Facile fabrication of uniform hierarchical structured (UHS) nanocomposite surface with high water repellency and self-cleaning properties

被引:40
作者
Bagheri, H. [1 ]
Aliofkhazraei, M. [1 ]
Forooshani, H. Mojiri [1 ]
Rouhaghdam, A. Sabour [1 ]
机构
[1] Tarbiat Modares Univ, Dept Mat Engn, POB 14115-143, Tehran, Iran
关键词
Electrodeposition; Superhydrophobic surfaces; TiO2; nanocomposite; Self-cleaning; Corrosion; RESISTANT SUPERHYDROPHOBIC SURFACE; STEP ELECTRODEPOSITION PROCESS; CORROSION; ALLOY; COATINGS; HYDROPHOBICITY; ANTICORROSION; TRANSITION; ROUGHNESS; SUBSTRATE;
D O I
10.1016/j.apsusc.2017.12.156
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the present study, two-stage process for the fabrication of superhydrophobic Ni-Cu-TiO2 nanocomposite coatings on the copper substrate has been introduced. Surface modification was performed on the electrodeposited coatings by myristic acid-ethanol solution to achieve superhydrophobicity. Additionally, in order to further study the roughness effect, instead of addition of copper ions in electrodeposition bath, three substrates were roughened by electrochemical etching method. Water repellency properties were studied through measurement of static and dynamic contact angles, and performing bouncing test, self-cleaning and water-jet evaluation. The samples were electrodeposited in various current densities, and the highest corrosion resistance and water repellency properties were obtained for the sample which was electrodeposited in two consecutive steps and modified by a fatty acid called myristic acid (which significantly reduces surface energy of the coating). The highest water contact angle (161 degrees) and the lowest contact angle hysteresis (3 degrees) were obtained for the sample which was coated by 10 mA/cm(2) (144 min) and 20 mA/cm(2) (18 min), respectively. Since this approach does not require any sophisticated equipment and materials, it shows promising future in the fabrication of superhydrophobic coatings. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1134 / 1146
页数:13
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