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首页> 外文期刊>Materials >The Evolution of Complex Carbide Precipitates in a Low Alloy Cr–Mo–V Steel after Long-Term Aging Treatment
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The Evolution of Complex Carbide Precipitates in a Low Alloy Cr–Mo–V Steel after Long-Term Aging Treatment

机译:长期时效处理后低合金Cr-Mo-V钢中复合碳化物的析出

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Complex carbide precipitates in a quenched and tempered low alloy Cr–Mo–V steel after long-term aging at 650 °C for 13,000 h and 30,000 h were investigated in this study. The mass fraction and sizes of precipitates were quantified by electrolytical extraction technique. The types of precipitate were further studied by combined X-ray diffraction and transmission electron microscopy with selected area electron diffraction and energy dispersive spectrometry. A series of carbide precipitates, namely MC, M 7 C 3 , M 6 C, and M 2 C, were found existing in the near-equilibrium state. The precipitate sequence of these carbides was identified as MC + M 7 C 3 + M 2 C → MC + M 2 C + M 7 C 3 + M 6 C → MC + M 7 C 3 + M 6 C. It was clarified that the stable phases for the investigated steel aged at 650 °C were composed of MC, M 7 C 3 , and M 6 C. For the first time, the in-situ transformations of M 2 C to M 6 C and M 7 C 3 to M 6 C were directly observed. It was also observed that the nucleation site of the M 6 C was located at the interface of M 7 C 3 carbides and the matrix. The orientation relationships between the secondary phases of the in-situ transforming carbides aged for 13,000 h and 30,000 h at 650 °C were established. The coherent interfaces between these secondary phases became incoherent with prolonged aging treatment due to the exerted strain field of the growing carbides.
机译:在本研究中,研究了在650°C长期老化13,000 h和30,000 h后,在调质低合金Cr-Mo-V钢中的复杂碳化物沉淀。沉淀物的质量分数和大小通过电解萃取技术定量。通过结合X射线衍射和透射电子显微镜以及选择区域电子衍射和能量色散光谱法进一步研究了沉淀物的类型。发现一系列碳化物沉淀,即MC,M 7 C 3,M 6 C和M 2 C处于接近平衡状态。将这些碳化物的析出顺序确定为MC + M 7 C 3 + M 2 C→MC + M 2 C + M 7 C 3 + M 6 C→MC + M 7 C 3 + M 6C。被研究钢在650°C时的稳定相由MC,M 7 C 3和M 6 C组成。这是首次将M 2 C原位转变为M 6 C和M 7 C 3直接观察到M 6 C至M 6C。还观察到,M 6 C的成核位点位于M 7 C 3碳化物与基体的界面。建立了在650°C时效13000 h和30,000 h的原位相变碳化物的第二相之间的取向关系。这些二级相之间的相干界面由于碳化物的不断增加的应变场而随着长时间的时效处理变得不相干。

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