Microstructure and mechanical properties of boron carbide/graphene nanoplatelets composites fabricated by hot pressing

In this study, boron carbide (B₄C)-graphene nanoplatelets (GNPs) composites, with enhanced strength and toughness, were fabricated by hot pressing at 1950 °C under a pressure of 30 MPa for 1 h. Microstructure analysis revealed that the GNPs are homogenously dispersed within the B₄C matrix. Raman spectroscopy and electron microscopy showed the orientation of the GNPs in the composites. The effects of the amount of GNPs on the microstructure and mechanical properties of the composites were also investigated. The optimal mechanical properties were achieved using 1 wt% GNPs. The relative density, Vickers hardness, flexure strength, and fracture toughness of the B₄C-GNPs composite ceramic were found to be 99.12%, 32.8 GPa, 508 MPa, and 4.66 MPa m^1/2, respectively. The main toughening mechanisms included crack deflection in three dimensions, GNPs pull-out, and crack bridging. The curled and semi-wrapped GNPs encapsulated individual B₄C grains to resist GNPs pull-out and to deflect propagating cracks.     

Microstructures and mechanical properties of B4C-TiB2-SiC composites fabricated by ball milling and hot pressing

B₄C-TiB₂-SiC composites were fabricated via hot pressing using ball milled B₄C, TiB₂, and SiC powder mixtures as the starting materials. The impact of ball milling on the densification behaviors, mechanical properties, and microstructures of the ceramic composites were investigated. The results showed that the refinement of the powder mixtures and the removal of the oxide impurities played an important role in the improvement of densification and properties. Moreover, the formation of the liquid phases during the sintering was deemed beneficial for densification. The typical values of relative density, hardness, bending strength, and fracture toughness of the composites reached 99.20%, 32.84?GPa, 858?MPa and 8.21?MPa?m^1/2, respectively. Crack deflection, crack bridging, crack branching, and microcracking were considered to be the potential toughening mechanisms in the composites. Furthermore, numerous nano-sized intergranular/intragranular phases and twin structures were observed in the B₄C-TiB₂-SiC composite.     

Microstructure and properties of HfC and TaC-based ceramics obtained by ultrafine powder

HfC and TaC-based ceramics were hot pressed at 1900 °C for 5-20 min starting from synthesized ultrafine powders. The addition of 5 vol.% of MoSi₂ improved the densification, which increased from around 85-90% for the pure matrices to 95% for the composites. The flexural strength was measured at room temperature and at 1500 °C under protective atmosphere. The added value of this work consists in the utilization of cheap synthesized powders for the realization of the composites with properties comparable to those obtained using more expensive commercial powders. The effect of the nanometric size of the starting powder showed to have the potential to improve the densification behavior and the mechanical properties, however it is necessary a further optimization of the synthesis condition in order to avoid the formation of agglomerates of unreacted powder.     

Fabrication and mechanical behavior of ZrB2 strengthened SiCf/SiC composites prepared by hybrid processing route

A SiC fiber-reinforced composite containing a SiC-ZrB₂ mixed matrix (SiC_f/(SiC-ZrB₂)) with high density and enhanced mechanical properties was fabricated. ZrB₂ at 5 or 40?vol% was added to a (SiC + C) slurry to be infiltrated into the voids of 2D woven Tyranno?-SA grade-3 fabrics by electrophoretic deposition. Subsequent hot pressing at 1300?°C and 10?MPa for 1?h, followed by liquid silicon infiltration (LSI) at 1600?°C for 5?h in an Ar atmosphere resulted in the formation of the reaction-bonded SiC matrix, which revealed a composite density close to 97%. SiC_f/(SiC-ZrB₂) having open porosities of 0.2–0.6% showed peak strengths of 398 and 320?MPa for 5 and 40?vol% ZrB₂ addition, respectively. The large mismatch in the coefficient of thermal expansion and Young's modulus between the SiC and ZrB₂ phases was attributed to a reverse trend in the strength of composites. Brittle behavior of the composites in flexure can be explained by the strong bonding between the matrix and fibers formed by the reaction of interphase with molten Si during LSI. Strength retention after oxidation at 1000 and 1400?°C for 2?h was also compared in terms of ZrB₂ amount contained in the composites.     

