Eco-Friendly Hybrid Materials for Steel Protection Using a Water-Soluble Polyamic Acid as Chelating Agent
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide In this study, an environmentally friendly waterborne coating was developed as a corrosion inhibitor for mild steel (MS) through the synthesis of a polymeric dispersion. Initially, a water-soluble polyamic acid (PAmA) solution was synthesized utilizing ethylenediaminetetraacetic dianhydride and 2,2-(ethylenedioxy)bis(ethylamine). The incorporation of ether linkages and amic acid functional groups into the polymer backbone generates numerous polar sites, thereby facilitating the formation of a stable aqueous organosilane dispersion predominantly composed of 3-glycidoxypropyl trimethoxysilane (GPTMS), without the use of surfactants or additional salts. Additionally, 25 wt % of GPTMS can be replaced with tetraethyl orthosilicate (TEOS), which serves primarily as a crosslinking agent and a precursor for nanosilica, resulting in an aqueous organic/inorganic dispersion under optimized conditions. Comparative analyses with reference samples, such as polyacrylic acid dispersion, demonstrated a higher degree of condensation of 94.6% for the organic/inorganic dispersion in PAmA, as confirmed by Raman spectroscopy and 29 Si-NMR following sol-gel reactions. These results indicate the formation of extensive cross-linking sites and a silica network, which serves as passive layers, yielding a thermal decomposition temperature exceeding 380 °C for the organic/inorganic layer produced by the PAmA polymer. Notably, the application of the PAmA solution not only enhanced cross-linking density and facilitated the formation of a silica network for the organic/inorganic dispersion but also provided the formation of imide structures, leading to a robust sol-gel-derived hybrid coating system, consistent with findings from FTIR and DSC analyses. Consequently, this study demonstrates the successful development of an eco-friendly corrosion inhibitor that exhibits outstanding performance in salt spray tests and superior corrosion protection efficiency (η = 99.7%), as determined by electrochemical impedance spectroscopy for MS.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Material Properties and Applications · biodegradable polymer synthesis and properties · Corrosion Behavior and Inhibition
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Polymer Science and Engineering
National Taiwan University
Advanced Research Center for Green Materials Science and Technology
Department of Materials Engineering
Ming Chi University of Technology
Department of Chemical Engineering
Funding
National Science and Technology Council · Ministry of Education, Taiwan
References (51)
Show source-provided references
1. 10.1021/acsapm.3c0233510.1021/acsapm.3c02335 ↗
2. 10.1016/j.surfcoat.2024.13059610.1016/j.surfcoat.2024.130596 ↗
3. 10.1021/acs.macromol.7b0213810.1021/acs.macromol.7b02138 ↗
4. 10.1016/j.cej.2022.13905510.1016/j.cej.2022.139055 ↗
5. 10.1149/2.0491706jes10.1149/2.0491706jes ↗
6. 10.1016/j.electacta.2004.01.05110.1016/j.electacta.2004.01.051 ↗
7. Davis, J. R. Corrosion of Aluminum and Aluminum Alloys; ASM International: Materials Park, 1999; 210–211.10.31399/asm.tb.caaa.9781627082990 ↗
8. 10.1007/s11998-014-9595-610.1007/s11998-014-9595-6 ↗
9. 10.1007/s10971-010-2173-110.1007/s10971-010-2173-1 ↗
10. 10.1016/S0300-9440(01)00134-510.1016/S0300-9440(01)00134-5 ↗
11. 10.1007/s10971-012-2838-z10.1007/s10971-012-2838-z ↗
12. 10.1007/BF0243688010.1007/BF02436880 ↗
13. 10.1016/j.jnoncrysol.2006.05.04210.1016/j.jnoncrysol.2006.05.042 ↗
14. 10.1016/j.jpowsour.2008.12.12610.1016/j.jpowsour.2008.12.126 ↗
15. 10.1016/j.surfcoat.2012.04.06110.1016/j.surfcoat.2012.04.061 ↗
16. 10.1016/S0169-4332(98)00254-210.1016/S0169-4332(98)00254-2 ↗
17. 10.1016/S0022-3093(02)01431-X10.1016/S0022-3093(02)01431-X ↗
18. 10.1016/j.electacta.2005.09.01710.1016/j.electacta.2005.09.017 ↗
19. 10.3390/coatings912080710.3390/coatings9120807 ↗
20. 10.1021/acsapm.0c0126610.1021/acsapm.0c01266 ↗
21. 10.1016/j.scp.2024.10153510.1016/j.scp.2024.101535 ↗
22. 10.1016/j.porgcoat.2024.10836510.1016/j.porgcoat.2024.108365 ↗
23. 10.1016/j.cscee.2023.10059110.1016/j.cscee.2023.100591 ↗
24. 10.1016/j.porgcoat.2023.10813510.1016/j.porgcoat.2023.108135 ↗
25. 10.3144/expresspolymlett.2019.6610.3144/expresspolymlett.2019.66 ↗
26. 10.1002/app.3266910.1002/app.32669 ↗
27. 10.1016/j.polymer.2011.03.03010.1016/j.polymer.2011.03.030 ↗
28. 10.1002/pc.2363710.1002/pc.23637 ↗
29. 10.1007/s13233-011-0603-810.1007/s13233-011-0603-8 ↗
30. 10.1016/j.matdes.2013.12.04610.1016/j.matdes.2013.12.046 ↗
31. 10.1007/s00396-013-3019-510.1007/s00396-013-3019-5 ↗
32. 10.2147/IJN.S7650210.2147/IJN.S76502 ↗
33. Brinker C. J. · 2013
34. 10.1002/(SICI)1099-0518(20000601)38:11<1972::AID-POLA60>3.0.CO;2-510.1002/(SICI)1099-0518(20000601)38:11<1972::AID-POLA60>3.0.CO;2-5 ↗
35. 10.1016/j.compositesb.2021.10942710.1016/j.compositesb.2021.109427 ↗
36. 10.1179/1743284715Y.000000008110.1179/1743284715Y.0000000081 ↗
37. 10.1155/2022/189141910.1155/2022/1891419 ↗
38. 10.1021/j100182a06810.1021/j100182a068 ↗
39. 10.1016/S0022-3093(97)00487-010.1016/S0022-3093(97)00487-0 ↗
40. 10.1016/S0022-3093(05)80622-210.1016/S0022-3093(05)80622-2 ↗
41. 10.1007/s12034-011-0064-x10.1007/s12034-011-0064-x ↗
42. 10.1016/0022-3093(84)90140-610.1016/0022-3093(84)90140-6 ↗
43. 10.1021/acs.langmuir.5b0450610.1021/acs.langmuir.5b04506 ↗
44. 10.1039/C5RA24008E10.1039/C5RA24008E ↗
45. 10.1016/j.corsci.2017.09.01910.1016/j.corsci.2017.09.019 ↗
46. 10.1016/j.porgcoat.2023.10805110.1016/j.porgcoat.2023.108051 ↗
47. 10.1021/acsapm.3c0242410.1021/acsapm.3c02424 ↗
48. 10.1016/j.ijbiomac.2024.13002410.1016/j.ijbiomac.2024.130024 ↗
49. 10.46754/jssm.2021.06.00410.46754/jssm.2021.06.004 ↗
50. 10.1016/j.porgcoat.2024.10857210.1016/j.porgcoat.2024.108572 ↗
51. 10.1016/j.porgcoat.2023.10763810.1016/j.porgcoat.2023.107638 ↗