TiB-Ti基金属陶瓷的燃烧合成

通过自蔓延高温燃烧合成 ,结合准热等静压工艺 (SHS/PHIP)制备了相对密度超过 94%的TiB xTi基金属陶瓷复合材料 ,研究了金属Ti含量对燃烧合成TiB Ti基金属陶瓷复合材料的影响。研究结果表明 :随着Ti含量的增加 ,绝热温度、燃烧温度和燃烧速度均降低 ,反应产物主要由TiB和Ti两相组成 ,部分产物还有TiB2 相存在 ,产物组织中 ,TiB相主要有针状、棒状和片状等形态 ,增强相的尺寸随Ti含量的增加而减小 ;随Ti含量的增加 ,产物的抗弯强度、抗拉强度、抗压强度和断裂韧性提高 ,且在Ti含量为 40 % (质量分数 )时达到最大值     

放电等离子烧结TiB/Ti-1.5Fe-2.25Mo复合材料的微观组织与力学性能

采用放电等离子烧结技术原位合成了TiB增强Ti?1.5Fe?2.25Mo复合材料,研究了烧结温度对复合材料微观组织和力学性能的影响规律。结果表明,随着烧结温度的升高,钛合金中 TiB 晶须的长细比迅速减小;然而,复合材料的相对密度及TiB的体积含量随着烧结温度的升高而不断增大。由于TiB晶须长细比的减小会导致复合材料强度的降低,而复合材料的相对密度及TiB体积含量的增大又会带来复合材料强度的增加,因此,在这两种因素的共同作用下,最终导致 TiB/Ti?1.5Fe?2.25Mo复合材料的弯曲强度随着烧结温度的升高而缓慢增大。在烧结温度为1150°C 时,TiB/Ti?1.5Fe?2.25Mo复合材料具有最大的弯曲强度1596 MPa。     

Microstructure and mechanical properties of magnesium composites prepared by spark plasma sintering technology

Spark plasma sintering (SPS) technology was used to determine the appropriate conditions for SPS sintering of commercially pure magnesium as well as the magnesium alloy AZ31. It was found that the sintering temperatures of 585 °C and 552 °C were the most suitable sintering temperatures for the magnesium and the AZ31 alloy, respectively. Magnesium matrix and AZ31 alloy matrix composites reinforced with SiC particles were then successfully fabricated by the SPS method at sintering temperatures of 585 °C and 552 °C, respectively. A uniform distribution of SiC particles was observed along the boundary between matrix particles. The mechanical properties, i.e. hardness and tensile strength increased with increasing SiC content up to 10 wt%. However, when the SiC content was larger than 10 wt%, the tensile strength decreased due to the agglomeration of SiC particles. The agglomeration of SiC particles was found to lead to the degradation of the interfacial bonding strength between matrix and reinforcement.     

Densification and compressive strength ofin-situ processed Ti/TiB composites by powder metallurgy

In the present study, the densification of Ti/TiB composites, the growth behavior ofin-situ formed TiB reinforcement, the effects of processing variables — such as reactant powder (TiB₂, B₄C), sintering temperature and time — on the microstructures and the mechanical properties ofin-situ processed Ti/TiB composites have been investigated. Mixtures of TiB₂ or B₄C powder with pure titanium powder were compacted and presintered at 700°C for 1 hr followed by sintering at 900, 1000, 1100, 1200, and 1300°C, respectively, for 3hrs. Some specimens were sintered at 1000°C for various times in order to study the formation behavior of TiB reinforcementin-situ formed within the pure Ti matrix. TiB reinforcements were formed through different mechanisms, such as the formation of fine TiB and the formation of coarse TiB by Ostwald ripening or the coalescence of fine TiB. There was no crystallographic relationship between TiB reinforcement and the matrix. There were voids at the interface between the TiB reinforcement and the Ti matrix due to the preferential growth of coarse TiB without a particular crystallographic relationship with pure Ti matrix and the surface energy between the Ti matrix and TiB reinforcements. Therefore, the densification of Ti/TiB₂ compacts was hindered by the preferential growth of coarse TiB reinforcements. The mechanical properties ofin-situ processed composites were evaluated by measuring the compressive yield strength at ambient and high temperatures. The compressive yield strength of thein situ processed composites was higher than that of the Ti-6A1-4V alloy. It was also found that the compressive yield strength of the composite made from TiB₂ reactant powder was higher than that of the composite made from B₄C at the same volume fraction of reinforcement. A crack path examination suggested that the bonding nature of interface between matrix and reinforcement made from TiB₂ reactant powder was better than that made from B₄C.     

