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Characterization of network structure and chain dynamics of elastomeric ionomers by means of 1H Low-Field NMR

机译:通过1H低场NMR表征弹性体离聚物的网络结构和链动力学

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摘要

The network structure and chain dynamics of ionic elastomers based on carboxylated nitrile rubber (XNBR) cross-linked with different content of magnesium oxide (MgO) have been studied by different low-field time-domain NMR experiments. Ionic contacts created during the vulcanization tend to aggregate trapping some polymer segments that show restricted mobility as it was quantified by analyses of refocused free induction decays. Increasing the MgO content above the stoichiometric fraction has no effect on the amount of trapped polymer segments, but it increases the network cross-link density as measured by multiple-quantum (MQ) NMR experiments. The central finding of this work is that MgO addition above the stoichiometric content enhances the mechanical properties by creating a larger number of smaller ionic clusters, which act as dynamic cross-links, but are not readily seen by other techniques. Changes in the network structure and morphology of segregated thermolabile ionic domains have an impact on the ionic rearrangement dynamics and, in consequence, on the thermoplastic behavior of these materials at elevated temperatures.
机译:通过不同的低场时域NMR实验研究了基于羧基化丁腈橡胶(XNBR)与不同含量的氧化镁(MgO)交联的离子弹性体的网络结构和链动力学。硫化过程中产生的离子接触往往会聚集一些聚合物片段,这些片段显示出受限的迁移率,这是通过对重新聚焦的自由感应衰变进行分析来量化的。将MgO含量增加到化学计量分数以上对捕获的聚合物链段的数量没有影响,但是通过多量子(MQ)NMR实验测量,它会增加网络交联密度。这项工作的主要发现是,MgO的添加量超过化学计量含量,可以通过产生大量较小的离子簇来增强机械性能,这些较小的离子簇起着动态交联的作用,但其他技术却不易发现。分离的热不稳定离子域的网络结构和形态的变化会影响离子重排动力学,进而影响这些材料在高温下的热塑性。

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