材料科学
纳米纤维素
生物高聚物
羧甲基纤维素
复合数
生物相容性
碳酸钙
纤维素
无定形固体
化学工程
细菌纤维素
复合材料
纳米复合材料
聚合物
化学
有机化学
冶金
钠
工程类
作者
Wanlin Wu,Zhixing Lu,Canhui Lu,Xunwen Sun,Bing Ni,Helmut Cölfen,Rui Xiong
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-03-22
卷期号:17 (7): 6664-6674
被引量:37
标识
DOI:10.1021/acsnano.2c12385
摘要
Nature builds numerous structurally complex composites with fascinating mechanical robustness and functionalities by harnessing biopolymers and amorphous calcium carbonate (ACC). The key to successfully mimicking these natural designs is efficiently stabilizing ACC, but developing highly efficient, biodegradable, biocompatible, and sustainable stabilizing agents remains a grand challenge since anhydrous ACC is inherently unstable toward crystallization in the wet state. Inspired by the stabilized ACC in crustacean cuticles, we report the efficient stabilization ability of the most abundant biopolymer-cellulose nanofibrils (CNFs) for ACC. Through the cooperative stabilizing effect of surface carboxyl groups and a rigid segregated network, the CNFs exhibit long-term stability (more than one month) and achieved a stabilization efficiency of 3.6 and 4.4 times that of carboxymethyl cellulose (CMC) and alginate, respectively, even higher than poly(acrylic acid). The resulting CNF/ACC dispersions can be constructed into transparent composite films with the high strength of 286 MPa and toughness up to 28.5 MJ/m3, which surpass those of the so far reported synthetic biopolymer-calcium carbonate/phosphate composites. The dynamic interfacial interaction between nanocomponents also provides the composite films with good self-healing properties. Owing to their good wet stability, the composite films present high humidity sensitivity for monitoring respiration and finger contact.
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