Fabrication of Alloyed Aluminum Nickelides by Metallothermy
of Metals Oxides
V. V. Gostishcheva,*, I. A. Astapova,b,**, A. V. Mednevab,***,
Ri Khosenb,****, and S. N. Khimukhina,b,*****
aInstitute of Materials Science, Khabarovsk Scientific Center, Far East Branch, Russian Academy of Sciences,
ul. Tikhookeanskaya 153, Khabarovsk, 680042 Russia
bPacific State University, Far East Branch, Russian Academy of Sciences,
ul. Tikhookeanskaya 136, Khabarovsk, 680035 Russia
*e-mail: Gost.v.v@mail.ru
**e-mail: immaterial_khv@mail.ru
***e-mail: anasta-91@mail.ru
****e-mail: opirus@bk.ru
*****e-mail: ximuxin@mail.ru
Received April 24, 2014; in final form, August 1, 2014; accepted for publication, August 15, 2014
AbstractFabrication conditions of NiAl, NiAlCr, and NiAlCrMoW alloys by joint aluminothermic
reduction of initial metal oxides are investigated. Thermodynamic characteristics of accompanying reactions
are determined. The temperature dependence of the change in the isobaric potential (
G
, kJ/mol) of reduction
reactions of oxides points to the high formation probability of alloys. It is revealed by differential thermal anal-
ysis that the reduction of metal oxides enters the active phase after aluminum is melted at ~650
C and
progresses according to the heterogeneous mechanism in a temperature range of 8001100
C. The optimal
composition of the initial charge, which provides the maximal yield of metals into alloys, is established. It is
found experimentally that the yield of metals into alloys constitutes 8592 wt %. Synthesis products are iden-
tified by the elemental and X-ray phase analyses as intermetallics of the NiAl system, which contain inclusions
of chromium, molybdenum, and tungsten. It is shown that the concentration of inclusions varies in a range of
1.56.5 wt %. The microhardness of alloys is determined to vary from 3546 to 7436 MPa, depending on the
content of alloying elements.
Keywords: aluminum nickelides, metallothermy, oxides, alloying elements, chromium, molybdenum, X-ray
phase analysis, microstructure
DOI: 10.3103/S1067821216010065
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