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首页> 外文期刊>Macromolecules >Hydrogen-Bonding Assembly of Rigid-Rod Poly(p-sulfophenylene terephthalamide) and Flexible-Chain Poly(vinyl alcohol) for Transparent, Strong, and Tough Molecular Composites
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Hydrogen-Bonding Assembly of Rigid-Rod Poly(p-sulfophenylene terephthalamide) and Flexible-Chain Poly(vinyl alcohol) for Transparent, Strong, and Tough Molecular Composites

机译:刚性杆状聚对对苯二甲撑对苯二甲酰胺和柔性链状聚乙烯醇的氢键键合,用于透明,强韧的分子复合材料

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摘要

Molecular composites comprising poly(p-sulfophenylene terephthalamide) (sPPTA), a sulfonated polyaramid rigid-rod polyelectrolyte, and flexible-chain poly(vinyl alcohol) (PVA) were prepared by a green and easy-to-scale-up water casting method. Influence of sPPTA on the microstructure and properties of the molecular composites was systematically investigated. Fourier transform infrared spectroscopy confirms the existence of hydrogen bonding between sPPTA and PVA. Wide-angle X-ray diffraction patterns do not show the characteristic of neat sPPTA crystalline aggregates in the composites even when the sPPTA content is as high as 33 wt %, suggesting that the strong interaction between sPPTA and PVA prevents the self-aggregation of sPPTA and leads to the formation of PVA/sPPTA complexes inside the composites. Transmission electron microscopy shows that sPPTA has good compatibility with PVA, and nanoscale fibril-like supramolecular assemblies dispersing uniformly in the composites become observable with the increase of sPPTA content. Moreover, the PVA/sPPTA complexes have a strong effect on the melt point, crystallinity, mechanical properties, and thermal stability of PVA. The PVA/sPPTA composites exhibit both high strength and high ductility. When the content of sPPTA is 5 wt %, the PVA/sPPTA composite exhibits the best mechanical properties, with a tensile strength of 169 +/- 13 MPa, which is 54% higher than that of neat PVA (110 +/- 10 MPa). Surprisingly, the reinforcement factor is even superior to that of multiwalled carbon nanotubes, vapor grown carbon fibers, and nanodiamonds previously reported for the reinforcement of PVA nanocomposites. Moreover, the PVA/sPPTA molecular composites have a relatively low modulus but a much larger elongation at break than prefabricated nanocomposites, showing good ductility. The strong and tough PVA/sPPTA molecular composites can be potentially used as high performance membranes or fibers in the future.
机译:通过绿色且易于放大的水铸法制备包含聚对对苯二甲撑对苯二甲酰胺(sPPTA),磺化聚芳酰胺硬棒聚电解质和柔性链聚乙烯醇(PVA)的分子复合材料。系统地研究了sPPTA对分子复合材料的微观结构和性能的影响。傅立叶变换红外光谱证实了sPPTA和PVA之间存在氢键。即使当sPPTA含量高达33 wt%时,广角X射线衍射图也不显示出纯净的sPPTA结晶聚集体的特征,这表明sPPTA与PVA之间的强相互作用阻止了sPPTA的自聚集并导致在复合材料内部形成PVA / sPPTA复合物。透射电子显微镜显示,sPPTA与PVA具有良好的相容性,并且随着sPPTA含量的增加,可以观察到均匀分布在复合物中的纳米级原纤维状超分子组装体。此外,PVA / sPPTA配合物对PVA的熔点,结晶度,机械性能和热稳定性有很大影响。 PVA / sPPTA复合材料同时具有高强度和高延展性。当sPPTA的含量为5 wt%时,PVA / sPPTA复合材料表现出最佳的机械性能,抗张强度为169 +/- 13 MPa,比纯PVA(110 +/- 10 MPa)高54% )。令人惊讶地,增强因子甚至优于先前报道的用于增强PVA纳米复合材料的多壁碳纳米管,气相生长的碳纤维和纳米金刚石。此外,与预制的纳米复合材料相比,PVA / sPPTA分子复合材料具有相对较低的模量,但断裂伸长率大得多,显示出良好的延展性。强韧的PVA / sPPTA分子复合材料将来可能会用作高性能膜或纤维。

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