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In situ fibrillation of CO_2-philic polymers: Sustainable route to polymer foams in a continuous process

机译:亲CO_2聚合物的原位原纤化:连续过程中聚合物泡沫的可持续发展途径

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摘要

In this study, in situ polymer-fibrillar blends of polypropylene (PP)/polytetrafluoroethylene (PTFE) are prepared. Dynamic oscillatory shear experiments confirm that the PTFE elongates into fibrils during blending and forms a physical network of entanglements in the melt which results in gel-like properties. Uniaxial extensional flow experiments show strain-induced hardening behaviour. CO_2 solvency in the PP/PTFE fibrillar blend is enhanced due to the CO_2-philic character of PTFE. Remarkably, adding only 0.3 wt% of PTFE is sufficient to markedly enhance the CO_2 sorption capacity of the matrix. Continuous foam extrusion of the in situ fibrillar blend reveals a three orders of magnitude increase in bubble density, a ten-fold increase in volume expansion ratio, and a marked broadening of the foaming window with respect to neat PP. These improvements are attributed to the simultaneous enhancement in CO_2 solvency and strain-hardening behaviour of the melt in the in situ fibrillar blend.
机译:在这项研究中,准备了聚丙烯(PP)/聚四氟乙烯(PTFE)的原位聚合物-原纤维共混物。动态振荡剪切实验证实,PTFE在共混过程中会伸长成原纤维,并在熔体中形成缠结的物理网络,从而形成凝胶状特性。单轴拉伸流动实验表明应变引起的硬化行为。 PP / PTFE纤维状共混物中的CO_2溶解度由于PTFE的亲CO_2特性而提高。显着地,仅添加0.3重量%的PTFE足以显着增强基质的CO 2吸附能力。原位纤维共混物的连续泡沫挤出显示气泡密度增加了三个数量级,体积膨胀比增加了十倍,并且相对于纯PP而言,发泡窗口显着加宽了。这些改善归因于原位原纤共混物中熔体的CO_​​2溶解能力和应变硬化行为的同时提高。

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