Ti-xCr-yCu钛基材料的制备及组织性能研究

通过粉末冶金法制备了Ti-xCr、Ti-yCu及Ti-xCr-yCu钛基材料,研究了Cr、Cu含量对其相组成、显微组织、压缩屈服强度、弹性模量以及切削加工性能的影响规律。结果表明:随Cr含量的增加,Ti-xCr钛基材料依次出现了Ti_4Cr、TiCr_2及Cr相,其压缩屈服强度表现出先增大后减小的趋势,当Cr含量为10%时其屈服强度达到最大值(710 MPa),同时,添加Cr元素有利于降低钛基材料的弹性模量,最低可达25 GPa。添加Cu元素的钛基材料,随Cu含量的增加,Ti_2Cu相增加,并且显微组织细化,屈服强度降低;弹性模量受Cu含量影响较小而受烧结温度影响较大。添加Cr和Cu元素的钛基材料,其显微组织主要为网篮组织,弹性模量低于纯钛,其中添加Cu元素有利于细化层片,添加Cr元素有利于细化等轴组织。此外,Cr含量为5%时,钛基材料具有较佳的切削加工性能。     

Oxidation‐led decomposition of hexagonal boron nitride coatings on alloy substrates at 900 °C: Ti‐6Al‐4V

Hexagonal boron nitride (h‐BN) coatings on Ti‐6Al‐4V substrates undergo complete decomposition in air at 900 °C. This fate is similar to that of this ceramic material on chromia‐former alloys, and unlike that of a mass of powder treated in isolation. As the ceramic and alloy oxidize concurrently, outwardly diffusing aluminum (III) ions but not the predominant titanium (IV) ions react with the boron trioxide that forms around the h‐BN basal plane peripheries. Resultant aluminum borate is incorporated into the growing scale and the boron trioxide diffusion barrier is depleted. By this mechanism, the oxidation of h‐BN is maintained at an enhanced rate, until both this material and its oxide completely decompose. Liberated nitrogen from the oxidation of h‐BN can enter the underlying scale as a randomly distributed solute in rutile solid solution. The post‐coating oxide‐atmosphere interface comprises elongated aluminum borate crystallites protruding through at the boundaries between 3–5 at% nitrogen‐doped rutile grains. It differs significantly from that of oxidized, uncoated Ti‐6Al‐4V, which is occupied by a thin α‐alumina layer atop rutile. This interface does not change with an additional 72 h of heat‐treatment.     

The isothermal reduction kinetics of chromium-bearing vanadium–titanium magnetite sinter

The reduction of chromium-bearing vanadium–titanium magnetite sinter (CVTMS) by CO was investigated at 1123–1223?K. The reduction degree increased with increasing temperature. The isothermal reduction kinetics of CVTMS was analysed, according to Sharp analysis and ln–ln analysis, the kinetic mechanism of reduction process for all samples in different basicity can be represented as f(α)?=?1.61(1?α)[?ln(1?α)]^1–1/1.61. The reaction activation energy of all samples (R?=?1.9, 2.1, 2.3, obtained according to the components of the materials burdening used in sintering process) at different reaction degrees were calculated by the model-free method. And the pre-exponential factors of reaction also were calculated by the mathematical method. The rate controlling step for the reduction process under the present reduction condition was chemical reaction.     

激光立体成形TC4钛合金的热力场演化

激光立体成形能够实现高性能复杂零件的精确成形，但成形过程中的高温度梯度极易导致残余应力和变形，最终影响构件的几何精度和力学性能。通过搭建基板单边夹持原位热变形测量系统，探究了多道多层TC4钛合金成形件在激光立体成形过程中基板温度、变形的演化规律，分析了不同扫描策略对构件热应力场的影响。研究结果表明，构件的变形发展受其热历史驱使，扫描策略对成形件的热变形具有显著影响。     

