Localized Corrosion Behavior of UNS N07718 in a Solution Simulating a Diluted-sour Environment

Abstract

The localized corrosion behavior of precipitation-hardened UNS N07718 was investigated by immersion tests in 6 wt% FeCl3 + 1.0 wt% HCl and the use of electrochemical techniques in a simulating solution of a diluted-sour environment of 25 wt% NaCl + 0.5 wt% CH3COOH. The Ti carbides and Nb-Mo carbides with 1-10 µm size were distributed in the alloy. After immersion at a solution temperature higher than 45oC, localized corrosion with a depth of over 25 µm was identified, and the critical pitting temperature was determined to be 45oC. Potentiodynamic polarization showed that the surface of the UNS N07718 was immediately passivated in the experimental solution. The passivity-maintaining current density was gradually increased with increasing solution temperature, and finally, localized corrosion was initiated or propagated at 0.5 VSSE in 80oC. The localized corrosion was initiated or propagated at the interface between the Ti and Nb-Mo carbides and the alloy substrate. Scanning Kelvin probe microscopic images revealed that the contact-potential difference values were in the order of Ti carbide > Nb-Mo carbide > alloy substrate, indicating that the carbides and alloy substrate act as a cathode and an anode, respectively, forming a micro-galvanic couple. Therefore, it is concluded that localized corrosion is initiated at the interface between the carbides and substrates in UNS N07718.