Crystallization behavior in a highly driven marginal glass forming alloy


Kalay Y. E., CHUMBLEY L. S., ANDERSON I. E.

JOURNAL OF NON-CRYSTALLINE SOLIDS, cilt.354, sa.26, ss.3040-3048, 2008 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 354 Sayı: 26
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1016/j.jnoncrysol.2007.12.006
  • Dergi Adı: JOURNAL OF NON-CRYSTALLINE SOLIDS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.3040-3048
  • Anahtar Kelimeler: amorphous metals, metallic glasses, alloys, crystallization, nanocrystals, synchrotron radiation, measurement techniques, STEM/TEM, TEM/STEM, nanoparticles, colloids and quantum structures, nanocrystals, time resolved measurements, rare earths in glasses, structure, long-range order, medium-range order, short-range order, thermal properties, calorimetry, X-rays, X-ray diffraction, AMORPHOUS-ALLOYS, METALLIC GLASSES, TENSILE-STRENGTH, AL, SYSTEMS, CU, NANOCRYSTALLIZATION, DEVITRIFICATION, AMORPHIZATION, ALUMINUM
  • Orta Doğu Teknik Üniversitesi Adresli: Hayır

Özet

Al90Sm10, a marginal glass former, was rapidly solidified using Cu-block single roller melt spinning at wheel speeds of 30 and 40 m/s. The product phases of rapid solidification were identified and analyzed using high energy synchrotron X-ray diffraction (HEXRD), high resolution transmission electron microscopy, and atom probe tomography. The as-quenched structure consists of a saturated amorphous phase and nanocrystalline Al with typical length scale of about 5 nm. The appearance of a pre-peak on HEXRD diffraction patterns and a low activation energy for first crystallization as determined using the Kissinger and Ozawa methods indicate some local ordering in the amorphous phase. The devitrification phase transformation path was determined using in situ high energy synchrotron radiation. Three phases, MS1, H1, and Al4Sm, were identified during decomposition of the amorphous phase. MS1, H1 and Al4Sm are cubic, hexagonal and orthorhombic metastable phases, respectively. Published by Elsevier B.V.