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Partially miscible blends of epoxy resin and epoxidized rubber: Structural characterization of the epoxidized rubber and mechanical properties of the blends

机译:环氧树脂和环氧橡胶的部分混溶混合物:环氧橡胶的结构表征和共混物的机械性能

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AbstractThe cure process and the mechanical properties of blends of diglycidyl ether of bisphenol‐A–based epoxy resin and hydroxyl terminated, internally epoxidized polybutadiene rubber have been studied. Internal oxirane groups are characterized by a main absorption at 885 cm−1in the infrared spectrum while the terminal oxirane groups of the diepoxide monomer absorb at 913 cm−1. In the absence of prereaction of the rubber, gelation of the epoxy matrix occurs much faster than any reaction involving the internal oxirane groups or the terminal hydroxyl groups. Therefore, only weak chemical bonding between the rubber particles and the epoxy matrix exists and the fracture toughness of the blends does not show any significant improvement. Upon prereaction of the rubber with an excess diepoxide monomers, a 40 improvement in the value of the critical stress intensity factor is obtained. However, dynamic mechanical spectra of these blends acquired in the rubbery plateau region uniquely demonstrate that this improvement is due to the incorporation of the rubber into the epoxy network rather than to the presence of phase‐separated rubber particles. © 1994 John Wiley
机译:摘要研究了双酚A基环氧树脂与羟基封端内环氧聚丁二烯橡胶共混物的固化工艺和力学性能.内部环氧乙烷基团的特征在于红外光谱中主吸收量为885 cm−1,而二环氧啶单体的末端环氧乙烷基团在913 cm−1处吸收。在没有橡胶预反应的情况下,环氧基质的凝胶化比任何涉及内部环氧乙烷基团或末端羟基的反应都要快得多。因此,橡胶颗粒与环氧基体之间仅存在弱化学键合,共混物的断裂韧性没有明显改善。在橡胶与过量的二环氧啶单体发生预反应后,临界应力强度因子的值提高了 40%。然而,在橡胶高原区域获得的这些混合物的动态力学光谱独特地表明,这种改进是由于橡胶掺入环氧树脂网络,而不是由于相分离橡胶颗粒的存在。© 1994 约翰·威利

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