Comparison of the decomposition and crystallization behavior of Zr and Pd based bulk amorphous alloys

被引:0
|
作者
Löffler, JF
Johnson, WL
Wagner, W
Thiyagarajan, P
机构
[1] CALTECH, WM Keck Lab, Pasadena, CA 91125 USA
[2] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[3] Argonne Natl Lab, Div Intense Pulsed Neutron Source, Argonne, IL 60439 USA
来源
METASTABLE, MECHANICALLY ALLOYED AND NANOCRYSTALLINE MATERIALS, PTS 1 AND 2 | 2000年 / 343-3卷
关键词
bulk amorphous materials; crystallization; glass transition; phase separation; small-angle neutron scattering; undercooled liquid;
D O I
暂无
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The best metallic glass formers known so far are Vit1 (and similar alloys with a slight variation in composition) and Pd40Cu30Ni10P20. having critical cooling rates of about 1 Ws and glass transition temperatures T-g of around 636 K and 582 K, respectively, at a heating rate of 10 K/min. To compare the decomposition and crystallization behavior of these alloys, we performed small-angle neutron scattering (SANS) on the Vit1 derivative Zr42.6Ti12.4Cu11.25Ni10Be23.75 (Vit1A) and on Pd40Cu30Ni10P20 (PCNP) at temperatures near their T-g. The samples of Vit1A show interference peaks when annealed for several hours between 603 K and 643 K, giving evidence for decomposition on the nanometer scale. The SANS intensity monotonically increases in this temperature regime. An in-situ experiment, performed for 15 h at 621 K, with an average acquisition time of 20 min, resolves the time evolution of this decomposition. The SANS experiment on PCNP shows a completely different behavior. An in-situ SANS experiment performed on PCNP for 10 h at 571 K produced no scattering, but the SANS intensity changed drastically when the temperature was raised to 586 K. However, no interference maximum was observed in the SANS data for PCNP. X-ray diffraction data, measured after the in-situ experiments, resolve nanocrystals in Vit1A but a coarse-grained structure in PCNP.
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页码:179 / 184
页数:6
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