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用于最大化全有机纳米复合材料性能的芳纶纳米纤维模板原位SAr聚合

Aramid Nanofiber Templated In Situ SAr Polymerization for Maximizing the Performance of All-Organic Nanocomposites.

作者信息

Park Seul-A, Eom Youngho, Jeon Hyeonyeol, Koo Jun Mo, Kim Taehyung, Jeon Jaemin, Park Moon Jeong, Hwang Sung Yeon, Kim Byeong-Su, Oh Dongyeop X, Park Jeyoung

机构信息

Research Center for Bio-based Chemistry, Korea Research Institute of Chemical Technology (KRICT), Ulsan 44429, Republic of Korea.

Department of Polymer Engineering, Pukyong National University, Busan 48513, Republic of Korea.

出版信息

ACS Macro Lett. 2020 Apr 21;9(4):558-564. doi: 10.1021/acsmacrolett.0c00156. Epub 2020 Mar 26.

Abstract

The performance limits of conventional super engineering plastics with inorganic nanofillers are surpassed by all-organic nanocomposites prepared via in situ SAr polymerization of polysulfone (PSU) in the presence of a highly dispersed aramid nanofiber (ANF) solution. The latter is directly used, bypassing the energy-consuming, nanostructure-damaging workup process. Using only a 0.15 wt % nanofiller, the all-organic nanocomposite shows an ultimate tensile strength 1.6× higher and 3.4× tougher than neat PSU and its blending counterpart due to the mutually interactive filler and maximally homogenized matrix. The exceptional toughness of the ANF/PSU nanocomposite originates from the grafted PSU on the surface of ANF; it drives stress-delocalized deformation, as revealed by stress-absorbable viscoelastic behavior and ductile elongation of materials. This material is a promising candidate for use as a filler-interactive, high-performance nanocomposite.

摘要

通过在高度分散的芳纶纳米纤维(ANF)溶液存在下对聚砜(PSU)进行原位SAr聚合制备的全有机纳米复合材料,超越了具有无机纳米填料的传统超级工程塑料的性能极限。后者可直接使用,绕过了耗能且会破坏纳米结构的后处理过程。仅使用0.15 wt%的纳米填料,这种全有机纳米复合材料的极限拉伸强度比纯PSU及其共混物高出1.6倍,韧性高出3.4倍,这归因于填料与基质之间的相互作用以及最大程度的均匀化。ANF/PSU纳米复合材料的卓越韧性源于ANF表面接枝的PSU;如材料的应力吸收粘弹性行为和韧性伸长所揭示的那样,它促使应力离域变形。这种材料是用作填料相互作用的高性能纳米复合材料的有前途的候选材料。

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