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Transient molecular orientation and rheology in flow aligning thermotropic liquid crystalline polymers

机译:流动取向热致液晶聚合物中的瞬态分子取向和流变学

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摘要

Quantitative measurements of molecular orientation and rheology are reported fro various transient shear flows of a nematic semiflexible copolyether. Unlike the case of lyotropic liquid crystalline polymers (LCPs), whose structure and rheology in shear are dominated by director tumbling, this material exhibits flow aligning behavior. The observed behavior is quite similar to that seen in a copolyester that we have recently studied [Ugaz and Burghardt (1998)], suggesting that flow aligning dynamics may predominate in main-chain thermotropes that incorporate significant chain flexibility. Since the flow aligning regime has received little attention in previous attempts to model the rheology of textured, polydomain LCPs, we attempt to determine whether available models are capable of predicting the orientation and stress response of this class of LCP. We first examine the predictions of the polydomain Ericksen model, an adaptation of Ericksen's transversely isotropic fluid model which accounts for the polydomain distribution of director orientation while neglecting distortional elasticity. This simple model captures a number of qualitative and quantitative features associated with the evolution of orientation and stress during shear flow inception, but cannot cope with reversing flows. To consider the possible role of distortional elasticity in the re-orientation dynamics upon reversal, we evaluate the mesoscopically averaged domain theory of Larson and Doi [Larson and Doi (1991)], which incorporates a phenomenological description of distortional elastic effects. To date, their approach to account for polydomain structure has only been applied to describe tumbling LCPs. We find that it captures the qualitative transient orientation response to flow reversals, but is less successful in describing the evolution of stresses. This is linked to the decoupling approximation adopted during the model's development. Finally, a modified polydomain Ericksen model is introduced that provides some of the benefits of the Larson-Doi model while offering more realistic stress predictions.
机译:据报道,向列型半柔性共聚醚的各种瞬时剪切流动都对分子取向和流变性进行了定量测量。与溶致液晶聚合物(LCP)的情况不同,该材料的剪切结构和流变特性受导向器翻滚的支配,该材料表现出流动对准行为。观察到的行为与我们最近研究的共聚酯中观察到的行为非常相似[Ugaz and Burghardt(1998)],这表明流动排列动力学可能在具有显着链柔性的主链热致变质中占主导地位。由于流动对准机制在先前对带纹理的多域LCP流变建模的尝试中很少受到关注,因此我们尝试确定可用的模型是否能够预测此类LCP的方向和应力响应。我们首先检查了多域Ericksen模型的预测,该模型是Ericksen的横向各向同性流体模型的改编,该模型考虑了指向矢取向的多域分布,而忽略了变形弹性。这个简单的模型捕获了与剪切流开始过程中取向和应力的演变相关的许多定性和定量特征,但是无法应对反向流动。为了考虑扭转弹性在反向时的重新定向动力学中的可能作用,我们评估了Larson和Doi的介观平均域理论[Larson and Doi(1991)],其中结合了畸变弹性效应的现象学描述。迄今为止,他们解决多域结构的方法仅用于描述翻转的LCP。我们发现它捕获了对流动逆转的定性瞬态定向响应,但是在描述应力的演化方面不太成功。这与模型开发过程中采用的解耦近似有关。最后,引入了经过修改的多域Ericksen模型,该模型提供了Larson-Doi模型的一些优点,同时提供了更为逼真的应力预测。

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