Microstructure and formation mechanisms of δ-hydrides in variable grain size Zircaloy-4 studied by electron backscatter diffraction
Abstract
Microstructure and crystallography of δ phase hydrides in as-received fine grain and 'blocky' alpha large grain Zircaloy-4 (average grain size ~11 μm and >200 μm, respectively) were examined using electron backscatter diffraction. Results suggest that the the matrix-hydride orientation relationship is 0001α||111δ;<11-20>α||<110>δ for all the cases studied. The habit plane of intragranular hydrides and some intergranular hydrides has been found to be 10-17 of the surrounding matrix. The morphology of intergranular hydrides can vary depending upon the angle between the grain boundary and the hydride habit plane. The misfit strain between α-Zr and δ-hydride is accommodated by high density of dislocations and twin structures in the hydrides, and a mechanism of twin formation in the hydrides has been proposed. The growth of hydrides across grain boundaries is achieved through an auto-catalytic manner similar to the growth pattern of intragranular hydrides. Easy collective shear along <1-100> makes it possible for hydride nucleation at any grain boundaries, while the process seems to favour grain boundaries with low (<40) and high (>80) c-axis misorientation angles. Moreover, the angle between the grain boundary and the adjacent basal planes does not influence the propensity for hydride nucleation.
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