Characterization of B4C-SiC ceramic composites prepared by ultra-high pressure sintering

Additive-free boron carbide (B₄C) – silicon carbide (SiC) ceramic composites with different B₄C and β-SiC powders ratio were densified using the high-pressure “anvil-type with hollows” apparatus at 1500 °C under a pressure of 4 GPa for 60 s in air. The effect of starting powders ratio on the composites sintering behavior, relative density, microstructural development, and thermomechanical properties was studied. The sintered samples hardness was found to be in the range from 24 to 31 GPa. The thermal conductivity measurements, conducted in the temperature range from room temperature to 1000 °C, showed that the thermal diffusivity of sintered samples was between 6 and 9.5 mm²/s whereas the thermal conductivity was in the range from 16 to 28 W/(m K). The results of this study show that the high-pressure sintering can be a very effective low-temperature densification method for the obtainment of additive-free B₄C - β-SiC ceramic composites.     

Synergistic effects of TiB2 and graphene nanoplatelets on the mechanical and electrical properties of B4C ceramic

Monolithic B₄C, B₄C–TiB₂, and B₄C–TiB₂–graphene nanoplatelets (GNPs) were fabricated by hot pressing (HP) at 1900 °C for 1 h under an axial pressure of 30 MPa. The microstructures and mechanical and electrical properties of the B₄C composites were investigated. The results show that the GNPs are distributed homogeneously in B₄C-based ceramic composites. Compared with monolithic B₄C, the TiB₂–GNPs-containing B₄C composite exhibits an approximately 68 % increase in flexural strength and a 169 % increase in fracture toughness due to the synergistic effects of TiB₂ particles and GNPs. The toughening mechanisms mainly include TiB₂ crack deflection, crack branching, transgranular fracture and GNPs crack deflection, crack bridging, and GNPs pull-out. Additionally, the electrical conductivity of the B₄C composite reinforced with dual fillers is three orders of magnitude higher than that of monolithic B₄C due to the establishment of a conductive network. The addition of GNPs can efficiently connect the isolated conductive TiB₂ particles in the B₄C matrix and provides an additional channel for electron migration.     

Microstructure and properties of diamond/SiC composites prepared by tape-casting and chemical vapor infiltration process

This article reported a novel method for preparing diamond/SiC composites by tape-casting and chemical vapor infiltration (CVI) process, and the advantages of this method were discussed. The diamond particle was proved to be thermally stable under CVI conditions and the CVI diamond/SiC composites only contained diamond and CVI-SiC phases. The SEM and TEM results showed a strong interfacial bonding existed between diamond and CVI-SiC matrix. Due to the strong bonding, the surface HRA hardness could reach up to 98.4 (HV 50 ± 5 GPa) and the thermal conductivity (TC) of composites was five times higher than that of pure CVI-SiC matrix. Additionally, the effects of diamond particle size on microstructure and properties of composites were also investigated. With the increasing of particle size, the density and TC of composites with the size 27 μm reached 2.940 g/cm³ and 82 W/(m K), respectively.     

Preparation and mechanical properties of SiCw-Al2O3-YAG ceramic composite by hot oscillatory pressing

SiC_w-Al₂O₃-YAG ceramic composites were prepared by hot oscillatory pressing (HOP) and traditional hot pressing (HP). The results showed that compared with static pressure, the oscillatory pressure could effectively promote densi?cation and mechanical properties of the composites. The sample prepared by HOP exhibited higher hardness (15.72 ± 0.20 GPa) and fracture toughness (7.13 ± 0.19 MPa m^1/2). The current work suggests that HOP could be an effective technique for the preparation of whisker reinforced ceramic composites.     

Effects of Ta2O5 on mechanical properties and elements diffusion of Ti/Al2O3 composites prepared via hot pressing sintering

Homogeneous Ti/Al₂O₃ composites with different volume percentages of Ta₂O₅ addition were prepared at different temperatures via hot pressing sintering. Laminated Ti/Al₂O₃ composites with different volume percentages of Ta₂O₅ added were prepared. The effects of Ta₂O₅ on the composition, microstructure, mechanical properties and elements diffusion of the composites were characterized and investigated. Ta₂O₅ inhibited the production of TiAl and Ti₃Al by forming solid solution with Ti or new reaction product of Al. This solid solution melted and filled the void of Al₂O₃ phase to increase the density of Ti/Al₂O₃ composites at high temperature. Mechanical properties had also been improved by this phenomenon. Because Al element couldn’t diffuse in Ta or react with it, Al couldn’t diffuse through the Ta-enriched area at the interface of Ti and Al₂O₃.     

