Tunable softening and toughening of individualized cellulose nanofibers-polyurethane urea elastomer composites

被引:39
作者
Lee, Minwoo [1 ]
Heo, Min Haeng [1 ,2 ]
Lee, Hwi-Hui [1 ,2 ]
Kim, Young-Wun [1 ,2 ]
Shin, Jihoon [1 ,2 ]
机构
[1] Korea Res Inst Chem Technol, Ctr Biobased Chem, 141 Gajeong Ro, Daejeon 34114, South Korea
[2] Univ Sci & Technol, Dept Green Chem & Environm Biotechnol, 217 Gajeong Ro, Daejeon 34113, South Korea
关键词
Cellulose nanofibers; Nanocomposites; Chemical cross-linking; Ductile; Toughening; CARBON NANOTUBE; PHASE-SEPARATION; GAS BARRIER; NANOCOMPOSITES; BEHAVIOR; NANOCRYSTALS; MORPHOLOGY; MODEL; REINFORCEMENT; SURFACE;
D O I
10.1016/j.carbpol.2016.12.019
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of elastomeric nanocomposites with superior tensile strength and extensibility, simultaneously exhibiting softening, was prepared using in situ polymerization by homogeneously dispersing TEMPO oxidized cellulose individualized nanofibers (TOCNs) in a polyurethane urea (PUU) matrix. The structure of these PUU composites covalently cross-linked with the TOCNs was characterized. It was interesting to find that the amount and size of the hard domains in the composites gradually decreased by introducing crosslinkable TOCNs. With only 2 wt% of TOCNs incorporated, a 10.4-fold increase in tensile strength, 5.5-fold increase in strain-to-failure, and a decrease of 35% in the coefficient of thermal expansion were achieved, compared with those of neat PUU. However, the elastic modulus of the nanocomposites gradually decreased with up to 1 wt% of TOCNs. Conversely, with 2 wt% of TOCNs, the stiffness of the elastomers again increased, due to filler-filler interaction over the CNFs percolation in the nanocomposites. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:125 / 135
页数:11
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