Search

Objectives: In this paper we propose embedding natural fillers, such as pristine and functionalized chitin nanocrystals, into resin adhesives to produce photopolymerizable dental filled adhesives with enhanced biocompatibility, hydrophobicity, mechanical resistance, and anti-bacterial properties., Methods: Chitin nanocrystals (ChNC) were functionalized with decanoyl chloride and methacrylic anhydride to produce ChNC-C10 and ChNC-MA, respectively. These hydrophobically functionalized chitin nanocrystals were incorporated into a resin adhesive at concentrations of 0.5-3.0 wt% to assess the materials' physical and mechanical properties through Fourier-transform infrared (FTIR) spectroscopy, solid-state NMR spectroscopy, X-ray diffraction (XRD), elemental analysis, scanning electron microscopy (SEM), thermogravimetric analysis (TGA), flexural strength, microhardness, and water sorption tests., Results: The analytical techniques confirmed the successful preparation of chitin nanocrystals from commercial chitin powder derived from shrimp shells and the efficient hydrophobization of their surface. Electron microscope images indicated that the increased hydrophobicity of ChNC-C10 promotes the formation of layered structures throughout the resin adhesive, while ChNC-MA tends to form aggregates in the matrix. Adhesives filled with ChNC-C10 enhanced their flexural strength, microhardness, and thermal stability and decreased their water sorption and degree of conversion. Adhesives filled with ChNC-MA resulted in improvements in microhardness, in water sorption and degree of conversion, although they did not exhibit augmentation of their flexural strength and thermal stability., Significance: In light of the improved physical and mechanical properties with respect to the control, resin adhesives filled with anti-bacterial chitin nanocrystals are promising new materials for dental applications, especially those filled with low/moderate amounts of ChNC-C10., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

The properties of chiral nematic and iridescent cellulose nanocrystal films with different monovalent cations (CNC-X) obtained through evaporation-induced self-assembly (EISA) can be modified by a variety of external stimuli. Here, we study the transformations of their optical and structural properties when the films are thermally annealed at 200 °C and 240 °C for up to 2 days. The chiral nematic structure of the most thermally stable films is not destroyed even after extensive heating due to the thermochemical stability of the cellulose backbone and the presence of surface alkali counterions, which suppress catalysis of early stage degradation. Despite the resilience of the cholesteric structure and the overall integrity of heated CNC-X films, thermal annealing is often accompanied by reduction of iridescence, birefringence, and transparency, as well as formation of degradation products. The versatility, sustainability, and stability of CNC-X films highlight their potential as temperature indicators and photonic devices., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Bioderived cellulose nanocrystals (CNCs) are used to create light, flexible, biocompatible, and biodegradable electronic devices. Herein, surface modification of cellulose nanocrystals was employed to fabricate cationic and anionic CNCs. Subsequently, we demonstrated rectification behavior from a fixed junction between two agarose hydrogels doped with cationic and anionic cellulose nanocrystals. The current rectification ratio reaches 70 reproducibly, which is significantly higher than that for analogous diodes generated with microfibrillated cellulose (∼15) and the first polyelectrolyte gel diode (∼40). The current-voltage characteristics of the CNC-hydrogel diode are influenced by concentration, gel thickness, scanning frequency, and applied voltage. The high surface area of CNC resulted in high charge density after surface modification, which in turn resulted in good rectification behavior from only small amounts of dopant material.

Cellulose-derived materials, such as microcellulose and nanocellulose, are sustainable materials with a wide range of applications. Here, through a multi-analytical approach, we investigate the thermal degradation of microfibrillar cellulose filaments (CFs); acidic cellulose nanocrystals (CNC-H), containing sulfate half-ester groups on the surface; and neutralized cellulose nanocrystals (CNC-Na), where the protons are replaced by sodium ions. CFs have a simple degradation mechanism, associated with extensive dehydration, decarboxylation, and decarbonylation, and the highest thermal stability of the three (∼325 °C) despite the abundance of amorphous regions and inhomogeneous fibrous mass that make them structurally and morphologically less homogeneous than high-crystallinity CNCs. CNC-H decompose in a complex way below 200 °C, with large char fractions and evaporation of sulfur compounds at high temperatures, while sodium counterions in CNC-Na can improve the thermal stability up to 300 °C, where the pyrolysis leads to partial rehydration and formation of sodium hydroxide on the surface.

The functionalization of cellulose nanocrystal (CNC) aerogels was achieved through a two-step synthetic procedure. CNC aerogels were prepared under hydrothermal conditions, followed by solvent exchange and critical point drying. The CNC aerogels were functionalized with a methacrylate group and then underwent thiol-ene click chemistry to impart a range of functionalities onto the surface of the CNC aerogel. The use of the functionalized aerogels as oil absorbents was then investigated, with the most hydrophobic CNC aerogel, 1 H,1 H,2 H,2 H-perfluorodecanethiol-functionalized CNC aerogel, exhibiting the highest absorption of xylenes at 2.9 mL g -1 .