An Ultrastrong Nanofibrillar Biomaterial: The Strength of Single Cellulose Nanofibrils Revealed via Sonication-Induced Fragmentation

被引:494
作者
Saito, Tsuguyuki [1 ,2 ]
Kuramae, Ryota [1 ]
Wohlert, Jakob [2 ]
Berglund, Lars A. [2 ,3 ]
Isogai, Akira [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Biomat Sci, Tokyo 1138657, Japan
[2] Royal Inst Technol, Wallenberg Wood Sci Ctr, SE-10044 Stockholm, Sweden
[3] Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
基金
日本学术振兴会;
关键词
ATOMIC-FORCE MICROSCOPY; TRANSMISSION ELECTRON-MICROSCOPY; TEMPO-OXIDIZED CELLULOSE; ELASTIC-MODULUS; CRYSTALLINE REGIONS; CARBON NANOTUBES; NATIVE CELLULOSE; INDUCED SCISSION; MECHANISM; BACTERIAL;
D O I
10.1021/bm301674e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the mechanical strength of native cellulose nanofibrils. Native cellulose nanofibrils, purified from wood and sea tunicate, were fully dispersed in water via a topochemical modification of cellulose nanofibrils using 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO) as a catalyst. The strength of individual nanofibrils was estimated based on a model for the sonication-induced fragmentation of filamentous nanostructures. The resulting strength parameters were then analyzed based on fracture statistics. The mean strength of the wood cellulose nanofibrils ranged from 1.6 to 3 GPa, depending on the method used to measure the nanofibril width. The highly crystalline, thick tunicate cellulose nanofibrils exhibited higher mean strength of 3-6 GPa. The strength values estimated for the cellulose nanofibrils in the present study are comparable with those of commercially available multiwalled carbon nanotubes.
引用
收藏
页码:248 / 253
页数:6
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