材料科学
复合材料
硅烷
环氧树脂
纤维
抗弯强度
聚乙烯
双层
傅里叶变换红外光谱
超高分子量聚乙烯
抗剪强度(土壤)
表面改性
X射线光电子能谱
膜
化学工程
化学
生物化学
环境科学
土壤科学
工程类
土壤水分
作者
Yao Zhang,Shao Cao,Xiaochen Zhou,Fanmin Kong,Huaidong Li,Guodong Jiang
摘要
Abstract A bilayer structure with polydopamine (PDA) transition layer and 3‐glycidyl ether oxy‐propyl trimethoxy silane (GOPTS) hydrolysis‐condensate strengthened layer on the surface of ultra‐high molecular weight polyethylene (UHMWPE) fiber is prepared to improve the damage resistance of composites and more efficient stress transmission in composites. PDA is covered on the surface of UHMWPE fiber and then GOPTS is hydrolyzed and condensed to form inorganic ‐O‐Si‐O‐ with epoxy groups on the PDA layer. In addition, the surface activated nano‐SiO 2 is dispersed in the epoxy resin to increase the strength of the matrix resin. The results show that the interfacial shear strength (IFSS), the impact strength, the flexural strength and flexural modulus of UHMWPE‐PDA‐GOPTS/EP‐SiO 2 increase by 99.1%, 54.1%, 76.8%, and 36.6% respectively compared with unmodified UHMWPE/EP. The chemical compositions of the treated fiber surface are characterized by X‐ray photoelectron spectroscopy and Fourier transform infrared spectroscopy (ATR‐FTIR). With the help of the scanning electron microscopy, the interface failure and reinforcement mechanism of the composites are further explored due to UHMWPE fiber shear yield deformation, UHMWPE fiber fracture, matrix resin cracking and the relative sliding friction between the fiber and matrix.
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