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Chitin nanocrystals (ChNCs) are unique to all other bio-derived nanomaterials in one aspect: the inherent presence of a nitrogen moiety. By tuning the chemical functionality of this nanomaterial, and thus its charge and hydrogen bonding capacity, one can heavily impact its macroscopic properties such as its rheological and self-assembly characteristics. In this study, two types of ChNCs are made using acid hydrolysis (AH-ChNCs) and oxidative (OX-ChNCs) pathways, unto which deacetylation using a solvent-free procedure is utilized to create chitosan nanocrystals (ChsNCs) of varying degree of deacetylation (DDA). These nanocrystals were then studied for their rheological behavior and liquid crystalline ordering. It was found that with both deacetylation and carboxylation of ChNCs, viscosity continually increased with increasing concentrations from 2 to 8 wt %, contrary to AH-ChNC dispersions in the same range. Interestingly, increasing the amine content of ChNCs was not proportional to the storage modulus, where a peak saturation of amines provided the most stiffness. Conversely, while the introduction of carboxylation increased the elastic modulus of OX-ChNCs by an order of magnitude from that of AH-ChNCs, it was decreased by increasing DDA. Deacetylation and carboxylation both inhibited the formation of a chiral nematic phase. Finally, these series of nanocrystals were incorporated into biodegradable pectin-alginate films as a physical reinforcement, which showed increased tensile strength and Young's modulus values for the films incorporated with ChsNCs. Overall, this study is the first to investigate how surface functionalization of chitin-derived nanocrystals can affect their rheological and liquid crystalline properties and how it augments pectin/alginate films as a physical reinforcement nanofiller.

In this study, we demonstrate for the first time the fabrication of carboxylated chitosan nanocrystals (ChsNC) with high degree of deacetylation (DDA) at >80% and narrow size distribution. We also studied its application as a sustainable support material for metal-based catalysts. Carboxylated chitin nanocrystals (ChNCs) were initially prepared through partial cleavage of glycosidic bonds in chitin by ammonium persulfate, with concurrent oxidation of chitin C6 primary alcohols to produce carboxylate groups on the surface of the ChNCs. ChsNCs were subsequently prepared using an alkaline deacetylation procedure in the presence of NaBH 4 to preserve the nanorod structure of the biomaterial. The resulting nanocrystals feature both carboxyl and amino functional groups. Transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier-transform infrared (FTIR) spectroscopy were used to determine the morphology and composition of these carboxylated ChNCs and ChsNCs. Subsequently, we tested the ability of the as-made ChsNCs as a biomass-based catalyst support for Au nanoparticles (NPs) using the 4-nitrophenol reduction and the aldehyde-amine-alkyne (A 3 ) coupling reactions to demonstrate its capabilities in regard to the ones of cellulose nanocrystals (CNCs). In particular, Au NPs over ChsNCs featured the highest turnover frequency (TOF) value for the 4-nitrophenol reduction reported for all Au-based catalysts supported on carbon-based systems. Spectroscopic and imaging techniques confirmed the importance of precisely controlling the redox state of Au as it is being deposited to afford a highly disperse active site on the bionano-support.

Chitosan is readily available from various biomass waste streams including crustaceans, cephalopods, insects, and fungus. The polymer possesses primary amine groups which are great handles for functionalization. Yet efficient functionalization with high degree of substitution is challenging to achieve via solvothermal methods due to limitations in chitosan solvation properties. Herein we report a mechanochemical and aging-based method directly addressing this point. Working in the solid phase helps stabilize the formation of Schiff bases from chitosan and aldehydes, affording a novel pathway to the green functionalization of chitosan by reductive alkylation, with unprecedentedly high degrees of substitution. The method showed great efficacy and compatibility for chitosan to be functionalized with 21 different aldehyde substrates and a low process mass intensity (PMI) of 36. This work also opens a new avenue for the development of mechanochemical and aging-based reductive amination transformations. [ABSTRACT FROM AUTHOR]

Marine biomass waste is a remarkable source of functional molecules and materials. Yet material extraction, conversion and processing are often chemically intensive, preventing the widespread and clean use of these abundant resources for high-end applications. Moreover, current challenges in biomedicine call for the design of novel materials with better functional and mechanical properties. Herein, we present a novel chemical process to afford chitosan nanocrystals (ChsNCs), which uniquely combine a high degree of deacetylation, rod shape and high crystallinity for mechanical robustness. This method is a simple solid-state aging process starting from chitin nanocrystals (ChNCs) and requiring limited chemical and energetic input, which we have quantified using process mass intensity as the sustainability metric. This method, as well as a previously reported solution-based method, afforded a family of novel nanomaterials, which we used to form alginate hydrogels. The resulting materials are the first examples of ChsNC-based hydrogels and featured superior performances in terms of both rheological properties, as well as sustained drug release, as compared to previously reported chitosan/alginate systems. This work opens an avenue for functional soft materials using a green resource via a clean process. [ABSTRACT FROM AUTHOR]