Interfacial microstructure and mechanical properties of ZTA/ZTA joints brazed with Ni-Ti filler metal

The reliable brazing of the ZTA ceramic joints was successfully obtained using Ni-Ti filler metal. The microstructure and mechanical properties of the joints brazed at different temperatures were investigated. During the process of brazing, both Al₂O₃ and ZrO₂ in the ZTA reacted with the Ni-Ti filler, resulting in the formation of the AlNi₂Ti + Ni₂Ti₄O reaction layer adjacent to the ZTA substrate when brazed at 1350 °C for 30 min. NiTi and Ni₃Ti compounds precipitated at the center of brazing seam. When the brazing temperature increased from 1320 °C to 1380 °C, the thickness of AlNi₂Ti + Ni₂Ti₄O layer increased gradually. As the brazing temperature varied from 1400 °C to 1450 °C, TiO was formed adjacent to the ZTA substrate, along with the reduction of Ni₂Ti₄O. AlNi₂Ti distributed at the interface and center of brazing seam. The maximum shear strength of 152 MPa was obtained when brazed at 1420 °C for 30 min.     

Interfacial microstructure and mechanical properties of zirconia ceramic and niobium joints vacuum brazed with two Ag-based active filler metals

Reliable brazing of a zirconia ceramic and pure niobium was achieved by using two Ag-based active filler metals, Ag-Cu-Ti and Ag-Cu-Ti+Mo. The effects of brazing temperature, holding time, and Mo content on the interfacial microstructure and mechanical properties of ZrO₂/Nb joints were investigated. Double reaction layers of TiO and Ti₃Cu₃O formed adjacent to the ZrO₂ ceramic, whereas TiCu₄+Ti₂Cu₃+TiCu compounds appeared in the brazing interlayer. With increasing brazing temperature and time, the thickness of the Ti₃Cu₃O layer increased with consumption of the TiO layer, and the total thickness of the reaction layers increased slightly. Meanwhile, the blocky Ti-Cu compounds in the brazing interlayer tended to accumulate and grow. This microstructural evolution and its formation mechanism are discussed. The maximum shear strength was 157 MPa when the joints were brazed with Ag-Cu-Ti at 900 °C for 10 min. The microstructure and bonding properties of the brazed joints were significantly improved when Mo particles were added into the Ag-Cu-Ti. The shear strength reached 310 MPa for joints brazed with 8.0 wt% Mo additive, which was 97% higher than that of joints brazed with single Ag-Cu-Ti filler metal.     

Effects of SiC whiskers on the mechanical properties and microstructure of SiC ceramics by reactive sintering

As-received and pre-coated SiC whiskers (SiC_w)/SiC ceramics were prepared by phenolic resin molding and reaction sintering at 1650 °C. The influence of SiC_w on the mechanical behaviors and morphology of the toughened reaction-bonded silicon carbide (RBSC) ceramics was evaluated. The fracture toughness of the composites reinforced with pre-coated SiC_w reached a peak value of 5.6 MPa m^1/2 at 15 wt% whiskers, which is higher than that of the RBSC with as-received SiC_w (fracture toughness of 3.4 MPa m^1/2). The surface of the whiskers was pre-coated with phenolic resin, which could form a SiC coating in situ after carbonization and reactive infiltration sintering. The coating not only protected the SiC whiskers from degradation but also provided moderate interfacial bonding, which is beneficial for whisker pull-out, whisker bridging and crack deflection.     

Interfacial microstructure and mechanical properties of TC4/Ti3SiC2 contact-reactive brazed joints using a Cu interlayer

