Investigation of local corrosion behavior and mechanism for TA2/HAl77-2/ 316L SS coupling systems under seawater liquid film

The behavior and mechanism of local corrosion for a TA2/HAl77-2/316L SS coupling system was investigated under a seawater liquid film using coupled multielectrode arrays (CMEAs) and Electrochemical Impedance Spectroscopy (EIS) technology. Local corrosion parameters, such as the maximum potential difference (Delta Emax), the maximum anode current density ( I a, max ), the local corrosion intensity factor (LCII), and the cathode to anode area ratio ( S c /S a ) were obtained to quantitatively characterize the local corrosion degree of microarray electrodes. The results showed that HAl77-2 and most of the 316L SS electrode wires in the microarray electrodes served as anodes, while TA2 and the remainder of the 316L SS electrode wires performed as cathodes. When the concentration of Cl increased from 1.9 to 4.3 wt%, the anode potential shifted negatively and the anode current tended to increase. Under a seawater liquid film with a thickness of 200 mu m and Cl concentrations of 3.1 and 4.3 wt%, the anodic galvanic current and corrosion driving force of CMEA were relatively high. Under a seawater liquid film with a thickness of 200 mu m, the anodic galvanic current, Delta E max , I a, max , and LCII all reached their maximum values at 60 degrees C. The electrochemical impedance modulus of HAl77-2 under coupled polarization conditions was smaller than that of HAl77-2 under uncoupled conditions, indicating that the polarization effect between the electrodes in the coupled state promoted the corrosion kinetics of HAl77-2.