The surface modification of cellulose nanocrystals (CNC) is a key intermediate step in the development of new functionalities and the tailoring of nanomaterial properties for specific applications. In the area of polymeric nanocomposites, apart from good interfacial adhesion, the high thermal stability of cellulose nanomaterial is vitally required for the stable processing and improvement of material properties. In this respect, the heterogeneous esterification of CNC with succinic anhydride was investigated in this work in order to obtain CNC with optimised surface and thermal properties. The influence of reaction parameters, such as time, temperature, and molar ratio of reagents, on the structure, morphology and thermal properties, were systematically studied over a wide range of values by DLS, FTIR, XPS, WAXD, SEM and TGA methods. It was found that the degree of surface substitution of CNC increased with the molar ratio of succinic anhydride to cellulose hydroxyl groups (SA:OH), as well as the reaction time, whilst the temperature of reaction showed a moderate effect on the degree of esterification in the range of 70–110 °C. The studies on the thermal stability of modified nanoparticles indicated that there is a critical extent of surface esterification below which only a slight decrease of the initial temperature of degradation was observed in pyrolytic and oxidative atmospheres. A significant reduction of CNC thermal stability was observed only for the longest reaction time (240 min) and the highest molar ratio of SA:OH. This illustrates the possibility of manufacturing thermally stable, succinylated, CNC by controlling the reaction conditions and the degree of esterification.

The wider use of renewable feedstock in structural applications, where high mechanical performance is required, can be achieved by the application of recently developed engineering biopolymers and their further modification by micro-and nanoparticles. In this review, we present the current state of the art of biopolyamide materials for structural and functional applications. The overview includes all stages of the manufacturing-from the synthesis of building blocks, through the synthesis of polymers and its physical modification, with special emphasis on the properties of the obtained engineering biocomposites as a final product of modern polymer technology. In the first part, the synthetic routes of bio-derived counterparts of common polyamides as well as specialty polymers with functional properties arising from the complex structure of biochemicals were exemplified. The development of environmentally friendly composites and nanocomposites based on biopolyamides and natural fillers, such as plant fibers or cellulosic nanofibers, was of particular interest due to preserved sustainable character of such materials.

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Nowadays, increasing attention is devoted to the search for polymeric composite materials that are characterized by reduced flammability. In this work, the layer-by-layer (LbL) technique was applied to form multilayered protective coatings for polyamide 6/montmorillonite (PA6/MMT) hybrid nanocomposites. This time, the double layers LbL deposition was used in order to improve the thermal properties or flammability of PA6 materials. Our goal was to check how five, 10, and 15 triple-layer deposition onto the surface of PA6 and PA6/MMT composites influenced these relevant properties. For this reason, disodium H-phosphonate, sodium montmorillonite, and iodo-bis(triphenylphosphino)copper were used for polyelectrolyte solution preparation. It was found that the LbL method could be successfully used to improve the flammability characteristics of polyamide 6-based composites. Nevertheless, the deposition of the copper complex should be combined with other flame retardants—preferentially containing phosphorus—which enable synergistic effects to occur. Moreover, microscopic observations confirmed that the surfaces on which the formation of interwoven fibrous crystal structures was observed had a tendency to protect the entire material against the destructive effects of heat, contributing, among other things, to reduce the maximum point of heat release rate (PHRR).