Fabrication of bioinspired, self-cleaning superliquiphilic/phobic stainless steel using different pathways

被引:54
作者
Cremaldi, Joseph [1 ]
Bhushan, Bharat [1 ]
机构
[1] Ohio State Univ, Nanoprobe Lab Bio & Nanotechnol & Biomimet NLBB, 201 W 19th Ave, Columbus, OH 43210 USA
关键词
Stainless steel; Chemical etching; Nanocomposite coating; Self-cleaning; Superoleophobic; Silane condensation; SOLUTION-IMMERSION PROCESS; SUPERHYDROPHOBIC SURFACES; WATER-REPELLENT; SCALABLE METHOD; WEAR-RESISTANT; CORROSION; SUBSTRATE; FACILE; NANOPARTICLES; DEPOSITION;
D O I
10.1016/j.jcis.2018.02.034
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
The mechanical properties, corrosion-resistance, and aesthetics of stainless steel make it one of the most important and widely used materials worldwide in the construction, food, and transportation industries just to name a few. In this paper we demonstrate how these properties can be further enhanced by changing the hydrophilic stainless steel surface to be superhydrophilic, superhydrophobic, or superliquiphobic. Creation of these functional surfaces requires hierarchical roughness and chemistry. Roughness is created using various pathways including sandblasting, chemical etching, and nanocomposite coatings. Surface chemistry is controlled using methylchlorosilane, nanoparticles in methylphenyl silicone, and fluorosilane treatment. The broad approach allows for direct comparisons of these pathways. Resulting treatments can create stainless steel surfaces with a hexadecane contact angle of 155 degrees and tilt angle of 7-10 degrees. Discussions of rust-avoidance and coating through condensation reactions are included. Enhanced properties of self-cleaning behavior, anti-icing behavior, wear resistance, and bending resistance are demonstrated on stainless steel 304 L. Stainless steel 430, which is more corrosion prone than stainless steel 304 L, is then used to demonstrate transferability of the treatments and corrosion resistance imparted through superliquiphobicity. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:284 / 297
页数:14
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