Department of Chemistry, Taibah University, 30002 Al-Madinah Al-Munawarah, Saudi Arabia.
Chemistry Department, Faculty of Science, Cairo University, Orman-Giza, P.O. 12613, Egypt.
Molecules. 2018 Oct 19;23(10):2703. doi: 10.3390/molecules23102703.
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 (t) 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.
阳离子环戊二烯基铁 (CpFe⁺) 是一种最有成效的有机金属基团之一,已被用于介导大量大分子的简便合成。然而,该化合物作为一种成核剂来改善其他大分子性质的能力尚未得到探索。本报告研究了阳离子配合物作为一种新型成核剂对聚(3-羟基丁酸酯) (PHB) 细菌来源的球晶形态、晶体结构以及等温和非等温结晶行为的影响。CpFe⁺的掺入使 PHB 材料的球晶数量显著增加,球晶尺寸显著减小。与其他成核剂不同,SEM 图像显示 CpFe⁺ 部分在 PHB 基质中分散良好,没有形成团聚体。此外,根据 FTIR 分析,阳离子有机铁配合物通过与酯羰基的配位与 PHB 聚合物链具有强烈的相互作用。然而,XRD 结果表明,这种掺入对 PHB 结晶结构没有显著影响。尽管 CpFe⁺ 对聚合物的晶体结构没有影响,但它显著加速了 PHB 的熔体结晶。同时,随着 CpFe⁺ 的加入,PHB 的结晶半衰期 (t) 急剧下降。PHB 的等温和非等温结晶过程成功地用 Avrami 模型和改进的 Avrami 模型以及 Avrami 和 Ozawa 方法的组合进行了描述。最后,PHB/CpFe⁺纳米复合材料的有效活化能明显低于纯 PHB 的活化能,这支持了有机金属基团的异相成核机制,表明 CpFe⁺ 是此类聚合物的优异成核剂。