Crystallization of amorphous Cu50Ti50 alloy prepared by high-energy ball milling

Amorphous Cu50Ti50 alloy was prepared by short-term (20 min) high-energy ball milling (HEBM). According to TEM, electron diffraction, and HAADF STEM results, the material was 93% amorphous with an admixture of nanocrystalline particles 2–8 nm in their size. Thermal stability and crystallization of a...

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Veröffentlicht in:Journal of alloys and compounds 2018-04, Vol.741, p.575-579
Hauptverfasser: Shkodich, N.F., Vadchenko, S.G., Nepapushev, A.A., Kovalev, D. Yu, Kovalev, I.D., Ruvimov, S., Rogachev, A.S., Mukasyan, A.S.
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Sprache:eng
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Zusammenfassung:Amorphous Cu50Ti50 alloy was prepared by short-term (20 min) high-energy ball milling (HEBM). According to TEM, electron diffraction, and HAADF STEM results, the material was 93% amorphous with an admixture of nanocrystalline particles 2–8 nm in their size. Thermal stability and crystallization of amorphous Cu50Ti50 was studied by differential scanning calorimetry (DSC) and time-resolved XRD (TRXRD). Depending on heating rate, the crystallization of Cu50Ti50 took place within the temperature range 298–397 °C. The activation energy (199 ± 4 kJ/mol) was found by using the Kissinger equation. Time-resolved diffraction patterns have revealed that the phase transition proceeds without melting within a time period of 20–30 s and the onset of crystallization gets started around 300 °C which is markedly lower than the melting temperature in the Cu–Ti system (982 °C). Based on our TRXRD results, a mechanism of the phase transition under study was suggested. •Amorphous Cu50Ti50 alloy was prepared by short-term (20 min) high-energy ball milling.•Cu50Ti50 consists of amorphous matrix (93%) with a nanocrystalline (2–8 nm) inclusions.•Activation energy of crystallization (199 kJ/mol) was obtained by Kissinger method.•The crystallization of Cu50Ti50 starts at 300 °C without melting within 20–30 s.•A mechanism of the phase transition under study was suggested.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2018.01.062