Densification and mechanical properties of fine-grained Al2O3-ZrO2 composites consolidated by spark plasma sintering

Alumina matrix composites containing 5 and 10 wt% of ZrO₂ were sintered under 100 MPa pressure by spark plasma sintering process. Alumina powder with an average particle size of 600 nm and yttria-stabilized zirconia with 16 at% of Y₂O₃ and with a particle size of 40 nm were used as starting materials. The influence of ZrO₂ content and sintering temperature on microstructures and mechanical properties of the composites were investigated. All samples could be fully densified at a temperature lower than 1400 °C. The microstructure analysis indicated that the alumina grains had no significant growth (alumina size controlled in submicron level 0.66-0.79 μm), indicating that the zirconia particles provided a hindering effect on the grain growth of alumina. Vickers hardness and fracture toughness of composites increased with increasing ZrO₂ content, and the samples containing 10 wt% of ZrO₂ had the highest Vickers hardness of 18 GPa (5 kg load) and fracture toughness of 5.1 MPa m^1/2.     

Effect of SPS process sintering on the microstructure and mechanical properties of nanocrystalline TiC for tools application

The most important spark plasma sintering (SPS) parameters (Temperature, holding time and pressure), have been reviewed to assess their effect on the densification, grain growth kinetics and mechanical properties of nanocrystalline TiC synthesized by mechanical alloying. Experiments were performed in the 1350-1800 °C temperature range with holding time from 1 to 10 min under various pressure values of 50, 80 and 100 MPa. The results of experiments revealed that the mechanical properties of the material were improved with raising the sintering temperature and extending the sintering time. However, a hardness decrease was observed as a result of abnormal grain growth under higher sintering temperatures. The optimized process parameters for SPS process are identified as a sintering temperature of 1650 °C, a pressure 100 MPa and a sintering time of 5 min. The resulting mechanical properties are: a relative density of 97.9%, a micro-hardness of 2570 Hv, a nano-hardness of 28 GPa, a fracture toughness of 4.9 MPa·m^1/2 and a compressive strength of about 2210 MPa.     

Comparison of ZrB2-SiC ceramics with Yb2O3 additive prepared by hot pressing and spark plasma sintering

This work compared phase composition, microstructures and mechanical properties of ZrB₂—20 vol.% SiC—5 vol.%Yb₂O₃ prepared by hot pressing (HP) and spark plasma sintering (SPS) in vacuum. Despite the same raw material composition, the two densification techniques led to the appearance of different secondary phases. The HP ceramics had coarsened microstructure, predominantly intergranular fracture characteristic and high fracture toughness. The SPS ceramics exhibited refined microstructure, transgranular fracture model and high bending strength.     

Fabrication of full density near-nanostructured cemented carbides by combination of VC/Cr3C2 addition and consolidation by SPS and HIP technologies

The aim of present work is to study the effect of VC and/or Cr₃C₂ in densification, microstructural development and mechanical behavior of nanocrystalline WC-12wt.%Co powders when they are sintered by spark plasma sintering (SPS) and hot isostatic pressing (HIP). The results were compared to those corresponding to conventional sintering in vacuum. The density, microstructure, X-ray diffraction, hardness and fracture toughness of the sintered materials were evaluated. Materials prepared by SPS exhibits full densification at lower temperature (1100 °C) and a shorter stay time (5 min), allowing the grain growth control. However, the effect of the inhibitors during SPS process is considerably lower than in conventional sintering. Materials prepared by HIP at 1100 °C and 30 min present full densification and a better control of microstructure in the presence of VC. The added amount of VC allows obtaining homogeneous microstructures with an average grain size of 120 nm. The hardness and fracture toughness values obtained were about 2100 HV₃₀ and close to 10 MPa m^1/2, respectively.     

