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Talebian, M.; Raeissi, K.; Atapour, M.; Fernández-Pérez, B.M.; Betancor-Abreu, A.; Llorente, I.; Fajardo, S.; Salarvand, Z.; Meghdadi, S.; Amirnasr, M.; Souto, R.M.
Corrosion science, November 2019, 2019-11-00, 20191101, Volume: 160Journal Article
•Synthesis and characterization of three Schiff base derivatives for pitting corrosion inhibition of 304 stainless steel•Enhanced pitting corrosion resistance in neutral chloride solution was provided by these inhibitors•Inhibition efficiency increased with the concentration of sodium (E)-4-(nitrobenzylidene-amino)-benzoate up to 10 mM•SVET revealed the inhibitive action of the Schiff base on both metastable pit nucleation and stable pit growth regimes•Metal-inhibitor interaction happened upon breakdown of the chromium-enriched passive surface releasing iron ions Three newly synthesized Schiff base derivatives, sodium (E)-4-(nitrobenzylideneamino)-benzoate (SNBB), sodium (E)-4-(benzylideneamino)-benzoate (SBB), and sodium (E)-4-(hydroxybenzylideneamino)-benzoate (SHBB) were investigated as pitting corrosion inhibitors for 304 stainless steel in neutral 0.1 M NaCl. Potentiodynamic polarization evidenced major shifts in pitting potential to more positive values with increasing inhibitor concentration. The scanning vibrating electrode technique (SVET) imaged metastable pitting in 0.1 M NaCl, but not in the presence of the inhibitor, indicating that it prevented pit nucleation. The inhibition performance was established under anodic polarization conditions, because only minute local anodic activity due to metastable pit formation could be observed when the steel was exposed to SNBB-containing solution, whereas the metal would undergo pit propagation at the same potential in the inhibitor-free solution. X-ray photoelectron spectroscopy (XPS) analysis evidenced chromium enrichment at weak points (pores) of the passive film at anodic polarization condition where sudden release of Fe cations is possible. In this way, the SNBB molecules will migrate to these sites to react with the Fe ions and form a chelate compound which will deposit finally at those sites and plug them, whereas no effect occurred at the open circuit potential (OCP).
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