Investigation on microstructure and internal friction for low density TiB_2/ZL114 composites

TiB2/ZL114 composites with the density of 2.733 g/cm3 were fabricated through reaction of K2TiF4 and KBF4 (LSM method). The composites were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). The internal friction measurements were performed on DTM-Ⅱ-J dynamic modulus damping an-alyzer and the mechanisms were investigated. Experimental results indicate that reinforced particles are well-distributed in the matrix and the internal friction value of TiB2/ZL114 composites is up to a maximum of 9.04x10-3, almost twice that of ZL114. The internal friction results form dislocation vibration within the material,the sliding of grain boundary and phase interface, and together with the micro-plastic deformation caused by difference in coefficients of thermal expansion and elasticity modulus of various phases. The average internal friction values of samples with the sizes of 40 min×4 mm×2 mm, 40 mm×8 mm×2 mm and 40 mm×25 mm×2 mm are 8.83x 10-3, 8.89x 10-3, and 8.93×10-3, respectively. Thus, the developed composites are of low density, high internal friction, and the sizes of samples have no relation to the internal friction behavior.     

Synthesis, microstructure and mechanical properties of reaction-infiltrated TiB2-SiC-Si composites

TiB₂-C preforms formed with different compositions and processing parameters were reactively infiltrated by Si melts at 1450 °C to fabricate TiB₂-SiC-Si composites. Phase constituent and microstructure of these composites were analyzed by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The resulting composites are generally composed of TiB₂ and reaction-formed β-SiC major phases, together with a quantity of residual Si. Unreacted carbon is detected in the samples with a starting composition of 2TiB₂ + 1C formed at higher pressure and in all of the ones at the composition of 1TiB₂ + 1C. The distribution of these phases is fairly homogeneous in microstructure. TiB₂-SiC-Si composites show good mechanical properties, with representative values of 19.9 GPa in hardness, 395 GPa in elastic modulus, 3.5 MPa m^1/2 in fracture toughness and 604 MPa in bending strength. The primary toughening and strengthening mechanism is attributed to the crack deflection of TiB₂ particles.     

Effect of ultrasonic vibration on microstructural evolution of the reinforcements and degassing of in situ TiB2p/Al-12Si-4Cu composites

Some issues such as clustering of TiB₂ particles, formation of long rod-like Al₃Ti particles, as well as high porosity level usually associate with the fabrication of in situ TiB_2p/Al-alloy composites via conventional stir casting technique using Ti and B as reactants. High-intensity ultrasonic vibration was introduced in our research to solve the above issues. The process involved that the original in situ TiB_2p/Al-12Si-4Cu sample with large clusters of TiB₂ particles, large long rod-like Al₃Ti particles and high porosity was remelted at 850 °C, and then ultrasonic vibration was applied to the melt with an ultrasonic probe. The microstructural evolution of the samples treated by ultrasonic vibration with different time was examined by using SEM. After treated by ultrasonic vibration for 12 min, large clusters of TiB₂ particles were broken up effectively and TiB₂ particles were dispersed uniformly in the matrix, and long rod-like Al₃Ti particles were turned into blocky ones with the size of 10 μm due to the effect of ultrasonic stirring. In the meantime, the porosity in the composites decreased from about 6.5% to 0.86% due to the effect of ultrasonic degassing. Microhardness test suggested that a homogeneous microstructure of the composite was achieved after ultrasonic treatment. An effective approach using high-intensity ultrasonic vibration to optimize the microstructures of the particulate reinforced Al-alloy composites was proposed, and the mechanism of the effect of high-intensity ultrasonic vibration on the microstructural evolution of the reinforcements and degassing of composites was also discussed in our research.     

