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首页> 外文期刊>Journal of Applied Polymer Science >Reactive Extrusion for the Synthesis of Nylon 12 and Maleated Low-Density Polyethylene Blends via the Anionic Ring-Opening Polymerization of Lauryllactam
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Reactive Extrusion for the Synthesis of Nylon 12 and Maleated Low-Density Polyethylene Blends via the Anionic Ring-Opening Polymerization of Lauryllactam

机译:通过十二烷基内酰胺的阴离子开环聚合反应合成尼龙12和马来酸低密度聚乙烯共混物的反应挤出

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摘要

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.
机译:尼龙12是通过月桂内酰胺(LL)的阴离子开环聚合反应在双螺杆挤出机中成功合成的。添加马来酸化低密度聚乙烯(LDPE-MAH)以改善尼龙12的机械性能。通过机械测试和扫描电子显微镜对尼龙12和LDPE-MAH的原位共混物进行表征。随着LDPE-MAH含量的增加,当LDPE-MAH的含量为30 wt%时,抗张强度和挠曲强度降低,而共混物则提高了冲击强度并获得了超韧性。在原位形成的低密度聚乙烯-g-PA12共聚物中,LDPE-MAH相的区域精细地分散在尼龙12基质中。两相之间的良好界面表明,LDPE-MAH可用作诱导LL聚合的大分子活化剂。

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