Institute of Physical Chemistry, University of Vienna, Währingerstrasse 42, A-1090 Wien, Austria.
Inorg Chem. 2011 May 16;50(10):4537-47. doi: 10.1021/ic200245m. Epub 2011 Apr 14.
Ti(2)(Ti(0.16)Ni(0.43)Al(0.41))(3) is a novel compound (labeled as τ(6)) in the Ti-rich region of the Ti-Ni-Al system in a limited temperature range 870 < T < 980 °C. The structure of τ(6)-Ti(2)(Ti,Ni,Al)(3) was solved from a combined analysis of X-ray single crystal and neutron powder diffracton data (space group C2/m, a = 1.85383(7) nm, b = 0.49970(2) nm, c = 0.81511(3) nm, and β = 99.597(3)°). τ(6)-Ti(2)(Ti,Ni,Al)(3) as a variant of the V(2)(Co(0.57)Si(0.43))(3)-type is a combination of slabs of the MgZn(2)-Laves type and slabs of the Zr(4)Al(3)-type forming a tetrahedrally close-packed Frank-Kasper structure with pentagon-triangle main layers. Titanium atoms occupy the vanadium sites, but Ti/Ni/Al atoms randomly share the (Co/Si) sites of V(2)(Co(0.57)Si(0.43))(3). Although τ(6) shows a random replacement on 6 of the 11 atom sites, it has no significant homogeneity range (~1 at. %). The composition of τ(6) changes slightly with temperature. DSC/DTA runs (1 K/min) were not sufficient to define proper reaction temperatures due to slow reaction kinetics. Therefore, phase equilibria related to τ(6) were derived from X-ray powder diffraction in combination with EPMA on alloys, which were annealed at carefully set temperatures and quenched. τ(6) forms from a peritectoid reaction η-(Ti,Al)(2)Ni + τ(3) + α(2) ↔ τ(6) at 980 °C and decomposes in a eutectoid reaction τ(6) ↔ η + τ(4) + α(2) at 870 °C. Both reactions involve the η-(Ti,Al)(2)Ni phase, for which the atom distribution was derived from X-ray single crystal intensity data, revealing Ti/Al randomly sharing the 48f- and 16c-positions in space group Fd3̅m (Ti(2)Ni-type, a = 1.12543(3) nm). There was no residual electron density at the octahedral centers of the crystal structure ruling out impurity stabilization. Phase equilibria involving the τ(6) phase have been established for various temperatures (T = 865, 900, 925, 950, 975 °C, and subsolidus). The reaction isotherms concerning the τ(6) phase have been established and are summarized in a Schultz-Scheil diagram.
Ti(2)(Ti(0.16)Ni(0.43)Al(0.41))(3) 是 Ti-Ni-Al 体系富 Ti 区在有限温度范围内(870 < T < 980°C)的一种新型化合物(标记为 τ(6))。τ(6)-Ti(2)(Ti,Ni,Al)(3) 的结构通过 X 射线单晶和中子粉末衍射数据的综合分析确定(空间群 C2/m,a = 1.85383(7) nm,b = 0.49970(2) nm,c = 0.81511(3) nm,β = 99.597(3)°)。τ(6)-Ti(2)(Ti,Ni,Al)(3) 作为 V(2)(Co(0.57)Si(0.43))(3)-type 的变体,是 MgZn(2)-Laves 型和 Zr(4)Al(3)-type 片层的组合,形成具有五边形-三角形主层的四面体密堆 Frank-Kasper 结构。钛原子占据钒原子的位置,但 Ti/Ni/Al 原子随机共享 V(2)(Co(0.57)Si(0.43))(3) 的(Co/Si)原子位置。尽管 τ(6) 在 11 个原子位置中的 6 个位置上表现出随机取代,但它没有显著的均匀范围(~1 原子%)。τ(6) 的组成随温度略有变化。由于反应动力学缓慢,1 K/min 的 DSC/DTA 运行不足以确定合适的反应温度。因此,τ(6) 相关的相平衡是通过仔细设定温度并淬火的合金的 X 射线粉末衍射和 EPMA 结合推导出来的。τ(6) 从包晶反应 η-(Ti,Al)(2)Ni + τ(3) + α(2) ↔ τ(6) 在 980°C 形成,并在 870°C 时在共晶反应 τ(6) ↔ η + τ(4) + α(2) 中分解。这两个反应都涉及 η-(Ti,Al)(2)Ni 相,其原子分布是从 X 射线单晶强度数据中推导出来的,揭示了 Ti/Al 随机共享空间群 Fd3̅m 中的 48f-和 16c-位置(Ti(2)Ni 型,a = 1.12543(3) nm)。晶体结构的八面体中心没有剩余的电子密度,排除了杂质稳定化的可能性。已经为不同温度(T = 865、900、925、950、975°C 和亚稳区)建立了涉及 τ(6) 相的相平衡。已经建立了有关 τ(6) 相的反应等温线,并总结在舒尔茨-谢勒图中。