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Cationic Cyclopentadienyliron Complex as a Novel and Successful Nucleating Agent on the Crystallization Behavior of the Biodegradable PHB Polymer

机译:阳离子环戊二烯基铁配合物作为新型和成功的成核剂对可生物降解PHB聚合物的结晶行为

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摘要

Cationic cyclopentadienyliron (CpFe+) is one of the most fruitful organometallic moieties that has been utilized to mediate the facile synthesis of a massive number of macromolecules. However, the ability of this compound to function as a nucleating agent to improve other macromolecule properties has not been explored. This report scrutinizes the influence of the cationic complex as a novel nucleating agent on the spherulitic morphology, crystal structure, and isothermal and non-isothermal crystallization behavior of the Poly(3-hydroxybutyrate) (PHB) bacterial origin. The incorporation of the CpFe+ into the PHB materials caused a significant increase in its spherulitic numbers with a remarkable reduction in the spherulitic sizes. Unlike other nucleating agents, the SEM imageries exhibited a good dispersion without forming agglomerates of the CpFe+ moieties in the PHB matrix. Moreover, according to the FTIR analysis, the cationic organoiron complex has a strong interaction with the PHB polymeric chains via the coordination with its ester carbonyl. Yet, the XRD results revealed that this incorporation had no significant effect on the PHB crystalline structure. Though the CpFe+ had no effect on the polymer’s crystal structure, it accelerated outstandingly the melt crystallization of the PHB. Meanwhile, the crystallization half-times (t0.5) of the PHB decreased dramatically with the addition of the CpFe+. The isothermal and non-isothermal crystallization processes were successfully described using the Avrami model and a modified Avrami model, as well as a combination of the Avrami and Ozawa methods. Finally, the effective activation energy of the PHB/CpFe+ nanocomposites was much lower than those of their pure counterparts, which supported the heterogeneous nucleation mechanism with the organometallic moieties, indicating that the CpFe+ is a superior nucleating agent for this class of polymer.
机译:阳离子环戊二烯基铁(CpFe + )是最有成果的有机金属部分之一,已被用来介导大量大分子的简便合成。但是,尚未探索该化合物用作成核剂以改善其他大分子性质的能力。该报告详细研究了阳离子络合物作为新型成核剂对聚(3-羟基丁酸)(PHB)细菌来源的球状形态,晶体结构以及等温和非等温结晶行为的影响。将CpFe + 掺入PHB材料中会导致其球体数显着增加,并且球体尺寸显着减小。与其他成核剂不同,SEM图像显示出良好的分散性,而没有在PHB基质中形成CpFe + 部分的附聚物。此外,根据FTIR分析,阳离子有机铁配合物通过与其酯羰基的配位与PHB聚合物链具有强相互作用。然而,XRD结果表明该掺入对PHB的晶体结构没有显着影响。尽管CpFe + 对聚合物的晶体结构没有影响,但它显着促进了PHB的熔融结晶。同时,随着CpFe + 的加入,PHB的结晶半衰期(t0.5)急剧下降。使用Avrami模型和改进的Avrami模型以及Avrami和Ozawa方法的组合成功地描述了等温和非等温结晶过程。最后,PHB / CpFe + 纳米复合材料的有效活化能远低于其纯复合材料,这支持了有机金属部分的异质成核机理,表明CpFe + < / sup>是这类聚合物的优良成核剂。

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