The incorporation of organic corrosion inhibitors into waterborne coatings is optimized in this work. Herein, p‐coumaric acid (4‐hydroxycinnamic acid) is modified by a butyl radical and its effectiveness as an anticorrosive free inhibitor in solution is confirmed by potentiodynamic polarization (PP). The molecule is then successfully incorporated into waterborne polymeric binders by employing different polymerization techniques in dispersed media. Whenever possible, the inhibitor is also blended into the bare latexes to compare the effect of the incorporating method. The anticorrosion performance of the obtained coatings is tested and compared by electrochemical analysis. Promising results are obtained for the coatings produced by semibatch emulsion polymerization even at the low concentration of 1.5 mg of inhibitor g−1 latex. The intact control coating without inhibitor shows an impedance of up to 106 Ω and a phase angle of 72° after 1 h of immersion in the corrosive medium, meanwhile the coating with inhibitor shows higher values, 106.7 Ω and 80°. Active corrosion inhibition is observed in the coating with inhibitor in which a defect has been done, as the impedances drop to 103.9 Ω after 24 h of immersion in the saline solution while in the control scratched coating it drops to 103.6 Ω.
One of the most widely applied methods for the mitigation
of corrosion
is to cover metallic surfaces with polymeric coatings; however, the
barrier properties provided by the polymer may not be enough to prevent
corrosion. To improve the performance of the coatings, the incorporation
of corrosion inhibitors in their formulation can be done to provide
active protection to the system. Among the organic corrosion inhibitors, p-coumaric acid (p-CA) is promising for
corrosion protection. Therefore, in this work, the corrosion protection
efficiency of four p-coumaric-based inhibitors, methyl
(H1), butyl (H4), trifluoromethoxy (HCF3), and p-4-ethyloxymethacrylate p-coumaric acid (HMA), is investigated. The inhibitors are
incorporated into environmentally friendly waterborne polymeric binders
by batch miniemulsion polymerization. The barrier corrosion protection
of the coatings produced from these hybrid latexes is analyzed by
electrochemical impedance spectroscopy (EIS) of the intact and scratched
coated steel substrates. Of the intact coatings, the one with H1 showed
the best response, with impedances of 106.3–106.7 Ω and phase angles of 82–84°, considerably
higher than the control without inhibitor (105–105.2 Ω and 60–66°, respectively). The better
performance of H1 has been attributed to its higher solubility in
the media. However, the best impedance results for the scratched films
have been obtained for the coating with HMA, as the impedance was
maintained at ∼104.3 Ω for 24 h, while the
impedance drops from ∼104.6 to 104.1 Ω
for the control scratched sample. As HMA is attached to the polymeric
chains, it is likely able to protect the exposed metallic area without
completely leaching from the coating, thus explaining why it is able
to maintain its performance. The EIS analysis also strongly suggests
that the inhibitors have an additional protective effect through increasing
pore resistance and decreasing metal corrosion as indicated from the
higher R
pore and lower C
dl data extracted from the fits.
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