Reliable contact-reactive brazed joints of TC4 alloy and Ti₃SiC₂ ceramic were obtained using a Cu interlayer. The interfacial microstructure of a TC4/Ti₃SiC₂ joint brazed at 920?°C for 10?min was TC4/Ti₂Cu +?α-Ti +?β-Ti/Ti₂Cu +?AlCu₂Ti +?Ti₅Si₃/Ti₅Si₃ +?Ti₅Si₄/Ti₃SiC₂. The interfacial microstructure and mechanical properties of TC4/Ti₃SiC₂ joints brazed at different temperatures were investigated. With increasing temperature, the shear strength of the brazed joints first increased and then decreased. The maximum shear strength was 132?±?8?MPa, and the corresponding fracture occurred along the Ti–Si reaction layer and the Ti₃SiC₂ substrate adjacent to the Ti–Si reaction layer. The microhardness test also demonstrated that the Ti–Si reaction layer possessed the highest microhardness, 812?±?22 HV. The Ti-Si reaction layer was the weakest part of the brazed joints. To eliminate the Ti-Si reaction layer and improve the mechanical properties of TC4/Ti₃SiC₂ brazed joints, a 40-μm Ni layer was plated on the surface of the Ti₃SiC₂ ceramic before brazing. The results showed that the Ti–Si reaction layer that formed adjacent to the Ti₃SiC₂ ceramic was thin and intermittent. Moreover, the interface between the Ti₃SiC₂ ceramic and the TC4 alloy became jagged. The shear strength of the TC4/nickel-plated Ti₃SiC₂ brazed joints improved to 148?±?8?MPa; the corresponding fracture occurred mainly in the Ti₃SiC₂ ceramic and only a small portion of the fracture occurred in the brazing seam.     

Interfacial microstructure and mechanical properties of porous-Si3N4 ceramic and TiAl alloy joints vacuum brazed with AgCu filler

Porous Si₃N₄ ceramic was firstly joined to TiAl alloy using an AgCu filler alloy. The effects of brazing temperature and holding time on the interfacial microstructure and mechanical properties of porous-Si₃N₄/AgCu/TiAl joints were studied. The typical interfacial microstructure of joints brazed at 880 °C for 15 min was TiAl/AlCu₂Ti/Ag-Cu eutectic/penetration layer (Ti₅Si₃+TiN, Si₃N₄, Ag (s, s), Cu (s, s))/porous-Si₃N₄. The penetration layer was formed firstly in the brazing process. With increasing brazing temperature and time, the thickness of the penetration layer increased. A large amount of element Ti was consumed in the penetration layer which suppressed the formation and growth of other intermetallic compounds. The penetration layer led the fracture to propagate in the porous Si₃N₄ ceramic substrate. The maximum shear strength was ~13.56 MPa.     

Microstructure evolution and mechanical properties of YAG/YAG joint using bismuth-borate glass

Joining of Y₃Al₅O₁₂ garnet single crystal (YAG) was achieved by using a bismuth-borate based glass filler. The thermal properties of glass filler were experimentally determined and the wettability of molten glass on YAG was investigated. The YAG reacted with glass to form ZnAl₂O₄ particles and Y₂O₃ nanowires successively as joining temperature is above 625℃. ZnAl₂O₄ preferentially nucleated and grew on Y₂O₃ nanowires. The cooperative growth of the two phases accelerated YAG decomposition, which in turn led to cluster growth of Y₂O₃ nanowires and aggregation of ZnAl₂O₄ particles at elevated temperature. The microstructure evolution and reaction mechanism were studied. The highest shear strength of 29.6 ± 5.2 MPa was obtained for the joint brazed at 650℃. The fracture morphology demonstrated that the dispersive strengthening of ZnAl₂O₄ and stress relief by Y₂O₃ nanowire network contributed to the superior mechanical performance.     

Effect of brazing parameters on microstructure and mechanical properties of Cf/SiC and Nb-1Zr joints brazed with Ti-Co-Nb filler alloy

Reliable brazing of carbon fiber reinforced SiC (C_f/SiC) composite to Nb-1Zr alloy was achieved by adopting a novel Ti45Co45Nb10 (at.%) filler alloy. The effects of brazing temperature (1270–1320 °C) and holding time (5–30 min) on the microstructure and mechanical properties of the joints were investigated. The results show that a continuous reaction layer (Ti,Nb)C was formed at the C_f/SiC/braze interface. A TiCo and Nb(s,s) eutectic structure was observed in the brazing seam, in which some CoNb₄Si phases were distributed. By increasing the brazing temperature or extending the holding time, the reaction layer became thicker and the amount of the CoNb₄Si increased. The optimized average shear strength of 242 MPa was obtained when the joints were brazed at 1280 °C for 10 min. The high temperature shear strength of the joints reached 202 MPa and 135 MPa at 800 °C and 1000 °C, respectively.     

