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The combination of topology and CO2 switchability could provide new options for amphiphilic copolymers. Cyclic molecules supply novel topologies, and CO2 switching provides stimulus responsiveness. Cyclic poly(2–(diethylamino)ethyl methacrylate)–b–poly(ethylene oxide) and their corresponding block copolymers were prepared from poly(ethylene oxide) and 2–(diethylamino)ethyl methacrylate via atom transfer radical polymerization and Keck allylation with a Hoveyda–Grubbs catalyst. Changes in conductivity, surface activity, and hydrodynamic size were examined to illustrate the switchability of the produced amphiphilic copolymers upon contact with CO2 in the presence of water. The reversible emulsification and switchable viscosity behaviors of the copolymers were also demonstrated. [ABSTRACT FROM AUTHOR]

Essential oils (EOs) have stability problems, including volatility, oxidation, photosensitivity, heat sensitivity, humidity sensitivity, pH sensitivity, and ion sensitivity. A drug delivery system is an effective way to stabilize EOs, especially due to the protective effect of polymeric drug carriers. Polysaccharides are frequently employed as drug carrier materials because they are highly safe, come in a variety of forms, and have plentiful sources. Interestingly, the EO drug delivery system is based on the biomimetic concept since it corresponds to the structure of plant tissue. In this paper, we associate the biomimetic plant-like structures of the EO drug delivery system with the natural forms of EO in plant tissues, and summarize the characteristics of polysaccharide-based drug carriers for EO protection. Thus, we highlight the research progress on polysaccharides and their modified materials, including gum arabic, starch, cellulose, chitosan, sodium alginate, pectin, and pullulan, and their use as biomimetic drug carriers for EO preparations due to their abilities and potential for EO protection. [ABSTRACT FROM AUTHOR]

To give full play to the advantages of polyurethane as a binder, such as mixing at room temperature, short curing time, and high curing strength, polyurethane was used as the binder of a waste asphalt mixture, and the pavement performance of PCRM (Polyurethane Cold-Recycled Mixture) was analyzed. Firstly, the adhesion performance of polyurethane binder with new and old aggregates was evaluated using the adhesion test. Then, the mix proportion was designed according to the material characteristics, and the reasonable molding process, maintenance conditions, design indexes, and the optimal binder ratio were proposed. Secondly, the high-temperature stability, low-temperature crack resistance, water stability, and compressive resilient modulus of the mixture were evaluated through laboratory tests. Finally, the pore structure and microscopic morphology of polyurethane cold-recycled mixture were analyzed by industrial CT (Computerized Tomography) scanning, and the failure mechanism of polyurethane cold-recycled mixture was revealed. The test results show that the adhesion between polyurethane and RAP (Reclaimed Asphalt Pavement) is good, and the splitting strength of the mixture increases greatly when the ratio of glue to stone reaches 9%. Polyurethane binder has low sensitivity to temperature and poor water stability. With the increase of RAP content, the high-temperature stability, low-temperature crack resistance, and compressive resilient modulus of PCRM showed a decreasing trend. When the RAP content was less than 40%, the freeze–thaw splitting strength ratio of the mixture was improved. After the incorporation of RAP, the interface was more complex and there were many micron-scale holes, cracks, and other defects; after high-temperature immersion, the polyurethane binder appeared to show a certain degree of peeling at the holes of the RAP surface. After freeze–thaw, the polyurethane binder on the surface of the mixture produced many cracks. The study of polyurethane cold-recycled mixture is of great significance to realize green construction. [ABSTRACT FROM AUTHOR]

Hydrogels based on nanocomposites (NC) structure have acquired a great deal of interest, but they are still limited by relatively low mechanical strength, inevitably losing elasticity when applied below subzero temperatures, due to the formation of ice crystallization. In this study, an anti-freezing and mechanically strong Laponite NC organohydrogel was prepared by a direct solvent replacement strategy of immersing Laponite NC pre-hydrogel into ethylene glycol (EG)/water mixture solution. In the organohydrogel, a part of water molecules was replaced by EG, which inhibited the formation of ice crystallization even at extremely low temperatures. In addition, the formation of hydrogen bonds between Laponite and the monomers of N-isopropylacrylamide (NIPAM) and hydroxyethyl acrylate (HEA) endowed the organohydrogels with high mechanical strength and toughness. The NC organohydrogel can maintain its mechanical flexibility even at −25 °C. The compressive stress, tensile stress, and elongation at the break of N5H5L reached 3871.71 kPa, 137.05 kPa, and 173.39%, respectively, which may be potentially applied as ocean probes in low temperature environment. [ABSTRACT FROM AUTHOR]

To develop a novel asymmetric nanofiber membrane with antioxidant and antibacterial activities, biocompatible polyvinyl pyrrolidone (PVP) and polycaprolactone (PCL) were used as carriers to load water-soluble tea tree extract (TTE) and hydrophobic tea tree oil (TTO) via electrospinning and electrostatic spraying, respectively, which was named as TTE-PVP-3/TTO-PCL. The results show that uniform TTE-PVP nanofibers with an average diameter of 95 ± 27 nm could be obtained when the mass ratio of TTE to PVP was set as 1:3. Homogeneous TTO/PCL microspheres with an average size of 4.38 ± 0.79 µm could be obtained when the propulsion speed was 0.08 mm/min and the voltage was 10 KV. The activity study showed that TTE could only improve the antioxidant activity of TTE-PVP-3/TTO-PCL, while TTO could improve the antibacterial activity effectively. Under experimental conditions, the inhibition zones of TTE-PVP-3/TTO-PCL against Staphylococcus aureus and Escherichia coli were 7.50 ± 0.48 mm and 9.55 ± 0.45 mm, respectively, and its scavenging rates for 2,2-diphenylpicrylhydrazyl (DHPP) and hydroxyl radical were 59.79 ± 4.10% and 61.02 ± 4.95%, respectively. In conclusions, TTE-PVP-3/TTO PCL can be potentially used as a new kind of anti-oxidative and antibacterial wound dressings. [ABSTRACT FROM AUTHOR]

Sustainable and affordable supply of clean, safe, and adequate water is one of the most challenging issues facing the world. Membrane separation technology is one of the most cost-effective and widely applied technologies for water purification. Polymeric membranes such as cellulose-based (CA) membranes and thin-film composite (TFC) membranes have dominated the industry since 1980. Although further development of polymeric membranes for better performance is laborious, the research findings and sustained progress in inorganic membrane development have grown fast and solve some remaining problems. In addition to conventional ceramic metal oxide membranes, membranes prepared by graphene oxide (GO), carbon nanotubes (CNTs), and mixed matrix materials (MMMs) have attracted enormous attention due to their desirable properties such as tunable pore structure, excellent chemical, mechanical, and thermal tolerance, good salt rejection and/or high water permeability. This review provides insight into synthesis approaches and structural properties of recent reverse osmosis (RO) and nanofiltration (NF) membranes which are used to retain dissolved species such as heavy metals, electrolytes, and inorganic salts in various aqueous solutions. A specific focus has been placed on introducing and comparing water purification performance of different classes of polymeric and ceramic membranes in related water treatment industries. Furthermore, the development challenges and research opportunities of organic and inorganic membranes are discussed and the further perspectives are analyzed. [ABSTRACT FROM AUTHOR]