首页> 外文会议>Symposium on Supercooled Liquid, Bulk Glassy and Nanocrystalline States of Alloys Nov 27-30, 2000, Boston, Massachusetts, U.S.A. >Formation of Nano Icosahedral Quasicrystalline Phase in Zr-based Binary and Ternary Glassy Alloys
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Formation of Nano Icosahedral Quasicrystalline Phase in Zr-based Binary and Ternary Glassy Alloys

机译:Zr基二元和三元玻璃态合金中纳米二十面体准晶相的形成

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It is found that a nano icosahedral phase with diameters below 50 nm is formed as a primary phase in the Zr_(70)Ni_(10)M_(20), Zr_(70)TM_(10)Pd_(20), Zr_(70)Au_(10)Pd_(20) and Zr_(75)Pt_(10)Pd_(15) ternary and Zr_(70)Pd_(30) binary glassy alloys. The nanoscale icosahedral phase in the diameter range below 10 nm was also found to be formed directly in the melt-spun Zr_(80)Pt_(20) binary alloy. These icosahedral phases transform to the crystalline phase(s) at the higher annealing temperature. The nucleation kinetics for the precipitation of the icosahedral phase from supercooled liquid were examined in the Zr_(70)Pd_(30) and Zr_(70)Ni_(10)Pd_(20) glassy alloys. It was clarified that the transformation of both alloys proceeds in the diffusion-controlled growth mode with increasing nucleation rate. The formation of the nanometer-scale icosahedral phase is due to the transformation mode. The activation energy of nucleation is evaluated to be 267 kJmol~(-1) for the binary alloy and 311 kJmol~(-1) for the ternary alloy. The difference between the two alloy systems seems to originate from the difference in the number of atoms for rearrangements in the nucleation mode. The short-range ordering is observed in the as-quenched Zr_(70)Pd_(30) glassy alloy, which is indicative of the icosahedral structure. The formation of the nano-scale icosahedral phase in the Zr-based binary and ternary alloys is due to the existence of an icosahedral short-range order in the glassy or liquid state. It is suggested that the icosahedral short-range order is stabilized by the restraint of the long-range atomic rearrangements that lead to the transition to a periodic structure by the strong chemical affinities of Pd or Pt with Zr.
机译:发现在Zr_(70)Ni_(10)M_(20),Zr_(70)TM_(10)Pd_(20),Zr_(70)中形成直径小于50nm的纳米二十面体相作为主相Au_(10)Pd_(20)和Zr_(75)Pt_(10)Pd_(15)三元和Zr_(70)Pd_(30)二元玻璃态合金。还发现在熔融纺丝的Zr_(80)Pt_(20)二元合金中直接形成了直径范围在10 nm以下的纳米二十面体相。这些二十面体相在较高的退火温度下转变为结晶相。在Zr_(70)Pd_(30)和Zr_(70)Ni_(10)Pd_(20)玻璃态合金中检查了从过冷液体中析出二十面体相的形核动力学。可以明确的是,两种合金的相变都随着成核速率的增加而以扩散控制的生长模式进行。纳米级二十面体相的形成归因于转变模式。二元合金的成核活化能估计为267 kJmol〜(-1),三元合金的成核活化能为311 kJmol〜(-1)。两种合金体系之间的差异似乎源自成核模式下重排原子数的差异。在淬火后的Zr_(70)Pd_(30)玻璃态合金中观察到短程有序,这表明是二十面体结构。 Zr基二元和三元合金中纳米级二十面体相的形成是由于存在玻璃态或液态的二十面体短程有序。建议通过限制远距离原子的重排来稳定二十面体的近距离有序,而远距离原子的重排可以通过Pd或Pt与Zr的强化学亲和力导致过渡到周期性结构。

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