Hydrazine and Hydrogen Coinjection to Mitigate Stress Corrosion Cracking of Structural Materials in Boiling Water Reactors (VII)-Effects of Bulk Water Chemistry on ECP Distribution inside a Crack

• Published in: Journal of nuclear science and technology Vol. 44; no. 11; pp. 1448 - 1457
• Main Authors: WADA, Yoichi, ISHIDA, Kazushige, TACHIBANA, Masahiko, AIZAWA, Motohiro, FUSE, Motomasa
• Format: Journal Article
• Language: English
• Published: Tokyo Taylor & Francis Group 01.11.2007; Atomic Energy Society of Japan
• Subjects: Applied sciences; boiling water reactor; crack water chemistry; electrochemical corrosion potential; Energy; Energy. Thermal use of fuels; Exact sciences and technology; Fission nuclear power plants; hydrazine; hydrogen water chemistry; Installations for energy generation and conversion: thermal and electrical energy; stress corrosion cracking; Measurement; crack water chemistry; Water chemistry; Oxygen; Corrosion potential; Hydrogen; Stress corrosion cracking; hydrogen water chemistry; Crack propagation; Nuclear reactor; electrochemical corrosion potential; Boiling water reactor; Platinum; Stainless steel; Hydrazine; Catalyst; Crack
• ISSN: 0022-3131; 1881-1248
• DOI: 10.1080/18811248.2007.9711392

Water chemistry in a simulated crack (crack) has been studied to understand the mechanisms of stress corrosion cracking in a boiling water reactor environment. Electrochemical corrosion potential (ECP) in a crack made in an austenite type 304 stainless steel specimen was measured. The ECP distribution along the simulated crack was strongly affected by bulk water chemistry and bulk flow. When oxygen concentration was high in the bulk water, the potential difference between the crack tip and the outside of the crack (ΔE), which must be one motive force for crack growth, was about 0.3V under a stagnant condition. When oxygen was removed from the bulk water, ECP inside and outside the crack became low and uniform and ΔE became small. The outside ECP was also lowered by depositing platinum on the steel specimen surface and adding stoichiometrically excess hydrogen to oxygen to lower ΔE. This was effective only when bulk water did not flow. Under the bulk water flow condition, water-borne oxygen caused an increase in ECP on the untreated surface inside the crack. This also caused a large ΔE. The ΔE effect was confirmed by crack growth rate measurements with a catalyst-treated specimen. Therefore, lowering the bulk oxidant concentration by such measures as hydrazine hydrogen coinjection, which is currently under development, is important for suppressing the crack growth.