Self-cleaning coated glass
Introduction
In physical chemistry, hydrophobicity is the physical property of a molecule that is apparently repelled by a mass of water (known as hydrophobic).[1] On the contrary, hydrophilic ones are attracted to water.
Hydrophobic molecules tend to be nonpolar and therefore prefer other neutral molecules and nonpolar solvents. Because water molecules are polar, hydrophobes do not dissolve well with each other. Hydrophobic molecules in water tend to clump together, forming micelles. Water on hydrophobic surfaces will show a high contact angle.
Examples of hydrophobic molecules are alkanes, oils, fats and fatty substances in general. Hydrophobic materials are used for oil removal from water, oil spill management, and chemical separation processes to remove non-polar substances from polar compounds.[2].
Hydrophobic is often used interchangeably with lipophilic, "grease-loving." However, both terms are not synonymous. Although hydrophobic substances are usually lipophilic, there are exceptions, such as silicones and fluorocarbons.
The term hydrophobic comes from the ancient Greek ὑδρόφόβος (hýdrophóbos), "being afraid of water", constructed (Greek ὕδωρ (húdōr) water and φόβος (phóbos) fear}}.[3].
Physicochemical foundations
In the case of small solutes, the hydrophobic interaction is mainly an entropic effect originated by the disruption of the highly dynamic hydrogen bonds between liquid water molecules by the nonpolar solute, causing the water to form a clathrate-like structure around the nonpolar molecules. This formed structure is more highly ordered than free water molecules because the water molecules are organized to interact as much as possible with themselves (thereby minimizing the breaking of hydrogen bonds), and therefore results in a loss of entropy at the interface. This causes the non-polar molecules to group together to reduce the surface area exposed to water, thus increasing the entropy of the system.[4][5] In such a way, the two immiscible phases (hydrophilic versus hydrophobic) will change so that their corresponding interfacial area will be minimal. This effect can be visualized in the phenomenon called phase separation "Phase (matter)").
On the other hand, for larger non-polar solutes, which cannot be adequately “clatrated” by the hydrogen bond network of water, the breaking of said bonds becomes inevitable, implying a high enthalpic cost. Under ambient conditions, this transition from a regime dominated by entropy to one governed by enthalpy occurs around a size of ~1 nm, reflecting a change in the behavior of the free energy of hydration, which goes from scaling with the volume of the solute to depending on the exposed surface area.[6][7].