氮化物
氮气
渗氮
材料科学
铁氧体(磁铁)
冶金
溶解度
热力学
化学
复合材料
物理化学
物理
有机化学
图层(电子)
作者
Marcel A.J. Somers,R. M. Lankreijer,E. J. Mittemeijer
标识
DOI:10.1080/01418618908205064
摘要
Abstract On nitriding ferritic Fe-M (M = Ti, V, Cr or Mo) alloys, three types of absorbed nitrogen atoms can be distinguished: (i) nitrogen incorporated in the stoichiometric nitride; (ii) nitrogen adsorbed at the nitride/matrix interface, and (iii) nitrogen dissolved in octahedral interstices of the ferrite lattice. As compared with pure ferrite, enhanced nitrogen lattice solubility is observed for the ferritic matrix of Fe-M alloys. This excess nitrogen can be ascribed to an average lattice dilation induced by the volume misfit between nitrides and matrix. A model is developed for a quantitative description of the amount of excess nitrogen in ferrite. The treatment originates from an application of a theory due to Eshelby, developed originally for the case of elastic distortions by point imperfections, in conjunction with the thermodynamics of stressed solids. The model is applied to published data on excess nitrogen in various Fe-M alloys where coherent nitrides develop. The dependence of the amount of excess nitrogen in Fe-M alloys on the type of alloying element can be explained in terms of an interaction parameter, weighing up the contributions of chemical and strain energy changes occurring on precipitation of nitrides.
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