Microstructure and mechanical properties of hot-pressed WC–MgO composites with Cr3C2 or VC addition

The influence of Cr₃C₂ and VC addition on the microstructure and mechanical properties of WC–MgO composites hot-pressed at 1650 °C for 90 min was comprehensively investigated. The grain growth of WC was significantly retarded and the homogeneity of MgO particulate dispersion was effectively improved with the addition of 0.5 wt.% Cr₃C₂ or 0.5 wt.% VC. The indentation size effect (ISE) on hardness was restrained and the load-independent hardness was increased by doping grain growth inhibitors. Improvements on fracture toughness of hot-pressed samples were also observed due to the refined WC grains and uniformly dispersed MgO particulates. In addition, experimental results demonstrated that Niihara's equation was preferable for estimating the indentation fracture toughness, by comparing the fracture toughness evaluated using the single-edge V-notch beam (SEVNB) method with the values estimated through the Vickers indentation technique.     

Microstructures and properties of Ni based composite coatings prepared by plasma spray welding with mixed powders

The Ni based composite coatings have been obtained by using the plasma spray welding process and mixed powders (NiCrBSi + NiCr-Cr₃C₂ + WC). Their microstructures and properties were studied. The results showed that the coatings consist mainly of γ-Ni, WC, Cr₂₃C₆, Cr₇C₃, Ni₃Si, Cr₅B₃, CrB and FeNi₃ phases, and the Ni₃Si, Cr₅B₃, CrB and FeNi₃ phases mainly segregated between the carbide grains. The carbide contents in the coatings increased with increasing the mass fractions of NiCr-Cr₃C₂ and WC powders in the mixed powders, which results in enhancing the coating hardness. The abrasive wear resistance of the coatings depends on their hardness. The higher the coating hardness, the stronger the wear resistance is. When the mixed powder (15wt%WC + 30 wt% NiCr-Cr₃C₂ + 55wt%NiCrBSi) was used, the composite coating has higher hardness and more excellent wear resistance, and the coating hardness and weight loss after wear tests are 991 HV and 8.6 mg, respectively.     

Influence and effectivity of VC and Cr3C2 grain growth inhibitors on sintering of binderless tungsten carbide

For the production of hard, high temperature and abrasion resistant parts, like water-jet nozzles or pressing tools for forming glass lenses, binderless cemented carbide is used. In this work, the consolidation of tungsten carbide with additions of VC and Cr₃C₂ grain growth inhibitors is studied. Tungsten carbide powder dry or wet milled was consolidated by dry pressing, debindering and gas pressurized sintering and, alternatively, by spark plasma sintering. The effect of adding VC and Cr₃C₂ to binderless tungsten carbide on the grain growth was studied with contents being 0; 0.1; 0.3; 0.5; 0.7 and 1.0 wt.%. Samples with an ultrafine microstructure free of abnormal grain growth, a hardness of 25.5 GPa and a fracture toughness of 7.2 MPa·m^1/2 were archived by conventional sintering. Both carbides reduce grain growth, but with Cr₃C₂ a finer microstructure can be achieved at lower amounts. Compared to the same amount of Cr₃C₂, the addition of VC results in smaller grains but lower hardness and fracture toughness.     

Preparation of Al2O3–ZrO2–SiO2 ceramic composites by high-gravity combustion synthesis

By a furnace-free technique of high-gravity combustion synthesis, Al₂O₃–ZrO₂–SiO₂ ceramic composites were prepared via melt solidification instead of conventional powder sintering. The solidification kinetics and microstructure evolution of the ceramic composites in high-gravity combustion synthesis were discussed. The phase assemblage of the ceramic composites depended on the chemical composition, where both (Al₂O₃ + ZrO₂) and (mullite + ZrO₂) composites were obtained. The ceramic composites consisted of ultrafine eutectics and sometimes also large primary crystals. In the (mullite + ZrO₂) composites, two different morphologies and orientations were observed for the primary mullite crystals, and the volume fraction of mullite increased with increasing SiO₂ content. The ceramic composites exhibited a hardness of 11.2–14.8 GPa, depending on the chemical composition and phase assemblage.     

