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Applications ofNanochitin in Multidimensional Materials AK 5.1. Application of Nanochitins as Building Blocks AL 5.1.1. Nanochitin as a Pickering Stabilizer AL 5.
Micro- and nanofibrillated cellulose (MNFC) was extracted from pineapple stems by acid hydrolysis, then characterized and tested in two concentrations (0.5 and 1.0 wt%) in polyvinyl acetate (PVAc) and urea-formaldehyde (UF) adhesives. The modified adhesives were used to glue three tropical wood species (Vochysia ferruginea, Cordia alliodora, and Gmelina arborea), and their corresponding bond strength resistance was determined. MNFC and the correspondent adhesives were characterized by TGA, FTIR, SEM, TEM, AFM, and viscosity determination. The TGA analysis of MNFC showed three decomposition reactions. The SEM, TEM, and AFM evaluations demonstrated the presence of micro- and nanosized dimensions of particles after the acid hydrolysis of pineapple stems. Adding 1 wt% MNFC to PVAc and UF adhesives increased their thermal stability in similar manner. Viscosity diminished in both modified adhesives with MNFC; however, this reduction did not affect the adhesion properties in the tropical wood tested. MNFC added to PVAc and UF adhesives improved shear strength (SS) of the glue line in the three tropical species tested. The highest SS increase was obtained when adding 0.5 wt% MNFC to PVAc in V. ferruginea, and 1 wt% MNFC concentration in the case of C. alliodora and G. arborea. In the case of UF adhesives, the application of 1 wt% MNFC produced significant differences in SS for the three tropical species studied.
The long-term biodegradation of various polyurethanes with and without surface modifications was evaluated by implanting small porous filamentous patches of these materials subcutaneously in the backs of dogs for one month. Data were compared to those obtained with spun polyurethane vascular grafts of similar materials implanted in the aorto-iliac position in dogs. The extremely high surface area of approximately 7 m2/cm3 of these porous filamentous patches provided numerous sites for surface cracking and the very fine filaments (10 microns in diameter) provided an easily identifiable structure to study the cracking phenomenon. Results from numerous one month implants clearly demonstrated that the subcutaneous implant model effectively reproduced the biodegradation behavior observed in vascular graft implants. The degradation was most pronounced in the softer Shore 80A polyurethanes and less pronounced in the harder 55D and 75D polyurethanes. The degradation could not simply be stopped by stress annealing the polyurethane and the degradation did not require the presence of metallic ions. Antioxidants, surface adsorbed albumin, poly(2-hydroxyethyl-methacrylate) grafting, silicone copolymerization, tetrafluoroethylene plasma discharge and the addition of urea linkages to the polymer were also shown to be ineffective in stopping the biodegradation process. In contrast, covalent bonding or grafting of silicone polymer to the surface of the urethane successfully inhibited the biodegradation process.
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