材料科学
环氧树脂
甲基丙烯酸缩水甘油酯
纳米复合材料
天然橡胶
复合材料
共价键
丁苯橡胶
硅烷
极限抗拉强度
单体
苯乙烯
高分子化学
聚合物
共聚物
化学
有机化学
作者
He Qiao,Mingyuan Chao,David Hui,Jun Liu,Junchi Zheng,Liqun Zhang,Xinxin Zhou,Runguo Wang,Liqun Zhang
标识
DOI:10.1016/j.compositesb.2017.02.021
摘要
Epoxy group-functionalized styrene-butadiene rubbers (G-ESBRs) with different epoxy group contents were synthesized through emulsion polymerization using glycidyl methacrylate (GMA) as the epoxy group-included monomer, and the silica/G-ESBR nanocomposites without silane coupling agents were prepared. The covalent bonding interfaces, resulting from a ring-opening reaction between the hydroxyl groups on the silica surfaces and the epoxy groups of G-ESBR, were formed during the preparation of the silica/G-ESBR nanocomposites. By increasing the epoxy group content, the number of covalent bonds at the interface increases, contributing to an improvement of the interfacial interaction between the G-ESBR and silica and the dispersion of silica, which were verified and analyzed in detail by bound rubber measurement, transmission electron microscopy (TEM) and rubber process analyzer (RPA). The silica/G-ESBR nanocomposites with improved dispersion of silica and interfacial interaction showed decreased rolling resistance and increased wet skid resistance. The mechanical properties of the nanocomposites were greatly improved with increasing epoxy group contents. The highest tensile strength reached 29.4 MPa at a GMA content of 4.8 wt%, a 55.6% increase compared with that of the nanocomposite without epoxy group.
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