In situ synthesis,microstructure, mechanical properties and thermal shock resistance of (ZrB2 + SiC)/Zr2[Al(Si)]4C5 composites

Dense (ZrB₂ + SiC)/Zr₂[Al(Si)]₄C₅ composites with adjustable content of (ZrB₂ + SiC) reinforcements (0–30 vol.%) were prepared by in situ hot-pressing. The microstructure, room and high temperature mechanical and thermal physical properties, as well as thermal shock resistance of the composites were investigated and compared with monolithic Zr₂[Al(Si)]₄C₅ ceramic. ZrB₂ and SiC incorporated by in situ reaction significantly improve the mechanical properties of Z₂[Al(Si)]₄C₅ by the synergistic action of many mechanisms including particulate reinforcement, crack deflection, branching, bridging, “self-reinforced” microstructure and grain-refinement. With (ZrB₂ + SiC) content increasing, the flexural strength, toughness and Vickers hardness show a nearly linear increase from 353 to 621 MPa, 3.88 to 7.85 MPa·m^1/2, and 11.7 to 16.7 GPa, respectively. Especially, the 30 vol.% (ZrB₂ + SiC)/Zr₂[Al(Si)]₄C₅ composite retains a high modulus up to 1511 °C (357 GPa, 86% of that at 25 °C) and superior strength (404 MPa) at 1300 °C in air. The composite shows higher thermal conductivity (25–1200 °C) and excellent thermal shock resistance at ΔT up to 550 °C. Superior properties render the composites a promising prospect as ultra-high-temperature ceramics.     

Fine platelet-like grained WC–Co cemented carbides: Preparation,characterization, properties and application in PVD coating substrates

Strengthening of the adhesion strength and its stability of PVD coated cemented carbides has always been the focus of attention. Commercial ultrafine WC–12Co composite powder by spray conversion processing was used as the raw material. WC–12Co–0.05La₂O₃, WC–12Co–0.9Cr₃C₂–0.05La₂O₃, WC–12Co–0.5Cr₃C₂–0.4VC–0.05La₂O₃ and WC–12Co–0.9Cr₃C₂–0.4VC–0.05La₂O₃ alloys were prepared by a conventional long-time ball-milling. The results show that fine platelet-like grained WC–12Co–0.9Cr₃C₂–0.4VC–0.05La₂O₃ alloy is characterized with a homogenous microstructure, the best property combination of high strength, high hardness and high toughness and the highest WC (0001) texture coefficient. By using fine platelet-like grained WC–Co cemented carbides as the substrates, larger than 100 N adhesion strength expressed by critical load L_C2 for AlCrN, AlTiN and (AlCrSiWN + AlCrN) PVD coatings is achieved. The related strengthening mechanisms are discussed.     

Microstructure and mechanical properties of TiB2–SiC ceramic composites by Reactive Hot Pressing

TiB₂–SiC ceramic composites with different contents of Ni as additive were prepared by the Reactive Hot Pressing (RHP) process at 1700 °C under a pressure of 32 MPa for 30 min. For comparison, a monolithic TiB₂ ceramic and TiB₂–SiC ceramic composite were also fabricated under the identical temperature, pressure and holding time by the Hot Pressing (HP) process. The effects of the fabrication process and Ni on the microstructure and mechanical properties of the composites were investigated. About 8 vol.% of elongated TiB₂ grains with an aspect ratio of 3–6 and a diameter of 0.5–1 μm were produced in the composite prepared by the RHP process. The improvement of the fracture toughness was attributed to the toughening and strengthening effects of SiC particles and the elongated TiB₂ grains such as crack deflection. The TiB₂–SiC–5 wt.% Ni ceramic composite had the optimum mechanical properties with a flexural strength of 858 ± 87 MPa, fracture toughness of 8.6 ± 0.54 MPa·m^1/2 and hardness of 20.2 ± 0.94GPa. The good mechanical properties were ascribed to the relatively fine and homogeneous microstructure and the strengthening effect of Ni. Ni inhibited the anisotropic growth of TiB₂.     

