Sweet Corrosion Inhibition by CO2 Capture

The most practical and economical way to combat the problems derived from CO2 corrosion (sweet corrosion) is the use of corrosion inhibitors of organic origin. Its main protection mechanism is based on its ability to adsorb on the metal surface, forming a barrier between the metal surface and the aggressive medium. However, despite its excellent performance, its inhibition efficiency can be compromised with the increase in temperature as well as the shear stresses. In this study, the use of an inorganic inhibitor is proposed that has not been considered as an inhibitor of sweet corrosion. The reported studies are based on using LaCl3 as a corrosion inhibitor. Its behavior was evaluated on 1018 carbon steel using electrochemical measurements, such as potentiodynamic polarization curves, open-circuit potential measurements, linear polarization resistance measurements, and electrochemical impedance. The results showed an inhibition efficiency of the sweet corrosion process greater than 95%, and that the inhibition mechanism was different from the classic corrosion process in CO2-free electrolytes. In this case, it was observed that the inhibitory capacity of the La3+ cations is based on a CO2-capture process and the precipitation of a barrier layer of lanthanum carbonate (La2(CO3)3)

Pouteria sapota as green CO2-corrosion inhibition of carbon steel

Imidazoline obtained from the essential oil contained in Pouteria sapota seed was tested as an environmentally-friendly corrosion inhibitor of 1018 carbon steel in a CO2 saturated 3.5 % NaCl solution using electrochemical techniques. This imidazoline contains fatty acids with long hydrophobic chains, with 52.73 % of unsaturated (oleic and linolenic acids) and 40 % of saturated (palmitic and myristic acids) compounds. Polarization curves revealed that this inhibitor is a highly efficient mixed-type of inhibitor with the inhibitor efficiency of 99.9 % reached at 25 ppm. Also, the lowest pitting potential value was observed at 25 ppm of inhibitor, making the carbon steel highly susceptible to the pitting type of corrosion. Corrosion current density value decreased by nearly four orders of magnitude, and a passive film formation was induced for inhibitor concen­tra­tions higher than 5 ppm. Accordingly, polarization resistance values were increased from 100 W cm2 up to about 106 W cm2 at 25 ppm of inhibitor. The inhibitor forms a protective film of corrosion products adsorbed on the metal surface in a very strong chemical way, following a Langmuir type of adsorption isotherm. This was supported by electrochemical impedance spectra that showed two relaxation processes ascribed to electrode interface and film regions. In agre­ement with polarization resistance data, the total electrode resistance determined by inter­facial charge transfer and film resistance increased up to 8.2 ´ 105 W cm2 in the presence of 25 ppm of inhibitor. SEM images additionally showed that type of corrosion was fully changed from uniform to a localized type when 25 ppm of inhibitor was added into the solution

Corrosion Inhibition in CO₂-Saturated Brine by Nd³⁺ Ions

This study reports the use of an inorganic corrosion inhibitor to mitigate dissolved CO2-induced corrosion. Using electrochemical techniques (polarization curves, open circuit potential, polarization resistance, and electrochemical impedance), the effect of adding Nd3+ ions on the corrosion resistance of X52 steel immersed in CO2-saturated brine at 20 °C and 60 °C was evaluated. The polarization curves showed that the Icorr values tend to decrease with increasing Nd3+ ion concentration, up to the optimal inhibition concentration, and that the corrosion potential increases at nobler values. Open circuit potential measurements showed a large increase in potential values immediately after the addition of the Nd3+ ions. Similarly, polarization resistance measurements showed similar trends. It was observed that regardless of temperature, Nd3+ ions can reduce the corrosion rate by more than 97% at doses as low as 0.001 M. Electrochemical impedance measurements confirmed the formation of a protective layer on the steel surface, which caused an increase in the magnitude of the impedance module and phase angle, which indicates an increase in the resistance to charge transfer and capacitive properties of the metallic surface. The characterization of the metallic surface showed that the protective layer was formed by Nd carbonates, whose formation was due to a CO2 capture process

Behavior of Ni20Cr Alloy in Molten Nitrate Salts

This study reports the behavior of the Ni20Cr alloy in molten nitrate salts. Its behavior was evaluated in the eutectic mixture called Solar Salt (binary salt) and in a ternary mixture (90% Solar Salt and 10% lanthanum nitrate). The addition of lanthanum nitrate was performed to determine if the presence of the La3+ cation could act as a corrosion inhibitor. Through mass loss and potentiodynamic polarization studies, the effects of both electrolytes on the corrosion resistance of the alloy at 300, 400, and 500 °C and at exposure times of 250, 500, 750, and 1000 h were determined. The results showed an increase in the corrosivity of the ternary salt, due to a decrease in its melting point and an increase in the concentration of nitrate ions. However, it was observed that the La3+ cations formed a protective layer (La2O3) on the alloy surface. In both corrosive media, the Ni20Cr alloy showed excellent corrosion resistance, due to its ability to form protective layers of Cr2O3, NiO, and NiCr2O4, in addition to the presence of a layer of La2O3 in the case of the ternary salt