Walterarmstrong7632

To fabricate antibacterial activity and simultaneous strengthened and toughened carboxylated nitrile butadiene rubber (XNBR) composites, starch was oxidized by H2O2 to achieve oxidized starch (OST) with different carboxyl content, meanwhile, ZnO were utilized to promote the in-situ interfacial reaction for improving compatibility of starch and XNBR. The formation of ionic cross-link networks and "Zinc-carboxylate polymers" in the XNBR/OST/ZnO composites were confirmed by FT-IR, XRD, XPS, SEM-EDS and TEM. Interestingly, because of the carboxyl groups of OSTs which provided a low pH surroundings to inhibit the growth of bacteria, XNBR/OST/ZnO composites achieved a significant antibacterial activity. Noteworthy, the sulfur-free XNBR composites achieved 3.04 and 1.99 times increase for tensile strength and elongation at break compared with neat XNBR. The mechanism of simultaneous strengthened and toughened for composites had been proposed. These new sustainable, green and facile fabricated XNBR/OST/ZnO could be utilized as the medical protective appliance to against the bacteria.Tough hydrogels with shape memory property are highly desirable for actuators and smart engineering materials. Herein, super-tough polyacrylamide/iota-carrageenan double-network hydrogels were synthesized via a one-pot radical polymerization and strengthened by incorporating bacterial cellulose microclusters, through the intermolecular hydrogen bonds and topological interlock between microclusters and polymer network. Such hydrogels were able to withstand over 200 kPa of tensile stress, or be stretched over 27 times of initial length, and reached a high toughness of ∼2000 kJ/m3. By tension-drying and post-annealing treatments on the strongest hydrogel, dry strands were fabricated to withstand over 100 MPa of tensile stress. Moreover, these strands presented water-stimulated shape memory by a recovery ratio of 84.3 % in 4 min. Based on these characteristics, this super-tough hydrogel may serve as smart textile or actuator for a variety of applications.Wood is actually a natural polymers composite that is easy to process, mainly constituted of cellulose, hemicellulose and lignin. However, most wood-based functional materials are prepared by physical methods, which undoubtedly limit the application of wood-based materials. Herein, the wood aerogel (WA) was obtained from wood by delignification and freezing dried. Selleck Elacridar The WA then was fabricated into an unexpected photochromic wood aerogel (PWA) via surface-initiated atom transfer radical polymerization (SI-ATRP) covalently grafting poly6-[4-(4-methoxyphenyl-azo)phenoxy]hexyl methacrylate (PMAZOM). Both WA and PWA showed good compression resilience. The hydrophobicity of PWA was obviously enhanced because of the surface modification. The color of PWA can change from yellow to orange-red after being irradiated by UV light for 30 s. The color of sample can be reversibly changed to yellow under sunlight for 200 s. The lightweight and photosensitive wood aerogel is potential to apply for optical information storage materials and photosensitive devices.This review examines investigations into the functionalization of polysaccharides by substituents containing multiple (CC) bonds and thiol (SH) groups that are prone to (co)polymerization in the presence of thermal, redox and photoinitiators or Michael addition reactions. A comparative analysis of the approaches to grafting the mentioned substituents onto the polysaccharide macromolecules was conducted. The use of the modified polysaccharides for the design of the 3D structures, including for the development of the pore bearing matrixes of cells or scaffolds utilized in regenerative medicine was examined. These modified polymers were also examined toward the design of excipient matrixes in pharmacological compositions, including with controllable release of active pharmaceuticals, as wel as of antibacterial and antifungal agents and others. In addition, a few examples of the use of modified derivatives in other areas are given.Oligosaccharides are one of the most important components in mammalian milk. Milk oligosaccharides can promote colonization of gut microbiota and protect newborns from infections. The diversity and structures of MOs differ among mammalian species. MOs in human and farm animals have been well-documented. However, the knowledge on MOs in rat and mouse have been very limited even though they are the most-widely used models for studies of human physiology and disease. Herein, we use a high-sensitivity online solid-phase extraction and HILIC coupled with electrospray tandem mass spectrometry to analyze the acidic MOs in rat and mouse. Among the fifteen MOs identified, twelve were reported for the first time in rat and mouse together with two novel sulphated oligosaccharides. The complete list of acidic oligosaccharides present in rat and mouse milk is the baseline information of these animals and should contribute to biological/biomedical studies using rats and mice as models.In this work, hydroxypropyl-β-cyclodextrin-polyurethane magnetic nanoconjugates/reduced graphene oxide (HPMNPU/GO) supramolecules were prepared. The adsorbent was characterized using FTIR and SEM. The adsorbent was evaluated for its efficiency to remove Cr6+ and Pb2+ from aqueous solutions through batch adsorption studies following a Definitive Screening Design (DSD). Effects of solution pH, contact time, adsorbent dosage, initial metal concentration, ionic strength, GO/NC ratio and temperature on Cr 6+ and Pb 2+ adsorption were investigated. Optimization of the adsorption process was done using a desirability function of the Design Expert V11 software. A good agreement between experimental and predicted data proved the efficiency of this model for prediction of real optimum point. The batch experiments implied that the pseudo-second-order model (lowest sum of square error (SSE) values and correlation coefficients (R2) > 0.999) was better to describe the adsorption kinetics of Cr6+ and Pb2+ onto the HPMNPU/GO.The polysaccharide from Ribes nigrum L. (RCP) was modified by nitric acid-sodium selenite method. After purification by Sepharose-6B, high purity native (PRCP) and three selenized polysaccharides (PRSPs) with different selenium contents were obtained. Compared with PRCP, PRSPs possessed the lower molecular weight, better water-solubility, physical stability and rheological properties. FT-IR and NMR spectra confirmed PRSPs had the characteristic absorption peaks of polysaccharides and the glycosidic bond types were not changed after selenylation modification, whereas the selenyl groups existing in PRSPs were mainly introduced at the C-6 position of sugar residue →4)-β-d-Manp-(1→. Moreover, PRSPs displayed obviously smoother and smaller flaky structure than PRCP, and their inhibitory effects on α-amylase and α-glucosidase also were greater than PRCP. PRSPs exhibited a reversible inhibition on two enzymes in competitive manner and quenched their fluorescence through the static quenching mechanism. The polysaccharide-enzyme complex was spontaneously formed mainly driven by the hydrophobic interaction and hydrogen bonding.