Phase transformations in Cd–Ni nanostructured system at elevated temperatures
- Авторлар: 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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Мекемелер:
- 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
- Шығарылым: Том 68, № 1 (2019)
- Беттер: 17-23
- Бөлім: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/243271
- DOI: https://doi.org/10.1007/s11172-019-2410-x
- ID: 243271
Дәйексөз келтіру
Аннотация
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.
Авторлар туралы
V. Pugachev
Kemerovo State University
Email: bic@catalysis.ru
Ресей, 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
Хат алмасуға жауапты Автор.
Email: zaharov@kemsu.ru
Ресей, 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
Ресей, 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
Ресей, 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
Ресей, 18 prosp. Sovetskiy, Kemerovo, 650000
S. Yashnik
G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: bic@catalysis.ru
Ресей, 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
Ресей, 18 prosp. Sovetskiy, Kemerovo, 650000; 5 prosp. Lavrentieva, Novosibirsk, 630090
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