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.     

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.     

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.     

Fabrication of Ti3SiC2 and Ti4SiC3 MAX phase ceramics through reduction of TiO2 with SiC

Ti₃SiC₂ and Ti₄SiC₃ MAX phase ceramics were fabricated through high-temperature vacuum reduction of TiO₂ using SiC as a reductant, followed by hot pressing of the products under 25 MPa of pressure at 1600 °C. It was found that both Ti₃SiC₂ and Ti₄SiC₃ may be obtained in good yields, depending on the annealing time during the reduction step. In addition to MAX phases, the products contained some amounts of TiC. The hot pressing step did not significantly affect the composition of the products, indicating good stability of Ti₃SiC₂ and Ti₄SiC₃ under these conditions. Analysis of the densification behavior of the samples revealed lower ductility in Ti₄SiC₃ compared to Ti₃SiC₂. The samples prepared herein exhibited the flexural strength, fracture toughness and microhardness typical of coarse-grained MAX-phase ceramics.     

Fabrication of TiC coated short carbon fiber reinforced Ti3SiC2 composites: Process,microstructure and mechanical properties

The C_f/Ti₃SiC₂ composites were fabricated through spark plasma sintering (SPS) and hot isostatic pressing (HIP), TiC coated C_f and Ti₃SiC₂ powder were used as starting materials. The improved fracture toughness (K_IC) and Vickers hardness (HV₁) of the TiC coated C_f/Ti₃SiC₂ composite fabricated by SPS were 7.59 MPa·m^1/2 and 7.28 GPa. On this foundation, taking the advantage of better sintering process of HIP, the highest K_IC and HV₁ achieved 8.32 MPa·m^1/2 and 9.24 GPa with fiber content of 10 vol%, which increased by 40% and 65% compared with that of monolithic Ti₃SiC₂. The reasonable control of reactive interface is the main factor for the improved mechanical properties of the composites, the TiC coating effectively protected the fiber structure from interfacial reaction compared with that of the non-coated C_f/Ti₃SiC₂. Meanwhile, the artificially designed and weakly bonded TiC coated C_f can fully exert the toughening mechanisms like fiber pull-out and debonding.     

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.     

Highly transparent LiAlON ceramic prepared by reaction sintering and post hot isostatic pressing

A highly transparent polycrystalline LiAlON ceramic with the size of Φ57?mm?×?6?mm was successfully fabricated by reaction sintering (1750?°C, 20?h) and post hot isostatic pressing (HIP, 1850?°C, 3?h, 180?MPa) using AlN, Al₂O₃ and LiAl₅O₈ powders. Related mechanism on the reaction sintering and densification were studied via the analysis of phase and microstructural evolution. High transparency was resulted from full elimination of Al₂O₃ secondary phase and residual pores. It has excellent optical transparency from the visible to middle infrared (IR) bands with the maximum transmittance of ～ 85.5%. The flexural strength and Vikers hardness reach ～303?MPa and ～15.0?GPa, respectively.     

Effect of Al2O3 particle size on the microstructure,phase transformation and mechanical properties of hot pressed Al2O3-CA6-ZrO2/Ni multi-phase composites

Al₂O₃-CA6-ZrO₂/Ni multi-phase composites were fabricated by vacuum hot pressing sintering at 1650 °C under the pressure of 30 MPa for 30 min. The microstructural evolution rule of the composites was investigated as a function of Al₂O₃ particle size. Upon increasing the Al₂O₃ particle size to 30 μm, the generated CA6 underwent a transformation from unfixed type to a plate-like pattern and to a combined CA6-Al₂O₃ matrix, whereas the fracture mode of m-ZrO₂ changed from an intergranular fracture to an intergranular and transgranular mixed type due to the improved interface binding energy. Additionally, satisfactory mechanical properties of the composites were achieved when the Al₂O₃ particle size was 30 μm. Under the synergistic effect of different strengthening and reinforcing phases, the inhomogeneous distribution caused by poor wettability between Al₂O₃ and Ni was effectively solved by the distributions of “intercrystalline type” and “intracrystalline type” for the Ni phase. The mechanisms of the microstructural evolution, phase transformation and improved mechanical properties are discussed in detail.     

