Polyethyleneimine‐Modified Cellulose Nanofibers for Toughening Acid‐Cured Epoxy Resins

Guangming Zhou, Simiao Yu, Lihu Fu, Bingyan Yu, Tao Liu, Zian Xu, Jie Liu, Ning Qiao, Gang Lu
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Abstract

ABSTRACT Weak interfacial bonding between the two phases limited the toughening efficacy of carboxylated cellulose nanofibers (CNF‐C) on epoxy resin. To address this interfacial incompatibility, surface modification of CNF‐C was implemented through polyethyleneimine (PEI) functionalization. The toughening mechanism of PEI‐modified CNF‐C was systematically investigated through Fourier transform infrared spectroscopy (FT‐IR), scanning electron microscopy (SEM), and dynamic mechanical analysis (DMA). Optimal composite performance was achieved at a CNF‐C:PEI mass ratio of 1:1, where the impact strength of the epoxy resin increased significantly from 15.7 to 37.2 kJ/m 2 , representing a 136.9% enhancement. At the same time, the effect of using high molecular weight PEI is significantly higher than that of low molecular weight PEI. The toughening mechanism analysis revealed that stress dispersion and transfer were significantly enhanced by the long‐chain PEI structure, while the amine groups on PEI were found to participate in the epoxy‐curing reaction. Through these dual mechanisms, the interfacial bonding strength of CNF‐C was effectively reinforced. This systematic investigation provided both theoretical validation and experimental evidence to support the application of CNF‐C in composite materials.
聚乙烯亚胺改性纤维素纳米纤维增韧酸固化环氧树脂
两相之间的弱界面结合限制了羧化纤维素纳米纤维(CNF - C)对环氧树脂的增韧效果。为了解决这种界面不相容性,通过聚乙烯亚胺(PEI)功能化对CNF - C进行了表面改性。通过傅里叶变换红外光谱(FT - IR)、扫描电镜(SEM)和动态力学分析(DMA)对PEI改性CNF - C的增韧机理进行了系统的研究。当CNF - C:PEI质量比为1:1时,复合材料性能达到最佳,环氧树脂的冲击强度从15.7 kJ/ m2显著提高到37.2 kJ/ m2,提高了136.9%。同时,使用高分子量PEI的效果明显高于低分子量PEI。增韧机理分析表明,长链PEI结构显著增强了应力分散和传递,同时发现PEI上的胺基参与了环氧固化反应。通过这两种机制,CNF - C的界面结合强度得到了有效增强。该系统的研究为CNF - C在复合材料中的应用提供了理论验证和实验证据。
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