Quantifying the Shape Memory Performance of a Three-Dimensional-Printed Biobased Polyester/Cellulose Composite Material

被引:11
作者
Barbier, Maxime [1 ]
Le Guen, Marie Joo [1 ]
McDonald-Wharry, John [2 ]
Bridson, James H. [1 ]
Pickering, Kim L. [2 ]
机构
[1] Scion, Private Bag 3020, Rotorua 3010, New Zealand
[2] Univ Waikato, Fac Sci & Engn, Hamilton, New Zealand
关键词
smart materials; 4D printing; thermosetting resin; thermomechanical properties; additive manufacturing;
D O I
10.1089/3dp.2020.0166
中图分类号
T [工业技术];
学科分类号
08 ;
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 degrees in a single cantilever setup. Extending curing duration increased the material's glass-transition temperature from -26 degrees C after 6 h to 13 degrees 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.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 52 条
[1]   Biodegradable, amorphous copolyester-urethane networks having shape-memory properties [J].
Alteheld, A ;
Feng, YK ;
Kelch, S ;
Lendlein, A .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (08) :1188-1192
[2]   Characterization of nanocellulose-reinforced shape memory polyurethanes [J].
Auad, Maria L. ;
Contos, Vasili S. ;
Nutt, Steve ;
Aranguren, Mirta I. ;
Marcovich, Norma E. .
POLYMER INTERNATIONAL, 2008, 57 (04) :651-659
[3]   Exploring mechanical properties of fully compostable flax reinforced composite filaments for 3D printing applications [J].
Badouard, Celine ;
Traon, Fanny ;
Denoual, Clement ;
Mayer-Laigle, Claire ;
Paes, Gabriel ;
Bourmaud, Alain .
INDUSTRIAL CROPS AND PRODUCTS, 2019, 135 :246-250
[4]   4D Printing with Mechanically Robust, Thermally Actuating Hydrogels [J].
Bakarich, Shannon E. ;
Gorkin, Robert, III ;
Panhuis, Marc In Het ;
Spinks, Geoffrey M. .
MACROMOLECULAR RAPID COMMUNICATIONS, 2015, 36 (12) :1211-1217
[5]   Actively moving polymers [J].
Behl, Marc ;
Lendlein, Andreas .
SOFT MATTER, 2007, 3 (01) :58-67
[6]   Shape-memory polymers [J].
Behl, Marc ;
Lendlein, Andreas .
MATERIALS TODAY, 2007, 10 (04) :20-28
[7]   Shape-memory effect of poly (glycerol-sebacate) elastomer [J].
Cai, Wei ;
Liu, Lili .
MATERIALS LETTERS, 2008, 62 (14) :2171-2173
[8]   Using cellulose nanocrystals as sustainable additive to enhance mechanical and shape memory properties of PLA/ENR thermoplastic vulcanizates [J].
Cao, Liming ;
Liu, Cong ;
Zou, Dijia ;
Zhang, Shuidong ;
Chen, Yukun .
CARBOHYDRATE POLYMERS, 2020, 230
[9]   Thermo-responsive shape memory polymer blends based on alpha olefin and ethylene propylene diene rubber [J].
Chatterjee, Tuhin ;
Dey, Pranab ;
Nando, Golok Behari ;
Naskar, Kinsuk .
POLYMER, 2015, 78 :180-192
[10]   Gelation of cellulose nanocrystal suspensions in glycerol [J].
Dorris, Annie ;
Gray, Derek G. .
CELLULOSE, 2012, 19 (03) :687-694