The effect of oxide,carbide, nitride and boride additives on properties of pressureless sintered SiC: A review

Properties such as high hardness, low density, and high elastic modulus have made SiC ceramics proper choices for a variety of industrial applications. However, disadvantages such as low sinterability, and low fracture toughness have limited the fabrication of these ceramics. Past researches show that the use of Al₂O₃-Y₂O₃ additives play an important role in improving the sinterability and the properties of the composites. The use of oxide, carbide, nitride and boride additives results in improved sinterability, physical and mechanical properties. The investigations show that the microstructure, porosities, amount of additives, reaction of additives with the matrix, grain size and, finally, the sintering temperature are the most important factors affecting the properties of SiC ceramics. In this paper, the effect of using various additives, the sintering temperature and the annealing heat treatment on sinterability, microstructure and properties of the SiC matrix composites fabricated by pressureless sintering method have been investigated.     

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.     

Graphene nanoplatelets reinforced AgCuTi composite filler for brazing SiC ceramic

Graphene nanoplatelets (GNPs) were used as reinforcement in AgCuTi filler for brazing SiC ceramic. Ti from the filler reacted with SiC ceramic to form TiC and Ti₅Si₃ adjacent to the SiC ceramic. According to the TEM and HRTEM results, TiC layer exhibited good lattice matching with SiC substrate. TiC particles synthesized by the reaction between Ti and GNPs in situ promoted the heterogeneous nucleation of TiCu and Cu(s,s), and contributed to the refinement of microstructure. Shear tests results indicated that the adoption of GNPs affected the joint property significantly. The TiC particles and an appropriate TiC + Ti₅Si₃ layer thickness both relieved the residual stress of the brazed joint and thereby increased the joint strength. The shear strength of the joint reached the maximum value of 38 MPa when using AgCuTi/GNPs (GNPs reinforced AgCuTi) composite filler containing 1% GNPs, which was ～139% higher than that of the joint brazed with AgCuTi filler.     

Zirconia ceramic and Nb joints brazed with Mo-particle-reinforced Ag-Cu-Ti composite fillers: Interfacial microstructure and formation mechanism

Zirconia (ZrO₂) ceramic and Nb were successfully brazed using a Mo-particle -reinforced Ag-Cu-Ti composite filler. The effect of the Mo content of the composite filler on the interfacial microstructures and mechanical properties of ZrO₂/Nb-brazed joints was investigated. The calculated Ti activity initially increased and then decreased as the Mo content was increased from 1 to 40 wt%, and played a decisive role in the evolution of interfacial products formed adjacent to the ZrO₂ ceramic. When 40 wt% Mo particles were added to the composite filler, TiO+Ti₃Cu₃O reaction layers formed adjacent to the ceramic substrate. By decreasing the Mo content of the filler, the TiO layer became thinner or even vanished, whereas the thickness of the Ti₃Cu₃O reaction layer increased gradually with decreasing Mo content. Concurrently, a bulky TiCu compound grew near to the ZrO₂ ceramic, and further fine TiCu particles were observed in the brazing seam. This microstructure evolution, as well as the mechanism for the formation of joints brazed with composite fillers of differing Mo content, is discussed based on TEM analyses. The shear strength of the brazed joint is clearly improved when a suitable amount of Mo is added to the Ag-Cu-Ti filler. A maximum shear strength of 370 MPa was obtained when ZrO₂/Nb joints were brazed with Ag-Cu-Ti+5 wt% Mo composite filler.     

Interfacial microstructure and mechanical properties of Ti3SiC2 ceramic and TC11 alloy joint diffusion bonded with a Cu interlayer

Reliable joints of Ti₃SiC₂ ceramic and TC11 alloy were diffusion bonded with a 50 μm thick Cu interlayer. The typical interfacial structure of the diffusion boned joint, which was dependent on the interdiffusion and chemical reactions between Al, Si and Ti atoms from the base materials and Cu interlayer, was TC11/α-Ti + β-Ti + Ti₂Cu + TiCu/Ti₅Si₄ + TiSiCu/Cu(s, s)/Ti₃SiC₂. The influence of bonding temperature and time on the interfacial structure and mechanical properties of Ti₃SiC₂/Cu/TC11 joint was analyzed. With the increase of bonding temperature and time, the joint shear strength was gradually increased due to enhanced atomic diffusion. However, the thickness of Ti₅Si₄ and TiSiCu layers with high microhardness increased for a long holding time, resulting in the reduction of bonding strength. The maximum shear strength of 251 ± 6 MPa was obtained for the joint diffusion bonded at 850 °C for 60 min, and fracture primarily occurred at the diffusion layer adjacent to the Ti₃SiC₂ substrate. This work provided an economical and convenient solution for broadening the engineering application of Ti₃SiC₂ ceramic.     

