低密度聚乙烯
材料科学
聚乙烯
极限抗拉强度
反应挤出
尼龙6
复合材料
聚合
艾氏冲击强度试验
聚合物
扫描电子显微镜
高分子化学
摘要
Abstract Nylon 12 was successfully synthesized in a twin‐screw extruder via the anionic ring‐opening polymerization of lauryllactam (LL). Maleated low‐density polyethylene (LDPE–MAH) was added to improve the mechanical properties of nylon 12. The in situ blends of nylon 12 and LDPE–MAH were characterized by mechanical testing and scanning electron microscopy. With increasing LDPE–MAH content, the tensile strength and flexural strength decreased, whereas the blend had improved impact strength and achieved supertoughness when the content of LDPE–MAH was 30 wt %. In the in situ formed low‐density polyethylene‐ g ‐PA12 copolymer, the domain of the LDPE–MAH phase was finely dispersed in the nylon 12 matrix. The good interface between the two phases demonstrated that LDPE–MAH could be used as a macromolecular activator to induce the polymerization of LL. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009
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