Characteristics of SiCf/SiC hybrid composites fabricated by hot pressing and spark plasma sintering

Abstract

Abstract

SiC fibre reinforced SiC–matrix ceramic composites were fabricated by electrophoretic deposition (EPD) combined with ultrasonication. Fine β-SiC powder and Tyranno-SA fabrics were used as the matrix and fibre for reinforcement, respectively. Different amounts of fine Al₂O₃–Y₂O₃ were added for liquid phase assisted sintering. For EPD, highly dispersed slurry was prepared by adjusting the zeta potentials of the constituent particles to ?+40 mV for homogeneous deposition. The composite properties were compared after using two different consolidation methods: hot pressing for 2 h at 20 MPa and spark plasma sintering (SPS) for 3 min at 45 MPa at 1750°C to minimise the damage to the SiC fibre. The maximum flexural strength and density for the 45 vol.-% fibre content composites were 482 MPa and 98% after hot pressing, respectively, whereas those for SPS were 561 MPa and 99·5%, indicating the effectiveness of SPS.     

Oxidation and hot corrosion behaviors of MAX-phase Ti3SiC2, Ti2AlC,Cr2AlC

Oxidation and hot corrosion behaviours of Ti₃SiC₂, Ti₂AlC and Cr₂AlC at 750 °C were investigated in this work. Ti₃SiC₂ and Ti₂AlC showed a linear increase in mass gain and a relatively poor oxidation resistance. This might be attributed to the porous TiO₂ scale. A dense α-Al₂O₃ layer was formed during the oxidation test. Cr₂AlC exhibited the best oxidation resistance. This dense oxide scale can effectively isolate the substrate from contact with oxygen leading to excellent oxidation resistance. In contrast to the oxidation test, Ti₃SiC₂ and Ti₂AlC showed relatively better resistance to hot corrosion, while Cr₂AlC showed inferior resistance to NaCl introduced hot corrosion. The hot corrosion mechanism of the MAX phases was analyzed. Due to the formation of Na₂TiO₃, Ti containing MAX phases showed a continuous increase in the mass gain. The corrosion products of Cr₂AlC were Al₂O₃, Cr₂O₃ and Na₂CrO₄. However, due to the volatilization of Na₂CrO₄, Cr₂AlC showed a mass loss during the hot corrosion test. The chemical reaction process of the MAX phase was also analyzed.     

Investigation of preparation and properties of Ti3SiC2/Al2O3 multilayered composites

Ti₃SiC₂/Al₂O₃ multilayered composites were prepared by the combination of tape casting and hot pressing sintering. The slurry was produced by adjusting the amounts of each organic material, including triethyl phosphate (TEP) as a dispersion, polyvinyl butyrate (PVB) as a binder, dioctyl phthalate (DOP) as a plasticizer, and anhydrous ethanol as an organic solvent. When TEP content was 3 wt.%, PVB content was 4.5 wt.%, R-value (DOP/PVB) was 1.4, and solid content was 38 wt.%; the cast film with a smooth surface, good flexibility, and uniform thickness was obtained after defoaming, tape casting, and drying. Three samples were prepared, namely, S1–S3. The S1 was monolithic Ti₃SiC₂/Al₂O₃ (mass ratio is 1:1) composites. S2 and S3 were Ti₃SiC₂/Al₂O₃ multilayered composites, which matrix layers were Ti₃SiC₂/Al₂O₃ composites (mass ratio is 1:1) and Al₂O₃, respectively, and their interface layer was Ti₃SiC₂. S1–S3 were also sintered at 1550°C. The bending strength of multilayered materials were lower than that of monolithic material, but the fracture toughness of multilayered materials significantly increased. Due to the introduction of Ti₃SiC₂ interface layer, the friction coefficient and wear rate of Ti₃SiC₂/Al₂O₃ multilayered composites were reduced by 30.7% and 33.8%, respectively, compared with monolithic material.     

