Experimental investigation of the Mg-Zn-Zr ternary system at 450 degree C
The Mg-Zn-Zr ternary system was experimentally investigated at 450 degree C using six diffusion couples and 16 key alloys. Four new ternary compounds, IM1, IM2, IM3 and IM4 were detected. The compositions, homogeneity ranges, phase relationships and the X-ray diffraction patterns of these compounds...
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Published in | Journal of alloys and compounds Vol. 680; pp. 212 - 225 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
25.09.2016
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Subjects | |
Online Access | Get full text |
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Summary: | The Mg-Zn-Zr ternary system was experimentally investigated at 450 degree C using six diffusion couples and 16 key alloys. Four new ternary compounds, IM1, IM2, IM3 and IM4 were detected. The compositions, homogeneity ranges, phase relationships and the X-ray diffraction patterns of these compounds were identified using scanning electron microscopy coupled with energy-dispersive x-ray spectrometer and x-ray diffraction techniques. The homogeneity ranges of IM1, IM2, IM3 and IM4 are Mg sub((23-26))Zn sub(66)Zr sub((8-11)), Mg sub((15-16))Zn sub(66)Zr sub((18-19)), Mg sub((10-11))Zn sub(66)Zr sub((23-24)), and Mg sub((9-13))Zn sub((79-87))Zr sub((5-8)), respectively. IM1 compound crystallizes in an MgZn sub(2) structure type with hexagonal structure and P6 sub(3)/mmc space group. The Mg-Zn and Zn-Zr binary compounds do not have extended solid solubility into the ternary system. The phase boundaries of Mg-Zn-Zr liquid phase at 450 degree C were determined by several key alloys. The single phase liquid region extended into the ternary phase diagram only to around 1 at.% Zr. However, phase regions containing liquid along with other phases existed in the vicinity of the Mg-Zn side up to 10 at% Zr. Based on the current experimental results, the isothermal section of the Mg-Zn-Zr ternary system at 450 degree C was constructed. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 0925-8388 |
DOI: | 10.1016/j.jallcom.2016.04.081 |