材料科学
复合材料
降级(电信)
极限抗拉强度
纤维
耐久性
水解降解
模数
各向异性
现象学模型
拉伸应变
弹性模量
水分
基质(化学分析)
杨氏模量
拉伤
玻璃纤维
变形(气象学)
蠕动
含水量
化学分解
动能
可塑性
纤维类型
天然纤维
作者
Gyeong-min Park,Jeong-Moo Lee,Jung-Hwan Lee,Jung-Wook Wee
标识
DOI:10.1038/s41529-026-00774-z
摘要
Abstract This study examines the degradation behavior of PC/GF composites with varying short glass fiber (SGF) contents (10, 20, and 30 wt%) and fiber orientations (0°, 45°, and 90°) when exposed to conditions of 85 °C/85% RH. Although the elastic modulus remained largely unchanged, both tensile strength and strain at break exhibited significant deterioration as a result of moisture ingress, which promoted interfacial debonding (after 1008 h, tensile strength decreased by up to 27.7% and strain at break by up to 45.8%). To quantify chemical degradation, a hydroxyl index (HI) was derived from ATR-FTIR spectroscopy. The temporal evolution of HI followed a power-law kinetic model that was independent of fiber content, indicating that matrix hydrolysis governs the degradation rate, with HI increasing by up to 3.57×, while the bulk-average molecular weight decreased by 5.8–8.7%. Furthermore, a phenomenological model was developed linking the HI to macroscopic mechanical properties. This model accurately captured time-dependent, anisotropic degradation based on the material’s chemical state, yielding cross-validation errors under 5%. Ultimately, these findings demonstrate that non-destructive spectroscopic techniques can reliably estimate structural integrity, providing a robust framework for durability assessment and lifetime prediction in harsh environments.
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