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Dissolution of chitosan with low degradation enabled by aqueous amino acid salt solutions at room-temperature
Xiaona Huang1, Yuxing Wu1, Binqi Wang2
1College of Chemistry and Molecular Sciences, Henan University, Kaifeng, 475004, China; Longzihu New Energy Laboratory, Zhengzhou Institute of Emerging Industrial Technology, Zhengzhou, 450000, China.
Abstract:
The efficient dissolution of chitosan (CS) is an essential prerequisite for high-value-added applications. However, conventional solvents are plagued by high viscosity, notable CS degradation, and an unclear dissolution mechanism. Herein, two aqueous nitrate-based amino acid salt solutions-glycine nitrate ([Gly]NO3) and proline nitrate ([Pro]NO3) systems-were employed to dissolve CS at room temperature. Spectroscopic analysis and molecular dynamics (MD) simulations of the [Gly]NO3 system suggest that the dissolution process is primarily driven by the protonation of amino groups, which disrupts the intra- and inter-molecular hydrogen bond networks of CS while simultaneously strengthening its interactions with [Gly]NO3. The structure-property relationship between amino acid-based ionic liquid (AAILs) and regenerated chitosan (RCS) degradation was investigated under various dissolution conditions, revealing that the [Pro]NO3 system induces less polymer degradation than the [Gly]NO3 system. Using aqueous [Pro]NO3 salt solution as the solvent, regenerated chitosan fibers (RCFs) were successfully fabricated via microfluidic wet-spinning. The resulting fibers were characterized by a dense morphology and acceptable mechanical properties (tensile strength: 1.51 cN·dtex-1; elongation: 3.50%).
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