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Coating solid surfaces with cellulose nanofibril (CNF) monolayers via physical deposition was found to keep the surfaces free of a variety of oils, ranging from viscous engine oil to polar n-butanol, upon water action. The self-cleaning function was well correlated with the unique molecular structure of the CNF, in which abundant surface carboxyl and hydroxy groups are uniformly, densely, and symmetrically arranged to form a polar corona on a crystalline nanocellulose strand. This isotropic core-corona configuration offers new and easily adoptable guidance to design self-cleaning surfaces at the molecular level. Thanks to its excellent self-cleaning behavior, the CNF coating converted conventional meshes into highly effective membranes for oil-water separation with no prior surface treatment required. [ABSTRACT FROM AUTHOR]

In this work, graphene oxide (GO)-loaded agarose hydrogel was transferred into oil such as hexadecane via stepwise solvent exchange with no chemical modification of the GO hydrophilic surface and the agarose network. After transfer, the GOs, loaded in the agarose network, could effectively and efficiently adsorb lipophilic dyes in oil via hydrogen bonding between the polar groups of the GOs and the dyes. The maximum adsorption capacity was 355.9 mg g−1 for Nile red for instance, which is substantially larger than that of pristine agarose hydrogel and hydrophilic GO powder. The dye concentration for effective adsorption can be as low as 0.5 ppm. Thus, the present work demonstrates the promising potential of using hydrophilic adsorbents for efficient removal of polar impurities from oil. [ABSTRACT FROM AUTHOR]

Groß und klein, kurz und lang: Mit einem pH ‐ sensitiven Polymer beschichtete Nanopartikel (NPs) gehen ein reversibles Kettenwachstum ein, das von der pH ‐ abhängigen elektrostatischen Interpartikelabstoßung bestimmt wird. Durch stufenweise Änderung des pH ‐ Wertes konnten unterschiedlich große NPs zu linearen Ketten gekuppelt werden, die an Blockcopolymere erinnern (siehe Bild). [ABSTRACT FROM AUTHOR]

Organic–inorganic metal‐halide materials (OIMMs) with zero‐dimensional (0D) structures offer useful optical properties with a wide range of applications. However, successful examples of 0D structural OIMMs with well‐defined optical performance at the micro‐/nanometer scale are limited. We prepared one‐dimensional (1D) (DTA)2SbCl5⋅DTAC (DTAC=dodecyl trimethyl ammonium chloride) single‐crystal microrods and 2D microplates with a 0D structure in which individual (SbCl5)2− quadrangular units are completely isolated and surrounded by the organic cation DTA+. The organic molecular unit with a long alkyl chain (C12) and three methyl groups enables microrod and ‐plate formation. The single‐crystal microrods/‐plates exhibit a broadband orange emission peak at 610 nm with a photoluminescence quantum yield (PLQY) of ca. 90 % and a large Stokes shift of 260 nm under photoexcitation. The broad emission originates from self‐trapping excitons. Spatially resolved PL spectra confirm that these microrods exhibit an optical waveguide effect with a low loss coefficient (0.0019 dB μm−1) during propagation, and linear polarized photoemission with a polarization contrast (0.57). [ABSTRACT FROM AUTHOR]

The counterions of polydiallyldimethylammonium (PDADMA) coatings were altered by incubation in aqueous solutions of different electrolytes. Oil de‐wetting on the resulting polycationic surfaces upon water action exhibited a straightforward connection with the Jones–Dole viscosity B‐coefficient (Bη) sign of surface counteranions. Upon water action, surface counteranions with negative Bη render PDADMA coatings oil‐adhering, but those with positive Bη furnish PDADMA coatings with excellent self‐cleaning. The oil‐adhering PDADMA surfaces can become self‐cleaning upon water action in response to the Bη of surface counteranions sign‐switching with increasing water temperature. Courtesy of surface counter‐anions with Bη>0, self‐cleaning PDADMA coatings enable not only conversion of conventional meshes into self‐cleaning membranes for oil/water separation, but also regioselective maneuver of oil flow on polycationic surfaces according to the Bη sign of surface counteranions patterned atop. [ABSTRACT FROM AUTHOR]

Abstract: Hydrophobic reduced graphene oxides (rGOs) were generated in agarose hydrogel beads (AgarBs) by NaBH4 reduction of graphene oxides (GOs) initially loaded in the AgarBs. The resulting rGO‐loaded AgarBs were able to effectively adsorb organic compounds in water as a result of the attractive hydrophobic force between the rGOs in the AgarBs and the organic compounds dissolved in aqueous media. The adsorption capacity of the rGOs was fairly high even toward reasonably water‐soluble organic compounds such as rhodamine B (321.7 mg g−1) and aspirin (196.4 mg g−1). Yet they exhibited salinity‐enhanced adsorption capacity and preferential adsorption of organic compounds with lower solubility in water. Such peculiar adsorption behavior highlights the exciting possibility for adopting an adsorption strategy, driven by hydrophobic forces, in practical wastewater treatment processes. [ABSTRACT FROM AUTHOR]

Abstract: Surface‐inactive, highly hydrophilic particles are utilized to effectively and reversibly stabilize oil‐in‐water emulsions. This is a result of attractive van der Waals forces between particles and oil droplets in water, which are sufficient to trap the particles in close proximity to oil–water interfaces when repulsive forces between particles and oil droplets are suppressed. The emulsifying efficiency of the highly hydrophilic particles is determined by van der Waals attraction between particle monolayer shells and oil droplets enclosed therein and is inversely proportional to the particle size, while their stabilizing efficiency is determined by van der Waals attraction between single particles and oil droplets, which is proportional to the particle size. This differentiation in mechanism between emulsification and stabilization will significantly advance our knowledge of emulsions, thus enabling better control and design of emulsion‐based technologies in practice. [ABSTRACT FROM AUTHOR]

Surface wetting on polyelectrolyte multilayers (PEMs), prepared by alternating deposition of polydiallyldimethylammonium chloride (PDDA) and poly(styrene sulfonate) (PSS), was investigated mainly in water-solid-oil systems. The surface-wetting behavior of as-prepared PEMs was well correlated to the molecular structures of the uncompensated ionic groups on the PEMs as revealed by sum frequency generation vibrational and X-ray photoelectron spectroscopies. The orientation change of the benzenesulfonate groups on the PSS-capped surfaces causes poor water wetting in oil or air and negligible oil wetting in water, while the orientation change of the quaternized pyrrolidine rings on the PDDA-capped surfaces hardly affects their wetting behavior. The underwater oil repellency of PSS-capped PEMs was successfully harnessed to manufacture highly efficient filters for oil-water separation at high flux. [ABSTRACT FROM AUTHOR]