The Synthesis and Inhibitory Action of Some amido carboxylic acids on Mild Steel Corrosion Protection in Hydrochloric Acid | ||||
Egyptian Journal of Chemistry | ||||
Volume 66, Issue 5, May 2023, Page 35-53 PDF (946.32 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/ejchem.2022.156862.6802 | ||||
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Authors | ||||
Mohamed Abd El-Moneim1; Mahmoud M ElDesouky2; ElSayed Fouad3; Wagdy Ibrahim Eldougdoug 4 | ||||
1Chemistry Department, Faculty of Science, Port Said Univeristy | ||||
2Higher Institute of Engineering and Technology | ||||
3Faculty of Engineering, Banha University. | ||||
4Chemistry, Faculty of Science, Benha University, Benha, Egypt | ||||
Abstract | ||||
Mild steel has been utilized in a variety of applications, including reaction vessels, tanks, and other structures, however the fundamental issue with this material is that it is quickly impacted by corrosive solutions. We tried to solve this problem by producing new inhibitors. From the interaction of benzoic acid derivatives and aminoacetophenone with various quinazoline derivatives, a range of amido carboxylic acids have been produced. The corrosion inhibition capabilities of the novel compounds for mild steel corrosion in HCl solution were examined. The results of these techniques showed that increasing the concentration of inhibitor and reducing the temperature boosted inhibition efficiency. From data acquired at various temperatures, some thermodynamic parameters were derived and discussed for the examined systems. Using 1000 ppm of the newly synthesized derivative, around 94 percent inhibitory efficiency was determined. According to the polarization data, the newly synthesized compounds exhibit a mixed inhibitory effect. The Langmuir isotherm was determined to be the best fit for representing the inhibitor's adsorption behavior. | ||||
Keywords | ||||
potentiodynamic polarization; quinazoline derivatives; nitrogen nucleophiles; steel; HCl | ||||
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