Cellulose Nanofiber Orientation in Nanopaper and Nanocomposites by Cold Drawing

被引:294
作者
Sehaqui, Houssine [1 ]
Mushi, Ngesa Ezekiel [1 ]
Morimune, Seira [3 ]
Salajkova, Michaela [2 ]
Nishino, Takashi [3 ]
Berglund, Lars A. [1 ,2 ]
机构
[1] Royal Inst Technol, Dept Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
[2] Royal Inst Technol, Wallenberg Wood Sci Ctr, SE-10044 Stockholm, Sweden
[3] Kobe Univ, Dept Chem Sci & Engn, Kobe, Hyogo 6578501, Japan
关键词
nanopaper; cellulose nanofibers; orientation; cold drawing; nanocomposites; nanofibrillated cellulose; NATIVE CELLULOSE; HIGH TOUGHNESS; SURFACE-AREA; CELL-WALLS; COMPOSITES; AEROGELS; MICROFIBRILS; TEMPLATES; OXIDATION; POROSITY;
D O I
10.1021/am2016766
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To exploit the mechanical potential of native cellulose fibrils, we report on the preparation of nanopaper with preferred orientation of nanofibrillated cellulose (TEMPO-NFC) by cold drawing. The preparation route is papermaking-like and includes vacuum filtering of a TEMPO-oxidated NFC water dispersion, drawing in wet state and drying. The orientation of the fibrils in the nanopaper was assessed by AFM and wide-angle Xray diffraction analysis, and the effect on mechanical properties of the resulting nanopaper structure was investigated by tensile tests. At high. draw ratio, the degree of orientation is as high as 82 and 89% in and cross-sectional planes of the nanopaper, respectively, and the Young's modulus is 33 GPa. This is much higher than mechanical properties of isotropic nanopaper. The cold drawing method can be also applied to NFC nanocomposites as demonstrated, by preparation of TEMPO-NFC/hydroxyethyl cellulose (HEC) nanocomposites. The introduction of the soft HEC matrix allows further tailoring of the mechanical properties.
引用
收藏
页码:1043 / 1049
页数:7
相关论文
共 38 条
[1]   Orientation of native cellulose in an electric field [J].
Bordel, Damien ;
Putaux, Jean-Luc ;
Heux, Laurent .
LANGMUIR, 2006, 22 (11) :4899-4901
[2]   High-performance composites from low-cost plant primary cell walls [J].
Bruce, DM ;
Hobson, RN ;
Farrent, JW ;
Hepworth, DG .
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING, 2005, 36 (11) :1486-1493
[3]   Individualization of cellulose nanofibers from wood using high-intensity ultrasonication combined with chemical pretreatments [J].
Chen, Wenshuai ;
Yu, Haipeng ;
Liu, Yixing ;
Chen, Peng ;
Zhang, Mingxin ;
Hai, Yunfei .
CARBOHYDRATE POLYMERS, 2011, 83 (04) :1804-1811
[4]  
Gindl A.W., 2011, ANN M LAWS, P90
[5]   Drawing of self-reinforced cellulose films [J].
Gindl, Wolfgang ;
Keckes, Jozef .
JOURNAL OF APPLIED POLYMER SCIENCE, 2007, 103 (04) :2703-2708
[6]   An environmentally friendly method for enzyme-assisted preparation of microfibrillated cellulose (MFC) nanofibers [J].
Henriksson, M. ;
Henriksson, G. ;
Berglund, L. A. ;
Lindstrom, T. .
EUROPEAN POLYMER JOURNAL, 2007, 43 (08) :3434-3441
[7]   Cellulose nanopaper structures of high toughness [J].
Henriksson, Marielle ;
Berglund, Lars A. ;
Isaksson, Per ;
Lindstrom, Tom ;
Nishino, Takashi .
BIOMACROMOLECULES, 2008, 9 (06) :1579-1585
[8]   Structure and Mechanical Properties of Wet-Spun Fibers Made from Natural Cellulose Nanofibers [J].
Iwamoto, Shinichiro ;
Isogai, Akira ;
Iwata, Tadahisa .
BIOMACROMOLECULES, 2011, 12 (03) :831-836
[9]   Elastic Modulus of Single Cellulose Microfibrils from Tunicate Measured by Atomic Force Microscopy [J].
Iwamoto, Shinichiro ;
Kai, Weihua ;
Isogai, Akira ;
Iwata, Tadahisa .
BIOMACROMOLECULES, 2009, 10 (09) :2571-2576
[10]   Clay Nanopaper with Tough Cellulose Nanofiber Matrix for Fire Retardancy and Gas Barrier Functions [J].
Liu, Andong ;
Walther, Andreas ;
Ikkala, Olli ;
Belova, Lyuba ;
Berglund, Lars A. .
BIOMACROMOLECULES, 2011, 12 (03) :633-641