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Updated: Oct 20, 2025

Dynamic Electrochemical Measurement of Chloride Ions
Published on: February 5, 2016
Control of chloride ion corrosion by MgAlOx/MgAlFeOx in the process of chloride deicing
Dongdong Wang1,2, Qi Zhu3,4, Zipeng Xing5,6
1School of Chemistry and Materials Science, Heilongjiang University, Harbin, China.
Abstract:
Adding a corrosion inhibitor to the chloride deicing salt can prevent the corrosion and pollution of Cl-, which is very important. Layered double hydroxide (LDHs), calcined at high temperature is used as adsorbents to remove various anionic contaminants, and it can reduce the freezing point of solution after adsorbing anions. Therefore, this paper reports the use of calcined LDHs as corrosion inhibitors in deicing salts, which are denoted as MgAlOx or MgAlFeOx depending on the preparation element. By analyzing the removal efficiency and the freezing point of MgAlOx and MgAlFeOx to Cl-, the feasibility of the study was determined. Resulted that the removal efficiency to Cl- of MgAlFeOx at low temperature (0 ± 2 °C) and room temperature (25 ± 2 °C) was higher than that of MgAlOx, reaching 39.4% and 85.60%, respectively. And the freezing point of MgAlFeOx was lower than that of MgAlOx, the value was -12.0 °C. At the same time, we also found that CaCl2-MgAlOx and CaCl2-MgAlFeOx significantly reduced the corrosion of carbon steel and concrete compared with chloride salts, and CaCl2-MgAlFeOx had the lowest corrosion degree. Hence, MgAlFeOx was chosen as the corrosion inhibitor in chloride deicing salt. The metal molar ratio, synthesis temperature, and calcination temperature for preparation of MgAl/MgAlFe-LDHs were determined by XRD and TG-DSC analysis that were 9/2/1, 120 °C, and 500 °C, respectively. Characterization methods such as Zeta, XRD, XPS, BET, and SEM were used to study in detail the characteristic changes of MgAlFe-LDHs and MgAlFeOx after Fe3+ was added, and the mechanism of corrosion inhibitors was further determined that was achieved by adsorption and neutralization.
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