TEMPO-oxidized cellulose nanofibers

被引:2491
作者
Isogai, Akira [1 ]
Saito, Tsuguyuki [1 ]
Fukuzumi, Hayaka [1 ]
机构
[1] Univ Tokyo, Dept Biomat Sci, Bunkyo Ku, Tokyo 1138657, Japan
基金
日本学术振兴会;
关键词
PRIMARY ALCOHOL GROUPS; MEDIATED SELECTIVE OXIDATION; REGENERATED CELLULOSE; NATIVE CELLULOSE; MICROFIBRILLATED CELLULOSE; CATALYZED OXIDATION; CARBOXYLATE GROUPS; CELLOURONIC ACID; WOOD CELLULOSE; FIBRIN FIBERS;
D O I
10.1039/c0nr00583e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 (similar to 74%) or crystal width of wood celluloses. Electrostatic repulsion and/or osmotic effects working between anionically-charged cellulose microfibrils, the zeta-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 200-300 MPa 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-based nanomaterials in high-tech fields.
引用
收藏
页码:71 / 85
页数:15
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