首页> 外文会议>Annual Technical Conference of the Society of Plastics Engineers >PREPARATION OF HIGH MELT STRENGTH POLYPROPYLENE BY THE REACTIVE EXTRUSION PROCESS AND ITS FOAMING APPLICATION
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PREPARATION OF HIGH MELT STRENGTH POLYPROPYLENE BY THE REACTIVE EXTRUSION PROCESS AND ITS FOAMING APPLICATION

机译:用反应挤出工艺制备高熔点聚丙烯及其发泡施用

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The reactive extrusion of maleic anhydride grafted polypropylene (PP-g-MAH) with ethylenediamine (EDA) as coupling agent was carried out in a co-rotating twin-screw extruder to produce long chain branched polypropylene (LCBPP). Part of PP-g-MAH was replaced by maleic anhydride grafted high-density polyethylene (HDPE-g-MAH) or linear low-density polyethylene (LLDPE-g-MAH) to obtain hybrid long chain branched (LCB) polymers. Compared with the linear PP, PE and their blends, the LCB polyolefins exhibit excellent dynamic shear and transient extensional rheological characteristics such as increased dynamic modulus, higher low-frequency complex viscosity, significantly enhanced melt strength and strain-hardening behaviors. LCB polymers also have higher tensile strength, tensile modulus, impact strength and lower elongation at break than linear polymer and their blends. Supercritical carbon dioxide (scCO2) was introduced in the reactive extrusion process. With the presence of scCO2, the motor current of twin extruder was decreased and LCB polyolefins with lower MFR, higher complex viscosity and increased tensile strength and modulus were obtained. This indicates that the application of scCO2 can reduce the viscosity of melt in extruder, enhance the diffusion of reactive species, facilitate the reaction between functional groups, and increase the LCB density. The foaming behavior of both linear and LCB polyolefins were studied. The results show that cellular materials produced from the LCB polyolefins have higher weight reduction, smaller cell size and better mechanical properties than those produced from the linear polymers.
机译:在共旋转的双螺杆挤出机中进行马来酸酐接枝聚丙烯(EDA)作为偶联剂的马来酸酐接枝聚丙烯(PP-G-MAH)的反应性挤出,以产生长链支化聚丙烯(LCBPP)。 PP-G-MAH的一部分被马来酸酐接枝的高密度聚乙烯(HDPE-G-MAH)或线性低密度聚乙烯(LLDPE-G-MAH)所取代,得到杂化长链支链(LCB)聚合物。与线性PP,PE及其共混物相比,LCB聚烯烃具有出色的动态剪切和瞬态延伸流变学特性,例如动态模量增加,低频复合粘度较高,显着增强的熔体强度和应变硬化行为。 LCB聚合物还具有较高的拉伸强度,拉伸模量,冲击强度和下伸长的伸长率,而不是线性聚合物及其共混物。在反应挤出过程中引入超临界二氧化碳(SCCO2)。随着SCCO2的存在,获得双挤出机的电动机电流降低,得到了具有较低MFR,更高的复合粘度和增加的拉伸强度和模量的LCB聚烯烃。这表明SCCO2的应用可以降低挤出机中熔体的粘度,增强反应性物质的扩散,促进官能团之间的反应,并增加LCB密度。研究了线性和LCB聚烯烃的发泡行为。结果表明,由LCB聚烯烃产生的细胞材料重量减轻较高,细胞尺寸较小,力学性能更高,而不是由线性聚合物产生的物质。

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