4.7 Article

Super-hydrophobicity and oleophobicity of silicone rubber modified by CF4 radio frequency plasma

Journal

APPLIED SURFACE SCIENCE
Volume 257, Issue 11, Pages 4945-4950

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2011.01.001

Keywords

Super-hydrophobicity and oleophobicity; CF4 radio frequency plasma; Silicone rubber; Surface morphology; XPS

Funding

  1. Scientific Research Special Foundation of Science and Technology Bureau of Sanming, Fujian Province, China [2009-G-4]
  2. Scientific Research Special Foundation of Provincial University of Education Department of Fujian Province, China [JA10268]

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Owing to excellent electric properties, silicone rubber (SIR) has been widely employed in outdoor insulator. For further improving its hydrophobicity and service life, the SIR samples are treated by CF4 radio frequency (RF) capacitively coupled plasma. The hydrophobic and oleophobic properties are characterized by static contact angle method. The surface morphology of modified SIR is observed by atom force microscope (AFM). X-ray photoelectron spectroscopy (XPS) is used to test the variation of the functional groups on the SIR surface due to the treatment by CF4 plasma. The results indicate that the static contact angle of SIR surface is improved from 100.7 degrees to 150.2 degrees via the CF4 plasma modification, and the super-hydrophobic surface of modified SIR, which the corresponding static contact angle is 150.2 degrees, appears at RF power of 200 W for a 5 min treatment time. It is found that the super-hydrophobic surface ascribes to the coaction of the increase of roughness created by the ablation action and the formation of [-SiFx(CH3)(2-x)-O-](n), (x = 1, 2) structure produced by F atoms replacement methyl groups reaction, more importantly, the formation of [-SiF2-O-](n) structure is the major factor for super-hydrophobic surface, and it is different from the previous studies, which proposed the fluorocarbon species such as C-F, C-F-2, C-F-3, CF-CFn, and C-CFn, were largely introduced to the polymer surface and responsible for the formation of low surface energy. (C) 2011 Elsevier B.V. All rights reserved.

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