Microstructure and mechanical properties of hot-pressed SiC nanofiber reinforced SiC composites

This study reports on the preparation and mechanical properties of a novel SiC_nf/SiC composite. The single crystal SiC nanofiber(SiC_nf) reinforced SiC ceramic matrix composites (CMC) were successfully fabricated by hot pressing the mixture of β-SiC powders, SiC_nf and Al–B–C powder. The effects of SiC_nf mass fraction as well as the hot-pressing temperature on the microstructure and mechanical properties of SiC_nf/SiC CMC were systematically investigated. The results demonstrated that the 15 wt% SiC_nf/SiC CMC obtained by hot pressing (HP) at 1850 °C with 30 MPa for 60 min possessed the maximum flexural strength and fracture toughness of 678.2 MPa and 8.33 MPa m^1/2, respectively. The nanofibers pull out, nanofibers bridging and cracks deflection were found by scanning electron microscopy, which are believed can strengthen and toughen the SiC_nf/SiC CMC via consuming plenty of the fracture energy. Besides, although the relative density of the prepared SiC_nf/SiC CMC further increased with the sintering temperature rose to 1900 °C, the further coarsend composites grains results in the deterioration of the mechanical properties for the obtained composites compared to 1850 °C.     

The microstructure and mechanical properties of Ni/Al2O3 composites by in-situ generated CaAl12O19 and ZrO2 via hot pressing sintering

Ni/Al₂O₃ composites with a varying mass fraction of CaZrO₃ (0–12 wt%) were prepared by vacuum hot pressing sintering at 1650 °C under a pressure of 30 MPa for 30 min to investigate how CaZrO₃ affect the mechanical properties and morphology of the composites. The results show that CaZrO₃ can react with Al₂O₃ and form new strengthening and reinforcing phases of CaAl₁₂O₁₉ and ZrO₂, which can promote complete densification and solve the problem of uneven distribution due to the poor wettability between Al₂O₃ and Ni. Additionally, composites showed satisfactory mechanical properties when 6.0–9.0 wt% CaZrO3 was added and the major toughening mechanism involved the typical fracture of delamination and the transgranular mode.     

Microstructure and mechanical properties of reaction bonded B4C-SiC composites: The effect of polycarbosilane addition

Reaction bonded B₄C-SiC composites were prepared by infiltrating silicon melt into porous B₄C-SiC green preforms at 1500 °C in vacuum. The porous green preform was obtained from a mixture of polycarbosilane (PCS) and particle size graded B₄C after pre-sintering at 1600 °C. For the first time, PCS was used to adjust the phase composition and microstructure of the reaction bonded boron carbide composites. It is indicated that the addition of PCS and its content has a significant influence on the microstructure as well as the mechanical properties of the subsequent reaction bonded B₄C-SiC composites. For the B₄C-SiC composite with 5 wt% PCS added, a flexural strength of 319±12 MPa, and an elastic modulus of 402±18 GPa can be achieved, which is 23% and 15% higher than those of the composite without PCS addition, respectively. While, with the higher content of PCS addition, the mechanical properties of the composites are decreased drastically due to the large amount of residual Si agglomeration in the composites. The reaction mechanisms as well as their microstructure evolution processes correlated with the mechanical properties of the reaction bonded B₄C-SiC composites are further discussed in our work.     

