Abstract
Phase transformation mechanisms in a variety of non-metals can be studied from the point of view of structural aspects and nucleation, and compared with metallurgical classification schemes.(1–3) In a “reconstructive” transformation first coordination bonds or nearest-neighbor interactions are broken and remade when converting to a new structure. Such processes require a high activation energy and are usually slow and sluggish. They proceed by thermally-activated growth across an interface. “Displacive” transformations on the other hand, involve no rupture of first cordinations, but merely a distortion of the crystal lattice. The activation energy is much lower and the kinetics are fast. Displacive transformations are not necessarily martensitic. This has been a frequent source of confusion, evident in the literature. Martensitic transformations are a subset of displacive transformations.(2) A martensitic mechanism is a “lattice-distortive, virtually diffusionless structure change having a dominant deviatoric component and associated shape change, such that strain energy dominates the kinetics and morphology during the transformation.”(2)
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Kriven, W.M. (1986). Displacive Transformation Mechanisms in Zirconia Ceramics and Other Non-Metals. In: Tressler, R.E., Messing, G.L., Pantano, C.G., Newnham, R.E. (eds) Tailoring Multiphase and Composite Ceramics. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-2233-7_18
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DOI: https://doi.org/10.1007/978-1-4613-2233-7_18
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