Dielectric and microwave properties of ZrO2 doped CaO-SiO2-B2O3 ceramic matrix composites

The behavior of dielectric and microwave properties against sintering temperature has been carried out on CaO-SiO₂-B₂O₃ ceramic matrix composites with ZrO₂ addition. The results indicated that ZrO₂ addition was advantageous to improve the dielectric and microwave properties. X-ray diffraction (XRD) patterns show that the major crystalline β-CaSiO₃ and a little SiO₂ phase existed at the temperature ranging from 950 °C to 1050 °C. At 0.5 wt% ZrO₂, CaO-SiO₂-B₂O₃ ceramic matrix composites sintered at 1000 °C possess good dielectric properties: ?_r = 5.85, tan δ = 1.59 × 10⁻⁴ (1 MHz) and excellent microwave properties: ?_r = 5.52, Q · f = 28,487 GHz (11.11 GHz). The permittivity of Zr-doped CaO-SiO₂-B₂O₃ ceramic matrix composites exhibited very little temperature dependence, which was less than ±2% over the temperature range of −50 to 150 °C. Moreover, the ZrO₂-doped CaO-SiO₂-B₂O₃ ceramic matrix composites have low permittivity below 5.5 over a wide frequency range from 20 Hz to 1 MHz.     

Effect of ball milling the hybrid reinforcements on the microstructure and mechanical properties of Mg-(Ti + n-Al2O3) composites

In this study, composites containing pure magnesium and hybrid reinforcements (5.6 wt.% titanium (Ti) particulates and 2.5 wt.% nanoscale alumina (n-Al₂O₃) particles) were synthesized using the disintegrated melt deposition technique followed by hot extrusion. The hybrid reinforcement addition into the Mg matrix was carried out in two ways: (i) by direct addition of the reinforcements into the Mg-matrix, Mg-(5.6Ti + 2.5n-Al₂O₃) and (ii) by pre-synthesizing the composite reinforcement by ball milling and its subsequent addition into the Mg-matrix, Mg-(5.6Ti + 2.5n-Al₂O₃)_BM. Microstructural characterization revealed significant grain refinement due to reinforcement addition. The evaluation of mechanical properties indicated a significant improvement in microhardness, tensile and compressive properties of the composites when compared to monolithic magnesium. For the Mg-(5.6Ti + 2.5n-Al₂O₃) composite, wherein the reinforcements were directly added into the matrix, the improvement in strength properties occurred at the expense of ductility. For the Mg-(5.6Ti + 2.5n-Al₂O₃)_BM composites with pre-synthesized ball-milled reinforcements, the increase in strength properties was accompanied by an increase/retention of ductility. The observed difference in behaviour of the composites is primarily attributed to the morphology and distribution of the reinforcements obtained due to the ball-milling process, thereby resulting in composites with enhanced toughness.     

The effect of heat treatment on thermal stability of Ti matrix composite

The microstructures of in situ synthesized (TiB + La₂O₃)/Ti composite after β and TRIPLEX heat treatment are investigated. The room temperature tensile properties of the titanium matrix composites (TMCs) are tested, and thermal stability is carried out at 600, 650 and 700 °C for 100 h, respectively. The results show that the microstructure of specimen after β heat treatment is widmanstätten, while it is similar to basketweave after TRIPLEX heat treatment. Room tensile properties of specimen after TRIPLEX heat treatment are better than those of β heat treatment. After thermal exposure, the strength of specimens treated by β and TRIPLEX heat treatment increases, while the ductility decreases sharply, this is attributed to the precipitation of Ti₃Al and silicides. The thermal stability of specimen after TRIPLEX heat treatment is better than that after β heat treatment.     

