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Updated: Dec 11, 2025

Highly Stable, Functional Hairy Nanoparticles and Biopolymers from Wood Fibers: Towards Sustainable Nanotechnology
Published on: July 20, 2016
Patience is a virtue: self-assembly and physico-chemical properties of cellulose nanocrystal allomorphs
Gwendoline Delepierre1, Samuel Eyley2, Wim Thielemans2
1Adolphe Merkle Institute, University of Fribourg, Chemin des Verdiers 4, 1700 Fribourg, Switzerland and University of British Columbia, 2424 Main Mall, Vancouver, BC V6 T 1Z4, Canada. emily.cranston@ubc.ca.
Abstract:
Cellulose nanocrystals (CNCs) are bio-based rod-like nanoparticles with a quickly expanding market. Despite the fact that a variety of production routes and starting cellulose sources are employed, all industrially produced CNCs consist of cellulose I (CNC-I), the native crystalline allomorph of cellulose. Here a comparative study of the physico-chemical properties and liquid crystalline behavior of CNCs produced from cellulose II (CNC-II) and typical CNC-I is reported. CNC-I and CNC-II are isolated by sulfuric acid hydrolysis of cotton and mercerized cotton, respectively. The two allomorphs display similar surface charge densities and ζ-potentials and both have a right-handed twist, but CNC-II have a slightly smaller average length and aspect ratio, and are less hygroscopic. Interestingly, the self-assembly behavior of CNC-I and CNC-II in water is different. Whilst CNC-I forms a chiral nematic phase, CNC-II initially phase separates into an upper isotropic and a lower nematic liquid crystalline phase, before a slow reorganization into a large-pitch chiral nematic texture occurs. This is potentially caused by a combination of factors, including the inferred faster rotational diffusion of CNC-II and the different crystal structures of CNC-I and CNC-II, which are responsible for the presence and absence of a giant dipole moment, respectively.
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