超音速大气等离子喷涂TiB2-SiC涂层的抗氧化性及耐熔盐腐蚀性能

采用超音速大气等离子喷涂制备全包覆TiB₂-SiC涂层,研究了TiB₂-SiC涂层在400和800 ℃的氧化性能,并探究其氧化机理。对TiB₂-SiC涂层在900 ℃下的抗铝熔盐腐蚀性能进行研究,并探讨其耐熔盐腐蚀机理。结果表明,超音速大气等离子喷涂制备的TiB₂-SiC涂层具有良好的抗氧化性,在400 ℃的氧化速率常数为1.92×10^-5 mg²·cm^-4·s^-1,在800 ℃的氧化速率常数为1.82×10^-4 mg²·cm^-4·s^-1。超音速大气等离子喷涂制备的TiB₂-SiC涂层在900 ℃下具有良好的抗熔盐腐蚀性能,熔盐腐蚀后TiB₂-SiC涂层都保持致密结构,未发生涂层的开裂及剥落。     

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.     

自反应电弧喷涂原位合成Ti(C,N)-TiB2-Al2O3复相陶瓷涂层

以Ti+B4C为反应药芯、Al为外皮材料制备反应型喷涂丝材,探讨利用自反应电弧喷涂技术在45钢基体表面制备复相陶瓷涂层的可行性。以X射线衍射仪(XRD)、扫描电子显微镜(SEM)和能谱仪(EDS)等方法分析、观察了涂层的组织与结构,测试了涂层的主要力学性能。结果表明:利用制备的药芯丝材进行喷涂试验,可获得由TiB2、TiB、TiC0.3N0.7、TiN、Al2O3、AlN等多相组成的复相陶瓷涂层。涂层呈典型的层状结构,其连续的基体相内弥散分布着离散的第二、第三相。涂层与基体间的结合强度为18.9MPa,涂层的平均显微硬度与弹性模量分别为735.4HV0.2和461.4GPa,摩擦因数在0.45～0.50之间,耐磨性能较基体材料提高3倍以上。     

Effects of sintering additives on microstructure and mechanical properties of TiB2-WC ceramic-metal composite tool materials

TiB₂-WC ceramic-metal composite tool materials were fabricated using Co, Ni and (Ni, Mo) as sintering additives by vacuum hot-pressing technique. The microstructure and mechanical properties of the composite were investigated. The composite was analyzed by the observations of scanning electron microscope (SEM), X-ray diffraction (XRD) and energy dispersive spectrometry (EDS). The microstructure of TiB₂-WC ceramic-metal composites consisted of the fine WC grains and uniform TiB₂ grains. The brittle phase of Ni₃B₄ and a few pores were found in TiB₂-WC-Ni ceramic-metal composite. A lot of pores and brittle phases such as W₂CoB₂ and Co₂B were formed in TiB₂-WC-Co ceramic-metal composite. The liquid phase of Co was consumed by the reaction which led to the formation of the pores and the coarse grains of TiB₂. The pores, brittle phases and coarse grains of TiB₂ were harmful to the improvement of the mechanical properties of the composite. The sintering additive of (Ni, Mo) had a significant effect on the density and the mechanical properties of TiB₂-WC ceramic-metal composite. The formation of intermetallic compound of MoNi₄ inhibited the consumption of liquid phase of (Ni, Mo). The liquid phase of (Ni, Mo) not only inhibited the formation of the pores and the coarse grains of TiB₂ but also strengthened the interface energy between WC and TiB₂ grains. The grain size was fine and the average relative density of TiB₂-WC-(Ni, Mo) ceramic-metal composite reached 99.1%. The flexural strength, fracture toughness and Vickers hardness of TiB₂-WC-(Ni, Mo) ceramic-metal composite were 1307.0 ± 121.4 MPa, 8.19 ± 0.29 MPa m^1/2 and 22.71 ± 0.82 GPa, respectively.     

