TY - JOUR
T1 - Effect of synthesis pressure on hydride phases in Mg-M systems (M = Mn, Y)
AU - Goto, Yasuyuki
AU - Kakuta, Hirofumi
AU - Kamegawa, Atsunori
AU - Takamura, Hitoshi
AU - Okada, Masuo
N1 - Funding Information:
This work has been supported in part by ‘Giant-in-Aids for Scientific Research’ on the Priority Group of ‘New Protium Function’ and on the Priority Group of ‘Platform Science and Technology for Advanced Magnesium Alloys’ from the Ministry of Culture, Science, and Education.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2003/7/1
Y1 - 2003/7/1
N2 - High-pressure synthesis of the hydrides in Mg-M (M = Mn, Y) systems and the influence of applied pressures during synthesis on present phases and their crystal structures have been studied. In Mg-Mn system, it was found that the crystal structure of Mg3MnHy changed from hexagonal structure (a = 0.47107(4) nm and c = 1.0297(1) nm) to monoclinic structure (a = 0.8819(8) nm, b = 0.4658(4) nm, c = 0.4678(5) nm and β = 105.6(1)°) in a pressure range of 3-3.5 GPa. This crystal structural change was reversible with respect to pressure. The Mg3MnHy synthesized under 5 GPa was stable up to around 620 K. From thermogravimetric and fusion extraction analyses, the hydrogen content was determined as Mg3MnH 5.0-5.6. In Mg-Y system, the high-pressure hydride (MgY 2Hy) with yellowish color was synthesized at 1073 K for 2 h under 3 GPa or higher. This phase exhibited an FCC-type structure with a cell parameter of a = 0.516 nm. Its hydrogen content was determined to be about 3.7 mass%, corresponding to a chemical formula of MgY2H7.8. The hydride was partially dehydrogenated at around 600 K, and the amount of hydrogen partially desorbed was 1.4 mass%. The FCC-type structure was stable even after the partial dehydrogenation.
AB - High-pressure synthesis of the hydrides in Mg-M (M = Mn, Y) systems and the influence of applied pressures during synthesis on present phases and their crystal structures have been studied. In Mg-Mn system, it was found that the crystal structure of Mg3MnHy changed from hexagonal structure (a = 0.47107(4) nm and c = 1.0297(1) nm) to monoclinic structure (a = 0.8819(8) nm, b = 0.4658(4) nm, c = 0.4678(5) nm and β = 105.6(1)°) in a pressure range of 3-3.5 GPa. This crystal structural change was reversible with respect to pressure. The Mg3MnHy synthesized under 5 GPa was stable up to around 620 K. From thermogravimetric and fusion extraction analyses, the hydrogen content was determined as Mg3MnH 5.0-5.6. In Mg-Y system, the high-pressure hydride (MgY 2Hy) with yellowish color was synthesized at 1073 K for 2 h under 3 GPa or higher. This phase exhibited an FCC-type structure with a cell parameter of a = 0.516 nm. Its hydrogen content was determined to be about 3.7 mass%, corresponding to a chemical formula of MgY2H7.8. The hydride was partially dehydrogenated at around 600 K, and the amount of hydrogen partially desorbed was 1.4 mass%. The FCC-type structure was stable even after the partial dehydrogenation.
KW - High-pressure hydride
KW - Magnesium-manganese system
KW - Magnesium-yttrium system
KW - Thermal stability
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U2 - 10.1016/S1468-6996(03)00057-3
DO - 10.1016/S1468-6996(03)00057-3
M3 - Article
AN - SCOPUS:0242551670
SN - 1468-6996
VL - 4
SP - 333
EP - 338
JO - Science and Technology of Advanced Materials
JF - Science and Technology of Advanced Materials
IS - 4
ER -