Effect of High Molecular Weight PPTA on Liquid Crystalline Phase and Spinning Process of Aramid Fibers.

High molecular weight poly (-phenylene-terephthalamide) (h-PPTA) was blended with the commercial PPTA in concentrated sulfuric acid to improve the spinnability of the polymer solutions and the mechanical properties of the as-spun fibers. h-PPTA in the solution has an influence on the temperature of the formation of liquid crystalline phenomenon. The temperature range with the existence of the liquid crystalline phase increases upon the contents of h-PPTA in the solution, and the extended temperature window is helpful for the preparation of PPTA fibers by the dry-jet wet-spinning technology.

Layer-by-Layer Self-Assembly Strategy for Surface Modification of Aramid Fibers to Enhance Interfacial Adhesion to Epoxy Resin.

In this work, the layer-by-layer self-assembly technology was used to modify aramid fibers (AFs) to improve the interfacial adhesion to epoxy matrix. By virtue of the facile layer-by-layer self-assembly technique, poly(l-3,4-Dihydroxyphenylalanine) (l-PDOPA) was successfully coated on the surface of AFs, leading to the formation of AFs with controllable layers (nL-AF). Then, a hydroxyl functionalized silane coupling agent (KH550) was grafted on the surface of l-PDOPA coated AFs.

Simple Synthesis of Hydroxyl and Ethylene Functionalized Aromatic Polyamides as Sizing Agents to Improve Adhesion Properties of Aramid Fiber/Vinyl Epoxy Composites.

To improve interfacial adhesion between aramid fibers and vinyl epoxy resins, a series of hydroxyl and ethylene-functional aromatic polyamides ((ClPPTA)-R') with different chain segments were successfully synthesized via a one-pot low-temperature polycondensation. The hydroxyl and ethylene-functional aromatic polyamides were characterized by Fourier transform infrared spectroscopy (FT-IR), solid-state C CP/MAS nuclear magnetic resonance spectroscopy (C CP/MAS NMR), thermal gravimetric analysis (TGA), and wide-angle X-ray diffraction (WXRD). The contact angle of the hydroxyl and ethylene-functional aromatic polyamides films were measured.