The recent progress of oil/water separation technologies using various materials that possess surface superwetting properties is summarized.

“Self-lubricating organogels (SLUGs)”showing exceptional surface properties are preparedviaa crosslinking of polydimethylsiloxanes in the presence of organic liquids.

Highly transparent antifogging films were successfully prepared on various substrates, including glass slides, silicon, copper and PMMA, by spin-coating a mixture of polyvinylpyrrolidone and aminopropyl-functionalized, nanoscale clay platelets. The resulting films were superhydrophilic and showed more than 90% transmission of visible light, as well as excellent antifogging and self-healing properties.

We report a novel oil/water separation device, allowing continuous, high-speed, and highly efficient purification of large volumes of oily water. This device uses a pair of hydrophilic/hydrophobic polymer-brush-functionalized stainless steel meshes, which have antagonistic wetting properties, i.e., superoleophobic and superhydrophobic properties, when submerged in the opposite liquid phase. This device can purify large volumes of n-hexadecane/water mixture (∼1000 L) in a continuous process rather than in batches, to high purities (∼99.9% mol/mol) at high flow rates (∼5 mL s(-1) cm(-2)), unlike the oil/water separation meshes reported so far.

SummaryThe attachment ability of ladybird beetles Coccinella septempunctata was systematically investigated on eight types of surface, each with different chemical and topographical properties. The results of traction force tests clearly demonstrated that chemical surface properties, such as static/dynamic de-wettability of water and oil caused by specific chemical compositions, had no significant effect on the attachment of the beetles. Surface roughness was found to be the dominant factor, strongly affecting the attachment ability of the beetles.

No abstract

Superhydrophobic coatings/materials are important for a wide variety of applications, but the majority of these man-made coatings/materials still suffer from poor durability because of their lack of self-healing ability. Here, we report novel superhydrophobic materials which can quickly self-heal from various severe types of damage. In this study, we used poly(dimethylsiloxane) (PDMS) infused with two liquids: trichloropropylsilane, which reacts with ambient moisture to self-assemble into grass-like microfibers (named silicone micro/nanograss) on the surfaces and low-viscosity silicone oil (SO), which remains within the PDMS matrices and acts as a self-healing agent. Because of the silicone micro/nanograss structures on the PDMS surfaces and the effective preserve/protection system of a large quantity of SO within the PDMS matrices, our superhydrophobic materials showed quick superhydrophobic recovery under ambient conditions (within 1-2 h) even after exposure to plasma (24 h), boiling water, chemicals, and outside environments. Such an ability is superior to the best self-healing superhydrophobic coatings/materials reported so far.

Metal‐infiltrated protein crystals form a novel class of bio‐nanomaterials of great interest for applications in biomedicine, chemistry, and optoelectronics. As yet, very little is known about the internal structure of these materials and the interconnectivity of the metallic network. Here, the optical response of individual Au‐ and Ag‐infiltrated cross‐linked lysozyme crystals is investigated using angle‐ and polarization‐dependent spectroscopy. The measurements unequivocally show that metallic inclusions formed inside the nanoporous solvent channels do not connect into continuous nanowires, but rather consist of ensembles of isolated spheroidal nanoclusters with aspect ratios as high as a value of four, and which exhibit a pronounced plasmonic response that is isotropic on a macroscopic length scale. Fluorescence measurement in the visible range show a strong contribution from the protein host, which is quenched by the Au inclusions, and a weaker contribution attributed to the molecule‐like emission from small Au‐clusters.