Improvement in the corrosion resistance of TiB2/A356 composite by molten-salt electrodeposition and anodization

This study reported a novel treatment to improve the corrosion resistance of TiB₂/A356 composites. The method was employed in combination of the molten-salt electrodeposition and subsequent electrochemical anodization technique. By means of molten-salt electrodeposition, the Al coatings were deposited on the surface of TiB₂/A356 composites. It was found that the morphology of the Al coatings is closely related to the current density. Thus, under the suitable condition, a dense and uniform Al coating can be obtained, with the crystal size in the range of 0.5–2 μm and the coating thickness of ~ 9 μm. This continuous Al layer can eliminate the adverse corrosion contribution of TiB₂ particles in Al matrix. The following step of anodization was designed to convert the Al film to an anodized Al oxide film for further corrosion protection. The electrochemical corrosion behavior was evaluated by potentiodynamic polarization curves and electrochemical impedance spectroscopy. These results showed the corrosion resistance was greatly enhanced in TiB₂/A356 composites with an anodized Al-coating than that of the anodized composites. It is evident that the new treatment of metal electrodeposition in molten salts and following anodization is an effective method of anti-corrosion in composites.     

Ti 元素对B4C/Al复合材料力学性能的改善作用研究

B₄C/Al复合材料是目前最理想的中子吸收材料,广泛用于乏燃料储存。本文利用液态搅拌法制备B₄C/Al复合材料,通过添加Ti元素,探讨了界面反应对材料的界面结构和力学性能的影响。研究发现,Ti元素通过参与界面反应,改变了界面结构,在B₄C颗粒表面形成了紧密结合的纳米TiB₂界面层;Ti的添加消除了界面微裂纹、微孔、分离等缺陷。随着界面反应程度的加强,材料强度提高,尤其反应脱落的纳米TiB₂颗粒作为原位第二强化相进一步增强基体。B₄C/Al复合材料断裂过程表现为韧窝延性断裂;TiB₂界面层增强了B₄C颗粒与基体的结合,断裂行为从B₄C-Al界面脱落转变为B₄C颗粒断裂;但过渡的界面反应会形成微韧窝,引起材料延伸率下降。     

Magnetomechanical properties of epoxy-bonded Sm1−xNdxFe1.55 (0 ≤ x ≤ 0.56) pseudo-1-3 magnetostrictive particulate composites

Pseudo-1-3 magnetostrictive particulate composites consisting of light rare earth (Sm and Nd)-based magnetostrictive Sm_1−xNd_xFe_1.55 particles with the Nd content x of 0-0.56 and randomly distributed sizes of 10-180 μm embedded and aligned in a passive epoxy matrix are fabricated using the particulate volume fraction of 0.5. The quasistatic magnetomechanical properties of the composites are investigated and the results are compared with their monolithic alloys for various x. The composites exhibit similar qualitative trends in properties with the alloys for all x. The Sm_0.92Nd_0.08Fe_1.55 composite shows a large unsaturated magnetostriction λ of −530 ppm at 500 kA/m and a high piezomagnetic coefficient d₃₃ of −2.0 nm/A at 100 kA/m as a result of the magnetocrystalline anisotropy compensation between Sm³⁺ and Nd³⁺ ions in the Sm_0.92Nd_0.08Fe_1.55 alloy.     

Cyclic oxidation behavior of TiAl composites incorporated with TiB2 dispersoids

TiAl alloys incorporated in (0,3,5,10) wt.% TiB₂ dispersoids were manufactured via mechanical alloyingspark plasma sintering (MA-SPS), and their cyclic oxidation characteristics were studied at 800, 900 and 1000°C in air. The cyclic oxidation resistance of the prepared TiAl-TiB₂ composites effectively increased with increases in TiB₂ content. The oxide scale formed consisted of an outer TiO₂ layer, an intermediate Al₂O₃ layer, and an inner (Al₂O₃+TiO₂) mixed layer. The scale adherence was relatively good, and much thinner oxide scales, when compared to TiB₂-free TiAl alloys, were formed on the prepared composites. The incorporated TiB₂ dispersoids oxidized to TiO₂ and B₂O₃ which evaporated during oxidation.     

