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Perfluorinated ProDOT monomers for superhydrophobic/oleophobic surfaces elaboration.

Authors :
Godeau, Guilhem
Ben Taher, Yosra
Pujol, Manon
Guittard, Frédéric
Darmanin, Thierry
Source :
Journal of Fluorine Chemistry. Nov2016, Vol. 191, p90-96. 7p.
Publication Year :
2016

Abstract

Here, we report for the first time the use of the Staudinger-Vilarrasa reaction to synthesize perfluorinated 3,4-propylenedioxythiophene (ProDOT) monomers for preparing hydrophobic/oleophobic surfaces. The efficiency of this reaction is shown with various perfluorinated chains. The prepared monomers are nicely polymerized to form homogeneous perfluorinated surfaces. The study of these surfaces reveal extremely high hydrophobic features with para and superhydrophobic properties (high and low water adhesion). Using different organic probe liquids (diiodomethane and hexadecane), it has been shown that the surfaces present also high oleophobic features. This work also shows a nice impact of the perfluorinated chain length on the surface morphologies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221139
Volume :
191
Database :
Academic Search Index
Journal :
Journal of Fluorine Chemistry
Publication Type :
Academic Journal
Accession number :
119288472
Full Text :
https://doi.org/10.1016/j.jfluchem.2016.09.019