ABSTRACT
HYPOTHESIS: When they are used alone, some polymers, such as polypropylene, Carnauba wax or polycarbonate allow the creation of superhydrophobic surfaces by spin coating or casting. On the other hand, some other polymers, such as polystyrene, polyvinylacetate or polychloroprene, are unable to render a superhydrophobic surface by these techniques. Using binary mixtures of these two types of polymers in a single common solvent, superhydrophobic composite surfaces can be created. We aim to show that superhydrophobicity is depending on the ratio between the two polymers in the initial blend and their intrinsic wettability. EXPERIMENTS: The transition towards superhydrophobicity is studied on composite surfaces made of various polymers. Surfaces are created with simple coating methods, such as casting or spin-coating, of polymer solutions and letting the solvent evaporate at ambient conditions. FINDINGS: Transitions are sharp and the amount of polypropylene in the blend to achieve superhydrophobicity decreases with the hydrophobicity of the second polymer. Topographic and wettability measurements are performed that show that both effects, topographical and chemical, interplay in the property of superhydrophobicity.
ABSTRACT
The wettability of cross-linked poly(dimethylsiloxane) elastomer films and of octadecyltrichlorosilane self-assembled monolayers with water has been measured and compared using various methods. Contact angle hysteresis values were compared with values reported in the literature. A new method to characterize advancing, receding contact angles, and hysteresis using drop impact have been tested and compared with usual methods. It has been found that for the rigid surfaces the drop impact method is comparable with other methods but that for elastomer surfaces the hysteresis is function of the drop impact velocity which influences the extent of the deformation of the soft surface at the triple line.
ABSTRACT
Superhydrophobic surfaces are generated by chemisorption on aluminum substrates of fluorinated block copolymers synthesized by reversible addition-fragmentation chain transfer in supercritical carbon dioxide. In an appropriate solvent, those block copolymers can form micelles with a fluorinated corona, which are grafted on the aluminum substrate thanks to the presence of carboxylic acid groups in the corona. Water contact angle and drop impact analysis were used to characterize the wettability of the films at the macroscale, and atomic force microscopy measurements provided morphological information at the micro- and nanoscale. The simple solvent casting of the polymer solution on a hydroxylated aluminum surface results in a coating with multiscale roughness, which is fully superhydrophobic over areas up to 4 cm(2).