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Carbon dots (CDs) are spherical zero-dimensional carbon nanomaterials, generally below 10 nm in size, which have received increasing attention in the field of corrosion because of various advantages such as good water solubility, abundant raw materials, and environmental protection. In this work, water-soluble carbon dots (CDs) with particle sizes of 5–10 nm are obtained by electrochemical oxidation with anhydrous ethanol. FTIR, Raman, UV–Vis, XPS, and TEM are used to characterize the obtained CDs, and electrochemical tests are used to investigate the anti-corrosion performance of the CDs. The results reveal that the corrosion inhibition performance increased with the addition of CDs, and the highest corrosion inhibition efficiency reaches 98% when the addition amount is 200 mg/L. Moreover, the inhibition mechanism for CDs needs to be further investigated, and the stable adsorption of CDs on carbon steel to form adsorption film may be the key factor for its good corrosion inhibition performance. [ABSTRACT FROM AUTHOR]

In this work, high‐yield carbon quantum dots (CQDs) are successfully synthesized by a simple chemical oxidation method using acetaldehyde as raw material. Fourier‐transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), thermogravimetry (TGA), and XPS are used to analyze the structural characteristics of CQDs. The results demonstrate that many oxygen‐containing functional groups are on the surface of carbon nuclei. The inhibitive efficiency of electrochemical experiments and weight loss is 87.1 % and 95.3 %, respectively. SEM observes the surface morphology of the sample after 72 h corrosion with or without CQDs, and EDS analysis confirms that CQDs are effectively adsorbed on the surface of carbon steel. Furthermore, through calculation, the standard adsorption‐free energy of CQDs is −25 kJ/mol, concluding that the adsorption process is a combination of physisorption and chemisorption. This work is helping to solve the corrosion problem of metal equipment in the acid process. [ABSTRACT FROM AUTHOR]

The corrosion inhibition effect and synergistic mechanism of novel imidazoline derivative (SMIF) and benzimidazole (BMZ) in 3.5 wt% simulated concrete solution were studied experimentally and theoretically. The complex inhibitors have the most outstanding inhibition efficiency when SMIF concentration is 0.1 g/L and BMZ is 0.9 g/L, the corrosion inhibition efficiencies of weight loss, Electrochemical Impedance Spectroscopy and Potentiodynamic polarization curve (Tafel) were 88.81%, 86.27% and 90.22%, respectively. Electrochemistry analysis results proved that the corrosion inhibition mechanism of the inhibitors in the corrosion solution was mainly the formation of a protective film on the surface of carbon steel. FT-IR, Energy Dispersive Spectroscopy and X-ray Photoelectron Spectroscopy all proved the existence of the protective film. Molecular dynamics proved that the composite inhibitor molecules could be stable on the surface of carbon steel and when consist of complex inhibitor was 0.1 g/L SMIF and 0.9 g/L BMZ the stable adsorption morphology were the highest. This work confirmed that SMIF and BMZ inhibitors have a good synergistic effect, greatly improving the inhibition efficiency and reducing the cost of corrosion inhibition, and has a certain guiding significance for synergistic inhibition. [ABSTRACT FROM AUTHOR]