钛铝固相反应中金属间化合物的形成顺序及反应层生长动力学

A. Kar, S. Kailas, S. Suwas
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引用次数: 18

摘要

摘要了解不同材料搅拌摩擦焊(FSW)中金属间化合物形成的反应动力学以及不同温度下固相反应产物演化的机理,对于选择最佳操作条件控制金属间化合物的产生具有重要意义。本文研究了Ti和Al在固相反应过程中金属间化合物的演化顺序和反应动力学。发现Al和Ti的机械混合影响了反应层(RL)和金属间化合物的演化。RL的厚度随反应温度的升高而增加,在较高温度(650℃)下形成的有序相只有三铝化钛(Al3Ti)。与常规焊接相比,反应层生长的活化能明显降低。这些金属间化合物的形成顺序是基于动力学和热力学原理,如相互扩散和形成自由能。FSW过程中发生的机械混合导致的Al/Ti界面化学计量的变化以及Al和Ti通过反应层的扩散率的差异被认为是这些层相演化和生长的原因。反应活化能降低的机理是材料的破碎、机械混合、位错和孪晶的发展、剧烈变形引起的原子活化和晶界扩散。
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Formation Sequence of Intermetallics and Kinetics of Reaction Layer Growth During Solid State Reaction between Titanium and Aluminum
Abstract Understanding on the reaction kinetics associated with the formation of intermetallic compounds and the mechanisms involved in evolution of the reaction product at different temperatures due to solid state reaction in Friction Stir Welding (FSW) of dissimilar materials is very important in selecting optimum operating condition to control intermetallic compounds for safety-critical applications. In this study, the evolution sequence of intermetallic compounds and reaction kinetics during the solid state reaction between Ti and Al has been investigated. It was found that the mechanical mixing of Al and Ti affects evolution of reaction layers (RL) and intermetallic compounds. The thickness of the RL increases with reaction temperature and titanium trialuminide (Al3Ti) was found to be the only ordered phase that is formed at a higher temperature (650 °C). The activation energy for the growth of the reaction layer was found to be significantly lower when compared to conventional welding. The sequence of formation of these intermetallic compounds is proposed based on kinetics and thermodynamic principles such as inter-diffusion and free energy of formation. The variation in stoichiometry at the Al/Ti interfaces due to mechanical mixing as occurred during FSW and difference in diffusivity of Al and Ti through reaction layers are considered responsible for the phase evolution and growth of these layers. The mechanism of the reaction with the reduced activation energy was attributed to fragmentation, mechanical mixing, development of dislocation and twinning in materials, activation of atoms due to severe deformation and grain boundary diffusion.
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