Enzymatic Hydrolysis Combined with Mechanical Shearing and High-Pressure Homogenization for Nanoscale Cellulose Fibrils and Strong Gels
Top Cited Papers
- 3 May 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Biomacromolecules
- Vol. 8 (6) , 1934-1941
- https://doi.org/10.1021/bm061215p
Abstract
Toward exploiting the attractive mechanical properties of cellulose I nanoelements, a novel route is demonstrated, which combines enzymatic hydrolysis and mechanical shearing. Previously, an aggressive acid hydrolysis and sonication of cellulose I containing fibers was shown to lead to a network of weakly hydrogen-bonded rodlike cellulose elements typically with a low aspect ratio. On the other hand, high mechanical shearing resulted in longer and entangled nanoscale cellulose elements leading to stronger networks and gels. Nevertheless, a widespread use of the latter concept has been hindered because of lack of feasible methods of preparation, suggesting a combination of mild hydrolysis and shearing to disintegrate cellulose I containing fibers into high aspect ratio cellulose I nanoscale elements. In this work, mild enzymatic hydrolysis has been introduced and combined with mechanical shearing and a high-pressure homogenization, leading to a controlled fibrillation down to nanoscale and a network of long and highly entangled cellulose I elements. The resulting strong aqueous gels exhibit more than 5 orders of magnitude tunable storage modulus G‘ upon changing the concentration. Cryotransmission electron microscopy, atomic force microscopy, and cross-polarization/magic-angle spinning (CP/MAS) 13C NMR suggest that the cellulose I structural elements obtained are dominated by two fractions, one with lateral dimension of 5−6 nm and one with lateral dimensions of about 10−20 nm. The thicker diameter regions may act as the junction zones for the networks. The resulting material will herein be referred to as MFC (microfibrillated cellulose). Dynamical rheology showed that the aqueous suspensions behaved as gels in the whole investigated concentration range 0.125−5.9% w/w, G‘ ranging from 1.5 Pa to 105 Pa. The maximum G‘ was high, about 2 orders of magnitude larger than typically observed for the corresponding nonentangled low aspect ratio cellulose I gels, and G‘ scales with concentration with the power of approximately three. The described preparation method of MFC allows control over the final properties that opens novel applications in materials science, for example, as reinforcement in composites and as templates for surface modification.Keywords
This publication has 13 references indexed in Scilit:
- Homogeneous Suspensions of Individualized Microfibrils from TEMPO-Catalyzed Oxidation of Native CelluloseBiomacromolecules, 2006
- Rheological Properties and Molecular Structure of Tunicate Cellulose in LiCl/1,3-Dimethyl-2-imidazolidinoneBiomacromolecules, 2004
- Assignment of non-crystalline forms in cellulose I by CP/MAS 13C NMR spectroscopyCarbohydrate Research, 1998
- Enhanced Ordering of Liquid Crystalline Suspensions of Cellulose Microfibrils: A Small Angle Neutron Scattering StudyMacromolecules, 1998
- A CP/MAS13C NMR investigation of molecular ordering in cellulosesCarbohydrate Research, 1997
- In Reply: Crystalline Form of Native CellulosesScience, 1985
- Native Cellulose: A Composite of Two Distinct Crystalline FormsScience, 1984
- Rheology and Rheo-Optics of Polymer Liquid CrystalsPublished by Springer Nature ,1980
- Dynamics of concentrated polymer systems. Part 3.—The constitutive equationJournal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics, 1978
- Hydrolysis and Crystallization of CelluloseIndustrial & Engineering Chemistry, 1950