TY - JOUR
T1 - Facile synthesis of regenerated chitosan nanowhiskers with concentration-dependent self-assembly behavior
AU - Xia, Ruicai
AU - Wang, Li
AU - Chen, Lei
AU - Liu, Xiaodi
AU - Chang, Yuqing
AU - Tian, Yichen
AU - Jin, Zhiping
AU - Zhang, Qiang
N1 - Publisher Copyright:
© 2025 Elsevier Ltd.
PY - 2026/2/1
Y1 - 2026/2/1
N2 - The conversion of chitosan into nanowhiskers significantly enhances its application potential and value. However, current methods for producing chitosan nanowhiskers (CNWs) typically involve harsh acid/base treatments, chemical modifications, or toxic solvents, resulting in demanding processing conditions, high costs, structural alterations, and environmental concerns. Here, we present a mild, cost-effective, and eco-friendly approach that eliminates the need for chemical modification. Raw chitosan was dissolved in dilute acetic acid, regenerated via pH adjustment, and mechanically processed to obtain CNWs. The resulting CNWs, with a 95 % degree of deacetylation, exhibited diameters of ∼7.4 nm and lengths of ∼93.6 nm. The CNWs displayed concentration-dependent self-assembly in water, forming interconnected nanofibrous networks at high concentrations while remaining well-dispersed as individual nanowhiskers at low concentrations. Leveraging this behavior, CNWs served as effective suspending agents and Pickering emulsifiers, stabilizing particles for over 72 h and emulsions for over 30 d at additive concentrations of 5–10 mg/mL. Additionally, CNW films and aerogels prepared through self-assembly demonstrated excellent water stability and mechanical strength, with Young's modulus and compressive modulus reaching ∼3.5 GPa and ∼110.2 KPa, respectively. This study establishes a foundation for the facile and large-scale production of CNWs and their high-value applications.
AB - The conversion of chitosan into nanowhiskers significantly enhances its application potential and value. However, current methods for producing chitosan nanowhiskers (CNWs) typically involve harsh acid/base treatments, chemical modifications, or toxic solvents, resulting in demanding processing conditions, high costs, structural alterations, and environmental concerns. Here, we present a mild, cost-effective, and eco-friendly approach that eliminates the need for chemical modification. Raw chitosan was dissolved in dilute acetic acid, regenerated via pH adjustment, and mechanically processed to obtain CNWs. The resulting CNWs, with a 95 % degree of deacetylation, exhibited diameters of ∼7.4 nm and lengths of ∼93.6 nm. The CNWs displayed concentration-dependent self-assembly in water, forming interconnected nanofibrous networks at high concentrations while remaining well-dispersed as individual nanowhiskers at low concentrations. Leveraging this behavior, CNWs served as effective suspending agents and Pickering emulsifiers, stabilizing particles for over 72 h and emulsions for over 30 d at additive concentrations of 5–10 mg/mL. Additionally, CNW films and aerogels prepared through self-assembly demonstrated excellent water stability and mechanical strength, with Young's modulus and compressive modulus reaching ∼3.5 GPa and ∼110.2 KPa, respectively. This study establishes a foundation for the facile and large-scale production of CNWs and their high-value applications.
KW - Aerogel
KW - Chitosan nanowhisker
KW - Dissolution/regeneration method
KW - Film
KW - Pickering emulsion
KW - Self-assembly
UR - https://www.scopus.com/pages/publications/105020916464
U2 - 10.1016/j.carbpol.2025.124615
DO - 10.1016/j.carbpol.2025.124615
M3 - 文章
AN - SCOPUS:105020916464
SN - 0144-8617
VL - 373
JO - Carbohydrate Polymers
JF - Carbohydrate Polymers
M1 - 124615
ER -