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In recent years, various hydrogels with a wide range of functionalities have been developed. However, owing to the two major drawbacks of hydrogels—air‐drying and water‐swelling—hydrogels developed thus far have yet to achieve most of their potential applications. Herein, a bioinspired, facile, and versatile method for fabricating hydrogels with high stability in both air and water is reported. This method includes the creation of a bioinspired homogeneous fusion layer of a hydrophobic polymer and oil in the outermost surface layer of the hydrogel via a double‐hydrophobic‐coating produced through quenching. As a proof‐of‐concept, this method is applied to a polyacrylamide hydrogel without compromising its mechanical properties. The coated hydrogel exhibits strong resistance to both drying in air and swelling in multiple aqueous environments. Furthermore, the versatility of this method is demonstrated using different types of hydrogels and oils. Because this method is easy to apply and is not dependent on hydrogel surface chemistry, it can significantly broaden the scope of next‐generation hydrogels for real‐world applications in both wet and dry environments. A double‐hydrophobic‐coating method using a hydrophobic polymer and a viscous oil prepared via quenching is developed to fabricate hydrogels with strong resistance to drying in air and swelling in multiple aqueous environments. The method is not dependent on the type of oil or the surface chemistry of the hydrogel used; therefore, it is applicable to a wide range of hydrogels.

Cellulose-based materials represent a renewable, biodegradable, and environmentally friendly alternative to plastic from fossil resources. Nanopaper is a strong and lightweight material formed from cellulose nanofibrils (CNFs). Paper and nanopaper have been considered as excellent alternatives to plastics for use in agriculture and for packaging applications. However, common for both paper and nanopaper is their hydrophilic character, and consequently, poor water-resistance properties. ORMOCER®s are a class of inorganic–organic polymers with excellent barrier and protective properties used for a range of coating applications. Here we present ORMOCER®-coated paper and nanopaper. The coated papers and nanopapers are characterized, both in terms of their morphology, hydrophobicity, and mechanical properties. We demonstrate that the pressure used during the pressing and drying of paper and nanopaper influence their tear and tensile—properties, and that the morphology of the coated nanopaper differs significantly from that of the coated paper. While the ORMOCER® was impregnated within the porous network of the paper, a well-defined two-layered morphology was obtained with the coated nanopaper. Further, the biodegradability of the nanopaper with and without coating was assessed. The degradation study demonstrated that both the pressure used during the pressing and drying of the nanopaper, and the composition of the ORMOCER®, influenced the rate of degradation. Taken together, ORMOCER®-coated paper and nanopaper are promising for the preparation of materials that are both water-resistant, renewable, and biodegradable.

Selective oxidation of methane to organic oxygenates over metal—organic frameworks (MOFs) catalysts at low temperature is a challenging topic in the field of C1 chemistry because of the inferior stability of MOFs. Modifying the surface of Cu-BTC via hydrophobic polydimethylsiloxane (PDMS) at 235 °C under vacuum not only can dramatically improve its catalytic cycle stability in a liquid phase but also generate coordinatively unsaturated Cu(I) sites, which significantly enhances the catalytic activity of Cu-BTC catalyst. The results of spectroscopy characterizations and theoretical calculation proved that the coordinatively unsaturated Cu(I) sites made H₂O₂ dissociative into •OH, which formed Cu(II)-O active species by combining with coordinatively unsaturated Cu(I) sites for activating the C—H bond of methane. The high productivity of C1 oxygenates (CH₃OH and CH₃OOH) of 10.67 mmol gcat. −1h−1 with super high selectivity of 99.6% to C1 oxygenates was achieved over Cu-BTC-P-235 catalyst, and the catalyst possessed excellent reusability.

