Degradation mechanisms of corrosion and biofouling resistance of superhydrophobic coatings in harsh marine conditions

被引:20
作者
Cao, Xiangkang [1 ]
Pan, Jinglong [1 ]
Cai, Guangyi [2 ]
Hu, Yunfei [1 ]
Zhang, Xinxin [1 ]
Dong, Zehua [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China
[2] Naval Univ Engn, Natl Key Lab Sci & Technol Vessel Integrated Power, Wuhan 430033, Peoples R China
基金
中国国家自然科学基金;
关键词
Superhydrophobicity; Coating; Corrosion; Biofouling; Failure mechanisms; SURFACES; COST;
D O I
10.1016/j.porgcoat.2022.107222
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The easy loss of non-wettability of superhydrophobic coatings (SHPs) severely hinders their applications in practice, and an understanding of their degradation mechanism would be helpful to solve this problem. In this work, we studied the degradation process of superhydrophobicity of SHPs subjected to static salt spray and dynamic abrasion tests, and found that most SHPs feature a considerable anti-corrosion and anti-biofouling ability in the initial period. Unfortunately, with prolonged aging tests, the air cushion on the surface of SHPs is depleted due to static saline corrosion and/or dynamic erosion. Morphological and chemical observations suggest that there are two mechanisms to explain the static and dynamic degradation of SHPs, respectively. First, due to the chemical or photo-oxidation of coatings, the SHPs become more hydrophilic and prone to capture hygroscopic salt particles instead of air bubbles during salt spray tests, leading to the depletion of air cushion. Second, the micro-nano rough structures of SHPs may be polished away due to solid particle abrasion or flowing water erosion, causing non-wettability loss. Therefore, to sustain a reliable superhydrophobic surface, it is necessary to armor the micro-nano structures with a hard coating or shell. Finally, a mathematical model was proposed to explain the non-wettability of SHPs based on their roughness and surface energy.
引用
收藏
页数:13
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