Microstructure and mechanical properties of plasma sprayed TiC/Ti5Si3/Ti3SiC2 composite coatings with Al additions

The mass production of MAX phase coatings such as Ti₃SiC₂ and Ti₃AlC₂ using the plasma spraying method is highly challenging due to its ultra-high temperature and short reaction time. In this study, agglomerate powders of 3Ti/SiC/C/xAl with various Al contents (x = 0–1.5) were prepared to form TiC/Ti₅Si₃/Ti₃SiC₂ composite coatings using the plasma spraying technique. The effect of the Al addition on the microstructures and mechanical performances of the as-sprayed coatings was investigated. The addition of Al decreased the TiC content of the coatings while increasing their Ti₃SiC₂ content significantly. The addition of even small amounts of Al improved the MAX phase fraction of the coatings from 8.95 wt% (x = 0) to 34.05 wt% (x = 0.2) and 41.60 wt% (x = 0.5). Excess Al did not affect the Ti₃SiC₂ content of the coatings. The composite coatings showed a lamellar structure with pores and microcracks. With the addition of Al, the microhardness of the coatings increased slightly, while the fracture toughness improved significantly. The composite coatings with Al showed better wear resistance than those without Al. The wear mechanism of the coatings was a combination of adhesive wear, abrasive wear, and oxidative wear.     

Comparison of hydrothermal corrosion behavior of SiC with Al2O3 and Al2O3 + Y2O3 sintering additives

Fully dense SiC bulks with Al₂O₃ and Al₂O₃ + Y₂O₃ sintering additives were prepared by spark plasma sintering and the effect of sintering additives on the hydrothermal corrosion behavior of SiC bulks was investigated in the static autoclave at 400°C/10.3 MPa. The SiC specimen with Al₂O₃ sintering additive exhibited a higher weight loss and followed a linear law. However, the SiC specimen with Al₂O₃ + Y₂O₃ additive exhibited a lower weight loss and followed a parabolic law, indicating that the corrosion kinetic and mechanism were different for these two SiC bulks. Further examination revealed that, a deposited layer was formed on the surface of SiC specimen with Al₂O₃ + Y₂O₃ sintering additive after corrosion, which can effectively protect the SiC specimen from further corrosion, and thereby improved the corrosion resistance of the SiC specimen with Al₂O₃ + Y₂O₃ sintering additive.     

Exploring processing,reactivity and performance of novel MAX phase/ultra-high temperature ceramic composites: The case study of Ti3SiC2

The reactivity behaviour between a MAX phase and ZrB₂ or WC was explored with the aim of developing novel composites by merging the benefits of the individual constituents. Hot pressing of Ti₃SiC₂ with 30 vol% ZrB₂ at 1450 °C led to notable microstructure re-assessment with formation of inter-locked sub-micrometric boride grains. This composite displayed enhanced hardness and showed a strength over 430 MPa up to 1200 °C, which is a great achievement considering the ductile behaviour of typical pure MAX compounds. However, addition of WC led to a highly porous composite with poor performance. These findings set a first basis for the progress of original light ceramics with combined hardness and failure tolerance over a broad temperature range.     

热压烧结Al2O3-ZrB2-SiC复相陶瓷的高温力学性能研究

为提高Al2O3陶瓷的高温力学性能,采用热压烧结工艺(烧结温度1 800℃,烧结压力20 MPa,保温1 h)制备了Al2O3-ZrB2-SiC复相陶瓷(简称AZS),并研究了ZrB2含量对Al2O3基陶瓷高温抗折强度和抗热震性的影响。结果表明:1)在Al2O3基陶瓷中加入第二相ZrB2能有效改善材料的高温抗折强度和高温强度保持率,在1 000和1 200℃时,加入20%体积分数ZrB2的AZS陶瓷试样具有最高的高温抗折强度,而加入24%体积分数ZrB2的AZS陶瓷试样具有最高的高温强度保持率。2)AZS陶瓷的抗热震性能优于纯Al2O3陶瓷。经100℃温差急冷后,加入20%体积分数ZrB2的AZS陶瓷具有最高的残余强度,比纯Al2O3陶瓷提高了17.2%;经300和500℃温差急冷后,加入24%体积分数ZrB2的AZS陶瓷都具有最高的残余强度,比Al2O3陶瓷分别提高了35.3%和20.9%。     

Synthesis,microstructure and mechanical properties of Cr2AlC/Al2O3 in situ composites by reactive hot pressing