Fe–W–C thermodynamics and in situ preparation of tungsten carbide-reinforced iron-based surface composites by solid-phase diffusion

Tungsten carbide (WC)-reinforced Fe-based surface composites were prepared by in situ solid-phase diffusion at 1423 K for 4, 6, and 8 h. The thermodynamics, phase composition, microstructure, microhardness, and wear-resistance of the Fe–W–C ternary system of the samples were examined by X-ray diffraction, scanning electron microscopy, Vickers hardness test, and wear test, respectively. Thermodynamic calculations showed that the thermodynamically favored products of the Fe–W–C system were W₂C, WC, and Fe₃C. W also exhibited a stronger carbide-forming tendency than Fe. The Gibbs free-energies of W₂C and WC, which were stable carbides, significantly decreased with increased temperature. The main phases of the composite were WC, γ-Fe, Fe₃C, graphite, and η-carbide (M₆C) with fishbone-like morphology. The longitudinal section of the composite could be easily divided into three reaction zones, namely, WC layer, “no graphite area,” and M₆C-reinforced area. WC particles in the WC layer were irregularly shaped with 0.3–12 μm particle size, with volume fraction of up to > 80%. The average microhardness value of the dense ceramic layer was 2152 HV_0.1. The maximum relative wear-resistance, which was 230.4 times higher than that of gray cast iron, was obtained at 20 N. The high wear-resistance of the composite was due to the in situ formation of dense and hard WC particulates that acted as a reinforcement phase.     

Chromium carbide–CNT nanocomposites with enhanced mechanical properties

Chromium carbide is widely used as a tribological coating material in high-temperature applications requiring high wear resistance and hardness. Herein, an attempt has been made to further enhance the mechanical and wear properties of chromium carbide coatings by reinforcing carbon nanotubes (CNTs) as a potential replacement of soft binder matrix using plasma spraying. The microstructures of the sprayed CNT-reinforced Cr₃C₂ coatings were characterized using transmission electron microscopy and scanning electron microscopy. The mechanical properties were assessed using micro-Vickers hardness, nanoindentation and wear measurements. CNT reinforcement improved the hardness of the coating by 40% and decreased the wear rate of the coating by almost 45–50%. Cr₃C₂ reinforced with 2 wt.% CNT had an elastic modulus 304.5 ± 29.2 GPa, hardness of 1175 ± 60 VH_0.300 and a coefficient of friction of 0.654. It was concluded that the CNT reinforcement increased the wear resistance by forming intersplat bridges while the improvement in the hardness was attributed to the deformation resistance of CNTs under indentation.     

Effects of Ti addition on microstructure homogenization and wear resistance of wide-band laser clad Ni60/WC composite coatings

Ni60/WC composite coatings were fabricated by wide-band laser cladding. The effects of Ti addition on microstructure homogenization and coating properties were investigated. Coating microstructure, phase constitution, microhardness and wear resistance were studied and grading analysis of in-situ synthesized ceramic particles was carried out. Results indicated that ceramics particles of Cr₅B₃ and M₂₃C₆ (M represents for Cr and W) carbides were in-situ synthesized in original Ni60-20WC coatings. With Ti addition, dissolution of original WC was facilitated and lots of TiC particles were synthesized instead of M₂₃C₆ carbides. Furthermore, the block Cr₅B₃ particles were greatly homogenized due to the net structure formed by dispersive TiC particles. With Ti addition, D50 of particle size decreased from 8.94 μm to 4.45 μm and particle morphologies were transformed from star-like shapes to uniform square blocks. Microhardness distribution became more uniform with average value decreased from 799 ± 89 HV_0.2 to 744 ± 77 HV_0.2. Due to the homogenized ceramic particles, wear resistance of coatings with Ti addition was enhanced to 2.6 times that of the original coatings.     

Effect of Ni content on the compression properties and abrasive wear behavior of the (TiB2–TiCxNy)/Ni composites

The (TiB₂–TiC_xN_y)/Ni composites were fabricated by the method of combustion synthesis and hot press consolidation in a Ni–Ti–B₄C–BN system. The effect of Ni content on the microstructure, hardness, compression properties and abrasive wear behavior of the composites has been investigated. The results indicate that with the increase in Ni content from 30 wt.% to 60 wt.%, the average size of the ceramic particles TiB₂ and TiC_xN_y decreases from 5 μm to ≤ 1 μm, while the hardness and the abrasive wear resistance of the composites decrease. The composite with the Ni content of 30 wt.% Ni possesses the highest hardness (1560.8 Hv) and the best abrasive wear resistance. On another hand, with the increase in the Ni content, the compression strength increases firstly, and then decreases. The composite with 50 wt.% Ni possesses the highest compression strength (3.3 GPa). The hardness and fracture strain of the composite with 50 wt.% Ni are 1251.2 Hv and 3.9%, respectively.     