Microstructure and mechanical properties of B4C matrix composites prepared via hot-pressing sintering with Pr6O11 as additive

High-performance B₄C-PrB₆ composites were prepared via hot-pressing sintering with matrix phase B₄C and with 2–5 wt% Pr₆O₁₁ as additive. The effects of different sintering processes and Pr₆O₁₁ content on the microstructure and mechanical properties of the composites were studied in detail. It is found that increasing sintering temperature and pressure will contribute to the densification of B₄C-PrB₆ composites. Coarse grains are formed in B₄C without additives at high temperature conditions, resulting in the decrease of the densification. Pr₆O₁₁ can effectively hinder the formation of coarse grains and finally promote the densification of the composites. The main toughening mechanisms of composites was crack deflection. The composites with 4 wt% Pr₆O₁₁ prepared at 2050 °C and 25 MPa had the best comprehensive mechanical properties. The relative density, hardness, flexural strength and fracture toughness reached to 98.9%, 37.6 GPa, 339 MPa and 4.4 MP am^1/2, respectively.     

Effect of Ge on microstructure and mechanical properties of Ti3SiC2/Al2O3 composites

Owing to the good physicochemical compatibility and complementary mechanical properties of Ti₃SiC₂ and Al₂O₃, Ti₃SiC₂/Al₂O₃ composites are considered as ideal structural materials. However, TiC and TiSi₂ typically coexist during the synthesis of Ti₃SiC₂/Al₂O₃ composites through an in-situ reaction, which adversely affects the mechanical properties of the resulting composites. In this study, Ti₃SiC₂/Al₂O₃ composites were prepared via in-situ hot pressing sintering at 1450 °C. Ge, which was used as a sintering aid, improved the purity and mechanical properties of the Ti₃SiC₂/Al₂O₃ composites. This is because Ge replaced some of the Si atoms to compensate the evaporation loss of Si to form Ti₃(Si_1-xGe_x)C₂, which showed a crystal structure similar to that of Ti₃SiC₂. Furthermore, the molten Ge accelerated the diffusion reaction of the raw materials, increasing the overall density of the Ti₃SiC₂/Al₂O₃ composites. The optimum Ge amount for improving the mechanical properties of the composites was found to be 0.3 mol. The flexural strength, fracture toughness, and microhardness of the composite with the optimum Ge amount were 640.2 MPa, 6.57 MPa m^1/2, and 16.21 GPa, respectively. The formation of Ti₃(Si_1-xGe_x)C₂ was confirmed by carrying out X-ray diffraction, energy dispersive spectroscopy, and transmission electron microscopy analyses. A model crystal structure of Ti₃(Si_1-xGe_x)C₂ doped with 0.3 mol Ge was established by calculating the solid solubility of Ge.     

Microstructure, magnetic and mechanical properties of Ni-Zn ferrites prepared by powder injection moulding

Nowadays, the electronic industry demands small and complex parts as a consequence of the miniaturization of electronic devices. Powder injection moulding (PIM) is an emerging technique for the manufacturing of magnetic ceramics. In this paper, we analyze the sintering process, between 900 °C and 1300 °C, of Ni-Zn ferrites prepared by PIM. In particular, the densification behaviour, microstructure and mechanical properties of samples with toroidal and bar geometry were analyzed at different temperatures. Additionally, the magnetic behaviour (complex permeability and magnetic losses factor) of these compacts was compared with that of samples prepared by conventional powder compaction. Finally, the mechanical behaviour (elastic modulus, flexure strength and fracture toughness) was analyzed as a function of the powder loading of feedstock. The final microstructure of prepared samples was correlated with the macroscopic behaviour. A good agreement was established between the densities and population of defects found in the materials depending on the sintering conditions. In general, the final mechanical and magnetic properties of PIM samples were enhanced relative those obtained by uniaxial compaction.     

Microstructure and properties of WB/Al nuclear shielding composites prepared by spark plasma sintering

In this paper, a novel nuclear shielding material capable of shielding neutrons and gamma rays, WB-reinforced Al (WB/Al) composites, was prepared by spark plasma sintering (SPS) process. The microstructure of the composites was characterized, and the effects of WB content, heat treatment and matrix type on the properties of the composites were discussed. The results demonstrate that the WB particles are uniformly dispersed in the aluminum matrix and formed a good binding interface with the matrix. WAl₁₂ as an interfacial reaction product is identified, and segregation of Si and Mg elements at the reinforcement/matrix interface occurs. The mechanical properties of the WB/Al composites are sensitive to the WB content. The hardness, elastic modulus and bending strength of the composites increase monotonously as the WB volume fraction increasing, up to 234%, 107% and 91.6% higher respectively than those of the monolithic 6061Al. However, the tensile strength reaches a peak point when the volume fraction is 20%. The effects of T6 treatment and matrix type are not pronounced, especially for the composites with high WB content. The thermal neutron and gamma ray shielding properties of the composites both increase with the increase of material thickness and WB content. The WB/Al composites developed in this work show good application prospects in the field of nuclear radiation protection, due to their good mechanical properties and well neutron and gamma-ray shielding performance.     

