Hot water corrosion behaviour of Zr-Cu-Al-Ni bulk metallic glass

Citation
A. Gebert et al., Hot water corrosion behaviour of Zr-Cu-Al-Ni bulk metallic glass, MAT SCI E A, 316(1-2), 2001, pp. 60-65
Citations number
12
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING
ISSN journal
09215093 → ACNP
Volume
316
Issue
1-2
Year of publication
2001
Pages
60 - 65
Database
ISI
SICI code
0921-5093(20011015)316:1-2<60:HWCBOZ>2.0.ZU;2-S
Abstract
Cylindrical Zr55Cu30Al10Ni5 (numbers indicate at.%) alloy specimens with 3 mm diameter were prepared by copper mould casting and characterised concern ing their microstructure and thermal stability by X-ray diffraction, optica l and scanning electron microscopy and by differential scanning calorimetry . The samples revealed an amorphous structure except for a few micro-crysta lline inclusions. The hot water corrosion behaviour was studied in comparis on to that at room temperature using an autoclave cell at 150 and 250 degre esC, respectively. Applying potentiodynamic and potentiostatic polarisation measurements, the anodic behaviour of the samples was investigated in 0.1 in Na2SO4 Solution and in 0.001 m NaCl solution (both with pH(25 degreesC) = 8) regarding oxide layer formation and pitting susceptibility. Furthermor e, electrochemically treated sample surfaces were characterised by scanning electron microscopy and Auger electron spectroscopy. With increasing tempe rature the Zr55Cu30Al10Ni5 alloy forms thicker but more porous and, thus, m ore permeable oxide layers as compared to barrier-type films formed at 25 d egreesC. A change from a high field-controlled layer growth at 25 degreesC to a diffusion-controlled oxide layer formation already at 150 degreesC was detected. Also at elevated temperatures, the surface layer formed in aqueo us electrolyte consists mainly of zirconium oxides, Under hydrothermal cond itions pitting processes mainly initiated at the transition zone between cr ystalline and amorphous phase are strongly enhanced. (C) 2001 Elsevier Scie nce B.V. All rights reserved.