Effects of Cr3C2 addition on the corrosion behavior of Ti(C,N)-based cermets

The Ti(C, N)-based cermets with different Cr₃C₂ addition were prepared and the effects of Cr₃C₂ addition on the microstructure and properties of cermets were discussed. The corrosion behavior of the cermets with different Cr₃C₂ addition was investigated emphatically in 2 mol/L HNO₃ solution. The results indicate that there is no obvious effect of Cr₃C₂ addition on the densification of the cermets, and all cermets are almost fully densified during sintering. The thickness of rim phase is reduced and the core size is increased remarkably in the cermets with 1 wt.% and 3 wt.% Cr₃C₂ addition; the grains are refined significantly in the cermets with the increase of Cr₃C₂ addition to 5 wt.%. The hardness and transverse rapture strength of the cermets are improved with Cr₃C₂ added properly. In HNO₃ solution, the corrosion resistance of cermets is improved remarkably by Cr₃C₂ addition. The corrosion of binder phase is predominant in the cermets in which the Ni binder phase without Cr has lower corrosion resistance than the rim phase; whereas the corrosion resistance of binder phase with high Cr content is better compared to the rim phase, so that the degradation of rim phase is predominant and a reticulate binder phase forms. With the increase of Cr₃C₂ addition, the Mo content in rim increases, and it is bad for the corrosion resistance of rim phase. Additionally, the inner rim phase has lower corrosion resistance than the outer rim phase owing to the higher Mo content.     

Investigation on the preparation and machinability of the B4C/BN nanocomposites by hot-pressing process

The machinable B₄C/BN nanocomposites were fabricated by the hot-pressing process using the B₄C/BN nanocomposite powders at 1850 °C for 1 h under the pressure of 30 MPa. The nanocomposite powders with the microstructure of micro-sized B₄C particles coated with amorphous nano-sized BN particles were prepared by the chemical reaction of H₃BO₃ and CO(NH₂)₂ on the surface of B₄C particles at high temperature. Then the amorphous BN transformed into the hexagonal-BN (h-BN) after the hot-pressing process at 1850 °C. The microstructure investigations of the B₄C/BN nanocomposites sintered samples showed that the nano-sized h-BN particles were homogenously distributed within the matrix grains as well as at the matrix grains boundaries. With the increasing content of h-BN, the relative density of the B₄C/BN nanocomposites decreased gradually. The fracture strength and fracture toughness of the B₄C/BN nanocomposites decreased gradually, the fracture strength and fracture toughness of the B₄C/BN nanocomposites with the h-BN content of 10 wt.% and 20 wt.% achieved high values. The Vickers hardness of the B₄C/BN nanocomposites decreased remarkably with the increasing content of h-BN, while the drilling rates and machinability of the B₄C/BN nanocomposites increased significantly. The B₄C/BN nanocomposites with the h-BN content more than 20 wt.% exhibited excellent machinability.     

Mullite/molybdenum ceramic–metal composites

Dense (>98 th%) homogeneous mullite/Mo (32 vol.%) composites with two different Mo average grain sizes (1.4 and 3 μm) have been obtained at 1650°C in vacuum and in reducing condition. Depending on the Mo grain size and processing atmosphere, the K_IC ranges from 4 to 7 MPa m^1/2 and σ_f from 370 to 530 MPa. The MoO₂–2SiO₂·3Al₂O₃–Mo system was found to be compatible in solid state, and a solid solution of ≈4 wt% of MoO₂ in mullite at 1650°C was detected. A solid state dewetting of MoO₂ from the surface of the Mo particle takes place during sintering. It was found that the absence of MoO₂ in the mullite/Mo composites by processing in reducing conditions increases the strength of the metal/ceramic interface and the plasticity of the Mo metal particles, thus strengthening the composite by a crack bridging mechanism. As a result, the K_IC and the σ_f values of the ceramic–metal composite were found to be ≈4 times and ≈2 times higher than the ones corresponding to the mullite matrix.     

