Isogai, Akira and Saito, Tsuguyuki and Fukuzumi, Hayaka (2010) TEMPO-oxidized cellulose nanofibers. Nanoscale .
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Abstract
Native wood celluloses can be converted to individual nanofibers 3–4 nm wide that are at least several microns in length, i.e. with aspect ratios >100, by TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl radical)-mediated oxidation and successive mild disintegration in water. Preparation methods and fundamental characteristics of TEMPO-oxidized cellulose nanofibers (TOCN) are reviewed in this paper. Significant amounts of C6 carboxylate groups are selectively formed on each cellulose microfibril surface by TEMPO-mediated oxidation without any changes to the original crystallinity ( 74%) or crystal width of wood celluloses. Electrostatic repulsion and/or osmotic effects working between anionically-charged cellulose microfibrils, the z-potentials of which are approximately 75 mV in water, cause the formation of completely individualized TOCN dispersed in water by gentle mechanical disintegration treatment of TEMPO-oxidized wood cellulose fibers. Self-standing TOCN films are transparent and flexible, with high tensile strengths of 200–300MPa and elastic moduli of 6–7 GPa. Moreover, TOCN-coated poly(lactic acid) films have extremely low oxygen permeability. The new cellulose-based nanofibers formed by size reduction process of native cellulose fibers by TEMPO- mediated oxidation have potential application as environmentally friendly and new bio-basednanomaterials in high-tech fields.
| Item Type: | Article |
|---|---|
| Subjects: | Material Science > Nanochemistry |
| ID Code: | 9969 |
| Deposited By: | CSMNT |
| Deposited On: | 28 Nov 2010 15:16 |
| Last Modified: | 28 Nov 2010 15:16 |
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