Synthesis, Characterization, and Corrosion Inhibition Properties of a Novel Quaternary Ammonium Salt Containing...

A novel dual-imidazoline ring quaternary ammonium salt corrosion inhibitor (TN-IM) was rationally synthesized via a three-step sequential reaction, using hydroxyethyl ethylenediamine and tetradecanedioic acid as starting materials, with benzyl chloride as the quaternizing reagent. The synthetic process involved amidation at 160 °C for 4 h, cyclization at 220 °C for 3 h, and quaternization at 70 °C for 3 h, respectively. Fourier transform infrared spectroscopy and proton nuclear magnetic resonance were employed to characterize the chemical structure of TN-IM, confirming its successful synthesis. The corrosion inhibition performance of TN-IM was evaluated by the static weight loss method and electrochemical measurements, while the corrosion products and surface morphology of N80 carbon steel were analyzed via energy-dispersive X-ray spectroscopy and scanning electron microscopy. Static weight loss tests conducted in 3.5 wt% of a NaCl solution saturated with 0.6 MPa CO₂ at 60 °C for 24 h revealed that TN-IM at a concentration of 0.15 mmol/L exhibited a corrosion inhibition efficiency 1.86% higher than that of a single-imidazoline ring quaternary ammonium salt inhibitor. Potentiodynamic polarization measurements demonstrated that TN-IM functions as a mixed-type corrosion inhibitor, with a predominant inhibitory effect on the anodic reaction on N80 steel. Electrochemical impedance spectroscopy results indicated that TN-IM molecules can adsorb onto the active sites of the N80 surface, thereby retarding the corrosion process by suppressing the charge transfer step in the electrochemical corrosion reaction. This study establishes a new paradigm for the synthesis of high-efficiency imidazoline-based CO₂ corrosion inhibitors with multiple adsorption sites, holding significant implications for corrosion control in harsh industrial environments.