Phase transformations in Cd–Ni nanostructured system at elevated temperatures
- 作者: Pugachev V.M.1, Zakharov Y.A.1,2, Valnyukova A.S.1,2, Popova A.N.2, Khitsova L.M.2, Yashnik S.A.3, Ismagilov Z.R.2,3
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隶属关系:
- Kemerovo State University
- The Federal Research Center of Coal and Coal Chemistry, Siberian Branch of the Russian Academy of Sciences
- G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences
- 期: 卷 68, 编号 1 (2019)
- 页面: 17-23
- 栏目: Full Articles
- URL: https://bakhtiniada.ru/1066-5285/article/view/243271
- DOI: https://doi.org/10.1007/s11172-019-2410-x
- ID: 243271
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详细
Using X-ray diffraction (both in vacuum and in air), derivatomass-spectrometry and thermo-programmed oxidation, phase transformations in nanostructured Cd–Ni system occurring while heating up 720 °C were described. These metal powders were obtained by joint reduction from aqueous solutions of salts with hydrazine. When study their composition, earlier unknown phases were detected (intermetallide CdNi3 and solid solution CdxNi1–x with face centered cubic structure) and among the known intermetallides (Cd5Ni and CdNi), only Cd5Ni was found. As a consequence, phase transformations in the obtained nanostructured powders were remarkably different from those present on the Cd–Ni phase diagram. The intermediates and FCC phase decompose independently with formation of individual initial components (Cd and Ni) without intermediate product. At relatively high Cd concentration in the system, intermediate CdNi3 phase formation from Cd5Ni and CdxNi1–x phases, which are polar opposites in composition, is possible. The decomposition temperatures of Cd5Ni and melting point of Cd in the nanostructured state were lower than those specified by the phase diagram by 170 and 70 °C, respectively, which well corresponded to the concept of effective (high) temperatures attributed to the nanostructured systems due to the energy saturation of the con stituent nanocrystallites.
作者简介
V. Pugachev
Kemerovo State University
Email: bic@catalysis.ru
俄罗斯联邦, 6 ul. Krasnaya., Kemerovo, 650000
Yu. Zakharov
Kemerovo State University; The Federal Research Center of Coal and Coal Chemistry, Siberian Branch of the Russian Academy of Sciences
编辑信件的主要联系方式.
Email: zaharov@kemsu.ru
俄罗斯联邦, 6 ul. Krasnaya., Kemerovo, 650000; 18 prosp. Sovetskiy, Kemerovo, 650000
A. Valnyukova
Kemerovo State University; The Federal Research Center of Coal and Coal Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: bic@catalysis.ru
俄罗斯联邦, 6 ul. Krasnaya., Kemerovo, 650000; 18 prosp. Sovetskiy, Kemerovo, 650000
A. Popova
The Federal Research Center of Coal and Coal Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: bic@catalysis.ru
俄罗斯联邦, 18 prosp. Sovetskiy, Kemerovo, 650000
L. Khitsova
The Federal Research Center of Coal and Coal Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: bic@catalysis.ru
俄罗斯联邦, 18 prosp. Sovetskiy, Kemerovo, 650000
S. Yashnik
G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences
编辑信件的主要联系方式.
Email: bic@catalysis.ru
俄罗斯联邦, 5 prosp. Lavrentieva, Novosibirsk, 630090
Z. Ismagilov
The Federal Research Center of Coal and Coal Chemistry, Siberian Branch of the Russian Academy of Sciences; G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences
Email: bic@catalysis.ru
俄罗斯联邦, 18 prosp. Sovetskiy, Kemerovo, 650000; 5 prosp. Lavrentieva, Novosibirsk, 630090
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