Polyester coatings containing metal-organic framework (MOF) corrosion inhibitors were studied for their ability to protect carbon steel. The polyester coating was synthesized in the laboratory using microwave (MW) radiation to polycondense soy fatty acids, phthalic anhydride, and pentaerythritol-type polyols. The incorporation of these inhibitors into the polyester coating altered the behavior of the carbon steel, resulting in enhanced corrosion protection compared with uncoated carbon steel and polyester alone. Polyester with a 49% oil content, prepared using fatty acids from soybeans, phthalic anhydride, and pentaerythritol synthesized under microwave irradiation, and with a content of 3 mM Mg(GLY), exhibited a notable enhancement in the anticorrosive properties of the alkyd coating. The inhibition mechanism of corrosion was investigated through electrochemical impedance spectroscopy analysis.

This work investigates the physicochemical characterization of two poly(styrene-co-divinylbenzene) copolymer supports, containing 6.7% and 15% divinylbenzene, functionalized with glycine. The resulting copolymers were characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis, energy-dispersive X-ray spectroscopy, and scanning electron microscopy. The degree of amino acid functionalization was estimated by statistical modeling of the repeating structural units and through analysis of nitrogen content. Thermogravimetric analysis (TGA) was further employed to investigate the impact of grafted amino acid groups on the thermal stability and decomposition behavior of the copolymers.

The investigation primarily focuses on synthesizing Polyvinyl Chloride (PVC)-coordination polymer (CP) polymeric membranes that employ L-Cu-NO₃ (¹_∞[Cu₃L₂(NO₃)]NO₃·2MeOH·2H₂O based on the Schiff base H₂L, where H₂L stands for N,N’-bis[(2-hydroxybenzilideneamino)-propyl]-piperazine)) as a coordination polymer. The membrane’s capacity to hold moisture is greatly improved by the addition of CPs. The water contact angle dropped from 73.4° for the PVC to about 71° for the composite membrane, indicating that the CP–PVC polymer interactions improved the hydrophilicity. Impedance spectroscopy (EIS) was used to determine the membranes response to the tested concentrations of phenol solution at pH 9.11 in the concentration range of 10⁻¹⁰ to 10⁻² mol·L⁻¹. A PVC membrane with a 0.6 wt% L-Cu-NO₃ deposit on a Cu electrode yields the best response. Between 10⁻⁸ and 10⁻⁵ mol·L⁻¹ phenol, a linear dependence was found. The detection limit was 4.64 × 10⁻⁸ mol·L⁻¹.

The corrosion inhibitory performance of a coordination polymer, ¹_∞[Cu₃L¹₂(NO₃)](NO₃)·2H₂O and a complex compound, [Zn₂L²(CH₃COO)₂]·2H₂O, toward iron corrosion in a saline medium at pH 2.5 was investigated. Here, L¹ and L² stand for N,N’-bis[(2-hydroxybenzylideneamino)-propyl]-piperazine and N,N’-bis[(3-methoxysalicylideneamino)-propyl]-piperazine, respectively. This study was motivated by the recognized potential of organic compounds incorporating N, S, and O heteroatoms and π-conjugated electronic systems as effective corrosion inhibitors. The evaluation of the performance is determined using electrochemical impedance spectroscopy (EIS) and potentiometric methods (CP). The experimental findings reveal that an optimal inhibitor concentration of 100 ppm ensures enhanced corrosion protection. For both inhibitors, the corrosion rate decreased by two orders of magnitude compared with the untreated iron sample.