天冬酰胺低分子量凝胶和碳酸丙烯酯高温超分子体系的平移动力学和结构增强效应

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Farooq Ahmad, , , Natalia Bielejewska, , , Dawid Pakulski, , and , Michał Bielejewski*, 
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引用次数: 0

摘要

化学工程为设计具有目标性能的新材料铺平了道路。超分子化学允许基于组件之间的非共价相互作用(例如氢键和色散或静电力)从小分子创建分子组装,从而导致自组装结构的模板化。可逆键相互作用允许优化最终结构和增强性能。在这项研究中,我们使用这种方法来设计和制备在超过100°C极限温度下工作的超分子膜。该系统以低分子量凝胶(lmwg)为基础,具有多功能性、灵活性、可调性能和可持续性。基于lmwg的系统大多具有凝胶样特征,提供了一种具有增强响应性、自愈能力、可回收性和粘弹性的替代方案。在这种情况下,我们开发了一种凝胶状膜,使用阿斯巴甜衍生物作为低分子转移物,碳酸丙烯酯作为液相,制备了一种可以固化化学工业中广泛使用的碳酸盐溶剂的体系。采用热重分析(TGA/DTG)和差热分析(DSC)对体系的高温性能进行了评价。用不同的核磁共振方法研究了分子间相互作用、凝胶机理和溶剂动力学。用荧光共聚焦扫描显微镜研究了所得膜的微观结构。所获得的结果表明,经过适当的热处理路线,所设计的系统可以获得增强的结构稳定性,使它们能够在超过100°C的极限温度下连续工作。核磁共振研究表明,固化液体的平动动力学与观察到的液体状态相当,同时防止了大块流动并补偿了热对流效应。所进行的矩阵分析显示了凝胶的自组装超分子聚集体是如何随着膜的组成而进化的。我们已经证明所研究的膜在某些浓度阈值以上表现出有效的自愈效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Translational Dynamics and Structural Enhancement Effect in High-Temperature Supramolecular Systems of Asparaginyl Low-Molecular-Weight Gelators and Propylene Carbonate

Translational Dynamics and Structural Enhancement Effect in High-Temperature Supramolecular Systems of Asparaginyl Low-Molecular-Weight Gelators and Propylene Carbonate

Chemical engineering paves the way for the design of new materials with targeted properties. Supramolecular chemistry allows the creation of molecular assemblies from small molecules based on noncovalent interactions between the components, e.g., hydrogen bonds and dispersive or electrostatic forces, leading to the templating of self-assembly structures. The reversible bonding interaction allows for optimization of the final structure and enhancement of the properties. In this study, we have used this approach to design and prepare supramolecular membranes that work at temperatures exceeding the 100 °C limit. The system is based on low molecular weight gelators (LMWGs), which provide versatility of compositions, flexibility, tunable properties, and improved sustainability. LMWG-based systems mostly exhibit gel-like features, offering an alternative with enhanced responsiveness, self-healing abilities, recyclability, and viscoelastic properties. In this context, we developed a gel-like membrane using an aspartame derivative as the LMWG and propylene carbonate as a liquid phase to prepare systems that can solidify carbonate solvents widely used in the chemical industry. The TGA/DTG and DSC thermal analyses were used to evaluate the system’s performance at high temperatures. The intermolecular interactions, gelation mechanism, and solvent dynamics were examined using different nuclear magnetic resonance methods. The microstructures of the obtained membranes were studied by using a fluorescence confocal scanning microscope. The obtained results have shown that the designed systems subjected to proper thermal processing routes can achieve enhanced structural stability, allowing them to work continuously at temperatures exceeding the 100 °C limit. The NMR studies showed that translational dynamics of the solidified liquid remain comparable to those observed for the liquid state, preventing the bulk flow simultaneously and compensating for the thermal convection effects. The performed matrix analysis showed how the self-assembled supramolecular aggregates of the gelator evolve with the membrane composition. We have demonstrated that the investigated membranes exhibit efficient self-healing effects above some concentration threshold.

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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