Improved thermal conductivity and mechanical properties of SiC/SiC composites using pitch-based carbon fibers

Pitch-based carbon fibers were assembled in horizontal and thickness directions of SiC/SiC composites to form three-dimensional heat conduction networks. The effects of heat conduction networks on microstructures, mechanics, and thermal conductivities were investigated. The results revealed the benefit of introducing heat conduction networks in the densification of composites. The maximum bending strength and interlaminar shear strength of the modified composites reached 568.67 MPa and 68.48 MPa, respectively. These values were equivalent to 18.6% and 69.4% increase compared to those of composites without channels. However, channels in thickness direction destroyed the continuity of fibers and matrix, creating numerous defects. As the volume fraction of heat conduction channels rose, the pinning strengthening effect of channels and influence of defects competed with each other to result in first enhanced mechanical properties followed by a decline. The in-plane thermal conductivity was found anisotropic with a maximum value reaching 86.20 W/(m·K) after introducing pitch-based carbon unidirectional tapes. The thermal conductivity in thickness direction increased with volume fraction of pitch-based carbon fibers and reached 19.13 W/(m·K) at 3.87 vol% pitch-based carbon fibers in the thickness direction. This value was 90.75% higher than that of composites without channels.     

Effect of adding of SiC particulate on the microstructure and shear strength of SiC ceramic joint brazed with Si-24Ti alloy

In order to refine the grain size of TiSi₂ silicide and reduce the formation of micro-defects in the joint, and thereby increasing the joint strength of SiC ceramic brazed with Si-24Ti (wt.%), a small amount of SiC particulates were added in the brazing alloy. The microstructure and mechanical strength of SiC joints was investigated by using field emission scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction spectrometer, and shear strength test. The results indicated that SiC particulates enhanced the nucleation and grain refinement of the TiSi₂ and Si phase. The adding of appropriate content of SiC (<1 wt.%) could effectively refine the size of TiSi₂ phase and increase the fraction of Si-TiSi₂ eutectic zone. However, excess addition of 1.5 wt.% SiC caused the coarsening of TiSi₂ phase due to the clustering of added fine SiC particulates. With the increasing of SiC particulate content, the shear strength of the joints increased at first and then decreased. The maximum shear strength of 106.3 MPa of SiC joint was obtained for the joint brazed with 1 wt.% SiC addition, which was ~19% higher than that of the joint brazed without SiC particulates.     

Wetting behavior and brazing of titanium-coated SiC ceramics using Sn0.3Ag0.7Cu filler

By coating active titanium, Sn0.3Ag0.7Cu (SAC) filler wetted SiC effectively, as the contact angle decreased significantly from ~145° to ~10°. Ti₃SiC₂ and TiO_x (x ≤ 1) reaction layers were formed at the droplet/SiC interface, leading to the reduction of contact angle. Reliable brazing of SiC was achieved using titanium deposition at 900°C for 10 minutes, and the typical interfacial microstructure of Ti-coated SiC/SAC was SiC/TiO_x + Ti₃SiC₂/Sn(s,s). Comparing to direct brazing, Ti–Sn compounds in the brazing seam were effectively reduced and the mechanical property of joints was dramatically improved by titanium coating. The optimal average shear strength of SiC joints reached 25.3 MPa using titanium coating- assisted brazing, which was ∼62% higher than that of SiC brazed joints using SAC-Ti filler directly.     

Ti3SiC2-Cf composites by spark plasma sintering: Processing,microstructure and thermo-mechanical properties

MAX phases, and particularly Ti₃SiC₂, are interesting for high temperature applications. The addition of carbon fibers can be used to reduce the density and to modify the properties of the matrix. This work presents the densification and characterization of Ti₃SiC₂ based composites with short carbon fibers using a fast and simple fabrication approach: dry mixing and densification by Spark Plasma Sintering. Good densification level was obtained below 1400 °C even with a high amount of fibers. The reaction of the fibers with the matrix is limited thanks to the fast processing time and depends on the amount of fibers in the composite. Bending strength at room temperature, between 437 and 120 MPa, is in the range of conventional CMCs with short fibers and according to the resistance of the matrix and the presence of residual porosity. Thermo-mechanical properties of the composites up to 1500 °C are also presented.     

