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氨基功能化多壁碳纳米管促进聚(ε-己内酯)的开环聚合:增强的界面结合和优化的力学性能。

Amino-Functionalized Multiwalled Carbon Nanotubes Lead to Successful Ring-Opening Polymerization of Poly(ε-caprolactone): Enhanced Interfacial Bonding and Optimized Mechanical Properties.

机构信息

⊥Polymers' Laboratory, Department of Materials Science Engineering, University of Ioannina, 45110 Ioannina, Greece.

出版信息

ACS Appl Mater Interfaces. 2015 Jun 3;7(21):11683-94. doi: 10.1021/acsami.5b03693. Epub 2015 May 20.

Abstract

In this work, the synthesis, structural characteristics, interfacial bonding, and mechanical properties of poly(ε-caprolactone) (PCL) nanocomposites with small amounts (0.5, 1.0, and 2.5 wt %) of amino-functionalized multiwalled carbon nanotubes (f-MWCNTs) prepared by ring-opening polymerization (ROP) are reported. This method allows the creation of a covalent-bonding zone on the surface of nanotubes, which leads to efficient debundling and therefore satisfactory dispersion and effective load transfer in the nanocomposites. The high covalent grafting extent combined with the higher crystallinity provide the basis for a significant enhancement of the mechanical properties, which was detected in the composites with up to 1 wt % f-MWCNTs. Increasing filler concentration encourages intrinsic aggregation forces, which allow only minor grafting efficiency and poorer dispersion and hence inferior mechanical performance. f-MWCNTs also cause a significant improvement on the polymerization reaction of PCL. Indeed, the in situ polymerization kinetics studies reveal a significant decrease in the reaction temperature, by a factor of 30-40 °C, combined with accelerated the reaction kinetics during initiation and propagation and a drastically reduced effective activation energy.

摘要

本文报道了通过开环聚合(ROP)制备的小含量(0.5、1.0 和 2.5wt%)氨基功能化多壁碳纳米管(f-MWCNTs)的聚己内酯(PCL)纳米复合材料的合成、结构特征、界面键合和力学性能。该方法在纳米管表面形成了共价键结合区,从而实现了有效的解缠结,因此在纳米复合材料中实现了良好的分散和有效的负载传递。高共价接枝程度和较高的结晶度为力学性能的显著提高提供了基础,在添加高达 1wt%f-MWCNTs 的复合材料中可以检测到这种提高。增加填充剂浓度会促进内在的聚集力,这会导致接枝效率较低、分散性较差,从而导致力学性能较差。f-MWCNTs 还显著改善了 PCL 的聚合反应。实际上,原位聚合动力学研究表明,反应温度显著降低,降低了 30-40°C,同时在引发和增长阶段加快了反应动力学,有效活化能也大大降低。

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