Changes in Electrochemical Properties of Directionally Solidified Ni-base Superalloy Due to Creep and Damage Evaluation

Changes in electrochemical properties of directionally solidified Ni-base superalloy CM 247 LC due to creep have been investigated. The electrochemical polarization technique has been applied to creep-ruptured and creep-interrupted specimens under various creep condition in order to examine a detect...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:TRANSACTIONS OF THE JAPAN SOCIETY OF MECHANICAL ENGINEERS Series A 1998/07/25, Vol.64(623), pp.1997-2004
Hauptverfasser: KOMAZAKI, Shinichi, SHOJI, Tetsuo, TAKEICHI, Tetsuya, SATO, Minoru
Format: Artikel
Sprache:eng ; jpn
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Changes in electrochemical properties of directionally solidified Ni-base superalloy CM 247 LC due to creep have been investigated. The electrochemical polarization technique has been applied to creep-ruptured and creep-interrupted specimens under various creep condition in order to examine a detectability of creep damage. Experimental results on electrochemical polarization measurements revealed that the peak current density "Ip" and "Ipr" which appeared at a specific potential during potentiodynamic polarization reactivation measurements in dilute glyceregia solution increased with increased thermal history and showed a good correlation with Larson-Miller Parameter value. Ip and Ipr value reflected both a thermal aging effect and a stress effect, and increased with a creep life fraction. The increases in Ip and Ipr were mainly corresponded to increases in preferential dissolution rate of γ' phase at γ/γ' interface. This preferential dissolution was considered as a result from degradation of corrosion resistance of γ'phase at γ/γ'interface which may be attributable to creep damage accumulation. As a consequence, the creep damage in CM 247 LC can be quantitatively evaluated by the electrochemical technique.
ISSN:0387-5008
1884-8338
DOI:10.1299/kikaia.64.1997