材料科学
复合材料
固化(化学)
聚酯纤维
纤维素
玻璃化转变
傅里叶变换红外光谱
复合数
动态力学分析
柠檬酸
聚合物
化学工程
化学
有机化学
工程类
作者
Maxime Barbier,Marie-Joo Le Guen,John McDonald‐Wharry,James H. Bridson,K.L. Pickering
出处
期刊:3D printing and additive manufacturing
[Mary Ann Liebert, Inc.]
日期:2021-02-04
卷期号:8 (3): 193-200
被引量:13
标识
DOI:10.1089/3dp.2020.0166
摘要
A biobased composite material with heat-triggered shape memory ability was successfully formulated for three-dimensional (3D) printing. It was produced from cellulose nanocrystals and cellulose micro-powder particles within a bioderived thermally cured polyester matrix based on glycerol, citric acid, and sebacic acid. The effect of curing duration on the material's shape memory behavior was quantified by using two thermo-mechanical approaches to measure recovery: (1) displacement in three-point bending and (2) angular recovery from a beam bent at 90° in a single cantilever setup. Extending curing duration increased the material's glass-transition temperature from -26°C after 6 h to 13°C after 72 h of curing. Fourier-transform infrared spectroscopy confirmed the associated progressive conversion of functional groups consistent with polyester formation. Slow recovery rates and low levels of shape recovery (22-70%) were found for samples cured less than 24 h. Those results also indicated a high dependence on the measurement approach. In contrast, samples cured for 48 and 72 h exhibited faster recovery rates, a significantly higher recovery percentage (90-100%) and were less sensitive to the measurement approach. Results demonstrated that once a sufficient curing threshold was achieved, additional curing time could be used to tune the material glass-transition temperature and create heat-triggered 3D-printed products.
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