A stable superhydrophobic and superoleophilic Cu mesh based on copper hydroxide nanoneedle arrays
- Authors
- La, Duc-Duong; Tuan Anh Nguyen; Lee, Sungho; Kim, Jeong Won; Kim, Yong Shin
- Issue Date
- Apr-2011
- Publisher
- Elsevier BV
- Keywords
- Superhydrophobicity; Copper mesh; Electrochemical anodization
- Citation
- Applied Surface Science, v.257, no.13, pp 5705 - 5710
- Pages
- 6
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Applied Surface Science
- Volume
- 257
- Number
- 13
- Start Page
- 5705
- End Page
- 5710
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/38135
- DOI
- 10.1016/j.apsusc.2011.01.078
- ISSN
- 0169-4332
1873-5584
- Abstract
- A superhydrophobic and superoleophilic copper mesh was prepared via a simple electrochemical route. Copper substrates were anodized in a 1 mol/L NaOH aqueous solution to produce a rough thin film of Cu(OH)(2) nanoneedle arrays and then the film was reacted with 1H,1H,2H,2H-perfluorooctyltriethoxysilane to form a very thin and stable hydrophobic coating layer. X-ray photoelectron spectroscopy (XPS) data revealed the coordination of silicon atoms with cuprate (CuO) molecules present on the anodized substrate. The water contact angle of the perfluoroalkylsilane-modified nanoneedle surface was approximately 170 degrees. Furthermore, the superhydrophobicity was maintained after wet treatments in aqueous solutions with a wide pH range of 2-14 and after a long storage time of 4 months. This excellent durability and long-term reliability, which was unattainable in comparable samples modified with n-dodecanethiol or n-dodecanoic acid, could be interpreted with the formation of a stable and dense surface modification layer via a condensation reaction between -SiOEt and -CuOH and subsequent polymerization among the ethoxysilane adsorbates. Preliminary studies of the dynamic permeation behaviors of water and non-polar solvents exhibited a potential use of the hybrid copper mesh as a filtering layer for oil and water separation. (C) 2011 Elsevier B. V. All rights reserved.
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