纳米纤维素
材料科学
热固性聚合物
复合材料
蠕动
热塑性塑料
纤维素
聚合物
挤压
动态力学分析
丙烯酸酯
共聚物
化学工程
工程类
作者
Anna Peterson,Ida Östergren,A. Lotsari,Abhijit Venkatesh,Johannes Thunberg,Anna Ström,Ramiro Rojas,Martin Andersson,Lars A. Berglund,Antal Boldizar,Christian Müller
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2019-09-17
卷期号:20 (10): 3924-3932
被引量:14
标识
DOI:10.1021/acs.biomac.9b00993
摘要
Many polymers, including polyethylene, feature a relatively low melting point and hence must be cross-linked to make them viable for applications that demand a high stiffness and creep resistance at elevated temperatures. The resulting thermoset plastics cannot be recycled, and therefore alternative materials with a reconfigurable internal network structure are in high demand. Here, we establish that such a thermoset-like yet recyclable material can be realized through the addition of a nanocellulose reinforcing agent. A network consisting of cellulose nanocrystals, nano- or microfibrils imparts many of the characteristics that are usually achieved through chemical cross-linking. For instance, the addition of only 7.5 wt % of either nanocellulose material significantly enhances the melt stiffness of an otherwise molten ethylene-acrylate copolymer by at least 1 order of magnitude. At the same time, the nanocellulose network reduces the melt creep elongation to less than 10%, whereas the neat molten matrix would rupture. At high shear rates, however, the molten composites do not display a significantly higher viscosity than the copolymer matrix, and therefore retain the processability of a thermoplastic material. Repeated re-extrusion at 140 °C does not compromise the thermomechanical properties, which indicates a high degree of recyclability. The versatility of dynamic nanocellulose networks is illustrated by 3D printing of a cellulose composite, where the high melt stiffness improves the printability of the resin.
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