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首页> 外文期刊>Rheologica Acta >The effect of 1,3:2,4- bis - O -( p -methylbenzylidene)-d -sorbitol (PDTS) on uniaxial elongational viscosity of polypropylene
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The effect of 1,3:2,4- bis - O -( p -methylbenzylidene)-d -sorbitol (PDTS) on uniaxial elongational viscosity of polypropylene

机译:1,3:2,4-双-O-(对甲基苄叉基)-d-山梨糖醇(PDTS)对聚丙烯单轴拉伸粘度的影响

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摘要

We investigated the dynamic viscoelasticity and elongational viscosity of polypropylene (PP) containing 0.5 wt% of 1,3:2,4-bis-O-(p-methylbenzylidene)-d-sorbitol (PDTS). The PP/PDTS system exhibited a sol–gel transition (T gel) at 193 °C. The critical exponent n was nearly equal to 2/3, in agreement with the value predicted by a percolation theory. This critical gel is due to a three-dimensional network structure of PDTS crystals. The elongational viscosity behavior of neat PP followed the linear viscosity growth function 3η + (t), where η + (t) is the shear stress growth function in the linear viscoelastic region. The elongational viscosity of the PP/PDTS system also followed the 3η + (t) above T gel but did not follow the 3η + (t) and exhibited strong strain-softening behavior below T gel. This strain softening can be attributed to breakage of the network structure of PDTS with a critical stress (σ c) of about 104 Pa.
机译:我们研究了含有0.5 wt%的1,3:2,4-双-O-(对甲基苄叉基)-d-山梨醇(PDTS)的聚丙烯(PP)的动态粘弹性和伸长粘度。 PP / PDTS系统在193°C时出现了溶胶-凝胶转变(T gel )。临界指数n几乎等于2/3,与渗流理论预测的值一致。这种关键的凝胶归因于PDTS晶体的三维网络结构。纯聚丙烯的伸长粘度行为遵循线性粘度增长函数3η + (t),其中η + (t)是线性粘弹性区域中的剪切应力增长函数。 PP / PDTS系统的伸长粘度也遵循高于T gel 的3η + (t),但不遵循3η + (t ),并在T gel 以下表现出较强的应变软化行为。这种应变软化可以归因于PDTS网络结构的破坏,其临界应力(σ c )约为10 4 Pa。

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