Scalable processing of thermoplastic polyurethane nanocomposites toughened with nanocellulose

被引:53
作者
Amin, Khairatun Najwa Mohd [1 ,2 ]
Amiralian, Nasim [1 ]
Annamalai, Pratheep K. [1 ]
Edwards, Grant [1 ]
Chaleat, Celine [1 ]
Martin, Darren J. [1 ]
机构
[1] Univ Queensland, AIBN, Brisbane, Qld 4072, Australia
[2] Univ Malaysia Pahang, Fac Chem Engn & Nat Resources, Gambang Kuantan 26300, Pahang Dm, Malaysia
关键词
Nanocomposites; Polyurethane; Nanocellulose; Reactive extrusion; CELLULOSE NANOCRYSTALS; POLYMER NANOCOMPOSITES; MECHANICAL-PROPERTIES; MODEL COMPOUNDS; ELASTOMERS; BEHAVIOR; NANOFIBRES; MORPHOLOGY; SEPARATION; RUBBER;
D O I
10.1016/j.cej.2016.05.067
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The production of strong and elastic polyurethane nanocomposites toughened with nanocellulose (NC) and their widespread application in many engineering fields are currently limited by poor processability via classical industrial processing methods and/or the usage of large amount of solvents. In this report, we demonstrate a scalable, organic solvent-free incorporation of nanocellulose into thermoplastic polyurethane (TPU) and a remarkable reinforcement without compromising elastic properties. The nanocomposites were prepared via water-assisted dispersion of nanocellulose in polyether polyol by bead milling, drying and reactive extrusion of this dispersion with comonomers. Upon the incorporation of nanocellulose (0.5 wt.%), as observed from infrared spectroscopic and thermal analysis, the phase mixing of hard and soft segments in the TPU matrix and the primary relaxation temperature have slightly increased due to the hydrogen bonding, interfacial area and nucleation-enhanced by long polar nanocrystals. The TPU/nanocellulose nanocomposites prepared with an appropriate stoichiometric ratio (determined through appropriate process control) showed a remarkable improvement (up to 43%) in ultimate tensile strength without compromising the elastic properties including elongation, creep and hysteresis. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:406 / 416
页数:11
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