{"title":"DL@Ti3C2Tx enhanced waterborne epoxy coating with superior active/passive anti-corrosion properties under 30 MPa hydrostatic pressure","authors":"Yangmin Wu , Changchun Zhao , Wenjie Zhao","doi":"10.1016/j.corcom.2024.08.006","DOIUrl":null,"url":null,"abstract":"<div><div>It is challenging for organic coatings with solely physical barrier property to achieve long-term corrosion protection on metal equipment, especially in harsh deep sea environments. Here, we utilized DL-phenylalanine to modify Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> nanosheets via noncovalent interaction to obtain DL@Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> hybrid additives, which significantly improved the corrosion protection ability of epoxy coating (EP). The impedance modulus of DL@Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub>/EP composite coating with a thickness of 50 μm was two orders of magnitude higher than that of pure EP after 240 h immersion under 30 MPa hydrostatic pressure. The adhesion strength of DL@Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub>/EP composite coating remained at a favorable value of 1.84 MPa after long-term immersion in a harsh environment, which was twice as high as that of pure EP coating. In addition, the active corrosion resistance property of DL@Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub>/EP coating was investigated via the local electrochemical impedance spectroscopy (LEIS) measurement. The improved protection ability of DL@Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub>/EP was benefited from the synergistic effects of the superior physical barrier property of Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> nanosheets and the self-healing feature provided by DL molecules. The corrosion protection and failure mechanisms of composite coating were discussed in detail, supplying broader platforms for constructing active/passive integrated anti-corrosion coatings in harsh deep sea environments.</div></div>","PeriodicalId":100337,"journal":{"name":"Corrosion Communications","volume":"20 ","pages":"Pages 1-12"},"PeriodicalIF":10.7000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Corrosion Communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S266726692500057X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/22 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
It is challenging for organic coatings with solely physical barrier property to achieve long-term corrosion protection on metal equipment, especially in harsh deep sea environments. Here, we utilized DL-phenylalanine to modify Ti3C2Tx nanosheets via noncovalent interaction to obtain DL@Ti3C2Tx hybrid additives, which significantly improved the corrosion protection ability of epoxy coating (EP). The impedance modulus of DL@Ti3C2Tx/EP composite coating with a thickness of 50 μm was two orders of magnitude higher than that of pure EP after 240 h immersion under 30 MPa hydrostatic pressure. The adhesion strength of DL@Ti3C2Tx/EP composite coating remained at a favorable value of 1.84 MPa after long-term immersion in a harsh environment, which was twice as high as that of pure EP coating. In addition, the active corrosion resistance property of DL@Ti3C2Tx/EP coating was investigated via the local electrochemical impedance spectroscopy (LEIS) measurement. The improved protection ability of DL@Ti3C2Tx/EP was benefited from the synergistic effects of the superior physical barrier property of Ti3C2Tx nanosheets and the self-healing feature provided by DL molecules. The corrosion protection and failure mechanisms of composite coating were discussed in detail, supplying broader platforms for constructing active/passive integrated anti-corrosion coatings in harsh deep sea environments.