TY - JOUR
T1 - Low Alloy X100 Pipeline Steel Corrosion and Passivation Behavior in Bicarbonate-Based Solutions of pH 6.7 to 8.9 with Groundwater Anions
T2 - An Electrochemical Study
AU - Gadala, Ibrahim M.
AU - Alfantazi, Akram
N1 - Funding Information:
This work was funded by Qatar National Research Fund (QNRF) 6-027-2-010. The authors express their appreciation for this support.
Publisher Copyright:
© 2015, The Minerals, Metals & Materials Society and ASM International.
PY - 2015/7/26
Y1 - 2015/7/26
N2 - This research investigates the fundamental corrosion and passivation processes occurring on API-X100 pipeline steels before, during, and after passive layer formation in bicarbonate-based simulated soil solutions of pH 6.7 to 8.9. Free corrosion potentials decrease exponentially with bicarbonate (and pH), owing to increased water and bicarbonate reduction in more alkaline conditions and the coupled iron oxidation reaction. Active corrosion rates at potentials slightly above open circuit potential increase with bicarbonate, until a concentration of 1.68 g L−1 sodium bicarbonate (plus dilute amounts of chlorides/sulfate) at which first signs of film formation appear. Thereon, increased bicarbonate concentration generally decreases current densities and resists ferrous-oxide product formations due to improved iron carbonate formation conditions precipitating more durable passive layers. Potentiodynamic polarization in the anodic regime reveals varying electrochemical processes involving interactions between hydroxide, carbonate, and oxide complexes with ferrous, with diverse pH and potential dependencies. The products of corrosion reactions were investigated by scanning electron microscopy, X-ray diffraction, and/or X-ray photoelectron spectroscopy.
AB - This research investigates the fundamental corrosion and passivation processes occurring on API-X100 pipeline steels before, during, and after passive layer formation in bicarbonate-based simulated soil solutions of pH 6.7 to 8.9. Free corrosion potentials decrease exponentially with bicarbonate (and pH), owing to increased water and bicarbonate reduction in more alkaline conditions and the coupled iron oxidation reaction. Active corrosion rates at potentials slightly above open circuit potential increase with bicarbonate, until a concentration of 1.68 g L−1 sodium bicarbonate (plus dilute amounts of chlorides/sulfate) at which first signs of film formation appear. Thereon, increased bicarbonate concentration generally decreases current densities and resists ferrous-oxide product formations due to improved iron carbonate formation conditions precipitating more durable passive layers. Potentiodynamic polarization in the anodic regime reveals varying electrochemical processes involving interactions between hydroxide, carbonate, and oxide complexes with ferrous, with diverse pH and potential dependencies. The products of corrosion reactions were investigated by scanning electron microscopy, X-ray diffraction, and/or X-ray photoelectron spectroscopy.
UR - http://www.scopus.com/inward/record.url?scp=84929707676&partnerID=8YFLogxK
U2 - 10.1007/s11661-015-2891-7
DO - 10.1007/s11661-015-2891-7
M3 - Article
AN - SCOPUS:84929707676
SN - 1073-5623
VL - 46
SP - 3104
EP - 3116
JO - Metallurgical and Materials Transactions A: Physical Metallurgy and Materials Science
JF - Metallurgical and Materials Transactions A: Physical Metallurgy and Materials Science
IS - 7
M1 - 2891
ER -