A Polymethylvinylsiloxane/Low Density Polyethylene Blending Melt: Dynamic Rheological Behavior and Relaxation Time

Hua-yong Liao
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引用次数: 1

Abstract

The dynamic rheological behavior of a polymethylvinylsiloxane (PMVS)/ low density polyethylene (LDPE) blending melts at 150,180 and 210 ℃ is investigated by small amplitude oscillatory shear on a rotational rheometer. LDPE has higher viscosity than PMVS at three temperatures, which affects the morphology and rheological response of the blends. The LDPE-rich blends have smaller dispersed droplets and longer relaxation time than the PMVS-rich blends. Higher temperature means less viscosity as well as dynamic modulus difference between the LDPE-rich blend and the PMVS-rich blend. Increasing temperature fastens relaxation of polymer samples thus relaxation time at higher temperature is shorter than that at low temperature. Phase separation can be shown at some weight ratio of PMVS/LDPE through the failure of time-temperature superposition principle and double peaks of relaxation time including the form relaxation time peak due to relaxation of dispersed droplets.
聚甲基硅氧烷/低密度聚乙烯共混熔体:动态流变行为和弛豫时间
在旋转流变仪上用小振幅振荡剪切法研究了聚甲基乙烯硅氧烷(PMVS)/低密度聚乙烯(LDPE)共混熔体在150,180和210℃下的动态流变行为。LDPE在三个温度下的粘度都高于PMVS,这影响了共混物的形貌和流变响应。富ldpe共混物比富pmvs共混物具有更小的分散液滴和更长的松弛时间。更高的温度意味着更小的粘度和动态模量差异之间的ldpe富共混物和pmvs富共混物。温度升高使聚合物样品的弛豫加快,在高温下的弛豫时间比在低温下的弛豫时间短。在PMVS/LDPE的一定质量比下,由于时间-温度叠加原理失效,弛豫时间出现双峰,包括分散液滴弛豫形成的弛豫时间峰。
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