轧制与退火对T9S钛合金板材组织与性能的影响

研究了轧制变形量及退火温度对T9S钛合金板材显微组织和室温力学性能的影响。结果表明:增加成品轧制变形量,板材组织破碎更充分,退火后形成等轴α相、拉长α相和晶间β相组织形貌,变形流线比较明显,板材室温强度和硬度升高,伸长率降低,弹性模量增加。随着退火温度升高,板材室温强度和硬度逐渐降低,伸长率逐渐提高,横向弹性模量逐渐减小,纵向弹性模量先增加后减小。经(750~790) ℃×45 min空冷退火处理后的板材可以获得较好的强度和塑性的匹配。     

Synthesis and performance of TiB2–B4C composites by high pressure of TiC–B mixture

TiB₂–B₄C composites were in situ synthesized and consolidated by high pressure synthesis method from a mixture of TiC and B powders at the pressure and temperature of 5.0 GPa and 1500℃-1900℃. The phase composition, microstructure, density, hardness, thermal conductivity, and electrical resistivity of TiB₂–B₄C composites were analyzed. As the increase in the synthesis temperature, the products were TiB₂ and B₄C phases and that crystallinity improved. TiB₂–B₄C composites were dense without obvious pores. TiB₂–B₄C composites synthesized at 1800℃ obtained the optimized performance, including the relative density of 98.2%, the Vickers hardness of 31.7 ± 1.2 GPa with the load of 9.8 N, the thermal conductivity of 30.3 ± 0.7 W/(m K), and the electrical resistivity of 3.3 × 10⁻³ Ω cm, respectively. The grain size of the TiB₂–B₄C composites changed with the increase in synthesis temperature, leading to the changes in hardness, thermal conductivity, and electrical resistivity.     

柔性钙钛矿太阳能电池的制备及性能研究

采用钛箔作为衬底,原位生长二氧化钛薄膜,然后制备有机钙钛矿吸收层及固态空穴传输层,组装成太阳能电池。通过电压-电流曲线测试,结果表明,这种钙钛矿太阳能电池的光生电压达到0.8 V、光生电流达到16 mA/cm²、光电转化效率为10.2%。进一步对电池进行弯折试验,弯折20次后,光电转化效率能达到初始值的85%,表现出良好的柔性特征。     

Effects of hydrogen content on powder metallurgy characteristic of titanium hydrides

The titanium dihydride (TiH₂) powder metallurgy has been attracted a lot of attention, but TiH₂ powder is difficult to press moulding. In this paper, the titanium hydride powder metallurgy including TiH₂ and unsaturated titanium hydrides (TiH_1.5) was investigated simultaneously compared with pure titanium metal powder metallurgy. The results indicates that the titanium hydride powder metallurgy is accompanied by the deoxidation self-purification effect during dehydrogenation process for both of TiH₂ and TiH_1.5, which have higher sintering density than pure titanium. There are the three stages relative to densification rate, namely the slow, rapid and full densification stages for all of three materials. The compressive yield strengths increase rapidly in the rapid densification stage and are unchangeable almost in the full densification stage after holding 2 h at 1300 °C. The titanium hydride powder metallurgy is helpful to obtain much better mechanical properties than the pure titanium metal powder metallurgy. Here the compressive yield strength of the as-sintered TiH₂ compact with the maximum hydrogen content is the best but has very small difference compared with that of the as-sintered TiH_1.5 compact after full sintering densification.     

Precipitation location of secondary phase and microstructural evolution during static recrystallization of as-cast Ti-25V-15Cr-0.3Si titanium alloy

The microstructural evolution and precipitation location of the secondary phase of an as-cast Ti-25V-15Cr-0.3Si titanium alloy were investigated via isothermal compression experiments and heat treatment. The average aspect (length-to-width) ratio, average area and size of the grains at different heat treatment temperatures and holding time were analyzed and the effects of deformation and annealing time on the grain area and size were considered. It was found that the grain size was strongly influenced by the height reduction and holding time. Grain growth was significant when annealing time increased from 10 min to 2 h at 950 °C and height reduction of 30%; however, grain growth was minimal at annealing time between 2 and 4 h. Many dispersion particles were observed to form in continuous chains; the precipitation location was confirmed to be along initial grain boundaries, and the dispersion particles were identified to be Ti₅Si₃ phase by TEM.