Al₂O₃ particle-reinforced Cr₂AlC in situ composites were successfully fabricated from powder mixtures of Cr₃C₂, Cr, Al, and Cr₂O₃ by a reactive hot-pressing method at 1400 °C. A possible synthesis mechanism was proposed to explain the formation of the composites in which Al₂O₃ was formed by the aluminothermic reaction between Al and Cr₂O₃, meanwhile, Cr₃C₂, Al, together with Cr reacted to form Cr₂AlC in a shortened reaction route. The effect of Al₂O₃ addition on the microstructure and mechanical properties of Cr₂AlC/Al₂O₃ composites was investigated. The results indicated that the as-sintered products consisted of Cr₂AlC matrix and Al₂O₃ reinforcement, and the in situ formed fine Al₂O₃ particles dispersed at the matrix grain boundaries. The flexural strength and Vickers hardness of the composites increased gradually with increasing Al₂O₃ content. But the fracture toughness peaked at 6.0 MPa m^1/2 when the Al₂O₃ content reached 11 vol.%. The strengthening and toughening mechanism was also discussed.     

Grain size dependence,mechanical properties and surface nanoeutectic modification of Al2O3-ZrO2 ceramic

The present work aims to provide fundamental insights into the grain size dependence and mechanical behavior of hot-pressed Al₂O₃-ZrO₂ ceramic at its eutectic composition, and further to explore the hardening effect of laser-induced surface nanoeutectic layer. The underlying correlations between densification behavior, grain size distribution and mechanical properties were elucidated. Sintering at 1550 °C promotes the densification without extensive grain growth, and in this case the sample exhibits a critical density of 99.3 %. The average grain size is tailored into a range of 0.6–0.9 μm, and the measured flexural strength and toughness reach 1100 MPa and 11 MPa·m^1/2, respectively. The metastable t-ZrO₂ grains indeed play a pivotal role in energy dissipation at the crack tip through crack deflection and branching. In addition, the mechanical behavior is reasonably explained through constructing a multilevel toughening mechanism map associated with grain size distribution of ZrO₂. Particularly, surface nanocrystallized Al₂O₃-ZrO₂ eutectic layer with a thickness of 1000 μm free of pores and cracks is achieved by a rapid laser melting process. The outmost laser-modified nanoeutectic layer exhibits a fine cellular structure with an interphase spacing of only 105 nm and a hardness of as high as 26.1 GPa, which provides a promising potential in enhancing significantly the hardness and wear resistance for applications as sliding ceramic components.     

Microstructure evolution,mechanical and tribological properties of Ti3(Al,Sn)C2/Al2O3 composites

In this paper, in situ formed Ti₃(Al,Sn)C₂/Al₂O₃ composites were fabricated by sintering the mixture of Ti₃AlC₂ and SnO₂. The Al atoms could diffuse out of the Ti₃AlC₂ layered structure to react with SnO₂, resulting in the formation of Ti₃(Al,Sn)C₂ solid solution and Al₂O₃. When the SnO₂ content was 20?wt.%, the sintered Ti₃(Al,Sn)C₂/Al₂O₃ composite exhibited the best overall mechanical properties, because of the optimized cooperative strengthening effect of solution strengthening and Al₂O₃ enhancement. When the SnO₂ content increased up to 30?wt.%, the flexural strength and fracture toughness of Ti₃(Al,Sn)C₂/Al₂O₃ composite dramatically decreased on account of the large accumulation of generated Al₂O₃. Moreover, according to the SiC ball-on-flat wear tests, it was found that the wear resistance of Ti₃(Al,Sn)C₂/Al₂O₃ composites was significantly improved as the SnO₂ content increased.     

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.     

Microstructure and properties of Al2O3-TiC-Ti3SiC2 composites fabricated by spark plasma sintering

Abstract

Abstract

Highly densified Al₂O₃-TiC-Ti₃SiC₂ composites were fabricated by spark plasma sintering technique and subsequently characterised. From fracture surface observation, it is found that Al₂O₃ is 0·2-0·4?μm, TiC is 1-1·5?μm and Ti₃SiC₂ is 1·5-5?μm in grain size. With the increase in Ti₃SiC₂ volume contents, Vickers hardness of the composites decreases because of the low hardness of monolithic Ti₃SiC₂. The fracture toughness rises remarkably when the contents of Ti₃SiC₂ increase, which is attributed to the pullout and microplastic deformation of Ti₃SiC₂ grains. At the same time, the flexural strength of the composites shows a considerable improvement as well. The electrical conductivity rises significantly as the Ti₃SiC₂ contents increase because of the formation of Ti₃SiC₂ network and the increase in conductive phase contents.