TY - JOUR
T1 - Identification and quantification of hydride phases in Zircaloy-4 cladding using synchrotron X-ray diffraction
AU - Daum, R. S.
AU - Chu, Y. S.
AU - Motta, A. T.
N1 - Funding Information:
The authors would like to acknowledge Yong Yan and Yuncheng Zhong of Argonne National Laboratory for their assistance with the experimental work of this study. The authors also acknowledge helpful discussions with D. Koss. The authors also thank NDC, Areva and Sandvik for supplying the hydrided Zircaloy and Zircaloy samples used in this study. This research was supported by US Nuclear Regulatory Commission, Office of Nuclear Regulatory Research. Usage of the Advanced Photon Source was supported by the US Department of Energy, Office of Basic Energy Sciences under Contract No. DE-AC02-06CH11357.
Funding Information:
The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory (‘Argonne’). Argonne, a US Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357. The US Government retains for itself, and others acting on its behalf, a paid-up nonexclusive, irrevocable worldwide license in said article to reproduce, prepare derivative works, distribute copies to the public, and perform publicly and display publicly, by or on behalf of the Government.
PY - 2009/8/1
Y1 - 2009/8/1
N2 - Zirconium hydrides precipitate in fuel cladding alloys as a result of hydrogen uptake from the high-temperature corrosion environment of light water reactors. Synchrotron X-ray diffraction was performed at room temperature on stress-relieved Zircaloy-4 cladding with two distributions of hydrides - (1) uniformly distributed hydrides across the entire cladding wall and (2) hydride rim next to the outer surface. The δ-hydride phase was found to be the predominant hydride phase to precipitate for hydrogen contents up to 1250 weight parts per million (wt ppm). At a higher content, about 3000 wt ppm, although δ-hydride is still the majority phase, a significant amount of γ-hydride is also observed. At even higher hydrogen contents, in excess of approximately 6000 wt ppm, such as can occur in a highly dense hydride layer, peaks associated with the ε-hydride phase are also observed in the diffraction pattern. The volume fraction of hydrides was estimated as a function of hydrogen content using the integrated intensities of select diffraction peaks corresponding to the α-Zr matrix and the hydride phases. These estimated values agree well with calculated values from the independently measured concentrations. The results of this study indicate that hydride precipitation in Zircaloy-4 is a complex process of evolving hydride phases with increasing local hydrogen content.
AB - Zirconium hydrides precipitate in fuel cladding alloys as a result of hydrogen uptake from the high-temperature corrosion environment of light water reactors. Synchrotron X-ray diffraction was performed at room temperature on stress-relieved Zircaloy-4 cladding with two distributions of hydrides - (1) uniformly distributed hydrides across the entire cladding wall and (2) hydride rim next to the outer surface. The δ-hydride phase was found to be the predominant hydride phase to precipitate for hydrogen contents up to 1250 weight parts per million (wt ppm). At a higher content, about 3000 wt ppm, although δ-hydride is still the majority phase, a significant amount of γ-hydride is also observed. At even higher hydrogen contents, in excess of approximately 6000 wt ppm, such as can occur in a highly dense hydride layer, peaks associated with the ε-hydride phase are also observed in the diffraction pattern. The volume fraction of hydrides was estimated as a function of hydrogen content using the integrated intensities of select diffraction peaks corresponding to the α-Zr matrix and the hydride phases. These estimated values agree well with calculated values from the independently measured concentrations. The results of this study indicate that hydride precipitation in Zircaloy-4 is a complex process of evolving hydride phases with increasing local hydrogen content.
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U2 - 10.1016/j.jnucmat.2009.04.004
DO - 10.1016/j.jnucmat.2009.04.004
M3 - Article
AN - SCOPUS:67651003296
SN - 0022-3115
VL - 392
SP - 453
EP - 463
JO - Journal of Nuclear Materials
JF - Journal of Nuclear Materials
IS - 3
ER -