Synthesis of centimeter-scale monolithic SiC nanofoams and pore size effect on mechanical properties

By pressure infiltrating pre-ceramic polymer polycarbosilane (PCS) into thermally and mechanically stable silica nanofoam, followed by PCS pyrolysis and silica template removal, synthesis of large-scale monolithic SiC nanofoams has been accomplished. Tailoring of the porosity and cell size of the SiC nanofoam has been realized by dissociating the porosity and pore size of the silica nanofoam. Because of the surface hardening and increased surface volume ratio of deformable nanopores, with the same porosity, the decrease of nanopore size has led to an increase in the quasi-static and dynamic indentation resistance for SiC nanofoams.     

Mechanical properties and strengthening mechanism of SiCf/SiC mini-composites modified by SiC nanowires

The effects of the SiC nanowires (SiCNWs) and PyC interface layers on the mechanical and anti-oxidation properties of SiC fiber (SiC_f)/SiC composites were investigated. To achieve this, the PyC layer was coated on the SiC_f using a chemical vapour infiltration (CVI) method. Then, SiCNWs were successfully coated on the surface of SiC_f/PyC using the electrophoretic deposition method. Finally, a thin PyC layer was coated on the surface of SiC_f/PyC/SiCNWs. Three mini-composites, SiC_f/PyC/SiC, SiC_f/PyC/SiCNWs/SiC, and SiC_f/PyC/SiCNWs/PyC/SiC, were fabricated using the typical precursor infiltration and pyrolysis method. The morphologies of the samples were examined using scanning electron microscopy and energy dispersive X-ray spectrometry. Tensile and single-fibre push-out tests were carried out to investigate the mechanical performance and interfacial shear strength of the composites before and after oxidization at 1200 °C. The results revealed that the SiC_f/PyC/SiCNWs/SiC composites showed the best mechanical and anti-oxidation performance among all the composites investigated. The strengthening and toughening is mainly achieved by SiCNWs optimization of the interfacial bonding strength of the composite and its own nano-toughening. On the basis of the results, the effects of SiCNWs on the oxidation process and retardation mechanism of the SiC_f/SiC mini-composites were investigated.     

Joining of SiCf/SiC using a layered Ti3SiC2-SiCw and TiC gradient filler

A layered filler consisting of Ti₃SiC₂-SiC whiskers and TiC transition layer was used to join SiC_f/SiC. The effects of SiC_w reinforcement in Ti₃SiC₂ filler were examined after joining at 1400 or 1500 °C in terms of the microstructural evolution, joining strength, and oxidation/chemical resistances. The TiC transition layer formed by an in-situ reaction of Ti coating resulted in a decrease in thermal expansion mismatch between SiC_f/SiC and Ti₃SiC₂, revealing a sound joint without cracks formation. However, SiC_f/SiC joint without TiC layer showed formation of cracks and low joining strength. The incorporation of SiC_w in Ti₃SiC₂ filler showed an increase in joining strength, oxidation, and chemical etching resistance due to the strengthening effect. The Ti₃SiC₂ filler containing 10 wt.% SiC_w along with the formation of TiC was the optimal condition for joining of SiC_f/SiC at 1400 °C, showing the highest joining strength of 198 MPa as well as improved oxidation and chemical resistance.     

Effect of SiC nanowhisker addition on microstructure and mechanical properties of regenerated cemented carbides by low-pressure sintering

The hardness and toughness of regenerated cemented carbides, in general, are contradictory. Therefore, it is critical to explore regenerated cemented carbides with both high hardness and high toughness. In this study, regenerated WC-8-wt% Co cemented carbide with SiC nanowhisker were prepared by low-pressure sintering. The influence of SiCw contents on the microstructure and mechanical properties of regenerated WC-8-wt% Co cemented carbide was investigated. The results indicated that the hardness, density, flexural strength, and fracture toughness of regenerated cemented carbide first increased and then decreased with the addition of SiCw. The Vickers hardness, density, flexural strength, and fracture toughness could reach 1575 HV, 14.6 g/cm³, 2204 MPa, 16.85 MPa·m^1/2, respectively, with SiCw content 0.5 wt%, which were increased by 14.4%, 0.7%, 12.2%, and 17.3%, respectively, when compared with the regenerated cemented carbide without SiCw. The lowest friction coefficient and the best wear resistance could be also reached when 0.5-wt% SiCw was added. The fracture mechanism of the regenerated cemented carbide contained both transgranular and intergranular fracture through the microscopic observation of fracture surface via scanning electron microscope.