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It is well known that metal corrosion causes serious economy losses worldwide. One of the most effective ways to prevent corrosion is the continuous development of high-efficient and environment-friendly corrosion inhibitors. Among the widely used organic and inorganic corrosion inhibitors, plant extracts are top candidates due to their nontoxic nature. The present study reports a novel application of the methanolic extract of Terminalia bellerica fruits as an environment friendly corrosion inhibitor for steel in sulphuric acid medium. The phytochemicals of the extract, namely Ellagic, Gallic, and Malic acids, play a key role of the anti-corrosive behavior of the extract. The corrosion prevention activity was studied on the steel in 1 M H2SO4 using a variety of approaches including weight loss analysis (WL), scanning electron microscope (SEM), electrochemical impedance spectroscopy (EIS), density functional theory (DFT), natural bond orbital analysis (NBO), Fukui function and Monte Carlo simulations (MC). In 1 M H2SO4 solution, the maximum electrochemical inhibition efficiency of 91.79% was observed at 4000 mg/L concentration of the extract. The NBO analysis showed that the charge density of the double bonds and the oxygen atoms of carbonyl and hydroxyl groups of the phytochemicals lies on the top of the natural bond orbitals which promotes the anticorrosive properties of the investigated inhibitors. The surface coverage of steel was validated by SEM measurements. According to DFT studies, numerous nucleophilic regions were present in the active phytochemical constituents of the inhibitor, demonstrating their favorable nucleophilicity. The computed electronic structure of the phytochemicals revealed band gaps of 4.813, 5.444, and 7.562 eV for Ellagic, Gallic, and Malic acids respectively suggesting effective metal-inhibitor interactions. A good correlation between experimental and theoretical findings was addressed. [ABSTRACT FROM AUTHOR]

The studied Schiff-base compounds in this work are multitasked investigated as corrosion inhibitors and also, to improve the physical and mechanical properties of reinforced concrete. The efficiency inhibition of the two novel Schiff-base compounds named (DHSiMF) and (DHSiB) for corrosion of carbon-steel in aqueous media of 1 M HCl was assessed via electrochemical methods and loss in weight. FT-IR, 1H-NMR spectra and elemental analysis were used to confirm the structure of such compounds. It was found to have successful inhibition even at low concentrations in tested media, as an increase in inhibitor concentration led to an improvement in the inhibition efficiency. The weight loss results clearly demonstrate that DHSiMF of C-steel in 1 M HCl has a higher inhibition efficiency than DHSiB, with a maximum inhibition efficiency (85%) attained at 1 × 10–2 M from DHSiMF. Electrochemical experiments likewise revealed the same order, but with a maximal inhibitory efficiency of 98.1%. The addition of inhibitors to the corrosive media dramatically changed the anodic Tafel constants (βa) and cathodic Tafel constants (βc), indicating a mixed type nature. Electrochemical polarization curves illustrated the functions of mixed-type inhibition and the action of adsorption matching with the Langmuir adsorption isotherm. The ∆Gads values for DHSiMF and DHSiB at temperatures (ranging from 303 to 333 K) are − 34.42 kilojoule/mole to − 37.51 kilojoule/mole. These values indicate that the compounds' adsorption types are chemo-physical adsorption. X-ray diffraction (XRD) and Scanning electron microscopy (SEM) experiments were used to check the existence of the protection layer on the surface of carbon steel by analyzing the morphologies of the corrosion effects and the formed chemical compositions of the corrosion outcomes. For the concrete, the findings suggest that the chemical reaction that takes place between the DHSiMF and DHSiB and the concrete mix will result in an increase in the flexural strength, the compressive strength, and the indirect tensile strength of the concrete that is made of the gravel and dolomite aggregate. [ABSTRACT FROM AUTHOR]

The influence of branched N, N′-bis(p-hydroxybenzoyl) containing propylenediamine (PDA) and triethylenetetramine (TETA) composites for corrosion inhibition of carbon steel in acidic solution (1 M HCl) was investigated using several quantum chemical, electrochemical impedance spectroscopy and potentiodynamic polarization as electrochemical techniques. The investigated molecules were posteriorly characterized by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared spectroscopy (FTIR) while the surfaces of carbon steel test coupons were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The obtained results revealed that the two amino compounds, N, N′-bis(p-hydroxybenzoyl) propanediamine (N, N′-HBPDA) and N, N′-bis(p-hydroxybenzoyl) triethylenetetramine (N, N′-HBTETA), have significant efficiency toward steel corrosion attack and its inhibition performance was significantly boosted by increasing concentration of di- and tetramine containing inhibitors. The two inhibitors achieved a maximum corrosion inhibition efficiency of 99.1% as indicated from polarization measurements. The isotherm feature of Langmuir adsorption appeared to be proper factor for associating the experimental gains with an applicable mechanism of inhibition process. The free energy ∆Gads was calculated to be − 27.5, 29.1 kJ/mol based on the adsorption isotherm model, indicating physical adsorption on the carbon steel surface. Further, images of the morphological analysis exhibited various features of attack owing to the aggressive medium and the employed concentration of the inhibitor. These synthesized amines supplied many favorable scores in the fabrication of functional mixed-type inhibitors. The computational studies reveal that N, N′-HBPDA and N, N′-HBTETA molecules could absorb via several lone pairs and π clouds, confirming their ability to be good corrosion inhibitors. [ABSTRACT FROM AUTHOR]

This document is a correction notice for an article titled "Synthesis and applications of novel Schiff base derivatives as corrosion inhibitors and additives for improvement of reinforced concrete" published in Scientific Reports. The correction addresses errors in the affiliations of the authors. Ehab S. Gad's affiliation was incorrectly listed as 'Department of Chemistry, Faculty of Science (Men's Campus), Al-Azhar University, Nasr City 11884, Cairo, Egypt', but the correct affiliation is Chemistry Department, College of Science and Arts, Jouf University, Alqurayat, Saudi Arabia. The incorrect affiliation was also removed. The original article has been corrected. [Extracted from the article]