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Thermal, Dynamic Mechanical and Dielectric Behavior of Liquid-Crystalline Linear and Crosslinked Polyurethanes with Mesogenic Group in Side Chains

机译:侧链中介质基团与介质组的热,动态机械和介电行为

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This paper describes DSC, dielectric and dynamic mechanical behavior of linear and crosslinked liquid crystalline (LC) polyurethanes based on LC diols with a mesogenic group in the side chain, diisocyanates of various flexibility and two triols. From our investigations it follows: a) Linear polymers prepared from diols with simple end side chain substituents (as hydrogen, nitro and nitril group) exhibit only amorphous behavior regardless of the structure of used diisocyanate; generally, the most pronounced LC behavior exhibited polymers prepared from a diol with phenyl substituent. b) Investigation of the curing reaction showed that rheological power-law parameters, which are characteristic of the structure at the gel point, are dependent on the initial ratio of the reactants (amount of LC diol in EANCs). c) Strong physical interactions between the mesogens support the cyclization in the course of crosslinking reaction. d) Introduction of chemical junctions (amount of triols) suppresses LC ordering in the networks.
机译:本文介绍了基于LC二醇的直链和交联液晶(LC)聚氨酯的DSC,介电和动态力学行为,所述LC二醇在侧链中具有介于链中的介晶基团,各种柔性的二异氰酸酯和两个三醇。从我们的调查中,如下:a)用简单的末端侧链取代基制备的直链聚合物(作为氢,硝基和硝基组),无论二异氰酸酯的结构如何,都表现出非晶行为;通常,最明显的LC行为表现出由二醇用苯基取代基制备的聚合物。 b)固化反应的研究表明,凝胶点处的结构特征的流变能量 - 法参数取决于反应物的初始比(EANC中的LC二醇的量)。 c)蛋白质之间的强烈物理相互作用支持交联反应过程中的环化。 d)化学连接的引入(三醇的量)抑制网络中的LC排序。

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