Protection of passivated iron against corrosion in a 0.1M NaNO3 solution by coverage with an ultrathin polymer coating of carboxylate SAM
Source abstract
Abstract
An ultrathin, ordered and two-dimensional polymer coating was prepared on passivated iron by modification of 16-hydroxyhexadecanoate ion HO(CH2)15CO2− self-assembled monolayer (SAM) with 1,2-bis(triethoxysilyl)ethane (C2H5O)3Si(CH2)2Si(OC2H5)3 and octadecyltriethoxysilane C18H37Si(OC2H5)3. Protection of passivated iron against passive film breakdown and corrosion of iron was examined by monitoring of the open-circuit potential and repeated polarization measurements in an aerated 0.1 M NaNO3 solution during immersion for many hours. Passive film breakdown on the polymer-coated electrode in the solution was not observed during immersion for 480 h, whereas that of the passivated one occurred at 18.1 h, indicating protection of the passive film from breakdown by coverage with the polymer coating. The protective efficiencies of the passive film covered with the coating were extremely high, around 99.9% in the initial region of the immersion time up to 72 h and more than 98.3% thereafter, indicating prominent cooperative suppression of iron corrosion in 0.1 M NaNO3 by coverage with the passive film and polymer coating. The polymer-coated surface was characterized by contact angle measurement and electron-probe microanalysis.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Corrosion Behavior and Inhibition · Electrochemical Analysis and Applications · Analytical Chemistry and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (24)
Show source-provided references
1. Aramaki · Corros. Sci. · 2006 · 48 · 20910.1016/j.corsci.2004.11.016 ↗
2. Aramaki · Corros. Sci. · 2005 · 47 · 290110.1016/j.corsci.2005.05.037 ↗
3. K. Aramaki, T. Shimura, Proceedings of the 10th European Symposium on Corrosion and Scale Inhibitors, vol. 1, University of Ferrara, Ferrara, 2005, p. 63.
4. Aramaki · Corros. Sci. · 2005 · 47 · 158210.1016/j.corsci.2004.07.046 ↗
5. Aramaki · Corros. Sci. · 2008 · 50 · 354210.1016/j.corsci.2008.07.026 ↗
6. Toušek · 1985
7. Sastri · 1998
8. Aramaki · J. Electrochem. Soc. · 1991 · 138 · 39410.1149/1.2085596 ↗
9. Fujioka · Corros. Sci. · 1996 · 38 · 191510.1016/S0010-938X(96)00075-3 ↗
10. Rosenfeld · 1981
11. Aramaki · Corrosion · 1999 · 55 · 102010.5006/1.3283939 ↗
12. Aramaki · Corrosion · 2000 · 56 · 90110.5006/1.3280593 ↗
13. Aramaki · Corros. Sci. · 2000 · 42 · 197510.1016/S0010-938X(00)00031-7 ↗
14. Aramaki · Corros. Sci. · 2000 · 42 · 202310.1016/S0010-938X(00)00037-8 ↗
15. Pearson · J. Am. Chem. Soc. · 1963 · 85 · 353310.1021/ja00905a001 ↗
16. Higashi · Boshoku-Gijutsu · 1985 · 34 · 599
17. K. Aramaki, H. Nishihara, Proceedings of the 6th European Symposium on Corrosion Inhibitors, vol. 1, Università Degli Studi di Ferrara, 1985, p. 67.
18. Aramaki · J. Electrochem. Soc. · 1969 · 116 · 56810.1149/1.2411965 ↗
19. Aramaki · Corros. Sci. · 1987 · 27 · 48910.1016/0010-938X(87)90092-8 ↗
20. Ohi · Corrosion · 1994 · 50 · 22610.5006/1.3293514 ↗
21. Suzuki · Corros. Sci. · 1996 · 38 · 122310.1016/0010-938X(95)00172-G ↗
22. Aramaki · Corros. Sci. · 1999 · 41 · 171510.1016/S0010-938X(99)00008-6 ↗
23. Haneda · J. Electrochem. Soc. · 1997 · 144 · 121510.1149/1.1837575 ↗
24. Aramaki · Corros. Sci. · 2004 · 46 · 31310.1016/S0010-938X(03)00156-2 ↗