Effect of partial substitution of Cr for Ni on densification behavior, microstructure evolution and mechanical properties of Ti(C,N)-Ni-based cermets

Four cermets of composition TiC-10TiN-16Mo-6.5WC-0.8C-0.6Cr₃C₂-(32 − x)Ni-xCr (x = 0, 3.2, 6.4 and 9.6 wt%) were prepared, to investigate the effect of the partial substitution of Cr for Ni on densification behavior, microstructure evolution and mechanical properties of Ti(C,N)-Ni-based cermets. The partial substitution of Cr for Ni decreased full densification temperature, and the higher the content of Cr additive was, the lower full densification temperature was. The partial substitution of Cr for Ni had no significant effect of the formation of Mo₂C and Ti(C,N) and the dissolution of WC, and however, it had a significant effect on the dissolution of Mo₂C. Cr in Ni-based binder phase diffused into undissolved Mo₂C to form (Mo,Cr)₂C above 1000 °C at 6.4-9.6 wt% Cr additive, and a small amount of (Mo,Cr)₂C did not dissolve after sintering at 1410 °C for 1 h at 9.6 wt% Cr additive. In the final microstructure, Cr content in Ni-based binder phase increased with increasing the content of Cr additive, and however, regardless of the content of Cr additive, coarse Ti(C,N) grains generally consisted of black core, white inner rim and grey outer rim, and fine Ti(C,N) grains generally consisted of white core and grey rim. The partial substitution of Cr for Ni increased hardness and decreased transverse rupture strength (TRS). Ni-based binder phase became hard with increasing the content of Cr additive, therefore resulting in the increase of hardness and the decrease of TRS. TRS was fairly low at 9.6 wt% Cr additive, which was mainly attributed hardening of Ni-based binder phase and undissolved (Mo,Cr)₂C.     

Thermal stability of in situ synthesized high temperature titanium matrix composites

TiB and La₂O₃ reinforced high temperature titanium matrix composites are in situ synthesized by common casting technology. Microstructure of the matrix alloys and composites before and after thermal exposure are characterized, tensile properties of the specimens are tested. Both the strength and ductility of the composites are enhanced by the reinforcements. Titanium matrix composites show better thermal stability than the matrix alloys because of the reduction of oxygen and microstructure refinement without Ti₃Al agglomeration.     

Ti-coated SiC particle reinforced sintered Fe-Cu-Sn alloy

Ti-coated SiC particles were developed to improve the wear resistance of Fe-Cu-Sn alloy metal matrices designed for diamond tools. The phase structure of the Ti-coated SiC particles was investigated by X-ray diffraction. Ti coating on SiC was composed of Ti₅Si₃, TiC, and Ti. Excellent interfacial bonding between SiC and the matrix was realized. The SiC/iron alloy composites, prepared by hot pressing at 820 °C, were studied by wear and bending strength tests, and scanning electron microscope. For the composites reinforced by uncoated SiC particles, the wear resistance was improved, but the bending strength decreased. The composites with Ti-coated SiC particles outperformed the composites with uncoated SiC particles in both wear resistance and bending strength tests.     

高分数GNFs/6061Al基复合材料的放电等离子体烧结制备及其显微组织与性能

采用放电等离子体烧结(SPS)工艺在610℃制备30％～50％(质量分数)纳米石墨片(GNF)/6061Al基复合材料,研究烧结压力及GNF含量对复合材料显微组织和力学、热学性能的影响.结果表明,SPS有效抑制GNFs/6061Al基复合材料中Al4C3等界面反应产物的生成.随着GNF含量的增加,GNFs团聚程度增加,...     

Cu + TiB2 composite filler for brazing Al2O3 and Ti-6Al-4V alloy

Al₂O₃ and Ti-6Al-4V alloy were brazed using Cu + TiB₂ composite filler, which manufactured by mechanical milling of Cu and TiB₂ powders. Typical interface microstructure of joint was Al₂O₃/Ti₄(Cu,Al)₂O/Ti₂Cu + Ti₃Al + Ti₂(Cu,Al)/Ti₂(Cu,Al) + AlCu₂Ti/Ti₂Cu + AlCu₂Ti + Ti₃Al + Ti₂(Cu,Al) + TiB/Ti(s.s) + Ti₂Cu/Ti-6Al-4V alloy. Based on temperature- and time-dependent compositional change, the formation of intermetallics in joint was basically divided into four stages: formation of interfacial Ti₄(Cu,Al)₂O in Al₂O₃ side, formation of Ti₂Cu, Ti₃Al, TiB, Ti₂Cu, and AlCu₂Ti in layers II and IV, formation of Ti₂(Cu,Al) and AlCu₂Ti in layer III, formation of Ti + Ti₂Cu hypereutectoid organization adjacent to Ti-6Al-4V alloy. TiB in situ synthesized in joint not only acted as low thermal expansion coefficient reinforcement to improve the mechanical properties at room temperature, but also as skeleton ceramic of joint to increase high temperature mechanical properties of Al₂O₃/Ti-6Al-4V alloy joint increasing. When the joint containing 30 vol.% TiB brazed at 930 °C and 10 min of holding time, the maximum room temperature shear strength of joint was 96.76 MPa, and the high temperature shear strength of joint was 115.16 MPa at 800 °C.     