ZrB2-ZrSi2-SiC composites prepared by reactive spark plasma sintering

ZrSi₂ and SiC are good candidates to improve both sinterability and mechanical properties of ZrB₂ ceramics, which were synthesized simultaneously by an in-situ reaction of ZrC and Si additives during the sintering processing in this work. The ZrB₂ ceramic composites with different amount of ZrSi₂ and SiC were fabricated by reactive spark plasma sintering (RSPS) method. X-ray diffraction, scanning microscopy and Archimedes's method are used to characterize the phase, microstructure and density of the composites. Meanwhile, fracture toughness and flexural strength of the obtained composites were investigated too. It's found that a fully dense composite can be achieved at 1500 °C by SPS. Both fracture toughness and flexural strength of ZrB₂ ceramics increased with increasing the concentration of ZrSi₂ and SiC additives and reached a maximum of 7.33 ± 0.24 MPa·m^1/2 and 471 ± 15 MPa, respectively, with the ZrSi₂ + SiC content of 30 wt%.     

Microstructure and tribological performance of NbC-Ni cermets modified by VC and Mo2C

The current study reports on the influence of the addition of 5–15 vol% VC or/and Mo₂C carbide on the microstructure and mechanical properties of nickel bonded NbC cermets, which are compared to cobalt bonded NbC cermets. The NbC, Ni and secondary carbides powder mixtures were liquid phase sintered for 1 h at 1420 °C in vacuum. The fully densified cermets are composed of a cubic NbC grains matrix and an evenly distributed fcc Ni binder. NbC grain growth was significantly inhibited and a homogeneous NbC grain size distribution was obtained in the cermets with VC/Mo₂C additions. The mechanical properties of the NbC-Ni matrix cermets are strongly dependent on the carbide and Ni binder content and are directly compared to their NbC-Co equivalents. The liquid phase sintered NbC-12 vol% Ni cermet had a modest Vickers hardness (HV₃₀) of 1077 ± 22 kg/mm² and an indentation toughness of 9.1 ± 0.5 MPa·m^1/2. With the addition of 10–15 vol% VC, the hardness increased to 1359 ± 15 kg/mm², whereas the toughness increased to 11.3 ± 0.1 MPa·m^1/2. Addition of 5 and 10 vol% Mo₂C into a NbC-12 vol% Ni mixtures generated the same values in HV₃₀ and K_IC when compared to VC additions. A maximum flexural strength of 1899 ± 77 MPa was obtained in the cermet with 20 vol% Ni binder and 4 vol% VC + 4 vol% Mo₂C addition, exhibiting a high fracture toughness of 15.0 ± 0.5 MPa·m^1/2, but associated with a loss in hardness due to the high Ni content. The dry sliding wear behaviour was established at room temperature and 400 °C from 0.1 to 10 m/s.     

Mechanical and thermal properties of hot pressed ZrB2 system with TiB2

ZrB₂-TiB₂-based ceramics with varying amount of TiB₂ (up to 30 wt%) were hot pressed at 2200 °C in Ar atmosphere, and the effect of the TiB₂ addition on mechanical properties like hardness, fracture toughness, scratch resistance, wear resistance and thermal conductivity of the system was compared to monolithic ZrB₂ ceramic. It was found from X-ray diffraction that TiB₂ completely entered into the structure and formed solid solution with ZrB₂. Addition of TiB₂ in ZrB₂ system improves the mechanical and wear resistance properties. ZrB₂-TiB₂ (30 wt%) ceramic, for example, showed highest hardness of 22.34 GPa, fracture toughness 3.01 MPa(m)^1/2 and lowest coefficient of friction (0.398 at 10 N load). The addition of TiB₂ in ZrB₂ system showed lower thermal conductivity than monolithic ZrB₂ by increasing grain boundary thermal resistance.     

