Abstract

The effect of heat treatments on delayed hydride cracking (DHC) in Zr-2.5 wt pct Nb has been studied. Crack velocities were measured in hydrided specimens, which were cooled from solution-treatment temperatures at different rates by water-quenching, oil-quenching, liquid-nitrogen quenching, and furnace cooling. The resulting hydride size, morphology, and distributions were examined by optical metallography. It was found that fast cooling rates, which produce very finely dispersed hydrides, result in higher crack growth rates and a stronger dependence of the crack velocity on the applied-stress intensity factor. Also, the incubation period before cracking commences was found to be relatively short for specimens with fine hydrides, whereas specimens with coarse hydrides required considerably longer incubation periods. These results can be explained by rapid growth of preexisting hydrides within the crack-tip plastic zone. In addition, different solution temperatures were used to investigate the effect of the continuity of the grain-boundary phase(β-phase) on the crack velocity. Transmission electron microscopy was used to examine the structure of this grain-boundary phase. It was found that for heat treatments, which destroyed theβ-phase continuity, the crack velocity was significantly reduced, as would be expected from the theory of enhanced diffusion through grain boundaries.

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