An experimental study was carried out to determine the hydrogen concentration limit as a function of temperature at which delayed hydride cracking (DHC) commences in Zr-2.5Nb pressure tube material. For a given hydrogen content of the specimen, two critical temperatures were observed in this work - a DHC initiation temperature, T-c, at which DHC would initiate when approaching the test temperature from above the solvus (or terminal solid solubility) for hydride dissolution (TSSD) and a DHC arrest temperature, T-h, obtained by heating the same specimen from T-c after DHC had started. Both of T-c and T-h are close to, but below, the temperatures defined by TSSD for the specific hydrogen content of the specimen. A theoretical analysis was carried out to quantitatively derive the hydrogen concentration limit and these critical temperatures. The theoretical prediction for T-c depends sensitively on the particular solvus or terminal solid solubility curve for hydride precipitation (TSSP) used, since there is a wide range of values for TSSP depending on the thermal-mechanical history of the material. It is also suggested that T-h is governed by the TSSP for hydride growth, in contrast to T-c, which is governed by the TSSP for hydride nucleation. A model for a previously observed critical temperature (T-A) is also proposed. T-A is a DHC arrest temperature, obtained by approaching the test temperature from a lower temperature. The model suggests that T-A is controlled by the energy difference between TSSD, TSSP and the hydrostatic stress at the crack tip. [References: 16]
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