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Preparation of polypropylene/montmorillonite nanocomposites by intercalative polymerization: Effect of in situ polymer matrix functionalization on the stability of the nanocomposite structure

机译:插层聚合制备聚丙烯/蒙脱土纳米复合材料:原位聚合物基体官能化对纳米复合材料结构稳定性的影响

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摘要

The copolymerization of propylene and 5-hexenyl-9-borabicyclo[3.3.1]nonane (5-hexenyl-9-BBN) has been conducted with an MgCl_2/TiCl_4 catalyst intercalated in an organically modified montmorillonite (OMMT) with triethylaluminum (AIEt_3) cocatalyst and diphenyldimethoxysilane (DDS) external donor. This polymerization process simultaneously results in both the exfoliation of MMT layers to realize the preparation of polypropylene (PP)/MMT nanocomposites and the implantation of reactive borane groups in the formed PP matrix. The polymer-borne borane groups have been able to undergo an efficient hydrolysis process under very mild reaction conditions (40℃, 3 h, in THF), introducing hydroxy groups into PP without sacrificing the polymerization-formed nanocomposite structure (the exfoliation of MMT). The resultant hydroxyl-functionalized PP/MMT nanocomposites exhibit enhanced structural stability against processing compared with those based on unfunctionalized PP matrix.
机译:丙烯和5-己烯基-9-硼环[3.3.1]壬烷(5-己烯基-9-BBN)的共聚反应是通过将MgCl_2 / TiCl_4催化剂插入有机改性的蒙脱土(OMMT)和三乙基铝(AIEt_3)中进行的助催化剂和二苯基二甲氧基硅烷(DDS)的外部供体。该聚合过程同时导致MMT层剥离以实现聚丙烯(PP)/ MMT纳米复合材料的制备以及反应性硼烷基团在形成的PP基体中的植入。聚合物中的硼烷基团已经能够在非常温和的反应条件下(在THF中40℃,3小时)进行有效的水解过程,在不牺牲聚合反应形成的纳米复合结构(MMT剥离)的情况下,将羟基引入PP中。 。与基于未官能化的PP基质的那些相比,所得的羟基官能化的PP / MMT纳米复合材料对加工显示出增强的结构稳定性。

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