Metallic glass formation in multicomponent (Ti, Zr, Hf, Nb)–(Ni, Cu, Ag)–Al alloys
A wide range of novel multicomponent amorphous alloys have been manufactured by a new method of equiatomic substitution for the early and late transition metals in Zr-based amorphous alloys. (Ti 33Zr 33Hf 33) 90− x (Ni 50Cu 50) x Al 10, (Ti 33Zr 33Hf 33) 90− x (Ni 33Cu 33Ag 33) x Al 10, (Ti 25Zr 25H...
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Veröffentlicht in: | Journal of non-crystalline solids 2003-03, Vol.317 (1), p.17-22 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A wide range of novel multicomponent amorphous alloys have been manufactured by a new method of equiatomic substitution for the early and late transition metals in Zr-based amorphous alloys. (Ti
33Zr
33Hf
33)
90−
x
(Ni
50Cu
50)
x
Al
10, (Ti
33Zr
33Hf
33)
90−
x
(Ni
33Cu
33Ag
33)
x
Al
10, (Ti
25Zr
25Hf
25Nb
25)
90−
x
(Ni
50Cu
50)
x
Al
10 and (Ti
25 Zr
25Hf
25Nb
25)
90−
x
(Ni
33Cu
33Ag
33)
x
Al
10 alloys with composition range
x=20–70 at.% have been prepared by melt-spinning and the range of glass formation characterized by X-ray diffraction and differential scanning calorimetry. Amorphous alloys were formed over the composition range
x=20–70 at.% for the (Ti
33Zr
33Hf
33)
90−
x
(Ni
50Cu
50)
x
Al
10 and (Ti
25Zr
25Hf
25Nb
25)
90−
x
(Ni
50Cu
50)
x
Al
10 alloys. Addition of Nb with a higher melting point than Ti, Zr and Hf increased the thermal stability of the amorphous phase for the whole composition range
x=20–70 at.%. The most stable amorphous alloy was (Ti
33Zr
33Hf
33)
40(Ni
50Cu
50)
50Al
10 with a crystallisation temperature of
T
x
=545 °C. Addition of Ag decreased the composition range of the amorphous phase to
x=20–40 at.% for the (Ti
33Zr
33Hf
33)
90−
x
(Ni
33Cu
33Ag
33)
x
Al
10 and (Ti
25Zr
25Hf
25Nb
25)
90−
x
(Ni
33Cu
33Ag
33)
x
Al
10 alloys. However the amorphous alloy with the largest supercooled liquid region was (Ti
33Zr
33Hf
33)
50(Ni
33Cu
33Ag
33)
40Al
10 with a crystallisation–glass transition temperature difference of
T
x
−
T
g=103 °C. |
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ISSN: | 0022-3093 1873-4812 |
DOI: | 10.1016/S0022-3093(02)02002-1 |