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Thermomechanical-induced polyelectrolyte complexation between chitosan and carboxymethyl cellulose enabling unexpected hydrolytic stability

Lookup NU author(s): Professor David XieORCiD

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

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.


Publication metadata

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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