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

The effect of added salt on the propulsion of Janus platinum-polystyrene colloids in hydrogen peroxide solution is studied experimentally. It is found that micromolar quantities of potassium and silver nitrate salts reduce the swimming velocity by similar amounts, while leading to significantly different effects on the overall rate of catalytic breakdown of hydrogen peroxide. It is argued that the seemingly paradoxical experimental observations could be theoretically explained by using a generalised reaction scheme that involves charged intermediates and has the topology of two nested loops.

In this paper we show that processes such as Brownian motion, convection, sedimentation, and bacterial contamination can cause small particles to move through liquids in a fashion which may be mistaken as nanopropulsion. It is shown that particle tracking and subsequent statistical analysis is essential to ascertain if small particles actually propel themselves, or if they are propelled by another process. Specifically we find that it is necessary to calculate the mean-squared displacement of particles at both short and long time intervals, to show that the direction of propulsion changes coincident with rotation of the particle by Brownian motion, as this allows nanopropulsion to be differentiated from Brownian motion, convection and sedimentation. We also find that bacteria can attach themselves to particles and cause them to be propelled. This leads to motion which appears very similar to nanopropulsion and cannot be differentiated using particle tracking and therefore find that carefully designed control experiments must be performed. Finally, we suggest an experimental protocol which can be used to investigate the motion of small objects and prove if they move due to nanopropulsion.

“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.

Contrary to conventional ATRP, aqueous A(R)GET-ATRP at ambient temperature without deoxygenating reaction solutions is an extremely facile method to create polymer brushes. Using these techniques, extremely thick poly[2-(dimethylamino)ethyl methacrylate] polymer brushes can be prepared (∼700 nm), or reaction solutions can be low chemical-content, consisting of 99% v/v water. Based on these techniques, we have also developed an easy and inexpensive method, referred to as "paint on"-ATRP, that directly pastes reaction solutions onto various large-scale real-life substrates open to the air. The resulting brush surfaces possess excellent oil-repellent properties, which can be activated or deactivated in response to solution pH.

Synthetic polymers are thoroughly embedded in the modern society and their consumption grows annually. Efficient routes to their production and processing have never been more important. In this respect, silk protein fibrillation is superior to conventional polymer processing, not only by achieving outstanding physical properties of materials, such as high tensile strength and toughness, but also improved process energy efficiency. Natural silk solidifies in response to flow of the liquid using conformation-dependent intermolecular interactions to desolvate (denature) protein chains. This mechanism is reproduced here by an aqueous poly(ethylene oxide) (PEO) solution, which solidifies at ambient conditions when subjected to flow. The transition requires that an energy threshold is exceeded by the flow conditions, which disrupts a protective hydration shell around polymer molecules, releasing them from a metastable state into the thermodynamically favoured crystalline state. This mechanism requires vastly lower energy inputs and demonstrates an alternative route for polymer processing.

We demonstrated for the first time a facile and reproducible preparation of large-scale (∼40 m2) initiator layers for surface-initiated atom transfer radical polymerization (SI-ATRP) using a simple sol–gel solution of (p-chloromethyl)­phenyl­trimethoxysilane and tetraethoxysilane. Highly smooth and transparent initiator layers could be formed on various inorganic/organic substrates via a spin-, wire-bar-, or roll-to-roll-coating without any marked change in surface morphology or bulk properties at room temperature. Combining the advantages of this sol–gel approach and subsequent “paint on” SI-ATRP using a variety of waterborne monomers, we have succeeded in the formation of polymer brushes on large-scale real-life substrates (i.e., maximum 50 × 50 cm2) under ambient conditions (room temperature and open to the air) without any complicated apparatus or harsh reaction conditions.