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Nitriding of ternary iron-based alloys: metastable mixed nitrides, excess nitrogen and stress-depth profile

机译:三元铁基合金的氮化:亚稳态混合氮化物,过量氮和应力深度分布

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For the first time it could be shown that, upon nitriding Fe-Cr-Al alloys, the thermodynamical stable cubic CrN and hexagonal A1N nitrides do not develop. Instead, a mixed Cr_xAl_(1-x)N nitride develops of rock-salt crystal-structure type exhibiting a Bain orientation relationship with the ferritic matrix: the Al atoms are "dragged" into the developing cubic CrN precipitates. Similar observations were made upon nitriding Fe-Cr-Ti alloys. The formation of these mixed Cr_xAl_(1-x)N precipitates is associated with the incorporation of large amounts of (mobile and immobile) "excess nitrogen" and the development of large residual stresses. Creep, associated with residual stress relaxation, occurs during nitriding, giving rise to complex residual stress-depth profiles.
机译:首次可以证明,在氮化Fe-Cr-Al合金时,没有形成热力学稳定的立方CrN和六方AlN氮化物。相反,混合的Cr_xAl_(1-x)N氮化物形成了盐岩晶体结构类型,与铁素体基体表现出贝恩取向关系:Al原子被“拖延”到正在形成的立方CrN沉淀物中。对Fe-Cr-Ti合金进行渗氮也得到了类似的观察结果。这些混合的Cr_xAl_(1-x)N沉淀物的形成与大量(活动和不活动的)“过量氮”的掺入和大量残余应力的产生有关。在渗氮过程中会发生与残余应力松弛相关的蠕变,从而产生复杂的残余应力深度分布。

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