High water vapor flux at low brine temperatures without surface fouling is needed in membrane distillation-based desalination. Brine crossflow over surface-modified hydrophobic hollow fiber membranes (HFMs) yielded fouling-free operation with supersaturated solutions of scaling salts and their precipitates. Surface modification involved an ultrathin porous polyfluorosiloxane or polysiloxane coating deposited on the outside of porous polypropylene (PP) HFMs by plasma polymerization. The outside of hydrophilic MicroPES HFMs of polyethersulfone was also coated by an ultrathin coating of porous plasma-polymerized polyfluorosiloxane or polysiloxane rendering the surface hydrophobic. Direct contact membrane distillation-based desalination performances of these HFMs were determined and compared with porous PP-based HFMs. Salt concentrations of 1, 10, and 20 wt% were used. Leak rates were determined at low pressures. Surface and cross-sections of two kinds of coated HFMs were investigated by scanning electron microscopy. The HFMs based on water-wetted MicroPES substrate offered a very thin gas gap in the hydrophobic surface coating yielding a high flux of 26.4–27.6 kg/m2-h with 1 wt% feed brine at 70 °C. The fluxes of HFMs on porous PP substrates having a long vapor diffusion path were significantly lower. Coated HFM performances have been compared with flat hydrophilic membranes of polyvinylidene fluoride having a similar plasma-polymerized hydrophobic polyfluorosiloxane coating.

Soiling of solar module cover glass is a serious problem for solar asset managers. It causes a reduction in power output due to attenuation of the incident light, and reduces the return on investment. Regular cleaning is required to mitigate the effect but this is a costly procedure. The application of transparent hydrophobic, anti-soiling coatings to the cover glass is a promising solution. These coatings have low surface energy and contaminants do not adhere well. Even if soiling does remain on the coated surface, it is much more easily removed during cleaning. The performance of the coatings is determined using the water contact angle and roll-off angle measurements. However, although hydrophobic coatings hold out great promise, outdoor testing revealed degradation that occurs surprisingly quickly. In this study, we report on results using laboratory-based damp heat and UV exposure environmental tests. We used SEM surface imaging and XPS surface chemical analysis to study the mechanisms that lead to coating degradation. Loss of surface fluorine from the coatings was observed and this appeared to be a major issue. Loss of nanoparticles was also observed. Blistering of surfaces also occurs, leading to loss of coating material. This was probably due to the movement of retained solvents and was caused by insufficient curing. This mechanism is avoidable if care is taken for providing and carrying out carefully specified curing conditions. All these symptoms correlate well with observations taken from parallel outdoor testing. Identification of the mechanisms involved will inform the development of more durable anti-soiling, hydrophobic coatings for solar application.

Antioxidant activity is an important feature for food contact materials such as packaging, aiming to preserve freshness and retard food spoilage. Common bioactive agents are highly susceptible to various forms of degradation; therefore, protection is required to maintain functionality and bioavailability. Poly(ε-caprolactone) (PCL), a biodegradable GRAS labeled polymer, was used in this study for encapsulation of α-tocopherol antioxidant, a major component of vitamin E, in the form of electrospun fibers. Rheological properties of the fiber forming solutions, which determine the electrospinning behavior, were correlated with the properties of electrospun fibers, e.g., morphology and surface properties. Interactions through hydrogen bonds were evidenced between the two components. These have strong effect on structuration of macromolecular chains, especially at low α-tocopherol amounts, decreasing viscosity and elastic modulus. Intra-molecular interactions in PCL strengthen at high α-tocopherol amounts due to decreased solvation, allowing good structural recovery after cease of mechanical stress. Morphologically homogeneous electrospun fibers were obtained, with ~6 μm average diameter. The obtained fibers were highly hydrophobic, with fast release in 95% ethanol as alternative simulant for fatty foods. This induced good in vitro antioxidant activity and significant in vivo reduction of microbial growth on cheese, as determined by respirometry. Therefore, the electrospun fibers from PCL entrapping α-tocopherol as bioactive agent showed potential use in food packaging materials.

