TY - JOUR
T1 - In-situ synchrotron X-ray diffraction investigation of the hydriding and dehydriding properties of a cast Mg-Ni alloy
AU - Tran, X. Q.
AU - McDonald, S. D.
AU - Gu, Q. F.
AU - Nogita, K.
N1 - Publisher Copyright:
© Elsevier B.V. All rights reserved.
PY - 2015/3
Y1 - 2015/3
N2 - Abstract In previous research, it has been demonstrated that the hydrogenation kinetics of Mg-Ni alloys is significantly improved by elemental Na doping. To clarify the underlying mechanisms in terms of crystallographic phase changes during the reactions, in-situ hydrogen absorption and desorption as a function of temperature under constant hydrogen atmospheres of 2 MPa and 0.2 MPa, respectively, was studied. The experiments were performed at the Powder Diffraction beamline of the Australian Synchrotron facility with a gas flow cell and a hot air blower. This study showed that the hydrogenation of Na-doped Mg-Ni alloys can be identified at a temperature as low as 260 °C via an interface-controlled nucleation and growth mechanism without any prior activation whilst the dehydrogenation occurred at about 370 °C. The sequence of phase transformations associated with these reactions as well as associated expansion properties of individual phases during hydrogen sorption reactions as provided by the high resolution X-ray diffraction data are discussed.
AB - Abstract In previous research, it has been demonstrated that the hydrogenation kinetics of Mg-Ni alloys is significantly improved by elemental Na doping. To clarify the underlying mechanisms in terms of crystallographic phase changes during the reactions, in-situ hydrogen absorption and desorption as a function of temperature under constant hydrogen atmospheres of 2 MPa and 0.2 MPa, respectively, was studied. The experiments were performed at the Powder Diffraction beamline of the Australian Synchrotron facility with a gas flow cell and a hot air blower. This study showed that the hydrogenation of Na-doped Mg-Ni alloys can be identified at a temperature as low as 260 °C via an interface-controlled nucleation and growth mechanism without any prior activation whilst the dehydrogenation occurred at about 370 °C. The sequence of phase transformations associated with these reactions as well as associated expansion properties of individual phases during hydrogen sorption reactions as provided by the high resolution X-ray diffraction data are discussed.
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U2 - 10.1016/j.jallcom.2015.02.044
DO - 10.1016/j.jallcom.2015.02.044
M3 - Article
AN - SCOPUS:84924308898
SN - 0925-8388
VL - 636
SP - 249
EP - 256
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
M1 - 33418
ER -