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Lookup NU author(s): Professor David XieORCiD
This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).
Natural biopolymers such as chitosan and cellulose have demonstrated huge potential in important and rapidly growing environmental and biomedical applications. However, it is always challenging to create advanced functional biopolymer materials with enhanced hydrolytic stability cost-effectively. Here, we report an advance in preparing biopolymer polyelectrolyte complexed materials based on chitosan and carboxymethyl cellulose (CMC) using a “dry”, thermo-mechanical kneading method. Despite the high hydrophilicity of chitosan and CMC, the resulting films showed excellent dimensional stability and structural integrity (27% dimensional expansion and 94% weight increase after hydration for one day). In comparison, chitosan-only films were swollen dramatically under the same conditions, with a 138% dimensional expansion and a 913% rise in weight, which were also fragile. We propose that our processing method led to polyelectrolyte complexation between chitosan and CMC generating physical crosslinking points in the materials, which stabilised the films in water. Interestingly, the greater hydrolytic stability of chitosan/CMC films is in contrast with their higher surface hydrophilicity, a contribution from CMC. Our simple approach to engineering high-performance biopolymer materials without resorting to complex chemistries can be envisioned to bring about a new direction in the design of advanced functional materials where sustainability and cost-effectiveness are priorities.
Author(s): Chen P, Xie F, Tang F, McNally T
Publication type: Article
Publication status: Published
Journal: Composites Science and Technology
Year: 2020
Volume: 189
Print publication date: 22/03/2020
Online publication date: 24/01/2020
Acceptance date: 21/01/2020
Date deposited: 23/05/2023
ISSN (print): 0266-3538
ISSN (electronic): 1879-1050
Publisher: Elsevier
URL: https://doi.org/10.1016/j.compscitech.2020.108031
DOI: 10.1016/j.compscitech.2020.108031
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