Synthesis and consolidation of TiN/TiB2 ceramic composites via reactive spark plasma sintering

The simultaneous synthesis and densification of TiN/TiB₂ ceramic composites via reactive spark plasma sintering (RSPS) was investigated. Different component ratios (TiH₂/BN (TiN, B)) and heating rates (112.5-300 °C/min) were used to initiate the chemical reaction for TiN/TiB₂ synthesis. The omit RSPS process was revealed to have three stages, which are described separately. The relationships between the RSPS conditions, the microstructure and the properties of sintered ceramic composites were established. A Vickers hardness of 16-25 GPa and a fracture toughness of 4-6.5 MPa m^1/2 were measured for various compositions. Sintered ceramic composites containing 36 wt% TiB₂ with the highest relative density of 97.4 ± 0.4% and an average grain size of 150-550 nm have been obtained.     

Densification of Al-doped ZnO via preliminary heat treatment under external pressure

With the doping of Al in ZnO for the preparation of a bulk transparent conductor target, deteriorations were observed in sinterability and uniformity. The doping of 3 wt% Al resulted in the predominance of open pores after sintering at 1300 °C. Less open pores were observed in the ZnO with 2 wt% Al, but the porosity between the inner and outer regions was not uniform due to the preferential evaporation near the surface. To improve both the sinterability and uniformity, mild (<2 MPa) pressure was applied during the preliminary heat treatment at 900 °C, before pressureless final sintering. The pressed specimens showed increased density and uniformity after the final sintering, which were higher than those of the unpressed specimens. The improvements were particularly noticeable in the 3 wt% Al and at 1250 °C, wherein the conventional densification was not successful.     

Identification of microstructural mechanisms during densification of a TiAl alloy by spark plasma sintering

This work aims at identifying, by coupled scanning and transmission electron microscopy (SEM and TEM) observations, the densification mechanisms occurring when an atomized Ti-47Al-1W-1Re-0.2Si powder is densified by spark plasma sintering (SPS). For this purpose, interruptions of the SPS cycle have been performed to follow the evolution of the microstructure step by step. The powder particles exhibit a classical dendritic microstructure containing a large amount of out-of-equilibrium α phase. During heating-up, the microstructure undergoes successive transformations. At T = 525-875 °C the α phase transforms into γ. The γ phase formed is supersaturated in W and Re. It de-saturates for T above 875 °C by discontinuous precipitation of W and Re-rich B2 phase. Densification takes place for T between 900 °C and 1150 °C by plastic deformation of the powder particles. TEM observations show that the repartition of the plastic deformation is correlated to the dendritic microstructure, and that dynamic recrystallization mechanisms occur. Microstructural phenomena directly resulting from the high currents involved in the SPS process have not been observed.     

Effects of adding yttrium nitrate on the mechanical properties of hot-pressed AlN ceramics

Aluminum nitride (AlN) ceramics were prepared by hot-pressing with Y(NO₃)₃·6H₂O as sintering additive. The mechanical properties including flexural strength, Vickers’ hardness, and fracture toughness were studied. The relative density and mechanical property of the monolithic AlN were improved by adding Y(NO₃)₃·6H₂O, which decreased the porosity. At 2 wt% Y₂O₃, the AlN ceramic exhibited the highest strength of 383 MPa, the highest hardness of 15.39 GPa, and the highest fracture toughness of 3.1 MPa m^1/2. However, doping with more additive, the strength, hardness, and toughness of AlN ceramics decreased because of the weak interfacial bonding between AlN matrix and the yttrium aluminates phase.