Zirconium alloys are widely used in the nuclear industry because of their high strength, good corrosion resistance and low neutron absorption cross-section. Zirconium has a strong affinity for hydrogen, however, and if hydrogen concentration builds up, the material will gradually degrade. In one class of such hydrogen caused degradation, called hydride induced embrittlement, hydrogen chemically reacts with zirconium forming one, or several, crystal phases of zirconium hydride. These hydrides play a primary, but sometime not fully understood, role in crack initiation and propagation within these materials. Despite the fact that hydride induced embrittlement in zirconium have been studied for several decades, there are still some unresolved issues. It has been the aim of the research presented in this thesis to provide the research community with new and updated data of the hydrides themselves in order to aid further studies within the field of hydride induced embrittlement in general, and the mechanism of delayed hydride cracking in particular. To that end, the research presented here proceeded, in short, as follows: First, zirconium hydride powder, of well defined hydrogen concentration, was produced from commercial grade zirconium. This powder was subjected to heat treatment and the hydride phases were characterized both in situ and ex situ using neutron, synchrotron X-ray, and conventional laboratory X-ray based diffraction techniques. Next, most of the low-pressure zirconium hydride phases were produced under hydrogen/argon atmosphere from commercial grade zirconium powder. This process was simultaneously monitored and recorded in real time using synchrotron X-ray diffraction. These experiments have produced new data of the behavior of different hydride phases during thermal treatment and in situ hydrogenation. For the first time all commonly reported zirconium hydride phases and the complete transformation between two different hydride phases were recorded with a single experimental arrangement. The phase transformation between δ and ε zirconium hydride was recorded in detail and presented. Finally, the controversial γ zirconium hydride was observed both in situ and ex situ and the preparation route, its crystal structure, and formation mechanisms were analyzed and presented.

Zirconium alloys are widely used in the nuclear industry because of their high strength, good corrosion resistance and low neutron absorption cross-section. However, zirconium has strong affinity for hydrogen, which may lead to hydrogen concentration build-up over time during a corrosion reaction when exposed to water. Hydrogen stays in solution at higher temperature but precipitates as zirconium hydrides at ambient temperatures. The formation of zirconium hydrides is considered to be a major cause of embrittlement, in particular as a key step in the mechanism of delayed hydride cracking. Despite the fact that zirconium hydrides have been studied for several decades, the basic nature and mechanisms of hydride formation, transformation and exact structure are not yet fully understood. In order to find the answer to some of these problems, the precipitation and dissolution of hydrides in commercial grade Zr powder were monitored in real time with high resolution synchrotron and neutron radiations, and the whole pattern crystal structure analysis, using Rietveld and Pawley refinements, were performed. For the first time all commonly reported zirconium hydride phases and complete reversible transformation between two different Zr-hydride phases were recorded with a single setup and their phase transformation type have been analyzed. In addition, the preparation route of controversial γ-zirconium hydride (ZrH), its crystal structure and formation mechanisms are also discussed.