The Oxidation of TiB2 Particle-Reinforced TiAl Intermetallic Composites

The oxidation kinetics of TiAl alloys with and without (3, 5, 10 wt.%) TiB₂ dispersoids were studied between 1073 and 1273 K in atmospheric air. The inert TiB₂ dispersoids effectively increased the oxidation resistance of TiAl alloys. The higher the TiB₂ dispersoids content, the more pronounced the effect. The oxide scale formed on TiAl–TiB₂ composites was triple-layered, consisting mainly of an outer TiO₂ layer, an intermediate Al₂O₃ layer, and an inner (TiO₂+Al₂O₃) mixed layer. No B₂O₃ was observed within the oxide scale because of its high vapor pressure. A thin Ti₃Al sublayer and discrete TiN particles were found at the oxide–substrate interface. During the oxidation of TiAl alloys with and without TiB₂ dispersoids, titanium ions diffused outwardly to form the outer TiO₂ layer, while oxygen ions transported inwardly to form the inner (TiO₂+Al₂O₃) mixed layer. The increased oxidation resistance by the addition of TiB₂ was attributed to the enhanced alumina-forming tendency and thin and dense scale formation.     

热喷涂TiB2-Ni复合涂层组织结构和力学性能

采用团聚烧结方法制备TiB₂-Ni复合粉末喂料,并采用大气等离子喷涂和高速火焰喷涂两种喷涂方法制备了TiB₂-Ni涂层,比较分析了两种涂层的显微组织、物相组成、孔隙率、硬度和断裂韧性.结果表明,与等离子喷涂相比,高速火焰喷涂制备的TiB₂-Ni涂层具有更高的致密度,TiB₂含量,硬度和断裂韧性.两种涂层中TiB₂都没有发生明显的脱硼,氧化,但等离子喷涂过程中TiB₂向金属相中发生了溶解生成了大量脆性Ni₂₀Ti₃B₆相,并降低了涂层中TiB₂的含量,这是涂层硬度和断裂韧性相对较低的主要原因.     

Thermal and electrical properties of TiB2–MoSi2

The present communication reports the effect of MoSi₂ addition on high temperature thermal conductivity and room temperature (RT) electrical properties of TiB₂. The thermal diffusivity and the thermal conductivity of the hot pressed TiB₂–MoSi₂ samples were measured over a range from room temperature to 1000 °C using the laser-flash technique, while electrical resistivity was measured at RT using a four linear probe method. The reciprocal of thermal diffusivity of TiB₂ samples exhibit linear dependence on temperature and the measured thermal conductivity of TiB₂-2.5% MoSi₂ composites correlate well with the theoretical predictions from Hashin’s model and Hasselman and Johnson’s model. A common observation is that the thermal conductivity of all the samples slightly increases with temperature (up to 200 °C) and then decreases with further increasing temperature. It is interesting to note that both the thermal conductivity and electrical conductivity of TiB₂ samples enhanced with the addition of 2.5 wt.% MoSi₂ sinter additive. Among all the samples, TiB₂-2.5 wt.% MoSi₂ ceramics measured with high thermal conductivity (77 W/mK) and low electrical resistivity (12 μΩ-cm) at room temperature. Such an improvement in properties can be attributed to its high density and low volume fraction of porosity. On the other hand, both the thermal and electrical properties of TiB₂ were adversely affected with further increasing the amount of MoSi₂ (10 wt.%).     

Electromagnetic wave absorption properties of mechanically mixed Nd2Fe14B/C microparticles

Nd₂Fe₁₄B/C microparticles were prepared by a mechanical mixing technique using a weight ratio of 2:1. Paraffin-bonded Nd₂Fe₁₄B/C composites were fabricated using 40 wt% microparticles, and their electromagnetic wave absorption properties were studied and compared with those of the paraffin-bonded Nd₂Fe₁₄B composites in the 2-18 GHz frequency range and for 1-5 mm thickness. The Nd₂Fe₁₄B/C-paraffin composites exhibit dual dielectric resonance in complex relative permittivity (?_r) and essentially flat response in complex relative permeability (μ_r) rather than showing an abrupt change in both ?_r and μ_r as in the Nd₂Fe₁₄B-paraffin composites. The results are ascribed to the increased electrical resistivity in the Nd₂Fe₁₄B/C-paraffin composites and the protection on the magnetic properties of the Nd₂Fe₁₄B microparticles at 2-18 GHz by the presence of the C phase. Large reflection loss (RL) exceeding −10 dB and an optimal RL of −13.2 dB are achieved in the Nd₂Fe₁₄B/C-paraffin composites from 9.6 to 18 GHz at a thickness of 1.4-2.6 mm and at 18 GHz at a thickness of 1.4 mm, respectively.     

