Mechanism of solid-gas reaction for formation of metastable niobium-nitride alloy powders by reactive ball milling

IF 0.7 4区 材料科学 Q4 METALLURGY & METALLURGICAL ENGINEERING
El Sherif, K. Sumiyama, K. Aoki, T. Masumoto, Kenji Suzuki
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引用次数: 32

Abstract

We report on the formation of a new metastable phase of niobium-nitride (Nb-N) alloy powders. This nonequilibrium phase has been synthesized by milling elemental niobium (Nb) powders under purified nitrogen gas flow using a high energy ball mill at room temperature. The progress of the solid-gas reaction for the Nb-N system has been followed by means of x-ray diffraction, differential thermal analysis, transmission electron microscopy, and chemical analysis. After 720 ks of milling, the initial bcc-Nb is completely transformed to nonequilibrium-fcc-NbN containing about 50 at. % N. The lattice parameter of the end product fcc-NbN was calculated to be 0.433 nm. In addition, the particle and grain sizes of the completely reacted alloy powders are 3 μm and 5 nm, respectively. This transforms to a mixture of hcp-Nb_4N_3 and hcp-NbN at the high temperatures, as high as 1150 K.
反应球磨形成亚稳氮化铌合金粉末的固气反应机理
本文报道了氮化铌(Nb-N)合金粉末亚稳相的形成。采用高能球磨机在纯净氮气流下,在室温条件下对铌粉进行研磨,合成了这种非平衡相。通过x射线衍射、差热分析、透射电镜和化学分析等手段跟踪了Nb-N体系固气反应的进展。铣削720 ks后,初始bcc-Nb完全转变为含有约50 at的非平衡态fcc- nbn。计算得到最终产物fcc-NbN的晶格参数为0.433 nm。完全反应合金粉末的粒径为3 μm,晶粒尺寸为5 nm。在高达1150 K的高温下转变为hcp-Nb_4N_3和hcp-NbN的混合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.30
自引率
12.50%
发文量
119
审稿时长
6.4 months
期刊介绍: The International Journal of Materials Research (IJMR) publishes original high quality experimental and theoretical papers and reviews on basic and applied research in the field of materials science and engineering, with focus on synthesis, processing, constitution, and properties of all classes of materials. Particular emphasis is placed on microstructural design, phase relations, computational thermodynamics, and kinetics at the nano to macro scale. Contributions may also focus on progress in advanced characterization techniques. All articles are subject to thorough, independent peer review.
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