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电场辅助相转化提高 PA6 与壳聚糖的相容性。

Improved miscibility of PA6 and chitosan by the electric-field assisted phase inversion.

机构信息

Department of Polymer Science and Engineering, School of Material Science and Chemical Engineering, Ningbo University, Ningbo 315211, Zhejiang, PR China; School of Materials and Chemical Engineering, Ningbo University of Technology, Ningbo 315016, Zhejiang, PR China.

School of Materials and Chemical Engineering, Ningbo University of Technology, Ningbo 315016, Zhejiang, PR China.

出版信息

Carbohydr Polym. 2018 Jun 1;189:15-21. doi: 10.1016/j.carbpol.2018.02.020. Epub 2018 Feb 7.

Abstract

A facile and efficient method for the improved miscibility of natural polymer/synthetic polymer blends is reported here based on the electric-field-driven phase inversion. We have employed bioderived chitosan (CS) and Polyamide-6 (PA6) as an example since their blends are known to always result in a large scale phase separation (i.e. CS settles to the bottom of the blends as sediment) during phase inversion procedure. The condensed structure of the polymer blends has been well characterized, notably by the polarized attenuated total reflectance infrared spectroscopy and proton longitudinal relaxation time (T) distribution. The application of an electric field can orient the polar groups which will hinder the crystallization of blends and also increase the interphase interaction between PA6 and CS. The miscibility of the PA6/CS blends has been characterized by scanning electron microscopy and confocal Raman spectroscopy. It is shown that this controllable hydrogen bonding environment, induced by the presence of electric field, indeed greatly hinder the sedimentation of CS without destroying its chemical structure. The improved miscibility of PA6/CS blends can thus significantly increase the toughness and generate a somewhat larger tensile strength.

摘要

本文报道了一种基于电场驱动相转化的提高天然聚合物/合成聚合物共混物混溶性的简便有效方法。我们选择生物衍生壳聚糖 (CS) 和聚酰胺-6 (PA6) 作为示例,因为它们的共混物在相转化过程中总是会导致大规模相分离(即 CS 作为沉淀物沉降到底部)。聚合物共混物的凝聚结构已通过偏光衰减全反射红外光谱和质子纵向弛豫时间 (T) 分布得到很好的表征。施加电场可以使极性基团取向,这将阻碍共混物的结晶,并增加 PA6 和 CS 之间的相间相互作用。扫描电子显微镜和共焦拉曼光谱表征了 PA6/CS 共混物的混溶性。结果表明,电场诱导的这种可控氢键环境确实极大地阻碍了 CS 的沉淀,而不会破坏其化学结构。因此,PA6/CS 共混物的混溶性得到改善,从而显著提高了韧性,并产生了稍大的拉伸强度。

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