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Solid-State Polymerization as a Vitrimerization Tool Starting from Available Thermoplastics: The Effect of Reaction Temperature

机译:用可用的热塑性塑料开始的固态聚合作为葡萄质化工具:反应温度的影响

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摘要

In the current work, solid-state polymerization (SSP) was studied for the synthesis of poly(butylene terephthalate), PBT-based vitrimers. A two-step process was followed; the first step involved alcoholysis reactions and the incorporation of glycerol in the polymer chains. The second step comprised transesterification reactions in the solid state (SSP) in the presence of zinc(II) catalyst resulting in the formation of a dynamic crosslinked network with glycerol moieties serving as the crosslinkers. The optimum SSP conditions were found to be 3 h at 180 °C under N2 flow (0.5 L/min) to reach high vitrimer insolubility (up to 75%) and melt strength (2.1 times reduction in the melt flow rate) while increasing the crosslinker concentration (from 3.5 to 7 wt.%) improved further the properties. Glass transition temperature (Tg) was almost tripled in vitrimers compared to initial thermoplastic, reaching a maximum of 97 °C, whereas the melting point (Tm) was slightly decreased, due to loss of symmetry perfection under the influence of the crosslinks. Moreover, the effect of the dynamic crosslinked structure on PBT crystallization behavior was investigated in detail by studying the kinetics of non-isothermal crystallization. The calculated effective activation energy using the Kissinger model and the nucleating activity revealed that the higher crosslinker content impeded and slowed down vitrimers melt crystallization, also inducing an alteration in the crystallization mechanism towards sporadic heterogeneous growth.
机译:在当前的工作中,研究了固态聚合(SSP),用于合成聚(丁二醇酯),基于基于乙酸酯的PBT基富矿体。遵循两步过程;第一步涉及醇解反应和聚合物链中的甘油掺入。第二步包括在锌(II)催化剂存在下固态(SSP)中的酯交换反应,导致形成用作交联剂的甘油部分的动态交联网络。在N 2流动(0.5L / min)下,在180℃下发现最佳SSP条件为3小时,以达到高virimer不溶性(高达75%)和熔体强度(熔体流速降低2.1倍),同时增加交联剂浓度(从3.5至7重量%)进一步改善了性质。与初始热塑性塑料相比,玻璃化转变温度(Tg)几乎三倍于六叠玻璃,最大达到97℃,而在交联的影响下,熔点(Tm)略微降低。此外,通过研究非等温结晶的动力学,详细研究了动态交联结构对PBT结晶行为的影响。使用基辛格模型的计算有效活化能量和成核活性表明,较高的交联剂含量妨碍和减慢了virimers熔融结晶,也诱导了散发致散发性非均相生长的结晶机制的改变。

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