We discuss mechanical forces that act upon a water droplet and a piece of ice on a rough solid surface and the difference between dewetting and ice fracture. The force needed to detach a water droplet depends on contact angle (CA) hysteresis and can be reduced significantly in the case of a superhydrophobic surface. The force needed to detach a piece of ice depends on the receding CA and the initial size of interfacial cracks. Therefore, even surfaces with very high receding CA may have strong adhesion to ice if the size of the cracks is small.
The term “icephobicity” has emerged in the literature recently. An extensive discussion took place on whether the icephobicity is related to the superhydrophobicity, and the consensus is that there is no direct correlation. Besides the parallel between the icephobicity and superhydrophobicity for water/ice repellency, there are similarities on other levels including the hydrophobic effect/hydrophobic interactions, mechanisms of protein folding and ice crystal formation. In this paper, we report how ice adhesion is different from water using force balance analysis, and why superhydrophobic surfaces are not necessary icephobic. We also present experimental data on anti-icing of various surfaces and suggest a definition of icephobicity, which is broad enough to cover a variety of situations relevant to de-icing including low adhesion strength and delayed ice crystallization and bouncing.
We discuss wetting of rough surfaces with two-phase (solid-liquid), three-phase (solid-water-air and solid-oil-water), and four-phase (solid-oil-water-air) interfaces mimicking fish scales. We extend the traditional Wenzel and Cassie-Baxter models to these cases. We further present experimental observations of two-, three-, and four-phase systems in the case of metal-matrix composite solid surfaces immersed in water and in contact with oil. Experimental observations show that wetting transitions can occur in underwater oleophobic systems. We also discuss wetting transitions as phase transitions using the phase-field approach and show that a phenomenological gradient coefficient is responsible for wetting transition, energy barriers, and wetting/dewetting asymmetry (hysteresis).
We report here, for the first time in the literature, a method to synthesize hydrophobic and superhydrophobic concrete. Concrete is normally a hydrophilic material, which significantly reduces the durability of concrete structures and pavements. To synthesize water-repellent concrete, hydrophobic emulsions were fabricated and applied on portland cement mortar tiles. The emulsion was enriched with the polymethyl-hydrogen siloxane oil hydrophobic agent as well as metakaolin (MK) or silica fume (SF) to induce the microroughness and polyvinyl alcohol (PVA) fibers to create hierarchical surfaces. Various emulsion types were investigated by using different mixing procedures, and single-and double-layer hydrophobic coatings were applied. The emulsions and coatings were characterized with optical microscope and scanning electron microscope (SEM), and their wetting properties, including the water contact angle (CA) and roll-off angle, were measured. A theoretical model for coated and non-coated concrete, which can be generalized for other types of materials, was developed to predict the effect of surface roughness and composition on the CA. An optimized distance between the aggregates was found where the CA has the highest value. The maximal CA measured was 156°for the specimen with PVA fibers treated with MK based emulsion. Since water penetration is the main factor leading to concrete deterioration, hydrophobic waterrepellent concretes have much longer durability then regular concretes and can have a broad range of applications in civil and materials engineering.
The Wenzel and Cassie-Baxter models are almost exclusively used to explain the contact angle dependence of the structure of rough and patterned solid surfaces. However, these two classical models do not always accurately predict the wetting properties of surfaces since they fail to capture the effect of many interactions occurring during wetting, including, for example, the effect of the disjoining pressure and of crystal microstructure, grains, and defects. We call such effects the second-order effects and present here a model showing how the disjoining pressure isotherm can affect wettability due to the formation of thin liquid films. We measure water contact angles on pairs of metallic surfaces with nominally the same Wenzel roughness obtained by abrasion and by chemical etching. These two methods of surface roughening result in different rough surface structure, thus leading to different values of the contact angle, which cannot be captured by the Wenzel- and Cassie-type models. The chemical and physical changes that occur on the stainless steel and aluminum alloy surfaces as a result of intergranular corrosion, along with selective intermetallic dissolution, lead to a surface roughness generated on the nano- and microscales.
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