In-situ time resolved X-ray diffraction study of the formation of the nanocrystalline NbAl3 phase by mechanically activated self-propagating high-temperature synthesis reaction

被引:55
作者
Gauthier, V
Bernard, F
Gaffet, E
Josse, C
Larpin, JP
机构
[1] Univ Bourgogne, CNRS, UMR 5613, Lab Rech React Solides, F-21078 Dijon, France
[2] Univ Technol Belfort Montbeliard, CNRS, UPR A0806, Far Equilibrium Phase Transit Grp, F-90010 Belfort, France
来源
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING | 1999年 / 272卷 / 02期
关键词
mechanical activation; NbAl3; nanostructured intermetallic; self-propagating high-temperature synthesis; in-situ time resolved X-ray diffraction;
D O I
10.1016/S0921-5093(99)00488-8
中图分类号
TB3 [工程材料学];
学科分类号
0805 [材料科学与工程]; 080502 [材料学];
摘要
The mechanically activated self-propagating high-temperature synthesis (MASHS) technique was used to produce a NbAl3 intermetallic compound. This process results from the combination of two steps: a mechanical activation of the Nb + 3Al powder mixture which is followed by a self-propagating high-temperature synthesis (SHS) reaction, induced by the exothermal character of the reaction Nb + 3Al. An original experiment was designed to study in-situ the formation of the NbAl3 phase in the combustion front: time-resolved X-ray diffraction coupled with an infrared imaging technique and a thermocouple measurement were performed to monitor the structural and thermal evolution during the SHS reaction. Owing to the temporal resolution of 100 ms between two consecutive diffraction patterns, it was possible to observe several steps before obtaining the niobium aluminide compound. Indeed, the phase transformations corresponding to the aluminum melting plateau, the subsequent temperature increase to the ignition temperature, and the fast reaction between niobium and molten aluminum at such a temperature were well-identified. The NbAl3 intermetallic compound resulting from the MASHS process is nanostructured. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:334 / 341
页数:8
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