Mechanical properties and microstructure of TiB2–TiC composite ceramic cutting tool material

TiB₂–TiC composite ceramic cutting tool material was prepared by sintering during hot-pressing in vacuum. The effects of nano-scale Ni and Mo additives and sintering heating rate on mechanical properties and grain characteristics were investigated. TiB₂ and TiC grains exhibited prismatic and equiaxed shapes respectively. The diameter and aspect ratio of prismatic TiB₂ grains were influenced by nano-scale Ni/Mo additives. A higher heating rate could cause a higher aspect ratio of prismatic TiB₂ grains. The good mechanical properties of TN1((TiB₂–TiC)/Ni composite ceramic sintered at a heating rate of 50 °C/min) were ascribed to a relatively fine and homogenous microstructure. And a brittle B₄MoTi solid solution phase and wider distribution of grain size induced the lower flexural strength of TNM2((TiB₂–TiC)/(Ni,Mo) composite ceramic sintered at heating rate of 100 °C/min), but the higher aspect ratio of TiB₂ grains could prevent cracks from propagating and ameliorated the fracture toughness. The optimum resultant mechanical properties were obtained by (TiB₂–TiC)/Ni composite ceramic sintered at a heating rate of 50 °C/min.     

Diffusion and solubility of Cr in WC

Although no detailed study on the Cr solubility in WC exists the compilation on the various C–Cr–W phase diagrams [1] suggests this behaviour. In order to prove this and to estimate the diffusivity of Cr in WC we prepared diffusion couples of the type Cr₃C₂–WC by joining and annealing polished fully dense counterparts of the two carbides (temperature range 1550–1750 °C). After thermal treatment the diffusion couples were cut, polished and investigated by metallography. For the measurement of the diffusion profiles the couples were subjected to WDS-EPMA (Cameca SX 100 microprobe). W, Cr, and C concentration profiles were obtained from line scans performed perpendicular to the interface. The analysis of diffusion couples of WC contacted to other carbides used for doping of hardmetals (VC, TaC, NbC, and TiC) did not yield perceptible solubility of the respective metals in WC with respect to the detection limit of EPMA.From the Cr diffusion profiles a diffusion coefficient of Cr in WC of approximately D = 1.70–2.20 × 10^?11cm²/s and an activation energy of E_A = 0.75 eV was estimated. In addition the composition of the ternary phase (W,Cr)₂C in equilibrium with WC and Cr₃C₂ could be measured. For example, in couples annealed at 1750 °C the composition reaches from (W_0.5Cr_0.5)₂C (in equilibrium with WC) to (W_0.2Cr_0.8)₂C (in equilibrium with Cr₃C₂).With the results obtained from the analysis of diffusion couples, the Cr uptake of WC powder as a function of grain size, time and temperature was calculated. Cr saturation in idealised spherical particles of 1 μm occurs only within a few minutes.     

Effects of ZrC and SiC addition on the microstructures and mechanical properties of binderless WC

ZrC-added WC ceramics and SiC-added WC–2 mol% ZrC ceramics were sintered at 1800 °C using a resistance-heated hot-pressing machine. Dense WC ceramics containing 0–1 mol% ZrC and WC–2 mol% ZrC ceramics containing 1–6 mol% SiC were obtained. The reaction products W₂C, ZrO₂ and ZrC-based solid solutions were formed in the ZrC-added WC ceramics during sintering. The relative amount of W₂C reached zero at 2 mol% ZrC, increased in the range of 2–6 mol% ZrC, and decreased again above 6 mol% ZrC. The average WC grain size decreased from 0.49 μm for the WC ceramic to 0.24 μm at 4 mol% ZrC. The SiC addition of 1–2 mol% to the WC–2 mol% ZrC ceramics caused abnormal growth of WC grains. The Vickers hardness of the ZrC-added WC ceramics decreased to 17 GPa at 2 mol% ZrC. The hardness of the SiC-added WC–2 mol% ZrC ceramics increased from 12.4 at 2 mol% SiC to 21.5 GPa at 6 mol% SiC. The fracture toughness of the ZrC-added WC ceramics decreased from 6.2 MPa m^0.5 for the WC ceramic to 5.2 MPa m^0.5 at 4 mol% added ZrC. The fracture toughness of the WC–2 mol% ZrC ceramics with 6 mol% SiC were relatively high at 6.7 MPa m^0.5. The addition of SiC to WC-based ceramics thus improved both hardness and fracture toughness.