Abstract
A spontaneous transformation has been observed in thin foils of metastable β-phase (b.c.c.) niobium 16–60% zirconium alloys during electro-polishing. The product has a f.c.c. crystal structure and a plate-like morphology. The transformation is governed by the concentration of both hydrogen, which has to exceed a critical value and zirconium. Consequently the spontaneously formed plates are only stable at room temperature in foils where the zirconium concentration exceeds 40%. The hydride plates have a habit plane close to {133} β and contain either slip dislocations, stacking faults or fine twins on {111} h planes or mixtures of these. The orientation relationship between the hydride plates and the β-matrix corresponds closely with the Kurdjumov-Sachs relationship. Complex interactions between plates result in a further transformation which has been interpreted as a reverse transformation (f.c.c. → b.c.c.). The results have been considered in terms of the phenomenological crystallographic theory for martensite formation. Satisfactory agreement between theory and experiment has been established.
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