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.     

激光热喷涂Co30Cr8W1.6C3Ni1.4Si涂层在PAO+2.5%MoDTC油中摩擦学特性

为了提高TC4合金的耐磨性能,采用激光热喷涂技术在其表面制备了Co₃₀Cr₈W_1.6C₃Ni_1.4Si涂层。通过扫描电子显微镜（SEM）和X射线衍射（XRD）分析了涂层的形貌和物相,并通过摩擦磨损实验研究了涂层在PAO+2.5% MoDTC（质量分数）油中的磨损行为。结果表明,激光热喷涂的Co₃₀Cr₈W_1.6C₃Ni_1.4Si涂层主要由Ti、WC_1-x、CoO、Co₂Ti₄O和CoAl相组成,在涂层界面形成冶金结合。在激光功率为1000、1200和1400 W时所制备的涂层平均摩擦因数分别为0.151、0.120和0.171,其对应的磨损率分别为1.17×10^-6、1.33×10^-6和2.80×10^-6 mm³?N^-1?m^-1,磨损机理为磨粒磨损,其枝晶尺寸对降磨起主要作用。     

Effects of CeO2 additive on the microstructure and mechanical properties of in situ TiB2/Al composite

In this paper, CeO₂ was investigated as an additive for in situ preparation of TiB₂/Al composite using an exothermic reaction process via K₂TiF₆ and KBF₄ salts. Experimental results indicated that when 0.5 wt.% CeO₂ additive was added, the dispersion of TiB₂ particles was improved significantly. Meanwhile, α-Al matrix grain was further refined. Compared with the composite without CeO₂, the ultimate tensile strength, yield strength, elastic modulus and tensile elongation increased by 8%, 7%, 26% and 14%, respectively in as-cast condition, and the tensile fracture behavior of the composite with CeO₂ belonged to a typical ductile fracture with microvoid coalescence.     

FRICTION WELDING OF Zr55Al10Ni5Cu30 BULK METALLIC GLASS

采用摩擦焊对Zr₅₅Al₁₀Ni₅Cu₃₀块体金属玻璃进行了焊接, 当焊机主轴转速为4.0×10³---5.0×10³ r/min, 摩擦压力为80---100 MPa, 摩擦时间为0.2---0.4 s, 顶锻压力和保压时间分别为200 MPa和2 s时, 能够成功实施Zr₅₅Al₁₀Ni₅Cu₃₀金属玻璃的焊接. 用SEM, XRD和TEM观察分析未检测到晶化相, 焊缝处金属仍保持非晶状态. 金属玻璃的塑性在玻璃转变点T_g附近随温度变化很大, 在T_g以上具有良好的塑性变形能力, 这是实施摩擦焊焊接的重要基础.     

The study of NiAl-TiB2 coatings prepared by electro-thermal explosion ultrahigh speed spraying technology

NiAl-TiB₂ composite coatings with 0, 10 and 20 wt.% TiB₂ were synthesized on the Ni-based superalloy substrate using electro-thermal explosion ultrahigh speed spraying technology. The microstructure analysis shows that the coatings consist of submicron grains. The bond between coatings and substrate is metallic cohesion. TiB₂ as a powerful reinforcement is doped in NiAl for increasing its hardness. The isothermal oxidation test is carried out for the composite coatings at 1100 °C in air. The result shows that the oxidation resistance of NiAl coating is higher than that of NiAl-10TiB₂ and NiAl-20TiB₂ coatings. The phases of oxides on the coatings during the process at high temperature have been analyzed by X-ray diffraction. The results show that Al₂O₃ and Cr₂O₃ coexistence on surface of NiAl coating, while Al₂O₃, Cr₂O₃, TiO₂ and a small amount of NiO form on surface of NiAl-10TiB₂ and NiAl-20TiB₂ coatings after oxidation for 4 h.