硅烷化
硅烷
表面改性
嫁接
化学
接触角
高分子化学
粘附
光引发剂
硅烷
傅里叶变换红外光谱
化学工程
X射线光电子能谱
核化学
聚合物
材料科学
有机化学
复合材料
单体
物理化学
工程类
作者
Mohammad Sayyadian,Masoud Jamshidi,Reza Ghamarpoor,Mahmoud Razavizadeh
标识
DOI:10.1016/j.arabjc.2023.105098
摘要
Surface modification could increase affinity of PET fibers to polymer matrix by changing the interfacial physical interactions to covalent bonds. In this research, surface modification of a superfine polyethylene terephthalate (PET) fabric was performed by bis(triethoxysilylpropyl)tetrasulfide (TESPT). The surface grafting was performed at different silane concentrations (i.e. 1, 5 and 10X). Before silanization, the fabrics were functionalized using photochemical method (i.e. irradiation of UV light in presence of glutaric acid peroxide (GAP)) and also hydrolysis by Sodium hydroxide (NaOH). Due to functionalization, carboxyl and hydroxyl groups were formed on the PET surface that made it ready to condense with hydrolyzed silane molecules. The fabrics were characterized using FTIR, TGA, FE-SEM, XPS analysis for evaluation of grafting performances. XPS analysis confirmed the presence of new peaks of Si and S after surface modification with TESPT. Comparing the results of TESPT-grafted functionalized PETs, it was found that the silane grafting content on PET surface is dependent not only to the silane concentration but also to the functionalization method. Finally, the influences of silane grafting on the functionalized PET fabrics to NBR adhesion were evaluated using H-pull and T-peel tests. The results showed that silane grafted-carboxylated PET fabric illustrated more adhesion to NBR than silane grafted-hydroxylated PET (i.e. 33 and 12% improvement in the pullout strength and T-peel adhesion, respectively).
科研通智能强力驱动
Strongly Powered by AbleSci AI