Microstructure and mechanical properties of Nb4AlC3 MAX phase synthesized by reactive hot pressing

The present study aims at synthesizing the Nb₄AlC₃ MAX phase by reactive hot pressing using Nb:Al:NbC as starting materials. In order to identify the reaction path, interrupted tests at intermediate temperatures were performed as well as differential thermal analyses (DTA) of powders. Coupling between DTA and XRD data and SEM/EDS analyses of the samples allows a better understanding of the reaction mechanisms. Pure and fully dense Nb₄AlC₃ samples were obtained and characterized for the first time by EBSD and SEM to assess, using an original method, grain size and microstructure. For instance, in the present study, an average grain length of 5–7?µm was obtained.Standard mechanical characterizations showed interesting properties: K_Ic≈?6?MPa?m^1/2, E?≈?350?GPa and α?≈?7.10^?6 °C^?1. Oxidation performance of Nb₄AlC₃ was evaluated at 1100?°C under cyclic conditions. A breakaway regime was instantaneously established for this condition, thus demonstrating the impossibility of using such an unprotected material for structural applications at high temperature in air environment.     

Fe doping and magnetic properties of zincblende SiC ceramics

Fe-doped SiC bulk ceramics were fabricated by hot-pressing, and their magnetic and electronic properties were investigated. Si_1−xFe_xC (x ≤ 0.04) samples having a zincblende crystal structure exhibited ferromagnetic hysteresis at room temperature with the saturation magnetization increasing with x. X-ray diffraction measurements revealed the creation of a Fe₃Si phase in the samples with its density increasing with x. The samples were found to be p-type semiconductors with a hole concentration (electrical resistivity) of ∼10¹⁹ cm⁻³ (∼10⁰ Ω cm) at room temperature. The observed magnetic properties of the samples are mainly ascribed to the presence of ferromagnetic Fe₃Si crystallites. The high carrier concentration of the samples likely implies the existence of acceptors due to individual Fe³⁺ occupation of the Si sites in the lattice. The randomly distributed Fe³⁺ ions represent a minor contribution to the magnetization of the samples through the formation of magnetic polarons with the carriers.     

Mechanical and tribological properties of alumina-MWCNTs composites sintered by rapid hot-pressing

Alumina – MWCNTs composites were prepared using a novel approach. This process comprises functionalization of MWCNTs and stabilization of alumina-MWCNTs dispersion with subsequent freezing, which resulted in formation of granulated powders with homogeneous distribution of MWCNTs. The granulated powders were sintered by rapid hot pressing (RHP) at 1550 °C. Relative densities, microstructural analysis, tribological properties, fracture toughness and bending strength of prepared composites were investigated to reveal the effect of MWCNTs. Compared to pure alumina, bending strength and fracture toughness of dense alumina-5 vol.% MWCNTs composites decreased about 37% and 18%, respectively. At higher MWCNT contents, strength remained almost constant and fracture toughness slightly increased. Thus, the positive effect of CNTs on fracture toughness was demonstrated despite their counteracting effect on the refinement of the microstructure.     

Microstructure and mechanical properties of Si3N4f/Si3N4 composites with different coatings

The Si₃N₄ coating and Si₃N₄ coating with Si₃N₄ whiskers as reinforcement (Si₃N_4w-Si₃N₄) were prepared by chemical vapor deposition (CVD) on two-dimensional silicon nitride fiber reinforced silicon nitride ceramic matrix composites (2D Si₃N_4f/Si₃N₄ composites). The effects of process parameters of as-prepared coating including the preparation temperature and volume fraction of Si₃N_4w on the microstructure and mechanical properties of the composites were investigated. Compared with Si₃N₄ coating, Si₃N_4w-Si₃N₄ coating shows more significant effect on the strength and toughness of the composites, and both strengthening and toughening mechanism were analyzed.