Coatings are often applied in the materials industry to impart hydrophobic properties to the produced materials. Commonly used coatings contain plastics as well as perfluorinated compounds, which pose challenges for environmental sustainability due to their persistence and end-of-life impacts. Coatings based on natural wax, such as rapeseed, soy, palm or beeswax, constitute a key bio-based and more sustainable alternative. These waxes exhibit high hydrophobicity while also being biodegradable, offering opportunities to replace fossil-derived coatings within circular-economy material systems. Wax coating constitutes a protective layer that undergoes biodegradation after a certain amount of time. This paper presents the results of studies concerning the development of a wax coating characterized by a coarse microstructure that increases water resistance, and an appropriate susceptibility to biodegradation. It was revealed that all the analysed coatings were susceptible to biodegradation, although their rates varied markedly depending on wax type and form. The biodegradation of palm wax in bulk form and as a thick layer was 17% and 80%, respectively, after 180 days. Palm wax exhibited a pronounced ability to bind inorganic and organic matter deposits, which reduced the degradation rate. When applied as a thin coating, palm wax did not form such a barrier. Palm wax significantly influences coating durability because its surface undergoes morphic changes induced by bio-surfactants secreted by microorganisms. These changes the adhesion of organic and inorganic matter particles, and the layer thus established limits the diffusion of oxygen, enzymes and microorganisms to the wax coating. The tests demonstrated that the addition of palm wax to wax mixtures allows the degradation rate to be controlled, and that its inhibitory effect is strongly dependent on the geometry of the material.

The presence of soiling on photovoltaic modules reduces light transmission through the front cover glass to the active absorber, thereby reducing efficiency and performance. Current soiling mitigation techniques are expensive and/or ineffective. However, anti-soiling coatings applied to the solar cover glass have the potential to reduce soiling for long periods of time without continuous maintenance. This paper reports the performance of two transparent hydrophobic coatings (A and B) exposed to the outdoor environment of coastal Denmark for 24 weeks. A comparison was made between the performance of coated and uncoated glass coupons, periodically cleaned coupons, and accelerated laboratory tests. Although initial results were promising, water contact angle and transmittance values were found to decline continuously for all coated and uncoated coupons. Surface blisters, film thickness reduction, changes in surface chemistry (fluorine loss), and abrasion damage following cleaning were observed. Coupons cleaned every 4 weeks showed a restoration in transmittance. Cycles of light rainfall and evaporation combined with a humid and salty environment led to cementation occurring on all coupons. The development of an abrasion-resistant, super-hydrophobic coating with a low roll-off angle and high water contact angle is more likely to provide an anti-soiling solution by reducing the build-up of cementation.

Despite their effectiveness in preventing icing, hydrophobic coatings possess drawbacks such as susceptibility to detachment and limited wear resistance, leading to inadequate longevity in melting ice/snow. To enhance the surface stability and durability of superhydrophobic coatings, nanoparticle/epoxy formulations were developed using three types of nanoparticles, two dispersion techniques, three application methods, and two epoxy resin introduction approaches. Testing encompassed water contact angle measurements, assessment of ice adhesion force, and determination of icing rates on asphalt concrete coated with these hydrophobic formulations. Fourier-transform infrared spectroscopy was employed to analyze the molecular structures of the coatings, while scanning electron microscopy facilitated observation of the surface morphology of the hydrophobic coatings. The findings indicated that nano-ZnO, TiO2, and SiO2 particles could be modified into hydrophobic forms using stearic acid. Application of the hydrophobic coating improved the concrete’s hydrophobicity, reduced ice adhesion strength on both concrete and asphalt, and delayed the onset of icing. Furthermore, optimal dosages of stearic acid, nanoparticles, and epoxy resin were identified as crucial parameters within specific ranges to ensure the optimal hydrophobicity and durability of the coatings.

Water repellency has significant potential in applications like self-cleaning coatings, anti-staining textiles, and electronics. This study introduces a novel nanocomposite system incorporating functionalized Al2O3 and CeO2 nanoparticles within a polyurethane matrix to achieve hydrophobic and UV-blocking properties. The nanoparticles were functionalized using an octadecyl phosphonic acid solution and characterized by FTIR and XPS, confirming non-covalent functionalization. Spin-coated polyurethane coatings with functionalized and non-functionalized Al2O3, CeO2, and binary Al2O3-CeO2 nanoparticles were analyzed. The three-layered Al2O3-CeO2-ODPA binary system achieved a contact angle of 166.4° and 85% transmittance in the visible range. Incorporating this binary functionalized system into a 0.4% w/v polyurethane solution resulted in a nanocomposite with 75% visible transmittance, 60% at 365 nm UV, and a 147.7° contact angle after three layers. These findings suggest that ODPA-functionalized nanoparticles, when combined with a polymer matrix, offer a promising approach to developing advanced hydrophobic and UV-protective coatings with potential applications across various industrial sectors.