidation and cracks formation were found to be the primary cause of the strength degradation of porous Si₃N₄ ceramics. The phase composition variation in the surface was also characterized by X-ray diffraction.     

Joining of Cf/SiC composites and Si3N4 ceramic with Y2O3–Al2O3–SiO2 glass filler for high-temperature applications

C_f/SiC composites and Si₃N₄ ceramics are candidate materials for applications in thermal protection system. This paper investigated the joining of C_f/SiC and Si₃N₄ using Y₂O₃–Al₂O₃–SiO₂ glass. The reliability of joints was evaluated by thermal shock tests. In this present work, the typical joint structure was C_f/SiC-glass-Si₃N₄. The results demonstrate that Direct bonding has been identified as the interfacial bonding mechanism at the SiC/glass and glass/Si₃N₄ interfaces. The maximum shear strength of the C_f/SiC–Si₃N₄ joint was ~34 MPa, which delivered an effective method to achieve strong, reliable bonding between the dissimilar materials. In addition, after thermal shock for 10 cycles, the residual strength remained ~13 MPa. Bubbles instead of microcracks formed in the glass filler, which was the main factor causing the degradation of the joint performance. It is suggested that improving the high temperature resistance of joining materials is the key to realize the application of this joint structure.     

Toughness and R-curve behaviour of laminated Si3N4/SiCw ceramics

Laminated Si₃N₄/SiC_w ceramics were successfully prepared by tape casting and hot-pressing. Its mechanical properties were measured and the impact resistance was discussed. The toughness of the laminated Si₃N₄/SiC_w ceramics was 13.5 MPa m^1/2, which was almost 1.6 times that of Si₃N₄/SiC_w composite ceramics, namely 8.5 MPa m^1/2. Moreover, the indentation strength of laminated Si₃N₄/SiC_w ceramics was not sensitive to increasing indentation loads and exhibited a rising R-curve behaviour, indicating that the laminated Si₃N₄/SiC_w ceramics had excellent impact resistance. The improved toughness and impact resistance of laminated Si₃N₄/SiC_w ceramics was attributed to the residual stress caused by a thermal expansion coefficient mismatch between the different layers, resulting in crack deflection and bridging of SiC whiskers in the interface layer, thus consuming a large amount of fracture work.     

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.     

Recent advances and perspectives in carbon-based fillers reinforced Si3N4 composite for high power electronic devices

New advances in carbon-based fillers (CBFs) as reinforcing agents have gained worldwide attention due to their novel properties and promising applications to obtain advanced composite materials with superior electrical, mechanical and thermal performance. These CBFs (carbon nanotubes (CNTs), carbon nanofibers (CNFs), graphene, graphene oxide, and graphite) are important for ceramic materials to make them more attractive for modern industry. These materials in the ceramic matrix can enhance various properties, such as mechanical, thermal, and electrical conductivity, as a sensor material for pressure and other environmental changes. This overview introduces the latest developments in the fabrication of Si₃N₄ ceramics and the effect of CBFs as well SiC and SiC_w on structural, mechanical, and thermal properties of Si₃N₄ ceramics for next-generation electronic power devices. Moreover, we summarized the key aspects such as the fabrication approaches, influence of additive composition and concentration, and sintering parameters on the microstructure and overall performance of Si₃N₄ ceramics. In particular, design strategies for scientists and engineers concerned about the manufacture of Si₃N₄ substrate and active regeneration for the first time are proposed and discussed extensively.