An investigation of novel approaches in order to provide crosslinked fully aromatic polyamide chains

摘要

Two different, novel approaches to crosslink fully aromatic, rigid-rod aramid chains were studied. First, the new rigid-rod aramid poly1,4-phenylen-2,5-bis(prop-2-ynyloxy)-terephthalamide with an inherent viscosity of eta(inh) = 2.74 dL/g was synthesized by low temperature polycondensation of p-phenylendiamine and 2,5-bis(prop-2-ynyloxy)-terephthaloylchloride. The pendant alkinyl moieties allowed thermally induced crosslinking at temperatures higher than 200 degrees C, No weight loss was found due to this treatment, but curing gave rise to the formation of stable radicals. However, no fiber spinning experiments were carried out using this material due to the insufficient stability of the polymer chains against degradation when being dissolved in sulfuric acid. Furthermore, fibers of a rigid rod polyamide containing pyrimidine moieties, produced by polycondensation of bis-silylated 2,5-diaminoprimidine and terephthaloyl. dichloride, were spun from nematic solutions. Fibers were crosslinked by complexation with nickel(II)-ions in the swollen state. Both crosslinked and non-crosslinked, otherwise identically processed samples, were characterized by wide-angle X-ray-diffraction (WAXD) measurements and mechanical tests. A post-spin heat treatment was employed to improve the low degrees of orientation 1 and crystallinity that the untreated fibers in general showed. The dominating crystal structures of both fiber samples are similar to "Modification II" of the well characterized fibers from poly(p-phenylene-terephthalamide) (PPTA). The number and size of the morphological; defects in the crosslinked fibers was significantly higher than in the non-crosslinked samples. The influence of the annealing on the mechanical fiber properties and the molecular order in the fibers was investigated. The values of all mechanical parameters were considerably lower in the case of the crosslinked fibers, probably due to the collapse of the entire supramolecular order and fiber morphology. References: 71